Predicted mutation | ||||||
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evidence | seq id | position | mutation | annotation | gene | description |
RA | NC_000913 | 3,728,118 | (C)8→9 | coding (1254/1455 nt) | xylB ← | xylulokinase |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_000913 | 3,728,110 | 1 | . | C | 100.0% | 81.7 / NA | 24 | D421G (GAT→GGT) | xylB | xylulokinase |
Reads supporting (aligned to +/- strand): ref base . (0/0); new base C (13/11); total (13/11) |
AGCGGCATAACGCTGCGCATCTGGTAGATGCGACTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACAT‑‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCAATCAACGTAACACTTTGCGGTTTAATACCGCAGGCATGCAC > NC_000913/3727980‑3728234 | aGCGGCATAACGCTGCGCATCTGGTAGATGCGACTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACAT‑‑cccccccc < 1:203737/139‑1 (MQ=255) cATAACGCTGCGCATCTGGTAGATGCGACTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACAT‑‑ccccccccccgta < 2:281078/139‑6 (MQ=255) cgcATCTGGTAGATGCGACTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAg < 2:1126685/139‑1 (MQ=255) cTGGTAGATGCGACTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAgctgct < 1:778418/139‑1 (MQ=255) cTGGTAGATGCGACTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACAT‑‑c > 1:1122622/1‑112 (MQ=255) cTGGTAGATGCGACTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACAT‑‑c < 2:1122622/112‑1 (MQ=255) aTGCTACTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATCCCCCCCCCCGTACGGGAATCTAGCTGCTGACCGc < 1:866852/139‑1 (MQ=255) cTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATc > 1:346900/1‑139 (MQ=255) atGTTCTAACGGTAGTTGCGGCAAAAATTCAATGAGCGATTTCTCTGGGTTCGCCGCGTTCCGCGTCCGCCTTGCTGCGCCCGGAGGTGGCCCCACATCCCCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGatat < 2:955278/138‑1 (MQ=255) aCGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATCCCCCCCCCCGTCCGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGc > 1:78278/1‑139 (MQ=255) gTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACAT‑‑ccccc > 1:198710/1‑92 (MQ=255) gTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACAT‑‑ccccc < 2:198710/92‑1 (MQ=255) aGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATCCCCCCCCCCGTACGGTAATCCAGCGGCTGACCGCTGATATCCGCCAGCATCTg > 1:497255/1‑139 (MQ=255) aGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGa > 2:260508/1‑139 (MQ=255) gCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATCCCCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGc < 2:78278/139‑1 (MQ=255) gCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGt > 1:949089/1‑139 (MQ=255) aGCGATTTCTCTGGATTCGCCGCGAACTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGTTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGcg‑cc > 2:70506/1‑139 (MQ=255) gCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGata > 2:647420/1‑102 (MQ=255) gCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGata < 1:647420/102‑1 (MQ=255) tctGGATTTGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGACCCACATC‑CCCCCCCCGTACGGTAATCGCGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCa < 1:675601/139‑1 (MQ=255) tGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCAAt < 1:241873/139‑1 (MQ=255) tGGATTCGCCGCGAACTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGTTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCAAt < 1:70506/139‑1 (MQ=255) gccgcGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCAATCAACGTa > 1:634857/1‑139 (MQ=255) ccgcGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCCCATCCCCCCCCCCGCCCGGCAATCGCGCCGCTCACCGCTGATTTTCCCCACCACCTCTCTCCCGTCCCCCCTACCCGCCCCCGCCCCCatcccccca > 2:753238/1‑131 (MQ=255) ccgcGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATCCCCCCCCCCCTACGGTAACCGCACTGCCGGCCCCTGCGATCCGCCAGCATCCTGCGCCAGTACTCACCCCCCG‑cccccccccccaccaccgca > 2:462050/1‑129 (MQ=255) gcCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCa < 2:130253/93‑1 (MQ=255) gcCAGCCTTGCTGCGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCa > 1:130253/1‑93 (MQ=255) tgctgcGCCCAGTGCTGGCCCCACATCCCCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCAATCAACGTAACACTTTGCGGTTTAATAc < 1:462050/139‑1 (MQ=255) gctggGCCCAGTGCTGGCCCCACAT‑‑cccccccccc < 1:112574/35‑3 (MQ=255) gctgcGCCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCAATCAACGTAACACTTTGCGGTTTAATACCg > 2:929325/1‑139 (MQ=255) gctgcGCCCAGTGCTGGCCCCACAT‑‑cccccccccc > 2:112574/1‑33 (MQ=255) gcgcCCAGTGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCAATCAACGTAACACTTTGCGGTTTAATACCGCAg < 2:949089/139‑1 (MQ=255) tGCTGGCCCCACATC‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCAATCAACGTAACACTTTGCGGTTTAATACCGCAGGCATGCAc > 1:157352/1‑139 (MQ=255) | AGCGGCATAACGCTGCGCATCTGGTAGATGCGACTGTTCTAACGGTAGTTGCGGCAACAATTCAATGAGCGATTTCTCTGGATTCGCCGCGATCTGCGCCAGCCTTGCTGCGCCCAGTGCTGGCCCCACAT‑‑CCCCCCCCGTACGGTAATCGAGCTGCTGACCGCTGATATCCGCCAGCATCTGACGCCAGTACTCACTACGCG‑CCCCGCCCCCAATCAACGTAACACTTTGCGGTTTAATACCGCAGGCATGCAC > NC_000913/3727980‑3728234 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 28 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |