Run ID: SRR25827674
Sample name:
Date: 16-03-2024 00:34:19
Number of reads: 3877980
Percentage reads mapped: 98.32
Strain: lineage3;lineage2.2.1.1
Drug-resistance: XDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Ser450Leu (1.00) |
Isoniazid | R | fabG1 c.-15C>T (0.24), katG p.Ser315Thr (0.99) |
Ethambutol | R | embB p.Met306Val (0.56), embB p.Gln497Arg (0.37) |
Pyrazinamide | R | pncA p.Gly132Ala (0.26), pncA c.-11A>G (0.45) |
Streptomycin | R | rpsL p.Lys43Arg (0.89), rpsL p.Lys88Arg (0.18) |
Fluoroquinolones | R | gyrA p.Asp94Gly (0.80) |
Moxifloxacin | R | gyrA p.Asp94Gly (0.80) |
Ofloxacin | R | gyrA p.Asp94Gly (0.80) |
Levofloxacin | R | gyrA p.Asp94Gly (0.80) |
Ciprofloxacin | R | gyrA p.Asp94Gly (0.80) |
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | R | fabG1 c.-15C>T (0.24) |
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid | R | rplC p.Cys154Arg (0.43) |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.15 |
lineage2 | East-Asian | Beijing | RD105 | 0.84 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.84 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.85 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 0.58 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.8 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.89 | streptomycin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.18 | streptomycin |
rplC | 801268 | p.Cys154Arg | missense_variant | 0.43 | linezolid |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.24 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.99 | isoniazid |
pncA | 2288847 | p.Gly132Ala | missense_variant | 0.26 | pyrazinamide |
pncA | 2289252 | c.-11A>G | upstream_gene_variant | 0.45 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 0.56 | ethambutol |
embB | 4248003 | p.Gln497Arg | missense_variant | 0.37 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.99 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.99 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491290 | p.Val170Met | missense_variant | 0.25 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.89 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.9 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.14 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764723 | p.Phe452Leu | missense_variant | 0.5 |
rpoC | 764840 | p.Ile491Val | missense_variant | 0.28 |
rpoC | 767123 | p.Val1252Leu | missense_variant | 0.21 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.81 |
mmpR5 | 779156 | p.Leu56Arg | missense_variant | 0.54 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.89 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.83 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.86 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.23 |
eis | 2714846 | p.Val163Ile | missense_variant | 0.56 |
folC | 2747195 | p.Asp135Gly | missense_variant | 0.51 |
Rv2752c | 3064700 | p.Ser498Pro | missense_variant | 0.15 |
Rv2752c | 3065864 | p.Ala110Ser | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473820 | c.-187C>A | upstream_gene_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568425 | c.255T>G | synonymous_variant | 0.24 |
whiB7 | 3568874 | c.-195C>T | upstream_gene_variant | 0.49 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.86 |
alr | 3840259 | p.Tyr388Asp | missense_variant | 0.43 |
embC | 4241022 | p.Ala387Val | missense_variant | 0.24 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243190 | c.-43G>C | upstream_gene_variant | 0.38 |
embA | 4243216 | c.-17G>A | upstream_gene_variant | 0.4 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.85 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.18 |
embB | 4248115 | c.1602C>T | synonymous_variant | 0.55 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.86 |
ethA | 4326593 | p.Cys294Phe | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407620 | p.Tyr195His | missense_variant | 0.22 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.86 |