Run ID: ERR4820362
Sample name:
Date: 01-04-2023 16:38:15
Number of reads: 113025
Percentage reads mapped: 97.21
Strain: lineage4.2
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 | 0.08 |
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 | 9224 | p.Asp641Glu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.14 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.14 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.15 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.14 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474181 | n.524_525insT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918698 | c.759C>A | synonymous_variant | 0.5 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.4 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
Rv1979c | 2221797 | c.1368C>T | synonymous_variant | 0.29 |
Rv1979c | 2223284 | c.-120C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2859408 | c.1011C>T | synonymous_variant | 1.0 |
Rv2752c | 3065541 | c.651A>G | synonymous_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
fbiD | 3339564 | c.447G>T | synonymous_variant | 0.4 |
rpoA | 3877494 | p.Glu338Asp | missense_variant | 0.5 |
rpoA | 3877503 | c.1005G>C | synonymous_variant | 0.4 |
rpoA | 3877507 | p.Gly334Ala | missense_variant | 0.4 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.4 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.5 |
embC | 4241572 | c.1710C>T | synonymous_variant | 0.5 |
embB | 4247705 | p.Phe398Ile | missense_variant | 0.5 |
whiB6 | 4338585 | c.-64G>A | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338666 | c.-145G>A | upstream_gene_variant | 0.4 |