SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8170417 | snp | A/G | | | intron-variant | Wsb2 | Rn_Celera | 12:44962240 | GAAAGCTCAAAGTGA[A/G]AGCATGGGATGAACT | 288692 |
rs8173652 | snp | C/T | 0 | 0 | downstream-variant-500B | Rfc5, Wsb2 | Rn_Celera | 12:44941247 | GTTTGCCCCATCCCT[C/T]CCCAACAAGGCAGGC | 288692 |
rs104912772 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44945663 | CACACACACGCACGC[A/G]CACACGCTGGAGGCT | 288692 |
rs104930411 | snp | A/C | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44954332 | CCACAGGAGGCAGCC[A/C]ACCAGTCACTCTGGA | 288692 |
rs105156825 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44954671 | GCACCTGAGCATCAG[A/G]GTGCACCTGAGCATC | 288692 |
rs105213705 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44945655 | CACACACACACACAC[A/G]CGCACGCGCACACGC | 288692 |
rs105223199 | snp | C/T | 0 | 0 | downstream-variant-500B | Wsb2 | Rn_Celera | 12:44941624 | CGTCTTTGCTTCTTT[C/T]GTAATAGGAAAAAAA | 288692 |
rs105293422 | snp | A/T | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44958493 | ACAGGTTTTTTTTTT[A/T]AATTTATTTATTTAT | 288692 |
rs105315868 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44954687 | GTGCACCTGAGCATC[A/G]GAGGTGCACCTGAGC | 288692 |
rs105537342 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44944805 | TGGAAATCTGGCCAT[A/G]ACTACATCTGACCAA | 288692 |
rs105704838 | snp | A/T | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44955636 | CACACACACACACAC[A/T]CTCTCCAAGTGCCAG | 288692 |
rs105748781 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44943182 | GCGTGAGGAGGTTCT[A/G]AGTAACACAGTAACA | 288692 |
rs105844060 | snp | C/T | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44953706 | GAATGACTGTGTACT[C/T]GCTTCTGAGAAAGTC | 288692 |
rs106028799 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44953835 | TGCGTCCTGTTTCCT[A/G]CTCGGTGGCTCAGGC | 288692 |
rs106093599 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44946215 | GCATGGTCAGGCACC[A/G]AGCATCATCTTCTCA | 288692 |
rs106142961 | snp | C/T | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44948288 | CTAGCCTGTGCACTC[C/T]ACATGCTGAGCGGCA | 288692 |
rs106160613 | snp | C/T | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44948475 | GTCTGAGAGCAGTCC[C/T]GAGGGGGCTTCCTGA | 288692 |
rs106172857 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44955487 | ACCCTGGAGGCCTGC[A/G]CCTACTGGATGTGTC | 288692 |
rs106451812 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44950360 | ACTCAATTGGAGGAA[A/G]GCAGATGAGGACACC | 288692 |
rs106575800 | snp | C/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44944647 | ACTCAACACTGCAAA[C/G]TGCTTTCTGACCCTT | 288692 |
rs106612179 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44954653 | GCACCTGAGCATCAG[A/G]GTGCACCTGAGCATC | 288692 |
rs106654613 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44945651 | CACACACACACACAC[A/G]CACACGCACGCGCAC | 288692 |
rs106939473 | snp | A/T | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44961216 | CACGTGGTGCAGACA[A/T]ACTGGCAGTTTAAAA | 288692 |
rs107074011 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | Wsb2 | Rn_Celera | 12:44958320 | TTAAACACCCACTGA[A/G]CAATCTCACTGAACC | 288692 |
rs107192482 | snp | C/T | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44954240 | TCTAGCTCTAGGTAC[C/T]ACATTCGTAGAGAAC | 288692 |
rs107212758 | snp | A/C | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44948720 | GGGGCATGTGATAGC[A/C]CCCCCCCCCACACAC | 288692 |
rs107339275 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44944657 | GCAAACTGCTTTCTG[A/G]CCCTTGCTTGAGATG | 288692 |
rs107505688 | snp | A/G | 0 | 0 | intron-variant | Wsb2 | Rn_Celera | 12:44955187 | ACATCAACCAGGAGA[A/G]AAACACTGGCACCAC | 288692 |