Run ID: SRR6896539
Sample name:
Date: 04-04-2023 18:09:15
Number of reads: 689648
Percentage reads mapped: 84.57
Strain: lineage3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761109 | p.Asp435Tyr | missense_variant | 1.0 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.47 | streptomycin |
inhA | 1674319 | p.Gly40Trp | missense_variant | 0.12 | isoniazid |
katG | 2155793 | p.Trp107Arg | missense_variant | 0.2 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8056 | p.Arg252Leu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620062 | p.Ser58Arg | missense_variant | 0.2 |
ccsA | 620209 | c.323delG | frameshift_variant | 0.18 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761297 | p.Tyr497* | stop_gained | 0.12 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 779157 | c.-677C>A | upstream_gene_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303646 | p.Ala239Glu | missense_variant | 0.17 |
embR | 1417102 | c.246C>A | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472826 | n.981G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472836 | n.991G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472838 | n.993A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472845 | n.1000G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472873 | n.1028C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472875 | n.1030T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472877 | n.1032T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472880 | n.1035_1036insA | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474053 | n.396G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474903 | n.1246T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673515 | p.Gly26Arg | missense_variant | 0.12 |
fabG1 | 1673518 | p.Ile27Val | missense_variant | 0.12 |
rpsA | 1834909 | c.1368G>A | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101679 | p.Ser455* | stop_gained | 0.18 |
ndh | 2102583 | p.Ala154Ser | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.92 |
pncA | 2289478 | c.-237T>A | upstream_gene_variant | 0.17 |
kasA | 2518647 | p.Ile178Thr | missense_variant | 0.11 |
eis | 2715139 | p.Met65Thr | missense_variant | 0.12 |
eis | 2715311 | p.Pro8Thr | missense_variant | 0.12 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2859620 | p.Gly267Cys | missense_variant | 0.12 |
pepQ | 2860113 | c.306C>A | synonymous_variant | 0.13 |
pepQ | 2860184 | c.229_234delCGCGCG | conservative_inframe_deletion | 0.12 |
pepQ | 2860201 | c.216_217delAG | frameshift_variant | 0.12 |
pepQ | 2860207 | c.211_212insGCGCGC | conservative_inframe_insertion | 0.13 |
thyA | 3074424 | c.48G>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339324 | c.207G>A | synonymous_variant | 0.12 |
Rv3083 | 3448897 | p.Thr132Ala | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474655 | p.Asp217His | missense_variant | 0.1 |
Rv3236c | 3612843 | c.273delG | frameshift_variant | 0.13 |
fbiB | 3640629 | c.-906T>C | upstream_gene_variant | 0.14 |
fbiB | 3642412 | p.Arg293Pro | missense_variant | 0.11 |
clpC1 | 4038843 | p.Val621Ala | missense_variant | 0.11 |
clpC1 | 4039669 | p.Gln346* | stop_gained | 0.17 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243285 | p.Val18Ala | missense_variant | 0.11 |
embA | 4243292 | c.60G>T | synonymous_variant | 0.12 |
embA | 4244480 | c.1248G>A | synonymous_variant | 0.13 |
embA | 4244638 | p.Val469Ala | missense_variant | 0.21 |
embB | 4245824 | c.-690G>A | upstream_gene_variant | 0.17 |
embB | 4247141 | p.Phe210Leu | missense_variant | 0.11 |
aftB | 4268683 | p.Gly52Cys | missense_variant | 0.18 |
ethA | 4328212 | c.-740delC | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |