Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 1,677,320 | T→C | D195G (GAC→GGC) | pntA ← | pyridine nucleotide transhydrogenase subunit alpha |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 1,677,320 | 0 | T | C | 100.0% | 36.2 / NA | 12 | D195G (GAC→GGC) | pntA | pyridine nucleotide transhydrogenase subunit alpha |
Reads supporting (aligned to +/- strand): ref base T (0/0); new base C (6/6); total (6/6) |
GGAGTCAACCATTTCACGGGTAATTAGCTTCGGCGCTGGTTTGCCTGGAATAAGCGCGGTGGTGACAATGATATCGACCTCTTTTGCCTGGGCGGCAAAGAGTTCCATTTCCGCTTTGATGAACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGTCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCAACACCCGCACCAATCACCATCACTTTTGCCGGTGGCACTTTCCCGGCCGCAGTAATTTGCCCGGTAAAGAAGCGCCCAAATTCATGTGCCGCTTCAACAATGGCGCGATAACCGGCGATGTTCGCCATCGAGCTTAGTGCGTCCAGCGATTGTGCGCGTGAGATACGCGGCACAGAGTCCATCG > NC_000913/1677082‑1677563 | ggAGTCAACCATTTCACGGGTAATTAGCTTCGGCGCTGGTTTGCCTGGAATAAGCGCGGTGGTGACAATGATATCGACCTCTTTGGCCTGGGCGGCAAAGAGTTCCATTTCCGCGTTGATGAACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAAGTCCGCGCGCATACTTTGAACGTGTGCTTTCACTTCCTGGCGGGTGCCGAATtcacgc < 2:156290/250‑1 (MQ=255) gCTTCGGCGCTGGTTTGCCTGGAATAAGCGCGGTGGTGACAATGATATCGACCTCTTTTGCCTGGGCGGCAAAGAGTTCCATTTCCGCTTTGATGAACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTgcg < 1:169914/251‑1 (MQ=255) tGGAATAAGCGCGGTGGTGACAATGATATCGACCTCTTTTGCCTGGGCGGCAAAGAGTTCCATTTCCGCTTTGATGAACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTg > 1:217343/1‑251 (MQ=255) aGCGCGGTGGTGACAATGATATCGACCTCTTTTGCCTGGGCGGCAAAGAGTTCCATTTCCGCTTTGATGAACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCaaaaac > 1:126538/1‑247 (MQ=255) cGACCTCTTTTGCCTGGGCGGCAAAGAGTTCCATTTCCGCTTTGATGAACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCAACACCCGCACCAATCACCATCACtttt < 1:192621/251‑1 (MQ=255) gcggcAAAGAGTTCCATTTCCGCTTTGATGAACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACGTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCAACACCCGCACCAATCACCATCACTTTTGCCGGTGGCACTTTccc < 2:80920/251‑1 (MQ=255) tCCATTTCCGCTTTGATGAACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCAACACCCGCACCAATCTCCATCACTTTTGCCGGTGGCACTTTCCCCGCCGCAGTAAt > 2:31630/1‑251 (MQ=255) gaACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCAACACCCGCACCAATCACCATCCCTTTTGCCCGTGGCACTTTCCCGGCCGCAGTAATTTGCCCGGTAAagcagc > 2:62544/1‑251 (MQ=255) tCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCAACACCCGCACCAATCACCATCACTTTTGCCGGTGGCACTTTCCCGGCCGCAGTAATTTGCCCGGTAAAGAAGCACCCaa > 1:137504/1‑250 (MQ=255) aGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCAACACCCGCACCAATCACCATCACTTTTGCCGGTGGCACTTTCCCGGCCGCAGTAATTTGCCCGGTAAAGAAGCGCCCAAATTCATGTGCCGCTTCAACAATGGCGCGATAACCgg > 2:57588/1‑251 (MQ=255) cAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGCCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCAACACCCGCACCAATCACCATCACTTTTGCCGGTGGCACTTTCCCGGCCGCAGTAATTTGCCCGGTAAAGAAGCGCCCAAATTCATGTGCCGCTTCAACAATGGCGCGATAACCGGCGATGTTCGCCATCGAGc < 1:214596/251‑1 (MQ=255) gcgggTGCCGAATGCCCGCACAATCGCGCCGTGACTGTTTGCTGCGCCAATGGCGGTCAGACCTGCAACACCCGCACCAATCACCATCACTTTTGCCGGTGGCACTTTCCCGGCCGCAGTAATTTGCCCGGTAAAGAAGCGCCCAAATTCATGTGCCGCTTCAACAATGGCGCGATAACCGGCGATGTTCGCCATCGAGCTTAGTGCGTCCAGCGATTGTGCGCGTGAGATACGCGGCACAGAGTCCATCg < 2:281622/251‑1 (MQ=255) | GGAGTCAACCATTTCACGGGTAATTAGCTTCGGCGCTGGTTTGCCTGGAATAAGCGCGGTGGTGACAATGATATCGACCTCTTTTGCCTGGGCGGCAAAGAGTTCCATTTCCGCTTTGATGAACGCGTCCGACATCACTTTGGCATAGCCATCGCCGCTGCCAGCTTCCTCTTTAAAATCCAGCTCGAGGAATTCCGCGCCCATACTTTGAACTTGTTCTTTCACTTCCGGGCGGGTGTCGAATGCACGCACAATCGCGCCGAGACTGTTTGCTGCGCCAATGGCGGCCAGACCTGCAACACCCGCACCAATCACCATCACTTTTGCCGGTGGCACTTTCCCGGCCGCAGTAATTTGCCCGGTAAAGAAGCGCCCAAATTCATGTGCCGCTTCAACAATGGCGCGATAACCGGCGATGTTCGCCATCGAGCTTAGTGCGTCCAGCGATTGTGCGCGTGAGATACGCGGCACAGAGTCCATCG > NC_000913/1677082‑1677563 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |