Run ID: ERR2679303
Sample name:
Date: 31-03-2023 23:01:39
Number of reads: 242082
Percentage reads mapped: 99.51
Strain: lineage4.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6507 | p.Ala423Val | missense_variant | 0.96 |
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 | 9656 | c.2355C>G | synonymous_variant | 0.86 |
fgd1 | 491078 | p.Asn99Ser | missense_variant | 0.15 |
rpoB | 760341 | p.Val179Leu | missense_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765187 | c.1818C>T | synonymous_variant | 1.0 |
rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777217 | c.1258_1263delTACCTG | conservative_inframe_deletion | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155824 | c.288C>T | synonymous_variant | 1.0 |
katG | 2156007 | c.105C>T | synonymous_variant | 1.0 |
PPE35 | 2168448 | p.Gln722Arg | missense_variant | 0.93 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715432 | c.-100C>T | upstream_gene_variant | 0.4 |
eis | 2715436 | c.-104G>A | upstream_gene_variant | 0.4 |
eis | 2715440 | c.-108A>C | upstream_gene_variant | 0.33 |
eis | 2715445 | c.-113C>T | upstream_gene_variant | 0.33 |
eis | 2715447 | c.-115T>A | upstream_gene_variant | 0.33 |
eis | 2715450 | c.-118T>C | upstream_gene_variant | 0.33 |
eis | 2715451 | c.-119C>A | upstream_gene_variant | 0.33 |
eis | 2715454 | c.-122T>G | upstream_gene_variant | 0.33 |
eis | 2715455 | c.-123G>A | upstream_gene_variant | 0.33 |
eis | 2715458 | c.-126T>A | upstream_gene_variant | 0.33 |
eis | 2715460 | c.-128A>G | upstream_gene_variant | 0.33 |
eis | 2715465 | c.-133G>T | upstream_gene_variant | 0.33 |
eis | 2715469 | c.-137T>C | upstream_gene_variant | 0.33 |
eis | 2715473 | c.-141A>G | upstream_gene_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087893 | p.Asp358Glu | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embC | 4240394 | p.Glu178* | stop_gained | 0.25 |
embC | 4240646 | p.Phe262Leu | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242708 | p.Asp949Ala | missense_variant | 0.33 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 0.2 |
embA | 4244262 | c.1030C>T | synonymous_variant | 0.82 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |