Run ID: SRR18002879
Sample name:
Date: 03-04-2023 19:07:31
Number of reads: 4124895
Percentage reads mapped: 88.89
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 | 0.94 |
lineage4.4 | Euro-American | S;T | None | 0.92 |
lineage4.4.2 | Euro-American | T1;T2 | None | 0.92 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.97 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.98 | isoniazid |
pncA | 2288740 | p.Thr168Pro | missense_variant | 0.93 | pyrazinamide |
embA | 4243217 | c.-16C>T | upstream_gene_variant | 0.87 | ethambutol |
embB | 4248003 | p.Gln497Arg | missense_variant | 0.96 | ethambutol |
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 | 575254 | c.-94C>T | upstream_gene_variant | 0.93 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.32 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.16 |
rpoC | 764724 | p.Phe452Cys | missense_variant | 0.95 |
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 |
katG | 2155854 | c.258C>A | synonymous_variant | 0.92 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3066099 | p.Met31Ile | missense_variant | 0.91 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448348 | c.-156G>A | upstream_gene_variant | 0.86 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246508 | c.-6G>A | upstream_gene_variant | 0.95 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.13 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.18 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.17 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.2 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.25 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.21 |
embB | 4247249 | p.Gly246Arg | missense_variant | 0.95 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.12 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 0.92 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 0.95 |
ethA | 4327058 | p.Gly139Val | missense_variant | 0.99 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407712 | p.Gly164Ala | missense_variant | 0.94 |