Run ID: SRR5818670
Sample name:
Date: 04-04-2023 11:41:51
Number of reads: 1465713
Percentage reads mapped: 84.07
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 | 0.11 | 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 | 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 | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473316 | n.1471C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473318 | n.1473G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474722 | n.1065T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475897 | n.2240T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475938 | n.2281C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | 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 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
ethA | 4328094 | c.-621C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |