Run ID: ERR7801150
Sample name:
Date: 02-04-2023 05:56:33
Number of reads: 32096
Percentage reads mapped: 88.55
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8195 | c.894C>A | synonymous_variant | 0.4 |
fgd1 | 491280 | c.498C>T | synonymous_variant | 1.0 |
fgd1 | 491326 | p.Ala182Ser | missense_variant | 0.67 |
mshA | 575820 | p.Ser158* | stop_gained | 1.0 |
rpoC | 763333 | c.-37G>A | upstream_gene_variant | 0.5 |
rpoC | 767083 | c.3714C>T | synonymous_variant | 1.0 |
mmpL5 | 776462 | c.2019G>T | synonymous_variant | 0.67 |
mmpL5 | 776483 | p.Met666Ile | missense_variant | 1.0 |
fbiC | 1303818 | c.888C>T | synonymous_variant | 1.0 |
rrl | 1474239 | n.582G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474642 | n.985G>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155086 | c.1026G>A | synonymous_variant | 0.67 |
PPE35 | 2168434 | p.Gly727Trp | missense_variant | 1.0 |
PPE35 | 2169776 | p.Phe279Leu | missense_variant | 0.67 |
Rv1979c | 2222226 | c.939C>T | synonymous_variant | 1.0 |
kasA | 2519236 | p.Glu374Asp | missense_variant | 1.0 |
kasA | 2519255 | p.Asp381Tyr | missense_variant | 1.0 |
eis | 2714645 | p.Arg230Cys | missense_variant | 1.0 |
thyX | 3067229 | c.717C>T | synonymous_variant | 1.0 |
thyA | 3073838 | p.His212Asn | missense_variant | 0.5 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449692 | c.1189C>T | synonymous_variant | 0.67 |
ddn | 3987264 | p.Asp141Tyr | missense_variant | 0.67 |
embC | 4240681 | c.819G>T | synonymous_variant | 1.0 |
embA | 4245359 | c.2127G>T | synonymous_variant | 0.5 |
embB | 4247359 | c.846G>T | synonymous_variant | 0.67 |
embB | 4248028 | c.1515C>A | synonymous_variant | 0.67 |
embB | 4248228 | p.Trp572Leu | missense_variant | 0.67 |
aftB | 4269522 | c.-686C>A | upstream_gene_variant | 0.67 |
ethR | 4326583 | c.-966G>T | upstream_gene_variant | 1.0 |
gid | 4408439 | c.-237G>A | upstream_gene_variant | 1.0 |