B0432.13
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193323323snpG/T0.0103090.0710509synonymous-codon?WS195II:279326CACATTTTCAGTTTT[G/T]GGAGCTTCTGTGGGT173412
rs193323324snpC/T0.0101520.0705191missense?WS195II:279337TTTTTGGAGCTTCTG[C/T]GGGTTTTGATGACGT173412
rs193323325snpA/G0.0101520.0705191synonymous-codon?WS195II:279359TGATGACGTTTTGGC[A/G]CTTAAATTCGGGATT173412
rs193323326snpC/T0.01025610.0708723synonymous-codon?WS195II:279389TTTTGGATATTTTTT[C/T]GCAGGTTGTGCAGTA173412
rs193323327snpA/T0.0101520.0705191synonymous-codon?WS195II:279392TGGATATTTTTTTGC[A/T]GGTTGTGCAGTAGTT173412
rs193323328snpA/T0.01010080.0703445intron-variant?WS195II:279471TCGAATGAGCTGAAA[A/T]TTTTAACGAATTAAT173412
rs193323329snpG/T0.010050.0701712intron-variant?WS195II:279475ATGAGCTGAAAATTT[G/T]AACGAATTAATTATG173412
rs193323330snpA/G0.010050.0701712intron-variant?WS195II:279476TGAGCTGAAAATTTT[A/G]ACGAATTAATTATGG173412
rs193323331snpA/T0.010050.0701712intron-variant?WS195II:279493CGAATTAATTATGGT[A/T]AAAAAGAATTTGTCG173412
rs353103362snpA/Gintron-variant?WS195II:282075TGGGTCTGCTAAATC[A/G]AAACTTGTAGTTTGT173412
rs353104479in-del-/GCTGTintron-variant?WS195II:281299CTTAAATTTTAATTA[-/GCTGT]GCTCCCTAATTCAGT173412
rs353107775snpA/Gmissense?WS195II:279210ATAACGTATTCCGTA[A/G]GATTCGACGTAGAAG173412
rs353148468snpA/Tintron-variant?WS195II:281857AACTACAAATTTCGA[A/T]TTAGCAGACCCAAGT173412
Full records
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