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 |
rs46204976 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14899607 | GGCTTACAGTTACAC[A/C]GAGGATGGCTGAGAA | 71682 |
rs46209581 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14884128 | TCTCAGCCTACGTAA[C/G]TGTGCTCTGTGACTA | 71682 |
rs46227210 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14795936 | CCTCACTCTGTTGTT[C/T]TTCTGATTATAGAGA | 71682 |
rs46238625 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14917603 | GTTCTTTCATATAGC[A/T]TTAGTGTGGTTGAGA | 71682 |
rs46243204 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14825092 | AAGAGGCACTGTGGG[A/G]AACACAGCTTGAGCT | 71682 |
rs46245814 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14918382 | TGCTGGCGAGGGTGT[A/G]CAGCCAGAGCCCGCA | 71682 |
rs46253436 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14785541 | GCTGTTGCTAAAGAA[A/G]GCCAGTACATCTGAC | 71682 |
rs46268330 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14822320 | TGCTCTGCTGACCTC[A/G]TTCATTCAGTAGTAA | 71682 |
rs46268635 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14931489 | TGTGGCCACACCTGC[A/G]CCATCAGCCGCAACT | 71682 |
rs46293404 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14935835 | TCGAGTGGCCTTGCT[G/T]GGTGAAAACACATGT | 71682 |
rs46307779 | snp | G/T | 0.132653 | 0.220748 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14944205 | CACAAACCCTTATTT[G/T]CACAGAGCGATTACA | 71682 |
rs46324764 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14878326 | ACATTTGCCTAAATC[C/T]CTTCCTTCATTTAAG | 71682 |
rs46333069 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14835700 | TACTCATTTTTGTTG[A/G]CTATTGTACGGGACT | 71682 |
rs46343878 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14934164 | GGAGGCCTCATTAAG[C/T]TACGATGGGTCTTTT | 71682 |
rs46348919 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14887288 | AGTGTCTAATAGCTG[A/G]GCCAAACTAACAGCT | 71682 |
rs46351055 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14841859 | ATAGCCTACATGGTA[A/C]CCGAGGGAGATCTGA | 71682 |
rs46352129 | snp | C/G | 0.32 | 0.24 | missense, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14908557 | AAAAGGCAGCCGGTG[C/G]TCCTGAAAGGCTGGC | 71682 |
rs46362097 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14935520 | GGGAGGGGAGGCTAC[A/G]ACTGAGCATAGCCAA | 71682 |
rs46374341 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14899716 | CGCAGAGGCAAGGAC[A/G]AGAAAGAGAACCCAA | 71682 |
rs46374774 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr27 | Mm_Celera | 17:14884925 | TATAGTCAAGAAATC[A/G]GATCCATGGTGGTAT | 71682 |
rs46385708 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14816768 | CTATCCATTTTTAGC[C/T]GGCTGACCAGGTTAA | 71682 |
rs46411212 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14827049 | GAAACAATGGTCTCT[C/T]GGTCACACAGGGTCA | 71682 |
rs46460419 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14811365 | ATTTGGTTTTGCTCT[A/C]AGGTTAAATACAGTA | 71682 |
rs46462837 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14846732 | CTTGAGTAAAACATA[C/T]TTGCCATTCTTATAA | 71682 |
rs46541479 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr27 | GRCm38.p3 | 17:14901531 | AAGAGCACAGAGAAG[A/T]GTGTTACAGCCAGGG | 71682 |
rs46559597 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14940797 | ATTAACTTTTAAATG[A/G]CAAAAATACACAGAG | 71682 |
rs46587044 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14814997 | CCTGGAGGGCACTGG[C/T]ATCTCAAGTGACTTT | 71682 |
rs46587374 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14799636 | CCTATCATCCTGCCA[C/T]TCCCACTGCTGCTGC | 71682 |
rs46601996 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14826591 | CAGCCACTGGAGAGC[A/G]ACCAGTGTAAGCATG | 71682 |
rs46615901 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14885151 | AGTGCCTATACTCCA[C/T]TAAGAAATACTCCAC | 71682 |
rs46625615 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14821228 | GGCAGATTCAGTCCA[A/G]GAAATGATAGGCTGA | 71682 |
rs46640535 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14826201 | GTTTAAAAGCTGGCA[C/T]GTGGCAATGTAGGAA | 71682 |
rs46646100 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14865030 | GGTTTCAATATAGAA[A/G]GGGCTTTCTTTTTTT | 71682 |
rs46673069 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14913493 | TGTCCACTAAGAAGC[A/C]GCGTTAAAGCAGCAT | 71682 |
rs46687227 | snp | C/T | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14883475 | ATCCCAAAGTGACTG[C/T]GTCAAATCTGTATAG | 71682 |
rs46705919 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14940408 | GCAAACAAACAGCGC[G/T]CAGGACTCAGAATTT | 71682 |
rs46717215 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14817760 | GATGACAGCAACATG[C/T]GCAAGGTTCTGTGTT | 71682 |
rs46721512 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14908648 | TGAAAAATAAACAGC[A/T]CTATAAAATCAAAGC | 71682 |
rs46722262 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14824342 | CTCCTTTAAGACTAC[A/C]CCAGGTCTTGCTTTC | 71682 |
rs46724943 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14816879 | ATCAACTGGTGGCCA[A/G]TACAACATTATCAGT | 71682 |
rs46750655 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14859341 | AAACTAAAGTCTGAG[A/G]CAGAATGAACACAAC | 71682 |
rs46752946 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14939072 | CCATATCTCAGGTAA[A/G]ACAGCACAAGCACAG | 71682 |
rs46753511 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14876254 | CCAGCTCCAAACTAC[A/G]GCTCAGCTATGCTCT | 71682 |
rs46755347 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14899228 | GTGTGTCCTCAAACA[G/T]GTGGTAGAAGGTATC | 71682 |
rs46756483 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14816340 | GGCAGTGCTGCTTCT[A/G]AAGCTTGGCAAGCTA | 71682 |
rs46783130 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14821208 | ACTCTAGCAAAGATC[C/T]GAATGGCAGATTCAG | 71682 |
rs46804424 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14931385 | GTTTCTGGCATACGC[A/C]ATTCGCTCACAGCAG | 71682 |
rs46815155 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14918621 | CAGAGAAGAACGGAG[A/G]CACACAAGAGCATGG | 71682 |
rs46820566 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14917493 | TAATGGAACTGCTAC[A/C]TTAGAATTTATGTTG | 71682 |
rs46830553 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14810311 | ATCTTTATGACCATT[C/T]ATGTCTACACATGGA | 71682 |
rs46839349 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14829127 | AGAGACCAATGTGGG[A/G]CATCTGGGTGAACAC | 71682 |
rs46872585 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14821251 | TAGGCTGACACCCTC[A/G]AGAGGAGCCTCATTT | 71682 |
rs46893942 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14835526 | CCAGAACAGGGTCCA[A/G]GAATGAAGTCATGTG | 71682 |
rs46918415 | snp | C/G | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14829462 | TGGAAACTGCCCATC[C/G]ACTTCAATAGCTAAG | 71682 |
rs46919257 | snp | A/G | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime, splice-donor-variant | Wdr27 | Mm_Celera | 17:14916560 | AAGGTAAGGATACAT[A/G]CAGATGCGGTACATA | 71682 |
rs46924162 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14901370 | GCCACTTAACACACA[C/T]TTGTTACTCATCTTC | 71682 |
rs46935024 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14909921 | AGAGAATCCTGACCA[C/T]ATCAACCAAGACTCA | 71682 |
rs46971582 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14822363 | TTACCACCTCCATAT[A/G]TGATAGCTGTATGTA | 71682 |
rs46998865 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14907805 | GTGTACACCTCTGAT[C/T]GTAAGCATGACCTTA | 71682 |
rs47004896 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14811754 | AATCCTCAGGAACAT[A/T]GCTCCAAGTCACTGA | 71682 |
rs47014617 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14884932 | AAGAAATCAGATCCA[C/T]GGTGGTATCATAGCT | 71682 |
rs47020400 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14820800 | CTCCCAGTGTCTCAG[A/G]CCTCCTGTTTGGTCT | 71682 |
rs47055223 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14790746 | AGCTTGGTGAAGATT[A/G]GATGACATGCATGGG | 71682 |
rs47058115 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14812990 | GGATTGAAATGGGAT[A/T]CGCAAGACTCTAAAT | 71682 |
rs47065522 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14887115 | TCCAGGGGAAGTCCA[A/G]TAATCCCACATACAC | 71682 |
rs47090545 | snp | A/C/G | 0.336735 | 0.234472 | intron-variant | Wdr27 | GRCm38.p3 | 17:14876274 | AGCTATGCTCTGTGG[A/C/G]TGACCCAGAATACAG | 71682 |
rs47107622 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14859204 | AGTGGATGTGGAACA[A/G]AACAACTGTGAGCTG | 71682 |
rs47113021 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14900319 | TCGGCTCCACACTGG[C/T]TCTGACATTGCAACT | 71682 |
rs47142335 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14795893 | TCGACAGTCACCATC[C/T]ACCCTATCTCACACC | 71682 |
rs47153117 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14793887 | CTGTGCAGTTATCCA[C/T]AGTCACCTTCTATGC | 71682 |
rs47160745 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14824908 | GGAAGCTGCTGCACC[A/G]GGTGGTCCCATGGAA | 71682 |
rs47170409 | snp | A/G | 0.244898 | 0.249948 | intron-variant, utr-variant-5-prime | Wdr27 | Mm_Celera | 17:14924231 | TACAACCTAATCCAT[A/G]GACTGCATGCTGTCC | 71682 |
rs47186901 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14887233 | AGATGCAAAGTTCAG[G/T]CACTGTGCTTCGTGC | 71682 |
rs47201413 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14821247 | ATGATAGGCTGACAC[A/C]CTCGAGAGGAGCCTC | 71682 |
rs47210956 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14822512 | CCATTCCATGTACTT[A/C]TGACCCAGGTGCTCT | 71682 |
rs47269264 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14918883 | GACACAAAGATGGAA[A/G]GAGAGCATCACGGGA | 71682 |
rs47286705 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14928162 | TCGACCCAAACTGCC[A/G]TTTTAAAGAGGGAAG | 71682 |
rs47286801 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14921585 | TGGCTTAATACATTC[A/G]TGGAAAGGGAGCTAT | 71682 |
rs47287690 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Wdr27 | Mm_Celera | 17:14876511 | CAGAATCCATGGTTC[A/G]TACCCATCAATCCCT | 71682 |
rs47303085 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14827033 | CCAATCAGAAACTGT[G/T]GAAACAATGGTCTCT | 71682 |
rs47307592 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14824433 | ATTACAGATCTCAGA[A/G]CATCCACGCTATGAA | 71682 |
rs47324226 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14824475 | GCACTCAGGCTACAG[A/G]CCCACTTGTGGCCAC | 71682 |
rs47332067 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14848062 | CAGTTAAATGAGCTG[C/T]CTCTGTTTTGCACCT | 71682 |
rs47346083 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14821013 | GATCTCCTCTGGCAG[A/G]TGGGAGCAACACACC | 71682 |
rs47364079 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14883622 | GCTGGCCTTACCTCA[A/G]GTTCCTCAAGTCCCA | 71682 |
rs47375140 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14898585 | TTTATATGCCCCAGT[A/G]TAGTGGAACACCAGG | 71682 |
rs47382533 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14918781 | GCGCACACGTGAAGA[A/G]GAGAGCCTGCGGGAG | 71682 |
rs47383598 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14816148 | TTAAAGCCACAGGGG[C/T]TTTGAGTCACTGGAA | 71682 |
rs47388134 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr27 | Mm_Celera | 17:14848978 | CAGCATCTGACACAG[A/G]AACTGGCACTCAGAG | 71682 |
rs47390081 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14923338 | ATAAGATGGTGTATA[C/T]GAATTACAGCTGGCT | 71682 |
rs47411933 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14810003 | ACACGGGTGGGAGAC[A/G]AAATACATAACTGTC | 71682 |
rs47422038 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14909374 | TCACAGAAGGTATGT[A/G]TGAGCCATCCTGGCA | 71682 |
rs47428866 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14815192 | CGAGACTCACTCCAC[G/T]GTTCACAGTGGCACA | 71682 |
rs47437932 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14879038 | ACTATGATACCCTCT[A/G]CTTCTCTCCGATAGC | 71682 |
rs47444152 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14902191 | AGCTAGCTCAGAAGA[C/T]TGGAAAAGTGGAGGG | 71682 |
rs47466227 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14857089 | GGTTCTATAGCACAA[A/G]CAAAGCTTAAGATGT | 71682 |
rs47475782 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14796539 | ATACTACAGGGCTTT[C/G]TCTTAGAATCTCAAT | 71682 |
rs47485292 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14817188 | CCAAGGAAGGAATTG[C/T]TAAAATCTGTAGAGA | 71682 |
rs47485783 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14918983 | GAGCCTGAGAGACAT[A/G]TTTGAAAAACGGAGG | 71682 |
rs47499520 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14814453 | TAAATGCTAGTAAAC[C/G/T]TCAGAGAATAGGCTG | 71682 |
rs47513327 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14795981 | TACTCCATGTTACCA[A/G]CCAGCATGCCCAGAG | 71682 |
rs47514979 | snp | C/T | 0.42 | 0.183303 | intron-variant | Wdr27 | Mm_Celera | 17:14918416 | GAGAGGAACACATAG[C/T]ATAATACATATGTTA | 71682 |
rs47527911 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14797237 | ACATCTGTGTTGTGT[A/G]GCTCCCTTCGGCAGT | 71682 |
rs47536579 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14917141 | AGTGACTTCACAAAG[G/T]GATTCAGCAATGTTG | 71682 |
rs47553325 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14928466 | GAATGGGTCCTGCGT[A/G]CAGTCCTGTGAAGTT | 71682 |
rs47557533 | snp | A/C | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Wdr27 | Mm_Celera | 17:14926637 | CACACCACACACTAC[A/C]CCTTCCAGATTTGGA | 71682 |
rs47566883 | snp | A/C | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14810194 | TGCATGACATCAGAC[A/C]TAGGGAGCTGAGATC | 71682 |
rs47567837 | snp | A/T | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14841047 | CTAGTGTGAGTTGCT[A/T]TACATTTACTAAGAG | 71682 |
rs47568090 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14884203 | CTAGCAGGGTAACTA[A/G]GCAAGAACACTCTAA | 71682 |
rs47610243 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14843449 | GAACGCCATCCACTG[C/T]CTCTAGTCTCCCAAC | 71682 |
rs47614381 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14797119 | AAGTGGCTTTAGACT[A/G]AGGGCTTCGGTGCCA | 71682 |
rs47616223 | snp | G/T | 0.124444 | 0.216185 | missense, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14908617 | AGCCACAGGCCAGCT[G/T]CTGTCCATCCCCTGT | 71682 |
rs47620235 | snp | A/G | 0.152778 | 0.230321 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14908092 | CAGTAGCAACATAAC[A/G]TGGCTGTTTTTACTT | 71682 |
rs47625332 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14842177 | ATTGCCGATAGATCT[A/G]CATCAATAAAGGGCT | 71682 |
rs47634594 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14847880 | CTTATACACACACTC[A/G]TTGCTGAGGTCAGCA | 71682 |
rs47652712 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14919077 | CCCAGCAGTCTGAGC[C/G]TGTGCCATGTTTGGT | 71682 |
rs47661260 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14892328 | GGAGAACCATTCATC[C/T]GACCTTTATGTCCAG | 71682 |
rs47690430 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14794555 | AAATGCTGACTACTT[A/C]TGTTTCCCTATTTCC | 71682 |
rs47693629 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14875089 | TGCTGTTACACACAG[A/G]ACATGCTAAGTATAC | 71682 |
rs47707635 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14923706 | GTTCCTCAAATTGTT[C/T]CACAAGATGGTCTTC | 71682 |
rs47715381 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14844037 | ACTGCCTGTGGCGGA[C/T]ACAAACTCCTGTTCC | 71682 |
rs47724398 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14824588 | AGGGTAACTCTGGGG[A/C]CCCACTCCTGAAGGC | 71682 |
rs47756713 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14816435 | AACAGTGAGTGCTCA[C/T]AGCCACCACAGATTT | 71682 |
rs47757416 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14811563 | CTTCTGATACAACCT[A/T]TCAGAGCCAGGCACA | 71682 |
rs47765250 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14899330 | CCATACAGAGACAGA[A/C]GCAGTGCAGCTGAGT | 71682 |
rs47769455 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14812696 | ATCCCTACTGAGAAA[G/T]AGAAAGACAGAAGAC | 71682 |
rs47789782 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14931701 | TCTTACTATTCACCC[A/G]TGTGATCTATGCAGT | 71682 |
rs47801433 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14907145 | AAGAGTCAAAGCCCT[A/G]GGAAATGGCACTGTG | 71682 |
rs47809992 | snp | A/C | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14840597 | CTCCAAACTCGAGCC[A/C]TTGAGAAAAGGAGGA | 71682 |
rs47850974 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14856744 | GAAATGTGAAAGAGA[A/G]ATCACTGAAGAAAAG | 71682 |
rs47875971 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14902256 | TGTTGAAGCAGAGAA[C/T]GTGCTCTGAAACACA | 71682 |
rs47885829 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14814548 | ATTTTCTCTGAAACG[G/T]TAATGAAAACCTAGT | 71682 |
rs47888565 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wdr27 | Mm_Celera | 17:14874532 | TTGGAAGAGGGAAAG[A/G]AAATGATCAAAAAAT | 71682 |
rs47895185 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14814516 | TTACCACTATGGGCA[C/G]AGTTTACTGAATATC | 71682 |
rs47924738 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14887052 | CAGAGCACACCACAG[A/G]AAGCAAACAGTGACT | 71682 |
rs47964297 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14827567 | ATAAAAAAACACTAT[A/C]TTACAGAGATACTTC | 71682 |
rs47967791 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14817622 | GGCCAAGTCTTTAGC[A/G]GGAACTTGAACATGC | 71682 |
rs47971371 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14841931 | CTGCACATCTAGACC[C/T]TGGTTCCTGACATCC | 71682 |
rs48057417 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14794608 | GCCATGGATTTGAAT[A/G]GCCTTGATCTAGCGT | 71682 |
rs48061688 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14827491 | AAGTAACCAATGAGT[C/T]AGCCCTGTCTCCTAA | 71682 |
rs48085941 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14884088 | AGATAACAGAGTGCA[C/T]GTGCAACAAGGTTGA | 71682 |
rs48103630 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14817476 | GGAATGGAGTAGGTG[C/T]TGCCTGAAGAGGGCA | 71682 |
rs48123144 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14928752 | GGCCTCTAAGGCTCT[G/T]ATACCATGACATCAC | 71682 |
rs48131623 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14810092 | GCTCACAACATTGCA[A/T]TTTGCTTTTGCAACA | 71682 |
rs48139195 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14826042 | CATTCAGACTGAATC[A/G]ATGGTAACTATAACA | 71682 |
rs48147218 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14934784 | ATACCACGCTTACCC[A/G]TTCACCCCAACTCCC | 71682 |
rs48170112 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14821959 | ACATCATGGTAGGAA[A/G]TGTGTGTTGGAGCAA | 71682 |
rs48183410 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14813009 | AAGACTCTAAATATC[G/T]TTCCAACCAATATAA | 71682 |
rs48185552 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14904636 | CTCCTGGGCGAGCCA[A/G]TGGAAACAGGTAGAC | 71682 |
rs48186125 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14919342 | CTAATCTTAGGAAAA[A/G]AGAAACAAACAGTCT | 71682 |
rs48197599 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14874697 | GACATAGCAACTCAA[A/C]ATCAAATAGAGTAGT | 71682 |
rs48243355 | snp | C/T | 0.32 | 0.24 | missense, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14918112 | TGGGCTCGCTCACCA[C/T]TGCACACGACCCAGC | 71682 |
rs48249012 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14811602 | CATGTTGTAACTGGT[C/T]GAGTTCCTGGTCCAG | 71682 |
rs48257508 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14901692 | AGAGTGGGAAAGTGG[A/G]CTGGCTCTTTGGGAT | 71682 |
rs48269753 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14878468 | ACAGTAAAGACCAGA[C/T]AAATATCACTCCTGC | 71682 |
rs48301169 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14907768 | TCAAGCTAGGCCAGG[C/G]ACCCAACATGCATGG | 71682 |
rs48301905 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14785477 | GCAAAGATTGGCAGC[C/T]AAAAATTATGTGGGC | 71682 |
rs48313014 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14796096 | TCTTTGTTGATATAT[C/T]ACTTCAGATTAGTGA | 71682 |
rs48323041 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14910259 | ATCATGAATAACTCT[C/T]TAAAACAAATTTGTA | 71682 |
rs48329621 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14829444 | GTGCAGCAAGGCCTC[C/T]TATGGAAACTGCCCA | 71682 |
rs48368258 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14822830 | ATCTCTGAGGTTAGT[A/G]CTCCCTTAGTATCAC | 71682 |
rs48379372 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14858802 | TATGCACCCTAGCTC[A/G]CTGGGCTCAAAACAT | 71682 |
rs48391406 | snp | C/T | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14841073 | AAGAGGGTGTGGGAA[C/T]CTAGGAACTGCATAG | 71682 |
rs48394367 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14858782 | AAAATTACAGCACAT[A/G]GGAGTATGCACCCTA | 71682 |
rs48396523 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr27 | Mm_Celera | 17:14859794 | TGACAATCTGGAAAA[A/G]GTGTCTGAAGCTACA | 71682 |
rs48403258 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14899912 | GAATAGTGAAACTCT[A/G]GCTAGACTGGAGCCT | 71682 |
rs48404753 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14826228 | GGAACTGCGCTCATA[A/G]AATCTGAACCAATCC | 71682 |
rs48406830 | snp | C/G/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | GRCm38.p3 | 17:14793043 | CCACAGGTGATACAC[C/G/T]GACTACAGAACCAAC | 71682 |
rs48408812 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14902705 | GCCAAGAAAAGGTCA[A/G]GCTTCAATGTACAAT | 71682 |
rs48417707 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14816784 | GGCTGACCAGGTTAA[A/G]CAGGCCTATACTTGC | 71682 |
rs48439290 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14796817 | TTTATCCTCTAATAC[G/T]TGTGGCAGTGAATCA | 71682 |
rs48441854 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14902230 | ATTGACTATTAAGGA[C/T]AGTCAACCACTGTTG | 71682 |
rs48460653 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14886126 | CACTTGAGCACACAG[A/C]AGTCACTGCACAGAA | 71682 |
rs48470981 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14859951 | AGCTTTCTGAACAGA[C/T]AGACATATCTTTATA | 71682 |
rs48472443 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14826253 | CAATCCACAGAAATA[A/G]CTTAGGTGGCAGACT | 71682 |
rs48496721 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14930767 | CAATGGCAGTAGCCT[A/G]TCTTTTTATAGCTGG | 71682 |
rs48504743 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14821067 | TGACCCTCTGAAATA[C/G]AACAGGACTTTGTTG | 71682 |
rs48523569 | snp | A/G | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14883476 | TCCCAAAGTGACTGC[A/G]TCAAATCTGTATAGG | 71682 |
rs48557192 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr27 | Mm_Celera | 17:14821699 | CTTGCATATTGGTTG[C/T]TATTTCCCAGCTGTA | 71682 |
rs48557197 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14899759 | CAGATGACCCCACAG[A/G]GACAAACACAGTCAC | 71682 |
rs48571138 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14929086 | GGATGTTAAGACATT[A/G]ATGTGAGAATCCAGA | 71682 |
rs48580151 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14811306 | CATTCACTTATCCAT[A/T]TAGACTCTCAAATGT | 71682 |
rs48588228 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14901399 | TCCCATTTGTCCACG[A/G]GGATGCAGAGGCACA | 71682 |
rs48590666 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14916676 | CTTGACGGGGACACA[A/G]AGGAGCATCAGTCAC | 71682 |
rs48594885 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14797182 | ATGGTTTGGGAGAGC[A/G]AGGGCCTCTTTCCTT | 71682 |
rs48599691 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14919051 | CCTTCAGGTTCCGCA[A/G]CACAGGGGGTCCCAG | 71682 |
rs48600811 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14821134 | TCCTGGAGGCAGGCT[G/T]CGTCCAGCTGCAATT | 71682 |
rs48621552 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14812003 | TTTCTCATCAACTCA[A/G]AACATTCAAGTGCCA | 71682 |
rs48623538 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14825099 | ACTGTGGGGAACACA[A/G]CTTGAGCTCCAGCTG | 71682 |
rs48625555 | snp | A/G | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14848318 | CACAGCCTGTTGCCA[A/G]GGATGTGCTGCAAGC | 71682 |
rs48636670 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Wdr27, Gm34975 | Mm_Celera | 17:14934897 | CTACATCTCTTTCGG[A/G]ACTGTGAAGGTGACC | 71682 |
rs48659355 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14898267 | ACCAAACGCAGACAC[C/T]ATTACATATGCCAGC | 71682 |
rs48661073 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14815660 | CAAGGGAGAAGGAGG[C/T]GTGAAAGGGAGGAAC | 71682 |
rs48686518 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14926698 | GATTCGGAATCTCTG[C/T]GGGAGGGAGGTGCAC | 71682 |
rs48690637 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14820829 | CTCCCAGCTGTGACT[A/G]GAAGCATGGTCACAC | 71682 |
rs48697168 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Wdr27 | Mm_Celera | 17:14925655 | AGAAAATAGCCTCCT[C/T]GGGTGCATGCTTTAT | 71682 |
rs48722954 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14932958 | GTGTACTGAGTACTC[C/T]ATGGATGCAGATGTG | 71682 |
rs48733455 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14828121 | TGGCTTCTGTGGCTC[A/G]ACTTGAAAGTCCTCT | 71682 |
rs48733895 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Wdr27 | Mm_Celera | 17:14835842 | TAAAAGGTATTATTG[C/G]CAGGCTAAGCACACA | 71682 |
rs48750024 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14815277 | CATATAGTAGAACCC[A/G]AGGATCAATAGATCT | 71682 |
rs48767992 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14887491 | CCCTTTGCTTCACCA[C/T]CAGAACATAACACCC | 71682 |
rs48781828 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14938707 | GTGAGCCGTGCTCTC[C/T]AGTGGATGACAGGGG | 71682 |
rs48787302 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14922489 | CTTCAGGTGTTCCTA[C/G]GTTCTCTCAGACACT | 71682 |
rs48798765 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14921622 | AGGTTAGGACTTTCT[G/T]ACCTCACTGAAAAAC | 71682 |
rs48812115 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14942520 | ACTGTTGCCTTCACA[C/T]AGGTTAACCCGGAAG | 71682 |
rs48819609 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14828544 | GAACACACTCAAACG[A/G]GGCGCTTCTACAGGT | 71682 |
rs48829104 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14874975 | CTGATTATATCATTT[C/G]ACAGGACATCAAGAT | 71682 |
rs48836070 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Wdr27 | Mm_Celera | 17:14797144 | GTGCCAACCAGCTTC[G/T]GGAGTAACGTCTACA | 71682 |
rs48836450 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14903319 | CTAAGCAGTCTGGAT[A/C]TATTGCTGGTCTCCC | 71682 |
rs48854041 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14901502 | ATCAGGGTAAAATCA[A/G]TGAACAAAAGGTTAA | 71682 |
rs48870860 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14880672 | AGACTGAATCATTGT[A/G]GTTTTGGATACATCA | 71682 |
rs48894022 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14814927 | TGGCGTATCCCGGTT[C/T]GTGAAACATTTTCCT | 71682 |
rs48916114 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Wdr27 | Mm_Celera | 17:14810227 | CTGGTTGTTGTATGC[A/G]GACTCTCAAGAGAGA | 71682 |
rs48917589 | snp | A/C | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14934127 | CATTACAAAGCAAAA[A/C]AGCTCAAGCTGGCAT | 71682 |
rs48930393 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14890548 | CCTAAGAGAGGACGC[A/G]GTCCATCACACTGTT | 71682 |
rs48931559 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14825830 | TAAAGGCTCTGCTAC[C/T]GTATGCCATAGGAAA | 71682 |
rs49042627 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14918925 | TCGGAGAAAGGAGGG[C/T]TCCACAGACTCCTGA | 71682 |
rs49046971 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14888044 | CAGCTAAAGAAGAAG[A/G]AGCTCTTAAAGAAGA | 71682 |
rs49055402 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr27 | Mm_Celera | 17:14914450 | GGCCACTCCTGGGAC[A/G]CACTCATCCTTCTGT | 71682 |
rs49065645 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14816052 | TGTGGAATTAACCAG[A/C]CTTATGCCCTCTGAA | 71682 |
rs49071483 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14883588 | CTCCAATTTCCCTCA[A/G]GGCAGTGCCGTGATG | 71682 |
rs49082540 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14859282 | ACATAGAAACCAAGA[G/T]GGCCTCTGAGAGAAG | 71682 |
rs49126062 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14823985 | AGGTCCTGAATTCAA[C/T]TCCCAGCAACCACAT | 71682 |
rs49126821 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14828668 | CTATGTGCTCGCCAA[A/G]ACCCACAAATGTCTG | 71682 |
rs49142478 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14884511 | ATATGTCAAGAACAC[C/T]GAGCTGCACCTTGGC | 71682 |
rs49144670 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14824904 | GTCTGGAAGCTGCTG[C/T]ACCAGGTGGTCCCAT | 71682 |
rs49167665 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14821117 | GAAGATCCTAGGGAA[A/G]ATCCTGGAGGCAGGC | 71682 |
rs49210088 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14922859 | TACAACGCTGGTGCT[A/G]ACAGCTGTGCCAGCA | 71682 |
rs49241456 | snp | A/C | 0.152778 | 0.230321 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14840959 | AAGAGAAATCAACAC[A/C]GTTGTACTTCAAGAT | 71682 |
rs49250444 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14816899 | ACATTATCAGTGCAA[C/G]GAGAGAAAGCCAAAG | 71682 |
rs49305053 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14933328 | GAAGAAGGGAAACGT[A/G]CAGAGGAAGAGAGCG | 71682 |
rs49313817 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14855013 | AAAGTTGGGTAATGG[C/T]GACCTAGAAAAGGTG | 71682 |
rs49331329 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | GRCm38.p3 | 17:14902676 | CAGAAAGTATTGCAT[C/T]CTTAGGTCTCTAAGC | 71682 |
rs49334570 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14889535 | CCACATGTGTGTTGC[C/G]GGATATGTCTAGAGC | 71682 |
rs49361071 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14916887 | TTCTAATTGTGACAG[A/G]ATATGACTGTGGCTA | 71682 |
rs49414690 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14841736 | GTGGCAGCAGAGTGT[A/G]TCCCACAGCAGATGT | 71682 |
rs49463361 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14902331 | GACCCTAGGATAATC[C/G]ACCAGCATTTAAAAG | 71682 |
rs49505653 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14829832 | ACTTAGACCTTAGAA[G/T]CATTCTGAGTTTAAG | 71682 |
rs49518459 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14875016 | CAACATGTCAGGCAC[C/T]GCAGCAAGCCTTGGA | 71682 |
rs49558277 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14875402 | TCACATTTAGATTAG[A/G]CAGAACCATATCTAT | 71682 |
rs49613313 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14931510 | AGCCGCAACTAGGAA[A/C]GCTCTCAGAACACGT | 71682 |
rs49620219 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14826879 | CAGTCATACTTGTTG[C/T]TTAACACAAAGGATA | 71682 |
rs49636085 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14919981 | CCCCGGCTTTGCCTG[C/T]AAGAACTCCCAATAC | 71682 |
rs49647490 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14810597 | GATGACCTGTTCACA[C/T]AGTGATGGTGACTGC | 71682 |
rs49650024 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14846690 | TGCCTCCCTTCAAAG[C/T]CTGTTGCTCTCTTTA | 71682 |
rs49661133 | snp | A/G | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14829387 | CAAGGGTCTTCTTGA[A/G]AGGAAGGACTCTCAG | 71682 |
rs49664345 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14918551 | CCTGCTCACCATCAA[C/G]AGCAGGCAAGCCTCA | 71682 |
rs49675690 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14854299 | ATACTCGCTCTAAGG[G/T]CTAGAAAGCATCAGC | 71682 |
rs49680164 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14930655 | GTATAGGTCCTTCTA[A/G]CTCAGAAGTGTCTAC | 71682 |
rs49684269 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14810372 | GAATTTCTAACCTTG[C/G]AAATTTCTCTGACCT | 71682 |
rs49684570 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Wdr27 | Mm_Celera | 17:14820697 | ATGAAGAAGATAAGG[C/G]TGACCTTAGTTCTTA | 71682 |
rs49702769 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14823285 | GGTTTTCTGGCCTGG[C/T]AATTCCACATGTGGG | 71682 |
rs49703704 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14877250 | ATGAATGCTTCATTT[A/G]AAGGACAAAATCTGG | 71682 |
rs49711009 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14915891 | TGACCTCTGACCTCT[A/G]AAATGAAGAGGCTCT | 71682 |
rs49714564 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14859804 | GAAAAGGTGTCTGAA[A/G]CTACATCTCAAGACA | 71682 |
rs49732054 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14814717 | GTGCCAGGATAAGTC[A/G]TTTCTGGCTCGTGCC | 71682 |
rs49740453 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14826129 | GGCATTAAAGAGTCA[A/G]AGCACCCCCATGTCA | 71682 |
rs49745774 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14856638 | AAGAGGGCAACTCTG[C/T]GGTCACTCTTGAGAA | 71682 |
rs49750023 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14874949 | TTCTGGCAACTACAC[A/G]GCAAGCTTTACTGAT | 71682 |
rs49752008 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14907907 | CTGTCCACGACTACC[C/T]AAGCGGGCATATAAG | 71682 |
rs49763603 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14887788 | AGCAGTGTTAAGGTG[A/G]AGGAGATGATATAAG | 71682 |
rs49766892 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14890774 | TTCACAATTAGTCAA[A/C]GACAACCAACAAAAA | 71682 |
rs49800444 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14908684 | AAGCCCACTGGCCAA[A/C]TGACAGAGTAGAGAA | 71682 |
rs49800860 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14879269 | GACCAGAGTATGATG[C/T]TGAATAAGACCGTTG | 71682 |
rs49811707 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14922443 | CTCACTGCAAAAGCC[A/G]AAGGGAAGTGGGGCA | 71682 |
rs49825287 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14794974 | AGGCTCTAGACATGC[A/G]AGAATTTATAACTAT | 71682 |
rs49831642 | snp | A/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14908258 | CCGAAGCTGTTCCAA[A/T]GCTTTTGCCCAGGAA | 71682 |
rs49867295 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14921321 | GGATGTTTCAGAAAT[A/T]CATGTTGATAGAATG | 71682 |
rs49890357 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14930201 | TTTCCACTTGACAAC[A/G]CAGAGAACCATCTCC | 71682 |
rs49892202 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14890707 | CCATCACATGGGCAT[C/G]CAGACTGACCCCAGC | 71682 |
rs49892542 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14902713 | AAGGTCAGGCTTCAA[C/T]GTACAATTTCTATCA | 71682 |
rs49918894 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Wdr27 | Mm_Celera | 17:14789061 | CTCTATATTGTTGGC[A/C]ACCACATCTCCATGT | 71682 |
rs49956328 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14918748 | TAGACCTTGTCAGGT[A/G]TTAAATCAGTACTGA | 71682 |
rs49965901 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14815754 | GCAAATGATGACATC[A/G]GCTTGGTGGTGTCCT | 71682 |
rs49970619 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14812814 | CAAAGCCAAACCTTA[C/G]CAGCCACGCCCTCTG | 71682 |
rs49981256 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14824012 | AGCAACCACATGGTG[G/T]CTCACAACCATCTGT | 71682 |
rs49987391 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14809842 | GGATGTTCTAGAAAC[C/T]TTTTAGACCTAATCT | 71682 |
rs49994239 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14829660 | CTACGAGGTTTACAC[A/G]ATATTTGTAATGTTC | 71682 |
rs49994738 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14854674 | ATCAAGGGTGTAGCA[A/G]TACAGACCATTTCCT | 71682 |
rs50039800 | snp | C/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Wdr27 | GRCm38.p3 | 17:14828763 | TTCCCAGAGCAGGCT[C/T]GGAATGCAGAGTAGT | 71682 |
rs50041615 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14887853 | TACTAAACTAAGAGT[C/T]AATCACAAAGACAGA | 71682 |
rs50051586 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14890653 | GCTCAGGGAGAGACT[A/G]CCACAGCCTGCAGTG | 71682 |
rs50053813 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14928569 | TTTTCAGTACAGGAT[A/C]AATGCCATATGGAAA | 71682 |
rs50101476 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14933437 | TGCAAACAAAGGGGC[A/G]GCCCCTGACATGCAC | 71682 |
rs50122326 | snp | C/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14892400 | CCAAAAAGCCATGCT[C/T]GGTGCAAGGCACATC | 71682 |
rs50130898 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14817719 | GCATTGAGCATGGCT[C/T]AATATAATGCAGAAT | 71682 |
rs50158612 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14916630 | CTTCTTAACTAAGCC[A/C/G]ATCAGGAGACTATGA | 71682 |
rs50162830 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14923775 | CCAAAGCTTGGTGAA[C/T]AACTGCAGGCTGTCA | 71682 |
rs50165536 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14938867 | TGGCATTCTCTAGGC[A/T]CGGAATCCAACTTTC | 71682 |
rs50182320 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14817333 | ATCACTAACACATTA[C/T]TTTACCATCATCTGT | 71682 |
rs50216165 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Wdr27 | Mm_Celera | 17:14874555 | CAAAAAATATATACG[A/T]GAAAGCAAATTAAAA | 71682 |
rs50242046 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14884473 | CCCATGGCACGAAGA[A/G]CACTGAGCCACTTGC | 71682 |
rs50260576 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14811809 | GTGACTTGGTCAACA[A/G]ATCCACAAATATTTG | 71682 |
rs50301389 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14823567 | CTGTAGCCACCTCAG[A/C]CTCATGCATCAATTA | 71682 |
rs50321064 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14818022 | GGATGTCCACCATAA[A/G]GTGATGTCAGAGCTG | 71682 |
rs50330292 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14913559 | AAATGCTTCTCAGGG[A/G]TGGTCAGCCATCAAA | 71682 |
rs50346892 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14857503 | TCAAGGTACAGAGCA[C/T]CTGGCACATACCTGA | 71682 |
rs50347649 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14918767 | AATCAGTACTGATGG[A/C]GCACACGTGAAGAGG | 71682 |
rs50359253 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14816653 | GTGGAGGCTCCATAG[A/G]CTGTGAGAAGGATGT | 71682 |
rs50361473 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14813547 | CTCTGGGGACAATAC[A/G]CCCTAAAGCTGAGAG | 71682 |
rs50364179 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14827602 | TCAAGCCATAAAAAT[A/G]CTAACATAAAACTTA | 71682 |
rs50365966 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14939048 | ATGGCAGTGACACTC[A/G]CCAGGACACCATATC | 71682 |
rs50366976 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14827076 | GTCAGCAACAAAGGT[A/G]TTCACCCTGGGGTCT | 71682 |
rs50367953 | snp | C/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14933011 | GAGGAGCTGGAAGAG[C/G]ATGAACACATTTGGG | 71682 |
rs50373549 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14859353 | GAGACAGAATGAACA[A/C]AACTCATGAGCTGGC | 71682 |
rs50385508 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14887719 | AAGTTACTAAGCAGT[A/G]TGCAAACATAGATAT | 71682 |
rs50436507 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14827096 | CCCTGGGGTCTAATC[C/G]TCTGGCGGTCTTACT | 71682 |
rs50452968 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14826978 | CAAAAGAGGAAGCCT[G/T]CAAAAAATAGTCTTT | 71682 |
rs50465503 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr27 | Mm_Celera | 17:14900039 | CTGTGGTATTCCTGA[A/G]AAGAGCTGCCAATCA | 71682 |
rs50476603 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14898539 | GCCTAGTCGGCCATC[A/C]TTGGTAAGAGAGGCC | 71682 |
rs50552087 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14826604 | GCAACCAGTGTAAGC[A/T]TGGGCCAACCCTAGC | 71682 |
rs50554882 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14921647 | AAAAACAAATCATTT[A/C]AAACCACACAAAAAT | 71682 |
rs50565677 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14810116 | TGCAACAATGAAAGT[C/T]TTGAGAAGGAGAGAG | 71682 |
rs50570734 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Wdr27 | Mm_Celera | 17:14836055 | GAACCTCATCTTTAG[C/G]AGATTTTATCAGAGA | 71682 |
rs50572425 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14877315 | TGTCAAAGGCGCTCT[C/G]TAAAAGTCTGCTGCT | 71682 |
rs50580599 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14887991 | GAAAGAGATGAGTTA[A/C]TGAAAATGTTTAAGT | 71682 |
rs50633391 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14918722 | GCTAGAGAGGAGAAC[G/T]CTAGGCTGTTTAGAC | 71682 |
rs50635105 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14853946 | TAACTACACACACAA[C/T]TAAGGGATCACTTTA | 71682 |
rs50653696 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14849406 | CTAAGGTCTAAGTGA[A/G]TGGAGAAAGACAGGA | 71682 |
rs50703592 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14858035 | TTGCCAGGATCCCTG[A/G]AAACCAAGTACAGAG | 71682 |
rs50719221 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14853407 | AAAAAGGATTCTTAG[A/G]TTCAGTGATGGGGAA | 71682 |
rs50729903 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14918067 | GACACACTGCCCATG[A/G]CACGAGTTTCACACT | 71682 |
rs50734140 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14815643 | GTGGAAAGAACAGTG[A/G]CCAAGGGAGAAGGAG | 71682 |
rs50735619 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr27 | Mm_Celera | 17:14794684 | AGAAGAACACTCCCT[A/G]CCAGGATGGAATCAG | 71682 |
rs50738816 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14827548 | CATCCATCTGGGAAC[A/G]AGTATAAAAAAACAC | 71682 |
rs50744720 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14849496 | GAGGATGACCATGGA[C/T]GTGGGAACTCAAGAC | 71682 |
rs50749103 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14795195 | TTTTAAAAATAGTTA[G/T]TTAAAGAGAGAAAAG | 71682 |
rs50783496 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14941842 | TCCTTGATGCGATTG[A/G]TGTTCTTGTAAAATG | 71682 |
rs50785090 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14886405 | TGTCATCTTCAGGCT[A/T]TATCTACTATCTGAC | 71682 |
rs50785400 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14829340 | GAAAGAGGCACTGGC[C/T]CATCTTTATTGAAGA | 71682 |
rs50786622 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14859920 | CTGAAAAGAAAAGGT[C/T]TATAACCAGGTTAGT | 71682 |
rs50789785 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14904120 | GCCTACTGATGAGGG[C/T]TGGAGAGGAGGCCTC | 71682 |
rs50790268 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14854479 | TATGATGCAGATGAC[A/G]TAAAGCATGAAGAAG | 71682 |
rs50794166 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14849787 | TGAACAGGAAGAAGG[C/T]AACAGAGACTATTTC | 71682 |
rs50802493 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14829720 | TAAAGTCTGCTGCAA[C/G]TGTGATTCTTGCACT | 71682 |
rs50817247 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wdr27 | Mm_Celera | 17:14797202 | CCTCTTTCCTTTGCG[A/G]GGCCTTTGAGGGCTT | 71682 |
rs50818158 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr27 | Mm_Celera | 17:14854851 | CTTATTCACCATGCA[A/G]TCTTAGGATAGAGAC | 71682 |
rs50829774 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14821937 | TTTGGGGCCTGAGGT[A/G]AGGCAGACATCATGG | 71682 |
rs50834090 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14918951 | CCTGACACACAAGGA[C/T]GGGGGCGAGCCTCAC | 71682 |
rs50835032 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14811620 | GTTCCTGGTCCAGAA[G/T]TTTCTCCCTAGAAGT | 71682 |
rs50850893 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14911515 | TTCCCGGTTCCTACA[C/T]TCTAAAGGGGCCTTG | 71682 |
rs50854376 | snp | A/G | 0.124444 | 0.216185 | missense, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14917246 | TATTGGCAAGCTTAG[A/G]AAATTTTTCCTTAAT | 71682 |
rs50865269 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14919691 | CATGTGCTCACATCA[A/G]TGTCGCCAATGTACC | 71682 |
rs50866829 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14810526 | GCATGTATAAAACTA[C/T]CCACTTATTCAAGGT | 71682 |
rs50868455 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14891474 | GAAAGTTTAGCATAG[C/T]TTGATTATCAGAAAA | 71682 |
rs50875756 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14810034 | TCCTTAGGTTGTCTG[C/T]CAGATAGTGTGGTCA | 71682 |
rs50888288 | snp | A/C/T | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14819159 | ATCCCTCTGTGAGTG[A/C/T]CCCCTCTTTCCATTT | 71682 |
rs50942228 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Wdr27 | Mm_Celera | 17:14829527 | TTACCAGCATGACGG[C/T]CATCACTCAGCCACA | 71682 |
rs50952031 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14910453 | AAATGCCCAGCATTT[A/G]TGTCAGTGCTAAGGA | 71682 |
rs50969173 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14810566 | ACCTCTGATAGGCTG[A/G]TATTCACATATCCCT | 71682 |
rs50986743 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14918840 | GTGTGATTGGCACAG[A/G]GAGAAGGGAGAGCCT | 71682 |
rs50990970 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14812541 | AGCATCTCTTTCTCC[A/G]TGTTCTGGAAATAGC | 71682 |
rs50991315 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14826951 | GAAAGCTCACATTTG[C/T]ATTTGTTGAGGCAAA | 71682 |
rs50991595 | snp | C/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14891525 | ATAGTTACAAAATTG[C/G]ATCATACTACATTTA | 71682 |
rs50997640 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14878987 | CCAGCCTAGCTTCCT[A/G]CTTCTCTATTATGAC | 71682 |
rs50997922 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14890128 | TGACTACCCTTGTTG[A/G]TTGTTTTTGTTACTG | 71682 |
rs51005517 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | GRCm38.p3 | 17:14886950 | AAGCAGGACCACATG[C/T]ATCATACACTCCTGT | 71682 |
rs51046255 | snp | A/G | 0.297521 | 0.245442 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14840866 | ACATAACAATTAGAA[A/G]AGACTTTAGTTGTTT | 71682 |
rs51056668 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14789782 | ACTCAGGCTCCTTCT[A/G]TGCTGTGACAAGCCC | 71682 |
rs51057305 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14884064 | CATGAATAGCACAAC[A/C]ACCTATGTAGATAAC | 71682 |
rs51065488 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14901977 | TCATCTTGCACACGT[C/T]TTATCACCACCAACT | 71682 |
rs51072939 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14919624 | CTGAGTTTATAAAAG[C/T]AGTTGATGCCCAAGT | 71682 |
rs51089736 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14828627 | AATACTGAAAATGGG[C/T]TTCTGGAGGGCCTGT | 71682 |
rs51091106 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14917795 | CAAGTCAATTTCCAA[C/T]ACAGCAATCTTACTC | 71682 |
rs51106895 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14922070 | TCATAGTCCCTGGGT[A/G]AGAGCCAGCCTCCAG | 71682 |
rs51157228 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14863605 | AAAGCAGAGAGGACC[A/C]CAGTAGAACCAACAA | 71682 |
rs51158900 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14879060 | TCCGATAGCCTCATC[A/G]TATGGCTTCTTTCAT | 71682 |
rs51161398 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14927021 | ACTTTATCCAGAAGG[C/T]TCCCATACACCTCTG | 71682 |
rs51163585 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14917067 | TATTCCCTAACAAAG[A/G]TAACGCAGTAACTCC | 71682 |
rs51163826 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14876544 | GACTTCGCCTCAGGC[A/G]TTTAGTCCCAGGCTA | 71682 |
rs51169520 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14810248 | TCAAGAGAGAAACCC[C/T]GGCCTTTTCTGATTA | 71682 |
rs51170535 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14899128 | GGTTGGCCAGGGCAC[A/G]GCAAAATGTCAAGAG | 71682 |
rs51188304 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14874682 | TCAACTCATTAAGAG[A/G]ACATAGCAACTCAAA | 71682 |
rs51197196 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14929143 | GCACTTCCAGATGTG[A/T]GAGAGATGCCCAAAT | 71682 |
rs51208978 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14856307 | ATATTTAGCAAAAGT[C/T]GAGGAGTGATTGTGG | 71682 |
rs51253957 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14810562 | TGAAACCTCTGATAG[A/G]CTGGTATTCACATAT | 71682 |
rs51258732 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Wdr27 | Mm_Celera | 17:14899701 | CCAGAAAGGTAGCCA[A/C]GCAGAGGCAAGGACG | 71682 |
rs51263848 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14846949 | CCACAGTGTGCTCAG[A/G]GCTGGAGGCCACAGC | 71682 |
rs51267935 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14922892 | TCTAACTTTTGCTCA[A/T]TCAAATACTACCTAG | 71682 |
rs51286270 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14823046 | TGGAATTGTGCCACC[A/G]AGGCTGTGACCCTCA | 71682 |
rs51291152 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14928148 | ACATACAAAATACAT[C/T]GACCCAAACTGCCGT | 71682 |
rs51298747 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14828642 | TTTCTGGAGGGCCTG[A/T]CACTTGTGGCCTATG | 71682 |
rs51323844 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14847947 | CAGTAGGTCCATCCT[C/T]CATCCTTACTTATCA | 71682 |
rs51331001 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14823988 | TCCTGAATTCAACTC[C/T]CAGCAACCACATGGT | 71682 |
rs51347764 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14792943 | CTGTCCACAGAGGCA[G/T]CCCTGTCCACAGATG | 71682 |
rs51355283 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14920014 | TACGACTGCAGTGCA[A/G]AAACCAGCCTATAGC | 71682 |
rs51360923 | snp | C/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14848283 | GGGGTTCATCGTCTG[C/T]GGTATGGGCCCACCG | 71682 |
rs51361186 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14927796 | CGCTCTCCCCAGGGA[A/G]TTTGTGTAGCACAGG | 71682 |
rs51375713 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14929567 | CAGCAGCAAGTGTCT[A/G]GAGGCTAAATTAGAA | 71682 |
rs51382348 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Wdr27 | Mm_Celera | 17:14925029 | TCCAACCATGACAGC[C/T]ACGTGTGTTTGTTGT | 71682 |
rs51384677 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14828350 | TGAGAATAGGGCATC[G/T]GAAAGCTAACCCCAC | 71682 |
rs51399721 | snp | A/T | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14840525 | AGAAAACTGAAAAAA[A/T]AATAGAAGCCAATGA | 71682 |
rs51405814 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14900381 | CAGTCAACTAGCAGT[C/T]CTCACTCTAACTCGG | 71682 |
rs51411599 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14888069 | AGAAGACAGATGCAT[C/T]CTAAGAAATGCTGTA | 71682 |
rs51411718 | snp | A/G | 0.244898 | 0.249948 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14840922 | AGGAGCTAAATACTT[A/G]CTTTGGCTGGTTCTT | 71682 |
rs51434300 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14789787 | GGCTCCTTCTGTGCT[A/G]TGACAAGCCCACTGT | 71682 |
rs51466548 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14920249 | CACATCTATTTCTAT[C/T]ACGCTCACAGAGGAG | 71682 |
rs51486637 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14825679 | CTTCAAAAACAATAG[A/T]GTGATATAAAATTCC | 71682 |
rs51495788 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14824831 | TTGTGAAATATGTGA[A/C]GAGGCTTTGGGTCAG | 71682 |
rs51496404 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14859111 | TCTGGAAATGGAGGA[C/T]GATGGTAGAGGGGAG | 71682 |
rs51502829 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14908749 | AATAACTGGGTACAG[C/G]ACATAACAAGGCCCA | 71682 |
rs51503236 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14919635 | AAAGCAGTTGATGCC[C/T]AAGTCATTCAGGAGC | 71682 |
rs51511960 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14929005 | CAATAGACAGCGATG[A/C]CTAACTTTGAGAGTA | 71682 |
rs51513948 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14851417 | CTATGAGCTCTTACT[G/T]GGTTGGGAAATGGTT | 71682 |
rs51519827 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14810731 | TTGTACCTTCATGCC[A/G]ACGCTGACTGGTACA | 71682 |
rs51536631 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | GRCm38.p3 | 17:14928077 | AATTTGTGTAAACAC[C/T]AATTCTGGTGGCTTA | 71682 |
rs51542684 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14812991 | GATTGAAATGGGATT[C/T]GCAAGACTCTAAATA | 71682 |
rs51551128 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14876294 | CCAGAATACAGTGAC[A/C]TCTAACAAGACTGAC | 71682 |
rs51559450 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14810471 | GGGTGTTTCTCCTGA[A/T]TTAAGAAAATTTTCT | 71682 |
rs51569643 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14793869 | CTTCAACTATTGCAG[G/T]ATCTGTGCAGTTATC | 71682 |
rs51585222 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14935926 | TGGAACATACTGCAG[C/T]CAAGGCCATAGAATC | 71682 |
rs51590421 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14922532 | GTGCTGCTTTTAGTC[C/G]CTTCCTGAACGCTGC | 71682 |
rs51592007 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14940838 | TTAATTAGTGAAGGT[G/T]CCACAGCAGTAATGC | 71682 |
rs51599806 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14900503 | CCAGCAGACATCAGG[A/G]CACATTTTCACCTGT | 71682 |
rs51610689 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14810515 | TAATTGGAATTGCAT[C/G]TATAAAACTACCCAC | 71682 |
rs51612168 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14888013 | TGTTTAAGTCAGCTA[A/G]CACTTACTTTTGTCT | 71682 |
rs51616382 | snp | A/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14915863 | TCCCCAAACCAGGCA[A/T]AGTCAAACAAAATGA | 71682 |
rs51623640 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14826631 | TAGCCTAGCAGTTCA[A/G]CCAGACTGAAAGCTT | 71682 |
rs51640849 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14814772 | ATATTGTACTGAACG[A/G]TCAAAGGCCAACTCG | 71682 |
rs51642160 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14880652 | GATGTCTATGCTTCT[C/T]GAGGAGACTGAATCA | 71682 |
rs51646089 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14922402 | AATCAAAAAATGTGG[A/C]TACAGATCTCTTTCA | 71682 |
rs51657150 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14825743 | AAAGAGCAAGAGAAA[A/G]AAGAGACAGATGGGA | 71682 |
rs51657975 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14820858 | ACCATTCTCCTGAGA[A/C]TCTGAACAGGCAAGT | 71682 |
rs51666124 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14815958 | TGGTCCTGGGCCCTA[A/T]GGGATAAATGCCTAA | 71682 |
rs51685213 | snp | A/G | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14873107 | GACTAACAAAATTAA[A/G]TATAGCCAAGAGTAT | 71682 |
rs51685482 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14812648 | GTTAGGAGGCTAAGA[A/C]AAGAGGTAGCTGCCA | 71682 |
rs51692930 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14831022 | CTCACCCTTCCGTGC[A/C]TCTCTGCCCTTTCTT | 71682 |
rs51693458 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14794035 | CTCAGGGGCAGCTCA[G/T]AAACAGACTTTGGAA | 71682 |
rs51721268 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14922109 | ACAAACCTATGGGGC[G/T]CAGTGGTGTCAGAGG | 71682 |
rs51724485 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14795605 | GCTGTTTTTCTGAGT[C/T]TGGCTATGTTGCTTG | 71682 |
rs51754810 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14814307 | AGTATATTTGTATTG[C/T]GTAGCTATTCCCATT | 71682 |
rs51774947 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14821912 | AGGACAGGGTCCACC[A/G]ACTCCATTGTTTGGG | 71682 |
rs51775653 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14854781 | GTATATATCATATAG[C/T]CACAACTTGCATGAT | 71682 |
rs51779445 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14927880 | CCCCAACCTTGGAGA[C/T]ATTTACATAAACTGT | 71682 |
rs51804489 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14829747 | CACTCCATTCGTCCA[A/G]CACACACAGGGTAAT | 71682 |
rs51808406 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14907580 | CAGAGATGCTTTCTA[C/T]GAGCAGTCACAGCCT | 71682 |
rs51819735 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr27 | Mm_Celera | 17:14819048 | ACATGTGATGAAGGC[A/G]AGGACTTTAAAAATA | 71682 |
rs51823631 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14821182 | GCCTGGAGCAGCAGA[A/G]CACTGGTGTGACTCT | 71682 |
rs51829813 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14854594 | AAGGCAAGCAATAGT[C/T]TAAGCTCTAGGGTTT | 71682 |
rs51832833 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14909279 | GATGCTTTGAGAACA[C/T]CATAAGGTGGCCAGG | 71682 |
rs51833208 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14815552 | AACACATAGCCCTTT[C/T]CACAGCTCTTCCTGA | 71682 |
rs51850080 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14905588 | ATGGAATGGTATAAA[G/T]AGCCGGGCAGTGGTG | 71682 |
rs51859410 | snp | C/T | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14848360 | AAGAAGGACCTTTCA[C/T]ACCAACAGCTTCCTT | 71682 |
rs51869911 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14927721 | AACCTGAAAAAGCGG[C/T]GTAAGACAGCTATTT | 71682 |
rs51894440 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14846326 | GCTGGGATTACAGAC[C/G]CGATGACCACACCTG | 71682 |
rs51911531 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14904499 | TGCTGTCTCCTAATC[C/T]CACCTTTGCCCTTAC | 71682 |
rs51926472 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14918732 | AGAACGCTAGGCTGT[C/T]TAGACCTTGTCAGGT | 71682 |
rs51952921 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14863755 | GAGGCAGGCGGATTT[C/T]TGAGTTTGAGGCCAG | 71682 |
rs51954595 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14914923 | CTGTTAAAGGAATGG[G/T]TATGATGTATGTAGT | 71682 |
rs51959766 | snp | A/G | 0.391111 | 0.206368 | missense, downstream-variant-500B, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14915702 | ACTCACTGTGGTGCC[A/G]ATGTATAGCCGGACG | 71682 |
rs51981541 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14906039 | TGATTACCACTTTTG[A/G]ACTTACTGGCCACTG | 71682 |
rs51988601 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14849378 | GGTTCAGCATTGTGA[A/C]AGAACCTCTAATCTA | 71682 |
rs51991719 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wdr27 | Mm_Celera | 17:14821285 | GGCATTTATTAACTT[A/G]GAATCCCACTGAACA | 71682 |
rs51995576 | snp | A/C | 0.32 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14919095 | TGCCATGTTTGGTTA[A/C]TGATAAACTCATCCT | 71682 |
rs52010705 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr27 | Mm_Celera | 17:14794809 | TGTCCTTGCTAATGC[G/T]GAATACCCTTACCCA | 71682 |
rs52024210 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr27 | Mm_Celera | 17:14826301 | TGACACAGACTAAAA[C/T]TAGGGCTGGTCCTCA | 71682 |
rs52027357 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Wdr27 | Mm_Celera | 17:14841901 | CTAGCAGATGCATAT[C/G]AAAGGTGGTTGCAAC | 71682 |
rs52030495 | snp | C/T | 0.18 | 0.24 | intron-variant | Wdr27 | Mm_Celera | 17:14815232 | TCAGATTTAAGTAAA[C/T]TAAGTCTAGTTACCA | 71682 |
rs52030866 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14918952 | CTGACACACAAGGAT[A/G]GGGGCGAGCCTCACA | 71682 |
rs52042957 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14935901 | GTTTATGCTCACACT[C/T]ACTCTAAAGTGGAAC | 71682 |
rs52054464 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14899396 | CACAGAGATGGCTAT[A/G]AAACACCACTTACAG | 71682 |
rs52098699 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14900222 | CAAAGAGGCAGATGG[C/G]ATAAGGTAGGATATG | 71682 |
rs52124584 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14900207 | GAATGAGATCAGATG[C/G]AAAGAGGCAGATGGC | 71682 |
rs52129961 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Wdr27 | Mm_Celera | 17:14821623 | CACACACACACACAC[A/T]ACTTCTGGTATTCTT | 71682 |
rs52153869 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Wdr27 | Mm_Celera | 17:14850406 | CTGATGACCCCCAAA[A/G]CAAACACAAATCTCC | 71682 |
rs52162966 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Wdr27 | Mm_Celera | 17:14861621 | AAATAAGAGCAGCAA[C/G]GCATTTGAATGTGTC | 71682 |
rs52172489 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr27 | Mm_Celera | 17:14819331 | ACCATCACACACCAC[C/T]ACTATCACCACGATC | 71682 |
rs52230050 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14790874 | GTGTGCATGCACGCA[C/T]GGGAGCATGTGTATA | 71682 |
rs52230757 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14833568 | TCTTGGTTTAATTTT[A/G]GTGGTTTGGGTCAAT | 71682 |
rs52235087 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr27 | Mm_Celera | 17:14821999 | CCTCAGAATGGGCAG[C/T]AAAAGAGAAGAGACA | 71682 |
rs52249792 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14900201 | ATGGTAGAATGAGAT[C/G]AGATGCAAAGAGGCA | 71682 |
rs52363997 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14790831 | TATGTGCCTGTGTGT[A/G]TGTGTGTGTGTGTGT | 71682 |
rs52377210 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14900215 | TCAGATGCAAAGAGG[C/G]AGATGGCATAAGGTA | 71682 |
rs52416216 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14833154 | ATATCGAATCACTGT[G/T]GCATTCAAATATATA | 71682 |
rs52422034 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr27 | Mm_Celera | 17:14821969 | AGGAAATGTGTGTTG[A/G]AGCAAAGAAATCCAC | 71682 |
rs52432055 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14933751 | GAAGGAAGGAAGGAA[A/G]GAAAGAAAGAAAGAA | 71682 |
rs52435881 | snp | C/T | | | intron-variant | Wdr27 | GRCm38.p3 | 17:14790823 | TGCATGTGTATGTGC[C/T]TGTGTGTATGTGTGT | 71682 |
rs52535101 | snp | A/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14915996 | TATACTAAACCATAT[A/T]ATGTGTGGCACTGTT | 71682 |
rs107596978 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14853655 | CTATCTGCTAGGCTC[A/G]TGACCACCCACACTT | 71682 |
rs107599652 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14861244 | ATGTCAGCACAGAGA[C/T]AATGAAGTGAATGAA | 71682 |
rs107600027 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14901706 | GGCTGGCTCTTTGGG[A/G]TCAGAGCAGGAAGGC | 71682 |
rs107600075 | snp | G/T | | | upstream-variant-2KB, intron-variant | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14941579 | GTTGGTTGGTTTTTT[G/T]TTGTTGTTGTTGTTG | 71682 |
rs107600367 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14909215 | TTCAGACTCTAGATC[G/T]GGAACAGTGTGAGCG | 71682 |
rs107603104 | snp | G/T | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14937843 | TGTTTAATTTTTTTT[G/T]GGGGGGGGAGCCTTT | 71682 |
rs107603352 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14913105 | ACTCATATGTGTAAT[C/T]TCAACAAGTTGACCT | 71682 |
rs107603714 | snp | C/T | | | intron-variant, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14908781 | TCGCCTTTCTCACGC[C/T]CTCCTTCCCAAGGAG | 71682 |
rs107603889 | snp | G/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14915636 | AAACCCTATTCCTAT[G/T]GTATACCTGCAGCTC | 71682 |
rs107605833 | snp | C/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14829087 | GGCTCAGCCATCGTC[C/T]ACCCTTGGGTTGTGC | 71682 |
rs107605853 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14901145 | CCAAGAAGTGGGAGT[A/G]AGTGGGTAGGAGAGC | 71682 |
rs107610018 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14822123 | AACGACCTACTTCCT[C/T]CCAACAGCCTGTTAG | 71682 |
rs107618560 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14862287 | GGAAAGGTTTTATTC[A/G]GCTTACACTTCCTGC | 71682 |
rs107619024 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14902118 | CCTCACACTGGCTTG[C/G]AGGATCACCCGTCCT | 71682 |
rs107620919 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14834788 | AAGAATTGCGGCCAT[G/T]GATACTTCAAAGTTA | 71682 |
rs107622289 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14914754 | TGGGAAAGTTCTGAG[C/T]GGGGACTTGAGGTTG | 71682 |
rs107624173 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14851525 | TTGGTAATAAAGAAC[C/T]GCCTTATAGCCAATG | 71682 |
rs107624672 | snp | C/T | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14873485 | CTGCTGCTGCTGCTG[C/T]TCAGTTGAGCCGTAA | 71682 |
rs107625640 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14820467 | GAGTTTGGAGGGACA[A/G]GGTGTGGGAAAATGG | 71682 |
rs107626806 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14819814 | TCCCCCCAGTATCAT[G/T]AGACCTAGTCCTCAG | 71682 |
rs107631837 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14878541 | ATCATTCTTCAGGAG[A/T]CCAATCTGGGAAATA | 71682 |
rs107632468 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14788008 | TTAGGCTCAGCCTAT[A/T]TTGAGCAATTCCACG | 71682 |
rs107633112 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14799521 | TTGTTAAAGATATTA[A/G]TGCTGCTATAAAGAC | 71682 |
rs107635711 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14820006 | TTGTTAGATGGCATT[C/T]GGATCTTGGAGAGAG | 71682 |
rs107637242 | snp | A/G | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14939323 | AATCCACATAAAAAA[A/G]GGGATTTATTAAAGT | 71682 |
rs107638252 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14931160 | GATGGGCGGACGGAC[A/G]GATGGATGGATAGAT | 71682 |
rs107638695 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14910940 | TCCCACAAGCTCAGC[A/G]CAGGCACAAAGACCT | 71682 |
rs107639772 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14823926 | GTTGGATTAGGGGGC[C/T]GGAGAGATTGATCAG | 71682 |
rs107641353 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14809770 | AATTATGGCTTAAAT[A/C]TCAAATGTCCCTTAT | 71682 |
rs107641422 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14861849 | AGATGGAGGAAGGAT[A/G]AGGAATTGTTACTAT | 71682 |
rs107641456 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831160 | TGCTGGTTTCTGCAG[A/T]TACTCCAGGGTATGT | 71682 |
rs107641934 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14814379 | CTTCATCCCTGCACC[C/T]TCCTTGCAACTTTTT | 71682 |
rs107642216 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14831910 | TTGGGAAAGTGAAGT[C/G]TTCTTTTCCTACATC | 71682 |
rs107642988 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14901165 | GGTAGGAGAGCAGGG[A/C]GGGGGGAGGGTATAG | 71682 |
rs107644880 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14789502 | GACACTGGAGTTACC[A/G]CAAGGAACTCAGAGT | 71682 |
rs107646309 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14834829 | GTGTGAGTTAATTGT[C/T]GCCATTATGTTTAGC | 71682 |
rs107646925 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14864724 | AAGCATGCTGGACAG[G/T]GCACAGTATCCAGGA | 71682 |
rs107647293 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14836162 | AGCACAAACTCTACA[A/G]CCAGTCCCACAACAC | 71682 |
rs107656032 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14862613 | ACAAGCACCTAAAGG[C/T]CAAAAGGAGTAAAGG | 71682 |
rs107658406 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14797385 | CATAGTTTACTAGGG[A/G]TGGTTTCCTGAGTGT | 71682 |
rs107658838 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14827486 | GTGTCAAGTAACCAA[C/T]GAGTTAGCCCTGTCT | 71682 |
rs107660019 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14850414 | CCCCAAAGCAAACAC[A/G]AATCTCCTTTTGATA | 71682 |
rs107662513 | snp | C/G/T | | | intron-variant | Wdr27 | GRCm38.p3 | 17:14817784 | CTGTGTTACCAGCCC[C/G/T]GACTGCTGCTGATGC | 71682 |
rs107663341 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14912832 | AAGAAAGAAAGGAAG[A/G]AAGAAAGAAAGAAAG | 71682 |
rs107666379 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14791799 | CCTCCCTGCCAAGGA[C/T]CTGCCTCAGCTTGGT | 71682 |
rs107672440 | snp | A/G | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14936171 | AGGGGAAGATGGTAA[A/G]GAGGCAGAGAAAGGG | 71682 |
rs107673854 | snp | A/C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14855469 | GTAAAGGATGTAAAA[A/C/G]GGTATCCAAGCAAAT | 71682 |
rs107674646 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831822 | GGGCTTCCTCTTCAT[C/T]TAGTTCAGTGCTGCA | 71682 |
rs107674763 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14905996 | CTAGATACCATAGGC[C/T]AACAAATGAAAAGCC | 71682 |
rs107675419 | snp | A/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14871814 | TCACATGTTTTTTTT[A/T]AAAAAAAGTGAATAG | 71682 |
rs107675901 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14902570 | TAATTCAATGCCTAG[A/C]CAACCATGCAGCATC | 71682 |
rs107676076 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14876035 | GAGACAGAATAAACT[A/G]GAGAGGTCTTGCTCA | 71682 |
rs107677854 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14878676 | TATCTTAGGCATACA[A/G]ATTTTTTTTAAGCAA | 71682 |
rs107680761 | snp | C/G | | | utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14785869 | TACATCTGGAAATGA[C/G]TCTGGCACACTGGAG | 71682 |
rs107682727 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14831835 | ATTTAGTTCAGTGCT[A/G]CAGCTCTGCAGGGTT | 71682 |
rs107683341 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14864773 | GTCTTTCTGTGTGGT[A/G]AAGATTTCAGTGGCC | 71682 |
rs107687512 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14827304 | CATCATAGCTTTGCT[C/T]GGCCTACATTCTTAT | 71682 |
rs107689845 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14850187 | GAAGCAAGCCAATAC[A/G]CCTCTATAGCCTTTG | 71682 |
rs107690360 | snp | A/C | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14916216 | TCTGCCTCGTGGGTG[A/C]TGGGATTAAAGGCAT | 71682 |
rs107691994 | snp | A/C | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14873304 | TACATGATCCCCCCC[A/C]AAAATGGAAAATGAA | 71682 |
rs107694080 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14876997 | ATAAAAACAAGAACT[A/G]ACTGTTTACATGTTC | 71682 |
rs107695630 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14822218 | CCTCTGCGTATTGCT[C/G]CCCTTGAGACCAAGC | 71682 |
rs107696687 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14793517 | TCTTTCCTTTTGTTA[A/C]AAAATACTTGACCCA | 71682 |
rs107698223 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14788318 | TCTTTAAAGTATATT[A/G]ACTTAGCACACCACT | 71682 |
rs107699594 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14836323 | ACCCAACCAGTGGCA[C/T]GGGTCCCTTCTGGTC | 71682 |
rs107701248 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14846026 | TTTCTTCACCTGTGG[A/G]TGTATATAAGTATAA | 71682 |
rs107702026 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14828048 | TGGGGGTGGGGGTGG[A/G]GGCAGAACCTTAGGC | 71682 |
rs107704114 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14839072 | AATATTAAAATCATG[C/T]TCTACAAACATCATG | 71682 |
rs107705257 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14788384 | ACCTCTGAGGCCTAG[A/G]GCAGATTATTTCCCT | 71682 |
rs107706881 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14912828 | GAAAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG | 71682 |
rs107707874 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14817814 | CGTCTGCTCTCACCA[C/T]CACTCCTGCGCTCTG | 71682 |
rs107708787 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14875835 | AGACTGTATGAATTG[A/G]AGAGGCCCTCCCTGC | 71682 |
rs107710221 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14856692 | CTCACCAGGAAGCTG[A/T]CCCTCTGCTTCTGGT | 71682 |
rs107712166 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14800090 | GCCACCATGCCTGGC[A/G]ATGTCAAAGAATTTA | 71682 |
rs107712931 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14817357 | CATCTGTAGTGCATA[C/G]AGAGTTGTGGAAGTA | 71682 |
rs107713831 | snp | C/T | | | synonymous-codon, downstream-variant-500B, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14915695 | TGCTTATACTCACTG[C/T]GGTGCCAATGTATAG | 71682 |
rs107719135 | snp | A/C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14903888 | TAGCTAGTTACCCCA[A/C/T]CCCCTTTGGTCCCAG | 71682 |
rs107719823 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14810243 | GACTCTCAAGAGAGA[A/G]ACCCCGGCCTTTTCT | 71682 |
rs107720238 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14859310 | AAGAAGGTGCAAATG[A/G]CGACAGCTACTGCAC | 71682 |
rs107721056 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14902370 | CTTTTAATTTTCAAG[G/T]AAGGCCAACTTTGTG | 71682 |
rs107721902 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14907529 | GCCTCCTTGAATCTG[A/G]AAGGCAGCGCAGGCA | 71682 |
rs107724910 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14820008 | GTTAGATGGCATTTG[C/G]ATCTTGGAGAGAGTC | 71682 |
rs107728356 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14878159 | AGCCACCTCTCCAGA[A/C]ATGCCCCTGGTCTTT | 71682 |
rs107729392 | snp | A/T | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14872164 | TTACTTACTTACACG[A/T]CTCAGAACCACCTGC | 71682 |
rs107731129 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14878450 | TAACTAGACATGCAG[C/T]CCACAGTAAAGACCA | 71682 |
rs107732896 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14863701 | CAAGCTAAACCAGGC[A/G]TGGTGGTGCACACCT | 71682 |
rs107735114 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14927227 | TAAGAATGCCCCCCC[A/C]CACACAGGTTCATAC | 71682 |
rs107736880 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14852050 | GACCCTTTTTGGTCC[C/T]TGTCTGCGTAGAATG | 71682 |
rs107738665 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831474 | GCATGTGCCAAGAAA[G/T]GAACTATTTGAGTTA | 71682 |
rs107739086 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14836423 | CCACTCCCAGGCACT[C/G]TAATATGCCCAGGAC | 71682 |
rs107742229 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14834899 | TTTAAATAATTATGG[A/C]ATCATATTTCTCTCC | 71682 |
rs107743837 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14828050 | GGGGTGGGGGTGGGG[A/G]CAGAACCTTAGGCAC | 71682 |
rs107744524 | snp | G/T | | | upstream-variant-2KB, intron-variant | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14941582 | GGTTGGTTTTTTGTT[G/T]TTGTTGTTGTTGTTT | 71682 |
rs107749989 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14930063 | TGTGTCTGATTCAGT[C/T]AAATATTCCTTCATG | 71682 |
rs107751557 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14877816 | GTTTTTTTGAGGGCA[C/T]ACCATACTGTCTGCA | 71682 |
rs107753126 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14813091 | GAATTTATTTTCTTT[A/G]ATTTTCCTTTTGGCT | 71682 |
rs107753488 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14823942 | GGAGAGATTGATCAG[C/T]GGTTAAGAGCACTGA | 71682 |
rs107753552 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14830565 | ATTCTTAACCACTGA[A/G]CCATTTCTTCAGGCC | 71682 |
rs107754366 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14814384 | TCCCTGCACCTTCCT[G/T]GCAACTTTTTTAGTG | 71682 |
rs107755292 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14878903 | TCAGGACCTCTGGAA[A/G]AGCAGTCAGTATTCT | 71682 |
rs107755490 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14825541 | ATACATACACACACA[C/T]ATACACACACACACT | 71682 |
rs107756558 | snp | A/T | | | intron-variant, stop-lost | Wdr27 | Mm_Celera | 17:14873488 | CTGCTGCTGCTGCTC[A/T]GTTGAGCCGTAAAAA | 71682 |
rs107756732 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14902052 | AAGACAATCTGAGAA[A/T]TTGGAGGGAAAGGAA | 71682 |
rs107760644 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14819730 | CTGGTCACCATCGTG[A/G]TTCATAATCATCATA | 71682 |
rs107760739 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14902768 | TAGTATAAGTCAAAA[C/T]ATCCAGACTCAGGCT | 71682 |
rs107761907 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14853883 | TTGTCCCTGTCAAAC[A/C]CAAGCAAGTCCTTCC | 71682 |
rs107764483 | snp | G/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14829084 | TATGGCTCAGCCATC[G/T]TCCACCCTTGGGTTG | 71682 |
rs107764515 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14830025 | CCCATCCATGATGTA[A/G]GTAATATCCCAGAGC | 71682 |
rs107765009 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14849834 | AAGACATTTCCAACT[A/T]GAAACTCACAAGTTT | 71682 |
rs107771966 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14821210 | TCTAGCAAAGATCTG[A/G]ATGGCAGATTCAGTC | 71682 |
rs107776912 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14846716 | CTTTAATCTGCTTGT[C/T]CTTGAGTAAAACATA | 71682 |
rs107776927 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14907089 | AAAAACAAATAAATA[A/G]GCAACACTGACAAAC | 71682 |
rs107777857 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14836387 | ACTCTGCTGCCAGTC[C/T]CACAACACCCAGAAG | 71682 |
rs107779477 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14929312 | AAAGAAACCCTGTCT[A/C]AAAAAAACAAAAATA | 71682 |
rs107781672 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14790903 | TATGCATGTGATGCA[C/T]ATGAGTGTGTGTGCA | 71682 |
rs107782104 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14830875 | GGGTACAGAGCTAAA[A/C]AAAAAATTCTCAACT | 71682 |
rs107785921 | snp | A/G | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14908529 | AAAAAAAAAAAAAAC[A/G]TAAGGAAACCTGAAA | 71682 |
rs107788412 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14822066 | GGGGTCAGAAGAGAG[A/T]GTGTGCCCTAATGTC | 71682 |
rs107788601 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14840377 | TATTTATTAATGATA[A/G]TTTTAGGGTATGAAA | 71682 |
rs107790401 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14906551 | GCCTCTCAGCCTTCA[G/T]CACATTCACTGCCGT | 71682 |
rs107791759 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14829614 | CACTGTATTAATTAT[C/T]CTTCTTTTATTGAGT | 71682 |
rs107793408 | snp | C/T | | | intron-variant, missense, synonymous-codon | Wdr27 | Mm_Celera | 17:14848524 | TTGCACATAACATGT[C/T]CCTCTCTGCAGCTGT | 71682 |
rs107793676 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14906773 | AGGGCAGTTGGCATA[C/T]AAACACACAGCAGTT | 71682 |
rs107793853 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14903953 | CGGCATTTCCCTGAG[C/T]TCATTTACCTGCTGG | 71682 |
rs107794789 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14795476 | GCCTTTACTTCCCAA[A/G]CCTTCACACCTGAGC | 71682 |
rs107794845 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14856933 | GTAAATATCTGATAT[G/T]TAGGATATCTGATAT | 71682 |
rs107797254 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14787609 | GAGGCATTTTCTCAA[C/T]TGAGGTTCCCTCCTT | 71682 |
rs107799887 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14841406 | TGTAAACATACAAAA[A/T]TAATATACAAAAATT | 71682 |
rs107801181 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14821700 | TTGCATATTGGTTGC[C/T]ATTTCCCAGCTGTAT | 71682 |
rs107802349 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14821009 | ACTGGATCTCCTCTG[A/G]CAGATGGGAGCAACA | 71682 |
rs107802366 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14795131 | TCAAGGTATTTTTTT[A/T]AACTGATAGTGGGTT | 71682 |
rs107803844 | snp | A/C/G | | | intron-variant | Wdr27 | GRCm38.p3 | 17:14907026 | TGTGAAGAGTTGGGG[A/C/G]GAGGAATATGATCAA | 71682 |
rs107804808 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14878570 | TAAGCCTTAACATGG[A/G]GACTGTGCCGTCATT | 71682 |
rs107807106 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831517 | TTAACGTTTGAAAAT[C/T]ATTTTCCTACATGCT | 71682 |
rs107807464 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14905671 | GTTCAAGACCAGCCT[A/G]GTCTACAGTGTGAAT | 71682 |
rs107809149 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14910583 | AACTACAGGTACTTT[C/T]CAACTTACAGTGGAG | 71682 |
rs107809179 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14855403 | CAGGACCATCTTTCT[G/T]CTTCATTCCAAGTAA | 71682 |
rs107809471 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14854186 | CGCAACTGTAGTATT[A/T]GACCAGGGTCATCTC | 71682 |
rs107809547 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14906301 | AACTCTGAATGCTGC[A/C]ATCAGCCTGACAGGA | 71682 |
rs107811197 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14799599 | TTTCAGTGTTAGAGA[A/G]CATTGGGGCGGAGCT | 71682 |
rs107817467 | snp | A/G | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14936542 | GAGAGAGAGAGAGAG[A/G]GAAAGGGAGGAAAGA | 71682 |
rs107817984 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14877591 | CTCCAAGTCTGACAC[A/T]GCCAGGCCAAGCCAG | 71682 |
rs107818217 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14903917 | AGCCTGCTTCTTCCT[C/T]TGTGTCTCCTCAGCA | 71682 |
rs107818368 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14942884 | AAGTGTCCCTCCCGG[C/T]GCTGCCCGCACTCAG | 71682 |
rs107822454 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14835807 | TGGACCCAATAGAAG[A/T]CTGATGTAAAAAATA | 71682 |
rs107823294 | snp | C/T | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14938147 | GACAGACTTGACACA[C/T]CAGGCACTTTGTGCA | 71682 |
rs107824116 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14832060 | ATTCTTCTGCATGTG[C/G]ACATACGGTTTTCCC | 71682 |
rs107827422 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14793260 | TCTTTCTTTCTCTCT[C/T]TCTTTCTTTCTTTCT | 71682 |
rs107836570 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14862300 | TCGGCTTACACTTCC[C/T]GCATTACTGTTCATC | 71682 |
rs107836973 | snp | A/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14943389 | CCTGTCCTAAGGTCC[A/C]TCTTACCGCTTCCCT | 71682 |
rs107839809 | snp | C/G/T | | | intron-variant | Wdr27 | GRCm38.p3 | 17:14905281 | TATGGAAACAGCCTG[C/G/T]GTGTCTATCAACTCA | 71682 |
rs107840602 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14796265 | TTTTCCTTTTTACAC[A/G]TTTATGTCTGGTTTT | 71682 |
rs107840875 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14809425 | ATTCAAATTGGTTCA[A/G]TATACCCTAGATGGC | 71682 |
rs107842617 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14793202 | TTTATGAAAAATTTT[C/T]TTTCTTTCTTTCTTT | 71682 |
rs107849700 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14834572 | CTGAAGTATCCCTCC[A/G]TATGTCTTCTGTTTA | 71682 |
rs107852450 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14920633 | TTCGAGGCCAGCCTG[A/G]TCTACAAAGTGAGTT | 71682 |
rs107854403 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14814685 | CCTGAGCAGCTCCCC[A/G]TCTTTCAAGAAATCG | 71682 |
rs107855153 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14861578 | AAACAAGAACAAAAA[A/C]CAAAATCCCCCAAAA | 71682 |
rs107856196 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14797484 | CCTGCCATATAACAC[A/T]GCTGCCATGATGTTC | 71682 |
rs107856853 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14814546 | CAATTTTCTCTGAAA[A/C]GGTAATGAAAACCTA | 71682 |
rs107858189 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14853482 | TTATCTATTATAAAT[C/T]ATAGAAAACCAAAGA | 71682 |
rs107861460 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14910632 | ATGTTCTTCTAGTTG[C/T]GCTGCCTTGTCTGGC | 71682 |
rs107862518 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14852083 | TCTCTAGTTGCAGGT[A/G]GACAAGGAGTCATCA | 71682 |
rs107865549 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14877362 | ATTTAACAAGTATCC[C/T]CTTGGAACTGACTCC | 71682 |
rs107865894 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14860974 | AAGCTGTGTGGCTCT[A/G]AATGTGCGGTGGGAA | 71682 |
rs107866166 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14830100 | TCACCAAACTATGGC[A/G]GTTGACAGACTAAAA | 71682 |
rs107867932 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14830746 | TTAGCACATTATATA[A/G]TGACTGTAATCTTTA | 71682 |
rs107868138 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831811 | TTCCACACCGTGGGC[G/T]TCCTCTTCATTTAGT | 71682 |
rs107869250 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14903426 | GGCACAGGTGCTCAC[A/G]TACACATTACCAAAA | 71682 |
rs107872257 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14854998 | ATCCCATAGAATGGC[A/C]AAGTTGGGTAATGGC | 71682 |
rs107872765 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14793256 | TCTTTCTTTCTTTCT[C/T]TCTCTCTTTCTTTCT | 71682 |
rs107874263 | snp | C/T | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14938278 | CTGTTGCTTTGTGAA[C/T]TAACAGTGTGATCTA | 71682 |
rs107874356 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14799603 | AGTGTTAGAGAGCAT[C/T]GGGGCGGAGCTTGCT | 71682 |
rs107878164 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14834735 | TTTCTTATAGACAGC[G/T]GATAGATGTATTCTA | 71682 |
rs107878901 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14841410 | AACATACAAAATTAA[C/T]ATACAAAAATTAATA | 71682 |
rs107880361 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14878764 | CCAGTGTACTTTGAT[A/G]GTGTCTCTTTTTTCT | 71682 |
rs107880588 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14890546 | GACCTAAGAGAGGAC[G/T]CGGTCCATCACACTG | 71682 |
rs107882480 | snp | A/C | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14872213 | ACAGTGGGCTGGATA[A/C]TCCCACCATCAATTA | 71682 |
rs107884157 | snp | C/T | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14829274 | AGTGCTACTTCATGC[C/T]CCACCCTTTCTTCCC | 71682 |
rs107885346 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14850222 | AGCTCCTGCCTCCAG[A/G]TTCCTACTCTGTTTG | 71682 |
rs107889764 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14836284 | GTAACTGGATCCAAC[A/G]GGATCCAGGCACCCA | 71682 |
rs107890694 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14822532 | CCAGGTGCTCTGATG[C/T]CAACTTATATACCCA | 71682 |
rs107894106 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14905605 | GCCGGGCAGTGGTGG[C/T]GCACGCCTTTAATCC | 71682 |
rs107894520 | snp | C/T | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14873058 | CAAACTAAAAACAAC[C/T]CTATACATCTACTTT | 71682 |
rs107897572 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14860126 | GGCTAATGCAGGGAA[C/T]CCTGCTTCCTAGATA | 71682 |
rs107898294 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14884984 | CCTAGAGCTATCTCG[A/C]AGCAAAGCCTAACTG | 71682 |
rs107898511 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14791478 | GGTAGTGTAGACATA[G/T]ATTTGCCCAATCTAG | 71682 |
rs107898757 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14889986 | GCCTCCCACTGCCCT[A/G]ATGTGATTGGACAGG | 71682 |
rs107899232 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14795463 | CAAGGCTCATGGGGC[C/T]TTTACTTCCCAAGCC | 71682 |
rs107900329 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14819790 | CTTTGGAAGCTTGCA[C/T]TACCTTCTTCCCCCC | 71682 |
rs107902103 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14905806 | AAGGTTAAATGGGGT[A/G]GAGGCTGGGAACAAA | 71682 |
rs107902935 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14855715 | AATGATTGCTTCAGT[A/G]CCCCAACAGACAGTC | 71682 |
rs107903001 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14832067 | TGCATGTGCACATAC[A/G]GTTTTCCCAGCACCA | 71682 |
rs107903667 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14888497 | ATCCCCTGAGCCCAT[A/G]GGGCAGGAGGAGAAA | 71682 |
rs107904192 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14813203 | TCAGATGCCAGAAAG[A/G]AATAGACAGGCTATA | 71682 |
rs107906950 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14850462 | GTGTGTGTGTGTGTA[A/T]GTGTGTGAGAGAGAC | 71682 |
rs107907101 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14811052 | AAGAAAGCAAACTGA[A/G]CAAATCGAGGCAAGT | 71682 |
rs107907594 | snp | C/T | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14872181 | TCAGAACCACCTGCA[C/T]AGGGGTAGCACTGCC | 71682 |
rs107909450 | snp | A/T | | | intron-variant | Wdr27 | GRCm38.p3 | 17:14899260 | GAGGCTGAGGAACTC[A/T]GGGCGACAGAATGTA | 71682 |
rs107913526 | snp | A/C | | | intron-variant, downstream-variant-500B | Wdr27 | GRCm38.p3 | 17:14908528 | AAAAAAAAAAAAAAA[A/C]GTAAGGAAACCTGAA | 71682 |
rs107914180 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14844757 | GATGTCAATACCCCA[A/G]TCTAAGGCCCCAGGA | 71682 |
rs107915185 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14891857 | ACAACTCTACCACAC[C/T]CGCCTCCCAGCTCGG | 71682 |
rs107916167 | snp | A/C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14878063 | AGCTGCTAGGAACCA[A/C/T]GAGGAGCCCACACTC | 71682 |
rs107916469 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14792247 | ATTTTTATGTGAGAA[A/G]GCTTTCTGTTTTTTG | 71682 |
rs107918801 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14911907 | TCCTTATGGAAGAAA[A/T]CAGAAGGAAAAGCAC | 71682 |
rs107919544 | snp | A/G/T | | | intron-variant | Wdr27 | GRCm38.p3 | 17:14876918 | ACCAAAGCATCTTAA[A/G/T]AAAAAAAGGTTATTT | 71682 |
rs107922917 | snp | C/T | | | downstream-variant-500B, intron-variant | Wdr27 | Mm_Celera | 17:14818546 | ACAAACATACTTTTC[C/T]ACCTACCTAATCAAT | 71682 |
rs107923693 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14806827 | AGGCCGATAACTATA[G/T]TATTAATTACCTAGC | 71682 |
rs107923727 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14909424 | CCCTGTGCAACTACA[A/G]TCTCACTCCACTCCG | 71682 |
rs107927585 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14828263 | AAAGAAAAAAATAAA[A/C]CAAAAACAAAACCTC | 71682 |
rs107930916 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14931795 | ACACAAACCTCGAGG[A/G]TACCTCCACATGAGC | 71682 |
rs107931056 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14900738 | TCTCATTAGTTAAGA[C/T]GAAAGGATGGACTAT | 71682 |
rs107934086 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14833258 | AATATATATTTTTGA[A/G]AATTTCTTCATAAAT | 71682 |
rs107934133 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14876745 | GGAAAAGATGCCACA[G/T]TGTCTCCGTCTTTGG | 71682 |
rs107935820 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14821165 | CAGTGATGAGGGCTG[C/G]TGCCTGGAGCAGCAG | 71682 |
rs107941322 | snp | A/C | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14873303 | CTACATGATCCCCCC[A/C]CAAAATGGAAAATGA | 71682 |
rs107941665 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14824034 | CAATCTGTAATGGGA[C/T]CTGATGCCCTCCTCT | 71682 |
rs107943282 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831256 | AGGGTCTGGATCATC[C/T]CACTCAATATGATGT | 71682 |
rs107945151 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14862301 | CGGCTTACACTTCCT[A/G]CATTACTGTTCATCA | 71682 |
rs107946843 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14907442 | AGAAGTGGATGACCC[A/T]TTCAGAGCTGCAATA | 71682 |
rs107948105 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14827437 | GAAGGCATTTTCCTA[A/G]TTGAGGTTTCCTCCT | 71682 |
rs107948394 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14821453 | AAGGCATCCACCATG[C/T]ACATATACTCATACA | 71682 |
rs107948459 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14910713 | TGGCGAGATACCCAG[A/G]GGGACCCAACTGCTC | 71682 |
rs107950704 | snp | C/T | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14936282 | ATTAAAGTGACCCTG[C/T]CAATATTCTGGCATG | 71682 |
rs107951208 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14836275 | ACACCGGAAGTAACT[G/T]GATCCAACGGGATCC | 71682 |
rs107955366 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14864715 | AATAAAGGCAAGCAT[A/G]CTGGACAGTGCACAG | 71682 |
rs107956263 | snp | C/T | | | intron-variant, nc-transcript-variant | Wdr27 | Mm_Celera | 17:14908818 | AGGCCCTGAACTAAC[C/T]CTCCATCAGGACCAT | 71682 |
rs107957937 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14820334 | AGACCAAGCACCTAC[A/G]CATTTAGGGGTGTGT | 71682 |
rs107958883 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14877748 | ATAAAGGCCCAGTAG[C/T]GACATTGCTGAATAA | 71682 |
rs107960515 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14875483 | TTTAATTACAAAAAT[C/T]CCAGATTTCTCTTTC | 71682 |
rs107962046 | snp | A/G | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14935511 | TAAGGCTGGGGGAGG[A/G]GAGGCTACGACTGAG | 71682 |
rs107964267 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14813979 | CATCAATCAATCAAT[A/C]AATCAATCAACGTCC | 71682 |
rs107969508 | snp | A/T | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14939909 | TTGTTTTTTTTTTTT[A/T]AAATAACCCATGGTG | 71682 |
rs107969638 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14920704 | AAACTAAAAGAAATA[A/T]AAAAAAGTTAGAAGG | 71682 |
rs107970863 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831714 | CATGTCTTGAATGGG[C/T]CATTACTTGCTGTTT | 71682 |
rs107971010 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14933198 | CAGGACGATCCTAGG[A/G]TGCATTTGTGTATGC | 71682 |
rs107972545 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14933188 | TAAGTCCAAGCAGGA[C/T]GATCCTAGGATGCAT | 71682 |
rs107972925 | snp | A/G | | | utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14785283 | CCACCCCAGCTATCT[A/G]GTCATAACTAAAACA | 71682 |
rs107973251 | snp | C/G | | | utr-variant-3-prime, intron-variant | Wdr27 | Mm_Celera | 17:14818873 | CACAGTGATCTGAAT[C/G]CTCCAACATCAATCA | 71682 |
rs107975319 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14904727 | CTGAACCATCACATT[C/T]CACCCCAAGGTGCCC | 71682 |
rs107977071 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14905096 | TACTCACTACTGTGG[A/G]AACACAACGTGGAGC | 71682 |
rs107978222 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831525 | TGAAAATTATTTTCC[C/T]ACATGCTGTTTAGAA | 71682 |
rs107978510 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14861535 | CTGAGCCAATCCCTT[C/T]CCACAGCCAAAAAAC | 71682 |
rs107979240 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14791505 | CTAGGCGCACAACAT[A/G]TATTCATATTAACTG | 71682 |
rs107980647 | snp | C/T | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14829308 | CCATCTCTACCCTCA[C/T]CCCAAGGCACAGTCA | 71682 |
rs107981418 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14864500 | AATCCAACACCCACT[C/T]ATTGAGACAACAGCA | 71682 |
rs107981681 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14822130 | TACTTCCTTCCAACA[A/G]CCTGTTAGACCAGAA | 71682 |
rs107985146 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14831999 | TGCTTAGTTTCTAAT[C/G]CATTTGAGGTTAGTT | 71682 |
rs107986121 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14808007 | AAGTGCCTTTCAATT[A/C]ATACAGTCAGCCTTC | 71682 |
rs107987276 | snp | A/G | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14847774 | CTACAGTGTACTTAT[A/G]TATAATAAATAAATA | 71682 |
rs107987568 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14928267 | CATGGGGAGGGGGGG[A/G]CAGTCTTACCTCCAC | 71682 |
rs107989523 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14796833 | TGTGGCAGTGAATCA[C/T]TGAGGAAAAGAGAGA | 71682 |
rs107992476 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14855490 | CCAAGCAAATGGACT[A/G]AAGAAAGCTTGCATA | 71682 |
rs107992987 | snp | A/T | | | intron-variant | Wdr27 | GRCm38.p3 | 17:14792163 | AAGAACATTTTTTTT[A/T]AATATAGCAAGCCCT | 71682 |
rs107993384 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14877689 | TGTTGCCATAAGCAC[C/T]GAGATACAATGATCT | 71682 |
rs107993973 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14860385 | ATTTTCCTCAGGAGG[C/T]CTGAGGTAATGAGCT | 71682 |
rs107998684 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14905361 | CTTAAGAAAAGCACA[A/G]TTATGAAATCCCCAG | 71682 |
rs107999831 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14864642 | GGGTATCTCTTCTCA[A/C]CATTCTTTGCTGCAT | 71682 |
rs108000555 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr27, Gm34975 | Mm_Celera | 17:14933187 | TTAAGTCCAAGCAGG[A/G]CGATCCTAGGATGCA | 71682 |
rs108003517 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14877530 | CTGTTTTTCTTGTTT[A/G]GAAAGTATACTTTTC | 71682 |
rs108004510 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14902308 | AAAGGAGTGTACAGA[C/T]ACCTCCAGACCCTAG | 71682 |
rs108005197 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14824210 | GGATTTTTGTGAGTT[C/T]CAGGGTAGCAAAGGC | 71682 |
rs108021171 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14817894 | TGCAGAGAGGTTTCT[A/T]GAAGCCCCACATTTG | 71682 |
rs108021320 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14914780 | GGTTGAGGTGAGAGT[A/G]GGTGGGCAAGAGGGA | 71682 |
rs108021642 | snp | A/G | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14871958 | ATTTAGGTTTCTGTT[A/G]TTGTAATAAACACCA | 71682 |
rs108022631 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14907082 | GTTAATTAAAAACAA[A/G]TAAATAGGCAACACT | 71682 |
rs108025825 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14799324 | AAAGTAATGGGCTAA[C/T]CAAGTTGACACGGGA | 71682 |
rs108027381 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14821176 | GCTGGTGCCTGGAGC[A/G]GCAGAGCACTGGTGT | 71682 |
rs108028218 | snp | C/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14871739 | ATGACACAAGAGGTG[C/T]ATGCTATAGCCATAC | 71682 |
rs108028289 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14796389 | GGGTTTTAGGCATGT[A/G]CCACCACACCCAGTT | 71682 |
rs108030074 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14863368 | CCAGAATAAATAATA[C/T]ACTTCACAGAAAAAA | 71682 |
rs108030215 | snp | C/T | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14938167 | CACTTTGTGCATAGC[C/T]GTGAGGAGCCTGCAT | 71682 |
rs108033360 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14831902 | TTTCATCCTTGGGAA[A/G]GTGAAGTGTTCTTTT | 71682 |
rs108036504 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14849104 | CCTTTAGAGGAGCCC[A/G]GCTGAGGGTCAGCCT | 71682 |
rs108036683 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14792322 | GACAGACCTTGAGAT[C/T]GGAGATATGCCTGTT | 71682 |
rs108036702 | snp | A/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14847744 | GACTCCCTCTTCTGG[A/T]GTGTCTGAAGACAGC | 71682 |
rs108040135 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14900571 | AAACATGTTAAAACT[A/G]GACAACAACATGTTT | 71682 |
rs108040834 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14861133 | ACAGACTGAATGGAA[A/G]TCAGAAAGAGAAAAG | 71682 |
rs108042444 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14820048 | CCGGTGGGAAATTTT[C/T]CTTTAGAATATTGAC | 71682 |
rs108044434 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14823956 | GTGGTTAAGAGCACT[A/G]ACTGCTCTTCCAGAG | 71682 |
rs108044492 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831021 | TCTCACCCTTCCGTG[C/T]ATCTCTGCCCTTTCT | 71682 |
rs108044542 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14834471 | TCCAGTAGTAGATTT[C/T]TTTTAAAGAAATTGG | 71682 |
rs108045433 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14798645 | CTCTCTTATCTATAC[A/T]GTTCTTGTGTGAGTT | 71682 |
rs108046003 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831252 | TTTCAGGGTCTGGAT[C/T]ATCCCACTCAATATG | 71682 |
rs108047010 | snp | C/T | | | intron-variant | Wdr27 | GRCm38.p3 | 17:14795823 | ATCTAGGCCCTCAAA[C/T]ACACACACACACACA | 71682 |
rs108047636 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14823821 | AGCTTCTGCTCCATC[A/C]CCTACTGGATGCTGC | 71682 |
rs108047967 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14910478 | TAAGGATTCAGACTC[C/G]GGCCCCTTTCTTTGC | 71682 |
rs108049393 | snp | C/T | | | utr-variant-3-prime, intron-variant | Wdr27 | Mm_Celera | 17:14829521 | GCATTCTTACCAGCA[C/T]GACGGTCATCACTCA | 71682 |
rs108050682 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14831433 | GGGCAGCAATGAACA[C/T]GGCTGAGCAAGTATC | 71682 |
rs108054683 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14861466 | TTCAGATCCAAGTAA[A/T]ACTAAGCATCAAAGG | 71682 |
rs108059822 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14901938 | AACACCACACACACA[A/C]ACACACACACACACA | 71682 |
rs108060042 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14850322 | CCCTAACTTACTTTA[C/T]CATGGTGTTTTGTTG | 71682 |
rs108061173 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14875947 | CTCACACTGGGAGAT[A/G]GTGGGAACTGGAGAA | 71682 |
rs108062039 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14919583 | GACCACTGCTCAACT[A/C]TGATCTGTGTGATTT | 71682 |
rs108062535 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14860982 | TGGCTCTAAATGTGC[A/G]GTGGGAATACTGGCC | 71682 |
rs108064192 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14862937 | AAAGTTACCAGAGCT[A/C]GATAAAGGCATTAGG | 71682 |
rs108064257 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14900886 | GCAAATACAGAAGTG[A/G]ATGGAACAGTCATCT | 71682 |
rs108068070 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14841750 | TATCCCACAGCAGAT[C/G]TCAGAGCAGTAGATC | 71682 |
rs108068447 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14794488 | GTATGATGTGCTGTT[A/C]CAATAATACCTGAGT | 71682 |
rs108070289 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14903833 | ATTTCCTGACTAGCT[C/T]ATAACATATTTAACC | 71682 |
rs108070383 | snp | A/G | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14936832 | AGCTGGGCATATGTA[A/G]TCTGTCAGCTTCCTG | 71682 |
rs108070672 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14787904 | ATTGTCTAAAAACAG[C/T]CCTGCATGCAAATTG | 71682 |
rs108071101 | snp | A/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14871763 | GCCATACATGACAGT[A/T]ATAAAACATTATTTT | 71682 |
rs108073724 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14877944 | TATGTGTACACATCT[A/G]TCGAGAGATAGATGC | 71682 |
rs108074567 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14826699 | CTGCCCCACAACCAG[G/T]CCATGGTAGAGTTTA | 71682 |
rs108075152 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14910784 | CAGGATATAAAGTGA[A/G]TAAATAAAAATTAAT | 71682 |
rs108076703 | snp | A/G | | | utr-variant-3-prime, intron-variant | Wdr27 | Mm_Celera | 17:14818977 | ACTCCAACTTGTGTA[A/G]AGTTGATATAAAACT | 71682 |
rs108078488 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14851111 | ACCCATAGAGTAATA[C/T]ATGGCAATGATCATT | 71682 |
rs108079464 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14841465 | ATAGGAGAGAGCCTC[A/G]TGTGGCTCAGCACAA | 71682 |
rs108082779 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14913104 | CACTCATATGTGTAA[G/T]TTCAACAAGTTGACC | 71682 |
rs108083019 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14830474 | GGAGATGGTGTCAGA[A/T]TGCCTGGACTGGATG | 71682 |
rs108083386 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14876752 | ATGCCACATTGTCTC[C/T]GTCTTTGGTCTGAGA | 71682 |
rs108083703 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14799039 | CTGTGACTAAACCTG[C/T]CTGGTTCTTATGCCT | 71682 |
rs108092713 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14898609 | TGCCAGGGCCAGGAA[G/T]TGGGAGTGGGTGGGT | 71682 |
rs108093922 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14863164 | GATATCATTGATGTT[G/T]GCAGTGTGCTTCATC | 71682 |
rs108094031 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14880929 | TCTGTAATGAGATCT[A/G]ATGCCCTCTTCTGGT | 71682 |
rs108095010 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14858547 | GACAGCGCAGAATAC[C/G]CAGAATGATAAAGAA | 71682 |
rs108095589 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14819861 | TCAGTTCTATATTAG[A/G]GACTTCTAGGTCCTC | 71682 |
rs108095982 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14820465 | GAGAGTTTGGAGGGA[C/T]AAGGTGTGGGAAAAT | 71682 |
rs108096586 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14850905 | TGCACACAGCACTTT[A/T]AATGAGCATAAGGTC | 71682 |
rs108097661 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14910747 | GGACAAGGGGAAGGG[G/T]ATATTGGAAGGGGGC | 71682 |
rs108100402 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14931495 | CACACCTGCGCCATC[A/T]GCCGCAACTAGGAAA | 71682 |
rs108102587 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14809307 | AAACACGGACTATCT[C/T]TCATGGAAAGCTATA | 71682 |
rs108103481 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14792385 | GATCCTGCCCTGAGA[G/T]CACCACTACCTCACT | 71682 |
rs108107836 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14905569 | TCAAGGGAGCAAAGA[C/G]CAAATGGAATGGTAT | 71682 |
rs108111793 | snp | A/T | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14939934 | ATGGTGTCCAATTAG[A/T]ACAAGCAGTGTATGC | 71682 |
rs108112986 | snp | C/T | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14935668 | CACGATGTCTATACC[C/T]CTCTACAAACGGCTG | 71682 |
rs108114778 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14929310 | ACAAAGAAACCCTGT[A/C]TCAAAAAAACAAAAA | 71682 |
rs108117658 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14797083 | TTGTGTTCTTTTTAG[A/G]GATGTACTGTAAAGT | 71682 |
rs108120806 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14910568 | TGGTATTATAATACT[A/C]ACTACAGGTACTTTT | 71682 |
rs108128733 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14887826 | AAATTTAACCAAGCT[C/T]CTAGGAGTGGATACT | 71682 |
rs108128780 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14809465 | GCTGCAGGTTGTACT[A/G]CTTGCCCTGTTGGGG | 71682 |
rs108130434 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14819253 | TTAACCCACACCTTT[C/T]CTCCTCCTCCTTCTC | 71682 |
rs108130677 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14887759 | TGCATGGCCATATGT[C/G]TCCACAGATACAAAG | 71682 |
rs108131841 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14905717 | GCTATACAGAGAAAC[C/G]CTGTCTCGAAAAACA | 71682 |
rs108135304 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14899975 | TGACACAGAGCAGTT[C/T]ATCAATGGCTGGAAG | 71682 |
rs108136704 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14796375 | CCTCTCATCTGCAAG[A/G]GTTTTAGGCATGTGC | 71682 |
rs108137196 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14796902 | TTCAGAGGAACCCAA[G/T]ATGTGTAAGCCTACT | 71682 |
rs108139774 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14835479 | TTCTCTATATTTTTT[A/G]AAAATTCTTCATATT | 71682 |
rs108140718 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14796962 | CATAAAAGCCACAAA[C/T]GTTTACCAACTCACA | 71682 |
rs108142650 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14899793 | CCCCAGCCATCTTTC[A/G]GAAGGGAAAGCACTT | 71682 |
rs108144523 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14809754 | GGGAGATCTGTGGTG[A/G]AATTATGGCTTAAAT | 71682 |
rs108146500 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14912790 | AGTGCAATTACTTTA[C/T]AAAACAATTTGTCTT | 71682 |
rs108146714 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14904523 | CCCTTACAGTCTCTA[C/T]AAAGCAAACTTGAAA | 71682 |
rs108146764 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14909705 | TACTGCTGAAGCATT[C/T]TTTCGCTGGTATTAG | 71682 |
rs108150457 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14835106 | TCAGGACTTGAAATA[C/T]GTTGTTCCACATTCA | 71682 |
rs108153167 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14855555 | CAAAAGTAATCAAGA[A/G]ATAAGGAAGTATACG | 71682 |
rs108156133 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14862906 | CATGGCAGACACAAC[A/G]GATTTCAAAGCAAGA | 71682 |
rs108156928 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14879398 | GTGTCACCATAATGG[G/T]TGGGACAAGCTCTCC | 71682 |
rs108156935 | snp | G/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14871757 | GCTATAGCCATACAT[G/T]ACAGTAATAAAACAT | 71682 |
rs108160410 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14856592 | AAAAAAGAAGACTTG[A/G]TCTTATTTCTGTGTG | 71682 |
rs108161210 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14820284 | CCAATACCATATGGT[A/C]AGTCCTGAAAACAAG | 71682 |
rs108164658 | snp | C/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14892058 | GTAGACACAGCACAG[C/T]AAGTGCTCTGTCTTA | 71682 |
rs108165256 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14874503 | GTATAGAAGTGAGGA[A/G]GAGCTGGAAAGAGTT | 71682 |
rs108166844 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14878685 | CATACAGATTTTTTT[A/T]AAGCAATGTGTCTTA | 71682 |
rs108168306 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14798752 | CACTTTCAAACATGG[A/C]TGCTTCCTTCTACAA | 71682 |
rs108177394 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14822468 | AAACTTACTCTCTCC[G/T]TGTATGCTGCCTGAC | 71682 |
rs108177767 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14931144 | CTCAGATGGATGGAT[A/G]GATGGGCGGACGGAC | 71682 |
rs108179690 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14906986 | AGAACATAAAGCAGC[A/T]GGGTGGGTAAAGAAG | 71682 |
rs108181598 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14900992 | TAGGTGGAACAACAA[C/T]ATGAACTAACAAGTA | 71682 |
rs108181609 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14853224 | CCAGCTCAGGCCTGC[C/T]GAGGCCTCTGTGGTC | 71682 |
rs108186106 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14793214 | TTTCTTTCTTTCTTT[C/T]TTTCTTTCTTTCTTT | 71682 |
rs108186454 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14929298 | CAGCCAGGTTACACA[A/G]AGAAACCCTGTCTCA | 71682 |
rs108187015 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14902580 | CCTAGCCAACCATGC[A/T]GCATCTCCACTCAGC | 71682 |
rs108187317 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14829978 | ACATCTGTGCTCAAC[A/G]AGCTCCTGAGATAAA | 71682 |
rs108187447 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14861456 | GGTTTGGAAATTCAG[A/G]TCCAAGTAATACTAA | 71682 |
rs108189923 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14789364 | CATTCAGTAAGTAGA[A/G]TGTGCAGATGGCTAG | 71682 |
rs108190701 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14855401 | AACAGGACCATCTTT[C/T]TGCTTCATTCCAAGT | 71682 |
rs108191049 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14910764 | TATTGGAAGGGGGCA[G/T]TGAGCAGGATATAAA | 71682 |
rs108194517 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14864271 | GAAAGAAAATACAGC[C/G]CAATATACTTCATGA | 71682 |
rs108196251 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14903408 | GATGTCACTGACCAC[C/T]ATGGCACAGGTGCTC | 71682 |
rs108197231 | snp | A/G | | | utr-variant-3-prime, intron-variant | Wdr27 | Mm_Celera | 17:14818916 | ACGCACCACAGGCCA[A/G]GCTGGTGGGGGCATT | 71682 |
rs108197995 | snp | G/T | | | utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14785769 | GTATGTGCTGGGGGG[G/T]GGTGAAGTGTCTTCA | 71682 |
rs108198253 | snp | A/G | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14938201 | CACCACGCACTAGGA[A/G]ATTTCCCTCCTCTTC | 71682 |
rs108198713 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14796771 | CCCAAACACACTGGC[A/T]CATCATTGGCTTTCC | 71682 |
rs108200334 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14858538 | AGTAAGACAGACAGC[A/G]CAGAATACGCAGAAT | 71682 |
rs108201434 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14836299 | GGGATCCAGGCACCC[A/G]GGAACTGCACCCAAC | 71682 |
rs108202476 | snp | A/T | | | intron-variant | Wdr27 | GRCm38.p3 | 17:14797723 | AATCTGATTTTTTTT[A/T]AATTGGATATTTTCT | 71682 |
rs108203726 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14845946 | AATGGTCATCCTAAA[A/T]TTAACTTTAAAAATA | 71682 |
rs108204150 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14877731 | TGATTCCAATTCTTT[A/G]AATAAAGGCCCAGTA | 71682 |
rs108206385 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14856078 | TTCCTGGCATTGGGT[A/G]TTTCGCTTGATGGCA | 71682 |
rs108212218 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14808748 | AGTCAAGAACTGACA[C/T]CTGCAAAGTAGTCTC | 71682 |
rs108219122 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14860892 | AATCGAGATCAAGGA[A/C]TATCCAGAAACAAAT | 71682 |
rs108219800 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14899696 | ACTTTCCAGAAAGGT[A/G]GCCACGCAGAGGCAA | 71682 |
rs108220768 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14791852 | TTTGGAAGTGGTGGA[A/C]GCAATGACTCAGAGT | 71682 |
rs108221605 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14849077 | AAAGAAGAGGCCTGC[A/C]TCACACACAACCCTT | 71682 |
rs108221916 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14842870 | CCAGAAGGAAACAAA[C/T]GTTTATAACAGCTTC | 71682 |
rs108224805 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14902098 | TCACTCTGTAAGCAT[A/G]CTGCCCTCACACTGG | 71682 |
rs108227581 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14902373 | TTAATTTTCAAGGAA[G/T]GCCAACTTTGTGTCT | 71682 |
rs108228216 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14904059 | CACTGGCCATTAGCT[C/T]TTTTATTGACAGGTA | 71682 |
rs108233416 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14905445 | AAACACCAACTTTGC[A/G]TGTTTTCTCAAATCC | 71682 |
rs108233542 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14914748 | GAGGCCTGGGAAAGT[C/T]CTGAGTGGGGACTTG | 71682 |
rs108234991 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14863297 | TAAAAATTATACAAT[G/T]CCTACTCTATATACC | 71682 |
rs108236352 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14817091 | GTAGACATGTACACA[A/C]ACACACACACACACA | 71682 |
rs108237877 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14900103 | AGGGTAGAATAGGAT[A/G]AGGTGGGATGGGGTG | 71682 |
rs108238374 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14852761 | GTGAGTGCTTCCAGG[C/T]CTCTCAGCCTGCCCA | 71682 |
rs108239370 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14860895 | CGAGATCAAGGACTA[A/T]CCAGAAACAAATGCT | 71682 |
rs108241447 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14864584 | TTACAAGTAGCATCT[A/T]CACTCAACCTGGAAA | 71682 |
rs108241723 | snp | G/T | | | intron-variant, downstream-variant-500B | Wdr27 | Mm_Celera | 17:14916144 | TAACAGTCCTGGCTG[G/T]CCTGGAACTCACTTA | 71682 |
rs108241903 | snp | C/T | | | intron-variant, splice-acceptor-variant | Wdr27 | Mm_Celera | 17:14893224 | ATACCCCAACACACC[C/T]GAAAAGCAAGACTCA | 71682 |
rs108244574 | snp | A/G | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14872359 | TAATGTATCAATTTT[A/G]TATCAATATGGATGA | 71682 |
rs108244870 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14892549 | ACCTGGAAGAAAGGG[A/G]AAAGGAAAGAAATGA | 71682 |
rs108247511 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14822134 | TCCTTCCAACAGCCT[A/G]TTAGACCAGAATTAA | 71682 |
rs108247611 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14830654 | TAATATTGTAACTTA[G/T]ATTTATAACTATATT | 71682 |
rs108247630 | snp | A/G | | | intron-variant | Wdr27, Gm34975 | Mm_Celera | 17:14937299 | AATATAGATAGGTAG[A/G]TAGGTACATACATAC | 71682 |
rs108252767 | snp | A/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14917402 | AAGATTAACTCATGT[A/T]AAAAAGTATACATGT | 71682 |
rs108253783 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14860847 | GGAGGTCAGGAAGTA[A/C]CCAGAGGAGATACAC | 71682 |
rs108256830 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14863224 | ACTTGTATGGGACAC[G/T]GACCAAGAGAGACAA | 71682 |
rs108257653 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14931789 | CATGAAACACAAACC[C/T]CGAGGGTACCTCCAC | 71682 |
rs108260321 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14794475 | AGGAGCATCTGTTGT[A/G]TGATGTGCTGTTACA | 71682 |
rs108263217 | snp | A/C | | | intron-variant | Wdr27 | Mm_Celera | 17:14791854 | TGGAAGTGGTGGAAG[A/C]AATGACTCAGAGTCA | 71682 |
rs108264591 | snp | C/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14849052 | AGGACGTGCTTACAA[C/G]TCTAAGCAGAAAGAA | 71682 |
rs108267466 | snp | G/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14879289 | TAAGACCGTTGGAAT[G/T]GCGTTCTTTTAATAC | 71682 |
rs108268288 | snp | C/T | | | downstream-variant-500B, intron-variant | Wdr27 | Mm_Celera | 17:14818397 | CATTCAACCCCAACT[C/T]TCCTTTCAGGAACCC | 71682 |
rs108275485 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14834469 | ATTCCAGTAGTAGAT[C/T]TTTTTTAAAGAAATT | 71682 |
rs108279137 | snp | A/G | | | intron-variant | Wdr27 | Mm_Celera | 17:14834782 | CTTTTGAAGAATTGC[A/G]GCCATTGATACTTCA | 71682 |
rs108279173 | snp | C/T | | | intron-variant, utr-variant-3-prime | Wdr27 | Mm_Celera | 17:14872162 | ACTTACTTACTTACA[C/T]GACTCAGAACCACCT | 71682 |
rs108280967 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14876983 | CACAGTAGCAGGTAA[C/T]AAAAACAAGAACTAA | 71682 |
rs108282567 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14798794 | TAGGGATTGATAGTG[C/T]GTAGTAAGAGCATGT | 71682 |
rs108282577 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | 1600012H06Rik, Wdr27, Gm34975 | Mm_Celera | 17:14943537 | GTGGACGAGCACCTC[C/G]GGTCACGCCTGTCAC | 71682 |
rs108283408 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14819396 | GATACTTTGTACATG[C/T]ATCCATTGTGACTGG | 71682 |
rs108287140 | snp | C/T | | | intron-variant | Wdr27 | Mm_Celera | 17:14799475 | GGCCAAAAAGAGAAA[C/T]CTGAGCCCTTTCAAA | 71682 |