Epn2
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs8143209snpC/Tutr-variant-3-primeEpn2Rn_Celera10:47795713ATGCGCTGGGTGGCC[C/T]GTGGGAGGAAGAGCC60443
rs8143276snpC/T0.50utr-variant-3-primeEpn2Rn_Celera10:47795540ACAGTAAAGTATCAA[C/T]AGTCAACACAAATCC60443
rs8143277snpA/C00utr-variant-3-primeEpn2Rn_Celera10:47795825GGCCCTAGCCTATAC[A/C]ATCTGAAGGAAGCAG60443
rs8144703snpA/Tdownstream-variant-500BEpn2Rn_Celera10:47795492GACACAGCCAAAACC[A/T]ACATCATGATACAAA60443
rs8163832snpC/T00synonymous-codonEpn2Rn_Celera10:47797892TCCTGTCAATCCCTT[C/T]CAGGTCAACCAGCCC60443
rs8168422snpC/T0.4734760.112064utr-variant-3-primeEpn2Rn_Celera10:47796361CTCCAAAATAGGATA[C/T]GGTTACTTCCTGGTC60443
rs13457223snpC/Tutr-variant-3-primeEpn2Rn_Celera10:47796878ATTTTGCTTAGTTTT[C/T]CATAAGGCATATTTT60443
rs13457224snpC/G0.480.0979796utr-variant-3-primeEpn2Rn_Celera10:47797159ATAGGGCAGGGTCGC[C/G]CTCCAGTCAGCTTAA60443
rs66029466snpA/G0.2373360.249679intron-variantEpn2Rn_Celera10:47807939AGGACAGCTGCTGAA[A/G]AGCTAGTGGCCCAGT60443
rs104954915snpC/T0.50intron-variantEpn2Rn_Celera10:47819671GATTGACAGCACCCA[C/T]CTAGGACAAACCACC60443
rs105022018snpC/T0.50intron-variantEpn2Rn_Celera10:47817383ATGAGATGGAAACTC[C/T]ACCTTCATTCTTTCT60443
rs105386145snpA/C00intron-variant, upstream-variant-2KBEpn2Rn_Celera10:47825655GGGGCAACAAAGCCT[A/C]ATTTCGAGAATACCT60443
rs105538168snpC/T00missenseEpn2Rn_Celera10:47799850ACTGAGCTGGTGGAT[C/T]AGGCTTAGTCACCAG60443
rs105606956snpA/G00intron-variantEpn2Rn_Celera10:47806775CAAACAGTTAAACCC[A/G]GGGCTGGGGATTTGG60443
rs105665651snpC/T00intron-variantEpn2Rn_Celera10:47832619CTGGCCCCTCTGAAC[C/T]GCTGCACTGCCCAAA60443
rs106155970snpA/C0.50intron-variantEpn2Rn_Celera10:47824192GACAGACATTCTTGG[A/C]CAAAAAAAAAAAAAA60443
rs106252351snpA/C00intron-variantEpn2Rn_Celera10:47808599TCCAACAAATGAAGG[A/C]CACAGTAATGTGACT60443
rs106680037snpA/G0.50intron-variantEpn2Rn_Celera10:47827306GAGCTGGTCTGGAGA[A/G]CTATTGAGCCGTACA60443
rs106783921snpC/T00intron-variantEpn2Rn_Celera10:47829567ACATTTCCACCAGTA[C/T]CATGCCAATATGTTC60443
rs107003709snpG/T00missenseEpn2Rn_Celera10:47799849GACTGAGCTGGTGGA[G/T]TAGGCTTAGTCACCA60443
rs107083654snpA/C00intron-variantEpn2Rn_Celera10:47823338AATTCTAACAGTGGT[A/C]CAAAGAAAGTCAGAC60443
rs107259717snpC/G0.50intron-variantEpn2Rn_Celera10:47830995CAGGGAAACAAGAGA[C/G]CACACTACTGAAGGT60443
rs198326904snpC/T00intron-variantEpn2Rn_Celera10:47802037ACACACACATACACA[C/T]ACACACACACACGAA60443
rs198803318snpC/T00intron-variantEpn2Rn_Celera10:47802031ACACACACACACACA[C/T]ACACACACACACACA60443
Full records
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