SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6217060 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Wdr27 | Mm_Celera | 17:14811974 | GCCTGCAGAGAAAGC[C/T]GCTTTGTGTTATTTT | 71682 |
rs6217097 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Wdr27 | Mm_Celera | 17:14812001 | TTTTTCTCATCAACT[C/G]AAAACATTCAAGTGC | 71682 |
rs6217523 | snp | C/T | 0.5 | 0 | intron-variant | Wdr27 | Mm_Celera | 17:14812049 | TGGAGAGAGCATAAT[C/T]GTTACTCTAAANGCG | 71682 |
rs6217542 | snp | C/T | 0.5 | 0 | intron-variant | Wdr27 | Mm_Celera | 17:14812061 | AATNGTTACTCTAAA[C/T]GCGGCCCTTTGTGCA | 71682 |
rs6217580 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Wdr27 | Mm_Celera | 17:14812090 | CAGAAATGGCCTCTT[C/T]CCTTATCCTTGTGCA | 71682 |
rs6232569 | snp | A/G | 0.5 | 0 | intron-variant | Wdr27 | Mm_Celera | 17:14812478 | TAGAAATGTGTATGC[A/G]TTAACATTGTAAGTA | 71682 |
rs6280790 | snp | C/T | 0.5 | 0 | intron-variant | Wdr27 | Mm_Celera | 17:14857186 | TAAGAATTGCAATGC[C/T]CTAGGGCCATCTGGC | 71682 |
rs6280838 | snp | A/G | 0.5 | 0 | intron-variant | Wdr27 | Mm_Celera | 17:14857209 | CATCTGGCAAGATAT[A/G]TACTTTGCTAAATCG | 71682 |
rs6302985 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14937954 | GTCTTTCTTAGGCCC[A/C]AGTGTGAAGCTTATG | 71682 |
rs6351251 | snp | C/T | 0.5 | 0 | intron-variant | Wdr27 | Mm_Celera | 17:14831619 | tgttttatgtatgta[C/T]ttctagttatgatta | 71682 |
rs13482888 | snp | A/G | 0.334252 | 0.235376 | intron-variant | Wdr27 | Mm_Celera | 17:14923629 | AGGCTGAGAAACACT[A/G]TATGTCCTAACTAAG | 71682 |
rs29504097 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr27 | Mm_Celera | 17:14832756 | GATCCCTAATGTAAA[A/G]TGTCACGTCATCAGC | 71682 |
rs29522298 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr27 | Mm_Celera | 17:14851623 | GGGAGGAGAATTGCT[A/G]TAAAACTCAAAGGCA | 71682 |
rs29528537 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Wdr27 | Mm_Celera | 17:14793877 | ATTGCAGGATCTGTG[C/T]AGTTATCCACAGTCA | 71682 |
rs33062015 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Wdr27 | Mm_Celera | 17:14925854 | TGCATGCTTTAAATT[A/G]CATTCATTTTTATTT | 71682 |
rs33083132 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Wdr27 | Mm_Celera | 17:14820912 | GAATCATGCCCTTGC[C/T]GCCAACATCCATGTT | 71682 |
rs33091770 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14785007 | AGTTATAAGGCTCTG[C/T]GTGTGCAGTACAATC | 71682 |
rs33092670 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Wdr27 | GRCm38.p3 | 17:14926544 | GCTCATGTGTATATG[C/T]GCACAAACATACATA | 71682 |
rs33120017 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14941586 | GGTTTTTTGTTGTTG[G/T]TGTTGTTGTTTGTTT | 71682 |
rs33126047 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Wdr27 | Mm_Celera | 17:14789261 | TTCATTCTGCTTAAT[A/T]GTAGCATCATATGCA | 71682 |
rs33137434 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr27 | GRCm38.p3 | 17:14797200 | GGCCTCTTTCCTTTG[C/T]GGGGCCTTTGAGGGC | 71682 |
rs33138338 | snp | A/G | 0.255 | 0.24995 | intron-variant, upstream-variant-2KB | Wdr27 | Mm_Celera | 17:14924998 | TTGTAGAGGGTGACC[A/G]CCTGCAGGACTGCAT | 71682 |
rs33144195 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr27 | Mm_Celera | 17:14923293 | ATGAGCCAAAGGGGG[A/G]GAAAAAAAAAAAAAG | 71682 |
rs33149778 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Wdr27 | Mm_Celera | 17:14784506 | CCATTTAACAATTTT[A/G]TTTTGTTTTGTTTTT | 71682 |
rs33156099 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | GRCm38.p3 | 17:14789827 | TCTACAGAAGGGCTT[C/T]TTAAACTTCTCCACC | 71682 |
rs33190987 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Wdr27 | Mm_Celera | 17:14925832 | TGCGCCACCACTGCC[A/C]GGCGGGTGCATGCTT | 71682 |
rs33204834 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14786240 | TCAGAGTCTAAAACC[A/C]CCATAGATGGGAAGA | 71682 |
rs33217027 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14791501 | CAATCTAGGCGCACA[A/G]CATATATTCATATTA | 71682 |
rs33225576 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr27 | Mm_Celera | 17:14923294 | TGAGCCAAAGGGGGG[A/G]AAAAAAAAAAAAAGG | 71682 |
rs33240239 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | GRCm38.p3 | 17:14819749 | ATAATCATCATAGCT[A/G]GGTCAGACTGTTGGT | 71682 |
rs33281112 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr27 | Mm_Celera | 17:14793620 | GGGAATATGCAGTGG[C/G]TGGTTATACCATCTC | 71682 |
rs33284799 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14922938 | CACGTCAGGGTCCCC[G/T]CTGCAGACCAAAGGT | 71682 |
rs33292187 | snp | A/G | 0.487535 | 0.077957 | intron-variant, downstream-variant-500B | Wdr27 | GRCm38.p3 | 17:14915518 | ATATGCTACCCTTGT[A/G]GTGACTGTGGCATGC | 71682 |
rs33297708 | snp | C/T | 0.493827 | 0.0552116 | downstream-variant-500B | Wdr27 | Mm_Celera | 17:14784431 | TAGACTTCAGCTCCA[C/T]GGCTTTCCCTTTCTC | 71682 |
rs33308424 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14790126 | AAAATTCTCAGTGCT[A/G]AGAAGGCTGTTTTGC | 71682 |
rs33317958 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr27 | Mm_Celera | 17:14798861 | TGTCTGCATTCTGAC[A/G]GGATCATATAGAACT | 71682 |
rs33333499 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr27 | Mm_Celera | 17:14821601 | CACGCACACGCACAC[A/G]CGCACACGCACACAC | 71682 |
rs33379727 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Wdr27 | Mm_Celera | 17:14887593 | AATCAGAGTCTGTGT[A/G]ATTATACACCCTTTG | 71682 |
rs33399525 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14789879 | TTTACAAGGCCTGAA[A/G]TATATAGGCATAAAA | 71682 |
rs33412784 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14789967 | CAATTATTTGTATAC[A/G]ATTTTGCCATTTATT | 71682 |
rs33427243 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14799669 | GCCAACTAGCTGTTC[C/T]GGACCTATCACGTGT | 71682 |
rs33450635 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr27 | Mm_Celera | 17:14791369 | AAGAGGGAGAGGACA[C/T]AGAGGAGGAGGAGGA | 71682 |
rs33487240 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Wdr27 | Mm_Celera | 17:14821193 | CAGAGCACTGGTGTG[A/G]CTCTAGCAAAGATCT | 71682 |
rs33555902 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14799646 | TGCCACTCCCACTGC[C/T]GCTGCCTGCCAACTA | 71682 |
rs33568691 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Wdr27 | Mm_Celera | 17:14795347 | GCCTTCCATTCTGCA[C/T]AGTTCTTTAACCCAC | 71682 |
rs33598757 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14922940 | CGTCAGGGTCCCCGC[C/T]GCAGACCAAAGGTCC | 71682 |
rs33600726 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14788267 | CTCCGTAGGAGCTGC[C/T]TCGGTGTCTAAAATC | 71682 |
rs33621209 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Wdr27 | GRCm38.p3 | 17:14786832 | GGAATACCCAAGATA[A/C/T]AATTCACAGACCATA | 71682 |
rs33632107 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14789004 | TGGACAAAATGACTA[A/C]GATCTGCAATGGTAT | 71682 |
rs33632652 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Wdr27 | GRCm38.p3 | 17:14785097 | AACTCCTTTCTGTGA[C/T]TGCTCCTTTTCTCTG | 71682 |
rs33668229 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Wdr27 | Mm_Celera | 17:14925269 | TCAAATAAGTATTTT[C/T]AAATGACCATAGAAT | 71682 |
rs33670132 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr27 | Mm_Celera | 17:14799683 | CTGGACCTATCACGT[A/G]TTCACCTGCAACTTT | 71682 |
rs33693469 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Wdr27 | Mm_Celera | 17:14840178 | ACAGATATATAATGC[A/G]TTTTAATTACTCTTA | 71682 |
rs45632300 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14812514 | TCTTCATGTTTTTGT[A/G]ATACTTTAAGTAGCA | 71682 |
rs45637457 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14812822 | AACCTTAGCAGCCAC[A/G]CCCTCTGAGCACAGT | 71682 |
rs45670532 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14811720 | GATTAGAGATTGTAC[C/T]GCAGGTCAGAACCAG | 71682 |
rs45675425 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14785323 | TCACTGACTGTGAGG[C/T]GGTGATCATGTCATT | 71682 |
rs45677796 | snp | A/C/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14921500 | AGCTAAGGTGCAATA[A/C/G]ACAACGAGTGACTGT | 71682 |
rs45705935 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14794349 | ACCATGGTGTTGTCT[C/T]CATCTTCTAAAATTT | 71682 |
rs45710992 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14810429 | GTAGAAGTTTTACTG[C/T]AACTTGCTAGACAGA | 71682 |
rs45742301 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14877275 | ATCTGGTAGCGTAGT[C/T]TATCCTATTGGGATG | 71682 |
rs45752654 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Wdr27 | Mm_Celera | 17:14821108 | CAGCTGAGGGAAGAT[C/G]CTAGGGAAGATCCTG | 71682 |
rs45755047 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14918989 | GAGAGACATATTTGA[A/G]AAACGGAGGTGCCGG | 71682 |
rs45758371 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14849749 | TGTTGACATTTTCCT[A/G]GTGTCAGAGTAACAG | 71682 |
rs45769276 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14854506 | GAAGCATGCTAGAAA[C/T]ATTAACCTCACGACT | 71682 |
rs45776845 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14899902 | CCGAACCCAGGAATA[C/G]TGAAACTCTAGCTAG | 71682 |
rs45779198 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14820963 | CCCACACTGCCAGTT[C/T]TGTCACAAGAATAAG | 71682 |
rs45790620 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14922597 | TGTCCAGAACCTTAG[C/T]TCAGACACAGCTATG | 71682 |
rs45791162 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14814847 | TATTGAGGACTTTGG[C/T]GTTTGATGATCTGTA | 71682 |
rs45819943 | snp | C/T | 0.497778 | 0.0332592 | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | GRCm38.p3 | 17:14934726 | ACGGTCTCATGTAGT[C/T]CATGAAGGTCCAGTT | 71682 |
rs45825884 | snp | G/T | 0.244898 | 0.249948 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14872815 | TCCTGTACAAAATAC[G/T]AGCCATGGATAATGT | 71682 |
rs45827171 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14916992 | TGCCCAAACTATCAC[A/G]TCAGCATTGAGACAC | 71682 |
rs45836554 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14859087 | GTGACATTGTAGACA[C/T]GAGGCCTTTCTGGAA | 71682 |
rs45840674 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14890075 | ACAGATCTTTTTAAA[A/G]TCAGCATTTTTCATG | 71682 |
rs45842329 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14899977 | ACACAGAGCAGTTCA[C/T]CAATGGCTGGAAGGC | 71682 |
rs45855306 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14853569 | GCTGCCCTGCTGCCC[A/G]GATGAACTTAATAGG | 71682 |
rs45858214 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14900281 | TGGCCTGGGGTGAGC[A/G]GGATCAAAGACGTAG | 71682 |
rs45861541 | snp | A/G | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14883606 | CAGTGCCGTGATGCA[A/G]GCTGGCCTTACCTCA | 71682 |
rs45870787 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14910173 | ATCTACAAATTAAGT[A/G]CATTTCCCTTTATAT | 71682 |
rs45879055 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14942639 | CGTGCTGGGCCCTAA[A/G]TCTGTGGCTCGCGTT | 71682 |
rs45886743 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14920450 | ATTTTAGGAGCATTT[A/G]CAGTCGGTAATAATA | 71682 |
rs45900700 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14928962 | AGACTCTTTCTCTAC[A/C]TAAGTAAGTAGCTGG | 71682 |
rs45900772 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14817962 | AGCTCAGGGACAGCA[C/T]GGCGCTCCTGTGACC | 71682 |
rs45905274 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14820987 | GAATAAGGCCATTAC[C/T]CTGGCGACTGGATCT | 71682 |
rs45906888 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | GRCm38.p3 | 17:14853850 | GAAAATGCCAGTCCC[A/G]AGCCACTGCTCTAGA | 71682 |
rs45919436 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14817165 | AAGCCTGGAGAGTGA[C/T]CTGAATCCCAAGGAA | 71682 |
rs45995761 | snp | A/C | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14847961 | TCCATCCTTACTTAT[A/C]ATATCTGCCCATATG | 71682 |
rs46011349 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14847381 | ATCACTCATATTGCA[G/T]AGCTGGCTCCACCGT | 71682 |
rs46012738 | snp | A/C | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14891494 | TTATCAGAAAAAGCT[A/C]ATATTGGACCTGGCA | 71682 |
rs46028253 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14857536 | TACACAGAGCCCTAG[C/T]ATATGGAGCATATCT | 71682 |
rs46034638 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14828315 | CTCACCCTCGCTGGT[A/G]CTGGAACTTCCCTGA | 71682 |
rs46044083 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14795401 | AAGTCATCTCTTTGC[A/G]ACACTCTCACTCAGC | 71682 |
rs46048634 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14900582 | AACTGGACAACAACA[C/T]GTTTTATTGTCTAAG | 71682 |
rs46089203 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14886819 | CTATGTATAGGAAAT[A/G]AAACACTGAGTTCCA | 71682 |
rs46130050 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14796925 | AGCCTACTGAGTGTT[C/G]TCATGAATTAGCATA | 71682 |
rs46147068 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14856343 | TATACCTGATAATTG[C/T]CAAATAAGGTACAGA | 71682 |
rs46156120 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14919043 | AGCTCCGTCCTTCAG[A/G]TTCCGCAGCACAGGG | 71682 |
rs46158718 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14810322 | CATTTATGTCTACAC[A/G]TGGACGCTTTGGTTA | 71682 |
rs46176030 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14935580 | AATGGCTCCACTCAT[C/T]CCATCCCACTGTGGG | 71682 |
rs46191236 | snp | A/G | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14840903 | TTTAAGGTCCAGATC[A/G]TTTAGGAGCTAAATA | 71682 |