Run ID: SRR10809051
Sample name:
Date: 02-04-2023 19:20:48
Number of reads: 2994698
Percentage reads mapped: 99.61
Strain: lineage4.9;lineage4.3
Drug-resistance: HR-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 | 0.13 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.85 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.22 | isoniazid, ethionamide |
pncA | 2288997 | p.His82Arg | missense_variant | 0.14 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.12 |
gyrA | 9074 | c.1773G>A | synonymous_variant | 0.16 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.11 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.27 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777182 | c.1299C>T | synonymous_variant | 0.83 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406785 | p.Leu186Phe | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472179 | n.334C>T | non_coding_transcript_exon_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154350 | p.Glu588Lys | missense_variant | 0.86 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3066335 | c.-144T>G | upstream_gene_variant | 0.16 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.21 |
Rv3236c | 3612176 | p.Arg314Gln | missense_variant | 0.15 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.81 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243081 | c.-152T>G | upstream_gene_variant | 0.81 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.18 |
ethA | 4326423 | p.Gly351Trp | missense_variant | 0.87 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.25 |