Run ID: SRR5818400
Sample name:
Date: 04-04-2023 11:21:42
Number of reads: 659590
Percentage reads mapped: 99.78
Strain: lineage4.9
Drug-resistance: Other
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 | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.17 | streptomycin |
ethA | 4326444 | c.1029dupG | frameshift_variant | 0.99 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
rplC | 801093 | c.285C>T | synonymous_variant | 0.22 |
rrs | 1471860 | n.15T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472286 | n.441C>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472297 | n.453_461delGTCCGGGTT | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472309 | n.464C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472311 | n.466C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472312 | n.468_470delGAT | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472328 | n.483G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476164 | n.2507A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476194 | n.2537A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673770 | p.Ala111Pro | missense_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ahpC | 2726184 | c.-9A>C | upstream_gene_variant | 0.19 |