Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 1,197,502 | C→T | G11R (GGA→AGA) | ymfD ← | e14 prophage; putative SAM‑dependent methyltransferase |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 1,197,502 | 0 | C | T | 100.0% | 63.5 / NA | 22 | G11R (GGA→AGA) | ymfD | e14 prophage; putative SAM‑dependent methyltransferase |
Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (6/16); total (6/16) |
CTCGCAAAGATATCTAGAGGGCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCCGTGCATATTATAGTTCAAAGCAAGTACCATTCAATTAATGTTATTTTTAGTGAAAAATTCTTT > NC_000913/1197437‑1197565 | ctctCAAAGATATCTAGTGGTCATCGTATGAGTTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGt < 2:382790/68‑1 (MQ=255) cTCGCAAAGATATCTAGAGGGCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGt < 2:628596/68‑1 (MQ=255) cTCGCAAAGATATCTAGAGGGCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGt < 2:60830/68‑1 (MQ=255) cTCGCAAAGATATCTAGAGGGCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGt < 1:598626/68‑1 (MQ=255) cTCGCAAAGATATCTAGAGGGCATCGTACGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGt < 2:450301/68‑1 (MQ=255) cGCAAAGATATCTAGAGGGCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGc < 2:280406/68‑1 (MQ=255) cGCAAAGATATCTAGAGGGCATCGTACGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGc < 2:489443/68‑1 (MQ=255) cAAAGATATCTAGAGGGCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCat < 2:174608/68‑1 (MQ=255) aGATATCTAGAGGGCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCAtatt < 1:64982/68‑1 (MQ=255) agagGGCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCATATTATAGTTCa > 2:140018/1‑68 (MQ=255) agagGGCATAGGATGAGGTTTTGCAGCATTCTCTGAGCGAATTTTAACTCTGTGCATATTATAGTTCa > 2:507410/1‑68 (MQ=255) gggCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCATATTATAGTTCAAAg > 2:633679/1‑68 (MQ=255) gggCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCATATTATAGTTCAAAg < 1:134624/68‑1 (MQ=255) gggCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCATATTATAGTTCAAAg < 2:411915/68‑1 (MQ=255) gggCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCATATTATAGTTCAAAg < 2:208335/68‑1 (MQ=255) gTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCATATTATAGTTCAAAGCAAGTAc > 1:171840/1‑68 (MQ=255) tATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCATATTATAGTTCAAAGCAAGTAcc < 2:138558/68‑1 (MQ=255) tATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCATATTATAGTTCAAAGCAAGTAcc < 2:584400/68‑1 (MQ=255) gTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCat < 2:383542/40‑1 (MQ=255) gTTTTGCTGCATTCTCTGAGCGAATATTAACTCTGTGCat > 1:383544/1‑40 (MQ=255) gCGAATATTAACTCTGTGCATATTATAGTTCAAAGCAAGTACCATTCAATTAATGTTATTTTTAGTGa < 1:626524/68‑1 (MQ=255) aCTCTGTGCATATTATAGTTCAAAGCAAGTACCATTCAATTAATGTTATTTTTAGTGAAAAATTCttt > 1:181073/1‑68 (MQ=255) | CTCGCAAAGATATCTAGAGGGCATCGTATGAGGTTTTGCTGCATTCTCTGAGCGAATATTAACTCCGTGCATATTATAGTTCAAAGCAAGTACCATTCAATTAATGTTATTTTTAGTGAAAAATTCTTT > NC_000913/1197437‑1197565 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |