Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 1,935,789 | C→G | 15.4% | A16A (GCC→GCG) | PP_1736 → | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 1,935,789 | 0 | C | G | 15.4% | 62.2 / 4.1 | 26 | A16A (GCC→GCG) | PP_1736 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base C (11/11); new base G (2/2); total (13/13) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.46e-01 |
TACCTGTGGGCGCACCGCCGGTTCAAGTCGCGGCCCGAGGGTTCGCCGCGGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCATCAACGCCGTCACCCTGGCCAGTGGTGCGGTGCACTTCAATG > NC_002947/1935640‑1935934 | tACCTGTGGGCGCACCGCCGGTTCAAGTCGCGGCCCGAGGGTTCGCCGCGGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGcc > 1:443492/1‑150 (MQ=255) aCCTGTGGGCGCACCGCCGGTTCAAGTCGCGGCCCGAGGGTTCGCCGCGGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGccc > 2:146729/1‑150 (MQ=255) ccGAGGGTTCGCCGCGGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCa > 1:592795/1‑150 (MQ=255) ccGAGGGTTCGCCGCGGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTCGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCa > 1:476802/1‑150 (MQ=255) cGAGGGTTCGCCGCGGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCAt < 1:382352/150‑1 (MQ=255) gAGGGTTCGCCGCGGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCGTACCAGGTCGGTGTGCTGGCGGGCATc < 1:579871/150‑1 (MQ=255) gcgGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGAGGCGGCGCGGGCgccgccgcc < 2:291860/115‑4 (MQ=255) gcgGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGAGGCGGCGCGGGCgccgccgcc > 1:291860/1‑112 (MQ=255) gACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCGGGCgccgccgcca > 2:463545/1‑102 (MQ=255) gACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCGGGCgccgccgcca < 1:463545/106‑5 (MQ=255) tGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCtttt > 2:756461/1‑150 (MQ=255) acacATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGt < 1:146729/150‑1 (MQ=255) acaTCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCgg > 1:290209/1‑132 (MQ=255) acaTCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCgg < 2:290209/132‑1 (MQ=255) tACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCAtcgtc < 2:443492/150‑1 (MQ=255) ccAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCa > 1:842240/1‑150 (MQ=255) aggaaggaCGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCAcc > 1:616878/1‑150 (MQ=255) gaCGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTccgcc > 1:212333/1‑150 (MQ=255) ccATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCgggg < 2:774393/150‑1 (MQ=255) aTGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGcc < 2:842240/150‑1 (MQ=255) gCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCATc > 1:522090/1‑150 (MQ=255) accaccCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCa < 2:476922/146‑1 (MQ=255) accaccCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCa > 1:476922/1‑146 (MQ=255) cccccGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCATCAACGcc < 2:592795/150‑1 (MQ=255) aTCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCATCaa < 2:186647/128‑1 (MQ=255) aTCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCATCaa > 1:186647/1‑128 (MQ=255) aatgccggcgtctCCCGCGCTGCCTACTAGTTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCATCAACGCCGTCACCCTGGCCAGTggtgcggtg < 2:476802/145‑1 (MQ=255) gcgcCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCATCAACGCCGTCACCCTGGCCAGTGGTGCGGTGCACTTCAATg > 1:593852/1‑150 (MQ=255) | TACCTGTGGGCGCACCGCCGGTTCAAGTCGCGGCCCGAGGGTTCGCCGCGGCTGTATGACAAGAAGAAGCGCTGAAAACACATCTACCCCAGGAAGGACGCCATGGCACCACCCCCGGTAACCGGTCTCATCCTGTCTGGCGGCGGCGCCCGCGCCGCCTACCAGGTCGGTGTGCTGGCGGGCATCGCCGAGTTGCTGCCCGCCGGCGCGGACAACCCTTTTCCGGTCATCGTCGGCACCTCCGCCGGGGCCATCAACGCCGTCACCCTGGCCAGTGGTGCGGTGCACTTCAATG > NC_002947/1935640‑1935934 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |