Run ID: ERR1199132
Sample name:
Date: 31-03-2023 12:36:52
Number of reads: 3753191
Percentage reads mapped: 87.28
Strain: lineage4.6.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.1 | Euro-American (Uganda) | T2 | RD724 | 0.99 |
lineage4.6.1.1 | Euro-American | T2-Uganda | RD724 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6190 | c.951A>G | synonymous_variant | 0.18 |
gyrB | 6196 | c.957C>A | synonymous_variant | 0.14 |
gyrB | 6208 | c.969G>A | synonymous_variant | 0.15 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.16 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.15 |
gyrB | 6229 | c.990G>A | synonymous_variant | 0.15 |
gyrA | 6622 | c.-680C>T | upstream_gene_variant | 0.11 |
gyrA | 6634 | c.-668T>C | upstream_gene_variant | 0.12 |
gyrA | 6649 | c.-653T>G | upstream_gene_variant | 0.16 |
gyrB | 6663 | p.Phe475Tyr | missense_variant | 0.23 |
gyrA | 6667 | c.-635G>A | upstream_gene_variant | 0.24 |
gyrA | 6673 | c.-629A>T | upstream_gene_variant | 0.23 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.16 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.14 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.16 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.16 |
gyrA | 6715 | c.-587C>G | upstream_gene_variant | 0.16 |
gyrA | 6722 | c.-580C>A | upstream_gene_variant | 0.14 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.15 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.17 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.15 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7442 | c.141G>T | synonymous_variant | 0.13 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.12 |
gyrA | 7475 | c.174A>C | synonymous_variant | 0.13 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.14 |
gyrA | 7514 | c.213C>G | synonymous_variant | 0.12 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.15 |
gyrA | 7526 | c.225G>T | synonymous_variant | 0.15 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.14 |
gyrA | 7539 | p.Thr80Ala | missense_variant | 0.85 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.17 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.19 |
gyrA | 7703 | c.402G>C | synonymous_variant | 0.21 |
gyrA | 7710 | c.409_411delTTGinsCTC | synonymous_variant | 0.21 |
gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 0.25 |
gyrA | 7763 | c.462T>G | synonymous_variant | 0.27 |
gyrA | 7775 | c.474C>T | synonymous_variant | 0.28 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.25 |
gyrA | 7787 | c.486G>A | synonymous_variant | 0.24 |
gyrA | 7793 | c.492G>C | synonymous_variant | 0.24 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.2 |
gyrA | 7832 | c.531G>C | synonymous_variant | 0.24 |
gyrA | 7835 | c.534A>C | synonymous_variant | 0.24 |
gyrA | 7841 | c.540C>T | synonymous_variant | 0.22 |
gyrA | 7847 | c.546G>C | synonymous_variant | 0.24 |
gyrA | 7853 | c.552C>G | synonymous_variant | 0.23 |
gyrA | 7859 | c.558A>G | synonymous_variant | 0.22 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.23 |
gyrA | 7886 | c.585T>C | synonymous_variant | 0.18 |
gyrA | 7889 | c.588G>A | synonymous_variant | 0.19 |
gyrA | 7892 | c.591G>C | synonymous_variant | 0.18 |
gyrA | 7898 | p.Asp199Glu | missense_variant | 0.2 |
gyrA | 7906 | p.Phe202Tyr | missense_variant | 0.2 |
gyrA | 7919 | p.Glu206Asp | missense_variant | 0.13 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.18 |
gyrA | 8327 | c.1026C>T | synonymous_variant | 0.18 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.19 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.15 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.18 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.14 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.13 |
gyrA | 8408 | c.1107A>G | synonymous_variant | 0.13 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.14 |
gyrA | 8585 | c.1284C>T | synonymous_variant | 0.11 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.14 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.12 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.12 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.15 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 0.18 |
gyrA | 9056 | c.1755C>G | synonymous_variant | 0.17 |
gyrA | 9062 | c.1761C>T | synonymous_variant | 0.17 |
gyrA | 9065 | c.1764C>G | synonymous_variant | 0.17 |
gyrA | 9068 | c.1767G>C | synonymous_variant | 0.17 |
gyrA | 9071 | c.1770G>C | synonymous_variant | 0.17 |
gyrA | 9080 | c.1779G>C | synonymous_variant | 0.16 |
gyrA | 9089 | c.1788G>C | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.99 |
fgd1 | 491316 | c.534C>G | synonymous_variant | 0.16 |
fgd1 | 491321 | p.Ala180Val | missense_variant | 0.16 |
fgd1 | 491343 | c.561C>T | synonymous_variant | 0.16 |
fgd1 | 491349 | c.567T>C | synonymous_variant | 0.16 |
fgd1 | 491355 | c.573C>A | synonymous_variant | 0.2 |
fgd1 | 491364 | c.582T>C | synonymous_variant | 0.15 |
fgd1 | 491367 | c.585G>A | synonymous_variant | 0.14 |
fgd1 | 491370 | c.588C>G | synonymous_variant | 0.14 |
fgd1 | 491563 | p.Ser261Cys | missense_variant | 0.12 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.13 |
rpoB | 760092 | p.Ser96Thr | missense_variant | 0.13 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.13 |
rpoB | 760106 | c.300G>C | synonymous_variant | 0.15 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.15 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.16 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.16 |
rpoB | 760130 | c.324T>C | synonymous_variant | 0.17 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.15 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.14 |
rpoB | 760148 | p.Asp114Glu | missense_variant | 0.15 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.15 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.14 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.15 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.17 |
rpoB | 760208 | p.Ile134Met | missense_variant | 0.15 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.14 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.14 |
rpoB | 760265 | p.Met153Ile | missense_variant | 0.12 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.12 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.18 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.19 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.2 |
rpoB | 760457 | c.651C>G | synonymous_variant | 0.23 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.23 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.23 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.21 |
rpoB | 760485 | p.Pro227Ser | missense_variant | 0.21 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.16 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.16 |
rpoB | 760616 | p.Asp270Glu | missense_variant | 0.15 |
rpoB | 760643 | c.837G>A | synonymous_variant | 0.16 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.15 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.15 |
rpoB | 760668 | p.Thr288Ala | missense_variant | 0.14 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.13 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.13 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.12 |
rpoB | 760845 | p.Thr347Val | missense_variant | 0.12 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.16 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.16 |
rpoB | 760869 | p.Val355Phe | missense_variant | 0.17 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.16 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.16 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.17 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.19 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.18 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.19 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.18 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.24 |
rpoB | 760964 | c.1158C>G | synonymous_variant | 0.25 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.25 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.26 |
rpoB | 760985 | c.1179G>T | synonymous_variant | 0.29 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.27 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.28 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.27 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.22 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.23 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.22 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.14 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.14 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.15 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.15 |
rpoB | 761150 | c.1344A>G | synonymous_variant | 0.15 |
rpoB | 761282 | c.1476C>G | synonymous_variant | 0.12 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 0.14 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.12 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.13 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.13 |
rpoB | 761627 | c.1821C>T | synonymous_variant | 0.12 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.12 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.12 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.12 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.13 |
rpoB | 762170 | c.2364C>G | synonymous_variant | 0.13 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.12 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.15 |
rpoB | 762314 | c.2508C>G | synonymous_variant | 0.14 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.14 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.15 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.15 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.16 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.23 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.17 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.15 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.12 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.16 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.14 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.12 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.15 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.16 |
rpoC | 763082 | c.-288C>G | upstream_gene_variant | 0.16 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.15 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.15 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.16 |
rpoC | 763115 | c.-255T>G | upstream_gene_variant | 0.13 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.12 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.14 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.15 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.14 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.12 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.12 |
rpoC | 763208 | c.-162T>C | upstream_gene_variant | 0.13 |
rpoC | 763430 | c.61A>C | synonymous_variant | 0.12 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.19 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.17 |
rpoC | 763489 | c.120G>A | synonymous_variant | 0.17 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.18 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.22 |
rpoC | 763597 | c.228G>A | synonymous_variant | 0.13 |
rpoC | 763606 | c.237C>T | synonymous_variant | 0.12 |
rpoC | 763609 | c.240C>G | synonymous_variant | 0.12 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.12 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.12 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.12 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.12 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.14 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.14 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.16 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.15 |
rpoC | 763782 | p.Ser138Trp | missense_variant | 0.12 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.14 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.15 |
rpoC | 764060 | p.Pro231Ile | missense_variant | 0.16 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.18 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.23 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.24 |
rpoC | 764134 | c.765C>G | synonymous_variant | 0.15 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.12 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.13 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.15 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.15 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.13 |
rpoC | 764284 | c.915G>C | synonymous_variant | 0.14 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.17 |
rpoC | 764347 | c.978G>C | synonymous_variant | 0.14 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.12 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.15 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.14 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.14 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.14 |
rpoC | 764443 | p.Ile358Met | missense_variant | 0.14 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.14 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.13 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.14 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.13 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.14 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.14 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.17 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.19 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.19 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.19 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.19 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.2 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.2 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.2 |
rpoC | 764713 | c.1344G>A | synonymous_variant | 0.16 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.15 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.22 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.21 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.21 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.19 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.13 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.14 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.14 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.15 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.14 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.14 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.12 |
rpoC | 765435 | p.His689Pro | missense_variant | 0.85 |
rpoC | 765454 | c.2085C>G | synonymous_variant | 0.2 |
rpoC | 765466 | c.2097C>T | synonymous_variant | 0.19 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.2 |
rpoC | 765493 | c.2124G>C | synonymous_variant | 0.21 |
rpoC | 765544 | c.2175C>G | synonymous_variant | 0.13 |
rpoC | 765547 | c.2178C>T | synonymous_variant | 0.13 |
rpoC | 765548 | c.2179_2180delAGinsTC | synonymous_variant | 0.13 |
rpoC | 765553 | c.2184C>G | synonymous_variant | 0.13 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.13 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.13 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.14 |
rpoC | 765781 | p.Asp804Glu | missense_variant | 0.14 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.15 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.13 |
rpoC | 765814 | c.2445A>C | synonymous_variant | 0.13 |
rpoC | 765823 | c.2454C>G | synonymous_variant | 0.15 |
rpoC | 765826 | c.2457T>G | synonymous_variant | 0.15 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.17 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.18 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.16 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.16 |
rpoC | 765898 | c.2529C>T | synonymous_variant | 0.16 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.15 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.15 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.15 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.13 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.14 |
rpoC | 765967 | c.2598C>G | synonymous_variant | 0.15 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.14 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.15 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.15 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.16 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.14 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.16 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 0.13 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.13 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.13 |
rpoC | 766517 | p.Thr1050Ser | missense_variant | 0.12 |
rpoC | 766522 | c.3153C>T | synonymous_variant | 0.12 |
rpoC | 766525 | c.3156G>C | synonymous_variant | 0.12 |
rpoC | 766526 | p.Val1053Ile | missense_variant | 0.12 |
rpoC | 766534 | c.3165C>G | synonymous_variant | 0.13 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.14 |
rpoC | 766542 | p.Gly1058Asp | missense_variant | 0.14 |
rpoC | 766714 | c.3345G>C | synonymous_variant | 0.12 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.12 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.14 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.19 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.2 |
rpoC | 766775 | p.Arg1136Lys | missense_variant | 0.2 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.18 |
rpoC | 766813 | c.3444G>C | synonymous_variant | 0.17 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.12 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.17 |
rpoC | 766996 | c.3627C>G | synonymous_variant | 0.21 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.24 |
rpoC | 767011 | c.3642G>C | synonymous_variant | 0.25 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.2 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.2 |
rpoC | 767059 | c.3690T>C | synonymous_variant | 0.14 |
rpoC | 767062 | c.3693C>G | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.15 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.14 |
rplC | 801249 | c.441T>C | synonymous_variant | 0.13 |
rplC | 801252 | c.444G>C | synonymous_variant | 0.13 |
fbiC | 1304403 | c.1473T>C | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1471936 | n.91A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472031 | n.186G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472033 | n.188A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472106 | n.261G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472489 | n.644A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473677 | n.20C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473758 | n.101G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473937 | n.280C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473941 | n.284T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473965 | n.308G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474105 | n.448T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474106 | n.449A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474107 | n.450T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474109 | n.452A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474110 | n.453A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474498 | n.841G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474505 | n.848C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474712 | n.1055G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474715 | n.1061delA | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475030 | n.1373_1374insT | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475217 | n.1560T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475429 | n.1772G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475430 | n.1773T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475453 | n.1796T>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475586 | n.1929C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476085 | n.2428G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476105 | n.2448G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476256 | n.2599A>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476262 | n.2605G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476540 | n.2883C>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476665 | n.3008T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476691 | n.3034T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476692 | n.3035T>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.24 |
inhA | 1674503 | p.Thr101Ser | missense_variant | 0.13 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.14 |
inhA | 1674513 | c.312C>G | synonymous_variant | 0.15 |
inhA | 1674514 | p.Ile105Val | missense_variant | 0.15 |
inhA | 1674534 | c.333G>C | synonymous_variant | 0.21 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.22 |
inhA | 1674546 | c.345T>C | synonymous_variant | 0.21 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.17 |
inhA | 1674550 | p.Ser117Ala | missense_variant | 0.17 |
inhA | 1674573 | c.372G>C | synonymous_variant | 0.18 |
inhA | 1674576 | c.375T>C | synonymous_variant | 0.19 |
inhA | 1674585 | c.384T>G | synonymous_variant | 0.24 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.24 |
inhA | 1674601 | p.Leu134Val | missense_variant | 0.21 |
inhA | 1674610 | p.Ile137Val | missense_variant | 0.19 |
inhA | 1674621 | c.420C>G | synonymous_variant | 0.21 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.19 |
inhA | 1674630 | c.429C>G | synonymous_variant | 0.17 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.16 |
inhA | 1674656 | p.Ser152Thr | missense_variant | 0.19 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.12 |
rpsA | 1833691 | c.150G>A | synonymous_variant | 0.13 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.14 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.14 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.18 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.17 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.17 |
rpsA | 1833733 | c.192C>G | synonymous_variant | 0.15 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.16 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.18 |
rpsA | 1833770 | p.Asn77His | missense_variant | 0.17 |
rpsA | 1833778 | c.237C>G | synonymous_variant | 0.14 |
rpsA | 1833781 | c.240T>G | synonymous_variant | 0.14 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.15 |
rpsA | 1833806 | c.265C>T | synonymous_variant | 0.13 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.13 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.14 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.12 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.12 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.12 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.15 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.14 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.12 |
rpsA | 1834573 | c.1032G>C | synonymous_variant | 0.13 |
rpsA | 1834579 | c.1038C>G | synonymous_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.13 |
kasA | 2518612 | c.498C>G | synonymous_variant | 0.12 |
eis | 2715188 | p.Arg49Cys | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877710 | c.798C>G | synonymous_variant | 0.13 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.14 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.14 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.13 |
rpoA | 3877788 | c.720G>A | synonymous_variant | 0.12 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.14 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.14 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.14 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.14 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.16 |
rpoA | 3878145 | c.363C>G | synonymous_variant | 0.17 |
rpoA | 3878159 | p.Thr117Ala | missense_variant | 0.17 |
rpoA | 3878163 | c.345C>G | synonymous_variant | 0.17 |
rpoA | 3878185 | p.Gly108Ala | missense_variant | 0.17 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.16 |
rpoA | 3878202 | c.306G>A | synonymous_variant | 0.17 |
rpoA | 3878205 | c.303T>G | synonymous_variant | 0.17 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.19 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.18 |
rpoA | 3878253 | c.255G>C | synonymous_variant | 0.18 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.18 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.15 |
rpoA | 3878270 | p.Leu80Ile | missense_variant | 0.14 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.14 |
rpoA | 3878276 | c.232C>T | synonymous_variant | 0.15 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.16 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.12 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.19 |
clpC1 | 4038905 | c.1800A>G | synonymous_variant | 0.2 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.19 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.16 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.16 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.16 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.14 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.14 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.13 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.13 |
clpC1 | 4038974 | c.1731T>G | synonymous_variant | 0.13 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.12 |
clpC1 | 4039823 | c.882T>G | synonymous_variant | 0.13 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.13 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.12 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.18 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.18 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.18 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.13 |
clpC1 | 4039901 | c.804C>G | synonymous_variant | 0.13 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.12 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.12 |
clpC1 | 4039970 | c.735G>A | synonymous_variant | 0.13 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.12 |
clpC1 | 4040498 | c.207G>A | synonymous_variant | 0.13 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.12 |
clpC1 | 4040531 | c.174T>G | synonymous_variant | 0.13 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.15 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.15 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.13 |
ethA | 4328329 | c.-856C>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |