SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8150166 | snp | A/C | | | utr-variant-3-prime | Enc1 | Rn_Celera | 2:28060808 | CTCCCCTGTCTTATG[A/C]CAGGGTTTTTGTGTG | 294674 |
rs8166156 | snp | C/T | 0 | 0 | synonymous-codon | Enc1 | Rn_Celera | 2:28053705 | TGTCTGCAACAGTTC[C/T]GGGAGGTAACAGTAG | 294674 |
rs8167649 | snp | A/C | 0.3588 | 0.225084 | utr-variant-5-prime | Enc1 | Rn_Celera | 2:28049359 | AGCCACTACCCGGGA[A/C]GCCATCGCCTCCCTT | 294674 |
rs8167958 | snp | A/T | | | utr-variant-3-prime | Enc1 | Rn_Celera | 2:28060815 | GAAGAACCTCCCCTG[A/T]CTTATGCCAGGGTTT | 294674 |
rs13450789 | snp | C/T | 0.462701 | 0.131371 | utr-variant-3-prime | Enc1 | Rn_Celera | 2:28059942 | TGTAAACGTTAGTGT[C/T]CACCCTTAGATACAT | 294674 |
rs105785468 | snp | A/G | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28050673 | TTTCGGGGGGGGGGG[A/G]CTTAGAAAACACAGA | 294674 |
rs105884235 | snp | C/T | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28056948 | ATTGCCAGGGGTGAT[C/T]GGTGGCAGTAGGTCA | 294674 |
rs106093202 | snp | C/G | 0 | 0 | missense | Enc1 | Rn_Celera | 2:28053027 | CAAAATGTCCGTCAG[C/G]GTGCATGAGAACCGC | 294674 |
rs106646718 | snp | C/T | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28058448 | TGGGTGTGCACATTT[C/T]CTACTGAACACAATT | 294674 |
rs106939984 | snp | C/T | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28051861 | AATCAATCTCTCTCT[C/T]TCTCACTCTCTCTCT | 294674 |
rs106986271 | snp | C/T | 0 | 0 | utr-variant-3-prime | Enc1 | Rn_Celera | 2:28059978 | AAGAGAGCTTTGGTA[C/T]GCGGAAGTGGCATCT | 294674 |
rs107406765 | snp | A/T | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28051866 | ATCTCTCTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 294674 |
rs197375304 | snp | A/G | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28055503 | CTATTCCGATTTCAC[A/G]TCTTCAGATCTTTCT | 294674 |
rs197423281 | snp | C/T | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28051229 | GCTTTCTTAGTTCTC[C/T]TTGGCCTTGTTTACT | 294674 |
rs197530361 | snp | C/T | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28047421 | GTATCTTTCTCTCCT[C/T]GGGAACTAAATTGAG | 294674 |
rs197835874 | snp | G/T | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28051628 | GAGCCCTAGAAGAGT[G/T]CTGTCAGAAGGGGGA | 294674 |
rs198048921 | snp | C/G | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28047748 | TTTCAGCAGGCTGTG[C/G]TCTCAGGAAGCGCCA | 294674 |
rs198403676 | snp | A/G | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28050645 | GGTGATAGGGTAGAC[A/G]GTGCCTTCTGGTTTT | 294674 |
rs198444883 | snp | A/C | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28047664 | CTTTGCGATGAGCAA[A/C]ATTTATCAGCCTGGA | 294674 |
rs198472160 | snp | G/T | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28048189 | GTGTGTGTGTGTGTG[G/T]GGTGGGGTACTATTT | 294674 |
rs198577560 | snp | C/G | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28055386 | CGTAAGGAATCCACC[C/G]GGGGAGCCTGAGCCC | 294674 |
rs198772734 | snp | A/G | 0 | 0 | downstream-variant-500B | Enc1 | Rn_Celera | 2:28061141 | CTCTTCATTGTATGT[A/G]TGAGTTTTTATTTGA | 294674 |
rs199199096 | snp | A/T | 0 | 0 | intron-variant | Enc1 | Rn_Celera | 2:28051647 | TCAGAAGGGGGAGTT[A/T]ATTCCATTTTTCAAG | 294674 |