Run ID: SRR7131047
Sample name:
Date: 04-04-2023 18:43:13
Number of reads: 2815987
Percentage reads mapped: 100.0
Strain: lineage4.3.3
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 |
lineage4.3 | 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 |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.87 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.73 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289099 | p.Lys48Thr | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326341 | p.Pro378Leu | missense_variant | 1.0 | ethionamide |
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 | 1.0 |
mshA | 576516 | p.Val390Ala | missense_variant | 1.0 |
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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472415 | n.570T>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472880 | n.1035_1036insA | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473201 | n.1357C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.45 |
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 |
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 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243392 | p.Asn54Asp | missense_variant | 1.0 |
ubiA | 4269731 | p.Ala35Ser | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407986 | p.Gly73Arg | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |