SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3658901 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63981666 | TATCTATTAAAAAAA[C/T]GGACAAGCCAAGCCT | 104082 |
rs3660169 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63981905 | TTCTCCACTCCCATC[C/G]AGATTCTCTACCCAC | 104082 |
rs3660789 | snp | G/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63981978 | AAGATGGTGCAGTCT[G/T]GATTTCCCATCTAGT | 104082 |
rs3660814 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63981991 | CTTGATTTCCCATCT[A/C]GTCCCTCTCTGCCGG | 104082 |
rs3661374 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63982079 | AAGACCCCCTGCTCC[A/G]AAGGCTGCTTGGTGC | 104082 |
rs3665839 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63974874 | AATGCAGTGTGGGGG[A/G]TTGGGCTTAAAGTCA | 104082 |
rs3665904 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63974909 | AGGTGATGTCTGCAC[C/T]AGTCCTCAAGTCCAG | 104082 |
rs3667642 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63975192 | TGTGCACACGTGTGT[A/G]TGCCTGTGTGTGCAC | 104082 |
rs3671132 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63978612 | AGGTTCAAGAATCCA[A/G]TAGCTGTTCAGTCCA | 104082 |
rs3673006 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63978943 | CTCACAAGTGTACCC[A/G]GTCATTTGGTTTTTA | 104082 |
rs3679845 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63896684 | CTGTTTCAGACAAGG[A/G]TGACCTTCCGCCTCC | 104082 |
rs3698319 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63897325 | TGCCCTCCTTCTTGC[C/T]GTCAGTCCTGCAGCT | 104082 |
rs3698321 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63897326 | GCCCTCCTTCTTGCT[A/G]TCAGTCCTGCAGCTA | 104082 |
rs3698344 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63897342 | TCAGTCCTGCAGCTA[C/T]GCTGGTTTTCAGTGT | 104082 |
rs3698434 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63897387 | CAGGCAACTTTCTCA[C/T]GCCTCTTCCACATCA | 104082 |
rs3698953 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63897445 | GCTCTGAGCCATCTT[C/G]TACTCTCCTGTCTCT | 104082 |
rs3699002 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63897479 | ACTCATAGGCTCCTG[A/T]GTTTATTTTTCTGCC | 104082 |
rs3703820 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63976530 | TAAGTGCCAGACAAC[A/C]TTTAATATTTTTAAT | 104082 |
rs3708852 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63884570 | TGGACTCTTAGACGC[A/C]CATAATCTAAACATC | 104082 |
rs3724035 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63755293 | TAAAAATGTGGAAAT[A/G]TACAGAGGTTTTTAA | 104082 |
rs4211918 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Wdr7 | GRCm38.p3 | 18:63947086 | CTAGGGGTGTTCCAT[A/G]AAAATGTGGATGCCT | 104082 |
rs4211919 | snp | G/T | 0.46875 | 0.121031 | intron-variant | Wdr7 | GRCm38.p3 | 18:63946991 | AGAGTGAATGTGAAA[G/T]AAACCCCTAGCCAGA | 104082 |
rs4211920 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63946931 | TACATAAAGGAGACA[C/T]TGGCTTAGTGTTCTA | 104082 |
rs6161522 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63899176 | TAGTCAAGTACCCGT[A/G]TGAAGCAGAGCAATA | 104082 |
rs6162031 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63899230 | CCCTGTTCTTTGATG[C/G]ACATAGCAACTGGGA | 104082 |
rs6163136 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63899507 | TCTAAGGCCACCGAT[C/T]GAGGTTGCTGTGACT | 104082 |
rs6165125 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63899849 | TTCTCTTGATGTCTC[C/T]TCCACCGTCCTCCCT | 104082 |
rs6185980 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63822684 | gagtgtaatcttccc[A/G]tattcccnattatag | 104082 |
rs6185992 | snp | G/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63822692 | tcttcccntattccc[G/T]attatagggtgatgg | 104082 |
rs6186465 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63822748 | aaatgttagctgcag[A/G]ttttcntagaCATCT | 104082 |
rs6186466 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63822754 | tagctgcagnttttc[C/T]tagaCATCTTACACA | 104082 |
rs6190782 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63973857 | AGTACCAAGAAAGTG[C/T]CCATGTTGCTAGTTC | 104082 |
rs6200803 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63823146 | tcgtgagaactgtga[A/T]taaaggcatttacca | 104082 |
rs6217451 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63758620 | tgagttccaggacag[C/T]cagggctatacagag | 104082 |
rs6218023 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63758726 | ACTAAAGCCAATATA[A/G]CCCTTAATGATGAAA | 104082 |
rs6218567 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63758813 | AGGGCATCTAACCTA[A/G]AATCAGCAGAGCTGG | 104082 |
rs6260017 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63877925 | TATTTTAAATTGAGT[A/G]TTTTATGGTAGTTCT | 104082 |
rs6273961 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63762005 | GTTTCTCTCACTGAT[C/T]GTGCACGCTGTCACA | 104082 |
rs6274624 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63762156 | aggggtttgctaaaa[A/C]cattcctcttagggc | 104082 |
rs6280386 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63846046 | CTACTCACAGTTCAT[C/G]CATTATTTTGGTAAT | 104082 |
rs6281026 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63846203 | CAAGGTCTGAAGTTA[C/T]TCAGCATATGCAGAT | 104082 |
rs6287804 | snp | A/G/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63762283 | gcaatgaactggccc[A/G/T]tggatgtagcagtat | 104082 |
rs6338225 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63744571 | TTAAATTCTACTTAT[A/G]CCTNTCTGTTCCTTN | 104082 |
rs6338227 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63744575 | ATTCTACTTATNCCT[C/T]TCTGTTCCTTNTCTG | 104082 |
rs6338247 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63744586 | NCCTNTCTGTTCCTT[A/G]TCTGAAATTGAGATT | 104082 |
rs6338768 | snp | G/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63744653 | GTTTGTCATCCCCCA[G/T]TGTGGATCACAGAGG | 104082 |
rs6348742 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63855994 | GATGGCTAATGATTA[C/T]TTAATGACAGATCTC | 104082 |
rs6356581 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63850907 | TATTGCTATGGGGAC[C/T]GTAACTGAAGAAGAC | 104082 |
rs6369427 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63850944 | AAATACAGATGCGCT[C/T]TCTAAAGCTGAGTGT | 104082 |
rs6369468 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63850964 | AAGCTGAGTGTCTGC[A/G]GGAAACAGAATGGGA | 104082 |
rs6369543 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63851001 | GGCCGACCCTGCAGG[A/G]CAGGCTCAGTCTTNC | 104082 |
rs6369572 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63851015 | GNCAGGCTCAGTCTT[C/T]CTCACTGCANGNAGG | 104082 |
rs6369973 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63851025 | GTCTTNCTCACTGCA[A/G]GNAGGTAGAGGCTGA | 104082 |
rs6369974 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63851027 | CTTNCTCACTGCANG[A/G]AGGTAGAGGCTGATG | 104082 |
rs6370009 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63851045 | GTAGAGGCTGATGTG[C/T]GCCTTACTTCCTCTT | 104082 |
rs6370028 | snp | G/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63851064 | TTACTTCCTCTTATG[G/T]CAGATGTGCTTACAN | 104082 |
rs6370066 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63851079 | NCAGATGTGCTTACA[C/T]GAGTAGAATGTGGGT | 104082 |
rs6371061 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63851248 | CAGTCTCTGCCTGAC[C/T]CTGACCACTCCCACC | 104082 |
rs6371111 | snp | A/C/G | 0.489796 | 0.070696 | intron-variant | Wdr7 | GRCm38.p3 | 18:63779340 | GCTCTGTTCTGGTTA[A/C/G]TTTTATAAAAATTCA | 104082 |
rs13462275 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime | Wdr7 | GRCm38.p3 | 18:63988044 | CATCACTACTCACCA[A/T]GCAGTGACTATAGCC | 104082 |
rs13483401 | snp | C/G | 0.493343 | 0.057307 | missense | Wdr7 | GRCm38.p3 | 18:63779921 | AGGGATTCCCCTCCA[C/G]CCTCCAGTAACATTG | 104082 |
rs29537754 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63824428 | CATACTTCTTTTAAA[A/C]ACTTGATGAGAAATT | 104082 |
rs29538310 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63730877 | AGACCCGCTGCGCAC[C/T]CTGGTCAGTGTTGGG | 104082 |
rs29539603 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63972002 | CCACACGCTCAGCAC[G/T]TAAGCCCCTTGGTGA | 104082 |
rs29539816 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63871414 | CCAGGTGTCATGTTC[C/T]ACACTGCAAACGTGC | 104082 |
rs29540093 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63901930 | GAAGTCAGCTTCCAC[A/G]AGTCACTTTTTCTCC | 104082 |
rs29540142 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63828599 | CACTGTAGAGCAATG[C/G]CTGTGTGCTTTTGAA | 104082 |
rs29541454 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63818548 | GTGTCAAAGATAAGA[C/T]GCTCTGCGTGGGTGA | 104082 |
rs29541663 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63722683 | CAAGGTGTGGTGGTG[C/T]ATGCCTGACACACCT | 104082 |
rs29541964 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63900296 | AAGCATGCTTTTCTT[A/C]AGGCCTGTTGTGTTT | 104082 |
rs29542586 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63794491 | CCATCTTCCTCCTGT[A/G]TCTCTGAAGTAAACA | 104082 |
rs29543145 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63926350 | ATGGTGATGGTGATG[A/G]TGATGATGCACAAGG | 104082 |
rs29543678 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63778530 | CGTATGTACGTATGT[A/G]GATACATTTAGTTGC | 104082 |
rs29552793 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63731716 | ATTTATCCAGCTCTC[A/G]ATATTCCCCAGTTTC | 104082 |
rs29552890 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63837214 | CATACTAATTCATTA[A/C]GGCAGTAAAGAAACA | 104082 |
rs29555135 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63878755 | ACCTAGGGAGGAAAG[C/G]ATTAGGTTTTAGATC | 104082 |
rs29555536 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63950966 | CGACAGGACTGGGGC[A/G]GGCTGATTGCAGCCA | 104082 |
rs29557127 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63763860 | TGTTAGTCTTTTTTT[G/T]GGGGGGGGGTTGGTT | 104082 |
rs29557358 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63939015 | TAATATACTGCTAGA[A/T]TATTTCTGAGTAAAG | 104082 |
rs29557841 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63959979 | CATGTGAAATAAGTT[A/G]AAGGAAGCAAAGTCA | 104082 |
rs29558483 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63958747 | TTAAAGCCTGTTTGG[A/G]CTGGAGAGATGGCTC | 104082 |
rs29558879 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63983338 | GCTGGCAGTGGTTGT[C/T]ACAAGAAAGTAAGAT | 104082 |
rs29559007 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63754164 | CTGGAACAAGAGCTA[A/C/T]GCAGCATTACGGGCC | 104082 |
rs29559554 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63745029 | CACCTGGGGTTCCAG[A/T]GTATGCTGATAACTC | 104082 |
rs29559723 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63890260 | GAAATAATGTCAGAG[A/G]CATGTAATCGTCAGA | 104082 |
rs29561106 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63731676 | GCACTGGGTTGAATC[A/G]ACGCGCCTTTCCCTG | 104082 |
rs29561273 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63970963 | GTCCCTAGAACTCAT[A/G]TTAAAGGTTAGATGG | 104082 |
rs29561389 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63836245 | TAAATCACGTAACTA[A/G]AGAAACTTATCTATA | 104082 |
rs29561458 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63981432 | AACAATATGAACTAA[A/C]CAGTACCCCCAGAGC | 104082 |
rs29561563 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63767558 | CTGAAAGTATTGCAG[A/C]CGTCTTCCTAGCCCG | 104082 |
rs29562584 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63876815 | TAATGAATCTCCTTC[A/C]TAAATTTTATTACAT | 104082 |
rs29562851 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63776443 | AGACTCATGCCAAAG[A/G]ACAGGTGGAAGGGCC | 104082 |
rs29563032 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63875330 | TTTATATGTAACATG[C/T]GGTTTGAGGGTTATT | 104082 |
rs29564204 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63873800 | TACTACGTATGATCT[A/C]CCTCTTGTGGAGCTG | 104082 |
rs29564969 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63918158 | GGGCTCTCTGTAGGT[A/G]CAGCTCAACCTCTCT | 104082 |
rs29565231 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime, downstream-variant-500B | Wdr7 | GRCm38.p3 | 18:63987581 | CAACAGGATGCGACC[A/G]TTCTGTCACTAGGTA | 104082 |
rs29567130 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63823268 | CCAAGTTTTATAACC[C/T]CTTTTTCTGAGACAC | 104082 |
rs29570739 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63955873 | AGCAATAAGGCTTGA[C/G]AGGAAGTATGGTTAT | 104082 |
rs29571701 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63719559 | GAGAGTAAGGCAGAC[C/T]ATAGGTTCTGGCGTC | 104082 |
rs29572458 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63841812 | GTGAGCAGGAAATGT[C/T]TCCTGTGTACTGATT | 104082 |
rs29572576 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63761260 | TTAGGGAATGCTGGC[A/C]GTGGAAGAGAATCCA | 104082 |
rs29573320 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63882714 | GAATCGGGAGGACGG[C/T]TTACTAGATACATTT | 104082 |
rs29573414 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63821089 | CTCCAGTGTGGCAGC[A/G]TTGAGAGATGGAGGA | 104082 |
rs29573534 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63829460 | CTTCATTTAAAAAAA[A/T]TTTTTTAGAGGTCAG | 104082 |
rs29575554 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63983296 | ATGGGTGAGTGTTAG[C/T]GAGGTCCAAAAGCTG | 104082 |
rs29576068 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63725695 | GCTACCCTAGACCCA[A/G]TGGGGGAGTGGCCCC | 104082 |
rs29576473 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63964736 | TTTTTTTCGAGACAG[A/G]GTTTCTCTGTGTAGC | 104082 |
rs29576759 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63976001 | ATAATCAGTTCCAAG[A/T]GCACGGAGCAAATGG | 104082 |
rs29577221 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63722534 | ACTCAGGATCTTTGG[A/G]ATAGCAGTCATTGCT | 104082 |
rs29577282 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Wdr7 | GRCm38.p3 | 18:63904154 | GGAGCCCTACATGGA[C/T]GTGTCCGCTGTCCTG | 104082 |
rs29577318 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63950198 | TTGTAAGCTACCCTA[C/T]GTGTATATAATTAAG | 104082 |
rs29577989 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63735164 | CCAAGTAAGATAATT[C/T]TACTGAACAGAAAAT | 104082 |
rs29578083 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63781960 | TTTCTATGGAGTTTG[A/C]ATAGCTGAATATGAC | 104082 |
rs29578232 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr7 | GRCm38.p3 | 18:63936523 | AAAATATACCCAGTG[A/G]GTAGATAAGGCAGGT | 104082 |
rs29578396 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63827519 | ACACAATTACAAACT[C/T]ATGAGGTTGTATCAA | 104082 |
rs29579126 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63805263 | TCAGAACTATCTGAA[A/G]AAATTGTAGTCATCT | 104082 |
rs29580063 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63972426 | ATAAACTAACTGACA[C/T]TGATGAATTAAATAG | 104082 |
rs29581228 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63847451 | GGTGAACCAGGAAGC[C/T]AGGAACTCAGGAAAA | 104082 |
rs29581526 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63893229 | GGCATGGTGGCGCAC[C/G]CCTTTAATCCCAGCA | 104082 |
rs29581568 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63842237 | GAAAATATTTCCTTC[C/T]TATTACACGCAGATA | 104082 |
rs29581809 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63764951 | CAGAGATGAGATTAG[A/G]CAGTGAAGATAAAGA | 104082 |
rs29582427 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63799601 | TATATCTTAGTATAT[A/C]ATATATTTTATACAT | 104082 |
rs29582721 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63730444 | TGAAGTCTGAACCTC[A/G]ATGGTCATAATTCAC | 104082 |
rs29596428 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63891381 | GCCTTTCTCTGCCTT[C/G]TTTGGATGTGCTAAT | 104082 |
rs29619497 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63804353 | CTTTCTGAGATAACC[A/G]AGTTAGGGGAATGAC | 104082 |
rs29620638 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63956777 | AATTCAGGTTAATGT[A/G]TTATCCTCTGAGTCA | 104082 |
rs29622312 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63733896 | AGAATAACTGCTCAC[A/G]GTTTTAGTAAAAACA | 104082 |
rs29623252 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63731472 | ATTTGAAAAACTATT[C/T]CTTTTGTTTTAATAA | 104082 |
rs29624190 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63976341 | TAATAATCTGGCTTC[A/G]ATGATCCTCTATTAT | 104082 |
rs29624375 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63815007 | TCAGTGTCTTTGCTG[C/T]TAAAGCCTTATTGTT | 104082 |
rs29625599 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63820384 | ACATAATGTTGCTGT[A/G]TATATTTATGGGTTA | 104082 |
rs29626010 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63729261 | GGCCATGGCTGGCCT[C/T]TCTCTTCCTACCTTC | 104082 |
rs29626319 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63952440 | ATTTAAGTTGAACTT[C/G]AATTTTAGGATGACT | 104082 |
rs29627025 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63742551 | GTATAATGAAAAAGC[C/T]TTCCTACCCTTCCAA | 104082 |
rs29627026 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63753085 | CATGAGTTGAAGCAG[C/T]AAAACCACAAGTAGT | 104082 |
rs29627395 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63970872 | ATAGACATGCTAACA[C/T]AGTCTGGAAGATGGG | 104082 |
rs29628400 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63929878 | TAGGGCTTGGGATAT[C/T]ATCAAGTAAGTTGGT | 104082 |
rs29628445 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63722028 | CATCGATGTCTCAGT[C/T]GGGTCCAGAGTGGGA | 104082 |
rs29628462 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63740634 | AACAGTAATGTAGGC[A/G]GCTAGTGTGATCATG | 104082 |
rs29628659 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63825358 | TAGGAATCTTTCTTT[A/G]TTTGTTTGTTTGTTT | 104082 |
rs29628748 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63819117 | TTCCTGAAAACAGTC[A/G]GCAAGAATGCCTTTG | 104082 |
rs29629661 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63949970 | TTACTGTAAACCACT[G/T]TGACAAGCATCCCAT | 104082 |
rs29630216 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63977430 | GTTATGTGATTGTTA[A/G]AATTTGTGTGGTTAT | 104082 |
rs29631005 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63741556 | GGAAGCAGGATGTTA[C/T]TGTTTATTAAGAAGA | 104082 |
rs29631122 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63935083 | CTTGGTCAGTTTCAC[A/G]GTATTTTTTTTTTTC | 104082 |
rs29631497 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63809154 | AATCAAAACCTGGAC[A/G]TGGATCTGAACAGGG | 104082 |
rs29634823 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63927997 | TTGTAAGACAGGCTC[C/T]GTGACAGCCACCTTT | 104082 |
rs29636997 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63765387 | AAGCCACTCTCGTGG[C/T]GCCTGCGTCTCTGGG | 104082 |
rs29645084 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63721103 | CCTTAAAAAGGAAAA[A/C]GAAAAAGAAAAGGAT | 104082 |
rs29670977 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63793450 | TTTATAATATATAAT[A/G]TATATTATATATAAT | 104082 |
rs29671364 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63823287 | TTTCTGAGACACATC[A/T]ATCAAAGCGACAATG | 104082 |
rs29671764 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63839375 | TTAAACAAAAGCAGG[C/T]CATATCACCCAGGGA | 104082 |
rs29672125 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63960315 | CTGGTCTACCTAAAG[A/G]ATTCTGGGTTAGCAG | 104082 |
rs29672791 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63733914 | TTTAGTAAAAACAGG[C/T]GATAAGGTGGCCTCG | 104082 |
rs29673196 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63890564 | TAATAGTCTTGTGGG[G/T]TTTTTTTTTGTGTGT | 104082 |
rs29673476 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63848346 | TACAAATGCGCATCT[A/G]TATGCATGTACTATA | 104082 |
rs29673556 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63949054 | ATACCTACTAAACAG[C/T]CATGAGCAGACGATA | 104082 |
rs29673882 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63952956 | CTTCACACACCACAA[C/T]GTTGCAGGAGAACAT | 104082 |
rs29674206 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63838500 | TGGCATTTCCCTACA[C/G]TGGGCATCCAAAGAT | 104082 |
rs29674429 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63742740 | CCTTTGTGTGTGTGT[A/G]TATTTTTGTGCTTTG | 104082 |
rs29676197 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63853983 | ACCCTGTCTCGAAAA[A/C]CCAAAAAAAAAAAAA | 104082 |
rs29676521 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63723443 | TTTCTGTTAAGTAAA[C/T]CTTATTTCTTTAAAA | 104082 |
rs29677302 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63834061 | TGACTAAAAGACTAG[C/T]CTCAGAGTGTTTCCT | 104082 |
rs29677748 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63865757 | TTTTTGATCAAGGTT[C/T]TTCTCCAAAATGTTT | 104082 |
rs29677813 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63745026 | AGCCACCTGGGGTTC[C/T]AGAGTATGCTGATAA | 104082 |
rs29680016 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63926561 | AGCAGCCTCTGCAGC[A/G]TGACAACTCTTTTGT | 104082 |
rs29683991 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63822988 | TATATTGCAGACTTA[C/G]TTGTTTAATTTATCA | 104082 |
rs29686765 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63973940 | CCATCTCCAGTCTAT[C/G]TCTTGCTTCCATAGA | 104082 |
rs29718641 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63938374 | TCTCCCATGGTCTAT[C/T]CTGGTCTAACCACAC | 104082 |
rs29718733 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63949198 | GCCATCGCTTCATGA[A/G]CATGCTCAGCGTCTA | 104082 |
rs29719623 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63836733 | ATGCATATGAAAAGT[A/T]TAAAAATTATTATTG | 104082 |
rs29721346 | snp | A/C | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63827062 | TAGAGCCTGCTTAGT[A/C]TATAATGTTACCAAT | 104082 |
rs29721448 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63835381 | AGCTATTGTATATCT[A/G]AGTGTTAGGTGATGC | 104082 |
rs29721876 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63890572 | TTGTGGGGTTTTTTT[G/T]TGTGTGTTTGTGTGT | 104082 |
rs29722336 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63828703 | ACGTTTATTTGGGTG[C/T]ACTGACATTTTTACA | 104082 |
rs29722514 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63820595 | CTCTTTTTTTTTCTC[A/G]TCTGTGTCTTGCCCT | 104082 |
rs29723020 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63877051 | AAGAGAGAAAGGAAG[A/G]AAGGAAGGAAGGAAG | 104082 |
rs29723498 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63985452 | TAGGTTTTATAGATG[C/T]GAGACTACCTAATCG | 104082 |
rs29724236 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63972301 | AAGGGAGCTATCATA[A/C]GTTTTATTATAAGAT | 104082 |
rs29724246 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63891154 | ATACAGTTTTATAAG[C/T]GCGCACTTGACTGGT | 104082 |
rs29724602 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63805281 | ATTGTAGTCATCTTA[C/T]ACTGAGTACTATATG | 104082 |
rs29725065 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63781527 | TGCTATGCATTATAC[A/T]GTTGAATGAATAGAC | 104082 |
rs29725133 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Wdr7 | GRCm38.p3 | 18:63777758 | TGGGAAGCGAGCAGC[A/G]GTTCTTTTCCAGCAA | 104082 |
rs29725514 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63974290 | TATCATCTACCAACC[A/G]GTCATCTATCTACTT | 104082 |
rs29726003 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63766336 | GTGGCATGTCTCCTT[C/T]TAAGATCAGTCTTAA | 104082 |
rs29726126 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63818642 | CAGGCACACCTATAT[A/C]CATCTTCACATATGT | 104082 |
rs29726430 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63803054 | CTGAATGCCTTGTGA[C/T]TTATGCTTCCGGTGG | 104082 |
rs29727101 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63740664 | GAGTGTTTGTACCTT[C/T]GTTTGACAATGTTGG | 104082 |
rs29727160 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63877810 | AATTACAGGAGGATA[C/T]GGCACATCTGGCTAT | 104082 |
rs29727713 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63757184 | AACCGGAATGGGAGC[C/T]GTCCTAAAAGCTGTT | 104082 |
rs29727918 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63929674 | AGTGACAGCAGGGAC[A/G]GACGTAGAAGAGTTT | 104082 |
rs29731616 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63926344 | ATGATGATGGTGATG[A/G]TGATGATGATGATGC | 104082 |
rs29732633 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63724639 | TCAAGCTCATCATAC[A/G]TAATTACCTTGATTT | 104082 |
rs29734449 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63747167 | AACTTAGAATTTGAG[A/G]TCATAACTATATATT | 104082 |
rs29735204 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63864805 | GTGGGAATAGGTAAT[A/G]TTATAATATTGATTG | 104082 |
rs29743496 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63778405 | CACTTTAGTCATGTT[A/T]GTGATTTCCCATTTC | 104082 |
rs29765290 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63893930 | TTGAGCTTGACCTGG[C/G]TTTTCCTTTGTTACA | 104082 |
rs29766018 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63712670 | ATGGTAAGACTGCAG[C/G]AGCCAGTGCAGCGCA | 104082 |
rs29766344 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63803791 | ATACTGATAGAAAGC[A/G]TGTAACACGTGTGTT | 104082 |
rs29766501 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63797405 | GGTTTTGGTTTGTTT[A/G]TTTGTTTGTTTGTTT | 104082 |
rs29768532 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63846560 | TGTTCGGAAAAATTC[A/G]GGTTTTTGTTTTGTT | 104082 |
rs29769123 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63927578 | ACGGGTGGTTATGAG[C/T]CACCACGTGGTTGCT | 104082 |
rs29769428 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63753053 | AGTCCTTTTTATTGG[A/G]GATTTTAGAGAGCTC | 104082 |
rs29769486 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63801135 | ATATGGGGGGAGGGG[A/G]CAGGAGAGAAGCCTA | 104082 |
rs29769694 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63883907 | GTTCCATAAATAGGA[A/G]CTAGAAAGAAAGCTC | 104082 |
rs29769900 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63831704 | GGTTCCCCAGGTCTG[C/T]CTTTTGCTGGCTGTG | 104082 |
rs29769944 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63803828 | ATCCCGATGTCATCA[A/G]GCAGCTTGATCCTTT | 104082 |
rs29770048 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63929802 | CTTCCTATTCCTCGT[A/G]CCTAAAAAATCTCCC | 104082 |
rs29770200 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63938788 | GATCTTTTCCCTCAC[A/G]CTATTTCAGTTAACC | 104082 |
rs29770733 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63723744 | GCCGGGCCAACTGCC[A/G]GGTTGGCTCTGCTTC | 104082 |
rs29770951 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63823590 | GAACTTAGCAGTGTC[G/T]TTCCGTTGAGCACTT | 104082 |
rs29771147 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63962803 | ATGACTTGGCAGAAC[A/G]GAATCCTTTTCAGCC | 104082 |
rs29771211 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63813546 | TAGTCTCTGGGAGCC[A/G]GAGTCAGGTGGGTCT | 104082 |
rs29771340 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63819850 | TTGTTGAAAGTGTTC[A/G]CCTGAAAGTGATCCG | 104082 |
rs29771450 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63819905 | ATGCCCCACTCCTGC[C/T]CATCCGTAGGTCAGT | 104082 |
rs29773963 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63818805 | TGGTTATGAACAATA[C/T]GTTTGGTCACATTCA | 104082 |
rs29773996 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63809176 | TGAACAGGGAGTTCT[C/T]AAGAGAAGTTAAAAT | 104082 |
rs29775635 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63753542 | TATCGTGGCTAAATA[A/T]GAATTAGTGTTTTAG | 104082 |
rs29775891 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63855537 | GATAATAATTATATT[A/G]ATATAGGAAGCTTTG | 104082 |
rs29776177 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63886058 | TCGAAAAGCAATGGC[G/T]ATAGCCTGTAATGTG | 104082 |
rs29777509 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63890406 | AGTCCATGAAAATAA[G/T]TAGTTATGGAAAGAA | 104082 |
rs29784396 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63974134 | AGCATCCTCAAATTA[C/T]ATCTGCCTTATTATT | 104082 |
rs29793015 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63778352 | AGGGCTAAGAGAACC[A/G]TGCTATGTATTTGTT | 104082 |
rs29808017 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63728832 | AGAGCTCCAAGGGGC[C/T]AAACCACCAACCAAA | 104082 |
rs29811255 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63734140 | AACAGTTCTGACAAA[C/T]AGTAGTACAAACAAA | 104082 |
rs29813013 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63719683 | TATATCTACACCTAC[A/G]CGGTGCTGGAGAGGA | 104082 |
rs29814713 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63756711 | GAGTGCCAAGGCAGT[A/G]GCCTTGATGTGATCT | 104082 |
rs29816062 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63974267 | GTCCATCCATCCATC[A/C]ATCTATCTATCATCT | 104082 |
rs29816310 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63844095 | CTCCCAAATCTAGCT[A/G]AGGGTTTAGTCGGTC | 104082 |
rs29816446 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63810942 | TATTTTTTAAATTTT[G/T]CTTATGAGCCTATTA | 104082 |
rs29817898 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63831802 | AAATCGCAGTAAGCC[A/G]CCATTACCCATGCTT | 104082 |
rs29818498 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63954618 | TGGTAAGTGCCATAA[C/G]CCTCTTGCTTCTCGC | 104082 |
rs29818519 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63878616 | TATGTATATATATAT[A/G]TATATATATATACAC | 104082 |
rs29818744 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63971589 | AGGGTCTGCAGGTCA[A/G]GAAACAGCAATCAGT | 104082 |
rs29818827 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63742591 | CTCTATCTCTTAAAA[A/C]AACAACAACAACAAC | 104082 |
rs29819164 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63988393 | AGTGAAAGTGTCCAC[A/G]CTTCAACCCAAACTT | 104082 |
rs29820067 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63813600 | TCTACATGGTGAGTT[A/C]TAGGTTCACAAAGGT | 104082 |
rs29821063 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63882603 | AACACATCTAACAAG[A/T]CTCAAGATAGCAGAA | 104082 |
rs29821964 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63883796 | TGTTGTTACCTAGCT[C/T]AATCCATGCGGGTTT | 104082 |
rs29822579 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63938656 | GTATTATAATAAGCA[C/T]GAGCCAAGGCTGGTA | 104082 |
rs29823222 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63831911 | ACAGAAGCTGGGACG[C/T]CGTAGTTCTCCGAGT | 104082 |
rs29823280 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Wdr7 | GRCm38.p3 | 18:63922696 | GCCCGGTCTTCACCC[A/C/T]GCAGACCCTAGGCGG | 104082 |
rs29823714 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63900693 | TTTGGTTTTTCTTGC[C/T]AGTTTATGATTGAGT | 104082 |
rs29824253 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63936482 | TGATTTTTTTTTTTG[A/G]CTTTGCTCTTGTTTA | 104082 |
rs29826016 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63842572 | AACTTTCCTAAAGAC[A/C]CTATGTTCATTCTTC | 104082 |
rs29826694 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63858064 | GACATGTGCAAGACT[G/T]GTAACTAATATGCAC | 104082 |
rs29827229 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63893824 | GACTCCACAAGGAAG[G/T]CTCACTGTGGGGCAT | 104082 |
rs29828353 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63802153 | TACACTTTCTTTTAT[C/T]GGAAGCTTCCTGAAG | 104082 |
rs29831317 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63971471 | ATAATTGAAGCACTC[A/T]GGAGGCTGAGGCAAA | 104082 |
rs29832856 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63852555 | AATCTTTGATAGTTG[C/T]ACTTTGATAAATAAA | 104082 |
rs29832881 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63760842 | AGGGTTATTTAGTAA[A/C]ATAGGTGTTTCCAAT | 104082 |
rs29858951 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63819257 | AGTGTTATGGGGGTT[A/G]TGACTTTGAGCTTAT | 104082 |
rs29859704 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63900375 | AAGAGTGTAGATGTT[A/T]TTGAAAAGGAATGAT | 104082 |
rs29861055 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63864601 | GTGCCTGCTAAGTAC[A/G]TAAATAAGGCTGGGT | 104082 |
rs29861969 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63823657 | TCCTTCTCATCCACT[A/G]TGTTCACTTTCACTG | 104082 |
rs29863861 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63714968 | AACTGCTAAAGTTGA[C/T]GCTCACGTCTGATGG | 104082 |
rs29865101 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63776716 | GCGTGTTAATGATGT[A/G]CAATTTTATATATAT | 104082 |
rs29866365 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63952323 | TTTTTTACTTATGTG[C/T]CCTTCTTGTGGTAAG | 104082 |
rs29866566 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63846304 | AAGTAGACTTAGCGG[C/T]GTATGACATAGTTCC | 104082 |
rs29867290 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63958433 | TCTGGCTCCTTCATT[A/G]GGGACCTTCTGCTCT | 104082 |
rs29867388 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63802419 | CTATTTCTGGCATGA[C/G]ACTCTTAGAAAGTAC | 104082 |
rs29867566 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63729331 | CATGAAAAAAAAGTT[A/C/T]GAAGGGCTTGCTTGA | 104082 |
rs29868528 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63723032 | ACAATGGTACAGAGA[C/T]AGGGTGAGGAGAGAA | 104082 |
rs29869047 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63974223 | CTGTGGCATGTAGGC[C/T]GTGCTCCTATCTCTG | 104082 |
rs29869984 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63891746 | CACCCTTAAAAAAAA[A/T]AAAGAAAAGAAAAGA | 104082 |
rs29871921 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63793420 | TACATAATTTGAGAT[A/G]AGGCATTCATTGAAT | 104082 |
rs29871963 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63801560 | CCTCAGAGAGGCCCT[A/G]CCAACAGCTGACTGT | 104082 |
rs29873419 | snp | G/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63724818 | AGATGCCTTTTGGCA[G/T]ATTCGTGGGAATTAT | 104082 |
rs29874242 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63797899 | AGGTGTACAGATTGG[C/T]ACCAACTCACGGTAA | 104082 |
rs29874628 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63740767 | AATGTTCACTGCCAG[C/T]GAGAATGGCTAACAA | 104082 |
rs29875760 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63845632 | AATTATTTTCTTTTT[G/T]TGTGTGTGTGTTTTC | 104082 |
rs29876010 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63878807 | TCAGAGCAGAAATTC[A/G]AGGCAGGGCTAAAAG | 104082 |
rs29877304 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63903373 | AATTGCTTTCTTTTT[G/T]AATGTCAAAGCGCCC | 104082 |
rs29878345 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63809952 | GGATTGTGTAAATTT[G/T]CTGTAGAGTAGCATG | 104082 |
rs29878618 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63723903 | CCAGTGAGGAATCAG[G/T]AGTGCATCTCTGTTA | 104082 |
rs29879185 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63824261 | CACTCATAGTGCTGA[A/G]TAAGTTAAGGATGAT | 104082 |
rs29879851 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63861316 | TCAGTTAAAATAGGA[A/G]TCAGTCAAAAGGAAG | 104082 |
rs29882800 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63741816 | GTCTTTTTTTCTTTA[C/T]ACTTAATTCATTATA | 104082 |
rs29883029 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63757595 | GCAAAGAAATCACCA[A/G]TAAGTACAGAAACTC | 104082 |
rs29884426 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63753381 | TCATACACATTCAAG[A/G]CTTGCACTTTATTAA | 104082 |
rs29885537 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63820422 | TGAGGACATGGTTTC[A/C]TTCCCTGGCAGTAGT | 104082 |
rs29885944 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63924799 | TTTTCCTTTTTGCCC[A/G]CTCCCTGTTTAGCAT | 104082 |
rs29903841 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63725336 | TTGTCCTCTTGTGCT[A/G]TAATTATTATTGTTT | 104082 |
rs29907978 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63765870 | TATTTATATTATTGT[C/T]CCTTTAAGATAGGGC | 104082 |
rs29908676 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63958371 | GTTAGTTCATATTGA[C/T]GTTCCTCCTATGAGG | 104082 |
rs29912682 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63789100 | GACCAGGCTGACCTC[A/G]AACTTAGAAATCTGC | 104082 |
rs29912700 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63749542 | GCACCAGCTCATATC[C/T]ATGTTTAATGAGTTG | 104082 |
rs29915577 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63898262 | GACGGCTACTTATTT[A/C]TTTATTTTACTTTAC | 104082 |
rs29917790 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63818445 | GAAGCCTGTGATCCC[A/G]GGGTTGCTGGAAGCA | 104082 |
rs29917921 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63723077 | ATGAAGACAGGACAA[C/T]GCAGAGAATAAGAGG | 104082 |
rs29919253 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63730527 | TAAGGTACCACCTCC[C/T]ACAGCCCCCACAAGG | 104082 |
rs29919646 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63946952 | CCTTTATGTAGTGTT[A/G]CAGGGGGACTTAGCA | 104082 |
rs29920106 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63955877 | ATAAGGCTTGACAGG[A/G]AGTATGGTTATCGTG | 104082 |
rs29920119 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63825251 | CAGGTAAGCCTGGGC[A/G]GAGGAGGAGCGCGCT | 104082 |
rs29923272 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63830472 | ATTCTTGCCCAGCAT[A/G]CTTAAAGCTTCAGGT | 104082 |
rs29924486 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63782627 | AATGATTGTATTCTT[C/T]TTTAATTTTTCCAAT | 104082 |
rs29924630 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63839376 | TAAACAAAAGCAGGC[C/T]ATATCACCCAGGGAC | 104082 |
rs29927611 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63730954 | AGGTAGCTCCAGGGT[C/T]CCAGGTCGAGGGCTG | 104082 |
rs29927651 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63750489 | CTATTTTTTTCTAGT[G/T]TGTATGTTCAGATTC | 104082 |
rs29929925 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63951090 | GAGCCGCTTCTTAAA[C/T]GCTTCGTGTCATGGG | 104082 |
rs29931568 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63760957 | ATATTATAAAAAAAA[A/C]CACAGTTTTTTAACC | 104082 |
rs29933670 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63802783 | TATGGGTTTGTGTGA[A/G]AGAATGGAAAGCATA | 104082 |
rs29934361 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr7 | GRCm38.p3 | 18:63723389 | AGACAGCAGTTACAT[C/T]AGGTGCATAAAAGTT | 104082 |
rs29936234 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63938755 | TTGGTGTAACTTTCT[C/T]CTCGGGATTTTTCTG | 104082 |
rs29948582 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63926563 | CAGCCTCTGCAGCGT[G/T]ACAACTCTTTTGTAG | 104082 |
rs29951818 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr7 | GRCm38.p3 | 18:63936556 | ATCTCTATTTGAGAT[A/G]GAAAAGGAGTTGAAG | 104082 |
rs29956642 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63730992 | CCCACCCTCTGCCTC[A/G]TGGGTCAGGCATGCT | 104082 |
rs29958253 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63716461 | TGCTGTTTGATAAGG[A/G]TGTTGTGTTTATCCT | 104082 |
rs29958348 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63951034 | TTAACACAAAGTCTC[A/G]AACAATAGGGAAGTG | 104082 |
rs29958516 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63725318 | CACCCACTTCTCACA[C/T]TCTTGTCCTCTTGTG | 104082 |
rs29959075 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63963891 | CAATCAAGGAATGAT[A/G]TAACCATAACTAATT | 104082 |
rs29961644 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63975863 | TAATGCCTTCTGGGT[G/T]AATGTTGAGAGTCAC | 104082 |
rs29961653 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63790046 | AGCCAGGCTCCTGAT[A/T]CTCTCTCTCGAATAT | 104082 |
rs29962089 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63875322 | GGGTTCCCTTTATAT[A/G]TAACATGTGGTTTGA | 104082 |
rs29962160 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63951165 | TACATATTGTAATTA[C/T]GTAGTACATAAGTGA | 104082 |
rs29964101 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63710768 | TTCTGGCCTCTCTGC[C/T]TCTATAAGATTACCT | 104082 |
rs29964700 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63734281 | CTGGGGTTGGCCTTG[A/C]AGCCCTGGCTTACAG | 104082 |
rs29965511 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63908840 | GGTTTAATTTCAGAT[C/T]TAGCTTCTAAAGCTA | 104082 |
rs29967635 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63883687 | AGTTCCCAAATAAAA[A/G]ACATACACCCTAGAT | 104082 |
rs29972919 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63849748 | ATTCAGTGAGAGACT[C/T]TGTTTCAAATATAAG | 104082 |
rs29973359 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63900496 | CTTTAATAAATAGAG[C/T]CTGTGCTTTGTAATA | 104082 |
rs29973500 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63960815 | GTAAAGTGAGCAGTC[A/G]TCCCCCTGGGATGCT | 104082 |
rs29974399 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63958929 | TAAGAATTCTTTTTT[A/T]AAAAAAACCTGTTTA | 104082 |
rs29976078 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63804397 | AGATTTTTTTTTTTT[A/T]AATTACAAATTAGGT | 104082 |
rs29977565 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63778333 | CTCATTCTTTGTTTT[C/T]GAGAGGGCTAAGAGA | 104082 |
rs29979275 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr7 | GRCm38.p3 | 18:63922662 | TAATGCAAGAAGACA[C/T]GACATAGGGGGAAGC | 104082 |
rs29979863 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63725448 | ACTGAAGAAAACCAA[C/T]TCACGCTCCCTTAGC | 104082 |
rs29980011 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63733399 | AGGAGAGAGCCAGGT[A/G]AATGTAAGAAAAGTG | 104082 |
rs29980752 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63875694 | CCATTCATTCTCCTT[G/T]TAGGGCTTTCCTTTG | 104082 |
rs29981285 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63907047 | GGGAGAGCAGACAGT[A/G]GAGTGGTCTCTCTCT | 104082 |
rs29996481 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63801250 | GGAGGTGAGACACTA[A/C]CAGGATTCATTTGGA | 104082 |
rs30001615 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63829678 | CAGCCAAACATTATG[C/T]GGAGTGAGATACCTT | 104082 |
rs30004266 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63820070 | GAGGGCATCGGGTCC[C/T]ATTACAGATGGTTGT | 104082 |
rs30004267 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63781721 | TTCTCTATTTTCTTC[A/G]TGAGGTGAACAATAT | 104082 |
rs30006622 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63815834 | AGTGTTAGTGTTAGT[A/G]TTAGTGTTAGTGTTA | 104082 |
rs30007910 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63820584 | TCTCTCTCTCTCTCT[C/T]TTTTTTTCTCGTCTG | 104082 |
rs30009766 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63789369 | GAATGGTGACATGCC[A/G]CCTATCTGCTGTCAT | 104082 |
rs30010069 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63918051 | CATCTAAAGTAGCCA[C/T]AGAGGCCGTAAAAGT | 104082 |
rs30010204 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63816621 | GCTTTAATTAGATCA[C/T]GGGAACACCACAGTT | 104082 |
rs30010212 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63724673 | TACAATTTGCAGCTA[C/T]GGCTTAAAAACTTCT | 104082 |
rs30010440 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63813502 | TTAAAGGAGTCATGC[A/T]TATGAGCTGGTAGGG | 104082 |
rs30012771 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63725277 | TCACACTTCCCCACT[C/T]CCAAGTTCTCCTGAG | 104082 |
rs30014840 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63891046 | ATCTACACAGAGGAC[C/T]GTGGGCCATGGGCAG | 104082 |
rs30015711 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63817081 | TGTGTCCAGGTGTTT[A/T]GCCTGCACACACCTC | 104082 |
rs30018400 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63883569 | GTGAAGGAAGCTTGT[A/G]GTGAGACTGACTCCT | 104082 |
rs30018490 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63811504 | TGCTCCTAGAGACAC[A/T]TTATACTCATTACAG | 104082 |
rs30018896 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63844884 | AGGTCCTCTGCGAGG[A/G]CCCAATGGGCTCTTA | 104082 |
rs30021137 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63922742 | CTTCTGGATTGAGCT[C/T]TGCCAGCGAGGGATG | 104082 |
rs30021755 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63822862 | AATAATTCCTATGAT[C/T]GCTTGCTTTTGTTTA | 104082 |
rs30022658 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63949025 | GTAGTTCAAATTTTG[C/T]TGTTAGCCTGGAGAT | 104082 |
rs30024162 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63743305 | GTTCTATATGACTTA[C/T]ATACTCAGATTTTAT | 104082 |
rs30024515 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63870098 | AAGGCCATTAACATG[C/T]AATATTTGATGAACT | 104082 |
rs30025126 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63749173 | GGGGGAAGCATCTCT[G/T]ATGATGGCTGAGCAA | 104082 |
rs30025369 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63729857 | ATGCTGACTTACCAT[C/T]GCCATCAGGGTTTAC | 104082 |
rs30026873 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63724744 | ATTTTTGAGTACTTT[A/T]AAAAAATCTAATTCT | 104082 |
rs30027047 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63729499 | GCATGACTGACTGGC[C/T]AGTAGTGAGTGACAT | 104082 |
rs30028013 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63982638 | AGAAAACAGTCTTCA[C/T]ATAAGTAGTGATGCA | 104082 |
rs30028813 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63743669 | TGATTAAATTTAATC[C/T]AGCCAGAGAGTCAGA | 104082 |
rs30029257 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63740809 | TTTTCTTTATTTTTA[C/T]TTTTTAGAATTTTAT | 104082 |
rs30031152 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63924798 | TTTTTCCTTTTTGCC[C/T]GCTCCCTGTTTAGCA | 104082 |
rs30032330 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63892096 | AAAGAGAACCTGCCC[A/C]CTGTTTGCAGGGCAT | 104082 |
rs30050539 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63736149 | CTTAAAAATCCCATT[C/T]TTGTCTATTGTCATA | 104082 |
rs30051087 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63715313 | TTGTCAGCTGTGTGG[C/T]GCTAGAAGGTTGGGT | 104082 |
rs30054219 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime | Wdr7 | GRCm38.p3 | 18:63988250 | CTGGCCTTCCAGATT[A/C]TGACCAGTGAAAGAA | 104082 |
rs30057174 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63761702 | AAAATAATTTTCTAA[C/T]ACATAGCTGGAAAGC | 104082 |
rs30057241 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63760479 | AATAAGACATTCCTC[C/T]AAATATGCTATACCA | 104082 |
rs30058119 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63939055 | AATCCATAGTAGACC[A/C]CTTTCAAAACAGTTT | 104082 |
rs30058125 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63973994 | TTCCCCATGTTTGTG[C/T]GTATGAAACATGAGA | 104082 |
rs30059616 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63982440 | AGTCTTATTAATACA[A/T]AGCCTTACTAAAACT | 104082 |
rs30060016 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63854091 | GGACAGGTAGCCTAA[C/G]TTTTGAGTCCATGGT | 104082 |
rs30061557 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63741553 | GCAGGAAGCAGGATG[C/T]TATTGTTTATTAAGA | 104082 |
rs30062672 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63956206 | ATAACCTCGCTTTTT[C/G]TTTTTGTTTTTTTTT | 104082 |
rs30063688 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63945195 | TGGGCCGATGACCAG[A/G]GAAAAGGTACGGGCC | 104082 |
rs30064258 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63926361 | GATGATGATGATGCA[C/T]AAGGAGGTGATGGCG | 104082 |
rs30064398 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63917712 | CTGATGCTGTACCGC[A/G]CCATACCTGCCCCAT | 104082 |
rs30064422 | snp | A/C/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63917555 | AAAAGATTTGTAGCA[A/C/G]ACAAATAAGAGAGGC | 104082 |
rs30067153 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63892809 | CAGATTTAGTGAAAA[A/G]GAGCTATATTTGAAA | 104082 |
rs30067950 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63812130 | AGTCCGGGGACTGGG[G/T]GTACATCCTGCTCCT | 104082 |
rs30068516 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63804527 | GCCATGCTGAGGGGT[A/G]ACTACTGCTTGCTTC | 104082 |
rs30068522 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63829409 | GTATAAAGGAAAAGT[C/T]AGTCACACAGAATAC | 104082 |
rs30069469 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63819221 | TAAGGAGTCGCAGGG[A/G]GTTGGCTGCCATCAC | 104082 |
rs30070947 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63977495 | TTGCTGAATTTATTA[C/T]GTACTAAGAATTGTA | 104082 |
rs30072356 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63785823 | CTGTACATGTGCATG[A/T]GCCGAAGGTTAGGGG | 104082 |
rs30073310 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63801692 | ATACGAAGACCAGCA[A/G]TCTCAACTAACCCAG | 104082 |
rs30073705 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63796658 | GGCAGTGGTGGCGCA[C/T]GCCTCTAATCCCAGC | 104082 |
rs30074239 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63758127 | AGGAGGAGATGGACA[A/C]CCTAACCAGACCTAC | 104082 |
rs30074550 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63781545 | TGAATGAATAGACCA[C/T]TTATATATGTTTTTC | 104082 |
rs30075156 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63919542 | TACTCTACTCAGAAC[A/G]TCAGAACTGTGCCGA | 104082 |
rs30075159 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63845531 | TCACAGAAAAACATC[C/T]ATTTTAATCAGATCA | 104082 |
rs30077078 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63752646 | AGCCCAAACTAGCTT[A/C]TAACTATCACCACTA | 104082 |
rs30077755 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63802810 | CATAGGCCAAGGCCA[A/G]CTGCCTTTCTTGGGG | 104082 |
rs30080532 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63749123 | TTTCTGCATCACATC[A/G]TGCTGTAGGTCTGCA | 104082 |
rs30095400 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63882616 | AGTCTCAAGATAGCA[A/G]AAAGAAAATTACAAA | 104082 |
rs30097242 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63970339 | ACTTGTCTTTTTTTG[A/T]TTGCTGATTGACAAG | 104082 |
rs30099212 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63950199 | TGTAAGCTACCCTAC[A/G]TGTATATAATTAAGG | 104082 |
rs30099698 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63812769 | TTGGATCTTTAGGGT[A/G]TGACACATTACTAGA | 104082 |
rs30099745 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63796621 | GTATAGAGACCTTTC[A/G]CAAGTTAAGATTACA | 104082 |
rs30102541 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63948684 | TATGCACTGAGGACC[A/G]TCGAGTTTTGAGCAA | 104082 |
rs30104846 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63952218 | AGTGTTGCTCTCAGA[A/G]CCAGTGGGCCACACT | 104082 |
rs30106013 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63813463 | TCTTCTGCTCTTTCT[A/G]CCGCATGGTGCCAGG | 104082 |
rs30107244 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63714666 | GGGCTTAGAGGCAGC[C/T]ACTAGGAGAGCTGGC | 104082 |
rs30109146 | snp | G/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63723311 | GGCCTAGAGAAGGTT[G/T]CTCAGAGGTTAGAAG | 104082 |
rs30109675 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63852400 | TTTCCTTCATTCTTT[C/G]TTACCAGCTTTTGTT | 104082 |
rs30110528 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63767093 | GTGAGATACATCAGG[A/G]TTTTTAAATCACTCC | 104082 |
rs30110658 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63834688 | TAATAACACCACAGT[C/T]GACTGGATTCTCTTA | 104082 |
rs30111013 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63804380 | TGACGTTTCTGGATA[C/G]TAAGATTTTTTTTTT | 104082 |
rs30111300 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63852229 | ATTCAGTTTTATAAT[A/T]TCTTTTCTTACCCTT | 104082 |
rs30111518 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63776681 | ATTTTATAGTTTTAA[C/T]TTTCTAGTTATGAAA | 104082 |
rs30112509 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63760847 | TATTTAGTAAAATAG[C/G]TGTTTCCAATCCTGA | 104082 |
rs30112755 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63812016 | GGCTGTTTTCTGGCA[C/T]GTGCTCTGTATCTCT | 104082 |
rs30113888 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr7 | GRCm38.p3 | 18:63980007 | TGCTGGGATTGTAGG[C/T]GTGCCCTACCAGGCT | 104082 |
rs30114416 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63842774 | GGCTATTCATTCCTT[A/C]AAATGCTCTGTTACC | 104082 |
rs30114966 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Wdr7 | GRCm38.p3 | 18:63922710 | CCGCAGACCCTAGGC[A/G/T]GGGCCGCGTTCTTTT | 104082 |
rs30115400 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63873747 | CTCTTCCAAGATCCC[A/C]GATGTCACTAGCCCC | 104082 |
rs30118387 | snp | G/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Wdr7, LOC105246469 | Mm_Celera | 18:63707655 | AGACTGGGGCTCATG[G/T]GGTCTTGCCAAGATC | 104082 |
rs30118529 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63960738 | AAGCAAGGGGGGTGC[A/G]TGTCTCTCTTTCCTG | 104082 |
rs30118676 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63830396 | CAGTATGGTGTGTAT[C/T]CTGTCTCATTGTGAA | 104082 |
rs30120084 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63761046 | TTGCTGCTTCTCTGT[C/T]TGCCAGAAGGATGTC | 104082 |
rs30120803 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63763393 | TCCTTTGAGCTTAAG[C/T]TCAGGAAACTTGTAG | 104082 |
rs30120931 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63835629 | TGAAATCTGCCAGTC[G/T]TGTTGAATCATGATT | 104082 |
rs30121607 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63888083 | CTCGTGCAGCATTGG[G/T]TTGATTGGAGCAGGC | 104082 |
rs30122923 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63726358 | TCTAGGGGTCCCGGG[A/C]GGCTGCTTTGGTGGT | 104082 |
rs30126016 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63964338 | AAAAGTGCAGATGCC[A/G]CTTAGGGAGAAGCTA | 104082 |
rs30128346 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63802218 | GCATTTAACAGAGGA[C/G]GAGTGAGCACAGAGG | 104082 |
rs30129175 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63918970 | AAAGGACAAAGTTAT[C/G]TCCAGCTGGGACTCT | 104082 |
rs30130026 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63977431 | TTATGTGATTGTTAA[A/C]ATTTGTGTGGTTATT | 104082 |
rs30132540 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63801891 | CACCCACTCAGGGGG[A/G]GGAAGAATGGAATGA | 104082 |
rs30145798 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63719344 | AACATTAAGGACACC[C/G]CCCCCCCTCCAGGTT | 104082 |
rs30149704 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63796695 | GAGGCAGAGGCAGGA[C/G]GATTTCTGAGTTCAA | 104082 |
rs30152339 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63894562 | CAGCTCCAGGCTGCA[C/T]GTGCAGCTGTCTTGG | 104082 |
rs30153464 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63749031 | TGTGGTGTCCTCCAT[C/T]CCCTCGGGCTCCTTC | 104082 |
rs30153482 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63882554 | GCTAATAATAGTGAA[C/T]ATGATAGAAAGTCAT | 104082 |
rs30153779 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63823394 | TGTCTTCAGTGGAAT[A/G]AATGCCTTGTACAGC | 104082 |
rs30154740 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63725552 | ACAAACACACACACA[C/T]AACCTTTATATTTTA | 104082 |
rs30156610 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63747779 | AAAAAAAAAAGGAAA[C/T]CCAGAAAAGCTCAAG | 104082 |
rs30156690 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63948506 | TTATGGAAGCATCAA[A/G]TGAAAGGATGCTTCA | 104082 |
rs30159177 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63735830 | AATATTTAGCTTCAG[A/G]ATGTCTTAAGTGTTG | 104082 |
rs30159277 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63875969 | GTTCTTTTAAATCCT[C/G]TGTCCTGAAGTTCAT | 104082 |
rs30159959 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63830137 | AGTATTGTCCTTATA[C/T]ATAAATGGGGAAATA | 104082 |
rs30160159 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63882705 | ATAGTCAAAGAATCG[A/G]GAGGACGGTTTACTA | 104082 |
rs30161639 | snp | A/T | 0.32 | 0.24 | synonymous-codon | Wdr7 | GRCm38.p3 | 18:63924851 | CCCTGCAGCTGACTC[A/T]GCCCGCTCCGCAAGG | 104082 |
rs30162104 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63798017 | CGATTTGAGTACCAG[A/G]TGTTTATTGAGTAAA | 104082 |
rs30162594 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63742593 | CTATCTCTTAAAAAA[A/G]CAACAACAACAACAA | 104082 |
rs30162714 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63824358 | AGAAATCCCTCAGTA[C/T]CTATAGCATTCAGTT | 104082 |
rs30163294 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63807822 | GAGGAAAGAGAGCTA[A/G]TCTAGAATCAGTACA | 104082 |
rs30164532 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63861248 | GCCTATACTGATGAG[A/G]AAACAGCATACCTTA | 104082 |
rs30164997 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63883408 | AATTGATAAGGCAAG[A/T]AAGTTTAATAATACT | 104082 |
rs30165048 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63957429 | GCTCGTACAAGTCAG[A/G]ACTGTTTACGTCTTG | 104082 |
rs30165113 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63852040 | CCACAGCCTTAAAAC[C/T]AGACGATGTGCAGCA | 104082 |
rs30165845 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63948390 | TCACACTAGAGAGTG[C/T]GAGTATAAAACAAGG | 104082 |
rs30167320 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63816014 | GGAAAATGTATTTCC[A/G]TAATTATGCATCAAT | 104082 |
rs30167637 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63747608 | TAGCTCAGTGGTTAA[A/G]AGCACTGACTGCTCT | 104082 |
rs30167851 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63922902 | GATTAAAAATAAGGT[A/G]CAAGGTATCTAAAAT | 104082 |
rs30169482 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63823537 | TTCCTAGCAAACCTT[A/G]TGATGAAATGATGTG | 104082 |
rs30170025 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63785115 | GGACAGTGTCCCAAT[A/G]TAATTGCCATTTTTT | 104082 |
rs30170590 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63809474 | GAACTATATTGGAAA[A/G]AAGAATTTATTGGAT | 104082 |
rs30171135 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63971591 | GGTCTGCAGGTCAAG[A/C]AACAGCAATCAGTGA | 104082 |
rs30172569 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63843521 | AACTTGGATTTGAAT[C/T]CCTTCCTTGGCTCAC | 104082 |
rs30173437 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63782657 | TTTACTGTATTTGCT[G/T]CTTCAAAAATAATTG | 104082 |
rs30177636 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63743622 | ATTCAGTTGTGTGGG[A/C]CTGTAATTGTGGATG | 104082 |
rs30178630 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63891047 | TCTACACAGAGGACT[C/G]TGGGCCATGGGCAGA | 104082 |
rs30179867 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63949266 | GACATGGAGGAAATC[C/T]GCCTTAGATCTACTT | 104082 |
rs30179996 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63883712 | CTAGATTCAAGCCAA[A/G]TCAGATTCAAGCCAA | 104082 |
rs30184027 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63954864 | ACTTAAGCCTAAGTA[C/T]GCCCCTTTGTCTCAG | 104082 |
rs30197150 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63927930 | GTCCTATTAATATAA[A/G]GATTTCCCCTGAGAG | 104082 |
rs30203992 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63710699 | CAGCACAGGTGTCAT[C/T]TAATCAGAGATGGGA | 104082 |
rs30208597 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63802365 | GGTTTGTGGAGCCAA[A/C]CATCACTGTGAGTTT | 104082 |
rs30209275 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63725970 | GCACAAATCAAATCC[C/G]CAACAGTGGGTCCTC | 104082 |
rs30210171 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63814723 | GCTAATCACTGCATC[C/T]AGTCACACATCGTTC | 104082 |
rs30210595 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63836485 | CCCTGGCCCTCATAG[A/G]TAGGAAGCTATTCTA | 104082 |
rs30211194 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63774871 | CTTGAGTTAGTGCTC[A/G]TCTGTACCAAAGCAT | 104082 |
rs30213235 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63803189 | TACTGCATCAAATAA[A/T]GCAACATGGGAGCAT | 104082 |
rs30214593 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63788792 | TGTGAAAGTTTAGGT[A/G]CTCTTTGGGTATATA | 104082 |
rs30214646 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63852785 | CTGTATTCAGCACTA[A/C]GGCTATTGATAAAGC | 104082 |
rs30214745 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63876748 | TCCTGTGATTTCTAA[G/T]CCTGAAGAGTATATT | 104082 |
rs30214747 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63722422 | GTATTTATTATTATA[A/T]ATTAGTACACTGTAG | 104082 |
rs30215090 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63850482 | GCCGTCTCACCAGCC[C/T]GTGAATGCATTTTAA | 104082 |
rs30215532 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr7 | GRCm38.p3 | 18:63723620 | CTGGCTTTAGCTGGC[C/T]GTGTTTCTCAGTGCT | 104082 |
rs30216734 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr7 | GRCm38.p3 | 18:63808903 | GTAGAAGAAAATATA[C/G]ATGTAGGAAAGTTCT | 104082 |
rs30220061 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63827891 | TCTTTTTATTGACTG[A/G]AATCCTATATAAATT | 104082 |
rs30222514 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63711607 | GTCATCACATGTTGC[A/G]ATCCAGTTTCTTTTC | 104082 |
rs30225133 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63746304 | CTCTCTTTTTTTTTA[C/T]ATAAAAGTTTCATTT | 104082 |
rs30225423 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63961372 | TCCATCGCTTAGTCC[C/T]CTGAACCCCGTGTTA | 104082 |
rs30227017 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63758268 | AATTCTCACAAACTA[A/G]TTACAGGCATGCATG | 104082 |
rs30247258 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63791282 | ACTGTGTATGTACTT[C/T]ACAAGTTGTTATATT | 104082 |
rs30252366 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63800157 | ATAAAATGGAGTCTT[C/T]CCCAGTCATGTTATC | 104082 |
rs30253149 | snp | C/G | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63829180 | TATTATATTAAGTAG[C/G]AGACAAGGCATTAGA | 104082 |
rs30253846 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63794992 | ATTTGATGGGCCCTC[A/T]GAATGTCTGTTCTAC | 104082 |
rs30254595 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63785351 | CCTGGCTTCCGGGAG[C/T]GCTTACACCCATTGA | 104082 |
rs30256384 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63848274 | CCTTAGAGCATAGAA[C/G]ATATTGGCATAGAAC | 104082 |
rs30256496 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63801408 | GAACTGCAGGGACAG[A/C]AATGGAGAAGAGACT | 104082 |
rs30257788 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63892547 | TATCAAATTAAATCC[A/T]TATGTTAAAAATATT | 104082 |
rs30258844 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63947106 | AACACCCCTAGGTAA[A/C]TCCATGGCAGGCTAC | 104082 |
rs30260752 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63761294 | CTGTCCCACTGACCC[A/G]TAGCCGCCATAATTG | 104082 |
rs30261849 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63733143 | GAAGGTGGCAAAATG[A/G]AGTTTGTTGGGTAGG | 104082 |
rs30262590 | snp | A/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63955993 | AACAAAGCACGTGGC[A/T]GCTCATTGATACCGT | 104082 |
rs30263779 | snp | A/C | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63722438 | ATTAGTACACTGTAG[A/C]TGCTCTTCAGATGCA | 104082 |
rs30264129 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr7 | Mm_Celera | 18:63903286 | GGCCAGGATAGAGAA[A/G]AATCTGTCTGAAAAA | 104082 |
rs30265069 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63945428 | AGGTGCTCCTTTCTC[A/G]CTCACATTGAACGTG | 104082 |
rs30270389 | snp | G/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63762663 | TCAGGTTGTAGAAGG[G/T]AACCAGCAGTATCGG | 104082 |
rs30270572 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63888074 | TCCCTTTGCCTCGTG[C/T]AGCATTGGGTTGATT | 104082 |
rs30271199 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63820088 | TACAGATGGTTGTCA[C/T]GCACCATGTGGTTGC | 104082 |
rs30271377 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63845403 | GATCCCTCAGTTTCA[C/T]GGGATGACACACAAC | 104082 |
rs30272144 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63976061 | CTGTGTTCTGTGGGT[A/G]AACTCATGTAGCCCA | 104082 |
rs30273295 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63847260 | CAGGCTTGGCTGGAG[A/T]CCACTCTTCCCCTGT | 104082 |
rs30273301 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63872423 | TCTGAGAGAGGAATT[C/T]CTCCTTCCTCCTAGA | 104082 |
rs30273926 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63938885 | CCTATTCCTGCCCAT[C/T]TCTGTTTAATACATT | 104082 |
rs30273928 | snp | C/T | 0.5 | 0 | intron-variant | Wdr7 | GRCm38.p3 | 18:63907470 | TTGTGTGGAGAAGAG[C/T]AATGGCGCCCAACAG | 104082 |
rs30274969 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63938231 | TCTTTGCAGTAGACC[C/T]GGCATCCTGGGGCCT | 104082 |
rs30275634 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63764252 | CTTTGTCAAAAATTA[C/T]GCATCCATAGGTGTG | 104082 |
rs30277306 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr7 | Mm_Celera | 18:63972635 | TGGGCAAAATGATTG[C/T]GTTAAAGATAGGAAA | 104082 |
rs30277652 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63979429 | CCTTCTGGCAGGTAA[G/T]CCAGTCTTAAATATG | 104082 |
rs30277875 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr7 | GRCm38.p3 | 18:63813576 | TCTATAAACACAAAA[C/G]TAGCTTGATCTACAT | 104082 |
rs30280117 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr7 | GRCm38.p3 | 18:63803201 | TAATGCAACATGGGA[A/G]CATACTGTACATCTT | 104082 |
rs30280291 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63961481 | ACTAGATAGTATAGT[A/G]CCAGCAATGTATTAA | 104082 |
rs30303198 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr7 | Mm_Celera | 18:63799650 | ATATACAAAATATAT[A/G]GCTATATAATTTTAT | 104082 |
rs30303679 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63835327 | GTGAGCTGTGAGATG[C/T]CTCAGAGAAGGAACT | 104082 |
rs30304325 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Wdr7 | GRCm38.p3 | 18:63781005 | AGTGGGACTCAGGTG[C/G/T]TGCTACTGAACTCCC | 104082 |
rs30308925 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63757797 | GAAGTCAGAGCACAC[A/G]TGAGGGACTTGATGA | 104082 |
rs33851591 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr7 | Mm_Celera | 18:63834827 | TGGCTCACTGATAGG[C/T]AATGGTGAAATGAAG | 104082 |
rs45635029 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63780892 | GAGGTATTGAGATAA[C/T]TACATTGAATGCATA | 104082 |
rs45639547 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63848472 | TAAGATTCTGTTACT[A/G]AGGGAAAGACACACA | 104082 |
rs45644656 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63937377 | AAACTTCCTTGTTTG[C/T]TTGTTTGTTTGCATA | 104082 |
rs45645366 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63885357 | GTCATACGTGCAACT[A/G]TCCTGTTATGACCTT | 104082 |
rs45646567 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63854579 | TTACAGTGTGTGTTA[A/G]TTCTGGCATGGCAGT | 104082 |
rs45654939 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63714842 | GTAGGAGGGAAATAG[G/T]AGAACTGATTGGAGG | 104082 |
rs45655876 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63803069 | CTTATGCTTCCGGTG[C/G]TGCATTTTTGTCTTG | 104082 |
rs45655933 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63803486 | CGCTGGTTTATGAAC[A/G]ATGCCTGCCTGTGCC | 104082 |
rs45659159 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63977960 | GATTCATTCCCTGCT[C/T]CACTATAGACAAAGA | 104082 |
rs45666797 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63935247 | ATCCTCATTTCTGCT[C/T]AGATAGAAGTGTTGC | 104082 |
rs45667214 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63842583 | AGACCCTATGTTCAT[G/T]CTTCCTGTTGTTTGC | 104082 |
rs45668176 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63770027 | CAAACTAGTAATGAA[A/G]CTGGCAGTATATTTT | 104082 |
rs45672463 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63907390 | AGTGGAAAAGGGTGA[A/G]CAGGCCTGTTGAGAT | 104082 |
rs45675073 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63982739 | TAGTCTGGCAGCCAC[A/G]CACCATATTGCTACA | 104082 |
rs45686795 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63785986 | TTTTTGGTGTTAGTA[A/G]TGAAGATGTTTTAAA | 104082 |
rs45689346 | snp | C/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63986178 | ACAAATAATGCGTAT[C/G]AAAGTCGTTTAAGTA | 104082 |
rs45689818 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63861744 | CAACAAAAGAAAGTT[A/T]TTTCTAAAAAACAGC | 104082 |
rs45699436 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63755715 | CAAAAAGCACAGGCA[C/T]TGATAAATGTGCACA | 104082 |
rs45707254 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63879303 | AATAACTTACAACTT[C/G]TTAATATAAGGCGGA | 104082 |
rs45708623 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63808171 | TTCTGGCTTTGGAGC[A/G]TCCCTTCATTATACA | 104082 |
rs45722537 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63738445 | ATAAGTAACTTTCCC[C/T]GTGATTGGTAAACCA | 104082 |
rs45726394 | snp | A/C | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63772990 | GTATATCTACATGTC[A/C]TGACTTTTTCTGCTG | 104082 |
rs45729767 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63936258 | AAGAAAGGTGGGTGC[C/T]ACCTGTGAGGAGGTG | 104082 |
rs45730274 | snp | G/T | | | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63989171 | GGGACTGGAGGTCAA[G/T]GACAGATGGTATCAC | 104082 |
rs45731558 | snp | A/G/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63928808 | GTGTATCAAGGGCTC[A/G/T]ATATTCTCTGGGGAA | 104082 |
rs45733250 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63723939 | CTGATAGAGACTGAA[A/G]TGGGGCATTGACAGG | 104082 |
rs45744424 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63937260 | GAGTCAGTTCTCCGC[C/T]CCTTGCATGTGGACT | 104082 |
rs45746666 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63771710 | TACCAAATCAAGGGG[A/G]AAATTATTGTTCCTT | 104082 |
rs45748138 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63767247 | GTTATTGTGATAGAC[A/G]TATAAAGGGTTTGAC | 104082 |
rs45757726 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63934007 | TATATTTTTAATTTA[C/T]GTGTGAGTCATACCA | 104082 |
rs45758676 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63972762 | TTCCATTGAAGCAAA[A/T]TTTTTGAGAAATCTA | 104082 |
rs45761148 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63886552 | CTGACATTTCTATGG[A/G]GAAGTGCAGCTGATT | 104082 |
rs45769781 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63760491 | CTCCAAATATGCTAT[A/G]CCATTTTTTTTCTGT | 104082 |
rs45776407 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63767856 | TTACCTCAGTGGCTT[C/T]CAAAAATTAAAAAAA | 104082 |
rs45777305 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63928886 | GAGAGGAGATTATGT[C/T]GGTTCACTGGACTAC | 104082 |
rs45777843 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63884509 | CTGGGTGTTACAGAG[A/T]CACTAGCCCTTCTCA | 104082 |
rs45778829 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63844046 | CACGTTGGAGTCCTA[C/T]ACATGGTCTGTGGCC | 104082 |
rs45781785 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63856444 | AATTAATGATTTTGT[A/G]TATGCCCCACTGAGT | 104082 |
rs45788188 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63841349 | GACTGTTGTGTCTAA[C/T]AGAGTTACTGAAATC | 104082 |
rs45792041 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63880033 | TGAAAACTATGTTCG[A/T]CAGAGACCTACAGTT | 104082 |
rs45792184 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63894095 | GTAAGCACTGACACC[C/T]TTTGCATCCTAGAGC | 104082 |
rs45796824 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63738968 | AACATATTTACGTAT[C/T]GCTTTCTCCTAAGTA | 104082 |
rs45801168 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63766098 | GAATCTGCAGGTGGT[C/G]CTCAGCACTCACTCA | 104082 |
rs45801498 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63933919 | TGGATGAGGCTTATG[A/G]GTAAGGCAAAACATC | 104082 |
rs45802068 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63890071 | ACAATAGTGTTCTAC[A/C]CAATAAATGAAGATG | 104082 |
rs45805911 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63746706 | CAGACTAGGAAAACT[C/T]GATAATAAAAATGAA | 104082 |
rs45816491 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63872919 | AAAAGAAAGTCTTTA[C/T]AAGAATAATGGATAA | 104082 |
rs45828252 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63793841 | CAAGTGAGACCTGTG[C/T]GGATGTCTGTGTGAA | 104082 |
rs45830518 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63787618 | TGAAATATATGTGTA[A/G]TCAAATTAGAAGAGT | 104082 |
rs45830697 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63715297 | ACAGGAAAGGCTGGC[G/T]TTGTCAGCTGTGTGG | 104082 |
rs45831337 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63921724 | AGCCACTCAGCGAAG[G/T]CCATTTGGTCATGTT | 104082 |
rs45833090 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63896588 | ATACTGAGATGGAAG[G/T]CAGAGGCAGGTATAT | 104082 |
rs45836200 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63973995 | TCCCCATGTTTGTGC[A/G]TATGAAACATGAGAT | 104082 |
rs45836263 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63760815 | TAGTTTCATTGTCCG[C/T]GGGTTCCATGGAGGG | 104082 |
rs45838300 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63848231 | GGGACAGAAGTACTA[A/G]CTAGTGGTTTCTGAT | 104082 |
rs45846566 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63843655 | AGGGCTCAGTCCCGA[A/T]GCTTCTTCCTCCCCA | 104082 |
rs45854096 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63770379 | CCACAGGTCATGAGC[C/T]GAAGGCCTCTGATCT | 104082 |
rs45866216 | snp | C/T | | | synonymous-codon | Wdr7 | Mm_Celera | 18:63777935 | CCTTACTATGGATAC[C/T]GCAAAATTATTCATG | 104082 |
rs45869749 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63897991 | TGACTTAACCAAAAG[C/G]AAAATGAGACTGAAT | 104082 |
rs45877042 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63755701 | AAATAATGCTCAACC[A/G]AAAAGCACAGGCATT | 104082 |
rs45879779 | snp | C/G | | | intron-variant, upstream-variant-2KB | Wdr7, LOC105246469 | Mm_Celera | 18:63708952 | CCTCCTTGTGAAAAC[C/G]CAGCTTTAGAGCTTA | 104082 |
rs45883150 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63854328 | GGAGCGCACTGTGTT[G/T]CAGTCTTGATATTAT | 104082 |
rs45883416 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63852505 | TTCTTATGCAGAATA[C/G]TAAAAGATCAAGGTA | 104082 |
rs45884348 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63885193 | GAAAACCATAGAAAT[C/G]GGCTCTTCCTCTTCT | 104082 |
rs45885870 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63737706 | CCCAGTCCGTCTTGG[C/T]GGTGACATCTCAGGC | 104082 |
rs45886736 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63965175 | TGGGCAGATTGGCAT[C/T]TCCTCCCTGTGCTGC | 104082 |
rs45889622 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63834891 | GACTTTTGATTGGAA[A/G]GAATTTGCCTGAAAC | 104082 |
rs45896291 | snp | A/G | | | downstream-variant-500B | Wdr7 | Mm_Celera | 18:63990148 | CTTCAGTTTGAAGTC[A/G]AATTTGAATGCTGAG | 104082 |
rs45910369 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63941861 | CCTACAGGGATAGAC[A/G]TTCAGAAGACAATGT | 104082 |
rs45911027 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63883754 | CTGGGTTGCCATAAA[A/G]CATAATAAAATTAAA | 104082 |
rs45914427 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63881191 | AATCTATCCAGAATG[C/T]ATCTGTTTCATTCCC | 104082 |
rs45916407 | snp | A/C | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63737712 | CCGTCTTGGCGGTGA[A/C]ATCTCAGGCAGCGGC | 104082 |
rs45917903 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63775518 | TGCTCCCTTCGTTTC[A/T]TATTGACTGTTAAGT | 104082 |
rs45940357 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63853249 | TGGATGCTTAGTAAC[A/C]TCAAGTGTAATGTAA | 104082 |
rs45942856 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63947429 | ATCGTGGTCCACACA[A/C]CCTGGTGGAGCTCAC | 104082 |
rs45943338 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63814380 | GGAAGGTTCCACCTC[A/G]ACTTCTTGTTCGTAC | 104082 |
rs45943897 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63982849 | TCCAGAAATCACCAA[A/T]ACCACCTAACAAATA | 104082 |
rs45944273 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63711000 | ACGTGTTCATCTGAA[C/T]ATGACCAGCGTTTCC | 104082 |
rs45952448 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63871331 | CACTTGAAGGTAAAT[A/T]TTTTTTTCTCACCTG | 104082 |
rs45955859 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63844505 | CTTCTACTCATATCT[C/T]AATACTCAGATCTTT | 104082 |
rs45962728 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63770711 | AGGAGAGTAGTGTGT[A/G]TGTTACCTATCAGCC | 104082 |
rs45964727 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63891786 | TGTATTCCTCACAAA[A/C]CTATTTTCAGAATAA | 104082 |
rs45965897 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63942605 | GACACCTGGCTCAAA[A/G]CGTCTTCCAATTCTG | 104082 |
rs45971430 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63906797 | CGGGGCACACAGCAG[C/T]TAAAGGGCGGCTCTC | 104082 |
rs45971760 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63888860 | AGTGGCTGTCCTCTC[A/G]GCATGAGGTACAGCA | 104082 |
rs45972349 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63930992 | CTGACTGGGAAATAG[C/T]GACTCCTAAGCAGAA | 104082 |
rs45972715 | snp | C/G | | | synonymous-codon | Wdr7 | Mm_Celera | 18:63924893 | TCTCATCGCCACAGC[C/G]AGACCACCCGCCTTC | 104082 |
rs45996833 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63739654 | ACTCTTCTAAAACAG[C/T]GCTGTTGAACTAATG | 104082 |
rs46004652 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63809338 | ATTTTCCCATTTATT[A/C]ATGAATTAATATTTA | 104082 |
rs46008169 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63967016 | CACCTAGTACAGGCT[A/G]TCTTTTTTAGGTTCA | 104082 |
rs46010264 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63895763 | CAGTAACTTACACAG[C/G]GGCAATCCCATTATC | 104082 |
rs46010612 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63885087 | ATAACATTGTGTTCA[A/G]TTTGTGTTGCCACAA | 104082 |
rs46013320 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63985392 | TAACTAACAATTTCC[C/T]GGATCAATTGGATCT | 104082 |
rs46016029 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63770858 | TGTTTGGTACTCTTG[A/G]TTCTTTGGCTGGAGT | 104082 |
rs46016082 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63881633 | AGTATTCATGGCAGT[A/G]GTGACTAAACACTGA | 104082 |
rs46023062 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63881029 | CCTCCAGGAGAGAAC[A/G]TTTTAATCCAGAGGA | 104082 |
rs46023861 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63940313 | GTGTGGTTGCTGGGA[A/T]TTGAACTCAGGACCT | 104082 |
rs46025767 | snp | C/G/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63798862 | TAGGACCTCTAACAC[C/G/T]TGTTCACGTCATTTA | 104082 |
rs46027822 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63970353 | GATTGCTGATTGACA[A/G]GGCCTGGGGCAGTTC | 104082 |
rs46036425 | snp | C/G/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63939210 | GAGCTTTCATGGCTG[C/G/T]AGCTGCTGAAGCACT | 104082 |
rs46043183 | snp | G/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63930894 | GCCACAGTTGCTGTG[G/T]TATAGTAGCCTCCTC | 104082 |
rs46045363 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63770990 | AAGAAATACCTTCAA[A/G]AAATGTTTCCTATGT | 104082 |
rs46052566 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63737481 | TAAAATCCTACATAA[A/G]TGATTTTCTTTCTAC | 104082 |
rs46053886 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63966526 | TACTGTGTACTGAGT[C/T]ATCTCAAGCCAGCAC | 104082 |
rs46055721 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63776113 | AATGAATAAAGCATA[A/G]TTAGTTTGTTCATGT | 104082 |
rs46058486 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63723801 | GATGCGGGAACAGCC[A/G]CTATCAGAAACCTCT | 104082 |
rs46069402 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63886575 | AGCTGATTTGGAGCC[A/G]TTCAGGAGGAATAAT | 104082 |
rs46072148 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63860314 | TAGGCTGCTCACACT[G/T]CACATACCTACTTTA | 104082 |
rs46076614 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63889634 | TCTCACCCCAAAGTG[C/T]GGCAGGATCTCTGTG | 104082 |
rs46077466 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63720191 | TTTTAGGGAGAATAT[C/T]TGACATTACTCTTAC | 104082 |
rs46080057 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63793334 | GCTTTCTCATCCAGT[C/T]CTGATTATTTGCCTC | 104082 |
rs46082118 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63850613 | TCTGTTTTCTATTTT[G/T]TATGCACTCCCCTTT | 104082 |
rs46089392 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63948147 | GTCTCTGCAAAGAGT[A/G]CTTTTCAGGATTGAG | 104082 |
rs46089824 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63759539 | ACATGCAGGCAAAAA[G/T]TCATACACATAAGAA | 104082 |
rs46097510 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63941489 | TGCTTAGCGTAGCTT[C/T]GTTAGTAAGTTGTGT | 104082 |
rs46099269 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63900536 | TCCAGAATACAAATT[C/T]GTTACATAGCTTTGT | 104082 |
rs46105153 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63802942 | TGTTTTGATGGCTTG[A/G]ATTTTCTTATCCTAC | 104082 |
rs46109700 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63771246 | CCAAGAATAGTCTGT[C/T]AGGAGAAGTGTAGTA | 104082 |
rs46111966 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63721885 | TTTTTAAGAAACTCA[A/G]GTGATGCCATGTGGA | 104082 |
rs46116358 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63838623 | AGTCACTGTTTGGAT[C/T]AAGCTTTCTGTGGAT | 104082 |
rs46125731 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63744535 | AGGTCTTATTGCCTC[C/T]TAATTTCTTAGAAAA | 104082 |
rs46131722 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63851450 | CTGGAAGAAGGGAGC[A/G]TGAGAAAGGGTTTCC | 104082 |
rs46134567 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63954553 | ATATTTTATTAGTGT[A/G]TATTCATTGAGTGAG | 104082 |
rs46139402 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63794551 | CTTCCTTAAAATTCA[C/T]TGAGTATTTCATTAA | 104082 |
rs46145980 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63905363 | GGAGCCTTGCATCCT[C/G]TGGTGTTTTATGGTT | 104082 |
rs46148029 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63809685 | TGCTAGTTACTGGTC[A/C]CGTTTAGCATGTGTT | 104082 |
rs46148471 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63717152 | ATTAATTGTTTTGCT[C/T]TTGACCTTTCCATGT | 104082 |
rs46149379 | snp | A/C | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63901722 | TTTCGTGTGGCACTT[A/C]CAGCCATTTTCATGG | 104082 |
rs46149804 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63893576 | GCTTTCTGTCGGGAA[C/T]GGGCCACTGAAACCA | 104082 |
rs46151737 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63944733 | AGTCAGGATTCTGGA[A/C]CGCCTAGAGGAAAGG | 104082 |
rs46154471 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63843765 | TTTATTTCCTTGCTT[A/G]TTCTCTGATACACAA | 104082 |
rs46166113 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63891504 | GACTGTAAAACAGCA[C/T]GTCACTGTGGCCTTG | 104082 |
rs46166586 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63854529 | AACATTCGTGCTGAG[C/T]CTGGACAGATCTCCG | 104082 |
rs46168504 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63739423 | TGCGGGGAATTTCTC[C/T]ATGCCATAATTTAAG | 104082 |
rs46169568 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63885207 | TCGGCTCTTCCTCTT[C/T]TAGCAGCTATCAAAT | 104082 |
rs46171109 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63972176 | AACCAATCAGTGAAC[C/T]GAATTATTCCCTATC | 104082 |
rs46204520 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63931047 | TACATCTTCTATTTG[A/G]CCTTTTGAGCTGATA | 104082 |
rs46215442 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63772078 | GGCCATTATATAAGA[A/G]TCTGAGTTTGAGTCC | 104082 |
rs46216579 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63951636 | TCTTACTACTTGATA[A/G]CAGTCAGCAAATAGA | 104082 |
rs46222414 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63934400 | AAATACCCGAAAGGG[C/T]AATCCAATGGAGGCA | 104082 |
rs46222426 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63753149 | TGATGGGAGCACACG[A/G]TCAGAGCAAGAGCAG | 104082 |
rs46224029 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63775604 | AAGATTTGTATCCTC[C/T]TATAAACGCCATTCA | 104082 |
rs46226364 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63921466 | CTCATGATTGTGGGG[C/T]AAGCCTTTTTTACTG | 104082 |
rs46226420 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63760564 | ACGTGGAGGTGCTGC[C/T]TTCCAGGTGCGCTGG | 104082 |
rs46227958 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63790768 | CTCTTAGTCCTGCTG[A/G]GCACCTCACACGTGC | 104082 |
rs46234877 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63881807 | TAATCTAAACTTCAG[C/T]TTTTATGTGACTTTT | 104082 |
rs46236277 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63956766 | GTCTTAATATAAATT[C/T]AGGTTAATGTGTTAT | 104082 |
rs46236844 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63871441 | GTGCTAGCTTAGTCT[A/G]TTATAGGGCATGGAT | 104082 |
rs46238511 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63754477 | ATAGGCAAATACCAC[A/G]AAGGGAGCAGGGGTG | 104082 |
rs46239577 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63958975 | GAATATCTCTGTAAA[A/G]AAGAGTTGTCTGCAA | 104082 |
rs46243057 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr7, LOC105246469 | Mm_Celera | 18:63709416 | AGGCTCATCTTTGAA[C/T]TGCCACTTGGCTGCT | 104082 |
rs46253474 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63723850 | TCTGGAGAGCCCCAC[A/T]TAAGTTCTGCCAAGA | 104082 |
rs46260858 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63938865 | GAATATACCCACCTT[A/G]CTGACCTATTCCTGC | 104082 |
rs46263825 | snp | C/T | | | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63989597 | AAAGGTGACATGATG[C/T]GACACTTGTGTGAAA | 104082 |
rs46267964 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63972056 | GTGTGTTTTAACAAT[C/T]GCTTTCTCTTCTTTC | 104082 |
rs46274723 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63788471 | CCAAATGCTAGGCCT[A/G]GTGCAGAAGATCTTC | 104082 |
rs46286287 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63986552 | TGGAATCCCAGCTCT[C/T]GGTGGGCAAGTGGAT | 104082 |
rs46286681 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63888710 | TGTGCAAGCTCATGG[A/G]TTAGTTATGACTCAG | 104082 |
rs46286804 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63758961 | TCAAATCCTGCCTGA[A/G]TCTGATTTATAGAGC | 104082 |
rs46292839 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63797910 | TTGGCACCAACTCAC[A/G]GTAAGCATTGATTTG | 104082 |
rs46293805 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63904935 | ATGCACATGCACAGA[C/T]AGTAAATGAAATCAA | 104082 |
rs46310588 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63893989 | GCCCCTCTGCTAAAA[A/G]ATAGAGAAACTTGAA | 104082 |
rs46312206 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63746778 | CCCAGGGAGCTAGTG[A/G]CTGGGCTACACTGGC | 104082 |
rs46312701 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63909677 | AGAAAACTCCTATGC[G/T]GCTGGAAGACTAGAC | 104082 |
rs46314761 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63769906 | AGACAGCTACAGTGT[A/G]CTTACATATAATAAA | 104082 |
rs46332756 | snp | A/C | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63928752 | CAAAAAGCAATAGTA[A/C]TTTGTTTATTGATTT | 104082 |
rs46339570 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63947278 | TGTAGACTATAACAG[A/C]GTTTAGGACGACTGG | 104082 |
rs46339592 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63851926 | TAAAAAAAAATCAAT[A/G]TACGTACCAAACACT | 104082 |
rs46340864 | snp | C/T | | | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63989660 | TGAGTTAAAATGTCT[C/T]GTCTCCTACGACATT | 104082 |
rs46347684 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63710981 | ATCTTTGTCGTCAAT[A/C]TGGACGTGTTCATCT | 104082 |
rs46347821 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63881237 | TTGCTTTGGTTTCCC[A/G]TTCATGTATTGGCAA | 104082 |
rs46350626 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63718509 | CCTTTAACTTGAGTT[C/G]GGTTTTGAGTGGATC | 104082 |
rs46355754 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63740984 | CCTACCTTACACAAT[C/T]CGTTTAGTGTTGGTT | 104082 |
rs46366838 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63896278 | CCAGAAGGTCCTTGA[A/G]CCCATTGGTGCAGTT | 104082 |
rs46367481 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63981579 | GAAGCAGGAGTGGGT[G/T]GGTAAGGGAGCAGGG | 104082 |
rs46369695 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63885489 | AGTCTCTTATTCTTC[A/G]CATGTTGCCGCATGG | 104082 |
rs46381760 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63965706 | GACATGCGCAGATCT[A/G]CTACAGAGTGATAGA | 104082 |
rs46395474 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63776273 | CAGGCTTTCTCTGGG[A/G]AAATTAAGAGTCCTC | 104082 |
rs46396013 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63847716 | AGTAAAAGACCTGTT[A/G]TAGTGTAAATGTCTT | 104082 |
rs46397847 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63941351 | ACAAAGCCCATACAC[A/G]AACAACACAGGCCTG | 104082 |
rs46398072 | snp | C/T | | | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63989756 | TAAAACTGAAGTGTA[C/T]TAAAGGTGGTTTTTA | 104082 |
rs46400827 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63881727 | AAGTACTCATGGCAG[C/T]AGTGACTAAGTACTC | 104082 |
rs46401699 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63931533 | ACTGCAGAGGAACAA[C/T]GGGAGGCAGTATATG | 104082 |
rs46402316 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63845386 | AATGCCTATGCCTAC[A/G]TGATCCCTCAGTTTC | 104082 |
rs46402557 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63767966 | TGGAGAATTTAAACT[C/T]GATAGTTGAATTGAG | 104082 |
rs46403980 | snp | A/C | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63936783 | GGGGTCTAAGACTTT[A/C]GATTATTTCTCCAAT | 104082 |
rs46404388 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63715728 | TGACCTTGACACTCT[C/T]TCTTGACAAGTGATG | 104082 |
rs46405529 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63767623 | AGCGGAATATATTTA[A/G]AGTTTGAATGGAGAA | 104082 |
rs46405934 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Wdr7, LOC105246469 | Mm_Celera | 18:63708892 | TCCCCTACAGACATG[A/G]TTATCGCCTGAGGTG | 104082 |
rs46406673 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63768529 | AAGGGAGCATGATGA[C/G]GAAGGATTAGGTAGG | 104082 |
rs46409204 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63884897 | GTCAATAGTATTTCA[C/T]AGTAGAATGTGGTTT | 104082 |
rs46410558 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63879464 | TCAGACTCTGCTGTC[C/T]TCAGCACACATAGCT | 104082 |
rs46417211 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63862531 | AATACAATAACAAGC[G/T]TCTATCAATATATGG | 104082 |
rs46422029 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63738962 | GAATTGAACATATTT[A/T]CGTATTGCTTTCTCC | 104082 |
rs46422644 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63773813 | TCAGTCGGGTCCCAG[A/G]TGTGCATATTTTATC | 104082 |
rs46425691 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63737009 | TCTATAATTGAATTG[C/T]GTGGGCTGGAGAGAT | 104082 |
rs46430153 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63716650 | ATGGGATAGGAATAG[G/T]CACCTCCTTTGGAAA | 104082 |
rs46430216 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63769999 | AAATTCATGCAGATA[A/G]CCTCCCTTTGAACAA | 104082 |
rs46430500 | snp | C/T | | | synonymous-codon | Wdr7 | Mm_Celera | 18:63777863 | GCAGAGCAGGGAGGA[C/T]AGTGACCCTGAGTAC | 104082 |
rs46434218 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63976193 | TAGAAATGCAGGCAC[A/G]AACCTTCTTAAACAG | 104082 |
rs46438643 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63794732 | GATGGAAGGAAGGTT[C/T]CTATGTTACATAAAA | 104082 |
rs46440526 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63787938 | CATAATAGGTTAATC[A/G]GCATAGATTTCCATT | 104082 |
rs46441809 | snp | C/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63784069 | CCTCTACACACTGAG[C/G]CCTCTGGTTTGCTAG | 104082 |
rs46444690 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63770983 | TTTTTAGAAGAAATA[C/T]CTTCAAAAAATGTTT | 104082 |
rs46445951 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63793970 | AGAAATGTGTTTTCT[A/G]TGGGAATTTGGCAAA | 104082 |
rs46447798 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63870106 | TAACATGCAATATTT[A/G]ATGAACTTTAATTGC | 104082 |
rs46448764 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63900201 | AAAGTCAATATATGG[C/T]GAAATGAGTATATAG | 104082 |
rs46453951 | snp | A/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63771368 | CCGCTTAAACTAGCA[A/T]GAAGGAACACTAGTG | 104082 |
rs46454938 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63747139 | CTGTTGCTTATTGTT[A/T]GCTTCTACTTTTAAC | 104082 |
rs46460564 | snp | A/C | | | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63988466 | TAATAGAAGAAAAAA[A/C]TCTATAACAATGTTT | 104082 |
rs46468565 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63782246 | ATAGCCTAGTATAAA[A/G]CAATTTTCAGGTCGT | 104082 |
rs46471064 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63772895 | TAAAACATAATCTTG[A/G]TATTCAGAGACAAAG | 104082 |
rs46473804 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63775239 | GGCCCAGGAGCCTGT[A/C]TTTCACCAGAGGTCC | 104082 |
rs46480438 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63907377 | CTGAGGACGTGGGAG[C/T]GGAAAAGGGTGAACA | 104082 |
rs46485430 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63929963 | TTAAGATAATATAAA[A/G]AATGCAAGTTTAAGC | 104082 |
rs46485929 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63738257 | TCTCAACCTGATGGC[A/G]TCCTCCTCTTTCGTT | 104082 |
rs46489461 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63928866 | TCCAGGATCCAGTGG[C/T]TAACGAGAGGAGATT | 104082 |
rs46492452 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63884112 | ATAAAAAGATGATAA[A/G]GTAAACACAAGCTGT | 104082 |
rs46496583 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63805445 | TCTAGAGTGTCAGGG[A/G]ACTTGAGCTTAATTT | 104082 |
rs46497272 | snp | C/T | | | downstream-variant-500B | Wdr7 | Mm_Celera | 18:63990056 | CATTGTACGGAATTG[C/T]ATCTTGTCAGCCCTC | 104082 |
rs46515171 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63964868 | CACGCCCAGCTTGGC[A/G]TATTTGCATTTAATT | 104082 |
rs46515475 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63889552 | TCTGCTGCGTGGACA[A/G]GATGTGGAAGGCAGA | 104082 |
rs46531882 | snp | A/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63769779 | GAGAGATGGCTCAGC[A/T]GTTAAGAGCACTGAC | 104082 |
rs46535064 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63930855 | AGGCTCACAAGCATA[C/T]GCAGTCCTTTCTTTA | 104082 |
rs46544811 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63884960 | TATTTTTATTAATTT[A/C]AAAGTACAATGTATT | 104082 |
rs46546633 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63863215 | TGGATCTCTATGTCA[C/T]CCTTTAGCATGATTA | 104082 |
rs46556377 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63714179 | CTGGTATGTGATTGC[C/T]GAGTCTCACTGCTAC | 104082 |
rs46557227 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63769934 | AAATAAATAAATCTT[A/T]AAAAAAAAAGAATAG | 104082 |
rs46557556 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63797879 | GGAGTGAGTTGACCC[A/T]TGGTAGGTGTACAGA | 104082 |
rs46561157 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63803029 | TACCTGATAGCCGCA[A/C]ATTTCTGTACTGAAT | 104082 |
rs46572803 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63859480 | ATGGGGTTTTTAGAG[A/C]AACAAACAAGTAGAA | 104082 |
rs46573388 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63860117 | TACAAATTAATAGCA[C/T]GTTTGTTTACTCGGG | 104082 |
rs46576139 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63777302 | AGCTTTTATTAATGT[A/G]TACTTGGTTTTAATT | 104082 |
rs46577599 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63928888 | GAGGAGATTATGTTG[A/G]TTCACTGGACTACGG | 104082 |
rs46577957 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63934751 | ATATAATGTGACTGG[A/G]AAGGATGTCTTCAAA | 104082 |
rs46584182 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63980067 | ACTATCCAAGACATT[A/T]AAAAAAAAACTTGAA | 104082 |
rs46585193 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63938968 | TTGTTTGGCAACTTT[A/T]AAAAACTTATATACT | 104082 |
rs46590030 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63962864 | TGGGAAAGTCTTTGT[A/G]AAGAGTAAAAACACA | 104082 |
rs46594071 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63762780 | TTTTCACTTCATATC[A/C]TATGATGTCTAGTTT | 104082 |
rs46618778 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63855435 | AGAATATCTTGATTT[C/T]CTCCCTCAGTTTCAT | 104082 |
rs46625586 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63866667 | CAAAAATCCTCCTTC[A/G]GGTAAGGCCAGCGTC | 104082 |
rs46629469 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63736521 | GGTAAAGTTCTTCAG[A/G]TATCATTTATTTATA | 104082 |
rs46639241 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63774975 | CTTGCTTTGTCCCAT[C/T]GCTCACATTTCTTGG | 104082 |
rs46643139 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63837321 | AGGAGTAGGATATGG[G/T]AAAACTAGTTGGAAA | 104082 |
rs46649367 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63869794 | TATTCACTGGTGATG[A/G]ACTTGCCTATAATAA | 104082 |
rs46649851 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63885255 | CGCTTGGTGGAATTT[C/T]ACATCCACTTTCCCT | 104082 |
rs46669362 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63954641 | CTTCTCGCAGAGACC[C/T]GTTCAATTCTAGGCT | 104082 |
rs46671216 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63741479 | CAAGAAAATGCTTAT[A/G]AACCTAGCACAATGT | 104082 |
rs46672848 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63934339 | CTGCATAGGGTGTTA[C/G]CTCCTGCAGTGGGCC | 104082 |
rs46682520 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63755666 | TTCAGTTTTATGTAT[A/G]TATGGGTCTAGTTTA | 104082 |
rs46685001 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63965474 | TTCTGATCTCTCACA[C/T]ATAGAAGTTTGAACT | 104082 |
rs46686134 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63935177 | TGTTCTGTGAGAATG[C/T]ATATTTCAATAGTTG | 104082 |
rs46688580 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63808244 | AGCCATAATCAGTTG[A/T]AATAATTACTTTCTG | 104082 |
rs46692072 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63931291 | AGCTGTGGCATCTCC[A/G]TGACTGGTGGCCTGC | 104082 |
rs46702838 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63736577 | AGGCACTTGAGAGAT[A/T]CAGTAAAATCCAGCA | 104082 |
rs46703674 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63872908 | ATCCCGTTTCCAAAA[A/G]AAAGTCTTTATAAGA | 104082 |
rs46708076 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63739600 | ACAAATTATTAGTTG[A/G]ATTGATTAGTATATA | 104082 |
rs46710655 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63881973 | CTAGAATCTTTTCTG[C/T]ATAAGAACACTTAAT | 104082 |
rs46717418 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63717176 | TCCATGTATATATGA[A/G]TATTTTCTTTTTGTT | 104082 |
rs46737033 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63892689 | AACAGAAAAATAAAT[G/T]TCTTAGCTTGATTAA | 104082 |
rs46737902 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63833963 | GGACATCTGTGAGTA[C/T]GTAACTTACGGACAC | 104082 |
rs46739154 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63930407 | TTATACTTGTAAAGA[A/G]TAGGTCTTTAAAAAT | 104082 |
rs46741055 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63744375 | ATGGTTGTGAGCCAC[A/C]ATGTGGTTGCTGGGA | 104082 |
rs46744243 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63741461 | GATTTGAATGTCATG[C/T]TTCAAGAAAATGCTT | 104082 |
rs46745580 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63931206 | GTGTACAGCTTGGAT[A/G]ACTAGAATTCTTAGG | 104082 |
rs46749655 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63738976 | TACGTATTGCTTTCT[C/T]CTAAGTATTTATTAT | 104082 |
rs46755776 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63799368 | AAGCAGAGATGGGAG[A/T]ATTCCTGTGTCCTAA | 104082 |
rs46756977 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63979034 | GTTGCAAAATTACAC[C/T]CTTTAATGTAAAAAA | 104082 |
rs46757976 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63872182 | TTCCAGGACTGTGAA[C/T]GCTAGGTACTAGGGA | 104082 |
rs46774923 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63882426 | CACTGGTCCAATTAC[C/T]AAGATGAAAGTTGCA | 104082 |
rs46776102 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63754761 | CCAGTTTTGCCTTTG[C/T]GGATGTAGCAATTGT | 104082 |
rs46778792 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63712144 | GTCATTCAGAGGAAT[C/T]CGGAGTTCAGAAGAC | 104082 |
rs46785942 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63743992 | TTTGTCCAGGTTAAG[C/T]GTGAGCCTCCTCTTT | 104082 |
rs46786032 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63782180 | TATGGAATTCTTAAA[A/T]TTTTCTTTTTCATTT | 104082 |
rs46795649 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63933805 | GAAATAGAATAACAT[G/T]CCACTTTCTGTGGAC | 104082 |
rs46801167 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63891153 | AATACAGTTTTATAA[A/G]CGCGCACTTGACTGG | 104082 |
rs46808957 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63895818 | GTCTGTCCTGTGTTA[C/T]AGTTCTAGTTCTGCT | 104082 |
rs46810090 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63738597 | TACATGAAAATACAC[C/T]GAATAACCATGCTGT | 104082 |
rs46810333 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63755774 | ACAGATCAATATAGT[C/T]TTTACCAGGAATATT | 104082 |
rs46816168 | snp | G/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63889062 | TTCATCTATCTTATA[G/T]CCTGTTAACTTCTAA | 104082 |
rs46817461 | snp | A/C | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63755457 | ATGTGCAGATGAGGA[A/C]GACAGGCAGTGATGC | 104082 |
rs46834359 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63946671 | CTCATGTTTGACACA[C/G]TTGTACTACTAACCA | 104082 |
rs46845639 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63738937 | TACTCTAACATTTTG[A/T]GTTATAACAGAATTG | 104082 |
rs46845676 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63872581 | GCTGGTGCAAAGACT[A/G]AGGATGTTCAGTGAG | 104082 |
rs46848165 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63953954 | ACACACATTCACCTT[C/T]GTGAAGTATCTATAA | 104082 |
rs46858366 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63743764 | TCACCCCATCACAGT[A/G]CTTTGAGAACACAAG | 104082 |
rs46859806 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63884452 | CATTGGAAGGGTTCC[A/C]ATTCTAGGTGTGCAT | 104082 |
rs46860694 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63850538 | AGAGCAAGGTAAAGA[A/G]GAATACAAGGAAAGA | 104082 |
rs46862253 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63756074 | CTGTAAGAGATATTA[A/G]TATTTTCTGTTATAT | 104082 |
rs46863233 | snp | A/C | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63771306 | TCAGGGTGGTGTGGT[A/C]ACGGACATATGTTGA | 104082 |
rs46865302 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63939375 | GATGACTGCAGCTCC[A/G]ATTCCATCTTCATAA | 104082 |
rs46866242 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63779563 | TAACAGGAAGAAGAG[A/G]AGGCTAAGATGATTT | 104082 |
rs46870150 | snp | A/G/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63779374 | TCCTTAATCCTGCAA[A/G/T]TGCTTTGATCTATGG | 104082 |
rs46870679 | snp | C/T | | | synonymous-codon | Wdr7 | Mm_Celera | 18:63738778 | TACTCGGTTTTTCTA[C/T]GGATGCAAGGAATAT | 104082 |
rs46889429 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63936932 | AAGGATGCTGTTTGA[A/G]TATTAAGTGCATTTC | 104082 |
rs46893792 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63890117 | GTTATGTTATTCCCC[A/G]GTGAATCAACAGACC | 104082 |
rs46899126 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63775749 | AGATGGAGAAGGAAC[A/G]TGGTCCTGGTGTAAA | 104082 |
rs46902853 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63964488 | TGGCAGAAACCATCT[A/G]TACAGCAGGTGCCTC | 104082 |
rs46903448 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63947026 | GCATTGAGACACAGC[A/G]GTATTCTTTCCAAAC | 104082 |
rs46903602 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63872613 | GCCAGGCTGTGTGCA[C/G]ATGTGAAGACCTTGA | 104082 |
rs46904350 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63938409 | CCAGCCACAGTTAGC[A/G]CTCACTCTCTGTAGA | 104082 |
rs46910617 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63937235 | GAGGAGATCAGAGGA[A/G]GCCTTGAAGGAGTCA | 104082 |
rs46912777 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63773392 | CAAAAGAAATCTCAC[A/G]TGGTTAAAGACATAC | 104082 |
rs46918243 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63762554 | TCATCTTCCAGTGCT[A/G]TGAGTGCGAGTCTGG | 104082 |
rs46918597 | snp | C/T | | | synonymous-codon | Wdr7 | Mm_Celera | 18:63904160 | CTACATGGATGTGTC[C/T]GCTGTCCTGATGGGG | 104082 |
rs46921711 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63850710 | CCACATCTCTAAATA[G/T]CCATGAGATTTTTCA | 104082 |
rs46946999 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63901803 | TGTCCTGCTGACTCC[C/T]TCTGCCAGTCTCCTC | 104082 |
rs46948574 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63888980 | TAAACTGAAAAGGCA[A/G]ACTTCAACCTTGATT | 104082 |
rs46953135 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63803000 | AGGGAGGAAGAAGCA[A/G]CAGCAGTCAGCCTTA | 104082 |
rs46958198 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63903047 | AGCATGGCCCTCTGT[G/T]TGCCTCTCTCTCAGC | 104082 |
rs46958386 | snp | C/T | | | upstream-variant-2KB | Wdr7, LOC105246469 | Mm_Celera | 18:63708577 | GCCATAGTAACCAGA[C/T]CACGCCTGCCTGGAC | 104082 |
rs46961457 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63773426 | CTCCACATAGAAAAT[A/G]AAAATTACAATAAAT | 104082 |
rs46962718 | snp | C/T | | | synonymous-codon | Wdr7 | Mm_Celera | 18:63720347 | TGTAACTGGATGCCA[C/T]GATGGACAAATATGT | 104082 |
rs46966653 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63844962 | AGCTCCTGGCCCATC[A/G]ACTTTAAACATGTAT | 104082 |
rs46975550 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63933670 | GATATGAGCACACCC[A/G]GTACTCAGACTGATA | 104082 |
rs46976547 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63986042 | GCATGATGTGGCCCA[C/T]GTAGATGAAGATGCT | 104082 |
rs46986217 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63974405 | CTTTGCTAAAAGAAG[C/T]AAAATGTTTTGTTTG | 104082 |
rs46986521 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63857606 | TCAGTTTCCTAGTTC[A/G]ATGAAATGATAGTCA | 104082 |
rs46988761 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63738567 | TAGTTGACATGAATA[C/T]TAACACTATTGAATT | 104082 |
rs46991554 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63932290 | TTGTTCTTATGAAAT[C/T]AGGAAGTGTTTCTAT | 104082 |
rs46992043 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63888993 | CAGACTTCAACCTTG[A/G]TTAAAATGATAGCAG | 104082 |
rs46994784 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63762647 | CTTCCGTGACTTACC[C/T]TCAGGTTGTAGAAGG | 104082 |
rs46997696 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63760029 | GGTGCTTTCTTCCTG[C/T]CTATCGTGAAAGAGG | 104082 |
rs46998960 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63982024 | TGTTGACAGGTCTGG[C/T]TTTTCTCCAGAACGT | 104082 |
rs46999860 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63793273 | TAAAACACAGAACTG[A/G]TAAAATACTGTGTTC | 104082 |
rs47005652 | snp | A/C | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63950178 | TCTGATATTCATAAA[A/C]GGAATTGTAAGCTAC | 104082 |
rs47014874 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63782644 | TTAATTTTTCCAATT[C/T]ACTGTATTTGCTTCT | 104082 |
rs47015495 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63776623 | CAGGGCTCACAGATA[C/T]GGTTTAGGAGCCCGA | 104082 |
rs47015787 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63797010 | TTGCATTTTTGGGAA[A/C]TTTGTGAAAGTTACA | 104082 |
rs47016178 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63907632 | GTGAAGGTTAGACAC[A/C]AGATGGGTTTAAGCT | 104082 |
rs47023855 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63891272 | GATTCCCCCTCTACA[A/G]ATTTTGAAAGGAAGA | 104082 |
rs47028112 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63893873 | CGAGTGTAAATTGTC[A/G]TCTAGGAGTTTAGCC | 104082 |
rs47030854 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63781935 | GTTAGGGAAAGAGGA[C/T]TCTTGGGCTTTTCTA | 104082 |
rs47032824 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63961546 | AACAAGTGTTTTGAT[A/G]AAGAGTGCTGCATTT | 104082 |
rs47035472 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63984953 | GAAATCCATTGAGCT[C/T]ATAGGTCTTCATCTC | 104082 |
rs47037542 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63882003 | TGACTTTAAGCTGGA[C/T]CTCAAAAGACACATT | 104082 |
rs47059236 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63922763 | GCGAGGGATGGAGTC[C/T]CCAGGAAGCTGATGT | 104082 |
rs47062025 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63729342 | AGTTTGAAGGGCTTG[C/T]TTGAATGAACTAAAT | 104082 |
rs47062868 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63737974 | TGAAATGTATGTGTG[C/T]TATAGTGAGAGACAC | 104082 |
rs47066883 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63891927 | TTCCTTATTGTTTGC[C/T]GAGATGTTTTGTAAT | 104082 |
rs47068551 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63780814 | TCCCATTTCTCTGTC[C/T]CTTAGTAAAGTTATA | 104082 |
rs47069364 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63773522 | GCAAGTTGGAGACTC[A/G]ATCATTTGTCTATAC | 104082 |
rs47072793 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63932441 | AGAACTATTTCTAGA[C/T]CCTGTAGTTGAATAG | 104082 |
rs47076423 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63736180 | AACCTTGGCATAAAA[C/T]ATTTCATCTCATTTA | 104082 |
rs47077255 | snp | G/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63928647 | CAGACATCCCTGACT[G/T]TTGGCTGAGTTGCCC | 104082 |
rs47086652 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63777040 | CCACTCTCACAGGCT[C/G]ACTAAGCAGGACAGT | 104082 |
rs47086947 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63973241 | TCCTGAGAGTGCTTG[C/T]ACAGGGAGGCTTGAG | 104082 |
rs47089606 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63880391 | ACAAAGAAATTATTC[C/T]AGCCACATCCAGATA | 104082 |
rs47097187 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63761062 | TGCCAGAAGGATGTC[C/T]TACTAATGAGCTGCA | 104082 |
rs47099786 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63940659 | GAAACACATGGAGGC[C/T]TGAAGACAATTGTTT | 104082 |
rs47102101 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63720422 | TGCTGTACATTTGAA[A/G]CAATGACTGCTCCAC | 104082 |
rs47116410 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63859800 | TCAGGGGTTAAGCTT[G/T]GTTTGGCAGCGCCTG | 104082 |
rs47122676 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63775493 | TCACCCGAGATAGAC[G/T]GCTTTGCTCTGCTCC | 104082 |
rs47125732 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63869897 | GTTTGGAAATAGATG[C/T]CTAACTGCCTGGTAT | 104082 |
rs47127035 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63934236 | CCTGGGAGGAAAGGG[C/T]TTGCTTCAGCTTAGG | 104082 |
rs47130567 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63972114 | GATTACGCCAAGTCT[A/G]GAAGGAGGGCCAACC | 104082 |
rs47131763 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63802006 | TTTGAATTGTATCTT[C/T]AACTATAATTTTGTG | 104082 |
rs47133268 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63755445 | CAGTGGAGGGAGATG[A/T]GCAGATGAGGAAGAC | 104082 |
rs47148321 | snp | C/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63930903 | GCTGTGTTATAGTAG[C/G]CTCCTCTCTCCAGAA | 104082 |
rs47149378 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63736631 | TGATATGGTGAGTTA[C/T]AAGCACATTTCAAAA | 104082 |
rs47153574 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63855679 | AAAGGTAGGAAAGAC[A/C]CTGAGTTTTATACGT | 104082 |
rs47154181 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63932261 | CATGTGCAATAAAAT[A/G]TGACATTTACATTTT | 104082 |
rs47174855 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63985941 | AGTAACACATCTTAA[A/G]GGTCCGAAGATCCGC | 104082 |
rs47176014 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63899216 | GGGCACTCTGCCATC[C/T]CTGTTCTTTGATGCA | 104082 |
rs47176519 | snp | C/T | | | synonymous-codon | Wdr7 | Mm_Celera | 18:63924860 | TGACTCTGCCCGCTC[C/T]GCAAGGCACGCCCTG | 104082 |
rs47176881 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63881991 | AAGAACACTTAATGA[C/T]TTTAAGCTGGATCTC | 104082 |
rs47180611 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63939265 | AGTACATGCACACTC[A/G]CAGCCTTGCGCACAC | 104082 |
rs47185946 | snp | C/T | | | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63987890 | CCTTCTCGGTAACAT[C/T]AATTCTGATCTGAGG | 104082 |
rs47186906 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63717582 | TAATTTAGTGATGTA[C/T]GTAAGGCACATTGTC | 104082 |
rs47193074 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63759850 | GTCTTGAAATTGGAA[C/T]CAATCAATCAATCAA | 104082 |
rs47204829 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63939978 | CCCACACGTTTATGC[A/G]CACTTGCTTCCCACG | 104082 |
rs47211543 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63930863 | AAGCATATGCAGTCC[C/T]TTCTTTACCTCCCTA | 104082 |
rs47211949 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63976455 | TGTTGTTTTTCAGAC[C/T]TGGGTACTAATTTTG | 104082 |
rs47214450 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63753215 | AGGAGCTCTGCTTCA[G/T]GTGGCAGAAATACAG | 104082 |
rs47216664 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63861331 | GTCAGTCAAAAGGAA[A/G]GTGGTTTTGATTACT | 104082 |
rs47217583 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63844286 | TCAGTGAGTGTTTGG[C/T]GCCTTCGACATAAAT | 104082 |
rs47223895 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63793895 | CACATGTGTAGCTCT[C/T]GCGTGTGTTTATTCC | 104082 |
rs47229899 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63907678 | GGTTGTTACAGGAAG[C/T]TCCTTGCTGTACCAC | 104082 |
rs47232306 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63833673 | TGGTTGCTGCCTCTT[C/T]TCCTCCACTCTGTGC | 104082 |
rs47233714 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63881022 | CCTTCTCCCTCCAGG[A/T]GAGAACATTTTAATC | 104082 |
rs47239332 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63771226 | ATCATGAATTCTCAT[C/T]CCACCCAAGAATAGT | 104082 |
rs47251646 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63738639 | AAACGGGGGTATGAT[C/G]AAAGCATCTAAATAC | 104082 |
rs47258038 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63940273 | AGAGGGCATCAGATC[C/T]CATTACAGATGGTTG | 104082 |
rs47264041 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63769883 | ACACCCTCTTCTGGG[A/G]TGTCTGAAGACAGCT | 104082 |
rs47267221 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63788923 | AAGATGGAGTTTATA[A/G]TCAACCTTGAATGAG | 104082 |
rs47269354 | snp | A/G | | | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63987965 | AAAGTTTTCTAGATA[A/G]CTAGCTTTTTGAATG | 104082 |
rs47272288 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63923857 | ATGAATGTAATAAAA[A/T]ACTTTCTTTGCATAA | 104082 |
rs47275729 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63742997 | TAGTTCATGCAGTTT[G/T]GTGTTTTCCAGTCTT | 104082 |
rs47280786 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63908025 | AATGTCTGGAGTCCC[A/G]ATGTGTTAAGGAATG | 104082 |
rs47292635 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63865570 | GAATATCAGAGTATT[A/G]ACTGTATCCTGAGAC | 104082 |
rs47307046 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63803136 | ATTTTAAAAAATGTG[A/G]AATTTAAAGATAGCT | 104082 |
rs47308389 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63744449 | GCTGAGCCATCGCTT[A/C]AGCCCCAACTCTGCA | 104082 |
rs47318335 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63907780 | TATGTACACGGGGAT[C/T]CACCTCTTAGAGTTC | 104082 |
rs47324518 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63715686 | AACAGTAATGGCCAC[C/T]TCGTTGATGACATAA | 104082 |
rs47327851 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63776055 | AATTTTGTAAGATTT[C/T]TAGTGTTCTTTGTTC | 104082 |
rs47329760 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63861749 | AAAGAAAGTTTTTTC[A/T]AAAAAACAGCCTGTA | 104082 |
rs47330102 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63715283 | TTCTTGCCATCCACA[C/T]AGGAAAGGCTGGCGT | 104082 |
rs47330799 | snp | G/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63885307 | ATGGCTTGAGCATGC[G/T]CAGGTCTCGTGCATC | 104082 |
rs47335060 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63753731 | TTAAGCAAAGTTTGT[A/G]GTCTCTCTCTGCACT | 104082 |
rs47337810 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63762846 | TAAATTCCATTTACA[C/T]ACGTTATATGTATAT | 104082 |
rs47341285 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63877842 | TTTGCTAGTTTAAAA[A/T]TTTTCACAGGTAATT | 104082 |
rs47344440 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63879700 | CCAGTGCCCTGTCAC[A/G]GTGCCAACCCTCAAC | 104082 |
rs47353176 | snp | A/G | | | intron-variant, upstream-variant-2KB | Wdr7, LOC105246469 | Mm_Celera | 18:63709674 | GTTTTCTTGCTGCTG[A/G]CTTTAGTGCTTAGTC | 104082 |
rs47357321 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63715375 | TTAAGGAAGCAGCTA[A/C]GGACTCAATTTCTTC | 104082 |
rs47358898 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63716339 | TTTGAGTCCACAACA[A/G]GAAAGTACATTGCAT | 104082 |
rs47364360 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63947941 | CATAAGCCACTGAGC[A/G]TTTAGTTTCTTACCA | 104082 |
rs47365341 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63901026 | CCAGTGCTGGACTTC[G/T]GTCTGTTCAGCTTTT | 104082 |
rs47366369 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63940564 | ACAGCATGACTTTTG[G/T]GCACATAAATTCTCA | 104082 |
rs47369144 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63735796 | TATAACTCTAAAGTA[A/C]GAGCATTTATGAATT | 104082 |
rs47377360 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63982707 | AGTCCATTTATATAA[C/T]CAGCTGTTAGATAGC | 104082 |
rs47381490 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63905867 | GTAAGGTCCTCCTGT[C/T]CTTTGCTAGAGTACA | 104082 |
rs47384874 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63973297 | ACCTGAGCCTTGTGA[C/G]TGGCCATAGCCAGAT | 104082 |
rs47385293 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63773907 | TAGGCCTGAGAGTGA[C/T]GAGCTCAGCCATTTC | 104082 |
rs47385658 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63783672 | TGAGCCTCTCCTTTG[A/C]TGTATTTCTCATTGT | 104082 |
rs47394450 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63952681 | TTTGGGAGTGTTTTC[C/T]TCAAGTCGCCATGGT | 104082 |
rs47398640 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63788302 | TAGCTGGCACTTCAG[C/T]TAGATCTTAGGGAAA | 104082 |
rs47401482 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63770142 | GTGCCATCGCCTGTG[A/G]TGTCACGCGAGTGAC | 104082 |
rs47410273 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63962936 | ATAGTATTTTGTGGA[C/T]GTGAATATTACTTAA | 104082 |
rs47414371 | snp | G/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63740279 | AATGTGATTTCTCTA[G/T]GGTAAAGGAGGGCCT | 104082 |
rs47419185 | snp | C/T | | | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63989036 | CTCAGCGCAGGTTTA[C/T]TGTATGAACTTCAGA | 104082 |
rs47428450 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63930883 | TTACCTCCCTAGCCA[C/T]AGTTGCTGTGTTATA | 104082 |
rs47428583 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63770713 | GAGAGTAGTGTGTGT[A/G]TTACCTATCAGCCGC | 104082 |
rs47430634 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63753808 | AATAAAAGTACAGCT[A/C]ACTCCTGGTGGAGAG | 104082 |
rs47433639 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63898988 | GAGCCGTGAGGCCCC[A/G]TTCCCAGCTCTCAGC | 104082 |
rs47433663 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63937724 | CACTTTAAAGTGTAT[C/G]TTACATTGTACTGTA | 104082 |
rs47435652 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63715187 | CCCGCTGTTCTTCCC[A/G]CACACCCTTGTGAGC | 104082 |
rs47437961 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63851557 | TGCTGACCAGAAACA[C/T]AGGCCGGGTATGTGC | 104082 |
rs47442065 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63790223 | AAACAGAAATTAACA[C/T]TGTTTTCTAGAGAAT | 104082 |
rs47446211 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63739686 | AATTGTTTAGTAGTA[A/G]TTTTTATAGTAAAGT | 104082 |
rs47454418 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63904780 | CGAAGCCTGACTGAT[A/G]ATCTAAGTTCAATCC | 104082 |
rs47458097 | snp | A/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63928837 | AAGGAATGGTAGACT[A/T]GGTAACTCTGTACTC | 104082 |
rs47459028 | snp | A/G | 0.5 | 0 | intron-variant | Wdr7 | Mm_Celera | 18:63911015 | TCGAGGGAAATGCTC[A/G]GTAAGAGAGTCTGTG | 104082 |
rs47461557 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63738170 | TATTTGTTATGTTTT[C/G]AATTTCATACATGAG | 104082 |
rs47465436 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63714028 | GCAGAGTTCTCTATC[A/G]ACTTCAGTTACCTTT | 104082 |
rs47468742 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63715408 | TGAATTTTCTGGCCT[A/T]GCTGTCTCTTCATTG | 104082 |
rs47489451 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63777367 | TCTCATAATTGCATC[A/T]TTTACATGTTGCTGG | 104082 |
rs47493745 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63908097 | AACTCAGGAGAGCGG[A/G]CAGATCTACCAAGCT | 104082 |
rs47494022 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr7, LOC105246469 | Mm_Celera | 18:63708966 | CCCAGCTTTAGAGCT[C/T]AGCCTTGGAAGGCAG | 104082 |
rs47494459 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63953922 | GCGAACTATAATGGA[A/G]CTCCTATCTGCCTGT | 104082 |
rs47495176 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63746527 | TGATTCATGGGCAAA[A/G]AAGCTGGTCACTCAA | 104082 |
rs47498158 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63738938 | ACTCTAACATTTTGT[A/G]TTATAACAGAATTGA | 104082 |
rs47502062 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63775024 | TTGCTCACGTGGGTG[A/G]CATCTGCTGCCTCCC | 104082 |
rs47505980 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63891992 | CTTTAAAAAATTTTT[C/T]ACTCTAAAAGCTAAG | 104082 |
rs47508851 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63869880 | TTGAGTCTTGCTCTG[C/T]TGTTTGGAAATAGAT | 104082 |
rs47509664 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63947676 | GTCATCTCTATCTGG[C/T]TAGCCCCTTGTAGTT | 104082 |
rs47513367 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63743750 | CAGCAGGACACTTTT[C/T]ACCCCATCACAGTGC | 104082 |
rs47514071 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63723660 | GGGCACACTAATGGA[A/G]CCCCGGGCTCTCAGT | 104082 |
rs47514914 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63787961 | TTTCCATTATCTCTT[C/G]TGAACTAGGAAATAG | 104082 |
rs47516963 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63744954 | ATTGCAGCTCAGTCG[C/T]TTGACAGTGTTCGCG | 104082 |
rs47520077 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63713675 | TTATCTACACACATT[A/T]GGAAGTTGGGAGGAT | 104082 |
rs47520381 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63790875 | CCTCACCGCGTGCAA[A/C]GCAAATGTACTGTTC | 104082 |
rs47527058 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63959802 | AGGCACGAGGACCAT[A/C]GGGAGAGCAGGCACC | 104082 |
rs47543704 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63742922 | AGAGAATATATGAAA[A/G]TAAAGCACTGTCTAT | 104082 |
rs47545399 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63746023 | TTATAACTTTGGGAT[A/G]AAGATAAGAATAAGG | 104082 |
rs47549152 | snp | A/C | | | intron-variant | Wdr7 | Mm_Celera | 18:63865000 | AAATGAACACGTAAG[A/C]TTGTGCATGGTATTA | 104082 |
rs47550364 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63842659 | CATATCTGTTTTTCA[A/G]CTTTTAAAATGGCTG | 104082 |
rs47558421 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63832438 | TATAAACTGTTTGCC[C/T]AATTATCTCATTTCC | 104082 |
rs47561394 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63932828 | ACCTGAGAGTTTTCA[C/T]TGGGTGAAGATGAAA | 104082 |
rs47567512 | snp | C/T | | | utr-variant-3-prime | Wdr7 | Mm_Celera | 18:63988886 | TTTCACATGCATGTA[C/T]ATCGTACTTATAATG | 104082 |
rs47569352 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63959543 | CCATAAATGAAAAAA[C/G]TCTGACGTTTGGCCA | 104082 |
rs47572780 | snp | C/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63736627 | AAGCTGATATGGTGA[C/G]TTACAAGCACATTTC | 104082 |
rs47573617 | snp | A/G | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63928220 | GTTTAACTGTTGGAC[A/G]GTGCTGCCTAGATGG | 104082 |
rs47579545 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63719429 | GAAGTTTCTCACTAA[A/G]TATGTCCACTCAGTG | 104082 |
rs47583075 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63796960 | GTCTGAGGAGTCTTT[C/T]AGATGACTATGATTT | 104082 |
rs47584262 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63857813 | TTTTAGCCTATAACA[A/G]AAATAAATTGCTATT | 104082 |
rs47587518 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63739381 | TCTACCTATGTGCAC[C/T]GTGTTCTGAGAACTC | 104082 |
rs47594377 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63775871 | GGGCCAGCAGTGGTA[C/T]GTCCTGAACGATATC | 104082 |
rs47597661 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63895827 | GTGTTACAGTTCTAG[C/T]TCTGCTGGAACCTGA | 104082 |
rs47600157 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63944459 | TGGTGGAAATGGAGA[C/T]CAGAGAACCTCGGCT | 104082 |
rs47601991 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63896814 | TGCACCCTATTTACA[A/G]TCAGCAGGCAGATAG | 104082 |
rs47614651 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63737885 | CTGTCAAGTCGACAG[C/T]CGTTATTAGCCATCA | 104082 |
rs47615513 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63773010 | TTTTTCTGCTGAACA[A/G]TCTGGATTGTTACGT | 104082 |
rs47617640 | snp | A/G | | | intron-variant | Wdr7 | Mm_Celera | 18:63720400 | TAGAAGTGAGTATTG[A/G]AATGCTTGCTGTACA | 104082 |
rs47618636 | snp | C/T | | | intron-variant, upstream-variant-2KB | Wdr7, LOC105246469 | Mm_Celera | 18:63709002 | AAAGGTCAAGGGTCA[C/T]GAGCCCTCCCTAGCT | 104082 |
rs47621377 | snp | C/T | | | intron-variant | Wdr7 | GRCm38.p3 | 18:63736394 | GCGAACGCTTACTTT[C/T]CTGTTCCAGTTGCCT | 104082 |
rs47622773 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63962469 | TACCTTGTGTCCCTC[C/T]GTATCCTCTGTGGAG | 104082 |
rs47638223 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63759678 | AAAGTGGGGACAAAA[C/T]TTATGCTGGAAGAAG | 104082 |
rs47643657 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | Wdr7 | Mm_Celera | 18:63987541 | CATGGGCAGCCTGTC[G/T]ATTGAAAGGCACACA | 104082 |
rs47644770 | snp | C/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63859081 | CCCAGCAACTCCAGT[C/T]CCCTCCACAAAAGCC | 104082 |
rs47649923 | snp | A/T | | | intron-variant | Wdr7 | Mm_Celera | 18:63986107 | GTGAAGGAAGGAGAT[A/T]ATTTCCAGGGCTTCT | 104082 |