Run ID: ERR5866150
Sample name:
Date: 02-04-2023 00:32:11
Number of reads: 1586536
Percentage reads mapped: 99.38
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
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 |
rpsL | 781822 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
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 |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
katG | 2155734 | p.Met126Ile | missense_variant | 0.11 | isoniazid |
pncA | 2289030 | p.His71Arg | missense_variant | 0.98 | pyrazinamide |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247513 | p.Tyr334His | missense_variant | 1.0 | ethambutol |
thyA | 3072600 | c.-4122_*1079del | transcript_ablation | 1.0 | para-aminosalicylic_acid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491008 | c.231delC | frameshift_variant | 0.14 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575567 | p.Gln74Lys | missense_variant | 0.17 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 619822 | c.-69G>T | upstream_gene_variant | 0.33 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620854 | p.Gly322Ser | missense_variant | 0.13 |
rpoB | 762448 | p.Gly881Ala | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764817 | p.Val483Gly | missense_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
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 | 777536 | c.945G>C | synonymous_variant | 0.12 |
mmpL5 | 779049 | c.-569G>A | upstream_gene_variant | 0.12 |
mmpS5 | 779560 | c.-655C>G | upstream_gene_variant | 0.11 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674200 | c.-2A>T | upstream_gene_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101816 | c.1227C>A | synonymous_variant | 0.15 |
ndh | 2101931 | p.Ala371Val | missense_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746370 | p.Arg410Gln | missense_variant | 0.12 |
ribD | 2987337 | p.Gly167Ser | missense_variant | 0.12 |
ribD | 2987510 | c.672G>A | synonymous_variant | 0.2 |
ribD | 2987574 | p.Asp246Asn | missense_variant | 0.1 |
thyX | 3067356 | p.Ala197Glu | missense_variant | 0.11 |
thyX | 3067949 | c.-4C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087532 | p.Ala238Asp | missense_variant | 1.0 |
Rv3083 | 3449083 | p.Pro194Thr | missense_variant | 0.17 |
fprA | 3473981 | c.-26G>C | upstream_gene_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475065 | c.1059C>T | synonymous_variant | 0.11 |
whiB7 | 3568666 | p.Thr5Lys | missense_variant | 0.11 |
Rv3236c | 3612229 | c.888C>T | synonymous_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
clpC1 | 4039007 | c.1698G>A | synonymous_variant | 0.13 |
panD | 4044265 | p.Leu6Pro | missense_variant | 0.1 |
embC | 4241009 | p.Gly383Cys | missense_variant | 0.12 |
embC | 4242428 | p.Ala856Ser | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244185 | p.Ser318Ile | missense_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268488 | p.Met117Val | missense_variant | 0.1 |
ubiA | 4269303 | c.530delT | frameshift_variant | 0.12 |
ethA | 4327237 | p.Lys79Asn | missense_variant | 0.1 |
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 |