Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | REL606 | 474,211 | Δ2 bp | coding (1094‑1095/1677 nt) | ybaL ← | predicted transporter 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 | ||
* | REL606 | 474,211 | 0 | T | . | 100.0% | 123.9 / NA | 26 | coding (1095/1677 nt) | ybaL | predicted transporter with NAD(P)‑binding Rossmann‑fold domain |
Reads supporting (aligned to +/- strand): ref base T (0/0); new base . (13/13); total (13/13) | |||||||||||
* | REL606 | 474,212 | 0 | C | . | 100.0% | 123.9 / NA | 26 | coding (1094/1677 nt) | ybaL | predicted transporter with NAD(P)‑binding Rossmann‑fold domain |
Reads supporting (aligned to +/- strand): ref base C (0/0); new base . (13/13); total (13/13) |
CAGTAGTGCGAACAGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTGTCCGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTCACCAATCT > REL606/474145‑474278 || cAGTAGTGCGAACAGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCgg > 2:338808/1‑76 (MQ=255) tagtGCGAACAGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAg > 1:773455/1‑76 (MQ=255) agtGCGAACAGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGt > 2:478677/1‑76 (MQ=255) gtGCGAACAGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTa > 2:54493/1‑76 (MQ=255) cGAACAGTACCGGGTTGAGCATAATCGACAGGATCACCCCTGCCAGAACCAGGTTTTG‑‑CGGCCTGCGGCAGTaaaa > 1:313015/1‑75 (MQ=255) gAACAGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAAtt < 1:759552/76‑1 (MQ=255) aCAGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCa < 1:787276/76‑1 (MQ=255) aCAGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCa < 1:787282/76‑1 (MQ=255) aGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAAt > 1:247003/1‑76 (MQ=255) aCCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGcc > 2:12437/1‑76 (MQ=255) cGGGTTGACCATAATCGACAGGATCCCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCan < 1:722395/76‑2 (MQ=255) gggTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCAtt < 2:712985/76‑1 (MQ=255) tGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCa > 1:1110007/1‑76 (MQ=255) tGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCa > 1:88643/1‑76 (MQ=255) cATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTcc > 2:563479/1‑76 (MQ=255) gACAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAgg < 2:531812/76‑1 (MQ=255) cAGGATCGCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGAt > 2:765970/1‑76 (MQ=255) cAGGATCGCCCCTGCCAGCACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGAt < 2:1116505/76‑1 (MQ=255) cAGGATCCCCCCTGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGAt < 2:272917/76‑1 (MQ=255) tGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCCATGCCATTCCCCGTCCCGCCCGGCTACACGCGAACTc > 2:243178/1‑76 (MQ=255) tGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTc > 2:243168/1‑76 (MQ=255) tGCCAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTc < 2:370353/76‑1 (MQ=255) cAGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTCAcc > 2:583813/1‑76 (MQ=255) aGTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTCACCa < 2:510771/76‑1 (MQ=255) gTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTCACCaa > 1:225811/1‑76 (MQ=255) gTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTCACCaa < 1:715281/76‑1 (MQ=255) gTACCAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCACTCCCGCCAGGATAAACGCGAACTCACCaa < 1:715289/76‑1 (MQ=255) ccAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTCACCAATCt < 1:229459/76‑1 (MQ=255) ccAGGTTTTG‑‑CGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTCACCAATCt < 2:985639/76‑1 (MQ=255) || CAGTAGTGCGAACAGTACCGGGTTGAGCATAATCGACAGGATCGCCCCTGCCAGTACCAGGTTTTGTCCGGCCTGCGGCAGTAAATTCAATGCCATTCCCAGTCCCGCCAGGATAAACGCGAACTCACCAATCT > REL606/474145‑474278 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 30 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |