Run ID: ERR4813047
Sample name:
Date: 01-04-2023 12:30:11
Number of reads: 622145
Percentage reads mapped: 99.55
Strain: lineage4.3
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761101 | p.Gln432Pro | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288764 | p.Thr160Pro | missense_variant | 1.0 | pyrazinamide |
pncA | 2289213 | p.Gln10Arg | missense_variant | 0.11 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 763087 | p.Val1094Asp | missense_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765926 | p.Thr853Ala | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416324 | p.Asn342Asp | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 0.92 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155757 | p.Arg119Ser | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288692 | p.Cys184Arg | missense_variant | 0.2 |
eis | 2714276 | c.1057C>A | synonymous_variant | 0.11 |
pepQ | 2860387 | p.Lys11Ile | missense_variant | 0.14 |
ribD | 2987548 | p.Arg237Gln | missense_variant | 0.11 |
thyX | 3067817 | c.129C>T | synonymous_variant | 0.14 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074375 | p.Gln33Lys | missense_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449249 | p.Ala249Asp | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038384 | p.Arg774Gln | missense_variant | 0.11 |
embC | 4241966 | p.Gly702* | stop_gained | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247608 | c.1095G>A | synonymous_variant | 0.18 |
ubiA | 4269320 | p.Leu172Val | missense_variant | 1.0 |
ubiA | 4269954 | c.-121A>G | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407721 | p.Ala161Gly | missense_variant | 1.0 |
gid | 4408050 | p.Asn51Lys | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |