Run ID: SRR671725
Sample name:
Date: 04-04-2023 15:25:16
Number of reads: 5608809
Percentage reads mapped: 99.41
Strain: lineage4.4.2
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 |
lineage4.4 | Euro-American | S;T | None | 0.99 |
lineage4.4.2 | Euro-American | T1;T2 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.99 | rifampicin |
katG | 2155168 | p.Ser315Asn | missense_variant | 0.99 | isoniazid |
pncA | 2289072 | p.His57Arg | missense_variant | 0.99 | pyrazinamide |
embA | 4243217 | c.-16C>G | upstream_gene_variant | 0.98 | ethambutol |
ethA | 4326699 | c.774delG | frameshift_variant | 0.93 | ethionamide, ethionamide |
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 |
mshA | 576585 | p.Arg413Gln | missense_variant | 0.99 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2859381 | c.1038C>G | synonymous_variant | 0.27 |
Rv2752c | 3064552 | p.Arg547Pro | missense_variant | 0.2 |
Rv2752c | 3066099 | p.Met31Ile | missense_variant | 0.98 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448348 | c.-156G>A | upstream_gene_variant | 0.98 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.12 |
embC | 4240654 | c.792C>G | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.37 |
embB | 4246508 | c.-6G>A | upstream_gene_variant | 0.99 |
embB | 4248320 | p.Gly603Arg | missense_variant | 0.99 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 0.99 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 0.99 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.23 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |