Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 3,506,024 | T→C | intergenic (‑4/+8) | yhfS ← / ← yhfT | FNR‑regulated pyridoxal phosphate‑dependent aminotransferase family protein/inner membrane protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 3,506,024 | 0 | T | C | 100.0% | 110.5 / NA | 32 | intergenic (‑4/+8) | yhfS/yhfT | FNR‑regulated pyridoxal phosphate‑dependent aminotransferase family protein/inner membrane protein |
Reads supporting (aligned to +/- strand): ref base T (0/0); new base C (13/19); total (13/19) |
AATCACCGCCAGTAAGAAACTCGCTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGTGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGACGGCCCAGGGATTCGTTGAGGAAGTAAA > NC_000913/3505903‑3506156 | aaTCACCGCCAGTAAGAAGCTCGCTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAg > 1:559867/1‑134 (MQ=255) aaTCACCGCCAGTAAGAAACTCGCTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAg < 2:559867/134‑1 (MQ=255) aaTCACCGCCAGTAAGAAACTCGCTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGga < 2:887107/139‑1 (MQ=255) aTCACCGCCAGTAAGAAACTCGCTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGgaa > 2:853810/1‑139 (MQ=255) aGTAAGAAACTCGCTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGc < 1:25686/139‑1 (MQ=255) aGAAACTCGCTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCACGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAg > 1:612258/1‑139 (MQ=255) cTCGCTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGt < 1:246763/139‑1 (MQ=255) cTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAg < 1:1007215/130‑1 (MQ=255) cTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAg > 2:1007215/1‑130 (MQ=255) tGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGa < 1:146517/139‑1 (MQ=255) cAAATGCTATCCACCAGCTCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATAcc < 2:632724/139‑1 (MQ=255) aaaTGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCg < 2:612258/139‑1 (MQ=255) tATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATc > 2:767514/1‑139 (MQ=255) ccaGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACt > 1:528132/1‑139 (MQ=255) caGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGgaacgaa < 1:4852/89‑1 (MQ=255) caGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGgaacgaa > 2:4852/1‑89 (MQ=255) cgcAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGcc < 1:540604/67‑1 (MQ=255) cgcAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGcc > 2:540604/1‑67 (MQ=255) cAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACg > 2:870423/1‑139 (MQ=255) ttttGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTgc < 2:528132/139‑1 (MQ=255) ttGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACAATCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTgccg < 2:319209/139‑1 (MQ=255) atCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCgg > 2:914489/1‑139 (MQ=255) tCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGa < 1:767514/139‑1 (MQ=255) tCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGCGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGa < 1:853810/139‑1 (MQ=255) aGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGACGGcc < 2:558973/139‑1 (MQ=255) aGGCTTTGCAGAGGAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGACGGcc < 1:565531/139‑1 (MQ=255) ggAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTcag > 2:112548/1‑67 (MQ=255) ggAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTcag < 1:112548/67‑1 (MQ=255) gAAACGTCTTCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGACGGCCCAGGGATTCGTTg < 1:528883/139‑1 (MQ=255) ttCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGa < 2:391229/113‑1 (MQ=255) ttCATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGa > 1:391229/1‑113 (MQ=255) cATAGGCGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGACGGCCCAGGGATTCGTTGAGGAAGTaaa > 1:956700/1‑139 (MQ=255) | AATCACCGCCAGTAAGAAACTCGCTGCCGGGGAAATGGCGACAAATGCTATCCACCAGCGCAAACTGCTTTTGCTGCGCCTCAATAATCGTCAGGCTTTGCAGAGGAAACGTCTTCATAGGTGCCTTCCTTAAGCCGGAACGAACAGGCCAAGCCAGTAAAGAACATTCAGCAGAATACCGGTGATCATTACTGCCACGACCGGTGCCGCCATTTTCTGTACCGGACGGCCCAGGGATTCGTTGAGGAAGTAAA > NC_000913/3505903‑3506156 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 16 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |