Run ID: SRR24112527
Sample name:
Date: 16-04-2023 20:35:09
Number of reads: 5409462
Percentage reads mapped: 99.54
Strain: lineage2.2.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.His445Leu (0.98) |
Isoniazid | R | katG c.375_382dupCATGCAGC (0.24) |
Ethambutol | ||
Pyrazinamide | R | pncA c.-11A>C (0.94) |
Streptomycin | ||
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | R | ethA c.264delC (0.99) |
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.2 | East-Asian (Beijing) | Beijing-RD105/RD207 | RD105;RD207 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761140 | p.His445Leu | missense_variant | 0.98 | rifampicin |
katG | 2155729 | c.375_382dupCATGCAGC | frameshift_variant | 0.24 | isoniazid |
pncA | 2289252 | c.-11A>C | upstream_gene_variant | 0.94 | pyrazinamide |
ethA | 4327209 | c.264delC | frameshift_variant | 0.99 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5080 | c.-160_-159insGA | upstream_gene_variant | 0.99 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.99 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
fbiC | 1305026 | p.Glu699Gly | missense_variant | 0.95 |
Rv1258c | 1406145 | p.Ala399Val | missense_variant | 0.98 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155417 | p.Pro232Leu | missense_variant | 0.23 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.14 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289374 | c.-133T>G | upstream_gene_variant | 0.94 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.14 |
embC | 4240385 | p.Pro175Ala | missense_variant | 0.95 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243222 | c.-11C>T | upstream_gene_variant | 0.99 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.18 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.19 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.2 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.19 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.22 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.22 |
embB | 4247573 | p.Asp354Asn | missense_variant | 0.92 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4326130 | c.1344G>A | synonymous_variant | 0.98 |
whiB6 | 4338289 | p.Gly78Ala | missense_variant | 0.99 |
whiB6 | 4338480 | c.42T>C | synonymous_variant | 0.96 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4407931 | p.Leu91Pro | missense_variant | 0.98 |