Run ID: SRR13861329
Sample name:
Date: 03-04-2023 09:29:07
Number of reads: 451351
Percentage reads mapped: 45.18
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.47 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8393 | c.1092T>C | synonymous_variant | 0.13 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.14 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.12 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.12 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.12 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.12 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.13 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.13 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.13 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.18 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.19 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.19 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.12 |
gyrA | 9774 | p.Asp825Asn | missense_variant | 0.18 |
ccsA | 620144 | c.255dupT | frameshift_variant | 1.0 |
rpoB | 760191 | p.Val129Phe | missense_variant | 1.0 |
rpoB | 760311 | p.Val169Leu | missense_variant | 1.0 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.12 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.12 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.12 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.12 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.14 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.14 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.13 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.14 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.17 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.13 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.14 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.14 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.18 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.19 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.15 |
rpoB | 761732 | c.1926C>G | synonymous_variant | 0.15 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 0.14 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.16 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.15 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.18 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.18 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.19 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.12 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.16 |
rpoB | 761847 | p.Cys681Ser | missense_variant | 0.11 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.12 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.12 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.13 |
rpoB | 762805 | p.Gly1000Asp | missense_variant | 1.0 |
rpoB | 762963 | p.Gly1053Arg | missense_variant | 0.94 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.13 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.12 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.13 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.2 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.2 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.25 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.17 |
rpoC | 763662 | p.Ala98Asp | missense_variant | 0.82 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.2 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.27 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.27 |
rpoC | 763708 | c.339G>A | synonymous_variant | 0.27 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.27 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.27 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.27 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.27 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.27 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.33 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.31 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.23 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.23 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.2 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.2 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.13 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.13 |
mmpL5 | 776041 | p.Ala814Thr | missense_variant | 0.92 |
mmpL5 | 776070 | c.2410delA | frameshift_variant | 1.0 |
mmpL5 | 777800 | c.681C>T | synonymous_variant | 1.0 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.12 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.12 |
fbiC | 1304996 | p.Leu689Ser | missense_variant | 1.0 |
Rv1258c | 1407148 | p.Ala65Ser | missense_variant | 1.0 |
embR | 1416842 | p.Asp169Gly | missense_variant | 1.0 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.12 |
inhA | 1674940 | c.739_740insG | frameshift_variant | 1.0 |
rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 0.15 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.14 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.12 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.12 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.17 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.17 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.16 |
rpsA | 1834624 | c.1083G>C | synonymous_variant | 0.12 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.13 |
ndh | 2102590 | c.453A>C | synonymous_variant | 0.17 |
ndh | 2102694 | p.Val117Ile | missense_variant | 1.0 |
katG | 2155865 | p.Val83Met | missense_variant | 1.0 |
PPE35 | 2168123 | c.2489dupG | frameshift_variant | 1.0 |
PPE35 | 2170268 | c.345C>A | synonymous_variant | 1.0 |
kasA | 2518311 | p.Asp66Gly | missense_variant | 1.0 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.12 |
eis | 2714666 | p.Tyr223Asp | missense_variant | 1.0 |
ahpC | 2726589 | p.Arg133Ser | missense_variant | 1.0 |
pepQ | 2859467 | p.Ala318Thr | missense_variant | 0.14 |
Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.2 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.25 |
Rv2752c | 3065994 | c.198T>C | synonymous_variant | 0.23 |
Rv2752c | 3065997 | c.195C>G | synonymous_variant | 0.23 |
Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.21 |
Rv2752c | 3066024 | c.168T>C | synonymous_variant | 0.25 |
Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 0.15 |
Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.15 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.15 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.15 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.17 |
Rv2752c | 3066087 | c.105A>G | synonymous_variant | 0.14 |
Rv2752c | 3066289 | c.-98T>G | upstream_gene_variant | 1.0 |
thyA | 3074418 | p.Lys18Asn | missense_variant | 1.0 |
ald | 3087163 | c.344_345insC | frameshift_variant | 1.0 |
Rv3236c | 3612049 | c.1068G>C | synonymous_variant | 1.0 |
Rv3236c | 3612400 | c.717G>A | synonymous_variant | 1.0 |
fbiB | 3642445 | p.Ala304Gly | missense_variant | 1.0 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.92 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.18 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.18 |
clpC1 | 4040104 | p.Met201Leu | missense_variant | 0.92 |
embC | 4241480 | c.1618T>C | synonymous_variant | 1.0 |
embB | 4249483 | c.2970C>G | synonymous_variant | 1.0 |
aftB | 4268164 | c.672_673insA | frameshift_variant | 1.0 |
ethA | 4327641 | c.-168G>A | upstream_gene_variant | 1.0 |