Run ID: ERR11243566
Sample name:
Date: 21-04-2023 22:47:48
Number of reads: 493428
Percentage reads mapped: 99.56
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Ser450Leu (1.00) |
Isoniazid | R | fabG1 c.-15C>T (1.00), katG p.Ser315Thr (1.00), katG p.Met176Ile (0.20) |
Ethambutol | R | embA c.-12C>T (1.00), embB p.Tyr334His (1.00) |
Pyrazinamide | R | pncA p.His71Arg (1.00) |
Streptomycin | R | rpsL p.Lys88Arg (1.00) |
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | R | fabG1 c.-15C>T (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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
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 |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
katG | 2155584 | p.Met176Ile | missense_variant | 0.2 | isoniazid |
pncA | 2289030 | p.His71Arg | missense_variant | 1.0 | pyrazinamide |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247513 | p.Tyr334His | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5279 | p.Ala14Ser | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8276 | c.975G>A | synonymous_variant | 0.26 |
gyrA | 8277 | p.Val326Met | missense_variant | 0.22 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9789 | p.Ala830Ser | missense_variant | 0.15 |
fgd1 | 490597 | c.-186G>T | upstream_gene_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575992 | c.645C>A | synonymous_variant | 0.13 |
mshA | 576169 | c.822C>A | synonymous_variant | 0.13 |
ccsA | 619949 | p.Ser20* | stop_gained | 0.14 |
ccsA | 620029 | p.Leu47Met | missense_variant | 0.15 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759697 | c.-110A>G | upstream_gene_variant | 0.11 |
rpoB | 762292 | p.Thr829Asn | missense_variant | 0.13 |
rpoB | 762741 | p.Leu979Met | missense_variant | 0.15 |
rpoB | 763029 | p.Ala1075Ser | missense_variant | 0.2 |
rpoC | 764817 | p.Val483Gly | missense_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 767037 | p.Ala1223Glu | missense_variant | 0.15 |
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 | 777746 | c.735G>T | synonymous_variant | 0.17 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303458 | c.528G>T | synonymous_variant | 0.15 |
fbiC | 1305142 | p.Glu738Lys | missense_variant | 0.22 |
Rv1258c | 1406517 | p.Ala275Glu | missense_variant | 0.17 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407184 | c.157C>T | synonymous_variant | 0.5 |
embR | 1416770 | p.Glu193Gly | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473981 | n.324G>T | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673267 | c.-173C>A | upstream_gene_variant | 0.15 |
fabG1 | 1673393 | c.-47G>T | upstream_gene_variant | 0.18 |
fabG1 | 1673638 | p.Ala67Ser | missense_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918215 | c.276G>T | synonymous_variant | 0.18 |
katG | 2154418 | p.Val565Ala | missense_variant | 0.15 |
katG | 2154673 | p.Ala480Glu | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168944 | p.Gln557Lys | missense_variant | 0.14 |
Rv1979c | 2221918 | p.Val416Ala | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289239 | c.3G>T | start_lost | 0.14 |
eis | 2714766 | c.567G>T | synonymous_variant | 0.22 |
Rv2752c | 3067086 | c.-895A>G | upstream_gene_variant | 0.11 |
thyA | 3074573 | c.-102C>G | upstream_gene_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087532 | p.Ala238Asp | missense_variant | 1.0 |
fbiD | 3339285 | c.168G>C | synonymous_variant | 0.2 |
fbiD | 3339693 | c.576C>A | synonymous_variant | 0.2 |
Rv3083 | 3449946 | c.1443C>A | synonymous_variant | 0.18 |
fprA | 3473879 | c.-128T>G | upstream_gene_variant | 0.15 |
fprA | 3473927 | c.-79delT | upstream_gene_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612229 | c.888C>T | synonymous_variant | 1.0 |
Rv3236c | 3612287 | p.Gly277Val | missense_variant | 0.16 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3841272 | p.Arg50Leu | missense_variant | 0.12 |
alr | 3841512 | c.-92C>A | upstream_gene_variant | 0.13 |
clpC1 | 4040778 | c.-74G>T | upstream_gene_variant | 0.2 |
panD | 4044147 | c.135C>A | synonymous_variant | 0.18 |
embC | 4241105 | c.1246dupG | frameshift_variant | 0.22 |
embC | 4241391 | p.Leu510Pro | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242913 | c.-320C>A | upstream_gene_variant | 0.12 |
embA | 4243385 | c.153C>A | synonymous_variant | 0.12 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245076 | p.Ala615Glu | missense_variant | 0.29 |
embB | 4245692 | c.-822G>T | upstream_gene_variant | 0.4 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268400 | p.Ala146Asp | missense_variant | 0.13 |
aftB | 4268493 | p.Ala115Glu | missense_variant | 0.15 |
ubiA | 4269535 | p.Trp100* | stop_gained | 0.2 |
ethA | 4328455 | c.-982G>A | upstream_gene_variant | 0.25 |
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 |