Run ID: SRR6831950
Sample name:
Date: 04-04-2023 17:08:10
Number of reads: 2394279
Percentage reads mapped: 89.65
Strain: lineage4.3.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.99 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247448 | p.His312Arg | missense_variant | 0.16 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6133 | c.894G>C | synonymous_variant | 0.13 |
gyrB | 6136 | c.897G>A | synonymous_variant | 0.13 |
gyrB | 6217 | c.978G>C | synonymous_variant | 0.12 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.15 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.12 |
gyrA | 7198 | c.-104C>A | upstream_gene_variant | 0.12 |
gyrA | 7216 | c.-86G>C | upstream_gene_variant | 0.12 |
gyrA | 7237 | c.-65C>T | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.14 |
gyrA | 7626 | c.325C>T | synonymous_variant | 0.14 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.15 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.15 |
gyrA | 7683 | c.382A>C | synonymous_variant | 0.13 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.13 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.17 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.19 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.21 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.19 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.19 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.12 |
gyrA | 7892 | c.591G>C | synonymous_variant | 0.14 |
gyrA | 7898 | p.Asp199Glu | missense_variant | 0.15 |
gyrA | 7919 | p.Glu206Asp | missense_variant | 0.17 |
gyrA | 7923 | p.His208Tyr | missense_variant | 0.12 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8069 | c.768T>C | synonymous_variant | 0.15 |
gyrA | 8078 | c.777A>G | synonymous_variant | 0.16 |
gyrA | 8090 | c.789C>G | synonymous_variant | 0.16 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.16 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.14 |
gyrA | 8237 | c.936A>G | synonymous_variant | 0.14 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.21 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.17 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.17 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.17 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.14 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.19 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.19 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.19 |
gyrA | 8327 | c.1026C>A | synonymous_variant | 0.19 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.16 |
gyrA | 8342 | c.1041G>C | synonymous_variant | 0.15 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.25 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.25 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.3 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.31 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.29 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.29 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.34 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.37 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.28 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.25 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.19 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.12 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.24 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.27 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.28 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.28 |
gyrA | 8537 | c.1236G>A | synonymous_variant | 0.3 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.3 |
gyrA | 8552 | c.1251C>G | synonymous_variant | 0.29 |
gyrA | 8556 | p.Ala419Gln | missense_variant | 0.28 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.28 |
gyrA | 8562 | c.1261C>T | synonymous_variant | 0.28 |
gyrA | 8576 | c.1275C>G | synonymous_variant | 0.28 |
gyrA | 8597 | c.1296C>G | synonymous_variant | 0.25 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.17 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.15 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.13 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.13 |
gyrA | 8717 | c.1416C>G | synonymous_variant | 0.13 |
gyrA | 8720 | c.1419G>A | synonymous_variant | 0.13 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.14 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.13 |
gyrA | 8735 | c.1434C>T | synonymous_variant | 0.15 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.14 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.14 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.13 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.13 |
gyrA | 8945 | c.1644G>C | synonymous_variant | 0.12 |
gyrA | 8948 | p.Leu549Phe | missense_variant | 0.14 |
gyrA | 8951 | c.1650G>A | synonymous_variant | 0.12 |
gyrA | 8966 | c.1665C>G | synonymous_variant | 0.16 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.16 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.16 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.15 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.16 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.14 |
fgd1 | 491196 | c.414A>G | synonymous_variant | 0.15 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.15 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.15 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.13 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.14 |
fgd1 | 491532 | c.750G>T | synonymous_variant | 0.12 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.14 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.13 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.12 |
ccsA | 620703 | c.813G>C | synonymous_variant | 0.12 |
ccsA | 620710 | p.Val274Met | missense_variant | 0.12 |
ccsA | 620721 | c.831G>C | synonymous_variant | 0.12 |
ccsA | 620730 | c.840C>T | synonymous_variant | 0.12 |
ccsA | 620733 | c.843G>C | synonymous_variant | 0.12 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.12 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.12 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.12 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.12 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.13 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.15 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.14 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.13 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.12 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.12 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.12 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.16 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.16 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.17 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.16 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.21 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.2 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.21 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.21 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.19 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.19 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.16 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.17 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.17 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.18 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.17 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.15 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.16 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.19 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.18 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.15 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.14 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.16 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.18 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.13 |
rpoB | 762148 | c.2343G>C | synonymous_variant | 0.12 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.23 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.23 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.23 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.26 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.27 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.27 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.32 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.25 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.19 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.16 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.12 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.13 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.25 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.27 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.27 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.32 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.32 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.29 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.29 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.15 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.17 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.17 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.23 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.23 |
rpoC | 763708 | c.339G>A | synonymous_variant | 0.23 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.23 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.25 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.26 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.3 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.37 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.35 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.35 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.37 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.35 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.31 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.29 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.25 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.24 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.23 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.14 |
rpoC | 763836 | p.Ala156Val | missense_variant | 0.12 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.14 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.12 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.12 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.12 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.12 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.12 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.12 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.15 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.18 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.17 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.21 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.25 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.24 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.25 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.19 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.18 |
rpoC | 764195 | p.Ser276Gln | missense_variant | 0.16 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.16 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.15 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.38 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.32 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.32 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.29 |
rpoC | 764282 | c.913_915delTCGinsAGC | synonymous_variant | 0.28 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.17 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.12 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.13 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.17 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.18 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.19 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.21 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.22 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.93 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.13 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.15 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.15 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.15 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.14 |
rpoC | 765085 | c.1716T>G | synonymous_variant | 0.14 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.14 |
rpoC | 765103 | c.1734G>A | synonymous_variant | 0.14 |
rpoC | 765287 | c.1918C>T | synonymous_variant | 0.15 |
rpoC | 765292 | c.1923G>T | synonymous_variant | 0.12 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.2 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.18 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.17 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.16 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.18 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.18 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.18 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.19 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.17 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.2 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.19 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.17 |
rpoC | 765985 | c.2616C>T | synonymous_variant | 0.19 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.18 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.12 |
rpoC | 766069 | c.2700G>A | synonymous_variant | 0.14 |
rpoC | 766444 | c.3075C>G | synonymous_variant | 0.14 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.14 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.13 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.15 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.14 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.12 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.17 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.13 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.14 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.14 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.17 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.17 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.17 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.15 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.12 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.14 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.14 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.17 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.2 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.15 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.16 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.12 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.17 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.2 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.21 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.13 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.17 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.26 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.2 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.2 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.15 |
fbiC | 1303095 | c.165G>A | synonymous_variant | 0.96 |
fbiC | 1303534 | p.Ser202Ala | missense_variant | 0.12 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.12 |
fbiC | 1303929 | c.999G>C | synonymous_variant | 0.14 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.13 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.13 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.17 |
fbiC | 1303973 | p.Gly348Ala | missense_variant | 0.17 |
fbiC | 1303981 | p.Val351Ile | missense_variant | 0.17 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.19 |
atpE | 1461152 | c.108C>T | synonymous_variant | 0.16 |
atpE | 1461159 | p.Val39Ile | missense_variant | 0.16 |
atpE | 1461185 | c.141G>C | synonymous_variant | 0.22 |
atpE | 1461189 | c.145C>T | synonymous_variant | 0.21 |
atpE | 1461194 | c.150C>T | synonymous_variant | 0.18 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.16 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.16 |
atpE | 1461224 | c.180T>C | synonymous_variant | 0.17 |
atpE | 1461233 | c.189A>G | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474959 | n.1302C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474962 | n.1306delG | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475271 | n.1614A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475273 | n.1616T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.2 |
inhA | 1673574 | c.-628C>G | upstream_gene_variant | 0.13 |
inhA | 1674285 | c.84A>G | synonymous_variant | 0.12 |
inhA | 1674295 | p.Gln32Ala | missense_variant | 0.17 |
inhA | 1674300 | c.99C>G | synonymous_variant | 0.18 |
inhA | 1674303 | c.102C>G | synonymous_variant | 0.17 |
inhA | 1674307 | c.106C>T | synonymous_variant | 0.17 |
inhA | 1674315 | c.114C>G | synonymous_variant | 0.26 |
inhA | 1674321 | c.120G>C | synonymous_variant | 0.3 |
inhA | 1674342 | c.141T>C | synonymous_variant | 0.21 |
inhA | 1674352 | p.Thr51Val | missense_variant | 0.18 |
inhA | 1674368 | p.Ala56Glu | missense_variant | 0.13 |
inhA | 1674379 | c.178C>T | synonymous_variant | 0.14 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.12 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.16 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.21 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.22 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.15 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.13 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.17 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.21 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.19 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.18 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.21 |
inhA | 1674630 | c.429C>G | synonymous_variant | 0.21 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.19 |
inhA | 1674639 | c.438C>T | synonymous_variant | 0.18 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.18 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.12 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.12 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.14 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.14 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.12 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102050 | c.993T>C | synonymous_variant | 0.12 |
ndh | 2102053 | c.990G>C | synonymous_variant | 0.13 |
ndh | 2102059 | c.984T>C | synonymous_variant | 0.16 |
ndh | 2102065 | c.978G>C | synonymous_variant | 0.16 |
ndh | 2102068 | c.975T>C | synonymous_variant | 0.14 |
ndh | 2102076 | p.Met323Leu | missense_variant | 0.14 |
ndh | 2102077 | c.966T>C | synonymous_variant | 0.15 |
ndh | 2102083 | p.Val320Ile | missense_variant | 0.14 |
ndh | 2102218 | c.825C>G | synonymous_variant | 0.12 |
ndh | 2102233 | c.810G>A | synonymous_variant | 0.13 |
ndh | 2102242 | c.801G>A | synonymous_variant | 0.19 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518468 | c.354A>T | synonymous_variant | 0.15 |
kasA | 2518475 | c.361A>C | synonymous_variant | 0.15 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.15 |
kasA | 2518483 | c.369C>G | synonymous_variant | 0.14 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.16 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.15 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.24 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.22 |
kasA | 2518540 | c.426T>G | synonymous_variant | 0.21 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.21 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.12 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.12 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.13 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.13 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.12 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.12 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.13 |
kasA | 2518717 | c.603C>T | synonymous_variant | 0.14 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.18 |
kasA | 2518741 | c.627G>C | synonymous_variant | 0.17 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.17 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.16 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 0.94 |
kasA | 2519008 | c.894C>T | synonymous_variant | 0.13 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.12 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.12 |
ahpC | 2726681 | c.489A>G | synonymous_variant | 0.13 |
ahpC | 2726687 | c.495C>G | synonymous_variant | 0.13 |
ahpC | 2726690 | c.498C>T | synonymous_variant | 0.12 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
folC | 2746594 | c.1005T>C | synonymous_variant | 0.12 |
folC | 2746597 | c.1002C>A | synonymous_variant | 0.12 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.14 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.16 |
thyA | 3073824 | c.648A>C | synonymous_variant | 0.12 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.14 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.19 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.8 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.2 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.22 |
thyA | 3073902 | c.570C>G | synonymous_variant | 0.15 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.16 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.17 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.19 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.19 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.19 |
thyA | 3074172 | c.300G>C | synonymous_variant | 0.15 |
thyA | 3074175 | c.297A>G | synonymous_variant | 0.13 |
thyA | 3074199 | c.273G>A | synonymous_variant | 0.16 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.17 |
thyA | 3074214 | c.258T>C | synonymous_variant | 0.17 |
thyA | 3074217 | c.255T>C | synonymous_variant | 0.21 |
thyA | 3074349 | c.123T>C | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475036 | p.Val344Thr | missense_variant | 0.16 |
fprA | 3475047 | c.1041A>G | synonymous_variant | 0.15 |
fprA | 3475048 | p.Ile348Val | missense_variant | 0.14 |
fprA | 3475051 | p.Asn349Glu | missense_variant | 0.14 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.13 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.12 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.14 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.12 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.16 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.16 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.16 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.16 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.14 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.14 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.12 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.12 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.15 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.15 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.12 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.16 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.17 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.18 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.14 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.14 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.15 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.2 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.21 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.21 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.18 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.18 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.18 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.16 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.16 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.14 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.13 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.15 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.15 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.13 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.16 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.15 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.17 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.13 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.17 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.14 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.13 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.14 |
clpC1 | 4038212 | c.2493T>C | synonymous_variant | 0.14 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 0.17 |
clpC1 | 4038272 | p.Gly811Ser | missense_variant | 0.17 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.18 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.87 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.17 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.16 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.17 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.13 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.17 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.17 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.23 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.2 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.22 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.22 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.16 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.13 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 0.92 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.13 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.14 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.13 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.17 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.16 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.16 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.18 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.17 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.17 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.16 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.13 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.13 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.15 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.14 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.14 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.12 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.21 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.17 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.15 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.12 |
panD | 4044478 | c.-197G>A | upstream_gene_variant | 0.12 |
embC | 4240979 | p.Thr373Gln | missense_variant | 0.14 |
embC | 4240983 | p.Ser374Asn | missense_variant | 0.13 |
embC | 4240990 | c.1128A>G | synonymous_variant | 0.13 |
embC | 4240996 | c.1134G>C | synonymous_variant | 0.14 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.17 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.15 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.15 |
embC | 4241035 | c.1173G>A | synonymous_variant | 0.13 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.17 |
embC | 4241086 | c.1224G>C | synonymous_variant | 0.22 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.24 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.21 |
embC | 4241137 | c.1275G>C | synonymous_variant | 0.19 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.16 |
embC | 4241141 | p.Ile427Val | missense_variant | 0.16 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.13 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.13 |
embC | 4241509 | c.1647A>G | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.13 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.12 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.16 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.17 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.16 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.17 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.16 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.15 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.15 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.15 |
embB | 4247536 | c.1023C>G | synonymous_variant | 0.15 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.14 |
embB | 4247566 | c.1053C>G | synonymous_variant | 0.14 |
embB | 4247567 | c.1054C>T | synonymous_variant | 0.15 |
embB | 4247572 | c.1059A>G | synonymous_variant | 0.14 |
embB | 4247579 | p.Ala356Phe | missense_variant | 0.15 |
embB | 4248035 | p.Val508Ile | missense_variant | 0.14 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.15 |
embB | 4248044 | p.Lys511Ala | missense_variant | 0.16 |
embB | 4248052 | c.1539G>A | synonymous_variant | 0.15 |
embB | 4248055 | c.1542G>C | synonymous_variant | 0.14 |
embB | 4248064 | c.1551G>C | synonymous_variant | 0.17 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.16 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.16 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.14 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.13 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.16 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.16 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.15 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.13 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.13 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.16 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |