Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 3,002,885 | G→C | 19.1% | D295H (GAC→CAC) ‡ | PP_2626 → | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 3,002,885 | 0 | G | C | 19.1% | 40.5 / 6.4 | 21 | D295H (GAC→CAC) ‡ | PP_2626 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base G (8/9); new base C (2/2); total (10/11) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 6.99e-01 |
TACCGGCTACCAGTTACGGCGTTTCGGTTTGTGGGCGCACATTCAGGTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGAAAAGAGCCTGACGGCTTGCCCCTTCTGGATTCGTGGCAGCTTTCTGGCTGCGACCGTCGCCACACAGCTGGCGATGTGCGAGGTGGCCGAAGCCATCCGTTGTGCCACCGCCCGGTTTGTACA > NC_002947/3002740‑3003033 | tACCGGCTACCAGTTACGGCGTTTCGGTTTGTGGGCGCACATTCAGGTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCc < 2:587507‑M2/150‑2 (MQ=255) ggCGTTTCGGTTTGTGGGCGCACATTCAGGTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTa > 2:276471/1‑150 (MQ=255) cGGTTTGTGGGCGCACATTCAGGTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGaaaa < 1:276471/150‑1 (MQ=255) ggCGCACATTCAGGTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGAAAAGAGCCTGAc < 1:739055/150‑1 (MQ=255) aGGTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTg < 1:24711/126‑1 (MQ=255) aGGTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTg > 2:24711/1‑126 (MQ=255) aGGTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGAAAAGAGCCTGACGGCTTGCCCCt > 1:293024/1‑150 (MQ=255) ggTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGAAAAGAGCCTGACGGCTTGCCCCtt > 2:493057/1‑150 (MQ=255) cccAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTAtt < 1:43173/116‑1 (MQ=255) cccAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTAtt > 2:43173/1‑116 (MQ=255) ccAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGGGG‑TCAACcgccttactggcaatg > 2:74733‑M2/1‑96 (MQ=255) ccAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGGGG‑TCAACcgccttactggcaatg < 1:74733‑M2/112‑17 (MQ=255) cAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGGGG‑TCAACcgccttactggcaatg > 1:114466‑M2/1‑95 (MQ=255) cAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑GGTCAACcgccttactggcaatg < 2:114466‑M2/111‑17 (MQ=255) gggCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGAAAAGAGCCTGACGGCTTGCCCCTTCTGGATTCGTGGCAGCTTTCt > 2:665561/1‑150 (MQ=255) cACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGAAAAGAGCCTGACGGCTTGCCCCTTCTGGATTCGTGGCAGCTTTCTGGCTGCGACCGTCGCCACACAGCTGGCGATGTGCGAGGt < 1:493057/150‑1 (MQ=255) cgaggTTCTATGAAGAGGGCATTGCGAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCATCGTATTGAAAAGAGCCTGACTGATTGCCCCTCCTGGATTCCTGGCAGCTTTCTGGCTGCGACCTTCGCCAGACAGCTGGCGATGTGCGAGGTgg < 2:375423/147‑1 (MQ=255) gAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGAAAAGAGCCTGACGGCTTGCCCCTTCTGGATTCGTGGCAGCTTTCTGGCTGCGACCGTCGc < 2:556036/113‑1 (MQ=255) gAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGAAAAGAGCCTGACGGCTTGCCCCTTCTGGATTCGTGGCAGCTTTCTGGCTGCGACCGTCGc > 1:556036/1‑113 (MQ=255) cAGTAAGGCGG‑T‑TGACCccgccttgctggcaatggcctcttcatagaaccgcgtgatatccagcggcaccgccatcaattccgtacggttgccctgcctgacttggggagcaacctgaatgtgcgcccacaaaccgaaacgcagtaactg < 2:916‑M2/150‑134 (MQ=255) tGACCccgccttgctggcaatggcctcttcatagaaccgcgtgatatccagcggcaccgccatcaattccgtacggttgccctgcctgacttggggagcaacctgaatgtgcgcccacaaaccgaaacgccgtaactggtagccggtagc > 1:916‑M2/1‑5 (MQ=255) | TACCGGCTACCAGTTACGGCGTTTCGGTTTGTGGGCGCACATTCAGGTTGCTCCCCAAGTCAGGCAGGGCAACCGTACGGAATTGATGGCGGTGCCGCTGGATATCACGCGGTTCTATGAAGAGGCCATTGCCAGTAAGGCGG‑T‑TGACCCCGCCTTGCTGCAGCGTATTGAAAAGAGCCTGACGGCTTGCCCCTTCTGGATTCGTGGCAGCTTTCTGGCTGCGACCGTCGCCACACAGCTGGCGATGTGCGAGGTGGCCGAAGCCATCCGTTGTGCCACCGCCCGGTTTGTACA > NC_002947/3002740‑3003033 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |