Run ID: ERR4819400
Sample name:
Date: 01-04-2023 16:05:14
Number of reads: 584466
Percentage reads mapped: 98.34
Strain: lineage4.3.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | 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 |
rpoB | 759952 | p.Asp49Gly | missense_variant | 0.14 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765964 | p.Leu865Phe | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776085 | p.Val799Ala | missense_variant | 0.17 |
mmpL5 | 778061 | p.Gln140His | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304689 | c.1762delG | frameshift_variant | 0.12 |
embR | 1416864 | c.483dupC | frameshift_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673193 | c.-247T>C | upstream_gene_variant | 0.12 |
rpsA | 1834035 | p.Ile165Asn | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154226 | p.Gly629Asp | missense_variant | 0.18 |
katG | 2154816 | c.1296C>A | synonymous_variant | 0.18 |
PPE35 | 2168774 | c.1838delC | frameshift_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073849 | c.622delA | frameshift_variant | 0.22 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086915 | c.96G>A | synonymous_variant | 0.29 |
ald | 3086922 | p.Ile35Val | missense_variant | 0.25 |
Rv3083 | 3449854 | p.Met451Val | missense_variant | 0.1 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568471 | p.Ile70Thr | missense_variant | 0.18 |
Rv3236c | 3613275 | c.-159C>T | upstream_gene_variant | 0.14 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.22 |
clpC1 | 4040540 | c.164delC | frameshift_variant | 0.22 |
panD | 4044179 | p.Ala35Ser | missense_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246286 | c.-228G>A | upstream_gene_variant | 0.14 |
aftB | 4268781 | p.Trp19Leu | missense_variant | 0.29 |
whiB6 | 4338248 | p.Leu92Met | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408110 | c.93G>A | synonymous_variant | 0.29 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |