Run ID: ERR4423486
Sample name:
Date: 01-04-2023 05:50:56
Number of reads: 738849
Percentage reads mapped: 99.22
Strain: lineage4.6.2.2
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 | 0.99 |
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 |
---|---|---|---|---|---|
rpoB | 761140 | p.His445Leu | missense_variant | 1.0 | rifampicin |
katG | 2154642 | c.1469delG | frameshift_variant | 0.14 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8114 | c.813C>A | synonymous_variant | 0.19 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490960 | p.Ala60Ser | missense_variant | 0.14 |
fgd1 | 491192 | p.Gly137Val | missense_variant | 0.13 |
fgd1 | 491408 | p.Pro209Gln | missense_variant | 0.17 |
fgd1 | 491691 | p.Trp303Cys | missense_variant | 0.14 |
rpoB | 761709 | p.Val635Phe | missense_variant | 0.2 |
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 |
fbiC | 1304258 | p.Ser443Tyr | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673393 | c.-809G>C | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102361 | p.Leu228Ile | missense_variant | 0.14 |
katG | 2154296 | p.Ala606Ser | missense_variant | 0.12 |
katG | 2155005 | c.1107C>A | synonymous_variant | 0.15 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyX | 3067261 | p.Asp229Tyr | missense_variant | 0.18 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568639 | p.Arg14Ile | missense_variant | 0.12 |
rpoA | 3878394 | c.114G>T | synonymous_variant | 0.25 |
ddn | 3987011 | c.168C>T | synonymous_variant | 1.0 |
embC | 4241502 | p.Ser547* | stop_gained | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244840 | c.1608G>A | synonymous_variant | 0.2 |
embA | 4245317 | c.2085G>T | synonymous_variant | 0.17 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 1.0 |
aftB | 4268605 | p.Arg78Ser | missense_variant | 0.15 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 1.0 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338440 | p.Glu28Lys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |