Run ID: ERR1035138
Sample name:
Date: 18-08-2022 11:53:02
Number of reads: 1028351
Percentage reads mapped: 16.86
Strain:
Drug-resistance: MDR-TB
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage6.3.1 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
| lineage5.1.2 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 1.0 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| rpoB | 761154 | p.Ser450Asn | missense_variant | 1.0 | rifampicin |
| katG | 2155108 | p.Ile335Thr | missense_variant | 1.0 | isoniazid |
| embB | 4248488 | p.Ala659Thr | missense_variant | 1.0 | ethambutol |
| ethA | 4326636 | c.837_838insC | frameshift_variant | 1.0 | ethionamide |
| ethA | 4326639 | c.834delG | frameshift_variant | 1.0 | ethionamide |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5510 | p.Ser91Thr | missense_variant | 1.0 |
| gyrB | 5518 | p.Ile93Met | missense_variant | 1.0 |
| gyrB | 5521 | c.282G>C | synonymous_variant | 0.91 |
| gyrB | 5542 | c.303A>C | synonymous_variant | 0.91 |
| gyrB | 5545 | c.306A>G | synonymous_variant | 0.91 |
| gyrB | 5548 | c.309A>G | synonymous_variant | 0.91 |
| gyrB | 5551 | c.312T>C | synonymous_variant | 0.91 |
| gyrB | 5992 | c.753T>C | synonymous_variant | 1.0 |
| gyrB | 5998 | c.759T>C | synonymous_variant | 1.0 |
| gyrB | 6001 | c.762G>C | synonymous_variant | 1.0 |
| gyrB | 6004 | c.765T>C | synonymous_variant | 1.0 |
| gyrB | 6013 | c.774G>C | synonymous_variant | 1.0 |
| gyrB | 6022 | c.783G>C | synonymous_variant | 1.0 |
| gyrB | 6025 | c.786A>G | synonymous_variant | 1.0 |
| gyrB | 6047 | p.Ala270Pro | missense_variant | 1.0 |
| gyrB | 6052 | c.813T>C | synonymous_variant | 0.97 |
| gyrB | 6055 | c.816T>C | synonymous_variant | 1.0 |
| gyrB | 6067 | c.828G>C | synonymous_variant | 1.0 |
| gyrB | 6073 | c.834T>C | synonymous_variant | 1.0 |
| gyrB | 6085 | c.846C>T | synonymous_variant | 1.0 |
| gyrB | 6086 | p.Thr283Pro | missense_variant | 1.0 |
| gyrB | 6091 | c.852G>C | synonymous_variant | 1.0 |
| gyrB | 6094 | c.855C>T | synonymous_variant | 1.0 |
| gyrB | 6100 | c.861G>C | synonymous_variant | 1.0 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6160 | c.921C>G | synonymous_variant | 1.0 |
| gyrB | 6172 | c.933C>T | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>T | synonymous_variant | 1.0 |
| gyrB | 6202 | c.963C>G | synonymous_variant | 1.0 |
| gyrB | 6203 | p.Ser322Ala | missense_variant | 1.0 |
| gyrB | 6223 | c.984G>C | synonymous_variant | 1.0 |
| gyrB | 6235 | c.996C>G | synonymous_variant | 1.0 |
| gyrB | 6250 | c.1011A>G | synonymous_variant | 1.0 |
| gyrB | 6253 | c.1014G>C | synonymous_variant | 1.0 |
| gyrB | 6256 | c.1017G>A | synonymous_variant | 1.0 |
| gyrB | 6280 | c.1041T>A | 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 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 1.0 |
| gyrA | 6319 | c.-983G>C | upstream_gene_variant | 1.0 |
| gyrA | 6331 | c.-971A>G | upstream_gene_variant | 1.0 |
| gyrA | 6355 | c.-947G>A | 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 | 6376 | c.-926G>A | upstream_gene_variant | 1.0 |
| gyrA | 6382 | c.-920A>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 | 6421 | c.-881C>T | upstream_gene_variant | 1.0 |
| gyrA | 6427 | c.-875T>C | upstream_gene_variant | 1.0 |
| gyrA | 6430 | c.-872A>G | upstream_gene_variant | 1.0 |
| gyrA | 6436 | c.-866C>T | upstream_gene_variant | 1.0 |
| gyrA | 6577 | c.-725T>C | upstream_gene_variant | 1.0 |
| gyrA | 6583 | c.-719G>C | upstream_gene_variant | 1.0 |
| gyrA | 6598 | c.-704C>G | upstream_gene_variant | 1.0 |
| gyrA | 6604 | c.-698G>T | upstream_gene_variant | 1.0 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 1.0 |
| gyrA | 6613 | c.-689A>G | upstream_gene_variant | 1.0 |
| gyrA | 6622 | c.-680C>T | upstream_gene_variant | 1.0 |
| gyrA | 6631 | c.-671C>T | upstream_gene_variant | 1.0 |
| gyrA | 6634 | c.-668T>C | upstream_gene_variant | 1.0 |
| gyrA | 6637 | c.-665T>G | upstream_gene_variant | 1.0 |
| gyrA | 6640 | c.-662A>C | upstream_gene_variant | 1.0 |
| gyrA | 6643 | c.-659A>G | upstream_gene_variant | 1.0 |
| gyrA | 6655 | c.-647T>C | upstream_gene_variant | 1.0 |
| gyrA | 6673 | c.-629A>C | upstream_gene_variant | 1.0 |
| gyrA | 6676 | c.-626T>G | upstream_gene_variant | 1.0 |
| gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrA | 6721 | c.-581C>T | upstream_gene_variant | 1.0 |
| gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.97 |
| gyrA | 6733 | c.-569G>A | upstream_gene_variant | 1.0 |
| gyrA | 6742 | c.-560A>G | upstream_gene_variant | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Ser | missense_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>C | upstream_gene_variant | 1.0 |
| gyrA | 6853 | c.-449A>G | upstream_gene_variant | 1.0 |
| gyrA | 6856 | c.-446T>C | upstream_gene_variant | 1.0 |
| gyrA | 6859 | c.-443T>C | upstream_gene_variant | 1.0 |
| gyrA | 6862 | c.-440C>G | upstream_gene_variant | 1.0 |
| gyrA | 6869 | c.-433T>C | upstream_gene_variant | 1.0 |
| gyrA | 6872 | c.-430T>C | upstream_gene_variant | 1.0 |
| gyrA | 6877 | c.-425G>T | 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 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>G | upstream_gene_variant | 1.0 |
| gyrA | 6934 | c.-368A>G | upstream_gene_variant | 1.0 |
| gyrA | 6949 | c.-353A>G | upstream_gene_variant | 1.0 |
| gyrA | 6967 | c.-335T>C | upstream_gene_variant | 1.0 |
| gyrB | 6970 | p.Asp577Glu | missense_variant | 1.0 |
| gyrA | 6976 | c.-326A>G | upstream_gene_variant | 1.0 |
| gyrA | 6982 | c.-320A>G | upstream_gene_variant | 1.0 |
| gyrA | 6994 | c.-308C>G | upstream_gene_variant | 1.0 |
| gyrA | 7006 | c.-296T>A | upstream_gene_variant | 1.0 |
| gyrA | 7007 | c.-295C>T | 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>A | upstream_gene_variant | 1.0 |
| gyrB | 7023 | p.Leu595Gln | missense_variant | 1.0 |
| gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
| gyrA | 7060 | c.-242T>C | upstream_gene_variant | 1.0 |
| gyrA | 7066 | c.-236G>C | upstream_gene_variant | 1.0 |
| gyrA | 7078 | c.-224A>G | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>C | upstream_gene_variant | 1.0 |
| gyrA | 7114 | c.-188C>G | upstream_gene_variant | 1.0 |
| gyrA | 7120 | c.-182T>C | upstream_gene_variant | 1.0 |
| gyrA | 7123 | c.-179C>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 | 7150 | c.-152G>C | upstream_gene_variant | 1.0 |
| gyrA | 7153 | c.-149G>C | upstream_gene_variant | 1.0 |
| gyrA | 7190 | c.-112C>T | upstream_gene_variant | 1.0 |
| gyrA | 7213 | c.-89G>C | upstream_gene_variant | 1.0 |
| gyrA | 7216 | c.-86G>T | upstream_gene_variant | 1.0 |
| gyrA | 7225 | c.-77T>C | upstream_gene_variant | 1.0 |
| gyrA | 7231 | c.-71C>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 | 7313 | c.12G>C | synonymous_variant | 1.0 |
| gyrA | 7317 | c.16T>C | synonymous_variant | 1.0 |
| gyrA | 7324 | c.23_24insAGGCGG | disruptive_inframe_insertion | 1.0 |
| gyrA | 7330 | p.Asp10Ala | missense_variant | 1.0 |
| gyrA | 7332 | p.Ser11Ala | missense_variant | 1.0 |
| gyrA | 7333 | c.33_35delGCT | disruptive_inframe_deletion | 1.0 |
| gyrA | 7343 | c.42G>C | synonymous_variant | 1.0 |
| gyrA | 7344 | p.Ile15Val | missense_variant | 1.0 |
| gyrA | 7355 | c.54T>C | synonymous_variant | 1.0 |
| gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 7415 | c.114C>G | synonymous_variant | 1.0 |
| gyrA | 7418 | c.117C>T | synonymous_variant | 1.0 |
| gyrA | 7427 | c.126G>C | synonymous_variant | 1.0 |
| gyrA | 7430 | c.129G>A | synonymous_variant | 1.0 |
| gyrA | 7433 | c.132G>T | synonymous_variant | 1.0 |
| gyrA | 7442 | c.141G>C | synonymous_variant | 1.0 |
| gyrA | 7451 | c.150C>G | synonymous_variant | 1.0 |
| gyrA | 7454 | c.153G>C | 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>G | synonymous_variant | 1.0 |
| gyrA | 7484 | c.183T>C | synonymous_variant | 1.0 |
| gyrA | 7490 | c.189C>G | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>G | synonymous_variant | 1.0 |
| gyrA | 7526 | c.225G>C | synonymous_variant | 1.0 |
| gyrA | 7532 | c.231T>C | synonymous_variant | 1.0 |
| gyrA | 7541 | c.240C>G | synonymous_variant | 1.0 |
| gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
| gyrA | 7556 | c.255C>T | synonymous_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7595 | c.294C>G | synonymous_variant | 1.0 |
| gyrA | 7601 | c.300C>G | synonymous_variant | 1.0 |
| gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
| gyrA | 7613 | c.312G>T | synonymous_variant | 1.0 |
| gyrA | 7625 | c.324G>C | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | 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 | 7697 | c.396C>G | synonymous_variant | 1.0 |
| gyrA | 7700 | c.399G>A | synonymous_variant | 1.0 |
| gyrA | 7710 | c.409T>C | synonymous_variant | 1.0 |
| gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 1.0 |
| gyrA | 7758 | p.Ile153Ala | missense_variant | 1.0 |
| gyrA | 7763 | c.462T>C | synonymous_variant | 1.0 |
| gyrA | 7776 | c.475C>A | synonymous_variant | 1.0 |
| gyrA | 7784 | c.483A>G | synonymous_variant | 1.0 |
| gyrA | 7787 | c.486G>A | synonymous_variant | 1.0 |
| gyrA | 7796 | c.495G>A | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7802 | c.501C>A | synonymous_variant | 1.0 |
| gyrA | 7811 | c.510C>T | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>G | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>C | synonymous_variant | 1.0 |
| gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
| gyrA | 7881 | c.580C>T | synonymous_variant | 1.0 |
| gyrA | 7886 | c.585T>C | synonymous_variant | 1.0 |
| gyrA | 7892 | c.591G>C | synonymous_variant | 1.0 |
| gyrA | 7898 | p.Asp199Glu | missense_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 | 8071 | p.Val257Ala | missense_variant | 1.0 |
| gyrA | 8076 | p.Val259Ile | missense_variant | 1.0 |
| gyrA | 8084 | c.783G>A | synonymous_variant | 1.0 |
| gyrA | 8090 | c.789C>G | synonymous_variant | 1.0 |
| gyrA | 8096 | c.795T>C | synonymous_variant | 1.0 |
| gyrA | 8099 | c.798T>C | synonymous_variant | 1.0 |
| gyrA | 8102 | c.801C>A | synonymous_variant | 1.0 |
| gyrA | 8156 | c.855T>G | synonymous_variant | 1.0 |
| gyrA | 8168 | c.867A>G | synonymous_variant | 1.0 |
| gyrA | 8177 | c.876A>C | synonymous_variant | 1.0 |
| gyrA | 8186 | c.885G>A | synonymous_variant | 1.0 |
| gyrA | 8189 | c.888G>C | synonymous_variant | 1.0 |
| gyrA | 8192 | c.891C>G | synonymous_variant | 1.0 |
| gyrA | 8198 | c.897T>C | synonymous_variant | 1.0 |
| gyrA | 8199 | p.Ser300Ala | missense_variant | 1.0 |
| gyrA | 8207 | c.906T>C | synonymous_variant | 1.0 |
| gyrA | 8210 | c.909G>A | synonymous_variant | 1.0 |
| gyrA | 8219 | c.918T>C | synonymous_variant | 1.0 |
| gyrA | 8225 | c.924T>C | synonymous_variant | 1.0 |
| gyrA | 8228 | c.927G>C | synonymous_variant | 1.0 |
| gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 1.0 |
| gyrA | 8252 | c.951G>A | 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>T | synonymous_variant | 1.0 |
| gyrA | 8270 | c.969G>C | synonymous_variant | 1.0 |
| gyrA | 8283 | p.Ile328Leu | missense_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8294 | c.993T>C | synonymous_variant | 1.0 |
| gyrA | 8306 | c.1005C>T | synonymous_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>G | synonymous_variant | 1.0 |
| gyrA | 8360 | c.1059G>A | synonymous_variant | 1.0 |
| gyrA | 8366 | c.1065G>C | synonymous_variant | 1.0 |
| gyrA | 8369 | c.1068G>T | 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 | 8408 | c.1107A>G | synonymous_variant | 1.0 |
| gyrA | 8417 | c.1116C>G | synonymous_variant | 1.0 |
| gyrA | 8420 | c.1119T>C | synonymous_variant | 1.0 |
| gyrA | 8426 | c.1125G>C | synonymous_variant | 1.0 |
| gyrA | 8438 | c.1137C>T | synonymous_variant | 1.0 |
| gyrA | 8447 | c.1146C>G | synonymous_variant | 1.0 |
| gyrA | 8450 | c.1149G>A | synonymous_variant | 1.0 |
| gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
| gyrA | 8462 | c.1161A>G | 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 | 8501 | c.1200G>C | synonymous_variant | 1.0 |
| gyrA | 8504 | c.1203G>C | synonymous_variant | 1.0 |
| gyrA | 8510 | c.1209G>A | synonymous_variant | 1.0 |
| gyrA | 8513 | c.1212C>G | synonymous_variant | 1.0 |
| gyrA | 8516 | c.1215T>C | synonymous_variant | 1.0 |
| gyrA | 8531 | c.1230G>A | synonymous_variant | 1.0 |
| gyrA | 8537 | c.1236G>A | synonymous_variant | 1.0 |
| gyrA | 8546 | c.1245T>C | synonymous_variant | 1.0 |
| gyrA | 8576 | c.1275C>G | synonymous_variant | 1.0 |
| gyrA | 8597 | c.1296C>G | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>C | synonymous_variant | 1.0 |
| gyrA | 8619 | c.1318T>C | synonymous_variant | 1.0 |
| gyrA | 8630 | c.1329G>T | synonymous_variant | 1.0 |
| gyrA | 8633 | c.1332C>G | synonymous_variant | 1.0 |
| gyrA | 8636 | c.1335A>C | synonymous_variant | 1.0 |
| gyrA | 8637 | c.1336C>T | synonymous_variant | 1.0 |
| gyrA | 8642 | c.1341A>G | synonymous_variant | 1.0 |
| gyrA | 8645 | c.1344C>T | synonymous_variant | 1.0 |
| gyrA | 8666 | c.1365G>C | synonymous_variant | 1.0 |
| gyrA | 8672 | c.1371A>G | synonymous_variant | 1.0 |
| gyrA | 8678 | c.1377G>A | synonymous_variant | 1.0 |
| gyrA | 8684 | c.1383G>A | synonymous_variant | 1.0 |
| gyrA | 8693 | c.1392T>C | synonymous_variant | 1.0 |
| gyrA | 8705 | c.1404C>T | synonymous_variant | 1.0 |
| gyrA | 8706 | c.1405C>T | synonymous_variant | 1.0 |
| gyrA | 8711 | c.1410A>G | synonymous_variant | 1.0 |
| gyrA | 8717 | c.1416C>G | synonymous_variant | 1.0 |
| gyrA | 8723 | c.1422G>C | synonymous_variant | 1.0 |
| gyrA | 8732 | c.1431G>C | synonymous_variant | 1.0 |
| gyrA | 8767 | p.Arg489Lys | missense_variant | 1.0 |
| gyrA | 8783 | c.1482G>T | synonymous_variant | 1.0 |
| gyrA | 8786 | c.1485T>C | synonymous_variant | 1.0 |
| gyrA | 8792 | c.1491G>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 | 8828 | c.1527T>C | synonymous_variant | 1.0 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>G | 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 | 8906 | c.1605C>G | synonymous_variant | 1.0 |
| gyrA | 8912 | c.1611G>A | synonymous_variant | 1.0 |
| gyrA | 8918 | c.1617C>G | synonymous_variant | 1.0 |
| gyrA | 8930 | c.1629C>T | synonymous_variant | 1.0 |
| gyrA | 8939 | c.1638T>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 | 8975 | c.1674C>T | synonymous_variant | 1.0 |
| gyrA | 8978 | c.1677C>T | synonymous_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 | 9017 | c.1716C>G | synonymous_variant | 1.0 |
| gyrA | 9023 | c.1722A>C | synonymous_variant | 1.0 |
| gyrA | 9026 | c.1725G>C | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>G | synonymous_variant | 1.0 |
| gyrA | 9044 | c.1743C>T | synonymous_variant | 1.0 |
| gyrA | 9056 | c.1755C>G | synonymous_variant | 1.0 |
| gyrA | 9062 | c.1761C>G | synonymous_variant | 1.0 |
| gyrA | 9065 | c.1764C>G | synonymous_variant | 1.0 |
| gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
| gyrA | 9080 | c.1779G>C | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9182 | c.1881T>C | synonymous_variant | 1.0 |
| gyrA | 9200 | c.1899A>G | synonymous_variant | 1.0 |
| gyrA | 9204 | p.Ser635Thr | missense_variant | 1.0 |
| gyrA | 9212 | c.1911G>C | synonymous_variant | 1.0 |
| gyrA | 9218 | c.1917C>T | synonymous_variant | 1.0 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 1.0 |
| gyrA | 9233 | c.1932C>G | synonymous_variant | 1.0 |
| gyrA | 9242 | c.1941A>C | synonymous_variant | 1.0 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 1.0 |
| gyrA | 9258 | c.1957C>T | synonymous_variant | 1.0 |
| gyrA | 9267 | p.Asn656Gly | missense_variant | 1.0 |
| gyrA | 9284 | c.1983T>C | synonymous_variant | 1.0 |
| gyrA | 9296 | c.1995T>C | synonymous_variant | 1.0 |
| gyrA | 9300 | p.Ala667Ser | missense_variant | 1.0 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9335 | c.2034G>C | synonymous_variant | 1.0 |
| gyrA | 9356 | c.2055G>C | synonymous_variant | 1.0 |
| gyrA | 9368 | c.2067G>A | 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>G | synonymous_variant | 1.0 |
| gyrA | 9389 | c.2088C>G | synonymous_variant | 1.0 |
| gyrA | 9395 | c.2094G>C | synonymous_variant | 1.0 |
| gyrA | 9398 | c.2097T>A | synonymous_variant | 1.0 |
| gyrA | 9419 | c.2118T>C | synonymous_variant | 1.0 |
| gyrA | 9421 | p.Ile707Thr | missense_variant | 1.0 |
| gyrA | 9429 | p.Arg710Tyr | missense_variant | 1.0 |
| gyrA | 9446 | c.2145C>T | synonymous_variant | 1.0 |
| gyrA | 9585 | c.2284T>C | synonymous_variant | 1.0 |
| gyrA | 9621 | p.Leu774Val | missense_variant | 1.0 |
| gyrA | 9626 | c.2325T>C | synonymous_variant | 1.0 |
| gyrA | 9630 | p.Val777Ile | missense_variant | 1.0 |
| gyrA | 9635 | c.2334T>C | synonymous_variant | 1.0 |
| gyrA | 9647 | c.2346C>G | synonymous_variant | 1.0 |
| gyrA | 9665 | c.2364A>G | synonymous_variant | 1.0 |
| gyrA | 9668 | c.2367C>G | synonymous_variant | 1.0 |
| gyrA | 9671 | c.2370G>A | synonymous_variant | 1.0 |
| gyrA | 9674 | c.2373T>C | synonymous_variant | 1.0 |
| gyrA | 9683 | c.2382G>C | synonymous_variant | 1.0 |
| gyrA | 9692 | c.2391G>A | synonymous_variant | 1.0 |
| gyrA | 9701 | c.2400T>C | synonymous_variant | 1.0 |
| gyrA | 9716 | c.2415T>C | synonymous_variant | 1.0 |
| gyrA | 9717 | c.2416C>T | synonymous_variant | 1.0 |
| gyrA | 9740 | c.2439G>A | synonymous_variant | 1.0 |
| gyrA | 9749 | c.2448G>A | synonymous_variant | 1.0 |
| gyrA | 9752 | c.2451C>T | synonymous_variant | 1.0 |
| fgd1 | 490818 | c.36C>G | synonymous_variant | 1.0 |
| fgd1 | 490830 | c.48A>G | synonymous_variant | 1.0 |
| fgd1 | 490836 | c.54C>G | synonymous_variant | 1.0 |
| fgd1 | 490839 | c.57G>A | synonymous_variant | 1.0 |
| fgd1 | 490849 | c.67_69delCTAinsTTG | synonymous_variant | 1.0 |
| fgd1 | 490854 | c.72C>G | synonymous_variant | 1.0 |
| fgd1 | 490869 | c.87C>G | synonymous_variant | 1.0 |
| fgd1 | 490890 | c.108C>G | synonymous_variant | 1.0 |
| fgd1 | 490905 | c.123T>C | synonymous_variant | 1.0 |
| fgd1 | 490911 | c.129T>G | synonymous_variant | 1.0 |
| fgd1 | 490917 | c.135C>G | synonymous_variant | 1.0 |
| fgd1 | 490921 | p.Gln47Lys | missense_variant | 1.0 |
| fgd1 | 490929 | c.147C>G | synonymous_variant | 1.0 |
| fgd1 | 490932 | c.150T>C | synonymous_variant | 1.0 |
| fgd1 | 490948 | p.Ser56Ala | missense_variant | 1.0 |
| fgd1 | 490962 | c.180T>G | synonymous_variant | 1.0 |
| fgd1 | 491133 | c.351A>C | synonymous_variant | 1.0 |
| fgd1 | 491144 | p.Ala121Glu | missense_variant | 1.0 |
| fgd1 | 491166 | c.384G>C | synonymous_variant | 1.0 |
| fgd1 | 491175 | c.393G>C | synonymous_variant | 1.0 |
| fgd1 | 491181 | c.399T>C | synonymous_variant | 1.0 |
| fgd1 | 491184 | c.402A>G | synonymous_variant | 1.0 |
| fgd1 | 491191 | p.Gly137Arg | missense_variant | 1.0 |
| fgd1 | 491196 | c.414A>G | synonymous_variant | 1.0 |
| fgd1 | 491202 | c.420G>C | synonymous_variant | 1.0 |
| fgd1 | 491203 | p.Gln141Glu | missense_variant | 1.0 |
| fgd1 | 491212 | p.Ser144Arg | missense_variant | 1.0 |
| fgd1 | 491217 | c.435T>C | synonymous_variant | 1.0 |
| fgd1 | 491220 | c.438C>T | synonymous_variant | 1.0 |
| fgd1 | 491232 | c.450T>C | synonymous_variant | 1.0 |
| fgd1 | 491244 | c.462T>C | synonymous_variant | 1.0 |
| fgd1 | 491256 | c.474G>A | synonymous_variant | 1.0 |
| fgd1 | 491259 | c.477T>C | synonymous_variant | 1.0 |
| fgd1 | 491283 | p.Asp167Glu | missense_variant | 1.0 |
| fgd1 | 491285 | p.Gly168Asp | missense_variant | 1.0 |
| fgd1 | 491295 | c.513C>A | synonymous_variant | 1.0 |
| fgd1 | 491296 | p.Val172Ile | missense_variant | 1.0 |
| fgd1 | 491310 | c.528C>G | synonymous_variant | 1.0 |
| fgd1 | 491331 | c.549G>A | synonymous_variant | 1.0 |
| fgd1 | 491340 | c.558C>T | synonymous_variant | 1.0 |
| fgd1 | 491343 | c.561C>G | synonymous_variant | 1.0 |
| fgd1 | 491349 | c.567T>C | synonymous_variant | 1.0 |
| fgd1 | 491364 | c.582T>C | synonymous_variant | 1.0 |
| fgd1 | 491367 | c.585G>C | synonymous_variant | 1.0 |
| fgd1 | 491392 | p.Thr204Arg | missense_variant | 1.0 |
| fgd1 | 491453 | p.Gly224Asp | missense_variant | 1.0 |
| fgd1 | 491472 | c.690A>G | synonymous_variant | 1.0 |
| fgd1 | 491499 | c.717G>C | synonymous_variant | 1.0 |
| fgd1 | 491500 | p.Glu240Lys | missense_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 | 1.0 |
| fgd1 | 491547 | c.765A>C | synonymous_variant | 1.0 |
| fgd1 | 491550 | c.768T>C | synonymous_variant | 1.0 |
| fgd1 | 491601 | c.819T>C | synonymous_variant | 0.98 |
| fgd1 | 491604 | c.822G>A | synonymous_variant | 1.0 |
| fgd1 | 491610 | c.828A>G | synonymous_variant | 1.0 |
| fgd1 | 491616 | c.834A>G | synonymous_variant | 1.0 |
| fgd1 | 491620 | p.Ile280Val | missense_variant | 1.0 |
| fgd1 | 491640 | c.858G>C | synonymous_variant | 1.0 |
| fgd1 | 491643 | c.861G>A | synonymous_variant | 1.0 |
| fgd1 | 491649 | c.867C>T | synonymous_variant | 1.0 |
| fgd1 | 491658 | c.876A>G | synonymous_variant | 1.0 |
| mshA | 575512 | c.165A>G | synonymous_variant | 1.0 |
| mshA | 575521 | c.174A>G | synonymous_variant | 1.0 |
| mshA | 575536 | c.189T>G | synonymous_variant | 1.0 |
| mshA | 575548 | c.201C>A | synonymous_variant | 1.0 |
| mshA | 575561 | p.Met72Val | missense_variant | 1.0 |
| mshA | 575569 | c.222A>G | synonymous_variant | 1.0 |
| mshA | 575572 | c.225T>C | synonymous_variant | 1.0 |
| mshA | 575581 | c.234C>T | synonymous_variant | 1.0 |
| mshA | 575587 | c.240C>G | synonymous_variant | 1.0 |
| mshA | 575590 | c.243T>C | synonymous_variant | 1.0 |
| mshA | 575593 | c.246G>C | synonymous_variant | 1.0 |
| mshA | 575597 | p.Ile84Val | missense_variant | 1.0 |
| mshA | 575600 | p.Glu85Gln | missense_variant | 1.0 |
| mshA | 575629 | c.282A>G | synonymous_variant | 1.0 |
| mshA | 575633 | p.Ala96Thr | missense_variant | 1.0 |
| mshA | 575641 | c.294A>G | synonymous_variant | 1.0 |
| mshA | 575644 | c.297G>C | synonymous_variant | 0.96 |
| mshA | 575647 | c.300G>C | synonymous_variant | 1.0 |
| mshA | 575659 | c.312A>G | synonymous_variant | 1.0 |
| mshA | 575665 | c.318G>T | 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 | 575734 | c.387T>G | synonymous_variant | 1.0 |
| mshA | 575737 | c.390T>C | synonymous_variant | 1.0 |
| mshA | 575770 | c.423G>C | synonymous_variant | 1.0 |
| mshA | 575772 | p.Val142Ala | missense_variant | 1.0 |
| mshA | 575779 | c.432A>G | synonymous_variant | 1.0 |
| mshA | 575782 | c.435G>C | synonymous_variant | 1.0 |
| mshA | 575788 | c.441C>T | synonymous_variant | 1.0 |
| mshA | 575821 | c.474G>C | synonymous_variant | 1.0 |
| mshA | 575824 | c.477T>G | synonymous_variant | 1.0 |
| mshA | 575839 | c.492G>T | synonymous_variant | 1.0 |
| mshA | 575842 | c.495G>C | synonymous_variant | 1.0 |
| mshA | 575845 | c.498C>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 | 575908 | c.561A>G | synonymous_variant | 1.0 |
| mshA | 575925 | p.Gly193Ala | missense_variant | 1.0 |
| mshA | 575944 | c.597T>C | synonymous_variant | 1.0 |
| mshA | 575953 | c.606G>C | synonymous_variant | 1.0 |
| mshA | 575980 | c.633T>C | synonymous_variant | 1.0 |
| mshA | 575984 | c.637T>C | synonymous_variant | 1.0 |
| rpoB | 759616 | c.-191C>T | upstream_gene_variant | 1.0 |
| rpoB | 759643 | c.-164T>C | upstream_gene_variant | 1.0 |
| rpoB | 759647 | c.-160T>C | upstream_gene_variant | 1.0 |
| rpoB | 759655 | c.-151delA | upstream_gene_variant | 1.0 |
| rpoB | 759661 | c.-146G>T | upstream_gene_variant | 1.0 |
| rpoB | 759672 | c.-135G>A | upstream_gene_variant | 1.0 |
| rpoB | 759674 | c.-133T>C | upstream_gene_variant | 1.0 |
| rpoB | 759678 | c.-129T>C | upstream_gene_variant | 1.0 |
| rpoB | 759679 | c.-128T>C | upstream_gene_variant | 1.0 |
| rpoB | 759681 | c.-126C>T | upstream_gene_variant | 1.0 |
| rpoB | 759693 | c.-114C>T | upstream_gene_variant | 1.0 |
| rpoB | 759694 | c.-113C>T | upstream_gene_variant | 1.0 |
| rpoB | 760046 | c.240G>C | synonymous_variant | 1.0 |
| rpoB | 760055 | c.249G>C | synonymous_variant | 1.0 |
| rpoB | 760059 | p.Tyr85Asp | missense_variant | 1.0 |
| rpoB | 760067 | c.261G>C | synonymous_variant | 1.0 |
| rpoB | 760070 | c.264T>C | 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>C | synonymous_variant | 1.0 |
| rpoB | 760112 | c.306T>C | synonymous_variant | 1.0 |
| rpoB | 760118 | c.312T>G | synonymous_variant | 1.0 |
| rpoB | 760121 | c.315T>C | synonymous_variant | 1.0 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760133 | c.327C>G | synonymous_variant | 1.0 |
| rpoB | 760172 | c.366G>C | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>G | synonymous_variant | 0.99 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760199 | c.393C>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 | 760271 | c.465C>G | 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 | 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 | 760388 | c.582C>T | synonymous_variant | 1.0 |
| rpoB | 760389 | c.583_585delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760457 | c.651C>T | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760528 | p.Gln241Arg | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243Thr | missense_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760634 | c.828T>C | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760649 | c.843G>C | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
| rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760718 | c.912C>A | synonymous_variant | 1.0 |
| rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760796 | c.990A>G | synonymous_variant | 1.0 |
| rpoB | 760805 | c.999G>C | synonymous_variant | 1.0 |
| rpoB | 760817 | c.1011A>G | synonymous_variant | 1.0 |
| rpoB | 760820 | c.1014T>C | synonymous_variant | 1.0 |
| rpoB | 760823 | c.1017G>C | synonymous_variant | 1.0 |
| rpoB | 760826 | c.1020C>G | synonymous_variant | 1.0 |
| rpoB | 760830 | c.1024T>C | synonymous_variant | 1.0 |
| rpoB | 760841 | c.1035T>C | synonymous_variant | 1.0 |
| rpoB | 760844 | p.Gln346His | missense_variant | 1.0 |
| rpoB | 760845 | p.Thr347Ala | missense_variant | 1.0 |
| rpoB | 760859 | c.1053T>C | synonymous_variant | 1.0 |
| rpoB | 760862 | c.1056G>C | synonymous_variant | 1.0 |
| rpoB | 760868 | c.1062C>T | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>G | synonymous_variant | 1.0 |
| rpoB | 760920 | p.Leu372Ile | missense_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761051 | c.1245G>T | synonymous_variant | 1.0 |
| rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
| rpoB | 761063 | c.1257C>G | synonymous_variant | 1.0 |
| rpoB | 761066 | c.1260G>C | synonymous_variant | 1.0 |
| rpoB | 761096 | c.1290G>C | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761129 | c.1323G>C | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
| rpoB | 761162 | c.1356G>C | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>T | synonymous_variant | 1.0 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 1.0 |
| rpoB | 761171 | c.1365C>T | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761183 | c.1377T>C | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>T | synonymous_variant | 1.0 |
| rpoB | 761198 | c.1392G>T | synonymous_variant | 1.0 |
| rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761252 | c.1446C>G | synonymous_variant | 1.0 |
| rpoB | 761255 | c.1449T>G | synonymous_variant | 1.0 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
| rpoB | 761279 | c.1473C>T | synonymous_variant | 1.0 |
| rpoB | 761282 | c.1476C>G | synonymous_variant | 1.0 |
| rpoB | 761289 | p.Ser495Ala | missense_variant | 1.0 |
| rpoB | 761300 | c.1494G>C | synonymous_variant | 1.0 |
| rpoB | 761318 | c.1512G>C | synonymous_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761330 | c.1524G>C | synonymous_variant | 1.0 |
| rpoB | 761355 | p.Val517Arg | missense_variant | 1.0 |
| rpoB | 761360 | c.1554T>G | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761370 | p.Ile522Val | missense_variant | 1.0 |
| rpoB | 761408 | c.1602G>C | synonymous_variant | 1.0 |
| rpoB | 761411 | c.1605G>C | synonymous_variant | 1.0 |
| rpoB | 761414 | c.1608A>G | synonymous_variant | 1.0 |
| rpoB | 761423 | c.1617T>C | synonymous_variant | 1.0 |
| rpoB | 761465 | c.1659G>C | synonymous_variant | 1.0 |
| rpoB | 761477 | c.1671C>T | synonymous_variant | 1.0 |
| rpoB | 761482 | p.Ala559Gly | missense_variant | 1.0 |
| rpoB | 761492 | c.1686G>C | synonymous_variant | 1.0 |
| rpoB | 761502 | p.Pro566Ser | missense_variant | 1.0 |
| rpoB | 761510 | c.1704T>C | synonymous_variant | 1.0 |
| rpoB | 761516 | c.1710G>C | synonymous_variant | 1.0 |
| rpoB | 761519 | p.Asp571Glu | missense_variant | 1.0 |
| rpoB | 761521 | p.Tyr572Phe | missense_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>G | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761655 | p.Ala617Arg | missense_variant | 1.0 |
| rpoB | 761663 | c.1857G>C | synonymous_variant | 1.0 |
| rpoB | 761666 | c.1860G>C | synonymous_variant | 1.0 |
| rpoB | 761672 | c.1866C>T | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761690 | c.1884G>C | synonymous_variant | 1.0 |
| rpoB | 761705 | c.1899C>T | synonymous_variant | 1.0 |
| rpoB | 761723 | p.Glu639Asp | missense_variant | 1.0 |
| rpoB | 761724 | p.Glu640Lys | missense_variant | 1.0 |
| rpoB | 761735 | c.1929C>G | synonymous_variant | 1.0 |
| rpoB | 761736 | p.Ile644Val | missense_variant | 1.0 |
| rpoB | 761745 | p.Val647Leu | missense_variant | 1.0 |
| rpoB | 761750 | c.1944G>C | synonymous_variant | 1.0 |
| rpoB | 761765 | c.1959T>G | synonymous_variant | 1.0 |
| rpoB | 761772 | p.His656Ala | missense_variant | 1.0 |
| rpoB | 761778 | p.Asn658Asp | missense_variant | 1.0 |
| rpoB | 761791 | p.Arg662Gln | missense_variant | 1.0 |
| rpoB | 761794 | p.Thr663Ser | missense_variant | 1.0 |
| rpoB | 761802 | p.Met666Leu | missense_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761834 | c.2028T>C | synonymous_variant | 1.0 |
| rpoB | 761847 | p.Cys681Arg | missense_variant | 1.0 |
| rpoB | 761852 | c.2046C>G | synonymous_variant | 1.0 |
| rpoB | 761864 | c.2058G>C | synonymous_variant | 1.0 |
| rpoB | 761868 | p.Asp688Gln | missense_variant | 1.0 |
| rpoB | 761873 | c.2067A>T | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761906 | c.2100C>G | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761990 | c.2184G>C | synonymous_variant | 1.0 |
| rpoB | 762002 | c.2196C>G | synonymous_variant | 1.0 |
| rpoB | 762008 | c.2202C>T | synonymous_variant | 1.0 |
| rpoB | 762011 | c.2205G>C | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762029 | c.2223C>G | synonymous_variant | 1.0 |
| rpoB | 762038 | c.2232C>T | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762122 | c.2316C>T | synonymous_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 | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762236 | c.2430G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
| rpoB | 762275 | c.2469C>T | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>G | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 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>G | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
| rpoC | 762467 | c.-903C>T | upstream_gene_variant | 1.0 |
| rpoC | 762491 | c.-879T>C | upstream_gene_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.99 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 0.99 |
| 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 | 762545 | c.-825C>G | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>G | upstream_gene_variant | 1.0 |
| rpoC | 762581 | c.-789T>C | upstream_gene_variant | 1.0 |
| rpoC | 762582 | c.-788T>C | upstream_gene_variant | 1.0 |
| rpoC | 762587 | c.-783G>A | upstream_gene_variant | 1.0 |
| rpoC | 762599 | c.-771T>C | upstream_gene_variant | 1.0 |
| rpoC | 762608 | c.-762C>G | upstream_gene_variant | 1.0 |
| rpoC | 762710 | c.-660G>C | upstream_gene_variant | 1.0 |
| rpoC | 762737 | c.-633C>G | upstream_gene_variant | 1.0 |
| rpoC | 762749 | c.-621C>T | upstream_gene_variant | 1.0 |
| rpoC | 762753 | c.-617T>C | upstream_gene_variant | 1.0 |
| rpoC | 762758 | c.-612G>C | upstream_gene_variant | 1.0 |
| rpoB | 762760 | p.Cys985Ser | missense_variant | 1.0 |
| rpoC | 762782 | c.-588T>C | upstream_gene_variant | 1.0 |
| rpoB | 762799 | p.Ala998Gly | missense_variant | 1.0 |
| rpoC | 762812 | c.-558C>G | upstream_gene_variant | 1.0 |
| rpoB | 762815 | p.Met1003Ile | missense_variant | 1.0 |
| rpoC | 762818 | c.-552C>G | upstream_gene_variant | 1.0 |
| rpoB | 762820 | p.Phe1005Tyr | missense_variant | 1.0 |
| rpoC | 762827 | c.-543G>C | upstream_gene_variant | 1.0 |
| rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 1.0 |
| rpoC | 762836 | c.-534C>T | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoC | 762860 | c.-510G>C | upstream_gene_variant | 1.0 |
| rpoB | 762861 | p.Val1019Thr | missense_variant | 1.0 |
| rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763082 | c.-288C>G | upstream_gene_variant | 1.0 |
| rpoC | 763085 | c.-285C>G | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>G | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>C | 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 | 763208 | c.-162T>C | upstream_gene_variant | 1.0 |
| rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
| rpoC | 763220 | c.-150G>C | upstream_gene_variant | 1.0 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoB | 763227 | p.Leu1141Met | missense_variant | 1.0 |
| rpoB | 763235 | p.Glu1143Asp | missense_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoB | 763241 | p.Glu1145Asp | missense_variant | 1.0 |
| rpoC | 763250 | c.-120C>T | upstream_gene_variant | 1.0 |
| rpoC | 763253 | c.-117G>C | upstream_gene_variant | 1.0 |
| rpoC | 763259 | c.-111G>C | upstream_gene_variant | 1.0 |
| rpoC | 763268 | c.-102C>G | upstream_gene_variant | 1.0 |
| rpoC | 763375 | c.6C>A | synonymous_variant | 0.97 |
| rpoC | 763396 | c.27A>G | synonymous_variant | 0.98 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 0.98 |
| rpoC | 763411 | c.42T>G | synonymous_variant | 0.98 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 0.98 |
| rpoC | 763420 | c.51G>C | synonymous_variant | 0.97 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 1.0 |
| rpoC | 763430 | c.61_63delAGGinsCGT | synonymous_variant | 1.0 |
| rpoC | 763435 | c.66A>G | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763483 | c.114G>A | synonymous_variant | 1.0 |
| rpoC | 763484 | c.115_117delCTTinsTTG | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763636 | c.267T>C | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 0.99 |
| rpoC | 763666 | c.297G>C | synonymous_variant | 0.99 |
| rpoC | 763669 | c.300C>G | synonymous_variant | 0.97 |
| rpoC | 763672 | c.303C>G | synonymous_variant | 0.99 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 0.99 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 0.99 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 0.99 |
| rpoC | 763735 | c.366G>C | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>G | synonymous_variant | 1.0 |
| rpoC | 763768 | c.399C>G | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
| rpoC | 763781 | c.412_414delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 763801 | c.432C>G | synonymous_variant | 1.0 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 763813 | c.444C>G | synonymous_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 | 763891 | c.522G>C | synonymous_variant | 1.0 |
| rpoC | 763900 | c.531G>C | synonymous_variant | 1.0 |
| rpoC | 763939 | c.570G>A | synonymous_variant | 1.0 |
| rpoC | 763978 | c.609C>T | synonymous_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764002 | c.633C>G | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655_657delTTGinsCTC | 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 | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764194 | p.Glu275Asp | missense_variant | 0.97 |
| rpoC | 764195 | p.Ser276Ala | missense_variant | 0.99 |
| rpoC | 764203 | c.834G>T | synonymous_variant | 1.0 |
| rpoC | 764206 | p.Asp279Glu | missense_variant | 1.0 |
| rpoC | 764242 | c.873C>T | synonymous_variant | 1.0 |
| rpoC | 764248 | c.879C>G | synonymous_variant | 1.0 |
| rpoC | 764254 | c.885G>T | synonymous_variant | 1.0 |
| rpoC | 764255 | c.886C>T | synonymous_variant | 1.0 |
| rpoC | 764266 | c.897T>G | synonymous_variant | 1.0 |
| rpoC | 764269 | c.900G>T | synonymous_variant | 1.0 |
| rpoC | 764278 | c.909A>G | synonymous_variant | 1.0 |
| rpoC | 764287 | c.918C>T | synonymous_variant | 1.0 |
| rpoC | 764290 | c.921C>T | synonymous_variant | 1.0 |
| rpoC | 764317 | c.948C>G | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>T | synonymous_variant | 1.0 |
| rpoC | 764383 | c.1014C>T | synonymous_variant | 1.0 |
| rpoC | 764386 | c.1017C>T | 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 | 764476 | c.1107C>T | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764572 | c.1203G>T | synonymous_variant | 1.0 |
| rpoC | 764578 | c.1209C>A | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>C | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764656 | c.1287C>G | synonymous_variant | 0.99 |
| rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
| rpoC | 764749 | c.1380G>C | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764755 | c.1386C>T | synonymous_variant | 1.0 |
| rpoC | 764761 | c.1392C>T | 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 | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764851 | c.1482C>T | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>G | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764896 | c.1527C>T | 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>G | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764983 | c.1614T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765013 | c.1644C>T | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
| rpoC | 765034 | c.1665T>G | 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 | 765076 | c.1707A>G | synonymous_variant | 1.0 |
| rpoC | 765079 | c.1710T>G | synonymous_variant | 1.0 |
| rpoC | 765082 | c.1713G>C | synonymous_variant | 1.0 |
| 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 | 765122 | c.1753C>T | synonymous_variant | 1.0 |
| rpoC | 765142 | c.1773G>A | synonymous_variant | 1.0 |
| rpoC | 765145 | c.1776C>T | synonymous_variant | 1.0 |
| rpoC | 765151 | c.1782G>C | synonymous_variant | 1.0 |
| rpoC | 765350 | p.Ala661Ser | missense_variant | 1.0 |
| rpoC | 765397 | c.2028G>T | synonymous_variant | 1.0 |
| rpoC | 765403 | c.2034G>C | synonymous_variant | 0.95 |
| rpoC | 765404 | p.Leu679Val | missense_variant | 1.0 |
| rpoC | 765409 | c.2040T>G | synonymous_variant | 1.0 |
| rpoC | 765421 | c.2052C>G | synonymous_variant | 1.0 |
| rpoC | 765451 | c.2082C>T | synonymous_variant | 1.0 |
| rpoC | 765454 | c.2085C>G | synonymous_variant | 1.0 |
| rpoC | 765469 | c.2100G>C | synonymous_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 | 765548 | c.2179_2180delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 765553 | c.2184C>G | synonymous_variant | 1.0 |
| rpoC | 765578 | c.2209C>T | synonymous_variant | 1.0 |
| rpoC | 765596 | p.Lys743Gln | missense_variant | 1.0 |
| rpoC | 765611 | p.His748Ser | missense_variant | 1.0 |
| rpoC | 765625 | c.2256C>G | synonymous_variant | 1.0 |
| rpoC | 765628 | c.2259G>C | synonymous_variant | 1.0 |
| rpoC | 765658 | c.2289C>T | synonymous_variant | 1.0 |
| rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
| rpoC | 765727 | c.2358T>C | synonymous_variant | 1.0 |
| rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
| rpoC | 765739 | c.2370G>C | synonymous_variant | 1.0 |
| rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
| rpoC | 765784 | c.2415C>G | synonymous_variant | 1.0 |
| rpoC | 765787 | c.2418C>T | synonymous_variant | 1.0 |
| rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
| rpoC | 765796 | c.2427C>T | synonymous_variant | 1.0 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
| rpoC | 765814 | c.2445A>G | synonymous_variant | 1.0 |
| rpoC | 765826 | c.2457T>C | synonymous_variant | 1.0 |
| rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
| rpoC | 765871 | c.2502T>G | synonymous_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765883 | c.2514C>G | synonymous_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765904 | c.2535C>G | synonymous_variant | 1.0 |
| rpoC | 765908 | c.2539C>T | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765946 | c.2577C>T | 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 | 765986 | c.2617C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766003 | c.2634G>C | synonymous_variant | 1.0 |
| rpoC | 766009 | c.2640G>C | synonymous_variant | 1.0 |
| rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766027 | c.2658G>T | synonymous_variant | 1.0 |
| rpoC | 766079 | p.Arg904Val | missense_variant | 1.0 |
| rpoC | 766084 | c.2715A>G | synonymous_variant | 1.0 |
| rpoC | 766096 | c.2727G>C | synonymous_variant | 1.0 |
| rpoC | 766113 | p.Tyr915Phe | missense_variant | 1.0 |
| rpoC | 766126 | c.2757G>C | synonymous_variant | 1.0 |
| rpoC | 766129 | c.2760C>G | synonymous_variant | 1.0 |
| rpoC | 766135 | c.2766G>C | synonymous_variant | 1.0 |
| rpoC | 766138 | c.2769G>C | synonymous_variant | 1.0 |
| rpoC | 766141 | c.2772C>T | synonymous_variant | 1.0 |
| rpoC | 766142 | c.2773C>T | synonymous_variant | 1.0 |
| rpoC | 766270 | c.2901G>C | synonymous_variant | 1.0 |
| rpoC | 766273 | c.2904T>C | synonymous_variant | 1.0 |
| rpoC | 766276 | c.2907C>G | synonymous_variant | 1.0 |
| rpoC | 766280 | p.Ser971Gly | missense_variant | 1.0 |
| rpoC | 766297 | c.2928G>C | synonymous_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 | 766321 | c.2952C>G | synonymous_variant | 1.0 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766393 | c.3024C>G | synonymous_variant | 1.0 |
| rpoC | 766456 | c.3087C>T | synonymous_variant | 1.0 |
| rpoC | 766459 | c.3090G>T | synonymous_variant | 1.0 |
| rpoC | 766486 | c.3117A>G | synonymous_variant | 1.0 |
| rpoC | 766492 | c.3123T>A | synonymous_variant | 1.0 |
| rpoC | 766495 | c.3126C>T | synonymous_variant | 1.0 |
| rpoC | 766510 | c.3141C>A | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>G | synonymous_variant | 1.0 |
| rpoC | 766531 | c.3162G>C | synonymous_variant | 1.0 |
| rpoC | 766534 | c.3165C>G | synonymous_variant | 1.0 |
| rpoC | 766540 | p.Asp1057Glu | missense_variant | 1.0 |
| rpoC | 766549 | c.3180G>C | synonymous_variant | 1.0 |
| rpoC | 766570 | c.3201T>C | synonymous_variant | 1.0 |
| rpoC | 766573 | c.3204T>C | synonymous_variant | 1.0 |
| rpoC | 766585 | c.3216T>C | synonymous_variant | 1.0 |
| rpoC | 766600 | c.3231C>T | synonymous_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766621 | c.3252G>A | synonymous_variant | 1.0 |
| rpoC | 766624 | c.3255G>C | synonymous_variant | 1.0 |
| rpoC | 766645 | c.3276A>G | synonymous_variant | 1.0 |
| rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
| rpoC | 766652 | p.Ser1095Thr | missense_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766661 | p.Val1098Leu | missense_variant | 1.0 |
| rpoC | 766667 | p.Ser1100Ala | missense_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766690 | c.3321G>C | synonymous_variant | 1.0 |
| rpoC | 766714 | c.3345G>C | synonymous_variant | 1.0 |
| rpoC | 766726 | c.3357T>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 | 766798 | c.3429C>G | synonymous_variant | 1.0 |
| rpoC | 766801 | c.3432C>G | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766843 | c.3474T>C | synonymous_variant | 1.0 |
| rpoC | 766846 | c.3477C>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 | 0.99 |
| rpoC | 766903 | c.3534C>T | synonymous_variant | 1.0 |
| rpoC | 766933 | c.3564A>G | synonymous_variant | 1.0 |
| rpoC | 766942 | c.3573C>T | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>G | synonymous_variant | 1.0 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
| rpoC | 766978 | c.3609C>T | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>G | synonymous_variant | 1.0 |
| rpoC | 767002 | c.3633G>C | synonymous_variant | 1.0 |
| rpoC | 767035 | c.3666G>C | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
| rpoC | 767062 | c.3693C>A | synonymous_variant | 1.0 |
| rpoC | 767068 | c.3699G>C | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767158 | c.3789T>G | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767200 | c.3831G>A | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>G | synonymous_variant | 1.0 |
| rpoC | 767209 | c.3840T>C | synonymous_variant | 1.0 |
| rpoC | 767221 | c.3852C>G | 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 | 767278 | c.3909T>C | synonymous_variant | 1.0 |
| rpoC | 767281 | c.3912C>G | synonymous_variant | 1.0 |
| rpoC | 767284 | c.3915C>T | synonymous_variant | 1.0 |
| rpsL | 781571 | c.12C>T | synonymous_variant | 1.0 |
| rpsL | 781592 | c.33T>G | synonymous_variant | 1.0 |
| rpsL | 781595 | c.36T>C | synonymous_variant | 1.0 |
| rpsL | 781598 | c.39G>C | synonymous_variant | 1.0 |
| rpsL | 781608 | p.Ser17Gly | missense_variant | 1.0 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781649 | c.90T>C | synonymous_variant | 1.0 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
| rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
| rpsL | 781664 | c.105C>G | synonymous_variant | 1.0 |
| rpsL | 781679 | c.120C>G | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>G | synonymous_variant | 1.0 |
| rpsL | 781718 | c.159C>G | synonymous_variant | 1.0 |
| rpsL | 781724 | c.165G>C | synonymous_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781733 | c.174G>C | synonymous_variant | 1.0 |
| rpsL | 781736 | c.177T>C | synonymous_variant | 1.0 |
| rpsL | 781742 | c.183C>T | synonymous_variant | 1.0 |
| rpsL | 781745 | c.186G>A | synonymous_variant | 1.0 |
| rpsL | 781751 | c.192G>C | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>A | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781778 | c.219C>T | synonymous_variant | 1.0 |
| rpsL | 781779 | c.220C>T | synonymous_variant | 1.0 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781835 | c.276T>C | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781901 | c.342C>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 | 0.98 |
| rplC | 800618 | c.-191T>A | upstream_gene_variant | 1.0 |
| rplC | 800630 | c.-179G>C | upstream_gene_variant | 1.0 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
| rplC | 800642 | c.-167C>T | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>T | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800702 | c.-107G>A | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800726 | c.-83G>A | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
| rplC | 800753 | c.-56C>T | upstream_gene_variant | 1.0 |
| rplC | 800759 | c.-50C>T | upstream_gene_variant | 1.0 |
| rplC | 800762 | c.-47T>G | upstream_gene_variant | 1.0 |
| rplC | 800796 | c.-13A>T | upstream_gene_variant | 1.0 |
| rplC | 800798 | c.-10_-8delGGA | upstream_gene_variant | 1.0 |
| rplC | 800804 | c.-4_-1delAGCA | upstream_gene_variant | 1.0 |
| rplC | 800815 | c.7C>A | synonymous_variant | 1.0 |
| rplC | 800820 | c.12G>A | synonymous_variant | 1.0 |
| rplC | 800829 | c.21C>G | synonymous_variant | 1.0 |
| rplC | 800832 | c.24T>C | synonymous_variant | 1.0 |
| rplC | 800844 | c.36T>C | synonymous_variant | 1.0 |
| rplC | 800856 | c.48A>G | synonymous_variant | 1.0 |
| rplC | 800865 | c.57A>G | synonymous_variant | 1.0 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
| rplC | 800872 | c.64_66delAGAinsCGG | synonymous_variant | 1.0 |
| rplC | 800877 | c.69A>T | synonymous_variant | 1.0 |
| rplC | 800880 | c.72A>T | synonymous_variant | 1.0 |
| rplC | 800910 | c.102C>T | synonymous_variant | 1.0 |
| rplC | 800916 | c.108A>G | synonymous_variant | 1.0 |
| rplC | 800922 | c.114C>T | synonymous_variant | 1.0 |
| rplC | 800931 | c.123G>A | synonymous_variant | 1.0 |
| rplC | 800934 | c.126C>G | synonymous_variant | 1.0 |
| rplC | 800937 | c.129A>G | synonymous_variant | 1.0 |
| rplC | 800940 | c.132C>T | synonymous_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 | 800970 | c.162T>C | synonymous_variant | 1.0 |
| rplC | 800982 | c.174C>T | synonymous_variant | 1.0 |
| rplC | 800985 | c.177A>C | synonymous_variant | 1.0 |
| rplC | 801141 | c.333C>T | synonymous_variant | 1.0 |
| rplC | 801147 | c.339T>C | synonymous_variant | 1.0 |
| rplC | 801153 | c.345G>C | synonymous_variant | 1.0 |
| rplC | 801156 | c.348T>C | synonymous_variant | 1.0 |
| rplC | 801162 | c.354C>G | synonymous_variant | 1.0 |
| rplC | 801174 | c.366T>C | synonymous_variant | 1.0 |
| rplC | 801177 | c.369C>T | synonymous_variant | 1.0 |
| rplC | 801186 | c.378C>G | synonymous_variant | 1.0 |
| rplC | 801201 | c.393C>T | synonymous_variant | 1.0 |
| rplC | 801210 | c.402T>C | synonymous_variant | 1.0 |
| rplC | 801222 | c.414T>C | synonymous_variant | 1.0 |
| rplC | 801228 | c.420T>C | synonymous_variant | 1.0 |
| rplC | 801231 | c.423C>G | synonymous_variant | 1.0 |
| rplC | 801249 | c.441T>C | synonymous_variant | 1.0 |
| rplC | 801252 | c.444G>C | synonymous_variant | 1.0 |
| rplC | 801267 | c.459A>C | synonymous_variant | 1.0 |
| rplC | 801270 | c.462T>C | synonymous_variant | 1.0 |
| rplC | 801276 | c.468G>C | synonymous_variant | 1.0 |
| rplC | 801312 | c.504G>C | synonymous_variant | 1.0 |
| rplC | 801321 | c.513C>T | synonymous_variant | 1.0 |
| rplC | 801324 | c.516T>C | synonymous_variant | 1.0 |
| rplC | 801337 | p.Val177Thr | missense_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 | 801366 | c.558T>C | synonymous_variant | 1.0 |
| rplC | 801372 | p.Glu188Asp | missense_variant | 1.0 |
| rplC | 801396 | c.588T>C | synonymous_variant | 1.0 |
| rplC | 801399 | c.591G>C | synonymous_variant | 1.0 |
| rplC | 801402 | c.594T>C | synonymous_variant | 1.0 |
| rplC | 801405 | c.597T>C | synonymous_variant | 1.0 |
| rplC | 801413 | p.Thr202Asn | missense_variant | 1.0 |
| rplC | 801420 | c.612A>G | synonymous_variant | 1.0 |
| rplC | 801423 | c.615G>C | synonymous_variant | 1.0 |
| rplC | 801438 | c.630T>C | synonymous_variant | 1.0 |
| rplC | 801461 | c.653G>A | splice_region_variant&stop_retained_variant | 1.0 |
| fbiC | 1303242 | c.312T>C | synonymous_variant | 1.0 |
| fbiC | 1303251 | c.321C>T | synonymous_variant | 1.0 |
| fbiC | 1303272 | c.342A>G | synonymous_variant | 1.0 |
| fbiC | 1303284 | c.354T>C | synonymous_variant | 1.0 |
| fbiC | 1303285 | p.Ser119Ala | missense_variant | 1.0 |
| fbiC | 1303288 | p.Ser120Gly | missense_variant | 1.0 |
| fbiC | 1303292 | p.Thr121Met | missense_variant | 1.0 |
| fbiC | 1303297 | p.Met123Leu | missense_variant | 1.0 |
| fbiC | 1303311 | c.381G>A | synonymous_variant | 1.0 |
| fbiC | 1303321 | p.Val131Ile | missense_variant | 1.0 |
| fbiC | 1303326 | c.396C>G | synonymous_variant | 1.0 |
| fbiC | 1303332 | c.402A>C | synonymous_variant | 1.0 |
| fbiC | 1303337 | p.Ala136Gly | missense_variant | 1.0 |
| fbiC | 1303342 | p.Phe138Leu | missense_variant | 1.0 |
| fbiC | 1303440 | c.510G>C | synonymous_variant | 1.0 |
| fbiC | 1303446 | c.516C>G | synonymous_variant | 1.0 |
| fbiC | 1303449 | c.519C>T | synonymous_variant | 1.0 |
| fbiC | 1303455 | c.525C>G | synonymous_variant | 1.0 |
| fbiC | 1303464 | c.534A>G | synonymous_variant | 1.0 |
| fbiC | 1303470 | c.540T>G | synonymous_variant | 1.0 |
| fbiC | 1303479 | c.549G>A | synonymous_variant | 1.0 |
| fbiC | 1303480 | p.Gln184Glu | missense_variant | 1.0 |
| fbiC | 1303488 | c.558G>C | synonymous_variant | 1.0 |
| fbiC | 1303506 | c.576C>T | synonymous_variant | 1.0 |
| fbiC | 1303509 | c.579G>C | synonymous_variant | 1.0 |
| fbiC | 1303512 | c.582T>C | synonymous_variant | 1.0 |
| fbiC | 1303531 | p.Met201Leu | missense_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303584 | c.654C>G | synonymous_variant | 1.0 |
| fbiC | 1303590 | c.660A>G | synonymous_variant | 1.0 |
| fbiC | 1303605 | c.675C>T | synonymous_variant | 1.0 |
| fbiC | 1303606 | p.Lys226Arg | missense_variant | 1.0 |
| fbiC | 1303611 | c.681G>T | synonymous_variant | 1.0 |
| fbiC | 1303629 | c.699C>T | 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 | 1303681 | c.751T>C | synonymous_variant | 1.0 |
| fbiC | 1303686 | c.756C>G | synonymous_variant | 1.0 |
| fbiC | 1303695 | c.765T>C | synonymous_variant | 1.0 |
| fbiC | 1303708 | c.778T>C | synonymous_variant | 1.0 |
| fbiC | 1303713 | c.783C>G | synonymous_variant | 1.0 |
| fbiC | 1303722 | c.792C>T | synonymous_variant | 1.0 |
| fbiC | 1303725 | c.795G>A | synonymous_variant | 1.0 |
| fbiC | 1303737 | c.807G>A | synonymous_variant | 1.0 |
| fbiC | 1303746 | p.Asp272Glu | missense_variant | 1.0 |
| fbiC | 1303752 | c.822A>G | synonymous_variant | 1.0 |
| fbiC | 1303755 | c.825T>C | synonymous_variant | 1.0 |
| fbiC | 1303761 | c.831T>C | synonymous_variant | 1.0 |
| fbiC | 1303788 | c.858T>C | synonymous_variant | 1.0 |
| fbiC | 1303794 | c.864A>G | synonymous_variant | 1.0 |
| fbiC | 1303824 | c.894G>A | synonymous_variant | 1.0 |
| fbiC | 1303827 | c.897A>G | synonymous_variant | 1.0 |
| fbiC | 1303884 | c.954T>G | synonymous_variant | 1.0 |
| fbiC | 1303887 | c.957G>C | synonymous_variant | 1.0 |
| fbiC | 1303890 | c.960G>C | synonymous_variant | 1.0 |
| fbiC | 1303908 | c.978C>T | synonymous_variant | 0.96 |
| fbiC | 1303914 | c.984C>A | synonymous_variant | 1.0 |
| fbiC | 1303947 | c.1017T>G | synonymous_variant | 1.0 |
| fbiC | 1303948 | p.Gly340Arg | missense_variant | 1.0 |
| fbiC | 1303956 | c.1026A>G | synonymous_variant | 1.0 |
| fbiC | 1303961 | p.Arg344Leu | missense_variant | 1.0 |
| fbiC | 1303965 | c.1035G>T | synonymous_variant | 1.0 |
| fbiC | 1303969 | p.Val347Ile | missense_variant | 1.0 |
| fbiC | 1303973 | p.Gly348Ala | missense_variant | 1.0 |
| fbiC | 1303980 | c.1050G>C | synonymous_variant | 1.0 |
| fbiC | 1303998 | c.1068T>C | synonymous_variant | 1.0 |
| fbiC | 1304004 | c.1074A>G | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304565 | c.1635C>G | synonymous_variant | 1.0 |
| fbiC | 1304568 | c.1638T>C | synonymous_variant | 1.0 |
| fbiC | 1304574 | c.1644C>G | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304634 | c.1704C>T | synonymous_variant | 1.0 |
| fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
| fbiC | 1304658 | c.1728C>G | synonymous_variant | 1.0 |
| fbiC | 1304661 | c.1731C>T | synonymous_variant | 1.0 |
| fbiC | 1304667 | c.1737G>C | synonymous_variant | 1.0 |
| fbiC | 1304694 | c.1764A>G | synonymous_variant | 1.0 |
| fbiC | 1304703 | c.1773C>G | synonymous_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| fbiC | 1304763 | c.1833C>G | synonymous_variant | 1.0 |
| fbiC | 1304775 | c.1845C>G | synonymous_variant | 1.0 |
| fbiC | 1304784 | c.1854T>G | 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 | 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 | 1304870 | c.1941_1945delGAGCA | frameshift_variant | 1.0 |
| fbiC | 1304877 | c.1949_1950insGTCCG | frameshift_variant | 1.0 |
| fbiC | 1304893 | p.Gly655Ser | missense_variant | 1.0 |
| fbiC | 1304904 | c.1974G>A | synonymous_variant | 1.0 |
| fbiC | 1304910 | c.1980G>C | synonymous_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 | 1304937 | c.2007G>C | synonymous_variant | 1.0 |
| fbiC | 1304940 | c.2010A>G | synonymous_variant | 1.0 |
| fbiC | 1304943 | c.2013C>T | synonymous_variant | 1.0 |
| fbiC | 1304946 | c.2016G>C | synonymous_variant | 1.0 |
| fbiC | 1304958 | c.2028T>G | synonymous_variant | 1.0 |
| fbiC | 1304970 | c.2040G>C | synonymous_variant | 1.0 |
| fbiC | 1304994 | c.2064A>G | synonymous_variant | 1.0 |
| fbiC | 1304995 | p.Leu689Met | missense_variant | 1.0 |
| fbiC | 1305006 | c.2076A>G | synonymous_variant | 1.0 |
| fbiC | 1305015 | c.2085G>C | synonymous_variant | 1.0 |
| fbiC | 1305021 | c.2091C>G | synonymous_variant | 1.0 |
| fbiC | 1305033 | c.2103T>G | synonymous_variant | 1.0 |
| fbiC | 1305042 | c.2112A>G | synonymous_variant | 1.0 |
| fbiC | 1305045 | c.2115A>G | synonymous_variant | 1.0 |
| fbiC | 1305063 | c.2133G>C | synonymous_variant | 1.0 |
| fbiC | 1305069 | c.2139G>C | synonymous_variant | 1.0 |
| fbiC | 1305168 | c.2238C>T | synonymous_variant | 1.0 |
| fbiC | 1305173 | p.Asn748Ser | missense_variant | 1.0 |
| fbiC | 1305177 | c.2247A>G | synonymous_variant | 1.0 |
| fbiC | 1305181 | c.2251T>C | synonymous_variant | 1.0 |
| fbiC | 1305186 | c.2256C>T | synonymous_variant | 1.0 |
| fbiC | 1305195 | c.2265T>C | synonymous_variant | 1.0 |
| fbiC | 1305199 | p.Ala757Ser | missense_variant | 1.0 |
| fbiC | 1305204 | c.2274C>G | synonymous_variant | 1.0 |
| fbiC | 1305219 | c.2289T>C | synonymous_variant | 1.0 |
| fbiC | 1305231 | c.2301C>G | synonymous_variant | 1.0 |
| fbiC | 1305237 | c.2307A>G | synonymous_variant | 1.0 |
| fbiC | 1305240 | c.2310T>C | synonymous_variant | 1.0 |
| fbiC | 1305243 | c.2313T>G | synonymous_variant | 1.0 |
| fbiC | 1305244 | c.2314T>C | synonymous_variant | 1.0 |
| fbiC | 1305268 | c.2338_2340delCGCinsAGG | synonymous_variant | 1.0 |
| fbiC | 1305276 | c.2346G>T | synonymous_variant | 1.0 |
| fbiC | 1305279 | c.2349C>T | synonymous_variant | 1.0 |
| fbiC | 1305300 | c.2370A>G | synonymous_variant | 1.0 |
| fbiC | 1305303 | c.2373T>C | synonymous_variant | 1.0 |
| fbiC | 1305306 | c.2376A>T | synonymous_variant | 1.0 |
| fbiC | 1305310 | p.Arg794Glu | missense_variant | 1.0 |
| fbiC | 1305318 | c.2388C>G | synonymous_variant | 1.0 |
| fbiC | 1305331 | p.Glu801Asn | missense_variant | 1.0 |
| fbiC | 1305336 | c.2406T>C | synonymous_variant | 1.0 |
| fbiC | 1305342 | c.2412C>G | synonymous_variant | 1.0 |
| fbiC | 1305349 | c.2419C>T | synonymous_variant | 1.0 |
| fbiC | 1305393 | c.2463T>C | synonymous_variant | 1.0 |
| fbiC | 1305396 | c.2466C>G | synonymous_variant | 1.0 |
| fbiC | 1305399 | c.2469A>G | synonymous_variant | 1.0 |
| fbiC | 1305405 | c.2475A>C | synonymous_variant | 1.0 |
| fbiC | 1305417 | c.2487C>G | synonymous_variant | 1.0 |
| fbiC | 1305423 | c.2493T>G | synonymous_variant | 1.0 |
| fbiC | 1305444 | c.2514A>G | synonymous_variant | 1.0 |
| fbiC | 1305459 | c.2529G>C | synonymous_variant | 1.0 |
| fbiC | 1305462 | c.2532G>C | synonymous_variant | 1.0 |
| atpE | 1460852 | c.-193C>G | upstream_gene_variant | 1.0 |
| atpE | 1460855 | c.-190T>C | upstream_gene_variant | 1.0 |
| atpE | 1460858 | c.-187C>G | upstream_gene_variant | 1.0 |
| atpE | 1460861 | c.-184C>G | upstream_gene_variant | 1.0 |
| atpE | 1460876 | c.-169G>C | upstream_gene_variant | 1.0 |
| atpE | 1460882 | c.-163T>C | upstream_gene_variant | 1.0 |
| atpE | 1460885 | c.-160G>C | upstream_gene_variant | 1.0 |
| atpE | 1460894 | c.-151A>G | upstream_gene_variant | 1.0 |
| atpE | 1461131 | c.87T>C | synonymous_variant | 1.0 |
| atpE | 1461132 | p.Val30Ile | missense_variant | 1.0 |
| atpE | 1461149 | c.105T>G | synonymous_variant | 1.0 |
| atpE | 1461161 | c.117C>A | synonymous_variant | 1.0 |
| atpE | 1461170 | c.126A>G | synonymous_variant | 1.0 |
| atpE | 1461179 | c.135G>A | synonymous_variant | 1.0 |
| atpE | 1461185 | c.141G>C | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>C | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461224 | c.180T>G | synonymous_variant | 1.0 |
| atpE | 1461254 | c.210T>C | synonymous_variant | 1.0 |
| atpE | 1461261 | c.217C>T | synonymous_variant | 1.0 |
| atpE | 1461275 | c.231T>C | synonymous_variant | 1.0 |
| atpE | 1461281 | c.237C>A | synonymous_variant | 1.0 |
| rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471936 | n.91A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471996 | n.151C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472028 | n.183A>G | non_coding_transcript_exon_variant | 0.45 |
| rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.45 |
| rrs | 1472056 | n.211G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472057 | n.212C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472298 | n.453G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472300 | n.455C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472489 | n.644A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473111 | n.1266A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473658 | n.1T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473668 | n.11C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473670 | n.13A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473701 | n.44A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473782 | n.125A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473788 | n.131A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473793 | n.136G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473936 | n.279A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473991 | n.334C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473992 | n.335A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474006 | n.349G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474026 | n.369C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474290 | n.633T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474293 | n.637_649delCCTCTCCGGAGGA | 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 | 1474350 | n.693G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474374 | n.718dupG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474381 | n.724T>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474446 | n.789C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474452 | n.795C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474638 | n.981C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474709 | n.1053_1054delTG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474715 | n.1058T>A | non_coding_transcript_exon_variant | 0.47 |
| rrl | 1474716 | n.1059A>G | non_coding_transcript_exon_variant | 0.46 |
| rrl | 1474717 | n.1060_1061insCG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060_1061insGACG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475008 | n.1351C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475016 | n.1359_1360insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475028 | n.1371G>T | non_coding_transcript_exon_variant | 0.92 |
| rrl | 1475029 | n.1372T>G | non_coding_transcript_exon_variant | 0.92 |
| rrl | 1475030 | n.1373G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475088 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475202 | n.1545G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475211 | n.1554G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475212 | n.1555A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475307 | n.1650T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475308 | n.1651C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475345 | n.1688T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475347 | n.1690A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475348 | n.1691G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475353 | n.1696A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475354 | n.1697A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475356 | n.1699A>G | non_coding_transcript_exon_variant | 0.93 |
| rrl | 1475375 | n.1718G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475376 | n.1719A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475379 | n.1722G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475433 | n.1776A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475458 | n.1801C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475479 | n.1822C>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475484 | n.1827A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475532 | n.1875A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475545 | n.1888T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475602 | n.1945G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475603 | n.1946G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475606 | n.1949T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475616 | n.1959A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475618 | n.1961C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475624 | n.1967G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475626 | n.1969T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475638 | n.1981C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475643 | n.1986C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475647 | n.1990G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475707 | n.2050T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475761 | n.2104C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475762 | n.2106_2107delCA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475766 | n.2109_2110insTAATTC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476025 | n.2368G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476045 | n.2388G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476108 | n.2451T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476246 | n.2589G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476692 | n.3035T>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 | 1476731 | n.3074G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476740 | n.3083G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476741 | n.3084G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476743 | n.3086A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476746 | n.3089T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476748 | n.3091A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476750 | n.3093T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476753 | n.3096T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476759 | n.3102T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476770 | n.3113T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476771 | n.3114G>A | non_coding_transcript_exon_variant | 1.0 |
| inhA | 1673526 | c.-676G>C | upstream_gene_variant | 1.0 |
| inhA | 1673535 | c.-667A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673537 | p.Gln33Arg | missense_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 | 1673586 | c.-616C>G | 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.Lys53Glu | missense_variant | 1.0 |
| inhA | 1673601 | c.-601G>A | upstream_gene_variant | 1.0 |
| inhA | 1673602 | c.-600C>T | upstream_gene_variant | 1.0 |
| inhA | 1673607 | c.-595T>C | upstream_gene_variant | 1.0 |
| inhA | 1673616 | c.-586A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673633 | p.Ser65Asn | missense_variant | 1.0 |
| inhA | 1673646 | c.-556T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673657 | p.Thr73Lys | missense_variant | 1.0 |
| fabG1 | 1673660 | p.Ala74Glu | missense_variant | 1.0 |
| inhA | 1673664 | c.-538A>C | upstream_gene_variant | 1.0 |
| inhA | 1673667 | c.-535A>G | upstream_gene_variant | 1.0 |
| inhA | 1673682 | c.-520G>C | upstream_gene_variant | 1.0 |
| inhA | 1673712 | c.-490A>G | upstream_gene_variant | 1.0 |
| inhA | 1673724 | c.-478A>T | upstream_gene_variant | 1.0 |
| inhA | 1673748 | c.-454A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673750 | p.Lys104Arg | missense_variant | 1.0 |
| fabG1 | 1673756 | p.Glu106Val | missense_variant | 1.0 |
| fabG1 | 1673767 | p.Asn110Asp | missense_variant | 1.0 |
| inhA | 1673802 | c.-400A>G | upstream_gene_variant | 1.0 |
| inhA | 1673808 | c.-394A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673816 | p.Ser126Thr | missense_variant | 1.0 |
| inhA | 1673841 | c.-361A>G | upstream_gene_variant | 1.0 |
| inhA | 1673847 | c.-355A>C | upstream_gene_variant | 1.0 |
| inhA | 1673853 | c.-349A>C | upstream_gene_variant | 1.0 |
| inhA | 1673856 | c.-346T>C | upstream_gene_variant | 1.0 |
| inhA | 1673865 | c.-337C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673870 | p.Ser144Thr | missense_variant | 1.0 |
| inhA | 1673895 | c.-307C>T | upstream_gene_variant | 1.0 |
| inhA | 1673916 | c.-286A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673917 | p.Val160Leu | missense_variant | 1.0 |
| inhA | 1673922 | c.-280T>C | upstream_gene_variant | 1.0 |
| inhA | 1673934 | c.-268C>T | upstream_gene_variant | 1.0 |
| inhA | 1673940 | c.-262C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673941 | p.Ala168Ser | missense_variant | 1.0 |
| inhA | 1673946 | c.-256C>G | upstream_gene_variant | 1.0 |
| inhA | 1673950 | c.-252C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673960 | p.Ala174Val | missense_variant | 1.0 |
| inhA | 1674024 | c.-178T>C | upstream_gene_variant | 1.0 |
| inhA | 1674030 | c.-172G>A | upstream_gene_variant | 1.0 |
| fabG1 | 1674037 | p.Gln200Ala | missense_variant | 1.0 |
| inhA | 1674042 | c.-160G>T | upstream_gene_variant | 1.0 |
| inhA | 1674045 | c.-157G>A | upstream_gene_variant | 1.0 |
| fabG1 | 1674049 | p.Gln204Glu | missense_variant | 1.0 |
| inhA | 1674054 | c.-148T>C | upstream_gene_variant | 1.0 |
| inhA | 1674060 | c.-142A>G | upstream_gene_variant | 1.0 |
| inhA | 1674072 | c.-130C>T | upstream_gene_variant | 1.0 |
| inhA | 1674096 | c.-106G>C | upstream_gene_variant | 1.0 |
| inhA | 1674108 | c.-94C>T | upstream_gene_variant | 1.0 |
| inhA | 1674109 | c.-93C>T | upstream_gene_variant | 1.0 |
| inhA | 1674114 | c.-88T>C | upstream_gene_variant | 1.0 |
| inhA | 1674123 | c.-79T>C | upstream_gene_variant | 1.0 |
| inhA | 1674126 | c.-76G>C | upstream_gene_variant | 1.0 |
| inhA | 1674127 | c.-75_-74delAGinsTC | upstream_gene_variant | 1.0 |
| inhA | 1674132 | c.-70T>C | upstream_gene_variant | 1.0 |
| inhA | 1674138 | c.-64C>A | upstream_gene_variant | 1.0 |
| inhA | 1674141 | c.-61T>C | upstream_gene_variant | 1.0 |
| inhA | 1674147 | c.-55C>G | upstream_gene_variant | 1.0 |
| inhA | 1674256 | p.Ser19Ala | missense_variant | 1.0 |
| inhA | 1674270 | c.69T>C | synonymous_variant | 1.0 |
| inhA | 1674279 | c.78A>C | synonymous_variant | 1.0 |
| inhA | 1674282 | c.81G>C | synonymous_variant | 1.0 |
| inhA | 1674285 | c.84A>C | synonymous_variant | 1.0 |
| inhA | 1674294 | c.93G>A | synonymous_variant | 1.0 |
| inhA | 1674303 | c.102C>G | synonymous_variant | 1.0 |
| inhA | 1674306 | c.105G>A | synonymous_variant | 1.0 |
| inhA | 1674309 | c.108G>C | synonymous_variant | 1.0 |
| inhA | 1674312 | c.111G>C | synonymous_variant | 1.0 |
| inhA | 1674313 | p.Leu38Cys | missense_variant | 1.0 |
| inhA | 1674321 | c.120G>A | synonymous_variant | 1.0 |
| inhA | 1674342 | c.141T>C | synonymous_variant | 1.0 |
| inhA | 1674343 | p.Gln48Glu | missense_variant | 1.0 |
| inhA | 1674352 | p.Thr51Leu | missense_variant | 1.0 |
| inhA | 1674368 | p.Ala56Glu | missense_variant | 1.0 |
| inhA | 1674373 | p.Ala58Pro | missense_variant | 1.0 |
| inhA | 1674384 | c.183C>G | synonymous_variant | 1.0 |
| inhA | 1674387 | c.186A>G | synonymous_variant | 1.0 |
| inhA | 1674519 | c.318C>T | synonymous_variant | 1.0 |
| inhA | 1674537 | c.336C>G | synonymous_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674555 | c.354G>A | synonymous_variant | 1.0 |
| inhA | 1674561 | c.360C>T | synonymous_variant | 1.0 |
| inhA | 1674567 | c.366C>T | synonymous_variant | 1.0 |
| inhA | 1674582 | c.381T>C | synonymous_variant | 1.0 |
| inhA | 1674585 | c.384T>G | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674604 | c.403C>T | synonymous_variant | 1.0 |
| inhA | 1674618 | c.417C>T | synonymous_variant | 1.0 |
| inhA | 1674620 | p.Pro140Arg | missense_variant | 1.0 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 1.0 |
| inhA | 1674627 | c.426T>C | synonymous_variant | 1.0 |
| inhA | 1674628 | p.Ser143Ala | missense_variant | 1.0 |
| inhA | 1674654 | c.453G>C | synonymous_variant | 1.0 |
| inhA | 1674656 | p.Ser152Thr | missense_variant | 1.0 |
| inhA | 1674660 | c.459G>C | synonymous_variant | 1.0 |
| inhA | 1674690 | c.489C>G | synonymous_variant | 1.0 |
| inhA | 1674703 | c.502T>C | synonymous_variant | 1.0 |
| inhA | 1674714 | c.513C>G | synonymous_variant | 1.0 |
| inhA | 1674718 | c.517A>C | synonymous_variant | 1.0 |
| inhA | 1674729 | c.528G>A | synonymous_variant | 1.0 |
| inhA | 1674735 | c.534G>A | synonymous_variant | 1.0 |
| inhA | 1674742 | p.Lys181Gln | missense_variant | 1.0 |
| inhA | 1674859 | p.Glu220Gln | missense_variant | 1.0 |
| inhA | 1674870 | c.669T>C | synonymous_variant | 1.0 |
| inhA | 1674879 | c.678T>G | synonymous_variant | 1.0 |
| inhA | 1674892 | p.Asn231Asp | missense_variant | 1.0 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 1.0 |
| inhA | 1674906 | c.705G>C | synonymous_variant | 1.0 |
| inhA | 1674909 | c.708G>C | synonymous_variant | 1.0 |
| inhA | 1674915 | c.714C>T | synonymous_variant | 1.0 |
| inhA | 1674934 | p.Leu245Val | missense_variant | 1.0 |
| inhA | 1674942 | c.741T>C | synonymous_variant | 1.0 |
| inhA | 1674957 | c.756G>C | synonymous_variant | 1.0 |
| rpsA | 1833568 | c.27G>C | synonymous_variant | 1.0 |
| rpsA | 1833589 | c.48A>C | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>G | synonymous_variant | 1.0 |
| rpsA | 1833616 | c.75A>C | synonymous_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833628 | c.87G>A | synonymous_variant | 1.0 |
| rpsA | 1833634 | c.93G>A | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>G | synonymous_variant | 1.0 |
| rpsA | 1833670 | c.129C>A | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>G | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833775 | c.234G>A | synonymous_variant | 1.0 |
| rpsA | 1833778 | c.237C>G | synonymous_variant | 1.0 |
| rpsA | 1833781 | c.240T>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833794 | p.Glu85Lys | missense_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
| rpsA | 1833820 | c.279G>A | synonymous_variant | 1.0 |
| rpsA | 1833832 | c.291G>A | 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>A | synonymous_variant | 1.0 |
| rpsA | 1833886 | c.345C>G | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833994 | c.453G>A | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834051 | c.510G>A | synonymous_variant | 1.0 |
| rpsA | 1834099 | c.558C>G | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>G | synonymous_variant | 1.0 |
| rpsA | 1834114 | c.573G>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 | 1834183 | c.642T>A | synonymous_variant | 1.0 |
| rpsA | 1834186 | c.645C>G | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>C | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>A | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834360 | c.819G>A | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>A | 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 | 1834429 | c.888C>T | synonymous_variant | 1.0 |
| rpsA | 1834435 | c.894G>C | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834456 | c.915T>G | 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 | 1834477 | c.936C>A | 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 | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834619 | c.1078T>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 | 1834669 | c.1128G>C | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834720 | c.1179C>G | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
| rpsA | 1834747 | c.1206A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| katG | 2155085 | c.1027C>T | synonymous_variant | 1.0 |
| katG | 2155113 | c.999C>G | synonymous_variant | 1.0 |
| katG | 2155119 | c.993T>C | synonymous_variant | 1.0 |
| katG | 2155131 | c.981A>G | synonymous_variant | 1.0 |
| katG | 2155143 | p.Asn323Pro | missense_variant | 1.0 |
| katG | 2155263 | c.849G>C | synonymous_variant | 1.0 |
| katG | 2155266 | c.846T>C | synonymous_variant | 1.0 |
| katG | 2155284 | c.828T>C | synonymous_variant | 1.0 |
| katG | 2155287 | c.825C>T | synonymous_variant | 1.0 |
| katG | 2155293 | c.819T>C | synonymous_variant | 1.0 |
| katG | 2155296 | p.Phe272Val | missense_variant | 1.0 |
| katG | 2155299 | c.813T>G | synonymous_variant | 1.0 |
| katG | 2155305 | c.807T>G | synonymous_variant | 1.0 |
| katG | 2155326 | c.786A>G | synonymous_variant | 1.0 |
| katG | 2155329 | c.783A>G | synonymous_variant | 1.0 |
| katG | 2155632 | c.480A>C | synonymous_variant | 1.0 |
| katG | 2155637 | p.Leu159Ile | missense_variant | 1.0 |
| katG | 2155656 | c.456G>A | synonymous_variant | 1.0 |
| katG | 2155677 | c.435C>G | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155693 | p.Ser140Ile | missense_variant | 1.0 |
| katG | 2155695 | p.Ala139Val | missense_variant | 1.0 |
| katG | 2155716 | c.396T>C | synonymous_variant | 1.0 |
| katG | 2155728 | c.384G>C | synonymous_variant | 1.0 |
| katG | 2155770 | c.342C>T | synonymous_variant | 1.0 |
| katG | 2155782 | c.330C>A | synonymous_variant | 1.0 |
| katG | 2155785 | c.327T>G | synonymous_variant | 1.0 |
| katG | 2155788 | c.324C>T | synonymous_variant | 1.0 |
| katG | 2155794 | p.Ala106Ser | missense_variant | 1.0 |
| katG | 2155803 | c.309C>T | synonymous_variant | 1.0 |
| katG | 2155806 | c.306T>C | synonymous_variant | 1.0 |
| katG | 2155811 | p.Leu101Met | missense_variant | 1.0 |
| kasA | 2517917 | c.-198G>T | upstream_gene_variant | 1.0 |
| kasA | 2517965 | c.-150C>A | upstream_gene_variant | 1.0 |
| kasA | 2517974 | c.-141T>C | upstream_gene_variant | 1.0 |
| kasA | 2517989 | c.-126T>C | upstream_gene_variant | 1.0 |
| kasA | 2517994 | c.-121C>A | 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 | 2518028 | c.-87G>A | upstream_gene_variant | 1.0 |
| kasA | 2518040 | c.-75G>C | upstream_gene_variant | 1.0 |
| kasA | 2518041 | c.-74_-72delTTGinsATC | upstream_gene_variant | 1.0 |
| kasA | 2518049 | c.-66G>C | upstream_gene_variant | 1.0 |
| kasA | 2518055 | c.-60T>C | upstream_gene_variant | 1.0 |
| kasA | 2518059 | c.-56T>G | 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 | 2518153 | c.39C>T | synonymous_variant | 1.0 |
| kasA | 2518162 | c.48G>A | synonymous_variant | 1.0 |
| kasA | 2518174 | c.60A>G | synonymous_variant | 1.0 |
| kasA | 2518186 | c.72G>A | synonymous_variant | 1.0 |
| kasA | 2518190 | p.Ser26Ala | missense_variant | 1.0 |
| kasA | 2518220 | c.106C>T | synonymous_variant | 1.0 |
| kasA | 2518248 | p.Ala45Val | missense_variant | 1.0 |
| kasA | 2518255 | c.141A>G | synonymous_variant | 1.0 |
| kasA | 2518268 | p.Thr52Ser | missense_variant | 1.0 |
| kasA | 2518282 | c.168A>G | synonymous_variant | 1.0 |
| kasA | 2518283 | p.Ala57Pro | missense_variant | 1.0 |
| kasA | 2518300 | c.186T>A | synonymous_variant | 1.0 |
| kasA | 2518312 | p.Asp66Glu | missense_variant | 1.0 |
| kasA | 2518315 | c.201G>C | synonymous_variant | 1.0 |
| kasA | 2518322 | p.Ser70Asp | missense_variant | 1.0 |
| kasA | 2518336 | c.222A>G | synonymous_variant | 1.0 |
| kasA | 2518339 | c.225C>G | synonymous_variant | 1.0 |
| kasA | 2518342 | p.Asp76Glu | missense_variant | 1.0 |
| kasA | 2518343 | p.Met77Leu | missense_variant | 1.0 |
| kasA | 2518348 | c.234A>G | synonymous_variant | 1.0 |
| kasA | 2518360 | c.246C>T | synonymous_variant | 1.0 |
| kasA | 2518374 | p.Gly87Ala | missense_variant | 1.0 |
| kasA | 2518379 | c.265T>C | synonymous_variant | 1.0 |
| kasA | 2518384 | c.270G>C | synonymous_variant | 1.0 |
| kasA | 2518390 | c.276A>C | synonymous_variant | 1.0 |
| kasA | 2518396 | c.282A>G | synonymous_variant | 1.0 |
| kasA | 2518403 | p.Ser97Thr | missense_variant | 1.0 |
| kasA | 2518406 | p.Ala98Thr | missense_variant | 1.0 |
| kasA | 2518417 | c.303G>C | synonymous_variant | 1.0 |
| kasA | 2518426 | c.312T>C | synonymous_variant | 1.0 |
| kasA | 2518429 | c.315A>C | synonymous_variant | 1.0 |
| kasA | 2518444 | c.330T>C | synonymous_variant | 1.0 |
| kasA | 2518447 | c.333T>G | synonymous_variant | 1.0 |
| kasA | 2518459 | c.345T>G | synonymous_variant | 1.0 |
| kasA | 2518462 | c.348A>G | synonymous_variant | 1.0 |
| kasA | 2518465 | c.351T>C | synonymous_variant | 1.0 |
| kasA | 2518468 | c.354A>C | synonymous_variant | 1.0 |
| kasA | 2518475 | c.361A>C | synonymous_variant | 1.0 |
| kasA | 2518480 | c.366T>C | synonymous_variant | 1.0 |
| kasA | 2518486 | c.372G>A | synonymous_variant | 1.0 |
| kasA | 2518506 | p.Ala131Glu | missense_variant | 1.0 |
| kasA | 2518513 | c.399C>T | synonymous_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 | 2518570 | c.456_457insACC | conservative_inframe_insertion | 1.0 |
| kasA | 2518573 | c.460_462delATC | conservative_inframe_deletion | 1.0 |
| kasA | 2518588 | c.474T>C | synonymous_variant | 1.0 |
| kasA | 2518591 | c.477G>C | synonymous_variant | 1.0 |
| kasA | 2518612 | c.498C>T | synonymous_variant | 1.0 |
| kasA | 2518624 | c.510C>G | synonymous_variant | 1.0 |
| kasA | 2518636 | c.522C>G | synonymous_variant | 1.0 |
| kasA | 2518642 | c.528A>G | synonymous_variant | 1.0 |
| kasA | 2518645 | c.531G>C | synonymous_variant | 1.0 |
| kasA | 2518648 | c.534C>T | synonymous_variant | 1.0 |
| kasA | 2518663 | c.549T>C | synonymous_variant | 1.0 |
| kasA | 2518678 | c.564C>T | synonymous_variant | 1.0 |
| kasA | 2518684 | c.570C>G | synonymous_variant | 1.0 |
| kasA | 2518688 | p.Val192Ile | missense_variant | 1.0 |
| kasA | 2518696 | c.582C>G | synonymous_variant | 1.0 |
| kasA | 2518699 | c.585C>T | synonymous_variant | 1.0 |
| kasA | 2518711 | c.597A>G | synonymous_variant | 1.0 |
| kasA | 2518714 | c.600A>C | synonymous_variant | 1.0 |
| kasA | 2518715 | p.Pro201Gly | missense_variant | 1.0 |
| kasA | 2518732 | c.618C>G | synonymous_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| kasA | 2518768 | c.654C>A | synonymous_variant | 1.0 |
| kasA | 2518780 | p.Glu222Asp | missense_variant | 1.0 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
| kasA | 2518787 | p.Arg225Gly | missense_variant | 1.0 |
| kasA | 2518792 | c.678C>G | synonymous_variant | 0.91 |
| kasA | 2518795 | c.681C>G | synonymous_variant | 0.92 |
| kasA | 2518798 | c.684G>C | synonymous_variant | 1.0 |
| kasA | 2518822 | c.708C>G | synonymous_variant | 0.79 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 0.98 |
| kasA | 2518840 | c.726C>G | synonymous_variant | 1.0 |
| kasA | 2518843 | c.729T>C | synonymous_variant | 1.0 |
| kasA | 2518846 | c.732G>A | synonymous_variant | 0.71 |
| kasA | 2518849 | c.735G>C | synonymous_variant | 1.0 |
| kasA | 2518853 | p.Leu247Val | missense_variant | 1.0 |
| kasA | 2518864 | c.750G>C | synonymous_variant | 1.0 |
| kasA | 2518879 | c.765A>G | synonymous_variant | 0.77 |
| kasA | 2518893 | p.Lys260Thr | missense_variant | 1.0 |
| kasA | 2518898 | c.784T>C | synonymous_variant | 1.0 |
| kasA | 2518906 | c.792A>G | synonymous_variant | 1.0 |
| kasA | 2518907 | p.Leu265Met | missense_variant | 1.0 |
| kasA | 2518910 | p.Leu266Met | missense_variant | 1.0 |
| kasA | 2518921 | c.807T>C | synonymous_variant | 1.0 |
| kasA | 2518930 | c.816G>C | synonymous_variant | 1.0 |
| kasA | 2519047 | c.933C>T | synonymous_variant | 1.0 |
| kasA | 2519049 | p.Gly312Ala | missense_variant | 1.0 |
| kasA | 2519056 | c.942G>C | synonymous_variant | 1.0 |
| kasA | 2519062 | c.948T>G | synonymous_variant | 1.0 |
| kasA | 2519068 | c.954C>T | synonymous_variant | 1.0 |
| kasA | 2519072 | p.Ala320Thr | missense_variant | 1.0 |
| kasA | 2519077 | c.963G>C | synonymous_variant | 1.0 |
| kasA | 2519092 | c.978C>T | synonymous_variant | 1.0 |
| kasA | 2519095 | c.981C>G | synonymous_variant | 1.0 |
| kasA | 2519104 | c.990T>C | synonymous_variant | 1.0 |
| kasA | 2519110 | p.Asp332Glu | missense_variant | 1.0 |
| kasA | 2519113 | p.Gln333His | missense_variant | 1.0 |
| kasA | 2519137 | c.1023T>G | synonymous_variant | 1.0 |
| kasA | 2519152 | c.1038G>C | synonymous_variant | 0.96 |
| kasA | 2519158 | c.1044C>A | synonymous_variant | 0.96 |
| kasA | 2519170 | c.1056G>T | synonymous_variant | 0.96 |
| kasA | 2519171 | c.1057_1059delCTCinsTTG | synonymous_variant | 0.96 |
| kasA | 2519183 | c.1069_1071delCTCinsTTG | synonymous_variant | 0.95 |
| kasA | 2519188 | c.1074G>C | synonymous_variant | 0.95 |
| kasA | 2519224 | c.1110C>G | synonymous_variant | 1.0 |
| kasA | 2519234 | p.Glu374His | missense_variant | 1.0 |
| ahpC | 2726237 | c.45C>G | synonymous_variant | 1.0 |
| ahpC | 2726243 | c.51T>C | synonymous_variant | 1.0 |
| ahpC | 2726246 | c.54C>G | synonymous_variant | 1.0 |
| ahpC | 2726264 | c.72C>G | synonymous_variant | 1.0 |
| ahpC | 2726285 | c.93C>G | synonymous_variant | 1.0 |
| ahpC | 2726303 | c.111T>C | synonymous_variant | 1.0 |
| ahpC | 2726312 | c.120T>C | synonymous_variant | 1.0 |
| ahpC | 2726340 | p.Val50Ile | missense_variant | 1.0 |
| ahpC | 2726348 | c.156T>C | synonymous_variant | 1.0 |
| ahpC | 2726357 | c.165A>G | synonymous_variant | 1.0 |
| ahpC | 2726378 | c.186T>G | synonymous_variant | 1.0 |
| ahpC | 2726390 | c.198G>C | synonymous_variant | 0.96 |
| ahpC | 2726397 | p.Ser69Gly | missense_variant | 1.0 |
| ahpC | 2726405 | c.213C>G | synonymous_variant | 1.0 |
| ahpC | 2726408 | c.216T>C | synonymous_variant | 1.0 |
| ahpC | 2726582 | c.390G>C | synonymous_variant | 1.0 |
| ahpC | 2726591 | c.399C>G | synonymous_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 | 2726657 | c.465A>C | synonymous_variant | 1.0 |
| ahpC | 2726669 | c.477T>C | synonymous_variant | 1.0 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
| ahpC | 2726681 | c.489A>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>C | synonymous_variant | 1.0 |
| ahpC | 2726729 | c.537C>T | synonymous_variant | 1.0 |
| ahpC | 2726735 | c.543C>T | synonymous_variant | 1.0 |
| ahpC | 2726745 | p.Leu185Ile | missense_variant | 1.0 |
| ahpC | 2726753 | c.561T>G | synonymous_variant | 1.0 |
| folC | 2746948 | c.651G>C | synonymous_variant | 1.0 |
| folC | 2746957 | c.642G>T | synonymous_variant | 1.0 |
| folC | 2746966 | c.633G>C | synonymous_variant | 1.0 |
| folC | 2746975 | c.624T>C | synonymous_variant | 1.0 |
| folC | 2746979 | p.Ala207Asp | missense_variant | 1.0 |
| folC | 2746981 | c.618T>C | synonymous_variant | 1.0 |
| folC | 2746984 | c.615C>G | synonymous_variant | 1.0 |
| folC | 2746987 | c.612T>C | synonymous_variant | 1.0 |
| folC | 2746999 | c.600T>C | synonymous_variant | 1.0 |
| folC | 2747002 | p.Ile199Val | missense_variant | 1.0 |
| folC | 2747032 | c.567A>G | synonymous_variant | 1.0 |
| folC | 2747037 | p.Asn188Asp | missense_variant | 1.0 |
| folC | 2747059 | c.540T>G | synonymous_variant | 1.0 |
| folC | 2747062 | c.537A>C | synonymous_variant | 1.0 |
| folC | 2747202 | p.Leu133Met | missense_variant | 1.0 |
| folC | 2747204 | p.Ala132Gln | missense_variant | 1.0 |
| folC | 2747209 | p.Leu130Phe | missense_variant | 1.0 |
| folC | 2747239 | c.360T>C | synonymous_variant | 1.0 |
| folC | 2747262 | p.Lys113Gln | missense_variant | 1.0 |
| folC | 2747263 | c.336C>G | synonymous_variant | 1.0 |
| folC | 2747359 | c.240C>G | synonymous_variant | 1.0 |
| folC | 2747374 | c.225G>A | synonymous_variant | 1.0 |
| folC | 2747389 | c.210G>C | synonymous_variant | 1.0 |
| folC | 2747395 | c.204T>C | synonymous_variant | 1.0 |
| folC | 2747398 | c.201C>T | synonymous_variant | 1.0 |
| folC | 2747404 | c.195G>A | synonymous_variant | 1.0 |
| folC | 2747416 | c.183A>G | synonymous_variant | 1.0 |
| folC | 2747419 | c.180C>G | synonymous_variant | 1.0 |
| folC | 2747428 | c.171G>C | synonymous_variant | 1.0 |
| folC | 2747452 | c.147G>A | synonymous_variant | 1.0 |
| folC | 2747464 | c.135G>C | synonymous_variant | 1.0 |
| folC | 2747467 | p.Asp44Glu | missense_variant | 1.0 |
| folC | 2747760 | c.-162G>T | upstream_gene_variant | 1.0 |
| folC | 2747766 | c.-168A>G | upstream_gene_variant | 1.0 |
| folC | 2747781 | c.-183G>A | upstream_gene_variant | 1.0 |
| folC | 2747787 | c.-190_-189delCCinsAG | upstream_gene_variant | 1.0 |
| folC | 2747790 | c.-192G>C | upstream_gene_variant | 1.0 |
| pepQ | 2859723 | c.696T>C | synonymous_variant | 1.0 |
| pepQ | 2859732 | c.687C>T | synonymous_variant | 1.0 |
| pepQ | 2859735 | c.684G>T | synonymous_variant | 1.0 |
| pepQ | 2859747 | c.672C>G | synonymous_variant | 1.0 |
| pepQ | 2859765 | c.654G>C | synonymous_variant | 1.0 |
| pepQ | 2859771 | c.648T>C | synonymous_variant | 1.0 |
| pepQ | 2859804 | c.615C>T | synonymous_variant | 1.0 |
| pepQ | 2859831 | c.588C>G | synonymous_variant | 1.0 |
| pepQ | 2859834 | c.585T>C | synonymous_variant | 1.0 |
| pepQ | 2859852 | c.567A>G | synonymous_variant | 1.0 |
| pepQ | 2859856 | p.Val188Pro | missense_variant | 1.0 |
| pepQ | 2859859 | p.Ala187Gly | missense_variant | 1.0 |
| pepQ | 2859864 | c.555T>C | synonymous_variant | 1.0 |
| pepQ | 2859870 | c.549T>C | synonymous_variant | 1.0 |
| pepQ | 2859873 | c.546T>C | synonymous_variant | 1.0 |
| thyX | 3067268 | c.678G>C | synonymous_variant | 1.0 |
| thyX | 3067277 | c.669C>A | synonymous_variant | 1.0 |
| thyX | 3067280 | c.666G>C | synonymous_variant | 1.0 |
| thyX | 3067284 | p.Ala221Asp | missense_variant | 1.0 |
| thyX | 3067287 | p.Ala220Val | missense_variant | 1.0 |
| thyX | 3067304 | p.Glu214Ala | missense_variant | 1.0 |
| thyX | 3067315 | c.631C>T | synonymous_variant | 1.0 |
| thyX | 3067316 | c.630A>G | synonymous_variant | 1.0 |
| thyX | 3067334 | c.612C>G | synonymous_variant | 1.0 |
| thyX | 3067340 | c.606G>A | synonymous_variant | 1.0 |
| thyX | 3067360 | p.Ile196Val | missense_variant | 1.0 |
| thyX | 3067373 | c.573C>T | synonymous_variant | 1.0 |
| thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
| thyX | 3067394 | c.552G>C | synonymous_variant | 1.0 |
| thyX | 3067430 | c.516C>T | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyX | 3067451 | c.495G>A | synonymous_variant | 1.0 |
| thyX | 3067457 | c.489C>G | synonymous_variant | 1.0 |
| thyX | 3067462 | c.484C>T | synonymous_variant | 1.0 |
| thyX | 3067463 | p.Ile161Val | missense_variant | 1.0 |
| thyX | 3067469 | c.477C>T | synonymous_variant | 1.0 |
| thyX | 3067472 | c.474C>G | synonymous_variant | 1.0 |
| thyX | 3067475 | c.471A>G | synonymous_variant | 1.0 |
| thyX | 3067498 | c.448C>T | synonymous_variant | 1.0 |
| thyX | 3067499 | c.447G>A | synonymous_variant | 1.0 |
| thyX | 3067511 | c.435G>A | synonymous_variant | 1.0 |
| thyX | 3067515 | p.Ser144Thr | missense_variant | 1.0 |
| thyX | 3067602 | p.Arg115Gln | missense_variant | 1.0 |
| thyX | 3067607 | p.Asp113Asn | missense_variant | 1.0 |
| thyX | 3067616 | c.330C>G | synonymous_variant | 1.0 |
| thyX | 3067631 | c.315C>G | synonymous_variant | 1.0 |
| thyX | 3067640 | c.306G>C | 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>A | synonymous_variant | 1.0 |
| thyX | 3067685 | c.261A>G | synonymous_variant | 1.0 |
| thyX | 3067688 | c.258G>C | synonymous_variant | 1.0 |
| thyX | 3067718 | c.228C>G | synonymous_variant | 1.0 |
| thyX | 3067721 | c.225T>C | synonymous_variant | 1.0 |
| thyX | 3067727 | c.219A>C | synonymous_variant | 1.0 |
| thyX | 3067742 | c.204A>G | synonymous_variant | 1.0 |
| thyX | 3067761 | p.Arg62Lys | missense_variant | 1.0 |
| thyX | 3067765 | p.Leu61Ile | missense_variant | 1.0 |
| thyX | 3067766 | c.180C>T | synonymous_variant | 1.0 |
| thyX | 3067769 | p.Gly59Ser | missense_variant | 1.0 |
| thyX | 3067778 | c.168C>G | synonymous_variant | 1.0 |
| thyX | 3067793 | c.153T>C | synonymous_variant | 1.0 |
| thyX | 3067814 | c.132T>C | synonymous_variant | 1.0 |
| thyX | 3067840 | p.Val36Leu | missense_variant | 1.0 |
| thyX | 3067847 | p.Pro33Gln | missense_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 | 3067886 | c.60A>C | synonymous_variant | 1.0 |
| thyX | 3067889 | c.57C>G | synonymous_variant | 1.0 |
| thyX | 3067898 | p.Asp16Glu | missense_variant | 1.0 |
| thyX | 3067915 | c.31C>T | synonymous_variant | 1.0 |
| thyX | 3067916 | c.30A>G | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073884 | c.588C>G | synonymous_variant | 1.0 |
| thyA | 3073888 | p.Ser195Gly | missense_variant | 1.0 |
| thyA | 3073890 | c.580_582delTTGinsCTC | synonymous_variant | 1.0 |
| thyA | 3073902 | c.570C>G | synonymous_variant | 1.0 |
| thyA | 3073917 | c.555C>T | synonymous_variant | 1.0 |
| thyA | 3073920 | c.552C>G | synonymous_variant | 1.0 |
| thyA | 3073925 | c.547T>C | synonymous_variant | 1.0 |
| thyA | 3073929 | c.543T>C | synonymous_variant | 1.0 |
| thyA | 3073950 | c.522G>A | synonymous_variant | 1.0 |
| thyA | 3073953 | c.519T>G | synonymous_variant | 1.0 |
| thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
| thyA | 3073959 | c.513T>C | synonymous_variant | 1.0 |
| thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
| thyA | 3074097 | c.375C>A | synonymous_variant | 1.0 |
| thyA | 3074100 | c.372T>C | synonymous_variant | 1.0 |
| thyA | 3074103 | c.369C>G | synonymous_variant | 1.0 |
| thyA | 3074106 | c.366T>C | synonymous_variant | 1.0 |
| thyA | 3074120 | c.352T>C | synonymous_variant | 1.0 |
| thyA | 3074121 | p.Asp117Glu | missense_variant | 1.0 |
| thyA | 3074130 | c.342G>C | synonymous_variant | 1.0 |
| thyA | 3074262 | c.210T>C | synonymous_variant | 1.0 |
| thyA | 3074268 | c.204T>C | synonymous_variant | 1.0 |
| thyA | 3074274 | c.198T>C | synonymous_variant | 1.0 |
| thyA | 3074376 | p.Gln32His | missense_variant | 1.0 |
| thyA | 3074379 | c.93C>T | synonymous_variant | 1.0 |
| thyA | 3074394 | c.78C>G | synonymous_variant | 1.0 |
| thyA | 3074397 | c.75A>C | synonymous_variant | 1.0 |
| thyA | 3074417 | p.Ser19Ala | missense_variant | 1.0 |
| ald | 3087176 | c.357C>G | synonymous_variant | 1.0 |
| fbiB | 3640554 | c.-981C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640562 | p.Ala7Val | missense_variant | 1.0 |
| fbiB | 3640566 | c.-969T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640569 | c.-966A>G | upstream_gene_variant | 1.0 |
| fbiB | 3640587 | c.-948C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640590 | c.-945G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640593 | c.-942C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640596 | c.-939G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640599 | c.-936C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640681 | p.Val47Ile | missense_variant | 1.0 |
| fbiA | 3640701 | p.Ile53Met | missense_variant | 1.0 |
| fbiB | 3640707 | c.-828G>A | upstream_gene_variant | 1.0 |
| fbiA | 3640708 | p.Leu56Val | missense_variant | 1.0 |
| fbiB | 3640713 | c.-822T>A | upstream_gene_variant | 1.0 |
| fbiA | 3640714 | p.Val58Ile | missense_variant | 1.0 |
| fbiB | 3640722 | c.-813G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640725 | c.-810T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640743 | c.-792T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640749 | c.-786G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640761 | c.-774G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640767 | c.-768C>G | upstream_gene_variant | 1.0 |
| fbiB | 3640782 | c.-753C>T | upstream_gene_variant | 1.0 |
| fbiA | 3640785 | p.Gln81His | missense_variant | 1.0 |
| fbiB | 3640788 | c.-747T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640797 | c.-738T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640803 | c.-732C>T | upstream_gene_variant | 1.0 |
| fbiA | 3640808 | p.Met89Lys | missense_variant | 1.0 |
| fbiA | 3640810 | p.Gln90Glu | missense_variant | 1.0 |
| fbiB | 3640821 | c.-714G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640827 | c.-708T>C | upstream_gene_variant | 1.0 |
| fbiA | 3640831 | p.Val97Met | missense_variant | 0.98 |
| fbiB | 3640851 | c.-684G>A | upstream_gene_variant | 1.0 |
| fbiB | 3640857 | c.-678G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640866 | c.-669T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640867 | c.-668C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640872 | c.-663C>G | upstream_gene_variant | 1.0 |
| fbiB | 3640879 | c.-656C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640890 | c.-645C>G | upstream_gene_variant | 1.0 |
| fbiB | 3641606 | c.72T>G | synonymous_variant | 1.0 |
| fbiB | 3641616 | p.Asp28Asn | missense_variant | 1.0 |
| fbiB | 3641622 | p.Ser30Gly | missense_variant | 1.0 |
| fbiB | 3641626 | p.Ala31Asp | missense_variant | 1.0 |
| fbiB | 3641633 | c.99C>T | synonymous_variant | 1.0 |
| fbiB | 3641638 | p.Ala35Glu | missense_variant | 1.0 |
| fbiB | 3641642 | c.108G>T | synonymous_variant | 1.0 |
| fbiB | 3641657 | c.123C>T | synonymous_variant | 1.0 |
| fbiB | 3641663 | c.129T>C | synonymous_variant | 1.0 |
| fbiB | 3641669 | c.135C>G | synonymous_variant | 1.0 |
| fbiB | 3641678 | c.144T>C | synonymous_variant | 1.0 |
| fbiB | 3641705 | p.Glu57Asp | missense_variant | 1.0 |
| fbiB | 3641711 | c.177G>C | synonymous_variant | 1.0 |
| fbiB | 3641717 | c.183T>G | synonymous_variant | 1.0 |
| fbiB | 3641723 | c.189T>G | synonymous_variant | 1.0 |
| fbiB | 3642578 | c.1044C>G | synonymous_variant | 1.0 |
| fbiB | 3642581 | c.1047A>C | synonymous_variant | 1.0 |
| fbiB | 3642602 | c.1068A>C | synonymous_variant | 1.0 |
| fbiB | 3642605 | c.1071A>C | synonymous_variant | 1.0 |
| fbiB | 3642614 | c.1080C>T | synonymous_variant | 1.0 |
| fbiB | 3642620 | c.1086T>C | synonymous_variant | 1.0 |
| fbiB | 3642635 | p.Asp367Glu | missense_variant | 1.0 |
| fbiB | 3642656 | c.1122G>C | synonymous_variant | 1.0 |
| alr | 3840956 | c.465C>G | synonymous_variant | 1.0 |
| alr | 3840980 | c.441G>C | synonymous_variant | 1.0 |
| alr | 3840994 | p.His143Asp | missense_variant | 1.0 |
| alr | 3840995 | c.424_426delTTGinsCTC | synonymous_variant | 1.0 |
| alr | 3841018 | p.Leu135Val | missense_variant | 1.0 |
| alr | 3841022 | c.399C>G | synonymous_variant | 1.0 |
| alr | 3841029 | p.Ala131Gly | missense_variant | 1.0 |
| alr | 3841033 | p.Val130Ile | missense_variant | 1.0 |
| alr | 3841037 | c.384G>C | synonymous_variant | 1.0 |
| ddn | 3986655 | c.-189A>T | upstream_gene_variant | 1.0 |
| ddn | 3986660 | c.-184C>T | upstream_gene_variant | 1.0 |
| ddn | 3986667 | c.-177_-176delCTinsAC | 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 |
| ddn | 3986705 | c.-139C>G | upstream_gene_variant | 1.0 |
| panD | 4044012 | c.270C>T | synonymous_variant | 1.0 |
| panD | 4044015 | c.267G>C | synonymous_variant | 1.0 |
| panD | 4044018 | c.264T>C | synonymous_variant | 1.0 |
| panD | 4044024 | c.258T>C | synonymous_variant | 1.0 |
| panD | 4044033 | c.249T>C | synonymous_variant | 1.0 |
| panD | 4044036 | c.246G>C | synonymous_variant | 1.0 |
| panD | 4044050 | c.232T>C | synonymous_variant | 1.0 |
| panD | 4044051 | c.231C>T | synonymous_variant | 1.0 |
| panD | 4044057 | c.225C>A | synonymous_variant | 1.0 |
| panD | 4044063 | c.219T>C | synonymous_variant | 1.0 |
| panD | 4044072 | c.210C>A | synonymous_variant | 1.0 |
| panD | 4044075 | c.207T>C | synonymous_variant | 1.0 |
| panD | 4044084 | c.198T>C | synonymous_variant | 1.0 |
| panD | 4044093 | c.189A>G | synonymous_variant | 1.0 |
| panD | 4044096 | c.186C>G | synonymous_variant | 1.0 |
| panD | 4044105 | c.177G>C | synonymous_variant | 1.0 |
| panD | 4044120 | c.162A>G | synonymous_variant | 1.0 |
| panD | 4044123 | c.159T>G | 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 | 4044156 | c.126A>G | synonymous_variant | 1.0 |
| panD | 4044159 | c.123C>T | synonymous_variant | 1.0 |
| panD | 4044162 | c.120A>G | synonymous_variant | 1.0 |
| panD | 4044165 | c.117G>T | synonymous_variant | 1.0 |
| panD | 4044168 | c.114G>C | synonymous_variant | 1.0 |
| panD | 4044188 | c.94T>C | synonymous_variant | 1.0 |
| panD | 4044195 | c.87T>C | synonymous_variant | 1.0 |
| panD | 4044237 | c.45G>C | synonymous_variant | 1.0 |
| panD | 4044240 | c.42G>C | synonymous_variant | 1.0 |
| panD | 4044243 | c.39C>G | synonymous_variant | 1.0 |
| panD | 4044246 | c.36C>G | synonymous_variant | 1.0 |
| panD | 4044264 | c.18G>C | synonymous_variant | 1.0 |
| panD | 4044270 | c.12G>A | synonymous_variant | 1.0 |
| embC | 4239677 | c.-186C>T | upstream_gene_variant | 1.0 |
| embC | 4239680 | c.-183C>G | upstream_gene_variant | 1.0 |
| embC | 4239686 | c.-177C>T | upstream_gene_variant | 1.0 |
| embC | 4239688 | c.-175A>G | upstream_gene_variant | 1.0 |
| embC | 4239696 | c.-167_-165delCATinsAAC | upstream_gene_variant | 1.0 |
| embC | 4239699 | c.-164A>G | upstream_gene_variant | 1.0 |
| embC | 4239703 | c.-160G>C | upstream_gene_variant | 1.0 |
| embC | 4239710 | c.-153C>G | upstream_gene_variant | 1.0 |
| embC | 4239723 | c.-140_-138delCAGinsGAA | upstream_gene_variant | 1.0 |
| embC | 4239749 | c.-114T>C | upstream_gene_variant | 1.0 |
| embC | 4239752 | c.-111T>G | upstream_gene_variant | 1.0 |
| embC | 4240726 | c.864G>C | synonymous_variant | 1.0 |
| embC | 4240736 | p.Ser292Ala | missense_variant | 0.98 |
| embC | 4240783 | c.921G>C | synonymous_variant | 0.99 |
| embC | 4240786 | c.924C>G | synonymous_variant | 1.0 |
| embC | 4240789 | c.927T>C | synonymous_variant | 1.0 |
| embC | 4240795 | c.933C>G | synonymous_variant | 1.0 |
| embC | 4240819 | c.957A>C | 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 | 4240875 | p.Ser338Thr | missense_variant | 1.0 |
| embC | 4240879 | c.1017G>C | synonymous_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 | 4240907 | c.1045C>T | synonymous_variant | 0.93 |
| embC | 4240910 | p.Ala350Leu | missense_variant | 1.0 |
| embC | 4241024 | p.Val388Phe | missense_variant | 1.0 |
| embC | 4241039 | p.Asp393Asn | missense_variant | 1.0 |
| embC | 4241047 | c.1185C>G | synonymous_variant | 1.0 |
| embC | 4241050 | c.1188T>G | synonymous_variant | 1.0 |
| embC | 4241071 | c.1209C>G | synonymous_variant | 1.0 |
| embC | 4241083 | c.1221G>T | synonymous_variant | 1.0 |
| embC | 4241084 | c.1222C>T | synonymous_variant | 1.0 |
| embC | 4241095 | c.1233C>T | synonymous_variant | 1.0 |
| embC | 4241122 | c.1260C>T | 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 | 4241167 | c.1305C>G | synonymous_variant | 1.0 |
| embC | 4241191 | c.1329C>T | synonymous_variant | 1.0 |
| embC | 4241194 | c.1332C>G | synonymous_variant | 1.0 |
| embC | 4241203 | c.1341T>C | synonymous_variant | 1.0 |
| embC | 4241207 | c.1345C>T | synonymous_variant | 1.0 |
| embC | 4241215 | c.1353C>G | synonymous_variant | 1.0 |
| embC | 4241230 | c.1368A>G | synonymous_variant | 1.0 |
| embC | 4241233 | c.1371G>C | synonymous_variant | 1.0 |
| embC | 4241236 | c.1374C>G | synonymous_variant | 1.0 |
| embC | 4241394 | p.Lys511Ser | missense_variant | 1.0 |
| embC | 4241407 | c.1545A>G | synonymous_variant | 1.0 |
| embC | 4241449 | c.1587C>G | synonymous_variant | 1.0 |
| embC | 4241453 | p.Ile531Val | missense_variant | 1.0 |
| embC | 4241457 | p.Ala532Gly | missense_variant | 1.0 |
| embC | 4241470 | c.1608C>G | synonymous_variant | 1.0 |
| embC | 4241479 | c.1617C>T | synonymous_variant | 1.0 |
| embC | 4241483 | p.Val541Leu | missense_variant | 1.0 |
| embC | 4241486 | p.Leu542Val | missense_variant | 0.97 |
| embC | 4241494 | c.1632C>G | synonymous_variant | 1.0 |
| embC | 4241500 | c.1638A>G | synonymous_variant | 1.0 |
| embC | 4241518 | c.1656A>G | synonymous_variant | 1.0 |
| embC | 4241521 | c.1659T>C | synonymous_variant | 1.0 |
| embC | 4241530 | c.1668C>G | synonymous_variant | 1.0 |
| embC | 4241536 | c.1674A>G | synonymous_variant | 1.0 |
| embC | 4241539 | c.1677T>C | synonymous_variant | 1.0 |
| embC | 4241545 | c.1683T>C | synonymous_variant | 1.0 |
| embC | 4241548 | c.1686T>C | synonymous_variant | 1.0 |
| embC | 4241551 | c.1689A>G | synonymous_variant | 1.0 |
| embC | 4241560 | c.1698C>G | 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.Leu577Ile | missense_variant | 1.0 |
| embC | 4241611 | c.1749G>C | synonymous_variant | 1.0 |
| embC | 4241614 | c.1752A>C | synonymous_variant | 0.98 |
| embC | 4241623 | c.1761C>A | synonymous_variant | 1.0 |
| embC | 4241644 | c.1782G>C | synonymous_variant | 1.0 |
| embC | 4241648 | c.1786T>C | synonymous_variant | 1.0 |
| embC | 4241653 | c.1791C>A | synonymous_variant | 1.0 |
| embC | 4241656 | c.1794G>C | synonymous_variant | 1.0 |
| embC | 4241665 | c.1803G>C | synonymous_variant | 1.0 |
| embC | 4241669 | c.1807_1809delCTTinsTTG | synonymous_variant | 1.0 |
| embC | 4241677 | c.1815G>C | synonymous_variant | 1.0 |
| embA | 4244154 | p.Thr308Pro | missense_variant | 1.0 |
| embA | 4244157 | p.Ser309Ala | missense_variant | 1.0 |
| embA | 4244178 | p.Ala316Thr | missense_variant | 1.0 |
| embA | 4244192 | c.960C>G | synonymous_variant | 1.0 |
| embA | 4244195 | c.963C>G | synonymous_variant | 1.0 |
| embA | 4244198 | c.966C>G | synonymous_variant | 1.0 |
| embA | 4244210 | c.978G>A | synonymous_variant | 1.0 |
| embA | 4244213 | c.981C>G | synonymous_variant | 1.0 |
| embA | 4244291 | c.1059G>C | synonymous_variant | 1.0 |
| embA | 4244306 | c.1074G>C | synonymous_variant | 1.0 |
| embA | 4244312 | c.1080T>G | synonymous_variant | 1.0 |
| embA | 4244317 | p.Phe362Trp | missense_variant | 1.0 |
| embA | 4244324 | c.1092T>C | synonymous_variant | 1.0 |
| embA | 4244327 | c.1095T>C | synonymous_variant | 1.0 |
| embA | 4244340 | p.Ser370Ala | missense_variant | 1.0 |
| embA | 4244366 | c.1134C>T | synonymous_variant | 1.0 |
| embA | 4244607 | c.1375C>T | synonymous_variant | 1.0 |
| embA | 4244610 | p.Ala460Thr | missense_variant | 1.0 |
| embA | 4244616 | p.Ala462Ser | missense_variant | 1.0 |
| embA | 4244645 | c.1413T>C | synonymous_variant | 1.0 |
| embA | 4244649 | p.Asp473Ser | missense_variant | 1.0 |
| embA | 4244669 | c.1437G>C | synonymous_variant | 1.0 |
| embA | 4244671 | p.Ala480Gly | missense_variant | 1.0 |
| embA | 4244675 | c.1443A>G | synonymous_variant | 1.0 |
| embA | 4244681 | c.1449A>G | synonymous_variant | 1.0 |
| embA | 4244708 | c.1476C>G | synonymous_variant | 1.0 |
| embA | 4244714 | c.1482C>G | synonymous_variant | 1.0 |
| embA | 4244720 | c.1488C>T | synonymous_variant | 1.0 |
| embA | 4244726 | p.Asp498Glu | missense_variant | 1.0 |
| embA | 4244728 | p.Phe499Trp | missense_variant | 1.0 |
| embA | 4244745 | p.Leu505Val | missense_variant | 1.0 |
| embA | 4244750 | c.1518C>G | synonymous_variant | 1.0 |
| embA | 4244838 | c.1606C>T | synonymous_variant | 1.0 |
| embA | 4244862 | c.1630C>T | synonymous_variant | 1.0 |
| embA | 4245041 | c.1809C>G | synonymous_variant | 1.0 |
| embA | 4245051 | p.Val607Ile | missense_variant | 1.0 |
| embA | 4245058 | p.Ala609Gly | missense_variant | 0.94 |
| embA | 4245060 | c.1828T>C | synonymous_variant | 1.0 |
| embA | 4245077 | c.1845G>C | synonymous_variant | 1.0 |
| embA | 4245083 | c.1851A>G | synonymous_variant | 1.0 |
| embA | 4245086 | c.1854C>A | synonymous_variant | 1.0 |
| embA | 4245092 | c.1860C>G | synonymous_variant | 1.0 |
| embA | 4245101 | c.1869G>C | synonymous_variant | 1.0 |
| embA | 4245107 | c.1875C>T | synonymous_variant | 1.0 |
| embA | 4245136 | p.Tyr635Phe | missense_variant | 1.0 |
| embA | 4245149 | c.1917C>G | synonymous_variant | 1.0 |
| embA | 4245167 | c.1935G>C | synonymous_variant | 1.0 |
| embA | 4245173 | c.1941G>A | synonymous_variant | 1.0 |
| embA | 4245285 | c.2053T>C | synonymous_variant | 1.0 |
| embA | 4245293 | c.2061T>C | synonymous_variant | 1.0 |
| embA | 4245296 | c.2064G>C | synonymous_variant | 1.0 |
| embA | 4245299 | c.2067A>G | synonymous_variant | 1.0 |
| embA | 4245311 | c.2079C>G | synonymous_variant | 1.0 |
| embA | 4245316 | p.Val695Ala | missense_variant | 1.0 |
| embA | 4245325 | c.2094delC | frameshift_variant | 1.0 |
| embA | 4245329 | c.2097A>T | synonymous_variant | 1.0 |
| embA | 4245331 | c.2100dupC | frameshift_variant | 1.0 |
| embA | 4245338 | c.2106C>G | synonymous_variant | 1.0 |
| embA | 4245772 | p.Asn847Ser | missense_variant | 1.0 |
| embB | 4245785 | c.-729G>C | upstream_gene_variant | 1.0 |
| embB | 4245791 | c.-723C>T | upstream_gene_variant | 1.0 |
| embB | 4245797 | c.-717C>G | upstream_gene_variant | 1.0 |
| embB | 4245806 | c.-708G>A | upstream_gene_variant | 1.0 |
| embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 1.0 |
| embB | 4245815 | c.-699C>G | upstream_gene_variant | 1.0 |
| embA | 4245820 | p.Ser863Thr | missense_variant | 1.0 |
| embB | 4245833 | c.-681G>A | upstream_gene_variant | 1.0 |
| embB | 4245839 | c.-675G>C | upstream_gene_variant | 1.0 |
| embB | 4245842 | c.-672G>C | upstream_gene_variant | 1.0 |
| embB | 4245845 | c.-669T>C | upstream_gene_variant | 1.0 |
| embB | 4245851 | c.-663G>C | upstream_gene_variant | 1.0 |
| embB | 4245878 | c.-636G>A | upstream_gene_variant | 1.0 |
| embB | 4245887 | c.-627T>C | upstream_gene_variant | 1.0 |
| embA | 4245891 | p.Ile887Ser | missense_variant | 1.0 |
| embA | 4245903 | p.Ser891Gln | missense_variant | 1.0 |
| embA | 4245915 | p.Gln895Glu | missense_variant | 1.0 |
| embB | 4246606 | c.93C>G | synonymous_variant | 1.0 |
| embB | 4246615 | c.102G>C | synonymous_variant | 1.0 |
| embB | 4246621 | c.108T>C | 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 | 4247068 | c.555T>C | synonymous_variant | 1.0 |
| embB | 4247077 | c.564G>A | synonymous_variant | 1.0 |
| embB | 4247095 | c.582G>T | synonymous_variant | 1.0 |
| embB | 4247370 | p.Gly286Ala | 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 | 4247398 | c.885G>C | synonymous_variant | 1.0 |
| embB | 4247401 | c.888T>C | synonymous_variant | 1.0 |
| embB | 4247407 | c.894G>C | synonymous_variant | 1.0 |
| embB | 4247437 | c.924A>C | synonymous_variant | 1.0 |
| embB | 4247440 | c.927C>T | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247491 | c.978G>C | synonymous_variant | 1.0 |
| embB | 4247494 | c.981G>A | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4247500 | c.987C>G | synonymous_variant | 1.0 |
| embB | 4247512 | c.999T>C | synonymous_variant | 1.0 |
| embB | 4247528 | c.1015C>T | synonymous_variant | 1.0 |
| embB | 4247539 | c.1026T>C | synonymous_variant | 1.0 |
| embB | 4247869 | c.1356G>C | synonymous_variant | 1.0 |
| embB | 4247876 | c.1363C>T | 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 | 4247905 | c.1392G>C | synonymous_variant | 1.0 |
| embB | 4247909 | c.1396T>C | synonymous_variant | 1.0 |
| embB | 4247917 | c.1404C>A | synonymous_variant | 1.0 |
| embB | 4247926 | c.1413C>T | synonymous_variant | 1.0 |
| embB | 4247938 | c.1425G>C | synonymous_variant | 1.0 |
| embB | 4247940 | p.Leu476Trp | missense_variant | 1.0 |
| embB | 4247951 | p.Ser480Ala | missense_variant | 1.0 |
| embB | 4247957 | p.Met482Leu | missense_variant | 1.0 |
| embB | 4247965 | c.1452C>A | synonymous_variant | 1.0 |
| embB | 4247972 | p.Thr487Phe | missense_variant | 1.0 |
| embB | 4247977 | c.1464C>G | synonymous_variant | 1.0 |
| embB | 4247984 | p.Thr491Pro | missense_variant | 1.0 |
| embB | 4248007 | c.1494C>A | synonymous_variant | 0.98 |
| embB | 4248022 | p.Leu503Phe | missense_variant | 1.0 |
| embB | 4248025 | c.1512A>G | synonymous_variant | 1.0 |
| embB | 4248035 | p.Val508Ile | missense_variant | 1.0 |
| embB | 4248042 | p.Ala510Gly | missense_variant | 1.0 |
| embB | 4248044 | p.Lys511Ala | missense_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 | 4248097 | c.1584C>G | synonymous_variant | 1.0 |
| embB | 4248118 | c.1605T>C | synonymous_variant | 1.0 |
| embB | 4248133 | c.1620C>G | synonymous_variant | 1.0 |
| embB | 4248173 | p.Val554Leu | missense_variant | 1.0 |
| embB | 4248178 | c.1665C>T | synonymous_variant | 1.0 |
| embB | 4248190 | c.1677G>C | synonymous_variant | 1.0 |
| embB | 4248199 | c.1686A>C | synonymous_variant | 1.0 |
| embB | 4248200 | p.Ile563Val | missense_variant | 1.0 |
| embB | 4248205 | c.1692C>G | synonymous_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248220 | c.1707A>C | synonymous_variant | 1.0 |
| embB | 4248232 | c.1719G>T | synonymous_variant | 1.0 |
| embB | 4248241 | c.1728C>T | synonymous_variant | 1.0 |
| embB | 4248277 | c.1764G>C | synonymous_variant | 1.0 |
| embB | 4248316 | c.1803C>G | synonymous_variant | 1.0 |
| embB | 4248319 | c.1806A>G | synonymous_variant | 1.0 |
| embB | 4248322 | c.1809G>T | synonymous_variant | 1.0 |
| embB | 4248334 | c.1821C>G | synonymous_variant | 1.0 |
| embB | 4248343 | c.1830G>C | synonymous_variant | 1.0 |
| embB | 4248346 | c.1833G>T | synonymous_variant | 1.0 |
| embB | 4248350 | c.1837T>C | synonymous_variant | 1.0 |
| embB | 4248355 | c.1842A>T | synonymous_variant | 1.0 |
| embB | 4248358 | c.1845C>G | synonymous_variant | 1.0 |
| embB | 4248361 | c.1848A>C | synonymous_variant | 1.0 |
| embB | 4248362 | p.Ser617Lys | missense_variant | 1.0 |
| embB | 4248388 | c.1875G>C | synonymous_variant | 1.0 |
| embB | 4248393 | p.Ala627Gly | missense_variant | 1.0 |
| embB | 4248398 | p.Leu629Val | missense_variant | 1.0 |
| embB | 4248406 | c.1893G>C | synonymous_variant | 1.0 |
| embB | 4248407 | p.Leu632Val | missense_variant | 1.0 |
| embB | 4248416 | c.1903C>T | synonymous_variant | 1.0 |
| embB | 4248430 | c.1917T>C | synonymous_variant | 1.0 |
| embB | 4248432 | p.Trp640Phe | missense_variant | 1.0 |
| embB | 4248457 | c.1944T>C | synonymous_variant | 1.0 |
| embB | 4248460 | c.1947C>G | synonymous_variant | 1.0 |
| embB | 4248472 | c.1959T>C | synonymous_variant | 1.0 |
| embB | 4248478 | c.1965G>A | synonymous_variant | 1.0 |
| embB | 4248496 | c.1983G>C | synonymous_variant | 1.0 |
| embB | 4248508 | c.1995G>A | synonymous_variant | 1.0 |
| embB | 4248514 | c.2001A>C | synonymous_variant | 1.0 |
| embB | 4248515 | p.Val668Ile | missense_variant | 1.0 |
| embB | 4248524 | p.Ile671Val | missense_variant | 1.0 |
| embB | 4248688 | c.2175G>C | synonymous_variant | 1.0 |
| embB | 4248697 | c.2184A>T | synonymous_variant | 1.0 |
| embB | 4248700 | c.2187G>A | synonymous_variant | 1.0 |
| embB | 4248706 | c.2193G>C | synonymous_variant | 1.0 |
| embB | 4248725 | p.Ser738Ala | missense_variant | 1.0 |
| embB | 4248730 | c.2217C>T | synonymous_variant | 1.0 |
| embB | 4248731 | p.Val740Leu | missense_variant | 1.0 |
| embB | 4249138 | c.2625C>G | synonymous_variant | 1.0 |
| embB | 4249141 | c.2628G>C | synonymous_variant | 1.0 |
| embB | 4249147 | c.2634C>G | synonymous_variant | 1.0 |
| embB | 4249150 | c.2637C>A | synonymous_variant | 1.0 |
| embB | 4249153 | c.2640G>C | synonymous_variant | 1.0 |
| embB | 4249186 | c.2673G>A | synonymous_variant | 1.0 |
| embB | 4249187 | p.Tyr892His | missense_variant | 1.0 |
| embB | 4249193 | p.Pro894Asp | missense_variant | 1.0 |
| embB | 4249204 | c.2691T>C | synonymous_variant | 1.0 |
| embB | 4249207 | c.2694G>C | synonymous_variant | 1.0 |
| embB | 4249381 | c.2868A>C | synonymous_variant | 1.0 |
| embB | 4249405 | c.2892C>T | synonymous_variant | 1.0 |
| embB | 4249417 | c.2904A>G | synonymous_variant | 1.0 |
| embB | 4249423 | p.Asp970Glu | 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 | 4249450 | c.2937C>G | synonymous_variant | 1.0 |
| embB | 4249454 | p.Thr981Ser | missense_variant | 1.0 |
| embB | 4249469 | p.Leu986Met | missense_variant | 1.0 |
| embB | 4249486 | c.2973T>G | synonymous_variant | 0.97 |
| embB | 4249487 | c.2974T>C | synonymous_variant | 1.0 |
| embB | 4249492 | c.2979C>T | 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 | 4249558 | c.3045A>C | synonymous_variant | 1.0 |
| embB | 4249568 | p.Ser1019Thr | missense_variant | 1.0 |
| embB | 4249573 | c.3060T>G | synonymous_variant | 1.0 |
| embB | 4249576 | c.3063G>A | synonymous_variant | 1.0 |
| embB | 4249581 | p.Leu1023Gln | missense_variant | 1.0 |
| embB | 4249594 | c.3081G>C | synonymous_variant | 1.0 |
| embB | 4249600 | c.3087A>G | synonymous_variant | 1.0 |
| ubiA | 4269039 | c.795C>T | synonymous_variant | 1.0 |
| ubiA | 4269042 | c.792G>C | synonymous_variant | 1.0 |
| ubiA | 4269051 | c.783C>G | synonymous_variant | 1.0 |
| ubiA | 4269066 | c.768C>G | synonymous_variant | 1.0 |
| ubiA | 4269077 | p.Ile253Val | missense_variant | 1.0 |
| ubiA | 4269081 | c.753G>C | synonymous_variant | 1.0 |
| ubiA | 4269084 | c.750G>C | synonymous_variant | 1.0 |
| ubiA | 4269088 | p.Ala249Met | missense_variant | 1.0 |
| ubiA | 4269102 | c.730_732delAGCinsTCG | synonymous_variant | 1.0 |
| ubiA | 4269142 | c.691_692insGG | frameshift_variant | 1.0 |
| ubiA | 4269145 | c.687_688delGG | frameshift_variant | 1.0 |
| ubiA | 4269156 | c.678C>G | synonymous_variant | 1.0 |
| ubiA | 4269159 | p.Ser225Ala | missense_variant | 1.0 |
| ubiA | 4269164 | p.Leu224Met | missense_variant | 1.0 |
| ubiA | 4269171 | c.663C>A | synonymous_variant | 1.0 |
| ubiA | 4269182 | c.652C>T | synonymous_variant | 1.0 |
| ubiA | 4269192 | c.642C>A | synonymous_variant | 1.0 |
| ubiA | 4269206 | c.628C>T | synonymous_variant | 1.0 |
| ubiA | 4269207 | c.627G>C | synonymous_variant | 1.0 |
| ubiA | 4269351 | c.483C>G | synonymous_variant | 1.0 |
| ubiA | 4269354 | c.480C>A | synonymous_variant | 1.0 |
| ubiA | 4269362 | c.472T>C | synonymous_variant | 1.0 |
| ubiA | 4269375 | c.459G>C | synonymous_variant | 1.0 |
| ubiA | 4269380 | p.Val152Ile | missense_variant | 1.0 |
| ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
| ubiA | 4269390 | p.Val148Ile | missense_variant | 1.0 |
| ubiA | 4269402 | c.432T>C | synonymous_variant | 0.97 |
| ubiA | 4269405 | c.429G>A | synonymous_variant | 0.97 |
| ubiA | 4269411 | c.423T>A | synonymous_variant | 0.97 |
| ubiA | 4269414 | c.420T>C | synonymous_variant | 0.97 |
| ubiA | 4269436 | p.Ala133Gly | missense_variant | 0.97 |
| ubiA | 4269440 | p.Leu132Ile | missense_variant | 0.97 |
| ubiA | 4269448 | p.Val129Ala | missense_variant | 0.95 |
| ubiA | 4269453 | c.381A>C | synonymous_variant | 0.93 |
| ubiA | 4269458 | p.Leu126Val | missense_variant | 0.9 |
| ubiA | 4269549 | c.285C>T | synonymous_variant | 1.0 |
| ubiA | 4269572 | c.262A>C | synonymous_variant | 1.0 |
| ubiA | 4269573 | c.261A>G | synonymous_variant | 1.0 |
| ubiA | 4269588 | c.246G>C | synonymous_variant | 1.0 |
| ubiA | 4269591 | c.243C>T | synonymous_variant | 1.0 |
| ubiA | 4269594 | c.240A>C | synonymous_variant | 1.0 |
| ubiA | 4269609 | c.225G>T | synonymous_variant | 1.0 |
| ubiA | 4269612 | c.222T>C | synonymous_variant | 1.0 |
| ubiA | 4269621 | c.213C>G | synonymous_variant | 1.0 |
| ubiA | 4269627 | c.207G>A | synonymous_variant | 1.0 |
| ubiA | 4269632 | p.Ala68Ser | missense_variant | 1.0 |
| ethA | 4326280 | c.1194G>A | synonymous_variant | 1.0 |
| ethA | 4326295 | c.1179G>C | synonymous_variant | 1.0 |
| ethA | 4326319 | c.1155C>G | synonymous_variant | 0.81 |
| ethA | 4326322 | p.Val384Ile | missense_variant | 1.0 |
| ethA | 4326329 | p.Tyr382Phe | missense_variant | 0.81 |
| ethA | 4326331 | c.1143C>G | synonymous_variant | 0.81 |
| ethA | 4326340 | c.1134C>G | synonymous_variant | 0.81 |
| ethA | 4326343 | p.Ile377Met | missense_variant | 1.0 |
| ethA | 4326351 | p.Ser375Thr | missense_variant | 0.81 |
| ethA | 4326352 | c.1122T>G | synonymous_variant | 0.81 |
| ethA | 4326547 | c.927G>A | synonymous_variant | 1.0 |
| ethR | 4326556 | c.-993A>G | upstream_gene_variant | 1.0 |
| ethR | 4326559 | c.-990A>G | upstream_gene_variant | 0.65 |
| ethA | 4326564 | p.Ala304Thr | missense_variant | 0.34 |
| ethR | 4326565 | c.-984C>A | upstream_gene_variant | 0.67 |
| ethA | 4326587 | p.Val296Ala | missense_variant | 0.34 |
| ethA | 4326589 | p.Leu295Val | missense_variant | 0.63 |
| ethR | 4326592 | c.-957G>A | upstream_gene_variant | 0.62 |
| ethR | 4326597 | c.-952A>G | upstream_gene_variant | 1.0 |
| ethR | 4326598 | c.-951T>C | upstream_gene_variant | 0.97 |
| ethR | 4326601 | c.-948C>T | upstream_gene_variant | 0.62 |
| ethR | 4326610 | c.-939G>C | upstream_gene_variant | 1.0 |
| ethA | 4326620 | p.His285Arg | missense_variant | 1.0 |
| ethR | 4326622 | c.-927C>T | upstream_gene_variant | 0.62 |
| ethR | 4326649 | c.-900C>G | upstream_gene_variant | 1.0 |
| ethR | 4326652 | c.-897C>T | upstream_gene_variant | 0.53 |
| ethR | 4327270 | c.-279G>C | upstream_gene_variant | 1.0 |
| ethR | 4327273 | c.-276A>G | upstream_gene_variant | 1.0 |
| ethR | 4327279 | c.-270T>G | upstream_gene_variant | 1.0 |
| ethR | 4327285 | c.-264A>G | upstream_gene_variant | 1.0 |
| ethR | 4327288 | c.-261T>C | upstream_gene_variant | 1.0 |
| ethR | 4327309 | c.-240G>A | upstream_gene_variant | 1.0 |
| ethR | 4327315 | c.-234A>G | upstream_gene_variant | 1.0 |
| ethR | 4327318 | c.-231T>G | upstream_gene_variant | 1.0 |
| ethR | 4327321 | c.-228G>C | upstream_gene_variant | 1.0 |
| ethA | 4327388 | p.Thr29Asn | missense_variant | 0.92 |
| ethR | 4327396 | c.-153A>G | upstream_gene_variant | 1.0 |
| ethR | 4327407 | c.-142G>A | upstream_gene_variant | 1.0 |
| ethA | 4327425 | p.Val17Ile | missense_variant | 1.0 |
| ethR | 4327426 | c.-123A>G | upstream_gene_variant | 1.0 |
| ethR | 4327435 | c.-114T>G | upstream_gene_variant | 1.0 |
| ethR | 4327438 | c.-111A>G | upstream_gene_variant | 1.0 |
| ethR | 4327459 | c.-90G>A | upstream_gene_variant | 1.0 |
| ethR | 4327465 | c.-84C>T | upstream_gene_variant | 1.0 |
| ethA | 4328429 | c.-956C>A | upstream_gene_variant | 1.0 |
| ethA | 4328435 | c.-962C>T | upstream_gene_variant | 1.0 |
| ethA | 4328461 | c.-989_-988delCCinsTG | upstream_gene_variant | 1.0 |
| ethA | 4328470 | c.-998_-997delAGinsGC | upstream_gene_variant | 1.0 |
| ethA | 4328473 | c.-1000G>C | upstream_gene_variant | 1.0 |
| rpoC | 767303 | c.3935_*2482del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |
| fabG1 | 1672169 | c.-1270_64del | frameshift_variant | 1.0 |
| alr | 3841283 | c.-9025_137del | frameshift_variant | 1.0 |
