Run ID: ERR2653022
Sample name:
Date: 31-03-2023 22:27:17
Number of reads: 1238205
Percentage reads mapped: 99.56
Strain: lineage4.3.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 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 | 8040 | p.Gly247Ser | missense_variant | 0.97 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575499 | p.Ala51Val | missense_variant | 0.11 |
mshA | 575579 | p.His78Tyr | missense_variant | 0.15 |
rpoB | 760318 | p.Ser171Asn | missense_variant | 0.11 |
rpoB | 760436 | c.630C>T | synonymous_variant | 0.11 |
rpoC | 764693 | p.Gly442Cys | missense_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406375 | c.966C>A | synonymous_variant | 0.13 |
Rv1258c | 1406413 | p.Pro310Ser | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674748 | p.Gly183Ser | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918726 | p.Ala263Thr | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518733 | p.Ile207Leu | missense_variant | 0.1 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
eis | 2715567 | c.-235G>A | upstream_gene_variant | 0.12 |
ribD | 2987388 | p.Ala184Pro | missense_variant | 0.12 |
Rv2752c | 3065771 | p.Cys141Ser | missense_variant | 0.12 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448910 | p.Leu136His | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878630 | c.-123G>C | upstream_gene_variant | 0.15 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
panD | 4044029 | p.Val85Met | missense_variant | 0.13 |
panD | 4044077 | p.Ile69Val | missense_variant | 0.12 |
panD | 4044372 | c.-91T>A | upstream_gene_variant | 0.15 |
panD | 4044397 | c.-116G>A | upstream_gene_variant | 0.14 |
embC | 4240006 | c.144A>G | synonymous_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245083 | c.1851A>G | synonymous_variant | 1.0 |
aftB | 4267180 | p.Tyr553His | missense_variant | 0.1 |
aftB | 4268665 | p.Asn58Tyr | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |