Run ID: SRR6046860
Sample name:
Date: 04-04-2023 12:24:34
Number of reads: 1044615
Percentage reads mapped: 92.43
Strain: lineage4.4.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 0.99 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.57 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.32 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407084 | p.Val86Gly | missense_variant | 0.24 |
Rv1258c | 1407407 | c.-67G>C | upstream_gene_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473078 | n.1233G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473289 | n.1444_1445insTTTTG | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475998 | n.2341C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.41 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102407 | c.636T>C | synonymous_variant | 0.1 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.14 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.29 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.14 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.14 |
PPE35 | 2170528 | p.Ser29Thr | missense_variant | 0.11 |
PPE35 | 2170532 | c.81G>C | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519172 | p.Leu353Arg | missense_variant | 0.17 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.24 |
folC | 2746648 | c.951G>A | synonymous_variant | 0.29 |
folC | 2746923 | p.Gly226Ser | missense_variant | 1.0 |
thyX | 3067464 | p.Ile161Thr | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339210 | c.93G>T | synonymous_variant | 0.15 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475006 | p.Phe334Leu | missense_variant | 0.13 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
rpoA | 3878486 | p.Thr8Ala | missense_variant | 0.11 |
embC | 4242557 | p.Gln899* | stop_gained | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243692 | p.Gly154Ser | missense_variant | 1.0 |
embB | 4246904 | p.Val131Met | missense_variant | 1.0 |
embB | 4248719 | p.Gly736Ser | missense_variant | 0.11 |
ethA | 4328252 | c.-779T>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |