Run ID: SRR14801688
Sample name:
Date: 03-04-2023 11:57:53
Number of reads: 1841676
Percentage reads mapped: 85.79
Strain: lineage4.3.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.99 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 | 9304 | p.Gly668Asp | missense_variant | 0.96 |
mshA | 576085 | c.738G>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.32 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.98 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472089 | n.244C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472518 | n.673G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472953 | n.1109dupT | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472958 | n.1114delT | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472967 | n.1122G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472970 | n.1125C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472971 | n.1126G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472973 | n.1129_1130delAT | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472977 | n.1132G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673266 | c.-174C>T | upstream_gene_variant | 1.0 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.67 |
fbiD | 3339744 | c.627A>T | synonymous_variant | 0.4 |
fbiD | 3339749 | p.Val211Gly | missense_variant | 0.27 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.27 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.5 |
embB | 4247237 | p.Leu242Val | missense_variant | 1.0 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.32 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408150 | p.Leu18Pro | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |