Run ID: SRR5818441
Sample name:
Date: 04-04-2023 11:30:32
Number of reads: 492943
Percentage reads mapped: 99.43
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 |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472296 | n.454_458delTCCGG | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472303 | n.458G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472332 | n.487A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472333 | n.488G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.97 |
ahpC | 2726389 | p.Ala66Val | missense_variant | 0.15 |
ahpC | 2726648 | c.456T>C | synonymous_variant | 0.18 |
ahpC | 2726701 | p.Ser170Phe | missense_variant | 0.22 |
ethA | 4326764 | p.Ala237Val | missense_variant | 0.22 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.95 |