Run ID: SRR7535045
Sample name:
Date: 04-04-2023 19:42:16
Number of reads: 1971647
Percentage reads mapped: 99.63
Strain: lineage4.3.4.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.95 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 0.96 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 0.98 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.93 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.98 | isoniazid |
pncA | 2289054 | p.Asp63Gly | missense_variant | 0.98 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 0.96 | ethambutol |
embB | 4247730 | p.Gly406Asp | missense_variant | 1.0 | ethambutol |
ethA | 4327033 | p.Tyr147* | stop_gained | 0.5 | ethionamide |
ethA | 4326694 | c.440_779del | frameshift_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 0.94 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.96 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.94 |
rpoC | 767083 | c.3714C>T | synonymous_variant | 0.96 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.95 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472753 | n.908A>C | non_coding_transcript_exon_variant | 0.9 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.31 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.15 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.97 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.99 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 0.96 |
alr | 3840869 | c.552C>G | synonymous_variant | 0.96 |
rpoA | 3877964 | p.Arg182Trp | missense_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ubiA | 4269311 | p.Trp175Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.88 |