Run ID: SRR3732595
Sample name:
Date: 04-04-2023 05:36:30
Number of reads: 550459
Percentage reads mapped: 99.49
Strain: lineage4
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
katG | 2155341 | p.Met257Ile | missense_variant | 0.2 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5710 | c.471C>A | synonymous_variant | 0.33 |
gyrB | 6719 | p.Asp494Tyr | missense_variant | 0.5 |
gyrB | 7154 | p.Asp639Tyr | missense_variant | 0.67 |
gyrA | 7520 | c.219G>T | synonymous_variant | 0.18 |
gyrA | 7544 | p.Met81Ile | missense_variant | 0.5 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490732 | c.-51C>A | upstream_gene_variant | 0.67 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491772 | c.990C>A | synonymous_variant | 1.0 |
mshA | 575255 | c.-93G>T | upstream_gene_variant | 1.0 |
mshA | 575591 | c.244C>A | synonymous_variant | 0.22 |
mshA | 575626 | c.279C>A | synonymous_variant | 0.18 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 575969 | p.Asp208Tyr | missense_variant | 0.29 |
mshA | 576032 | p.Gly229Cys | missense_variant | 0.33 |
mshA | 576373 | c.1026G>T | synonymous_variant | 0.17 |
mshA | 576459 | p.Ala371Gly | missense_variant | 0.33 |
rpoB | 760350 | p.Asp182Tyr | missense_variant | 0.67 |
rpoB | 760460 | c.654G>T | synonymous_variant | 0.33 |
rpoB | 761246 | c.1440C>A | synonymous_variant | 0.5 |
rpoB | 761428 | p.Pro541Leu | missense_variant | 0.18 |
rpoB | 761782 | p.Gly659Val | missense_variant | 0.67 |
rpoB | 762221 | p.Glu805Asp | missense_variant | 0.4 |
rpoB | 763290 | p.Arg1162Ser | missense_variant | 1.0 |
rpoC | 764041 | p.Ser224Arg | missense_variant | 1.0 |
rpoC | 765295 | c.1926G>T | synonymous_variant | 0.22 |
rpoC | 765378 | p.Arg670Leu | missense_variant | 0.25 |
rpoC | 765848 | p.Pro827Thr | missense_variant | 1.0 |
rpoC | 765904 | c.2535C>A | synonymous_variant | 0.5 |
rpoC | 766736 | p.Arg1123Trp | missense_variant | 0.33 |
rpoC | 766749 | p.Pro1127His | missense_variant | 0.29 |
rpoC | 766784 | p.Gln1139Lys | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776103 | p.Ile793Thr | missense_variant | 0.5 |
mmpL5 | 776499 | p.Gly661Val | missense_variant | 0.4 |
mmpL5 | 777342 | p.Arg380His | missense_variant | 0.22 |
mmpL5 | 777355 | p.Val376Leu | missense_variant | 0.17 |
mmpL5 | 777368 | p.Lys371Asn | missense_variant | 0.17 |
mmpS5 | 778792 | p.Leu38Phe | missense_variant | 0.4 |
mmpL5 | 779187 | c.-707C>T | upstream_gene_variant | 0.67 |
mmpS5 | 779620 | c.-715G>T | upstream_gene_variant | 0.67 |
rplC | 800624 | c.-185G>T | upstream_gene_variant | 0.5 |
fbiC | 1303197 | p.Lys89Asn | missense_variant | 0.22 |
fbiC | 1303217 | p.Arg96Leu | missense_variant | 0.25 |
fbiC | 1304133 | c.1203G>T | synonymous_variant | 0.17 |
fbiC | 1304355 | c.1425G>T | synonymous_variant | 0.33 |
fbiC | 1304362 | p.Glu478* | stop_gained | 0.5 |
fbiC | 1304649 | p.Asp573Glu | missense_variant | 0.4 |
Rv1258c | 1406755 | p.Ala196Thr | missense_variant | 0.5 |
Rv1258c | 1406767 | p.Gln192Lys | missense_variant | 0.4 |
Rv1258c | 1407157 | p.Ala62Ser | missense_variant | 0.2 |
embR | 1416468 | p.Asp294Tyr | missense_variant | 0.5 |
embR | 1417219 | c.129C>A | synonymous_variant | 0.5 |
atpE | 1461156 | p.Gly38Cys | missense_variant | 0.67 |
rrs | 1471718 | n.-128G>T | upstream_gene_variant | 1.0 |
fabG1 | 1673941 | p.Ala168Thr | missense_variant | 0.25 |
fabG1 | 1673947 | p.Glu170* | stop_gained | 0.25 |
inhA | 1674510 | p.Met103Ile | missense_variant | 0.5 |
rpsA | 1834406 | p.Arg289Ser | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918596 | c.657C>A | synonymous_variant | 0.33 |
ndh | 2101697 | p.Ala449Val | missense_variant | 0.5 |
ndh | 2102157 | p.Glu296* | stop_gained | 1.0 |
ndh | 2102188 | p.Leu285Phe | missense_variant | 0.67 |
ndh | 2102232 | p.Ser271Pro | missense_variant | 0.5 |
ndh | 2102254 | p.Asp263Glu | missense_variant | 1.0 |
ndh | 2102686 | c.357G>T | synonymous_variant | 1.0 |
ndh | 2102970 | p.Gly25Cys | missense_variant | 0.67 |
ndh | 2103123 | c.-81G>A | upstream_gene_variant | 0.5 |
katG | 2153982 | c.2130C>T | synonymous_variant | 0.29 |
katG | 2155354 | p.Arg253Leu | missense_variant | 0.22 |
katG | 2155419 | p.Asn231Lys | missense_variant | 0.25 |
katG | 2155448 | p.Ala222Thr | missense_variant | 0.67 |
PPE35 | 2167740 | p.Thr958Ile | missense_variant | 0.33 |
PPE35 | 2170107 | p.Ala169Val | missense_variant | 0.2 |
PPE35 | 2170293 | p.Pro107Leu | missense_variant | 0.67 |
Rv1979c | 2222501 | p.Ala222Thr | missense_variant | 1.0 |
Rv1979c | 2222548 | p.Ser206* | stop_gained | 0.5 |
Rv1979c | 2223130 | p.His12Arg | missense_variant | 0.5 |
Rv1979c | 2223152 | p.Arg5Trp | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288737 | p.Val169Ile | missense_variant | 0.33 |
pncA | 2288738 | c.504C>A | synonymous_variant | 0.33 |
pncA | 2288760 | p.Ala161Glu | missense_variant | 0.4 |
pncA | 2289415 | c.-174C>A | upstream_gene_variant | 0.67 |
pncA | 2289705 | c.-464G>T | upstream_gene_variant | 0.29 |
pncA | 2289733 | c.-492G>T | upstream_gene_variant | 0.33 |
pncA | 2289828 | c.-587C>A | upstream_gene_variant | 0.5 |
pncA | 2289839 | c.-598G>A | upstream_gene_variant | 0.4 |
pncA | 2290112 | c.-871C>T | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518456 | c.342C>A | synonymous_variant | 0.4 |
kasA | 2518738 | c.624G>T | synonymous_variant | 0.33 |
kasA | 2518755 | p.Arg214Leu | missense_variant | 0.33 |
kasA | 2519058 | p.Thr315Met | missense_variant | 0.18 |
eis | 2714902 | p.Arg144Gln | missense_variant | 0.67 |
eis | 2715054 | c.279G>A | synonymous_variant | 0.25 |
eis | 2715077 | p.Ala86Thr | missense_variant | 0.29 |
ahpC | 2726172 | c.-21G>A | upstream_gene_variant | 0.5 |
folC | 2747055 | p.Asp182Tyr | missense_variant | 1.0 |
folC | 2747696 | c.-98G>A | upstream_gene_variant | 0.22 |
pepQ | 2859321 | c.1098C>A | synonymous_variant | 0.5 |
pepQ | 2859666 | p.Gln251His | missense_variant | 0.5 |
pepQ | 2859789 | c.630G>T | synonymous_variant | 0.25 |
pepQ | 2859899 | p.Arg174Cys | missense_variant | 0.29 |
pepQ | 2860518 | c.-100C>A | upstream_gene_variant | 0.33 |
ribD | 2986721 | c.-118G>A | upstream_gene_variant | 0.25 |
ribD | 2986733 | c.-106C>A | upstream_gene_variant | 0.25 |
ribD | 2987064 | p.Glu76* | stop_gained | 0.33 |
Rv2752c | 3064589 | p.Arg535Ser | missense_variant | 0.4 |
Rv2752c | 3065172 | c.1020G>T | synonymous_variant | 0.4 |
Rv2752c | 3065438 | p.Ala252Thr | missense_variant | 1.0 |
thyX | 3067237 | p.Asp237Asn | missense_variant | 0.22 |
ald | 3086878 | p.Pro20Leu | missense_variant | 1.0 |
fbiD | 3339150 | c.33C>A | synonymous_variant | 0.25 |
fbiD | 3339198 | c.81C>A | synonymous_variant | 0.29 |
fbiD | 3339500 | p.Ala128Glu | missense_variant | 0.15 |
fbiD | 3339720 | c.603C>A | synonymous_variant | 0.29 |
Rv3083 | 3448315 | c.-189C>A | upstream_gene_variant | 0.18 |
Rv3083 | 3448703 | p.Arg67His | missense_variant | 1.0 |
Rv3083 | 3448730 | p.Ala76Asp | missense_variant | 0.67 |
Rv3083 | 3448909 | p.Leu136Ile | missense_variant | 0.67 |
Rv3083 | 3449943 | c.1440C>T | synonymous_variant | 0.67 |
fprA | 3475351 | p.Glu449* | stop_gained | 0.2 |
Rv3236c | 3612061 | c.1056C>A | synonymous_variant | 0.67 |
fbiA | 3641215 | p.Ala225Ser | missense_variant | 0.4 |
fbiA | 3641371 | p.Gly277Cys | missense_variant | 0.33 |
fbiA | 3641456 | p.Ser305* | stop_gained | 0.4 |
fbiB | 3641730 | p.Asp66Tyr | missense_variant | 0.5 |
fbiB | 3642317 | p.Arg261Ser | missense_variant | 0.17 |
fbiB | 3642611 | p.Ser359Arg | missense_variant | 0.25 |
alr | 3840923 | c.498C>A | synonymous_variant | 0.5 |
clpC1 | 4039682 | c.1023C>A | synonymous_variant | 0.67 |
embC | 4239859 | c.-4C>A | upstream_gene_variant | 0.5 |
embC | 4240340 | p.His160Asn | missense_variant | 0.29 |
embC | 4240360 | c.498C>A | synonymous_variant | 0.4 |
embC | 4240894 | p.Met344Ile | missense_variant | 0.67 |
embC | 4241642 | p.Ala594Thr | missense_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243015 | c.-218C>T | upstream_gene_variant | 0.67 |
embC | 4243070 | p.Ala1070Thr | missense_variant | 0.33 |
embA | 4244044 | p.Ser271* | stop_gained | 0.5 |
embA | 4244169 | p.Gln313Lys | missense_variant | 0.4 |
embA | 4244215 | p.Ala328Asp | missense_variant | 0.4 |
embA | 4245079 | p.Trp616* | stop_gained | 0.33 |
embB | 4247060 | p.Pro183Thr | missense_variant | 0.4 |
embB | 4247108 | p.Gly199Trp | missense_variant | 0.33 |
embB | 4247886 | p.Gly458Val | missense_variant | 0.29 |
embB | 4248590 | p.Ala693Ser | missense_variant | 0.29 |
embB | 4248981 | p.Ser823Ile | missense_variant | 1.0 |
embB | 4249184 | p.Gly891Trp | missense_variant | 0.5 |
embB | 4249334 | p.Ala941Thr | missense_variant | 0.25 |
aftB | 4267557 | p.Ala427Val | missense_variant | 0.5 |
aftB | 4267873 | p.Gln322Glu | missense_variant | 1.0 |
ethA | 4326740 | p.Arg245Leu | missense_variant | 0.67 |
ethA | 4326879 | p.Ala199Thr | missense_variant | 0.4 |
ethA | 4328214 | c.-741C>A | upstream_gene_variant | 0.33 |
whiB6 | 4338409 | p.Pro38His | missense_variant | 0.67 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407743 | p.Arg154Trp | missense_variant | 0.29 |