SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6164926 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Dcaf5 | Mm_Celera | 12:80358567 | GTAAGGTACATAATA[C/G]TAAGTCAGCTTTCTT | 320808 |
rs6213694 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Dcaf5 | Mm_Celera | 12:80432503 | CCTCTCCCTTGCTGT[C/T]CCTCACTGTCCTCTG | 320808 |
rs6214552 | snp | C/T | 0.5 | 0 | intron-variant | Dcaf5 | Mm_Celera | 12:80432644 | TTAGTTACAAAAAAG[C/T]GGGCCTGCCCAACTA | 320808 |
rs6214639 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Dcaf5 | Mm_Celera | 12:80432706 | TCTGTCAAGGGTATC[A/T]TGTCTCTCTAAGGGC | 320808 |
rs6215041 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Dcaf5 | Mm_Celera | 12:80432734 | GGCTTTCACCAATCC[A/T]GATCAAGATACAACA | 320808 |
rs6320240 | snp | C/T | 0.290657 | 0.246672 | synonymous-codon | Dcaf5 | GRCm38.p3 | 12:80339566 | AGTGGGCCGCTCATC[C/T]CGGGCTGTCTTTTGT | 320808 |
rs6321915 | snp | C/T | 0.5 | 0 | synonymous-codon | Dcaf5 | Mm_Celera | 12:80339851 | ATCCTCACATGTTGG[C/T]GTTGCTGGGGTTGAC | 320808 |
rs6321947 | snp | A/G | 0.359862 | 0.224567 | missense | Dcaf5 | GRCm38.p3 | 12:80339867 | GTTGCTGGGGTTGAC[A/G]CCACTGCATTTGTGG | 320808 |
rs6378815 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Dcaf5 | GRCm38.p3 | 12:80336920 | CCACCCTACTCAGGC[A/G]CCTTCCTTCCTCTCC | 320808 |
rs6379829 | snp | C/T | 0.359862 | 0.224567 | utr-variant-3-prime | Dcaf5 | GRCm38.p3 | 12:80337071 | GCACTGAGCAGCATC[C/T]GTCCGTCTGTCCGTC | 320808 |
rs13481555 | snp | C/T | 0.455 | 0.143091 | intron-variant | Dcaf5 | Mm_Celera | 12:80348923 | GATAACACAAAGAAC[C/T]CTTCCTTTGCCCTTG | 320808 |
rs29161575 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dcaf5 | Mm_Celera | 12:80352104 | AGTGAAAAGTGCTTA[C/T]TGCACATGTGTGAAG | 320808 |
rs29212408 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Dcaf5 | Mm_Celera | 12:80431588 | GTCACAAAACTATAC[A/G]GTCTGCCCAATTTGC | 320808 |
rs32635746 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Dcaf5 | Mm_Celera | 12:80426791 | ACTGATTGGTGTTTT[A/G]TCTACATGTGAGTCT | 320808 |
rs32635749 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80427487 | GCCACTACCCACCTA[A/C/T]CAGCACTTGGAGACT | 320808 |
rs32635751 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80427721 | TGATTGGACAAAAAG[G/T]TAGAGCCTAGGCAAG | 320808 |
rs32635753 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80427958 | CCTAGCCGGGTTATA[A/G]TAGTCTCAGAATCTT | 320808 |
rs32636536 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Dcaf5 | Mm_Celera | 12:80428088 | AAAAAAATTACTTCT[A/G]TAGGTAAACATACTT | 320808 |
rs32636539 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80428123 | CACAAGCCTGGAGAC[A/C]TGAATTCTATCCCTG | 320808 |
rs32636540 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80428474 | ATCACACACAGTCAA[C/T]TTATCTAACAGTAAG | 320808 |
rs32636542 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80428674 | CAAAGCCTACCCGGA[C/T]TTCATAAAACCAATC | 320808 |
rs32637395 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80428733 | TGACCAATATTCTAG[A/G]AAAAAAACAAAGACC | 320808 |
rs32637397 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80428780 | TAGCTCAGCTTCACA[A/C]TGGAGACTCAGCAGG | 320808 |
rs32637400 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80428814 | GACTGCCCAACTCTA[C/T]TCTGTAAAATCTCCC | 320808 |
rs32637403 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80428837 | AATCTCCCCTTATGG[A/G]ACACCATCAGTTTAA | 320808 |
rs32638105 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80429698 | ACTGCAAAGATTCTA[A/T]TTACACAAACCTTTA | 320808 |
rs32638108 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Dcaf5 | Mm_Celera | 12:80429947 | AAGAAGGTAATTTAT[A/G]AATCCATGTCCGATA | 320808 |
rs32638110 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80430305 | CAATCCTAATGCTAT[C/T]AATAAGGTTAGCACT | 320808 |
rs32638112 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80430700 | GTTTATGTGGTGCTA[A/G]TGCCAGGGCTCAGGG | 320808 |
rs32639024 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf5 | Mm_Celera | 12:80431202 | CTAACAGGTTAAATC[C/T]AGGTGTTCCCTATGG | 320808 |
rs32639027 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80431718 | ACAATAACCCCTCAG[G/T]TAGGCCTGAAATTCC | 320808 |
rs32639030 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Dcaf5 | Mm_Celera | 12:80432359 | CTCAGTCCCAAGGAG[C/G]TCCAAAGGCACCAGA | 320808 |
rs32639032 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80432383 | CACCAGACATAGACA[C/T]GGGACAGACATACAT | 320808 |
rs32639871 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Dcaf5, Gm30025 | Mm_Celera | 12:80432951 | AAGGAGTTCATTGGC[C/T]AACCTCAGCTACACA | 320808 |
rs32640382 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80424903 | CAAAAAGATTAAGAC[C/T]GAGTAATGGCAAGGC | 320808 |
rs32640644 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dcaf5, Gm30025 | Mm_Celera | 12:80433171 | CAAAAGCAAGCAGAA[C/T]GTATCGTTAACACAA | 320808 |
rs32640647 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dcaf5, Gm30025 | Mm_Celera | 12:80433306 | CAGGAAGGACTAAGA[A/G]CTGGGACAGGAGTAG | 320808 |
rs32640650 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dcaf5, Gm30025 | Mm_Celera | 12:80433492 | AGCCTGAGCCATGCG[C/T]CCAGTCCTTTCCTAC | 320808 |
rs32640653 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dcaf5, Gm30025 | Mm_Celera | 12:80433757 | TCAGGCCTGCCTGAA[C/T]TACAACAGACTCATT | 320808 |
rs32641175 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80424999 | TAGGAATCATTAGTA[A/G]GTTTTAGACTAGCCT | 320808 |
rs32641178 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80425244 | GTTTTTGAGAATTTC[A/G]TTTTACAGCAACTTT | 320808 |
rs32641181 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | GRCm38.p3 | 12:80426171 | TTTTCCTTTAATTAA[C/G/T]TGTGTTTGTGTATTT | 320808 |
rs32641465 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dcaf5, Gm30025 | Mm_Celera | 12:80434131 | TCATCCCAGCAGAGA[A/G]AGGCAGGCAGATCAA | 320808 |
rs32641467 | snp | C/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Dcaf5, Gm30025 | Mm_Celera | 12:80434153 | GCAGATCAAGGCCAG[C/T]AGAACTACACAGAGA | 320808 |
rs32641470 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dcaf5, Gm30025 | GRCm38.p3 | 12:80434361 | ATTAGTAATGATTAA[A/C/T]TAGTTCGTTATAAGA | 320808 |
rs32641472 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dcaf5, Gm30025 | Mm_Celera | 12:80434434 | GGGAGAGCCGCTCAT[C/T]GGTTAATACATTAAT | 320808 |
rs32641874 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Dcaf5 | Mm_Celera | 12:80426413 | TTTAGCAAATATTTG[C/T]AAAAATTATAACTAG | 320808 |
rs32641877 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80426498 | TTTCAATCTCCAACA[G/T]GCACGCGCATGCACA | 320808 |
rs32641880 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Dcaf5 | Mm_Celera | 12:80426780 | TTTTTATGTGCACTG[A/T]TTGGTGTTTTATCTA | 320808 |
rs45646958 | snp | G/T | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80355448 | TTAAGTTCCCAGCAG[G/T]GTTAAGGATCTGCCC | 320808 |
rs45664056 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80396859 | TAAATGAGAACCTTG[C/T]TTATTTTTCCATGGC | 320808 |
rs45666418 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80398018 | AAAGGGGAAAATGAG[C/T]TGTCTACAGAAGTAA | 320808 |
rs45686452 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Dcaf5 | Mm_Celera | 12:80411271 | AACACAGAAGACTTA[G/T]CTCAGCACACTTAGC | 320808 |
rs45719063 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Dcaf5 | GRCm38.p3 | 12:80376584 | GTAACCCTGATTGTC[A/G]AACTGGAACACTGGC | 320808 |
rs45726921 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80413803 | GCATCCAGAGATAGC[A/G]TAGAGGGCTGTCTTA | 320808 |
rs45783540 | snp | C/G | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80399211 | TGTTTTCATTTATCA[C/G]TTGTATGGAGATTTG | 320808 |
rs45801539 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80396333 | TGGGGATTCCAGGGG[C/T]AGATCAGAATTAAGA | 320808 |
rs45809169 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80364312 | TGGCATCACCGTTTC[C/T]GTGCCTCTCTTCCTC | 320808 |
rs45811483 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80390204 | GGGGCAAGCTTTTAA[A/G]GATCTGCCAGGGAGG | 320808 |
rs45824401 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Dcaf5 | Mm_Celera | 12:80407713 | GAAAACCATCTAAAC[A/G/T]CCTACCAACTGAAGT | 320808 |
rs45843682 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Dcaf5 | GRCm38.p3 | 12:80338197 | CAAGCCCACATGTGC[C/T]AGTGGACACACACAC | 320808 |
rs45860619 | snp | G/T | | | intron-variant | Dcaf5 | Mm_Celera | 12:80413298 | TTTTTGTTGTTGTTG[G/T]TTTTGGTTTTTCGAG | 320808 |
rs45891533 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80411470 | AATGTTGTTATGGAA[C/T]TGACAATCTAAAAAC | 320808 |
rs45903176 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80356534 | CAGTCTTCAGGTAAG[A/G]ACCACTAGGTCATTC | 320808 |
rs45940542 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80385860 | ATATCAGGGCTGGTT[C/T]TTACTGCAAGCAGAG | 320808 |
rs45957525 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80354034 | CACAGTAGTTCTCCC[A/C]ATTTCTCTCGTGAGA | 320808 |
rs45984674 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dcaf5 | Mm_Celera | 12:80350090 | CTTTTAGTTCTGTTG[C/T]TGAGACTCTGGGAGA | 320808 |
rs45986592 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80389699 | CTTTACTAGAATACC[C/T]GGCCTTGTCTCTTAC | 320808 |
rs46108804 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80349930 | AGTGAAGCTTGGCAC[A/G]TTATATCACAACATC | 320808 |
rs46109644 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Dcaf5 | Mm_Celera | 12:80375978 | AGAGGCAGTAACTTA[A/C]ATCCTCTTTCATCCA | 320808 |
rs46113236 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf5 | GRCm38.p3 | 12:80350876 | TGAACCTGAAAAAGG[C/T]TCTAATGATAGGACA | 320808 |
rs46127313 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf5 | GRCm38.p3 | 12:80375371 | GTCAGAGCCTATGAA[C/T]GAATCGAATCACCTT | 320808 |
rs46142086 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Dcaf5 | Mm_Celera | 12:80406707 | AGTTTTGTTGAAACG[C/T]TGGAATCTAAATGAA | 320808 |
rs46142201 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80355563 | CTTGGAGGAGGAAGC[G/T]AGAGCTATAACCTGC | 320808 |
rs46151698 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80363971 | GGGAACTGCATTCAA[A/G]CGGATTGGCACATCT | 320808 |
rs46178848 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Dcaf5 | Mm_Celera | 12:80335787 | TAAAACAGCAAAGAA[A/G]TGAAGGAAGAGGGTG | 320808 |
rs46207463 | snp | G/T | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80341696 | GACTTCCAGTTCACA[G/T]GAGGCTTATGACACC | 320808 |
rs46218078 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80401047 | CTCTCAAGTGCATAG[C/T]CCAAAGCCACCTAAG | 320808 |
rs46238425 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80341443 | TCTGCCTGACAGCCA[A/G]ACAGGTCCACAGGAT | 320808 |
rs46263043 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80376296 | TTCTCAGAGTCCATT[C/T]ACAAATGTGGCAGAG | 320808 |
rs46291698 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Dcaf5 | Mm_Celera | 12:80349849 | TACTGGTTAAAGTAG[A/G]CTGACATGGTGGGAT | 320808 |
rs46301059 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80361663 | GCTTAACAATCAAAA[A/T]CACTGCAAGTCAGGT | 320808 |
rs46336239 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80409666 | AATGAGATCCTGCTT[A/G]GGAAGAAGGGAAAAG | 320808 |
rs46368940 | snp | A/G | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80348159 | TTAACCTTGGCTCTA[A/G]GTGTCAGGTTTACAG | 320808 |
rs46371199 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80349320 | TGTTAATTGGACAGC[A/G]GATACTTTGTGCCTC | 320808 |
rs46389357 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80416760 | AACAAAAATAAAAAA[A/C]ATACCATCTTCATTT | 320808 |
rs46395641 | snp | C/T | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80348266 | TGTTCTAATTTCTTC[C/T]AGTTATGAACTACAA | 320808 |
rs46401012 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80360449 | GCAAGGCTAGACTCC[C/T]GAGAGAGGCAGGCTT | 320808 |
rs46414024 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80355942 | GTCTCTTTGGACACA[C/T]GTAACCACTTCAGAG | 320808 |
rs46433780 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80340625 | CAGCTTTCAGAGGTT[G/T]GTAAAAGCAGCTTAG | 320808 |
rs46435385 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Dcaf5 | GRCm38.p3 | 12:80340079 | GCCCTCAATTTCACG[A/G]CGCACCAAGGAGTCA | 320808 |
rs46444263 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80390048 | TTCTGGGTAGTGACC[C/T]TTGCACCTGGGAAAG | 320808 |
rs46473745 | snp | C/G | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80357820 | ATACCTTAGACAATA[C/G]CAGTTTTTGAGAATC | 320808 |
rs46580213 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf5 | Mm_Celera | 12:80353581 | TAACATGACAGCATG[C/T]GATGTTATCAGAGGC | 320808 |
rs46628641 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dcaf5 | Mm_Celera | 12:80352506 | TAAGATGCTCTGGCA[G/T]TGTAGGTACAGTGGG | 320808 |
rs46639476 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Dcaf5, Scarna3b, Mir1843a | Mm_Celera | 12:80392612 | CAGGCTGGCCATTCA[A/G]GTAAAGATGACCTTT | 320808 |
rs46692606 | snp | A/T | 0.32 | 0.24 | intron-variant | Dcaf5 | Mm_Celera | 12:80361989 | TTTGGTAGTGATGTT[A/T]TTCACTCAACAACAC | 320808 |
rs46759270 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Dcaf5 | Mm_Celera | 12:80337358 | AATCACCACTACACA[C/T]TGGAAGTTTGATATT | 320808 |
rs46764609 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Dcaf5 | Mm_Celera | 12:80408534 | CCTTTCAAATTCTTT[C/T]AGGTAATACAGGACT | 320808 |
rs46774297 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Dcaf5 | Mm_Celera | 12:80349274 | CAGCTAATAAGGCAG[A/C]GCATGAGGCATCCAG | 320808 |