Run ID: ERR8665555
Sample name:
Date: 02-04-2023 07:31:46
Number of reads: 831105
Percentage reads mapped: 99.55
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpoC | 764841 | p.Ile491Thr | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289040 | p.Trp68Gly | missense_variant | 1.0 | pyrazinamide |
folC | 2747471 | p.Ile43Ser | missense_variant | 1.0 | para-aminosalicylic_acid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
ethA | 4326087 | c.1386delA | frameshift_variant | 1.0 | ethionamide, 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 | 9642 | p.Gly781Cys | missense_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.93 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576456 | p.Val370Glu | missense_variant | 0.17 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764283 | p.Ser305* | stop_gained | 0.2 |
rpoC | 765704 | p.Lys779Glu | missense_variant | 0.12 |
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 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801211 | p.Gln135Lys | missense_variant | 0.19 |
fbiC | 1303526 | p.Ser199Trp | missense_variant | 0.1 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834495 | p.Glu318Asp | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.95 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2986917 | p.Glu27* | stop_gained | 0.18 |
Rv2752c | 3064808 | p.Leu462Met | missense_variant | 0.13 |
Rv2752c | 3065910 | c.282C>A | synonymous_variant | 0.19 |
Rv2752c | 3066304 | c.-113C>A | upstream_gene_variant | 0.18 |
thyX | 3067710 | p.Ser79Leu | missense_variant | 0.18 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568795 | c.-116A>G | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641504 | p.Arg321Leu | missense_variant | 0.13 |
fbiB | 3641537 | c.3G>T | start_lost | 0.23 |
fbiB | 3641695 | p.Ser54Tyr | missense_variant | 0.17 |
fbiB | 3641745 | p.Asp71Asn | missense_variant | 0.17 |
ddn | 3986675 | c.-169G>T | upstream_gene_variant | 0.17 |
clpC1 | 4040179 | p.Arg176Ser | missense_variant | 0.2 |
embC | 4242074 | c.2212C>A | synonymous_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242663 | p.Ser934Tyr | missense_variant | 0.22 |
embC | 4242812 | p.Asp984Tyr | missense_variant | 0.23 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244571 | p.Arg447Trp | missense_variant | 0.2 |
embA | 4244814 | p.Leu528Met | missense_variant | 0.14 |
embA | 4246297 | p.Gln1022Arg | missense_variant | 0.1 |
embB | 4247325 | p.Ala271Glu | missense_variant | 0.13 |
ubiA | 4269239 | p.Ala199Thr | missense_variant | 0.13 |
ethA | 4328019 | c.-546G>T | upstream_gene_variant | 0.14 |
whiB6 | 4338371 | p.Thr51Pro | missense_variant | 1.0 |
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 |