Run ID: ERR9806865
Sample name:
Date: 18-05-2023 17:15:13
Number of reads: 2014067
Percentage reads mapped: 99.55
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Ser450Leu (1.00) |
Isoniazid | R | fabG1 c.-15C>T (1.00) |
Ethambutol | R | embB p.Met306Val (1.00) |
Pyrazinamide | R | pncA c.459_466delCAGGGTGC (1.00), pncA c.459_466delCAGGGTGC (1.00) |
Streptomycin | R | rrs n.514A>C (1.00) |
Fluoroquinolones | R | gyrB p.Arg446Leu (0.15), gyrA p.Asp94Gly (0.94) |
Moxifloxacin | R | gyrB p.Arg446Leu (0.15), gyrA p.Asp94Gly (0.94) |
Ofloxacin | R | gyrB p.Arg446Leu (0.15), gyrA p.Asp94Gly (0.94) |
Levofloxacin | R | gyrB p.Arg446Leu (0.15), gyrA p.Asp94Gly (0.94) |
Ciprofloxacin | R | gyrB p.Arg446Leu (0.15), gyrA p.Asp94Gly (0.94) |
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | R | fabG1 c.-15C>T (1.00), ethA c.65delA (1.00), ethA c.65delA (1.00), ethR p.Ala95Thr (1.00) |
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 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrB | 6576 | p.Arg446Leu | missense_variant | 0.15 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.94 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rrs | 1472359 | n.514A>C | non_coding_transcript_exon_variant | 1.0 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
pncA | 2288775 | c.459_466delCAGGGTGC | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4327408 | c.65delA | frameshift_variant | 1.0 | ethionamide, ethionamide |
ethR | 4327831 | p.Ala95Thr | missense_variant | 1.0 | ethionamide |
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 |
gyrA | 9328 | p.Ala676Val | missense_variant | 0.14 |
gyrA | 9650 | c.2349G>A | synonymous_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763555 | c.186C>T | synonymous_variant | 1.0 |
rpoC | 765618 | p.Glu750Gly | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 778979 | c.-74G>T | upstream_gene_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407316 | p.Ala9Thr | missense_variant | 0.11 |
atpE | 1461185 | c.141G>A | synonymous_variant | 0.14 |
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 | 2155240 | p.Ala291Gly | missense_variant | 0.1 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746350 | p.Leu417Met | missense_variant | 0.12 |
folC | 2746704 | p.Ala299Ser | missense_variant | 0.18 |
folC | 2747731 | c.-133C>T | upstream_gene_variant | 0.13 |
pepQ | 2860189 | p.Arg77His | missense_variant | 0.13 |
thyX | 3067207 | p.Ala247Thr | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087504 | p.Val229Ile | missense_variant | 0.12 |
Rv3083 | 3449971 | c.1470delA | frameshift_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612533 | p.Ala195Val | missense_variant | 0.12 |
Rv3236c | 3612557 | p.Val187Ala | missense_variant | 0.18 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641990 | p.Met152Ile | missense_variant | 0.17 |
clpC1 | 4039540 | p.Tyr389Asn | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243159 | c.-74C>T | upstream_gene_variant | 0.12 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244149 | p.Trp306* | stop_gained | 0.12 |
embB | 4248685 | c.2172C>G | synonymous_variant | 0.1 |
embB | 4249054 | c.2541C>T | synonymous_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267679 | c.1158G>A | synonymous_variant | 0.12 |
aftB | 4268140 | p.Gly233Arg | missense_variant | 0.11 |
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 |