Run ID: ERR2041687
Sample name:
Date: 18-08-2022 09:22:55
Number of reads: 657686
Percentage reads mapped: 97.88
Strain: lineage4.2.2.1
Drug-resistance: HR-TB
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 | 1.0 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.97 |
lineage4.2.2.1 | Euro-American | LAM7-TUR | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4248003 | p.Gln497Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6026 | p.His263Asn | missense_variant | 0.12 |
gyrB | 6070 | c.831C>T | synonymous_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9525 | p.Val742Leu | missense_variant | 1.0 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
rpoC | 765421 | c.2052C>A | synonymous_variant | 0.12 |
rpoC | 766135 | c.2766G>T | synonymous_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305058 | p.Tyr710Asn | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473859 | n.202T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475241 | n.1584C>G | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673221 | c.-219C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.19 |
fabG1 | 1674133 | p.Ile232Val | missense_variant | 0.17 |
rpsA | 1833427 | c.-115G>T | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155465 | p.Leu216Pro | missense_variant | 0.13 |
pncA | 2289483 | c.-243delA | upstream_gene_variant | 0.12 |
kasA | 2518907 | c.793T>C | synonymous_variant | 0.15 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087284 | c.465C>G | synonymous_variant | 0.12 |
embC | 4240801 | c.939C>T | synonymous_variant | 0.18 |
embC | 4240803 | p.Tyr314Phe | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244958 | p.Ala576Thr | missense_variant | 1.0 |