Run ID: ERR11081537
Sample name:
Date: 09-04-2023 01:56:01
Number of reads: 1218335
Percentage reads mapped: 99.5
Strain: lineage4.2.2.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.98 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.96 |
lineage4.2.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.95 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6122 | p.Ala295Thr | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8688 | p.Ala463Ser | missense_variant | 0.92 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575455 | c.108G>T | synonymous_variant | 0.14 |
mshA | 576077 | c.730C>T | synonymous_variant | 0.94 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.15 |
mshA | 576448 | c.1101A>C | synonymous_variant | 0.19 |
mshA | 576489 | p.Val381Gly | missense_variant | 0.25 |
ccsA | 620839 | c.949C>T | synonymous_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417141 | c.207C>A | synonymous_variant | 0.11 |
atpE | 1461172 | p.Pro43Leu | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475959 | n.2302C>T | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.18 |
folC | 2747104 | p.Asp165Glu | missense_variant | 0.92 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.27 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 0.98 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.43 |
rpoA | 3878613 | c.-106A>C | upstream_gene_variant | 0.4 |
rpoA | 3878626 | c.-119A>C | upstream_gene_variant | 0.29 |
rpoA | 3878637 | c.-130G>C | upstream_gene_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.29 |
ethA | 4328212 | c.-740delC | upstream_gene_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |