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 |