Run ID: SRR4035722
Sample name:
Date: 04-04-2023 07:15:30
Number of reads: 1296558
Percentage reads mapped: 99.39
Strain: lineage4.1.2
Drug-resistance: Other
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 |
lineage4.1.2 | Euro-American | T;H | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4246734 | p.Leu74Arg | missense_variant | 0.11 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5130 | c.-110A>G | upstream_gene_variant | 0.13 |
gyrB | 5308 | c.69G>A | synonymous_variant | 0.13 |
gyrB | 7112 | p.Thr625Ala | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7590 | p.Val97Met | missense_variant | 0.12 |
gyrA | 7921 | p.Asn207Ile | missense_variant | 0.14 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.12 |
gyrA | 9036 | p.Ala579Thr | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9313 | p.Leu671Arg | missense_variant | 0.12 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575420 | p.Thr25Ala | missense_variant | 0.1 |
mshA | 575651 | p.Arg102Trp | missense_variant | 0.14 |
mshA | 576593 | p.Val416Met | missense_variant | 0.25 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760767 | p.Pro321Ser | missense_variant | 0.2 |
rpoB | 761136 | p.Thr444Ala | missense_variant | 0.18 |
rpoB | 761192 | c.1389delG | frameshift_variant | 0.2 |
rpoB | 762082 | p.Gly759Ala | missense_variant | 0.17 |
rpoB | 762306 | p.Pro834Ser | missense_variant | 0.22 |
rpoC | 763094 | c.-276G>T | upstream_gene_variant | 0.14 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.14 |
rpoC | 764210 | p.Ile281Val | missense_variant | 0.11 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 764399 | p.Tyr344His | missense_variant | 0.1 |
rpoC | 765137 | p.Thr590Ser | missense_variant | 0.17 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765438 | c.2070delG | frameshift_variant | 0.14 |
rpoC | 766073 | p.Ala902Pro | missense_variant | 0.11 |
rpoC | 766076 | p.Glu903Gln | missense_variant | 0.11 |
rpoC | 766862 | p.Val1165Leu | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776481 | p.Ala667Val | missense_variant | 0.14 |
mmpL5 | 776492 | p.Gln663His | missense_variant | 0.2 |
mmpL5 | 776714 | c.1766delA | frameshift_variant | 0.14 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
mmpL5 | 777437 | c.1044C>T | synonymous_variant | 0.17 |
mmpL5 | 777532 | p.Ile317Val | missense_variant | 0.17 |
mmpL5 | 777762 | p.Leu240Gln | missense_variant | 0.17 |
mmpL5 | 777986 | c.495C>T | synonymous_variant | 0.18 |
mmpL5 | 778188 | p.Gln98Arg | missense_variant | 0.11 |
mmpL5 | 778386 | p.Ala32Val | missense_variant | 0.17 |
mmpS5 | 779635 | c.-730G>C | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303442 | p.Leu171Ser | missense_variant | 0.13 |
fbiC | 1303794 | c.864A>G | synonymous_variant | 0.13 |
fbiC | 1303818 | c.889delG | frameshift_variant | 0.14 |
fbiC | 1303942 | p.Val338Met | missense_variant | 0.13 |
fbiC | 1304222 | c.1295delG | frameshift_variant | 0.25 |
fbiC | 1304434 | p.Ala502Ser | missense_variant | 0.15 |
embR | 1417112 | p.Leu79Pro | missense_variant | 0.15 |
atpE | 1460855 | c.-189delC | upstream_gene_variant | 0.12 |
atpE | 1461042 | c.-3G>A | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471789 | n.-57T>C | upstream_gene_variant | 0.11 |
rrs | 1471796 | n.-50A>G | upstream_gene_variant | 0.12 |
rrl | 1473684 | n.27G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474058 | n.401C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474296 | n.640delC | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474458 | n.801C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476173 | n.2516A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476306 | n.2649A>G | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673720 | p.Asp94Val | missense_variant | 0.17 |
inhA | 1674224 | p.Lys8Ile | missense_variant | 0.17 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.15 |
rpsA | 1833562 | c.21C>G | synonymous_variant | 0.14 |
rpsA | 1834017 | p.Arg159His | missense_variant | 0.22 |
rpsA | 1834218 | p.Val226Ala | missense_variant | 0.18 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.18 |
rpsA | 1834752 | p.Leu404Pro | missense_variant | 0.12 |
tlyA | 1917886 | c.-54C>A | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918421 | p.Ala161Asp | missense_variant | 0.13 |
ndh | 2101947 | p.Asp366Tyr | missense_variant | 0.14 |
ndh | 2102446 | c.597C>T | synonymous_variant | 0.13 |
ndh | 2102774 | p.Thr90Ser | missense_variant | 0.2 |
katG | 2154049 | p.Lys688Thr | missense_variant | 0.11 |
katG | 2154225 | c.1887T>C | synonymous_variant | 0.17 |
katG | 2154242 | p.Met624Leu | missense_variant | 0.17 |
katG | 2154343 | p.Lys590Arg | missense_variant | 0.12 |
katG | 2154516 | c.1596G>T | synonymous_variant | 0.17 |
katG | 2154540 | c.1572C>T | synonymous_variant | 0.22 |
katG | 2154626 | p.Arg496Ser | missense_variant | 0.25 |
katG | 2154670 | p.Ser481Leu | missense_variant | 0.29 |
katG | 2155723 | p.Ala130Gly | missense_variant | 0.11 |
katG | 2155851 | c.261G>A | synonymous_variant | 0.18 |
PPE35 | 2167868 | c.2744delG | frameshift_variant | 0.14 |
PPE35 | 2168195 | c.2418G>T | synonymous_variant | 0.12 |
PPE35 | 2168541 | p.Thr691Ile | missense_variant | 0.14 |
PPE35 | 2168790 | p.Pro608Leu | missense_variant | 0.15 |
PPE35 | 2168915 | c.1698G>A | synonymous_variant | 0.25 |
PPE35 | 2168964 | p.Val550Ala | missense_variant | 0.14 |
PPE35 | 2168991 | p.Ala541Asp | missense_variant | 0.13 |
PPE35 | 2169981 | p.Asn211Ile | missense_variant | 0.2 |
Rv1979c | 2222548 | p.Ser206* | stop_gained | 0.2 |
Rv1979c | 2223029 | p.Phe46Ile | missense_variant | 0.14 |
Rv1979c | 2223180 | c.-16A>G | upstream_gene_variant | 0.13 |
Rv1979c | 2223249 | c.-85G>T | upstream_gene_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223300 | c.-136G>C | upstream_gene_variant | 0.14 |
Rv1979c | 2223312 | c.-148C>A | upstream_gene_variant | 0.14 |
Rv1979c | 2223316 | c.-152T>A | upstream_gene_variant | 0.14 |
pncA | 2289796 | c.-555T>G | upstream_gene_variant | 0.12 |
pncA | 2290072 | c.-831T>C | upstream_gene_variant | 0.11 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518265 | p.Val51Leu | missense_variant | 0.11 |
kasA | 2518290 | p.Lys59Thr | missense_variant | 0.11 |
eis | 2714149 | p.Pro395Arg | missense_variant | 0.11 |
eis | 2714416 | p.Glu306Ala | missense_variant | 0.18 |
eis | 2715128 | p.Leu69Met | missense_variant | 0.17 |
eis | 2715137 | p.Asp66Asn | missense_variant | 0.15 |
eis | 2715147 | c.186G>A | synonymous_variant | 0.14 |
ahpC | 2726450 | c.258G>C | synonymous_variant | 0.11 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 0.11 |
folC | 2746570 | c.1029C>T | synonymous_variant | 0.25 |
folC | 2746816 | c.783C>A | synonymous_variant | 0.17 |
folC | 2747122 | c.477G>A | synonymous_variant | 0.17 |
folC | 2747201 | p.Leu133Pro | missense_variant | 0.15 |
folC | 2747496 | p.Asp35Asn | missense_variant | 0.12 |
pepQ | 2859575 | p.Ala282Pro | missense_variant | 0.2 |
pepQ | 2859580 | p.Leu280Pro | missense_variant | 0.18 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.22 |
ribD | 2986711 | c.-128G>A | upstream_gene_variant | 0.33 |
ribD | 2987158 | p.Gln107Arg | missense_variant | 0.17 |
Rv2752c | 3065376 | c.816C>T | synonymous_variant | 0.17 |
Rv2752c | 3066161 | p.Leu11Met | missense_variant | 0.12 |
thyX | 3067268 | c.678G>C | synonymous_variant | 0.15 |
thyX | 3067282 | p.Val222Met | missense_variant | 0.15 |
thyX | 3067701 | p.Ile82Thr | missense_variant | 0.15 |
thyX | 3067716 | p.Ser77Thr | missense_variant | 0.17 |
thyA | 3073901 | p.Gln191Glu | missense_variant | 0.11 |
thyA | 3074064 | c.408C>T | synonymous_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087788 | p.Glu323Asp | missense_variant | 0.11 |
fbiD | 3338999 | c.-119T>G | upstream_gene_variant | 0.11 |
fbiD | 3339041 | c.-77G>A | upstream_gene_variant | 0.14 |
fbiD | 3339579 | c.462C>T | synonymous_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474226 | p.Pro74Ser | missense_variant | 0.18 |
fprA | 3474764 | p.Arg253Leu | missense_variant | 0.14 |
whiB7 | 3568868 | c.-189G>T | upstream_gene_variant | 0.2 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
Rv3236c | 3612364 | c.753T>C | synonymous_variant | 0.15 |
fbiA | 3640642 | p.His34Asp | missense_variant | 0.11 |
fbiA | 3641075 | p.Ala178Asp | missense_variant | 0.13 |
fbiA | 3641510 | p.Gly323Glu | missense_variant | 0.17 |
fbiB | 3642209 | c.675C>T | synonymous_variant | 0.14 |
fbiB | 3642635 | p.Asp367Glu | missense_variant | 0.14 |
fbiB | 3642774 | p.Leu414Met | missense_variant | 0.13 |
alr | 3840701 | c.719_720insAGAC | frameshift_variant | 0.14 |
rpoA | 3877533 | c.975C>T | synonymous_variant | 0.14 |
rpoA | 3877907 | p.Ser201Pro | missense_variant | 0.11 |
rpoA | 3878013 | c.495T>C | synonymous_variant | 0.12 |
clpC1 | 4040806 | c.-102A>T | upstream_gene_variant | 0.2 |
panD | 4044195 | p.Asp29Glu | missense_variant | 0.17 |
embC | 4240025 | p.Thr55Ala | missense_variant | 0.18 |
embC | 4240814 | p.Gly318Ser | missense_variant | 0.17 |
embC | 4241231 | p.Arg457Trp | missense_variant | 0.13 |
embC | 4241234 | p.Thr458Ala | missense_variant | 0.14 |
embC | 4241279 | p.Val473Met | missense_variant | 0.12 |
embC | 4241844 | p.Leu661His | missense_variant | 0.14 |
embC | 4242219 | p.Thr786Arg | missense_variant | 0.12 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242722 | p.Pro954Ser | missense_variant | 0.25 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244510 | c.1278G>A | synonymous_variant | 0.2 |
embA | 4245382 | p.Thr717Ile | missense_variant | 0.14 |
embB | 4246605 | p.Thr31Ile | missense_variant | 0.15 |
embB | 4246625 | p.Phe38Leu | missense_variant | 0.14 |
embB | 4246750 | c.237T>C | synonymous_variant | 0.12 |
embB | 4247986 | c.1473C>A | synonymous_variant | 0.12 |
embB | 4248708 | p.Thr732Ser | missense_variant | 0.12 |
embB | 4249062 | p.Thr850Ile | missense_variant | 0.17 |
aftB | 4267123 | c.1714C>A | synonymous_variant | 0.14 |
aftB | 4267756 | p.Lys361Glu | missense_variant | 0.12 |
aftB | 4268277 | p.Pro187Gln | missense_variant | 0.13 |
aftB | 4268297 | c.540A>G | synonymous_variant | 0.11 |
aftB | 4268384 | c.453G>A | synonymous_variant | 0.15 |
aftB | 4268406 | p.Val144Ala | missense_variant | 0.18 |
aftB | 4268547 | p.Leu97Pro | missense_variant | 0.11 |
ubiA | 4269407 | p.Lys143* | stop_gained | 0.15 |
ubiA | 4269617 | p.Asn73Tyr | missense_variant | 0.17 |
ubiA | 4269634 | p.Ser67Leu | missense_variant | 0.25 |
ethA | 4326345 | p.Ile377Val | missense_variant | 0.29 |
ethA | 4327614 | c.-141G>C | upstream_gene_variant | 0.15 |
whiB6 | 4338569 | c.-48A>G | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |