Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 248,122 | T→C | R162R (CGT→CGC) | rayT → | RAYT REP element‑mobilizing transposase, TnpA(REP) |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 248,122 | 0 | T | C | 100.0% | 124.7 / NA | 35 | R162R (CGT→CGC) | rayT | RAYT REP element‑mobilizing transposase, TnpA(REP) |
Reads supporting (aligned to +/- strand): ref base T (0/0); new base C (18/17); total (18/17) |
TCCAGTAAAGCATGGTTGGGTAAAGCAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGTATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACAAACTTGTGCCGGATCGGTAGGCCGGATAAGGCGTTTATGCCGCATCCGGCAGTTATGCGCAG > NC_000913/247993‑248245 | tCCAGTAAAGCATGGTTGGGTAAAGCAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCa > 2:991315/1‑139 (MQ=255) tCCAGTAAAGCATGGTTGGGTAAAGCAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCa < 2:835608/139‑1 (MQ=255) cATGGTTGGGTAAAGCAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTgcg > 2:851838/1‑139 (MQ=255) ttGGGTAAAGCAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCa < 2:421315/119‑1 (MQ=255) ttGGGTAAAGCAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCa > 1:421315/1‑119 (MQ=255) ggTAAAGCAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGcc > 2:794579/1‑139 (MQ=255) aGCAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATg < 2:41270/139‑1 (MQ=255) cAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCa > 2:1029476/1‑109 (MQ=255) cAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCa < 1:1029476/109‑1 (MQ=255) gtgagtgaTTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACg > 1:160076/1‑139 (MQ=255) tgagtgaTTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGc > 2:419010/1‑139 (MQ=255) tGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGt < 2:160076/139‑1 (MQ=255) ggCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTc > 1:122289/1‑139 (MQ=255) ttCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATc > 2:516950/1‑139 (MQ=255) tctcAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCa > 1:1015002/1‑139 (MQ=255) ctcAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTCTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCAt < 1:991315/139‑1 (MQ=255) aaCGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGcc > 1:821173/1‑139 (MQ=255) ccATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCa > 1:416603/1‑85 (MQ=255) ccATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCa < 2:416603/85‑1 (MQ=255) ccATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACaaa > 1:91204/1‑139 (MQ=255) cATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACAAAc < 2:122289/139‑1 (MQ=255) aTGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACAAAc < 2:357455/132‑1 (MQ=255) aTGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACAAAc > 1:357455/1‑132 (MQ=255) tGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATc > 1:1047316/1‑119 (MQ=255) tGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATc < 2:1047316/119‑1 (MQ=255) ttATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACAAACTTGTGCCGGATCGGTAGGCCg < 1:851838/139‑1 (MQ=255) cATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCa < 1:886037/50‑1 (MQ=255) cATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCa > 2:886037/1‑50 (MQ=255) aTCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCa < 2:851817/49‑1 (MQ=255) aTCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGCATCa > 1:851817/1‑49 (MQ=255) gggACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCa > 2:12232/1‑53 (MQ=255) gggACGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCa < 1:12232/53‑1 (MQ=255) aCGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACAAACTTGTGCCGGATCGGTAGGCCGGATAAGGCGTTTATGCCGCATCCgg < 1:794579/139‑1 (MQ=255) aCGTAACGGATTTTAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACAAACTTGTGCCGGATCGGTAGGCCGGATAAGGCGTTTATGCCGCATCCgg < 2:821173/139‑1 (MQ=255) tAGTGCCGGGGAGCGCATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACAAACTTGTGCCGGATCGGTAGGCCGGATAAGGCGTTTATGCCGCATCCGGCAGTTATGCGCAg < 1:516950/139‑1 (MQ=255) | TCCAGTAAAGCATGGTTGGGTAAAGCAAGTGAGTGATTGGCCATTCTCAACGTTCCATCGCGATGTCGCGCGAGGGTTATATCCCATCGATTGGGCGGGGGACGTAACGGATTTTAGTGCCGGGGAGCGTATCATTTCATAATTGTGCGCAGATGCCTGATGCGACGCTAGCGCGTCTTATCATGCCTACAAACTTGTGCCGGATCGGTAGGCCGGATAAGGCGTTTATGCCGCATCCGGCAGTTATGCGCAG > NC_000913/247993‑248245 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |