Run ID: SRR6824434
Sample name:
Date: 20-10-2023 19:36:57
Number of reads: 10855674
Percentage reads mapped: 99.4
Strain: lineage4.4.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Leu452Pro (1.00) |
Isoniazid | R | katG c.371delG (1.00), katG c.371delG (1.00), ahpC c.-52C>T (1.00) |
Ethambutol | R | embA c.-12C>T (1.00), embB p.Gln497Arg (0.99) |
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.2 | Euro-American | T1;T2 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761161 | p.Leu452Pro | missense_variant | 1.0 | rifampicin |
katG | 2155740 | c.371delG | frameshift_variant | 1.0 | isoniazid, isoniazid |
ahpC | 2726141 | c.-52C>T | upstream_gene_variant | 1.0 | isoniazid |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 1.0 | ethambutol |
embB | 4248003 | p.Gln497Arg | missense_variant | 0.99 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779177 | p.Ser63Asn | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.99 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746936 | c.663T>C | synonymous_variant | 0.17 |
Rv2752c | 3066051 | c.88_140delAACATGACGGTTTTCGAACACCTGGGCCGACTGTTGATTATCGACTGCGGTGT | frameshift_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448348 | c.-156G>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038194 | c.2511G>A | synonymous_variant | 0.99 |
clpC1 | 4039376 | p.Asp443Glu | missense_variant | 0.99 |
clpC1 | 4039873 | p.Thr278Ser | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246508 | c.-6G>A | upstream_gene_variant | 0.99 |
embB | 4247249 | p.Gly246Arg | missense_variant | 0.99 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 0.99 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338422 | p.Cys34Ser | missense_variant | 0.11 |
whiB6 | 4338460 | p.Met21Thr | missense_variant | 0.86 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv2752c | 3066051 | c.87_140delNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNG | disruptive_inframe_deletion | 1.0 |