Run ID: SRR7131198
Sample name:
Date: 04-04-2023 18:48:48
Number of reads: 2327748
Percentage reads mapped: 99.99
Strain: lineage4.3.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.19 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7803 | p.Ser168Gly | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.16 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417339 | c.9T>C | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475177 | n.1520G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475760 | n.2103C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476194 | n.2537A>G | 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 | 0.16 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.23 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |