Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 6,112,033 | T→A | 14.3% | H118Q (CAT→CAA) | PP_5362 → | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 6,112,033 | 0 | T | A | 14.3% | 64.7 / 6.0 | 28 | H118Q (CAT→CAA) | PP_5362 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base T (13/11); new base A (2/2); total (15/13) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 3.81e-01 |
CACAAACCAACAGCCGCTATGGCACATTGACTTTTTTTACCGGCCTGGCCAGCGATGGTGAGGCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACGCGCTGAAAACACCAGCCTTGACCAACCCTTTGTCAGACCGAAAAG > NC_002947/6111888‑6112168 | cacaAACCAACAGCCGCTATGGCACATTGACTTTTTTTACCGGCCTGGCCAGCGATGGTGAGGCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCAATGCa > 2:141492/1‑150 (MQ=255) cAACAGCCGCTATGGCACATTGACTTTTTTTACCGGCCTGGCCAGCGATGGTGAGGCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGAt > 1:167097/1‑150 (MQ=255) cAACAGCCGCTATGGCACATTGACTTTTTTTACCGGCCTGGCCAGCGATGGTGAGGCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGAt > 2:610661/1‑150 (MQ=255) cAACAGCCGCTATGGCACATTGACTTTTTTTACCGGCCTGGCCAGCGATGGTGAGGCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCAATGCAGCTTGaa < 1:141492/150‑2 (MQ=255) gACTTTTTTTACGGGCCTGGCCAGCGATGGTGAGGCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCa > 2:469602/1‑122 (MQ=255) gACTTTTTTTACCGGCCTGGCCAGCGATGGTGAGGCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCa < 1:469602/122‑1 (MQ=255) ccGGCCTAGCCAGCGATGGTGAGGCCTGGGTGCGCTACAGCCGACGCGTAGGCTGGACCCCCTTGAACCGCGTACCCAGTCCCAGCGGCGAGCTCTTCAAGCTGCATTGCAGCTTGATCGAGCGGTGCCGTTCACGCCTCCTTTCAtttt < 2:742698/150‑1 (MQ=255) aGCGATGGTGAGGCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGtttttt > 1:523552/1‑150 (MQ=255) tGAGGCCTGGGTGGGCTACAGCCGCCGCATAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGa > 2:746252/1‑115 (MQ=255) tGAGGCCTGGGTGGGCTACAGCCGCCGCATAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGa < 1:746252/115‑1 (MQ=255) ggCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCt > 1:386075/1‑150 (MQ=255) tgggtgggCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTTAACGTTTTTTCTCTGCTGCCTAttt < 1:313563/150‑1 (MQ=255) cTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCAATGCAGCTTGaa > 2:24314/1‑83 (MQ=255) cTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCAATGCAGCTTGaa < 1:24314/84‑2 (MQ=255) ggCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGCACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACgcgc < 1:168366/150‑1 (MQ=255) gCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACGCGCt > 1:548667/1‑150 (MQ=255) ccTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGACTATTTTGTAAGTGAGCTTCGAGCACGCGCTAAAAACAcc > 1:206369/1‑150 (MQ=255) gcgTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTc > 1:327153/1‑115 (MQ=255) gcgTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTc < 2:327153/115‑1 (MQ=255) gcgTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACGCGCTGAAAACACCAGCCTTGAc < 2:523552/150‑1 (MQ=255) cAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACGCGCTGAAAACACCAGCCTTGACCAACCCt < 2:167097/150‑1 (MQ=255) tCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCAtttt > 1:572626/1‑70 (MQ=255) tCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCAtttt < 2:572626/70‑1 (MQ=255) tCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACGCGCTGAAAACACCAGCCTTGACCAACCCTTTGt < 2:548667/150‑1 (MQ=255) cAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACGCGCTGAAAACACCAGCCTTGACCAACCCTTTGTCa > 2:721679/1‑150 (MQ=255) gCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCAATCCCGCGCTGAAAACACCAGCCTTGACCAACCCTTTGTCata > 1:529421/1‑148 (MQ=255) aGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACGCGCTGAAAACACCAGCCTTGACCAACCCTTTGTCAGACCGAAAAg > 2:422915/1‑143 (MQ=255) aGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACGCGCTGAAAACACCAGCCTTGACCAACCCTTTGTCAGACCGAAAAg < 1:422915/143‑1 (MQ=255) | CACAAACCAACAGCCGCTATGGCACATTGACTTTTTTTACCGGCCTGGCCAGCGATGGTGAGGCCTGGGTGGGCTACAGCCGCCGCGTAGGCTGGACCACCTTGAACCGCGTATCCAGTTCCAGCGGGGAGCGCTTCAAGCTGCATTGCAGCTTGATCGAGGGGTGCCGTTGACGCCTCCTTTCATTTTGAACGTTTTTTCTCTGCTGCCTATTTTGTAAGTCAGCTTCGAGCACGCGCTGAAAACACCAGCCTTGACCAACCCTTTGTCAGACCGAAAAG > NC_002947/6111888‑6112168 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |