Run ID: SRR7131109
Sample name:
Date: 04-04-2023 18:45:32
Number of reads: 1379974
Percentage reads mapped: 100.0
Strain: lineage4.8
Drug-resistance: Pre-XDR-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 |
---|---|---|---|---|---|
gyrB | 6735 | p.Asn499Thr | missense_variant | 0.98 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781821 | p.Lys88Gln | missense_variant | 1.0 | streptomycin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.1 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.14 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155167 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289038 | p.Trp68* | stop_gained | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
embB | 4247729 | p.Gly406Cys | missense_variant | 1.0 | ethambutol |
ethA | 4326969 | c.504delC | frameshift_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5078 | c.-162_-161insG | upstream_gene_variant | 0.36 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.22 |
rpoB | 759955 | p.Val50Gly | missense_variant | 1.0 |
rpoC | 765713 | p.Thr782Ala | missense_variant | 1.0 |
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 | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473845 | n.188G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474074 | n.417C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474221 | n.564T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474269 | n.612C>A | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474630 | n.973T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474660 | n.1003G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475244 | n.1587A>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475760 | n.2103C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475812 | n.2157delA | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476381 | n.2724G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476514 | n.2857C>G | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3087251 | c.434dupG | frameshift_variant | 1.0 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fbiA | 3640901 | p.Gln120Arg | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |