Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 3,120,178 | C→A | 13.7% | E184* (GAG→TAG) | PP_2736 ← | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 3,120,178 | 0 | C | A | 13.7% | 90.5 / 2.3 | 34 | E184* (GAG→TAG) | PP_2736 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base C (14/15); new base A (2/3); total (16/18) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00 |
GTAAACCTTGCAGTTGAGGCGGATGCGCTCAGCGAACGGCCGGCACAGCGGTGCGACATAGCTGCGCGAGCCGCCTTTGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGATGAAGCGTTGCCCATAGCGGTTCGCTTGAAGGTAGTCGCCCAGCGTGGTGCTGGCATCGATACGCTGGTTGTCC > NC_002947/3120029‑3120326 | gTAAACCTTGCAGTTGAGGCGGATGCGCTCAGCGAACGGCCGGCACAGCGGTGCGAAATAGCTGGGCGAGCCGCCTTTGATCACGCGCCACTGTGGACGTTGGTTGACCGACATCAAGCCGTGGTTACGGCAGAAGCGCACGAAGAACTc > 2:61470/1‑150 (MQ=255) cTTGCAGTTGAGGCGGGTGCGCTCAGCGAACGGCCGGCACAGCGGTGCGACATAGCTGCGCGAGCCGCCTTGGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCgg > 2:613229/1‑150 (MQ=255) cTTGCAGTTGAGGCGGATGCGCTCAGCGAACGGCCGGCACAGCGGTGCGACATAGCTGCGCGAGCCGCCTTTGATCACCCGCCACTGTGGACGTTGGTTTACCGACAGCTAGCCGTGGTTGCGGCAGGAGCGCACTAAGAACTAAAGCgg > 2:366160/1‑150 (MQ=255) cTTGCAGTTGAGGCGGATGCGCTCAGCGAACGGCCGGCACAGCGGTGCGACATAGCTGCGCGAGCCGCCTTTGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTAAAGCgg > 2:366027/1‑150 (MQ=255) gTTGACGCGGATGCGCTCAGCGAACGGCCGGCACAGCGGTGCGACATAGCTGCGCGAGCCGCCTGTGATCGCCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTg < 1:409816/150‑1 (MQ=255) tCAGCGAGCGGCCGGCACAGCGGTGCGACATAGCTGCGCGAGCCGCCTTTGATCACCAGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCga < 2:779394/150‑1 (MQ=255) ggccggcACAGCGGTGCGACATAGCTGCGCGAGCCGCCTTTGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGAc > 2:557462/1‑150 (MQ=255) cacaGCGGTGCGACATAGCTGCGCGAGCCGCCTTTGATCCCCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTAAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATc < 1:366160/150‑1 (MQ=255) cacaGCGGTGCGACATAGCTGCGCGAGCCGCCTTTGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTAAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATc < 1:366027/150‑1 (MQ=255) gACATAGCTGCGCGAGCCGCCTTTGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCAt < 1:457299/150‑1 (MQ=255) aGCTGCGCGAGCCGCCTTTGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTa < 2:375727/150‑1 (MQ=255) gAGCCGCCTTTGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTaa < 1:606138/150‑1 (MQ=255) cgccTTTGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGAt > 2:697828/1‑150 (MQ=255) tttGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCa < 2:320886/92‑1 (MQ=255) tttGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCa > 1:320886/1‑92 (MQ=255) gATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCa > 2:443424/1‑89 (MQ=255) gATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCa < 1:443424/89‑1 (MQ=255) tCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCg > 2:115873/1‑105 (MQ=255) tCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCg < 1:115873/105‑1 (MQ=255) aCCCGCCACTGTGGACGTTGGTTGACCTACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGAc < 1:138537/105‑1 (MQ=255) aCCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGAc > 2:138537/1‑105 (MQ=255) cccGCCACTGTGGACGTTGGTTGACCGACAGCAAGCTGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGAGCGAATTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGATGAAGCGtt < 1:775453/150‑1 (MQ=255) gACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAGGCGCACGAAGACCCCGGGCTGGAAGTGGAGCATGTCGGCGCGAGACATCGACCAGTCCGCCGCCCCCATCGGTACGATGTAATGATCGATGAAGCGTTGCCCATAGCGGt < 2:189606/150‑1 (MQ=255) gACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGAc > 2:493914/1‑92 (MQ=255) gACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGAc < 1:493914/92‑1 (MQ=255) ggttgAGCGACAGCAAGGCGGGGTTGCGGCAGAGGCCCATTAGGAAACAAAGCGGGAAGTGGACCTCGGAGGCGAAAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGATGAAGCGTTGCCCATAGCGGTTCGCtt < 1:613229/150‑1 (MQ=255) cGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGa > 2:396381/1‑116 (MQ=255) cGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGa < 1:396381/116‑1 (MQ=255) gTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGa > 1:747771/1‑104 (MQ=255) gTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGa < 2:747771/104‑1 (MQ=255) gTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGATGAAGCGTTGCCCATAGCGGTTCGCTTGAAGGTAGTCGc > 2:30533/1‑140 (MQ=255) gTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGATGAAGCGTTGCCCATAGCGGTTCGCTTGAAGGTAGTCGc < 1:30533/140‑1 (MQ=255) cAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGATGAAGCGTTGCCCATAGCGGTTCGCTTGAAGGTAGTCGCCCAGCGTGGTGCTGGCa > 2:611386/1‑150 (MQ=255) cgcACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGATGAAGCGTTGCCCATAGCGGTTCGCTTGAAGGTAGTCGCCCAGCGTGGTGCTGGCATCGATa > 2:704491/1‑150 (MQ=255) tCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGATGAAGCGTTGCCCATAGCGGTTCGCTTGAAGGTAGTCGCCCAGCGTGGTGCTGGCATCGATACGCTGGTTGTcc > 2:657696/1‑150 (MQ=255) | GTAAACCTTGCAGTTGAGGCGGATGCGCTCAGCGAACGGCCGGCACAGCGGTGCGACATAGCTGCGCGAGCCGCCTTTGATCACCCGCCACTGTGGACGTTGGTTGACCGACAGCAAGCCGTGGTTGCGGCAGAAGCGCACGAAGAACTCAAGCGGGAAGTGGAGCATGTCTGCGCGAGACATCGACCAGATCGCCGACCCCATCGGTACGATGTAATGATCGATGAAGCGTTGCCCATAGCGGTTCGCTTGAAGGTAGTCGCCCAGCGTGGTGCTGGCATCGATACGCTGGTTGTCC > NC_002947/3120029‑3120326 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |