Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 2,863,165 | T→C | R277R (CGT→CGC) | ygbK → | FliA‑regulated DUF1537 family protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 2,863,165 | 0 | T | C | 100.0% | 66.9 / NA | 19 | R277R (CGT→CGC) | ygbK | FliA‑regulated DUF1537 family protein |
Reads supporting (aligned to +/- strand): ref base T (0/0); new base C (13/6); total (13/6) |
AAACGGTAACCAGGCTCGCAAAGCAGGGCGTCCGCTCGCTGGGCGCGGCGTAGTGCTCTCCGGTTCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGTGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCAGGAAAGTGTACTTGCTCCACTGGTTTTTGCCACCGCCAGCACTGA > NC_000913/2863042‑2863290 | aaaCGGTAACCAGGCTCGCAAAGCAGGGCGTCCGCTCGCTGGGCGCGGCGTAGTGCTCTCCGGTTCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCa < 2:248576/139‑1 (MQ=255) gCTCGCAAAGCAGGGCGTCCGCTCGCTGGGCGCGGCGTAGTGCTCTCCGGTTCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCaa > 1:313491/1‑139 (MQ=255) ggCGTCCGCTCGCTGGGCGCGGCGTAGTGCTCTCCGGTTCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGc < 2:589586/139‑1 (MQ=255) gctcgctGGGCGCGGCGTAGTGCTCTCCGGTTCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTAt > 1:578501/1‑139 (MQ=255) cgctGGGCGCGGCGTAGTGCTCTCCGGTTCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGca > 2:1005804/1‑139 (MQ=255) ctGGGCGCGGCGTAGTGCTCTCCGGTTCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGcaca < 1:1005804/139‑1 (MQ=255) tcCGGTTCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTc > 1:536027/1‑139 (MQ=255) ttCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGaa < 2:442985/118‑1 (MQ=255) ttCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGaa > 1:442985/1‑118 (MQ=255) cATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCa > 2:878319/1‑139 (MQ=255) tGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAg > 1:694918/1‑61 (MQ=255) tGCTCTCAAATGACCAACCGCCAGGTAGCACAGTACCGTCAAATTGCACCAGCCCGCGAAg < 2:694918/61‑1 (MQ=255) tctcAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCAGGaaa > 1:42477/1‑139 (MQ=255) tGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCAGGAAAGTGTACt < 2:663567/139‑1 (MQ=255) aaCCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCAGGGAAGTGTACTTGCTc > 1:580467/1‑139 (MQ=255) aaCCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCAGGAAAGTGTACTTGCTc > 1:320305/1‑139 (MQ=255) tACCGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCAGGAAAGTGTACTTGCTGCACTGGTTTTTGCCACCg > 2:752574/1‑139 (MQ=255) cGTCAAATTGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCAGGAAAGTGTACTTGCTCCACTGGTTTTTGCCACCGCCa > 2:595512/1‑139 (MQ=255) ttGCACCAGCCCGCGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCAGGAAAGTGTACTTGCTCCACTGGTTTTTGCCACCGCCAGCACTGa > 1:414242/1‑139 (MQ=255) | AAACGGTAACCAGGCTCGCAAAGCAGGGCGTCCGCTCGCTGGGCGCGGCGTAGTGCTCTCCGGTTCATGCTCTCAAATGACCAACCGCCAGGTAGCACATTACCGTCAAATTGCACCAGCCCGTGAAGTTGATGTGGCACGCTGCCTCTCAATTGAAACTCTGGCCGCTTATGCACACGAACTGGCAGAGTGGGTTCTGGGCCAGGAAAGTGTACTTGCTCCACTGGTTTTTGCCACCGCCAGCACTGA > NC_000913/2863042‑2863290 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |