Run ID: SRR5818391
Sample name:
Date: 04-04-2023 11:17:04
Number of reads: 320191
Percentage reads mapped: 83.03
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 |
rpoB | 760294 | p.Asn163Ile | missense_variant | 0.41 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472296 | n.454_458delTCCGG | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472303 | n.458G>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476164 | n.2507A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476194 | n.2537A>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ahpC | 2726184 | c.-9A>C | upstream_gene_variant | 0.32 |
embC | 4239705 | c.-158T>C | upstream_gene_variant | 0.67 |
ethA | 4326764 | p.Ala237Val | missense_variant | 0.28 |