Run ID: SRR6045910
Sample name:
Date: 04-04-2023 12:07:40
Number of reads: 2035228
Percentage reads mapped: 93.09
Strain: lineage3.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.5 | 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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | 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 | 1471935 | n.90T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472108 | n.263C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474673 | n.1016T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474674 | n.1018delC | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475752 | n.2095C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475776 | n.2119G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475998 | n.2341C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155334 | p.Val260Ile | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.21 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.24 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.24 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.11 |
whiB6 | 4338592 | c.-71G>C | upstream_gene_variant | 0.99 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338706 | c.-185C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |