Predicted mutation | ||||||
---|---|---|---|---|---|---|
evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 3,920,104 | A→G | R100R (CGT→CGC) | atpH ← | ATP synthase F1 complex subunit delta |
Read alignment evidence... | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 3,920,104 | 0 | A | G | 100.0% | 55.4 / NA | 16 | R100R (CGT→CGC) | atpH | ATP synthase F1 complex subunit delta |
Reads supporting (aligned to +/- strand): ref base A (0/0); new base G (6/10); total (6/10) |
ATCGATTTTGCAATTCAGCTTAACTTTGCGTGACAGACGTTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCACGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAACCCGAATCAGGTTCTGACCGTTTTCGTCCAGTTGCTCACCACAAACTGCGATAAACGACTCGGCGAGCGTT > NC_000913/3919972‑3920239 | aTCGATTTTGCAATTCAGCTTAACTTTGCGTGACAGACGCTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCATCCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGAAGCCTCACACACTGCGCGCAGGt > 2:258396/1‑140 (MQ=255) tttGCAATTCAGCTTAACTTTGCGTGACAGACGTTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGt < 2:111273/134‑1 (MQ=255) tttGCAATTCAGCTTAACTTTGCGTGACAGACGTTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGt > 1:111273/1‑134 (MQ=255) ttGCAATTCAGCTTAACTTTGCGTGACAGACGTTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATaaa < 2:3442/140‑1 (MQ=255) cTTAACTTTGCGTGACAGACGTTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGaa > 1:194198/1‑140 (MQ=255) tGCGTGACAGACGTTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCggg > 2:336694/1‑140 (MQ=255) cGTGACAGACGTTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAg > 2:240265/1‑140 (MQ=255) aCGTTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTaa < 2:47957/140‑1 (MQ=255) tttCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAAccc < 1:62773/140‑1 (MQ=255) tttCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAAccc < 2:150795/140‑1 (MQ=255) gcgAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAACCCGAAt < 2:194198/140‑1 (MQ=255) gcgAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAACCCGAAt < 2:229517/140‑1 (MQ=255) aCTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAACCCGAATCATGTTCTGACCGt < 2:300073/140‑1 (MQ=255) gCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAACCCGAATCAGGTTCTGACCGTTTTCGTc < 1:258396/140‑1 (MQ=255) gAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAACCCGAATCAGGTTCTGACCGTTTTCGTCCAGTTGCTc < 1:240265/140‑1 (MQ=255) gCCTCACTCACGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAACCCGAATCAGGTTCTGACCGTTTTCGTCCAGTTGCTCACCACAAACTGCGATAAACGACTc > 2:26405/1‑140 (MQ=255) cGGCGCGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAACCCGAATCAGGTTCTGACCGTTTTCGTCCAGTTGCTCACCACAAACTGCGATAAACGACTCGGCGAGCGtt > 1:189761/1‑140 (MQ=255) | ATCGATTTTGCAATTCAGCTTAACTTTGCGTGACAGACGTTTTTCCATCGCAGCAGAAATTTTCGCGAGCTGTTGTTCACTCAGTGCGGCAGCGGAAATGACGTCTACCTCAGCGGTAGCCTCACTCACGGCACGCAGGTGAATAAACTGCTCCAGAACATCCGGGAGCGCGTTAAGACGACCATTTTCAGCCATAACCCGAATCAGGTTCTGACCGTTTTCGTCCAGTTGCTCACCACAAACTGCGATAAACGACTCGGCGAGCGTT > NC_000913/3919972‑3920239 |
Alignment Legend |
---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |