Run ID: SRR6045022
Sample name:
Date: 04-04-2023 11:51:35
Number of reads: 1534902
Percentage reads mapped: 81.21
Strain: lineage3.1.1
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 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.3 | 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 | 491027 | p.Asn82Thr | missense_variant | 0.14 |
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 |
rpoC | 765916 | c.2547C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775647 | p.Gln945Arg | 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 | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.29 |
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 | 0.25 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474674 | n.1017A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474675 | n.1018C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474694 | n.1037C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.6 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 0.88 |
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 |
thyX | 3067442 | c.504C>G | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.22 |
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 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |