Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 4,494,386 | G→T | 26.6% | P824Q (CCA→CAA) | PP_3982 ← | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 4,494,386 | 0 | G | T | 26.6% | 31.4 / 2.8 | 15 | P824Q (CCA→CAA) | PP_3982 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base G (4/7); new base T (2/2); total (6/9) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.97e-01 |
CGACATCTTCAACCAAGCCCGCATCAAAATCTTCTCGATCGATTTCCTCATGGGTGCCCTTGTTCAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTCAGGCCAGGTTGATCTCCGTCACGAGCCAGCTGGACGGTCAAGACACCCTGACTGCATCTTCCCA > NC_002947/4494258‑4494521 | cgacATCTTCAACCAAGCCCGCATCAAAATCTTCTCGATCGATTTCCTCATGGGTGCCCTTGTTCAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCtt > 2:400117/1‑136 (MQ=255) gatcgatTTCCTCATTGGTGCCCTTGTTCAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTTGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCtt > 1:377102/1‑136 (MQ=255) gatcgatTTCCTCATTGGTGCCCTTGTTCAGATAACTCCAGATCAAGGTCTGCTAGCCGATTAAGAGGATTCGAACCAGTGCATCGATAAGTTGCTCCTTGTCTGCATGCTCAAACGAGTTGGCTCCTCGAAGCtt > 1:377101/1‑136 (MQ=255) gatcgatTTCCTCATGGGTGCCCTTGTTCAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCtt < 1:488507/136‑1 (MQ=255) tGGGTGCCCTTGTTCAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATg < 2:382947/136‑1 (MQ=255) tGCCCTTGTTCAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCa < 2:359840/136‑1 (MQ=255) ttGTTCAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGATGATTCGAACCAGTGCATCGATCAGTGgc > 1:365347/1‑72 (MQ=255) ttGTTCAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGATGATTCGAACCAGTGCATCGATCAGTGgc < 2:365347/72‑1 (MQ=255) cAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTTGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTc < 2:377102/136‑1 (MQ=255) cAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTc < 1:331822/136‑1 (MQ=255) cAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCAGCGATCAGTTGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTc < 2:377101/136‑1 (MQ=255) ttCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTCAGGCCAGGTTGAt < 1:326772/135‑1 (MQ=255) tCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTCAGGCCAGGTTGATCTCCGTc > 2:479232/1‑136 (MQ=255) cGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTCAGGCCAGGTTGATCTCCGTCACGAGc > 1:113586/1‑136 (MQ=255) gATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTCAGGCCAGGTTGATCTCCGTCACGAGCCAGc < 2:417941/136‑1 (MQ=255) ggCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTCAGGCCAGGTTGATCTCCGTCACGAGCCAGCTGGACGGTCAAGACACCCTGACTGCATCTTCCCa > 2:485881/1‑136 (MQ=255) | CGACATCTTCAACCAAGCCCGCATCAAAATCTTCTCGATCGATTTCCTCATGGGTGCCCTTGTTCAGATACCTCCAGATCAAGGTCTGCTCGCCGATTCCGAGGATTCGAACCAGTGCATCGATCAGTGGCTGCTTGTCTGCATGCTCAAACGTGTTGGCTCCTCGAAGCTTTGAACAGATAGATGCGCAGAGGTTACTCAGGCCAGGTTGATCTCCGTCACGAGCCAGCTGGACGGTCAAGACACCCTGACTGCATCTTCCCA > NC_002947/4494258‑4494521 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |