Run ID: ERR1035239
Sample name:
Date: 18-08-2022 11:46:42
Number of reads: 1264518
Percentage reads mapped: 20.45
Strain:
Drug-resistance: HR-TB
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage6.1.3 | West-Africa 2 | AFRI_1 | RD702 | 0.96 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
| katG | 2155108 | p.Ile335Thr | missense_variant | 0.98 | isoniazid |
| katG | 2155161 | p.Ile317Leu | missense_variant | 1.0 | isoniazid |
| katG | 2155810 | c.300_301delGC | frameshift_variant | 1.0 | isoniazid |
| katG | 2155815 | c.296_297insTG | frameshift_variant | 1.0 | isoniazid |
| embB | 4247448 | p.His312Arg | missense_variant | 1.0 | ethambutol |
| embB | 4247588 | p.Leu359Ile | missense_variant | 1.0 | ethambutol |
| embB | 4247663 | p.Tyr384Asn | missense_variant | 1.0 | ethambutol |
| embB | 4247676 | p.Ala388Gly | missense_variant | 1.0 | ethambutol |
| embB | 4247708 | p.Asn399Asp | missense_variant | 1.0 | ethambutol |
| embB | 4248488 | p.Ala659Thr | missense_variant | 1.0 | ethambutol |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5314 | c.75C>G | synonymous_variant | 1.0 |
| gyrB | 5326 | c.87T>C | synonymous_variant | 1.0 |
| gyrB | 5341 | c.102T>C | synonymous_variant | 1.0 |
| gyrB | 5347 | c.108G>C | synonymous_variant | 1.0 |
| gyrB | 5353 | c.114T>C | synonymous_variant | 1.0 |
| gyrB | 5359 | c.120C>A | 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 | 5772 | p.Ala178Asp | missense_variant | 1.0 |
| gyrB | 5774 | p.Val179Ile | missense_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 | 5806 | c.567C>G | synonymous_variant | 1.0 |
| gyrB | 5809 | c.570C>G | synonymous_variant | 1.0 |
| gyrB | 5815 | c.576C>G | synonymous_variant | 1.0 |
| gyrB | 5824 | c.585A>G | synonymous_variant | 1.0 |
| gyrB | 5827 | c.588G>A | synonymous_variant | 1.0 |
| gyrB | 5848 | c.609G>C | synonymous_variant | 0.98 |
| gyrB | 5863 | c.624G>C | synonymous_variant | 1.0 |
| gyrB | 5873 | c.634A>C | synonymous_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 | 1.0 |
| gyrB | 6100 | c.861G>C | synonymous_variant | 1.0 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6123 | p.Ala295Gly | missense_variant | 1.0 |
| gyrB | 6127 | c.888G>C | synonymous_variant | 1.0 |
| gyrB | 6130 | c.891T>C | synonymous_variant | 1.0 |
| gyrB | 6133 | c.894G>C | synonymous_variant | 1.0 |
| gyrB | 6136 | c.897G>A | synonymous_variant | 1.0 |
| gyrB | 6169 | c.930C>G | synonymous_variant | 1.0 |
| gyrB | 6190 | c.951A>G | synonymous_variant | 0.98 |
| gyrB | 6214 | c.975G>C | synonymous_variant | 1.0 |
| gyrB | 6217 | c.978G>C | synonymous_variant | 1.0 |
| gyrB | 6223 | c.984G>C | synonymous_variant | 1.0 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
| gyrB | 6250 | c.1011A>G | synonymous_variant | 1.0 |
| gyrB | 6253 | c.1014G>C | synonymous_variant | 1.0 |
| gyrB | 6274 | c.1035C>G | synonymous_variant | 1.0 |
| gyrB | 6280 | c.1041T>C | synonymous_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6292 | c.1053G>C | synonymous_variant | 1.0 |
| gyrB | 6295 | c.1056A>G | synonymous_variant | 1.0 |
| gyrB | 6298 | c.1059C>T | synonymous_variant | 1.0 |
| gyrB | 6299 | c.1060C>T | synonymous_variant | 1.0 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 1.0 |
| gyrA | 6319 | c.-983G>C | upstream_gene_variant | 1.0 |
| gyrA | 6325 | c.-977C>G | upstream_gene_variant | 1.0 |
| gyrA | 6361 | c.-941G>A | upstream_gene_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | 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 | 6400 | c.-902C>G | upstream_gene_variant | 1.0 |
| gyrA | 6403 | c.-899T>C | upstream_gene_variant | 1.0 |
| gyrA | 6415 | c.-887G>C | upstream_gene_variant | 1.0 |
| gyrA | 6427 | c.-875T>C | upstream_gene_variant | 1.0 |
| gyrA | 6602 | c.-700C>T | upstream_gene_variant | 1.0 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 1.0 |
| gyrA | 6613 | c.-689A>C | upstream_gene_variant | 1.0 |
| gyrA | 6616 | c.-686A>G | 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 | 6652 | c.-650C>G | 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 | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6706 | c.-596G>A | 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 | 6730 | c.-572A>G | 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 | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6778 | c.-524C>T | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Thr | missense_variant | 1.0 |
| gyrA | 6824 | c.-478C>T | upstream_gene_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>G | 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 | 6878 | c.-424T>C | upstream_gene_variant | 1.0 |
| gyrA | 6881 | c.-421T>C | upstream_gene_variant | 1.0 |
| gyrA | 6904 | c.-398C>G | upstream_gene_variant | 1.0 |
| gyrA | 6910 | c.-392G>A | upstream_gene_variant | 1.0 |
| gyrB | 6911 | p.Asn558His | missense_variant | 1.0 |
| gyrA | 6919 | c.-383T>C | upstream_gene_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>C | upstream_gene_variant | 1.0 |
| gyrA | 6934 | c.-368A>G | upstream_gene_variant | 1.0 |
| gyrA | 6937 | c.-365G>A | 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 | 6955 | c.-347G>A | upstream_gene_variant | 1.0 |
| gyrA | 6967 | c.-335T>C | upstream_gene_variant | 1.0 |
| gyrA | 6970 | c.-332C>T | upstream_gene_variant | 1.0 |
| gyrA | 6973 | c.-329G>C | upstream_gene_variant | 1.0 |
| gyrA | 6976 | c.-326A>G | upstream_gene_variant | 1.0 |
| gyrA | 6982 | c.-320A>C | upstream_gene_variant | 1.0 |
| gyrA | 7000 | c.-302C>G | upstream_gene_variant | 1.0 |
| gyrA | 7006 | c.-296T>G | upstream_gene_variant | 1.0 |
| gyrA | 7012 | c.-290G>C | upstream_gene_variant | 1.0 |
| gyrA | 7018 | c.-284G>C | upstream_gene_variant | 1.0 |
| gyrA | 7021 | c.-281G>C | upstream_gene_variant | 1.0 |
| gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
| gyrA | 7060 | c.-242T>C | upstream_gene_variant | 1.0 |
| gyrA | 7066 | c.-236G>C | upstream_gene_variant | 1.0 |
| gyrA | 7075 | c.-227T>G | upstream_gene_variant | 1.0 |
| gyrA | 7078 | c.-224A>G | upstream_gene_variant | 1.0 |
| gyrA | 7081 | c.-221T>C | upstream_gene_variant | 1.0 |
| gyrA | 7084 | c.-218A>G | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>C | 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>G | upstream_gene_variant | 1.0 |
| gyrA | 7132 | c.-170T>G | upstream_gene_variant | 1.0 |
| gyrA | 7136 | c.-166T>C | upstream_gene_variant | 1.0 |
| gyrA | 7141 | c.-161T>C | upstream_gene_variant | 1.0 |
| gyrA | 7144 | c.-158A>G | upstream_gene_variant | 1.0 |
| gyrA | 7147 | c.-155G>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 | 7216 | c.-86G>C | upstream_gene_variant | 1.0 |
| gyrA | 7225 | c.-77T>C | upstream_gene_variant | 1.0 |
| gyrA | 7237 | c.-65C>T | upstream_gene_variant | 1.0 |
| gyrA | 7243 | c.-59G>A | upstream_gene_variant | 1.0 |
| gyrA | 7246 | c.-56T>C | upstream_gene_variant | 1.0 |
| gyrA | 7355 | c.54T>C | 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 | 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 | 7472 | c.171T>C | synonymous_variant | 1.0 |
| gyrA | 7475 | c.174A>C | synonymous_variant | 1.0 |
| gyrA | 7480 | p.Phe60Tyr | missense_variant | 1.0 |
| gyrA | 7484 | c.183T>C | synonymous_variant | 1.0 |
| gyrA | 7487 | c.186C>G | synonymous_variant | 0.98 |
| gyrA | 7490 | c.189C>T | synonymous_variant | 0.98 |
| gyrA | 7517 | c.216G>A | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>G | synonymous_variant | 1.0 |
| gyrA | 7532 | c.231T>C | synonymous_variant | 1.0 |
| gyrA | 7538 | c.237G>A | synonymous_variant | 1.0 |
| gyrA | 7541 | c.240C>G | 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 | 1.0 |
| gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
| gyrA | 7622 | c.321C>T | synonymous_variant | 1.0 |
| gyrA | 7626 | c.325C>T | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 7637 | c.336C>G | synonymous_variant | 1.0 |
| gyrA | 7646 | c.345C>T | synonymous_variant | 1.0 |
| gyrA | 7649 | c.348C>T | synonymous_variant | 1.0 |
| gyrA | 7652 | c.351C>T | synonymous_variant | 1.0 |
| 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.382A>C | synonymous_variant | 1.0 |
| gyrA | 7694 | c.393A>G | synonymous_variant | 1.0 |
| gyrA | 7697 | c.396C>G | synonymous_variant | 1.0 |
| gyrA | 7710 | c.409T>C | synonymous_variant | 1.0 |
| gyrA | 7715 | c.414G>C | synonymous_variant | 1.0 |
| gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 1.0 |
| gyrA | 7731 | p.Glu144Gln | missense_variant | 1.0 |
| gyrA | 7760 | c.459C>T | synonymous_variant | 1.0 |
| gyrA | 7763 | c.462T>C | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>G | synonymous_variant | 1.0 |
| gyrA | 7838 | c.537C>G | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>C | synonymous_variant | 1.0 |
| gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
| gyrA | 7883 | c.582G>C | synonymous_variant | 1.0 |
| gyrA | 7884 | p.Arg195Gly | missense_variant | 1.0 |
| gyrA | 7892 | c.591G>C | synonymous_variant | 1.0 |
| gyrA | 7898 | p.Asp199Glu | missense_variant | 1.0 |
| gyrA | 7919 | p.Glu206Asp | missense_variant | 1.0 |
| gyrA | 7923 | p.His208Tyr | missense_variant | 1.0 |
| gyrA | 7928 | p.Asp209Glu | missense_variant | 1.0 |
| gyrA | 7942 | p.Glu214Ala | missense_variant | 1.0 |
| gyrA | 7955 | c.654G>C | synonymous_variant | 1.0 |
| gyrA | 7958 | c.657C>G | synonymous_variant | 1.0 |
| gyrA | 7963 | p.Gly221Glu | missense_variant | 0.92 |
| gyrA | 7970 | c.669T>G | synonymous_variant | 0.92 |
| gyrA | 7976 | c.675C>A | synonymous_variant | 0.92 |
| gyrA | 7979 | c.678G>C | synonymous_variant | 0.92 |
| gyrA | 8039 | c.738T>C | synonymous_variant | 1.0 |
| gyrA | 8054 | c.753T>C | synonymous_variant | 1.0 |
| gyrA | 8057 | c.756A>G | synonymous_variant | 1.0 |
| gyrA | 8069 | c.768T>C | synonymous_variant | 1.0 |
| gyrA | 8078 | c.777A>G | synonymous_variant | 1.0 |
| gyrA | 8090 | c.789C>G | synonymous_variant | 1.0 |
| gyrA | 8099 | c.798T>C | synonymous_variant | 1.0 |
| gyrA | 8111 | c.810G>C | synonymous_variant | 1.0 |
| gyrA | 8156 | c.855T>C | synonymous_variant | 0.99 |
| gyrA | 8168 | c.867A>G | synonymous_variant | 0.99 |
| gyrA | 8174 | c.873C>G | synonymous_variant | 0.99 |
| gyrA | 8177 | c.876A>C | synonymous_variant | 0.99 |
| gyrA | 8198 | c.897T>C | synonymous_variant | 0.99 |
| gyrA | 8207 | c.906T>C | synonymous_variant | 0.99 |
| gyrA | 8219 | c.918T>C | synonymous_variant | 0.98 |
| gyrA | 8225 | c.924T>C | synonymous_variant | 0.98 |
| gyrA | 8234 | c.933T>G | synonymous_variant | 1.0 |
| gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 1.0 |
| gyrA | 8253 | p.Ile318Leu | 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 | 0.98 |
| 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 | 8339 | c.1038A>G | synonymous_variant | 1.0 |
| gyrA | 8342 | c.1041G>C | synonymous_variant | 1.0 |
| gyrA | 8351 | c.1050C>T | synonymous_variant | 1.0 |
| gyrA | 8366 | c.1065G>C | synonymous_variant | 1.0 |
| gyrA | 8375 | c.1074G>C | synonymous_variant | 1.0 |
| gyrA | 8391 | p.Tyr364His | missense_variant | 1.0 |
| gyrA | 8399 | c.1098T>C | synonymous_variant | 1.0 |
| gyrA | 8420 | c.1119T>C | synonymous_variant | 1.0 |
| gyrA | 8423 | c.1122G>C | synonymous_variant | 1.0 |
| gyrA | 8442 | c.1141C>T | synonymous_variant | 1.0 |
| gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
| gyrA | 8462 | c.1161A>G | synonymous_variant | 1.0 |
| gyrA | 8471 | c.1170T>C | synonymous_variant | 1.0 |
| gyrA | 8480 | c.1179C>T | synonymous_variant | 1.0 |
| gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
| gyrA | 8489 | c.1188A>G | synonymous_variant | 1.0 |
| gyrA | 8498 | c.1197C>T | 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 | 8537 | c.1236G>A | synonymous_variant | 1.0 |
| gyrA | 8546 | c.1245T>C | synonymous_variant | 1.0 |
| gyrA | 8552 | c.1251C>G | synonymous_variant | 1.0 |
| gyrA | 8556 | p.Ala419Gln | missense_variant | 1.0 |
| gyrA | 8561 | c.1260A>C | synonymous_variant | 1.0 |
| gyrA | 8562 | c.1261C>T | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>G | synonymous_variant | 1.0 |
| gyrA | 8619 | c.1318T>C | synonymous_variant | 1.0 |
| gyrA | 8624 | c.1323G>C | synonymous_variant | 1.0 |
| gyrA | 8627 | c.1326C>G | synonymous_variant | 1.0 |
| gyrA | 8636 | c.1335A>C | synonymous_variant | 1.0 |
| gyrA | 8642 | c.1341A>G | synonymous_variant | 1.0 |
| gyrA | 8645 | c.1344C>G | synonymous_variant | 1.0 |
| gyrA | 8672 | c.1371A>G | synonymous_variant | 1.0 |
| gyrA | 8693 | c.1392T>C | synonymous_variant | 1.0 |
| gyrA | 8699 | c.1398A>G | synonymous_variant | 1.0 |
| gyrA | 8711 | c.1410A>C | synonymous_variant | 1.0 |
| gyrA | 8714 | c.1413A>G | synonymous_variant | 1.0 |
| gyrA | 8717 | c.1416C>G | synonymous_variant | 0.94 |
| gyrA | 8720 | c.1419G>A | synonymous_variant | 1.0 |
| gyrA | 8726 | c.1425G>A | synonymous_variant | 1.0 |
| gyrA | 8729 | c.1428T>C | synonymous_variant | 1.0 |
| gyrA | 8732 | c.1431G>C | synonymous_variant | 1.0 |
| gyrA | 8735 | c.1434C>T | synonymous_variant | 1.0 |
| gyrA | 8747 | c.1446A>G | synonymous_variant | 1.0 |
| gyrA | 8756 | c.1455A>G | synonymous_variant | 1.0 |
| gyrA | 8762 | c.1461G>C | synonymous_variant | 1.0 |
| gyrA | 8765 | p.Asp488Glu | missense_variant | 1.0 |
| gyrA | 8767 | p.Arg489Lys | missense_variant | 1.0 |
| gyrA | 8779 | p.Asp493Ala | missense_variant | 1.0 |
| gyrA | 8786 | c.1485T>C | synonymous_variant | 1.0 |
| gyrA | 8796 | p.Ile499Val | missense_variant | 1.0 |
| gyrA | 8801 | c.1500G>C | synonymous_variant | 1.0 |
| gyrA | 8810 | c.1509A>C | synonymous_variant | 1.0 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>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 | 8897 | c.1596T>C | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8918 | c.1617C>G | synonymous_variant | 1.0 |
| gyrA | 8939 | c.1638T>C | synonymous_variant | 1.0 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 1.0 |
| gyrA | 8945 | c.1644G>C | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 8951 | c.1650G>A | 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>G | 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 | 9023 | c.1722A>C | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>C | synonymous_variant | 1.0 |
| gyrA | 9032 | c.1731T>C | synonymous_variant | 1.0 |
| gyrA | 9035 | c.1734G>C | synonymous_variant | 1.0 |
| gyrA | 9050 | p.Asp583Glu | missense_variant | 1.0 |
| gyrA | 9051 | c.1750T>C | synonymous_variant | 1.0 |
| gyrA | 9062 | c.1761C>G | synonymous_variant | 1.0 |
| gyrA | 9065 | c.1764C>T | synonymous_variant | 1.0 |
| gyrA | 9068 | c.1767G>C | synonymous_variant | 1.0 |
| gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
| gyrA | 9074 | c.1773G>C | synonymous_variant | 1.0 |
| gyrA | 9080 | c.1779G>T | 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 | 9134 | c.1833C>G | synonymous_variant | 1.0 |
| gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
| gyrA | 9147 | p.Gly616Ser | missense_variant | 1.0 |
| gyrA | 9152 | c.1851C>T | synonymous_variant | 1.0 |
| gyrA | 9153 | p.Thr618Glu | missense_variant | 1.0 |
| gyrA | 9164 | c.1863G>C | 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 | 9227 | c.1926C>G | synonymous_variant | 1.0 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 1.0 |
| gyrA | 9233 | c.1932C>T | synonymous_variant | 1.0 |
| gyrA | 9242 | c.1941A>C | synonymous_variant | 1.0 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 1.0 |
| gyrA | 9275 | c.1974G>A | synonymous_variant | 1.0 |
| gyrA | 9278 | c.1977G>C | synonymous_variant | 1.0 |
| gyrA | 9281 | c.1980C>G | 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 | 9304 | p.Gly668Glu | missense_variant | 1.0 |
| gyrA | 9311 | c.2010C>T | synonymous_variant | 1.0 |
| gyrA | 9323 | c.2022C>G | synonymous_variant | 1.0 |
| gyrA | 9335 | c.2034G>C | synonymous_variant | 1.0 |
| gyrA | 9345 | c.2044A>C | 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>C | synonymous_variant | 1.0 |
| gyrA | 9386 | c.2085T>C | synonymous_variant | 1.0 |
| gyrA | 9395 | c.2094G>C | synonymous_variant | 1.0 |
| gyrA | 9626 | c.2325T>C | synonymous_variant | 1.0 |
| gyrA | 9629 | c.2328C>G | synonymous_variant | 1.0 |
| gyrA | 9630 | p.Val777Ile | missense_variant | 1.0 |
| gyrA | 9635 | c.2334T>C | synonymous_variant | 1.0 |
| gyrA | 9644 | c.2343T>C | synonymous_variant | 1.0 |
| gyrA | 9647 | c.2346C>T | synonymous_variant | 0.96 |
| gyrA | 9650 | c.2349G>C | synonymous_variant | 1.0 |
| gyrA | 9665 | c.2364A>G | synonymous_variant | 1.0 |
| gyrA | 9666 | p.Arg789Gly | missense_variant | 1.0 |
| gyrA | 9674 | c.2373T>C | synonymous_variant | 1.0 |
| gyrA | 9677 | c.2376C>T | synonymous_variant | 1.0 |
| gyrA | 9701 | c.2400T>C | synonymous_variant | 1.0 |
| gyrA | 9704 | c.2403T>C | synonymous_variant | 1.0 |
| gyrA | 9708 | c.2407T>C | synonymous_variant | 1.0 |
| gyrA | 9722 | c.2421C>T | synonymous_variant | 1.0 |
| gyrA | 9734 | c.2433A>G | synonymous_variant | 1.0 |
| gyrA | 9738 | c.2437T>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 | 490833 | c.51G>C | synonymous_variant | 1.0 |
| fgd1 | 490842 | c.60C>G | synonymous_variant | 1.0 |
| fgd1 | 490851 | c.69A>C | synonymous_variant | 1.0 |
| fgd1 | 490887 | c.105G>C | synonymous_variant | 1.0 |
| fgd1 | 490902 | c.120T>C | 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>A | synonymous_variant | 1.0 |
| fgd1 | 490921 | p.Gln47Glu | missense_variant | 1.0 |
| fgd1 | 490932 | c.150T>C | synonymous_variant | 1.0 |
| fgd1 | 490948 | p.Ser56Ala | missense_variant | 1.0 |
| fgd1 | 491038 | p.Ile86Val | missense_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 | 491077 | p.Asn99Gly | missense_variant | 1.0 |
| fgd1 | 491082 | c.300T>G | synonymous_variant | 1.0 |
| fgd1 | 491083 | p.Val101Ile | missense_variant | 1.0 |
| fgd1 | 491091 | c.309T>C | synonymous_variant | 1.0 |
| fgd1 | 491094 | c.312C>G | synonymous_variant | 1.0 |
| fgd1 | 491106 | c.324T>C | synonymous_variant | 1.0 |
| fgd1 | 491121 | c.339A>G | synonymous_variant | 1.0 |
| fgd1 | 491137 | p.Glu119Gln | missense_variant | 1.0 |
| fgd1 | 491144 | p.Ala121Glu | missense_variant | 1.0 |
| fgd1 | 491166 | c.384G>C | synonymous_variant | 1.0 |
| fgd1 | 491181 | c.399T>C | synonymous_variant | 1.0 |
| fgd1 | 491191 | p.Gly137Arg | missense_variant | 1.0 |
| fgd1 | 491196 | c.414A>G | synonymous_variant | 1.0 |
| fgd1 | 491202 | c.420G>C | synonymous_variant | 1.0 |
| fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.99 |
| fgd1 | 491212 | p.Ser144Arg | missense_variant | 1.0 |
| fgd1 | 491217 | c.435T>C | synonymous_variant | 1.0 |
| fgd1 | 491232 | c.450T>C | synonymous_variant | 1.0 |
| fgd1 | 491241 | p.Asp153Glu | missense_variant | 1.0 |
| fgd1 | 491244 | c.462T>C | synonymous_variant | 1.0 |
| fgd1 | 491250 | c.468G>A | synonymous_variant | 1.0 |
| fgd1 | 491259 | c.477T>C | synonymous_variant | 1.0 |
| fgd1 | 491286 | c.504G>C | synonymous_variant | 1.0 |
| fgd1 | 491292 | c.510G>C | synonymous_variant | 1.0 |
| fgd1 | 491295 | c.513C>G | synonymous_variant | 0.93 |
| fgd1 | 491296 | p.Val172Ile | missense_variant | 0.98 |
| fgd1 | 491319 | c.537G>C | synonymous_variant | 1.0 |
| fgd1 | 491331 | c.549G>A | synonymous_variant | 1.0 |
| fgd1 | 491343 | c.561C>G | synonymous_variant | 1.0 |
| fgd1 | 491349 | c.567T>C | synonymous_variant | 1.0 |
| fgd1 | 491359 | p.Ile193Val | missense_variant | 1.0 |
| fgd1 | 491364 | c.582T>C | synonymous_variant | 1.0 |
| fgd1 | 491367 | c.585G>C | synonymous_variant | 1.0 |
| fgd1 | 491388 | c.606C>G | synonymous_variant | 1.0 |
| fgd1 | 491453 | p.Gly224Asp | missense_variant | 1.0 |
| fgd1 | 491472 | c.690A>G | synonymous_variant | 1.0 |
| fgd1 | 491502 | c.720G>A | synonymous_variant | 1.0 |
| fgd1 | 491508 | c.726A>G | synonymous_variant | 1.0 |
| fgd1 | 491509 | c.727T>C | synonymous_variant | 1.0 |
| fgd1 | 491512 | p.Asn244Glu | missense_variant | 1.0 |
| fgd1 | 491526 | c.744T>C | synonymous_variant | 1.0 |
| fgd1 | 491542 | c.760T>C | synonymous_variant | 0.99 |
| fgd1 | 491547 | c.765A>C | synonymous_variant | 0.99 |
| fgd1 | 491550 | c.768T>C | synonymous_variant | 0.99 |
| fgd1 | 491583 | c.801G>A | synonymous_variant | 0.98 |
| fgd1 | 491595 | c.813C>G | synonymous_variant | 0.98 |
| fgd1 | 491601 | c.819T>C | synonymous_variant | 0.98 |
| fgd1 | 491610 | c.828A>C | synonymous_variant | 0.98 |
| fgd1 | 491616 | c.834A>G | synonymous_variant | 0.97 |
| fgd1 | 491620 | p.Ile280Val | missense_variant | 0.97 |
| fgd1 | 491643 | c.861G>C | synonymous_variant | 1.0 |
| mshA | 575153 | c.-195C>G | upstream_gene_variant | 1.0 |
| mshA | 575154 | c.-194_-192delGTGinsCTC | upstream_gene_variant | 1.0 |
| mshA | 575161 | c.-187_-186delTTinsCC | upstream_gene_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 | 575554 | c.207C>T | 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 | 575575 | c.228G>C | synonymous_variant | 1.0 |
| mshA | 575587 | c.240C>A | synonymous_variant | 1.0 |
| mshA | 575590 | c.243T>C | synonymous_variant | 1.0 |
| mshA | 575593 | c.246G>C | synonymous_variant | 1.0 |
| mshA | 575623 | c.276C>G | synonymous_variant | 1.0 |
| mshA | 575629 | c.282A>C | synonymous_variant | 1.0 |
| mshA | 575635 | c.288A>C | synonymous_variant | 1.0 |
| mshA | 575638 | c.291T>C | synonymous_variant | 1.0 |
| mshA | 575641 | c.294A>G | synonymous_variant | 1.0 |
| mshA | 575648 | p.Val101Gln | missense_variant | 1.0 |
| mshA | 575659 | c.312A>G | synonymous_variant | 1.0 |
| mshA | 575665 | c.318G>C | synonymous_variant | 1.0 |
| mshA | 575689 | c.342G>C | synonymous_variant | 1.0 |
| mshA | 575695 | c.348C>G | synonymous_variant | 1.0 |
| mshA | 575704 | c.357T>C | 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 | 1.0 |
| mshA | 575734 | c.387T>G | synonymous_variant | 1.0 |
| mshA | 575737 | c.390T>C | synonymous_variant | 1.0 |
| mshA | 575746 | c.399C>G | synonymous_variant | 1.0 |
| mshA | 575752 | c.405G>A | synonymous_variant | 1.0 |
| mshA | 575767 | c.420G>A | synonymous_variant | 1.0 |
| mshA | 575771 | p.Val142Ser | missense_variant | 0.99 |
| mshA | 575779 | c.432A>G | synonymous_variant | 1.0 |
| mshA | 575821 | c.474G>C | synonymous_variant | 0.98 |
| mshA | 575824 | c.477T>G | synonymous_variant | 1.0 |
| mshA | 575864 | c.517T>C | synonymous_variant | 1.0 |
| mshA | 575878 | c.531A>G | synonymous_variant | 1.0 |
| mshA | 575884 | c.537G>C | synonymous_variant | 1.0 |
| mshA | 575893 | c.546C>G | synonymous_variant | 1.0 |
| mshA | 575944 | c.597T>C | synonymous_variant | 1.0 |
| mshA | 575950 | c.603C>G | synonymous_variant | 1.0 |
| mshA | 575953 | c.606G>C | synonymous_variant | 1.0 |
| mshA | 575965 | c.618C>G | synonymous_variant | 1.0 |
| mshA | 575977 | c.630G>C | synonymous_variant | 1.0 |
| mshA | 575980 | c.633T>C | synonymous_variant | 1.0 |
| mshA | 575984 | c.637T>C | synonymous_variant | 1.0 |
| mshA | 576004 | c.657T>C | synonymous_variant | 1.0 |
| mshA | 576010 | c.663C>G | synonymous_variant | 1.0 |
| mshA | 576011 | c.664A>C | synonymous_variant | 1.0 |
| mshA | 576017 | p.Val224Leu | missense_variant | 1.0 |
| mshA | 576163 | c.816A>C | synonymous_variant | 1.0 |
| mshA | 576184 | c.837A>C | synonymous_variant | 1.0 |
| mshA | 576193 | c.846T>C | synonymous_variant | 1.0 |
| mshA | 576197 | c.850C>T | synonymous_variant | 1.0 |
| mshA | 576205 | c.858G>C | synonymous_variant | 1.0 |
| mshA | 576211 | c.864C>G | synonymous_variant | 1.0 |
| mshA | 576214 | c.867G>A | synonymous_variant | 1.0 |
| mshA | 576215 | c.868T>C | synonymous_variant | 1.0 |
| mshA | 576233 | p.Ile296Val | missense_variant | 1.0 |
| mshA | 576247 | c.900A>G | synonymous_variant | 1.0 |
| rpoB | 759644 | c.-163T>A | upstream_gene_variant | 1.0 |
| rpoB | 759647 | c.-160T>C | upstream_gene_variant | 1.0 |
| rpoB | 759914 | c.108T>C | synonymous_variant | 0.9 |
| rpoB | 759929 | c.123A>G | synonymous_variant | 0.9 |
| rpoB | 759932 | c.126T>C | synonymous_variant | 0.9 |
| rpoB | 760070 | c.264T>G | synonymous_variant | 1.0 |
| rpoB | 760088 | c.282C>G | synonymous_variant | 1.0 |
| rpoB | 760091 | c.285G>C | synonymous_variant | 1.0 |
| rpoB | 760101 | c.295T>C | synonymous_variant | 1.0 |
| rpoB | 760106 | c.300G>T | synonymous_variant | 1.0 |
| rpoB | 760112 | c.306T>C | synonymous_variant | 1.0 |
| rpoB | 760118 | c.312T>C | 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 | 760253 | c.447T>C | synonymous_variant | 1.0 |
| rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
| rpoB | 760331 | c.525G>C | synonymous_variant | 1.0 |
| rpoB | 760337 | c.531C>G | synonymous_variant | 0.97 |
| rpoB | 760340 | c.534G>C | synonymous_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_variant | 1.0 |
| rpoB | 760418 | c.612G>C | synonymous_variant | 0.97 |
| 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 | 760514 | c.708C>T | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 0.99 |
| rpoB | 760533 | p.Val243Thr | missense_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 0.99 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 0.99 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 0.99 |
| rpoB | 760634 | c.828T>C | synonymous_variant | 0.99 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 0.99 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 0.99 |
| 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 | 0.99 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760718 | c.912C>G | synonymous_variant | 0.98 |
| rpoB | 760721 | c.915C>G | synonymous_variant | 1.0 |
| rpoB | 760724 | c.918T>C | synonymous_variant | 0.99 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760751 | c.945G>C | synonymous_variant | 0.98 |
| rpoB | 760757 | c.951T>C | synonymous_variant | 0.97 |
| rpoB | 760759 | p.Val318Ala | missense_variant | 0.97 |
| rpoB | 760763 | c.957C>T | synonymous_variant | 0.97 |
| rpoB | 760769 | c.963C>G | synonymous_variant | 0.97 |
| rpoB | 760775 | c.969G>C | synonymous_variant | 0.96 |
| rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 0.96 |
| rpoB | 760793 | c.987A>G | synonymous_variant | 0.98 |
| rpoB | 760805 | c.999G>C | synonymous_variant | 0.98 |
| rpoB | 760817 | c.1011A>G | synonymous_variant | 0.98 |
| rpoB | 760820 | c.1014T>C | synonymous_variant | 0.98 |
| rpoB | 760826 | c.1020C>G | synonymous_variant | 0.98 |
| rpoB | 760830 | c.1024T>C | synonymous_variant | 0.98 |
| rpoB | 760845 | p.Thr347Pro | missense_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 | 760919 | c.1113C>G | synonymous_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760934 | c.1128C>T | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760970 | c.1164G>C | 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 | 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 | 0.99 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 0.99 |
| rpoB | 761051 | c.1245G>T | synonymous_variant | 0.99 |
| rpoB | 761054 | c.1248G>C | synonymous_variant | 0.99 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 0.99 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 0.99 |
| rpoB | 761063 | c.1257C>G | synonymous_variant | 0.99 |
| rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.99 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 0.99 |
| rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>C | synonymous_variant | 0.96 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 0.97 |
| rpoB | 761171 | c.1365C>T | synonymous_variant | 0.99 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761183 | c.1377T>G | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>G | synonymous_variant | 1.0 |
| rpoB | 761222 | c.1416G>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 | 761327 | c.1521A>G | synonymous_variant | 0.99 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 0.99 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 0.99 |
| rpoB | 761373 | p.Val523His | missense_variant | 0.99 |
| rpoB | 761414 | c.1608A>G | synonymous_variant | 1.0 |
| rpoB | 761423 | c.1617T>C | synonymous_variant | 1.0 |
| rpoB | 761434 | c.1629_1630delTG | frameshift_variant | 1.0 |
| rpoB | 761444 | c.1638T>C | synonymous_variant | 1.0 |
| rpoB | 761447 | c.1641C>G | synonymous_variant | 1.0 |
| rpoB | 761452 | p.Val549Ala | missense_variant | 1.0 |
| rpoB | 761457 | p.Pro551Ala | missense_variant | 1.0 |
| rpoB | 761462 | c.1656C>G | synonymous_variant | 1.0 |
| rpoB | 761492 | c.1686G>C | synonymous_variant | 1.0 |
| rpoB | 761510 | c.1704T>C | synonymous_variant | 1.0 |
| rpoB | 761531 | c.1725C>G | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 0.99 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 0.99 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 0.99 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 0.99 |
| rpoB | 761612 | c.1806G>C | synonymous_variant | 0.99 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 0.99 |
| 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 | 0.99 |
| rpoB | 761690 | c.1884G>C | synonymous_variant | 0.98 |
| rpoB | 761732 | c.1926C>G | synonymous_variant | 0.97 |
| rpoB | 761735 | c.1929C>G | synonymous_variant | 0.97 |
| 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 | 761847 | p.Cys681Ser | missense_variant | 1.0 |
| rpoB | 761852 | c.2046C>G | synonymous_variant | 1.0 |
| rpoB | 761858 | c.2052G>C | synonymous_variant | 1.0 |
| rpoB | 761864 | c.2058G>C | synonymous_variant | 1.0 |
| rpoB | 761873 | c.2067A>G | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761891 | c.2085G>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 | 761931 | c.2125C>T | synonymous_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761999 | c.2193G>C | synonymous_variant | 1.0 |
| rpoB | 762008 | c.2202C>G | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>T | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762027 | c.2221_2223delCTCinsTTG | synonymous_variant | 0.98 |
| rpoB | 762032 | c.2226C>G | synonymous_variant | 0.97 |
| rpoB | 762035 | c.2229G>C | synonymous_variant | 0.97 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 0.97 |
| 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 | 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 | 762218 | c.2412T>G | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | 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 | 0.99 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 0.99 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 0.99 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 0.99 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 0.97 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762374 | c.-996G>C | upstream_gene_variant | 1.0 |
| rpoC | 762380 | c.-990T>G | upstream_gene_variant | 1.0 |
| rpoC | 762395 | c.-975G>C | upstream_gene_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 | 762443 | c.-927G>C | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.99 |
| rpoB | 762489 | p.Val895Gln | missense_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.97 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 0.97 |
| rpoC | 762521 | c.-849C>G | 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>T | 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 | 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 | 0.91 |
| rpoB | 762799 | p.Ala998Gly | missense_variant | 0.92 |
| rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.93 |
| rpoB | 762813 | p.Met1003Val | missense_variant | 0.93 |
| rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.93 |
| rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.93 |
| rpoC | 762830 | c.-540C>G | upstream_gene_variant | 0.93 |
| rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.93 |
| rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.95 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.98 |
| rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.98 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.98 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.99 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.98 |
| 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 | 1.0 |
| rpoC | 763076 | c.-294C>G | upstream_gene_variant | 1.0 |
| rpoC | 763085 | c.-285C>G | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| 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 | 763169 | c.-201A>G | upstream_gene_variant | 1.0 |
| rpoC | 763202 | c.-168A>C | upstream_gene_variant | 1.0 |
| rpoC | 763205 | c.-165G>C | upstream_gene_variant | 1.0 |
| rpoC | 763206 | c.-164_-162delAGTinsTCC | 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 | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoC | 763268 | c.-102C>G | upstream_gene_variant | 1.0 |
| rpoC | 763283 | c.-87T>C | upstream_gene_variant | 1.0 |
| rpoC | 763284 | c.-86C>T | 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 | 0.99 |
| rpoC | 763441 | c.72C>G | synonymous_variant | 0.99 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 0.99 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 0.99 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 0.99 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 0.99 |
| 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 | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 0.99 |
| rpoC | 763636 | c.267T>C | synonymous_variant | 0.99 |
| rpoC | 763642 | c.273G>C | synonymous_variant | 0.99 |
| rpoC | 763658 | c.289_291delCTTinsTTG | 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 | 763708 | c.339G>A | synonymous_variant | 1.0 |
| rpoC | 763709 | c.340C>T | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | 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 | 0.98 |
| rpoC | 763735 | c.366G>C | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 0.99 |
| rpoC | 763768 | c.399C>G | synonymous_variant | 1.0 |
| rpoC | 763780 | c.411C>G | synonymous_variant | 1.0 |
| rpoC | 763783 | c.414G>C | synonymous_variant | 1.0 |
| rpoC | 763801 | c.432C>G | synonymous_variant | 1.0 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 763819 | c.450G>C | synonymous_variant | 1.0 |
| rpoC | 763831 | c.462A>G | synonymous_variant | 1.0 |
| rpoC | 763835 | p.Ala156Met | 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 | 763885 | c.516C>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 | 763945 | c.576T>C | synonymous_variant | 1.0 |
| rpoC | 763960 | c.591T>C | synonymous_variant | 1.0 |
| rpoC | 763967 | p.Gly200Ser | missense_variant | 1.0 |
| rpoC | 763978 | c.609C>G | synonymous_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_variant | 1.0 |
| rpoC | 764011 | c.642T>C | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655T>C | synonymous_variant | 1.0 |
| rpoC | 764040 | p.Ser224Asn | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>C | 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 | 764110 | c.741C>T | synonymous_variant | 1.0 |
| rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764161 | c.792G>C | synonymous_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764195 | p.Ser276Gln | missense_variant | 1.0 |
| rpoC | 764203 | c.834G>T | synonymous_variant | 1.0 |
| rpoC | 764206 | c.837T>C | 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 | 764282 | c.913_915delTCGinsAGC | 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 | 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 | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>C | synonymous_variant | 0.99 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764573 | c.1204_1206delCTTinsTTG | synonymous_variant | 1.0 |
| rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 0.99 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764695 | c.1326T>C | synonymous_variant | 1.0 |
| rpoC | 764716 | c.1347G>C | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764812 | c.1443C>G | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764830 | c.1461C>G | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764878 | c.1509C>G | synonymous_variant | 1.0 |
| rpoC | 764893 | c.1524T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>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 | 765052 | c.1683C>G | 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 | 1.0 |
| rpoC | 765082 | c.1713G>C | synonymous_variant | 0.98 |
| rpoC | 765085 | c.1716T>C | synonymous_variant | 1.0 |
| rpoC | 765089 | c.1720T>C | synonymous_variant | 1.0 |
| rpoC | 765103 | c.1734G>A | synonymous_variant | 1.0 |
| rpoC | 765208 | c.1839T>C | synonymous_variant | 0.91 |
| rpoC | 765220 | c.1851A>G | synonymous_variant | 0.92 |
| rpoC | 765223 | c.1854G>C | synonymous_variant | 0.92 |
| rpoC | 765232 | c.1863G>C | synonymous_variant | 0.92 |
| rpoC | 765244 | c.1875T>G | synonymous_variant | 1.0 |
| rpoC | 765245 | c.1877_1878insGCT | disruptive_inframe_insertion | 1.0 |
| rpoC | 765249 | p.Leu627Ser | missense_variant | 1.0 |
| rpoC | 765250 | c.1882_1884delAGC | conservative_inframe_deletion | 1.0 |
| rpoC | 765287 | c.1918C>T | synonymous_variant | 1.0 |
| rpoC | 765292 | c.1923G>T | synonymous_variant | 1.0 |
| rpoC | 765298 | c.1929G>T | synonymous_variant | 1.0 |
| rpoC | 765300 | p.Val644Ala | missense_variant | 0.97 |
| rpoC | 765319 | c.1950A>G | synonymous_variant | 0.98 |
| rpoC | 765325 | c.1956C>T | synonymous_variant | 0.98 |
| rpoC | 765326 | p.His653Ala | missense_variant | 0.98 |
| rpoC | 765330 | p.Ser654Asn | missense_variant | 0.98 |
| rpoC | 765349 | c.1980T>C | synonymous_variant | 0.99 |
| rpoC | 765352 | c.1983G>C | synonymous_variant | 0.99 |
| rpoC | 765383 | p.Met672Leu | missense_variant | 0.99 |
| rpoC | 765404 | p.Leu679Val | missense_variant | 1.0 |
| rpoC | 765409 | c.2040T>C | synonymous_variant | 1.0 |
| rpoC | 765412 | c.2043T>C | synonymous_variant | 1.0 |
| rpoC | 765421 | c.2052C>G | synonymous_variant | 1.0 |
| rpoC | 765451 | c.2082C>G | synonymous_variant | 1.0 |
| rpoC | 765452 | p.Ala695Ser | missense_variant | 1.0 |
| rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
| rpoC | 765493 | c.2124G>C | synonymous_variant | 1.0 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
| rpoC | 765508 | c.2139C>G | 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 | 765573 | p.Asp735Gly | missense_variant | 1.0 |
| rpoC | 765577 | c.2208G>C | synonymous_variant | 1.0 |
| rpoC | 765578 | c.2209C>T | synonymous_variant | 1.0 |
| rpoC | 765583 | c.2214G>T | synonymous_variant | 1.0 |
| rpoC | 765613 | p.His748Gln | missense_variant | 1.0 |
| rpoC | 765625 | c.2256C>G | synonymous_variant | 1.0 |
| rpoC | 765628 | c.2259G>C | synonymous_variant | 1.0 |
| rpoC | 765631 | p.Asp754Glu | missense_variant | 1.0 |
| rpoC | 765658 | c.2289C>T | synonymous_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>C | 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 | 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 | 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 | 765928 | c.2559C>G | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>T | synonymous_variant | 1.0 |
| rpoC | 765985 | c.2616C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766009 | c.2640G>C | synonymous_variant | 1.0 |
| rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 766015 | c.2646G>A | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766043 | p.Gln892Glu | missense_variant | 1.0 |
| rpoC | 766054 | c.2685C>G | synonymous_variant | 1.0 |
| rpoC | 766069 | c.2700G>A | synonymous_variant | 1.0 |
| rpoC | 766082 | p.Ala905Gln | missense_variant | 0.99 |
| rpoC | 766096 | c.2727G>C | synonymous_variant | 1.0 |
| rpoC | 766105 | c.2736C>T | synonymous_variant | 1.0 |
| rpoC | 766129 | c.2760C>G | synonymous_variant | 1.0 |
| rpoC | 766135 | c.2766G>A | synonymous_variant | 1.0 |
| rpoC | 766141 | c.2772C>T | synonymous_variant | 1.0 |
| rpoC | 766142 | c.2773C>T | synonymous_variant | 1.0 |
| rpoC | 766299 | p.Thr977Ile | missense_variant | 1.0 |
| rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
| rpoC | 766312 | c.2943T>G | synonymous_variant | 1.0 |
| rpoC | 766315 | c.2946C>G | synonymous_variant | 1.0 |
| rpoC | 766327 | c.2958C>G | synonymous_variant | 1.0 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766363 | c.2994G>C | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766444 | c.3075C>G | synonymous_variant | 1.0 |
| rpoC | 766447 | c.3078T>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 | 766495 | c.3126C>T | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>G | synonymous_variant | 1.0 |
| rpoC | 766543 | c.3174C>T | synonymous_variant | 1.0 |
| rpoC | 766573 | c.3204T>C | 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 | 766645 | c.3276A>G | synonymous_variant | 1.0 |
| rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766738 | c.3369G>T | synonymous_variant | 1.0 |
| rpoC | 766750 | c.3381C>G | synonymous_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766769 | c.3400C>T | 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 | 766894 | c.3525T>C | synonymous_variant | 1.0 |
| rpoC | 766895 | c.3526T>C | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766933 | c.3564A>G | synonymous_variant | 0.99 |
| rpoC | 766945 | c.3576A>G | synonymous_variant | 0.98 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 0.98 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 0.98 |
| rpoC | 766978 | c.3609C>G | synonymous_variant | 0.98 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 0.98 |
| 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 | 767074 | c.3705T>C | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 0.99 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 0.99 |
| rpoC | 767134 | c.3765C>G | synonymous_variant | 0.99 |
| rpoC | 767158 | c.3789T>G | synonymous_variant | 1.0 |
| rpoC | 767167 | c.3798C>G | 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>G | synonymous_variant | 1.0 |
| rpsL | 781571 | c.12C>T | synonymous_variant | 1.0 |
| rpsL | 781608 | p.Ser17Gly | missense_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781649 | c.90T>C | synonymous_variant | 0.99 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 0.98 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 0.99 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781736 | c.177T>C | synonymous_variant | 1.0 |
| rpsL | 781751 | c.192G>C | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781793 | c.234G>C | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>G | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| 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 | 0.99 |
| rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.99 |
| rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.99 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.99 |
| rplC | 800690 | c.-119C>T | 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 | 800738 | c.-71T>C | 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 | 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 | 800877 | c.69A>C | synonymous_variant | 1.0 |
| rplC | 800880 | c.72A>G | synonymous_variant | 1.0 |
| rplC | 800889 | c.81C>G | synonymous_variant | 1.0 |
| rplC | 800907 | c.99C>G | synonymous_variant | 1.0 |
| rplC | 800916 | c.108A>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 | 800955 | c.147C>G | 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 | 800994 | c.186C>G | synonymous_variant | 1.0 |
| rplC | 801004 | p.Leu66Val | missense_variant | 1.0 |
| rplC | 801114 | c.306C>G | 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 | 801171 | c.363A>G | synonymous_variant | 1.0 |
| rplC | 801174 | c.366T>C | synonymous_variant | 1.0 |
| rplC | 801183 | c.375C>A | synonymous_variant | 1.0 |
| rplC | 801222 | c.414T>C | synonymous_variant | 1.0 |
| rplC | 801228 | c.420T>C | synonymous_variant | 1.0 |
| rplC | 801246 | c.438C>G | synonymous_variant | 1.0 |
| rplC | 801249 | c.441T>G | synonymous_variant | 1.0 |
| rplC | 801255 | c.447C>T | synonymous_variant | 1.0 |
| rplC | 801301 | c.493C>A | synonymous_variant | 1.0 |
| rplC | 801312 | c.504G>C | synonymous_variant | 1.0 |
| rplC | 801324 | c.516T>C | synonymous_variant | 1.0 |
| rplC | 801336 | c.528C>G | 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 | 801396 | c.588T>C | synonymous_variant | 1.0 |
| rplC | 801402 | c.594T>C | synonymous_variant | 1.0 |
| rplC | 801405 | c.597T>C | synonymous_variant | 1.0 |
| rplC | 801417 | c.609T>C | synonymous_variant | 1.0 |
| rplC | 801423 | c.615G>C | synonymous_variant | 1.0 |
| rplC | 801438 | c.630T>C | synonymous_variant | 1.0 |
| rplC | 801442 | p.Ile212Val | missense_variant | 1.0 |
| rplC | 801461 | c.653G>A | splice_region_variant&stop_retained_variant | 1.0 |
| fbiC | 1303200 | c.270G>T | synonymous_variant | 1.0 |
| fbiC | 1303203 | c.273T>C | synonymous_variant | 1.0 |
| fbiC | 1303217 | p.Arg96His | missense_variant | 1.0 |
| fbiC | 1303219 | c.289_291delTTAinsCTG | synonymous_variant | 1.0 |
| fbiC | 1303233 | c.303T>C | synonymous_variant | 1.0 |
| fbiC | 1303242 | c.312T>C | synonymous_variant | 1.0 |
| fbiC | 1303248 | c.318G>C | synonymous_variant | 1.0 |
| fbiC | 1303269 | c.339G>A | synonymous_variant | 1.0 |
| fbiC | 1303455 | c.525C>G | synonymous_variant | 0.94 |
| fbiC | 1303464 | c.534A>G | synonymous_variant | 0.95 |
| fbiC | 1303470 | c.540T>G | synonymous_variant | 0.96 |
| fbiC | 1303476 | c.546G>C | synonymous_variant | 0.96 |
| fbiC | 1303480 | p.Gln184Glu | missense_variant | 0.96 |
| fbiC | 1303509 | c.579G>C | synonymous_variant | 1.0 |
| fbiC | 1303512 | c.582T>C | synonymous_variant | 1.0 |
| fbiC | 1303534 | p.Ser202Ala | missense_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303560 | c.630G>C | synonymous_variant | 1.0 |
| fbiC | 1303575 | c.645G>C | synonymous_variant | 1.0 |
| fbiC | 1303584 | c.654C>G | 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 | 1303611 | c.681G>C | 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 | 1303638 | c.708A>G | synonymous_variant | 1.0 |
| fbiC | 1303659 | c.729T>C | synonymous_variant | 1.0 |
| fbiC | 1303660 | p.Val244Thr | missense_variant | 1.0 |
| fbiC | 1303674 | c.744C>G | synonymous_variant | 1.0 |
| fbiC | 1303686 | c.756C>G | synonymous_variant | 1.0 |
| fbiC | 1303695 | c.765T>C | synonymous_variant | 1.0 |
| fbiC | 1303701 | c.771C>G | synonymous_variant | 1.0 |
| fbiC | 1303708 | c.778T>C | synonymous_variant | 1.0 |
| fbiC | 1303716 | c.786C>T | 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 | 1.0 |
| fbiC | 1303746 | c.816T>C | synonymous_variant | 1.0 |
| fbiC | 1303749 | c.819G>C | synonymous_variant | 1.0 |
| fbiC | 1303752 | c.822A>G | synonymous_variant | 0.99 |
| fbiC | 1303755 | c.825T>C | synonymous_variant | 1.0 |
| fbiC | 1303785 | c.855G>C | synonymous_variant | 1.0 |
| fbiC | 1303789 | p.Ile287Val | missense_variant | 1.0 |
| 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 | 1303881 | c.951G>C | synonymous_variant | 1.0 |
| fbiC | 1303884 | c.954T>G | synonymous_variant | 1.0 |
| fbiC | 1303900 | p.Val324Met | missense_variant | 1.0 |
| fbiC | 1303911 | c.981G>C | synonymous_variant | 0.93 |
| fbiC | 1303914 | c.984C>G | synonymous_variant | 1.0 |
| fbiC | 1303920 | c.990C>G | synonymous_variant | 1.0 |
| fbiC | 1303923 | c.993C>T | synonymous_variant | 1.0 |
| fbiC | 1303929 | c.999G>C | synonymous_variant | 1.0 |
| fbiC | 1303947 | c.1017T>C | synonymous_variant | 1.0 |
| fbiC | 1303948 | p.Gly340Arg | missense_variant | 1.0 |
| fbiC | 1303969 | p.Val347Ile | missense_variant | 1.0 |
| fbiC | 1303973 | p.Gly348Ala | missense_variant | 1.0 |
| fbiC | 1303981 | p.Val351Ile | missense_variant | 1.0 |
| fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.99 |
| fbiC | 1304001 | c.1071C>G | synonymous_variant | 0.99 |
| fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.99 |
| 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>G | 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 | 1304080 | p.Ala384Ser | missense_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 | 1304127 | c.1197A>G | synonymous_variant | 1.0 |
| fbiC | 1304192 | p.Ala421Val | missense_variant | 0.91 |
| fbiC | 1304199 | c.1269C>T | synonymous_variant | 0.92 |
| fbiC | 1304217 | c.1287C>T | synonymous_variant | 0.92 |
| fbiC | 1304226 | c.1296C>G | synonymous_variant | 0.9 |
| fbiC | 1304227 | p.Met433Leu | missense_variant | 0.9 |
| fbiC | 1304464 | p.Gly512Ser | missense_variant | 1.0 |
| fbiC | 1304469 | c.1539G>A | synonymous_variant | 1.0 |
| fbiC | 1304472 | c.1542T>C | synonymous_variant | 1.0 |
| fbiC | 1304476 | p.Ala516Ser | missense_variant | 1.0 |
| fbiC | 1304481 | c.1551T>G | synonymous_variant | 1.0 |
| fbiC | 1304499 | c.1569T>G | synonymous_variant | 1.0 |
| fbiC | 1304520 | c.1590A>C | synonymous_variant | 1.0 |
| fbiC | 1304523 | c.1593G>T | synonymous_variant | 0.98 |
| fbiC | 1304526 | c.1596T>A | synonymous_variant | 0.98 |
| fbiC | 1304544 | c.1614T>C | synonymous_variant | 1.0 |
| fbiC | 1304545 | p.Val539Thr | missense_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 | 1304574 | c.1644C>G | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| fbiC | 1304628 | c.1698G>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 | 1304670 | c.1740G>T | synonymous_variant | 1.0 |
| fbiC | 1304671 | p.Val581Thr | missense_variant | 1.0 |
| fbiC | 1304675 | p.Gly582Glu | missense_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 | 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 | 1304748 | c.1818T>C | synonymous_variant | 1.0 |
| fbiC | 1304754 | c.1824G>A | synonymous_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| fbiC | 1304784 | c.1854T>C | synonymous_variant | 1.0 |
| fbiC | 1304787 | c.1857T>C | synonymous_variant | 1.0 |
| fbiC | 1304790 | c.1860C>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>G | synonymous_variant | 1.0 |
| fbiC | 1304853 | c.1923C>G | synonymous_variant | 1.0 |
| fbiC | 1304856 | c.1926C>G | synonymous_variant | 1.0 |
| fbiC | 1304872 | c.1942_1944delAGCinsTCG | synonymous_variant | 1.0 |
| fbiC | 1304877 | c.1947T>C | synonymous_variant | 1.0 |
| fbiC | 1304878 | c.1948_1950delCGCinsAGG | synonymous_variant | 1.0 |
| fbiC | 1304889 | c.1959G>A | synonymous_variant | 1.0 |
| fbiC | 1304893 | p.Gly655Ser | missense_variant | 1.0 |
| fbiC | 1304916 | c.1986T>C | synonymous_variant | 1.0 |
| fbiC | 1304925 | c.1995G>C | synonymous_variant | 1.0 |
| fbiC | 1304928 | c.1998T>C | synonymous_variant | 1.0 |
| fbiC | 1304934 | c.2004C>G | synonymous_variant | 1.0 |
| fbiC | 1304937 | c.2007G>C | synonymous_variant | 1.0 |
| fbiC | 1304940 | c.2010A>G | synonymous_variant | 1.0 |
| fbiC | 1304946 | c.2016G>C | synonymous_variant | 1.0 |
| fbiC | 1304958 | c.2028T>G | synonymous_variant | 1.0 |
| fbiC | 1304961 | c.2031C>T | synonymous_variant | 1.0 |
| fbiC | 1304991 | c.2061G>C | synonymous_variant | 1.0 |
| fbiC | 1304994 | c.2064A>G | synonymous_variant | 1.0 |
| fbiC | 1304995 | c.2065T>C | synonymous_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>A | synonymous_variant | 1.0 |
| fbiC | 1305027 | c.2097G>A | synonymous_variant | 1.0 |
| fbiC | 1305033 | c.2103T>G | 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 | 1305300 | c.2370A>G | synonymous_variant | 1.0 |
| fbiC | 1305303 | c.2373T>C | synonymous_variant | 1.0 |
| fbiC | 1305311 | p.Arg794Gln | missense_variant | 1.0 |
| fbiC | 1305331 | p.Glu801Asn | missense_variant | 1.0 |
| fbiC | 1305336 | c.2406T>C | synonymous_variant | 1.0 |
| fbiC | 1305381 | c.2451G>C | synonymous_variant | 1.0 |
| fbiC | 1305393 | c.2463T>C | synonymous_variant | 1.0 |
| fbiC | 1305405 | c.2475A>G | synonymous_variant | 1.0 |
| fbiC | 1305420 | c.2490C>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 |
| atpE | 1460852 | c.-193C>G | upstream_gene_variant | 0.91 |
| 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 | 1461159 | p.Val39Ile | missense_variant | 1.0 |
| atpE | 1461185 | c.141G>C | synonymous_variant | 1.0 |
| atpE | 1461189 | c.145C>T | synonymous_variant | 1.0 |
| atpE | 1461194 | c.150C>T | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>G | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461224 | c.180T>C | synonymous_variant | 1.0 |
| atpE | 1461233 | c.189A>G | synonymous_variant | 1.0 |
| atpE | 1461254 | c.210T>C | synonymous_variant | 1.0 |
| atpE | 1461275 | c.231T>C | synonymous_variant | 1.0 |
| rrs | 1471923 | n.78T>C | 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 | 0.99 |
| rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.99 |
| 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 | 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 | 1473104 | n.1259C>T | 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 |
| 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 | 1473436 | n.-222T>C | 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 | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473839 | n.182G>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 | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474025 | n.368T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474249 | n.592G>T | 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 | 0.99 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.99 |
| 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 | 1.0 |
| rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474959 | n.1302C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474962 | n.1306delG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475006 | n.1349A>T | 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 | 1.0 |
| 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 | 1475271 | n.1614A>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475273 | n.1616T>A | non_coding_transcript_exon_variant | 0.97 |
| 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 | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475369 | n.1712G>C | 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 | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475638 | n.1981C>T | 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 | 1475763 | n.2106C>T | 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 | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476030 | n.2373A>G | 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 | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.99 |
| 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 | 1476384 | n.2727G>A | non_coding_transcript_exon_variant | 0.99 |
| 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 | 1476597 | n.2940G>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 | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476725 | n.3068C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476732 | n.3075T>C | 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 | 0.96 |
| inhA | 1673487 | c.-715T>C | upstream_gene_variant | 1.0 |
| inhA | 1673490 | c.-712A>C | upstream_gene_variant | 1.0 |
| inhA | 1673499 | c.-703T>G | upstream_gene_variant | 1.0 |
| inhA | 1673517 | c.-685G>C | upstream_gene_variant | 1.0 |
| inhA | 1673523 | c.-679G>T | upstream_gene_variant | 1.0 |
| inhA | 1673535 | c.-667A>C | upstream_gene_variant | 1.0 |
| inhA | 1673547 | c.-655T>C | upstream_gene_variant | 1.0 |
| inhA | 1673574 | c.-628C>G | upstream_gene_variant | 1.0 |
| inhA | 1673580 | c.-622T>C | upstream_gene_variant | 1.0 |
| inhA | 1673589 | c.-613A>G | upstream_gene_variant | 1.0 |
| inhA | 1673595 | c.-607A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673596 | p.Lys53Asp | missense_variant | 1.0 |
| inhA | 1673607 | c.-595T>C | upstream_gene_variant | 1.0 |
| inhA | 1673610 | c.-592C>T | upstream_gene_variant | 1.0 |
| inhA | 1673616 | c.-586A>G | upstream_gene_variant | 1.0 |
| inhA | 1673619 | c.-583T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673633 | p.Ser65Asn | missense_variant | 1.0 |
| inhA | 1673646 | c.-556T>C | upstream_gene_variant | 1.0 |
| inhA | 1673658 | c.-544G>A | upstream_gene_variant | 1.0 |
| fabG1 | 1673660 | p.Ala74Glu | missense_variant | 1.0 |
| inhA | 1673664 | c.-538A>G | upstream_gene_variant | 1.0 |
| inhA | 1673667 | c.-535A>G | upstream_gene_variant | 1.0 |
| inhA | 1673679 | c.-523T>G | upstream_gene_variant | 1.0 |
| inhA | 1673709 | c.-493C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673710 | p.Leu91Ile | missense_variant | 1.0 |
| fabG1 | 1673716 | p.Ala93Lys | missense_variant | 1.0 |
| inhA | 1673730 | c.-472C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673733 | p.Met98Ile | missense_variant | 1.0 |
| fabG1 | 1674098 | p.Val220Ala | missense_variant | 1.0 |
| inhA | 1674114 | c.-88T>C | 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 | 1674237 | c.36T>C | synonymous_variant | 1.0 |
| inhA | 1674239 | p.Ser13Thr | missense_variant | 1.0 |
| inhA | 1674243 | c.42A>G | synonymous_variant | 1.0 |
| inhA | 1674279 | c.78A>C | synonymous_variant | 1.0 |
| inhA | 1674280 | p.Arg27Lys | missense_variant | 0.96 |
| inhA | 1674285 | c.84A>G | synonymous_variant | 1.0 |
| inhA | 1674301 | c.102_103delCC | frameshift_variant | 1.0 |
| inhA | 1674307 | c.106C>T | synonymous_variant | 1.0 |
| inhA | 1674315 | c.114C>G | synonymous_variant | 1.0 |
| inhA | 1674321 | c.120G>C | synonymous_variant | 1.0 |
| inhA | 1674342 | c.141T>C | synonymous_variant | 1.0 |
| inhA | 1674352 | p.Thr51Val | missense_variant | 1.0 |
| inhA | 1674368 | p.Ala56Glu | missense_variant | 1.0 |
| inhA | 1674379 | c.178C>T | 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 | 1674440 | p.Glu80Ala | missense_variant | 1.0 |
| inhA | 1674443 | p.Ala81Glu | missense_variant | 1.0 |
| inhA | 1674450 | c.249G>C | synonymous_variant | 1.0 |
| inhA | 1674452 | p.Ala84Glu | missense_variant | 1.0 |
| inhA | 1674480 | c.279T>C | synonymous_variant | 1.0 |
| inhA | 1674486 | c.285T>C | synonymous_variant | 1.0 |
| inhA | 1674489 | c.288G>C | synonymous_variant | 1.0 |
| inhA | 1674507 | c.306G>C | synonymous_variant | 1.0 |
| inhA | 1674537 | c.336C>G | synonymous_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_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 | 1.0 |
| inhA | 1674585 | c.384T>C | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 0.99 |
| inhA | 1674627 | c.426T>G | synonymous_variant | 1.0 |
| inhA | 1674630 | c.429C>G | synonymous_variant | 1.0 |
| inhA | 1674636 | c.435C>G | synonymous_variant | 1.0 |
| inhA | 1674654 | c.453G>C | synonymous_variant | 1.0 |
| inhA | 1674693 | c.492C>G | synonymous_variant | 1.0 |
| inhA | 1674703 | c.502T>C | synonymous_variant | 1.0 |
| inhA | 1674718 | c.517A>C | synonymous_variant | 1.0 |
| inhA | 1674741 | c.540C>G | synonymous_variant | 1.0 |
| inhA | 1674742 | p.Lys181Pro | missense_variant | 1.0 |
| inhA | 1674745 | p.Tyr182His | missense_variant | 1.0 |
| inhA | 1674750 | c.549T>C | synonymous_variant | 1.0 |
| inhA | 1674756 | c.555T>C | synonymous_variant | 1.0 |
| inhA | 1674771 | c.570C>G | synonymous_variant | 1.0 |
| inhA | 1674774 | c.573A>G | synonymous_variant | 1.0 |
| inhA | 1674780 | c.579T>G | synonymous_variant | 1.0 |
| inhA | 1674786 | c.585G>C | synonymous_variant | 1.0 |
| inhA | 1674848 | p.Gln216Arg | missense_variant | 1.0 |
| inhA | 1674855 | c.654C>G | synonymous_variant | 1.0 |
| inhA | 1674876 | c.675C>G | synonymous_variant | 1.0 |
| inhA | 1674879 | c.678T>C | synonymous_variant | 1.0 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 1.0 |
| inhA | 1674904 | p.Ala235Pro | missense_variant | 1.0 |
| inhA | 1674909 | c.708G>C | synonymous_variant | 1.0 |
| inhA | 1674915 | c.714C>G | synonymous_variant | 1.0 |
| inhA | 1674942 | c.741T>C | synonymous_variant | 1.0 |
| inhA | 1674957 | c.756G>C | synonymous_variant | 1.0 |
| inhA | 1674963 | c.762G>C | synonymous_variant | 0.97 |
| inhA | 1674966 | c.765T>C | synonymous_variant | 0.97 |
| inhA | 1674967 | p.Asp256Thr | missense_variant | 0.97 |
| inhA | 1674993 | c.792G>C | synonymous_variant | 0.94 |
| inhA | 1674994 | p.His265Ser | missense_variant | 0.94 |
| inhA | 1675008 | c.807C>G | synonymous_variant | 1.0 |
| rpsA | 1833367 | c.-175G>T | upstream_gene_variant | 0.94 |
| rpsA | 1833489 | c.-53T>A | upstream_gene_variant | 1.0 |
| rpsA | 1833495 | c.-47_-46insAATC | upstream_gene_variant | 1.0 |
| rpsA | 1833500 | c.-41delC | upstream_gene_variant | 1.0 |
| rpsA | 1833541 | c.-1T>C | upstream_gene_variant | 1.0 |
| rpsA | 1833554 | p.Thr5Ala | missense_variant | 1.0 |
| rpsA | 1833568 | c.27G>C | synonymous_variant | 1.0 |
| rpsA | 1833589 | c.48A>T | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>C | synonymous_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
| rpsA | 1833667 | c.126C>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 | 1833787 | c.246C>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>A | synonymous_variant | 1.0 |
| rpsA | 1833793 | c.252C>T | synonymous_variant | 1.0 |
| rpsA | 1833799 | c.258C>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>C | 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 | 1833862 | c.321G>T | 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 | 1833970 | c.429G>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834150 | c.609G>C | synonymous_variant | 1.0 |
| rpsA | 1834153 | c.612T>C | synonymous_variant | 1.0 |
| rpsA | 1834154 | p.Asn205Gln | missense_variant | 1.0 |
| rpsA | 1834157 | c.616T>C | synonymous_variant | 1.0 |
| rpsA | 1834162 | c.621A>G | synonymous_variant | 1.0 |
| rpsA | 1834165 | c.624A>G | synonymous_variant | 1.0 |
| rpsA | 1834169 | p.Thr210Ala | missense_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834186 | c.645C>G | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>C | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834297 | c.756C>G | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>A | 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 | 1834474 | c.933C>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834498 | c.957C>T | synonymous_variant | 1.0 |
| rpsA | 1834513 | c.972C>G | synonymous_variant | 1.0 |
| rpsA | 1834528 | c.987T>G | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>C | synonymous_variant | 1.0 |
| rpsA | 1834558 | c.1017C>G | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>G | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834666 | c.1125G>C | synonymous_variant | 1.0 |
| rpsA | 1834669 | c.1128G>C | synonymous_variant | 1.0 |
| rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 1.0 |
| rpsA | 1834726 | c.1185C>A | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | c.1224A>G | synonymous_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834786 | c.1245A>G | synonymous_variant | 1.0 |
| rpsA | 1834789 | c.1248T>C | synonymous_variant | 1.0 |
| rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
| rpsA | 1834852 | c.1311C>G | synonymous_variant | 1.0 |
| tlyA | 1917929 | c.-11T>C | upstream_gene_variant | 1.0 |
| tlyA | 1917945 | c.6A>T | synonymous_variant | 1.0 |
| tlyA | 1917951 | c.12T>C | synonymous_variant | 1.0 |
| tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
| tlyA | 1917981 | c.42G>C | synonymous_variant | 1.0 |
| 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 | 1917999 | c.60T>C | synonymous_variant | 1.0 |
| tlyA | 1918002 | c.63A>G | synonymous_variant | 1.0 |
| tlyA | 1918015 | c.76T>C | synonymous_variant | 1.0 |
| tlyA | 1918036 | p.Arg33Ser | missense_variant | 1.0 |
| katG | 2155017 | c.1095G>C | synonymous_variant | 0.96 |
| katG | 2155020 | c.1092C>T | synonymous_variant | 1.0 |
| katG | 2155029 | c.1083C>G | synonymous_variant | 1.0 |
| katG | 2155032 | c.1080T>C | synonymous_variant | 1.0 |
| katG | 2155054 | p.Tyr353Phe | missense_variant | 0.98 |
| katG | 2155056 | c.1056A>G | synonymous_variant | 0.98 |
| katG | 2155062 | c.1050T>C | synonymous_variant | 0.98 |
| katG | 2155065 | c.1047C>G | synonymous_variant | 0.98 |
| katG | 2155068 | c.1044T>C | synonymous_variant | 0.98 |
| katG | 2155071 | c.1041T>C | synonymous_variant | 0.98 |
| katG | 2155080 | c.1032G>C | synonymous_variant | 0.97 |
| katG | 2155113 | c.999C>G | synonymous_variant | 0.98 |
| katG | 2155119 | p.Ser331Thr | missense_variant | 0.98 |
| katG | 2155131 | c.981A>G | synonymous_variant | 0.97 |
| katG | 2155134 | c.978G>C | synonymous_variant | 1.0 |
| katG | 2155144 | p.Asn323Pro | missense_variant | 1.0 |
| katG | 2155152 | c.960A>C | synonymous_variant | 1.0 |
| katG | 2155155 | c.957C>G | synonymous_variant | 1.0 |
| katG | 2155176 | c.936G>C | synonymous_variant | 1.0 |
| katG | 2155566 | c.546G>C | synonymous_variant | 1.0 |
| katG | 2155572 | c.540G>C | synonymous_variant | 1.0 |
| katG | 2155581 | c.531C>T | synonymous_variant | 1.0 |
| katG | 2155590 | c.522A>G | synonymous_variant | 1.0 |
| katG | 2155614 | p.Val166Ile | missense_variant | 1.0 |
| katG | 2155617 | c.495T>C | synonymous_variant | 1.0 |
| katG | 2155632 | c.480A>C | synonymous_variant | 1.0 |
| katG | 2155637 | p.Leu159Ile | missense_variant | 1.0 |
| katG | 2155641 | p.Lys157Asn | missense_variant | 0.97 |
| katG | 2155677 | c.435C>G | synonymous_variant | 1.0 |
| katG | 2155680 | c.432G>C | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155695 | p.Ala139Val | missense_variant | 1.0 |
| katG | 2155704 | c.408C>G | synonymous_variant | 1.0 |
| katG | 2155716 | c.396T>C | synonymous_variant | 1.0 |
| katG | 2155722 | c.390G>C | synonymous_variant | 1.0 |
| katG | 2155740 | p.Gly124Gln | missense_variant | 0.97 |
| katG | 2155747 | p.Ala122Gly | missense_variant | 1.0 |
| katG | 2155782 | c.330C>G | synonymous_variant | 1.0 |
| katG | 2155785 | c.327T>C | synonymous_variant | 1.0 |
| katG | 2155788 | c.324C>T | synonymous_variant | 1.0 |
| katG | 2155794 | p.Ala106Ser | missense_variant | 1.0 |
| katG | 2155806 | c.306T>C | synonymous_variant | 1.0 |
| pncA | 2289892 | c.-651C>G | upstream_gene_variant | 0.9 |
| pncA | 2289903 | c.-662C>T | upstream_gene_variant | 0.9 |
| pncA | 2289906 | c.-665T>C | upstream_gene_variant | 0.9 |
| pncA | 2289907 | c.-666A>G | upstream_gene_variant | 0.9 |
| pncA | 2289916 | c.-675A>G | 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 | 2289937 | c.-696C>G | upstream_gene_variant | 1.0 |
| pncA | 2289943 | c.-704_-702delTTTinsCTC | 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 | 2289958 | c.-717T>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 | 2290006 | c.-765T>C | upstream_gene_variant | 1.0 |
| pncA | 2290009 | c.-768A>G | upstream_gene_variant | 1.0 |
| pncA | 2290015 | c.-774A>C | upstream_gene_variant | 1.0 |
| pncA | 2290027 | c.-786G>A | 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>T | upstream_gene_variant | 1.0 |
| pncA | 2290042 | c.-801T>C | upstream_gene_variant | 1.0 |
| pncA | 2290071 | c.-830A>G | upstream_gene_variant | 1.0 |
| pncA | 2290072 | c.-831T>C | upstream_gene_variant | 1.0 |
| kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.99 |
| kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.99 |
| kasA | 2517989 | c.-126T>C | upstream_gene_variant | 1.0 |
| kasA | 2517992 | c.-123C>G | 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 | 1.0 |
| kasA | 2518035 | c.-80C>G | upstream_gene_variant | 1.0 |
| kasA | 2518049 | c.-66G>C | upstream_gene_variant | 1.0 |
| kasA | 2518053 | c.-62A>C | upstream_gene_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 | 0.98 |
| kasA | 2518190 | p.Ser26Ala | missense_variant | 0.99 |
| kasA | 2518199 | p.Ile29Val | missense_variant | 0.99 |
| kasA | 2518222 | c.108G>A | synonymous_variant | 0.98 |
| kasA | 2518223 | c.109_111delTTGinsCTC | synonymous_variant | 0.98 |
| kasA | 2518234 | c.120G>A | synonymous_variant | 0.98 |
| kasA | 2518248 | p.Ala45Val | missense_variant | 0.96 |
| kasA | 2518261 | p.Glu49Asp | missense_variant | 0.94 |
| kasA | 2518263 | p.Phe50Tyr | missense_variant | 1.0 |
| kasA | 2518265 | p.Val51Ile | missense_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 | 2518450 | c.336C>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>T | synonymous_variant | 1.0 |
| kasA | 2518475 | c.361A>C | 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>G | 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 | 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 | 2518621 | c.507G>A | synonymous_variant | 1.0 |
| kasA | 2518642 | c.528A>G | synonymous_variant | 1.0 |
| kasA | 2518663 | c.549T>C | synonymous_variant | 1.0 |
| kasA | 2518672 | c.558G>C | synonymous_variant | 1.0 |
| kasA | 2518687 | c.573C>T | synonymous_variant | 1.0 |
| kasA | 2518696 | c.582C>G | synonymous_variant | 1.0 |
| kasA | 2518702 | c.588C>T | 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 | 2518741 | c.627G>C | synonymous_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| kasA | 2518768 | c.654C>G | synonymous_variant | 1.0 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
| kasA | 2518792 | c.678C>G | synonymous_variant | 1.0 |
| kasA | 2518795 | c.681C>G | synonymous_variant | 1.0 |
| kasA | 2518816 | c.702C>A | synonymous_variant | 1.0 |
| kasA | 2518822 | c.708C>G | synonymous_variant | 1.0 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
| kasA | 2518855 | c.741C>G | 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 | 2518888 | c.774C>T | 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 | 2519095 | c.981C>G | synonymous_variant | 1.0 |
| kasA | 2519098 | c.984C>G | synonymous_variant | 1.0 |
| kasA | 2519104 | c.990T>A | synonymous_variant | 1.0 |
| kasA | 2519108 | p.Asp332Gln | missense_variant | 1.0 |
| kasA | 2519111 | p.Gln333Glu | missense_variant | 1.0 |
| kasA | 2519116 | c.1002C>G | synonymous_variant | 1.0 |
| kasA | 2519125 | c.1011C>T | synonymous_variant | 1.0 |
| kasA | 2519137 | c.1023T>C | synonymous_variant | 1.0 |
| kasA | 2519146 | c.1032C>A | synonymous_variant | 1.0 |
| kasA | 2519167 | c.1053T>C | synonymous_variant | 1.0 |
| kasA | 2519173 | c.1059C>G | synonymous_variant | 1.0 |
| kasA | 2519176 | c.1062G>A | synonymous_variant | 1.0 |
| kasA | 2519197 | c.1083G>C | synonymous_variant | 1.0 |
| kasA | 2519215 | c.1101C>T | synonymous_variant | 1.0 |
| kasA | 2519221 | c.1107G>C | synonymous_variant | 1.0 |
| kasA | 2519225 | c.1111C>T | synonymous_variant | 1.0 |
| ahpC | 2726255 | c.63T>C | synonymous_variant | 1.0 |
| ahpC | 2726288 | c.96C>T | synonymous_variant | 1.0 |
| ahpC | 2726303 | c.111T>C | synonymous_variant | 1.0 |
| ahpC | 2726312 | c.120T>C | synonymous_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 | 2726336 | c.144G>C | synonymous_variant | 1.0 |
| ahpC | 2726348 | c.156T>C | synonymous_variant | 1.0 |
| ahpC | 2726354 | c.162G>C | synonymous_variant | 1.0 |
| ahpC | 2726357 | c.165A>G | synonymous_variant | 1.0 |
| ahpC | 2726366 | c.174G>C | synonymous_variant | 1.0 |
| ahpC | 2726372 | c.180G>C | synonymous_variant | 1.0 |
| ahpC | 2726378 | c.186T>C | synonymous_variant | 1.0 |
| ahpC | 2726390 | c.198G>C | synonymous_variant | 1.0 |
| ahpC | 2726391 | p.Ala67Thr | missense_variant | 1.0 |
| ahpC | 2726397 | p.Ser69Gly | missense_variant | 1.0 |
| ahpC | 2726408 | c.216T>C | synonymous_variant | 1.0 |
| ahpC | 2726558 | c.366A>C | synonymous_variant | 1.0 |
| ahpC | 2726564 | c.372C>T | synonymous_variant | 1.0 |
| ahpC | 2726570 | c.378C>T | 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 | 2726612 | c.420C>G | synonymous_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 | 1.0 |
| ahpC | 2726672 | c.480G>A | synonymous_variant | 1.0 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
| ahpC | 2726681 | c.489A>G | synonymous_variant | 1.0 |
| ahpC | 2726687 | c.495C>G | synonymous_variant | 1.0 |
| ahpC | 2726693 | c.501C>G | synonymous_variant | 1.0 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 1.0 |
| ahpC | 2726717 | c.525A>G | synonymous_variant | 1.0 |
| folC | 2746555 | c.1044G>T | synonymous_variant | 1.0 |
| folC | 2746561 | c.1038C>A | synonymous_variant | 1.0 |
| folC | 2746564 | c.1035A>C | synonymous_variant | 1.0 |
| folC | 2746569 | p.Ser344Arg | missense_variant | 1.0 |
| folC | 2746576 | c.1023C>A | synonymous_variant | 1.0 |
| folC | 2746582 | c.1015_1017delTTGinsCTT | synonymous_variant | 1.0 |
| folC | 2746594 | c.1005T>C | synonymous_variant | 1.0 |
| folC | 2746597 | c.1002C>A | synonymous_variant | 1.0 |
| folC | 2746609 | c.990T>C | synonymous_variant | 1.0 |
| folC | 2746612 | c.987C>T | synonymous_variant | 1.0 |
| folC | 2746999 | c.600T>C | synonymous_variant | 1.0 |
| folC | 2747002 | c.597T>C | synonymous_variant | 1.0 |
| folC | 2747006 | c.592_593delAGinsTC | synonymous_variant | 1.0 |
| folC | 2747023 | c.576C>G | synonymous_variant | 1.0 |
| folC | 2747032 | c.567A>C | synonymous_variant | 1.0 |
| folC | 2747040 | p.Ile187Val | missense_variant | 1.0 |
| folC | 2747059 | c.540T>C | synonymous_variant | 1.0 |
| folC | 2747065 | c.534C>G | synonymous_variant | 1.0 |
| folC | 2747086 | c.513A>C | synonymous_variant | 1.0 |
| folC | 2747089 | c.510G>C | synonymous_variant | 1.0 |
| folC | 2747098 | c.501C>G | synonymous_variant | 1.0 |
| folC | 2747101 | c.498G>C | 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 | 2747149 | c.450C>T | synonymous_variant | 1.0 |
| folC | 2747264 | p.Gly112Ala | missense_variant | 1.0 |
| folC | 2747275 | c.324T>C | synonymous_variant | 1.0 |
| folC | 2747281 | c.318A>G | synonymous_variant | 1.0 |
| folC | 2747289 | p.Pro104Ala | missense_variant | 1.0 |
| folC | 2747290 | c.309A>C | synonymous_variant | 1.0 |
| folC | 2747293 | c.306G>A | synonymous_variant | 1.0 |
| folC | 2747302 | c.297A>G | synonymous_variant | 1.0 |
| folC | 2747314 | c.285A>C | synonymous_variant | 1.0 |
| folC | 2747317 | c.282C>G | synonymous_variant | 1.0 |
| folC | 2747355 | p.Val82Ile | missense_variant | 1.0 |
| folC | 2747359 | c.240C>G | synonymous_variant | 1.0 |
| folC | 2747362 | c.237G>C | synonymous_variant | 1.0 |
| folC | 2747394 | p.Ile69Val | missense_variant | 1.0 |
| folC | 2747395 | c.204T>C | synonymous_variant | 1.0 |
| folC | 2747401 | c.198G>C | synonymous_variant | 1.0 |
| folC | 2747407 | c.192T>C | synonymous_variant | 1.0 |
| folC | 2747411 | p.Ser63Ala | missense_variant | 1.0 |
| folC | 2747416 | c.183A>G | synonymous_variant | 1.0 |
| folC | 2747419 | c.180C>G | synonymous_variant | 1.0 |
| folC | 2747430 | c.169C>T | synonymous_variant | 1.0 |
| folC | 2747439 | p.Met54Leu | missense_variant | 0.95 |
| folC | 2747442 | c.157T>C | synonymous_variant | 1.0 |
| folC | 2747443 | c.156G>A | synonymous_variant | 1.0 |
| folC | 2747464 | c.135G>C | synonymous_variant | 1.0 |
| folC | 2747467 | p.Asp44Glu | missense_variant | 1.0 |
| folC | 2747473 | p.Arg42Lys | missense_variant | 1.0 |
| folC | 2747491 | c.108A>G | synonymous_variant | 1.0 |
| folC | 2747497 | c.102C>G | synonymous_variant | 1.0 |
| folC | 2747500 | c.99A>G | synonymous_variant | 1.0 |
| folC | 2747503 | c.96T>C | synonymous_variant | 1.0 |
| folC | 2747506 | c.93G>A | synonymous_variant | 1.0 |
| folC | 2747509 | c.90T>C | synonymous_variant | 1.0 |
| folC | 2747745 | c.-147A>C | upstream_gene_variant | 1.0 |
| folC | 2747752 | c.-154G>C | upstream_gene_variant | 1.0 |
| 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 | 2747778 | c.-180T>G | upstream_gene_variant | 1.0 |
| folC | 2747790 | c.-192G>C | upstream_gene_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 | 2859750 | c.669C>G | synonymous_variant | 1.0 |
| pepQ | 2859765 | c.654G>C | synonymous_variant | 1.0 |
| pepQ | 2859771 | c.648T>C | synonymous_variant | 1.0 |
| thyX | 3067220 | c.726G>C | synonymous_variant | 1.0 |
| thyX | 3067223 | c.723G>C | synonymous_variant | 1.0 |
| thyX | 3067244 | c.702C>G | synonymous_variant | 1.0 |
| thyX | 3067249 | p.Thr233Ala | missense_variant | 1.0 |
| thyX | 3067250 | p.Val232Ile | missense_variant | 1.0 |
| thyX | 3067277 | c.669C>G | synonymous_variant | 1.0 |
| thyX | 3067280 | c.666G>C | synonymous_variant | 1.0 |
| thyX | 3067284 | p.Ala221Asp | missense_variant | 1.0 |
| thyX | 3067286 | c.660C>G | synonymous_variant | 1.0 |
| thyX | 3067289 | c.657C>G | synonymous_variant | 1.0 |
| thyX | 3067293 | p.Gln218Arg | missense_variant | 1.0 |
| thyX | 3067304 | c.642A>G | synonymous_variant | 1.0 |
| thyX | 3067316 | c.630A>G | synonymous_variant | 1.0 |
| thyX | 3067325 | c.621A>G | synonymous_variant | 1.0 |
| thyX | 3067355 | c.591A>C | synonymous_variant | 1.0 |
| thyX | 3067367 | c.579G>C | synonymous_variant | 1.0 |
| thyX | 3067376 | c.570G>C | synonymous_variant | 1.0 |
| thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
| thyX | 3067394 | c.552G>C | synonymous_variant | 1.0 |
| thyX | 3067412 | c.534C>G | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyX | 3067445 | c.501C>G | synonymous_variant | 1.0 |
| thyX | 3067451 | c.495G>A | synonymous_variant | 1.0 |
| thyX | 3067457 | c.489C>G | synonymous_variant | 1.0 |
| thyX | 3067463 | p.Ile161Val | missense_variant | 1.0 |
| thyX | 3067466 | c.480G>C | synonymous_variant | 1.0 |
| thyX | 3067470 | p.Asn159Ser | missense_variant | 1.0 |
| thyX | 3067493 | c.453A>G | synonymous_variant | 1.0 |
| thyX | 3067500 | p.Lys149Arg | missense_variant | 1.0 |
| thyX | 3067515 | p.Ser144Thr | missense_variant | 1.0 |
| thyX | 3067586 | c.360C>G | synonymous_variant | 1.0 |
| thyX | 3067601 | c.345G>C | synonymous_variant | 1.0 |
| thyX | 3067604 | c.342G>C | synonymous_variant | 1.0 |
| thyX | 3067610 | p.Lys112Asn | missense_variant | 1.0 |
| thyX | 3067613 | c.333G>A | synonymous_variant | 1.0 |
| thyX | 3067619 | c.327A>C | synonymous_variant | 1.0 |
| thyX | 3067640 | c.306G>C | synonymous_variant | 1.0 |
| thyX | 3067643 | c.303C>T | synonymous_variant | 1.0 |
| thyX | 3067652 | c.294T>C | synonymous_variant | 1.0 |
| thyX | 3067661 | c.285C>G | synonymous_variant | 1.0 |
| thyX | 3067682 | c.264G>C | synonymous_variant | 1.0 |
| thyX | 3067685 | c.261A>G | synonymous_variant | 1.0 |
| thyX | 3067688 | c.258G>C | synonymous_variant | 1.0 |
| thyX | 3067694 | c.252G>C | synonymous_variant | 1.0 |
| thyX | 3067718 | c.228C>G | synonymous_variant | 1.0 |
| thyX | 3067721 | c.225T>C | synonymous_variant | 1.0 |
| thyX | 3067724 | c.222G>A | synonymous_variant | 1.0 |
| thyX | 3067727 | c.219A>C | synonymous_variant | 1.0 |
| thyX | 3067739 | c.207T>C | synonymous_variant | 1.0 |
| thyX | 3067742 | c.204A>C | synonymous_variant | 1.0 |
| thyX | 3067761 | p.Arg62Lys | missense_variant | 1.0 |
| thyX | 3067765 | p.Leu61Ile | missense_variant | 1.0 |
| thyX | 3067781 | c.165C>G | synonymous_variant | 1.0 |
| thyX | 3067787 | c.159G>A | 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 | 3067826 | c.120C>G | 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 | 0.98 |
| thyX | 3067886 | c.60A>C | synonymous_variant | 1.0 |
| thyX | 3067889 | c.57C>G | synonymous_variant | 1.0 |
| thyX | 3067894 | c.52T>C | synonymous_variant | 1.0 |
| thyX | 3067935 | p.Thr4Ile | missense_variant | 1.0 |
| thyA | 3073812 | c.660C>G | synonymous_variant | 1.0 |
| thyA | 3073815 | c.657G>A | synonymous_variant | 1.0 |
| thyA | 3073824 | c.648A>C | synonymous_variant | 1.0 |
| thyA | 3073827 | c.645A>G | synonymous_variant | 1.0 |
| thyA | 3073839 | c.633T>C | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073872 | p.Ile200Val | missense_variant | 1.0 |
| thyA | 3073878 | c.594G>A | synonymous_variant | 1.0 |
| thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
| thyA | 3073893 | c.579C>A | synonymous_variant | 1.0 |
| thyA | 3073925 | c.547T>C | synonymous_variant | 1.0 |
| thyA | 3073929 | c.543T>C | synonymous_variant | 1.0 |
| thyA | 3073953 | c.519T>C | synonymous_variant | 1.0 |
| thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
| thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
| thyA | 3074001 | c.471C>G | synonymous_variant | 1.0 |
| thyA | 3074004 | c.468T>C | synonymous_variant | 1.0 |
| thyA | 3074010 | c.462C>G | synonymous_variant | 1.0 |
| thyA | 3074031 | c.441T>C | synonymous_variant | 1.0 |
| thyA | 3074037 | c.435C>G | synonymous_variant | 1.0 |
| thyA | 3074056 | p.Glu139Pro | missense_variant | 1.0 |
| thyA | 3074061 | c.411A>G | synonymous_variant | 1.0 |
| thyA | 3074076 | c.396C>G | synonymous_variant | 1.0 |
| thyA | 3074082 | c.390G>C | synonymous_variant | 1.0 |
| thyA | 3074097 | c.375C>G | synonymous_variant | 1.0 |
| thyA | 3074100 | c.372T>C | synonymous_variant | 1.0 |
| thyA | 3074106 | c.366T>C | synonymous_variant | 1.0 |
| thyA | 3074117 | c.355C>T | synonymous_variant | 1.0 |
| thyA | 3074120 | c.352T>C | synonymous_variant | 1.0 |
| thyA | 3074130 | c.342G>C | synonymous_variant | 1.0 |
| thyA | 3074157 | c.315C>G | synonymous_variant | 1.0 |
| thyA | 3074160 | c.312A>G | synonymous_variant | 1.0 |
| thyA | 3074163 | 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 | 3074184 | c.288A>G | synonymous_variant | 1.0 |
| thyA | 3074187 | c.285T>C | synonymous_variant | 1.0 |
| thyA | 3074199 | c.273G>A | synonymous_variant | 1.0 |
| thyA | 3074205 | p.Glu89Asp | missense_variant | 0.97 |
| thyA | 3074214 | c.258T>C | synonymous_variant | 0.95 |
| thyA | 3074217 | c.255T>C | synonymous_variant | 0.95 |
| thyA | 3074235 | c.237C>T | synonymous_variant | 0.9 |
| thyA | 3074334 | c.138T>C | synonymous_variant | 1.0 |
| thyA | 3074339 | p.Leu45Ile | missense_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 | 3074372 | p.Met34Leu | missense_variant | 1.0 |
| thyA | 3074394 | c.78C>G | synonymous_variant | 1.0 |
| thyA | 3074397 | c.75A>G | synonymous_variant | 1.0 |
| ald | 3087608 | c.789A>G | synonymous_variant | 1.0 |
| ald | 3087617 | c.798T>C | synonymous_variant | 1.0 |
| ald | 3087620 | c.801A>C | synonymous_variant | 1.0 |
| ald | 3087621 | p.Ala268Ser | missense_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>C | 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 | 3087699 | p.Leu294Val | missense_variant | 1.0 |
| ald | 3087704 | c.885T>C | 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 |
| fbiB | 3641274 | c.-261G>C | 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 | 0.96 |
| fbiB | 3641328 | c.-207T>G | upstream_gene_variant | 0.95 |
| fbiA | 3641340 | p.Asp266Glu | missense_variant | 0.94 |
| fbiB | 3642110 | c.576C>G | synonymous_variant | 1.0 |
| fbiB | 3642113 | c.579A>G | synonymous_variant | 1.0 |
| fbiB | 3642114 | p.Val194Ile | missense_variant | 1.0 |
| fbiB | 3642143 | c.609C>T | synonymous_variant | 1.0 |
| fbiB | 3642144 | c.610T>C | synonymous_variant | 1.0 |
| fbiB | 3642149 | c.615C>G | synonymous_variant | 1.0 |
| fbiB | 3642152 | c.618A>G | synonymous_variant | 1.0 |
| fbiB | 3642169 | p.Thr212Met | missense_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 | 3642593 | c.1059G>C | synonymous_variant | 1.0 |
| fbiB | 3642602 | c.1068A>C | synonymous_variant | 1.0 |
| fbiB | 3642605 | c.1071A>G | synonymous_variant | 1.0 |
| fbiB | 3642614 | c.1080C>T | 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 | 3642662 | c.1128C>G | synonymous_variant | 1.0 |
| fbiB | 3642668 | c.1134A>C | synonymous_variant | 1.0 |
| fbiB | 3642677 | c.1143A>G | synonymous_variant | 1.0 |
| fbiB | 3642680 | c.1146A>G | synonymous_variant | 1.0 |
| fbiB | 3642684 | c.1150T>C | synonymous_variant | 1.0 |
| fbiB | 3642694 | p.Ala387Gly | missense_variant | 1.0 |
| fbiB | 3642696 | c.1162C>T | synonymous_variant | 1.0 |
| fbiB | 3642701 | c.1167C>G | synonymous_variant | 1.0 |
| alr | 3840215 | c.1206T>C | synonymous_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 | 3840287 | c.1134C>T | synonymous_variant | 1.0 |
| alr | 3840293 | c.1128T>C | synonymous_variant | 1.0 |
| alr | 3840296 | c.1125G>C | synonymous_variant | 1.0 |
| alr | 3840302 | c.1119G>A | synonymous_variant | 1.0 |
| alr | 3840308 | p.Arg371Asn | missense_variant | 1.0 |
| alr | 3840312 | p.Ile370Ser | missense_variant | 1.0 |
| alr | 3840328 | c.1093T>C | synonymous_variant | 1.0 |
| alr | 3840329 | c.1092T>C | synonymous_variant | 1.0 |
| alr | 3840344 | c.1077A>G | synonymous_variant | 1.0 |
| alr | 3840424 | c.997A>C | synonymous_variant | 1.0 |
| alr | 3840435 | p.Leu329Ser | missense_variant | 1.0 |
| alr | 3840442 | p.Glu327Gln | missense_variant | 1.0 |
| alr | 3840467 | p.Val318Ile | missense_variant | 1.0 |
| alr | 3840476 | c.945A>C | synonymous_variant | 1.0 |
| alr | 3840482 | c.939T>C | synonymous_variant | 1.0 |
| alr | 3840485 | p.Ile312Val | missense_variant | 1.0 |
| alr | 3841060 | p.Gly121Arg | missense_variant | 1.0 |
| alr | 3841100 | c.321A>G | synonymous_variant | 1.0 |
| alr | 3841104 | p.Thr106Ser | missense_variant | 1.0 |
| alr | 3841106 | c.315T>C | synonymous_variant | 1.0 |
| alr | 3841109 | c.312C>G | synonymous_variant | 1.0 |
| alr | 3841112 | p.Asp103Ala | missense_variant | 1.0 |
| alr | 3841115 | c.306T>C | synonymous_variant | 1.0 |
| alr | 3841127 | c.294A>G | synonymous_variant | 1.0 |
| alr | 3841148 | c.273C>G | synonymous_variant | 1.0 |
| ddn | 3986648 | c.-196C>G | upstream_gene_variant | 1.0 |
| ddn | 3986655 | c.-189A>T | upstream_gene_variant | 1.0 |
| ddn | 3986660 | c.-184C>T | upstream_gene_variant | 0.98 |
| ddn | 3986665 | c.-179G>C | upstream_gene_variant | 1.0 |
| ddn | 3986667 | c.-177_-176delCTinsAC | 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>T | upstream_gene_variant | 1.0 |
| ddn | 3986699 | c.-145C>G | upstream_gene_variant | 1.0 |
| panD | 4044057 | c.225C>A | 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>G | synonymous_variant | 1.0 |
| panD | 4044084 | c.198T>C | synonymous_variant | 1.0 |
| panD | 4044090 | c.192C>T | synonymous_variant | 1.0 |
| panD | 4044093 | c.189A>G | synonymous_variant | 1.0 |
| panD | 4044096 | c.186C>T | synonymous_variant | 1.0 |
| panD | 4044120 | c.162A>G | 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 | 4044150 | c.132A>G | synonymous_variant | 1.0 |
| panD | 4044162 | c.120A>G | synonymous_variant | 1.0 |
| panD | 4044165 | c.117G>C | synonymous_variant | 1.0 |
| panD | 4044188 | c.94T>C | 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 | 4044249 | c.33C>T | synonymous_variant | 1.0 |
| panD | 4044264 | c.18G>C | synonymous_variant | 1.0 |
| panD | 4044284 | c.-3C>T | upstream_gene_variant | 1.0 |
| panD | 4044287 | c.-6A>G | upstream_gene_variant | 1.0 |
| panD | 4044294 | c.-13A>C | upstream_gene_variant | 1.0 |
| embC | 4240010 | c.148C>T | synonymous_variant | 0.83 |
| embC | 4240019 | p.Asn53Asp | missense_variant | 0.96 |
| embC | 4240033 | c.171G>C | synonymous_variant | 0.96 |
| embC | 4240036 | c.174A>G | synonymous_variant | 0.96 |
| embC | 4240037 | c.175T>C | synonymous_variant | 0.96 |
| embC | 4240059 | p.Thr66Ser | missense_variant | 1.0 |
| embC | 4240065 | p.Ala68Gly | missense_variant | 1.0 |
| embC | 4240069 | c.207T>C | synonymous_variant | 1.0 |
| embC | 4240072 | c.210C>G | synonymous_variant | 1.0 |
| embC | 4240078 | c.216A>G | 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 | 4240123 | c.261C>G | synonymous_variant | 0.94 |
| embC | 4240183 | c.321A>G | synonymous_variant | 0.94 |
| embC | 4240204 | c.342T>C | synonymous_variant | 0.98 |
| embC | 4240210 | c.348C>G | synonymous_variant | 1.0 |
| embC | 4240216 | c.354T>C | synonymous_variant | 1.0 |
| embC | 4240229 | p.Leu123Ile | missense_variant | 1.0 |
| embC | 4240232 | p.Gln124Val | missense_variant | 1.0 |
| 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 | 4240285 | c.423C>G | synonymous_variant | 1.0 |
| embC | 4240297 | c.435T>C | synonymous_variant | 1.0 |
| embC | 4240306 | c.444C>G | synonymous_variant | 1.0 |
| embC | 4240313 | p.Thr151Ala | missense_variant | 1.0 |
| embC | 4240318 | c.456T>C | synonymous_variant | 1.0 |
| embC | 4240330 | c.468A>C | synonymous_variant | 1.0 |
| embC | 4240459 | c.597G>C | synonymous_variant | 1.0 |
| embC | 4240462 | c.600G>C | synonymous_variant | 1.0 |
| embC | 4240475 | p.Ala205Ser | missense_variant | 1.0 |
| embC | 4240480 | c.618G>A | synonymous_variant | 1.0 |
| embC | 4240489 | c.627A>G | synonymous_variant | 1.0 |
| embC | 4240495 | c.633T>C | synonymous_variant | 1.0 |
| embC | 4240512 | p.Ser217Thr | missense_variant | 1.0 |
| embC | 4240514 | p.Val218Ile | missense_variant | 1.0 |
| embC | 4240519 | c.657T>C | synonymous_variant | 1.0 |
| embC | 4240543 | c.681G>C | synonymous_variant | 1.0 |
| embC | 4240561 | c.699C>G | synonymous_variant | 1.0 |
| embC | 4240573 | c.711G>C | synonymous_variant | 1.0 |
| embC | 4240574 | p.Val238Leu | missense_variant | 1.0 |
| embC | 4240578 | p.Ala239Val | missense_variant | 1.0 |
| embC | 4240582 | c.720C>G | synonymous_variant | 1.0 |
| embC | 4240591 | c.729C>G | synonymous_variant | 1.0 |
| embC | 4240594 | c.732C>G | synonymous_variant | 1.0 |
| embC | 4240600 | c.738G>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 | 4240654 | c.792C>T | synonymous_variant | 1.0 |
| embC | 4240657 | c.795G>C | synonymous_variant | 1.0 |
| embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
| embC | 4240678 | c.816T>G | synonymous_variant | 1.0 |
| embC | 4240685 | p.Thr275Ala | missense_variant | 1.0 |
| embC | 4240693 | c.831T>C | synonymous_variant | 1.0 |
| embC | 4240706 | p.Val282Thr | missense_variant | 0.98 |
| embC | 4240726 | c.864G>C | synonymous_variant | 0.99 |
| embC | 4240780 | c.918T>C | synonymous_variant | 0.99 |
| embC | 4240783 | c.921G>C | synonymous_variant | 0.99 |
| embC | 4240789 | c.927T>C | synonymous_variant | 0.99 |
| embC | 4240819 | c.957A>G | synonymous_variant | 1.0 |
| embC | 4240831 | c.969T>G | synonymous_variant | 1.0 |
| embC | 4240867 | c.1005T>G | synonymous_variant | 1.0 |
| embC | 4240870 | c.1008T>C | 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 | 4240900 | c.1038A>G | synonymous_variant | 1.0 |
| embC | 4240919 | c.1057_1059delCTCinsTTG | synonymous_variant | 1.0 |
| embC | 4240936 | c.1074A>G | synonymous_variant | 1.0 |
| embC | 4240945 | c.1083T>C | synonymous_variant | 1.0 |
| embC | 4240951 | c.1089C>G | synonymous_variant | 1.0 |
| embC | 4240954 | p.Ile364Met | missense_variant | 1.0 |
| embC | 4240957 | c.1095C>G | synonymous_variant | 1.0 |
| embC | 4240966 | c.1104G>T | synonymous_variant | 1.0 |
| embC | 4240979 | p.Thr373Gln | missense_variant | 0.98 |
| embC | 4240983 | p.Ser374Asn | missense_variant | 0.98 |
| embC | 4240990 | c.1128A>G | synonymous_variant | 0.98 |
| embC | 4240996 | c.1134G>C | synonymous_variant | 0.98 |
| embC | 4241017 | c.1155T>C | synonymous_variant | 0.98 |
| embC | 4241023 | c.1161T>G | synonymous_variant | 0.98 |
| embC | 4241026 | c.1164C>G | synonymous_variant | 0.98 |
| embC | 4241035 | c.1173G>A | synonymous_variant | 0.98 |
| embC | 4241050 | c.1188T>G | synonymous_variant | 0.98 |
| embC | 4241104 | c.1242G>A | synonymous_variant | 1.0 |
| embC | 4241107 | c.1245G>C | synonymous_variant | 1.0 |
| embC | 4241137 | c.1275G>C | synonymous_variant | 1.0 |
| embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
| embC | 4241141 | p.Ile427Val | missense_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 | 4241203 | c.1341T>C | synonymous_variant | 0.98 |
| embC | 4241230 | c.1368A>G | synonymous_variant | 0.93 |
| embC | 4241233 | c.1371G>C | synonymous_variant | 0.92 |
| embC | 4241236 | c.1374C>G | synonymous_variant | 0.92 |
| embC | 4241361 | p.Asn500Ser | missense_variant | 0.91 |
| embC | 4241363 | p.Leu501Met | missense_variant | 0.91 |
| embC | 4241374 | c.1512T>C | synonymous_variant | 0.96 |
| embC | 4241380 | c.1518A>C | synonymous_variant | 0.96 |
| embC | 4241394 | p.Lys511Ser | missense_variant | 0.97 |
| embC | 4241443 | c.1581C>G | synonymous_variant | 1.0 |
| embC | 4241449 | c.1587C>G | synonymous_variant | 1.0 |
| embC | 4241453 | p.Ile531Val | missense_variant | 1.0 |
| embC | 4241473 | c.1611G>A | synonymous_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 | 4241560 | c.1698C>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 | 4241617 | c.1755G>A | synonymous_variant | 1.0 |
| embC | 4241623 | c.1761C>G | synonymous_variant | 1.0 |
| embC | 4241626 | c.1764T>C | synonymous_variant | 1.0 |
| embC | 4241644 | c.1782G>C | synonymous_variant | 1.0 |
| embC | 4241648 | c.1786T>C | synonymous_variant | 1.0 |
| embC | 4241657 | p.Ser599Pro | missense_variant | 1.0 |
| embC | 4241665 | c.1803G>T | synonymous_variant | 1.0 |
| embC | 4241671 | c.1809T>G | synonymous_variant | 1.0 |
| embA | 4242391 | c.-842G>C | upstream_gene_variant | 1.0 |
| embA | 4242400 | c.-833C>G | upstream_gene_variant | 1.0 |
| embA | 4242403 | c.-830T>C | upstream_gene_variant | 1.0 |
| embA | 4242406 | c.-827A>G | upstream_gene_variant | 1.0 |
| embA | 4242427 | c.-806A>C | upstream_gene_variant | 1.0 |
| embC | 4242428 | p.Ala856Ser | missense_variant | 1.0 |
| embC | 4242434 | p.Val858Ile | missense_variant | 1.0 |
| embC | 4242449 | p.Met863His | missense_variant | 1.0 |
| embA | 4242460 | c.-773G>C | 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 | 4242871 | c.-362C>G | upstream_gene_variant | 1.0 |
| embA | 4242880 | c.-353A>G | upstream_gene_variant | 1.0 |
| embA | 4242883 | c.-350C>G | upstream_gene_variant | 1.0 |
| embA | 4242886 | c.-347G>A | upstream_gene_variant | 1.0 |
| embA | 4242892 | c.-341G>C | upstream_gene_variant | 1.0 |
| embA | 4242907 | c.-326G>A | 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 | 4244298 | p.Ser356Ala | missense_variant | 1.0 |
| embA | 4244309 | c.1077C>G | 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 | 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 | 4244396 | c.1164T>C | synonymous_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 | 4244903 | c.1671G>C | synonymous_variant | 1.0 |
| embA | 4244919 | c.1687_1689delCTCinsTTG | synonymous_variant | 1.0 |
| embA | 4244933 | c.1701A>G | synonymous_variant | 1.0 |
| embA | 4244945 | c.1713C>G | synonymous_variant | 1.0 |
| embA | 4244948 | c.1716G>C | synonymous_variant | 1.0 |
| embA | 4244960 | c.1728A>C | synonymous_variant | 1.0 |
| embA | 4245038 | c.1806C>T | synonymous_variant | 1.0 |
| embA | 4245056 | c.1824C>G | synonymous_variant | 1.0 |
| embA | 4245077 | c.1845G>C | synonymous_variant | 1.0 |
| embA | 4245083 | c.1851A>C | synonymous_variant | 1.0 |
| embA | 4245089 | c.1857G>C | synonymous_variant | 0.96 |
| embA | 4245092 | c.1860C>G | synonymous_variant | 1.0 |
| embA | 4245101 | c.1869G>C | synonymous_variant | 1.0 |
| embA | 4245137 | c.1905T>C | synonymous_variant | 1.0 |
| embA | 4245149 | c.1917C>G | synonymous_variant | 1.0 |
| embA | 4245182 | c.1950T>C | synonymous_variant | 1.0 |
| embA | 4245194 | c.1962G>C | synonymous_variant | 1.0 |
| embA | 4245198 | p.Leu656Ile | missense_variant | 1.0 |
| embA | 4245206 | c.1974A>G | synonymous_variant | 1.0 |
| embA | 4245207 | c.1975T>C | synonymous_variant | 1.0 |
| embA | 4245215 | c.1983A>G | synonymous_variant | 1.0 |
| embA | 4245222 | p.Tyr664Gln | missense_variant | 1.0 |
| embA | 4245242 | c.2010C>T | synonymous_variant | 1.0 |
| embA | 4245245 | c.2013C>G | synonymous_variant | 1.0 |
| embA | 4245248 | c.2016G>C | synonymous_variant | 1.0 |
| embA | 4245461 | c.2229C>G | synonymous_variant | 1.0 |
| embA | 4245465 | p.Pro745Ala | missense_variant | 1.0 |
| embA | 4245470 | c.2238T>C | synonymous_variant | 1.0 |
| embA | 4245485 | c.2253A>G | synonymous_variant | 1.0 |
| embA | 4245489 | p.Val753Leu | missense_variant | 1.0 |
| embA | 4245501 | p.Ala757Thr | missense_variant | 1.0 |
| embA | 4245509 | c.2277A>G | synonymous_variant | 1.0 |
| embB | 4245518 | c.-996A>G | upstream_gene_variant | 1.0 |
| embB | 4245524 | c.-990G>C | upstream_gene_variant | 1.0 |
| embA | 4245557 | p.Glu775Asp | missense_variant | 1.0 |
| embA | 4245569 | p.Glu779Asp | missense_variant | 1.0 |
| embB | 4245587 | c.-927G>C | upstream_gene_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 | 4245617 | c.-897C>G | upstream_gene_variant | 1.0 |
| embB | 4245620 | c.-894T>C | upstream_gene_variant | 1.0 |
| embB | 4245623 | c.-891G>C | upstream_gene_variant | 1.0 |
| embB | 4245626 | c.-888G>C | upstream_gene_variant | 1.0 |
| embB | 4245659 | c.-855C>G | upstream_gene_variant | 1.0 |
| embA | 4245693 | p.Ile821Val | missense_variant | 1.0 |
| embB | 4245701 | c.-813G>C | upstream_gene_variant | 1.0 |
| embB | 4245716 | c.-798G>C | upstream_gene_variant | 1.0 |
| embB | 4245725 | c.-789A>C | upstream_gene_variant | 1.0 |
| embB | 4245726 | c.-788_-786delTTGinsCTC | 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 | 4245771 | p.Asn847Ser | missense_variant | 1.0 |
| embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 1.0 |
| embB | 4245830 | c.-684G>C | upstream_gene_variant | 1.0 |
| embB | 4245845 | c.-669T>G | upstream_gene_variant | 1.0 |
| embB | 4245848 | c.-666C>G | 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 | 4245905 | c.-609C>G | upstream_gene_variant | 0.98 |
| embB | 4245926 | c.-588C>G | upstream_gene_variant | 0.93 |
| embA | 4245927 | p.Thr899Ala | missense_variant | 0.92 |
| embA | 4245930 | p.Gly900Arg | missense_variant | 0.92 |
| embB | 4245983 | c.-531A>C | upstream_gene_variant | 0.93 |
| embB | 4245989 | c.-525A>G | upstream_gene_variant | 0.94 |
| embB | 4245992 | c.-522C>G | upstream_gene_variant | 0.95 |
| embB | 4246010 | c.-504G>C | upstream_gene_variant | 0.97 |
| embB | 4246013 | c.-501T>C | upstream_gene_variant | 0.98 |
| embA | 4246041 | p.Asp937Asn | missense_variant | 0.98 |
| embB | 4246055 | c.-459T>C | upstream_gene_variant | 0.98 |
| embB | 4246064 | c.-450T>C | upstream_gene_variant | 0.98 |
| embB | 4246079 | c.-435C>T | upstream_gene_variant | 0.97 |
| embA | 4246080 | p.Pro950Ser | missense_variant | 0.97 |
| embB | 4246088 | c.-426A>G | upstream_gene_variant | 1.0 |
| embB | 4246097 | c.-417C>G | upstream_gene_variant | 1.0 |
| embA | 4246264 | p.His1011Arg | missense_variant | 1.0 |
| embB | 4246274 | c.-240G>C | upstream_gene_variant | 1.0 |
| embB | 4246292 | c.-222A>G | upstream_gene_variant | 1.0 |
| embA | 4246303 | c.3073_3074delTC | frameshift_variant | 1.0 |
| embA | 4246308 | c.3076_3077insAG | frameshift_variant | 1.0 |
| embB | 4246316 | c.-198T>G | upstream_gene_variant | 1.0 |
| embA | 4246329 | p.Thr1033Leu | missense_variant | 1.0 |
| embB | 4246355 | c.-159G>C | upstream_gene_variant | 1.0 |
| embA | 4246359 | p.Ala1043Pro | missense_variant | 1.0 |
| embB | 4246364 | c.-150G>C | upstream_gene_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 |
| embA | 4246413 | p.His1061Phe | missense_variant | 1.0 |
| embB | 4246419 | c.-95C>T | upstream_gene_variant | 1.0 |
| embB | 4246603 | c.90C>G | 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 | 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 | 4247059 | c.546C>G | synonymous_variant | 1.0 |
| embB | 4247062 | c.549G>C | synonymous_variant | 1.0 |
| embB | 4247068 | c.555T>C | synonymous_variant | 1.0 |
| embB | 4247074 | c.561G>C | synonymous_variant | 1.0 |
| embB | 4247101 | c.588G>C | synonymous_variant | 1.0 |
| embB | 4247105 | p.Pro198Ala | missense_variant | 1.0 |
| embB | 4247110 | c.597G>C | synonymous_variant | 1.0 |
| embB | 4247114 | p.Ala201Lys | missense_variant | 1.0 |
| embB | 4247117 | p.Val202Leu | missense_variant | 1.0 |
| embB | 4247140 | c.627G>A | synonymous_variant | 1.0 |
| embB | 4247338 | c.825C>G | synonymous_variant | 1.0 |
| embB | 4247348 | p.Thr279Ala | missense_variant | 1.0 |
| embB | 4247355 | p.Ala281Val | missense_variant | 1.0 |
| embB | 4247358 | p.Val282Ala | missense_variant | 1.0 |
| embB | 4247365 | c.852A>C | synonymous_variant | 1.0 |
| embB | 4247371 | c.858C>G | synonymous_variant | 1.0 |
| embB | 4247375 | p.Leu288Val | missense_variant | 1.0 |
| embB | 4247386 | c.873T>C | synonymous_variant | 1.0 |
| embB | 4247389 | c.876C>G | synonymous_variant | 1.0 |
| embB | 4247395 | c.882C>G | synonymous_variant | 1.0 |
| embB | 4247401 | c.888T>C | synonymous_variant | 1.0 |
| embB | 4247437 | c.924A>G | synonymous_variant | 1.0 |
| embB | 4247440 | c.927C>G | 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 | 4247500 | c.987C>G | synonymous_variant | 1.0 |
| embB | 4247512 | c.999T>C | synonymous_variant | 1.0 |
| embB | 4247536 | c.1023C>G | synonymous_variant | 1.0 |
| embB | 4247554 | c.1041T>C | synonymous_variant | 1.0 |
| embB | 4247566 | c.1053C>G | synonymous_variant | 1.0 |
| embB | 4247567 | c.1054C>T | 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>C | synonymous_variant | 1.0 |
| embB | 4247614 | c.1101T>C | synonymous_variant | 1.0 |
| embB | 4247629 | c.1116C>G | synonymous_variant | 1.0 |
| embB | 4247632 | c.1119C>G | synonymous_variant | 1.0 |
| embB | 4247635 | c.1122G>A | synonymous_variant | 1.0 |
| embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
| embB | 4247655 | p.Lys381Arg | missense_variant | 1.0 |
| embB | 4247659 | c.1146C>G | 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>G | synonymous_variant | 1.0 |
| embB | 4247722 | c.1209G>C | synonymous_variant | 1.0 |
| embB | 4247725 | c.1212G>C | synonymous_variant | 0.95 |
| embB | 4247729 | p.Gly406Pro | missense_variant | 1.0 |
| embB | 4247743 | c.1230C>G | synonymous_variant | 1.0 |
| embB | 4247746 | c.1233C>A | synonymous_variant | 1.0 |
| embB | 4247776 | c.1263G>T | synonymous_variant | 1.0 |
| embB | 4247779 | c.1266C>G | synonymous_variant | 1.0 |
| embB | 4247785 | c.1272G>C | synonymous_variant | 1.0 |
| embB | 4247800 | c.1287A>C | synonymous_variant | 1.0 |
| embB | 4247806 | c.1293G>C | synonymous_variant | 1.0 |
| embB | 4247819 | p.Val436Ile | missense_variant | 0.98 |
| embB | 4247824 | c.1311C>G | synonymous_variant | 1.0 |
| embB | 4247830 | c.1317A>C | synonymous_variant | 1.0 |
| embB | 4247836 | c.1323A>G | synonymous_variant | 1.0 |
| embB | 4247842 | c.1329T>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 | 4247890 | c.1377C>T | synonymous_variant | 1.0 |
| embB | 4247899 | p.Met462Ile | missense_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 | 4247977 | c.1464C>G | synonymous_variant | 1.0 |
| embB | 4247986 | c.1473C>G | synonymous_variant | 1.0 |
| embB | 4248007 | c.1494C>G | synonymous_variant | 1.0 |
| embB | 4248011 | p.Ser500Ala | missense_variant | 1.0 |
| embB | 4248035 | p.Val508Ile | missense_variant | 1.0 |
| embB | 4248041 | p.Ala510Thr | missense_variant | 1.0 |
| embB | 4248044 | p.Lys511Ala | missense_variant | 1.0 |
| embB | 4248052 | c.1539G>A | synonymous_variant | 1.0 |
| embB | 4248055 | c.1542G>C | synonymous_variant | 1.0 |
| embB | 4248064 | c.1551G>C | synonymous_variant | 1.0 |
| embB | 4248070 | c.1557T>C | synonymous_variant | 1.0 |
| embB | 4248085 | c.1572T>C | synonymous_variant | 1.0 |
| embB | 4248095 | c.1582_1584delCTCinsTTG | synonymous_variant | 1.0 |
| embB | 4248118 | c.1605T>C | synonymous_variant | 1.0 |
| embB | 4248127 | c.1614G>C | synonymous_variant | 1.0 |
| embB | 4248133 | c.1620C>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 | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248220 | c.1707A>G | synonymous_variant | 1.0 |
| embB | 4248241 | c.1728C>T | synonymous_variant | 1.0 |
| embB | 4248265 | c.1752C>T | synonymous_variant | 1.0 |
| embB | 4248266 | c.1753C>T | synonymous_variant | 1.0 |
| embB | 4248277 | c.1764G>C | synonymous_variant | 1.0 |
| embB | 4248298 | c.1785C>T | synonymous_variant | 1.0 |
| embB | 4248304 | c.1791G>C | synonymous_variant | 1.0 |
| embB | 4248316 | c.1803C>G | synonymous_variant | 1.0 |
| embB | 4248319 | c.1806A>G | synonymous_variant | 1.0 |
| embB | 4248343 | c.1830G>C | synonymous_variant | 1.0 |
| embB | 4248346 | c.1833G>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>G | synonymous_variant | 1.0 |
| embB | 4248362 | p.Ser617Ala | missense_variant | 1.0 |
| embB | 4248398 | c.1885C>T | synonymous_variant | 1.0 |
| embB | 4248403 | c.1890G>C | synonymous_variant | 1.0 |
| embB | 4248407 | c.1894_1896delTTAinsCTG | synonymous_variant | 1.0 |
| embB | 4248410 | p.Phe633Leu | missense_variant | 1.0 |
| embB | 4248416 | p.Leu635Met | 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 | 4248460 | c.1947C>G | synonymous_variant | 1.0 |
| embB | 4248472 | c.1959T>G | synonymous_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 | 4248524 | p.Ile671Val | missense_variant | 1.0 |
| embB | 4249297 | c.2784G>C | synonymous_variant | 1.0 |
| embB | 4249369 | c.2856T>C | synonymous_variant | 1.0 |
| embB | 4249381 | c.2868A>G | synonymous_variant | 1.0 |
| embB | 4249417 | c.2904A>G | synonymous_variant | 1.0 |
| embB | 4249420 | c.2907G>C | synonymous_variant | 1.0 |
| embB | 4249423 | p.Asp970Glu | missense_variant | 1.0 |
| embB | 4249424 | p.Leu971Met | missense_variant | 1.0 |
| embB | 4249432 | c.2919A>G | synonymous_variant | 1.0 |
| embB | 4249441 | c.2928A>G | synonymous_variant | 1.0 |
| embB | 4249444 | c.2931T>C | synonymous_variant | 1.0 |
| embB | 4249447 | c.2934G>C | synonymous_variant | 1.0 |
| embB | 4249456 | c.2943G>C | synonymous_variant | 1.0 |
| embB | 4249469 | p.Leu986Met | missense_variant | 1.0 |
| embB | 4249483 | c.2970C>G | synonymous_variant | 1.0 |
| embB | 4249486 | c.2973T>G | synonymous_variant | 1.0 |
| embB | 4249487 | c.2974T>C | 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 | 1.0 |
| embB | 4249528 | c.3015C>G | synonymous_variant | 1.0 |
| embB | 4249529 | p.Ile1006Val | missense_variant | 1.0 |
| embB | 4249532 | p.Ala1007Thr | missense_variant | 1.0 |
| embB | 4249537 | c.3024A>G | synonymous_variant | 1.0 |
| embB | 4249543 | c.3030G>C | synonymous_variant | 1.0 |
| embB | 4249558 | c.3045A>C | synonymous_variant | 1.0 |
| embB | 4249564 | c.3051C>T | synonymous_variant | 1.0 |
| embB | 4249568 | p.Ser1019Thr | missense_variant | 0.96 |
| embB | 4249573 | c.3060T>C | synonymous_variant | 1.0 |
| embB | 4249580 | p.Leu1023Met | missense_variant | 1.0 |
| embB | 4249594 | c.3081G>C | synonymous_variant | 1.0 |
| embB | 4249600 | c.3087A>G | synonymous_variant | 1.0 |
| ubiA | 4268976 | c.858G>C | synonymous_variant | 1.0 |
| ubiA | 4268982 | p.Leu284Phe | missense_variant | 1.0 |
| ubiA | 4268985 | c.849A>G | synonymous_variant | 1.0 |
| ubiA | 4269001 | p.Ala278Val | missense_variant | 1.0 |
| ubiA | 4269006 | c.828T>C | synonymous_variant | 1.0 |
| ubiA | 4269009 | c.825A>G | synonymous_variant | 1.0 |
| ubiA | 4269012 | c.822G>C | synonymous_variant | 1.0 |
| ubiA | 4269033 | c.801T>C | synonymous_variant | 1.0 |
| ubiA | 4269036 | c.798C>G | synonymous_variant | 1.0 |
| ubiA | 4269042 | c.792G>C | synonymous_variant | 1.0 |
| ubiA | 4269075 | p.Ile253Val | missense_variant | 1.0 |
| ubiA | 4269081 | c.753G>C | synonymous_variant | 1.0 |
| ubiA | 4269088 | p.Ala249Val | missense_variant | 1.0 |
| ubiA | 4269123 | c.711T>C | synonymous_variant | 1.0 |
| ubiA | 4269132 | c.702G>C | synonymous_variant | 1.0 |
| ubiA | 4269141 | p.Leu231Val | missense_variant | 1.0 |
| ubiA | 4269144 | c.690C>G | synonymous_variant | 1.0 |
| ubiA | 4269149 | p.Val229Leu | missense_variant | 1.0 |
| ubiA | 4269183 | c.651T>C | synonymous_variant | 1.0 |
| ubiA | 4269201 | c.633A>G | synonymous_variant | 1.0 |
| ubiA | 4269209 | p.Ser209Ala | missense_variant | 1.0 |
| ubiA | 4269220 | p.Ala205Lys | missense_variant | 1.0 |
| ubiA | 4269222 | c.612T>G | synonymous_variant | 1.0 |
| ubiA | 4269225 | c.609C>G | synonymous_variant | 1.0 |
| ubiA | 4269231 | c.603C>G | synonymous_variant | 1.0 |
| ubiA | 4269234 | c.600A>G | synonymous_variant | 1.0 |
| ubiA | 4269243 | p.His197Gln | missense_variant | 1.0 |
| ubiA | 4269271 | p.Val188Ala | missense_variant | 1.0 |
| ubiA | 4269285 | c.549T>G | synonymous_variant | 1.0 |
| ubiA | 4269291 | c.543A>G | synonymous_variant | 1.0 |
| ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
| ubiA | 4269392 | p.Val148Met | missense_variant | 1.0 |
| ubiA | 4269402 | c.432T>C | synonymous_variant | 1.0 |
| ubiA | 4269405 | c.429G>A | synonymous_variant | 1.0 |
| ubiA | 4269411 | c.423T>C | synonymous_variant | 1.0 |
| ubiA | 4269414 | c.420T>C | synonymous_variant | 1.0 |
| ubiA | 4269420 | c.414T>C | synonymous_variant | 1.0 |
| ubiA | 4269423 | c.411G>C | synonymous_variant | 1.0 |
| ubiA | 4269428 | c.406T>C | synonymous_variant | 1.0 |
| ubiA | 4269432 | p.Met134Ile | missense_variant | 1.0 |
| ubiA | 4269440 | p.Leu132Ile | missense_variant | 1.0 |
| ubiA | 4269448 | p.Val129Ala | missense_variant | 1.0 |
| ubiA | 4269453 | c.381A>G | synonymous_variant | 1.0 |
| ubiA | 4269457 | p.Leu126Ala | missense_variant | 1.0 |
| ethA | 4328462 | c.-989C>T | upstream_gene_variant | 1.0 |
| ethA | 4328471 | c.-998A>G | upstream_gene_variant | 0.98 |
| ethA | 4328473 | c.-1000G>C | upstream_gene_variant | 1.0 |
