Run ID: SRR23310812
Sample name:
Date: 13-03-2023 22:58:49
Number of reads: 176644
Percentage reads mapped: 99.67
Strain: lineage2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ethA | 4327033 | p.Tyr147* | stop_gained | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5117 | c.-123G>A | upstream_gene_variant | 0.22 |
gyrA | 6631 | c.-671C>T | upstream_gene_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9513 | p.Glu738Lys | missense_variant | 0.33 |
fgd1 | 491617 | p.Gln279* | stop_gained | 0.5 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620539 | p.Arg217Trp | missense_variant | 0.29 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620660 | p.Arg257His | missense_variant | 1.0 |
rpoB | 760784 | c.978G>A | synonymous_variant | 0.4 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763870 | c.501C>T | synonymous_variant | 0.5 |
rpoC | 764840 | p.Ile491Val | missense_variant | 1.0 |
rpoC | 766041 | c.2674delC | frameshift_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775849 | p.Gly878Arg | missense_variant | 0.4 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776741 | c.1740C>T | synonymous_variant | 0.4 |
mmpL5 | 777584 | c.897C>T | synonymous_variant | 0.17 |
mmpL5 | 777649 | p.Ala278Thr | missense_variant | 0.15 |
mmpS5 | 779588 | c.-683C>A | upstream_gene_variant | 0.29 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305368 | p.Glu813Gly | missense_variant | 0.67 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407484 | c.-144C>A | upstream_gene_variant | 0.29 |
embR | 1416229 | c.1119C>T | synonymous_variant | 0.4 |
embR | 1417255 | c.90delG | frameshift_variant | 0.4 |
embR | 1417297 | c.49delG | frameshift_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472007 | n.162G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474930 | n.1273A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476024 | n.2367T>C | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673351 | c.-89G>A | upstream_gene_variant | 0.33 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102210 | p.Ala278Val | missense_variant | 0.67 |
katG | 2155118 | p.Phe332Leu | missense_variant | 0.33 |
PPE35 | 2167741 | p.Thr958Ala | missense_variant | 0.67 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222014 | p.Val384Ala | missense_variant | 0.18 |
Rv1979c | 2222962 | p.Ala68Val | missense_variant | 0.29 |
folC | 2746255 | c.1344C>T | synonymous_variant | 0.4 |
folC | 2746918 | c.681G>A | synonymous_variant | 0.4 |
pepQ | 2859329 | p.Arg364Trp | missense_variant | 0.25 |
pepQ | 2859466 | p.Ala318Val | missense_variant | 0.67 |
Rv2752c | 3065845 | p.Cys116Tyr | missense_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473837 | c.-170A>G | upstream_gene_variant | 0.25 |
fprA | 3473996 | c.-10_-9insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613199 | c.-83G>A | upstream_gene_variant | 0.29 |
alr | 3841476 | c.-56G>A | upstream_gene_variant | 0.5 |
rpoA | 3877750 | p.Asp253Gly | missense_variant | 1.0 |
clpC1 | 4038187 | p.Ala840Thr | missense_variant | 0.29 |
clpC1 | 4040198 | c.507G>A | synonymous_variant | 0.29 |
clpC1 | 4040536 | p.Glu57* | stop_gained | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243225 | c.-8C>A | upstream_gene_variant | 1.0 |
embA | 4244213 | c.981C>T | synonymous_variant | 0.2 |
embB | 4246806 | p.Val98Glu | missense_variant | 0.25 |
embB | 4247333 | p.Arg274Cys | missense_variant | 0.4 |
embB | 4248319 | c.1806A>T | synonymous_variant | 0.29 |
aftB | 4267334 | p.Asp501Glu | missense_variant | 0.29 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269947 | c.-114G>A | upstream_gene_variant | 0.67 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338684 | c.-163C>G | upstream_gene_variant | 0.5 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |