Run ID: SRR23861868
Sample name:
Date: 12-04-2023 07:50:25
Number of reads: 5422472
Percentage reads mapped: 99.78
Strain: lineage4.6.5
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | R | embB p.Ala313Val (1.00) |
Pyrazinamide | ||
Streptomycin | ||
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | R | tlyA p.Asn236Lys (1.00) |
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 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.5 | Euro-American | T;LAM | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918647 | p.Asn236Lys | missense_variant | 1.0 | capreomycin |
embB | 4247451 | p.Ala313Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.99 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576106 | c.759C>G | synonymous_variant | 0.14 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.14 |
rpoC | 763443 | p.Tyr25Cys | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777974 | c.507C>T | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304451 | c.1521C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154587 | p.Asp509Asn | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746995 | p.Val202Ile | missense_variant | 1.0 |
pepQ | 2859552 | c.867C>T | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568416 | p.Lys88His | missense_variant | 0.18 |
whiB7 | 3568428 | c.252A>C | synonymous_variant | 0.3 |
clpC1 | 4040235 | p.Gly157Ala | missense_variant | 0.16 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246574 | p.Ala21Ser | missense_variant | 0.16 |
embB | 4246993 | p.Asn160Lys | missense_variant | 0.13 |
embB | 4247013 | p.Pro167Arg | missense_variant | 0.2 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.16 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407914 | p.Arg97Cys | missense_variant | 1.0 |