Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | W3110S.gb | 2,427,890 | T→G | 100% | I246S (ATT→AGT) | yfcH → | conserved hypothetical protein with NAD(P)‑binding Rossmann‑fold domain |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | W3110S.gb | 2,427,890 | 0 | T | G | 96.5% | 91.7 / ‑4.7 | 28 | I246S (ATT→AGT) | yfcH | conserved hypothetical protein with NAD(P)‑binding Rossmann‑fold domain |
Reads supporting (aligned to +/- strand): ref base T (0/1); new base G (16/11); total (16/12) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 4.29e-01 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.97e-01 | |||||||||||
Rejected as polymorphism: E-value score below prediction cutoff. | |||||||||||
Rejected as polymorphism: Frequency below/above cutoff threshold. | |||||||||||
Rejected as polymorphism: Variant not supported by required number of reads on each strand. |
GAACAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCATTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGCGAATCTTCAGTACTGGTATTA > W3110S.gb/2427844‑2427951 | gAACAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCAt > 1:2677227/1‑71 (MQ=255) gAACAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCAt > 1:820693/1‑71 (MQ=255) gAACAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCAt > 1:3633623/1‑71 (MQ=255) gAACAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCAt > 1:319373/1‑71 (MQ=255) gAACAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCAt > 1:3010364/1‑71 (MQ=255) gAACAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCAt > 1:2935970/1‑71 (MQ=255) aaCAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGAGCGCCAtt > 1:2573292/1‑71 (MQ=255) aaCAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCAtt > 1:1896987/1‑71 (MQ=255) aaCAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCAtt > 1:1636900/1‑71 (MQ=255) aaCAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCAt > 1:2215369/1‑70 (MQ=255) cAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCg < 1:2189904/71‑1 (MQ=255) tGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGAc > 1:2407608/1‑68 (MQ=255) tGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGAc > 1:2799923/1‑68 (MQ=255) cccATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGtt < 1:1669365/70‑1 (MQ=255) cccATGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGtt < 1:674329/70‑1 (MQ=255) aTGCGCTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGtt < 1:1179522/67‑1 (MQ=255) cgcTCGGTCATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGc > 1:2052828/1‑71 (MQ=255) cATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGtt < 1:3176676/56‑1 (MQ=255) cATGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGtt < 1:74459/56‑1 (MQ=255) tGCGCTGCATCGCCCGGCCATTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGCGAATCTTCAg < 1:2730579/71‑1 (MQ=255) tGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTaa > 1:1581631/1‑56 (MQ=255) tGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTaa > 1:1180661/1‑56 (MQ=255) tGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGCGAATCTTCAg < 1:3624794/71‑1 (MQ=255) tGCGCTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGCGAATCTTCAg < 1:1941992/71‑1 (MQ=255) cgcTGCATCGCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGCGAATCTTCAGTa > 1:3423194/1‑71 (MQ=255) gCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGCGAATCTTCAGTACTGGTATTa < 1:1353021/71‑1 (MQ=255) gCCCGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGCGAATCTTCAGTACTGGTATTa < 1:569517/71‑1 (MQ=255) cccGGCCAGTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGCGAATCTTCAGTACTAGTATTa < 1:1725872/70‑1 (MQ=255) | GAACAATTTGCCCATGCGCTCGGTCATGCGCTGCATCGCCCGGCCATTTTGCGCGTCCCCGCGACCGCCATTCGACTGTTAATGGGCGAATCTTCAGTACTGGTATTA > W3110S.gb/2427844‑2427951 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |