Run ID: ERR501640
Sample name:
Date: 01-04-2023 21:48:19
Number of reads: 170069
Percentage reads mapped: 98.63
Strain: lineage4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 0.09 |
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 |
fgd1 | 491594 | p.Ala271Val | missense_variant | 0.29 |
rpoB | 761581 | p.Glu592Val | missense_variant | 0.4 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766389 | p.Gly1007Asp | missense_variant | 0.67 |
rpsL | 781928 | c.369G>A | synonymous_variant | 1.0 |
Rv1258c | 1406945 | c.396C>A | synonymous_variant | 0.29 |
Rv1258c | 1406959 | p.Leu128Met | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473708 | n.51G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1834137 | p.Arg199His | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170305 | p.Ala103Glu | missense_variant | 0.5 |
PPE35 | 2170577 | c.36G>A | synonymous_variant | 0.22 |
PPE35 | 2170666 | c.-54G>A | upstream_gene_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747505 | p.His32Asn | missense_variant | 0.5 |
folC | 2747587 | c.12G>A | synonymous_variant | 0.29 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.25 |
fbiB | 3641463 | c.-72G>A | upstream_gene_variant | 0.4 |
fbiB | 3641807 | c.273C>G | synonymous_variant | 1.0 |
alr | 3840789 | p.Gln211Arg | missense_variant | 0.67 |
alr | 3840802 | p.Ile207Phe | missense_variant | 0.67 |
ddn | 3986868 | c.25C>T | synonymous_variant | 0.5 |
ddn | 3986910 | c.67C>A | synonymous_variant | 0.67 |
panD | 4044420 | c.-139G>A | upstream_gene_variant | 0.67 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embC | 4242982 | p.Met1040Ile | missense_variant | 0.33 |
embC | 4243119 | p.Trp1086Ser | missense_variant | 1.0 |
embA | 4243746 | p.Gly172Ser | missense_variant | 0.25 |
embA | 4244816 | c.1584G>A | synonymous_variant | 0.4 |
embB | 4248604 | c.2091G>A | synonymous_variant | 0.67 |
embB | 4248763 | c.2250C>A | synonymous_variant | 0.5 |
embB | 4248790 | c.2277C>A | synonymous_variant | 0.67 |
ethR | 4327691 | p.Asp48Gly | missense_variant | 1.0 |
ethR | 4327732 | p.Tyr62Asn | missense_variant | 0.33 |
ethA | 4328294 | c.-821C>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408363 | c.-161G>A | upstream_gene_variant | 0.29 |