SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6378400 | snp | G/T | 0.359862 | 0.224567 | intron-variant, utr-variant-3-prime | Cdc16 | GRCm38.p3 | 8:13770386 | TTTCAAGTACTTCAC[G/T]TTAACTCTGTCCCTA | 69957 |
rs13465716 | snp | C/T | 0.42 | 0.183303 | synonymous-codon | Cdc16 | GRCm38.p3 | 8:13761114 | GGAGATGTCACAGTC[C/T]TCCGTGAGTGATATG | 69957 |
rs29977634 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756993 | GTGACAGCACAAATT[C/T]CCTTTATAAAACAAT | 69957 |
rs29977637 | snp | G/T | 0.165289 | 0.235211 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13757317 | TGGTGATGGACCTCT[G/T]TATTTCCAGCACCCA | 69957 |
rs29977640 | snp | A/G | 0.18 | 0.24 | upstream-variant-2KB | Cdc16 | GRCm38.p3 | 8:13757326 | ACCTCTTTATTTCCA[A/G]CACCCAAGGAGGTGT | 69957 |
rs29977643 | snp | A/G | 0.18 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13758012 | GCCGGACCGTAGGAC[A/G]TTTGGGAGGATTTAG | 69957 |
rs29978046 | snp | C/T | 0.32 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13780441 | TGCTTGTGTACGTTC[C/T]GTCCATGGAAACGGT | 69957 |
rs29978049 | snp | C/T | 0.165289 | 0.235211 | synonymous-codon | Cdc16 | Mm_Celera | 8:13781544 | TAAAGCTCCAGAGTC[C/T]AGACCTAACTTGGAA | 69957 |
rs29978052 | snp | C/T | 0.165289 | 0.235211 | utr-variant-3-prime | Cdc16 | Mm_Celera | 8:13781765 | CTACATCTCTACATT[C/T]AGGACCAGCAGCCTG | 69957 |
rs29978576 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Cdc16 | Mm_Celera | 8:13758101 | CTGGAAACAATACCC[C/G]GTGCTGGATCTTCAG | 69957 |
rs29978579 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Cdc16 | Mm_Celera | 8:13758196 | ACGTCATTGTCATGT[C/T]ATTTGGTTTTTTGCT | 69957 |
rs29978582 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Cdc16 | Mm_Celera | 8:13758303 | AAGGCTGCGTGCTAA[C/G]GGGCAGTCGGTTTGT | 69957 |
rs29979485 | snp | C/T | 0.18 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13758462 | GTTCTGACTATATCC[C/T]GAGGAACTGAGGCAG | 69957 |
rs29979488 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cdc16 | Mm_Celera | 8:13758826 | ATATGAAGTTCTTAC[A/G]GTAATGACGACCTAA | 69957 |
rs29979491 | snp | A/G | 0.165289 | 0.235211 | synonymous-codon, intron-variant | Cdc16 | GRCm38.p3 | 8:13759003 | TTGTATGCAGCAACA[A/G]TATCAAAGTGCTCTG | 69957 |
rs29980374 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Cdc16 | Mm_Celera | 8:13760946 | ATCTGGAAGACATGG[C/G]TGATGAATGGAACTT | 69957 |
rs29980377 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Cdc16 | Mm_Celera | 8:13761027 | CCTTGACATGGAGGA[A/G]CCAATTAACAGAAGG | 69957 |
rs29980380 | snp | A/G | 0.297521 | 0.245442 | synonymous-codon | Cdc16 | Mm_Celera | 8:13761078 | GGATGACAATGGCTC[A/G]AGAGACCCTTCCAGT | 69957 |
rs29980916 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cdc16 | Mm_Celera | 8:13767473 | TGTGTGAGAGTGGGT[A/G]AAAGGTCAGATGTGA | 69957 |
rs29980919 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Cdc16 | Mm_Celera | 8:13767905 | AGACAGAATTTCCTA[C/G]TTGTAGAGATAATAG | 69957 |
rs29980922 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Cdc16 | Mm_Celera | 8:13768199 | TAAGACAAAAGCCAG[C/T]GAGCAGAGGCCGATT | 69957 |
rs29980934 | snp | A/G | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Cdc16 | Mm_Celera | 8:13771699 | TGCACAAACTCCAGT[A/G]CCCACCATGTGGTCT | 69957 |
rs29980937 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Cdc16 | Mm_Celera | 8:13772077 | GGAGGAGAAAACAGT[A/G]CACTGCATCAGGCTC | 69957 |
rs29980940 | snp | C/G | 0.32 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13772086 | AACAGTACACTGCAT[C/G]AGGCTCTACCAAAGT | 69957 |
rs29980943 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cdc16 | Mm_Celera | 8:13772097 | GCATCAGGCTCTACC[A/G]AAGTGTAAGCACAGC | 69957 |
rs29981416 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Cdc16 | Mm_Celera | 8:13761801 | TCTCATGTTCATTTT[A/T]AAAAATACAGGAATT | 69957 |
rs29981419 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cdc16 | Mm_Celera | 8:13762296 | GCCAAGACAGATTAA[A/G]TCATCACACAGAAGC | 69957 |
rs29981422 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Cdc16 | Mm_Celera | 8:13762524 | CCACACTCCTGAGGT[A/G]CAAAGCTTCATTGGC | 69957 |
rs29981432 | snp | G/T | 0.231111 | 0.249285 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13755667 | TTAGTGCAAAAGCTA[G/T]CGATAATAAGTTCCA | 69957 |
rs29981645 | snp | G/T | 0.32 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13768205 | AAAAGCCAGTGAGCA[G/T]AGGCCGATTCTCAAG | 69957 |
rs29981648 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Cdc16 | Mm_Celera | 8:13768383 | GCGACCTTGGGAAAA[C/T]CACAATATCTGTTCC | 69957 |
rs29981651 | snp | A/C | 0.32 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13768658 | TTGTTTTCTTCTTTG[A/C]TCTGTAGTGAACCTA | 69957 |
rs29981756 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Cdc16 | Mm_Celera | 8:13772744 | AGTCTTTTGAGTGCT[C/G]TGGTTTTTCACAGCC | 69957 |
rs29981759 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Cdc16 | GRCm38.p3 | 8:13772826 | CTGCCTCTTGTGTAC[C/T]ATAAGTAGCCATCGT | 69957 |
rs29981762 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Cdc16 | Mm_Celera | 8:13773227 | TTCATAGTATAATCT[C/G]AGTTATTTTTAGCAG | 69957 |
rs29982175 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13755718 | CACAGCAAGGAGACA[C/T]TGACATCCCGTGCCC | 69957 |
rs29982178 | snp | C/T | 0.260355 | 0.249785 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13755939 | CCTTGAGTATCACAG[C/T]CCCTCAGGCAAGAGA | 69957 |
rs29982181 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13755996 | TACTCTGATGGATAC[A/G]ACAAGAAACATTCAG | 69957 |
rs29982375 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Cdc16 | Mm_Celera | 8:13763203 | AGTAAGCACATCACA[A/G]AATAGTGCGATGCAG | 69957 |
rs29982378 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Cdc16 | Mm_Celera | 8:13763309 | ATTAACCAAGATTCA[A/G]TGGTTTTTCATCCTA | 69957 |
rs29982381 | snp | A/T | 0.18 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13763460 | GTGTGACGTGGGTAA[A/T]CGAGAGAGCAGAGAA | 69957 |
rs29982404 | snp | A/G | 0.32 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13768698 | AATTGTTGCTCATAA[A/G]CTTGAATGCAGTGAG | 69957 |
rs29982407 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cdc16 | Mm_Celera | 8:13768804 | CTAGGATGCAGAGGT[A/G]AAGCAGGGTTGCAGG | 69957 |
rs29982409 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cdc16 | Mm_Celera | 8:13769124 | CAGAGTGGGCTACTG[C/T]GTAAATAGTATTTGT | 69957 |
rs29982412 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cdc16 | Mm_Celera | 8:13769521 | GGCACACGGCAGGAC[C/T]GCATGCCAGGAAGGG | 69957 |
rs29982625 | snp | A/G | 0.32 | 0.24 | intron-variant | Cdc16 | GRCm38.p3 | 8:13773471 | TAATGTTGGATGTGG[A/G]AAATGCAGGTAGTCT | 69957 |
rs29982628 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cdc16 | GRCm38.p3 | 8:13773553 | AGTCACCTATACCGA[A/G]AGAACATGAGCTCAG | 69957 |
rs29982631 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cdc16 | Mm_Celera | 8:13773648 | TCTGAAACAGTTTCC[A/G]ATGGCTAATCAAAGT | 69957 |
rs29983094 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756010 | CAACAAGAAACATTC[A/G]GGTGTTGTTGACACT | 69957 |
rs29983097 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756012 | ACAAGAAACATTCAG[A/G]TGTTGTTGACACTGG | 69957 |
rs29983100 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756204 | ATAAAACATCGCAAA[A/G]AACAAGGTGGCTTCC | 69957 |
rs29983103 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756225 | GGTGGCTTCCGATGA[A/G]GAAAAGCATTTAAAG | 69957 |
rs29983304 | snp | A/G | 0.18 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13763556 | TCTCAAGACAGGGAC[A/G]AGTAGGAAGCTGGCT | 69957 |
rs29983307 | snp | A/G | 0.32 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13763744 | GTACTTTGATTAGAG[A/G]ACTATAGAAGAGTAT | 69957 |
rs29983310 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Cdc16 | GRCm38.p3 | 8:13763977 | TCCTTAGCGTTGGCC[C/T]TTTTCCTTTTATCAG | 69957 |
rs29983313 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Cdc16 | Mm_Celera | 8:13764372 | TTCTGTCTTCTAAAC[G/T]TGTATGTGACATCCT | 69957 |
rs29983335 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cdc16 | Mm_Celera | 8:13769589 | GCTGTTACGGTTTGG[A/G]TCCTGAGTTAGAACT | 69957 |
rs29983338 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cdc16 | Mm_Celera | 8:13769612 | TTAGAACTGTCACAC[A/G]TGTGTTAGGTTAACA | 69957 |
rs29983341 | snp | C/T | 0.260355 | 0.249785 | intron-variant, synonymous-codon | Cdc16 | Mm_Celera | 8:13769688 | GTGATTCTCTTCCAG[C/T]CAGCTCGAGAGAAAA | 69957 |
rs29983454 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cdc16 | Mm_Celera | 8:13774069 | CGTTTCTCCACCTGG[A/G]ACAGTCTGCCTGACC | 69957 |
rs29983457 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cdc16 | Mm_Celera | 8:13774262 | CCAGTCCCCACATTC[C/T]GTCATTGAAACAATT | 69957 |
rs29983460 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cdc16 | Mm_Celera | 8:13774653 | AAATCCAGCCCTCAA[C/G]ACCTTGAAAAGATGA | 69957 |
rs29983463 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cdc16 | Mm_Celera | 8:13774911 | GCCACACCACATAGT[C/T]CATCCTTAGTATGCA | 69957 |
rs29984016 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756555 | CTCCTTAATATTCTG[C/T]AAGCATACACTTGTG | 69957 |
rs29984019 | snp | A/T | 0.48 | 0.0979796 | upstream-variant-2KB | Cdc16 | GRCm38.p3 | 8:13756604 | AAACCTGCAATGCAT[A/T]CTGCAAATAGCTCAA | 69957 |
rs29984022 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756638 | ATACACACTGCTAAT[C/T]GTTTGTTTGTCCCAA | 69957 |
rs29984126 | snp | C/G | 0.297521 | 0.245442 | synonymous-codon | Cdc16 | Mm_Celera | 8:13764589 | TAAGCCCAGTGAAAC[C/G]GTCATTCCCGAGTCA | 69957 |
rs29984129 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Cdc16 | Mm_Celera | 8:13765128 | CCCAAGAGGTGATAG[A/C]TTGAAATACCAATTT | 69957 |
rs29984132 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Cdc16 | Mm_Celera | 8:13765167 | GTTTTGTAAAATTTC[C/T]CATTGAGTACTGCTA | 69957 |
rs29984164 | snp | C/T | 0.336735 | 0.234472 | intron-variant, synonymous-codon | Cdc16 | GRCm38.p3 | 8:13769694 | CTCTTCCAGCCAGCT[C/T]GAGAGAAAAGGGAAT | 69957 |
rs29984167 | snp | A/G | 0.459184 | 0.136902 | intron-variant, synonymous-codon | Cdc16 | GRCm38.p3 | 8:13769751 | AGCCTTCTACTCTCC[A/G]TGCCCGTGAAGAATG | 69957 |
rs29984170 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Cdc16 | Mm_Celera | 8:13769769 | CCCGTGAAGAATGGA[C/T]GCCTTATAGTAAAAT | 69957 |
rs29984173 | snp | A/C | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Cdc16 | Mm_Celera | 8:13769815 | TTGCAGCTGTGTTCG[A/C]TGCTGTATATGCAGA | 69957 |
rs29984226 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cdc16 | Mm_Celera | 8:13775022 | GTTTTGGATTTGACA[C/T]TTCAGAGGATATCAA | 69957 |
rs29984229 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Cdc16 | GRCm38.p3 | 8:13775253 | ACTGAACAAACTCTA[G/T]AGAGTACTAGAAAGG | 69957 |
rs29984232 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cdc16 | Mm_Celera | 8:13775345 | CTAGAATGACCAAGG[A/G]AAGATGCATTGGTTT | 69957 |
rs29984835 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756745 | GAAGTGCAGGAGACA[C/T]ACGGAGACACAAACC | 69957 |
rs29984838 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756846 | TTGCTCTTTATAAGG[C/T]TTTCTTGGCTGGAGA | 69957 |
rs29984841 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB | Cdc16 | Mm_Celera | 8:13756983 | ACCATCTGTGGTGAC[A/C]GCACAAATTTCCTTT | 69957 |
rs29984886 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Cdc16 | Mm_Celera | 8:13770014 | TCACACCAGCTCTCA[C/T]GTGTTACTTTGCCAT | 69957 |
rs29984889 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Cdc16 | Mm_Celera | 8:13770055 | TCACCCTGCTGTAGT[A/G]TATAAACTGTCAGTC | 69957 |
rs29984892 | snp | C/T | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime | Cdc16 | Mm_Celera | 8:13770116 | AGCAACATACGGTTA[C/T]GTCATTTTTTTTTCT | 69957 |
rs29984995 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Cdc16 | Mm_Celera | 8:13775486 | TTAAATTTCTTTGGC[C/T]TGGCTGGACTCTGGG | 69957 |
rs29984998 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cdc16 | Mm_Celera | 8:13775504 | GCTGGACTCTGGGAT[A/G]AAACTGTGCTAGTTA | 69957 |
rs29985001 | snp | G/T | 0.32 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13776838 | GCTGGAGAATTTGAG[G/T]CTTGACTATCTGTTA | 69957 |
rs29985125 | snp | A/G | 0.18 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13765221 | GGTGCCCCGTCTTGC[A/G]TGTTAACTAGCTAAA | 69957 |
rs29985128 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Cdc16 | GRCm38.p3 | 8:13766284 | CCTTTATAATGAGCT[A/G]AAGTAAAGTGTTAGA | 69957 |
rs29985131 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cdc16 | Mm_Celera | 8:13766754 | AGAGCAAACTATTTC[C/T]CATCCTCCTGCTTCC | 69957 |
rs29985485 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-3-prime | Cdc16 | GRCm38.p3 | 8:13770197 | ATTTTTTACTGTAGT[A/G]TGTATTCACTTCCAC | 69957 |
rs29985489 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Cdc16 | Mm_Celera | 8:13770391 | AGTACTTCACTTTAA[C/T]TCTGTCCCTACGTGC | 69957 |
rs29985492 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Cdc16 | Mm_Celera | 8:13770552 | ACTGCAGTCACGTCA[C/T]TTATGTTGACTGACC | 69957 |
rs29985744 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cdc16 | Mm_Celera | 8:13777127 | CACCCAGATAAGGAC[A/G]TGCCAGGAAATAAAT | 69957 |
rs29985747 | snp | C/T | 0.32 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13777310 | TATGTTTTAAGATGG[C/T]GAAATCCATAAAAGT | 69957 |
rs29985750 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cdc16 | Mm_Celera | 8:13777369 | TATTTCTCAGGAAAG[A/G]CTGAAGATTCACAAG | 69957 |
rs29985753 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Cdc16 | Mm_Celera | 8:13777565 | AGGGTACATCCACAG[C/T]CTGATGGGCAACTTT | 69957 |
rs29985854 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cdc16 | Mm_Celera | 8:13766916 | GAAAGTGGAAAGGAG[C/T]AGATATTTCCCATGT | 69957 |
rs29985857 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Cdc16 | Mm_Celera | 8:13767162 | ATATGTGGCGGCTAT[A/G]GGATATGTTGCCATG | 69957 |
rs29985860 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Cdc16 | Mm_Celera | 8:13767196 | TGCTAAGACGTGCAC[A/G]TTTCTTTAGCACTTG | 69957 |
rs29985863 | snp | C/T | 0.18 | 0.24 | intron-variant | Cdc16 | Mm_Celera | 8:13767288 | CTGTGGCATGAGGAG[C/T]GTCAGTCTCTCAGAT | 69957 |
rs29986445 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Cdc16 | Mm_Celera | 8:13770567 | TTTATGTTGACTGAC[C/T]CACTTATTTTCCACG | 69957 |