Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 1,741,062 | T→C | C384C (TGT→TGC) | ydhC → | putative transporter YdhC |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 1,741,062 | 0 | T | C | 100.0% | 47.2 / NA | 13 | C384C (TGT→TGC) | ydhC | putative transporter YdhC |
Reads supporting (aligned to +/- strand): ref base T (0/0); new base C (6/7); total (6/7) |
AACAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGTGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTCA > NC_000913/1741020‑1741106 | aaCAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGaagaag > 1:917267/1‑50 (MQ=255) agtagtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTg > 1:290067/1‑50 (MQ=255) gtGCTGGTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTg < 1:263025/50‑1 (MQ=255) ggTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAg > 1:1546834/1‑49 (MQ=255) gTCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGaa < 1:165190/50‑1 (MQ=255) tCGCGCTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAAt < 1:905017/50‑1 (MQ=255) gcgcTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATc < 1:1800907/49‑1 (MQ=255) gcTGGGTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATg < 1:2205953/50‑1 (MQ=255) ggTTACATGATGCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGc < 1:1009194/48‑1 (MQ=255) atgatgCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCg > 1:405181/1‑49 (MQ=255) tgatgCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCg > 1:518082/1‑48 (MQ=255) tgatgCAACGTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGaa < 1:1652011/50‑1 (MQ=255) gTTGCGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTCa > 1:131333/1‑49 (MQ=255) | AACAGTAGTGCTGGTCGCGCTGGGTTACATGATGCAACGTTGTGAAGAAGTTGGCTGCCAGAATCATGGCAATGCCGAAGTCGCTCA > NC_000913/1741020‑1741106 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |