Run ID: ERR8025536
Sample name:
Date: 18-05-2023 01:07:17
Number of reads: 2709372
Percentage reads mapped: 99.73
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), inhA p.Ile194Thr (1.00), katG c.826delC (0.25) |
Ethambutol | R | embB p.Met306Val (1.00) |
Pyrazinamide | R | pncA p.Val130Ala (1.00) |
Streptomycin | ||
Fluoroquinolones | R | gyrA p.Asp94Gly (1.00) |
Moxifloxacin | R | gyrA p.Asp94Gly (1.00) |
Ofloxacin | R | gyrA p.Asp94Gly (1.00) |
Levofloxacin | R | gyrA p.Asp94Gly (1.00) |
Ciprofloxacin | R | gyrA p.Asp94Gly (1.00) |
Aminoglycosides | R | rrs n.1401A>G (1.00) |
Amikacin | R | rrs n.1401A>G (1.00) |
Capreomycin | R | rrs n.1401A>G (1.00) |
Kanamycin | R | rrs n.1401A>G (1.00) |
Cycloserine | ||
Ethionamide | R | fabG1 c.-15C>T (1.00), inhA p.Ile194Thr (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 |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
inhA | 1674782 | p.Ile194Thr | missense_variant | 1.0 | isoniazid, ethionamide |
katG | 2155285 | c.826delC | frameshift_variant | 0.25 | isoniazid |
pncA | 2288853 | p.Val130Ala | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethR | 4327831 | p.Ala95Thr | missense_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5617 | c.378G>T | synonymous_variant | 0.2 |
gyrB | 5758 | c.519C>T | synonymous_variant | 0.25 |
gyrA | 6334 | c.-968G>A | upstream_gene_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8173 | p.Val291Asp | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491126 | p.Ala115Asp | missense_variant | 0.17 |
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 | 759738 | c.-69G>T | upstream_gene_variant | 0.13 |
rpoB | 760286 | c.480C>T | synonymous_variant | 0.17 |
rpoB | 761482 | p.Ala559Val | missense_variant | 0.17 |
rpoB | 761817 | c.2011C>A | synonymous_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763555 | c.186C>T | synonymous_variant | 1.0 |
rpoC | 763771 | c.402C>T | synonymous_variant | 0.12 |
rpoC | 763848 | p.Lys160Met | missense_variant | 0.12 |
rpoC | 765617 | p.Glu750Gln | missense_variant | 1.0 |
rpoC | 766456 | c.3087C>A | synonymous_variant | 0.15 |
rpoC | 766742 | p.Gln1125* | stop_gained | 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 |
mmpL5 | 777151 | p.Asn444Tyr | missense_variant | 0.12 |
mmpL5 | 777256 | p.Pro409Ser | missense_variant | 0.11 |
mmpS5 | 778979 | c.-74G>T | upstream_gene_variant | 1.0 |
mmpR5 | 779363 | p.Leu125Pro | missense_variant | 0.11 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
mmpS5 | 779627 | c.-722T>C | upstream_gene_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305103 | c.2174delT | frameshift_variant | 0.11 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474666 | n.1012delG | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474911 | n.1254G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833414 | c.-127delT | upstream_gene_variant | 0.17 |
rpsA | 1833847 | c.306C>A | synonymous_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834646 | p.Tyr369His | missense_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102980 | c.63A>G | synonymous_variant | 0.11 |
katG | 2153979 | c.2133T>C | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155787 | p.Ala109Thr | missense_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168473 | c.2139dupC | frameshift_variant | 0.2 |
PPE35 | 2168752 | p.Ser621Gly | missense_variant | 0.12 |
Rv1979c | 2222081 | p.Ala362Thr | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289078 | p.Gly55Asp | missense_variant | 0.12 |
ahpC | 2726639 | c.447C>G | synonymous_variant | 0.12 |
ahpC | 2726758 | p.Glu189Gly | missense_variant | 0.15 |
ribD | 2986646 | c.-193G>T | upstream_gene_variant | 0.13 |
ald | 3086695 | c.-125C>A | upstream_gene_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449196 | c.693C>T | synonymous_variant | 0.15 |
fprA | 3473958 | c.-49C>A | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474089 | p.Thr28Met | missense_variant | 0.15 |
whiB7 | 3568699 | c.-20G>T | upstream_gene_variant | 0.15 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3640878 | c.-657T>C | upstream_gene_variant | 0.14 |
rpoA | 3877521 | c.987C>A | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243050 | p.Leu1063Ser | missense_variant | 0.12 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4249696 | p.Trp1061* | stop_gained | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267743 | p.Arg365Leu | missense_variant | 0.12 |
aftB | 4269003 | c.-167C>A | upstream_gene_variant | 0.12 |
ubiA | 4269373 | p.Ser154* | stop_gained | 0.13 |
ethA | 4326187 | c.1287G>A | synonymous_variant | 0.4 |
ethR | 4327633 | p.Ile29Phe | missense_variant | 0.18 |
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 |