Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 1,825,038 | (T)7→6 | intergenic (‑101/+102) | ves ← / ← spy | HutD family protein Ves/ATP‑independent periplasmic chaperone |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 1,825,032 | 0 | T | . | 100.0% | 19.4 / NA | 6 | intergenic (‑95/+108) | ves/spy | HutD family protein Ves/ATP‑independent periplasmic chaperone |
Reads supporting (aligned to +/- strand): ref base T (0/0); new base . (5/1); total (5/1) |
CACAGATTCACCGACATTTTACGCATATCAAAGTATTCCATACTCGCTCCCGGCCCGTTCTTTTCATTGTTATCGTTCAGGTAACCGTGGATGGTTATCGGCAACTCGGGTGATTTACGTTAGTGGTGATCAGGCTTTTTTTACAACTGTTTGAGAAGAGAAAAGAAAACCGCCGATCCTGTCCACCGCATTACTGCAAGGTAGTGGACAAGACCGGCGGTCTTAAGTTTTTTGGCTGAAAGATTATTCAGCAGTTGCAGGCATTTTACCTTT > NC_000913/1824897‑1825169 | cacaGATTCACCGACATTTTACGCATATCAAAGTATTCCATACTCGCTCCCGGCCCGTTCTTTTCATTGTTATCGTTCAGGTAACCGTGGATGGTTATCGGCAACTCGGGTGATTTACGTTAGTGGTGATCAGGCttttt > 1:335521/1‑140 (MQ=255) aCCGACATTTTACGCATATCAAAGTATTCCATACTCGCTCCCGGCCCGTTCTTTTCATTGTTATCGTTCAGGTAACCGTGGATGGTTATCGGCAACTCGGGTGATTTACGTTAGTGGTGATCAGGC‑TTTTTTACAACTg > 1:87889/1‑139 (MQ=255) aCCGACATTTTACGCATATCAAAGTATTCCATACTCGCTCCCGGCCCGTTCTTTTCATTGTTATCGTTCAGGTAACCGTGGATGGTTATCGGCAACTCGGGTGATTTACGTTAGTGGTGATCAGGC‑TTTTTTACAACTg < 2:87889/139‑1 (MQ=255) tCCATACTCGCTCCCGGCCCGTTCTTTTCATTGTTATCGTTCAGGTAACCGTGGATGGTTATCGGCAACTCGGGTGATTTACGTTAGTGGTGATCAGGC‑TTTTTTACAACTGTTTTAGAAGAGAAAAGAAAACCGCCGAt > 1:77824/1‑140 (MQ=255) tCCATACTCGCTCCCGGCCCGTTCTTTTCATTGTTATCGTTCAGGTAACCGTGGATGGTTATCGGCAACTCGGGTGATTTACGTTAGTGGTGATCAGGC‑TTTTTTACAACTGTTTGAGAAGAGAAAAGAAAACCGCCAAt > 2:160288/1‑140 (MQ=255) aCTCGCTCCCGGCCCGCTCTTTTCATTGTTATCGTTCAGGTAACCGTGGATGGTTATCGGCAACTCGGGTGATTTACGTTAGTGGTGATCAGGC‑TTTTTTACAACTGTTTGAGAAGAGAAAAGAAAACCGCCGATCCTGt > 1:19104/1‑140 (MQ=255) tCCCGGCCCGTTCTTTTCATTGTTATCGTTCAGGTAACCGTGGATGGTTATCGGCAACTCGGGTGATTTACGTTAGTGGTGATCAGGC‑TTTTTTACAACTGTTTGAGAAGAGAAAAGAAAACCGCCGATCCTGTCCACCg > 1:236021/1‑140 (MQ=255) cgccccGTTTTTTTATTTTTTATGGTTCAGGTACCGGTGGATGGTTCTCGGCAACGGGGGTGTTTTAGGTTAGTGGTAACCA‑GCTTTTTTAACACTTTTTTGAAAAGAAAAAAAAAAACCGCCGATCCTGTCCACCGCAt < 2:19104/137‑1 (MQ=255) cGGCCTTTTTTTTTATTTGTTATCGTTCAGGTACCGGTGGATGTTTATCGGCACCTGGGGTGTTTTAGGTTGGGGGTGATC‑GGTTTTTTTTACAATTTTTTGAAAAGAAAAAAAAAAACCGCCGATCCTGTCCACCGCAt < 2:236021/140‑1 (MQ=255) gttttttttACAATTGTTTGAAAAGAAAAAAAAAAACCGCCGATCCTGTCCACCGCATTACTGCAAGGTAGTGGACAAGACCGGCGGTCTTAAGTTTTTTGGCTGAAAGATTATTCAGCAGTTGCAGGCATTTTACCttt < 2:335521/138‑1 (MQ=255) | CACAGATTCACCGACATTTTACGCATATCAAAGTATTCCATACTCGCTCCCGGCCCGTTCTTTTCATTGTTATCGTTCAGGTAACCGTGGATGGTTATCGGCAACTCGGGTGATTTACGTTAGTGGTGATCAGGCTTTTTTTACAACTGTTTGAGAAGAGAAAAGAAAACCGCCGATCCTGTCCACCGCATTACTGCAAGGTAGTGGACAAGACCGGCGGTCTTAAGTTTTTTGGCTGAAAGATTATTCAGCAGTTGCAGGCATTTTACCTTT > NC_000913/1824897‑1825169 |
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 < 37 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |