Run ID: SRR7755704
Sample name:
Date: 04-04-2023 20:15:56
Number of reads: 3865418
Percentage reads mapped: 99.48
Strain: lineage4.2.1;lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.45 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.5 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.5 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.5 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.46 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 0.51 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.53 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.37 | streptomycin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.44 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.54 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288841 | p.Ala134Val | missense_variant | 0.56 | pyrazinamide |
pncA | 2289031 | p.His71Tyr | missense_variant | 0.49 | pyrazinamide |
pncA | 2289202 | p.Cys14Gly | missense_variant | 0.59 | pyrazinamide |
eis | 2715344 | c.-12C>T | upstream_gene_variant | 0.5 | kanamycin |
thyX | 3067961 | c.-16C>T | upstream_gene_variant | 0.61 | para-aminosalicylic_acid |
thyA | 3073808 | p.Arg222Gly | missense_variant | 0.78 | para-aminosalicylic_acid |
embB | 4247402 | p.Ser297Ala | missense_variant | 0.48 | ethambutol |
embB | 4248003 | p.Gln497Arg | missense_variant | 0.51 | ethambutol |
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 | 491247 | c.465C>T | synonymous_variant | 0.47 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.51 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.53 |
ccsA | 619969 | p.Val27Ile | missense_variant | 0.51 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.55 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.61 |
rpoC | 764817 | p.Val483Gly | missense_variant | 0.53 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.51 |
rpoC | 766779 | p.Glu1137Gly | missense_variant | 0.42 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.6 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.56 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.53 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.48 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.99 |
rrl | 1476091 | n.2434T>C | non_coding_transcript_exon_variant | 0.4 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.55 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.53 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.4 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 0.54 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 0.44 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.99 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.59 |
fbiB | 3641810 | c.276G>C | synonymous_variant | 0.43 |
rpoA | 3878642 | c.-135G>C | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.54 |
embB | 4249594 | c.3081G>A | synonymous_variant | 0.53 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.35 |
ubiA | 4269721 | p.Ala38Val | missense_variant | 0.41 |
ethA | 4326339 | p.Asn379Asp | missense_variant | 0.54 |
ethA | 4326632 | p.His281Pro | missense_variant | 0.53 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 0.51 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.43 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.32 |