Run ID: SRR22251315
Sample name:
Date: 10-02-2024 07:33:44
Number of reads: 1927807
Percentage reads mapped: 99.73
Strain: lineage4.8
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Ser450Leu (1.00), rpoC p.Asp735Asn (1.00) |
Isoniazid | R | katG p.Ser315Thr (0.98) |
Ethambutol | R | embB p.His1002Arg (1.00) |
Pyrazinamide | R | pncA p.Ala143Thr (1.00) |
Streptomycin | ||
Fluoroquinolones | R | gyrA p.Ala90Val (1.00) |
Moxifloxacin | R | gyrA p.Ala90Val (1.00) |
Ofloxacin | R | gyrA p.Ala90Val (1.00) |
Levofloxacin | R | gyrA p.Ala90Val (1.00) |
Ciprofloxacin | R | gyrA p.Ala90Val (1.00) |
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 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpoC | 765572 | p.Asp735Asn | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.98 | isoniazid |
pncA | 2288815 | p.Ala143Thr | missense_variant | 1.0 | pyrazinamide |
embB | 4249518 | p.His1002Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | 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 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289969 | c.-728G>C | upstream_gene_variant | 0.98 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.21 |
ubiA | 4269721 | p.Ala38Val | missense_variant | 0.97 |
ethR | 4326844 | c.-705G>C | upstream_gene_variant | 0.98 |
whiB6 | 4338362 | p.Arg54Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408061 | p.His48Asn | missense_variant | 0.97 |