Run ID: SRR4035789
Sample name:
Date: 04-04-2023 07:17:56
Number of reads: 711418
Percentage reads mapped: 99.4
Strain: lineage4.1
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 | Euro-American | T;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289090 | p.His51Arg | missense_variant | 0.2 | pyrazinamide |
ahpC | 2726142 | c.-51G>T | upstream_gene_variant | 0.22 | isoniazid |
embB | 4249071 | p.Gln853Pro | missense_variant | 0.29 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5582 | p.Ala115Thr | missense_variant | 0.17 |
gyrB | 5600 | p.His121Tyr | missense_variant | 0.15 |
gyrB | 5726 | p.Pro163Ser | missense_variant | 0.22 |
gyrB | 5732 | p.Lys165Glu | missense_variant | 0.22 |
gyrB | 6054 | p.His272Arg | missense_variant | 0.29 |
gyrB | 6179 | p.Gly314Arg | missense_variant | 0.2 |
gyrB | 6896 | p.Arg553Trp | missense_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7780 | p.Val160Ala | missense_variant | 0.25 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 8341 | p.Ala347Val | missense_variant | 0.13 |
gyrA | 8771 | p.His490Gln | missense_variant | 0.4 |
gyrA | 8923 | p.Gly541Asp | missense_variant | 0.15 |
gyrA | 9285 | p.Ala662Thr | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9708 | c.2407T>C | synonymous_variant | 0.5 |
fgd1 | 490908 | p.Gln42His | missense_variant | 0.17 |
fgd1 | 490994 | p.Gly71Asp | missense_variant | 0.18 |
fgd1 | 491175 | c.393G>A | synonymous_variant | 0.13 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575226 | c.-122C>T | upstream_gene_variant | 0.33 |
mshA | 575664 | p.Gly106Ala | missense_variant | 0.25 |
ccsA | 619806 | c.-85G>T | upstream_gene_variant | 0.33 |
ccsA | 620212 | p.Gly108Ser | missense_variant | 0.18 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760392 | p.Val196Ile | missense_variant | 0.17 |
rpoB | 760727 | c.921C>T | synonymous_variant | 0.14 |
rpoB | 761181 | p.Arg459Cys | missense_variant | 0.14 |
rpoB | 762637 | c.2836delG | frameshift_variant | 0.18 |
rpoC | 762686 | c.-684G>A | upstream_gene_variant | 0.22 |
rpoC | 764010 | p.Arg214His | missense_variant | 0.33 |
rpoC | 764147 | p.Ser260Thr | missense_variant | 0.25 |
rpoC | 764212 | c.843C>T | synonymous_variant | 0.14 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 764873 | p.Pro502Ser | missense_variant | 0.29 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765312 | p.Ala648Val | missense_variant | 0.18 |
rpoC | 765353 | p.Trp662Arg | missense_variant | 0.2 |
rpoC | 765363 | p.Glu665Gly | missense_variant | 0.2 |
rpoC | 765616 | c.2247C>T | synonymous_variant | 0.2 |
rpoC | 765792 | p.Thr808Ile | missense_variant | 0.17 |
rpoC | 766042 | p.Cys891* | stop_gained | 0.25 |
rpoC | 766119 | p.Glu917Gly | missense_variant | 0.18 |
rpoC | 766132 | p.Tyr921* | stop_gained | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776015 | c.2466C>A | synonymous_variant | 0.22 |
mmpL5 | 776407 | p.Pro692Ser | missense_variant | 0.4 |
mmpL5 | 776408 | c.2073G>T | synonymous_variant | 0.33 |
mmpL5 | 776511 | p.Ser657Phe | missense_variant | 0.12 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
mmpL5 | 777694 | p.Thr263Ala | missense_variant | 0.4 |
mmpL5 | 777721 | p.Arg254Trp | missense_variant | 0.33 |
mmpL5 | 777752 | c.729C>A | synonymous_variant | 0.29 |
mmpR5 | 778292 | c.-698C>T | upstream_gene_variant | 0.2 |
mmpR5 | 778990 | p.Val1Met | missense_variant | 0.25 |
mmpS5 | 779531 | c.-626T>A | upstream_gene_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781694 | c.135G>A | synonymous_variant | 0.33 |
rpsL | 781771 | p.Gly71Ala | missense_variant | 0.33 |
rplC | 801074 | p.Ser89Leu | missense_variant | 0.29 |
fbiC | 1303495 | p.Pro189Ser | missense_variant | 0.33 |
fbiC | 1303849 | p.Pro307Ser | missense_variant | 0.15 |
fbiC | 1305340 | p.Ala804Thr | missense_variant | 0.2 |
Rv1258c | 1406303 | c.1038C>A | synonymous_variant | 0.33 |
Rv1258c | 1406503 | p.Val280Met | missense_variant | 0.12 |
Rv1258c | 1407418 | c.-78T>C | upstream_gene_variant | 0.13 |
embR | 1416497 | p.Ser284Trp | missense_variant | 0.4 |
embR | 1416871 | c.477C>A | synonymous_variant | 0.29 |
embR | 1416940 | c.408C>A | synonymous_variant | 0.22 |
embR | 1416995 | p.Glu118Gly | missense_variant | 0.22 |
embR | 1417050 | p.Gly100Ser | missense_variant | 0.2 |
embR | 1417331 | p.Thr6Ile | missense_variant | 0.33 |
atpE | 1461005 | c.-40G>C | upstream_gene_variant | 0.12 |
atpE | 1461007 | c.-38T>C | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474879 | n.1222G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474899 | n.1242T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475931 | n.2274C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476177 | n.2520G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476432 | n.2775T>C | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673567 | p.Ala43Val | missense_variant | 0.29 |
fabG1 | 1673707 | p.Gly90Arg | missense_variant | 0.18 |
fabG1 | 1673819 | p.Met127Thr | missense_variant | 0.29 |
fabG1 | 1673933 | p.Arg165His | missense_variant | 0.17 |
inhA | 1674345 | p.Gln48His | missense_variant | 0.25 |
inhA | 1674348 | c.147C>T | synonymous_variant | 0.25 |
inhA | 1674468 | p.Asp89Glu | missense_variant | 0.29 |
inhA | 1674572 | p.Ala124Val | missense_variant | 0.25 |
rpsA | 1834557 | p.Ala339Val | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918606 | p.Val223Leu | missense_variant | 0.29 |
tlyA | 1918626 | c.687G>A | synonymous_variant | 0.22 |
ndh | 2101870 | c.1173C>A | synonymous_variant | 0.2 |
ndh | 2102801 | p.Asn81Ser | missense_variant | 0.4 |
ndh | 2102933 | p.Asp37Gly | missense_variant | 0.29 |
katG | 2154403 | p.Gly570Ala | missense_variant | 0.17 |
katG | 2154779 | p.Val445Phe | missense_variant | 0.33 |
katG | 2155145 | p.Asn323Tyr | missense_variant | 0.2 |
katG | 2155451 | p.Ala221Thr | missense_variant | 0.33 |
katG | 2155796 | p.Ala106Thr | missense_variant | 0.22 |
katG | 2155847 | p.Pro89Ser | missense_variant | 0.13 |
PPE35 | 2168233 | p.Ile794Phe | missense_variant | 0.17 |
PPE35 | 2168239 | p.Pro792Thr | missense_variant | 0.18 |
PPE35 | 2168244 | p.Ser790Asn | missense_variant | 0.18 |
PPE35 | 2168812 | c.1800delC | frameshift_variant | 0.2 |
PPE35 | 2169100 | p.Gly505Trp | missense_variant | 0.29 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.4 |
PPE35 | 2170085 | c.528G>T | synonymous_variant | 0.33 |
PPE35 | 2170114 | p.Ala167Thr | missense_variant | 0.29 |
Rv1979c | 2221902 | c.1263G>A | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518521 | p.Lys136Met | missense_variant | 0.22 |
kasA | 2518692 | p.Ala193Val | missense_variant | 0.67 |
kasA | 2519343 | p.Ala410Val | missense_variant | 0.15 |
eis | 2714586 | c.747T>C | synonymous_variant | 0.5 |
eis | 2714782 | p.Gln184Leu | missense_variant | 0.4 |
eis | 2714868 | c.465C>T | synonymous_variant | 0.4 |
eis | 2714872 | p.Pro154Leu | missense_variant | 0.4 |
folC | 2746528 | c.1071C>T | synonymous_variant | 0.29 |
folC | 2747136 | p.Leu155Ile | missense_variant | 0.13 |
folC | 2747152 | p.Met149Ile | missense_variant | 0.15 |
folC | 2747316 | p.Arg95Gly | missense_variant | 0.33 |
folC | 2747489 | p.Arg37His | missense_variant | 0.15 |
folC | 2747513 | p.Gln29Leu | missense_variant | 0.17 |
folC | 2747798 | c.-200A>T | upstream_gene_variant | 0.4 |
pepQ | 2859482 | p.Ala313Ser | missense_variant | 0.25 |
pepQ | 2860291 | p.Leu43* | stop_gained | 0.18 |
pepQ | 2860482 | c.-64A>G | upstream_gene_variant | 0.14 |
Rv2752c | 3065618 | p.Gly192Cys | missense_variant | 0.29 |
Rv2752c | 3065733 | c.459G>A | synonymous_variant | 0.2 |
Rv2752c | 3065901 | c.291A>G | synonymous_variant | 0.22 |
Rv2752c | 3066389 | c.-198C>T | upstream_gene_variant | 0.15 |
thyX | 3067526 | c.420C>A | synonymous_variant | 0.25 |
thyX | 3067610 | p.Lys112Asn | missense_variant | 0.15 |
thyX | 3067820 | c.126C>T | synonymous_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087486 | p.Tyr223His | missense_variant | 0.33 |
fbiD | 3339641 | p.Ala175Asp | missense_variant | 0.5 |
Rv3083 | 3448355 | c.-149C>A | upstream_gene_variant | 0.33 |
Rv3083 | 3448861 | p.Gly120Ser | missense_variant | 0.33 |
Rv3083 | 3448988 | p.Arg162Pro | missense_variant | 0.2 |
Rv3083 | 3449298 | p.Met265Ile | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568524 | c.156C>T | synonymous_variant | 0.18 |
whiB7 | 3568620 | c.60C>T | synonymous_variant | 0.33 |
whiB7 | 3568675 | p.Ser2Leu | missense_variant | 0.15 |
whiB7 | 3568859 | c.-181delA | upstream_gene_variant | 0.4 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
Rv3236c | 3612427 | c.690G>T | synonymous_variant | 0.17 |
fbiB | 3641754 | p.Arg74Cys | missense_variant | 0.25 |
fbiB | 3641900 | c.366G>C | synonymous_variant | 0.15 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.3 |
fbiB | 3642313 | p.Arg260His | missense_variant | 0.2 |
fbiB | 3642325 | p.Arg264His | missense_variant | 0.2 |
fbiB | 3642339 | p.Asp269Asn | missense_variant | 0.2 |
fbiB | 3642762 | p.Asp410Tyr | missense_variant | 0.25 |
alr | 3840438 | p.Val328Glu | missense_variant | 0.25 |
alr | 3840456 | p.Leu322Gln | missense_variant | 0.25 |
rpoA | 3877553 | p.Glu319* | stop_gained | 0.18 |
rpoA | 3877884 | c.624G>T | synonymous_variant | 0.22 |
rpoA | 3878068 | p.Val147Ala | missense_variant | 0.17 |
rpoA | 3878072 | p.Tyr146Asn | missense_variant | 0.18 |
rpoA | 3878186 | p.Gly108Ser | missense_variant | 0.29 |
rpoA | 3878422 | p.Gly29Glu | missense_variant | 0.25 |
rpoA | 3878452 | p.Ser19Tyr | missense_variant | 0.22 |
ddn | 3987215 | c.372A>G | synonymous_variant | 0.2 |
clpC1 | 4038234 | p.Arg824Pro | missense_variant | 0.25 |
clpC1 | 4038522 | p.Ile728Asn | missense_variant | 0.2 |
clpC1 | 4038573 | p.Asn711Ser | missense_variant | 0.33 |
clpC1 | 4038937 | p.Thr590Ala | missense_variant | 0.33 |
clpC1 | 4039283 | c.1422C>T | synonymous_variant | 0.33 |
clpC1 | 4039751 | p.Gln318His | missense_variant | 0.13 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.33 |
panD | 4044242 | p.Thr14Ala | missense_variant | 0.29 |
panD | 4044256 | p.Lys9Thr | missense_variant | 0.25 |
embC | 4239679 | c.-184T>A | upstream_gene_variant | 0.22 |
embC | 4240159 | c.297C>T | synonymous_variant | 0.17 |
embC | 4240236 | p.Arg125Gln | missense_variant | 0.18 |
embC | 4241037 | p.Leu392Pro | missense_variant | 0.25 |
embC | 4241065 | c.1203C>T | synonymous_variant | 0.22 |
embC | 4241074 | c.1212G>A | synonymous_variant | 0.25 |
embC | 4241083 | c.1221G>A | synonymous_variant | 0.22 |
embC | 4241435 | p.Ala525Thr | missense_variant | 0.22 |
embC | 4241673 | p.Ala604Val | missense_variant | 0.33 |
embA | 4242370 | c.-863C>T | upstream_gene_variant | 0.4 |
embC | 4242396 | p.Pro845Leu | missense_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embC | 4243044 | p.Gln1061Leu | missense_variant | 0.15 |
embA | 4244473 | p.Val414Glu | missense_variant | 0.15 |
embA | 4244479 | p.Thr416Lys | missense_variant | 0.17 |
embA | 4244720 | p.Tyr496* | stop_gained | 0.17 |
embA | 4245000 | p.Phe590Ile | missense_variant | 0.29 |
embA | 4245049 | p.Tyr606Phe | missense_variant | 0.17 |
embA | 4245052 | p.Val607Ala | missense_variant | 0.14 |
embA | 4245340 | p.Gly703Asp | missense_variant | 0.2 |
embB | 4246118 | c.-396G>T | upstream_gene_variant | 0.2 |
embA | 4246386 | p.Arg1052Cys | missense_variant | 0.18 |
embB | 4247100 | p.Ala196Val | missense_variant | 0.4 |
embB | 4249588 | c.3075C>T | synonymous_variant | 0.13 |
embB | 4249604 | p.Gly1031Ser | missense_variant | 0.2 |
embB | 4249613 | p.Gly1034Ser | missense_variant | 0.18 |
embB | 4249622 | p.Leu1037Ile | missense_variant | 0.2 |
aftB | 4267172 | c.1665C>T | synonymous_variant | 0.2 |
aftB | 4267561 | p.Ala426Thr | missense_variant | 0.17 |
aftB | 4267568 | c.1269G>A | synonymous_variant | 0.15 |
aftB | 4267636 | p.Arg401Gly | missense_variant | 0.25 |
aftB | 4269507 | c.-671G>A | upstream_gene_variant | 0.15 |
ubiA | 4269899 | c.-66A>G | upstream_gene_variant | 0.17 |
ubiA | 4269971 | c.-138A>T | upstream_gene_variant | 0.29 |
ethA | 4327725 | c.-252C>G | upstream_gene_variant | 0.18 |
ethR | 4328089 | p.Arg181Trp | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407951 | c.252G>T | synonymous_variant | 0.29 |