Run ID: ERR11044962
Sample name:
Date: 31-03-2023 12:03:40
Number of reads: 2483880
Percentage reads mapped: 99.52
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 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 |
mshA | 576113 | p.Arg256Trp | missense_variant | 0.25 |
mshA | 576117 | p.Ala257Val | missense_variant | 0.14 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.25 |
mshA | 576606 | p.Ala420Gly | missense_variant | 0.25 |
rpoC | 764298 | c.931_932dupGG | frameshift_variant | 0.11 |
rpoC | 766966 | p.Glu1199Asp | missense_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.23 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303157 | p.His76Pro | missense_variant | 0.19 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.23 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154915 | c.1197A>G | synonymous_variant | 1.0 |
PPE35 | 2170037 | c.576C>G | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087333 | p.Val172Met | missense_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474212 | p.Lys69Thr | missense_variant | 0.17 |
whiB7 | 3568433 | p.Arg83Gly | missense_variant | 0.2 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.75 |
clpC1 | 4038951 | p.Phe585Ser | missense_variant | 0.21 |
clpC1 | 4039702 | p.Asp335His | missense_variant | 0.17 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.46 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.17 |
whiB6 | 4338200 | p.Asp108His | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |