Run ID: SRR7517718
Sample name:
Date: 04-04-2023 19:33:43
Number of reads: 1834388
Percentage reads mapped: 94.37
Strain: lineage3
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8081 | c.780A>G | synonymous_variant | 1.0 |
gyrA | 8717 | c.1416C>A | synonymous_variant | 0.22 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491422 | p.Gly214Cys | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620456 | p.Ala189Val | missense_variant | 0.3 |
ccsA | 620464 | p.Ala192Ser | missense_variant | 0.22 |
ccsA | 620503 | p.Glu205* | stop_gained | 0.22 |
ccsA | 620766 | c.876C>T | synonymous_variant | 0.17 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 759760 | c.-47C>A | upstream_gene_variant | 0.29 |
rpoB | 761886 | p.Gln694Lys | missense_variant | 0.21 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764292 | p.Ser308* | stop_gained | 0.29 |
rpoC | 765502 | p.Gln711His | missense_variant | 0.18 |
rpoC | 766324 | c.2955C>T | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776150 | p.Met777Ile | missense_variant | 0.27 |
mmpL5 | 779010 | c.-530G>T | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781785 | p.Glu76* | stop_gained | 0.19 |
fbiC | 1304713 | p.Gly595Trp | missense_variant | 0.25 |
embR | 1416577 | p.Gln257His | missense_variant | 0.92 |
embR | 1416636 | p.Asp238Tyr | missense_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475417 | n.1760G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475961 | n.2304C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476018 | n.2361G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476051 | n.2394G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476149 | n.2492C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476663 | n.3006C>A | non_coding_transcript_exon_variant | 0.18 |
inhA | 1673868 | c.-334C>A | upstream_gene_variant | 0.27 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918533 | c.594C>A | synonymous_variant | 0.2 |
tlyA | 1918566 | c.627C>A | synonymous_variant | 0.2 |
katG | 2154711 | p.Leu467Phe | missense_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154991 | p.Ser374Tyr | missense_variant | 0.2 |
katG | 2155666 | p.Trp149Leu | missense_variant | 0.24 |
PPE35 | 2167670 | p.Phe981Leu | missense_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169552 | p.Pro354His | missense_variant | 0.23 |
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 |
pncA | 2289642 | c.-401A>G | upstream_gene_variant | 0.75 |
pncA | 2290033 | c.-792C>A | upstream_gene_variant | 0.2 |
kasA | 2518070 | c.-45C>A | upstream_gene_variant | 0.29 |
kasA | 2518690 | c.576C>A | synonymous_variant | 0.2 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2747026 | c.573C>A | synonymous_variant | 0.29 |
pepQ | 2859896 | p.Glu175* | stop_gained | 0.25 |
pepQ | 2859914 | p.Glu169* | stop_gained | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339507 | c.390G>T | synonymous_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568418 | c.250_261delGGACGTCCGCGC | conservative_inframe_deletion | 1.0 |
fbiA | 3641243 | p.Arg234Leu | missense_variant | 0.21 |
fbiA | 3641440 | p.Gly300Trp | missense_variant | 0.3 |
rpoA | 3878417 | p.Gly31Cys | missense_variant | 0.2 |
clpC1 | 4039017 | p.Ser563Tyr | missense_variant | 0.33 |
clpC1 | 4040169 | p.Thr179Met | missense_variant | 1.0 |
clpC1 | 4040788 | c.-84C>A | upstream_gene_variant | 0.2 |
embC | 4240306 | c.444C>A | synonymous_variant | 0.25 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244614 | p.Ala461Val | missense_variant | 0.18 |
embB | 4247932 | c.1419C>A | synonymous_variant | 0.24 |
aftB | 4267623 | p.Ser405* | stop_gained | 0.23 |
aftB | 4269024 | c.-188G>A | upstream_gene_variant | 1.0 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |