Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_002947 | 233,545 | C→T | G548G (GGC→GGT) | PP_0180 → | cytochrome c family protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 233,545 | 0 | C | T | 93.3% | 37.2 / ‑5.5 | 15 | G548G (GGC→GGT) | PP_0180 | cytochrome c family protein |
Reads supporting (aligned to +/- strand): ref base C (0/0); major base T (7/7); minor base A (0/1); total (7/8) | |||||||||||
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 |
TTGTTCGAAGTGATCCTGTTCTACGAGACCCTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGCTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGTGTGCTGGGCACACGG > NC_002947/233414‑233668 | ttGTTCGAAGTGATCCTGTTCTACGAGACCCTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCgg > 2:169492/1‑136 (MQ=255) ccTGTTCTACGAGACCCTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTa < 2:205017/136‑1 (MQ=255) cccTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAg < 2:116707/136‑1 (MQ=255) cccTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAg < 2:168769/136‑1 (MQ=255) cTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAAcg > 2:175663/1‑136 (MQ=255) gcaggcagGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAATCTGCCGCTATCGCTGTTCTTCAGCATCAAcgcc < 2:197282/136‑1 (MQ=255) gcaggcagGCCCCGCCGGGCAGCTGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCGTGGGTGATTCTGCGGGGATCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAAcgcc < 2:26568/136‑1 (MQ=255) gcaggcCCCGCCGGGCATCAGGCGGTGCTGACGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCgcgc > 1:154407/1‑136 (MQ=255) ggCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGgta < 1:74388/136‑1 (MQ=255) cGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCgg < 1:189903/136‑1 (MQ=255) ggtggGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGcc > 2:157811/1‑136 (MQ=255) cctggGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATGCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGTGTGCTggg < 1:88965/136‑1 (MQ=255) gATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGTGTGCTGGGCACACgg > 1:107826/1‑136 (MQ=255) gATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGTGTGCTGGGCACACgg > 1:230161/1‑136 (MQ=255) gATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTAGCAAGAGGCCGGTGTGCTGGGCACACgg > 2:186425/1‑136 (MQ=255) | TTGTTCGAAGTGATCCTGTTCTACGAGACCCTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGCTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGTGTGCTGGGCACACGG > NC_002947/233414‑233668 |
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: ‑ |