Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_002947 | 2,921,460 | G→A | G3494R (GGG→AGG) | PP_2561 → | hemolysin‑type calcium‑binding bacteriocin |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 2,921,460 | 0 | G | A | 96.8% | 95.0 / NA | 31 | G3494R (GGG→AGG) | PP_2561 | hemolysin‑type calcium‑binding bacteriocin |
Reads supporting (aligned to +/- strand): ref base G (0/0); major base A (20/10); minor base C (0/1); total (20/11) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 3.55e-01 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00 |
CACGTTGCTGGGGGAGGCCGGTAACGACAACCTGAACGGGGGCGCTGGCGATGACAGCCTGGATGGCGGCAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCGGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCAACGACCTGATCATCAAT > NC_002947/2921315‑2921603 | cacGTTGCTGGGGGAGGCCGGTAACGACAACCTGAACGGGGGCGCTGGCGATGACAGCCTGGATGGCGGCAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCaggg < 6:234116/149‑1 (MQ=255) ggggAGGCCGGTAACGACAACCTGAACGGGGGCGCTGGCGATGACAGCCTGGATGGCGGCAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCaa < 8:64864/149‑1 (MQ=255) gACAACCTGAACGGGGGCGCTGGCGATGACAGCCTGGATGGCGGCAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACgg > 1:26286/1‑149 (MQ=255) aCAACCGGCCCGGGCGCGCTGGCGCTGACCGCCAGGATGGCGGCACCGGCAATGTCACCCCGGAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCCGGGGGGCCGGCAACGACTTCCTCAACGGt < 8:204993/149‑1 (MQ=255) cTGAACGGGGGCGCTGGCGATGACAGCCTGGATGGCGGCAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGCCACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAATGGTGCgg > 8:98405/1‑148 (MQ=255) cgcTGGCGATGACAGCCTGGATGGCGGCAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATa < 1:1770/149‑1 (MQ=255) gcTGGCGATGACAGCCTGGATGGCGGCAACGGCAATGTCACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACCACTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATa < 1:91231/149‑1 (MQ=255) gATGACAGCCTGGATGGCGGCAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑Cggtggt > 4:176930/1‑149 (MQ=255) gCCTGGACGGCGGCCACGGCAAGGACACCCGGCAGGGCGGCGATGGTCACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGtgggtggg < 4:352859/149‑1 (MQ=255) ccTGGATGGCGGCAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTgggg > 2:104620/1‑149 (MQ=255) gcggcAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTaa < 2:26286/148‑1 (MQ=255) gcaaTGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCAt > 8:75823/1‑148 (MQ=255) ccTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCAcc > 5:44021/1‑148 (MQ=255) ccTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCAcc > 7:210701/1‑148 (MQ=255) aaCGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTc > 5:132480/1‑147 (MQ=255) aCGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCa < 6:44021/148‑1 (MQ=255) acaTTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGc < 7:75823/149‑1 (MQ=255) aTTGTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTg > 6:20688/1‑149 (MQ=255) gTTCGGCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAg > 6:141273/1‑149 (MQ=255) gCGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCttt < 6:132480/149‑1 (MQ=255) cGACGTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTg < 5:141273/149‑1 (MQ=255) gTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTACCGATA‑CGGTGGTGGGTGGGGCCGGTAACGCCACCATGATCGCCACGGATGGATGCGCTGTGTTCCAGTTCGCTGGAGGGTTTgggct > 6:238460/1‑146 (MQ=255) gTGGGTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGCAACGATAGTAGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCCCCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGc > 1:300820/1‑148 (MQ=255) ggTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCAACGa > 6:330611/1‑149 (MQ=255) gTACCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGGAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCAAGTTCGCTGCAGGCTTTGGCAACGAc > 8:72364/1‑149 (MQ=255) aCCGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCAACGACCt > 3:199175/1‑149 (MQ=255) cGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGCCACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCAACGACCTGa > 6:96560/1‑149 (MQ=255) cGACACC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCCACGACCTGa > 4:281270/1‑149 (MQ=255) cacC‑CTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCAACGACCTGatca < 5:20688/149‑1 (MQ=255) c‑cTGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCAACGACCTGatcatc > 5:180341/1‑148 (MQ=255) tGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCAACGACCTGATCATCAAt > 1:64042/1‑149 (MQ=255) tGATCAGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCAACGACCTGATCATCAAt > 1:58873/1‑149 (MQ=255) | CACGTTGCTGGGGGAGGCCGGTAACGACAACCTGAACGGGGGCGCTGGCGATGACAGCCTGGATGGCGGCAACGGCAATGACACCCTGCAGGGCGGCGATGGTAACGACACATTGTTCGGCGACGTGGGTACCGACACC‑CTGATCGGGGGGGCCGGCAACGACTTCCTCAACGGTGCGGCAGGTAACGATA‑CGGTGGTGGGTGGGGCCGGTAACGACACCATGATCGCCACCGATGGAAACGATGTGTTCCAGTTCGCTGCAGGCTTTGGCAACGACCTGATCATCAAT > NC_002947/2921315‑2921603 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |