Run ID: ERR8025484
Sample name:
Date: 17-05-2023 23:20:12
Number of reads: 3096237
Percentage reads mapped: 99.7
Strain: lineage2.2.2
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Asp435Val (1.00) |
Isoniazid | R | fabG1 c.-17G>T (1.00), katG p.Asp357Asn (0.29), katG p.Ser315Thr (1.00) |
Ethambutol | R | embB p.Met306Ile (1.00) |
Pyrazinamide | R | pncA c.517dupG (1.00), pncA c.517dupG (1.00) |
Streptomycin | R | rrs n.514A>C (1.00), gid p.Leu79Ser (1.00) |
Fluoroquinolones | R | gyrA p.Asp94Asn (1.00) |
Moxifloxacin | R | gyrA p.Asp94Asn (1.00) |
Ofloxacin | R | gyrA p.Asp94Asn (1.00) |
Levofloxacin | R | gyrA p.Asp94Asn (1.00) |
Ciprofloxacin | R | gyrA p.Asp94Asn (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.-17G>T (1.00), ethA p.Ala381Pro (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 |
lineage2.2.2 | East-Asian (Beijing) | Beijing-RD105/RD207 | RD105;RD207 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7581 | p.Asp94Asn | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
rrs | 1472359 | n.514A>C | non_coding_transcript_exon_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673423 | c.-17G>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155043 | p.Asp357Asn | missense_variant | 0.29 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288724 | c.517dupG | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
ethA | 4326333 | p.Ala381Pro | missense_variant | 1.0 | ethionamide |
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7199 | p.Glu654Lys | missense_variant | 0.22 |
gyrB | 7257 | p.Leu673Gln | missense_variant | 0.17 |
gyrA | 7342 | p.Arg14Leu | missense_variant | 0.12 |
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 | 9328 | p.Ala676Asp | missense_variant | 0.14 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491772 | c.990C>A | synonymous_variant | 0.15 |
mshA | 575397 | p.Arg17His | missense_variant | 0.13 |
mshA | 575498 | p.Ala51Ser | missense_variant | 0.13 |
rpoB | 760496 | c.690G>A | synonymous_variant | 0.15 |
rpoB | 760949 | c.1143C>T | synonymous_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764584 | c.1215G>A | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776338 | p.Ala715Ser | missense_variant | 0.18 |
mmpL5 | 776914 | p.Leu523Val | missense_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1461086 | c.42A>G | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472107 | n.262A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474789 | n.1137delC | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476055 | n.2398C>T | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673485 | p.Arg16Ser | missense_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834286 | p.Ser249Thr | missense_variant | 0.11 |
rpsA | 1834604 | p.Arg355Cys | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102504 | p.Pro180His | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155004 | p.Gly370Trp | missense_variant | 0.18 |
katG | 2155139 | p.Pro325Thr | missense_variant | 0.15 |
katG | 2155737 | c.375C>T | synonymous_variant | 0.13 |
katG | 2156093 | p.Pro7Ser | missense_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168904 | p.Ile570Thr | missense_variant | 0.17 |
PPE35 | 2169823 | p.Ala264Thr | missense_variant | 0.18 |
Rv1979c | 2221939 | p.Arg409Gln | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289667 | c.-426C>T | upstream_gene_variant | 0.12 |
kasA | 2517965 | c.-150C>A | upstream_gene_variant | 0.12 |
kasA | 2518005 | c.-110A>T | upstream_gene_variant | 0.14 |
thyA | 3074103 | c.369C>A | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086821 | c.2T>C | start_lost | 0.1 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
clpC1 | 4040754 | c.-50C>A | upstream_gene_variant | 0.12 |
clpC1 | 4040760 | c.-56C>T | upstream_gene_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245479 | p.Met749Ile | missense_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268022 | p.Leu272Gln | missense_variant | 0.12 |
ethA | 4326184 | c.1290C>A | synonymous_variant | 0.11 |
ethA | 4326422 | p.Gly351Val | missense_variant | 0.33 |
ethR | 4327672 | p.Leu42Met | missense_variant | 0.2 |
ethR | 4327682 | p.Ile45Asn | missense_variant | 0.2 |
ethR | 4327781 | p.Arg78Gln | missense_variant | 0.13 |
ethA | 4328115 | c.-642G>A | upstream_gene_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 |