Run ID: SRR5818469
Sample name:
Date: 04-04-2023 11:38:06
Number of reads: 592384
Percentage reads mapped: 94.67
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 | 1472119 | n.274G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472284 | n.439C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472332 | n.487A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472333 | n.488G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472436 | n.591G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472910 | n.1065G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473395 | n.-263G>A | upstream_gene_variant | 0.22 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.34 |
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 | 0.28 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ahpC | 2726184 | c.-9A>C | upstream_gene_variant | 0.36 |
ethA | 4326764 | p.Ala237Val | missense_variant | 0.32 |