Run ID: SRR5341333
Sample name:
Date: 04-04-2023 10:15:44
Number of reads: 1537788
Percentage reads mapped: 15.64
Strain:
Drug-resistance: HR-TB
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
| katG | 2155107 | p.Ile335Thr | missense_variant | 1.0 | isoniazid |
| katG | 2155163 | p.Ile317Leu | missense_variant | 1.0 | isoniazid |
| katG | 2155218 | c.893delT | frameshift_variant | 1.0 | isoniazid |
| panD | 4043869 | p.Val138Ala | missense_variant | 0.97 | pyrazinamide |
| embB | 4247448 | p.His312Arg | missense_variant | 1.0 | ethambutol |
| embB | 4247588 | p.Leu359Ile | missense_variant | 1.0 | ethambutol |
| embB | 4247708 | p.Asn399Asp | missense_variant | 0.96 | ethambutol |
| embB | 4248488 | p.Ala659Thr | missense_variant | 1.0 | ethambutol |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5353 | c.114T>C | synonymous_variant | 1.0 |
| gyrB | 5359 | c.120C>T | synonymous_variant | 1.0 |
| gyrB | 5363 | c.124_126delTTAinsCTG | synonymous_variant | 1.0 |
| gyrB | 5371 | c.132T>C | synonymous_variant | 1.0 |
| gyrB | 5377 | c.138T>C | synonymous_variant | 1.0 |
| gyrB | 5396 | p.Ala53Ser | missense_variant | 1.0 |
| gyrB | 5419 | c.180T>C | synonymous_variant | 1.0 |
| gyrB | 5776 | c.537T>C | synonymous_variant | 1.0 |
| gyrB | 5782 | c.543A>G | synonymous_variant | 1.0 |
| gyrB | 5788 | c.549G>C | synonymous_variant | 1.0 |
| gyrB | 5791 | c.552A>G | synonymous_variant | 1.0 |
| gyrB | 5803 | c.564A>G | synonymous_variant | 1.0 |
| gyrB | 5806 | c.567C>G | synonymous_variant | 1.0 |
| gyrB | 5809 | c.570C>G | synonymous_variant | 1.0 |
| gyrB | 5824 | c.585A>G | synonymous_variant | 1.0 |
| gyrB | 5827 | c.588G>A | synonymous_variant | 1.0 |
| gyrB | 5849 | c.610C>T | synonymous_variant | 1.0 |
| gyrB | 5854 | c.615C>A | synonymous_variant | 1.0 |
| gyrB | 5863 | c.624G>C | synonymous_variant | 1.0 |
| gyrB | 5873 | c.634A>C | synonymous_variant | 1.0 |
| gyrB | 5880 | p.Thr214Ser | missense_variant | 1.0 |
| gyrB | 5882 | p.Gln215Asn | missense_variant | 1.0 |
| gyrB | 5887 | p.Asp216Glu | missense_variant | 1.0 |
| gyrB | 5902 | c.663A>G | synonymous_variant | 1.0 |
| gyrB | 6086 | p.Thr283Pro | missense_variant | 1.0 |
| gyrB | 6091 | c.852G>C | synonymous_variant | 0.86 |
| gyrB | 6100 | c.861G>C | synonymous_variant | 0.95 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 0.97 |
| gyrB | 6123 | p.Ala295Gly | missense_variant | 0.97 |
| gyrB | 6127 | c.888G>C | synonymous_variant | 0.97 |
| gyrB | 6130 | c.891T>C | synonymous_variant | 0.97 |
| gyrB | 6136 | c.897G>A | synonymous_variant | 0.98 |
| gyrB | 6139 | c.900G>C | synonymous_variant | 0.98 |
| gyrB | 6238 | c.999G>A | synonymous_variant | 0.95 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 0.94 |
| gyrB | 6250 | c.1011A>G | synonymous_variant | 0.95 |
| gyrB | 6256 | c.1017G>A | synonymous_variant | 0.91 |
| gyrB | 6265 | c.1026C>T | synonymous_variant | 0.9 |
| gyrB | 6268 | c.1029C>G | synonymous_variant | 0.93 |
| gyrB | 6280 | c.1041T>C | synonymous_variant | 0.94 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 0.93 |
| gyrB | 6289 | c.1050C>T | synonymous_variant | 0.93 |
| gyrB | 6292 | c.1053G>C | synonymous_variant | 0.94 |
| gyrA | 6304 | c.-998C>G | upstream_gene_variant | 0.96 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.96 |
| gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.98 |
| gyrA | 6361 | c.-941G>A | upstream_gene_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 1.0 |
| gyrA | 6376 | c.-926G>A | upstream_gene_variant | 1.0 |
| gyrA | 6379 | c.-923C>G | upstream_gene_variant | 1.0 |
| gyrA | 6382 | c.-920A>G | upstream_gene_variant | 1.0 |
| gyrA | 6388 | c.-914T>C | upstream_gene_variant | 1.0 |
| gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.95 |
| gyrA | 6415 | c.-887G>C | upstream_gene_variant | 0.86 |
| gyrA | 6418 | c.-884C>G | upstream_gene_variant | 0.8 |
| gyrA | 6427 | c.-875T>C | upstream_gene_variant | 0.75 |
| gyrA | 6469 | c.-833T>G | upstream_gene_variant | 0.88 |
| gyrA | 6475 | c.-827C>G | upstream_gene_variant | 1.0 |
| gyrA | 6484 | c.-818A>G | upstream_gene_variant | 1.0 |
| gyrA | 6490 | c.-812T>G | upstream_gene_variant | 1.0 |
| gyrA | 6499 | c.-803A>G | upstream_gene_variant | 1.0 |
| gyrA | 6502 | c.-800T>C | upstream_gene_variant | 1.0 |
| gyrA | 6508 | c.-794A>G | upstream_gene_variant | 1.0 |
| gyrA | 6523 | c.-779G>C | upstream_gene_variant | 1.0 |
| gyrA | 6526 | c.-776T>C | upstream_gene_variant | 1.0 |
| gyrA | 6535 | c.-767C>G | upstream_gene_variant | 1.0 |
| gyrA | 6565 | c.-737G>C | upstream_gene_variant | 1.0 |
| gyrA | 6577 | c.-725T>C | upstream_gene_variant | 1.0 |
| gyrA | 6580 | c.-722C>G | upstream_gene_variant | 1.0 |
| gyrA | 6598 | c.-704C>G | upstream_gene_variant | 1.0 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 1.0 |
| gyrA | 6613 | c.-689A>G | upstream_gene_variant | 1.0 |
| gyrA | 6616 | c.-686A>G | upstream_gene_variant | 1.0 |
| gyrA | 6622 | c.-680C>T | upstream_gene_variant | 1.0 |
| gyrA | 6634 | c.-668T>C | upstream_gene_variant | 1.0 |
| gyrA | 6637 | c.-665T>G | upstream_gene_variant | 1.0 |
| gyrA | 6640 | c.-662A>G | upstream_gene_variant | 1.0 |
| gyrA | 6649 | c.-653T>C | upstream_gene_variant | 1.0 |
| gyrA | 6655 | c.-647T>C | upstream_gene_variant | 1.0 |
| gyrA | 6670 | c.-632G>C | upstream_gene_variant | 1.0 |
| gyrA | 6673 | c.-629A>C | upstream_gene_variant | 1.0 |
| gyrA | 6676 | c.-626T>G | upstream_gene_variant | 1.0 |
| gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 1.0 |
| gyrA | 6742 | c.-560A>G | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>G | upstream_gene_variant | 1.0 |
| gyrA | 6751 | c.-551G>C | upstream_gene_variant | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6763 | c.-539G>C | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Thr | missense_variant | 1.0 |
| gyrA | 6811 | c.-491C>T | upstream_gene_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>C | upstream_gene_variant | 1.0 |
| gyrA | 6853 | c.-449A>G | upstream_gene_variant | 1.0 |
| gyrA | 6856 | c.-446T>C | upstream_gene_variant | 1.0 |
| gyrA | 6859 | c.-443T>C | upstream_gene_variant | 1.0 |
| gyrA | 6862 | c.-440C>G | upstream_gene_variant | 1.0 |
| gyrA | 6865 | c.-437G>A | upstream_gene_variant | 1.0 |
| gyrA | 6878 | c.-424T>C | upstream_gene_variant | 1.0 |
| gyrA | 6881 | c.-421_-419delTTGinsCTC | upstream_gene_variant | 1.0 |
| gyrA | 6889 | c.-413G>C | upstream_gene_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>G | upstream_gene_variant | 1.0 |
| gyrA | 6949 | c.-353A>G | upstream_gene_variant | 1.0 |
| gyrA | 6952 | c.-350C>G | upstream_gene_variant | 1.0 |
| gyrA | 6967 | c.-335T>C | upstream_gene_variant | 1.0 |
| gyrA | 6973 | c.-329G>C | upstream_gene_variant | 1.0 |
| gyrA | 6982 | c.-320A>C | upstream_gene_variant | 1.0 |
| gyrA | 7007 | c.-295C>T | upstream_gene_variant | 1.0 |
| gyrA | 7010 | c.-292C>T | upstream_gene_variant | 1.0 |
| gyrB | 7023 | p.Leu595Gln | missense_variant | 1.0 |
| gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
| gyrA | 7066 | c.-236G>C | upstream_gene_variant | 1.0 |
| gyrA | 7078 | c.-224A>C | upstream_gene_variant | 1.0 |
| gyrA | 7084 | c.-218A>G | upstream_gene_variant | 1.0 |
| gyrA | 7090 | c.-212C>T | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>G | upstream_gene_variant | 1.0 |
| gyrA | 7099 | c.-203G>A | upstream_gene_variant | 1.0 |
| gyrA | 7108 | c.-194G>A | upstream_gene_variant | 1.0 |
| gyrA | 7114 | c.-188C>A | upstream_gene_variant | 1.0 |
| gyrB | 7124 | p.Ser629Thr | missense_variant | 1.0 |
| gyrA | 7129 | c.-173T>C | upstream_gene_variant | 1.0 |
| gyrA | 7132 | c.-170T>G | upstream_gene_variant | 1.0 |
| gyrA | 7141 | c.-161T>C | upstream_gene_variant | 1.0 |
| gyrA | 7165 | c.-137C>G | upstream_gene_variant | 1.0 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 1.0 |
| gyrA | 7186 | c.-116C>G | upstream_gene_variant | 1.0 |
| gyrA | 7216 | c.-86G>C | upstream_gene_variant | 1.0 |
| gyrA | 7228 | c.-74C>T | upstream_gene_variant | 1.0 |
| gyrA | 7234 | c.-68C>T | upstream_gene_variant | 1.0 |
| gyrA | 7246 | c.-56T>C | upstream_gene_variant | 1.0 |
| gyrA | 7252 | c.-50G>C | upstream_gene_variant | 1.0 |
| gyrA | 7256 | c.-46_-44delCTGinsTTA | upstream_gene_variant | 1.0 |
| gyrA | 7317 | c.16T>C | synonymous_variant | 1.0 |
| gyrA | 7324 | c.23_24insAGG | disruptive_inframe_insertion | 1.0 |
| gyrA | 7334 | c.33G>C | synonymous_variant | 1.0 |
| gyrA | 7335 | p.Leu12Val | missense_variant | 1.0 |
| gyrA | 7347 | p.Glu16Gln | missense_variant | 1.0 |
| gyrA | 7355 | c.54T>C | synonymous_variant | 1.0 |
| gyrA | 7361 | c.60C>T | synonymous_variant | 1.0 |
| gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
| gyrA | 7391 | c.90C>T | synonymous_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 7406 | c.105G>C | synonymous_variant | 1.0 |
| gyrA | 7427 | c.126G>C | synonymous_variant | 1.0 |
| gyrA | 7442 | c.141G>C | synonymous_variant | 1.0 |
| gyrA | 7451 | c.150C>G | synonymous_variant | 1.0 |
| gyrA | 7457 | c.156T>C | synonymous_variant | 1.0 |
| gyrA | 7475 | c.174A>G | synonymous_variant | 1.0 |
| gyrA | 7480 | p.Phe60Tyr | missense_variant | 1.0 |
| gyrA | 7484 | c.183T>C | synonymous_variant | 1.0 |
| gyrA | 7514 | c.213C>G | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>A | synonymous_variant | 1.0 |
| gyrA | 7532 | c.231T>C | synonymous_variant | 1.0 |
| gyrA | 7541 | c.240C>G | synonymous_variant | 1.0 |
| gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
| gyrA | 7562 | c.261C>T | synonymous_variant | 1.0 |
| gyrA | 7571 | c.270G>C | synonymous_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7595 | c.294C>G | synonymous_variant | 0.99 |
| gyrA | 7601 | c.300C>G | synonymous_variant | 0.99 |
| gyrA | 7607 | c.306C>G | synonymous_variant | 0.99 |
| gyrA | 7622 | c.321C>T | synonymous_variant | 0.98 |
| gyrA | 7625 | c.324G>C | synonymous_variant | 0.99 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 0.99 |
| gyrA | 7637 | c.336C>G | synonymous_variant | 0.99 |
| gyrA | 7658 | c.357A>G | synonymous_variant | 1.0 |
| gyrA | 7664 | c.363T>C | synonymous_variant | 1.0 |
| gyrA | 7670 | c.369A>G | synonymous_variant | 1.0 |
| gyrA | 7676 | c.375G>C | synonymous_variant | 1.0 |
| gyrA | 7683 | c.382_384delAGGinsCGC | synonymous_variant | 1.0 |
| gyrA | 7694 | c.393A>G | synonymous_variant | 1.0 |
| gyrA | 7697 | c.396C>A | synonymous_variant | 1.0 |
| gyrA | 7710 | c.409_411delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 7715 | c.414G>C | synonymous_variant | 1.0 |
| gyrA | 7721 | c.420G>A | synonymous_variant | 1.0 |
| gyrA | 7725 | c.424C>T | synonymous_variant | 1.0 |
| gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 1.0 |
| gyrA | 7784 | c.483A>G | synonymous_variant | 1.0 |
| gyrA | 7793 | c.492G>C | synonymous_variant | 1.0 |
| gyrA | 7796 | c.495G>C | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7814 | c.513C>G | synonymous_variant | 1.0 |
| gyrA | 7823 | c.522G>C | synonymous_variant | 0.98 |
| gyrA | 7832 | c.531G>T | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>G | synonymous_variant | 1.0 |
| gyrA | 7853 | c.552C>G | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>G | synonymous_variant | 1.0 |
| gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
| gyrA | 7886 | c.585T>C | synonymous_variant | 1.0 |
| gyrA | 7898 | p.Asp199Glu | missense_variant | 0.83 |
| gyrA | 7901 | c.600G>C | synonymous_variant | 0.8 |
| gyrA | 8069 | c.768T>C | synonymous_variant | 0.83 |
| gyrA | 8078 | c.777A>G | synonymous_variant | 0.92 |
| gyrA | 8090 | c.789C>A | synonymous_variant | 0.97 |
| gyrA | 8096 | c.795T>A | synonymous_variant | 0.97 |
| gyrA | 8099 | c.798T>C | synonymous_variant | 0.98 |
| gyrA | 8111 | c.810G>C | synonymous_variant | 1.0 |
| gyrA | 8121 | c.820T>C | synonymous_variant | 1.0 |
| gyrA | 8129 | c.828T>C | synonymous_variant | 1.0 |
| gyrA | 8135 | c.834C>G | synonymous_variant | 1.0 |
| gyrA | 8156 | c.855T>C | synonymous_variant | 0.99 |
| gyrA | 8168 | c.867A>G | synonymous_variant | 0.98 |
| gyrA | 8177 | c.876A>C | synonymous_variant | 0.98 |
| gyrA | 8189 | c.888G>C | synonymous_variant | 0.97 |
| gyrA | 8198 | c.897T>C | synonymous_variant | 0.97 |
| gyrA | 8207 | c.906T>C | synonymous_variant | 0.96 |
| gyrA | 8219 | c.918T>C | synonymous_variant | 0.93 |
| gyrA | 8225 | c.924T>C | synonymous_variant | 1.0 |
| gyrA | 8234 | c.933T>C | synonymous_variant | 1.0 |
| gyrA | 8237 | c.936A>G | synonymous_variant | 1.0 |
| gyrA | 8247 | p.Ile316Val | missense_variant | 1.0 |
| gyrA | 8264 | c.963T>C | synonymous_variant | 1.0 |
| gyrA | 8267 | c.966G>C | synonymous_variant | 1.0 |
| gyrA | 8270 | c.969G>C | synonymous_variant | 1.0 |
| gyrA | 8276 | c.975G>A | synonymous_variant | 1.0 |
| gyrA | 8283 | p.Ile328Leu | missense_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8294 | c.993T>C | synonymous_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8330 | c.1029C>G | synonymous_variant | 1.0 |
| gyrA | 8337 | c.1036_1038delCTAinsTTG | synonymous_variant | 1.0 |
| gyrA | 8342 | c.1041G>C | synonymous_variant | 1.0 |
| gyrA | 8366 | c.1065G>T | synonymous_variant | 0.97 |
| gyrA | 8367 | c.1066C>T | synonymous_variant | 0.97 |
| gyrA | 8372 | c.1071G>C | synonymous_variant | 0.97 |
| gyrA | 8375 | c.1074G>C | synonymous_variant | 0.97 |
| gyrA | 8382 | p.Leu361Met | missense_variant | 0.97 |
| gyrA | 8391 | p.Tyr364His | missense_variant | 0.96 |
| gyrA | 8399 | c.1098T>C | synonymous_variant | 0.95 |
| gyrA | 8400 | p.Asp367Asn | missense_variant | 0.95 |
| gyrA | 8417 | c.1116C>G | synonymous_variant | 0.8 |
| gyrA | 8442 | c.1141C>T | synonymous_variant | 1.0 |
| gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
| gyrA | 8459 | c.1158G>A | synonymous_variant | 1.0 |
| gyrA | 8462 | c.1161A>C | synonymous_variant | 1.0 |
| gyrA | 8465 | c.1164C>G | synonymous_variant | 1.0 |
| gyrA | 8471 | c.1170T>C | synonymous_variant | 1.0 |
| gyrA | 8472 | c.1171C>T | synonymous_variant | 1.0 |
| gyrA | 8480 | c.1179C>A | synonymous_variant | 1.0 |
| gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
| gyrA | 8504 | c.1203G>C | synonymous_variant | 1.0 |
| gyrA | 8516 | c.1215T>C | synonymous_variant | 1.0 |
| gyrA | 8519 | c.1218A>C | synonymous_variant | 1.0 |
| gyrA | 8520 | c.1219C>T | synonymous_variant | 1.0 |
| gyrA | 8528 | c.1227G>C | synonymous_variant | 1.0 |
| gyrA | 8531 | c.1230G>C | synonymous_variant | 1.0 |
| gyrA | 8543 | c.1242C>G | synonymous_variant | 1.0 |
| gyrA | 8546 | c.1245T>C | synonymous_variant | 1.0 |
| gyrA | 8553 | c.1252C>A | synonymous_variant | 0.99 |
| gyrA | 8561 | c.1260A>C | synonymous_variant | 0.99 |
| gyrA | 8588 | c.1287G>A | synonymous_variant | 0.99 |
| gyrA | 8603 | c.1302A>G | synonymous_variant | 0.99 |
| gyrA | 8619 | c.1318T>C | synonymous_variant | 0.99 |
| gyrA | 8624 | c.1323G>C | synonymous_variant | 0.99 |
| gyrA | 8636 | c.1335A>C | synonymous_variant | 1.0 |
| gyrA | 8642 | c.1341A>G | synonymous_variant | 1.0 |
| gyrA | 8672 | c.1371A>G | synonymous_variant | 1.0 |
| gyrA | 8678 | c.1377G>A | synonymous_variant | 1.0 |
| gyrA | 8693 | c.1392T>C | synonymous_variant | 1.0 |
| gyrA | 8696 | c.1395G>C | synonymous_variant | 1.0 |
| gyrA | 8699 | c.1398A>G | synonymous_variant | 1.0 |
| gyrA | 8708 | c.1407G>C | synonymous_variant | 1.0 |
| gyrA | 8711 | c.1410A>C | synonymous_variant | 1.0 |
| gyrA | 8714 | c.1413A>G | synonymous_variant | 1.0 |
| gyrA | 8729 | c.1428T>C | synonymous_variant | 1.0 |
| gyrA | 8731 | p.Gly477Ala | missense_variant | 1.0 |
| gyrA | 8740 | p.Arg480His | missense_variant | 1.0 |
| gyrA | 8747 | c.1446A>G | synonymous_variant | 1.0 |
| gyrA | 8750 | c.1449C>G | synonymous_variant | 1.0 |
| gyrA | 8751 | p.Ala484Ser | missense_variant | 1.0 |
| gyrA | 8762 | c.1461G>C | synonymous_variant | 1.0 |
| gyrA | 8767 | p.Arg489Lys | missense_variant | 1.0 |
| gyrA | 8780 | p.Asp493Glu | missense_variant | 1.0 |
| gyrA | 8786 | c.1485T>C | synonymous_variant | 1.0 |
| gyrA | 8801 | c.1500G>C | synonymous_variant | 1.0 |
| gyrA | 8807 | c.1506C>T | synonymous_variant | 1.0 |
| gyrA | 8810 | c.1509A>G | synonymous_variant | 1.0 |
| gyrA | 8816 | c.1515C>G | synonymous_variant | 1.0 |
| gyrA | 8818 | p.Ser506Asn | missense_variant | 1.0 |
| gyrA | 8828 | c.1527T>C | synonymous_variant | 1.0 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8867 | c.1566A>G | synonymous_variant | 1.0 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>C | synonymous_variant | 1.0 |
| gyrA | 8891 | c.1590G>A | synonymous_variant | 1.0 |
| gyrA | 8897 | c.1596T>C | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8933 | c.1632G>C | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 8966 | c.1665C>G | synonymous_variant | 1.0 |
| gyrA | 8967 | p.Ala556Arg | missense_variant | 1.0 |
| gyrA | 8987 | c.1686C>A | synonymous_variant | 1.0 |
| gyrA | 8990 | c.1689C>G | synonymous_variant | 1.0 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
| gyrA | 9017 | c.1716C>G | synonymous_variant | 1.0 |
| gyrA | 9023 | c.1722A>G | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>C | synonymous_variant | 1.0 |
| gyrA | 9032 | c.1731T>C | synonymous_variant | 1.0 |
| gyrA | 9050 | p.Asp583Glu | missense_variant | 1.0 |
| gyrA | 9051 | c.1750T>C | synonymous_variant | 1.0 |
| gyrA | 9056 | c.1755C>G | synonymous_variant | 1.0 |
| gyrA | 9062 | c.1761C>G | synonymous_variant | 1.0 |
| gyrA | 9065 | c.1764C>G | synonymous_variant | 1.0 |
| gyrA | 9068 | c.1767G>C | synonymous_variant | 1.0 |
| gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
| gyrA | 9080 | c.1779G>T | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 1.0 |
| gyrA | 9104 | c.1803C>G | synonymous_variant | 1.0 |
| gyrA | 9119 | c.1818A>G | synonymous_variant | 1.0 |
| gyrA | 9122 | c.1821C>G | synonymous_variant | 1.0 |
| gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
| gyrA | 9152 | c.1851C>T | synonymous_variant | 1.0 |
| gyrA | 9153 | p.Thr618Glu | missense_variant | 1.0 |
| gyrA | 9158 | c.1857C>T | synonymous_variant | 1.0 |
| gyrA | 9161 | c.1860C>G | synonymous_variant | 1.0 |
| gyrA | 9182 | c.1881T>C | synonymous_variant | 1.0 |
| gyrA | 9191 | c.1890G>C | synonymous_variant | 1.0 |
| gyrA | 9200 | c.1899A>G | synonymous_variant | 1.0 |
| gyrA | 9204 | p.Ser635Thr | missense_variant | 1.0 |
| gyrA | 9224 | c.1923C>T | synonymous_variant | 1.0 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 1.0 |
| gyrA | 9233 | c.1932C>G | synonymous_variant | 1.0 |
| gyrA | 9239 | c.1938C>T | synonymous_variant | 1.0 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 1.0 |
| gyrA | 9278 | c.1977G>T | synonymous_variant | 1.0 |
| gyrA | 9284 | c.1983T>C | synonymous_variant | 1.0 |
| gyrA | 9291 | c.1990C>T | synonymous_variant | 1.0 |
| gyrA | 9296 | c.1995T>C | synonymous_variant | 1.0 |
| gyrA | 9299 | c.1998G>C | synonymous_variant | 1.0 |
| gyrA | 9300 | p.Ala667Ser | missense_variant | 1.0 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9308 | p.Asp669Glu | missense_variant | 1.0 |
| gyrA | 9323 | c.2022C>G | synonymous_variant | 1.0 |
| gyrA | 9335 | c.2034G>C | synonymous_variant | 1.0 |
| gyrA | 9365 | c.2064G>A | synonymous_variant | 1.0 |
| gyrA | 9374 | c.2073G>C | synonymous_variant | 1.0 |
| gyrA | 9377 | c.2076A>G | synonymous_variant | 1.0 |
| gyrA | 9383 | c.2082T>G | synonymous_variant | 1.0 |
| gyrA | 9386 | c.2085T>C | synonymous_variant | 1.0 |
| gyrA | 9389 | c.2088C>T | synonymous_variant | 1.0 |
| gyrA | 9395 | c.2094G>C | synonymous_variant | 1.0 |
| gyrA | 9398 | c.2097T>C | synonymous_variant | 1.0 |
| gyrA | 9413 | c.2112G>C | synonymous_variant | 1.0 |
| gyrA | 9419 | c.2118T>C | synonymous_variant | 1.0 |
| fgd1 | 490782 | c.-1G>C | upstream_gene_variant | 1.0 |
| fgd1 | 490797 | c.15G>A | synonymous_variant | 1.0 |
| fgd1 | 490800 | c.18A>C | synonymous_variant | 1.0 |
| fgd1 | 490803 | c.21T>A | synonymous_variant | 1.0 |
| fgd1 | 490812 | c.30A>G | synonymous_variant | 1.0 |
| fgd1 | 490815 | c.33G>C | synonymous_variant | 1.0 |
| fgd1 | 490827 | c.45C>T | synonymous_variant | 1.0 |
| fgd1 | 490848 | c.66A>G | synonymous_variant | 1.0 |
| fgd1 | 490851 | c.69A>T | synonymous_variant | 1.0 |
| fgd1 | 490854 | c.72C>G | synonymous_variant | 1.0 |
| fgd1 | 490868 | p.Ala29Gly | missense_variant | 1.0 |
| fgd1 | 490887 | c.105G>A | synonymous_variant | 1.0 |
| fgd1 | 490890 | c.108C>G | synonymous_variant | 1.0 |
| fgd1 | 490896 | c.114C>T | synonymous_variant | 1.0 |
| fgd1 | 490905 | c.123T>C | synonymous_variant | 1.0 |
| fgd1 | 490911 | c.129T>G | synonymous_variant | 1.0 |
| fgd1 | 490917 | c.135C>G | synonymous_variant | 1.0 |
| fgd1 | 490921 | p.Gln47Glu | missense_variant | 1.0 |
| fgd1 | 490929 | c.147C>G | synonymous_variant | 1.0 |
| fgd1 | 490932 | c.150T>C | synonymous_variant | 1.0 |
| fgd1 | 490935 | c.153C>G | synonymous_variant | 1.0 |
| fgd1 | 490948 | p.Ser56Ala | missense_variant | 1.0 |
| fgd1 | 490962 | c.180T>G | synonymous_variant | 1.0 |
| fgd1 | 490988 | p.Leu69Pro | missense_variant | 1.0 |
| fgd1 | 490998 | c.216T>C | synonymous_variant | 1.0 |
| fgd1 | 491001 | c.219G>C | synonymous_variant | 1.0 |
| fgd1 | 491007 | c.225G>C | synonymous_variant | 1.0 |
| fgd1 | 491013 | c.231C>G | synonymous_variant | 1.0 |
| fgd1 | 491043 | c.261T>G | synonymous_variant | 1.0 |
| fgd1 | 491049 | c.267T>C | synonymous_variant | 1.0 |
| fgd1 | 491063 | p.Gly94Ala | missense_variant | 1.0 |
| fgd1 | 491067 | c.285C>T | synonymous_variant | 1.0 |
| fgd1 | 491106 | c.324T>C | synonymous_variant | 1.0 |
| fgd1 | 491121 | c.339A>G | synonymous_variant | 1.0 |
| fgd1 | 491130 | c.348C>G | synonymous_variant | 1.0 |
| fgd1 | 491144 | p.Ala121Asp | missense_variant | 1.0 |
| fgd1 | 491151 | c.369G>A | synonymous_variant | 1.0 |
| fgd1 | 491181 | c.399T>C | synonymous_variant | 1.0 |
| fgd1 | 491184 | c.402A>G | synonymous_variant | 1.0 |
| fgd1 | 491191 | p.Gly137Arg | missense_variant | 1.0 |
| fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 1.0 |
| fgd1 | 491202 | c.420G>C | synonymous_variant | 0.97 |
| fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.97 |
| fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.98 |
| fgd1 | 491217 | c.435T>C | synonymous_variant | 0.98 |
| fgd1 | 491232 | c.450T>C | synonymous_variant | 0.97 |
| fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.95 |
| fgd1 | 491244 | c.462T>C | synonymous_variant | 0.95 |
| fgd1 | 491259 | c.477T>C | synonymous_variant | 0.95 |
| fgd1 | 491283 | p.Asp167Glu | missense_variant | 0.92 |
| fgd1 | 491286 | c.504G>C | synonymous_variant | 0.88 |
| fgd1 | 491289 | c.507C>G | synonymous_variant | 1.0 |
| fgd1 | 491292 | c.510G>C | synonymous_variant | 1.0 |
| fgd1 | 491295 | c.513C>G | synonymous_variant | 1.0 |
| fgd1 | 491296 | p.Val172Ile | missense_variant | 1.0 |
| fgd1 | 491302 | p.Ile174Val | missense_variant | 1.0 |
| fgd1 | 491307 | c.525C>G | synonymous_variant | 1.0 |
| fgd1 | 491313 | c.531C>T | synonymous_variant | 1.0 |
| fgd1 | 491319 | c.537G>C | synonymous_variant | 1.0 |
| fgd1 | 491325 | c.543G>C | synonymous_variant | 1.0 |
| fgd1 | 491337 | c.555C>G | synonymous_variant | 1.0 |
| fgd1 | 491340 | c.558C>G | synonymous_variant | 1.0 |
| fgd1 | 491349 | c.567T>C | synonymous_variant | 1.0 |
| fgd1 | 491364 | c.582T>C | synonymous_variant | 1.0 |
| fgd1 | 491367 | c.585G>C | synonymous_variant | 1.0 |
| fgd1 | 491393 | p.Thr204Lys | missense_variant | 1.0 |
| fgd1 | 491397 | p.Glu205Asp | missense_variant | 1.0 |
| fgd1 | 491514 | p.Asn244Lys | missense_variant | 1.0 |
| fgd1 | 491523 | c.741G>A | synonymous_variant | 0.92 |
| fgd1 | 491526 | c.744T>C | synonymous_variant | 0.93 |
| fgd1 | 491542 | c.760T>C | synonymous_variant | 0.97 |
| fgd1 | 491547 | c.765A>C | synonymous_variant | 0.97 |
| fgd1 | 491550 | c.768T>C | synonymous_variant | 0.97 |
| fgd1 | 491553 | c.771G>A | synonymous_variant | 0.97 |
| fgd1 | 491607 | c.825G>C | synonymous_variant | 1.0 |
| fgd1 | 491610 | c.828A>G | synonymous_variant | 1.0 |
| fgd1 | 491616 | c.834A>G | synonymous_variant | 1.0 |
| fgd1 | 491620 | p.Ile280Val | missense_variant | 1.0 |
| fgd1 | 491643 | c.861G>A | synonymous_variant | 1.0 |
| fgd1 | 491646 | c.864G>C | synonymous_variant | 1.0 |
| fgd1 | 491649 | c.867C>T | synonymous_variant | 1.0 |
| fgd1 | 491658 | c.876A>G | synonymous_variant | 1.0 |
| fgd1 | 491661 | c.879C>G | synonymous_variant | 1.0 |
| fgd1 | 491673 | c.891A>C | synonymous_variant | 1.0 |
| fgd1 | 491676 | c.894T>C | synonymous_variant | 1.0 |
| fgd1 | 491679 | c.897A>G | synonymous_variant | 1.0 |
| fgd1 | 491687 | p.Thr302Lys | missense_variant | 1.0 |
| fgd1 | 491697 | c.915G>C | synonymous_variant | 1.0 |
| mshA | 575154 | c.-194_-192delGTGinsCTC | upstream_gene_variant | 1.0 |
| mshA | 575503 | c.156G>C | synonymous_variant | 1.0 |
| mshA | 575512 | c.165A>C | synonymous_variant | 1.0 |
| mshA | 575521 | c.174A>C | synonymous_variant | 1.0 |
| mshA | 575527 | c.180G>C | synonymous_variant | 1.0 |
| mshA | 575536 | c.189T>C | synonymous_variant | 1.0 |
| mshA | 575542 | c.195C>G | synonymous_variant | 1.0 |
| mshA | 575561 | p.Met72Val | missense_variant | 1.0 |
| mshA | 575569 | c.222A>G | synonymous_variant | 1.0 |
| mshA | 575571 | p.Ser75Thr | missense_variant | 1.0 |
| mshA | 575576 | c.229C>T | synonymous_variant | 1.0 |
| mshA | 575581 | c.234C>T | synonymous_variant | 1.0 |
| mshA | 575587 | c.240C>G | synonymous_variant | 1.0 |
| mshA | 575590 | c.243T>C | synonymous_variant | 1.0 |
| mshA | 575623 | c.276C>G | synonymous_variant | 1.0 |
| mshA | 575629 | c.282A>G | synonymous_variant | 0.93 |
| mshA | 575632 | c.285G>C | synonymous_variant | 0.92 |
| mshA | 575635 | c.288A>C | synonymous_variant | 0.92 |
| mshA | 575638 | c.291T>C | synonymous_variant | 0.92 |
| mshA | 575641 | c.294A>G | synonymous_variant | 0.92 |
| mshA | 575647 | c.300G>C | synonymous_variant | 0.93 |
| mshA | 575649 | p.Val101Ala | missense_variant | 0.93 |
| mshA | 575659 | c.312A>G | synonymous_variant | 0.96 |
| mshA | 575662 | c.315C>G | synonymous_variant | 0.97 |
| mshA | 575674 | c.327G>C | synonymous_variant | 0.98 |
| mshA | 575695 | c.348C>G | synonymous_variant | 0.98 |
| mshA | 575701 | c.354G>A | synonymous_variant | 0.98 |
| mshA | 575704 | c.357T>G | synonymous_variant | 1.0 |
| mshA | 575705 | c.358T>C | synonymous_variant | 1.0 |
| mshA | 575713 | c.366G>A | synonymous_variant | 1.0 |
| mshA | 575719 | c.372C>T | synonymous_variant | 0.98 |
| mshA | 575734 | c.387T>G | synonymous_variant | 0.98 |
| mshA | 575737 | c.390T>C | synonymous_variant | 0.95 |
| mshA | 575746 | c.399C>G | synonymous_variant | 0.97 |
| mshA | 575752 | c.405G>C | synonymous_variant | 0.95 |
| mshA | 575755 | c.408G>A | synonymous_variant | 0.95 |
| mshA | 575756 | c.409C>T | synonymous_variant | 0.95 |
| mshA | 575770 | c.423G>A | synonymous_variant | 0.96 |
| mshA | 575771 | p.Val142Ser | missense_variant | 0.96 |
| mshA | 575779 | c.432A>G | synonymous_variant | 0.97 |
| mshA | 575782 | c.435G>C | synonymous_variant | 0.97 |
| mshA | 575812 | c.465C>T | synonymous_variant | 1.0 |
| mshA | 575821 | c.474G>C | synonymous_variant | 0.98 |
| mshA | 575824 | c.477T>G | synonymous_variant | 1.0 |
| mshA | 575830 | c.483C>G | synonymous_variant | 1.0 |
| mshA | 575833 | c.486C>G | synonymous_variant | 1.0 |
| mshA | 575845 | c.498C>T | synonymous_variant | 1.0 |
| mshA | 575864 | c.517T>C | synonymous_variant | 0.98 |
| mshA | 575884 | c.537G>C | synonymous_variant | 1.0 |
| mshA | 575887 | c.540G>C | synonymous_variant | 1.0 |
| mshA | 575893 | c.546C>G | synonymous_variant | 1.0 |
| mshA | 575896 | c.549G>C | synonymous_variant | 1.0 |
| mshA | 575908 | c.561A>G | synonymous_variant | 1.0 |
| mshA | 575917 | p.Asp190Glu | missense_variant | 1.0 |
| mshA | 575920 | c.573C>G | synonymous_variant | 1.0 |
| mshA | 575924 | p.Gly193Ser | missense_variant | 1.0 |
| mshA | 575944 | c.597T>C | synonymous_variant | 0.98 |
| mshA | 575965 | c.618C>G | synonymous_variant | 0.98 |
| mshA | 575977 | c.630G>C | synonymous_variant | 0.98 |
| mshA | 575980 | c.633T>C | synonymous_variant | 0.98 |
| mshA | 575984 | c.637T>C | synonymous_variant | 0.98 |
| mshA | 576004 | c.657T>C | synonymous_variant | 0.96 |
| mshA | 576007 | c.660A>G | synonymous_variant | 1.0 |
| mshA | 576016 | c.669A>G | synonymous_variant | 1.0 |
| mshA | 576017 | p.Val224Leu | missense_variant | 1.0 |
| mshA | 576229 | c.882C>G | synonymous_variant | 1.0 |
| mshA | 576233 | p.Ile296Val | missense_variant | 1.0 |
| mshA | 576241 | c.894C>G | synonymous_variant | 1.0 |
| mshA | 576262 | c.915T>C | synonymous_variant | 1.0 |
| mshA | 576271 | c.924A>C | synonymous_variant | 1.0 |
| mshA | 576281 | c.934C>T | synonymous_variant | 1.0 |
| mshA | 576285 | p.Val313Ala | missense_variant | 1.0 |
| mshA | 576289 | c.942G>C | synonymous_variant | 1.0 |
| mshA | 576292 | c.945C>G | synonymous_variant | 1.0 |
| mshA | 576301 | c.954A>G | synonymous_variant | 1.0 |
| mshA | 576311 | p.Ser322Thr | missense_variant | 1.0 |
| ccsA | 619697 | c.-194_-192delAGGinsCGC | upstream_gene_variant | 1.0 |
| ccsA | 619705 | c.-186G>C | upstream_gene_variant | 1.0 |
| ccsA | 619735 | c.-156G>C | upstream_gene_variant | 1.0 |
| ccsA | 619744 | c.-147A>G | upstream_gene_variant | 1.0 |
| ccsA | 619762 | c.-129C>G | upstream_gene_variant | 1.0 |
| ccsA | 619766 | c.-125A>G | upstream_gene_variant | 1.0 |
| ccsA | 619794 | c.-97C>A | upstream_gene_variant | 0.97 |
| ccsA | 619807 | c.-84G>A | upstream_gene_variant | 0.96 |
| ccsA | 619808 | c.-83C>T | upstream_gene_variant | 0.96 |
| ccsA | 619815 | c.-76G>A | upstream_gene_variant | 0.91 |
| ccsA | 619891 | c.1T>A | initiator_codon_variant | 1.0 |
| ccsA | 619916 | p.Gly9Glu | missense_variant | 1.0 |
| ccsA | 619923 | c.33C>G | synonymous_variant | 1.0 |
| ccsA | 619947 | c.57C>G | synonymous_variant | 0.98 |
| ccsA | 619956 | c.66G>C | synonymous_variant | 0.98 |
| ccsA | 619959 | c.69G>C | synonymous_variant | 0.98 |
| ccsA | 619968 | c.78G>C | synonymous_variant | 0.95 |
| ccsA | 619969 | p.Val27Ile | missense_variant | 0.95 |
| ccsA | 619989 | c.99G>C | synonymous_variant | 0.88 |
| ccsA | 619996 | p.Phe36Leu | missense_variant | 0.5 |
| ccsA | 620175 | c.285C>G | synonymous_variant | 1.0 |
| ccsA | 620187 | c.297C>G | synonymous_variant | 1.0 |
| ccsA | 620196 | c.306C>G | synonymous_variant | 1.0 |
| ccsA | 620197 | p.Gln103Val | missense_variant | 1.0 |
| ccsA | 620226 | c.336G>A | synonymous_variant | 1.0 |
| ccsA | 620245 | c.355T>C | synonymous_variant | 1.0 |
| ccsA | 620249 | p.Ser120Cys | missense_variant | 1.0 |
| ccsA | 620254 | c.364_366delCTCinsTTG | synonymous_variant | 1.0 |
| ccsA | 620265 | c.375C>G | synonymous_variant | 1.0 |
| ccsA | 620268 | c.378G>C | synonymous_variant | 1.0 |
| ccsA | 620283 | c.393T>C | synonymous_variant | 1.0 |
| ccsA | 620284 | p.Ala132Pro | missense_variant | 1.0 |
| ccsA | 620288 | p.Arg133Gln | missense_variant | 1.0 |
| ccsA | 620295 | c.405G>T | synonymous_variant | 1.0 |
| ccsA | 620298 | c.408G>C | synonymous_variant | 1.0 |
| ccsA | 620310 | c.420C>T | synonymous_variant | 1.0 |
| ccsA | 620317 | p.Val143Leu | missense_variant | 1.0 |
| ccsA | 620340 | c.450C>G | synonymous_variant | 1.0 |
| ccsA | 620346 | c.456C>G | synonymous_variant | 1.0 |
| ccsA | 620362 | p.Ala158Thr | missense_variant | 1.0 |
| ccsA | 620367 | c.477T>C | synonymous_variant | 1.0 |
| ccsA | 620373 | c.483C>G | synonymous_variant | 0.97 |
| ccsA | 620376 | c.486G>C | synonymous_variant | 0.96 |
| ccsA | 620385 | c.495G>C | synonymous_variant | 1.0 |
| ccsA | 620388 | c.498A>G | synonymous_variant | 1.0 |
| ccsA | 620389 | c.499C>T | synonymous_variant | 1.0 |
| ccsA | 620412 | c.522T>C | synonymous_variant | 1.0 |
| ccsA | 620415 | c.525T>C | synonymous_variant | 1.0 |
| ccsA | 620424 | c.534G>C | synonymous_variant | 1.0 |
| ccsA | 620433 | c.543C>G | synonymous_variant | 1.0 |
| ccsA | 620436 | c.546T>A | synonymous_variant | 1.0 |
| ccsA | 620439 | c.549T>C | synonymous_variant | 1.0 |
| ccsA | 620442 | c.552G>C | synonymous_variant | 1.0 |
| ccsA | 620445 | c.555A>G | synonymous_variant | 1.0 |
| ccsA | 620460 | c.570T>G | synonymous_variant | 1.0 |
| ccsA | 620461 | p.Val191Ile | missense_variant | 1.0 |
| ccsA | 620481 | c.591T>G | synonymous_variant | 1.0 |
| ccsA | 620482 | p.Val198Leu | missense_variant | 1.0 |
| ccsA | 620490 | c.600A>C | synonymous_variant | 1.0 |
| ccsA | 620583 | c.693G>C | synonymous_variant | 1.0 |
| ccsA | 620586 | c.696C>G | synonymous_variant | 1.0 |
| ccsA | 620598 | c.708C>G | synonymous_variant | 1.0 |
| ccsA | 620601 | c.711C>T | synonymous_variant | 1.0 |
| ccsA | 620604 | c.714C>G | synonymous_variant | 1.0 |
| ccsA | 620607 | c.717T>C | synonymous_variant | 1.0 |
| ccsA | 620613 | c.723C>G | synonymous_variant | 1.0 |
| ccsA | 620622 | c.732G>C | synonymous_variant | 1.0 |
| ccsA | 620625 | c.735A>C | synonymous_variant | 1.0 |
| ccsA | 620631 | c.741T>G | synonymous_variant | 1.0 |
| ccsA | 620646 | c.756G>A | synonymous_variant | 1.0 |
| ccsA | 620649 | c.759A>G | synonymous_variant | 1.0 |
| ccsA | 620659 | c.769_771delCGCinsAGG | synonymous_variant | 1.0 |
| ccsA | 620664 | c.774C>T | synonymous_variant | 1.0 |
| ccsA | 620682 | c.792G>A | synonymous_variant | 1.0 |
| ccsA | 620688 | c.798G>C | synonymous_variant | 1.0 |
| ccsA | 620710 | p.Val274Ile | missense_variant | 1.0 |
| ccsA | 620718 | c.828G>C | synonymous_variant | 1.0 |
| ccsA | 620721 | c.831G>C | synonymous_variant | 1.0 |
| ccsA | 620733 | c.843G>C | synonymous_variant | 1.0 |
| ccsA | 620734 | c.844C>A | synonymous_variant | 1.0 |
| ccsA | 620739 | c.849A>G | synonymous_variant | 1.0 |
| ccsA | 620742 | c.852G>C | synonymous_variant | 1.0 |
| ccsA | 620745 | c.855G>C | synonymous_variant | 1.0 |
| ccsA | 620748 | c.858T>A | synonymous_variant | 1.0 |
| ccsA | 620763 | c.873G>A | synonymous_variant | 1.0 |
| ccsA | 620769 | c.879C>G | synonymous_variant | 1.0 |
| ccsA | 620778 | c.888T>C | synonymous_variant | 1.0 |
| ccsA | 620784 | c.894C>G | synonymous_variant | 1.0 |
| ccsA | 620790 | c.900C>T | synonymous_variant | 1.0 |
| ccsA | 620796 | c.906C>G | synonymous_variant | 1.0 |
| ccsA | 620809 | c.919C>T | synonymous_variant | 1.0 |
| ccsA | 620823 | c.933C>T | synonymous_variant | 1.0 |
| ccsA | 620832 | c.942C>T | synonymous_variant | 1.0 |
| ccsA | 620844 | c.954C>T | synonymous_variant | 1.0 |
| rpoB | 759629 | c.-178T>C | upstream_gene_variant | 1.0 |
| rpoB | 759644 | c.-163T>A | upstream_gene_variant | 1.0 |
| rpoB | 759647 | c.-160T>C | upstream_gene_variant | 1.0 |
| rpoB | 759896 | c.90A>C | synonymous_variant | 0.67 |
| rpoB | 759902 | c.96G>A | synonymous_variant | 0.67 |
| rpoB | 759905 | c.99C>T | synonymous_variant | 0.67 |
| rpoB | 759914 | c.108T>C | synonymous_variant | 0.8 |
| rpoB | 759920 | c.114G>T | synonymous_variant | 0.8 |
| rpoB | 759926 | c.120A>G | synonymous_variant | 0.8 |
| rpoB | 759929 | c.123A>C | synonymous_variant | 0.8 |
| rpoB | 759932 | c.126T>C | synonymous_variant | 0.8 |
| rpoB | 759944 | c.138A>C | synonymous_variant | 0.9 |
| rpoB | 759947 | c.141C>G | synonymous_variant | 0.9 |
| rpoB | 759956 | c.150C>G | synonymous_variant | 1.0 |
| rpoB | 759961 | p.Thr52Ile | missense_variant | 1.0 |
| rpoB | 759965 | c.159T>C | synonymous_variant | 1.0 |
| rpoB | 759968 | c.162G>C | synonymous_variant | 1.0 |
| rpoB | 759978 | c.172C>T | synonymous_variant | 1.0 |
| rpoB | 759986 | c.180T>C | synonymous_variant | 1.0 |
| rpoB | 759987 | p.Ser61Ala | missense_variant | 1.0 |
| rpoB | 759995 | c.189C>G | synonymous_variant | 1.0 |
| rpoB | 760030 | p.Asn75Thr | missense_variant | 0.75 |
| rpoB | 760034 | c.228A>G | synonymous_variant | 0.88 |
| rpoB | 760040 | c.234T>C | synonymous_variant | 0.92 |
| rpoB | 760046 | c.240G>C | synonymous_variant | 0.95 |
| rpoB | 760060 | p.Tyr85Leu | missense_variant | 0.97 |
| rpoB | 760067 | c.261G>C | synonymous_variant | 0.97 |
| rpoB | 760070 | c.264T>G | synonymous_variant | 0.98 |
| rpoB | 760091 | c.285G>C | synonymous_variant | 1.0 |
| rpoB | 760101 | c.295T>C | synonymous_variant | 0.99 |
| rpoB | 760112 | c.306T>C | synonymous_variant | 1.0 |
| rpoB | 760118 | c.312T>G | synonymous_variant | 1.0 |
| rpoB | 760121 | c.315T>C | synonymous_variant | 1.0 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760139 | c.333A>G | synonymous_variant | 1.0 |
| rpoB | 760142 | c.336C>G | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
| rpoB | 760223 | c.417T>C | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
| rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
| rpoB | 760331 | c.525G>C | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534G>T | synonymous_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760370 | c.564C>G | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760380 | p.Thr192Leu | missense_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_variant | 1.0 |
| rpoB | 760412 | c.606C>G | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243Thr | missense_variant | 1.0 |
| rpoB | 760541 | c.735G>C | synonymous_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760634 | c.828T>C | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
| rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760718 | c.912C>T | synonymous_variant | 1.0 |
| rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760751 | c.945G>C | synonymous_variant | 1.0 |
| rpoB | 760757 | c.951T>C | synonymous_variant | 1.0 |
| rpoB | 760759 | p.Val318Ala | missense_variant | 1.0 |
| rpoB | 760769 | c.963C>G | synonymous_variant | 1.0 |
| rpoB | 760775 | c.969G>C | synonymous_variant | 1.0 |
| rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 1.0 |
| rpoB | 760793 | c.987A>G | synonymous_variant | 1.0 |
| rpoB | 760856 | c.1050C>T | synonymous_variant | 1.0 |
| rpoB | 760859 | c.1053T>C | synonymous_variant | 1.0 |
| rpoB | 760862 | c.1056G>C | synonymous_variant | 1.0 |
| rpoB | 760869 | p.Val355Ile | missense_variant | 1.0 |
| rpoB | 760886 | c.1080A>G | synonymous_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760931 | c.1125C>G | synonymous_variant | 1.0 |
| rpoB | 760934 | c.1128C>T | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
| rpoB | 760985 | c.1179G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761006 | c.1200C>G | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761021 | c.1215G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761129 | c.1323G>C | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
| rpoB | 761153 | c.1347G>C | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>C | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761207 | c.1401C>T | synonymous_variant | 1.0 |
| rpoB | 761213 | c.1407G>C | synonymous_variant | 1.0 |
| rpoB | 761219 | c.1413G>C | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761255 | c.1449T>G | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>T | synonymous_variant | 1.0 |
| rpoB | 761306 | c.1500C>G | synonymous_variant | 0.99 |
| rpoB | 761312 | c.1506G>C | synonymous_variant | 0.99 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 0.99 |
| rpoB | 761330 | c.1524G>C | synonymous_variant | 0.99 |
| rpoB | 761354 | c.1548C>T | synonymous_variant | 1.0 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761373 | p.Val523His | missense_variant | 1.0 |
| rpoB | 761408 | c.1602G>C | synonymous_variant | 1.0 |
| rpoB | 761414 | c.1608A>G | synonymous_variant | 1.0 |
| rpoB | 761423 | c.1617T>C | synonymous_variant | 1.0 |
| rpoB | 761435 | c.1629T>C | synonymous_variant | 0.67 |
| rpoB | 761457 | p.Pro551Ser | missense_variant | 0.83 |
| rpoB | 761477 | c.1671C>G | synonymous_variant | 0.97 |
| rpoB | 761492 | c.1686G>C | synonymous_variant | 0.97 |
| rpoB | 761510 | c.1704T>C | synonymous_variant | 0.99 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 0.98 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 0.98 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 0.99 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 0.99 |
| rpoB | 761588 | c.1782C>T | synonymous_variant | 0.99 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 0.99 |
| rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761657 | c.1851C>G | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761727 | p.Ser641Gly | missense_variant | 1.0 |
| rpoB | 761728 | c.1923dupC | frameshift_variant | 1.0 |
| rpoB | 761732 | c.1926C>G | synonymous_variant | 1.0 |
| rpoB | 761735 | c.1929C>G | synonymous_variant | 1.0 |
| rpoB | 761747 | c.1941G>C | synonymous_variant | 1.0 |
| rpoB | 761750 | c.1944G>C | synonymous_variant | 1.0 |
| rpoB | 761765 | c.1959T>C | synonymous_variant | 1.0 |
| rpoB | 761772 | p.His656Ala | missense_variant | 1.0 |
| rpoB | 761778 | p.Asn658Asp | missense_variant | 1.0 |
| rpoB | 761791 | p.Arg662His | missense_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761815 | p.Ala670Glu | missense_variant | 1.0 |
| rpoB | 761834 | c.2028T>C | synonymous_variant | 1.0 |
| rpoB | 761848 | p.Cys681Ser | missense_variant | 0.98 |
| rpoB | 761852 | c.2046C>G | synonymous_variant | 1.0 |
| rpoB | 761858 | c.2052G>C | synonymous_variant | 1.0 |
| rpoB | 761873 | c.2067A>C | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761906 | c.2100C>G | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761915 | p.Asp703Glu | missense_variant | 1.0 |
| rpoB | 761916 | p.Asp704Asn | missense_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 762008 | c.2202C>T | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>T | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762032 | c.2226C>T | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
| rpoB | 762134 | c.2328C>G | synonymous_variant | 1.0 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762206 | c.2400C>G | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762246 | c.2440C>T | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762401 | c.-969G>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>C | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
| rpoC | 762449 | c.-921C>A | upstream_gene_variant | 1.0 |
| rpoC | 762467 | c.-903C>T | upstream_gene_variant | 1.0 |
| rpoC | 762488 | c.-882G>C | upstream_gene_variant | 1.0 |
| rpoB | 762489 | p.Val895Gln | missense_variant | 1.0 |
| rpoC | 762512 | c.-858C>G | upstream_gene_variant | 1.0 |
| rpoC | 762521 | c.-849C>T | upstream_gene_variant | 1.0 |
| rpoC | 762533 | c.-837T>C | upstream_gene_variant | 1.0 |
| rpoC | 762536 | c.-834T>C | upstream_gene_variant | 1.0 |
| rpoC | 762537 | c.-833T>C | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>G | upstream_gene_variant | 1.0 |
| rpoC | 762581 | c.-789T>C | upstream_gene_variant | 1.0 |
| rpoC | 762582 | c.-788T>C | upstream_gene_variant | 1.0 |
| rpoC | 762596 | c.-774G>C | upstream_gene_variant | 1.0 |
| rpoC | 762599 | c.-771T>G | upstream_gene_variant | 1.0 |
| rpoC | 762701 | c.-669T>C | upstream_gene_variant | 1.0 |
| rpoB | 762729 | p.Gln975Lys | missense_variant | 1.0 |
| rpoB | 762736 | p.Ala977Glu | missense_variant | 1.0 |
| rpoB | 762744 | p.Gln980Ala | missense_variant | 1.0 |
| rpoB | 762750 | p.Leu982Met | missense_variant | 1.0 |
| rpoC | 762753 | c.-617T>C | upstream_gene_variant | 1.0 |
| rpoC | 762758 | c.-612G>C | upstream_gene_variant | 1.0 |
| rpoC | 762782 | c.-588T>C | upstream_gene_variant | 1.0 |
| rpoB | 762785 | p.Asp993Glu | missense_variant | 1.0 |
| rpoC | 762788 | c.-582G>C | upstream_gene_variant | 1.0 |
| rpoB | 762789 | p.Leu995Met | missense_variant | 1.0 |
| rpoC | 762794 | c.-576C>G | upstream_gene_variant | 1.0 |
| rpoB | 762799 | p.Ala998Gly | missense_variant | 1.0 |
| rpoB | 762810 | p.Ala1002Ser | missense_variant | 1.0 |
| rpoB | 762813 | p.Met1003Val | missense_variant | 1.0 |
| rpoC | 762818 | c.-552C>G | upstream_gene_variant | 1.0 |
| rpoC | 762827 | c.-543G>C | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoC | 762860 | c.-510G>C | upstream_gene_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoC | 763013 | c.-357C>G | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.99 |
| rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.99 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.99 |
| rpoC | 763136 | c.-234C>T | upstream_gene_variant | 1.0 |
| rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
| rpoC | 763158 | c.-212C>T | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763190 | c.-180C>T | upstream_gene_variant | 1.0 |
| rpoC | 763202 | c.-168A>G | upstream_gene_variant | 1.0 |
| rpoC | 763205 | c.-165G>C | upstream_gene_variant | 1.0 |
| rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 1.0 |
| rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoC | 763227 | c.-143C>T | upstream_gene_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoC | 763253 | c.-117G>C | upstream_gene_variant | 1.0 |
| rpoC | 763256 | c.-114G>A | upstream_gene_variant | 1.0 |
| rpoC | 763268 | c.-102C>G | upstream_gene_variant | 1.0 |
| rpoC | 763283 | c.-87T>C | upstream_gene_variant | 0.91 |
| rpoC | 763284 | c.-86C>T | upstream_gene_variant | 0.91 |
| rpoC | 763338 | c.-32A>G | upstream_gene_variant | 0.8 |
| rpoC | 763351 | c.-19T>C | upstream_gene_variant | 1.0 |
| rpoC | 763352 | c.-18T>A | upstream_gene_variant | 1.0 |
| rpoC | 763402 | c.33C>G | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>G | synonymous_variant | 0.99 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763441 | c.72C>T | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>G | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763603 | c.234C>T | synonymous_variant | 1.0 |
| rpoC | 763636 | c.267T>C | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 763816 | c.447C>G | synonymous_variant | 1.0 |
| rpoC | 763825 | c.456G>A | synonymous_variant | 1.0 |
| rpoC | 763835 | p.Ala156Met | missense_variant | 1.0 |
| rpoC | 763853 | p.Val162Ile | missense_variant | 1.0 |
| rpoC | 763858 | c.489A>G | synonymous_variant | 1.0 |
| rpoC | 763872 | p.Gly168Ala | missense_variant | 1.0 |
| rpoC | 763876 | p.Glu169Asp | missense_variant | 1.0 |
| rpoC | 763879 | c.510A>G | synonymous_variant | 1.0 |
| rpoC | 763888 | c.519G>C | synonymous_variant | 1.0 |
| rpoC | 763891 | c.522G>C | synonymous_variant | 1.0 |
| rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
| rpoC | 763900 | c.531G>C | synonymous_variant | 1.0 |
| rpoC | 763936 | c.567C>G | synonymous_variant | 1.0 |
| rpoC | 763939 | c.570G>A | synonymous_variant | 1.0 |
| rpoC | 763942 | c.573C>G | synonymous_variant | 1.0 |
| rpoC | 763945 | c.576T>C | synonymous_variant | 1.0 |
| rpoC | 763948 | c.579G>A | synonymous_variant | 1.0 |
| rpoC | 763949 | c.580C>A | synonymous_variant | 1.0 |
| rpoC | 763954 | c.585C>G | synonymous_variant | 1.0 |
| rpoC | 763960 | c.591T>C | synonymous_variant | 1.0 |
| rpoC | 763987 | c.618C>T | synonymous_variant | 1.0 |
| rpoC | 763991 | p.Ile208Leu | missense_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764002 | c.633C>G | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764032 | p.Asp221Glu | missense_variant | 1.0 |
| rpoC | 764040 | p.Ser224Thr | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>T | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764098 | c.729A>G | synonymous_variant | 1.0 |
| rpoC | 764101 | c.732C>G | synonymous_variant | 1.0 |
| rpoC | 764102 | p.Val245Ile | missense_variant | 1.0 |
| rpoC | 764112 | p.Tyr248Phe | missense_variant | 1.0 |
| rpoC | 764116 | c.747C>T | synonymous_variant | 1.0 |
| rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764140 | c.771C>T | synonymous_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764195 | p.Ser276Ile | missense_variant | 1.0 |
| rpoC | 764203 | c.834G>C | synonymous_variant | 1.0 |
| rpoC | 764206 | c.837T>C | synonymous_variant | 1.0 |
| rpoC | 764215 | c.846A>G | synonymous_variant | 1.0 |
| rpoC | 764236 | c.867G>A | synonymous_variant | 1.0 |
| rpoC | 764248 | c.879C>G | synonymous_variant | 1.0 |
| rpoC | 764257 | c.888G>C | synonymous_variant | 1.0 |
| rpoC | 764266 | c.897T>C | synonymous_variant | 1.0 |
| rpoC | 764269 | c.900G>C | synonymous_variant | 1.0 |
| rpoC | 764272 | c.903G>C | synonymous_variant | 1.0 |
| rpoC | 764278 | c.909A>G | synonymous_variant | 1.0 |
| rpoC | 764338 | c.969G>A | synonymous_variant | 1.0 |
| rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036A>C | synonymous_variant | 1.0 |
| rpoC | 764419 | c.1050C>G | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
| rpoC | 764452 | c.1083T>C | synonymous_variant | 1.0 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764489 | c.1120C>T | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764510 | c.1141C>T | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>C | synonymous_variant | 0.98 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 0.97 |
| rpoC | 764554 | c.1185C>T | synonymous_variant | 0.98 |
| rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
| rpoC | 764593 | c.1224C>T | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 0.99 |
| rpoC | 764650 | c.1281G>C | synonymous_variant | 0.99 |
| rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.99 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 0.99 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 0.99 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 0.98 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 0.99 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
| rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
| rpoC | 765034 | c.1665T>C | synonymous_variant | 1.0 |
| rpoC | 765040 | c.1671T>C | synonymous_variant | 1.0 |
| rpoC | 765041 | c.1672T>C | synonymous_variant | 1.0 |
| rpoC | 765047 | c.1678T>C | synonymous_variant | 1.0 |
| rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 765073 | c.1704G>C | synonymous_variant | 1.0 |
| rpoC | 765076 | c.1707A>G | synonymous_variant | 1.0 |
| rpoC | 765079 | c.1710T>G | synonymous_variant | 0.98 |
| rpoC | 765082 | c.1713G>C | synonymous_variant | 1.0 |
| rpoC | 765089 | c.1720T>C | synonymous_variant | 1.0 |
| rpoC | 765103 | c.1734G>T | synonymous_variant | 1.0 |
| rpoC | 765146 | p.Pro593Asp | missense_variant | 1.0 |
| rpoC | 765156 | p.Thr596Lys | missense_variant | 1.0 |
| rpoC | 765165 | p.Tyr599Phe | missense_variant | 1.0 |
| rpoC | 765208 | c.1839T>G | synonymous_variant | 0.89 |
| rpoC | 765220 | c.1851A>G | synonymous_variant | 0.95 |
| rpoC | 765233 | p.Ala622Ser | missense_variant | 0.95 |
| rpoC | 765241 | c.1872C>T | synonymous_variant | 0.95 |
| rpoC | 765244 | c.1875T>C | synonymous_variant | 0.95 |
| rpoC | 765247 | c.1878C>G | synonymous_variant | 1.0 |
| rpoC | 765248 | c.1879T>C | synonymous_variant | 1.0 |
| rpoC | 765251 | c.1882_1884delAGCinsTCG | synonymous_variant | 1.0 |
| rpoC | 765292 | c.1923G>C | synonymous_variant | 1.0 |
| rpoC | 765298 | c.1929G>C | synonymous_variant | 1.0 |
| rpoC | 765300 | p.Val644Ala | missense_variant | 1.0 |
| rpoC | 765319 | c.1950A>G | synonymous_variant | 1.0 |
| rpoC | 765326 | p.His653Ala | missense_variant | 1.0 |
| rpoC | 765329 | p.Ser654Gly | missense_variant | 1.0 |
| rpoC | 765346 | c.1977C>G | synonymous_variant | 1.0 |
| rpoC | 765349 | c.1980T>C | synonymous_variant | 1.0 |
| rpoC | 765352 | c.1983G>C | synonymous_variant | 1.0 |
| rpoC | 765383 | p.Met672Leu | missense_variant | 0.99 |
| rpoC | 765404 | p.Leu679Val | missense_variant | 0.99 |
| rpoC | 765409 | c.2040T>C | synonymous_variant | 0.99 |
| rpoC | 765421 | c.2052C>G | synonymous_variant | 0.99 |
| rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
| rpoC | 765529 | c.2160C>T | synonymous_variant | 1.0 |
| rpoC | 765541 | c.2172C>G | synonymous_variant | 1.0 |
| rpoC | 765553 | c.2184C>T | synonymous_variant | 1.0 |
| rpoC | 765556 | c.2187G>C | synonymous_variant | 1.0 |
| rpoC | 765559 | c.2190G>C | synonymous_variant | 1.0 |
| rpoC | 765580 | c.2211G>C | synonymous_variant | 1.0 |
| rpoC | 765613 | p.His748Gln | missense_variant | 1.0 |
| rpoC | 765625 | c.2256C>G | synonymous_variant | 1.0 |
| rpoC | 765631 | p.Asp754Glu | missense_variant | 1.0 |
| rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
| rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
| rpoC | 765739 | c.2370G>T | synonymous_variant | 1.0 |
| rpoC | 765751 | c.2382C>G | synonymous_variant | 1.0 |
| rpoC | 765753 | p.Asp795Ala | missense_variant | 1.0 |
| rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
| rpoC | 765784 | c.2415C>G | synonymous_variant | 1.0 |
| rpoC | 765787 | c.2418C>T | synonymous_variant | 1.0 |
| rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
| rpoC | 765796 | c.2427C>T | synonymous_variant | 1.0 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
| rpoC | 765814 | c.2445A>G | synonymous_variant | 1.0 |
| rpoC | 765826 | c.2457T>C | synonymous_variant | 1.0 |
| rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
| rpoC | 765850 | c.2481G>C | synonymous_variant | 1.0 |
| rpoC | 765883 | c.2514C>G | synonymous_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765892 | c.2523T>C | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>G | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766027 | c.2658G>C | synonymous_variant | 1.0 |
| rpoC | 766043 | p.Gln892Glu | missense_variant | 1.0 |
| rpoC | 766054 | c.2685C>G | synonymous_variant | 1.0 |
| rpoC | 766082 | p.Ala905Gln | missense_variant | 1.0 |
| rpoC | 766096 | c.2727G>C | synonymous_variant | 1.0 |
| rpoC | 766129 | c.2760C>G | synonymous_variant | 0.99 |
| rpoC | 766135 | c.2766G>A | synonymous_variant | 0.99 |
| rpoC | 766141 | c.2772C>T | synonymous_variant | 0.98 |
| rpoC | 766142 | c.2773C>T | synonymous_variant | 0.98 |
| rpoC | 766168 | c.2799C>T | synonymous_variant | 0.97 |
| rpoC | 766174 | p.Asn935Lys | missense_variant | 0.97 |
| rpoC | 766178 | p.Ile937Val | missense_variant | 0.95 |
| rpoC | 766185 | p.Glu939Ala | missense_variant | 1.0 |
| rpoC | 766189 | c.2820T>C | synonymous_variant | 1.0 |
| rpoC | 766192 | c.2823T>C | synonymous_variant | 1.0 |
| rpoC | 766193 | p.Gln942Glu | missense_variant | 1.0 |
| rpoC | 766204 | c.2835C>T | synonymous_variant | 1.0 |
| rpoC | 766207 | c.2838T>C | synonymous_variant | 1.0 |
| rpoC | 766258 | c.2889T>C | synonymous_variant | 1.0 |
| rpoC | 766273 | c.2904T>C | synonymous_variant | 1.0 |
| rpoC | 766274 | p.Ala969Thr | missense_variant | 1.0 |
| rpoC | 766280 | p.Ser971Gly | missense_variant | 1.0 |
| rpoC | 766288 | c.2919C>G | synonymous_variant | 1.0 |
| rpoC | 766303 | c.2934C>T | synonymous_variant | 1.0 |
| rpoC | 766312 | c.2943T>G | synonymous_variant | 1.0 |
| rpoC | 766327 | c.2958C>A | synonymous_variant | 1.0 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 0.99 |
| rpoC | 766357 | c.2988C>T | synonymous_variant | 0.99 |
| rpoC | 766363 | c.2994G>C | synonymous_variant | 0.99 |
| rpoC | 766366 | c.2997C>G | synonymous_variant | 0.99 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 0.99 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 0.99 |
| rpoC | 766408 | c.3039C>G | synonymous_variant | 0.99 |
| rpoC | 766411 | c.3042C>G | synonymous_variant | 0.99 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766447 | c.3078T>C | synonymous_variant | 1.0 |
| rpoC | 766462 | c.3093G>C | synonymous_variant | 1.0 |
| rpoC | 766483 | c.3114G>C | synonymous_variant | 1.0 |
| rpoC | 766484 | p.Val1039Ile | missense_variant | 1.0 |
| rpoC | 766492 | c.3123T>C | synonymous_variant | 1.0 |
| rpoC | 766522 | c.3153C>G | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>C | synonymous_variant | 1.0 |
| rpoC | 766531 | c.3162G>C | synonymous_variant | 1.0 |
| rpoC | 766540 | p.Asp1057Glu | missense_variant | 1.0 |
| rpoC | 766549 | c.3180G>C | synonymous_variant | 1.0 |
| rpoC | 766573 | c.3204T>C | synonymous_variant | 1.0 |
| rpoC | 766582 | c.3213C>G | synonymous_variant | 1.0 |
| rpoC | 766583 | p.Gly1072Ser | missense_variant | 1.0 |
| rpoC | 766591 | c.3222A>G | synonymous_variant | 1.0 |
| rpoC | 766594 | c.3225G>C | synonymous_variant | 1.0 |
| rpoC | 766597 | c.3228C>G | synonymous_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766630 | c.3261G>C | synonymous_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766673 | p.Gly1102Asn | missense_variant | 1.0 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766738 | c.3369G>C | synonymous_variant | 1.0 |
| rpoC | 766747 | c.3378C>T | synonymous_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766801 | c.3432C>G | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
| rpoC | 766864 | c.3495G>C | synonymous_variant | 1.0 |
| rpoC | 766867 | c.3498C>G | synonymous_variant | 1.0 |
| rpoC | 766882 | c.3513C>T | synonymous_variant | 1.0 |
| rpoC | 766894 | c.3525T>C | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766933 | c.3564A>G | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>G | synonymous_variant | 1.0 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 1.0 |
| rpoC | 766987 | c.3618G>C | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 767014 | c.3645G>C | synonymous_variant | 1.0 |
| rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
| rpoC | 767062 | c.3693C>A | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>A | synonymous_variant | 1.0 |
| rpoC | 767158 | c.3789T>C | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>G | synonymous_variant | 1.0 |
| rpoC | 767209 | c.3840T>C | synonymous_variant | 1.0 |
| rpoC | 767212 | c.3843G>C | synonymous_variant | 1.0 |
| rpoC | 767221 | c.3852C>G | synonymous_variant | 1.0 |
| rpoC | 767230 | c.3861G>C | synonymous_variant | 1.0 |
| rpoC | 767233 | c.3864T>C | synonymous_variant | 1.0 |
| rpoC | 767263 | c.3894T>C | synonymous_variant | 1.0 |
| rpoC | 767264 | p.Ala1299Gln | missense_variant | 1.0 |
| rpoC | 767275 | c.3906T>C | synonymous_variant | 1.0 |
| rpoC | 767278 | c.3909T>C | synonymous_variant | 1.0 |
| rpoC | 767281 | c.3912C>G | synonymous_variant | 1.0 |
| rpoC | 767284 | c.3915C>T | synonymous_variant | 1.0 |
| rpoC | 767317 | c.3948C>G | synonymous_variant | 1.0 |
| mmpL5 | 775736 | c.2745C>G | synonymous_variant | 0.67 |
| mmpL5 | 775742 | c.2739C>T | synonymous_variant | 0.67 |
| mmpL5 | 775747 | p.Met912Leu | missense_variant | 0.67 |
| mmpL5 | 775748 | c.2733T>G | synonymous_variant | 1.0 |
| mmpL5 | 775817 | c.2664T>C | synonymous_variant | 1.0 |
| mmpL5 | 775826 | c.2655G>C | synonymous_variant | 1.0 |
| mmpL5 | 775832 | p.Ala883Ser | missense_variant | 1.0 |
| mmpL5 | 775838 | c.2643G>C | synonymous_variant | 1.0 |
| mmpL5 | 775847 | c.2634G>C | synonymous_variant | 1.0 |
| mmpL5 | 775851 | p.Ser877Thr | missense_variant | 1.0 |
| mmpL5 | 775856 | c.2625T>C | synonymous_variant | 1.0 |
| mmpL5 | 775864 | p.Ala873Ser | missense_variant | 0.8 |
| mmpL5 | 775865 | c.2616T>C | synonymous_variant | 0.8 |
| mmpL5 | 775883 | p.Ile866Leu | missense_variant | 0.86 |
| mmpL5 | 775886 | c.2595A>C | synonymous_variant | 0.86 |
| mmpL5 | 775901 | c.2580G>A | synonymous_variant | 0.88 |
| mmpL5 | 775909 | p.Leu858Phe | missense_variant | 0.83 |
| mmpL5 | 775913 | c.2568C>G | synonymous_variant | 0.83 |
| mmpL5 | 775916 | c.2565T>C | synonymous_variant | 0.83 |
| mmpL5 | 775937 | c.2544G>A | synonymous_variant | 0.75 |
| mmpL5 | 775946 | c.2535C>A | synonymous_variant | 0.9 |
| mmpL5 | 775952 | c.2529G>T | synonymous_variant | 0.69 |
| mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.38 |
| mmpL5 | 775966 | p.Ala839Ser | missense_variant | 0.89 |
| mmpL5 | 775972 | p.Ala837Pro | missense_variant | 0.48 |
| mmpL5 | 775973 | c.2506_2508delTTGinsCTC | synonymous_variant | 0.41 |
| mmpL5 | 775981 | p.Leu834Met | missense_variant | 1.0 |
| mmpL5 | 775987 | p.His832Tyr | missense_variant | 0.27 |
| mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.52 |
| mmpL5 | 775997 | c.2484T>C | synonymous_variant | 0.93 |
| mmpL5 | 776000 | p.Leu827Ile | missense_variant | 0.83 |
| mmpL5 | 776005 | p.Ile826Leu | missense_variant | 0.5 |
| mmpL5 | 776008 | p.His825Tyr | missense_variant | 0.5 |
| mmpL5 | 776009 | c.2472A>G | synonymous_variant | 1.0 |
| mmpL5 | 776030 | c.2451G>A | synonymous_variant | 0.72 |
| mmpL5 | 776048 | c.2433G>A | synonymous_variant | 0.26 |
| mmpL5 | 776053 | c.2428T>C | synonymous_variant | 1.0 |
| mmpL5 | 776056 | p.Val809Leu | missense_variant | 1.0 |
| mmpL5 | 776060 | c.2421C>G | synonymous_variant | 1.0 |
| mmpL5 | 776063 | c.2418C>T | synonymous_variant | 0.92 |
| mmpL5 | 776072 | c.2409C>G | synonymous_variant | 0.9 |
| mmpL5 | 776076 | p.Ala802Phe | missense_variant | 0.86 |
| mmpL5 | 776084 | c.2397C>G | synonymous_variant | 0.86 |
| mmpL5 | 776120 | c.2361C>T | synonymous_variant | 1.0 |
| mmpL5 | 776129 | c.2352C>G | synonymous_variant | 1.0 |
| mmpL5 | 776132 | p.Ala783Ser | missense_variant | 1.0 |
| mmpL5 | 776135 | p.Ser782Ala | missense_variant | 1.0 |
| mmpL5 | 776152 | p.Met777Leu | missense_variant | 1.0 |
| mmpL5 | 776155 | c.2326T>C | synonymous_variant | 1.0 |
| mmpL5 | 776159 | c.2322T>C | synonymous_variant | 1.0 |
| mmpL5 | 776646 | p.Val612Ala | missense_variant | 1.0 |
| mmpL5 | 776659 | p.Asp608Asn | missense_variant | 0.63 |
| mmpL5 | 776660 | c.1821C>G | synonymous_variant | 0.6 |
| mmpL5 | 776664 | p.Thr606Gly | missense_variant | 0.33 |
| mmpL5 | 776672 | c.1809G>C | synonymous_variant | 0.65 |
| mmpL5 | 776675 | c.1806G>A | synonymous_variant | 0.82 |
| mmpL5 | 776684 | c.1797G>A | synonymous_variant | 0.68 |
| mmpL5 | 776687 | p.Trp598Phe | missense_variant | 0.55 |
| mmpL5 | 776694 | p.Val596Thr | missense_variant | 0.44 |
| mmpL5 | 776705 | c.1776C>T | synonymous_variant | 0.33 |
| mmpL5 | 776738 | c.1743C>T | synonymous_variant | 0.5 |
| mmpL5 | 776741 | c.1740C>G | synonymous_variant | 0.56 |
| mmpL5 | 776744 | c.1735_1737delCGCinsAGA | synonymous_variant | 0.64 |
| mmpL5 | 776753 | c.1728T>C | synonymous_variant | 0.8 |
| mmpL5 | 776756 | p.Asp575Glu | missense_variant | 0.86 |
| mmpL5 | 776767 | p.Ala572Ser | missense_variant | 0.67 |
| mmpL5 | 777085 | p.Asn466Asp | missense_variant | 1.0 |
| mmpL5 | 777095 | c.1386T>C | synonymous_variant | 1.0 |
| mmpL5 | 777101 | c.1380C>G | synonymous_variant | 1.0 |
| mmpL5 | 777110 | c.1371T>G | synonymous_variant | 1.0 |
| mmpL5 | 777115 | p.Met456Leu | missense_variant | 1.0 |
| mmpL5 | 777116 | c.1365C>T | synonymous_variant | 1.0 |
| mmpL5 | 777133 | p.Val450Ile | missense_variant | 1.0 |
| mmpL5 | 777158 | c.1323C>G | synonymous_variant | 1.0 |
| mmpL5 | 777164 | c.1317C>G | synonymous_variant | 1.0 |
| mmpL5 | 777170 | c.1311T>C | synonymous_variant | 1.0 |
| mmpL5 | 777173 | c.1308C>G | synonymous_variant | 1.0 |
| mmpL5 | 777176 | p.Glu435Asp | missense_variant | 1.0 |
| mmpL5 | 777191 | c.1290C>G | synonymous_variant | 1.0 |
| mmpL5 | 777194 | c.1287A>G | synonymous_variant | 1.0 |
| mmpL5 | 777206 | c.1275A>G | synonymous_variant | 1.0 |
| mmpL5 | 777212 | p.Ala423Thr | missense_variant | 1.0 |
| mmpL5 | 777215 | c.1266C>G | synonymous_variant | 1.0 |
| mmpL5 | 777218 | c.1263G>A | synonymous_variant | 1.0 |
| mmpL5 | 777251 | c.1230C>G | synonymous_variant | 1.0 |
| mmpL5 | 777254 | c.1227G>C | synonymous_variant | 0.92 |
| mmpR5 | 778000 | c.-990G>A | upstream_gene_variant | 0.33 |
| mmpL5 | 778001 | p.Ser160Ala | missense_variant | 0.75 |
| mmpL5 | 778005 | p.Glu159Ser | missense_variant | 0.5 |
| mmpR5 | 778013 | c.-977A>G | upstream_gene_variant | 0.33 |
| mmpR5 | 778016 | c.-974G>A | upstream_gene_variant | 0.33 |
| mmpR5 | 778019 | c.-971C>G | upstream_gene_variant | 0.83 |
| mmpL5 | 778025 | p.Lys152Tyr | missense_variant | 0.83 |
| mmpR5 | 778028 | c.-962C>G | upstream_gene_variant | 0.83 |
| mmpR5 | 778034 | c.-956A>G | upstream_gene_variant | 0.33 |
| mmpL5 | 778056 | p.Ser142Asn | missense_variant | 0.33 |
| mmpR5 | 778064 | c.-926G>C | upstream_gene_variant | 1.0 |
| rpsL | 781571 | c.12C>T | synonymous_variant | 0.97 |
| rpsL | 781595 | c.36T>C | synonymous_variant | 0.96 |
| rpsL | 781605 | p.Ile16Val | missense_variant | 0.98 |
| rpsL | 781608 | p.Ser17Ala | missense_variant | 0.98 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 0.99 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 0.98 |
| rpsL | 781649 | c.90T>C | synonymous_variant | 0.99 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 0.99 |
| rpsL | 781700 | c.141G>C | synonymous_variant | 0.99 |
| rpsL | 781703 | c.144G>T | synonymous_variant | 0.99 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 0.99 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 0.99 |
| rpsL | 781736 | c.177T>C | synonymous_variant | 0.97 |
| rpsL | 781742 | c.183C>T | synonymous_variant | 0.97 |
| rpsL | 781748 | c.189C>G | synonymous_variant | 0.97 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 0.98 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 0.98 |
| rpsL | 781772 | c.213C>A | synonymous_variant | 0.99 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>C | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>G | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>C | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 0.99 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
| rplC | 800627 | c.-182C>T | upstream_gene_variant | 0.98 |
| rplC | 800648 | c.-161A>T | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
| rplC | 800771 | c.-38C>T | upstream_gene_variant | 1.0 |
| rplC | 800794 | c.-15A>G | upstream_gene_variant | 1.0 |
| rplC | 800796 | c.-13A>G | upstream_gene_variant | 1.0 |
| rplC | 800798 | c.-10_-9delGG | upstream_gene_variant | 1.0 |
| rplC | 800814 | c.6A>G | synonymous_variant | 1.0 |
| rplC | 800817 | c.9A>T | synonymous_variant | 1.0 |
| rplC | 800844 | c.36T>C | synonymous_variant | 1.0 |
| rplC | 800865 | c.57A>G | synonymous_variant | 1.0 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
| rplC | 800874 | c.66A>G | synonymous_variant | 1.0 |
| rplC | 800875 | p.Val23Ile | missense_variant | 1.0 |
| rplC | 800880 | c.72A>G | synonymous_variant | 1.0 |
| rplC | 800889 | c.81C>G | synonymous_variant | 1.0 |
| rplC | 800892 | c.84G>C | synonymous_variant | 1.0 |
| rplC | 800907 | c.99C>G | synonymous_variant | 1.0 |
| rplC | 800916 | c.108A>G | synonymous_variant | 1.0 |
| rplC | 800934 | c.126C>G | synonymous_variant | 1.0 |
| rplC | 800937 | c.129A>G | synonymous_variant | 1.0 |
| rplC | 800939 | p.Arg44Gln | missense_variant | 1.0 |
| rplC | 800946 | c.138T>C | synonymous_variant | 1.0 |
| rplC | 800949 | c.141T>C | synonymous_variant | 1.0 |
| rplC | 800967 | c.159C>G | synonymous_variant | 1.0 |
| rplC | 800970 | c.162T>C | synonymous_variant | 1.0 |
| rplC | 800982 | c.174C>T | synonymous_variant | 1.0 |
| rplC | 800985 | c.177A>G | synonymous_variant | 1.0 |
| rplC | 801004 | p.Leu66Val | missense_variant | 1.0 |
| rplC | 801009 | c.201A>C | synonymous_variant | 1.0 |
| rplC | 801019 | p.Thr71Ala | missense_variant | 1.0 |
| rplC | 801027 | c.219C>G | synonymous_variant | 1.0 |
| rplC | 801039 | c.231A>G | synonymous_variant | 1.0 |
| rplC | 801045 | c.237A>G | synonymous_variant | 1.0 |
| rplC | 801047 | p.Tyr80Phe | missense_variant | 1.0 |
| rplC | 801049 | c.241C>T | synonymous_variant | 1.0 |
| rplC | 801054 | c.246G>C | synonymous_variant | 1.0 |
| rplC | 801127 | p.Ala107Thr | missense_variant | 1.0 |
| rplC | 801132 | c.324T>C | synonymous_variant | 1.0 |
| rplC | 801147 | c.339T>C | synonymous_variant | 1.0 |
| rplC | 801150 | c.342G>C | synonymous_variant | 1.0 |
| rplC | 801153 | c.345G>C | synonymous_variant | 1.0 |
| rplC | 801156 | c.348T>A | synonymous_variant | 1.0 |
| rplC | 801168 | c.360C>G | synonymous_variant | 1.0 |
| rplC | 801171 | c.363A>G | synonymous_variant | 1.0 |
| rplC | 801174 | c.366T>C | synonymous_variant | 1.0 |
| rplC | 801180 | c.372C>G | synonymous_variant | 1.0 |
| rplC | 801195 | c.387G>C | synonymous_variant | 1.0 |
| rplC | 801201 | c.393C>T | synonymous_variant | 1.0 |
| rplC | 801207 | c.399C>T | synonymous_variant | 1.0 |
| rplC | 801246 | c.438C>T | synonymous_variant | 1.0 |
| rplC | 801249 | c.441T>C | synonymous_variant | 1.0 |
| rplC | 801255 | c.447C>T | synonymous_variant | 1.0 |
| rplC | 801264 | c.456C>T | synonymous_variant | 1.0 |
| rplC | 801267 | c.459A>T | synonymous_variant | 1.0 |
| rplC | 801270 | c.462T>C | synonymous_variant | 1.0 |
| rplC | 801276 | c.468G>C | synonymous_variant | 1.0 |
| rplC | 801279 | c.471G>C | synonymous_variant | 1.0 |
| rplC | 801282 | c.474G>C | synonymous_variant | 1.0 |
| rplC | 801285 | c.477G>C | synonymous_variant | 1.0 |
| rplC | 801300 | c.492C>G | synonymous_variant | 1.0 |
| rplC | 801309 | c.501C>G | synonymous_variant | 1.0 |
| rplC | 801312 | c.504G>C | synonymous_variant | 1.0 |
| rplC | 801321 | c.513C>T | synonymous_variant | 1.0 |
| rplC | 801324 | c.516T>C | synonymous_variant | 1.0 |
| rplC | 801339 | c.531T>C | synonymous_variant | 1.0 |
| rplC | 801341 | p.Leu178Gln | missense_variant | 1.0 |
| rplC | 801348 | c.540T>G | synonymous_variant | 1.0 |
| rplC | 801357 | c.549T>C | synonymous_variant | 1.0 |
| rplC | 801367 | p.Ala187Thr | missense_variant | 1.0 |
| rplC | 801402 | c.594T>C | synonymous_variant | 0.99 |
| rplC | 801405 | c.597T>C | synonymous_variant | 1.0 |
| rplC | 801423 | c.615G>C | synonymous_variant | 1.0 |
| rplC | 801426 | c.618C>G | synonymous_variant | 1.0 |
| rplC | 801427 | p.Met207Val | missense_variant | 1.0 |
| rplC | 801438 | c.630T>C | synonymous_variant | 1.0 |
| rplC | 801442 | p.Ile212Val | missense_variant | 1.0 |
| fbiC | 1303065 | c.135C>G | synonymous_variant | 1.0 |
| fbiC | 1303066 | p.Ile46Leu | missense_variant | 1.0 |
| fbiC | 1303080 | c.150A>G | synonymous_variant | 0.94 |
| fbiC | 1303088 | p.Asp53Ala | missense_variant | 0.94 |
| fbiC | 1303092 | p.Glu54Asp | missense_variant | 0.95 |
| fbiC | 1303116 | c.186C>G | synonymous_variant | 0.95 |
| fbiC | 1303119 | c.189G>A | synonymous_variant | 0.95 |
| fbiC | 1303131 | c.201T>C | synonymous_variant | 0.95 |
| fbiC | 1303137 | c.207T>C | synonymous_variant | 0.92 |
| fbiC | 1303140 | c.210C>G | synonymous_variant | 0.91 |
| fbiC | 1303142 | p.Val71Glu | missense_variant | 0.91 |
| fbiC | 1303152 | c.222C>A | synonymous_variant | 1.0 |
| fbiC | 1303157 | p.His76Arg | missense_variant | 1.0 |
| fbiC | 1303161 | c.231G>C | synonymous_variant | 1.0 |
| fbiC | 1303165 | p.Ser79Gly | missense_variant | 1.0 |
| fbiC | 1303299 | p.Met123Ile | missense_variant | 1.0 |
| fbiC | 1303321 | p.Val131Ile | missense_variant | 1.0 |
| fbiC | 1303327 | p.Arg133Cys | missense_variant | 1.0 |
| fbiC | 1303332 | c.402A>C | synonymous_variant | 1.0 |
| fbiC | 1303335 | c.405T>C | synonymous_variant | 1.0 |
| fbiC | 1303337 | p.Ala136Gly | missense_variant | 1.0 |
| fbiC | 1303342 | p.Phe138Leu | missense_variant | 1.0 |
| fbiC | 1303368 | c.438T>G | synonymous_variant | 1.0 |
| fbiC | 1303371 | c.441C>G | synonymous_variant | 1.0 |
| fbiC | 1303431 | c.501T>C | synonymous_variant | 1.0 |
| fbiC | 1303434 | c.504C>T | synonymous_variant | 1.0 |
| fbiC | 1303437 | c.507C>G | synonymous_variant | 1.0 |
| fbiC | 1303441 | c.511T>C | synonymous_variant | 1.0 |
| fbiC | 1303455 | c.525C>G | synonymous_variant | 1.0 |
| fbiC | 1303464 | c.534A>G | synonymous_variant | 1.0 |
| fbiC | 1303470 | c.540T>G | synonymous_variant | 1.0 |
| fbiC | 1303476 | c.546G>C | synonymous_variant | 1.0 |
| fbiC | 1303480 | p.Gln184Glu | missense_variant | 1.0 |
| fbiC | 1303489 | c.559C>T | synonymous_variant | 1.0 |
| fbiC | 1303497 | c.567G>A | synonymous_variant | 1.0 |
| fbiC | 1303501 | c.571C>T | synonymous_variant | 1.0 |
| fbiC | 1303509 | c.579G>C | synonymous_variant | 1.0 |
| fbiC | 1303512 | c.582T>C | synonymous_variant | 1.0 |
| fbiC | 1303521 | c.591C>T | synonymous_variant | 1.0 |
| fbiC | 1303530 | c.600G>A | synonymous_variant | 1.0 |
| fbiC | 1303534 | p.Ser202Ala | missense_variant | 1.0 |
| fbiC | 1303539 | c.609G>C | synonymous_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303575 | c.645G>C | synonymous_variant | 1.0 |
| fbiC | 1303590 | c.660A>G | synonymous_variant | 1.0 |
| fbiC | 1303602 | c.672A>G | synonymous_variant | 1.0 |
| fbiC | 1303605 | c.675C>G | synonymous_variant | 1.0 |
| fbiC | 1303608 | c.678G>A | synonymous_variant | 1.0 |
| fbiC | 1303614 | c.684C>T | synonymous_variant | 1.0 |
| fbiC | 1303617 | c.687C>G | synonymous_variant | 1.0 |
| fbiC | 1303632 | c.702T>G | synonymous_variant | 1.0 |
| fbiC | 1303641 | c.711C>T | synonymous_variant | 1.0 |
| fbiC | 1303671 | c.741C>T | synonymous_variant | 1.0 |
| fbiC | 1303674 | c.744C>G | synonymous_variant | 1.0 |
| fbiC | 1303681 | c.751T>C | synonymous_variant | 1.0 |
| fbiC | 1303686 | c.756C>G | synonymous_variant | 1.0 |
| fbiC | 1303695 | c.765T>C | synonymous_variant | 1.0 |
| fbiC | 1303704 | c.774T>C | synonymous_variant | 1.0 |
| fbiC | 1303708 | c.778T>C | synonymous_variant | 1.0 |
| fbiC | 1303728 | c.798G>A | synonymous_variant | 1.0 |
| fbiC | 1303731 | c.801A>C | synonymous_variant | 1.0 |
| fbiC | 1303732 | p.Ser268Ala | missense_variant | 1.0 |
| fbiC | 1303737 | c.807G>A | synonymous_variant | 0.98 |
| fbiC | 1303746 | c.816T>C | synonymous_variant | 0.98 |
| fbiC | 1303749 | c.819G>C | synonymous_variant | 0.97 |
| fbiC | 1303752 | c.822A>G | synonymous_variant | 0.97 |
| fbiC | 1303755 | c.825T>C | synonymous_variant | 0.98 |
| fbiC | 1303761 | c.831T>C | synonymous_variant | 0.98 |
| fbiC | 1303785 | c.855G>C | synonymous_variant | 0.98 |
| fbiC | 1303789 | p.Ile287Val | missense_variant | 0.98 |
| fbiC | 1303797 | c.867A>G | synonymous_variant | 0.98 |
| fbiC | 1303818 | c.888C>G | synonymous_variant | 1.0 |
| fbiC | 1303836 | c.906G>C | synonymous_variant | 1.0 |
| fbiC | 1303845 | c.915C>G | synonymous_variant | 1.0 |
| fbiC | 1303846 | p.Phe306Val | missense_variant | 1.0 |
| fbiC | 1303854 | c.924T>C | synonymous_variant | 1.0 |
| fbiC | 1303860 | c.930A>C | synonymous_variant | 1.0 |
| fbiC | 1303884 | c.954T>G | synonymous_variant | 0.99 |
| fbiC | 1303905 | c.975G>C | synonymous_variant | 0.99 |
| fbiC | 1303914 | c.984C>G | synonymous_variant | 0.99 |
| fbiC | 1303920 | c.990C>T | synonymous_variant | 0.98 |
| fbiC | 1303944 | c.1014G>C | synonymous_variant | 0.98 |
| fbiC | 1303947 | c.1017T>G | synonymous_variant | 0.98 |
| fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.98 |
| fbiC | 1303953 | p.Asp341Glu | missense_variant | 0.98 |
| fbiC | 1303956 | c.1026A>G | synonymous_variant | 0.98 |
| fbiC | 1303961 | p.Arg344Leu | missense_variant | 1.0 |
| fbiC | 1303971 | c.1041T>C | synonymous_variant | 1.0 |
| fbiC | 1303980 | c.1050G>A | synonymous_variant | 1.0 |
| fbiC | 1304004 | c.1074A>G | synonymous_variant | 1.0 |
| fbiC | 1304008 | c.1078T>C | synonymous_variant | 1.0 |
| fbiC | 1304022 | c.1092T>C | synonymous_variant | 1.0 |
| fbiC | 1304031 | c.1101C>G | synonymous_variant | 1.0 |
| fbiC | 1304034 | c.1104A>G | synonymous_variant | 1.0 |
| fbiC | 1304040 | c.1110C>G | synonymous_variant | 1.0 |
| fbiC | 1304046 | c.1116C>G | synonymous_variant | 1.0 |
| fbiC | 1304049 | c.1119T>C | synonymous_variant | 1.0 |
| fbiC | 1304050 | c.1120T>C | synonymous_variant | 1.0 |
| fbiC | 1304058 | c.1128G>A | synonymous_variant | 1.0 |
| fbiC | 1304059 | c.1129C>T | synonymous_variant | 1.0 |
| fbiC | 1304064 | c.1134G>C | synonymous_variant | 1.0 |
| fbiC | 1304067 | c.1137G>C | synonymous_variant | 1.0 |
| fbiC | 1304085 | c.1155C>T | synonymous_variant | 1.0 |
| fbiC | 1304091 | p.Asp387Glu | missense_variant | 1.0 |
| fbiC | 1304092 | p.Met388Leu | missense_variant | 1.0 |
| fbiC | 1304097 | c.1167G>C | synonymous_variant | 1.0 |
| fbiC | 1304106 | c.1176G>C | synonymous_variant | 1.0 |
| fbiC | 1304127 | c.1197A>G | synonymous_variant | 1.0 |
| fbiC | 1304142 | c.1212G>C | synonymous_variant | 1.0 |
| fbiC | 1304161 | p.Arg411Ser | missense_variant | 1.0 |
| fbiC | 1304169 | c.1239T>C | synonymous_variant | 1.0 |
| fbiC | 1304174 | p.Val415Ala | missense_variant | 1.0 |
| fbiC | 1304184 | c.1254G>C | synonymous_variant | 1.0 |
| fbiC | 1304187 | c.1257T>C | synonymous_variant | 1.0 |
| fbiC | 1304208 | c.1278C>T | synonymous_variant | 1.0 |
| fbiC | 1304226 | c.1296C>G | synonymous_variant | 1.0 |
| fbiC | 1304227 | p.Met433Leu | missense_variant | 1.0 |
| fbiC | 1304232 | c.1302G>A | synonymous_variant | 1.0 |
| fbiC | 1304526 | c.1596T>G | synonymous_variant | 1.0 |
| fbiC | 1304535 | c.1605G>A | synonymous_variant | 1.0 |
| fbiC | 1304544 | c.1614T>C | synonymous_variant | 1.0 |
| fbiC | 1304545 | p.Val539Thr | missense_variant | 1.0 |
| fbiC | 1304553 | c.1623C>T | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304565 | c.1635C>G | synonymous_variant | 1.0 |
| fbiC | 1304568 | c.1638T>C | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| fbiC | 1304634 | c.1704C>G | synonymous_variant | 1.0 |
| fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
| fbiC | 1304646 | c.1716T>C | synonymous_variant | 1.0 |
| fbiC | 1304658 | c.1728C>G | synonymous_variant | 1.0 |
| fbiC | 1304661 | c.1731C>T | synonymous_variant | 1.0 |
| fbiC | 1304691 | c.1761G>C | synonymous_variant | 1.0 |
| fbiC | 1304694 | c.1764A>C | synonymous_variant | 1.0 |
| fbiC | 1304703 | c.1773C>G | synonymous_variant | 1.0 |
| fbiC | 1304711 | p.Ala594Glu | missense_variant | 1.0 |
| fbiC | 1304715 | c.1785G>C | synonymous_variant | 1.0 |
| fbiC | 1304724 | c.1794A>G | synonymous_variant | 1.0 |
| fbiC | 1304727 | c.1797A>G | synonymous_variant | 1.0 |
| fbiC | 1304742 | c.1812T>C | synonymous_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| fbiC | 1304778 | c.1848T>C | synonymous_variant | 1.0 |
| fbiC | 1304784 | c.1854T>C | synonymous_variant | 1.0 |
| fbiC | 1304787 | c.1857T>G | synonymous_variant | 1.0 |
| fbiC | 1304808 | c.1878C>G | synonymous_variant | 1.0 |
| fbiC | 1304811 | c.1881C>G | synonymous_variant | 1.0 |
| fbiC | 1304817 | c.1887T>C | synonymous_variant | 1.0 |
| fbiC | 1304829 | c.1899T>C | synonymous_variant | 1.0 |
| fbiC | 1304832 | c.1902C>T | synonymous_variant | 1.0 |
| fbiC | 1304856 | c.1926C>G | synonymous_variant | 1.0 |
| fbiC | 1304869 | c.1939C>T | synonymous_variant | 1.0 |
| fbiC | 1304875 | p.Ile649Val | missense_variant | 1.0 |
| fbiC | 1304883 | p.Glu651Asp | missense_variant | 1.0 |
| fbiC | 1304891 | p.Ile654Thr | missense_variant | 1.0 |
| fbiC | 1304893 | p.Gly655Ser | missense_variant | 1.0 |
| fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.92 |
| fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.98 |
| fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.99 |
| fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.99 |
| fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.99 |
| fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.99 |
| fbiC | 1304983 | c.2053C>T | synonymous_variant | 1.0 |
| fbiC | 1304994 | c.2064A>G | synonymous_variant | 1.0 |
| fbiC | 1304995 | p.Leu689Met | missense_variant | 1.0 |
| fbiC | 1305006 | c.2076A>G | synonymous_variant | 1.0 |
| fbiC | 1305012 | c.2082G>C | synonymous_variant | 1.0 |
| fbiC | 1305015 | c.2085G>C | synonymous_variant | 1.0 |
| fbiC | 1305021 | c.2091C>G | synonymous_variant | 1.0 |
| fbiC | 1305030 | c.2100G>C | synonymous_variant | 1.0 |
| fbiC | 1305033 | c.2103T>G | synonymous_variant | 1.0 |
| fbiC | 1305042 | c.2112A>G | synonymous_variant | 1.0 |
| fbiC | 1305045 | c.2115A>G | synonymous_variant | 1.0 |
| fbiC | 1305114 | c.2184T>C | synonymous_variant | 1.0 |
| fbiC | 1305117 | c.2187T>C | synonymous_variant | 1.0 |
| fbiC | 1305126 | c.2196T>C | synonymous_variant | 0.95 |
| fbiC | 1305135 | c.2205C>T | synonymous_variant | 0.96 |
| fbiC | 1305150 | c.2220C>G | synonymous_variant | 0.96 |
| fbiC | 1305154 | c.2224_2226delTTGinsCTA | synonymous_variant | 0.96 |
| fbiC | 1305173 | p.Asn748Ser | missense_variant | 0.93 |
| fbiC | 1305177 | c.2247A>G | synonymous_variant | 0.93 |
| fbiC | 1305181 | c.2251T>C | synonymous_variant | 0.93 |
| fbiC | 1305186 | c.2256C>T | synonymous_variant | 0.93 |
| fbiC | 1305195 | c.2265T>C | synonymous_variant | 0.89 |
| fbiC | 1305201 | c.2271G>C | synonymous_variant | 1.0 |
| fbiC | 1305204 | c.2274C>G | synonymous_variant | 1.0 |
| fbiC | 1305210 | c.2280G>A | synonymous_variant | 1.0 |
| fbiC | 1305215 | p.Ser762Thr | missense_variant | 1.0 |
| fbiC | 1305231 | c.2301C>A | synonymous_variant | 1.0 |
| fbiC | 1305234 | c.2304G>C | synonymous_variant | 1.0 |
| fbiC | 1305240 | c.2310T>C | synonymous_variant | 1.0 |
| fbiC | 1305243 | c.2313T>G | synonymous_variant | 1.0 |
| fbiC | 1305244 | c.2314T>C | synonymous_variant | 1.0 |
| fbiC | 1305252 | c.2322G>A | synonymous_variant | 1.0 |
| fbiC | 1305276 | c.2346G>C | synonymous_variant | 1.0 |
| fbiC | 1305279 | p.His783Gln | missense_variant | 1.0 |
| fbiC | 1305282 | c.2352T>C | synonymous_variant | 1.0 |
| fbiC | 1305297 | c.2367G>C | synonymous_variant | 1.0 |
| fbiC | 1305318 | c.2388C>G | synonymous_variant | 1.0 |
| fbiC | 1305331 | p.Glu801Asn | missense_variant | 1.0 |
| fbiC | 1305336 | c.2406T>C | synonymous_variant | 1.0 |
| fbiC | 1305372 | c.2442G>A | synonymous_variant | 1.0 |
| fbiC | 1305384 | c.2454G>C | synonymous_variant | 1.0 |
| fbiC | 1305396 | c.2466C>G | synonymous_variant | 1.0 |
| fbiC | 1305405 | c.2475A>G | synonymous_variant | 1.0 |
| fbiC | 1305417 | c.2487C>G | synonymous_variant | 1.0 |
| fbiC | 1305423 | c.2493T>C | synonymous_variant | 1.0 |
| fbiC | 1305430 | p.Val834Thr | missense_variant | 1.0 |
| fbiC | 1305444 | c.2514A>G | synonymous_variant | 1.0 |
| fbiC | 1305453 | c.2523C>G | synonymous_variant | 1.0 |
| fbiC | 1305456 | c.2526C>A | synonymous_variant | 1.0 |
| fbiC | 1305459 | c.2529G>C | synonymous_variant | 1.0 |
| atpE | 1460852 | c.-193C>G | upstream_gene_variant | 1.0 |
| atpE | 1460855 | c.-190T>C | upstream_gene_variant | 0.93 |
| atpE | 1460882 | c.-163T>C | upstream_gene_variant | 1.0 |
| atpE | 1460894 | c.-151A>G | upstream_gene_variant | 1.0 |
| atpE | 1460897 | c.-148A>C | upstream_gene_variant | 1.0 |
| atpE | 1460900 | c.-145T>C | upstream_gene_variant | 1.0 |
| atpE | 1460915 | c.-130C>G | upstream_gene_variant | 1.0 |
| atpE | 1460918 | c.-127A>G | upstream_gene_variant | 1.0 |
| atpE | 1460933 | c.-112T>C | upstream_gene_variant | 1.0 |
| atpE | 1461089 | c.45G>C | synonymous_variant | 1.0 |
| atpE | 1461097 | p.Ala18Gly | missense_variant | 1.0 |
| atpE | 1461101 | c.57T>C | synonymous_variant | 1.0 |
| atpE | 1461107 | c.63C>G | synonymous_variant | 1.0 |
| atpE | 1461113 | c.69C>T | synonymous_variant | 1.0 |
| atpE | 1461132 | p.Val30Ile | missense_variant | 1.0 |
| atpE | 1461149 | c.105T>G | synonymous_variant | 1.0 |
| atpE | 1461150 | p.Ile36Val | missense_variant | 1.0 |
| atpE | 1461158 | c.114T>G | synonymous_variant | 1.0 |
| atpE | 1461159 | p.Val39Ile | missense_variant | 1.0 |
| atpE | 1461170 | c.126A>G | synonymous_variant | 1.0 |
| atpE | 1461185 | c.141G>T | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>G | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461233 | c.189A>C | synonymous_variant | 1.0 |
| atpE | 1461251 | c.207G>C | synonymous_variant | 1.0 |
| atpE | 1461254 | c.210T>C | synonymous_variant | 1.0 |
| atpE | 1461275 | c.231T>A | synonymous_variant | 1.0 |
| rrs | 1471647 | n.-199G>A | upstream_gene_variant | 1.0 |
| rrs | 1471648 | n.-198A>G | upstream_gene_variant | 1.0 |
| rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
| rrs | 1471665 | n.-181G>A | upstream_gene_variant | 1.0 |
| rrs | 1471668 | n.-178G>A | upstream_gene_variant | 1.0 |
| rrs | 1471673 | n.-172delG | upstream_gene_variant | 1.0 |
| rrs | 1471681 | n.-164_-159delGCAAGC | upstream_gene_variant | 1.0 |
| rrs | 1471720 | n.-126G>C | upstream_gene_variant | 1.0 |
| rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472044 | n.199G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472300 | n.455C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473403 | n.-255C>T | upstream_gene_variant | 1.0 |
| rrl | 1473408 | n.-250C>T | upstream_gene_variant | 1.0 |
| rrl | 1473417 | n.-241C>T | upstream_gene_variant | 1.0 |
| rrl | 1473419 | n.-239T>C | upstream_gene_variant | 1.0 |
| rrl | 1473420 | n.-238A>G | upstream_gene_variant | 1.0 |
| rrl | 1473421 | n.-237G>A | upstream_gene_variant | 1.0 |
| rrl | 1473437 | n.-221T>C | upstream_gene_variant | 1.0 |
| rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473938 | n.281G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473939 | n.282C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473981 | n.324G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474044 | n.387C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474091 | n.434C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474439 | n.782A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474961 | n.1304T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474963 | n.1306G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474964 | n.1307T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475028 | n.1371G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476031 | n.2374C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476048 | n.2391G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476717 | n.3060C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476755 | n.3098G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476759 | n.3102T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476770 | n.3113T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476771 | n.3114G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476790 | n.3134dupC | non_coding_transcript_exon_variant | 1.0 |
| fabG1 | 1673273 | c.-167C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673285 | c.-155A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673288 | c.-152G>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673301 | c.-138delT | upstream_gene_variant | 1.0 |
| fabG1 | 1673304 | c.-136_-135insCA | upstream_gene_variant | 1.0 |
| inhA | 1673468 | c.-734A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673473 | p.Pro12Ala | missense_variant | 1.0 |
| fabG1 | 1673482 | p.Ser15Ala | missense_variant | 1.0 |
| inhA | 1673487 | c.-715T>C | upstream_gene_variant | 1.0 |
| inhA | 1673490 | c.-712A>G | upstream_gene_variant | 1.0 |
| inhA | 1673523 | c.-679G>T | upstream_gene_variant | 1.0 |
| inhA | 1673535 | c.-667A>G | upstream_gene_variant | 1.0 |
| inhA | 1673547 | c.-655T>C | upstream_gene_variant | 1.0 |
| inhA | 1673556 | c.-646C>G | upstream_gene_variant | 1.0 |
| inhA | 1673568 | c.-634C>G | upstream_gene_variant | 1.0 |
| inhA | 1673574 | c.-628C>G | upstream_gene_variant | 1.0 |
| inhA | 1673580 | c.-622T>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673633 | p.Ser65Asn | missense_variant | 1.0 |
| fabG1 | 1673637 | p.Asp66Glu | missense_variant | 1.0 |
| fabG1 | 1673641 | p.Val68Ile | missense_variant | 1.0 |
| inhA | 1673646 | c.-556T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673657 | p.Thr73Lys | missense_variant | 1.0 |
| inhA | 1673660 | c.-542C>A | upstream_gene_variant | 1.0 |
| inhA | 1673664 | c.-538A>C | upstream_gene_variant | 1.0 |
| inhA | 1673667 | c.-535A>G | upstream_gene_variant | 1.0 |
| inhA | 1673679 | c.-523T>C | upstream_gene_variant | 1.0 |
| inhA | 1673685 | c.-517C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673710 | p.Leu91Ile | missense_variant | 1.0 |
| fabG1 | 1673716 | p.Ala93Lys | missense_variant | 1.0 |
| fabG1 | 1673733 | p.Met98Ile | missense_variant | 1.0 |
| inhA | 1673748 | c.-454A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673749 | p.Lys104Arg | missense_variant | 1.0 |
| fabG1 | 1673758 | p.Lys107Glu | missense_variant | 1.0 |
| inhA | 1673784 | c.-418G>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673797 | p.Ala120Thr | missense_variant | 1.0 |
| inhA | 1673802 | c.-400A>G | upstream_gene_variant | 1.0 |
| inhA | 1673805 | c.-397G>C | upstream_gene_variant | 1.0 |
| inhA | 1673808 | c.-394A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673809 | p.Ser124Ala | missense_variant | 1.0 |
| inhA | 1673856 | c.-346T>C | upstream_gene_variant | 1.0 |
| inhA | 1673862 | c.-340C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673890 | p.Ala151Ser | missense_variant | 1.0 |
| inhA | 1673901 | c.-301A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673905 | p.Ser156Ala | missense_variant | 1.0 |
| inhA | 1673916 | c.-286A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673917 | p.Val160Leu | missense_variant | 1.0 |
| inhA | 1673922 | c.-280T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673941 | p.Ala168Ser | missense_variant | 1.0 |
| inhA | 1673955 | c.-247G>C | upstream_gene_variant | 1.0 |
| inhA | 1673961 | c.-241A>C | upstream_gene_variant | 1.0 |
| inhA | 1673985 | c.-217C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1674006 | p.Asp189Glu | missense_variant | 1.0 |
| inhA | 1674015 | c.-187C>T | upstream_gene_variant | 1.0 |
| inhA | 1674018 | c.-184G>C | upstream_gene_variant | 1.0 |
| inhA | 1674021 | c.-181G>C | upstream_gene_variant | 1.0 |
| inhA | 1674024 | c.-178T>C | upstream_gene_variant | 1.0 |
| inhA | 1674033 | c.-169T>C | upstream_gene_variant | 1.0 |
| inhA | 1674054 | c.-148T>C | upstream_gene_variant | 1.0 |
| inhA | 1674060 | c.-142A>G | upstream_gene_variant | 1.0 |
| inhA | 1674063 | c.-139G>C | upstream_gene_variant | 1.0 |
| fabG1 | 1674079 | p.Pro214Ala | missense_variant | 1.0 |
| inhA | 1674114 | c.-88T>A | upstream_gene_variant | 1.0 |
| inhA | 1674123 | c.-79T>C | upstream_gene_variant | 1.0 |
| inhA | 1674126 | c.-76G>C | upstream_gene_variant | 1.0 |
| inhA | 1674132 | c.-70T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1674136 | p.Ser233Ala | missense_variant | 1.0 |
| inhA | 1674141 | c.-61T>C | upstream_gene_variant | 1.0 |
| inhA | 1674177 | c.-25C>T | upstream_gene_variant | 1.0 |
| inhA | 1674184 | c.-18C>T | upstream_gene_variant | 1.0 |
| inhA | 1674199 | c.-3C>G | upstream_gene_variant | 1.0 |
| inhA | 1674205 | p.Thr2Ala | missense_variant | 1.0 |
| inhA | 1674216 | c.15G>C | synonymous_variant | 1.0 |
| inhA | 1674231 | c.30T>C | synonymous_variant | 1.0 |
| inhA | 1674235 | p.Val12Ile | missense_variant | 1.0 |
| inhA | 1674238 | c.37_39delAGCinsTCG | synonymous_variant | 1.0 |
| inhA | 1674243 | c.42A>G | synonymous_variant | 1.0 |
| inhA | 1674331 | c.130C>T | synonymous_variant | 1.0 |
| inhA | 1674336 | c.135G>C | synonymous_variant | 1.0 |
| inhA | 1674352 | p.Thr51Ala | missense_variant | 1.0 |
| inhA | 1674368 | p.Ala56Glu | missense_variant | 1.0 |
| inhA | 1674375 | c.174C>G | synonymous_variant | 1.0 |
| inhA | 1674382 | p.Leu61Ile | missense_variant | 1.0 |
| inhA | 1674387 | c.186A>G | synonymous_variant | 1.0 |
| inhA | 1674399 | c.198A>G | synonymous_variant | 1.0 |
| inhA | 1674453 | c.252G>C | synonymous_variant | 1.0 |
| inhA | 1674471 | c.270G>C | synonymous_variant | 1.0 |
| inhA | 1674480 | c.279T>C | synonymous_variant | 1.0 |
| inhA | 1674486 | c.285T>C | synonymous_variant | 1.0 |
| inhA | 1674504 | c.303C>G | synonymous_variant | 0.99 |
| inhA | 1674507 | c.306G>T | synonymous_variant | 1.0 |
| inhA | 1674537 | c.336C>G | synonymous_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674546 | c.345T>C | synonymous_variant | 1.0 |
| inhA | 1674549 | c.348G>C | synonymous_variant | 1.0 |
| inhA | 1674555 | c.354G>A | synonymous_variant | 1.0 |
| inhA | 1674561 | c.360C>T | synonymous_variant | 1.0 |
| inhA | 1674582 | c.381T>C | synonymous_variant | 0.99 |
| inhA | 1674585 | c.384T>C | synonymous_variant | 0.99 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 0.99 |
| inhA | 1674601 | p.Leu134Thr | missense_variant | 0.98 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 0.99 |
| inhA | 1674630 | c.429C>G | synonymous_variant | 0.99 |
| inhA | 1674660 | c.459G>C | synonymous_variant | 1.0 |
| inhA | 1674672 | c.471C>G | synonymous_variant | 1.0 |
| inhA | 1674703 | c.502T>C | synonymous_variant | 1.0 |
| inhA | 1674708 | c.507G>A | synonymous_variant | 1.0 |
| inhA | 1674718 | c.517A>C | synonymous_variant | 1.0 |
| inhA | 1674738 | c.537C>G | synonymous_variant | 0.98 |
| inhA | 1674741 | c.540C>T | synonymous_variant | 0.98 |
| inhA | 1674746 | p.Tyr182Phe | missense_variant | 0.98 |
| inhA | 1674750 | c.549T>C | synonymous_variant | 0.98 |
| inhA | 1674753 | c.552G>C | synonymous_variant | 0.98 |
| inhA | 1674756 | c.555T>C | synonymous_variant | 0.98 |
| inhA | 1674759 | c.558G>C | synonymous_variant | 0.98 |
| inhA | 1674774 | c.573A>G | synonymous_variant | 0.98 |
| inhA | 1674780 | c.579T>G | synonymous_variant | 0.98 |
| inhA | 1674789 | c.588G>C | synonymous_variant | 0.98 |
| inhA | 1674801 | c.600T>C | synonymous_variant | 1.0 |
| inhA | 1674816 | c.615T>C | synonymous_variant | 1.0 |
| inhA | 1674822 | c.621C>G | synonymous_variant | 1.0 |
| inhA | 1674828 | c.627G>A | synonymous_variant | 1.0 |
| inhA | 1674846 | p.Ile215Met | missense_variant | 1.0 |
| inhA | 1674864 | c.663C>T | synonymous_variant | 1.0 |
| inhA | 1674870 | c.669T>C | synonymous_variant | 1.0 |
| inhA | 1674879 | c.678T>C | synonymous_variant | 1.0 |
| inhA | 1674888 | c.687C>G | synonymous_variant | 1.0 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 1.0 |
| inhA | 1674904 | p.Ala235Pro | missense_variant | 1.0 |
| inhA | 1674942 | c.741T>G | synonymous_variant | 1.0 |
| inhA | 1674954 | c.753G>C | synonymous_variant | 1.0 |
| inhA | 1674960 | c.759C>G | synonymous_variant | 1.0 |
| inhA | 1674966 | c.765T>G | synonymous_variant | 1.0 |
| inhA | 1674967 | p.Asp256Thr | missense_variant | 0.97 |
| inhA | 1674987 | c.786C>T | synonymous_variant | 1.0 |
| inhA | 1674993 | c.792G>C | synonymous_variant | 1.0 |
| rpsA | 1833367 | c.-175G>T | upstream_gene_variant | 0.95 |
| rpsA | 1833500 | c.-41delC | upstream_gene_variant | 1.0 |
| rpsA | 1833532 | c.-10A>C | upstream_gene_variant | 1.0 |
| rpsA | 1833554 | p.Thr5Ala | missense_variant | 1.0 |
| rpsA | 1833568 | c.27G>C | synonymous_variant | 0.99 |
| rpsA | 1833589 | c.48A>T | synonymous_variant | 0.99 |
| rpsA | 1833595 | c.54T>C | synonymous_variant | 0.99 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
| rpsA | 1833667 | c.126C>G | synonymous_variant | 1.0 |
| rpsA | 1833721 | c.180A>G | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>G | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833940 | c.399C>G | synonymous_variant | 1.0 |
| rpsA | 1833971 | c.430C>T | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 0.99 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 0.99 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 0.99 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 0.99 |
| rpsA | 1834099 | c.558C>G | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>G | synonymous_variant | 1.0 |
| rpsA | 1834108 | c.567C>G | synonymous_variant | 1.0 |
| rpsA | 1834123 | c.582C>G | synonymous_variant | 1.0 |
| rpsA | 1834150 | c.609G>C | synonymous_variant | 0.93 |
| rpsA | 1834153 | c.612T>C | synonymous_variant | 0.9 |
| rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.9 |
| rpsA | 1834157 | c.616T>C | synonymous_variant | 0.9 |
| rpsA | 1834162 | c.621A>G | synonymous_variant | 0.9 |
| rpsA | 1834165 | c.624A>G | synonymous_variant | 0.9 |
| rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.9 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 0.94 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 0.97 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 0.98 |
| rpsA | 1834210 | c.669C>T | synonymous_variant | 0.97 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834262 | c.721_723delTCGinsAGC | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834333 | c.792C>T | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834435 | c.894G>C | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpsA | 1834540 | c.999G>C | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>G | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834618 | c.1077G>C | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834654 | p.Glu371Asp | missense_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834733 | p.Ala398Ser | missense_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834775 | p.Ala412Thr | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834789 | c.1248T>C | synonymous_variant | 1.0 |
| rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
| rpsA | 1834849 | c.1308C>G | synonymous_variant | 1.0 |
| rpsA | 1834852 | c.1311C>G | synonymous_variant | 1.0 |
| rpsA | 1834864 | c.1323T>C | synonymous_variant | 1.0 |
| tlyA | 1917900 | c.-40T>C | upstream_gene_variant | 1.0 |
| tlyA | 1917908 | c.-32C>G | upstream_gene_variant | 1.0 |
| tlyA | 1917929 | c.-11T>C | upstream_gene_variant | 1.0 |
| tlyA | 1917937 | c.-3_-2insC | upstream_gene_variant | 1.0 |
| tlyA | 1917940 | p.Val1Met | missense_variant | 1.0 |
| tlyA | 1917943 | p.Ala2Ser | missense_variant | 1.0 |
| tlyA | 1917951 | c.12T>C | synonymous_variant | 1.0 |
| tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
| tlyA | 1917975 | c.36C>G | synonymous_variant | 1.0 |
| tlyA | 1917981 | c.42G>C | synonymous_variant | 0.97 |
| tlyA | 1917984 | c.45C>G | synonymous_variant | 0.96 |
| tlyA | 1917990 | c.51G>C | synonymous_variant | 1.0 |
| tlyA | 1917993 | c.54A>G | synonymous_variant | 1.0 |
| tlyA | 1917996 | c.57A>G | synonymous_variant | 1.0 |
| tlyA | 1918002 | c.63A>G | synonymous_variant | 1.0 |
| tlyA | 1918036 | p.Arg33Ser | missense_variant | 1.0 |
| tlyA | 1918048 | p.Leu37Met | missense_variant | 1.0 |
| tlyA | 1918053 | c.114G>C | synonymous_variant | 1.0 |
| tlyA | 1918057 | p.Val40Arg | missense_variant | 1.0 |
| tlyA | 1918065 | c.126G>C | synonymous_variant | 1.0 |
| tlyA | 1918067 | p.Ala43Gly | missense_variant | 1.0 |
| tlyA | 1918197 | c.258T>C | synonymous_variant | 1.0 |
| tlyA | 1918206 | c.267G>C | synonymous_variant | 1.0 |
| tlyA | 1918212 | c.273A>G | synonymous_variant | 1.0 |
| tlyA | 1918218 | c.279C>G | synonymous_variant | 1.0 |
| tlyA | 1918221 | c.282T>C | synonymous_variant | 1.0 |
| tlyA | 1918224 | c.285G>C | synonymous_variant | 1.0 |
| tlyA | 1918236 | c.297A>C | synonymous_variant | 1.0 |
| tlyA | 1918245 | c.306C>T | synonymous_variant | 1.0 |
| tlyA | 1918251 | c.312T>G | synonymous_variant | 1.0 |
| tlyA | 1918255 | p.Ala106Thr | missense_variant | 1.0 |
| tlyA | 1918258 | p.His107Glu | missense_variant | 1.0 |
| tlyA | 1918266 | c.327G>T | synonymous_variant | 1.0 |
| tlyA | 1918271 | p.Ala111Val | missense_variant | 1.0 |
| tlyA | 1918278 | c.339C>G | synonymous_variant | 1.0 |
| tlyA | 1918281 | c.342A>G | synonymous_variant | 1.0 |
| tlyA | 1918310 | p.Asn124Ser | missense_variant | 0.89 |
| tlyA | 1918315 | p.Pro126Ser | missense_variant | 0.89 |
| tlyA | 1918323 | c.384G>T | synonymous_variant | 0.88 |
| tlyA | 1918326 | c.387G>C | synonymous_variant | 0.88 |
| tlyA | 1918330 | p.Leu131Val | missense_variant | 0.88 |
| tlyA | 1918417 | c.478T>C | synonymous_variant | 1.0 |
| tlyA | 1918422 | c.483T>C | synonymous_variant | 1.0 |
| tlyA | 1918434 | c.495C>G | synonymous_variant | 1.0 |
| ndh | 2101732 | c.1311T>C | synonymous_variant | 1.0 |
| ndh | 2101735 | c.1308A>G | synonymous_variant | 1.0 |
| ndh | 2101744 | p.Asp433Glu | missense_variant | 1.0 |
| ndh | 2101756 | c.1287G>C | synonymous_variant | 1.0 |
| ndh | 2101765 | c.1278C>G | synonymous_variant | 1.0 |
| ndh | 2101768 | c.1275C>A | synonymous_variant | 1.0 |
| ndh | 2101771 | c.1272T>G | synonymous_variant | 1.0 |
| ndh | 2101774 | c.1269T>C | synonymous_variant | 1.0 |
| ndh | 2101777 | c.1266C>G | synonymous_variant | 1.0 |
| ndh | 2101783 | c.1260T>A | synonymous_variant | 1.0 |
| ndh | 2101804 | c.1239T>G | synonymous_variant | 1.0 |
| ndh | 2101808 | p.Thr412Ser | missense_variant | 1.0 |
| ndh | 2101830 | p.Ile405Val | missense_variant | 1.0 |
| ndh | 2101837 | p.Ala402Val | missense_variant | 1.0 |
| ndh | 2101858 | p.Ile395Met | missense_variant | 1.0 |
| ndh | 2101893 | c.1149delT | frameshift_variant | 1.0 |
| ndh | 2101912 | c.1131G>C | synonymous_variant | 1.0 |
| ndh | 2101920 | c.1123A>C | synonymous_variant | 1.0 |
| ndh | 2101924 | c.1119T>G | synonymous_variant | 1.0 |
| ndh | 2101939 | c.1104A>G | synonymous_variant | 1.0 |
| ndh | 2101960 | c.1083A>G | synonymous_variant | 1.0 |
| ndh | 2101963 | c.1080G>A | synonymous_variant | 1.0 |
| ndh | 2101966 | c.1077T>G | synonymous_variant | 1.0 |
| ndh | 2101972 | c.1071G>C | synonymous_variant | 1.0 |
| ndh | 2101988 | p.Ala352Asp | missense_variant | 1.0 |
| ndh | 2101990 | c.1053G>C | synonymous_variant | 1.0 |
| ndh | 2101993 | c.1050A>G | synonymous_variant | 1.0 |
| ndh | 2102011 | c.1032C>G | synonymous_variant | 1.0 |
| ndh | 2102014 | c.1029C>G | synonymous_variant | 1.0 |
| ndh | 2102020 | c.1023A>G | synonymous_variant | 1.0 |
| ndh | 2102023 | c.1020G>C | synonymous_variant | 1.0 |
| ndh | 2102026 | c.1017G>C | synonymous_variant | 1.0 |
| ndh | 2102038 | c.1005C>A | synonymous_variant | 1.0 |
| ndh | 2102194 | c.849T>C | synonymous_variant | 1.0 |
| ndh | 2102206 | c.837G>C | synonymous_variant | 1.0 |
| ndh | 2102212 | c.831G>C | synonymous_variant | 1.0 |
| ndh | 2102218 | c.825C>A | synonymous_variant | 1.0 |
| ndh | 2102227 | c.816C>T | synonymous_variant | 1.0 |
| ndh | 2102230 | c.813G>C | synonymous_variant | 0.98 |
| ndh | 2102233 | c.810G>A | synonymous_variant | 1.0 |
| ndh | 2102302 | c.741G>C | synonymous_variant | 1.0 |
| ndh | 2102305 | c.738T>C | synonymous_variant | 1.0 |
| ndh | 2102314 | c.729C>T | synonymous_variant | 1.0 |
| ndh | 2102317 | c.726A>G | synonymous_variant | 1.0 |
| ndh | 2102328 | p.Leu239Met | missense_variant | 1.0 |
| ndh | 2102332 | c.711G>A | synonymous_variant | 1.0 |
| ndh | 2102610 | c.433T>C | synonymous_variant | 1.0 |
| ndh | 2102623 | c.420C>G | synonymous_variant | 1.0 |
| ndh | 2102635 | c.408C>G | synonymous_variant | 0.96 |
| ndh | 2102638 | c.405A>C | synonymous_variant | 1.0 |
| ndh | 2102644 | c.399A>G | synonymous_variant | 1.0 |
| ndh | 2102671 | c.372T>G | synonymous_variant | 1.0 |
| ndh | 2102680 | c.363T>G | synonymous_variant | 1.0 |
| ndh | 2102683 | c.360T>C | synonymous_variant | 1.0 |
| ndh | 2102695 | c.348C>T | synonymous_variant | 1.0 |
| ndh | 2102700 | c.343C>T | synonymous_variant | 1.0 |
| ndh | 2102710 | c.333C>T | synonymous_variant | 1.0 |
| ndh | 2102718 | p.Gln109Glu | missense_variant | 1.0 |
| ndh | 2102728 | c.315T>C | synonymous_variant | 1.0 |
| ndh | 2102736 | c.307T>C | synonymous_variant | 1.0 |
| ndh | 2102737 | p.Glu102Asp | missense_variant | 1.0 |
| ndh | 2102743 | c.300C>G | synonymous_variant | 1.0 |
| ndh | 2102750 | p.Cys98Phe | missense_variant | 1.0 |
| ndh | 2102754 | p.Gln97Lys | missense_variant | 1.0 |
| ndh | 2102755 | c.288G>C | synonymous_variant | 1.0 |
| ndh | 2102758 | c.285C>G | synonymous_variant | 1.0 |
| ndh | 2102773 | c.270C>G | synonymous_variant | 1.0 |
| ndh | 2102781 | p.Asn88Asp | missense_variant | 1.0 |
| ndh | 2102785 | c.256_258delTTGinsCTC | synonymous_variant | 1.0 |
| ndh | 2102790 | c.253C>T | synonymous_variant | 1.0 |
| ndh | 2102791 | c.252A>G | synonymous_variant | 1.0 |
| ndh | 2102800 | c.243T>C | synonymous_variant | 1.0 |
| ndh | 2102810 | p.Lys78Arg | missense_variant | 1.0 |
| ndh | 2102812 | c.231T>C | synonymous_variant | 1.0 |
| ndh | 2102872 | c.171A>G | synonymous_variant | 1.0 |
| ndh | 2102893 | c.150G>C | synonymous_variant | 1.0 |
| ndh | 2102899 | c.144T>C | synonymous_variant | 1.0 |
| ndh | 2102902 | c.141C>G | synonymous_variant | 1.0 |
| ndh | 2102911 | c.132G>C | synonymous_variant | 1.0 |
| ndh | 2102920 | c.123G>A | synonymous_variant | 1.0 |
| ndh | 2102929 | c.114T>C | synonymous_variant | 1.0 |
| ndh | 2102934 | p.Asp37Asn | missense_variant | 1.0 |
| ndh | 2102938 | p.Arg35His | missense_variant | 1.0 |
| katG | 2154992 | p.Ser374Ala | missense_variant | 1.0 |
| katG | 2154993 | c.1119C>G | synonymous_variant | 1.0 |
| katG | 2155001 | p.Pro371Ala | missense_variant | 1.0 |
| katG | 2155002 | c.1110G>T | synonymous_variant | 1.0 |
| katG | 2155017 | c.1095G>C | synonymous_variant | 1.0 |
| katG | 2155023 | c.1089C>G | synonymous_variant | 1.0 |
| katG | 2155029 | c.1083C>G | synonymous_variant | 1.0 |
| katG | 2155035 | c.1077C>G | synonymous_variant | 1.0 |
| katG | 2155054 | p.Tyr353Phe | missense_variant | 1.0 |
| katG | 2155056 | c.1056A>G | synonymous_variant | 1.0 |
| katG | 2155062 | c.1050T>G | synonymous_variant | 1.0 |
| katG | 2155065 | c.1047C>G | synonymous_variant | 1.0 |
| katG | 2155068 | c.1044T>C | synonymous_variant | 1.0 |
| katG | 2155071 | c.1041T>C | synonymous_variant | 1.0 |
| katG | 2155080 | c.1032G>C | synonymous_variant | 1.0 |
| katG | 2155092 | c.1020G>A | synonymous_variant | 1.0 |
| katG | 2155106 | c.1006C>T | synonymous_variant | 1.0 |
| katG | 2155113 | c.999C>G | synonymous_variant | 1.0 |
| katG | 2155119 | c.993T>C | synonymous_variant | 1.0 |
| katG | 2155131 | c.981A>G | synonymous_variant | 1.0 |
| katG | 2155152 | c.960A>C | synonymous_variant | 1.0 |
| katG | 2155155 | c.957C>G | synonymous_variant | 1.0 |
| katG | 2155179 | c.933C>T | synonymous_variant | 1.0 |
| katG | 2155185 | c.927T>C | synonymous_variant | 1.0 |
| katG | 2155188 | p.Thr308Ser | missense_variant | 1.0 |
| katG | 2155191 | c.921A>T | synonymous_variant | 1.0 |
| katG | 2155200 | c.912T>C | synonymous_variant | 1.0 |
| katG | 2155626 | c.486G>C | synonymous_variant | 0.92 |
| katG | 2155632 | c.480A>C | synonymous_variant | 0.95 |
| katG | 2155637 | p.Leu159Ile | missense_variant | 0.96 |
| katG | 2155641 | p.Lys157Asn | missense_variant | 0.97 |
| katG | 2155661 | p.Val151Ile | missense_variant | 0.97 |
| katG | 2155668 | c.444G>T | synonymous_variant | 0.97 |
| katG | 2155677 | c.435C>A | synonymous_variant | 1.0 |
| katG | 2155680 | c.432G>C | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155695 | c.417C>G | synonymous_variant | 1.0 |
| katG | 2155704 | c.408C>G | synonymous_variant | 1.0 |
| katG | 2155716 | c.396T>G | synonymous_variant | 1.0 |
| katG | 2155722 | c.390G>C | synonymous_variant | 1.0 |
| katG | 2155728 | c.384G>C | synonymous_variant | 1.0 |
| katG | 2155740 | p.Gly124Gln | missense_variant | 1.0 |
| katG | 2155743 | c.369G>C | synonymous_variant | 1.0 |
| katG | 2155782 | c.330C>G | synonymous_variant | 1.0 |
| katG | 2155785 | c.327T>C | synonymous_variant | 1.0 |
| katG | 2155794 | p.Ala106Ser | missense_variant | 1.0 |
| katG | 2155806 | c.306T>C | synonymous_variant | 1.0 |
| katG | 2155812 | p.Pro100Ala | missense_variant | 1.0 |
| katG | 2155815 | c.297G>C | synonymous_variant | 1.0 |
| pncA | 2289858 | c.-617G>C | upstream_gene_variant | 1.0 |
| pncA | 2289871 | c.-632_-630delCTTinsTTG | upstream_gene_variant | 1.0 |
| pncA | 2289874 | c.-633C>G | upstream_gene_variant | 1.0 |
| pncA | 2289880 | c.-639T>C | upstream_gene_variant | 1.0 |
| pncA | 2289883 | c.-642C>G | upstream_gene_variant | 1.0 |
| pncA | 2289892 | c.-651C>G | upstream_gene_variant | 1.0 |
| pncA | 2289895 | c.-654C>G | upstream_gene_variant | 1.0 |
| pncA | 2289906 | c.-665T>C | upstream_gene_variant | 1.0 |
| pncA | 2289907 | c.-666A>C | upstream_gene_variant | 1.0 |
| pncA | 2289913 | c.-672T>C | upstream_gene_variant | 1.0 |
| pncA | 2289925 | c.-684T>C | upstream_gene_variant | 1.0 |
| pncA | 2289930 | c.-689A>G | upstream_gene_variant | 1.0 |
| pncA | 2289943 | c.-702T>G | upstream_gene_variant | 1.0 |
| pncA | 2289948 | c.-707C>T | upstream_gene_variant | 1.0 |
| pncA | 2289949 | c.-708A>G | upstream_gene_variant | 1.0 |
| pncA | 2289987 | c.-746C>T | upstream_gene_variant | 1.0 |
| pncA | 2289988 | c.-747G>C | upstream_gene_variant | 1.0 |
| pncA | 2289991 | c.-750G>C | upstream_gene_variant | 1.0 |
| pncA | 2289994 | c.-753A>G | upstream_gene_variant | 1.0 |
| pncA | 2289997 | c.-756G>C | upstream_gene_variant | 1.0 |
| pncA | 2290000 | c.-759C>T | upstream_gene_variant | 1.0 |
| pncA | 2290009 | c.-768A>C | upstream_gene_variant | 1.0 |
| pncA | 2290015 | c.-774A>C | upstream_gene_variant | 1.0 |
| pncA | 2290024 | c.-783C>G | upstream_gene_variant | 1.0 |
| pncA | 2290030 | c.-791_-789delAATinsCAC | upstream_gene_variant | 1.0 |
| pncA | 2290033 | c.-792C>G | upstream_gene_variant | 1.0 |
| pncA | 2290038 | c.-797G>A | upstream_gene_variant | 1.0 |
| pncA | 2290042 | c.-801T>C | upstream_gene_variant | 1.0 |
| pncA | 2290069 | c.-830_-828delAGCinsGGA | upstream_gene_variant | 1.0 |
| pncA | 2290072 | c.-831T>C | upstream_gene_variant | 1.0 |
| pncA | 2290075 | c.-834C>G | upstream_gene_variant | 1.0 |
| pncA | 2290084 | c.-843T>C | upstream_gene_variant | 1.0 |
| pncA | 2290087 | c.-846T>C | upstream_gene_variant | 1.0 |
| pncA | 2290107 | c.-866T>G | upstream_gene_variant | 1.0 |
| pncA | 2290108 | c.-868_-867delCCinsGG | upstream_gene_variant | 1.0 |
| pncA | 2290112 | c.-871C>A | upstream_gene_variant | 1.0 |
| pncA | 2290114 | c.-873T>C | upstream_gene_variant | 1.0 |
| pncA | 2290120 | c.-881_-879delAATinsGAC | upstream_gene_variant | 1.0 |
| pncA | 2290129 | c.-888C>G | upstream_gene_variant | 1.0 |
| pncA | 2290183 | c.-942T>C | upstream_gene_variant | 1.0 |
| pncA | 2290191 | c.-950C>T | upstream_gene_variant | 1.0 |
| pncA | 2290192 | c.-951A>G | upstream_gene_variant | 1.0 |
| pncA | 2290206 | c.-965C>T | upstream_gene_variant | 1.0 |
| pncA | 2290211 | c.-970G>C | upstream_gene_variant | 1.0 |
| pncA | 2290216 | c.-975T>C | upstream_gene_variant | 1.0 |
| pncA | 2290219 | c.-978C>G | upstream_gene_variant | 1.0 |
| pncA | 2290230 | c.-989T>C | upstream_gene_variant | 1.0 |
| pncA | 2290234 | c.-993T>C | upstream_gene_variant | 1.0 |
| kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.99 |
| kasA | 2517989 | c.-126T>C | upstream_gene_variant | 1.0 |
| kasA | 2517993 | c.-122G>T | upstream_gene_variant | 1.0 |
| kasA | 2518019 | c.-96A>G | upstream_gene_variant | 1.0 |
| kasA | 2518025 | c.-90G>C | upstream_gene_variant | 1.0 |
| kasA | 2518031 | c.-84G>T | upstream_gene_variant | 1.0 |
| kasA | 2518034 | c.-81T>C | upstream_gene_variant | 0.89 |
| kasA | 2518035 | c.-80C>G | upstream_gene_variant | 0.8 |
| kasA | 2518041 | c.-74T>C | upstream_gene_variant | 0.8 |
| kasA | 2518049 | c.-66G>C | upstream_gene_variant | 0.67 |
| kasA | 2518053 | c.-62_-60delATTinsCTG | upstream_gene_variant | 0.6 |
| kasA | 2518059 | c.-56_-54delTCGinsACC | upstream_gene_variant | 0.6 |
| kasA | 2518121 | p.Gln3Lys | missense_variant | 1.0 |
| kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
| kasA | 2518138 | c.24T>C | synonymous_variant | 1.0 |
| kasA | 2518146 | p.Phe11Tyr | missense_variant | 1.0 |
| kasA | 2518162 | c.48G>A | synonymous_variant | 1.0 |
| kasA | 2518174 | c.60A>G | synonymous_variant | 1.0 |
| kasA | 2518190 | p.Ser26Ala | missense_variant | 0.99 |
| kasA | 2518199 | p.Ile29Val | missense_variant | 0.98 |
| kasA | 2518220 | c.106C>T | synonymous_variant | 0.98 |
| kasA | 2518234 | c.120G>A | synonymous_variant | 0.98 |
| kasA | 2518248 | p.Ala45Val | missense_variant | 0.95 |
| kasA | 2518261 | p.Glu49Asp | missense_variant | 0.88 |
| kasA | 2518263 | p.Phe50Tyr | missense_variant | 1.0 |
| kasA | 2518265 | p.Val51Ile | missense_variant | 1.0 |
| kasA | 2518429 | c.315A>C | synonymous_variant | 1.0 |
| kasA | 2518439 | p.Ala109Ser | missense_variant | 1.0 |
| kasA | 2518444 | c.330T>C | synonymous_variant | 1.0 |
| kasA | 2518447 | c.333T>G | synonymous_variant | 1.0 |
| kasA | 2518459 | c.345T>C | synonymous_variant | 1.0 |
| kasA | 2518462 | c.348A>C | synonymous_variant | 1.0 |
| kasA | 2518468 | c.354A>C | synonymous_variant | 1.0 |
| kasA | 2518474 | c.360G>A | synonymous_variant | 1.0 |
| kasA | 2518480 | c.366T>C | synonymous_variant | 1.0 |
| kasA | 2518483 | c.369C>G | synonymous_variant | 1.0 |
| kasA | 2518504 | c.390T>C | synonymous_variant | 1.0 |
| kasA | 2518506 | p.Ala131Glu | missense_variant | 1.0 |
| kasA | 2518519 | c.405G>C | synonymous_variant | 1.0 |
| kasA | 2518528 | c.414C>G | synonymous_variant | 1.0 |
| kasA | 2518540 | c.426T>C | synonymous_variant | 1.0 |
| kasA | 2518561 | c.447T>C | synonymous_variant | 1.0 |
| kasA | 2518567 | c.453G>C | synonymous_variant | 1.0 |
| kasA | 2518570 | c.456G>C | synonymous_variant | 1.0 |
| kasA | 2518574 | p.Ile154Val | missense_variant | 1.0 |
| kasA | 2518579 | c.465T>C | synonymous_variant | 1.0 |
| kasA | 2518588 | c.474T>C | synonymous_variant | 1.0 |
| kasA | 2518591 | c.477G>C | synonymous_variant | 1.0 |
| kasA | 2518609 | p.Met165Ile | missense_variant | 1.0 |
| kasA | 2518624 | c.510C>G | synonymous_variant | 1.0 |
| kasA | 2518639 | c.525G>C | synonymous_variant | 1.0 |
| kasA | 2518657 | c.543G>C | synonymous_variant | 1.0 |
| kasA | 2518672 | c.558G>C | synonymous_variant | 1.0 |
| kasA | 2518678 | c.564C>T | synonymous_variant | 1.0 |
| kasA | 2518684 | c.570C>G | synonymous_variant | 1.0 |
| kasA | 2518693 | c.579C>G | synonymous_variant | 1.0 |
| kasA | 2518696 | c.582C>G | synonymous_variant | 1.0 |
| kasA | 2518702 | c.588C>T | synonymous_variant | 1.0 |
| kasA | 2518705 | c.591T>C | synonymous_variant | 1.0 |
| kasA | 2518711 | c.597A>G | synonymous_variant | 1.0 |
| kasA | 2518714 | c.600A>C | synonymous_variant | 1.0 |
| kasA | 2518732 | c.618C>G | synonymous_variant | 1.0 |
| kasA | 2518744 | c.630C>T | synonymous_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| kasA | 2518768 | c.654C>T | synonymous_variant | 1.0 |
| kasA | 2518777 | c.663C>T | synonymous_variant | 1.0 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
| kasA | 2518789 | c.675G>C | synonymous_variant | 1.0 |
| kasA | 2518792 | c.678C>A | synonymous_variant | 1.0 |
| kasA | 2518795 | c.681C>G | synonymous_variant | 1.0 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
| kasA | 2518864 | c.750G>C | synonymous_variant | 1.0 |
| kasA | 2518879 | c.765A>G | synonymous_variant | 1.0 |
| kasA | 2518885 | c.771T>C | synonymous_variant | 1.0 |
| kasA | 2518898 | c.784T>C | synonymous_variant | 1.0 |
| kasA | 2518906 | c.792A>G | synonymous_variant | 1.0 |
| kasA | 2518910 | p.Leu266Met | missense_variant | 1.0 |
| kasA | 2518921 | c.807T>C | synonymous_variant | 1.0 |
| kasA | 2518936 | c.822C>G | synonymous_variant | 1.0 |
| kasA | 2518939 | c.825T>C | synonymous_variant | 1.0 |
| kasA | 2518942 | c.828T>C | synonymous_variant | 1.0 |
| kasA | 2518951 | c.837G>C | synonymous_variant | 1.0 |
| kasA | 2518954 | c.840C>G | synonymous_variant | 1.0 |
| kasA | 2518963 | c.849T>C | synonymous_variant | 1.0 |
| kasA | 2518969 | c.855T>G | synonymous_variant | 1.0 |
| kasA | 2518975 | c.861C>G | synonymous_variant | 1.0 |
| kasA | 2518979 | c.865A>C | synonymous_variant | 1.0 |
| kasA | 2518990 | c.876T>G | synonymous_variant | 1.0 |
| kasA | 2518993 | c.879C>G | synonymous_variant | 1.0 |
| kasA | 2518999 | c.885G>C | synonymous_variant | 1.0 |
| kasA | 2519008 | c.894C>G | synonymous_variant | 1.0 |
| kasA | 2519017 | c.903G>C | synonymous_variant | 1.0 |
| kasA | 2519020 | c.906G>C | synonymous_variant | 1.0 |
| kasA | 2519021 | p.Ala303Lys | missense_variant | 1.0 |
| kasA | 2519027 | p.Ile305Val | missense_variant | 1.0 |
| kasA | 2519050 | c.936C>G | synonymous_variant | 1.0 |
| kasA | 2519053 | c.939G>C | synonymous_variant | 1.0 |
| kasA | 2519056 | c.942G>C | synonymous_variant | 1.0 |
| kasA | 2519062 | c.948T>G | synonymous_variant | 1.0 |
| kasA | 2519068 | c.954C>T | synonymous_variant | 1.0 |
| kasA | 2519072 | p.Ala320Thr | missense_variant | 1.0 |
| kasA | 2519095 | c.981C>A | synonymous_variant | 1.0 |
| kasA | 2519107 | c.993T>C | synonymous_variant | 1.0 |
| kasA | 2519108 | p.Asp332Gln | missense_variant | 1.0 |
| kasA | 2519116 | c.1002C>G | synonymous_variant | 1.0 |
| kasA | 2519122 | c.1008G>C | synonymous_variant | 1.0 |
| kasA | 2519137 | c.1023T>G | synonymous_variant | 1.0 |
| kasA | 2519158 | c.1044C>T | synonymous_variant | 1.0 |
| kasA | 2519167 | c.1053T>G | synonymous_variant | 1.0 |
| kasA | 2519173 | c.1059C>G | synonymous_variant | 1.0 |
| kasA | 2519196 | p.Thr361Ser | missense_variant | 1.0 |
| kasA | 2519215 | c.1101C>T | synonymous_variant | 1.0 |
| kasA | 2519218 | c.1104G>A | synonymous_variant | 1.0 |
| kasA | 2519221 | c.1107G>C | synonymous_variant | 1.0 |
| kasA | 2519227 | c.1113G>C | synonymous_variant | 1.0 |
| kasA | 2519230 | c.1116C>T | synonymous_variant | 1.0 |
| kasA | 2519236 | c.1122G>A | synonymous_variant | 1.0 |
| kasA | 2519239 | c.1125A>C | synonymous_variant | 1.0 |
| kasA | 2519245 | c.1131T>C | synonymous_variant | 1.0 |
| kasA | 2519260 | c.1146T>G | synonymous_variant | 1.0 |
| kasA | 2519263 | c.1149C>T | synonymous_variant | 1.0 |
| kasA | 2519266 | c.1152C>T | synonymous_variant | 1.0 |
| kasA | 2519269 | c.1155C>T | synonymous_variant | 1.0 |
| kasA | 2519272 | c.1158C>G | synonymous_variant | 1.0 |
| kasA | 2519281 | c.1167G>T | synonymous_variant | 1.0 |
| kasA | 2519287 | c.1173T>C | synonymous_variant | 1.0 |
| kasA | 2519295 | p.Tyr394Phe | missense_variant | 1.0 |
| kasA | 2519299 | c.1185C>T | synonymous_variant | 1.0 |
| kasA | 2519305 | c.1191A>G | synonymous_variant | 1.0 |
| kasA | 2519306 | p.Val398Ile | missense_variant | 1.0 |
| kasA | 2519323 | c.1209G>C | synonymous_variant | 1.0 |
| kasA | 2519329 | c.1215C>T | synonymous_variant | 1.0 |
| kasA | 2519338 | c.1224T>C | synonymous_variant | 1.0 |
| ahpC | 2726204 | c.12A>G | synonymous_variant | 1.0 |
| ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
| ahpC | 2726216 | c.24T>C | synonymous_variant | 1.0 |
| ahpC | 2726219 | c.27A>G | synonymous_variant | 1.0 |
| ahpC | 2726232 | p.Gln14Glu | missense_variant | 1.0 |
| ahpC | 2726243 | c.51T>G | synonymous_variant | 1.0 |
| ahpC | 2726244 | c.52_54delCTCinsTTG | synonymous_variant | 1.0 |
| ahpC | 2726251 | p.Gly20Ala | missense_variant | 1.0 |
| ahpC | 2726255 | c.63T>C | synonymous_variant | 1.0 |
| ahpC | 2726258 | c.66C>T | synonymous_variant | 1.0 |
| ahpC | 2726303 | c.111T>C | synonymous_variant | 1.0 |
| ahpC | 2726311 | p.Ser40Asn | missense_variant | 1.0 |
| ahpC | 2726315 | p.Asp41Glu | missense_variant | 1.0 |
| ahpC | 2726318 | p.Glu42Asp | missense_variant | 1.0 |
| ahpC | 2726322 | p.Pro44Ala | missense_variant | 1.0 |
| ahpC | 2726330 | c.138G>A | synonymous_variant | 1.0 |
| ahpC | 2726336 | c.144G>C | synonymous_variant | 1.0 |
| ahpC | 2726348 | c.156T>C | synonymous_variant | 1.0 |
| ahpC | 2726357 | c.165A>G | synonymous_variant | 1.0 |
| ahpC | 2726366 | c.174G>C | synonymous_variant | 1.0 |
| ahpC | 2726378 | c.186T>G | synonymous_variant | 1.0 |
| ahpC | 2726387 | c.195C>T | synonymous_variant | 1.0 |
| ahpC | 2726390 | c.198G>C | synonymous_variant | 1.0 |
| ahpC | 2726393 | c.201G>C | synonymous_variant | 1.0 |
| ahpC | 2726397 | p.Ser69Gly | missense_variant | 1.0 |
| ahpC | 2726408 | c.216T>C | synonymous_variant | 1.0 |
| ahpC | 2726414 | c.222G>A | synonymous_variant | 1.0 |
| ahpC | 2726419 | p.Glu76Ala | missense_variant | 1.0 |
| ahpC | 2726528 | c.336C>G | synonymous_variant | 1.0 |
| ahpC | 2726540 | c.348C>G | synonymous_variant | 1.0 |
| ahpC | 2726543 | c.351A>G | synonymous_variant | 1.0 |
| ahpC | 2726546 | c.354C>G | synonymous_variant | 1.0 |
| ahpC | 2726551 | p.Gln120Leu | missense_variant | 1.0 |
| ahpC | 2726556 | p.Ala122Thr | missense_variant | 1.0 |
| ahpC | 2726564 | c.372C>G | synonymous_variant | 1.0 |
| ahpC | 2726579 | c.387T>C | synonymous_variant | 1.0 |
| ahpC | 2726591 | c.399C>G | synonymous_variant | 1.0 |
| ahpC | 2726593 | p.Val134Ala | missense_variant | 1.0 |
| ahpC | 2726600 | c.408T>C | synonymous_variant | 1.0 |
| ahpC | 2726601 | p.Ile137Leu | missense_variant | 1.0 |
| ahpC | 2726638 | p.Ala149Val | missense_variant | 1.0 |
| ahpC | 2726645 | c.453C>G | synonymous_variant | 1.0 |
| ahpC | 2726657 | c.465A>C | synonymous_variant | 1.0 |
| ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.98 |
| ahpC | 2726672 | c.480G>A | synonymous_variant | 0.97 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 0.98 |
| ahpC | 2726681 | c.489A>C | synonymous_variant | 0.98 |
| ahpC | 2726693 | c.501C>G | synonymous_variant | 0.97 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 0.97 |
| ahpC | 2726717 | c.525A>G | synonymous_variant | 0.95 |
| ahpC | 2726747 | c.555A>C | synonymous_variant | 0.92 |
| folC | 2746138 | c.1461A>G | synonymous_variant | 0.93 |
| folC | 2746150 | c.1449T>G | synonymous_variant | 0.94 |
| folC | 2746158 | c.1441T>C | synonymous_variant | 0.94 |
| folC | 2746162 | c.1437G>C | synonymous_variant | 0.94 |
| folC | 2746165 | c.1434T>G | synonymous_variant | 0.94 |
| folC | 2746171 | c.1428G>C | synonymous_variant | 0.94 |
| folC | 2746174 | c.1425A>G | synonymous_variant | 0.94 |
| folC | 2746183 | c.1416T>C | synonymous_variant | 0.94 |
| folC | 2746264 | p.Ser445Ala | missense_variant | 1.0 |
| folC | 2746270 | c.1329C>G | synonymous_variant | 1.0 |
| folC | 2746273 | c.1326T>C | synonymous_variant | 1.0 |
| folC | 2746282 | c.1317T>C | synonymous_variant | 0.92 |
| folC | 2746285 | c.1314T>C | synonymous_variant | 0.92 |
| folC | 2746308 | p.Arg431Ser | missense_variant | 0.92 |
| folC | 2746321 | c.1278A>G | synonymous_variant | 0.91 |
| folC | 2746328 | p.Arg424Thr | missense_variant | 0.8 |
| folC | 2746335 | p.Gly422Arg | missense_variant | 0.8 |
| folC | 2746336 | c.1263C>G | synonymous_variant | 0.8 |
| folC | 2746345 | c.1254G>C | synonymous_variant | 0.67 |
| folC | 2746375 | c.1224G>C | synonymous_variant | 1.0 |
| folC | 2746390 | p.Val403Ile | missense_variant | 1.0 |
| folC | 2746393 | c.1206C>G | synonymous_variant | 1.0 |
| folC | 2746401 | p.Ser400Ala | missense_variant | 1.0 |
| folC | 2746402 | c.1197T>C | synonymous_variant | 1.0 |
| folC | 2746414 | p.Glu395Gln | missense_variant | 1.0 |
| folC | 2746420 | c.1179A>G | synonymous_variant | 1.0 |
| folC | 2746426 | c.1173G>C | synonymous_variant | 1.0 |
| folC | 2746438 | c.1161G>C | synonymous_variant | 1.0 |
| folC | 2746451 | p.Gly383Ala | missense_variant | 1.0 |
| folC | 2746478 | p.Phe374Tyr | missense_variant | 1.0 |
| folC | 2746480 | c.1119A>C | synonymous_variant | 1.0 |
| folC | 2746492 | c.1107G>A | synonymous_variant | 1.0 |
| folC | 2746525 | c.1074G>T | synonymous_variant | 1.0 |
| folC | 2746531 | c.1068G>C | synonymous_variant | 1.0 |
| folC | 2746564 | c.1035A>G | synonymous_variant | 1.0 |
| folC | 2746576 | c.1023C>G | synonymous_variant | 1.0 |
| folC | 2746584 | c.1015T>C | synonymous_variant | 1.0 |
| folC | 2746594 | c.1005T>C | synonymous_variant | 1.0 |
| folC | 2746598 | p.Thr334Val | missense_variant | 1.0 |
| folC | 2746714 | c.885T>A | synonymous_variant | 1.0 |
| folC | 2746728 | c.871T>C | synonymous_variant | 1.0 |
| folC | 2746734 | p.Ile289Val | missense_variant | 1.0 |
| folC | 2746741 | c.858C>T | synonymous_variant | 1.0 |
| folC | 2746744 | c.855T>G | synonymous_variant | 1.0 |
| folC | 2746753 | c.846C>G | synonymous_variant | 1.0 |
| folC | 2746756 | c.843C>G | synonymous_variant | 1.0 |
| folC | 2746765 | c.834A>G | synonymous_variant | 1.0 |
| folC | 2746771 | c.828A>G | synonymous_variant | 1.0 |
| folC | 2746777 | c.822T>G | synonymous_variant | 1.0 |
| folC | 2747007 | p.Ser198Gly | missense_variant | 1.0 |
| folC | 2747021 | p.Val193Ala | missense_variant | 1.0 |
| folC | 2747023 | c.576C>G | synonymous_variant | 1.0 |
| folC | 2747026 | c.573C>G | synonymous_variant | 1.0 |
| folC | 2747032 | c.567A>C | synonymous_variant | 1.0 |
| folC | 2747059 | c.540T>C | synonymous_variant | 1.0 |
| folC | 2747062 | c.537A>G | synonymous_variant | 1.0 |
| folC | 2747065 | c.534C>T | synonymous_variant | 1.0 |
| folC | 2747071 | c.528C>G | synonymous_variant | 1.0 |
| folC | 2747086 | c.513A>C | synonymous_variant | 1.0 |
| folC | 2747089 | c.510G>C | synonymous_variant | 1.0 |
| folC | 2747101 | c.498G>C | synonymous_variant | 1.0 |
| folC | 2747104 | c.495C>T | synonymous_variant | 1.0 |
| folC | 2747107 | c.492G>C | synonymous_variant | 1.0 |
| folC | 2747110 | c.489T>C | synonymous_variant | 1.0 |
| folC | 2747113 | c.486C>G | synonymous_variant | 1.0 |
| folC | 2747116 | c.483G>C | synonymous_variant | 1.0 |
| folC | 2747134 | c.465C>G | synonymous_variant | 1.0 |
| folC | 2747224 | c.375G>C | synonymous_variant | 0.89 |
| folC | 2747239 | c.360T>C | synonymous_variant | 1.0 |
| folC | 2747248 | c.351G>C | synonymous_variant | 1.0 |
| folC | 2747264 | p.Gly112Ala | missense_variant | 1.0 |
| folC | 2747275 | c.324T>C | synonymous_variant | 1.0 |
| folC | 2747289 | p.Pro104Ala | missense_variant | 1.0 |
| folC | 2747290 | c.309A>G | synonymous_variant | 1.0 |
| folC | 2747293 | c.306G>A | synonymous_variant | 1.0 |
| folC | 2747302 | c.297A>C | synonymous_variant | 1.0 |
| folC | 2747314 | c.285A>C | synonymous_variant | 1.0 |
| folC | 2747317 | c.282C>G | synonymous_variant | 1.0 |
| folC | 2747343 | p.Val86Ile | missense_variant | 1.0 |
| folC | 2747355 | p.Val82Ile | missense_variant | 1.0 |
| folC | 2747394 | p.Ile69Val | missense_variant | 0.94 |
| folC | 2747395 | c.204T>C | synonymous_variant | 0.94 |
| folC | 2747407 | c.192T>C | synonymous_variant | 0.83 |
| folC | 2747707 | c.-109C>A | upstream_gene_variant | 0.75 |
| folC | 2747718 | c.-120G>A | upstream_gene_variant | 0.83 |
| folC | 2747726 | c.-128G>A | upstream_gene_variant | 0.86 |
| folC | 2747736 | c.-138G>C | upstream_gene_variant | 0.86 |
| folC | 2747739 | c.-141G>A | upstream_gene_variant | 0.86 |
| folC | 2747745 | c.-147A>C | upstream_gene_variant | 0.88 |
| folC | 2747751 | c.-154_-153delGCinsCG | upstream_gene_variant | 0.88 |
| folC | 2747759 | c.-161T>C | upstream_gene_variant | 1.0 |
| folC | 2747760 | c.-162G>T | upstream_gene_variant | 1.0 |
| folC | 2747772 | c.-174C>G | upstream_gene_variant | 1.0 |
| folC | 2747790 | c.-192G>C | upstream_gene_variant | 1.0 |
| pepQ | 2859669 | c.750T>C | synonymous_variant | 1.0 |
| pepQ | 2859678 | c.741A>G | synonymous_variant | 1.0 |
| pepQ | 2859702 | c.715_717delTTGinsCTC | synonymous_variant | 1.0 |
| pepQ | 2859711 | c.708C>G | synonymous_variant | 1.0 |
| pepQ | 2859723 | c.696T>C | synonymous_variant | 1.0 |
| pepQ | 2859735 | c.684G>C | synonymous_variant | 1.0 |
| pepQ | 2859739 | p.Ala227Gly | missense_variant | 1.0 |
| pepQ | 2859747 | c.672C>G | synonymous_variant | 1.0 |
| pepQ | 2859765 | c.654G>C | synonymous_variant | 1.0 |
| pepQ | 2859891 | c.528G>C | synonymous_variant | 1.0 |
| pepQ | 2859897 | c.520_522delCGCinsAGG | synonymous_variant | 1.0 |
| pepQ | 2859903 | c.516G>C | synonymous_variant | 1.0 |
| pepQ | 2859908 | p.Gln171Glu | missense_variant | 1.0 |
| pepQ | 2859909 | c.510G>C | synonymous_variant | 1.0 |
| pepQ | 2859918 | c.501A>C | synonymous_variant | 1.0 |
| pepQ | 2859924 | c.495G>C | synonymous_variant | 1.0 |
| pepQ | 2859933 | c.486C>G | synonymous_variant | 1.0 |
| pepQ | 2859942 | c.477C>G | synonymous_variant | 1.0 |
| pepQ | 2859950 | c.469T>C | synonymous_variant | 1.0 |
| pepQ | 2859957 | c.462G>C | synonymous_variant | 1.0 |
| pepQ | 2859966 | c.453T>C | synonymous_variant | 1.0 |
| pepQ | 2859972 | c.447A>G | synonymous_variant | 0.67 |
| pepQ | 2859975 | c.444A>G | synonymous_variant | 0.67 |
| pepQ | 2860200 | c.219G>C | synonymous_variant | 1.0 |
| pepQ | 2860203 | c.216A>G | synonymous_variant | 1.0 |
| pepQ | 2860206 | c.211_213delCTCinsTTG | synonymous_variant | 1.0 |
| pepQ | 2860212 | c.207C>G | synonymous_variant | 1.0 |
| pepQ | 2860218 | c.201A>G | synonymous_variant | 1.0 |
| pepQ | 2860222 | p.Ser66Glu | missense_variant | 1.0 |
| pepQ | 2860233 | c.186T>C | synonymous_variant | 1.0 |
| pepQ | 2860254 | c.165C>G | synonymous_variant | 1.0 |
| pepQ | 2860259 | c.160T>C | synonymous_variant | 1.0 |
| pepQ | 2860407 | c.12C>A | synonymous_variant | 1.0 |
| pepQ | 2860420 | c.-2T>C | upstream_gene_variant | 1.0 |
| pepQ | 2860421 | c.-3G>C | upstream_gene_variant | 1.0 |
| pepQ | 2860422 | c.-4G>A | upstream_gene_variant | 1.0 |
| pepQ | 2860444 | c.-26C>A | upstream_gene_variant | 1.0 |
| pepQ | 2860445 | c.-27T>A | upstream_gene_variant | 1.0 |
| pepQ | 2860446 | c.-28T>A | upstream_gene_variant | 1.0 |
| pepQ | 2860447 | c.-29A>C | upstream_gene_variant | 1.0 |
| pepQ | 2860449 | c.-31G>C | upstream_gene_variant | 1.0 |
| pepQ | 2860456 | c.-38G>C | upstream_gene_variant | 1.0 |
| pepQ | 2860475 | c.-57C>T | upstream_gene_variant | 1.0 |
| pepQ | 2860480 | c.-62G>A | upstream_gene_variant | 1.0 |
| pepQ | 2860483 | c.-65A>T | upstream_gene_variant | 1.0 |
| pepQ | 2860490 | c.-72G>C | upstream_gene_variant | 1.0 |
| ribD | 2987026 | p.Ala63Gly | missense_variant | 1.0 |
| ribD | 2987033 | c.195C>G | synonymous_variant | 1.0 |
| ribD | 2987042 | c.204A>G | synonymous_variant | 1.0 |
| ribD | 2987046 | p.Val70Ile | missense_variant | 1.0 |
| ribD | 2987058 | c.220T>C | synonymous_variant | 1.0 |
| ribD | 2987066 | c.228A>G | synonymous_variant | 1.0 |
| ribD | 2987069 | c.231T>C | synonymous_variant | 1.0 |
| ribD | 2987092 | p.Val85Ala | missense_variant | 1.0 |
| ribD | 2987105 | c.267C>G | synonymous_variant | 1.0 |
| ribD | 2987108 | c.270T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064799 | c.1393C>A | synonymous_variant | 0.88 |
| Rv2752c | 3064800 | c.1392G>A | synonymous_variant | 0.89 |
| Rv2752c | 3064809 | c.1383C>G | synonymous_variant | 0.94 |
| Rv2752c | 3064815 | c.1377T>C | synonymous_variant | 0.94 |
| Rv2752c | 3064831 | p.Ala454Asn | missense_variant | 0.94 |
| Rv2752c | 3064838 | c.1354T>C | synonymous_variant | 0.97 |
| Rv2752c | 3064860 | c.1332G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064863 | c.1329G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064872 | c.1320T>G | synonymous_variant | 1.0 |
| Rv2752c | 3064877 | p.Ser439Ala | missense_variant | 1.0 |
| Rv2752c | 3064881 | p.Ser437Ala | missense_variant | 1.0 |
| Rv2752c | 3064887 | c.1305A>G | synonymous_variant | 1.0 |
| Rv2752c | 3064893 | c.1299C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064896 | c.1296T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064914 | c.1278T>G | synonymous_variant | 1.0 |
| Rv2752c | 3064941 | p.Gln417Glu | missense_variant | 0.86 |
| Rv2752c | 3064947 | c.1245A>G | synonymous_variant | 0.93 |
| Rv2752c | 3064956 | p.Ser412Arg | missense_variant | 0.96 |
| Rv2752c | 3064962 | c.1230C>G | synonymous_variant | 0.97 |
| Rv2752c | 3064973 | p.Ala407Ser | missense_variant | 0.98 |
| Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 0.98 |
| Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 0.98 |
| Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 0.98 |
| Rv2752c | 3065007 | c.1185G>C | synonymous_variant | 0.99 |
| Rv2752c | 3065013 | c.1179G>C | synonymous_variant | 0.99 |
| Rv2752c | 3065018 | p.Asn392His | missense_variant | 0.99 |
| Rv2752c | 3065028 | p.Val388Ile | missense_variant | 0.98 |
| Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 0.97 |
| Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.96 |
| Rv2752c | 3065052 | c.1140G>A | synonymous_variant | 0.96 |
| Rv2752c | 3065055 | c.1137T>C | synonymous_variant | 0.96 |
| Rv2752c | 3065064 | c.1128G>C | synonymous_variant | 0.96 |
| Rv2752c | 3065073 | c.1119C>G | synonymous_variant | 0.93 |
| Rv2752c | 3065079 | c.1113T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065082 | c.1110G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065085 | c.1105_1107delAGGinsCGC | synonymous_variant | 1.0 |
| Rv2752c | 3065088 | c.1104A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065109 | c.1081_1083delAGAinsCGC | synonymous_variant | 0.93 |
| Rv2752c | 3065115 | c.1077C>G | synonymous_variant | 0.93 |
| Rv2752c | 3065126 | p.Ser356Ala | missense_variant | 0.93 |
| Rv2752c | 3065127 | c.1065G>C | synonymous_variant | 0.93 |
| Rv2752c | 3065130 | p.Ala354Glu | missense_variant | 0.93 |
| Rv2752c | 3065133 | c.1059T>C | synonymous_variant | 0.93 |
| Rv2752c | 3065142 | c.1050A>C | synonymous_variant | 0.93 |
| Rv2752c | 3065146 | p.Phe349Tyr | missense_variant | 0.94 |
| Rv2752c | 3065151 | c.1041G>C | synonymous_variant | 0.95 |
| Rv2752c | 3065183 | p.Ser337Ala | missense_variant | 0.96 |
| Rv2752c | 3065186 | c.1006T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065190 | p.Ile334Val | missense_variant | 1.0 |
| Rv2752c | 3065196 | c.996T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065202 | c.990T>G | synonymous_variant | 1.0 |
| Rv2752c | 3065205 | c.987T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065210 | c.982T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065223 | c.969T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065229 | c.963G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065232 | c.960T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065241 | c.951A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065262 | c.930G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065268 | c.924A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065288 | c.904T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065292 | c.900T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065295 | p.Gln299Arg | missense_variant | 1.0 |
| Rv2752c | 3065298 | p.Asp298Glu | missense_variant | 1.0 |
| Rv2752c | 3065306 | p.Ala296Pro | missense_variant | 1.0 |
| Rv2752c | 3065311 | p.Thr294Met | missense_variant | 1.0 |
| Rv2752c | 3065313 | c.879A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065323 | p.Ala290Gly | missense_variant | 1.0 |
| Rv2752c | 3065334 | c.858C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065378 | p.Val272Ile | missense_variant | 1.0 |
| Rv2752c | 3065381 | p.Arg271Gly | missense_variant | 1.0 |
| Rv2752c | 3065397 | c.795G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065400 | c.792A>C | synonymous_variant | 1.0 |
| Rv2752c | 3065412 | c.780G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065418 | c.774A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065421 | c.771G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065442 | c.750T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065451 | c.741G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065457 | c.735A>C | synonymous_variant | 1.0 |
| Rv2752c | 3065463 | c.729T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065481 | c.711T>C | synonymous_variant | 0.95 |
| Rv2752c | 3065487 | c.705T>G | synonymous_variant | 0.86 |
| Rv2752c | 3065715 | p.Tyr159His | missense_variant | 1.0 |
| Rv2752c | 3065721 | c.471G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065727 | c.465C>G | synonymous_variant | 0.67 |
| Rv2752c | 3065732 | c.460T>C | synonymous_variant | 0.67 |
| Rv2752c | 3065739 | c.453G>C | synonymous_variant | 0.67 |
| Rv2752c | 3065742 | p.Thr150Ile | missense_variant | 0.67 |
| Rv2752c | 3065748 | c.444T>C | synonymous_variant | 0.67 |
| Rv2752c | 3065766 | p.Glu142Gln | missense_variant | 0.75 |
| Rv2752c | 3065772 | c.420G>A | synonymous_variant | 0.75 |
| Rv2752c | 3065775 | c.417T>C | synonymous_variant | 0.75 |
| Rv2752c | 3065785 | c.404_406delGGC | disruptive_inframe_deletion | 0.75 |
| Rv2752c | 3065794 | c.395_397dupAGA | conservative_inframe_insertion | 1.0 |
| Rv2752c | 3065806 | p.Arg129Ala | missense_variant | 1.0 |
| Rv2752c | 3065808 | c.384C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065874 | p.Lys106Arg | missense_variant | 1.0 |
| Rv2752c | 3065880 | c.312C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065915 | c.277C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065925 | p.Ala89Gly | missense_variant | 1.0 |
| Rv2752c | 3065928 | c.264G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065946 | p.Gly82Ala | missense_variant | 1.0 |
| Rv2752c | 3065955 | c.235_237delTTGinsCTC | synonymous_variant | 1.0 |
| Rv2752c | 3065979 | c.213T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.98 |
| Rv2752c | 3065994 | c.198T>C | synonymous_variant | 0.98 |
| Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.97 |
| Rv2752c | 3066009 | c.183G>C | synonymous_variant | 0.96 |
| Rv2752c | 3066018 | c.174T>C | synonymous_variant | 0.95 |
| Rv2752c | 3066024 | c.168T>G | synonymous_variant | 0.96 |
| Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 0.92 |
| Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.92 |
| Rv2752c | 3066045 | c.147T>C | synonymous_variant | 0.93 |
| Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.95 |
| Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.96 |
| Rv2752c | 3066066 | c.126T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066075 | c.117A>G | synonymous_variant | 1.0 |
| Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 1.0 |
| Rv2752c | 3066150 | c.42C>A | synonymous_variant | 0.96 |
| Rv2752c | 3066153 | p.Ser13Thr | missense_variant | 0.94 |
| Rv2752c | 3066158 | p.Thr12Ala | missense_variant | 0.94 |
| Rv2752c | 3066161 | c.31C>T | synonymous_variant | 0.94 |
| Rv2752c | 3066162 | c.30C>A | synonymous_variant | 0.94 |
| Rv2752c | 3066165 | c.27T>C | synonymous_variant | 0.94 |
| Rv2752c | 3066176 | p.Pro6Ala | missense_variant | 0.94 |
| Rv2752c | 3066177 | c.15T>C | synonymous_variant | 0.94 |
| Rv2752c | 3066196 | c.-5C>G | upstream_gene_variant | 0.67 |
| Rv2752c | 3066249 | c.-58C>T | upstream_gene_variant | 1.0 |
| Rv2752c | 3066261 | c.-70G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066270 | c.-79G>A | upstream_gene_variant | 1.0 |
| Rv2752c | 3066276 | c.-85G>A | upstream_gene_variant | 1.0 |
| Rv2752c | 3066279 | c.-88A>G | upstream_gene_variant | 1.0 |
| Rv2752c | 3066282 | c.-91G>T | upstream_gene_variant | 1.0 |
| Rv2752c | 3066287 | c.-96G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066290 | c.-99G>A | upstream_gene_variant | 1.0 |
| Rv2752c | 3066291 | c.-100G>A | upstream_gene_variant | 1.0 |
| Rv2752c | 3066309 | c.-118T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066315 | c.-124C>T | upstream_gene_variant | 1.0 |
| Rv2752c | 3066330 | c.-139G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066335 | c.-144T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066339 | c.-148G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066360 | c.-169T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066370 | c.-180_-179delAGinsGC | upstream_gene_variant | 1.0 |
| Rv2752c | 3066380 | c.-189A>G | upstream_gene_variant | 1.0 |
| Rv2752c | 3066994 | c.-804_-803delCAinsGC | upstream_gene_variant | 1.0 |
| Rv2752c | 3066996 | c.-805T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3067001 | c.-810G>A | upstream_gene_variant | 1.0 |
| thyX | 3067223 | c.723G>C | synonymous_variant | 1.0 |
| thyX | 3067232 | c.714C>G | synonymous_variant | 1.0 |
| thyX | 3067246 | p.Thr234Ala | missense_variant | 1.0 |
| thyX | 3067249 | p.Thr233Ser | missense_variant | 1.0 |
| thyX | 3067250 | p.Val232Ile | missense_variant | 1.0 |
| thyX | 3067274 | c.672C>G | synonymous_variant | 1.0 |
| thyX | 3067277 | c.669C>G | synonymous_variant | 1.0 |
| thyX | 3067281 | p.Val222Ala | missense_variant | 0.94 |
| thyX | 3067284 | p.Ala221Gly | missense_variant | 1.0 |
| thyX | 3067286 | c.660C>G | synonymous_variant | 1.0 |
| thyX | 3067289 | c.657C>G | synonymous_variant | 1.0 |
| thyX | 3067292 | c.654G>A | synonymous_variant | 1.0 |
| thyX | 3067295 | c.651C>T | synonymous_variant | 1.0 |
| thyX | 3067316 | c.630A>G | synonymous_variant | 1.0 |
| thyX | 3067325 | c.621A>G | synonymous_variant | 1.0 |
| thyX | 3067328 | c.618G>A | synonymous_variant | 1.0 |
| thyX | 3067349 | c.597G>C | synonymous_variant | 1.0 |
| thyX | 3067355 | c.591A>C | synonymous_variant | 1.0 |
| thyX | 3067367 | c.579G>C | synonymous_variant | 1.0 |
| thyX | 3067373 | c.573C>G | synonymous_variant | 1.0 |
| thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
| thyX | 3067394 | c.552G>C | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyX | 3067445 | c.501C>G | synonymous_variant | 1.0 |
| thyX | 3067457 | c.489C>G | synonymous_variant | 1.0 |
| thyX | 3067465 | p.Ile161Val | missense_variant | 1.0 |
| thyX | 3067466 | c.480G>C | synonymous_variant | 1.0 |
| thyX | 3067475 | c.471A>G | synonymous_variant | 1.0 |
| thyX | 3067490 | c.456C>G | synonymous_variant | 0.99 |
| thyX | 3067493 | c.453A>G | synonymous_variant | 0.99 |
| thyX | 3067515 | p.Ser144Thr | missense_variant | 0.99 |
| thyX | 3067530 | p.Ala139Ser | missense_variant | 0.98 |
| thyX | 3067545 | p.Glu134Ala | missense_variant | 0.99 |
| thyX | 3067549 | p.Thr133Ala | missense_variant | 0.99 |
| thyX | 3067556 | p.His130Gln | missense_variant | 1.0 |
| thyX | 3067559 | c.387C>G | synonymous_variant | 1.0 |
| thyX | 3067565 | p.Asp127Glu | missense_variant | 1.0 |
| thyX | 3067570 | p.Ala126Pro | missense_variant | 1.0 |
| thyX | 3067577 | c.369G>A | synonymous_variant | 1.0 |
| thyX | 3067601 | p.Arg115His | missense_variant | 1.0 |
| thyX | 3067611 | p.Lys112Thr | missense_variant | 1.0 |
| thyX | 3067619 | c.327A>C | synonymous_variant | 1.0 |
| thyX | 3067631 | c.315C>G | synonymous_variant | 1.0 |
| thyX | 3067634 | c.312C>G | synonymous_variant | 1.0 |
| thyX | 3067652 | c.294T>C | synonymous_variant | 1.0 |
| thyX | 3067661 | c.285C>G | synonymous_variant | 1.0 |
| thyX | 3067685 | c.261A>C | synonymous_variant | 1.0 |
| thyX | 3067691 | p.Ile85Leu | missense_variant | 1.0 |
| thyX | 3067694 | c.252G>C | synonymous_variant | 1.0 |
| thyX | 3067718 | c.228C>G | synonymous_variant | 0.98 |
| thyX | 3067721 | c.225T>C | synonymous_variant | 0.98 |
| thyX | 3067727 | c.219A>C | synonymous_variant | 0.98 |
| thyX | 3067736 | p.Phe70Leu | missense_variant | 0.91 |
| thyX | 3067739 | c.207T>C | synonymous_variant | 0.97 |
| thyX | 3067761 | p.Arg62Lys | missense_variant | 0.98 |
| thyX | 3067765 | p.Leu61Ile | missense_variant | 0.98 |
| thyX | 3067772 | c.174C>G | synonymous_variant | 0.98 |
| thyX | 3067781 | c.165C>G | synonymous_variant | 1.0 |
| thyX | 3067793 | c.153T>C | synonymous_variant | 1.0 |
| thyX | 3067799 | c.147G>A | synonymous_variant | 1.0 |
| thyX | 3067802 | c.144C>G | synonymous_variant | 1.0 |
| thyX | 3067814 | c.132T>C | synonymous_variant | 1.0 |
| thyX | 3067850 | c.96A>C | synonymous_variant | 1.0 |
| thyX | 3067869 | p.Thr26Ser | missense_variant | 1.0 |
| thyX | 3067874 | c.72C>G | synonymous_variant | 1.0 |
| thyX | 3067883 | c.63C>G | synonymous_variant | 0.97 |
| thyX | 3067886 | c.60A>C | synonymous_variant | 1.0 |
| thyX | 3067889 | c.57C>G | synonymous_variant | 1.0 |
| thyX | 3067898 | p.Asp16Glu | missense_variant | 1.0 |
| thyX | 3067935 | p.Thr4Ile | missense_variant | 1.0 |
| thyA | 3073787 | p.Lys229Glu | missense_variant | 0.67 |
| thyA | 3073791 | c.681T>C | synonymous_variant | 0.86 |
| thyA | 3073794 | c.678A>C | synonymous_variant | 0.86 |
| thyA | 3073812 | c.660C>G | synonymous_variant | 0.94 |
| thyA | 3073815 | c.657G>A | synonymous_variant | 0.95 |
| thyA | 3073824 | c.648A>G | synonymous_variant | 0.97 |
| thyA | 3073827 | c.645A>G | synonymous_variant | 0.97 |
| thyA | 3073839 | c.633T>C | synonymous_variant | 1.0 |
| thyA | 3073860 | c.612C>G | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073866 | c.606C>G | synonymous_variant | 1.0 |
| thyA | 3073872 | p.Ile200Val | missense_variant | 1.0 |
| thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
| thyA | 3073898 | p.Ala192Ser | missense_variant | 1.0 |
| thyA | 3073917 | c.555C>G | synonymous_variant | 1.0 |
| thyA | 3073920 | c.552C>G | synonymous_variant | 1.0 |
| thyA | 3073925 | c.547T>C | synonymous_variant | 1.0 |
| thyA | 3073929 | c.543T>C | synonymous_variant | 1.0 |
| thyA | 3073941 | c.531C>T | synonymous_variant | 1.0 |
| thyA | 3073953 | c.519T>C | synonymous_variant | 1.0 |
| thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
| thyA | 3073959 | c.513T>C | synonymous_variant | 0.94 |
| thyA | 3073977 | c.495A>G | synonymous_variant | 0.95 |
| thyA | 3073983 | c.489C>T | synonymous_variant | 0.95 |
| thyA | 3073989 | c.483T>C | synonymous_variant | 0.96 |
| thyA | 3074004 | c.468T>C | synonymous_variant | 0.95 |
| thyA | 3074010 | c.462C>G | synonymous_variant | 0.95 |
| thyA | 3074028 | c.444G>C | synonymous_variant | 0.96 |
| thyA | 3074031 | c.441T>C | synonymous_variant | 0.96 |
| thyA | 3074037 | c.435C>G | synonymous_variant | 1.0 |
| thyA | 3074053 | p.Arg140Gln | missense_variant | 1.0 |
| thyA | 3074055 | p.Glu139Pro | missense_variant | 1.0 |
| thyA | 3074061 | c.411A>G | synonymous_variant | 1.0 |
| thyA | 3074079 | c.393G>C | synonymous_variant | 1.0 |
| thyA | 3074097 | c.375C>G | synonymous_variant | 1.0 |
| thyA | 3074100 | p.Asp124Asn | missense_variant | 1.0 |
| thyA | 3074106 | c.366T>C | synonymous_variant | 1.0 |
| thyA | 3074127 | c.345G>C | synonymous_variant | 1.0 |
| thyA | 3074130 | c.342G>C | synonymous_variant | 1.0 |
| thyA | 3074147 | p.Ile109Val | missense_variant | 1.0 |
| thyA | 3074157 | c.315C>G | synonymous_variant | 1.0 |
| thyA | 3074165 | p.Ala103Thr | missense_variant | 1.0 |
| thyA | 3074172 | c.300G>C | synonymous_variant | 1.0 |
| thyA | 3074175 | c.297A>G | synonymous_variant | 1.0 |
| thyA | 3074181 | c.291A>G | synonymous_variant | 1.0 |
| thyA | 3074187 | c.285T>C | synonymous_variant | 1.0 |
| thyA | 3074205 | p.Glu89Asp | missense_variant | 1.0 |
| thyA | 3074208 | c.264C>T | synonymous_variant | 1.0 |
| thyA | 3074214 | c.258T>C | synonymous_variant | 1.0 |
| thyA | 3074241 | c.231C>G | synonymous_variant | 1.0 |
| thyA | 3074244 | c.228A>G | synonymous_variant | 1.0 |
| thyA | 3074254 | p.His73Arg | missense_variant | 1.0 |
| thyA | 3074262 | c.210T>C | synonymous_variant | 1.0 |
| thyA | 3074267 | p.Ile69Val | missense_variant | 1.0 |
| thyA | 3074268 | c.204T>C | synonymous_variant | 1.0 |
| thyA | 3074285 | c.187T>C | synonymous_variant | 1.0 |
| thyA | 3074286 | c.186T>C | synonymous_variant | 1.0 |
| thyA | 3074334 | c.138T>C | synonymous_variant | 1.0 |
| thyA | 3074346 | c.126C>T | synonymous_variant | 1.0 |
| thyA | 3074349 | c.123T>C | synonymous_variant | 1.0 |
| thyA | 3074360 | c.112T>C | synonymous_variant | 1.0 |
| thyA | 3074361 | c.111T>C | synonymous_variant | 1.0 |
| thyA | 3074364 | c.108T>C | synonymous_variant | 1.0 |
| thyA | 3074372 | p.Met34Leu | missense_variant | 1.0 |
| thyA | 3074377 | p.Gln32Arg | missense_variant | 1.0 |
| thyA | 3074391 | c.81C>A | synonymous_variant | 1.0 |
| thyA | 3074397 | c.75A>G | synonymous_variant | 1.0 |
| thyA | 3074448 | c.24G>T | synonymous_variant | 1.0 |
| thyA | 3074463 | c.9A>C | synonymous_variant | 1.0 |
| thyA | 3074470 | p.Val1Pro | missense_variant | 1.0 |
| thyA | 3074477 | c.-6T>C | upstream_gene_variant | 1.0 |
| thyA | 3074490 | c.-19G>A | upstream_gene_variant | 1.0 |
| ald | 3087641 | c.822T>C | synonymous_variant | 1.0 |
| ald | 3087647 | c.828A>G | synonymous_variant | 1.0 |
| ald | 3087649 | p.Gly277Asp | missense_variant | 1.0 |
| ald | 3087653 | c.834A>G | synonymous_variant | 1.0 |
| ald | 3087656 | c.837A>G | synonymous_variant | 1.0 |
| ald | 3087665 | c.846C>G | synonymous_variant | 1.0 |
| ald | 3087666 | p.Tyr283His | missense_variant | 1.0 |
| ald | 3087672 | p.His285Asp | missense_variant | 1.0 |
| ald | 3087680 | c.861G>C | synonymous_variant | 1.0 |
| ald | 3087704 | c.885T>C | synonymous_variant | 1.0 |
| ald | 3087716 | c.897G>C | synonymous_variant | 1.0 |
| ald | 3087726 | p.Ala303Ser | missense_variant | 0.94 |
| ald | 3087729 | p.Ser304Ala | missense_variant | 0.94 |
| ald | 3087737 | c.918G>C | synonymous_variant | 0.94 |
| ald | 3087749 | c.930C>G | synonymous_variant | 0.67 |
| ald | 3087761 | c.942C>G | synonymous_variant | 0.86 |
| ald | 3087770 | c.951G>C | synonymous_variant | 0.86 |
| ald | 3087787 | p.Glu323Ala | missense_variant | 0.86 |
| ald | 3087791 | c.972T>C | synonymous_variant | 0.86 |
| ald | 3087797 | p.Asp326Glu | missense_variant | 0.86 |
| ald | 3087799 | p.His327Arg | missense_variant | 1.0 |
| ald | 3087809 | c.990G>T | synonymous_variant | 1.0 |
| fbiD | 3339315 | p.Glu66Asp | missense_variant | 1.0 |
| fbiD | 3339318 | c.201C>G | synonymous_variant | 1.0 |
| fbiD | 3339324 | c.207G>C | synonymous_variant | 1.0 |
| fbiD | 3339327 | c.210T>G | synonymous_variant | 1.0 |
| fbiD | 3339333 | c.216G>C | synonymous_variant | 1.0 |
| fbiD | 3339338 | p.Gly74Glu | missense_variant | 1.0 |
| fbiD | 3339345 | c.228C>T | synonymous_variant | 1.0 |
| fbiD | 3339351 | c.234T>C | synonymous_variant | 1.0 |
| fbiD | 3339354 | c.237A>G | synonymous_variant | 1.0 |
| fbiD | 3339369 | c.252A>G | synonymous_variant | 1.0 |
| fbiD | 3339631 | p.Arg172Ser | missense_variant | 1.0 |
| fbiD | 3339639 | c.522C>T | synonymous_variant | 1.0 |
| fbiD | 3339642 | c.525T>G | synonymous_variant | 1.0 |
| fbiD | 3339643 | p.Val176Ile | missense_variant | 1.0 |
| fbiD | 3339654 | c.537A>C | synonymous_variant | 1.0 |
| fbiD | 3339657 | c.540A>C | synonymous_variant | 1.0 |
| fbiD | 3339660 | c.543C>G | synonymous_variant | 1.0 |
| fbiD | 3339666 | c.549G>C | synonymous_variant | 1.0 |
| fbiD | 3339678 | c.561C>T | synonymous_variant | 1.0 |
| fbiD | 3339681 | c.564T>C | synonymous_variant | 1.0 |
| fprA | 3473809 | c.-198G>C | upstream_gene_variant | 1.0 |
| fprA | 3473812 | c.-195G>A | upstream_gene_variant | 1.0 |
| fprA | 3473843 | c.-164C>G | upstream_gene_variant | 1.0 |
| fprA | 3473848 | c.-159_-157delCAAinsGAG | upstream_gene_variant | 1.0 |
| fprA | 3473878 | c.-129G>T | upstream_gene_variant | 1.0 |
| fprA | 3473887 | c.-120_-118delAGCinsCGA | upstream_gene_variant | 1.0 |
| fprA | 3473893 | c.-114G>C | upstream_gene_variant | 1.0 |
| fprA | 3473902 | c.-105C>G | upstream_gene_variant | 1.0 |
| fprA | 3474114 | c.108C>T | synonymous_variant | 0.67 |
| fprA | 3474130 | c.124_126delTTGinsCTC | synonymous_variant | 0.8 |
| fprA | 3474135 | c.129G>C | synonymous_variant | 0.8 |
| fprA | 3474138 | c.132T>C | synonymous_variant | 0.86 |
| fprA | 3474141 | c.135C>G | synonymous_variant | 0.89 |
| fprA | 3474156 | c.150C>G | synonymous_variant | 0.95 |
| fprA | 3474162 | c.156G>C | synonymous_variant | 0.95 |
| fprA | 3474171 | c.165G>C | synonymous_variant | 0.95 |
| fprA | 3474177 | c.171C>T | synonymous_variant | 0.95 |
| fprA | 3474180 | c.174C>G | synonymous_variant | 0.95 |
| fprA | 3474210 | c.204A>G | synonymous_variant | 1.0 |
| fprA | 3474220 | p.Glu72Gln | missense_variant | 1.0 |
| fprA | 3474225 | c.219C>T | synonymous_variant | 1.0 |
| fprA | 3474228 | c.222C>G | synonymous_variant | 1.0 |
| fprA | 3474231 | c.225C>G | synonymous_variant | 1.0 |
| fprA | 3474237 | c.231C>T | synonymous_variant | 1.0 |
| fprA | 3474249 | c.243T>C | synonymous_variant | 1.0 |
| fprA | 3474340 | c.334T>C | synonymous_variant | 1.0 |
| fprA | 3474345 | c.339C>T | synonymous_variant | 1.0 |
| fprA | 3474354 | c.348T>C | synonymous_variant | 1.0 |
| fprA | 3474360 | p.Asp118Glu | missense_variant | 1.0 |
| fprA | 3474361 | c.355C>T | synonymous_variant | 1.0 |
| fprA | 3474372 | c.366T>C | synonymous_variant | 1.0 |
| fprA | 3474393 | c.387C>G | synonymous_variant | 1.0 |
| fprA | 3474408 | c.402A>G | synonymous_variant | 1.0 |
| fprA | 3474411 | c.405T>C | synonymous_variant | 1.0 |
| fprA | 3474873 | c.867G>C | synonymous_variant | 1.0 |
| fprA | 3474888 | c.882G>C | synonymous_variant | 1.0 |
| fprA | 3474892 | p.Ser296Thr | missense_variant | 1.0 |
| fprA | 3474899 | p.Gly298Ala | missense_variant | 1.0 |
| fprA | 3474902 | p.Ser299Asn | missense_variant | 1.0 |
| fprA | 3474909 | c.903A>G | synonymous_variant | 1.0 |
| fprA | 3474912 | c.906G>C | synonymous_variant | 1.0 |
| fprA | 3474913 | p.Ala303Ser | missense_variant | 1.0 |
| fprA | 3474918 | c.912C>G | synonymous_variant | 1.0 |
| fprA | 3474921 | p.Lys305Asn | missense_variant | 1.0 |
| fprA | 3474948 | c.942A>G | synonymous_variant | 1.0 |
| fprA | 3474950 | p.Ala315Val | missense_variant | 1.0 |
| fprA | 3474960 | c.954C>G | synonymous_variant | 1.0 |
| fprA | 3474966 | c.960G>C | synonymous_variant | 1.0 |
| fprA | 3474975 | c.969C>T | synonymous_variant | 1.0 |
| fprA | 3474984 | c.978G>C | synonymous_variant | 1.0 |
| fprA | 3474996 | c.990C>G | synonymous_variant | 1.0 |
| fprA | 3475051 | p.Asn349Asp | missense_variant | 1.0 |
| fprA | 3475056 | c.1050C>G | synonymous_variant | 1.0 |
| fprA | 3475061 | p.Pro352Arg | missense_variant | 1.0 |
| fprA | 3475074 | c.1068C>G | synonymous_variant | 1.0 |
| fprA | 3475104 | c.1098G>C | synonymous_variant | 1.0 |
| fprA | 3475107 | c.1101G>C | synonymous_variant | 1.0 |
| fprA | 3475113 | c.1107G>C | synonymous_variant | 1.0 |
| fprA | 3475129 | p.Ala375Ser | missense_variant | 1.0 |
| fprA | 3475134 | c.1128A>G | synonymous_variant | 1.0 |
| fprA | 3475140 | c.1134C>G | synonymous_variant | 1.0 |
| fprA | 3475143 | c.1137C>G | synonymous_variant | 1.0 |
| fbiA | 3640347 | c.-196A>G | upstream_gene_variant | 1.0 |
| fbiA | 3640349 | c.-194A>G | upstream_gene_variant | 1.0 |
| fbiA | 3640350 | c.-193C>T | upstream_gene_variant | 1.0 |
| fbiA | 3640365 | c.-178C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640392 | c.-151A>G | upstream_gene_variant | 1.0 |
| fbiB | 3640683 | c.-852C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640689 | c.-846C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640707 | c.-828G>A | upstream_gene_variant | 1.0 |
| fbiB | 3640713 | c.-822T>A | upstream_gene_variant | 1.0 |
| fbiB | 3640722 | c.-813G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640726 | c.-809C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640827 | c.-708T>C | upstream_gene_variant | 0.86 |
| fbiB | 3640830 | c.-705C>G | upstream_gene_variant | 0.91 |
| fbiB | 3640839 | c.-696C>G | upstream_gene_variant | 0.95 |
| fbiA | 3640850 | p.Glu103Gly | missense_variant | 1.0 |
| fbiB | 3640857 | c.-678G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640866 | c.-669T>C | upstream_gene_variant | 1.0 |
| fbiA | 3640871 | p.Ala110Gly | missense_variant | 1.0 |
| fbiB | 3640878 | c.-657T>C | upstream_gene_variant | 0.98 |
| fbiB | 3640899 | c.-636G>C | upstream_gene_variant | 0.97 |
| fbiA | 3640900 | p.Gln120Asn | missense_variant | 0.97 |
| fbiB | 3640914 | c.-621C>G | upstream_gene_variant | 0.96 |
| fbiB | 3640920 | c.-615A>G | upstream_gene_variant | 0.96 |
| fbiA | 3640930 | p.Glu130Thr | missense_variant | 0.88 |
| fbiB | 3640935 | c.-600C>G | upstream_gene_variant | 0.83 |
| fbiB | 3640938 | c.-597A>G | upstream_gene_variant | 0.83 |
| fbiB | 3640944 | c.-591T>C | upstream_gene_variant | 0.83 |
| fbiB | 3641055 | c.-480G>A | upstream_gene_variant | 0.75 |
| fbiB | 3641073 | c.-462T>C | upstream_gene_variant | 0.75 |
| fbiB | 3641085 | c.-450G>C | upstream_gene_variant | 0.6 |
| fbiB | 3641088 | c.-447G>C | upstream_gene_variant | 0.6 |
| fbiB | 3641097 | c.-438T>C | upstream_gene_variant | 0.6 |
| fbiB | 3641100 | c.-435T>G | upstream_gene_variant | 0.6 |
| fbiB | 3641103 | c.-432T>C | upstream_gene_variant | 0.6 |
| fbiB | 3641112 | c.-423T>C | upstream_gene_variant | 0.75 |
| fbiA | 3641260 | p.Ile240Val | missense_variant | 1.0 |
| fbiB | 3641286 | c.-249C>T | upstream_gene_variant | 1.0 |
| fbiA | 3641288 | p.Glu249Gly | missense_variant | 1.0 |
| fbiA | 3641314 | p.Thr258Ala | missense_variant | 1.0 |
| fbiB | 3641322 | c.-213T>G | upstream_gene_variant | 1.0 |
| fbiB | 3641328 | c.-207T>G | upstream_gene_variant | 1.0 |
| fbiB | 3641334 | c.-201G>C | upstream_gene_variant | 1.0 |
| fbiB | 3641337 | c.-198G>C | upstream_gene_variant | 1.0 |
| fbiA | 3641340 | p.Asp266Glu | missense_variant | 1.0 |
| fbiB | 3641586 | p.Ile18Ala | missense_variant | 1.0 |
| fbiB | 3641606 | c.72T>G | synonymous_variant | 1.0 |
| fbiB | 3641609 | c.75C>G | synonymous_variant | 1.0 |
| fbiB | 3641622 | p.Ser30Gly | missense_variant | 1.0 |
| fbiB | 3641627 | c.93C>G | synonymous_variant | 1.0 |
| fbiB | 3641642 | c.108G>C | synonymous_variant | 1.0 |
| fbiB | 3641645 | c.111A>G | synonymous_variant | 1.0 |
| fbiB | 3641654 | c.120A>G | synonymous_variant | 1.0 |
| fbiB | 3641663 | c.129T>C | synonymous_variant | 1.0 |
| fbiB | 3641678 | c.144T>C | synonymous_variant | 1.0 |
| fbiB | 3641689 | p.Val52Ala | missense_variant | 1.0 |
| fbiB | 3641717 | c.183T>G | synonymous_variant | 1.0 |
| fbiB | 3641723 | c.189T>G | synonymous_variant | 1.0 |
| fbiB | 3641938 | p.Gly135Ala | missense_variant | 1.0 |
| fbiB | 3641961 | p.Thr143Glu | missense_variant | 1.0 |
| fbiB | 3641972 | c.438G>C | synonymous_variant | 1.0 |
| fbiB | 3641993 | c.459A>C | synonymous_variant | 1.0 |
| fbiB | 3642020 | c.486T>C | synonymous_variant | 1.0 |
| fbiB | 3642023 | c.489C>G | synonymous_variant | 1.0 |
| fbiB | 3642089 | c.555T>C | synonymous_variant | 1.0 |
| fbiB | 3642096 | p.Val188Leu | missense_variant | 1.0 |
| fbiB | 3642113 | c.579A>G | synonymous_variant | 1.0 |
| fbiB | 3642114 | p.Val194Ile | missense_variant | 1.0 |
| fbiB | 3642144 | c.610T>C | synonymous_variant | 1.0 |
| fbiB | 3642152 | c.618A>G | synonymous_variant | 1.0 |
| fbiB | 3642169 | p.Thr212Met | missense_variant | 1.0 |
| fbiB | 3642188 | c.654T>C | synonymous_variant | 1.0 |
| fbiB | 3642323 | c.789T>G | synonymous_variant | 1.0 |
| fbiB | 3642332 | c.798T>C | synonymous_variant | 1.0 |
| fbiB | 3642336 | p.Thr268Ala | missense_variant | 1.0 |
| fbiB | 3642341 | p.Asp269Glu | missense_variant | 1.0 |
| fbiB | 3642347 | c.813G>C | synonymous_variant | 1.0 |
| fbiB | 3642352 | p.Gly273Ala | missense_variant | 1.0 |
| fbiB | 3642356 | c.822C>T | synonymous_variant | 1.0 |
| fbiB | 3642359 | c.825C>G | synonymous_variant | 1.0 |
| fbiB | 3642362 | c.828C>G | synonymous_variant | 1.0 |
| fbiB | 3642368 | c.834T>G | synonymous_variant | 1.0 |
| fbiB | 3642371 | c.837G>C | synonymous_variant | 1.0 |
| fbiB | 3642395 | c.861A>G | synonymous_variant | 1.0 |
| fbiB | 3642542 | c.1008A>G | synonymous_variant | 1.0 |
| fbiB | 3642560 | c.1026T>C | synonymous_variant | 1.0 |
| fbiB | 3642566 | c.1032A>G | synonymous_variant | 1.0 |
| fbiB | 3642581 | c.1047A>C | synonymous_variant | 1.0 |
| fbiB | 3642587 | p.Met351Ile | missense_variant | 1.0 |
| fbiB | 3642593 | c.1059G>T | synonymous_variant | 1.0 |
| fbiB | 3642602 | c.1068A>C | synonymous_variant | 1.0 |
| fbiB | 3642605 | c.1071A>C | synonymous_variant | 1.0 |
| fbiB | 3642609 | c.1075_1076delAGinsTC | synonymous_variant | 1.0 |
| fbiB | 3642614 | c.1080C>T | synonymous_variant | 1.0 |
| fbiB | 3642617 | c.1083C>G | synonymous_variant | 1.0 |
| fbiB | 3642620 | c.1086T>C | synonymous_variant | 1.0 |
| fbiB | 3642656 | c.1122G>C | synonymous_variant | 1.0 |
| fbiB | 3642659 | c.1125C>G | synonymous_variant | 1.0 |
| fbiB | 3642668 | c.1134A>G | synonymous_variant | 1.0 |
| fbiB | 3642677 | c.1143A>G | synonymous_variant | 1.0 |
| fbiB | 3642680 | c.1146A>G | synonymous_variant | 0.97 |
| fbiB | 3642684 | c.1150T>C | synonymous_variant | 1.0 |
| fbiB | 3642701 | c.1167C>G | synonymous_variant | 1.0 |
| fbiB | 3642719 | c.1185T>C | synonymous_variant | 1.0 |
| fbiB | 3642731 | c.1197C>G | synonymous_variant | 1.0 |
| fbiB | 3642743 | c.1209T>C | synonymous_variant | 1.0 |
| fbiB | 3642749 | c.1215T>C | synonymous_variant | 1.0 |
| fbiB | 3642758 | c.1224C>G | synonymous_variant | 1.0 |
| fbiB | 3642763 | p.Asp410Ala | missense_variant | 1.0 |
| fbiB | 3642770 | c.1236G>C | synonymous_variant | 1.0 |
| fbiB | 3642779 | c.1245A>C | synonymous_variant | 0.94 |
| fbiB | 3642781 | p.Val416Ala | missense_variant | 1.0 |
| fbiB | 3642809 | c.1275G>C | synonymous_variant | 1.0 |
| fbiB | 3642815 | c.1281A>C | synonymous_variant | 1.0 |
| fbiB | 3642818 | c.1284T>C | synonymous_variant | 1.0 |
| fbiB | 3642823 | p.Asp430Ala | missense_variant | 1.0 |
| fbiB | 3642830 | c.1296G>C | synonymous_variant | 1.0 |
| alr | 3840215 | c.1206T>C | synonymous_variant | 1.0 |
| alr | 3840229 | p.Ile398Val | missense_variant | 1.0 |
| alr | 3840230 | c.1191T>G | synonymous_variant | 1.0 |
| alr | 3840233 | c.1188A>G | synonymous_variant | 1.0 |
| alr | 3840236 | c.1185A>C | synonymous_variant | 1.0 |
| alr | 3840239 | c.1182G>C | synonymous_variant | 1.0 |
| alr | 3840248 | c.1173C>G | synonymous_variant | 1.0 |
| alr | 3840274 | p.Val383Leu | missense_variant | 1.0 |
| alr | 3840275 | c.1146T>G | synonymous_variant | 1.0 |
| alr | 3840593 | c.828C>G | synonymous_variant | 1.0 |
| alr | 3840602 | c.819G>C | synonymous_variant | 1.0 |
| alr | 3840605 | p.Val272Ile | missense_variant | 1.0 |
| alr | 3840611 | c.810G>A | synonymous_variant | 1.0 |
| alr | 3840620 | c.801T>C | synonymous_variant | 1.0 |
| alr | 3840626 | p.Ala265Glu | missense_variant | 1.0 |
| alr | 3840632 | c.789A>G | synonymous_variant | 1.0 |
| alr | 3840641 | c.780A>G | synonymous_variant | 1.0 |
| alr | 3840647 | c.774T>C | synonymous_variant | 1.0 |
| alr | 3840662 | c.759G>C | synonymous_variant | 1.0 |
| alr | 3840665 | c.756G>C | synonymous_variant | 1.0 |
| alr | 3840673 | p.Leu250Met | missense_variant | 1.0 |
| alr | 3840926 | c.495T>C | synonymous_variant | 1.0 |
| alr | 3840932 | c.489C>T | synonymous_variant | 1.0 |
| alr | 3840944 | c.477T>C | synonymous_variant | 1.0 |
| alr | 3840947 | c.474G>C | synonymous_variant | 1.0 |
| alr | 3840959 | c.462G>C | synonymous_variant | 1.0 |
| alr | 3840968 | c.453G>C | synonymous_variant | 1.0 |
| alr | 3840980 | c.441G>C | synonymous_variant | 1.0 |
| alr | 3841010 | c.411A>G | synonymous_variant | 1.0 |
| alr | 3841017 | p.Leu135Glu | missense_variant | 1.0 |
| alr | 3841022 | c.399C>G | synonymous_variant | 1.0 |
| alr | 3841028 | c.393G>C | synonymous_variant | 1.0 |
| alr | 3841033 | p.Val130Ile | missense_variant | 1.0 |
| alr | 3841037 | p.Val128Ile | missense_variant | 1.0 |
| alr | 3841059 | p.Gly121Ala | missense_variant | 1.0 |
| alr | 3841069 | p.Ile118Phe | missense_variant | 1.0 |
| alr | 3841079 | c.342T>C | synonymous_variant | 1.0 |
| alr | 3841100 | c.321A>G | synonymous_variant | 0.91 |
| alr | 3841104 | p.Thr106Arg | missense_variant | 0.95 |
| alr | 3841106 | p.Ile105Val | missense_variant | 0.95 |
| alr | 3841112 | c.309T>C | synonymous_variant | 0.95 |
| alr | 3841115 | c.306T>C | synonymous_variant | 0.95 |
| alr | 3841127 | c.294A>G | synonymous_variant | 0.95 |
| alr | 3841148 | c.273C>G | synonymous_variant | 0.83 |
| alr | 3841151 | c.270C>T | synonymous_variant | 0.67 |
| alr | 3841214 | c.207C>G | synonymous_variant | 1.0 |
| alr | 3841229 | c.192G>C | synonymous_variant | 1.0 |
| alr | 3841232 | c.189G>C | synonymous_variant | 1.0 |
| alr | 3841240 | p.Leu61Val | missense_variant | 1.0 |
| alr | 3841248 | p.His58Gly | missense_variant | 1.0 |
| alr | 3841256 | p.His55Gln | missense_variant | 1.0 |
| alr | 3841262 | p.Arg53Cys | missense_variant | 1.0 |
| alr | 3841270 | p.Val51Leu | missense_variant | 0.67 |
| rpoA | 3877467 | c.1041T>C | synonymous_variant | 1.0 |
| rpoA | 3877482 | c.1026C>G | synonymous_variant | 1.0 |
| rpoA | 3877494 | p.Glu338Asp | missense_variant | 1.0 |
| rpoA | 3877503 | c.1005G>C | synonymous_variant | 1.0 |
| rpoA | 3877507 | p.Gly334Ala | missense_variant | 1.0 |
| rpoA | 3877515 | c.993G>C | synonymous_variant | 1.0 |
| rpoA | 3877553 | p.Glu319Gln | missense_variant | 1.0 |
| rpoA | 3877571 | p.Pro313Ala | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877613 | p.Ile299Val | missense_variant | 1.0 |
| rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
| rpoA | 3877679 | p.Ala277Ser | missense_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>C | synonymous_variant | 1.0 |
| rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
| rpoA | 3877764 | c.744C>G | synonymous_variant | 1.0 |
| rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
| rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
| rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
| rpoA | 3877791 | c.717C>G | synonymous_variant | 1.0 |
| rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
| rpoA | 3877839 | c.669G>C | synonymous_variant | 1.0 |
| rpoA | 3877848 | c.660C>T | synonymous_variant | 1.0 |
| rpoA | 3877857 | c.651G>A | synonymous_variant | 1.0 |
| rpoA | 3877866 | c.642G>C | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
| rpoA | 3877878 | c.630G>C | synonymous_variant | 1.0 |
| rpoA | 3877890 | c.618C>T | synonymous_variant | 1.0 |
| rpoA | 3877896 | c.612G>C | synonymous_variant | 1.0 |
| rpoA | 3877900 | p.Ser203Asn | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
| rpoA | 3877909 | p.Asn200Ser | missense_variant | 1.0 |
| rpoA | 3877920 | c.588G>C | synonymous_variant | 1.0 |
| rpoA | 3877923 | c.585C>T | synonymous_variant | 1.0 |
| rpoA | 3877926 | c.582G>C | synonymous_variant | 1.0 |
| rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
| rpoA | 3877986 | c.522G>C | synonymous_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878022 | c.486T>C | synonymous_variant | 1.0 |
| rpoA | 3878028 | c.480G>C | synonymous_variant | 1.0 |
| rpoA | 3878031 | c.477T>C | synonymous_variant | 1.0 |
| rpoA | 3878040 | c.468T>C | synonymous_variant | 1.0 |
| rpoA | 3878043 | c.465G>A | synonymous_variant | 1.0 |
| rpoA | 3878055 | c.453A>G | synonymous_variant | 1.0 |
| rpoA | 3878058 | c.450G>T | synonymous_variant | 1.0 |
| rpoA | 3878061 | c.447G>C | synonymous_variant | 1.0 |
| rpoA | 3878067 | c.441C>G | synonymous_variant | 1.0 |
| rpoA | 3878070 | c.438T>C | synonymous_variant | 1.0 |
| rpoA | 3878076 | c.432C>T | synonymous_variant | 1.0 |
| rpoA | 3878082 | c.426T>G | synonymous_variant | 1.0 |
| rpoA | 3878094 | c.414C>G | synonymous_variant | 1.0 |
| rpoA | 3878103 | c.405A>G | synonymous_variant | 1.0 |
| rpoA | 3878106 | c.402G>C | synonymous_variant | 1.0 |
| rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
| rpoA | 3878130 | c.378C>G | synonymous_variant | 1.0 |
| rpoA | 3878141 | p.Met123Leu | missense_variant | 1.0 |
| rpoA | 3878143 | p.Gly122Asp | missense_variant | 1.0 |
| rpoA | 3878157 | c.351C>G | synonymous_variant | 1.0 |
| rpoA | 3878163 | c.345C>T | synonymous_variant | 1.0 |
| rpoA | 3878169 | c.339G>C | synonymous_variant | 1.0 |
| rpoA | 3878172 | c.336G>C | synonymous_variant | 1.0 |
| rpoA | 3878181 | c.327C>T | synonymous_variant | 1.0 |
| rpoA | 3878187 | c.321C>G | synonymous_variant | 1.0 |
| rpoA | 3878193 | c.315T>C | synonymous_variant | 1.0 |
| rpoA | 3878199 | c.309T>C | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 1.0 |
| rpoA | 3878226 | c.282C>G | synonymous_variant | 1.0 |
| rpoA | 3878232 | c.276G>C | synonymous_variant | 1.0 |
| rpoA | 3878247 | c.261G>C | synonymous_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878284 | p.Glu75Ala | missense_variant | 1.0 |
| rpoA | 3878292 | c.216T>C | synonymous_variant | 1.0 |
| rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
| rpoA | 3878304 | c.204G>C | synonymous_variant | 1.0 |
| rpoA | 3878313 | c.195G>C | synonymous_variant | 1.0 |
| rpoA | 3878322 | c.186A>G | synonymous_variant | 1.0 |
| rpoA | 3878331 | c.177A>G | synonymous_variant | 1.0 |
| rpoA | 3878334 | c.174T>C | synonymous_variant | 1.0 |
| rpoA | 3878337 | c.171T>C | synonymous_variant | 1.0 |
| rpoA | 3878340 | c.168C>T | synonymous_variant | 1.0 |
| rpoA | 3878346 | c.162T>C | synonymous_variant | 1.0 |
| rpoA | 3878364 | c.144A>T | synonymous_variant | 1.0 |
| rpoA | 3878367 | c.141C>G | synonymous_variant | 1.0 |
| rpoA | 3878376 | c.132G>C | synonymous_variant | 1.0 |
| rpoA | 3878385 | c.123C>G | synonymous_variant | 1.0 |
| rpoA | 3878388 | c.120C>G | synonymous_variant | 1.0 |
| rpoA | 3878391 | c.117T>C | synonymous_variant | 1.0 |
| rpoA | 3878415 | c.93C>T | synonymous_variant | 1.0 |
| rpoA | 3878424 | c.84G>C | synonymous_variant | 1.0 |
| rpoA | 3878436 | c.72A>G | synonymous_variant | 1.0 |
| rpoA | 3878442 | c.66G>C | synonymous_variant | 1.0 |
| rpoA | 3878454 | c.54A>C | synonymous_variant | 0.99 |
| rpoA | 3878472 | p.Asp12Glu | missense_variant | 1.0 |
| rpoA | 3878478 | c.30C>G | synonymous_variant | 1.0 |
| rpoA | 3878484 | c.24C>A | synonymous_variant | 1.0 |
| rpoA | 3878490 | c.18C>A | synonymous_variant | 1.0 |
| rpoA | 3878496 | c.12A>T | synonymous_variant | 1.0 |
| rpoA | 3878658 | c.-151A>G | upstream_gene_variant | 1.0 |
| rpoA | 3878665 | c.-158A>G | upstream_gene_variant | 1.0 |
| rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 1.0 |
| rpoA | 3878683 | c.-176G>C | upstream_gene_variant | 1.0 |
| ddn | 3986648 | c.-196C>G | upstream_gene_variant | 1.0 |
| ddn | 3986665 | c.-179G>C | upstream_gene_variant | 1.0 |
| ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 1.0 |
| ddn | 3986672 | c.-172G>A | upstream_gene_variant | 1.0 |
| ddn | 3986673 | c.-171C>T | upstream_gene_variant | 1.0 |
| ddn | 3986681 | c.-163C>G | upstream_gene_variant | 1.0 |
| ddn | 3986690 | c.-154C>G | upstream_gene_variant | 1.0 |
| ddn | 3986696 | c.-148G>C | upstream_gene_variant | 1.0 |
| ddn | 3986726 | c.-118G>C | upstream_gene_variant | 1.0 |
| clpC1 | 4038197 | c.2508A>G | synonymous_variant | 1.0 |
| clpC1 | 4038200 | c.2505T>C | synonymous_variant | 1.0 |
| clpC1 | 4038212 | c.2493T>C | synonymous_variant | 1.0 |
| clpC1 | 4038239 | c.2466T>C | synonymous_variant | 1.0 |
| clpC1 | 4038255 | p.Val817Lys | missense_variant | 1.0 |
| clpC1 | 4038271 | p.Pro812Ala | missense_variant | 1.0 |
| clpC1 | 4038272 | p.Gly811Ser | missense_variant | 1.0 |
| clpC1 | 4038275 | c.2430A>G | synonymous_variant | 1.0 |
| clpC1 | 4038278 | c.2427T>C | synonymous_variant | 1.0 |
| clpC1 | 4038293 | c.2412G>C | synonymous_variant | 1.0 |
| clpC1 | 4038302 | c.2403C>G | synonymous_variant | 1.0 |
| clpC1 | 4038308 | c.2397G>T | synonymous_variant | 1.0 |
| clpC1 | 4038314 | c.2391T>C | synonymous_variant | 0.98 |
| clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.98 |
| clpC1 | 4038320 | c.2385G>C | synonymous_variant | 0.98 |
| clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.99 |
| clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.99 |
| clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.99 |
| clpC1 | 4038388 | c.2317T>C | synonymous_variant | 1.0 |
| clpC1 | 4038392 | c.2313C>T | synonymous_variant | 1.0 |
| clpC1 | 4038398 | c.2307G>T | synonymous_variant | 1.0 |
| clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
| clpC1 | 4038407 | c.2298G>C | synonymous_variant | 1.0 |
| clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.99 |
| clpC1 | 4038433 | c.2272C>T | synonymous_variant | 0.98 |
| clpC1 | 4038434 | c.2271G>A | synonymous_variant | 0.98 |
| clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.96 |
| clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.96 |
| clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.98 |
| clpC1 | 4038460 | p.Leu749Met | missense_variant | 0.98 |
| clpC1 | 4038486 | p.Gly740Asn | missense_variant | 1.0 |
| clpC1 | 4038489 | p.Ala739Gly | missense_variant | 1.0 |
| clpC1 | 4038494 | c.2211G>C | synonymous_variant | 1.0 |
| clpC1 | 4038497 | p.Ser736Gln | missense_variant | 0.98 |
| clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.99 |
| clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
| clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
| clpC1 | 4038640 | p.Asp689Asn | missense_variant | 1.0 |
| clpC1 | 4038653 | c.2052C>T | synonymous_variant | 1.0 |
| clpC1 | 4038658 | p.Lys683Gln | missense_variant | 1.0 |
| clpC1 | 4038661 | p.Ser682Thr | missense_variant | 1.0 |
| clpC1 | 4038662 | c.2043T>C | synonymous_variant | 1.0 |
| clpC1 | 4038671 | c.2034T>C | synonymous_variant | 1.0 |
| clpC1 | 4038683 | c.2022T>C | synonymous_variant | 1.0 |
| clpC1 | 4038695 | c.2010C>G | synonymous_variant | 1.0 |
| clpC1 | 4038701 | c.2004G>C | synonymous_variant | 1.0 |
| clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
| clpC1 | 4038707 | c.1998C>G | synonymous_variant | 1.0 |
| clpC1 | 4038710 | c.1995G>C | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038749 | c.1956C>G | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>T | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.99 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.99 |
| clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.99 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.99 |
| clpC1 | 4038821 | c.1884G>A | synonymous_variant | 0.99 |
| clpC1 | 4038845 | c.1860G>C | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.99 |
| clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.99 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.99 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.99 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.99 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.99 |
| clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.99 |
| clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.99 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039186 | c.1519C>T | synonymous_variant | 1.0 |
| clpC1 | 4039226 | c.1479T>C | synonymous_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.99 |
| clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.99 |
| clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.99 |
| clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.99 |
| clpC1 | 4039319 | c.1386T>C | synonymous_variant | 1.0 |
| clpC1 | 4039322 | c.1383T>C | synonymous_variant | 1.0 |
| clpC1 | 4039328 | c.1377A>C | synonymous_variant | 1.0 |
| clpC1 | 4039331 | c.1374C>G | synonymous_variant | 1.0 |
| clpC1 | 4039337 | p.Thr456Gln | missense_variant | 1.0 |
| clpC1 | 4039349 | c.1356C>T | synonymous_variant | 1.0 |
| clpC1 | 4039352 | c.1353C>G | synonymous_variant | 1.0 |
| clpC1 | 4039364 | c.1341C>G | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>G | synonymous_variant | 1.0 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 1.0 |
| clpC1 | 4039415 | p.Glu430Asp | missense_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>G | synonymous_variant | 1.0 |
| clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
| clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
| clpC1 | 4039480 | c.1225C>A | synonymous_variant | 1.0 |
| clpC1 | 4039481 | c.1224T>G | synonymous_variant | 1.0 |
| clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.9 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
| clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.89 |
| clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.89 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039576 | p.Ala377Pro | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039589 | c.1116G>C | synonymous_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.99 |
| clpC1 | 4039661 | c.1044T>G | synonymous_variant | 1.0 |
| clpC1 | 4039664 | c.1041G>C | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.74 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.99 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.99 |
| clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.98 |
| clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.98 |
| clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.98 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039775 | c.930G>C | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039781 | c.924G>C | synonymous_variant | 1.0 |
| clpC1 | 4039790 | c.915C>G | synonymous_variant | 1.0 |
| clpC1 | 4039805 | c.900C>T | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.99 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.98 |
| clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.97 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.97 |
| clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.98 |
| clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.98 |
| clpC1 | 4039951 | c.754C>T | synonymous_variant | 0.97 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.97 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.99 |
| clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.97 |
| clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.99 |
| clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.99 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040036 | c.669C>G | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.99 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.99 |
| clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.99 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
| clpC1 | 4040165 | c.540G>C | synonymous_variant | 1.0 |
| clpC1 | 4040171 | c.534C>G | synonymous_variant | 1.0 |
| clpC1 | 4040201 | c.504C>G | synonymous_variant | 1.0 |
| clpC1 | 4040204 | c.501G>C | synonymous_variant | 1.0 |
| clpC1 | 4040237 | c.468C>T | synonymous_variant | 1.0 |
| clpC1 | 4040246 | c.459C>G | synonymous_variant | 1.0 |
| clpC1 | 4040249 | c.456A>G | synonymous_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040273 | c.432T>C | synonymous_variant | 1.0 |
| clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 1.0 |
| clpC1 | 4040279 | c.426C>G | synonymous_variant | 1.0 |
| clpC1 | 4040291 | c.414G>C | synonymous_variant | 1.0 |
| clpC1 | 4040318 | c.387C>G | synonymous_variant | 1.0 |
| clpC1 | 4040330 | c.375C>G | synonymous_variant | 1.0 |
| clpC1 | 4040342 | c.363C>G | synonymous_variant | 1.0 |
| clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>T | synonymous_variant | 1.0 |
| clpC1 | 4040369 | c.336C>G | synonymous_variant | 1.0 |
| clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
| clpC1 | 4040381 | c.324T>C | synonymous_variant | 1.0 |
| clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
| clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
| clpC1 | 4040444 | c.261C>T | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
| clpC1 | 4040477 | c.228G>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>G | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040528 | c.177G>C | synonymous_variant | 1.0 |
| clpC1 | 4040531 | c.174T>C | synonymous_variant | 1.0 |
| clpC1 | 4040534 | c.171A>G | synonymous_variant | 1.0 |
| clpC1 | 4040537 | c.168G>C | synonymous_variant | 1.0 |
| clpC1 | 4040546 | c.159G>C | synonymous_variant | 1.0 |
| clpC1 | 4040551 | c.154T>C | synonymous_variant | 1.0 |
| clpC1 | 4040561 | c.144A>G | synonymous_variant | 1.0 |
| clpC1 | 4040567 | c.138C>G | synonymous_variant | 1.0 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
| clpC1 | 4040644 | c.61A>C | synonymous_variant | 1.0 |
| clpC1 | 4040654 | c.51G>A | synonymous_variant | 1.0 |
| clpC1 | 4040657 | c.48T>G | synonymous_variant | 1.0 |
| clpC1 | 4040695 | c.10C>A | synonymous_variant | 1.0 |
| clpC1 | 4040699 | c.6C>T | synonymous_variant | 0.98 |
| clpC1 | 4040706 | c.-4_-3delAC | upstream_gene_variant | 1.0 |
| clpC1 | 4040711 | c.-7G>A | upstream_gene_variant | 1.0 |
| clpC1 | 4040728 | c.-24G>T | upstream_gene_variant | 1.0 |
| clpC1 | 4040734 | c.-31delT | upstream_gene_variant | 1.0 |
| panD | 4043865 | p.Gly139Arg | missense_variant | 0.97 |
| panD | 4043872 | p.Gly137Val | missense_variant | 0.97 |
| panD | 4043876 | p.Leu136Ile | missense_variant | 0.97 |
| panD | 4043883 | c.399C>T | synonymous_variant | 0.97 |
| panD | 4043886 | c.396A>G | synonymous_variant | 0.97 |
| panD | 4043896 | p.Gly129Ala | missense_variant | 0.97 |
| panD | 4043903 | p.Asn127Asp | missense_variant | 0.96 |
| panD | 4043913 | c.369T>C | synonymous_variant | 0.94 |
| panD | 4043916 | c.366A>G | synonymous_variant | 0.85 |
| panD | 4043922 | c.360T>C | synonymous_variant | 0.88 |
| panD | 4043931 | p.Met117Leu | missense_variant | 0.88 |
| panD | 4043939 | p.Ile115Val | missense_variant | 1.0 |
| panD | 4043951 | p.Tyr111Asp | missense_variant | 1.0 |
| panD | 4043952 | c.330T>C | synonymous_variant | 1.0 |
| panD | 4043961 | c.321T>C | synonymous_variant | 1.0 |
| panD | 4043964 | c.318G>C | synonymous_variant | 1.0 |
| panD | 4044057 | c.225C>G | synonymous_variant | 1.0 |
| panD | 4044072 | c.210C>G | synonymous_variant | 1.0 |
| panD | 4044075 | c.207T>C | synonymous_variant | 1.0 |
| panD | 4044081 | c.201T>C | synonymous_variant | 1.0 |
| panD | 4044084 | c.198T>C | synonymous_variant | 1.0 |
| panD | 4044105 | c.177G>C | synonymous_variant | 1.0 |
| panD | 4044117 | c.165G>C | synonymous_variant | 1.0 |
| panD | 4044120 | c.162A>C | synonymous_variant | 1.0 |
| panD | 4044123 | c.159T>C | synonymous_variant | 1.0 |
| panD | 4044126 | c.156T>C | synonymous_variant | 1.0 |
| panD | 4044138 | c.144T>C | synonymous_variant | 1.0 |
| panD | 4044144 | c.138C>T | synonymous_variant | 0.98 |
| panD | 4044150 | c.132A>G | synonymous_variant | 1.0 |
| panD | 4044165 | c.117G>C | synonymous_variant | 1.0 |
| panD | 4044174 | c.108C>G | synonymous_variant | 1.0 |
| panD | 4044177 | c.105C>G | synonymous_variant | 1.0 |
| panD | 4044188 | c.94T>C | synonymous_variant | 1.0 |
| panD | 4044189 | c.93C>T | synonymous_variant | 1.0 |
| panD | 4044195 | c.87T>C | synonymous_variant | 1.0 |
| panD | 4044213 | c.69C>G | synonymous_variant | 1.0 |
| panD | 4044237 | c.45G>C | synonymous_variant | 1.0 |
| panD | 4044240 | c.42G>C | synonymous_variant | 1.0 |
| panD | 4044246 | c.36C>G | synonymous_variant | 1.0 |
| panD | 4044262 | p.Lys7Arg | missense_variant | 1.0 |
| embC | 4239994 | c.132C>G | synonymous_variant | 1.0 |
| embC | 4240006 | c.144A>G | synonymous_variant | 1.0 |
| embC | 4240019 | p.Asn53Asp | missense_variant | 1.0 |
| embC | 4240033 | c.171G>C | synonymous_variant | 1.0 |
| embC | 4240036 | c.174A>G | synonymous_variant | 1.0 |
| embC | 4240037 | c.175T>C | synonymous_variant | 1.0 |
| embC | 4240048 | c.186C>A | synonymous_variant | 1.0 |
| embC | 4240051 | c.189A>G | synonymous_variant | 1.0 |
| embC | 4240060 | c.198G>C | synonymous_variant | 1.0 |
| embC | 4240065 | p.Ala68Gly | missense_variant | 1.0 |
| embC | 4240069 | c.207T>C | synonymous_variant | 1.0 |
| embC | 4240078 | c.216A>G | synonymous_variant | 1.0 |
| embC | 4240081 | c.219G>C | synonymous_variant | 1.0 |
| embC | 4240087 | c.225T>C | synonymous_variant | 1.0 |
| embC | 4240090 | c.228C>T | synonymous_variant | 1.0 |
| embC | 4240105 | c.243C>T | synonymous_variant | 1.0 |
| embC | 4240249 | p.Asp129Glu | missense_variant | 0.88 |
| embC | 4240250 | c.388C>T | synonymous_variant | 0.88 |
| embC | 4240258 | c.396T>G | synonymous_variant | 1.0 |
| embC | 4240267 | c.405T>C | synonymous_variant | 1.0 |
| embC | 4240270 | c.408T>C | synonymous_variant | 1.0 |
| embC | 4240277 | p.Leu139Val | missense_variant | 1.0 |
| embC | 4240282 | c.420C>G | synonymous_variant | 1.0 |
| embC | 4240284 | p.Thr141Ser | missense_variant | 1.0 |
| embC | 4240288 | c.426C>G | synonymous_variant | 1.0 |
| embC | 4240297 | c.435T>C | synonymous_variant | 1.0 |
| embC | 4240313 | p.Thr151Ala | missense_variant | 1.0 |
| embC | 4240318 | c.456T>C | synonymous_variant | 1.0 |
| embC | 4240325 | c.463T>C | synonymous_variant | 1.0 |
| embC | 4240330 | c.468A>G | synonymous_variant | 1.0 |
| embC | 4240348 | c.486T>C | synonymous_variant | 1.0 |
| embC | 4240354 | c.492C>G | synonymous_variant | 1.0 |
| embC | 4240355 | p.Ala165Thr | missense_variant | 1.0 |
| embC | 4240363 | c.501A>G | synonymous_variant | 1.0 |
| embC | 4240484 | p.Ala208Thr | missense_variant | 1.0 |
| embC | 4240489 | c.627A>G | synonymous_variant | 1.0 |
| embC | 4240492 | c.630G>C | synonymous_variant | 0.79 |
| embC | 4240495 | c.633T>G | synonymous_variant | 1.0 |
| embC | 4240512 | p.Ser217Thr | missense_variant | 1.0 |
| embC | 4240516 | c.654G>C | synonymous_variant | 1.0 |
| embC | 4240519 | c.657T>C | synonymous_variant | 1.0 |
| embC | 4240543 | c.681G>C | synonymous_variant | 1.0 |
| embC | 4240558 | c.696C>G | synonymous_variant | 1.0 |
| embC | 4240561 | c.699C>G | synonymous_variant | 1.0 |
| embC | 4240570 | c.708C>G | synonymous_variant | 1.0 |
| embC | 4240600 | c.738G>C | synonymous_variant | 1.0 |
| embC | 4240610 | p.Ile250Arg | missense_variant | 1.0 |
| embC | 4240615 | c.753G>C | synonymous_variant | 1.0 |
| embC | 4240632 | p.Met257Thr | missense_variant | 1.0 |
| embC | 4240642 | c.780G>C | synonymous_variant | 1.0 |
| embC | 4240645 | c.783G>C | synonymous_variant | 1.0 |
| embC | 4240669 | c.807G>C | synonymous_variant | 1.0 |
| embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
| embC | 4240677 | p.Gly272Ala | missense_variant | 1.0 |
| embC | 4240685 | p.Thr275Ala | missense_variant | 1.0 |
| embC | 4240693 | c.831T>G | synonymous_variant | 1.0 |
| embC | 4240699 | c.837C>G | synonymous_variant | 0.99 |
| embC | 4240726 | c.864G>C | synonymous_variant | 1.0 |
| embC | 4240780 | c.918T>C | synonymous_variant | 1.0 |
| embC | 4240783 | c.921G>C | synonymous_variant | 1.0 |
| embC | 4240789 | c.927T>C | synonymous_variant | 1.0 |
| embC | 4240819 | c.957A>G | synonymous_variant | 1.0 |
| embC | 4240828 | c.966G>A | synonymous_variant | 1.0 |
| embC | 4240831 | c.969T>G | synonymous_variant | 1.0 |
| embC | 4240867 | c.1005T>C | synonymous_variant | 1.0 |
| embC | 4240870 | c.1008T>C | synonymous_variant | 1.0 |
| embC | 4240873 | c.1011C>G | synonymous_variant | 1.0 |
| embC | 4240879 | c.1017G>C | synonymous_variant | 1.0 |
| embC | 4240880 | p.Ala340Thr | missense_variant | 1.0 |
| embC | 4240885 | c.1023T>C | synonymous_variant | 1.0 |
| embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
| embC | 4240898 | c.1036_1038delCTAinsTTG | synonymous_variant | 1.0 |
| embC | 4240903 | c.1041C>G | synonymous_variant | 1.0 |
| embC | 4240911 | p.Ala350Val | missense_variant | 1.0 |
| embC | 4241002 | c.1140G>C | synonymous_variant | 1.0 |
| embC | 4241013 | p.Met384Thr | missense_variant | 1.0 |
| embC | 4241017 | c.1155T>C | synonymous_variant | 1.0 |
| embC | 4241023 | c.1161T>G | synonymous_variant | 1.0 |
| embC | 4241032 | c.1170G>C | synonymous_variant | 1.0 |
| embC | 4241038 | c.1176G>C | synonymous_variant | 1.0 |
| embC | 4241047 | c.1185C>G | synonymous_variant | 1.0 |
| embC | 4241050 | c.1188T>G | synonymous_variant | 1.0 |
| embC | 4241053 | c.1191G>C | synonymous_variant | 1.0 |
| embC | 4241089 | c.1227C>G | synonymous_variant | 1.0 |
| embC | 4241095 | c.1233C>T | synonymous_variant | 1.0 |
| embC | 4241107 | c.1245G>C | synonymous_variant | 1.0 |
| embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
| embC | 4241146 | c.1284C>G | synonymous_variant | 1.0 |
| embC | 4241158 | c.1296T>C | synonymous_variant | 1.0 |
| embC | 4241161 | c.1299C>G | synonymous_variant | 1.0 |
| embC | 4241162 | c.1300T>C | synonymous_variant | 1.0 |
| embC | 4241170 | c.1308G>C | synonymous_variant | 1.0 |
| embC | 4241173 | c.1311C>T | synonymous_variant | 1.0 |
| embC | 4241203 | c.1341T>C | synonymous_variant | 1.0 |
| embC | 4241206 | c.1344G>C | synonymous_variant | 1.0 |
| embC | 4241218 | c.1356G>C | synonymous_variant | 1.0 |
| embC | 4241230 | c.1368A>G | synonymous_variant | 1.0 |
| embC | 4241233 | c.1371G>C | synonymous_variant | 1.0 |
| embC | 4241344 | c.1482G>C | synonymous_variant | 0.67 |
| embC | 4241351 | p.Ile497Val | missense_variant | 1.0 |
| embC | 4241361 | p.Asn500Thr | missense_variant | 1.0 |
| embC | 4241363 | p.Leu501Met | missense_variant | 1.0 |
| embC | 4241374 | c.1512T>C | synonymous_variant | 1.0 |
| embC | 4241380 | c.1518A>C | synonymous_variant | 1.0 |
| embC | 4241383 | c.1521G>C | synonymous_variant | 1.0 |
| embC | 4241392 | c.1530G>C | synonymous_variant | 1.0 |
| embC | 4241394 | p.Lys511Ser | missense_variant | 1.0 |
| embC | 4241449 | c.1587C>G | synonymous_variant | 1.0 |
| embC | 4241453 | p.Ile531Val | missense_variant | 1.0 |
| embC | 4241479 | c.1617C>G | synonymous_variant | 1.0 |
| embC | 4241480 | c.1618T>C | synonymous_variant | 1.0 |
| embC | 4241488 | c.1626G>C | synonymous_variant | 1.0 |
| embC | 4241496 | p.Ala545Gly | missense_variant | 1.0 |
| embC | 4241500 | c.1638A>C | synonymous_variant | 1.0 |
| embC | 4241501 | p.Ser547Thr | missense_variant | 1.0 |
| embC | 4241506 | c.1644G>C | synonymous_variant | 1.0 |
| embC | 4241518 | c.1656A>G | synonymous_variant | 1.0 |
| embC | 4241521 | c.1659T>C | synonymous_variant | 1.0 |
| embC | 4241530 | c.1668C>G | synonymous_variant | 1.0 |
| embC | 4241536 | c.1674A>G | synonymous_variant | 1.0 |
| embC | 4241539 | c.1677T>C | synonymous_variant | 1.0 |
| embC | 4241545 | c.1683T>C | synonymous_variant | 1.0 |
| embC | 4241548 | c.1686T>C | synonymous_variant | 1.0 |
| embC | 4241551 | c.1689A>G | synonymous_variant | 1.0 |
| embC | 4241567 | p.Ile569Val | missense_variant | 1.0 |
| embC | 4241572 | c.1710C>G | synonymous_variant | 1.0 |
| embC | 4241578 | c.1716G>C | synonymous_variant | 1.0 |
| embC | 4241584 | c.1722T>C | synonymous_variant | 1.0 |
| embC | 4241587 | c.1725C>G | synonymous_variant | 1.0 |
| embC | 4241591 | p.Leu577Val | missense_variant | 1.0 |
| embC | 4241611 | c.1749G>C | synonymous_variant | 1.0 |
| embC | 4241614 | c.1752A>C | synonymous_variant | 1.0 |
| embC | 4241626 | c.1764T>C | synonymous_variant | 1.0 |
| embC | 4241635 | c.1773G>C | synonymous_variant | 1.0 |
| embC | 4241644 | c.1782G>C | synonymous_variant | 1.0 |
| embC | 4241648 | c.1786_1788delTTGinsCTC | synonymous_variant | 1.0 |
| embC | 4241657 | p.Ser599Pro | missense_variant | 1.0 |
| embC | 4241665 | c.1803G>C | synonymous_variant | 1.0 |
| embC | 4241671 | c.1809T>C | synonymous_variant | 1.0 |
| embC | 4241713 | c.1851G>C | synonymous_variant | 1.0 |
| embC | 4241719 | c.1857G>C | synonymous_variant | 1.0 |
| embC | 4241727 | p.Phe622Tyr | missense_variant | 1.0 |
| embC | 4241741 | p.Val627Leu | missense_variant | 1.0 |
| embC | 4241747 | p.Val629Leu | missense_variant | 1.0 |
| embC | 4241750 | p.Leu630Val | missense_variant | 1.0 |
| embC | 4241755 | c.1893C>G | synonymous_variant | 1.0 |
| embC | 4241770 | c.1908T>C | synonymous_variant | 1.0 |
| embC | 4241791 | c.1929G>C | synonymous_variant | 1.0 |
| embC | 4241794 | c.1932C>G | synonymous_variant | 1.0 |
| embC | 4241797 | c.1935C>T | synonymous_variant | 1.0 |
| embC | 4241809 | c.1947A>C | synonymous_variant | 1.0 |
| embC | 4241818 | c.1956C>T | synonymous_variant | 1.0 |
| embC | 4241819 | p.Ser653Ala | missense_variant | 1.0 |
| embC | 4241971 | c.2109T>C | synonymous_variant | 1.0 |
| embC | 4241972 | p.Val704Ile | missense_variant | 1.0 |
| embC | 4241995 | c.2133C>G | synonymous_variant | 1.0 |
| embC | 4242002 | p.Leu714Val | missense_variant | 1.0 |
| embC | 4242011 | p.Leu717Val | missense_variant | 1.0 |
| embC | 4242024 | p.Val721Ala | missense_variant | 1.0 |
| embC | 4242036 | p.Gln725Leu | missense_variant | 1.0 |
| embC | 4242045 | p.Ile728Thr | missense_variant | 1.0 |
| embC | 4242193 | c.2331G>C | synonymous_variant | 1.0 |
| embC | 4242196 | c.2334A>C | synonymous_variant | 1.0 |
| embC | 4242208 | c.2346T>G | synonymous_variant | 1.0 |
| embC | 4242220 | c.2358A>G | synonymous_variant | 1.0 |
| embC | 4242229 | c.2367C>A | synonymous_variant | 1.0 |
| embC | 4242245 | p.Thr795Arg | missense_variant | 1.0 |
| embA | 4242268 | c.-965T>G | upstream_gene_variant | 1.0 |
| embA | 4242271 | c.-962A>G | upstream_gene_variant | 1.0 |
| embA | 4242274 | c.-959G>T | upstream_gene_variant | 1.0 |
| embA | 4242277 | c.-956T>C | upstream_gene_variant | 1.0 |
| embC | 4242287 | p.Leu809Val | missense_variant | 1.0 |
| embA | 4242502 | c.-731G>A | upstream_gene_variant | 1.0 |
| embC | 4242519 | p.Thr886Ser | missense_variant | 1.0 |
| embA | 4242532 | c.-701A>T | upstream_gene_variant | 1.0 |
| embC | 4242539 | p.Ser893Pro | missense_variant | 1.0 |
| embA | 4242544 | c.-689C>T | upstream_gene_variant | 1.0 |
| embC | 4242552 | p.Arg897Gln | missense_variant | 1.0 |
| embC | 4242554 | p.Leu898Val | missense_variant | 1.0 |
| embA | 4242577 | c.-656A>G | upstream_gene_variant | 1.0 |
| embC | 4242585 | p.Ala908Gly | missense_variant | 1.0 |
| embA | 4242589 | c.-644A>G | upstream_gene_variant | 1.0 |
| embC | 4242594 | p.His911Pro | missense_variant | 0.86 |
| embC | 4242677 | p.Thr939Ser | missense_variant | 1.0 |
| embC | 4242689 | p.Val943Ile | missense_variant | 1.0 |
| embA | 4242694 | c.-539G>A | upstream_gene_variant | 1.0 |
| embC | 4242710 | p.Gln950Glu | missense_variant | 1.0 |
| embA | 4242715 | c.-518T>C | upstream_gene_variant | 1.0 |
| embA | 4242742 | c.-491C>G | upstream_gene_variant | 1.0 |
| embA | 4242748 | c.-485A>G | upstream_gene_variant | 1.0 |
| embA | 4242754 | c.-479G>C | upstream_gene_variant | 1.0 |
| embC | 4242764 | p.Val968Leu | missense_variant | 1.0 |
| embC | 4242779 | p.Asn973Asp | missense_variant | 1.0 |
| embC | 4242791 | p.Ala977Ser | missense_variant | 1.0 |
| embA | 4242796 | c.-437G>C | upstream_gene_variant | 1.0 |
| embA | 4242799 | c.-434T>C | upstream_gene_variant | 1.0 |
| embA | 4242820 | c.-413G>C | upstream_gene_variant | 1.0 |
| embA | 4242823 | c.-410G>C | upstream_gene_variant | 1.0 |
| embA | 4242832 | c.-401A>C | upstream_gene_variant | 1.0 |
| embA | 4242838 | c.-395C>G | upstream_gene_variant | 1.0 |
| embA | 4242841 | c.-392C>T | upstream_gene_variant | 1.0 |
| embA | 4242844 | c.-389A>G | upstream_gene_variant | 1.0 |
| embA | 4242847 | c.-386C>A | upstream_gene_variant | 1.0 |
| embA | 4242859 | c.-374C>T | upstream_gene_variant | 1.0 |
| embA | 4242862 | c.-371A>G | upstream_gene_variant | 1.0 |
| embC | 4242863 | p.Tyr1001Asn | missense_variant | 1.0 |
| embA | 4242883 | c.-350C>G | upstream_gene_variant | 1.0 |
| embA | 4242892 | c.-341G>C | upstream_gene_variant | 1.0 |
| embA | 4242901 | c.-332G>C | upstream_gene_variant | 1.0 |
| embA | 4242919 | c.-314A>G | upstream_gene_variant | 1.0 |
| embA | 4242928 | c.-305A>G | upstream_gene_variant | 1.0 |
| embA | 4242931 | c.-302G>C | upstream_gene_variant | 1.0 |
| embA | 4243553 | c.321C>G | synonymous_variant | 1.0 |
| embA | 4243559 | c.327C>G | synonymous_variant | 1.0 |
| embA | 4243563 | p.Gln111Lys | missense_variant | 1.0 |
| embA | 4243569 | p.Thr113Val | missense_variant | 1.0 |
| embA | 4243593 | p.Ser121Thr | missense_variant | 1.0 |
| embA | 4243598 | c.366G>C | synonymous_variant | 1.0 |
| embA | 4243601 | c.369C>G | synonymous_variant | 1.0 |
| embA | 4244189 | c.957C>G | synonymous_variant | 1.0 |
| embA | 4244192 | c.960C>G | synonymous_variant | 1.0 |
| embA | 4244207 | c.975C>G | synonymous_variant | 1.0 |
| embA | 4244219 | c.987C>G | synonymous_variant | 1.0 |
| embA | 4244228 | c.996A>G | synonymous_variant | 1.0 |
| embA | 4244233 | p.Ala334Gly | missense_variant | 1.0 |
| embA | 4244298 | p.Ser356Ala | missense_variant | 1.0 |
| embA | 4244306 | c.1074G>C | synonymous_variant | 1.0 |
| embA | 4244312 | c.1080T>G | synonymous_variant | 1.0 |
| embA | 4244315 | c.1083G>C | synonymous_variant | 1.0 |
| embA | 4244324 | c.1092T>G | synonymous_variant | 1.0 |
| embA | 4244327 | c.1095T>C | synonymous_variant | 1.0 |
| embA | 4244333 | c.1101G>T | synonymous_variant | 1.0 |
| embA | 4244337 | p.Leu369Val | missense_variant | 1.0 |
| embA | 4244340 | p.Ser370Ala | missense_variant | 1.0 |
| embA | 4244366 | c.1134C>G | synonymous_variant | 1.0 |
| embA | 4244372 | c.1140T>G | synonymous_variant | 1.0 |
| embA | 4244378 | c.1146G>A | synonymous_variant | 1.0 |
| embA | 4244381 | c.1149G>A | synonymous_variant | 1.0 |
| embA | 4244390 | c.1158G>C | synonymous_variant | 1.0 |
| embA | 4244393 | c.1161G>C | synonymous_variant | 1.0 |
| embA | 4244396 | c.1164T>C | synonymous_variant | 1.0 |
| embA | 4244408 | c.1176G>C | synonymous_variant | 1.0 |
| embA | 4244412 | p.Val394Met | missense_variant | 1.0 |
| embA | 4244415 | c.1183T>C | synonymous_variant | 1.0 |
| embA | 4244447 | c.1215G>C | synonymous_variant | 1.0 |
| embA | 4244462 | c.1230A>G | synonymous_variant | 1.0 |
| embA | 4244478 | p.Thr416Leu | missense_variant | 1.0 |
| embA | 4244483 | c.1251T>G | synonymous_variant | 1.0 |
| embA | 4244485 | p.Thr418Ser | missense_variant | 1.0 |
| embA | 4244498 | c.1266A>G | synonymous_variant | 1.0 |
| embA | 4244507 | c.1275G>T | synonymous_variant | 0.82 |
| embA | 4244508 | c.1276T>C | synonymous_variant | 1.0 |
| embA | 4244516 | c.1284G>C | synonymous_variant | 1.0 |
| embA | 4244517 | p.Leu429Val | missense_variant | 1.0 |
| embA | 4244523 | p.Pro431Ala | missense_variant | 1.0 |
| embA | 4244534 | c.1302T>C | synonymous_variant | 1.0 |
| embA | 4244537 | c.1305T>G | synonymous_variant | 1.0 |
| embA | 4244543 | c.1311C>G | synonymous_variant | 1.0 |
| embA | 4244547 | p.Ile439Val | missense_variant | 1.0 |
| embA | 4244557 | p.Arg442Thr | missense_variant | 1.0 |
| embA | 4244582 | c.1350T>C | synonymous_variant | 1.0 |
| embA | 4244585 | c.1353A>G | synonymous_variant | 1.0 |
| embA | 4244611 | p.Ala460Gly | missense_variant | 1.0 |
| embA | 4244616 | p.Ala462Ser | missense_variant | 1.0 |
| embA | 4244619 | c.1387_1389delTTGinsCTC | synonymous_variant | 1.0 |
| embA | 4244625 | p.Leu465Val | missense_variant | 1.0 |
| embA | 4244631 | p.Thr467Leu | missense_variant | 1.0 |
| embA | 4244645 | c.1413T>C | synonymous_variant | 1.0 |
| embA | 4244648 | c.1416G>C | synonymous_variant | 1.0 |
| embA | 4244649 | p.Asp473Ser | missense_variant | 1.0 |
| embA | 4244670 | p.Ala480Leu | missense_variant | 1.0 |
| embA | 4244675 | c.1443A>G | synonymous_variant | 1.0 |
| embA | 4244678 | c.1446G>C | synonymous_variant | 1.0 |
| embA | 4244681 | c.1449A>C | synonymous_variant | 1.0 |
| embA | 4244690 | c.1458G>A | synonymous_variant | 1.0 |
| embA | 4244702 | c.1470C>G | synonymous_variant | 1.0 |
| embA | 4244708 | c.1476C>G | synonymous_variant | 1.0 |
| embA | 4244728 | p.Phe499Trp | missense_variant | 1.0 |
| embA | 4244885 | c.1653A>G | synonymous_variant | 1.0 |
| embA | 4244897 | c.1665T>C | synonymous_variant | 1.0 |
| embA | 4244900 | c.1668G>C | synonymous_variant | 1.0 |
| embA | 4244904 | p.Val558Ile | missense_variant | 1.0 |
| embA | 4244918 | c.1686G>C | synonymous_variant | 1.0 |
| embA | 4244919 | p.Leu563Val | missense_variant | 1.0 |
| embA | 4244930 | c.1698G>C | synonymous_variant | 1.0 |
| embA | 4245032 | c.1800A>C | synonymous_variant | 0.8 |
| embA | 4245041 | c.1809C>G | synonymous_variant | 0.95 |
| embA | 4245044 | c.1812G>C | synonymous_variant | 0.96 |
| embA | 4245053 | c.1821G>C | synonymous_variant | 0.98 |
| embA | 4245060 | c.1828T>C | synonymous_variant | 0.98 |
| embA | 4245083 | c.1851A>C | synonymous_variant | 0.99 |
| embA | 4245089 | c.1857G>C | synonymous_variant | 0.99 |
| embA | 4245101 | c.1869G>C | synonymous_variant | 1.0 |
| embA | 4245137 | c.1905T>C | synonymous_variant | 1.0 |
| embA | 4245146 | c.1914G>A | synonymous_variant | 1.0 |
| embA | 4245149 | c.1917C>G | synonymous_variant | 1.0 |
| embA | 4245153 | p.Ile641Val | missense_variant | 1.0 |
| embA | 4245182 | c.1950T>C | synonymous_variant | 1.0 |
| embA | 4245189 | c.1957C>T | synonymous_variant | 1.0 |
| embA | 4245198 | p.Leu656Ile | missense_variant | 1.0 |
| embA | 4245207 | c.1975T>C | synonymous_variant | 1.0 |
| embA | 4245215 | c.1983A>C | synonymous_variant | 1.0 |
| embA | 4245222 | p.Tyr664Gln | missense_variant | 1.0 |
| embA | 4245248 | c.2016G>C | synonymous_variant | 1.0 |
| embA | 4245257 | c.2025A>G | synonymous_variant | 0.97 |
| embA | 4245263 | c.2031A>G | synonymous_variant | 0.97 |
| embA | 4245282 | p.Ile684Val | missense_variant | 0.91 |
| embA | 4245285 | c.2053T>C | synonymous_variant | 0.88 |
| embA | 4245290 | c.2058C>G | synonymous_variant | 0.87 |
| embA | 4245293 | c.2061T>G | synonymous_variant | 0.85 |
| embA | 4245296 | c.2064G>C | synonymous_variant | 0.85 |
| embA | 4245299 | c.2067A>G | synonymous_variant | 0.85 |
| embA | 4245328 | p.Ala699Val | missense_variant | 0.82 |
| embA | 4245335 | c.2103A>G | synonymous_variant | 1.0 |
| embA | 4245340 | p.Gly703Ala | missense_variant | 1.0 |
| embA | 4245345 | p.Met705Leu | missense_variant | 1.0 |
| embA | 4245348 | p.Ala706Thr | missense_variant | 1.0 |
| embA | 4245355 | p.Ala708Gly | missense_variant | 1.0 |
| embA | 4245368 | c.2136T>C | synonymous_variant | 1.0 |
| embA | 4245377 | c.2145T>C | synonymous_variant | 1.0 |
| embB | 4245557 | c.-957G>A | upstream_gene_variant | 1.0 |
| embB | 4245575 | c.-939C>G | upstream_gene_variant | 1.0 |
| embA | 4245576 | p.Lys782Gln | missense_variant | 1.0 |
| embB | 4245593 | c.-921C>G | upstream_gene_variant | 1.0 |
| embA | 4245594 | p.Ser788Thr | missense_variant | 1.0 |
| embB | 4245599 | c.-915A>G | upstream_gene_variant | 1.0 |
| embB | 4245602 | c.-912C>G | upstream_gene_variant | 1.0 |
| embB | 4245605 | c.-909G>A | upstream_gene_variant | 1.0 |
| embA | 4245652 | p.Thr807Ser | missense_variant | 1.0 |
| embB | 4245659 | c.-855C>G | upstream_gene_variant | 1.0 |
| embB | 4245674 | c.-840A>C | upstream_gene_variant | 1.0 |
| embB | 4245677 | c.-837G>C | upstream_gene_variant | 1.0 |
| embA | 4245693 | p.Ile821Val | missense_variant | 1.0 |
| embB | 4245701 | c.-813G>C | upstream_gene_variant | 1.0 |
| embB | 4245704 | c.-810G>C | upstream_gene_variant | 1.0 |
| embB | 4245725 | c.-789A>G | upstream_gene_variant | 1.0 |
| embB | 4245726 | c.-788T>C | upstream_gene_variant | 1.0 |
| embB | 4245737 | c.-777A>C | upstream_gene_variant | 1.0 |
| embB | 4245740 | c.-774T>C | upstream_gene_variant | 1.0 |
| embB | 4245764 | c.-750G>C | upstream_gene_variant | 1.0 |
| embA | 4245772 | p.Asn847Thr | missense_variant | 1.0 |
| embB | 4245785 | c.-729G>C | upstream_gene_variant | 1.0 |
| embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 1.0 |
| embB | 4245812 | c.-702G>C | upstream_gene_variant | 1.0 |
| embA | 4245813 | p.Pro861Ala | missense_variant | 1.0 |
| embA | 4245820 | p.Ser863Thr | missense_variant | 1.0 |
| embB | 4245824 | c.-690G>C | upstream_gene_variant | 1.0 |
| embB | 4245833 | c.-681G>C | upstream_gene_variant | 1.0 |
| embB | 4245842 | c.-672G>C | upstream_gene_variant | 1.0 |
| embB | 4245845 | c.-669T>C | upstream_gene_variant | 1.0 |
| embB | 4245851 | c.-663G>C | upstream_gene_variant | 1.0 |
| embB | 4245860 | c.-654C>G | upstream_gene_variant | 1.0 |
| embA | 4245885 | p.Asp885Thr | missense_variant | 1.0 |
| embA | 4245892 | p.Ile887Thr | missense_variant | 1.0 |
| embB | 4245899 | c.-615C>G | upstream_gene_variant | 1.0 |
| embB | 4245902 | c.-612G>A | upstream_gene_variant | 1.0 |
| embB | 4245905 | c.-609C>G | upstream_gene_variant | 1.0 |
| embB | 4245911 | c.-603A>G | upstream_gene_variant | 1.0 |
| embB | 4245917 | c.-597G>A | upstream_gene_variant | 1.0 |
| embA | 4245930 | p.Gly900Arg | missense_variant | 1.0 |
| embB | 4245983 | c.-531A>C | upstream_gene_variant | 1.0 |
| embB | 4245989 | c.-525A>G | upstream_gene_variant | 1.0 |
| embB | 4245992 | c.-522C>G | upstream_gene_variant | 1.0 |
| embB | 4246004 | c.-510T>C | upstream_gene_variant | 1.0 |
| embB | 4246010 | c.-504G>T | upstream_gene_variant | 1.0 |
| embB | 4246013 | c.-501T>C | upstream_gene_variant | 1.0 |
| embB | 4246022 | c.-492C>G | upstream_gene_variant | 1.0 |
| embB | 4246040 | c.-474C>G | upstream_gene_variant | 1.0 |
| embA | 4246041 | p.Asp937Asn | missense_variant | 1.0 |
| embB | 4246055 | c.-459T>C | upstream_gene_variant | 1.0 |
| embB | 4246064 | c.-450T>C | upstream_gene_variant | 1.0 |
| embA | 4246080 | p.Pro950Ser | missense_variant | 1.0 |
| embB | 4246088 | c.-426A>G | upstream_gene_variant | 1.0 |
| embB | 4246097 | c.-417C>G | upstream_gene_variant | 1.0 |
| embB | 4246103 | c.-411C>G | upstream_gene_variant | 1.0 |
| embB | 4246109 | c.-405C>G | upstream_gene_variant | 1.0 |
| embB | 4246115 | c.-399T>G | upstream_gene_variant | 1.0 |
| embB | 4246164 | c.-350T>C | upstream_gene_variant | 0.92 |
| embB | 4246184 | c.-330A>C | upstream_gene_variant | 0.93 |
| embB | 4246196 | c.-318C>G | upstream_gene_variant | 0.92 |
| embB | 4246205 | c.-309A>G | upstream_gene_variant | 0.92 |
| embB | 4246211 | c.-303T>C | upstream_gene_variant | 0.92 |
| embB | 4246217 | c.-297G>A | upstream_gene_variant | 0.92 |
| embB | 4246220 | c.-294T>C | upstream_gene_variant | 1.0 |
| embB | 4246223 | c.-291C>T | upstream_gene_variant | 1.0 |
| embA | 4246227 | p.Ile999Val | missense_variant | 1.0 |
| embB | 4246235 | c.-279G>A | upstream_gene_variant | 1.0 |
| embA | 4246242 | p.Gln1004Gly | missense_variant | 1.0 |
| embB | 4246250 | c.-264G>C | upstream_gene_variant | 1.0 |
| embB | 4246256 | c.-258G>T | upstream_gene_variant | 1.0 |
| embB | 4246259 | c.-255G>C | upstream_gene_variant | 1.0 |
| embA | 4246264 | p.His1011Arg | missense_variant | 1.0 |
| embB | 4246292 | c.-222A>G | upstream_gene_variant | 0.99 |
| embA | 4246305 | p.Ser1025Glu | missense_variant | 0.99 |
| embA | 4246308 | p.Thr1026Ala | missense_variant | 0.99 |
| embB | 4246316 | c.-198T>G | upstream_gene_variant | 0.97 |
| embB | 4246319 | c.-195G>C | upstream_gene_variant | 0.99 |
| embA | 4246329 | p.Thr1033Ala | missense_variant | 0.99 |
| embB | 4246349 | c.-165C>G | upstream_gene_variant | 0.99 |
| embA | 4246359 | p.Ala1043Ser | missense_variant | 1.0 |
| embB | 4246367 | c.-147C>T | upstream_gene_variant | 1.0 |
| embB | 4246373 | c.-141T>C | upstream_gene_variant | 1.0 |
| embB | 4246376 | c.-138G>C | upstream_gene_variant | 1.0 |
| embB | 4246379 | c.-135C>T | upstream_gene_variant | 1.0 |
| embB | 4246400 | c.-114G>C | upstream_gene_variant | 1.0 |
| embA | 4246413 | p.His1061Phe | missense_variant | 1.0 |
| embB | 4246419 | c.-95C>T | upstream_gene_variant | 1.0 |
| embB | 4246594 | c.81C>T | synonymous_variant | 1.0 |
| embB | 4246603 | c.90C>G | synonymous_variant | 1.0 |
| embB | 4246615 | c.102G>C | synonymous_variant | 1.0 |
| embB | 4246621 | c.108T>C | synonymous_variant | 1.0 |
| embB | 4246624 | c.111C>G | synonymous_variant | 1.0 |
| embB | 4246627 | c.114T>C | synonymous_variant | 1.0 |
| embB | 4246631 | c.118T>C | synonymous_variant | 1.0 |
| embB | 4246636 | c.123G>C | synonymous_variant | 1.0 |
| embB | 4246639 | c.126G>C | synonymous_variant | 1.0 |
| embB | 4246642 | c.129G>C | synonymous_variant | 1.0 |
| embB | 4246645 | c.132G>C | synonymous_variant | 1.0 |
| embB | 4246669 | c.156C>G | synonymous_variant | 1.0 |
| embB | 4247365 | c.852A>C | synonymous_variant | 0.89 |
| embB | 4247371 | c.858C>G | synonymous_variant | 0.89 |
| embB | 4247375 | p.Leu288Val | missense_variant | 0.89 |
| embB | 4247386 | c.873T>C | synonymous_variant | 0.89 |
| embB | 4247389 | c.876C>G | synonymous_variant | 0.89 |
| embB | 4247395 | c.882C>G | synonymous_variant | 0.94 |
| embB | 4247401 | c.888T>C | synonymous_variant | 0.95 |
| embB | 4247407 | c.894G>C | synonymous_variant | 0.95 |
| embB | 4247425 | c.912G>C | synonymous_variant | 0.97 |
| embB | 4247434 | c.921C>G | synonymous_variant | 1.0 |
| embB | 4247437 | c.924A>G | synonymous_variant | 1.0 |
| embB | 4247440 | c.927C>G | synonymous_variant | 1.0 |
| embB | 4247446 | c.933C>T | synonymous_variant | 1.0 |
| embB | 4247464 | c.951C>G | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247491 | c.978G>C | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4247512 | c.999T>C | synonymous_variant | 1.0 |
| embB | 4247539 | c.1026T>C | synonymous_variant | 1.0 |
| embB | 4247554 | c.1041T>C | synonymous_variant | 1.0 |
| embB | 4247566 | c.1053C>A | synonymous_variant | 1.0 |
| embB | 4247572 | c.1059A>G | synonymous_variant | 1.0 |
| embB | 4247579 | p.Ala356Phe | missense_variant | 1.0 |
| embB | 4247587 | c.1074G>A | synonymous_variant | 1.0 |
| embB | 4247603 | c.1090C>T | synonymous_variant | 1.0 |
| embB | 4247611 | c.1098G>T | synonymous_variant | 1.0 |
| embB | 4247614 | c.1101T>C | synonymous_variant | 1.0 |
| embB | 4247683 | c.1170C>G | synonymous_variant | 1.0 |
| embB | 4247692 | c.1179C>G | synonymous_variant | 1.0 |
| embB | 4247716 | c.1203C>T | synonymous_variant | 0.96 |
| embB | 4247722 | c.1209G>T | synonymous_variant | 0.91 |
| embB | 4247725 | c.1212G>C | synonymous_variant | 0.95 |
| embB | 4247729 | p.Gly406Pro | missense_variant | 0.95 |
| embB | 4247746 | c.1233C>T | synonymous_variant | 0.97 |
| embB | 4247761 | c.1248T>C | synonymous_variant | 0.98 |
| embB | 4247773 | c.1260G>A | synonymous_variant | 0.98 |
| embB | 4247776 | c.1263G>T | synonymous_variant | 0.98 |
| embB | 4247797 | c.1284C>G | synonymous_variant | 1.0 |
| embB | 4247800 | c.1287A>T | synonymous_variant | 1.0 |
| embB | 4247803 | c.1290G>C | synonymous_variant | 1.0 |
| embB | 4247815 | c.1302C>G | synonymous_variant | 1.0 |
| embB | 4247819 | p.Val436Ile | missense_variant | 1.0 |
| embB | 4247830 | c.1317A>G | synonymous_variant | 1.0 |
| embB | 4247836 | c.1323A>G | synonymous_variant | 1.0 |
| embB | 4247839 | c.1326G>C | synonymous_variant | 1.0 |
| embB | 4247866 | c.1353G>C | synonymous_variant | 1.0 |
| embB | 4247875 | c.1362G>C | synonymous_variant | 1.0 |
| embB | 4247876 | c.1363C>T | synonymous_variant | 1.0 |
| embB | 4247881 | c.1368G>C | synonymous_variant | 1.0 |
| embB | 4247887 | c.1374C>T | synonymous_variant | 1.0 |
| embB | 4247893 | c.1380C>T | synonymous_variant | 1.0 |
| embB | 4247899 | p.Met462Ile | missense_variant | 1.0 |
| embB | 4247905 | c.1392G>C | synonymous_variant | 1.0 |
| embB | 4247909 | c.1396T>C | synonymous_variant | 1.0 |
| embB | 4247932 | c.1419C>G | synonymous_variant | 1.0 |
| embB | 4247940 | p.Leu476Trp | missense_variant | 1.0 |
| embB | 4247945 | c.1432T>C | synonymous_variant | 1.0 |
| embB | 4247951 | p.Ser480Ala | missense_variant | 1.0 |
| embB | 4247956 | c.1443G>C | synonymous_variant | 1.0 |
| embB | 4247974 | c.1461C>G | synonymous_variant | 1.0 |
| embB | 4248007 | c.1494C>G | synonymous_variant | 1.0 |
| embB | 4248011 | p.Ser500Arg | missense_variant | 1.0 |
| embB | 4248014 | p.Thr501Ala | missense_variant | 1.0 |
| embB | 4248035 | p.Val508Ile | missense_variant | 1.0 |
| embB | 4248040 | c.1527C>G | synonymous_variant | 1.0 |
| embB | 4248041 | p.Ala510Thr | missense_variant | 1.0 |
| embB | 4248044 | p.Lys511Ala | missense_variant | 1.0 |
| embB | 4248070 | c.1557T>C | synonymous_variant | 1.0 |
| embB | 4248085 | c.1572T>C | synonymous_variant | 1.0 |
| embB | 4248097 | c.1584C>G | synonymous_variant | 1.0 |
| embB | 4248130 | c.1617G>C | synonymous_variant | 1.0 |
| embB | 4248133 | c.1620C>G | synonymous_variant | 1.0 |
| embB | 4248139 | c.1626C>G | synonymous_variant | 1.0 |
| embB | 4248142 | c.1629T>C | synonymous_variant | 1.0 |
| embB | 4248143 | c.1630T>C | synonymous_variant | 1.0 |
| embB | 4248157 | c.1644A>G | synonymous_variant | 1.0 |
| embB | 4248199 | c.1686A>G | synonymous_variant | 1.0 |
| embB | 4248200 | p.Ile563Val | missense_variant | 1.0 |
| embB | 4248205 | c.1692C>G | synonymous_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248220 | c.1707A>C | synonymous_variant | 1.0 |
| embB | 4248304 | c.1791G>C | synonymous_variant | 1.0 |
| embB | 4248319 | c.1806A>G | synonymous_variant | 1.0 |
| embB | 4248343 | c.1830G>C | synonymous_variant | 1.0 |
| embB | 4248350 | c.1837T>C | synonymous_variant | 1.0 |
| embB | 4248355 | c.1842A>G | synonymous_variant | 1.0 |
| embB | 4248358 | c.1845C>G | synonymous_variant | 1.0 |
| embB | 4248361 | c.1848A>C | synonymous_variant | 1.0 |
| embB | 4248362 | p.Ser617Ala | missense_variant | 1.0 |
| embB | 4248373 | c.1860C>G | synonymous_variant | 1.0 |
| embB | 4248386 | c.1873C>A | synonymous_variant | 1.0 |
| embB | 4248407 | p.Leu632Val | missense_variant | 1.0 |
| embB | 4248410 | p.Phe633Leu | missense_variant | 1.0 |
| embB | 4248419 | p.Leu636Met | missense_variant | 1.0 |
| embB | 4248425 | c.1912T>C | synonymous_variant | 1.0 |
| embB | 4248430 | c.1917T>C | synonymous_variant | 1.0 |
| embB | 4248432 | p.Trp640Phe | missense_variant | 1.0 |
| embB | 4248457 | c.1944T>C | synonymous_variant | 1.0 |
| embB | 4248472 | c.1959T>C | synonymous_variant | 1.0 |
| embB | 4248475 | c.1962G>C | synonymous_variant | 1.0 |
| embB | 4248500 | p.Ile663Phe | missense_variant | 1.0 |
| embB | 4248504 | p.Asp664Gly | missense_variant | 1.0 |
| embB | 4248508 | c.1995G>A | synonymous_variant | 1.0 |
| embB | 4248514 | c.2001A>G | synonymous_variant | 1.0 |
| embB | 4248535 | c.2022C>G | synonymous_variant | 1.0 |
| embB | 4248541 | c.2028T>C | synonymous_variant | 1.0 |
| embB | 4248659 | p.Ala716Leu | missense_variant | 1.0 |
| embB | 4248668 | p.Val719Ile | missense_variant | 1.0 |
| embB | 4248676 | c.2163C>G | synonymous_variant | 1.0 |
| embB | 4248688 | c.2175G>C | synonymous_variant | 1.0 |
| embB | 4248697 | c.2184A>C | synonymous_variant | 1.0 |
| embB | 4248706 | c.2193G>C | synonymous_variant | 1.0 |
| embB | 4249255 | c.2742G>A | synonymous_variant | 1.0 |
| embB | 4249259 | p.Met916Leu | missense_variant | 1.0 |
| embB | 4249268 | p.Asp919Tyr | missense_variant | 1.0 |
| embB | 4249276 | c.2763A>G | synonymous_variant | 1.0 |
| embB | 4249277 | p.Tyr922Asn | missense_variant | 1.0 |
| embB | 4249282 | c.2769A>C | synonymous_variant | 1.0 |
| embB | 4249291 | c.2778C>A | synonymous_variant | 1.0 |
| embB | 4249297 | c.2784G>C | synonymous_variant | 1.0 |
| embB | 4249312 | c.2799C>T | synonymous_variant | 1.0 |
| embB | 4249342 | c.2829C>G | synonymous_variant | 1.0 |
| embB | 4249348 | c.2835G>C | synonymous_variant | 1.0 |
| embB | 4249351 | c.2838C>G | synonymous_variant | 1.0 |
| embB | 4249369 | c.2856T>C | synonymous_variant | 0.96 |
| embB | 4249375 | c.2862G>C | synonymous_variant | 0.96 |
| embB | 4249381 | c.2868A>G | synonymous_variant | 0.92 |
| embB | 4249411 | c.2898G>A | synonymous_variant | 0.96 |
| embB | 4249417 | c.2904A>G | synonymous_variant | 0.96 |
| embB | 4249423 | p.Asp970Glu | missense_variant | 0.94 |
| embB | 4249424 | p.Leu971Met | missense_variant | 0.93 |
| embB | 4249429 | c.2916C>T | synonymous_variant | 0.97 |
| embB | 4249432 | c.2919A>G | synonymous_variant | 0.97 |
| embB | 4249441 | c.2928A>G | synonymous_variant | 0.97 |
| embB | 4249444 | c.2931T>C | synonymous_variant | 0.97 |
| embB | 4249447 | c.2934G>C | synonymous_variant | 0.97 |
| embB | 4249469 | p.Leu986Met | missense_variant | 1.0 |
| embB | 4249486 | c.2973T>G | synonymous_variant | 1.0 |
| embB | 4249498 | c.2985G>C | synonymous_variant | 1.0 |
| embB | 4249521 | p.Ala1003Val | missense_variant | 1.0 |
| embB | 4249525 | c.3012T>C | synonymous_variant | 0.97 |
| embB | 4249529 | p.Ile1006Val | missense_variant | 0.97 |
| embB | 4249532 | p.Ala1007Thr | missense_variant | 0.97 |
| embB | 4249537 | c.3024A>G | synonymous_variant | 0.97 |
| embB | 4249543 | c.3030G>C | synonymous_variant | 0.97 |
| embB | 4249546 | c.3033G>A | synonymous_variant | 0.97 |
| embB | 4249558 | c.3045A>C | synonymous_variant | 0.95 |
| embB | 4249568 | p.Ser1019Thr | missense_variant | 0.91 |
| embB | 4249573 | c.3060T>C | synonymous_variant | 0.83 |
| embB | 4249594 | c.3081G>C | synonymous_variant | 0.8 |
| embB | 4249606 | c.3093C>A | synonymous_variant | 1.0 |
| embB | 4249609 | c.3096T>C | synonymous_variant | 1.0 |
| embB | 4249615 | c.3102C>G | synonymous_variant | 1.0 |
| embB | 4249618 | c.3105C>G | synonymous_variant | 1.0 |
| embB | 4249624 | c.3111C>G | synonymous_variant | 0.8 |
| embB | 4249627 | c.3114G>C | synonymous_variant | 0.8 |
| embB | 4249640 | c.3127T>C | synonymous_variant | 0.83 |
| embB | 4249657 | c.3144C>G | synonymous_variant | 0.8 |
| embB | 4249661 | p.Ala1050Ser | missense_variant | 0.8 |
| embB | 4249666 | c.3153C>G | synonymous_variant | 0.8 |
| embB | 4249677 | p.Arg1055His | missense_variant | 0.8 |
| embB | 4249686 | p.Ala1058Gly | missense_variant | 0.8 |
| embB | 4249693 | c.3180T>C | synonymous_variant | 0.8 |
| embB | 4249699 | c.3186T>G | synonymous_variant | 1.0 |
| embB | 4249702 | c.3189C>G | synonymous_variant | 1.0 |
| aftB | 4267177 | p.Ile554Leu | missense_variant | 1.0 |
| aftB | 4267184 | c.1653C>G | synonymous_variant | 1.0 |
| aftB | 4267190 | c.1647T>A | synonymous_variant | 1.0 |
| aftB | 4267196 | c.1641C>T | synonymous_variant | 1.0 |
| aftB | 4267200 | p.Trp546Val | missense_variant | 1.0 |
| aftB | 4267214 | c.1623A>C | synonymous_variant | 1.0 |
| aftB | 4267241 | c.1596G>C | synonymous_variant | 1.0 |
| aftB | 4267244 | c.1593T>C | synonymous_variant | 1.0 |
| aftB | 4267256 | c.1581C>G | synonymous_variant | 1.0 |
| aftB | 4267262 | c.1575T>C | synonymous_variant | 1.0 |
| aftB | 4267266 | p.Ala524Gly | missense_variant | 1.0 |
| aftB | 4267268 | c.1569T>C | synonymous_variant | 1.0 |
| aftB | 4267274 | c.1563G>C | synonymous_variant | 1.0 |
| aftB | 4267289 | c.1548G>A | synonymous_variant | 1.0 |
| aftB | 4267316 | c.1521A>G | synonymous_variant | 1.0 |
| aftB | 4267325 | c.1512G>C | synonymous_variant | 1.0 |
| aftB | 4267334 | c.1503T>C | synonymous_variant | 1.0 |
| aftB | 4267355 | p.Leu494Val | missense_variant | 1.0 |
| aftB | 4267364 | p.Met491Leu | missense_variant | 1.0 |
| aftB | 4267382 | c.1455A>G | synonymous_variant | 1.0 |
| aftB | 4267394 | c.1443A>G | synonymous_variant | 1.0 |
| aftB | 4267574 | c.1263G>A | synonymous_variant | 1.0 |
| aftB | 4267580 | c.1257G>T | synonymous_variant | 0.97 |
| aftB | 4267604 | c.1233C>G | synonymous_variant | 1.0 |
| aftB | 4267607 | c.1230G>A | synonymous_variant | 1.0 |
| aftB | 4267625 | c.1212T>C | synonymous_variant | 1.0 |
| aftB | 4267628 | c.1209C>G | synonymous_variant | 1.0 |
| aftB | 4267634 | p.Arg401His | missense_variant | 1.0 |
| aftB | 4267649 | c.1188T>C | synonymous_variant | 1.0 |
| aftB | 4267658 | c.1179G>C | synonymous_variant | 1.0 |
| aftB | 4267822 | c.1015T>C | synonymous_variant | 0.75 |
| aftB | 4267829 | p.Gly336Ala | missense_variant | 0.75 |
| aftB | 4267838 | c.999T>C | synonymous_variant | 0.75 |
| aftB | 4267853 | c.984G>C | synonymous_variant | 0.5 |
| aftB | 4267856 | c.981T>C | synonymous_variant | 0.5 |
| aftB | 4267868 | c.969G>C | synonymous_variant | 0.5 |
| aftB | 4267876 | c.961C>T | synonymous_variant | 0.5 |
| aftB | 4267879 | p.Val320Leu | missense_variant | 0.5 |
| aftB | 4267916 | c.921T>C | synonymous_variant | 0.75 |
| aftB | 4267919 | p.Gln306His | missense_variant | 0.75 |
| aftB | 4267925 | c.912G>C | synonymous_variant | 1.0 |
| aftB | 4267940 | c.897T>G | synonymous_variant | 1.0 |
| aftB | 4267952 | c.885A>G | synonymous_variant | 1.0 |
| aftB | 4267959 | p.Val293Ala | missense_variant | 1.0 |
| aftB | 4267964 | c.873T>G | synonymous_variant | 1.0 |
| aftB | 4268096 | c.741C>G | synonymous_variant | 1.0 |
| aftB | 4268099 | c.738G>C | synonymous_variant | 1.0 |
| aftB | 4268102 | c.735C>G | synonymous_variant | 1.0 |
| aftB | 4268105 | c.732T>C | synonymous_variant | 1.0 |
| aftB | 4268117 | c.720G>C | synonymous_variant | 1.0 |
| aftB | 4268123 | p.Ser238Gly | missense_variant | 1.0 |
| aftB | 4268129 | c.708T>G | synonymous_variant | 1.0 |
| aftB | 4268138 | c.699A>C | synonymous_variant | 0.94 |
| aftB | 4268144 | c.693T>C | synonymous_variant | 0.95 |
| aftB | 4268164 | p.Gln225Glu | missense_variant | 0.92 |
| aftB | 4268169 | p.Ala223Gly | missense_variant | 0.92 |
| aftB | 4268171 | c.666G>C | synonymous_variant | 0.92 |
| aftB | 4268179 | c.658T>C | synonymous_variant | 0.89 |
| aftB | 4268182 | p.Phe219Leu | missense_variant | 0.89 |
| aftB | 4268183 | c.654A>T | synonymous_variant | 0.89 |
| aftB | 4268186 | c.651C>T | synonymous_variant | 0.9 |
| aftB | 4268193 | p.Leu215Ala | missense_variant | 0.92 |
| aftB | 4268205 | p.Val211Ala | missense_variant | 0.93 |
| aftB | 4268213 | c.624T>G | synonymous_variant | 1.0 |
| aftB | 4268225 | c.612G>C | synonymous_variant | 1.0 |
| aftB | 4268236 | c.601T>C | synonymous_variant | 1.0 |
| aftB | 4268258 | c.579C>T | synonymous_variant | 1.0 |
| aftB | 4268261 | p.Ile192Met | missense_variant | 1.0 |
| aftB | 4268264 | c.573G>C | synonymous_variant | 1.0 |
| aftB | 4268360 | p.Ser159Ala | missense_variant | 1.0 |
| aftB | 4268386 | c.451T>C | synonymous_variant | 1.0 |
| aftB | 4268393 | c.444G>C | synonymous_variant | 1.0 |
| aftB | 4268396 | c.441T>C | synonymous_variant | 1.0 |
| aftB | 4268404 | c.433T>C | synonymous_variant | 1.0 |
| aftB | 4268406 | p.Val144Ala | missense_variant | 1.0 |
| aftB | 4268410 | c.427C>T | synonymous_variant | 1.0 |
| aftB | 4268411 | c.426G>T | synonymous_variant | 1.0 |
| aftB | 4268417 | c.420G>A | synonymous_variant | 1.0 |
| aftB | 4268426 | c.411C>G | synonymous_variant | 1.0 |
| aftB | 4268638 | p.Leu67Met | missense_variant | 1.0 |
| aftB | 4268642 | c.195T>C | synonymous_variant | 1.0 |
| aftB | 4268651 | c.186G>C | synonymous_variant | 1.0 |
| aftB | 4268654 | c.183A>C | synonymous_variant | 1.0 |
| aftB | 4268657 | c.180G>C | synonymous_variant | 1.0 |
| aftB | 4268666 | c.171G>C | synonymous_variant | 1.0 |
| aftB | 4268669 | c.168A>G | synonymous_variant | 1.0 |
| aftB | 4268675 | c.162A>G | synonymous_variant | 1.0 |
| aftB | 4268699 | c.138A>G | synonymous_variant | 1.0 |
| aftB | 4268711 | c.124_126delTTGinsCTC | synonymous_variant | 1.0 |
| aftB | 4268714 | c.123A>G | synonymous_variant | 1.0 |
| aftB | 4268726 | c.111G>C | synonymous_variant | 1.0 |
| aftB | 4268729 | c.108G>C | synonymous_variant | 1.0 |
| aftB | 4268928 | c.-92C>T | upstream_gene_variant | 1.0 |
| aftB | 4268940 | c.-104T>C | upstream_gene_variant | 1.0 |
| aftB | 4268946 | c.-110G>A | upstream_gene_variant | 1.0 |
| ubiA | 4268951 | p.Val295Ile | missense_variant | 1.0 |
| aftB | 4268952 | c.-116G>C | upstream_gene_variant | 1.0 |
| aftB | 4268955 | c.-119A>G | upstream_gene_variant | 1.0 |
| aftB | 4268958 | c.-122A>C | upstream_gene_variant | 1.0 |
| ubiA | 4268969 | p.Leu289Val | missense_variant | 1.0 |
| aftB | 4268985 | c.-149A>G | upstream_gene_variant | 1.0 |
| aftB | 4268994 | c.-158T>G | upstream_gene_variant | 1.0 |
| aftB | 4268999 | c.-163C>T | upstream_gene_variant | 1.0 |
| aftB | 4269006 | c.-170T>C | upstream_gene_variant | 1.0 |
| aftB | 4269012 | c.-176G>C | upstream_gene_variant | 1.0 |
| aftB | 4269027 | c.-191C>T | upstream_gene_variant | 1.0 |
| aftB | 4269033 | c.-197T>C | upstream_gene_variant | 1.0 |
| aftB | 4269036 | c.-200C>G | upstream_gene_variant | 1.0 |
| aftB | 4269042 | c.-206G>C | upstream_gene_variant | 1.0 |
| ubiA | 4269075 | p.Ile253Val | missense_variant | 1.0 |
| aftB | 4269081 | c.-245G>C | upstream_gene_variant | 1.0 |
| aftB | 4269084 | c.-248G>C | upstream_gene_variant | 1.0 |
| aftB | 4269179 | c.-343C>A | upstream_gene_variant | 0.95 |
| aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.96 |
| aftB | 4269186 | c.-350C>G | upstream_gene_variant | 0.96 |
| aftB | 4269201 | c.-365A>G | upstream_gene_variant | 1.0 |
| ubiA | 4269220 | p.Ala205Lys | missense_variant | 1.0 |
| aftB | 4269222 | c.-386T>C | upstream_gene_variant | 1.0 |
| aftB | 4269242 | c.-406C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269243 | p.His197Gln | missense_variant | 1.0 |
| aftB | 4269249 | c.-413G>A | upstream_gene_variant | 1.0 |
| aftB | 4269258 | c.-422C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269329 | p.Lys169Glu | missense_variant | 0.75 |
| aftB | 4269342 | c.-506G>C | upstream_gene_variant | 0.92 |
| ubiA | 4269357 | p.Ile159Leu | missense_variant | 1.0 |
| aftB | 4269362 | c.-526T>C | upstream_gene_variant | 1.0 |
| aftB | 4269363 | c.-527T>C | upstream_gene_variant | 1.0 |
| ubiA | 4269380 | p.Val152Ile | missense_variant | 1.0 |
| ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
| ubiA | 4269390 | p.Val148Leu | missense_variant | 1.0 |
| aftB | 4269405 | c.-569G>A | upstream_gene_variant | 1.0 |
| aftB | 4269411 | c.-575T>G | upstream_gene_variant | 1.0 |
| aftB | 4269414 | c.-578T>C | upstream_gene_variant | 1.0 |
| aftB | 4269420 | c.-584T>C | upstream_gene_variant | 1.0 |
| aftB | 4269428 | c.-592T>C | upstream_gene_variant | 1.0 |
| ubiA | 4269436 | p.Ala133Gly | missense_variant | 1.0 |
| ubiA | 4269448 | p.Val129Ala | missense_variant | 1.0 |
| aftB | 4269453 | c.-617A>G | upstream_gene_variant | 1.0 |
| aftB | 4269458 | c.-622C>T | upstream_gene_variant | 1.0 |
| aftB | 4269459 | c.-623G>C | upstream_gene_variant | 1.0 |
| ubiA | 4269521 | p.Val105Met | missense_variant | 1.0 |
| ubiA | 4269522 | p.Thr104Ala | missense_variant | 1.0 |
| aftB | 4269528 | c.-692G>C | upstream_gene_variant | 1.0 |
| aftB | 4269549 | c.-713C>G | upstream_gene_variant | 1.0 |
| aftB | 4269552 | c.-716C>G | upstream_gene_variant | 1.0 |
| aftB | 4269555 | c.-719C>G | upstream_gene_variant | 1.0 |
| aftB | 4269564 | c.-728G>T | upstream_gene_variant | 1.0 |
| aftB | 4269573 | c.-737A>G | upstream_gene_variant | 1.0 |
| aftB | 4269585 | c.-749G>A | upstream_gene_variant | 1.0 |
| aftB | 4269588 | c.-752G>C | upstream_gene_variant | 1.0 |
| aftB | 4269594 | c.-758A>C | upstream_gene_variant | 1.0 |
| aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
| aftB | 4269612 | c.-776T>C | upstream_gene_variant | 1.0 |
| aftB | 4269621 | c.-785C>G | upstream_gene_variant | 1.0 |
| aftB | 4269624 | c.-788C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269627 | p.Val69Ile | missense_variant | 1.0 |
| ubiA | 4269632 | p.Ala68Ser | missense_variant | 1.0 |
| aftB | 4269636 | c.-800C>G | upstream_gene_variant | 1.0 |
| aftB | 4269639 | c.-803C>G | upstream_gene_variant | 1.0 |
| aftB | 4269660 | c.-824C>G | upstream_gene_variant | 1.0 |
| ubiA | 4269665 | p.Met57Leu | missense_variant | 1.0 |
| ubiA | 4269710 | p.Gly42Ser | missense_variant | 1.0 |
| aftB | 4269716 | c.-880T>C | upstream_gene_variant | 1.0 |
| ubiA | 4269718 | p.Ala39Gly | missense_variant | 1.0 |
| ubiA | 4269725 | p.Leu37Val | missense_variant | 1.0 |
| aftB | 4269743 | c.-907C>T | upstream_gene_variant | 1.0 |
| aftB | 4269744 | c.-908G>C | upstream_gene_variant | 1.0 |
| aftB | 4269750 | c.-914A>G | upstream_gene_variant | 1.0 |
| ubiA | 4269773 | p.Ile21Leu | missense_variant | 1.0 |
| ubiA | 4269782 | p.Val18Ile | missense_variant | 1.0 |
| ethR | 4327369 | c.-180C>G | upstream_gene_variant | 1.0 |
| ethR | 4327396 | c.-153A>T | upstream_gene_variant | 1.0 |
| ethA | 4327399 | p.Asp25Glu | missense_variant | 1.0 |
| ethR | 4327423 | c.-126G>C | upstream_gene_variant | 1.0 |
| ethR | 4327435 | c.-114T>G | upstream_gene_variant | 1.0 |
| ethR | 4327438 | c.-111A>G | upstream_gene_variant | 1.0 |
| ethA | 4327452 | p.Val8Leu | missense_variant | 1.0 |
| ethR | 4327453 | c.-96A>G | upstream_gene_variant | 1.0 |
| ethR | 4327459 | c.-90G>A | upstream_gene_variant | 1.0 |
| ethR | 4327468 | c.-81G>A | upstream_gene_variant | 1.0 |
| ethA | 4328449 | c.-976C>G | upstream_gene_variant | 1.0 |
| ethA | 4328463 | c.-990G>C | upstream_gene_variant | 1.0 |
| ethA | 4328467 | c.-994G>T | upstream_gene_variant | 1.0 |
| ethA | 4328470 | c.-998_-997delAGinsGC | upstream_gene_variant | 1.0 |
| gid | 4407603 | c.600G>A | synonymous_variant | 1.0 |
| gid | 4407609 | c.594G>C | synonymous_variant | 1.0 |
| gid | 4407652 | p.Val184Ala | missense_variant | 1.0 |
| gid | 4407654 | c.549G>C | synonymous_variant | 1.0 |
| gid | 4407666 | p.Ile179Ala | missense_variant | 1.0 |
| clpC1 | 4035711 | c.2515_*2446del | stop_lost&conservative_inframe_deletion&splice_region_variant | 1.0 |
