Run ID: SRR1173293
Sample name:
Date: 03-04-2023 03:21:01
Number of reads: 888127
Percentage reads mapped: 39.8
Strain: lineage4.6.1;lineage3.1.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.72 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.35 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 0.88 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 0.72 |
lineage4.6.1 | Euro-American (Uganda) | T2 | RD724 | 0.29 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.29 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.14 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 0.54 | ethambutol |
gid | 4407851 | c.351delG | frameshift_variant | 0.86 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7539 | p.Thr80Ala | missense_variant | 0.35 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7709 | c.408G>A | synonymous_variant | 0.36 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490599 | c.-184C>A | upstream_gene_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.74 |
mshA | 575320 | c.-28C>T | upstream_gene_variant | 0.12 |
mshA | 575640 | p.Pro98Gln | missense_variant | 0.15 |
ccsA | 620799 | p.Met303Ile | missense_variant | 0.15 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.64 |
rpoB | 761270 | c.1464C>A | synonymous_variant | 0.12 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.67 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.69 |
rpoC | 764021 | c.652C>A | synonymous_variant | 0.13 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.27 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.27 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.3 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.3 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.36 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.36 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.31 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.31 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.29 |
rpoC | 764641 | c.1272C>T | synonymous_variant | 0.26 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.29 |
rpoC | 764663 | p.Val432Thr | missense_variant | 0.18 |
rpoC | 764672 | p.Gln435Glu | missense_variant | 0.12 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.12 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.12 |
rpoC | 765191 | c.1823delA | frameshift_variant | 0.13 |
rpoC | 766488 | p.Pro1040Arg | missense_variant | 0.31 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.53 |
mmpL5 | 778516 | c.-36C>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406390 | p.Leu317Phe | missense_variant | 0.12 |
embR | 1416634 | p.Asp238Glu | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472264 | n.419T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472266 | n.421C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472427 | n.582T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472714 | n.869A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472814 | n.969G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475538 | n.1881T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475540 | n.1883C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475550 | n.1893A>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475551 | n.1894T>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475555 | n.1898T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475564 | n.1907C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475574 | n.1917C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475575 | n.1918C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475576 | n.1919C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476491 | n.2834T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.25 |
inhA | 1674281 | p.Arg27Leu | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102623 | c.420C>A | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.82 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.84 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.21 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 0.56 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.56 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.64 |
kasA | 2518593 | p.Ala160Asp | missense_variant | 0.14 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.71 |
folC | 2747535 | p.Asp22Tyr | missense_variant | 0.15 |
pepQ | 2860142 | p.Gly93Arg | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.7 |
fbiD | 3339140 | p.Gly8Asp | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474177 | c.171C>T | synonymous_variant | 0.24 |
Rv3236c | 3613149 | c.-33G>A | upstream_gene_variant | 0.15 |
Rv3236c | 3613153 | c.-37G>T | upstream_gene_variant | 0.15 |
fbiA | 3641494 | p.Glu318Lys | missense_variant | 0.15 |
rpoA | 3878703 | c.-196G>A | upstream_gene_variant | 0.14 |
ddn | 3987011 | c.168C>T | synonymous_variant | 0.12 |
embC | 4240172 | p.Val104Met | missense_variant | 0.64 |
embC | 4240728 | p.Ala289Val | missense_variant | 0.12 |
embC | 4241562 | p.Arg567His | missense_variant | 0.44 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4266975 | p.Pro621His | missense_variant | 0.12 |
ubiA | 4269670 | p.Val55Gly | missense_variant | 0.33 |
ethA | 4326038 | p.Arg479Leu | missense_variant | 0.12 |
ethA | 4328329 | c.-856C>G | upstream_gene_variant | 0.56 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.79 |
gid | 4407742 | p.Arg154Gln | missense_variant | 0.41 |