Run ID: SRR6045616
Sample name:
Date: 04-04-2023 12:02:34
Number of reads: 2895779
Percentage reads mapped: 90.67
Strain: lineage4.4.1.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.2 | Euro-American | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.14 | 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 |
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 | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474709 | n.1052G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476691 | n.3034T>C | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2167770 | p.Ser948Ile | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2860213 | p.Pro69Leu | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embC | 4241078 | p.Ile406Val | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247008 | c.495G>A | synonymous_variant | 1.0 |
embB | 4249012 | c.2499G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |