Run ID: SRR23311049
Sample name:
Date: 14-03-2023 08:12:07
Number of reads: 4581071
Percentage reads mapped: 99.52
Strain: lineage4.2.1;lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.32 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.68 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.31 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.3 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 0.68 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.7 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.61 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.63 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.71 | isoniazid |
eis | 2715344 | c.-12C>T | upstream_gene_variant | 0.69 | kanamycin |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 0.67 | ethambutol |
embB | 4247402 | p.Ser297Ala | missense_variant | 0.7 | 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 | 0.65 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.31 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.29 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.39 |
ccsA | 619969 | p.Val27Ile | missense_variant | 0.68 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.34 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.32 |
rpoC | 764817 | p.Val483Gly | missense_variant | 0.71 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.34 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.34 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.33 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.38 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.28 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.35 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.46 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 0.71 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.16 |
PPE35 | 2170623 | c.-11G>A | upstream_gene_variant | 0.31 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714955 | c.378C>T | synonymous_variant | 0.29 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 0.7 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339630 | c.513C>T | synonymous_variant | 0.32 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.24 |
fprA | 3473996 | c.-10_-9insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.31 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.32 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243157 | c.-76G>C | upstream_gene_variant | 0.34 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.34 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.32 |
embB | 4249594 | c.3081G>A | synonymous_variant | 0.65 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.34 |
ethA | 4326632 | p.His281Pro | missense_variant | 0.67 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 0.65 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.3 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.37 |