Run ID: ERR4132447
Sample name:
Date: 01-04-2023 04:30:27
Number of reads: 262894
Percentage reads mapped: 15.72
Strain: lineage4
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.39 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8086 | p.Asp262Val | missense_variant | 0.33 |
gyrA | 8984 | c.1683C>T | synonymous_variant | 0.22 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575230 | c.-118T>A | upstream_gene_variant | 0.4 |
mshA | 576089 | c.750_769delTGATCGGCGCGCGGCCCGGG | frameshift_variant | 0.29 |
ccsA | 620744 | c.857dupG | frameshift_variant | 0.17 |
rpoB | 762901 | p.Asp1032Gly | missense_variant | 0.15 |
rpoB | 762935 | p.Tyr1043* | stop_gained | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765748 | p.Tyr793* | stop_gained | 0.33 |
rpoC | 765823 | c.2454C>T | synonymous_variant | 0.25 |
rpoC | 766823 | p.Lys1152Glu | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775775 | c.2706G>C | synonymous_variant | 0.33 |
mmpS5 | 778584 | p.Asp108Asn | missense_variant | 0.5 |
mmpR5 | 779008 | p.Val7Ile | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781770 | p.Gly71Ser | missense_variant | 0.22 |
fbiC | 1303880 | p.Thr317Met | missense_variant | 0.29 |
fbiC | 1304159 | p.Val410Gly | missense_variant | 0.5 |
Rv1258c | 1406298 | c.1042delG | frameshift_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471878 | n.33C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.18 |
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 | 0.17 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473763 | n.106C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474255 | n.598C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474903 | n.1246T>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475047 | n.1390G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475163 | n.1506T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475895 | n.2238C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475897 | n.2240T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476213 | n.2556G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476602 | n.2945G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476608 | n.2951C>A | non_coding_transcript_exon_variant | 0.18 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.29 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
PPE35 | 2169386 | c.1227C>A | synonymous_variant | 0.25 |
PPE35 | 2169394 | p.Ala407Ser | missense_variant | 0.18 |
PPE35 | 2169397 | p.Gly406Ser | missense_variant | 0.18 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.15 |
PPE35 | 2169587 | c.1026G>A | synonymous_variant | 0.15 |
PPE35 | 2169602 | c.1011C>A | synonymous_variant | 0.14 |
PPE35 | 2169728 | c.885C>T | synonymous_variant | 0.12 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.62 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.71 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.2 |
PPE35 | 2170424 | c.189G>C | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289339 | c.-98C>A | upstream_gene_variant | 0.29 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
ahpC | 2725995 | c.-198A>G | upstream_gene_variant | 0.4 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.4 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
pepQ | 2860602 | c.-184A>C | upstream_gene_variant | 0.15 |
thyX | 3067540 | p.Ala136Thr | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087578 | c.759A>T | synonymous_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.33 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
clpC1 | 4039786 | p.Ile307Val | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245363 | p.Phe711Leu | missense_variant | 0.29 |
embB | 4247073 | p.Gly187Glu | missense_variant | 0.67 |
embB | 4248441 | p.Thr643Ile | missense_variant | 1.0 |
embB | 4249660 | p.Met1049Ile | missense_variant | 0.25 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.2 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.2 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.2 |
ethA | 4327093 | p.Ser127Arg | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |