SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6318812 | snp | C/T | 0.5 | 0 | intron-variant | Wdr66 | GRCm38.p3 | 5:123265594 | atgttctcttctact[C/T]cccgtgggtgcagag | 269701 |
rs6319258 | snp | A/G | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123265654 | caagcaccttcattc[A/G]ctgagccatntcacc | 269701 |
rs6319270 | snp | C/T | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123265664 | cattcnctgagccat[C/T]tcaccttccccAAAG | 269701 |
rs6319311 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Wdr66 | Mm_Celera | 5:123265692 | AAGTCTCTGTTTTTA[A/G]ACAACATTACCCTTT | 269701 |
rs6319844 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Wdr66 | GRCm38.p3 | 5:123265785 | CTGTGTGGGTCAGTG[C/G]GACATGGATCAGATA | 269701 |
rs13478499 | snp | A/G | 0.45088 | 0.14882 | synonymous-codon | Wdr66 | GRCm38.p3 | 5:123288711 | GGTCTGGGAGTATTT[A/G]GCAAGACTTCGCTCT | 269701 |
rs29507247 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr66 | Mm_Celera | 5:123257984 | CTTTGTTTTTATTTT[A/T]AAAATCTGCGGTGCC | 269701 |
rs29530419 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr66 | Mm_Celera | 5:123276024 | TTTATACCATCTTCA[A/G]TTCTTTTTTTGAGCA | 269701 |
rs29532708 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr66 | GRCm38.p3 | 5:123289141 | ATCTGCTGGCTTGCT[C/T]TCCATAGCGGCTTGC | 269701 |
rs29543113 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | Mm_Celera | 5:123269675 | GCCTCCCAAGTGCTG[A/G]GATTAAAGGTGTATA | 269701 |
rs29545289 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr66 | GRCm38.p3 | 5:123272657 | TGAATTCAATCACTT[C/T]CCCCAAATTGATCAT | 269701 |
rs29545670 | snp | A/G | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123263258 | CAGCCACTTAGACTC[A/G]GTTTCTCATTACTGT | 269701 |
rs29560212 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Wdr66 | GRCm38.p3 | 5:123259266 | TGGGTCCATGGTCTT[A/C]GACCAGCAGCCTTAG | 269701 |
rs29579326 | snp | G/T | 0.455 | 0.143091 | intron-variant | Wdr66 | GRCm38.p3 | 5:123259636 | ATACAAACACATGAG[G/T]TAACTTATACCCCAC | 269701 |
rs29581268 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr66 | GRCm38.p3 | 5:123291951 | ACCCCCTCACCCCCA[C/T]CCCCAAGCTCTTTTC | 269701 |
rs29582296 | snp | A/G | 0.5 | 0 | intron-variant | Wdr66 | GRCm38.p3 | 5:123289523 | GGTTGAATTAGTTCC[A/G]AAGGTAACGGGCAGA | 269701 |
rs29631146 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Wdr66 | GRCm38.p3 | 5:123292188 | AGGAGGAAAATGACC[A/G]CATCCTTACATCCAG | 269701 |
rs29631452 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Wdr66 | Mm_Celera | 5:123259754 | ATATGAAGGCAGTCC[C/T]GTGTTAATCTTGGAA | 269701 |
rs29639214 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Wdr66 | GRCm38.p3 | 5:123270925 | TGCCCTGCCAGAGAA[C/G]GTTTGGGGCTGCAGT | 269701 |
rs29671572 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123276666 | ACTTACAGTACAGGA[C/T]AGATCCCCACAGCAC | 269701 |
rs29677257 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr66 | Mm_Celera | 5:123276098 | TTAAATTTATTCCTG[C/T]ATCTTTTTTTTCTTC | 269701 |
rs29682473 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Wdr66 | GRCm38.p3 | 5:123263841 | CCTGTTGACTGGGTT[A/G]AGCTGAGATCACCAA | 269701 |
rs29683670 | snp | G/T | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123279189 | ATTTATTTATTATAT[G/T]TAAGTACACTGTAGC | 269701 |
rs29726651 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Wdr66 | GRCm38.p3 | 5:123294169 | AATCAGTTCCCAGCG[C/T]CTTGGCTAAACTTGA | 269701 |
rs29727342 | snp | A/G | 0.5 | 0 | intron-variant | Wdr66 | GRCm38.p3 | 5:123262355 | GTGTCTGAAGACAGC[A/G]ACAGTGTACTCATAC | 269701 |
rs29727565 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr66 | Mm_Celera | 5:123275997 | GTCTTGCTGTTTTGT[C/T]TTGTTTTGTTTTTTA | 269701 |
rs29733009 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr66 | GRCm38.p3 | 5:123293804 | GGTCTTGCCTCAGCA[C/T]ATGCATCTAATCAGC | 269701 |
rs29733489 | snp | A/T | 0 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123323606 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 269701 |
rs29733560 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123269232 | TTTTCTGGCCATGGA[C/G]CCCCCATTGCAGAGA | 269701 |
rs29778070 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Wdr66 | GRCm38.p3 | 5:123263535 | CCCCTCTCCTTGTGC[A/G]CATCCTCTAGGCCTG | 269701 |
rs29781646 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr66 | Mm_Celera | 5:123323608 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 269701 |
rs29781908 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123277599 | CCAAAGCCTCACGTT[C/T]GTTCCAAGATCTCCC | 269701 |
rs33056435 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Wdr66 | GRCm38.p3 | 5:123259710 | TTTGTTGTCAGAAAC[C/T]GTGAATGTAGTTCCA | 269701 |
rs33064123 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr66 | Mm_Celera | 5:123261568 | CCTAACCTTTCCATG[A/T]CCAATCTCTCCCTTT | 269701 |
rs33077754 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr66 | Mm_Celera | 5:123271256 | CAGAATAGGCTAACG[A/T]ACGTAAAAACAGGGA | 269701 |
rs33134256 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr66 | Mm_Celera | 5:123280651 | TGCGAAATACAGTCA[C/G]TGGTTATGACTCCTG | 269701 |
rs33138843 | snp | C/T | 0.49827 | 0.0293608 | synonymous-codon | Wdr66 | Mm_Celera | 5:123287250 | CGTGGAACCCAGGGA[C/T]GCTGTCTATGCCGTC | 269701 |
rs33143307 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123293841 | GCACAGAAGCAGCAA[A/G]AAACTGCAGTACATC | 269701 |
rs33147942 | snp | C/T | 0.255 | 0.24995 | intron-variant | Wdr66 | Mm_Celera | 5:123270808 | ACTTTTCTCATAATC[C/T]TCTCCACGAGTCAGT | 269701 |
rs33161796 | snp | A/G | 0.5 | 0 | intron-variant | Wdr66 | GRCm38.p3 | 5:123263886 | GAGGAAGCTGGCTGG[A/G]GTGGGCACACAACTC | 269701 |
rs33205013 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wdr66 | GRCm38.p3 | 5:123270325 | CTGGAATCCACTGTG[A/T]AGCCCAGACTAGCCT | 269701 |
rs33215288 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr66 | GRCm38.p3 | 5:123272658 | GAATTCAATCACTTC[C/T]CCCAAATTGATCATA | 269701 |
rs33248725 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Wdr66 | GRCm38.p3 | 5:123287901 | TTGCGGGCAGCAAGA[A/G]CAGGGCCTTAGAATG | 269701 |
rs33250161 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123263844 | GTTGACTGGGTTGAG[A/C]TGAGATCACCAAGTT | 269701 |
rs33298255 | snp | G/T | 0.42 | 0.183303 | intron-variant | Wdr66 | GRCm38.p3 | 5:123270878 | TCCCTCCGTGAACTC[G/T]GTGTTGCCATCCCAA | 269701 |
rs33317228 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Wdr66 | Mm_Celera | 5:123270597 | CAGAACAGCCTCTGA[A/G]TAATATTTTATGGGC | 269701 |
rs33329837 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | Mm_Celera | 5:123269694 | TAAAGGTGTATACCA[C/G]CAAGCCTGGCTAAAA | 269701 |
rs33342843 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr66 | Mm_Celera | 5:123272701 | TGGATGTTGAAGGTT[C/G]GAACCTTACAGTATC | 269701 |
rs33343476 | snp | C/T | 0.5 | 0 | intron-variant | Wdr66 | GRCm38.p3 | 5:123294042 | CGTTCCTTCACGAGT[C/T]GGCCTGAGCCCTTCA | 269701 |
rs33362448 | snp | C/T | 0 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123279313 | TGGAAGAGCAGTCGG[C/T]GCTCTTAACCACTGA | 269701 |
rs33391201 | snp | A/T | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123260187 | CCCCCCCCCTTTTTT[A/T]AAATTAATTTGTGAT | 269701 |
rs33393893 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123262231 | ACTCAGGGGCTGGAG[A/G]GAGCGGTTAAGAGCA | 269701 |
rs33405786 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr66 | Mm_Celera | 5:123270547 | CTTAAGGGGAAAAAA[A/T]TTTTTTTTCTCTTTG | 269701 |
rs33406679 | snp | A/C | 0.5 | 0 | intron-variant | Wdr66 | GRCm38.p3 | 5:123267716 | AAGAGGGCGTCAGAT[A/C]TCATTACAGATGGTT | 269701 |
rs33432628 | snp | C/G | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123260259 | CAGCTCCGTGGAGTT[C/G]CTTCTCTCCACTGTC | 269701 |
rs33463989 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Wdr66 | GRCm38.p3 | 5:123289527 | GAATTAGTTCCGAAG[A/G]TAACGGGCAGAAGTT | 269701 |
rs33476010 | snp | A/C | 0.42 | 0.183303 | intron-variant | Wdr66 | GRCm38.p3 | 5:123259690 | GTGAGCTATGAGCTT[A/C]ACCCTTTGTTGTCAG | 269701 |
rs33477647 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Wdr66 | Mm_Celera | 5:123271091 | GCCACTTGACCCTGG[C/T]TCCCAGTGACCTCCC | 269701 |
rs33497096 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr66 | Mm_Celera | 5:123270444 | ACAGTAGTTGCGAGC[C/T]AGTGTGGGATCTTGC | 269701 |
rs33504842 | snp | C/T | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Wdr66, LOC105246787 | Mm_Celera | 5:123253543 | ATGCATTTTGTTGCC[C/T]GTGGGAATATGAATT | 269701 |
rs33505680 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr66 | Mm_Celera | 5:123269697 | AGGTGTATACCAGCA[A/C]GCCTGGCTAAAAGAA | 269701 |
rs33519687 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123264149 | ACGCTAAGGAAGTCA[C/T]GATGAGAGACACTGT | 269701 |
rs33546289 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Wdr66 | Mm_Celera | 5:123270439 | TGGCTACAGTAGTTG[C/T]GAGCCAGTGTGGGAT | 269701 |
rs33550162 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123276751 | CTTCCGAGAAGGGAG[A/G]CAGTAACATGGCTCA | 269701 |
rs33550229 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr66 | Mm_Celera | 5:123259411 | TCAGCTTTCATTTTT[A/T]AAAAATATTTATTTA | 269701 |
rs33554347 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Wdr66 | Mm_Celera | 5:123271172 | GGTGTTTACAGCGGC[A/G]TCTGGTTGAATTCTG | 269701 |
rs33569302 | snp | A/G | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123272653 | CTTCTGAATTCAATC[A/G]CTTCCCCCAAATTGA | 269701 |
rs33581783 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123287827 | GGACAGTGGGGTTAC[A/G]TCCCAATCAAGCTGT | 269701 |
rs33582323 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123278974 | TTTTTAGTTTTGTGG[C/T]TTTTTTGTTTGTTTG | 269701 |
rs33587869 | snp | A/T | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123265084 | AACAGGAACCTTTTT[A/T]AAAAAGATTTATTTA | 269701 |
rs33593315 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Wdr66 | GRCm38.p3 | 5:123263651 | ATCCACTGCCGACGT[C/G]GTTATTCATTCTGCG | 269701 |
rs33622180 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Wdr66 | GRCm38.p3 | 5:123264055 | CGGAATTCCCAGTCT[A/G]TGATCCAAAGAGGCA | 269701 |
rs33629943 | snp | C/T | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123260384 | TTTTTAAAAAAAATT[C/T]ATTTATTTATTTATT | 269701 |
rs33650682 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr66 | Mm_Celera | 5:123260547 | CCCTTTAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 269701 |
rs33655245 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdr66 | Mm_Celera | 5:123264933 | CAGAGGATCGGCCCC[C/T]GTGGCCAGGAAAGGG | 269701 |
rs33657906 | snp | A/C | 0.32 | 0.24 | intron-variant | Wdr66 | Mm_Celera | 5:123270443 | TACAGTAGTTGCGAG[A/C]CAGTGTGGGATCTTG | 269701 |
rs33660855 | snp | A/C | 0.5 | 0 | intron-variant | Wdr66 | Mm_Celera | 5:123263358 | CTAGCCCAAACTGGG[A/C]TAATAATATAATTAT | 269701 |
rs33669951 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr66 | GRCm38.p3 | 5:123269395 | CGGTGTGGTGCTCGT[C/T]GTTGGGATAGCAGCA | 269701 |
rs33671758 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | Mm_Celera | 5:123270147 | AACTGAATATATCAC[A/G]TTTCTATATCCAGGT | 269701 |
rs33680118 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123276758 | GAAGGGAGGCAGTAA[C/G]ATGGCTCAGTGAGTA | 269701 |
rs33681054 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Wdr66 | GRCm38.p3 | 5:123286219 | ACTATGGAACAGCCT[G/T]GTGTTTTTCTCTATT | 269701 |
rs33681891 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr66 | Mm_Celera | 5:123294628 | CGCCCAACCACTGTT[G/T]GGGGGGGGGGTGTAA | 269701 |
rs33698733 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Wdr66 | GRCm38.p3 | 5:123269194 | CAGGCCTGAGGTCCC[C/T]GTGGGCTGTGTGGCG | 269701 |
rs33707354 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Wdr66 | GRCm38.p3 | 5:123263766 | ACTAGGTAGTACTCA[C/T]CGTTGGTACCGGTGA | 269701 |
rs33712228 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr66 | GRCm38.p3 | 5:123280058 | GTGTAGACTTAGTGG[A/G]TGTGGGCTATATCTT | 269701 |
rs33719180 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr66 | GRCm38.p3 | 5:123288858 | ATTGATCACCAGCAC[A/G]GTCCTCCTTCCCACC | 269701 |
rs33725165 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr66 | Mm_Celera | 5:123270154 | TATATCACGTTTCTA[C/T]ATCCAGGTTAATTTT | 269701 |
rs45650097 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr66 | Mm_Celera | 5:123304712 | TCAGGTGGGTGAGAT[A/G]GGATTTCTAACCCTC | 269701 |
rs45679815 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr66 | Mm_Celera | 5:123309787 | CTAGGTACAGCCTGA[A/G]GTCAGCTAGGGCCTC | 269701 |
rs45738309 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr66 | Mm_Celera | 5:123288469 | TGCCTTGATCTATGA[C/T]CCAGTAGCCTTAGTC | 269701 |
rs45803482 | snp | A/C/G/T | 0.459184 | 0.136902 | intron-variant | Wdr66 | GRCm38.p3 | 5:123276408 | ACACACAGCCCTTCC[A/C/G/T]TTCTTATAGCGGTTA | 269701 |
rs45825243 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr66 | Mm_Celera | 5:123274577 | AAAGTCACCCTGCCA[A/G]GCGTAGCGTTTCTTA | 269701 |
rs45940869 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr66 | Mm_Celera | 5:123299035 | CAGGAAGTGGTTCTC[A/G]GTATCTGCACATAGT | 269701 |
rs45972714 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr66 | Mm_Celera | 5:123262538 | TAACTTTCGTATAGA[C/T]TTTGCCTTGGATCCC | 269701 |
rs45973724 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr66 | Mm_Celera | 5:123300068 | CCCGAAAGGCACCCA[A/G]GCTGACCCTCTCATC | 269701 |
rs45989836 | snp | C/T | | | intron-variant | Wdr66 | GRCm38.p3 | 5:123290209 | TAACATAAGGCAAGG[C/T]GTATTCACCCAAGAG | 269701 |
rs45990592 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr66 | Mm_Celera | 5:123269057 | TGCCAAGCATAAATC[C/T]GATTTTGTAGCTCTC | 269701 |
rs46003628 | snp | A/C | 0.132653 | 0.220748 | synonymous-codon | Wdr66 | Mm_Celera | 5:123256180 | GAGTGCGGAGGAGTC[A/C]CTGGTGTCTGTCTCC | 269701 |
rs46005504 | snp | A/G | | | intron-variant | Wdr66 | GRCm38.p3 | 5:123266542 | CATTTATTTATTTGT[A/G]TGTGTCTGCCCATGC | 269701 |
rs46050649 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Wdr66 | Mm_Celera | 5:123271221 | ATGAACTGCACTGTT[C/G]GGGAGTCTCAGCAGT | 269701 |