Run ID: SRR833050
Sample name:
Date: 04-04-2023 20:59:12
Number of reads: 310934
Percentage reads mapped: 85.39
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 | 761110 | p.Asp435Gly | missense_variant | 1.0 | rifampicin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673432 | c.-8T>A | upstream_gene_variant | 0.83 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288785 | c.456dupC | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
ethA | 4327484 | c.-11A>G | upstream_gene_variant | 0.9 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9697 | p.Lys799Thr | missense_variant | 0.18 |
mshA | 575988 | p.Ile214Ser | missense_variant | 0.4 |
rpoB | 761299 | p.Ala498Val | missense_variant | 0.67 |
rpoB | 761353 | p.Gly516Ala | missense_variant | 0.4 |
rpoB | 761404 | p.His533Arg | missense_variant | 0.5 |
rpoB | 763123 | p.Ile1106Thr | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775618 | p.Pro955Ser | missense_variant | 0.5 |
mmpL5 | 776027 | c.2454G>T | synonymous_variant | 0.25 |
mmpL5 | 776925 | p.Thr519Met | missense_variant | 0.13 |
mmpR5 | 779487 | c.498A>C | stop_lost&splice_region_variant | 0.29 |
mmpS5 | 779511 | c.-606T>C | upstream_gene_variant | 0.33 |
mmpS5 | 779561 | c.-662_-657delGGGCAA | upstream_gene_variant | 0.33 |
mmpS5 | 779574 | c.-669T>A | upstream_gene_variant | 0.33 |
mmpS5 | 779578 | c.-673A>T | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302778 | c.-153G>T | upstream_gene_variant | 0.18 |
fbiC | 1302800 | c.-130_-121delGGTGCCGGAC | upstream_gene_variant | 0.33 |
fbiC | 1302818 | c.-113G>A | upstream_gene_variant | 0.33 |
fbiC | 1303181 | p.Ile84Ser | missense_variant | 0.25 |
fbiC | 1304605 | p.Tyr559His | missense_variant | 0.25 |
fbiC | 1305057 | p.Met709Ile | missense_variant | 0.25 |
embR | 1416245 | p.His368Arg | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101904 | p.Ala380Asp | missense_variant | 0.2 |
PPE35 | 2168402 | c.2211A>C | synonymous_variant | 0.22 |
PPE35 | 2168679 | c.1933delA | frameshift_variant | 0.33 |
Rv1979c | 2223051 | p.Glu38Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289658 | c.-417C>T | upstream_gene_variant | 0.2 |
eis | 2715405 | c.-73T>C | upstream_gene_variant | 0.22 |
pepQ | 2859793 | p.Asp209Ala | missense_variant | 0.67 |
pepQ | 2860022 | p.Glu133* | stop_gained | 0.4 |
pepQ | 2860289 | c.130C>T | synonymous_variant | 0.25 |
pepQ | 2860446 | c.-28T>G | upstream_gene_variant | 0.25 |
ribD | 2986990 | p.Gly51Ala | missense_variant | 0.67 |
Rv2752c | 3064646 | p.Glu516* | stop_gained | 0.4 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3640629 | c.-906T>C | upstream_gene_variant | 0.67 |
fbiB | 3641073 | c.-462T>G | upstream_gene_variant | 0.5 |
alr | 3840664 | p.Pro253Thr | missense_variant | 0.4 |
ddn | 3987183 | c.345_348dupCGAC | frameshift_variant | 0.29 |
clpC1 | 4039249 | p.Glu486Lys | missense_variant | 0.25 |
clpC1 | 4039254 | p.Ile484Thr | missense_variant | 0.29 |
clpC1 | 4040373 | p.Gly111Val | missense_variant | 0.43 |
embC | 4239967 | c.105G>A | synonymous_variant | 1.0 |
embC | 4240028 | p.Thr56Ala | missense_variant | 1.0 |
embC | 4242069 | p.Val736Gly | missense_variant | 0.33 |
embC | 4242072 | c.2212dupC | frameshift_variant | 0.4 |
embA | 4246141 | p.Leu970Trp | missense_variant | 0.67 |
ubiA | 4269271 | p.Val188Ala | missense_variant | 1.0 |
ethR | 4326703 | c.-846T>C | upstream_gene_variant | 0.17 |
ethA | 4326964 | p.Asp170Glu | missense_variant | 0.33 |
ethR | 4328129 | p.Val194Ala | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |