Run ID: ERR1750875
Sample name:
Date: 31-03-2023 14:57:38
Number of reads: 1155369
Percentage reads mapped: 99.2
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 | 0.99 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 0.92 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5723 | p.Ala162Ser | missense_variant | 0.9 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7775 | c.474C>T | synonymous_variant | 0.97 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 0.92 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575240 | c.-108G>A | upstream_gene_variant | 1.0 |
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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1674058 | p.Pro207Ser | missense_variant | 0.13 |
inhA | 1674952 | p.Pro251Ala | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102915 | p.Ile43Asn | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 0.92 |
Rv2752c | 3065737 | p.Asp152Gly | missense_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074519 | c.-48C>A | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877503 | c.1005G>T | synonymous_variant | 0.12 |
rpoA | 3877530 | p.Ala326Pro | missense_variant | 0.12 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4242182 | p.Ala774Ser | missense_variant | 0.92 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247155 | c.642G>A | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |