Run ID: SRR5818427
Sample name:
Date: 04-04-2023 11:27:51
Number of reads: 948435
Percentage reads mapped: 98.9
Strain: lineage4.9
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 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472359 | n.514A>C | non_coding_transcript_exon_variant | 0.89 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.96 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ahpC | 2726184 | c.-9A>C | upstream_gene_variant | 0.44 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ethA | 4326764 | p.Ala237Val | missense_variant | 0.25 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.99 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.98 |
gid | 4407935 | p.Leu90Val | missense_variant | 0.98 |
gid | 4407944 | p.Gln87Glu | missense_variant | 0.98 |