Run ID: ERR8025552
Sample name:
Date: 23-05-2023 03:03:12
Number of reads: 2631013
Percentage reads mapped: 99.61
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) |
Ethambutol | R | embB p.Met306Val (1.00) |
Pyrazinamide | R | pncA c.459_466delCAGGGTGC (1.00), pncA c.459_466delCAGGGTGC (1.00) |
Streptomycin | R | rrs n.514A>C (1.00) |
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 (0.91) |
Amikacin | R | rrs n.1401A>G (0.91) |
Capreomycin | R | rrs n.1401A>G (0.91) |
Kanamycin | R | rrs n.1401A>G (0.91) |
Cycloserine | ||
Ethionamide | R | fabG1 c.-15C>T (1.00), ethA c.65delA (1.00), ethA c.65delA (1.00), ethR p.Ala95Thr (1.00) |
Clofazimine | ||
Para-aminosalicylic_acid | R | thyX c.-16C>T (0.48) |
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 | 1.0 |
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 | 1472359 | n.514A>C | non_coding_transcript_exon_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.91 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
pncA | 2288775 | c.459_466delCAGGGTGC | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
thyX | 3067961 | c.-16C>T | upstream_gene_variant | 0.48 | para-aminosalicylic_acid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4327408 | c.65delA | frameshift_variant | 1.0 | ethionamide, ethionamide |
ethR | 4327831 | p.Ala95Thr | missense_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5273 | p.Tyr12His | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7935 | p.Glu212Lys | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575913 | p.Ala189Asp | missense_variant | 0.14 |
mshA | 575917 | c.570C>T | synonymous_variant | 0.14 |
mshA | 575986 | c.639G>A | synonymous_variant | 0.15 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760628 | p.Lys274Asn | missense_variant | 1.0 |
rpoB | 761396 | p.Glu530Asp | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763555 | c.186C>T | synonymous_variant | 1.0 |
rpoC | 767103 | p.Leu1245Arg | missense_variant | 0.21 |
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 | 777611 | c.870G>A | synonymous_variant | 0.17 |
mmpL5 | 778474 | p.Val3Leu | missense_variant | 0.12 |
mmpS5 | 778979 | c.-74G>T | upstream_gene_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304073 | c.1143C>T | synonymous_variant | 0.29 |
fbiC | 1304500 | p.Ala524Ser | missense_variant | 0.11 |
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 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103059 | c.-17G>A | upstream_gene_variant | 0.11 |
katG | 2153972 | p.Asp714Asn | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155797 | p.Met105Ile | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288906 | c.336C>T | synonymous_variant | 0.15 |
pncA | 2289785 | c.-544A>G | upstream_gene_variant | 0.13 |
kasA | 2518582 | c.468G>A | synonymous_variant | 0.13 |
folC | 2747205 | c.392_393dupTG | frameshift_variant | 0.11 |
thyX | 3067304 | p.Glu214Asp | missense_variant | 0.12 |
thyX | 3067946 | c.-1C>T | upstream_gene_variant | 0.17 |
thyX | 3067988 | c.-43A>C | upstream_gene_variant | 0.3 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339032 | c.-86C>T | upstream_gene_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3841029 | p.Ala131Val | missense_variant | 0.25 |
clpC1 | 4038745 | p.Thr654Ala | missense_variant | 0.12 |
embC | 4240793 | p.Ala311Thr | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244055 | p.Gly275Ser | missense_variant | 0.14 |
embA | 4245529 | p.Gly766Asp | missense_variant | 0.11 |
embA | 4245955 | c.2727delG | frameshift_variant | 0.14 |
aftB | 4267060 | p.His593Tyr | missense_variant | 0.13 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethR | 4326598 | c.-951T>A | upstream_gene_variant | 0.17 |
ethA | 4327454 | p.Val7Ala | missense_variant | 0.1 |
whiB6 | 4338296 | p.Trp76Gly | missense_variant | 0.36 |
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 |