Run ID: ERR2679261
Sample name:
Date: 31-03-2023 23:00:34
Number of reads: 269167
Percentage reads mapped: 99.49
Strain: lineage4.1.3
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.3 | Euro-American | T;X;H | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761161 | p.Leu452Pro | missense_variant | 1.0 | rifampicin |
inhA | 1674048 | c.-154G>A | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288746 | c.495delC | frameshift_variant | 0.9 | pyrazinamide, pyrazinamide |
embB | 4247730 | p.Gly406Ala | missense_variant | 0.89 | ethambutol |
gid | 4407967 | p.Leu79Ser | missense_variant | 0.94 | streptomycin |
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 |
gyrA | 9557 | c.2256G>C | synonymous_variant | 1.0 |
fgd1 | 490605 | c.-178G>A | upstream_gene_variant | 0.15 |
fgd1 | 490929 | c.147C>A | synonymous_variant | 0.17 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 1.0 |
rpsL | 781765 | p.Gly69Asp | missense_variant | 0.11 |
fbiC | 1303818 | c.888C>A | synonymous_variant | 0.22 |
fbiC | 1304610 | c.1680C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 0.13 |
PPE35 | 2167814 | p.Tyr933* | stop_gained | 0.11 |
PPE35 | 2170002 | p.Ala204Asp | missense_variant | 0.14 |
PPE35 | 2170749 | c.-137A>G | upstream_gene_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223354 | c.-190A>G | upstream_gene_variant | 0.11 |
pncA | 2288841 | p.Ala134Gly | missense_variant | 0.22 |
eis | 2714889 | c.444C>T | synonymous_variant | 0.2 |
Rv2752c | 3065536 | p.Gly219Asp | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449153 | p.Ile217Thr | missense_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474775 | p.Asp257Tyr | missense_variant | 0.17 |
fprA | 3475244 | p.Arg413His | missense_variant | 0.18 |
rpoA | 3878245 | p.Glu88Gly | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243217 | c.-16C>A | upstream_gene_variant | 1.0 |
aftB | 4269835 | c.-999G>T | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338661 | c.-140C>T | upstream_gene_variant | 1.0 |