Run ID: SRR10315640
Sample name:
Date: 02-04-2023 17:13:19
Number of reads: 4348718
Percentage reads mapped: 94.4
Strain: lineage4.8
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.37 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289067 | p.Ser59Pro | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6815 | p.Lys526Gln | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.34 |
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 | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472575 | n.730C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472591 | n.746G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472966 | n.1121A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474389 | n.732G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474483 | n.826C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474551 | n.894G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475683 | n.2026G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475760 | n.2103C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154769 | p.Asp448Ala | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.45 |
fbiD | 3339749 | p.Val211Gly | missense_variant | 0.29 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.22 |
alr | 3840764 | c.657G>C | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.23 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.24 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |