Run ID: SRR13861484
Sample name:
Date: 03-04-2023 09:32:59
Number of reads: 236310
Percentage reads mapped: 4.73
Strain: lineage4.9
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761131 | p.Gly442Glu | missense_variant | 0.36 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.38 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.25 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.25 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.25 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.25 |
gyrA | 6706 | c.-596G>A | upstream_gene_variant | 0.25 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.25 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.25 |
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.25 |
gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 0.25 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.25 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.29 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.29 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.25 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.29 |
gyrA | 7466 | c.165G>A | synonymous_variant | 0.22 |
gyrA | 7469 | c.168C>T | synonymous_variant | 0.2 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.2 |
gyrA | 7475 | c.174A>C | synonymous_variant | 0.2 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.2 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.25 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.25 |
gyrA | 7490 | c.189C>T | synonymous_variant | 0.25 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.29 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.25 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.25 |
fgd1 | 490955 | p.Met58Arg | missense_variant | 1.0 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.25 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.22 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.27 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.25 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.33 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.33 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.36 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.3 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.33 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.33 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.25 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.33 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.4 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.4 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.4 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.38 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.38 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.33 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.33 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.33 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.17 |
rpoB | 761126 | c.1320G>T | synonymous_variant | 0.33 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.36 |
rpoB | 761133 | p.Leu443Ile | missense_variant | 0.38 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.47 |
rpoB | 761151 | p.Leu449Val | missense_variant | 0.33 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.36 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.33 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.47 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.47 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.42 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.17 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.17 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.42 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.38 |
rpoB | 761196 | p.Leu464Phe | missense_variant | 0.36 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.36 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.36 |
rpoB | 761213 | c.1407G>A | synonymous_variant | 0.42 |
rpoB | 761220 | p.Ser472Thr | missense_variant | 0.42 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.38 |
rpoB | 761235 | p.Met477Val | missense_variant | 0.38 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.15 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.25 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.25 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.29 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.33 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.33 |
rpoB | 761373 | p.Val523His | missense_variant | 0.33 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.25 |
rpoB | 761423 | c.1617T>C | synonymous_variant | 0.29 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.25 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.29 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.3 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.3 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.38 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.38 |
rpoB | 762888 | p.His1028Asn | missense_variant | 0.42 |
rpoB | 762911 | p.Ile1035Met | missense_variant | 0.45 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.45 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.46 |
rpoB | 762930 | p.Pro1042Ser | missense_variant | 0.38 |
rpoC | 762936 | c.-434_-432delTCGinsAGC | upstream_gene_variant | 0.36 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.36 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.36 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.42 |
rpoC | 762971 | c.-399G>A | upstream_gene_variant | 0.42 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.42 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.55 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.5 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.18 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.17 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.18 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.2 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.2 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.2 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.2 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.2 |
rpoC | 763206 | c.-164_-162delAGTinsTCC | upstream_gene_variant | 0.2 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.2 |
rpoC | 763220 | c.-150G>C | upstream_gene_variant | 0.22 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.25 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.22 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.17 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.17 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.17 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.17 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.21 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.21 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.15 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.15 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.25 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.25 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.2 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.2 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.3 |
rpoC | 764401 | c.1032C>T | synonymous_variant | 0.5 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.5 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.5 |
rpoC | 764419 | c.1050C>T | synonymous_variant | 0.55 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 0.5 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.55 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.55 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.5 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.5 |
rpoC | 764451 | p.Gly361Ala | missense_variant | 0.5 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.5 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.5 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.5 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.5 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.6 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.6 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.6 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.6 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.6 |
rpoC | 764513 | p.Phe382Leu | missense_variant | 0.6 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.6 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.43 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.18 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.2 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.17 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.17 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.15 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.15 |
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 |
mmpL5 | 775883 | p.Ile866Leu | missense_variant | 0.2 |
mmpL5 | 775898 | c.2583G>A | synonymous_variant | 0.2 |
mmpL5 | 775901 | c.2580G>A | synonymous_variant | 0.2 |
mmpL5 | 775904 | c.2577G>A | synonymous_variant | 0.2 |
mmpL5 | 775909 | p.Leu858Phe | missense_variant | 0.22 |
mmpL5 | 775912 | c.2569C>A | synonymous_variant | 0.2 |
mmpL5 | 775916 | c.2565T>G | synonymous_variant | 0.22 |
mmpL5 | 775937 | c.2544G>C | synonymous_variant | 0.2 |
mmpL5 | 775966 | p.Ala839Ser | missense_variant | 0.29 |
mmpL5 | 775970 | c.2511G>C | synonymous_variant | 0.25 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.22 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.33 |
mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.2 |
mmpL5 | 775997 | c.2484T>C | synonymous_variant | 0.22 |
mmpL5 | 776000 | p.Leu827Ile | missense_variant | 0.3 |
mmpL5 | 776005 | p.Ile826Leu | missense_variant | 0.27 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.36 |
mmpL5 | 776066 | c.2415C>G | synonymous_variant | 0.18 |
mmpL5 | 776078 | c.2403C>G | synonymous_variant | 0.18 |
mmpL5 | 776087 | c.2394C>G | synonymous_variant | 0.22 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.22 |
mmpS5 | 779639 | c.-735dupG | upstream_gene_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.15 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.15 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.18 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.17 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.23 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.21 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.15 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.17 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.43 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.38 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.38 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.38 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.38 |
fbiC | 1304499 | c.1569T>G | synonymous_variant | 0.17 |
fbiC | 1304517 | c.1587C>T | synonymous_variant | 0.22 |
fbiC | 1304520 | c.1590A>C | synonymous_variant | 0.22 |
fbiC | 1304523 | c.1593G>T | synonymous_variant | 0.22 |
fbiC | 1304526 | c.1596T>G | synonymous_variant | 0.22 |
fbiC | 1304529 | c.1599T>C | synonymous_variant | 0.78 |
fbiC | 1304544 | c.1614T>C | synonymous_variant | 0.29 |
fbiC | 1304545 | p.Val539Thr | missense_variant | 0.33 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.5 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.33 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.33 |
fbiC | 1304574 | c.1644C>G | synonymous_variant | 0.33 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.25 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.22 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.25 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.25 |
Rv1258c | 1406845 | p.Ala166Pro | missense_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472108 | n.263C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472133 | n.288G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472135 | n.290C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472971 | n.1126G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.38 |
inhA | 1674480 | c.279T>C | synonymous_variant | 0.5 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.5 |
inhA | 1674489 | c.288G>C | synonymous_variant | 0.5 |
inhA | 1674498 | c.297G>A | synonymous_variant | 0.5 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.5 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.5 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.5 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.5 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.5 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.5 |
inhA | 1674564 | c.363C>T | synonymous_variant | 0.5 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.33 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.33 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.4 |
inhA | 1674607 | p.Pro136Ser | missense_variant | 0.57 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.29 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.29 |
inhA | 1674630 | c.429C>G | synonymous_variant | 0.29 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.29 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.25 |
inhA | 1674778 | p.Pro193Ala | missense_variant | 0.86 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.29 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.29 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.29 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.29 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.29 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.25 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.3 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.36 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.33 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.44 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.44 |
rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 0.33 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.33 |
rpsA | 1834150 | c.609G>C | synonymous_variant | 0.25 |
rpsA | 1834153 | c.612T>C | synonymous_variant | 0.25 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.25 |
rpsA | 1834157 | c.616T>C | synonymous_variant | 0.25 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.25 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.22 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.22 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.33 |
rpsA | 1834186 | c.645C>G | synonymous_variant | 0.38 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.33 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.33 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.33 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.33 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.33 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.25 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.29 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.25 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.25 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.29 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.22 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.22 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.22 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.25 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.2 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.18 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.18 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.25 |
PPE35 | 2169081 | p.Leu511Ser | missense_variant | 1.0 |
PPE35 | 2169202 | p.Ser471Pro | missense_variant | 1.0 |
Rv1979c | 2222091 | c.1074G>T | synonymous_variant | 1.0 |
Rv1979c | 2223306 | c.-142T>A | upstream_gene_variant | 1.0 |
pncA | 2289228 | p.Ile5Asn | missense_variant | 1.0 |
kasA | 2518176 | p.Ala21Gly | missense_variant | 1.0 |
eis | 2714755 | p.Pro193Gln | missense_variant | 1.0 |
ahpC | 2726324 | c.132A>G | synonymous_variant | 1.0 |
ahpC | 2726362 | p.Phe57Ser | missense_variant | 1.0 |
pepQ | 2859580 | p.Leu280Arg | missense_variant | 1.0 |
pepQ | 2859999 | c.420G>T | synonymous_variant | 1.0 |
Rv2752c | 3065553 | c.639A>C | synonymous_variant | 0.33 |
Rv2752c | 3065556 | c.636G>C | synonymous_variant | 0.4 |
Rv2752c | 3065562 | c.630T>C | synonymous_variant | 0.4 |
Rv2752c | 3065568 | p.Ile208Leu | missense_variant | 0.4 |
Rv2752c | 3065580 | c.612G>C | synonymous_variant | 0.29 |
Rv2752c | 3065586 | c.606C>T | synonymous_variant | 0.33 |
Rv2752c | 3065595 | p.Leu199Phe | missense_variant | 0.29 |
Rv2752c | 3065604 | c.588G>C | synonymous_variant | 0.29 |
Rv2752c | 3065607 | c.585C>G | synonymous_variant | 0.29 |
Rv2752c | 3065612 | p.Thr194Ala | missense_variant | 0.29 |
Rv2752c | 3065616 | c.576C>T | synonymous_variant | 0.25 |
Rv2752c | 3065634 | c.558G>C | synonymous_variant | 0.25 |
Rv2752c | 3065637 | c.555A>G | synonymous_variant | 0.22 |
Rv2752c | 3065649 | c.543T>G | synonymous_variant | 0.22 |
Rv2752c | 3065901 | c.291A>G | synonymous_variant | 0.29 |
Rv2752c | 3065916 | p.Phe92Tyr | missense_variant | 0.29 |
Rv2752c | 3065919 | c.273G>C | synonymous_variant | 0.29 |
Rv2752c | 3065925 | p.Ala89Gly | missense_variant | 0.25 |
Rv2752c | 3065928 | c.264G>C | synonymous_variant | 0.25 |
Rv2752c | 3065947 | p.Gly82Ala | missense_variant | 0.18 |
Rv2752c | 3065952 | c.240C>T | synonymous_variant | 0.2 |
Rv2752c | 3065955 | c.235_237delTTGinsCTC | synonymous_variant | 0.22 |
Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.25 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.27 |
Rv2752c | 3065994 | c.198T>C | synonymous_variant | 0.25 |
Rv2752c | 3065997 | c.195C>G | synonymous_variant | 0.25 |
Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.25 |
Rv2752c | 3066024 | c.168T>C | synonymous_variant | 0.23 |
Rv2752c | 3066040 | p.Gly51Ala | missense_variant | 0.17 |
thyX | 3067577 | p.Glu123Asp | missense_variant | 0.5 |
thyX | 3067582 | p.Met122Leu | missense_variant | 0.5 |
thyX | 3067586 | c.360C>G | synonymous_variant | 0.5 |
thyX | 3067601 | c.345G>C | synonymous_variant | 0.4 |
thyX | 3067604 | c.342G>C | synonymous_variant | 0.4 |
thyX | 3067610 | p.Lys112Asn | missense_variant | 0.5 |
thyX | 3067613 | c.333G>A | synonymous_variant | 0.5 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.5 |
thyX | 3067640 | c.306G>C | synonymous_variant | 0.4 |
thyX | 3067643 | c.303C>T | synonymous_variant | 0.4 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.4 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.4 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.33 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.33 |
thyX | 3067724 | c.222G>A | synonymous_variant | 0.33 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.33 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.43 |
thyX | 3067742 | c.204A>C | synonymous_variant | 0.38 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.43 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.43 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.43 |
thyX | 3067787 | c.159G>A | synonymous_variant | 0.43 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.38 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.38 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.38 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.33 |
thyX | 3067826 | c.120C>G | synonymous_variant | 0.33 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.18 |
thyX | 3067940 | c.6C>G | synonymous_variant | 1.0 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.5 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.5 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.4 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.5 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.5 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.5 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.29 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.38 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.33 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.33 |
thyA | 3074076 | c.396C>G | synonymous_variant | 0.33 |
thyA | 3074097 | c.375C>G | synonymous_variant | 0.33 |
thyA | 3074100 | c.372T>C | synonymous_variant | 0.33 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.25 |
thyA | 3074620 | c.-149C>A | upstream_gene_variant | 1.0 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.29 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.29 |
fprA | 3473836 | c.-171C>A | upstream_gene_variant | 0.25 |
fprA | 3473861 | c.-146T>G | upstream_gene_variant | 0.88 |
fprA | 3474953 | p.Gln316Arg | missense_variant | 1.0 |
ddn | 3986889 | p.Phe16Val | missense_variant | 1.0 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.22 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.25 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.25 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.33 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.33 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.29 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.25 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.18 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.25 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.33 |
embC | 4240900 | c.1038A>G | synonymous_variant | 0.22 |
embC | 4240919 | c.1057_1059delCTCinsTTG | synonymous_variant | 0.25 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.25 |
embC | 4240945 | c.1083T>C | synonymous_variant | 0.22 |
embC | 4240951 | c.1089C>G | synonymous_variant | 0.25 |
embC | 4240954 | p.Ile364Met | missense_variant | 0.29 |
embC | 4240957 | c.1095C>G | synonymous_variant | 0.29 |
embC | 4240966 | c.1104G>T | synonymous_variant | 0.29 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.4 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.4 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.5 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.5 |
embC | 4241137 | c.1275G>C | synonymous_variant | 0.5 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.5 |
embC | 4241141 | p.Ile427Val | missense_variant | 0.5 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.5 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.5 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.5 |
embC | 4242041 | p.Met727Leu | missense_variant | 1.0 |
embA | 4244228 | c.996A>G | synonymous_variant | 0.22 |
embA | 4244233 | p.Ala334Gly | missense_variant | 0.22 |
embA | 4244247 | p.Val339Ile | missense_variant | 0.22 |
embA | 4244254 | p.Arg341His | missense_variant | 0.22 |
embA | 4244257 | p.Phe342Trp | missense_variant | 0.2 |
embA | 4244267 | c.1035G>C | synonymous_variant | 0.22 |
embA | 4244276 | c.1044A>C | synonymous_variant | 0.22 |
embA | 4244284 | p.Pro351Arg | missense_variant | 0.2 |
embA | 4244298 | p.Ser356Ala | missense_variant | 0.17 |
embA | 4244309 | c.1077C>G | synonymous_variant | 0.2 |
embA | 4244312 | c.1080T>G | synonymous_variant | 0.22 |
embA | 4244315 | c.1083G>C | synonymous_variant | 0.22 |
embA | 4244324 | c.1092T>G | synonymous_variant | 0.25 |
embA | 4244327 | c.1095T>C | synonymous_variant | 0.25 |
embA | 4244337 | p.Leu369Val | missense_variant | 0.29 |
embA | 4244340 | p.Ser370Ala | missense_variant | 0.25 |
embA | 4244723 | p.Gln497His | missense_variant | 1.0 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.4 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.5 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.4 |
aftB | 4267979 | c.858G>C | synonymous_variant | 1.0 |
ethR | 4327804 | p.Ala86Thr | missense_variant | 0.5 |