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 | 100.0% | 33.8 / NA | 11 | G548G (GGC→GGT) | PP_0180 | cytochrome c family protein |
Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (9/2); total (9/2) |
GTTCGAAGTGATCCTGTTCTACGAGACCCTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGCTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGTGTGCTGGGCACACGG > NC_002947/233416‑233668 | gTTCGAAGTGATCCTGTTCTACGAGACCCTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGcc > 1:148110/1‑136 (MQ=255) aTCCTGTTCTACGAGACCCTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGc < 2:341749/136‑1 (MQ=255) ggCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCaa > 1:222594/1‑136 (MQ=255) ggCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCaa > 2:222322/1‑136 (MQ=255) cgccgGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTgc < 2:222594/136‑1 (MQ=255) gggCCTGGCCTGGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGgt > 2:1399/1‑136 (MQ=255) gcctggcctgGGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGgtgt > 1:390375/1‑136 (MQ=255) cctggcctggGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGtgtg > 1:184059/1‑136 (MQ=255) cctggcctggGTGATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGtgtg > 1:306475/1‑136 (MQ=255) gATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGTGTGCTGGGCACACgg > 1:264700/1‑136 (MQ=255) gATTCTGCGGGGTTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGTGTGCTGGGCACACgg > 2:384121/1‑136 (MQ=255) | GTTCGAAGTGATCCTGTTCTACGAGACCCTGTGGCTGCAGGCAGGCCCCGCCGGGCATCAGGCGGTGCTGGCGGGTGGCGCGACGGCACTGGTGCTGTTGGTGGGCCTGGCCTGGGTGATTCTGCGGGGCTCGGCCAAGCTGCCGCTATCGCTGTTCTTCAGCATCAACGCCGCGCTGCTGTGCGCGCTGTCGGTAGTATTCGCCGGGCATGGCGTGAAGGCGTTGCAAGAGGCCGGTGTGCTGGGCACACGG > NC_002947/233416‑233668 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |