| Predicted mutation | ||||||
|---|---|---|---|---|---|---|
| evidence | seq id | position | mutation | annotation | gene | description |
| RA | NC_000913 | 3,115,239 | G→A | P1292S (CCG→TCG) | yghJ ← | putative lipoprotein YghJ |
| Read alignment evidence... | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
| * | NC_000913 | 3,115,239 | 0 | G | A | 100.0% | 20.6 / NA | 10 | P1292S (CCG→TCG) | yghJ | putative lipoprotein YghJ |
| Reads supporting (aligned to +/- strand): ref base G (0/0); new base A (6/4); total (6/4) | |||||||||||
TGCCTGGTTGTTGCTCTCCTCCAGATATTCCGGTGCGACGGTAATATCGTCAGCGACACGGTTCATCTTGCCGAGATAACGATCCTGCATGTACAGCGCCAGCACGTTGTTAGCGACTTCAGTTGCACCCGGTACAGTCAACGGCGTTTCTGCGGCGTTATGACCGACTTCATGCCAGATCAGCCAGTCGTTCAGCGGCGTCGTCGGCAGCGTGGTGCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATCTGCACATCGTTGGTGAAACGATGTTTGTGGCCCGGCAAGTTTTTATAGGTAAACATCCGGTGCTTACCGTCTTCGCTATCACGGCCGTAGAAGTCATTCATCGAGCTGGCAAAGGTATCCAGATCGTTAGCGAATTGCTCCAGTCCGCCAGTGTAATTGC > NC_000913/3115033‑3115472 | nnnnngnTTNNTGCTNTCCTCCAGATATTCCGGTGCGACGNTAATATCGTCAGCGACACGGTTCATCTTGACNANATAACGATCCTGCATGTACAGCGCCAGCACGTTGTTAGCGACTTCAGTNGCACCCGGTANAGTNNACGGNGNTNCTGCGGCGTTATGACCGACTTCATGCCAGNTCAGCCAGTCGTTCAGCGGCGTCNNCGNNNGCNNGGTGc < 2:187678/213‑1 (MQ=255) ggTTCATCTTGCCGAGATAACGATCCTGCATGTACAGCGCCAGCACGTTGTTAGCGACTTCAGTTGCACCCGGTACAGTCAACGGCGTTTCTGCGGCGTTATGACCGACTTCATGCCAGATCAGCCAGTCGTTCAGCGGCGTCGTCGACAGCGTGGTGCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATCTGCACATCGTTGGTGAAACGATGTTTGTgg > 1:3973/1‑251 (MQ=255) cTTGCCGAGATAACGATCCTGCATGTACAGCGCCAGCACGTTGTTAGCGACTTCAGTTGCACCCGGTCCAGTCAACGCCGTTTCTGCGGCGTTATGACCGACTTCATGCCAGATCAGCCAGTCGTTCAGCGGCGTCGTCGACAGCGTGGTGCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATAACCGATGGAGATCTGCACATCGTTGGTGAAACGATGTTTGTGGCCCGGc > 1:138042/1‑250 (MQ=255) ccAGCACGTTGTTAGCGACTTCAGTTGCACCCGGTACAGTCAACGGCGTTTCTGCGGCGTTATGACCGACTTCATGCCAGATCAGCCAGTCGTTCAGCGGCGTCGTCGACAGCGTGGTGCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATCTGCACATCGTTGGTGAAACGATGTTTGTGGCCCGGCAAGTTTTTATAGGTAAACATCCGGTGCTTACCg < 1:2207/251‑1 (MQ=255) cTTCAGTTGCACCAGGTACAGTCAACGGCGTTTCTGCGGCGTTATGACCGACTTCATTCCAGATCAGCCAGTCGTTCAGCGGCGTCGTCGACAGCGTGGTGCTGTTCGGCGAGAAGCGGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATCTGCACATCGTTGGTGAAACGATGtt < 1:211853/189‑1 (MQ=255) ncccGGTACAGTCAACGGCGTTTCTGCGGCGTTATGACCGACTTCATGACAGATCAGCCAGTCGTTCAGCGGCGTCGTCGACAGCGTGGTGCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATCTGCACATCGTTGGTGAAAc > 1:28286/2‑173 (MQ=255) tGCGGCGTTATGAACGACTTCATGCCAGATCAGCCCGTAGTTCAGCGGCGTCGTCAAAAACGTGGTGCTGATCGGCGCGAAGCTGCTGTTCCTTACCGGATAACACGGATGCGCATCAACGATGGAGATCTGCACATCGTTGGTGAAACGATGTTTGTGGCCCGGAAAGTTTTTATAGGGAAACATCAGGTGCTTACCGTCTTCGCTATCAAGGCCGGAGAAGTCATTCATAGCGCTGGAACAGGTATcc > 1:185012/1‑250 (MQ=255) aCCGACTTCATGCCAGATCAGCCAGTCGTTCAGCGGCGTCGTCGACAGCGTGGTGCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATCTGCACATCGTTGGTGAAACGATGTTTGTGGCCCgg > 1:15170/1‑153 (MQ=255) aGCCAGTCGTTCAGCGGCGTCGTCGACAGCGTGGTGCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATCTGCACATCGTTGGTGAAACGATGTTTGTGGCCCg < 1:17456/133‑1 (MQ=255) gTTCAGCGGCGTCGTCGACAGCGTGGTTCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATCTGCACATCGTTGGTGAAACGATGTTTGTGGCCCGGCAAGTTTTTATAGGTAAACATCCGGTGCTTACCGTCTTCGCTATCACGGCCGGAGAAGTCATTCATCGAGCTGGCAAAGGTATCCAGATCGTTAGCGAATTGCTCCAGTCCGCCAGTGTAATTgn < 1:157523/251‑2 (MQ=255) ngtcgtcGACAGCGTGGTGCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATc > 1:66281/2‑82 (MQ=255) | TGCCTGGTTGTTGCTCTCCTCCAGATATTCCGGTGCGACGGTAATATCGTCAGCGACACGGTTCATCTTGCCGAGATAACGATCCTGCATGTACAGCGCCAGCACGTTGTTAGCGACTTCAGTTGCACCCGGTACAGTCAACGGCGTTTCTGCGGCGTTATGACCGACTTCATGCCAGATCAGCCAGTCGTTCAGCGGCGTCGTCGGCAGCGTGGTGCTGTTCGGCGAGAAGCTGCTGTTCATTACCGGATAACCCGAATGCGCATCACCGATGGAGATCTGCACATCGTTGGTGAAACGATGTTTGTGGCCCGGCAAGTTTTTATAGGTAAACATCCGGTGCTTACCGTCTTCGCTATCACGGCCGTAGAAGTCATTCATCGAGCTGGCAAAGGTATCCAGATCGTTAGCGAATTGCTCCAGTCCGCCAGTGTAATTGC > NC_000913/3115033‑3115472 |
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |