Run ID: ERR9806796
Sample name:
Date: 18-05-2023 14:56:58
Number of reads: 145608
Percentage reads mapped: 98.61
Strain: lineage4
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | R | fabG1 c.-15C>T (1.00), inhA p.Ile194Thr (1.00), katG p.Gln127Pro (1.00) |
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | ||
Fluoroquinolones | R | gyrB p.Arg446Cys (1.00) |
Moxifloxacin | R | gyrB p.Arg446Cys (1.00) |
Ofloxacin | R | gyrB p.Arg446Cys (1.00) |
Levofloxacin | R | gyrB p.Arg446Cys (1.00) |
Ciprofloxacin | R | gyrB p.Arg446Cys (1.00) |
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | R | fabG1 c.-15C>T (1.00), inhA p.Ile194Thr (1.00) |
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 |
---|---|---|---|---|---|
gyrB | 6575 | p.Arg446Cys | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
inhA | 1674782 | p.Ile194Thr | missense_variant | 1.0 | isoniazid, ethionamide |
katG | 2155732 | p.Gln127Pro | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8480 | c.1179C>A | synonymous_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781821 | p.Lys88Glu | missense_variant | 0.29 |
embR | 1416318 | p.Leu344Phe | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674253 | p.Asp18His | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169624 | p.Gly330Asp | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288944 | p.Thr100Pro | missense_variant | 1.0 |
ahpC | 2726137 | c.-56G>A | upstream_gene_variant | 0.33 |
Rv2752c | 3065616 | c.576C>T | synonymous_variant | 0.5 |
fbiD | 3339040 | c.-78T>C | upstream_gene_variant | 1.0 |
fbiB | 3642146 | p.Leu204Phe | missense_variant | 0.4 |
fbiB | 3642548 | c.1014C>T | synonymous_variant | 0.4 |
fbiB | 3642874 | p.Leu447Arg | missense_variant | 1.0 |
rpoA | 3878641 | c.-135delG | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248783 | p.Pro757Arg | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338599 | c.-78A>C | upstream_gene_variant | 1.0 |
gid | 4407766 | p.Thr146Lys | missense_variant | 1.0 |