Run ID: ERR4817283
Sample name:
Date: 01-04-2023 14:54:22
Number of reads: 1312439
Percentage reads mapped: 99.85
Strain: lineage4.6.2.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.2 | Euro-American | T;LAM | RD726 | 1.0 |
lineage4.6.2.2 | Euro-American (Cameroon) | LAM10-CAM | RD726 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7447 | p.Lys49Met | missense_variant | 0.14 |
gyrA | 7571 | c.270G>T | synonymous_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576263 | p.Leu306Met | missense_variant | 0.11 |
mshA | 576298 | p.Asp317Glu | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778298 | c.-692C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674280 | c.79C>A | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155381 | p.Ala244Val | missense_variant | 0.11 |
katG | 2155389 | c.723C>G | synonymous_variant | 1.0 |
katG | 2155503 | c.609C>A | synonymous_variant | 0.11 |
PPE35 | 2170176 | p.Leu146Arg | missense_variant | 0.1 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 0.97 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747008 | c.591C>T | synonymous_variant | 0.11 |
folC | 2747631 | c.-33C>T | upstream_gene_variant | 0.15 |
thyX | 3067335 | p.Ala204Asp | missense_variant | 0.1 |
thyX | 3067474 | p.Pro158Ala | missense_variant | 1.0 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612571 | c.546C>T | synonymous_variant | 1.0 |
Rv3236c | 3612910 | p.Leu69Phe | missense_variant | 1.0 |
fbiB | 3642005 | c.471C>T | synonymous_variant | 0.11 |
rpoA | 3878543 | c.-36G>A | upstream_gene_variant | 0.2 |
embA | 4242550 | c.-683C>G | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246652 | p.Leu47Met | missense_variant | 0.1 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 1.0 |
aftB | 4267819 | p.Leu340Met | missense_variant | 0.11 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 1.0 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |