SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6191941 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108603137 | CCATTGTTCTAAGTC[A/T]CGGGGCATCTCTCTA | 99512 |
rs6389549 | snp | A/G | 0.5 | 0 | intron-variant | Wdr47 | Mm_Celera | 3:108632920 | ACATTATAGTTAATT[A/G]GACTTGTCACTTAAA | 99512 |
rs6389608 | snp | C/T | 0.5 | 0 | intron-variant | Wdr47 | Mm_Celera | 3:108632963 | GCTACTATGAAATTA[C/T]CAAACAGGTATAATA | 99512 |
rs6390075 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr47 | Mm_Celera | 3:108632999 | ATTGATTTAAAGTGG[A/G]ATAAAGGTAACTCAA | 99512 |
rs6403267 | snp | A/G | 0.456747 | 0.140554 | synonymous-codon | Wdr47 | Mm_Celera | 3:108633072 | ATAGGATGACAAGTC[A/G]AAAAAGCAGTTTGTT | 99512 |
rs6403382 | snp | A/G/T | 0.456747 | 0.140554 | synonymous-codon | Wdr47 | GRCm38.p3 | 3:108633132 | TGTTAGAGCCGTGGC[A/G/T]TTTCATCCAAGTGGT | 99512 |
rs29638716 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr47 | Mm_Celera | 3:108602744 | GTGGGCTTTCTTGTA[C/T]TGTTTATCATGCCAC | 99512 |
rs29638719 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Wdr47 | Mm_Celera | 3:108602800 | GCTTCCGGGCAGTTC[A/G]GAGACCATGACACTT | 99512 |
rs29638722 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr47 | Mm_Celera | 3:108602828 | CTTTACCCATCTTGA[C/T]GGCGCCACAGGCACA | 99512 |
rs29639527 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr47 | Mm_Celera | 3:108603310 | ATGGGAATACTGACA[C/T]TGACACTACCCTATT | 99512 |
rs29639530 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wdr47 | Mm_Celera | 3:108605071 | CCTGTAAAGTATTTA[C/T]GTTGTACTACCTAAG | 99512 |
rs29639533 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr47 | Mm_Celera | 3:108606745 | TCTGCCAGCACCTGA[C/T]TCCGCAGGTACAGCA | 99512 |
rs29639645 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr47 | GRCm38.p3 | 3:108614852 | ATATTCTCCTTTAAG[A/G]TAAGTTAAACCAGGG | 99512 |
rs29639648 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr47 | Mm_Celera | 3:108615227 | GGAGTCCAGTTTGTC[C/T]TTATAGGCTGTCCTC | 99512 |
rs29639651 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Wdr47 | GRCm38.p3 | 3:108615238 | TGTCCTTATAGGCTG[C/G/T]CCTCCTTAGTTACTA | 99512 |
rs29640134 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Wdr47 | GRCm38.p3 | 3:108626550 | TCCTGCCTTAGCACC[C/G]CTCACGATGGATTAC | 99512 |
rs29640137 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr47 | Mm_Celera | 3:108626667 | TCAGGCTATGCAGAT[A/G]GAAGGATTGTTTAGA | 99512 |
rs29640140 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr47 | Mm_Celera | 3:108626759 | AATGATAGTTAAAGG[A/G]TGAGTGAATGAATAC | 99512 |
rs29640143 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr47 | Mm_Celera | 3:108626778 | GTGAATGAATACAGA[C/G]CTGAGTAATAGGCTA | 99512 |
rs29640216 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr47 | Mm_Celera | 3:108631627 | TGATTTTTGAGTTCT[C/T]AGGCTGTGTCCAGAG | 99512 |
rs29640219 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr47 | Mm_Celera | 3:108631722 | GCTGTCAGCCATGCT[A/G]TCTGTAGACCCCTGT | 99512 |
rs29640222 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr47 | Mm_Celera | 3:108631766 | CCTGCTCAAGTTAGC[A/G]GTGCTGTTTTAAAGG | 99512 |
rs29640236 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Wdr47 | Mm_Celera | 3:108645886 | CAGAGCACTTCTGTC[C/T]TCTCCATTCTTGCAC | 99512 |
rs29640239 | snp | A/C/G/T | 0.336735 | 0.234472 | downstream-variant-500B | Wdr47 | Mm_Celera | 3:108645905 | CCATTCTTGCACTCG[A/C/G/T]TAAGCAAGCAGTGTA | 99512 |
rs29640456 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr47 | Mm_Celera | 3:108607392 | ACCTCTTTATAGTCA[C/T]GTTAACCATCAGGTA | 99512 |
rs29640459 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr47 | Mm_Celera | 3:108607866 | TCAAGGATTAACTCA[C/T]CACCTGGGCTTGAGA | 99512 |
rs29640462 | snp | A/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108608038 | ACCATGGGAACCTAC[A/G]ACAAGCCTTCATTTT | 99512 |
rs29640554 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr47 | Mm_Celera | 3:108616835 | CTTCAGGGTAAAAGT[A/C]CGTGGAGGATGGCAG | 99512 |
rs29640557 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr47 | Mm_Celera | 3:108617159 | CTTTGAATTGAAATT[C/T]TTGAAGCAGAGTTGA | 99512 |
rs29640560 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Wdr47 | Mm_Celera | 3:108617531 | TATTTTTTTCCCATG[A/G]TGAAGAAATTTTTAC | 99512 |
rs29640563 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108617644 | ATTCAGTTTGTATTT[C/T]CAGTTAGGCCCATAT | 99512 |
rs29640614 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr47 | Mm_Celera | 3:108641881 | TTGCTTAGATTAATC[A/G]TGTATCATTCAGTTC | 99512 |
rs29640617 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108641976 | TTAGCGGTCTGGCCC[C/T]AGCCTGCCTGTCATG | 99512 |
rs29640620 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr47 | Mm_Celera | 3:108641986 | GGCCCTAGCCTGCCT[G/T]TCATGTCTCAGCTCC | 99512 |
rs29640623 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr47 | Mm_Celera | 3:108642107 | TATTTTCTTTTTTTT[C/T]TCCCAAAGTTTCAAG | 99512 |
rs29640685 | snp | A/T | 0.391111 | 0.206368 | synonymous-codon | Wdr47 | Mm_Celera | 3:108637147 | CTTCAATGCAGAGAC[A/T]TGTAATGCAACAGGT | 99512 |
rs29640688 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108637213 | GCATGTACGCTTGTC[C/T]CTCTGTCTCTCTGTC | 99512 |
rs29640691 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Wdr47 | Mm_Celera | 3:108637454 | CAGACATGAAAGAGA[C/G]AGACAGAGACTAAGA | 99512 |
rs29640855 | snp | A/C | 0.32 | 0.24 | intron-variant | Wdr47 | Mm_Celera | 3:108631777 | TAGCAGTGCTGTTTT[A/C]AAGGACATTGAGCAA | 99512 |
rs29640858 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr47 | Mm_Celera | 3:108631815 | GTGAGTCTTTGTATA[A/G]AATTGCTTCAACTCA | 99512 |
rs29640861 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr47 | Mm_Celera | 3:108631990 | TGATTTTAATTGTAA[G/T]TGTATCAAATTAATA | 99512 |
rs29640906 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Wdr47 | Mm_Celera | 3:108627236 | CGAATTAAATATTGG[A/G]ATGGATAGTCTTGGT | 99512 |
rs29640909 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr47 | Mm_Celera | 3:108627545 | TTGCTTTGGAGCCTT[A/C]CGGAATTGAGGGCTG | 99512 |
rs29640912 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr47 | Mm_Celera | 3:108627813 | TATAGGAAGACAATT[C/T]TGGCAACCGTGAAGA | 99512 |
rs29641215 | snp | C/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108609355 | CTATAATTGATATTA[C/T]CACTATGACACTGAT | 99512 |
rs29641218 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108610408 | ACTACATAGAAACAA[C/T]TGTGATTCTTACATT | 99512 |
rs29641221 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108610858 | GTAATTTTGTTTCAC[A/G]GGAATTCTCTGTGGT | 99512 |
rs29641456 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108617848 | CACAGGTTGTCATGC[A/T]GTCTGGGTATCTGAC | 99512 |
rs29641459 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr47 | Mm_Celera | 3:108617926 | TCTGCTCTTTCTACT[A/G]TTTTTGTAGTGTTTT | 99512 |
rs29641462 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Wdr47 | Mm_Celera | 3:108618062 | GCTAAACTAAATAAT[C/G]AAGTTTTTAAAACAA | 99512 |
rs29641564 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108637543 | CCTTTTTTGTTTGAA[A/G]TAAAAGACAGGGAAG | 99512 |
rs29641567 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108637642 | TGAAGTTTTATGTTC[A/C]GTAAATGAATTGATT | 99512 |
rs29641570 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108637731 | CATAGCCTAGCACAT[A/G]AGATAATGGGTTTCA | 99512 |
rs29641573 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108638087 | TACTCAGTCTTCCTT[C/T]TCTCAGTCTGTGCTG | 99512 |
rs29641586 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Wdr47 | GRCm38.p3 | 3:108642196 | ATTTATGCTGTTTAC[A/C/T]GTTTTTCAAGTTTTA | 99512 |
rs29641589 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr47 | Mm_Celera | 3:108642218 | CAAGTTTTAATTTAT[A/G]TCCTTTTATTTCTGT | 99512 |
rs29641592 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr47 | Mm_Celera | 3:108642648 | GTTAGGGCTATATCC[G/T]TCAGATTCAGAACTT | 99512 |
rs29641630 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108589327 | ACAACTTTTAAACTA[C/T]GACTTATCTTTTTGG | 99512 |
rs29641633 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108589330 | ACTTTTAAACTACGA[C/T]TTATCTTTTTGGGTT | 99512 |
rs29641634 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr47 | Mm_Celera | 3:108632031 | ATATTTCTTCTTCTT[C/T]TTTTCTTCCCGAGAG | 99512 |
rs29641637 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr47 | Mm_Celera | 3:108632039 | TCTTCTTCTTTTCTT[C/T]CCGAGAGAGCAGTCT | 99512 |
rs29641640 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr47 | Mm_Celera | 3:108632112 | TTCAACTAGCAGCCC[A/G]TGAATTTCCTATTAA | 99512 |
rs29641815 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr47 | Mm_Celera | 3:108627827 | TCTGGCAACCGTGAA[A/G]AGCATTATAGCAGCT | 99512 |
rs29641818 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr47 | Mm_Celera | 3:108628195 | AATACCCTGACCTCT[A/G]TATGCACAGCATTGC | 99512 |
rs29641821 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr47 | Mm_Celera | 3:108628265 | ACAAAACTCTCTCAG[C/T]ATTTTAAAAAGCATC | 99512 |
rs29642144 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108611194 | GATCCTTCTGCCCAT[C/T]CATCCATTTTATAAA | 99512 |
rs29642147 | snp | C/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108611259 | GTTATTGTAAAAGAA[C/T]ACTACTACTGTTTGA | 99512 |
rs29642150 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108611327 | TCTATTTTTGAATTG[A/G]TGAGCATTCTAGATT | 99512 |
rs29642153 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr47 | Mm_Celera | 3:108611453 | AGGTAGGATTTTATT[C/T]TAAAGTCTTAGTGTT | 99512 |
rs29642275 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr47 | Mm_Celera | 3:108642853 | ACTCACAGGACAGAC[A/G]TGTTTCATTTCTTCC | 99512 |
rs29642278 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108642914 | GATACAGTGGTTATT[A/G]GTTAATTTTGATTTT | 99512 |
rs29642281 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr47 | Mm_Celera | 3:108642980 | ATACCAGATCATTAG[C/T]GTGTGGTTCAGTGAA | 99512 |
rs29642345 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wdr47 | Mm_Celera | 3:108618078 | AAGTTTTTAAAACAA[A/G]CTATTGTCATCCTTC | 99512 |
rs29642348 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Wdr47 | Mm_Celera | 3:108618178 | GTTCCAGAGCAGCCC[A/G]GGCCACAGAGAGACC | 99512 |
rs29642351 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr47 | Mm_Celera | 3:108618446 | TTTCATTTTAAGGTG[A/G]TCATTTGCCTTGCAC | 99512 |
rs29642406 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr47 | Mm_Celera | 3:108638128 | TATCAGTGAGATCTC[C/G]TTGTAATGGATCTTT | 99512 |
rs29642409 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr47 | Mm_Celera | 3:108638220 | ATAGCACTACGATCC[A/G]TTTAGTCATCACGGG | 99512 |
rs29642412 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr47 | Mm_Celera | 3:108638452 | CCAAAGAAGGACTGA[A/C]TTTGTTCAGAGTGGT | 99512 |
rs29642486 | snp | C/T | 0.297521 | 0.245442 | upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108589797 | CTTTAAAGTATTGTA[C/T]TTATTTATTGGATAT | 99512 |
rs29642489 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108589838 | TACACAATGCTGTGA[C/T]TCACCTGGCCATTTA | 99512 |
rs29642492 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB | Wdr47 | Mm_Celera | 3:108589861 | GCCATTTATCTTGAA[C/T]TGGATTTTTTGTCTG | 99512 |
rs29642599 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr47 | Mm_Celera | 3:108633304 | TTTACTAATGTTCAC[C/T]TCTTCCTTTCCTTCT | 99512 |
rs29642602 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Wdr47 | Mm_Celera | 3:108633378 | GTAATTTATTCATTT[C/T]CCTATAAAATATTTC | 99512 |
rs29642644 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr47 | Mm_Celera | 3:108628287 | AAAAGCATCCAGTGA[A/G]TTGTTGTCTTCTTTC | 99512 |
rs29642647 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wdr47 | Mm_Celera | 3:108628314 | TTTCTCTCTGGGACA[C/T]GACTGGCGCCAGCAT | 99512 |
rs29642650 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr47 | Mm_Celera | 3:108628320 | TCTGGGACATGACTG[A/G]CGCCAGCATCGTTCT | 99512 |
rs29642653 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr47 | Mm_Celera | 3:108628661 | AAAGAAAAGGGATAT[A/G]TGTCAGAAGTAGTTT | 99512 |
rs29643106 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr47 | Mm_Celera | 3:108611591 | GTTACAGTTACAGTT[C/T]TTGGAAGTCTTTGTA | 99512 |
rs29643109 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108611605 | TCTTGGAAGTCTTTG[C/T]AAGTTCCATGAGCAG | 99512 |
rs29643112 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr47 | Mm_Celera | 3:108611674 | ATGAAGTAGTGAGGC[A/G]CATACTTCAGAGACA | 99512 |
rs29643204 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108643005 | AGTGAACTTGAGGAG[C/T]TACATTGTGGCATAA | 99512 |
rs29643207 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr47 | Mm_Celera | 3:108643032 | ATAAGTATTAATTTT[C/G]TGTGTTGCAACATTC | 99512 |
rs29643210 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr47 | Mm_Celera | 3:108643342 | TAGATTTTTTTTCTA[A/G]TATGATATGATTGAC | 99512 |
rs29643213 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdr47 | Mm_Celera | 3:108643401 | TTATTGCGAAGACTA[C/T]ATTAAGATTTCTTGT | 99512 |
rs29643355 | snp | A/T | 0.32 | 0.24 | intron-variant | Wdr47 | Mm_Celera | 3:108638480 | GGTTTTGATGAATTT[A/T]AAAAATCCTTAAATC | 99512 |
rs29643358 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr47 | Mm_Celera | 3:108638552 | GTTAGCTGGTGATGA[A/G]AAGAACTTGCTTTTA | 99512 |
rs29643361 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Wdr47 | Mm_Celera | 3:108638609 | ATCAGTGACTTCGTG[C/G]TTCTGGTCTTTTGTA | 99512 |
rs29643364 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Wdr47 | Mm_Celera | 3:108618660 | AGTTCACTGCTTTGA[A/G]GAGGTCTGTGTCATG | 99512 |
rs29643367 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Wdr47 | Mm_Celera | 3:108619385 | GTTCAGTACTTTGTA[A/G]TTTTAAGAATTTAAG | 99512 |
rs29643370 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr47 | Mm_Celera | 3:108619708 | ATAGGGAAAATGTAG[C/T]GTTTGTCTTTCTGAG | 99512 |