Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_000913 | 4,273,362 | T→A | 24.4% | A170A (GCA→GCT) | uvrA ← | excision nuclease subunit A |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 4,273,362 | 0 | T | A | 24.4% | 20.6 / 4.6 | 16 | A170A (GCA→GCT) | uvrA | excision nuclease subunit A |
Reads supporting (aligned to +/- strand): ref base T (8/4); new base A (2/2); total (10/6) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 6.04e-01 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 2.23e-01 |
AAGACGTTGGGTAAGATCGTCACGCACCTTGAAGCGATCAACCACCACTTCAATGGTATGTTTCTTTTGCAGTTCCAGTTTTGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCTTGCCAGGTTCTCCAGCGTTTTGGTGTGTTCGCCTTTGCGCTCTTTAATGATTGGCGCGAGTAGCATCAGACGCTTGCCTTCCGGCTGCGACAGCACGTTATCCACCATCTGGCTGACGGTTTGCGCCGCCAGCGGGACGTC > NC_000913/4273221‑4273502 | aaGACGTTGGGTAAGATCGTCACGCACCTTGAAGCGATCAACCACCACTTCAATGGTATGTTTCTTTTGCAGTTCCAGTTTTGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCTTg > 1:533437/1‑143 (MQ=255) aaGACGTTGGGTAAGATCGTCACGCACCTTGAAGCGATCAACCACCACTTCAATGGTATGTTTCTTTTGCAGTTCCAGTCTTGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATCCGAGCACGGATGTAGCCCGGGCTTg > 2:224397/1‑143 (MQ=255) ttGGGTAAGATCGTCACGCACCTTGAAGCGATCAACCACCACTTCAATGGTATGTTTCTTTTGCAGTTCCAGTTTTGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCTTGCCAggg > 1:585176/1‑142 (MQ=255) tGGGTAAGATCGTCACGCACCTTGAAGCGATCAACCACCACTTCAATGGTATGTTTCTTTTGCAGTTCCAGTTTTGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCAAGCCAgggc < 1:194411/143‑3 (MQ=255) tGGGGAAGATCGTCACGCACCTTGGAGCGATCAACTACCACTTCAATGGTATGTTTCTTTTGCAGTTCCAGGTTGGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCAAGCCAgggc < 1:286862/143‑3 (MQ=255) gTCACGCACCTTGAAGCGATCAACCACCACTTAAATGGTATGTTTCTTTTGAAGTTCCAGTTTTGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCTTGCCAGGTTCTCCAGCGtat > 2:351038/1‑141 (MQ=255) ttCAATGGTATGTTTCTTTTGCAGTTCCAGTTTTGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCTTGCCTGGTCCTCCAGCGTTTTGGTGTGTTCGCCTTGGCGCTCTTCAATGa > 2:438508/1‑143 (MQ=255) tCTTTTACCGTTCCCTTTTTGTCGGTTCGGAATGTTCGCAGTCTTCGCCATCTATACGAGCACGGATGTGGCCCTTGCTTGCCAGGTTTTTCAGCGTTTTGGTGTGTTCGCTTTTGCGCTCTTTAATGATTGGCGCGAGTAGc < 2:209648/143‑1 (MQ=255) tGCAGTTCCAGTTTTGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCTTGCCAGGTTCTCCAGCGTTTTGGTGTGTTCGCCTTTGCGCTCTCTAATGATTGGCGCGAGTAGCATCAg < 1:342661/143‑1 (MQ=255) tgagaggAGCGGAAAGACCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCTTGCCAGGTTCTCCAGCGTTTTGGTGTGTTCGCCTTTGCGCTCTTTAATGATTGGCGCGAGTAGCATCAGACGCTTGCCTTcc < 1:43063/138‑1 (MQ=255) gCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCTTGCCAGGTTCTCCAGCGTTTTGGTGTGTTCGCCTTTGCGCTCTTTAATGATTGGCGCGAGTAGCATCAGACGCTTGCCTTCCGGc > 2:245897/1‑143 (MQ=255) tCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGTCTAGCCAGGTTCTCCATCGTTTTGGTGTGTTCGCCTTTGCGCTCTTTAATGATTGGCGCGAGTGGCTTCAGACGCTTGCCTTCCGCCAGCGa > 2:336389/1‑143 (MQ=255) tCAATACGAGCACGGATGTAGCCCTGGCTTGCCCGGTTCTCCAGCGTTTTGGTGTGTTCGCCTTTGCGCTCTCTCCTGCTTGGCGCGAGTAGCTTCCCACGCTTGCCTTCCGGCTGCGTCCGCTCGTCGTCCACCGTcagcct > 1:78403/1‑138 (MQ=255) cACGGATGTAGCCCTGGCTTGCCAGGTTCTCCAGCGTTTTGGTGTGTTCGCCTTTGCGCTCTTTAATGCTTGTCGCGAGTAGCATCAGACGCTTGCCTTCCGGCTGCGACAGCACGCTATCCCCCACCTCGCTGCCgctccgc > 2:426083/1‑137 (MQ=255) gagaaccTGGCAAGCCAGGTTCTCCAGCGTTTTGGTGTGTTCGCCTTTGCGCTCTTTAATGAATGCGGCGGGGAGCACCAGACGCTTGCCTTCGGGCTGCGACAGCACGTTACCCACCATCTGGCTCACGGTTCGCGCCGCCa > 2:110943/6‑143 (MQ=255) cTTGCCAGGTTCTCCAGCGTTTTGGTGTGTTCGCCTTTGCGCTCTTTAATGATTGGCGCGAGTAGCATTAGACGCTTGCCTTCCGGCTGCGACAGCACGTTATCCACCATCTGGCTGACGGTTTGCGCCGCCAGCGGGAcgtc < 1:351038/143‑1 (MQ=255) | AAGACGTTGGGTAAGATCGTCACGCACCTTGAAGCGATCAACCACCACTTCAATGGTATGTTTCTTTTGCAGTTCCAGTTTTGGCGGATCGGAAAGATCGCAGACTTCGCCATCAATACGAGCACGGATGTAGCCCTGGCTTGCCAGGTTCTCCAGCGTTTTGGTGTGTTCGCCTTTGCGCTCTTTAATGATTGGCGCGAGTAGCATCAGACGCTTGCCTTCCGGCTGCGACAGCACGTTATCCACCATCTGGCTGACGGTTTGCGCCGCCAGCGGGACGTC > NC_000913/4273221‑4273502 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 8 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |