Run ID: SRR13861406
Sample name:
Date: 03-04-2023 09:30:55
Number of reads: 224204
Percentage reads mapped: 5.61
Strain: lineage4.9
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 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761131 | p.Gly442Glu | missense_variant | 0.4 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.76 | streptomycin |
katG | 2155185 | c.926_927insA | frameshift_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8396 | p.Tyr365* | stop_gained | 1.0 |
fgd1 | 490821 | p.Glu13Asp | missense_variant | 1.0 |
mshA | 575959 | p.Gln204His | missense_variant | 0.91 |
rpoB | 761126 | c.1320G>T | synonymous_variant | 0.4 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.4 |
rpoB | 761133 | p.Leu443Ile | missense_variant | 0.4 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.33 |
rpoB | 761151 | p.Leu449Val | missense_variant | 0.33 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.33 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.33 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.33 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.33 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.4 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.33 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.33 |
rpoB | 761196 | p.Leu464Phe | missense_variant | 0.33 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.29 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.29 |
rpoB | 761220 | p.Ser472Thr | missense_variant | 0.33 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.4 |
rpoB | 761235 | p.Met477Val | missense_variant | 0.33 |
rpoC | 764401 | c.1032C>T | synonymous_variant | 0.2 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.2 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.2 |
rpoC | 764419 | c.1050C>T | synonymous_variant | 0.22 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 0.25 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.22 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.25 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.22 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.25 |
rpoC | 764451 | p.Gly361Ala | missense_variant | 0.22 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.2 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.2 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.2 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.18 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.2 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.2 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.18 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.18 |
rpoC | 764513 | p.Phe382Leu | missense_variant | 0.18 |
rpoC | 766364 | p.Ala999Ser | missense_variant | 1.0 |
mmpL5 | 775945 | p.Val846Leu | missense_variant | 1.0 |
mmpL5 | 776248 | p.Ala745Pro | missense_variant | 0.4 |
mmpL5 | 778345 | p.Leu46Ile | missense_variant | 1.0 |
mmpL5 | 778992 | c.-512C>T | upstream_gene_variant | 1.0 |
mmpR5 | 779231 | p.Glu81Val | missense_variant | 1.0 |
fbiC | 1303186 | p.Tyr86His | missense_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.21 |
fabG1 | 1673157 | c.-283G>C | upstream_gene_variant | 1.0 |
ndh | 2101749 | p.Thr432Ser | missense_variant | 1.0 |
katG | 2155982 | p.Asn44His | missense_variant | 1.0 |
PPE35 | 2168042 | c.2571G>C | synonymous_variant | 1.0 |
PPE35 | 2169365 | c.1248C>T | synonymous_variant | 1.0 |
thyX | 3067878 | p.Val23Gly | missense_variant | 1.0 |
fbiD | 3339188 | p.Thr24Ser | missense_variant | 1.0 |
fprA | 3474999 | c.993G>T | synonymous_variant | 1.0 |
whiB7 | 3568496 | p.Pro62Ser | missense_variant | 1.0 |
Rv3236c | 3612323 | p.Pro265Gln | missense_variant | 1.0 |
fbiB | 3641121 | c.-414C>A | upstream_gene_variant | 1.0 |
clpC1 | 4038346 | p.Glu787* | stop_gained | 1.0 |
embC | 4239894 | p.Ala11Gly | missense_variant | 1.0 |
ethA | 4327073 | p.Leu134Pro | missense_variant | 1.0 |