Run ID: SRR23862011
Sample name:
Date: 12-04-2023 14:52:45
Number of reads: 6678157
Percentage reads mapped: 99.53
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | ||
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | ||
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6931 | c.-371A>G | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9098 | c.1797G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576100 | p.Asp251Glu | missense_variant | 0.22 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.2 |
mshA | 576626 | p.Thr427Pro | missense_variant | 0.17 |
mshA | 576732 | p.Asp462Gly | missense_variant | 1.0 |
ccsA | 619907 | p.Val6Ala | 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 |
rrl | 1475780 | n.2123A>G | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168214 | p.Thr800Arg | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339744 | c.627A>T | synonymous_variant | 0.44 |
Rv3083 | 3449582 | p.Val360Ala | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568425 | c.255T>G | synonymous_variant | 0.25 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.3 |
whiB7 | 3568441 | p.Lys80Thr | missense_variant | 0.14 |
rpoA | 3878608 | c.-101C>G | upstream_gene_variant | 0.45 |
rpoA | 3878613 | c.-106A>C | upstream_gene_variant | 0.55 |
rpoA | 3878615 | c.-108C>A | upstream_gene_variant | 0.18 |
rpoA | 3878618 | c.-111A>C | upstream_gene_variant | 0.45 |
rpoA | 3878629 | c.-122A>C | upstream_gene_variant | 0.18 |
rpoA | 3878637 | c.-130G>C | upstream_gene_variant | 0.17 |
rpoA | 3878640 | c.-133G>C | upstream_gene_variant | 0.21 |
rpoA | 3878653 | c.-146A>C | upstream_gene_variant | 0.18 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246974 | p.His154Pro | missense_variant | 0.17 |
embB | 4247010 | p.Asp166Ala | missense_variant | 0.16 |
embB | 4247015 | p.Ser168Ala | missense_variant | 0.27 |
whiB6 | 4338205 | p.Val106Gly | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |