Run ID: ERR3287777
Sample name:
Date: 01-04-2023 01:39:28
Number of reads: 4232446
Percentage reads mapped: 99.78
Strain: lineage4.9;lineage4.3.4.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.89 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.09 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 0.9 |
lineage4.3.4.1 | Euro-American (LAM) | LAM1;LAM2 | RD174 | 0.9 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761108 | p.Met434Ile | missense_variant | 0.85 | rifampicin |
rpoB | 761110 | p.Asp435Gly | missense_variant | 0.86 | rifampicin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.89 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.86 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.89 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.9 |
rpoB | 761167 | p.Pro454Leu | missense_variant | 0.89 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.94 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.92 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.96 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.99 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.91 |
katG | 2155787 | p.Ala109Thr | missense_variant | 0.84 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.86 |
ahpC | 2726323 | p.Pro44Arg | missense_variant | 0.89 |
thyX | 3067657 | p.Arg97Trp | missense_variant | 0.93 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.9 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.92 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.91 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 0.86 |
Rv3236c | 3612896 | p.Gly74Ala | missense_variant | 0.89 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.9 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.88 |
embB | 4248320 | p.Gly603Arg | missense_variant | 0.82 |
ubiA | 4269721 | p.Ala38Val | missense_variant | 0.89 |
ethA | 4327311 | p.Ser55Ala | missense_variant | 0.9 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.94 |
gid | 4407831 | c.371dupT | frameshift_variant | 0.88 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.92 |