Run ID: ERR8774327
Sample name:
Date: 02-04-2023 08:26:56
Number of reads: 442106
Percentage reads mapped: 99.46
Strain: lineage4.6.1
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 |
lineage4.6.1 | Euro-American (Uganda) | T2 | RD724 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5077 | c.-163_-162insC | upstream_gene_variant | 1.0 |
gyrB | 6151 | c.912C>T | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7539 | p.Thr80Ala | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490817 | p.Ala12Asp | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406189 | c.1152A>G | synonymous_variant | 1.0 |
Rv1258c | 1407057 | p.Gly95Glu | missense_variant | 0.13 |
embR | 1416294 | p.Val352Leu | missense_variant | 0.18 |
embR | 1416410 | p.Leu313Arg | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674465 | c.264C>T | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2153937 | c.2175C>A | synonymous_variant | 0.4 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.58 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.58 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746660 | c.938delT | frameshift_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840245 | c.1176C>A | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245055 | p.Thr608Asn | missense_variant | 1.0 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.67 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.67 |
whiB6 | 4338635 | c.-114A>C | upstream_gene_variant | 1.0 |