Run ID: ERR4812999
Sample name:
Date: 01-04-2023 12:28:07
Number of reads: 189866
Percentage reads mapped: 99.42
Strain: lineage4
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
pncA | 2289090 | p.His51Arg | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7824 | p.Ala175Ser | missense_variant | 0.22 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8730 | p.Gly477Trp | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9546 | p.Gly749Cys | missense_variant | 0.22 |
gyrA | 9659 | c.2358C>A | synonymous_variant | 0.22 |
fgd1 | 490977 | c.195C>A | synonymous_variant | 0.5 |
rpoB | 762021 | p.Asp739Tyr | missense_variant | 0.25 |
rpoB | 762640 | p.Gly945Val | missense_variant | 0.33 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766487 | p.Pro1040Ala | missense_variant | 1.0 |
mmpL5 | 776952 | p.Leu510Pro | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473384 | n.-274A>C | upstream_gene_variant | 0.33 |
rpsA | 1833404 | c.-138G>T | upstream_gene_variant | 0.4 |
rpsA | 1834683 | p.Ala381Val | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918034 | p.Val32Ala | missense_variant | 0.67 |
katG | 2156450 | c.-339T>C | upstream_gene_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
ahpC | 2726500 | p.Leu103His | missense_variant | 0.25 |
ribD | 2987159 | p.Gln107His | missense_variant | 0.67 |
Rv2752c | 3065558 | c.633delC | frameshift_variant | 0.22 |
Rv2752c | 3066038 | p.His52Tyr | missense_variant | 0.33 |
thyX | 3067377 | p.Arg190Gln | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3073938 | c.534C>A | synonymous_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embB | 4246764 | p.Pro84Gln | missense_variant | 0.67 |
embB | 4248797 | p.Gly762Cys | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |