Run ID: ERR5864460
Sample name:
Date: 01-04-2023 23:21:44
Number of reads: 2153017
Percentage reads mapped: 99.57
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 | 7563 | p.Gly88Cys | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
tlyA | 1918665 | c.728dupT | frameshift_variant | 1.0 | capreomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289030 | p.His71Arg | missense_variant | 1.0 | pyrazinamide |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 0.96 | ethambutol |
embB | 4247513 | p.Tyr334His | missense_variant | 1.0 | ethambutol |
ethA | 4326800 | c.672_673dupGC | frameshift_variant | 0.15 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5593 | c.354T>C | synonymous_variant | 0.1 |
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 | 9759 | p.Glu820Lys | missense_variant | 0.1 |
fgd1 | 491012 | p.Pro77His | missense_variant | 0.22 |
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 |
rpoB | 760089 | p.Gly95Arg | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764817 | p.Val483Gly | missense_variant | 1.0 |
rpoC | 765668 | p.His767Asn | missense_variant | 0.1 |
rpoC | 766222 | c.2853T>C | synonymous_variant | 0.12 |
rpoC | 766645 | p.Glu1092Asp | 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 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303078 | p.Ala50Thr | missense_variant | 0.14 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.307delC | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473969 | n.312G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473970 | n.313G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475445 | n.1788T>G | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1674029 | p.Arg197Gln | missense_variant | 0.12 |
inhA | 1674777 | c.576C>T | synonymous_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834892 | c.1353delC | frameshift_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102371 | c.671delT | frameshift_variant | 0.96 |
ndh | 2102845 | c.198A>T | synonymous_variant | 0.13 |
katG | 2154646 | p.Arg489His | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170241 | c.372C>T | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290007 | c.-766A>T | upstream_gene_variant | 0.11 |
kasA | 2518147 | c.33C>T | synonymous_variant | 0.3 |
eis | 2714579 | c.754T>C | synonymous_variant | 0.12 |
ahpC | 2726549 | p.Ser119Arg | missense_variant | 0.1 |
pepQ | 2859506 | p.Ala305Thr | missense_variant | 0.13 |
pepQ | 2860162 | p.Arg86Pro | missense_variant | 0.1 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 1.0 |
ribD | 2986976 | c.138C>T | synonymous_variant | 0.12 |
thyX | 3067283 | c.663C>T | synonymous_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087532 | p.Ala238Asp | missense_variant | 1.0 |
fbiD | 3338994 | c.-124G>C | upstream_gene_variant | 0.11 |
Rv3083 | 3448437 | c.-67C>T | upstream_gene_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612229 | c.888C>T | synonymous_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641265 | c.-270C>A | upstream_gene_variant | 0.11 |
fbiB | 3641540 | c.6C>A | synonymous_variant | 0.11 |
clpC1 | 4038242 | c.2463C>A | synonymous_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244604 | p.Val458Met | missense_variant | 0.2 |
embB | 4248630 | c.2119dupG | frameshift_variant | 0.11 |
embB | 4249707 | p.Arg1065Leu | missense_variant | 0.15 |
embB | 4249752 | p.Leu1080Ser | missense_variant | 0.11 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268500 | p.Arg113Cys | missense_variant | 0.12 |
aftB | 4269459 | c.-623G>T | upstream_gene_variant | 0.11 |
ubiA | 4269793 | c.40delG | frameshift_variant | 0.12 |
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 |