Run ID: ERR9117695
Sample name:
Date: 02-04-2023 09:28:43
Number of reads: 1408542
Percentage reads mapped: 88.17
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.31 | 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 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.98 |
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 | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473663 | n.6A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476214 | n.2557G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168892 | p.Thr574Lys | missense_variant | 0.98 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.11 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.11 |
Rv1979c | 2222142 | c.1023A>C | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878522 | c.-15G>T | upstream_gene_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338566 | c.-45A>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |