Run ID: SRR4035795
Sample name:
Date: 04-04-2023 07:18:12
Number of reads: 824605
Percentage reads mapped: 99.46
Strain: lineage4.1.2
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 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155165 | p.Gly316Asp | missense_variant | 0.18 | isoniazid |
ethA | 4326426 | c.1047delT | frameshift_variant | 0.14 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5667 | p.Gly143Ala | missense_variant | 0.18 |
gyrB | 7202 | p.Asp655Tyr | missense_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7418 | c.117C>T | synonymous_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 8173 | p.Val291Asp | missense_variant | 0.14 |
gyrA | 8182 | p.Gly294Asp | missense_variant | 0.15 |
gyrA | 8283 | c.983delT | frameshift_variant | 0.18 |
gyrA | 9056 | c.1755C>T | synonymous_variant | 0.15 |
gyrA | 9059 | p.Glu586Asp | missense_variant | 0.15 |
gyrA | 9078 | p.Gly593Arg | missense_variant | 0.17 |
gyrA | 9156 | p.Asp619Tyr | missense_variant | 0.29 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9390 | p.Thr697Ala | missense_variant | 0.25 |
fgd1 | 490700 | c.-83G>A | upstream_gene_variant | 0.13 |
fgd1 | 491054 | p.Ala91Val | missense_variant | 0.15 |
fgd1 | 491171 | p.Ala130Gly | missense_variant | 0.15 |
fgd1 | 491391 | c.609C>T | synonymous_variant | 0.33 |
fgd1 | 491483 | p.Ser234Tyr | missense_variant | 0.25 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491678 | p.Gln299Arg | missense_variant | 0.17 |
mshA | 575311 | c.-37A>T | upstream_gene_variant | 0.17 |
mshA | 575379 | p.Gly11Glu | missense_variant | 0.14 |
mshA | 575842 | c.495G>A | synonymous_variant | 0.2 |
ccsA | 619839 | c.-52C>T | upstream_gene_variant | 0.15 |
ccsA | 620017 | p.Gly43Arg | missense_variant | 0.2 |
ccsA | 620027 | p.Pro46Gln | missense_variant | 0.2 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760436 | c.630C>T | synonymous_variant | 0.15 |
rpoB | 760443 | p.Arg213Cys | missense_variant | 0.2 |
rpoB | 760860 | p.Pro352Thr | missense_variant | 0.15 |
rpoB | 761172 | p.Gly456Cys | missense_variant | 0.25 |
rpoB | 761535 | p.Pro577Ser | missense_variant | 0.2 |
rpoB | 762364 | p.Asp853Val | missense_variant | 0.15 |
rpoC | 763552 | c.183C>T | synonymous_variant | 0.17 |
rpoC | 763592 | p.Cys75Ser | missense_variant | 0.18 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.14 |
rpoC | 764104 | c.735C>G | synonymous_variant | 0.11 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 764922 | p.Glu518Val | missense_variant | 0.2 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765922 | c.2555delA | frameshift_variant | 0.17 |
rpoC | 766498 | p.Lys1043Asn | missense_variant | 0.18 |
rpoC | 766848 | p.Gln1160Arg | missense_variant | 0.17 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776025 | p.Ser819Leu | missense_variant | 0.17 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
mmpL5 | 778360 | p.Val41Ile | missense_variant | 0.22 |
mmpR5 | 779233 | p.Arg82Trp | missense_variant | 0.22 |
mmpR5 | 779285 | p.Ala99Val | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801272 | p.Ala155Val | missense_variant | 0.29 |
rplC | 801442 | p.Ile212Phe | missense_variant | 0.14 |
rplC | 801452 | p.Gly215Asp | missense_variant | 0.15 |
fbiC | 1302827 | c.-104A>G | upstream_gene_variant | 0.14 |
fbiC | 1303190 | p.Ser87Leu | missense_variant | 0.13 |
fbiC | 1303308 | c.378C>T | synonymous_variant | 0.14 |
fbiC | 1303697 | p.Thr256Ile | missense_variant | 0.33 |
fbiC | 1304147 | p.Ile406Asn | missense_variant | 0.25 |
fbiC | 1304216 | c.1289delC | frameshift_variant | 0.33 |
fbiC | 1304721 | c.1791C>T | synonymous_variant | 0.13 |
fbiC | 1304748 | c.1821delC | frameshift_variant | 0.15 |
fbiC | 1304820 | c.1890G>A | synonymous_variant | 0.29 |
fbiC | 1304835 | c.1905G>A | synonymous_variant | 0.4 |
Rv1258c | 1406548 | p.Met265Val | missense_variant | 0.25 |
Rv1258c | 1407276 | p.Gly22Asp | missense_variant | 0.12 |
embR | 1416870 | p.Glu160Gln | missense_variant | 0.15 |
embR | 1416882 | p.Phe156Ile | missense_variant | 0.17 |
embR | 1416900 | p.Leu150Val | missense_variant | 0.18 |
embR | 1416923 | p.Leu142Ser | missense_variant | 0.22 |
atpE | 1461049 | p.Asp2Gly | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471904 | n.59T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471918 | n.73A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472545 | n.700A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472873 | n.1028C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474020 | n.363A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475077 | n.1420C>A | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673319 | c.-121A>T | upstream_gene_variant | 0.25 |
inhA | 1674307 | p.Leu36Val | missense_variant | 0.17 |
inhA | 1674670 | p.Ala157Thr | missense_variant | 0.17 |
inhA | 1674871 | p.Gln224Lys | missense_variant | 0.17 |
rpsA | 1833401 | c.-141C>A | upstream_gene_variant | 0.2 |
rpsA | 1834063 | p.Ile174Met | missense_variant | 0.12 |
rpsA | 1834592 | p.Ile351Val | missense_variant | 0.13 |
rpsA | 1834818 | p.Lys426Arg | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918183 | p.Ala82Ser | missense_variant | 0.25 |
ndh | 2102438 | p.Arg202Leu | missense_variant | 0.18 |
ndh | 2103105 | c.-64_-63insG | upstream_gene_variant | 0.29 |
katG | 2154349 | p.Glu588Gly | missense_variant | 0.22 |
katG | 2155493 | p.Asp207His | missense_variant | 0.12 |
katG | 2155752 | c.360C>T | synonymous_variant | 0.18 |
katG | 2155939 | p.Met58Thr | missense_variant | 0.22 |
katG | 2156007 | c.105C>T | synonymous_variant | 0.12 |
katG | 2156538 | c.-427A>G | upstream_gene_variant | 0.12 |
PPE35 | 2167771 | p.Ser948Gly | missense_variant | 0.22 |
PPE35 | 2168397 | p.Ile739Asn | missense_variant | 0.17 |
PPE35 | 2168409 | p.Thr735Ile | missense_variant | 0.13 |
PPE35 | 2168415 | p.Gly733Ala | missense_variant | 0.14 |
PPE35 | 2170099 | p.Leu172Met | missense_variant | 0.33 |
PPE35 | 2170512 | p.Leu34Pro | missense_variant | 0.2 |
Rv1979c | 2221884 | c.1281G>A | synonymous_variant | 0.18 |
Rv1979c | 2222685 | p.Lys160Asn | missense_variant | 0.29 |
Rv1979c | 2222759 | p.Val136Met | missense_variant | 0.13 |
Rv1979c | 2222765 | p.Phe134Leu | missense_variant | 0.12 |
Rv1979c | 2222862 | c.303C>T | synonymous_variant | 0.17 |
Rv1979c | 2223251 | c.-87C>T | upstream_gene_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288875 | p.Arg123Ser | missense_variant | 0.14 |
pncA | 2288929 | p.Gly105Cys | missense_variant | 0.12 |
pncA | 2288999 | p.Phe81Leu | missense_variant | 0.17 |
pncA | 2289013 | p.Pro77Ser | missense_variant | 0.14 |
pncA | 2289415 | c.-174C>G | upstream_gene_variant | 0.29 |
pncA | 2289485 | c.-244A>G | upstream_gene_variant | 0.12 |
kasA | 2517927 | c.-188G>A | upstream_gene_variant | 0.17 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518280 | p.Leu56Ile | missense_variant | 0.18 |
kasA | 2518781 | p.Pro223Ala | missense_variant | 0.25 |
kasA | 2519320 | c.1206C>T | synonymous_variant | 0.12 |
kasA | 2519348 | p.Ala412Ser | missense_variant | 0.12 |
eis | 2714134 | p.Phe400Ser | missense_variant | 0.12 |
eis | 2714318 | p.Arg339Trp | missense_variant | 0.17 |
eis | 2714457 | p.Asp292Glu | missense_variant | 0.12 |
eis | 2714632 | p.Lys234Arg | missense_variant | 0.13 |
eis | 2714920 | p.His138Leu | missense_variant | 0.33 |
eis | 2715086 | p.Ser83Gly | missense_variant | 0.22 |
eis | 2715231 | c.102C>T | synonymous_variant | 0.22 |
eis | 2715584 | c.-252T>C | upstream_gene_variant | 0.17 |
ahpC | 2726635 | p.Ser148Leu | missense_variant | 0.13 |
ahpC | 2726644 | p.Ala151Val | missense_variant | 0.13 |
ahpC | 2726655 | p.Gly155Arg | missense_variant | 0.12 |
folC | 2747317 | c.282C>T | synonymous_variant | 0.29 |
folC | 2747363 | p.Ala79Glu | missense_variant | 0.22 |
folC | 2747377 | c.222C>T | synonymous_variant | 0.29 |
folC | 2747384 | p.Thr72Ser | missense_variant | 0.33 |
folC | 2747403 | p.Ser66Thr | missense_variant | 0.29 |
folC | 2747656 | c.-58G>A | upstream_gene_variant | 0.17 |
pepQ | 2859409 | p.Arg337Leu | missense_variant | 0.17 |
pepQ | 2860099 | p.Leu107Pro | missense_variant | 0.15 |
pepQ | 2860157 | p.Gly88Arg | missense_variant | 0.25 |
pepQ | 2860469 | c.-51C>T | upstream_gene_variant | 0.13 |
pepQ | 2860613 | c.-195C>A | upstream_gene_variant | 0.22 |
ribD | 2986835 | c.-4G>T | upstream_gene_variant | 0.25 |
Rv2752c | 3066177 | c.15T>C | synonymous_variant | 0.12 |
Rv2752c | 3067072 | c.-881C>T | upstream_gene_variant | 0.25 |
thyX | 3067941 | p.Ala2Val | missense_variant | 0.33 |
thyA | 3074165 | p.Ala103Thr | missense_variant | 0.25 |
thyA | 3074319 | p.His51Gln | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448635 | c.132C>A | synonymous_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474495 | c.489A>T | synonymous_variant | 0.13 |
fprA | 3474838 | p.Ile278Phe | missense_variant | 0.2 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
Rv3236c | 3612065 | c.1051delG | frameshift_variant | 0.33 |
Rv3236c | 3612491 | p.Leu209Ser | missense_variant | 0.12 |
fbiA | 3640346 | c.-197G>A | upstream_gene_variant | 0.18 |
fbiA | 3640353 | c.-190G>A | upstream_gene_variant | 0.18 |
fbiA | 3640412 | c.-131G>C | upstream_gene_variant | 0.14 |
fbiB | 3640605 | c.-930G>A | upstream_gene_variant | 0.22 |
fbiA | 3640907 | p.Gly122Asp | missense_variant | 0.2 |
fbiB | 3641031 | c.-504C>T | upstream_gene_variant | 0.14 |
fbiA | 3641050 | p.Gln170* | stop_gained | 0.14 |
fbiA | 3641392 | p.Ile284Leu | missense_variant | 0.18 |
fbiB | 3641762 | p.Lys76Asn | missense_variant | 0.17 |
fbiB | 3641922 | p.Ala130Pro | missense_variant | 0.15 |
fbiB | 3642645 | p.Thr371Ser | missense_variant | 0.14 |
fbiB | 3642813 | p.Gly427Arg | missense_variant | 0.25 |
alr | 3840416 | c.1005C>T | synonymous_variant | 0.2 |
alr | 3840429 | p.Asn331Ile | missense_variant | 0.25 |
alr | 3840436 | c.985C>T | synonymous_variant | 0.25 |
alr | 3840751 | p.Glu224* | stop_gained | 0.29 |
alr | 3841476 | c.-56G>C | upstream_gene_variant | 0.15 |
rpoA | 3877475 | p.Glu345Lys | missense_variant | 0.17 |
ddn | 3987012 | p.Gly57Ser | missense_variant | 0.15 |
clpC1 | 4038459 | p.Leu749Gln | missense_variant | 0.14 |
clpC1 | 4038616 | p.Val697Leu | missense_variant | 0.14 |
clpC1 | 4038724 | p.Val661Met | missense_variant | 0.15 |
clpC1 | 4038927 | p.Arg593Pro | missense_variant | 0.18 |
clpC1 | 4039345 | p.Glu454Lys | missense_variant | 0.17 |
clpC1 | 4039579 | p.Asp376Asn | missense_variant | 0.17 |
clpC1 | 4039608 | p.Tyr366Phe | missense_variant | 0.13 |
clpC1 | 4040308 | c.397C>A | synonymous_variant | 0.18 |
clpC1 | 4040560 | p.Leu49Val | missense_variant | 0.18 |
embC | 4239957 | p.Val32Ala | missense_variant | 0.11 |
embC | 4240872 | p.Val337Ala | missense_variant | 0.13 |
embC | 4240889 | p.Trp343Arg | missense_variant | 0.17 |
embC | 4240955 | p.Pro365Thr | missense_variant | 0.2 |
embC | 4241439 | p.Ser526Ile | missense_variant | 0.18 |
embC | 4241677 | c.1815G>A | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243497 | p.Val89Leu | missense_variant | 0.13 |
embA | 4245107 | p.Phe625Leu | missense_variant | 0.12 |
embA | 4245456 | p.Glu742Lys | missense_variant | 0.25 |
embB | 4247740 | c.1227G>T | synonymous_variant | 0.14 |
embB | 4248202 | c.1689T>A | synonymous_variant | 0.14 |
embB | 4248441 | p.Thr643Ile | missense_variant | 0.14 |
embB | 4248474 | p.Val654Glu | missense_variant | 0.29 |
embB | 4249436 | p.Gln975* | stop_gained | 0.13 |
ubiA | 4269602 | p.Val78Ile | missense_variant | 0.22 |
ethA | 4326694 | p.Met260Ile | missense_variant | 0.22 |
ethR | 4326799 | c.-750G>A | upstream_gene_variant | 0.18 |
ethA | 4326906 | p.Leu190Phe | missense_variant | 0.29 |
ethR | 4327574 | p.Ala9Val | missense_variant | 0.18 |
ethR | 4328186 | c.639delC | frameshift_variant | 0.29 |
whiB6 | 4338542 | c.-21A>G | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408349 | c.-147T>C | upstream_gene_variant | 0.29 |