SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8152925 | snp | A/T | | | intron-variant | Fbxw8 | Rn_Celera | 12:44127245 | ATGTGCTACATAGGT[A/T]TGCAAACTATCTATA | 304522 |
rs104989706 | snp | A/C | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44086202 | CCCTCCTCCCCAATG[A/C]GTGTGCACAGTAATA | 304522 |
rs105259175 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44058511 | AGCCGAGCAGCCTCC[A/G]CCCTGCTCTTTCCTC | 304522 |
rs105376648 | snp | C/T | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44062849 | CAGCCTTTGGTCAAA[C/T]GTTCTAGCTGTGTGT | 304522 |
rs105444652 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44059426 | GAACTGCACAGGAGC[A/G]TGTCATGCCGACTGA | 304522 |
rs105449463 | snp | A/T | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44049763 | CAAGGCAGCTCTTAT[A/T]AAAGAAAGCATTTAA | 304522 |
rs105514466 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44057170 | GTCGATGCTGGGAGC[A/G]TCTGCTTACAGTGGG | 304522 |
rs105587214 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44078677 | CTCTTTGAAAGTATC[A/G]AGCTCAGTGAATTTT | 304522 |
rs105833097 | snp | C/T | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44128942 | AGCTGGAGGATCCCT[C/T]CTGGTTCCCCCACGA | 304522 |
rs105908709 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44073578 | GAGGCCTGAAGTGAA[A/G]GTGGAGGGAAGGGAG | 304522 |
rs106127980 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44056243 | GACAAACACCATGAC[A/G]TGCTGAAGCTTCTAG | 304522 |
rs106229035 | snp | A/C | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44081007 | GCTCCGAAAAAAAGA[A/C]CCAAAAAAAAAAAAA | 304522 |
rs106418756 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44064237 | TTAGGATGGCTGGGA[A/G]CATGAGTGCTGTTTC | 304522 |
rs106525776 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44100317 | GTGGGTTTGGGTGTG[A/G]ATGTGTGGTCTGAAC | 304522 |
rs106619232 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44074709 | CTGGTCCCCTCTCCC[A/G]GGTTACTGAGGTCCT | 304522 |
rs106619342 | snp | A/G | 0.188602 | 0.242343 | intron-variant | Fbxw8 | Rn_Celera | 12:44121753 | ACTCTCCTCTGCTGA[A/G]GAAGAGGTGCAGCCA | 304522 |
rs106710588 | snp | C/T | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44061917 | TTTGGTTCTTTTTTT[C/T]GGAGCTGGGGACCGA | 304522 |
rs106744274 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44083924 | AGCTTGACTGGGAAA[A/G]CACATGGTTCTTCAT | 304522 |
rs106748714 | snp | C/T | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44073769 | GCGTGTGCGTGCGTG[C/T]GTGTGTGTGTGTGTG | 304522 |
rs106827393 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44059800 | AGGTGCGTGGGGAGC[A/G]GGACCCTCCAGTGAG | 304522 |
rs106848246 | snp | A/T | 0.441505 | 0.160704 | intron-variant | Fbxw8 | Rn_Celera | 12:44062154 | CCTTTACCCCTGAGA[A/T]AGTTTTTCCTGGGGT | 304522 |
rs106865209 | snp | C/T | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44121796 | ACAGTATCTGGAGCC[C/T]GCAGGCATCTGCTTG | 304522 |
rs107319091 | snp | C/T | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44051517 | CCACAAAGACACAGA[C/T]GCCCAACTCAAACTG | 304522 |
rs107405669 | snp | C/T | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44077805 | AGGCAGCTGCCTCTC[C/T]CCCACCGCCTTCTCT | 304522 |
rs197418658 | snp | C/G | 0 | 0 | missense | Fbxw8 | Rn_Celera | 12:44046295 | GGAGGAATTGGCGCA[C/G]TCGCAGGTGCTGAGG | 304522 |
rs197692639 | snp | A/G | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44079844 | AGGACAGCATTTCCC[A/G]CTTCTTAGGAAGAAA | 304522 |
rs198258316 | snp | C/T | 0 | 0 | missense | Fbxw8 | Rn_Celera | 12:44046303 | TGGCGCACTCGCAGG[C/T]GCTGAGGCGACGGCG | 304522 |
rs199033797 | snp | A/C | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44100207 | ACATGGTGAACGTGG[A/C]CCAGCTCAACTCAGT | 304522 |
rs199299653 | snp | C/T | 0 | 0 | intron-variant | Fbxw8 | Rn_Celera | 12:44079660 | GCTTGAACCTAGCAC[C/T]CAGGAGACTCTGAGA | 304522 |