Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 4,270,523 | C→A | L96M (CTG→ATG) | yjbQ → | thiamine phosphate synthase |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 4,270,523 | 0 | C | A | 100.0% | 92.1 / NA | 27 | L96M (CTG→ATG) | yjbQ | thiamine phosphate synthase |
Reads supporting (aligned to +/- strand): ref base C (0/0); new base A (14/13); total (14/13) |
GACACTTAATGAGAACTGCGATCCCACCGTACGCCACGACATGGAGCGTTTTTTCCTCCGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGCTGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTGGGGGAACATCGCATCCACGGCGGATCGCGTCGCATCATCGCGACACTACAAGGGGAGTAAAAAATGAC > NC_000913/4270384‑4270662 | gACACTTAATGAGAACTGCGATCCCACCGTACGCCACGACATGGAGCCTTTTTTCCTCAGAACCGTTCCCGAAAACGCAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATAAAATCCTCAATGATGGGaaaa > 7:45797/1‑146 (MQ=255) aTGAGAACTTCGATCCAAACTTACGCCACTTCATGGAGCGTTTTTTCCTCCGCACAGGTCCCGACAACGGAAATTATTAGCATGACTATGAGGGAGAATACGATATGCCTTCTCATATCAAATACTCAATGATGGTAACATAGCTTGTa < 8:45797/149‑1 (MQ=255) cTGCGATCCCACCGTACGCCACGACATGGAGCGTTTTTTCCTCCGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCgg < 7:7859/149‑1 (MQ=255) tGCGATCCCACCGTACGCCACGACATGGAGCGTTTTTTCCTCCGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCg < 8:114907/147‑1 (MQ=255) tGCGATCCCACCGTACGCCACGACATGGAGCGTTTTTTCCTCCGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCg > 7:114907/1‑147 (MQ=255) ccACGACATGGAGCGTTTTTTCCTCCGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTAtt > 8:48807/1‑148 (MQ=255) cACGACATGGAGCGTTTTTTCCTCCGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTAtt > 7:129211/1‑147 (MQ=255) gAGCGTTTTTTCCTCCGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCa < 1:162868/148‑1 (MQ=255) gAGCGTTTTTTCCTCCGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCa > 2:162868/1‑148 (MQ=255) tccGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGt < 8:2580/109‑1 (MQ=255) tccGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGt > 7:2580/1‑109 (MQ=255) gCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTgg < 8:129211/149‑1 (MQ=255) gTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTggg < 7:48807/149‑1 (MQ=255) gAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTGGGGGAACATCGCATc > 8:104360/1‑149 (MQ=255) gCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCa < 1:170215/96‑1 (MQ=255) gCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCa > 2:170215/1‑96 (MQ=255) tGAGGGCGCATACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTAGTCAGACCGGCACCTGGCAAGGCAGTTGGCTGGGGGCACATCGCCTCCACGGCGGATCGCGTCg > 6:101128/1‑147 (MQ=255) gggAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTGGGGGAACATCGCATCCACGGCGGATCGCGTCGca > 4:24926/1‑146 (MQ=255) gggAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTGGGGGAACATCGCATCCACGGCGGATCGCGTCGca < 3:24926/146‑1 (MQ=255) ggAGCAGACGATATGCCTTCTCATATCAGATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTgg > 6:4342/1‑96 (MQ=255) ggAGCAGACGATATGCCTTCTCATATCACATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTgg < 5:4342/96‑1 (MQ=255) aGACGATATGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTGGGGGAACATCGCATCCACGGCGGATCGCGTCGCATCATCGCGa < 7:104360/149‑1 (MQ=255) tatGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCgg < 6:67316/53‑1 (MQ=255) tatGCCTTCTCATATCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCgg > 5:67316/1‑53 (MQ=255) atCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTGGGGGAACATCGCATCCACGGCGGATCGCGTCGCATCATCGCGACACTACAAGGGGAGTaaa > 3:107346/1‑148 (MQ=255) tCAAATCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTGGGGGAACATCGCATCCACGGCGGATCGCGTCGCATCATCGCGACACTACAAGGGGAGTaaaa > 3:45793/1‑148 (MQ=255) tCCTCAATGATGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTGGGGGAACATCGCATCCACGGCGGATCGCGTCGCATCATCGCGACACTACAAGGGGAGTAAAAAATGAc < 5:101128/149‑1 (MQ=255) | GACACTTAATGAGAACTGCGATCCCACCGTACGCCACGACATGGAGCGTTTTTTCCTCCGCACCGTTCCCGACAACGGAAATTATGAGCATGACTATGAGGGAGCAGACGATATGCCTTCTCATATCAAATCCTCAATGCTGGGAACATCGCTTGTATTGCCGGTGCATAAAGGGCGTATTCAGACCGGCACCTGGCAAGGCATTTGGCTGGGGGAACATCGCATCCACGGCGGATCGCGTCGCATCATCGCGACACTACAAGGGGAGTAAAAAATGAC > NC_000913/4270384‑4270662 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |