Run ID: SRR7131221
Sample name:
Date: 04-04-2023 18:49:39
Number of reads: 1921709
Percentage reads mapped: 99.99
Strain: lineage4.6.2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.2 | Euro-American | T;LAM | RD726 | 1.0 |
lineage4.6.2.2 | Euro-American (Cameroon) | LAM10-CAM | RD726 | 1.0 |
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 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778298 | c.-692C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472502 | n.657G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472507 | n.662C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474483 | n.826C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474551 | n.894G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476701 | n.3044A>G | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3065258 | p.Met312Val | missense_variant | 1.0 |
thyX | 3067474 | p.Pro158Ala | missense_variant | 1.0 |
fbiD | 3339741 | c.624G>T | synonymous_variant | 0.11 |
fbiD | 3339744 | c.627A>C | synonymous_variant | 0.11 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612571 | c.546C>T | synonymous_variant | 1.0 |
embA | 4242550 | c.-683C>G | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246553 | c.40C>A | synonymous_variant | 0.17 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.24 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.17 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 1.0 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 1.0 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |