Run ID: ERR1633825
Sample name:
Date: 18-08-2022 14:49:21
Number of reads: 804193
Percentage reads mapped: 99.6
Strain: lineage4.3.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.99 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 0.99 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576548 | p.Ala401Thr | missense_variant | 0.17 |
rpoC | 763640 | p.Arg91Gly | missense_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765340 | p.Gln657His | missense_variant | 0.13 |
rpoC | 765652 | c.2283G>A | synonymous_variant | 0.13 |
rpoC | 765718 | p.Asp783Glu | missense_variant | 0.12 |
rpoC | 765805 | c.2436C>A | synonymous_variant | 0.12 |
rpsL | 781370 | c.-190G>A | upstream_gene_variant | 0.18 |
rpsL | 781386 | c.-174G>A | upstream_gene_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416830 | c.517delG | frameshift_variant | 0.17 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472940 | n.1095G>T | non_coding_transcript_exon_variant | 0.13 |
inhA | 1673691 | c.-511G>C | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154238 | p.Thr625Met | missense_variant | 0.11 |
thyX | 3067866 | p.Thr27Ile | missense_variant | 0.14 |
thyA | 3073722 | c.750C>T | synonymous_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
fbiB | 3641853 | p.Gly107Ser | missense_variant | 0.12 |
embC | 4240586 | p.Gly242Cys | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244570 | c.1338C>T | synonymous_variant | 0.12 |
embB | 4246811 | p.Gly100Ser | missense_variant | 0.22 |
embB | 4248827 | p.Gly772Ser | missense_variant | 0.12 |
ethR | 4327249 | c.-300G>A | upstream_gene_variant | 0.13 |
gid | 4407681 | p.His174Gln | missense_variant | 0.15 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |