Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | AP009048 | 3,684,870 | C→T | 100% | pseudogene (189/582 nt) pseudogene (1252/1645 nt) |
ilvG ← ilvG ← |
ECK3760:JW3741:b3768; acetolactate synthase II, large subunit, C‑ter fragment ECK3760:JW3740+JW3741:b4488; large subunit of acetolactate synthase II |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | AP009048 | 3,684,870 | 0 | C | T | 100.0% | 80.6 / NA | 28 | pseudogene (189/582 nt) pseudogene (1252/1645 nt) | ilvG ilvG | ECK3760:JW3741:b3768; acetolactate synthase II, large subunit, C‑ter fragment ECK3760:JW3740+JW3741:b4488; large subunit of acetolactate synthase II |
Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (12/16); total (12/16) | |||||||||||
Rejected as polymorphism: Frequency below/above cutoff threshold. | |||||||||||
Rejected as polymorphism: Variant not supported by required number of reads on each strand. |
GGTGCCCAGCTCTTGCACATTCATCATGAAAGAGCCGTCACCGGAGATACAGACAACGGTATCGTTCGGTCGCGCGACTTGTGCGCCAACCGCCGCCGGTAAACCAAAACCCATGGTACCTAAACCGCTGGAGG > AP009048/3684804‑3684937 | ggTGCCCAGCTCTTGCACATTCATCATGAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTc > 1:7569737/1‑71 (MQ=255) ggTGCCCAGCTCTTGCACATTCATCATGAAAGAGCCGGCACCGGAGATACAGACGACGGTATCGTTTGGt < 1:5221410/70‑1 (MQ=255) aGCTCTTGCACATTCATCATGAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGAc < 1:887216/71‑1 (MQ=255) ctctTGCACATTCATCATGAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACtt < 1:446026/71‑1 (MQ=255) tctTGCACATTCATCATGAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTtg > 1:3086933/1‑71 (MQ=255) ttGCACATTCATCATGAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTgg < 1:2490992/57‑1 (MQ=255) gCACATTCATCATGAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTTGcgcg > 1:6762192/1‑71 (MQ=255) acaTTCATCATGAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTTgcgcgc < 1:6498195/70‑1 (MQ=255) caTTCATCATGAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTTGCGCGcc < 1:5061906/70‑1 (MQ=255) tcatGAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTTGCGCGCCAAccgc > 1:3448159/1‑70 (MQ=255) tcatGAAAGAGCAGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTTGCGCGCCAAccgcc > 1:3051078/1‑71 (MQ=255) gAAAGAGCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACtt > 1:1549015/1‑53 (MQ=255) agagCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTTGCGCGCCAACCGCCGCCGGt > 1:7206406/1‑70 (MQ=255) agCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTcgcgcg < 1:170828/44‑1 (MQ=38) agCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTtgc < 1:7134414/50‑2 (MQ=255) agCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTTGCGCGCCa < 1:2111104/56‑1 (MQ=255) agCCGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACTTGCGCGCCAACCGCCGCCGGTaaa > 1:3706843/1‑71 (MQ=255) gCCGTAACCGGAGATACAGACGACGGTATCGTTTgg < 1:4641022/36‑1 (MQ=25) ccGTCACCGGAGATACAGACGACGGTATCGTTTGGTcgcgcg < 1:1994379/42‑1 (MQ=38) cGTCACCGGAGATACAGACGACGGTATCGTTTGGTCGCGCGACtt < 1:4436662/45‑1 (MQ=255) gagaTACAGACGACGGTATCGTTTGGTCGCGCGACTTGCGCGCCAAccgccg > 1:6883328/1‑52 (MQ=255) aGACGACGGTATCGTTTGGTCGCGCGACTTGCGCGCCAAccgccgc < 1:3683505/46‑1 (MQ=255) cgaCGGTATCGTTTGGTCGCGCGACTTGCGCGCCAACCGCCGCCGGTAAACCAAAACCCATGGTGCCt < 1:5949070/66‑1 (MQ=37) cgaCGGTATCGTTTGGTCGCGCGACTTGCGCGCCAACCGCCGCCGGTAAACCAAAACCCATGGTGCCTa < 1:1341997/67‑1 (MQ=38) gaCGGTATCGTTTGGTCGCGCGACTTGCGCGCCAACCGCCGCCGGTAAACCAAAACCCATGGTGCCTaagc < 1:7550797/70‑3 (MQ=38) aTCGTTTGGTCGCGCGACTTGCGCGCCAACCGCCGCCGGTAAACCAAAACCCATGGTGCCTaag > 1:4074509/1‑63 (MQ=37) tCGTTTGGTCGCGCGACTTGCGCGCCAACCGCCGCCGGTAAACCAAAACCCATGGTGCCTAAGCCGCTg > 1:2848318/1‑69 (MQ=37) gTTTGGTCGCGCGACTTGCGCGCCAACCGCCGCCGGTAAACCAAAACCCATGGTGCCTAAGCCGCTGGAgg > 1:349915/1‑71 (MQ=38) | GGTGCCCAGCTCTTGCACATTCATCATGAAAGAGCCGTCACCGGAGATACAGACAACGGTATCGTTCGGTCGCGCGACTTGTGCGCCAACCGCCGCCGGTAAACCAAAACCCATGGTACCTAAACCGCTGGAGG > AP009048/3684804‑3684937 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |