Rnf40
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs8154726snpC/Tsynonymous-codonRnf40Rn_Celera1:199041285GCAGAGCTCGAGAAG[C/T]TACAGGCTGAGCTTC266712
rs8154727snpC/Tsynonymous-codonRnf40Rn_Celera1:199051759CTTCTGCTTTGAATG[C/T]GTGCGGGGCCGCTAT266712
rs8168397snpA/Gdownstream-variant-500B, utr-variant-3-primeRnf40, Zfp629Rn_Celera1:199052369CAGAGTGTCCCTGAA[A/G]AGGGCAGACACCCAG266712
rs104935898snpC/T00intron-variantRnf40Rn_Celera1:199046303GGCTGGGCTTTTGGA[C/T]GTGGTAACTTGTGTG266712
rs105866806snpA/G00intron-variantRnf40Rn_Celera1:199042154TCGCTCTGCAGTCAC[A/G]GTGCTAAGGATTCAA266712
rs106055698snpA/G00synonymous-codonRnf40Rn_Celera1:199049756TGAGATCCTGCAGGA[A/G]GAGATCAAGGAGTAC266712
rs106308623snpA/G00intron-variantRnf40Rn_Celera1:199046504GTGCATCCATGTTGT[A/G]TGCATGTGTTTATGT266712
rs107321549snpA/C00intron-variantRnf40Rn_Celera1:199050422AACTAATATATAGCT[A/C]ACCCTATACCCAGAG266712
rs107390926snpC/T00intron-variantRnf40Rn_Celera1:199051085GGTAGTGACTAGAGC[C/T]GAATCTGAGGCCTCC266712
rs196999625snpC/T00intron-variantRnf40Rn_Celera1:199050012GGATGGGATGGAGAA[C/T]TGTGTAGCAACAGGC266712
rs198364515snpC/G00upstream-variant-2KB, intron-variantCcdc189, Rnf40Rn_Celera1:199037975GTGTGTGTATACACA[C/G]ACAAACGGGTGGTGA266712
rs198579754snpC/T00intron-variantRnf40Rn_Celera1:199041132TCTTCATAGGGAGCT[C/T]GGGTGGGATGCATGG266712
rs199292548snpA/C00upstream-variant-2KB, synonymous-codonCcdc189, Rnf40Rn_Celera1:199037802GGGCTCAGGACCCCC[A/C]GAGAAGAAGCTGAAC266712
rs199398733snpC/T00intron-variant, upstream-variant-2KBCcdc189, Rnf40Rn_Celera1:199035496ATCAGAAGGGGGATC[C/T]GGAGTTAGGGCATGG266712
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