Run ID: ERR4800390
Sample name:
Date: 01-04-2023 09:47:25
Number of reads: 3163267
Percentage reads mapped: 99.67
Strain: lineage4.3.3
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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.97 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.94 | rifampicin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.98 | isoniazid, ethionamide |
inhA | 1674262 | p.Ile21Val | missense_variant | 0.97 | isoniazid |
pncA | 2288704 | p.Val180Phe | missense_variant | 0.99 | pyrazinamide |
thyX | 3067961 | c.-16C>T | upstream_gene_variant | 1.0 | para-aminosalicylic_acid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.99 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.96 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 0.98 |
gyrA | 8095 | p.Gly265Asp | missense_variant | 0.97 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.97 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.17 |
rpoC | 764918 | p.Val517Leu | missense_variant | 0.98 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.99 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.99 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834346 | p.Arg269Cys | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.98 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
Rv2752c | 3066313 | c.-122T>G | upstream_gene_variant | 0.98 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.99 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.99 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.96 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.99 |
embC | 4242182 | p.Ala774Ser | missense_variant | 0.97 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338280 | c.241dupA | frameshift_variant | 0.95 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.99 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.89 |