Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 527,619 | (T)6→7 | coding (39/369 nt) | ybbC → | PF15631 family protein YbbC |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 527,613 | 1 | . | T | 100.0% | 35.3 / NA | 11 | S11S (TCA→TCT) | ybbC | PF15631 family protein YbbC |
Reads supporting (aligned to +/- strand): ref base . (0/0); new base T (4/7); total (4/7) |
TTAGTGGGGCCTATAAGGAGATTCAATGAAATATAGTTCAATATTTTCGATGCTTTCA‑TTTTTTATACTATTTGCCTGTAATGAGACAGCTGTTTACGGTTCTGATGAAAACATTATTTTTATGAG > NC_000913/527556‑527681 | ttaGTGGGGCCTATAAGGAGATTCAATGAAATATAGTTCAATATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGt < 1:117446/80‑1 (MQ=255) gTGGGGCCTATAAGGAGATTCAATGAAATATAGTTCAATATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGTAAt < 1:117447/80‑1 (MQ=255) ggCCTATAAGGAGATTCAATGAAATATAGTTCAATATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGTAATgaga > 1:117465/1‑80 (MQ=255) cTATAAGGAGATTCAATGAAATATAGTTCAATATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGTAATGAGACAGc < 1:117448/81‑1 (MQ=255) gagaTTCAATGAAATATAGTTCAATATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGTAATGAGACAGCTGTTTAc < 1:117449/81‑1 (MQ=255) gagaTTCAATGAAATATAGTTCAATATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGTAATGAGACAGCTGTTTAc > 1:117462/1‑81 (MQ=255) gAAATATAGTTCAATATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGTAATGAGACAGCTGTTTACGGTTCtgat > 1:117467/1‑80 (MQ=255) aaaTATAGTTCAATATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGTAATGAGACAGCTGTTTACGGTTCtgatga < 1:117450/81‑1 (MQ=255) aGTTCAATATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGTAATGAGACAGCTGTTTACGGTTCTGATGAAAACat > 1:117464/1‑81 (MQ=255) aaTATTTTCGATGCTTTCATTTTTTTATACTATTTGCCTGTAATGAGACAGCTGTTTACGGTTCTGATGAAAACattatt < 1:117451/80‑1 (MQ=255) cGATGCTTTCATTTTTTTATACTATTTGCCTGTAATGAGACAGCTGTTTACGGTTCTGATGAAAACATTATTTTTATGAg < 1:117452/80‑1 (MQ=255) | TTAGTGGGGCCTATAAGGAGATTCAATGAAATATAGTTCAATATTTTCGATGCTTTCA‑TTTTTTATACTATTTGCCTGTAATGAGACAGCTGTTTACGGTTCTGATGAAAACATTATTTTTATGAG > NC_000913/527556‑527681 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |