Run ID: SRR5818428
Sample name:
Date: 04-04-2023 11:27:15
Number of reads: 534773
Percentage reads mapped: 98.13
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 | 7585 | p.Ser95Thr | missense_variant | 1.0 |
rrs | 1471940 | n.95G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472284 | n.439C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472332 | n.487A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472333 | n.488G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 0.19 |
inhA | 1674896 | p.Met232Thr | missense_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
pncA | 2288942 | c.300C>G | synonymous_variant | 0.15 |
ahpC | 2726184 | c.-9A>C | upstream_gene_variant | 0.36 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.45 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 0.27 |
ethA | 4326388 | c.1086C>T | synonymous_variant | 0.25 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 0.25 |
ethA | 4326764 | p.Ala237Val | missense_variant | 0.23 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.9 |
gid | 4407742 | p.Arg154Pro | missense_variant | 0.53 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.53 |