Run ID: SRR5341249
Sample name:
Date: 04-04-2023 10:09:58
Number of reads: 918487
Percentage reads mapped: 99.45
Strain: lineage3.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
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 |
gyrA | 9788 | c.2487C>T | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575414 | c.69T>A | synonymous_variant | 0.15 |
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 | 763856 | p.Glu163Lys | missense_variant | 0.12 |
rpoC | 763998 | p.Asp210Gly | missense_variant | 0.13 |
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 |
fbiC | 1303428 | c.498C>A | synonymous_variant | 0.93 |
fbiC | 1304265 | c.1335C>T | synonymous_variant | 0.94 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473691 | n.34T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474425 | n.768A>G | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.14 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.15 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.15 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.23 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167770 | p.Ser948Ile | missense_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.63 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.68 |
Rv1979c | 2222561 | p.Ala202Thr | missense_variant | 0.12 |
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 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.14 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.14 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.96 |
pepQ | 2859833 | p.Ala196Ser | missense_variant | 0.17 |
thyA | 3073743 | c.729T>C | synonymous_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642005 | c.471C>G | synonymous_variant | 1.0 |
fbiB | 3642584 | c.1050G>T | synonymous_variant | 0.13 |
clpC1 | 4040276 | c.429C>A | synonymous_variant | 0.13 |
embC | 4240706 | p.Val282Met | missense_variant | 0.13 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.95 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242688 | p.Gln942His | missense_variant | 0.14 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.14 |
embB | 4246859 | p.Val116Ile | missense_variant | 0.12 |
ubiA | 4268992 | p.Asp281Val | missense_variant | 0.11 |
ethA | 4326912 | p.Val188Ile | missense_variant | 1.0 |
whiB6 | 4338364 | p.Cys53Phe | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.92 |