Run ID: ERR8774317
Sample name:
Date: 02-04-2023 08:27:06
Number of reads: 589736
Percentage reads mapped: 99.63
Strain: lineage4.6.2.2
Drug-resistance: Sensitive
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 | 0.99 |
lineage4.6.2.2 | Euro-American (Cameroon) | LAM10-CAM | RD726 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 |
rpoB | 761537 | c.1731C>A | synonymous_variant | 0.14 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778298 | c.-692C>T | upstream_gene_variant | 1.0 |
mmpR5 | 779005 | p.Gly6Arg | missense_variant | 0.17 |
mmpR5 | 779008 | p.Val7Ile | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303672 | p.Ala248Ser | missense_variant | 0.22 |
Rv1258c | 1406124 | p.Ala406Glu | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156487 | c.-376G>T | upstream_gene_variant | 0.22 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169059 | c.1554G>A | synonymous_variant | 1.0 |
PPE35 | 2169063 | p.Met517Thr | missense_variant | 1.0 |
PPE35 | 2169065 | p.Ala516Thr | missense_variant | 1.0 |
PPE35 | 2169068 | c.1545G>T | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.54 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.54 |
PPE35 | 2170332 | p.Val94Glu | missense_variant | 0.2 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 0.92 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.17 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.17 |
eis | 2715426 | c.-94G>T | upstream_gene_variant | 1.0 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 1.0 |
fprA | 3473962 | c.-45C>A | upstream_gene_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612760 | c.357C>A | synonymous_variant | 0.15 |
fbiB | 3641567 | c.33C>A | synonymous_variant | 0.14 |
clpC1 | 4040245 | p.Gly154Ser | missense_variant | 0.15 |
embC | 4241740 | c.1878G>T | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.2 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.2 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.2 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 1.0 |
aftB | 4268342 | c.495C>T | synonymous_variant | 0.17 |
ethA | 4326191 | p.Glu428Gly | missense_variant | 0.2 |
ethA | 4326535 | c.939G>T | synonymous_variant | 0.33 |
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 |