Run ID: SRR5341422
Sample name:
Date: 18-08-2022 09:29:57
Number of reads: 482114
Percentage reads mapped: 9.63
Strain: lineage2.1
Drug-resistance: HR-TB
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage2.1 | East-Asian (non-Beijing) | None | None | 0.93 |
| lineage4.3.1 | Euro-American (LAM) | LAM9 | None | 0.95 |
| lineage4.1.2 | Euro-American | T;H | None | 0.83 |
| lineage6.3.3 | West-Africa 2 | AFRI_1 | RD702 | 0.91 |
| lineage4.6.5 | Euro-American | T;LAM | None | 0.97 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| katG | 2155693 | p.Ser140Asn | missense_variant | 1.0 | isoniazid |
| katG | 2155734 | c.376_377delAT | frameshift_variant | 1.0 | isoniazid |
| katG | 2155739 | p.Gly125Cys | missense_variant | 1.0 | isoniazid |
| katG | 2155742 | c.369_370insCA | frameshift_variant | 1.0 | isoniazid |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6086 | p.Thr283Glu | missense_variant | 0.9 |
| gyrB | 6091 | c.852G>T | synonymous_variant | 0.9 |
| gyrB | 6097 | c.858G>A | synonymous_variant | 0.92 |
| gyrB | 6100 | c.861G>C | synonymous_variant | 0.92 |
| gyrB | 6110 | p.Met291Leu | missense_variant | 0.95 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 0.95 |
| gyrB | 6127 | c.888G>C | synonymous_variant | 0.96 |
| gyrB | 6160 | c.921C>G | synonymous_variant | 0.97 |
| gyrB | 6169 | c.930C>G | synonymous_variant | 0.97 |
| gyrB | 6172 | c.933C>T | synonymous_variant | 0.97 |
| gyrB | 6181 | c.942C>T | synonymous_variant | 0.97 |
| gyrB | 6203 | p.Ser322Ala | missense_variant | 0.98 |
| gyrB | 6217 | c.978G>C | synonymous_variant | 1.0 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
| gyrB | 6248 | c.1009_1011delCTAinsTTG | synonymous_variant | 1.0 |
| gyrB | 6253 | c.1014G>C | synonymous_variant | 1.0 |
| gyrB | 6265 | c.1026C>T | synonymous_variant | 1.0 |
| gyrB | 6268 | c.1029C>G | synonymous_variant | 1.0 |
| gyrB | 6280 | c.1041T>C | synonymous_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6292 | c.1053G>C | synonymous_variant | 1.0 |
| gyrB | 6295 | c.1056A>G | synonymous_variant | 1.0 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 1.0 |
| gyrA | 6319 | c.-983G>C | upstream_gene_variant | 1.0 |
| gyrB | 6326 | p.Ser363Ala | missense_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.96 |
| gyrA | 6367 | c.-935C>T | upstream_gene_variant | 0.98 |
| gyrA | 6379 | c.-923C>G | upstream_gene_variant | 0.97 |
| gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.97 |
| gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.97 |
| gyrB | 6398 | p.Val387Ile | missense_variant | 0.97 |
| gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.97 |
| gyrA | 6409 | c.-893A>G | upstream_gene_variant | 0.96 |
| gyrB | 6417 | p.Thr393Ser | missense_variant | 0.95 |
| gyrA | 6427 | c.-875T>C | upstream_gene_variant | 0.92 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 1.0 |
| gyrA | 6613 | c.-689A>G | upstream_gene_variant | 1.0 |
| gyrA | 6616 | c.-686A>G | upstream_gene_variant | 1.0 |
| gyrA | 6622 | c.-680C>T | upstream_gene_variant | 1.0 |
| gyrA | 6628 | c.-674C>A | upstream_gene_variant | 1.0 |
| gyrA | 6634 | c.-668T>C | upstream_gene_variant | 1.0 |
| gyrA | 6637 | c.-665T>G | upstream_gene_variant | 1.0 |
| gyrA | 6640 | c.-662A>G | upstream_gene_variant | 1.0 |
| gyrA | 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>C | upstream_gene_variant | 1.0 |
| gyrA | 6680 | c.-622C>T | upstream_gene_variant | 1.0 |
| gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrA | 6724 | c.-578G>C | upstream_gene_variant | 1.0 |
| gyrA | 6727 | c.-575G>C | upstream_gene_variant | 1.0 |
| gyrA | 6730 | c.-572A>G | upstream_gene_variant | 1.0 |
| gyrA | 6742 | c.-560A>G | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
| gyrA | 6751 | c.-551G>C | upstream_gene_variant | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6772 | c.-530C>G | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
| gyrA | 6778 | c.-524C>T | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Ser | missense_variant | 1.0 |
| gyrA | 6802 | c.-500G>A | upstream_gene_variant | 1.0 |
| gyrA | 6811 | c.-491C>T | upstream_gene_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>C | upstream_gene_variant | 1.0 |
| gyrA | 6853 | c.-449A>G | upstream_gene_variant | 1.0 |
| gyrA | 6856 | c.-446T>C | upstream_gene_variant | 1.0 |
| gyrA | 6859 | c.-443T>C | upstream_gene_variant | 1.0 |
| gyrA | 6862 | c.-440C>G | upstream_gene_variant | 1.0 |
| gyrA | 6869 | c.-433T>C | upstream_gene_variant | 1.0 |
| gyrA | 6872 | c.-430T>C | upstream_gene_variant | 1.0 |
| gyrA | 6878 | c.-424T>C | upstream_gene_variant | 1.0 |
| gyrB | 6896 | p.Arg553Lys | missense_variant | 1.0 |
| gyrA | 6904 | c.-398C>G | upstream_gene_variant | 1.0 |
| gyrA | 6916 | c.-386G>C | upstream_gene_variant | 1.0 |
| gyrA | 6919 | c.-383T>C | upstream_gene_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6926 | c.-376T>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 | 7391 | c.90C>T | synonymous_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 7406 | c.105G>C | synonymous_variant | 1.0 |
| gyrA | 7422 | c.121C>T | synonymous_variant | 1.0 |
| gyrA | 7442 | c.141G>C | synonymous_variant | 1.0 |
| gyrA | 7451 | c.150C>G | synonymous_variant | 1.0 |
| gyrA | 7457 | c.156T>C | synonymous_variant | 1.0 |
| gyrA | 7463 | c.162G>C | synonymous_variant | 1.0 |
| gyrA | 7469 | c.168C>G | 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 | 7487 | c.186C>G | synonymous_variant | 1.0 |
| gyrA | 7496 | c.195C>G | synonymous_variant | 0.95 |
| gyrA | 7499 | c.198G>C | synonymous_variant | 0.98 |
| gyrA | 7506 | p.Ser69Gly | missense_variant | 1.0 |
| gyrA | 7514 | c.213C>G | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>A | synonymous_variant | 1.0 |
| gyrA | 7526 | c.225G>A | synonymous_variant | 1.0 |
| gyrA | 7532 | c.231T>C | synonymous_variant | 1.0 |
| gyrA | 7541 | c.240C>G | synonymous_variant | 1.0 |
| gyrA | 7569 | p.Ala90Ser | missense_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7592 | c.291G>C | synonymous_variant | 1.0 |
| gyrA | 7601 | c.300C>G | synonymous_variant | 1.0 |
| gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 7637 | c.336C>T | synonymous_variant | 1.0 |
| gyrA | 7652 | c.351C>T | synonymous_variant | 1.0 |
| gyrA | 7760 | c.459C>T | synonymous_variant | 1.0 |
| gyrA | 7763 | c.462T>G | synonymous_variant | 1.0 |
| gyrA | 7775 | c.474C>G | synonymous_variant | 1.0 |
| gyrA | 7778 | c.477G>C | synonymous_variant | 1.0 |
| gyrA | 7784 | c.483A>G | synonymous_variant | 1.0 |
| gyrA | 7796 | c.495G>C | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7802 | c.501C>G | synonymous_variant | 1.0 |
| gyrA | 7811 | c.510C>T | synonymous_variant | 1.0 |
| gyrA | 7814 | c.513C>G | synonymous_variant | 1.0 |
| gyrA | 7823 | c.522G>C | synonymous_variant | 1.0 |
| gyrA | 7832 | c.531G>C | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>C | synonymous_variant | 1.0 |
| gyrA | 7838 | c.537C>T | synonymous_variant | 1.0 |
| gyrA | 7847 | c.546G>A | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>C | synonymous_variant | 1.0 |
| gyrA | 8156 | c.855T>C | synonymous_variant | 1.0 |
| gyrA | 8168 | c.867A>G | synonymous_variant | 1.0 |
| gyrA | 8177 | c.876A>C | synonymous_variant | 1.0 |
| gyrA | 8198 | c.897T>C | synonymous_variant | 1.0 |
| gyrA | 8201 | c.900C>G | synonymous_variant | 1.0 |
| gyrA | 8207 | c.906T>C | synonymous_variant | 1.0 |
| gyrA | 8213 | c.912C>T | synonymous_variant | 1.0 |
| gyrA | 8219 | c.918T>C | synonymous_variant | 1.0 |
| gyrA | 8222 | c.921C>T | synonymous_variant | 1.0 |
| gyrA | 8225 | c.924T>C | synonymous_variant | 1.0 |
| gyrA | 8228 | c.927G>C | synonymous_variant | 1.0 |
| gyrA | 8234 | c.933T>G | synonymous_variant | 1.0 |
| gyrA | 8237 | c.936A>G | synonymous_variant | 1.0 |
| gyrA | 8247 | p.Ile316Val | missense_variant | 1.0 |
| gyrA | 8253 | p.Ile318Leu | missense_variant | 1.0 |
| gyrA | 8264 | c.963T>C | synonymous_variant | 1.0 |
| gyrA | 8267 | c.966G>C | synonymous_variant | 1.0 |
| gyrA | 8270 | c.969G>C | synonymous_variant | 1.0 |
| gyrA | 8283 | p.Ile328Leu | missense_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8294 | c.993T>C | synonymous_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>G | synonymous_variant | 1.0 |
| gyrA | 8342 | c.1041G>C | synonymous_variant | 1.0 |
| gyrA | 8354 | c.1053G>C | synonymous_variant | 1.0 |
| gyrA | 8372 | c.1071G>C | synonymous_variant | 1.0 |
| gyrA | 8375 | c.1074G>C | synonymous_variant | 1.0 |
| gyrA | 8391 | p.Tyr364His | missense_variant | 1.0 |
| gyrA | 8399 | c.1098T>C | synonymous_variant | 1.0 |
| gyrA | 8400 | p.Asp367Asn | missense_variant | 1.0 |
| gyrA | 8405 | c.1104C>T | synonymous_variant | 1.0 |
| gyrA | 8414 | c.1113C>T | synonymous_variant | 1.0 |
| gyrA | 8420 | c.1119T>C | synonymous_variant | 1.0 |
| gyrA | 8432 | c.1131C>G | synonymous_variant | 1.0 |
| gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
| gyrA | 8459 | c.1158G>A | synonymous_variant | 1.0 |
| gyrA | 8462 | c.1161A>G | synonymous_variant | 1.0 |
| gyrA | 8471 | c.1170T>C | synonymous_variant | 1.0 |
| gyrA | 8480 | c.1179C>T | synonymous_variant | 1.0 |
| gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
| gyrA | 8489 | c.1188A>G | synonymous_variant | 1.0 |
| gyrA | 8498 | c.1197C>T | synonymous_variant | 1.0 |
| gyrA | 8501 | c.1200G>C | synonymous_variant | 1.0 |
| gyrA | 8504 | c.1203G>C | synonymous_variant | 1.0 |
| gyrA | 8513 | c.1212C>G | synonymous_variant | 1.0 |
| gyrA | 8516 | c.1215T>C | synonymous_variant | 1.0 |
| gyrA | 8519 | c.1218A>C | synonymous_variant | 1.0 |
| gyrA | 8546 | c.1245T>C | synonymous_variant | 1.0 |
| gyrA | 8547 | p.Ile416Val | missense_variant | 1.0 |
| gyrA | 8555 | c.1254G>C | synonymous_variant | 1.0 |
| gyrA | 8561 | c.1260A>C | synonymous_variant | 1.0 |
| gyrA | 8571 | c.1270C>T | synonymous_variant | 1.0 |
| gyrA | 8579 | c.1278C>T | synonymous_variant | 1.0 |
| gyrA | 8597 | c.1296C>G | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>C | synonymous_variant | 1.0 |
| gyrA | 8609 | c.1308G>C | synonymous_variant | 1.0 |
| gyrA | 8612 | c.1311C>T | synonymous_variant | 1.0 |
| gyrA | 8619 | c.1318T>C | synonymous_variant | 1.0 |
| gyrA | 8624 | c.1323G>C | synonymous_variant | 1.0 |
| gyrA | 8627 | c.1326C>G | synonymous_variant | 1.0 |
| gyrA | 8630 | c.1329G>C | synonymous_variant | 1.0 |
| gyrA | 8636 | c.1335A>C | synonymous_variant | 1.0 |
| gyrA | 8642 | c.1341A>G | synonymous_variant | 1.0 |
| gyrA | 8645 | c.1344C>T | synonymous_variant | 1.0 |
| gyrA | 8672 | c.1371A>G | synonymous_variant | 1.0 |
| gyrA | 8693 | c.1392T>C | synonymous_variant | 1.0 |
| gyrA | 8696 | c.1395G>C | synonymous_variant | 1.0 |
| gyrA | 8699 | c.1398A>G | synonymous_variant | 1.0 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 1.0 |
| gyrA | 8837 | c.1536C>G | synonymous_variant | 1.0 |
| gyrA | 8843 | c.1542G>A | synonymous_variant | 1.0 |
| gyrA | 8846 | p.Asp515Glu | missense_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 | 8873 | c.1572A>C | synonymous_variant | 1.0 |
| gyrA | 8885 | c.1584C>G | synonymous_variant | 1.0 |
| gyrA | 8892 | p.Thr531Ser | missense_variant | 1.0 |
| gyrA | 8900 | c.1599G>C | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8918 | c.1617C>T | synonymous_variant | 1.0 |
| gyrA | 8924 | c.1623C>T | synonymous_variant | 1.0 |
| gyrA | 8930 | c.1629C>T | synonymous_variant | 1.0 |
| gyrA | 8945 | c.1644G>C | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645T>C | synonymous_variant | 1.0 |
| gyrA | 8967 | p.Ala556Asn | missense_variant | 1.0 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
| gyrA | 9014 | c.1713C>G | synonymous_variant | 1.0 |
| gyrA | 9017 | c.1716C>G | synonymous_variant | 1.0 |
| gyrA | 9023 | c.1722A>C | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>C | synonymous_variant | 1.0 |
| gyrA | 9044 | c.1743C>G | synonymous_variant | 1.0 |
| gyrA | 9051 | c.1750T>C | synonymous_variant | 1.0 |
| gyrA | 9062 | c.1761C>A | synonymous_variant | 1.0 |
| gyrA | 9065 | c.1764C>G | synonymous_variant | 1.0 |
| gyrA | 9068 | c.1767G>C | synonymous_variant | 1.0 |
| gyrA | 9080 | c.1779G>T | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| fgd1 | 491016 | c.234C>G | synonymous_variant | 1.0 |
| fgd1 | 491031 | c.249C>G | synonymous_variant | 1.0 |
| fgd1 | 491034 | c.252C>G | synonymous_variant | 1.0 |
| fgd1 | 491043 | c.261T>C | synonymous_variant | 1.0 |
| fgd1 | 491049 | c.267T>C | synonymous_variant | 1.0 |
| fgd1 | 491064 | c.282A>G | synonymous_variant | 1.0 |
| fgd1 | 491067 | c.285C>T | synonymous_variant | 1.0 |
| fgd1 | 491073 | c.291C>T | synonymous_variant | 1.0 |
| fgd1 | 491076 | c.294G>C | synonymous_variant | 1.0 |
| fgd1 | 491077 | p.Asn99Asp | missense_variant | 1.0 |
| fgd1 | 491082 | c.300T>C | synonymous_variant | 1.0 |
| fgd1 | 491083 | p.Val101Ile | missense_variant | 1.0 |
| fgd1 | 491094 | c.312C>G | synonymous_variant | 1.0 |
| fgd1 | 491115 | c.333G>C | synonymous_variant | 1.0 |
| fgd1 | 491121 | c.339A>G | synonymous_variant | 1.0 |
| fgd1 | 491127 | c.345C>G | synonymous_variant | 1.0 |
| fgd1 | 491144 | p.Ala121Asp | missense_variant | 1.0 |
| fgd1 | 491500 | p.Glu240Lys | missense_variant | 1.0 |
| fgd1 | 491508 | c.726A>G | synonymous_variant | 1.0 |
| fgd1 | 491512 | p.Asn244Glu | missense_variant | 1.0 |
| fgd1 | 491526 | c.744T>C | synonymous_variant | 1.0 |
| fgd1 | 491532 | c.750G>T | synonymous_variant | 1.0 |
| fgd1 | 491538 | c.756G>T | 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 | 491569 | p.Asp263Asn | missense_variant | 1.0 |
| fgd1 | 491577 | c.795G>C | synonymous_variant | 1.0 |
| fgd1 | 491599 | p.Asp273Asn | missense_variant | 1.0 |
| fgd1 | 491603 | p.Ala274Glu | missense_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 | 491641 | p.Ala287Ser | missense_variant | 1.0 |
| fgd1 | 491649 | c.867C>T | synonymous_variant | 1.0 |
| mshA | 575803 | c.456C>T | synonymous_variant | 1.0 |
| mshA | 575833 | c.486C>T | synonymous_variant | 1.0 |
| mshA | 575842 | c.495G>A | synonymous_variant | 1.0 |
| mshA | 575845 | c.498C>G | synonymous_variant | 1.0 |
| mshA | 575848 | c.501C>T | synonymous_variant | 1.0 |
| mshA | 575851 | c.504C>G | synonymous_variant | 1.0 |
| mshA | 575864 | c.517_519delTTGinsCTC | synonymous_variant | 1.0 |
| mshA | 575875 | c.528C>G | synonymous_variant | 1.0 |
| mshA | 575878 | c.531A>G | 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 | 575939 | c.592C>T | synonymous_variant | 1.0 |
| rpoB | 760060 | p.Tyr85Ser | missense_variant | 1.0 |
| rpoB | 760067 | c.261G>C | synonymous_variant | 1.0 |
| rpoB | 760070 | c.264T>G | synonymous_variant | 1.0 |
| rpoB | 760088 | c.282C>G | synonymous_variant | 1.0 |
| rpoB | 760091 | c.285G>T | synonymous_variant | 1.0 |
| rpoB | 760094 | c.288G>C | synonymous_variant | 1.0 |
| rpoB | 760101 | c.295T>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 | 760139 | c.333A>C | synonymous_variant | 1.0 |
| rpoB | 760142 | c.336C>G | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>G | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760244 | c.438G>C | synonymous_variant | 1.0 |
| rpoB | 760253 | c.447T>C | synonymous_variant | 1.0 |
| rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>T | synonymous_variant | 1.0 |
| rpoB | 760316 | c.510C>G | synonymous_variant | 1.0 |
| rpoB | 760317 | c.511_512delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
| rpoB | 760331 | c.525G>C | synonymous_variant | 1.0 |
| rpoB | 760337 | c.531C>G | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534G>T | synonymous_variant | 1.0 |
| rpoB | 760357 | p.Thr184Ser | missense_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_variant | 1.0 |
| rpoB | 760407 | p.Ser201Gly | missense_variant | 1.0 |
| rpoB | 760415 | c.609C>T | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760454 | c.648C>G | synonymous_variant | 1.0 |
| rpoB | 760463 | c.657C>T | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760478 | c.672C>T | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>T | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760487 | c.681G>C | synonymous_variant | 1.0 |
| rpoB | 760508 | c.702G>A | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760535 | c.729C>G | synonymous_variant | 1.0 |
| rpoB | 760541 | c.735G>C | synonymous_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760561 | c.757_758delCG | frameshift_variant | 1.0 |
| rpoB | 760567 | p.Ser254Trp | missense_variant | 1.0 |
| rpoB | 760568 | c.762_763insGC | frameshift_variant | 1.0 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760634 | c.828T>C | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
| rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760736 | c.930C>G | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>T | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 0.97 |
| rpoB | 760961 | c.1155C>G | synonymous_variant | 0.97 |
| rpoB | 760965 | p.Met387Leu | missense_variant | 0.97 |
| rpoB | 760970 | c.1164G>C | synonymous_variant | 0.97 |
| rpoB | 760973 | c.1167G>C | synonymous_variant | 0.97 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 0.97 |
| rpoB | 760985 | c.1179G>C | synonymous_variant | 0.97 |
| rpoB | 760988 | c.1182C>G | synonymous_variant | 0.97 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 0.97 |
| rpoB | 761003 | c.1197C>G | synonymous_variant | 0.98 |
| rpoB | 761006 | c.1200C>T | synonymous_variant | 0.98 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 0.98 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 0.98 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 0.98 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 0.98 |
| rpoB | 761051 | c.1245G>T | synonymous_variant | 0.97 |
| rpoB | 761054 | c.1248G>C | synonymous_variant | 0.97 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 0.97 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 0.97 |
| rpoB | 761063 | c.1257C>G | synonymous_variant | 0.97 |
| 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 | 761132 | c.1326G>C | synonymous_variant | 1.0 |
| rpoB | 761147 | c.1341C>T | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>T | synonymous_variant | 1.0 |
| rpoB | 761153 | c.1347G>C | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>C | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761198 | c.1392G>C | synonymous_variant | 1.0 |
| rpoB | 761204 | c.1398C>G | synonymous_variant | 1.0 |
| rpoB | 761217 | p.Pro471Ser | missense_variant | 1.0 |
| rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 1.0 |
| rpoB | 761234 | c.1428G>C | 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 | 761258 | c.1452G>A | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>C | synonymous_variant | 1.0 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
| rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
| rpoB | 761306 | c.1500C>G | synonymous_variant | 1.0 |
| rpoB | 761312 | c.1506G>C | synonymous_variant | 1.0 |
| rpoB | 761318 | c.1512G>C | synonymous_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761333 | c.1527G>C | synonymous_variant | 1.0 |
| rpoB | 761345 | c.1539G>C | synonymous_variant | 1.0 |
| rpoB | 761346 | p.Val514Lys | missense_variant | 1.0 |
| rpoB | 761357 | c.1551G>C | synonymous_variant | 1.0 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761369 | p.Glu521Asp | missense_variant | 1.0 |
| rpoB | 761374 | p.Val523Glu | missense_variant | 1.0 |
| rpoB | 761408 | c.1602G>C | synonymous_variant | 1.0 |
| rpoB | 761414 | c.1608A>G | synonymous_variant | 1.0 |
| rpoB | 761516 | c.1710G>C | synonymous_variant | 1.0 |
| rpoB | 761531 | c.1725C>G | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761555 | c.1749G>C | synonymous_variant | 1.0 |
| rpoB | 761558 | c.1752C>G | synonymous_variant | 1.0 |
| rpoB | 761561 | c.1755C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | 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 | 761600 | c.1794T>C | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>T | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>G | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761657 | c.1851C>G | synonymous_variant | 1.0 |
| rpoB | 761666 | c.1860G>C | 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 | 761741 | c.1935G>A | synonymous_variant | 1.0 |
| rpoB | 761747 | c.1941G>A | synonymous_variant | 1.0 |
| rpoB | 761750 | c.1944G>C | synonymous_variant | 1.0 |
| rpoB | 761765 | c.1959T>C | synonymous_variant | 1.0 |
| rpoB | 761772 | p.His656Ala | missense_variant | 1.0 |
| rpoB | 761778 | p.Asn658Asp | missense_variant | 1.0 |
| rpoB | 761791 | p.Arg662His | missense_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761816 | c.2010C>G | 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 | 761858 | c.2052G>C | synonymous_variant | 1.0 |
| rpoB | 761864 | c.2058G>C | synonymous_variant | 1.0 |
| rpoB | 761873 | c.2067A>G | synonymous_variant | 1.0 |
| rpoB | 761876 | c.2070C>G | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761906 | c.2100C>G | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761915 | p.Asp703Glu | missense_variant | 1.0 |
| rpoB | 761916 | p.Asp704Asn | missense_variant | 1.0 |
| rpoB | 761930 | c.2124G>A | synonymous_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761972 | c.2166C>T | synonymous_variant | 1.0 |
| rpoB | 761999 | c.2193G>C | synonymous_variant | 1.0 |
| rpoB | 762002 | c.2196C>G | synonymous_variant | 1.0 |
| rpoB | 762008 | c.2202C>T | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
| rpoB | 762038 | c.2232C>T | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 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 | 762158 | c.2352G>T | synonymous_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762218 | c.2412T>C | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762251 | c.2445G>A | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762275 | c.2469C>G | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>G | synonymous_variant | 1.0 |
| rpoB | 762299 | c.2493G>C | synonymous_variant | 0.95 |
| rpoB | 762311 | c.2505C>T | synonymous_variant | 1.0 |
| rpoB | 762314 | c.2508C>T | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 0.9 |
| rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.9 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.9 |
| rpoC | 762431 | c.-939C>T | upstream_gene_variant | 0.91 |
| rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.91 |
| rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.85 |
| rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.87 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.92 |
| rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.96 |
| rpoC | 762491 | c.-879T>C | upstream_gene_variant | 0.96 |
| rpoC | 762503 | c.-867G>C | upstream_gene_variant | 0.96 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.96 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 0.96 |
| rpoC | 762521 | c.-849C>G | upstream_gene_variant | 0.96 |
| rpoC | 762524 | c.-846G>C | upstream_gene_variant | 0.96 |
| rpoC | 762527 | c.-843G>C | upstream_gene_variant | 0.96 |
| rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.96 |
| rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.96 |
| rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.96 |
| rpoC | 762545 | c.-825C>G | upstream_gene_variant | 0.96 |
| rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.96 |
| rpoC | 762581 | c.-789T>C | upstream_gene_variant | 0.92 |
| rpoC | 762582 | c.-788T>C | upstream_gene_variant | 0.9 |
| rpoB | 762761 | p.Cys985Trp | missense_variant | 1.0 |
| rpoC | 762782 | c.-588T>C | upstream_gene_variant | 1.0 |
| rpoB | 762786 | p.Val994Thr | missense_variant | 1.0 |
| rpoC | 762791 | c.-579G>C | upstream_gene_variant | 1.0 |
| rpoB | 762799 | p.Ala998Gly | missense_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762894 | c.-476C>T | upstream_gene_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.98 |
| rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.98 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.98 |
| rpoC | 762947 | c.-423C>T | upstream_gene_variant | 0.99 |
| rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.99 |
| rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.99 |
| rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.99 |
| 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 | 763052 | c.-318G>C | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>A | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
| rpoC | 763139 | c.-231C>T | upstream_gene_variant | 1.0 |
| rpoC | 763160 | c.-210G>T | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763169 | c.-201A>G | upstream_gene_variant | 1.0 |
| rpoC | 763172 | c.-198G>T | upstream_gene_variant | 1.0 |
| rpoC | 763202 | c.-168A>G | upstream_gene_variant | 0.97 |
| rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 0.97 |
| rpoC | 763217 | c.-153G>C | upstream_gene_variant | 0.97 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.97 |
| rpoB | 763227 | p.Leu1141Met | missense_variant | 0.97 |
| rpoB | 763235 | p.Glu1143Asp | missense_variant | 0.97 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.97 |
| rpoB | 763241 | p.Glu1145Asp | missense_variant | 0.97 |
| rpoC | 763259 | c.-111G>C | upstream_gene_variant | 0.95 |
| rpoC | 763262 | c.-108C>T | upstream_gene_variant | 0.95 |
| rpoC | 763265 | c.-105G>C | upstream_gene_variant | 0.95 |
| rpoC | 763268 | c.-102C>G | upstream_gene_variant | 0.95 |
| rpoC | 763283 | c.-87T>C | upstream_gene_variant | 0.93 |
| rpoC | 763373 | c.4_6delCTCinsTTA | synonymous_variant | 1.0 |
| rpoC | 763402 | c.33C>G | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>C | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>G | synonymous_variant | 0.97 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 0.97 |
| rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 0.97 |
| rpoC | 763433 | p.Gln22Asn | missense_variant | 0.89 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 0.98 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 0.98 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 0.99 |
| rpoC | 763486 | c.117T>A | synonymous_variant | 0.99 |
| rpoC | 763492 | c.123G>C | synonymous_variant | 0.99 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>T | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763615 | c.246G>C | synonymous_variant | 1.0 |
| rpoC | 763618 | c.249C>T | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>T | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763735 | c.366G>A | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>G | synonymous_variant | 1.0 |
| rpoC | 763781 | p.Ser138Ala | missense_variant | 1.0 |
| rpoC | 763792 | p.Glu141Asp | missense_variant | 0.99 |
| 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 | 0.98 |
| rpoC | 763816 | c.447C>G | synonymous_variant | 0.98 |
| rpoC | 763831 | c.462A>G | synonymous_variant | 0.96 |
| rpoC | 763837 | c.468G>C | synonymous_variant | 0.96 |
| rpoC | 763840 | c.471G>C | synonymous_variant | 0.96 |
| rpoC | 763852 | c.483C>T | synonymous_variant | 0.93 |
| rpoC | 763858 | c.489A>G | synonymous_variant | 0.92 |
| rpoC | 763861 | c.492C>T | synonymous_variant | 0.92 |
| rpoC | 763872 | p.Gly168Ala | missense_variant | 0.92 |
| rpoC | 763876 | p.Glu169Asp | missense_variant | 0.92 |
| rpoC | 763879 | c.510A>G | synonymous_variant | 0.92 |
| rpoC | 763894 | c.525A>G | synonymous_variant | 0.92 |
| rpoC | 763900 | c.531G>C | synonymous_variant | 0.9 |
| rpoC | 763910 | p.Leu181Met | missense_variant | 0.86 |
| rpoC | 763913 | p.Ala182Lys | missense_variant | 0.86 |
| rpoC | 763921 | c.552G>C | synonymous_variant | 0.86 |
| rpoC | 763926 | p.Ala186Asp | missense_variant | 0.86 |
| rpoC | 763940 | p.Ala191Ser | missense_variant | 0.9 |
| rpoC | 763944 | c.576_579delTGCG | frameshift_variant | 0.9 |
| rpoC | 763950 | c.581_582insTCAA | frameshift_variant | 0.9 |
| rpoC | 763960 | c.591T>G | synonymous_variant | 0.96 |
| rpoC | 763963 | c.594C>T | synonymous_variant | 0.96 |
| rpoC | 763987 | c.618C>T | synonymous_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764002 | c.633C>G | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_variant | 1.0 |
| rpoC | 764011 | c.642T>C | synonymous_variant | 1.0 |
| rpoC | 764023 | c.654G>T | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764032 | p.Asp221Glu | missense_variant | 1.0 |
| rpoC | 764040 | p.Ser224Thr | missense_variant | 0.97 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 0.97 |
| rpoC | 764059 | c.690G>T | synonymous_variant | 0.98 |
| rpoC | 764071 | c.702G>C | synonymous_variant | 0.98 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 0.98 |
| rpoC | 764084 | p.Asn239Val | missense_variant | 0.97 |
| rpoC | 764098 | c.729A>G | synonymous_variant | 0.97 |
| rpoC | 764107 | c.738C>T | synonymous_variant | 0.98 |
| rpoC | 764147 | p.Ser260Ala | missense_variant | 0.97 |
| rpoC | 764153 | p.Gln262Lys | missense_variant | 0.97 |
| rpoC | 764161 | c.792G>C | synonymous_variant | 0.97 |
| rpoC | 764170 | c.801C>T | synonymous_variant | 1.0 |
| rpoC | 764182 | c.813C>T | synonymous_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764194 | c.825G>A | synonymous_variant | 1.0 |
| rpoC | 764195 | p.Ser276Glu | missense_variant | 1.0 |
| rpoC | 764203 | c.834G>C | synonymous_variant | 1.0 |
| rpoC | 764206 | c.837T>C | synonymous_variant | 1.0 |
| rpoC | 764209 | c.840C>G | synonymous_variant | 1.0 |
| rpoC | 764215 | c.846A>T | synonymous_variant | 1.0 |
| rpoC | 764227 | c.858G>C | synonymous_variant | 1.0 |
| rpoC | 764242 | c.873C>T | synonymous_variant | 1.0 |
| rpoC | 764245 | c.876C>T | synonymous_variant | 1.0 |
| rpoC | 764248 | c.879C>G | synonymous_variant | 1.0 |
| rpoC | 764254 | c.885G>C | synonymous_variant | 1.0 |
| rpoC | 764263 | c.894G>C | synonymous_variant | 1.0 |
| rpoC | 764266 | c.897T>C | synonymous_variant | 0.96 |
| rpoC | 764275 | c.909_911delACA | disruptive_inframe_deletion | 1.0 |
| rpoC | 764320 | c.951C>T | synonymous_variant | 0.97 |
| rpoC | 764341 | c.972G>T | synonymous_variant | 0.94 |
| rpoC | 764353 | c.984G>T | synonymous_variant | 0.95 |
| rpoC | 764359 | c.990C>T | synonymous_variant | 0.95 |
| rpoC | 764362 | c.993C>T | synonymous_variant | 0.94 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 0.95 |
| rpoC | 764371 | c.1002G>C | synonymous_variant | 0.95 |
| rpoC | 764377 | c.1008C>G | synonymous_variant | 0.95 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 0.96 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 0.96 |
| rpoC | 764401 | c.1032C>T | synonymous_variant | 0.96 |
| rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 0.98 |
| rpoC | 764410 | c.1041G>C | synonymous_variant | 0.98 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 0.98 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 0.98 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 0.98 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 0.98 |
| rpoC | 764452 | c.1083T>C | synonymous_variant | 0.98 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
| rpoC | 764491 | c.1122G>T | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764500 | c.1131C>G | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764578 | c.1209C>G | synonymous_variant | 1.0 |
| rpoC | 764585 | c.1216_1218delCTCinsTTG | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
| rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
| rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764844 | p.Ala492Gly | missense_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>G | synonymous_variant | 1.0 |
| rpoC | 764878 | c.1509C>G | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764893 | c.1524T>C | synonymous_variant | 1.0 |
| rpoC | 764896 | c.1527C>T | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
| rpoC | 764917 | c.1548G>C | synonymous_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764983 | c.1614T>C | synonymous_variant | 1.0 |
| rpoC | 765004 | c.1635G>T | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765008 | c.1639T>C | synonymous_variant | 1.0 |
| rpoC | 765011 | c.1642_1644delAGCinsTCG | synonymous_variant | 1.0 |
| rpoC | 765016 | c.1647C>G | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 0.93 |
| 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 | 765055 | c.1686C>G | synonymous_variant | 1.0 |
| rpoC | 765079 | c.1710T>G | synonymous_variant | 1.0 |
| rpoC | 765292 | c.1923G>T | synonymous_variant | 0.92 |
| rpoC | 765298 | c.1929G>C | synonymous_variant | 0.92 |
| rpoC | 765300 | p.Val644Ala | missense_variant | 0.92 |
| rpoC | 765319 | c.1950A>G | synonymous_variant | 0.91 |
| rpoC | 765364 | p.Glu665Asp | missense_variant | 0.92 |
| rpoC | 765397 | c.2028G>T | synonymous_variant | 1.0 |
| rpoC | 765400 | c.2031G>C | synonymous_variant | 1.0 |
| rpoC | 765405 | p.Leu679Gln | missense_variant | 1.0 |
| rpoC | 765408 | p.Gly680Ala | missense_variant | 1.0 |
| rpoC | 765425 | p.Lys686Glu | missense_variant | 1.0 |
| rpoC | 765439 | c.2070G>A | synonymous_variant | 1.0 |
| rpoC | 765451 | c.2082C>G | synonymous_variant | 1.0 |
| rpoC | 765452 | p.Ala695Arg | missense_variant | 1.0 |
| rpoC | 765458 | p.Ile697Val | missense_variant | 1.0 |
| rpoC | 765466 | c.2097C>T | 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 | 765505 | c.2136C>G | synonymous_variant | 1.0 |
| rpoC | 765508 | c.2139C>G | synonymous_variant | 1.0 |
| rpoC | 765754 | p.Asp795Glu | missense_variant | 1.0 |
| rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
| rpoC | 765778 | c.2409C>G | synonymous_variant | 1.0 |
| rpoC | 765779 | p.Asp804Lys | missense_variant | 1.0 |
| rpoC | 765784 | c.2415C>G | synonymous_variant | 1.0 |
| rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
| rpoC | 765800 | p.Phe811Leu | missense_variant | 1.0 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
| rpoC | 765814 | c.2445A>C | synonymous_variant | 1.0 |
| rpoC | 765823 | c.2454C>G | synonymous_variant | 1.0 |
| rpoC | 765826 | c.2457T>C | synonymous_variant | 1.0 |
| rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765904 | c.2535C>G | synonymous_variant | 1.0 |
| rpoC | 765934 | c.2565C>T | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>G | synonymous_variant | 1.0 |
| rpoC | 765946 | c.2577C>T | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
| rpoC | 765958 | c.2589C>G | synonymous_variant | 1.0 |
| rpoC | 765961 | c.2592G>A | synonymous_variant | 1.0 |
| rpoC | 765962 | c.2593_2595delTTGinsCTT | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765973 | c.2604C>T | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766009 | c.2640G>C | synonymous_variant | 1.0 |
| rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 766369 | c.3000C>G | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
| rpoC | 766393 | c.3024C>G | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>G | synonymous_variant | 1.0 |
| rpoC | 766411 | c.3042C>G | synonymous_variant | 1.0 |
| rpoC | 766442 | p.Thr1025Val | missense_variant | 1.0 |
| rpoC | 766459 | c.3090G>C | synonymous_variant | 1.0 |
| rpoC | 766483 | c.3114G>T | synonymous_variant | 1.0 |
| rpoC | 766484 | p.Val1039Ile | missense_variant | 1.0 |
| rpoC | 766494 | p.Gly1042Asp | missense_variant | 1.0 |
| rpoC | 766645 | p.Glu1092Asp | missense_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 | 766666 | c.3297C>G | synonymous_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766720 | c.3351C>T | synonymous_variant | 1.0 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766735 | c.3366G>T | synonymous_variant | 1.0 |
| rpoC | 766738 | c.3369G>T | synonymous_variant | 1.0 |
| rpoC | 766741 | c.3372G>C | synonymous_variant | 1.0 |
| rpoC | 766747 | c.3378C>T | synonymous_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766771 | c.3402G>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766775 | p.Arg1136Lys | missense_variant | 1.0 |
| rpoC | 766801 | c.3432C>T | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766807 | c.3438T>C | synonymous_variant | 1.0 |
| rpoC | 766837 | c.3468G>C | synonymous_variant | 1.0 |
| rpoC | 766843 | c.3474T>C | synonymous_variant | 1.0 |
| rpoC | 766846 | c.3477C>G | synonymous_variant | 1.0 |
| rpoC | 766858 | c.3489C>G | synonymous_variant | 1.0 |
| rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
| rpoC | 766864 | c.3495G>C | synonymous_variant | 1.0 |
| rpoC | 766867 | c.3498C>G | synonymous_variant | 1.0 |
| rpoC | 766876 | c.3507C>T | synonymous_variant | 1.0 |
| rpoC | 766882 | c.3513C>T | synonymous_variant | 1.0 |
| rpoC | 766883 | p.Ser1172Ala | missense_variant | 1.0 |
| rpoC | 766894 | c.3525T>C | synonymous_variant | 1.0 |
| rpoC | 766895 | c.3526T>C | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766911 | p.Ile1181Thr | missense_variant | 1.0 |
| rpoC | 766915 | p.Asp1182Glu | missense_variant | 1.0 |
| rpoC | 766920 | p.Ala1184Gly | missense_variant | 0.96 |
| rpoC | 766931 | p.Ala1188Thr | missense_variant | 1.0 |
| rpoC | 766942 | c.3573C>T | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>G | synonymous_variant | 1.0 |
| rpoC | 766951 | c.3582G>C | synonymous_variant | 1.0 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
| rpoC | 766975 | c.3606C>G | synonymous_variant | 1.0 |
| rpoC | 766978 | c.3609C>T | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767008 | c.3639G>A | synonymous_variant | 1.0 |
| rpoC | 767020 | c.3651C>G | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
| rpoC | 767068 | c.3699G>C | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767104 | c.3735C>G | synonymous_variant | 1.0 |
| rpoC | 767105 | p.Asn1246Gln | missense_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767167 | c.3798C>G | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767200 | c.3831G>A | synonymous_variant | 1.0 |
| rpoC | 767203 | c.3834C>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 | 767230 | c.3861G>C | synonymous_variant | 1.0 |
| rpoC | 767233 | c.3864T>C | synonymous_variant | 1.0 |
| rpsL | 781571 | c.12C>T | 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.Ser17Ala | missense_variant | 1.0 |
| rpsL | 781616 | c.57C>G | synonymous_variant | 1.0 |
| rpsL | 781622 | c.63C>T | synonymous_variant | 1.0 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781652 | c.93T>C | synonymous_variant | 1.0 |
| rpsL | 781655 | c.96T>A | synonymous_variant | 1.0 |
| rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781709 | c.150G>C | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>C | 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 | 781751 | c.192G>C | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>C | synonymous_variant | 1.0 |
| rpsL | 781880 | c.321C>G | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781895 | c.336G>A | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>G | synonymous_variant | 1.0 |
| rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>C | upstream_gene_variant | 1.0 |
| rplC | 800690 | c.-119C>T | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.98 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.98 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.98 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.98 |
| rplC | 800744 | c.-65G>T | upstream_gene_variant | 0.97 |
| rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.94 |
| rplC | 800762 | c.-47T>G | upstream_gene_variant | 0.94 |
| rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.91 |
| rplC | 800904 | c.96G>C | synonymous_variant | 1.0 |
| rplC | 800913 | c.105G>C | synonymous_variant | 1.0 |
| rplC | 800916 | c.108A>C | synonymous_variant | 1.0 |
| rplC | 800928 | c.120C>T | synonymous_variant | 1.0 |
| rplC | 800931 | c.123G>A | 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 | 800950 | c.142_144delAGCinsTCG | synonymous_variant | 1.0 |
| rplC | 800964 | c.156G>C | synonymous_variant | 1.0 |
| rplC | 800967 | c.159C>G | synonymous_variant | 1.0 |
| rplC | 800970 | c.162T>C | synonymous_variant | 1.0 |
| rplC | 800994 | c.186C>G | synonymous_variant | 1.0 |
| rplC | 801004 | p.Leu66Val | missense_variant | 1.0 |
| rplC | 801009 | c.201A>G | synonymous_variant | 1.0 |
| rplC | 801127 | p.Ala107Ser | missense_variant | 1.0 |
| rplC | 801132 | c.324T>C | synonymous_variant | 1.0 |
| rplC | 801137 | p.Ser110Thr | missense_variant | 1.0 |
| rplC | 801141 | c.333C>T | synonymous_variant | 1.0 |
| rplC | 801147 | c.339T>C | synonymous_variant | 1.0 |
| rplC | 801156 | c.348T>G | synonymous_variant | 1.0 |
| rplC | 801162 | c.354C>G | synonymous_variant | 1.0 |
| rplC | 801168 | c.360C>T | synonymous_variant | 1.0 |
| rplC | 801171 | c.363A>G | synonymous_variant | 1.0 |
| rplC | 801174 | c.366T>C | synonymous_variant | 1.0 |
| rplC | 801195 | c.387G>T | synonymous_variant | 1.0 |
| rplC | 801205 | c.397_399delCGCinsAGG | synonymous_variant | 1.0 |
| rplC | 801210 | c.402T>C | synonymous_variant | 1.0 |
| rplC | 801222 | c.414T>C | synonymous_variant | 1.0 |
| rplC | 801249 | c.441T>C | synonymous_variant | 1.0 |
| rplC | 801255 | c.447C>T | synonymous_variant | 1.0 |
| fbiC | 1303464 | c.534A>G | synonymous_variant | 0.92 |
| fbiC | 1303470 | c.540T>G | synonymous_variant | 0.94 |
| fbiC | 1303480 | p.Gln184Glu | missense_variant | 0.95 |
| fbiC | 1303492 | c.562T>C | synonymous_variant | 0.97 |
| fbiC | 1303500 | c.570C>T | synonymous_variant | 0.97 |
| fbiC | 1303509 | c.579G>C | synonymous_variant | 0.98 |
| fbiC | 1303512 | c.582T>C | synonymous_variant | 0.98 |
| fbiC | 1303531 | p.Met201Leu | missense_variant | 0.98 |
| fbiC | 1303536 | c.606G>C | synonymous_variant | 0.98 |
| fbiC | 1303539 | c.609G>C | synonymous_variant | 0.98 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 0.98 |
| fbiC | 1303581 | c.651G>C | synonymous_variant | 0.96 |
| fbiC | 1303584 | c.654C>G | synonymous_variant | 0.96 |
| fbiC | 1303590 | c.660A>G | synonymous_variant | 0.98 |
| fbiC | 1303602 | c.672A>G | synonymous_variant | 0.97 |
| fbiC | 1303611 | c.681G>T | synonymous_variant | 0.96 |
| fbiC | 1303614 | c.684C>G | synonymous_variant | 0.96 |
| fbiC | 1304496 | c.1566T>C | synonymous_variant | 0.92 |
| fbiC | 1304499 | c.1569T>G | synonymous_variant | 0.92 |
| fbiC | 1304503 | c.1573C>T | synonymous_variant | 0.93 |
| fbiC | 1304508 | p.Glu526Asp | missense_variant | 0.94 |
| fbiC | 1304520 | c.1590A>G | synonymous_variant | 0.96 |
| fbiC | 1304526 | c.1596T>A | synonymous_variant | 0.96 |
| fbiC | 1304533 | c.1603T>C | synonymous_variant | 0.97 |
| fbiC | 1304547 | c.1617C>G | synonymous_variant | 1.0 |
| fbiC | 1304550 | c.1620C>G | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304562 | c.1632G>C | synonymous_variant | 1.0 |
| fbiC | 1304565 | c.1635C>G | synonymous_variant | 1.0 |
| fbiC | 1304568 | c.1638T>C | synonymous_variant | 1.0 |
| fbiC | 1304571 | c.1641G>C | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>G | synonymous_variant | 1.0 |
| fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.99 |
| fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.99 |
| fbiC | 1304652 | c.1722C>G | synonymous_variant | 0.99 |
| fbiC | 1304675 | p.Gly582Asp | missense_variant | 0.99 |
| fbiC | 1304694 | c.1764A>G | synonymous_variant | 0.98 |
| fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.98 |
| fbiC | 1304706 | c.1776C>T | synonymous_variant | 0.98 |
| fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.98 |
| fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.98 |
| fbiC | 1304742 | c.1812T>G | synonymous_variant | 0.98 |
| fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.98 |
| fbiC | 1304751 | c.1821C>G | synonymous_variant | 0.96 |
| 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>G | synonymous_variant | 1.0 |
| fbiC | 1304790 | c.1860C>G | synonymous_variant | 1.0 |
| fbiC | 1304797 | p.Ala623Lys | missense_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 | 1304826 | c.1896G>C | synonymous_variant | 1.0 |
| fbiC | 1304829 | c.1899T>C | synonymous_variant | 1.0 |
| fbiC | 1304832 | c.1902C>G | synonymous_variant | 1.0 |
| fbiC | 1304856 | c.1926C>T | synonymous_variant | 1.0 |
| fbiC | 1304946 | c.2016G>C | synonymous_variant | 1.0 |
| fbiC | 1304949 | c.2019C>T | synonymous_variant | 1.0 |
| fbiC | 1304958 | c.2028T>C | synonymous_variant | 1.0 |
| fbiC | 1304991 | c.2061G>A | 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 | 1305007 | p.Ile693Val | missense_variant | 1.0 |
| fbiC | 1305012 | c.2082G>C | synonymous_variant | 1.0 |
| fbiC | 1305015 | c.2085G>C | synonymous_variant | 1.0 |
| fbiC | 1305024 | c.2094C>T | synonymous_variant | 1.0 |
| fbiC | 1305030 | c.2100G>C | synonymous_variant | 1.0 |
| fbiC | 1305033 | c.2103T>C | synonymous_variant | 1.0 |
| atpE | 1461131 | c.87T>C | synonymous_variant | 1.0 |
| atpE | 1461132 | p.Val30Ile | missense_variant | 1.0 |
| atpE | 1461137 | c.93C>G | synonymous_variant | 1.0 |
| atpE | 1461149 | c.105T>G | synonymous_variant | 1.0 |
| atpE | 1461153 | p.Ser37Ala | missense_variant | 1.0 |
| atpE | 1461159 | p.Val39Ile | missense_variant | 1.0 |
| atpE | 1461167 | c.123G>T | synonymous_variant | 1.0 |
| atpE | 1461170 | c.126A>G | synonymous_variant | 1.0 |
| atpE | 1461179 | c.135G>T | synonymous_variant | 1.0 |
| atpE | 1461182 | c.138A>G | synonymous_variant | 1.0 |
| atpE | 1461185 | c.141G>C | synonymous_variant | 1.0 |
| atpE | 1461188 | c.144G>T | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>C | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461233 | c.189A>G | synonymous_variant | 1.0 |
| atpE | 1461251 | c.207G>C | synonymous_variant | 1.0 |
| atpE | 1461254 | c.210T>C | 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 | 1471926 | n.81C>T | 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 | 1471986 | n.141C>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 | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472327 | n.482G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472452 | n.607G>A | 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 | 0.99 |
| rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472973 | n.1128A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473670 | n.13A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473728 | n.71A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473788 | n.131A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473807 | n.150T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473813 | n.156C>A | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230T>G | 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 | 1.0 |
| rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474293 | n.637_647delCCTCTCCGGAG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474374 | n.717T>G | non_coding_transcript_exon_variant | 0.95 |
| rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1474629 | n.972G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474631 | n.974G>T | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474709 | n.1053_1059delTGGTGTA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474720 | n.1063C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475031 | n.1374G>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 | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475376 | n.1719A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475377 | n.1720G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475380 | n.1723C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475394 | n.1740_1743delGCTC | 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 | 1475430 | n.1773T>G | 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 | 1475480 | n.1823A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476105 | n.2448G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476665 | n.3008T>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 | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 1.0 |
| inhA | 1673706 | c.-496C>A | upstream_gene_variant | 1.0 |
| fabG1 | 1673710 | p.Leu91Ile | missense_variant | 1.0 |
| fabG1 | 1673716 | p.Ala93Lys | missense_variant | 1.0 |
| fabG1 | 1673728 | p.Leu97Met | missense_variant | 1.0 |
| fabG1 | 1673733 | p.Met98Ile | missense_variant | 1.0 |
| inhA | 1673748 | c.-454A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673749 | p.Lys104Arg | missense_variant | 1.0 |
| inhA | 1673757 | c.-445G>A | upstream_gene_variant | 1.0 |
| fabG1 | 1673758 | p.Lys107Glu | missense_variant | 1.0 |
| fabG1 | 1673770 | p.Ala111Thr | missense_variant | 1.0 |
| inhA | 1673784 | c.-418G>T | upstream_gene_variant | 1.0 |
| fabG1 | 1674006 | p.Asp189Glu | missense_variant | 1.0 |
| inhA | 1674024 | c.-178T>C | upstream_gene_variant | 1.0 |
| inhA | 1674030 | c.-172G>C | upstream_gene_variant | 1.0 |
| inhA | 1674033 | c.-169T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1674037 | p.Gln200Glu | missense_variant | 1.0 |
| inhA | 1674042 | c.-160G>T | upstream_gene_variant | 1.0 |
| fabG1 | 1674049 | p.Gln204Asp | missense_variant | 1.0 |
| inhA | 1674054 | c.-148T>C | upstream_gene_variant | 1.0 |
| inhA | 1674060 | c.-142A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1674079 | p.Pro214Ala | missense_variant | 1.0 |
| fabG1 | 1674083 | p.Ala215Glu | missense_variant | 0.95 |
| inhA | 1674090 | c.-112C>G | upstream_gene_variant | 1.0 |
| inhA | 1674096 | c.-106G>C | upstream_gene_variant | 1.0 |
| fabG1 | 1674098 | p.Val220Ala | missense_variant | 1.0 |
| inhA | 1674114 | c.-88T>A | upstream_gene_variant | 1.0 |
| fabG1 | 1674119 | p.Glu227Gly | missense_variant | 1.0 |
| inhA | 1674123 | c.-79T>C | upstream_gene_variant | 1.0 |
| inhA | 1674279 | c.78A>C | synonymous_variant | 1.0 |
| inhA | 1674280 | p.Arg27Lys | missense_variant | 1.0 |
| inhA | 1674285 | c.84A>G | synonymous_variant | 1.0 |
| inhA | 1674288 | c.87C>G | synonymous_variant | 1.0 |
| inhA | 1674295 | p.Gln32Ala | missense_variant | 1.0 |
| inhA | 1674313 | c.112_114delCTCinsTTG | synonymous_variant | 1.0 |
| inhA | 1674334 | p.Arg45Lys | missense_variant | 1.0 |
| inhA | 1674342 | c.141T>C | synonymous_variant | 1.0 |
| inhA | 1674352 | p.Thr51Ala | missense_variant | 1.0 |
| inhA | 1674363 | c.162G>T | synonymous_variant | 1.0 |
| inhA | 1674368 | p.Ala56Glu | missense_variant | 1.0 |
| inhA | 1674471 | c.270G>C | synonymous_variant | 1.0 |
| inhA | 1674473 | p.Val91Ala | missense_variant | 1.0 |
| inhA | 1674480 | c.279T>C | synonymous_variant | 1.0 |
| inhA | 1674486 | c.285T>C | synonymous_variant | 1.0 |
| inhA | 1674489 | c.288G>C | synonymous_variant | 1.0 |
| inhA | 1674507 | c.306G>A | synonymous_variant | 1.0 |
| inhA | 1674534 | c.333G>C | synonymous_variant | 1.0 |
| inhA | 1674537 | c.336C>G | synonymous_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674546 | c.345T>C | synonymous_variant | 1.0 |
| inhA | 1674549 | c.348G>C | synonymous_variant | 1.0 |
| inhA | 1674552 | c.351C>G | synonymous_variant | 1.0 |
| inhA | 1674570 | c.369G>C | synonymous_variant | 1.0 |
| inhA | 1674576 | c.375T>C | synonymous_variant | 1.0 |
| inhA | 1674585 | c.384T>C | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674597 | c.396G>A | synonymous_variant | 1.0 |
| inhA | 1674601 | p.Leu134Val | missense_variant | 1.0 |
| inhA | 1674609 | c.408G>C | synonymous_variant | 1.0 |
| inhA | 1674610 | p.Ile137Val | missense_variant | 1.0 |
| inhA | 1674618 | c.417C>T | synonymous_variant | 1.0 |
| inhA | 1674621 | c.420C>G | synonymous_variant | 1.0 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 1.0 |
| inhA | 1674627 | c.426T>C | synonymous_variant | 1.0 |
| inhA | 1674630 | c.429C>G | synonymous_variant | 1.0 |
| inhA | 1674656 | p.Ser152Thr | missense_variant | 1.0 |
| inhA | 1674660 | c.459G>C | synonymous_variant | 1.0 |
| inhA | 1674669 | c.468G>C | synonymous_variant | 1.0 |
| inhA | 1674699 | c.498C>T | synonymous_variant | 1.0 |
| inhA | 1674703 | c.502T>C | synonymous_variant | 1.0 |
| inhA | 1674708 | c.507G>A | synonymous_variant | 1.0 |
| inhA | 1674714 | c.513C>G | synonymous_variant | 1.0 |
| inhA | 1674718 | c.517_519delAGGinsCGC | synonymous_variant | 1.0 |
| inhA | 1674729 | c.528G>T | synonymous_variant | 1.0 |
| inhA | 1674738 | c.537C>G | synonymous_variant | 1.0 |
| inhA | 1674741 | c.540C>T | synonymous_variant | 1.0 |
| inhA | 1674742 | p.Lys181Pro | missense_variant | 1.0 |
| inhA | 1674745 | p.Tyr182His | missense_variant | 1.0 |
| inhA | 1674756 | c.555T>A | synonymous_variant | 1.0 |
| inhA | 1674774 | c.573A>G | synonymous_variant | 1.0 |
| inhA | 1674777 | c.576C>G | synonymous_variant | 1.0 |
| inhA | 1674780 | c.579T>G | synonymous_variant | 1.0 |
| inhA | 1674783 | c.582C>T | synonymous_variant | 1.0 |
| inhA | 1674786 | c.585G>C | synonymous_variant | 1.0 |
| inhA | 1674801 | c.600T>C | synonymous_variant | 1.0 |
| inhA | 1674804 | c.603G>C | synonymous_variant | 1.0 |
| inhA | 1674837 | c.636C>T | synonymous_variant | 1.0 |
| inhA | 1674846 | p.Ile215Met | missense_variant | 1.0 |
| inhA | 1674847 | p.Gln216Lys | missense_variant | 1.0 |
| inhA | 1674858 | c.657G>A | synonymous_variant | 1.0 |
| inhA | 1674870 | c.669T>C | synonymous_variant | 1.0 |
| inhA | 1674876 | c.675C>G | synonymous_variant | 1.0 |
| inhA | 1674879 | c.678T>G | synonymous_variant | 1.0 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 1.0 |
| inhA | 1674904 | p.Ala235Pro | missense_variant | 1.0 |
| inhA | 1674924 | c.723G>C | synonymous_variant | 1.0 |
| inhA | 1674933 | c.732G>T | synonymous_variant | 1.0 |
| inhA | 1674942 | c.741T>G | synonymous_variant | 1.0 |
| inhA | 1674945 | c.744C>T | synonymous_variant | 1.0 |
| rpsA | 1833547 | c.6G>A | synonymous_variant | 1.0 |
| rpsA | 1833554 | p.Thr5Ser | missense_variant | 1.0 |
| rpsA | 1833589 | c.48A>C | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>G | synonymous_variant | 1.0 |
| rpsA | 1833596 | p.Ser19Ala | missense_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>C | synonymous_variant | 1.0 |
| rpsA | 1833634 | c.93G>A | synonymous_variant | 1.0 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>A | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
| rpsA | 1833685 | c.144G>T | synonymous_variant | 1.0 |
| rpsA | 1833691 | c.150G>A | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
| rpsA | 1833709 | c.168C>T | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833733 | c.192C>T | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833739 | c.198C>T | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833781 | c.240T>C | synonymous_variant | 1.0 |
| rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833793 | c.252C>T | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
| rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
| rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>T | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>G | synonymous_variant | 1.0 |
| rpsA | 1833892 | c.351G>A | synonymous_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833898 | c.357C>T | synonymous_variant | 1.0 |
| rpsA | 1833901 | c.360G>A | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833958 | c.417C>T | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833991 | c.450C>G | synonymous_variant | 1.0 |
| rpsA | 1833995 | c.454C>T | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834009 | c.468C>T | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>T | 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 | 1834097 | c.556_557delTCinsAG | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834123 | c.582C>G | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834279 | c.738C>T | synonymous_variant | 1.0 |
| rpsA | 1834282 | c.741C>T | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
| rpsA | 1834297 | c.756C>G | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834345 | c.804C>T | synonymous_variant | 1.0 |
| rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834387 | c.846C>T | synonymous_variant | 1.0 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 0.99 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834456 | c.915T>G | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834498 | c.957C>T | synonymous_variant | 1.0 |
| rpsA | 1834520 | p.Ala327Ser | missense_variant | 1.0 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpsA | 1834540 | c.999G>C | synonymous_variant | 1.0 |
| rpsA | 1834543 | c.1002C>G | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 1.0 |
| rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 1.0 |
| rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834612 | c.1071G>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 | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | c.1224A>G | synonymous_variant | 1.0 |
| rpsA | 1834776 | p.Ala412Glu | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834786 | c.1245A>G | synonymous_variant | 1.0 |
| rpsA | 1834787 | p.Ala416Ser | missense_variant | 1.0 |
| rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
| rpsA | 1834804 | c.1263C>G | synonymous_variant | 1.0 |
| rpsA | 1834811 | c.1270C>A | synonymous_variant | 1.0 |
| rpsA | 1834849 | c.1308C>T | synonymous_variant | 1.0 |
| rpsA | 1834852 | c.1311C>A | synonymous_variant | 1.0 |
| katG | 2155661 | p.Val151Ile | missense_variant | 1.0 |
| katG | 2155671 | c.441G>C | synonymous_variant | 1.0 |
| katG | 2155677 | c.435C>T | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155704 | c.408C>A | synonymous_variant | 1.0 |
| katG | 2155716 | c.396T>C | synonymous_variant | 1.0 |
| katG | 2155722 | c.390G>A | synonymous_variant | 1.0 |
| katG | 2155728 | c.384G>C | synonymous_variant | 1.0 |
| katG | 2155740 | c.372C>G | synonymous_variant | 1.0 |
| katG | 2155766 | p.His116Tyr | missense_variant | 1.0 |
| katG | 2155776 | c.336C>G | synonymous_variant | 1.0 |
| katG | 2155782 | c.330C>G | synonymous_variant | 1.0 |
| kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
| kasA | 2517953 | c.-162C>T | upstream_gene_variant | 1.0 |
| kasA | 2517965 | c.-150C>G | 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 | 2517993 | c.-122G>A | upstream_gene_variant | 1.0 |
| kasA | 2518019 | c.-96A>G | upstream_gene_variant | 1.0 |
| kasA | 2518153 | c.39C>T | synonymous_variant | 1.0 |
| kasA | 2518162 | c.48G>C | synonymous_variant | 1.0 |
| kasA | 2518168 | c.54C>T | synonymous_variant | 1.0 |
| kasA | 2518174 | c.60A>C | synonymous_variant | 1.0 |
| kasA | 2518186 | c.72G>C | synonymous_variant | 1.0 |
| kasA | 2518190 | p.Ser26Ala | missense_variant | 1.0 |
| kasA | 2518219 | c.105T>C | synonymous_variant | 1.0 |
| kasA | 2518220 | c.106C>T | synonymous_variant | 1.0 |
| kasA | 2518223 | c.109T>C | synonymous_variant | 1.0 |
| kasA | 2518231 | c.117C>A | synonymous_variant | 1.0 |
| kasA | 2518248 | p.Ala45Val | missense_variant | 1.0 |
| kasA | 2518255 | c.141A>G | synonymous_variant | 1.0 |
| kasA | 2518732 | c.618C>G | synonymous_variant | 0.95 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 0.96 |
| kasA | 2518756 | c.642G>T | synonymous_variant | 0.96 |
| kasA | 2518759 | c.645C>G | synonymous_variant | 0.96 |
| kasA | 2518769 | p.Arg219Lys | missense_variant | 0.96 |
| kasA | 2518780 | p.Glu222Asp | missense_variant | 0.96 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 0.96 |
| kasA | 2518787 | p.Arg225Gly | missense_variant | 0.96 |
| kasA | 2518792 | c.678C>G | synonymous_variant | 0.96 |
| kasA | 2518796 | c.682C>A | synonymous_variant | 0.96 |
| kasA | 2518819 | c.705C>T | synonymous_variant | 0.97 |
| kasA | 2518822 | c.708C>G | synonymous_variant | 0.97 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 0.97 |
| kasA | 2518834 | c.720C>T | synonymous_variant | 0.97 |
| 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 | 1.0 |
| kasA | 2518882 | c.768C>A | synonymous_variant | 1.0 |
| kasA | 2518885 | c.771T>C | synonymous_variant | 1.0 |
| kasA | 2518891 | c.777C>A | synonymous_variant | 1.0 |
| kasA | 2518906 | c.792A>G | synonymous_variant | 1.0 |
| kasA | 2518910 | p.Leu266Met | missense_variant | 1.0 |
| folC | 2746708 | c.891C>T | synonymous_variant | 1.0 |
| folC | 2746714 | c.885T>C | synonymous_variant | 1.0 |
| folC | 2746722 | c.877C>T | synonymous_variant | 1.0 |
| folC | 2746730 | p.Tyr290Phe | missense_variant | 1.0 |
| folC | 2746739 | c.859_860delTCinsAG | synonymous_variant | 1.0 |
| folC | 2746746 | p.Val285Leu | missense_variant | 1.0 |
| folC | 2746756 | c.843C>T | synonymous_variant | 1.0 |
| folC | 2746765 | p.Gln278Glu | missense_variant | 1.0 |
| folC | 2746768 | c.831G>C | synonymous_variant | 1.0 |
| folC | 2746771 | p.Val276Leu | missense_variant | 1.0 |
| folC | 2746777 | c.822T>A | synonymous_variant | 1.0 |
| folC | 2746796 | c.802_803insA | frameshift_variant | 1.0 |
| folC | 2746800 | c.798delA | frameshift_variant | 1.0 |
| folC | 2746807 | c.792G>C | synonymous_variant | 1.0 |
| thyX | 3067355 | c.591A>G | synonymous_variant | 1.0 |
| thyX | 3067364 | c.582C>T | synonymous_variant | 1.0 |
| thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
| thyX | 3067394 | c.552G>C | synonymous_variant | 1.0 |
| thyX | 3067406 | c.540A>G | synonymous_variant | 1.0 |
| thyX | 3067418 | c.528C>G | synonymous_variant | 1.0 |
| thyX | 3067430 | c.516C>G | synonymous_variant | 1.0 |
| thyX | 3067433 | c.513C>G | synonymous_variant | 1.0 |
| thyX | 3067436 | c.510C>G | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyX | 3067442 | c.502_504delCGCinsAGA | synonymous_variant | 1.0 |
| thyX | 3067454 | c.492C>T | synonymous_variant | 1.0 |
| thyX | 3067465 | p.Ile161Val | missense_variant | 1.0 |
| thyX | 3067466 | c.480G>C | synonymous_variant | 1.0 |
| thyX | 3067469 | c.477C>T | synonymous_variant | 1.0 |
| thyA | 3073860 | c.612C>T | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073884 | c.588C>G | synonymous_variant | 1.0 |
| thyA | 3073886 | c.585_586insAG | frameshift_variant | 1.0 |
| thyA | 3073890 | p.Leu194Phe | missense_variant | 1.0 |
| thyA | 3073891 | c.579_580delCT | frameshift_variant | 1.0 |
| thyA | 3073902 | c.570C>G | synonymous_variant | 1.0 |
| thyA | 3073905 | c.567C>G | synonymous_variant | 1.0 |
| thyA | 3073917 | c.555C>G | synonymous_variant | 1.0 |
| thyA | 3073920 | c.550_552delCTCinsTTG | synonymous_variant | 1.0 |
| thyA | 3073925 | c.547T>C | synonymous_variant | 1.0 |
| thyA | 3073953 | c.519T>C | synonymous_variant | 1.0 |
| thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
| thyA | 3073971 | c.501C>T | synonymous_variant | 1.0 |
| thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
| thyA | 3073983 | c.489C>G | synonymous_variant | 1.0 |
| thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
| thyA | 3073995 | c.477G>C | synonymous_variant | 1.0 |
| thyA | 3074004 | c.468T>C | synonymous_variant | 1.0 |
| thyA | 3074013 | c.459C>T | synonymous_variant | 1.0 |
| thyA | 3074031 | c.441T>C | synonymous_variant | 1.0 |
| thyA | 3074034 | c.438T>C | synonymous_variant | 1.0 |
| thyA | 3074037 | c.435C>G | synonymous_variant | 1.0 |
| thyA | 3074040 | c.432G>C | synonymous_variant | 1.0 |
| thyA | 3074053 | p.Arg140Gln | missense_variant | 1.0 |
| thyA | 3074056 | p.Glu139Pro | missense_variant | 1.0 |
| thyA | 3074061 | c.411A>G | synonymous_variant | 1.0 |
| thyA | 3074076 | c.396C>G | synonymous_variant | 1.0 |
| ddn | 3986648 | c.-196C>G | upstream_gene_variant | 1.0 |
| ddn | 3986654 | c.-190C>G | upstream_gene_variant | 1.0 |
| ddn | 3986660 | c.-184C>T | upstream_gene_variant | 1.0 |
| ddn | 3986663 | c.-181G>A | upstream_gene_variant | 1.0 |
| ddn | 3986665 | c.-179G>C | upstream_gene_variant | 1.0 |
| ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 1.0 |
| ddn | 3986696 | c.-148G>C | upstream_gene_variant | 1.0 |
| ddn | 3986699 | c.-145C>G | upstream_gene_variant | 1.0 |
| ddn | 3986711 | c.-133C>A | upstream_gene_variant | 1.0 |
| ddn | 3986714 | c.-130C>G | upstream_gene_variant | 1.0 |
| panD | 4044108 | c.174C>T | synonymous_variant | 1.0 |
| panD | 4044111 | c.171C>T | synonymous_variant | 1.0 |
| panD | 4044114 | c.168C>G | synonymous_variant | 1.0 |
| panD | 4044117 | c.165G>T | synonymous_variant | 1.0 |
| panD | 4044123 | c.159T>G | synonymous_variant | 1.0 |
| panD | 4044138 | c.144T>C | synonymous_variant | 1.0 |
| panD | 4044141 | c.141C>G | synonymous_variant | 1.0 |
| panD | 4044147 | c.135C>G | synonymous_variant | 1.0 |
| panD | 4044150 | c.132A>C | synonymous_variant | 1.0 |
| panD | 4044156 | c.126A>G | synonymous_variant | 1.0 |
| panD | 4044162 | c.120A>G | synonymous_variant | 1.0 |
| panD | 4044165 | c.117G>C | synonymous_variant | 1.0 |
| panD | 4044171 | c.111C>T | synonymous_variant | 1.0 |
| panD | 4044177 | c.105C>T | synonymous_variant | 1.0 |
| panD | 4044188 | c.94T>C | synonymous_variant | 1.0 |
| panD | 4044189 | c.93C>T | synonymous_variant | 1.0 |
| panD | 4044195 | c.87T>C | synonymous_variant | 1.0 |
| panD | 4044225 | c.57C>T | synonymous_variant | 0.95 |
| panD | 4044231 | p.Cys17Gln | missense_variant | 0.94 |
| panD | 4044234 | c.48C>T | synonymous_variant | 0.94 |
| panD | 4044241 | p.Thr14Arg | missense_variant | 0.94 |
| panD | 4044243 | c.39C>G | synonymous_variant | 0.94 |
| panD | 4044246 | c.36C>T | synonymous_variant | 0.94 |
| panD | 4044264 | c.18G>C | synonymous_variant | 0.94 |
| panD | 4044270 | c.12G>C | synonymous_variant | 0.93 |
| embC | 4240726 | c.864G>C | synonymous_variant | 1.0 |
| embC | 4240736 | p.Ser292Ala | missense_variant | 1.0 |
| embC | 4240765 | c.903C>G | synonymous_variant | 1.0 |
| embC | 4240777 | c.915G>A | synonymous_variant | 1.0 |
| embC | 4240779 | p.His306Arg | missense_variant | 1.0 |
| embC | 4240783 | c.921G>C | 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 | 4240822 | c.960C>G | synonymous_variant | 0.97 |
| embC | 4240828 | c.966G>C | synonymous_variant | 1.0 |
| embC | 4240831 | c.969T>G | synonymous_variant | 1.0 |
| embC | 4240858 | c.996G>C | synonymous_variant | 1.0 |
| embC | 4240867 | c.1005T>G | synonymous_variant | 1.0 |
| embC | 4240870 | c.1008T>C | synonymous_variant | 1.0 |
| embA | 4242823 | c.-410G>C | upstream_gene_variant | 1.0 |
| embA | 4242826 | c.-407G>C | upstream_gene_variant | 1.0 |
| embA | 4242832 | c.-401A>C | upstream_gene_variant | 1.0 |
| embA | 4242838 | c.-395C>G | upstream_gene_variant | 1.0 |
| embA | 4242844 | c.-389A>G | upstream_gene_variant | 1.0 |
| embA | 4242847 | c.-386C>T | upstream_gene_variant | 1.0 |
| embA | 4242862 | c.-371A>G | upstream_gene_variant | 1.0 |
| embC | 4242872 | p.Asp1004Thr | missense_variant | 1.0 |
| embC | 4242878 | p.Thr1006Val | missense_variant | 1.0 |
| embA | 4242901 | c.-332G>C | upstream_gene_variant | 1.0 |
| embB | 4248277 | c.1764G>C | synonymous_variant | 1.0 |
| embB | 4248295 | c.1782C>T | synonymous_variant | 1.0 |
| embB | 4248304 | c.1791G>C | synonymous_variant | 1.0 |
| ubiA | 4269132 | c.702G>C | synonymous_variant | 0.92 |
| ubiA | 4269138 | c.696C>T | synonymous_variant | 1.0 |
| ubiA | 4269141 | c.691_693delTTGinsCTC | synonymous_variant | 1.0 |
| ubiA | 4269149 | p.Val229Leu | missense_variant | 1.0 |
| ubiA | 4269153 | c.681C>G | synonymous_variant | 1.0 |
| ubiA | 4269156 | c.678C>G | synonymous_variant | 1.0 |
| ubiA | 4269177 | c.657G>C | synonymous_variant | 1.0 |
| ubiA | 4269186 | p.Thr216Ser | missense_variant | 1.0 |
| ubiA | 4269189 | c.645C>T | synonymous_variant | 1.0 |
| ubiA | 4269192 | c.642C>G | synonymous_variant | 1.0 |
| ubiA | 4269201 | c.633A>G | synonymous_variant | 1.0 |
| ubiA | 4269220 | p.Ala205Lys | missense_variant | 1.0 |
| ubiA | 4269222 | c.612T>C | synonymous_variant | 1.0 |
| ubiA | 4269225 | c.609C>G | synonymous_variant | 1.0 |
| ubiA | 4269243 | p.His197Gln | missense_variant | 1.0 |
| ubiA | 4269246 | c.588G>C | synonymous_variant | 1.0 |
| ubiA | 4269249 | c.585G>A | synonymous_variant | 1.0 |
| ubiA | 4269258 | c.576C>G | synonymous_variant | 1.0 |
| ubiA | 4269267 | c.567C>G | synonymous_variant | 1.0 |
| ubiA | 4269271 | p.Val188Ala | missense_variant | 1.0 |
| pepQ | 2779779 | c.491_*79520del | exon_loss_variant | 1.0 |
