Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_012967 | 475,288:1 | +G | 100% | coding (18/1677 nt) | ybaL ← | Kef family K(+) transporter |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_012967 | 475,288 | 1 | . | G | 100.0% | 11.6 / NA | 5 | P6P (CCG→CCC) | ybaL | Kef family K(+) transporter |
Reads supporting (aligned to +/- strand): ref base . (0/0); new base G (1/4); total (1/4) | |||||||||||
Rejected as polymorphism: Frequency below/above cutoff threshold. | |||||||||||
Rejected as polymorphism: Variant not supported by required number of reads on each strand. | |||||||||||
Rejected as polymorphism: Polymorphic base substitution creates a homopolymer stretch. |
GCACAAGGCCGCCAACAATGGTGGTGATAAGC‑GGGGTGGCGTGATGCATTCCGTCTCCTTTT > NC_012967/475257‑475318 | gCACAAGGCCGCCAACAATGGTGGTGATAAGC‑gggg < 2:761601/36‑1 (MQ=255) ccAACAATGGTGGTGATAAGCGGGGGTGGCGTGATg < 2:415898/36‑1 (MQ=37) ggtggtGATAAGCGGGGGTGGCGTGATGCATTCCGt < 2:126244/36‑1 (MQ=37) ggtggtGATAAGCGGGGGTGGCGTGATGCATTCCGt < 2:700197/36‑1 (MQ=37) aTAAGCGGGGGTGGCGTGATGCATTCCGTCTCCttt > 1:359037/1‑36 (MQ=37) tAAGCGGGGGTGGCGTGATGCATTCCGTCTCCtttt < 2:547277/36‑1 (MQ=37) | GCACAAGGCCGCCAACAATGGTGGTGATAAGC‑GGGGTGGCGTGATGCATTCCGTCTCCTTTT > NC_012967/475257‑475318 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 9 ≤ ATCG/ATCG < 23 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |