SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8143209 | snp | C/T | | | utr-variant-3-prime | Epn2 | Rn_Celera | 10:47795713 | ATGCGCTGGGTGGCC[C/T]GTGGGAGGAAGAGCC | 60443 |
rs8143276 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Epn2 | Rn_Celera | 10:47795540 | ACAGTAAAGTATCAA[C/T]AGTCAACACAAATCC | 60443 |
rs8143277 | snp | A/C | 0 | 0 | utr-variant-3-prime | Epn2 | Rn_Celera | 10:47795825 | GGCCCTAGCCTATAC[A/C]ATCTGAAGGAAGCAG | 60443 |
rs8144703 | snp | A/T | | | downstream-variant-500B | Epn2 | Rn_Celera | 10:47795492 | GACACAGCCAAAACC[A/T]ACATCATGATACAAA | 60443 |
rs8163832 | snp | C/T | 0 | 0 | synonymous-codon | Epn2 | Rn_Celera | 10:47797892 | TCCTGTCAATCCCTT[C/T]CAGGTCAACCAGCCC | 60443 |
rs8168422 | snp | C/T | 0.473476 | 0.112064 | utr-variant-3-prime | Epn2 | Rn_Celera | 10:47796361 | CTCCAAAATAGGATA[C/T]GGTTACTTCCTGGTC | 60443 |
rs13457223 | snp | C/T | | | utr-variant-3-prime | Epn2 | Rn_Celera | 10:47796878 | ATTTTGCTTAGTTTT[C/T]CATAAGGCATATTTT | 60443 |
rs13457224 | snp | C/G | 0.48 | 0.0979796 | utr-variant-3-prime | Epn2 | Rn_Celera | 10:47797159 | ATAGGGCAGGGTCGC[C/G]CTCCAGTCAGCTTAA | 60443 |
rs66029466 | snp | A/G | 0.237336 | 0.249679 | intron-variant | Epn2 | Rn_Celera | 10:47807939 | AGGACAGCTGCTGAA[A/G]AGCTAGTGGCCCAGT | 60443 |
rs104954915 | snp | C/T | 0.5 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47819671 | GATTGACAGCACCCA[C/T]CTAGGACAAACCACC | 60443 |
rs105022018 | snp | C/T | 0.5 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47817383 | ATGAGATGGAAACTC[C/T]ACCTTCATTCTTTCT | 60443 |
rs105386145 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | Epn2 | Rn_Celera | 10:47825655 | GGGGCAACAAAGCCT[A/C]ATTTCGAGAATACCT | 60443 |
rs105538168 | snp | C/T | 0 | 0 | missense | Epn2 | Rn_Celera | 10:47799850 | ACTGAGCTGGTGGAT[C/T]AGGCTTAGTCACCAG | 60443 |
rs105606956 | snp | A/G | 0 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47806775 | CAAACAGTTAAACCC[A/G]GGGCTGGGGATTTGG | 60443 |
rs105665651 | snp | C/T | 0 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47832619 | CTGGCCCCTCTGAAC[C/T]GCTGCACTGCCCAAA | 60443 |
rs106155970 | snp | A/C | 0.5 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47824192 | GACAGACATTCTTGG[A/C]CAAAAAAAAAAAAAA | 60443 |
rs106252351 | snp | A/C | 0 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47808599 | TCCAACAAATGAAGG[A/C]CACAGTAATGTGACT | 60443 |
rs106680037 | snp | A/G | 0.5 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47827306 | GAGCTGGTCTGGAGA[A/G]CTATTGAGCCGTACA | 60443 |
rs106783921 | snp | C/T | 0 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47829567 | ACATTTCCACCAGTA[C/T]CATGCCAATATGTTC | 60443 |
rs107003709 | snp | G/T | 0 | 0 | missense | Epn2 | Rn_Celera | 10:47799849 | GACTGAGCTGGTGGA[G/T]TAGGCTTAGTCACCA | 60443 |
rs107083654 | snp | A/C | 0 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47823338 | AATTCTAACAGTGGT[A/C]CAAAGAAAGTCAGAC | 60443 |
rs107259717 | snp | C/G | 0.5 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47830995 | CAGGGAAACAAGAGA[C/G]CACACTACTGAAGGT | 60443 |
rs198326904 | snp | C/T | 0 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47802037 | ACACACACATACACA[C/T]ACACACACACACGAA | 60443 |
rs198803318 | snp | C/T | 0 | 0 | intron-variant | Epn2 | Rn_Celera | 10:47802031 | ACACACACACACACA[C/T]ACACACACACACACA | 60443 |