Run ID: SRR998698
Sample name:
Date: 04-04-2023 23:32:10
Number of reads: 1126024
Percentage reads mapped: 92.96
Strain: lineage4.6.2.2;lineage4.1.3
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 | Euro-American | T;LAM | None | 0.72 |
lineage4.1 | Euro-American | T;X;H | None | 0.31 |
lineage4.1.3 | Euro-American | T;X;H | None | 0.23 |
lineage4.6.2.2 | Euro-American (Cameroon) | LAM10-CAM | RD726 | 0.69 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Asp | missense_variant | 0.23 | rifampicin |
inhA | 1674048 | c.-154G>A | upstream_gene_variant | 0.3 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.34 | isoniazid |
pncA | 2288844 | p.Ile133Thr | missense_variant | 0.28 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 0.18 | ethambutol |
gid | 4407967 | p.Leu79Ser | missense_variant | 0.29 | streptomycin |
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 |
gyrA | 9557 | c.2256G>C | synonymous_variant | 0.24 |
mshA | 575313 | c.-35C>G | upstream_gene_variant | 0.4 |
rpoB | 762244 | c.2444_2446dupTGC | disruptive_inframe_insertion | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778298 | c.-692C>T | upstream_gene_variant | 0.62 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 0.33 |
fbiC | 1304610 | c.1680C>T | synonymous_variant | 0.39 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917894 | c.-46_-45insTGT | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 0.58 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715511 | c.-179C>T | upstream_gene_variant | 0.29 |
thyX | 3067238 | c.708C>T | synonymous_variant | 0.17 |
thyX | 3067474 | p.Pro158Ala | missense_variant | 0.67 |
thyX | 3067772 | c.174C>T | synonymous_variant | 0.12 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.26 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 0.77 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612571 | c.546C>T | synonymous_variant | 0.73 |
rpoA | 3878641 | c.-135delG | upstream_gene_variant | 0.12 |
embC | 4240986 | p.Arg375Gln | missense_variant | 0.22 |
embC | 4242220 | c.2361_2376delCAACGGCATTCCCGCC | frameshift_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.4 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 0.45 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 0.69 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 0.78 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |