Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | AM260480 | 69,908 | +G | intergenic (+89/‑184) | h16_B0060 → / → h16_B0061 | conserved hypothetical membrane protein/ABC‑type transporter, periplasmic component |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | AM260480 | 69,908 | 1 | . | G | 100.0% | 81.7 / NA | 22 | intergenic (+89/‑184) | h16_B0060/h16_B0061 | conserved hypothetical membrane protein/ABC‑type transporter, periplasmic component |
Reads supporting (aligned to +/- strand): ref base . (0/0); new base G (12/10); total (12/10) |
GTTGGACCCGGCTGTGCCGGCTTTCCCCTGAGCCGTCGGCGTATCGTCGCTTATTGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTA‑CGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGTTTGCCCCCATGAGACGCATGCGGTAACT > AM260480/69789‑70011 | gTTGGACCCGGCTGTGCCGGCTTTCCCCTGAGCCGTCGGCGTATCGTCGCTTATTGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTc > 1:784261/1‑134 (MQ=255) ggCTTTCCCCTGAGCCGTCGGCGTATCGTCGCTTATTGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTcg > 1:1058449/1‑134 (MQ=255) tGAGCCGTCGGCGTATCGTCGCTTATTGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGcccc < 1:172281/101‑1 (MQ=255) tGAGCCGTCGGCGTATCGTCGCTTATTGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGcccc > 2:172281/1‑101 (MQ=255) gCCGTCGGCGTATCGTCGCTTATTGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGtgtg < 2:450049/134‑1 (MQ=255) cGTCGGCGTATCGTCGCTTATTGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGAt < 1:901625/134‑1 (MQ=255) gTCGGCGTATCGTCGCTTATTGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATg > 2:1094468/1‑134 (MQ=255) ttGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATc < 2:784261/134‑1 (MQ=255) aCGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGtt < 2:1058449/134‑1 (MQ=255) aCGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGtt < 2:2945/134‑1 (MQ=255) aCGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGtt > 1:2945/1‑134 (MQ=255) aCGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGt < 1:756082/133‑1 (MQ=255) aCGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGt > 2:756082/1‑133 (MQ=255) cATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGAt < 1:770308/95‑1 (MQ=255) cATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGAt > 2:770308/1‑95 (MQ=255) gcgcgcCCTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGTTTGCCCCCATGAGACGCATGc > 2:1002563/1‑134 (MQ=255) cTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGTTTGCCCCCATGAGACGCATGCGGTAACt > 1:1064130/1‑134 (MQ=255) cTTGCGGCGCGCCCTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGTTTGCCCCCATGAGACGCATGCGGTAACt > 2:768914/1‑134 (MQ=255) cTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGcc > 1:785085/1‑45 (MQ=255) cTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGcc < 2:785085/45‑1 (MQ=255) cTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGgt > 2:51826/1‑59 (MQ=255) cTGACGCGCATCCTTTAGCGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGgt < 1:51826/59‑1 (MQ=255) | GTTGGACCCGGCTGTGCCGGCTTTCCCCTGAGCCGTCGGCGTATCGTCGCTTATTGTCGTTCAACGCGGTCGCATGTCTTTCCGCGCGCCCTTGCGGCGCGCCCTGACGCGCATCCTTTA‑CGCGCCCCGGCTCGCACCGGAACCGCCTTCGCGGTTCCGGTGTGATGCCGCTGCAACACTCCGATCTTTCCCGGTTTGCCCCCATGAGACGCATGCGGTAACT > AM260480/69789‑70011 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |