SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6270601 | snp | C/T | 0.5 | 0 | intron-variant | Wdr45b | Mm_Celera | 11:121344964 | CTTAAGGTATGAAGA[C/T]ATTAAGGCCCAAGGT | 66840 |
rs6271137 | snp | A/T | 0.5 | 0 | intron-variant | Wdr45b | Mm_Celera | 11:121345066 | CCTCTCTTCCACGTA[A/T]GTCCAGNCCCTAGCA | 66840 |
rs6271141 | snp | C/T | 0.5 | 0 | intron-variant | Wdr45b | Mm_Celera | 11:121345073 | TCCACGTANGTCCAG[C/T]CCCTAGCATCCAAAG | 66840 |
rs6271679 | snp | C/G | 0.5 | 0 | intron-variant | Wdr45b | Mm_Celera | 11:121345155 | GTGACAGCAGCATGC[C/G]TCTGACTGCTTTAGC | 66840 |
rs6272747 | snp | A/T | 0.5 | 0 | intron-variant | Wdr45b | Mm_Celera | 11:121345328 | actcactttgtagac[A/T]aggtttggccagaga | 66840 |
rs6272784 | snp | A/G | 0.5 | 0 | intron-variant | Wdr45b | Mm_Celera | 11:121345351 | gccagagatctgcct[A/G]cctctgcctctaacc | 66840 |
rs27000789 | snp | A/C | 0.244898 | 0.249948 | upstream-variant-2KB | Wdr45b | Mm_Celera | 11:121354848 | TTCCCAACCATCTGA[A/C]ACGTCCTCTCACAGA | 66840 |
rs27000790 | snp | C/T | 0.35503 | 0.226867 | upstream-variant-2KB | Wdr45b | Mm_Celera | 11:121354762 | GACCAGAAGCAGCCT[C/T]CGTGTAATGGTACCT | 66840 |
rs27000791 | snp | G/T | 0.165289 | 0.235211 | upstream-variant-2KB | Wdr45b | Mm_Celera | 11:121354541 | CGGGAAGTAGGTGGC[G/T]AGGGCTCGCCGGGCG | 66840 |
rs27000792 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Wdr45b | Mm_Celera | 11:121353433 | GAGTATCAGCCTTTA[C/G]CCTTTTCCCTTGAGG | 66840 |
rs27000793 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121351731 | GACTCAACTGTTTGA[A/T]GCGAGTTCATACTAT | 66840 |
rs27000794 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121350730 | CAGCTAATTGTGACA[C/T]ATCCTGACAAAGAAA | 66840 |
rs27000795 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121350303 | AAACGTAATTTATCC[A/G]GCCCAGAATCTGAAA | 66840 |
rs27000796 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121350104 | TCAATGTTTACAAAG[C/T]TTGGTTCCTTACAGC | 66840 |
rs27000797 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Wdr45b | Mm_Celera | 11:121349760 | TCTGCCGCTCTGCTC[C/T]ACATCTATGCCCAGA | 66840 |
rs27000798 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121349549 | GCACAGTCCTGGTCA[G/T]TGTGGACACAGCTTA | 66840 |
rs27000799 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr45b | Mm_Celera | 11:121349526 | ATGTATAGAGGCTCA[A/C]AATAAACGCACAGTC | 66840 |
rs27000800 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121346016 | GTACCAGTGCACAAC[G/T]CCCACATCACTATTC | 66840 |
rs27000801 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121345985 | ACAACACGGGGCTCA[G/T]ATAGAGGATGGTACT | 66840 |
rs27000802 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr45b | Mm_Celera | 11:121343644 | GCACAACACCTGAGC[A/G]CTTAAAGAAAGTGTG | 66840 |
rs27000803 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Wdr45b | Mm_Celera | 11:121343607 | GGACTCAGAGACAGC[G/T]CCCCAGACTGCAGCC | 66840 |
rs27000804 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr45b | Mm_Celera | 11:121343422 | TTCAGTCTCTGTTCC[A/G]ATGGAAGAGAAGTTT | 66840 |
rs27000805 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdr45b | Mm_Celera | 11:121343338 | TCCTCAATGCTGGTT[C/T]AACCAGTTTTAGAAA | 66840 |
rs27000806 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr45b | Mm_Celera | 11:121342942 | TACAGGAAGCCTCTA[C/T]GGAAGTCAAGTTAGA | 66840 |
rs27000807 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdr45b | Mm_Celera | 11:121342914 | ACGCTAGTACTCCAA[C/T]TGCAGGAGTGCCTAC | 66840 |
rs27000808 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr45b | Mm_Celera | 11:121341021 | TCAAAGGACTAGTAG[A/G]GAGGCTCTGCATGAC | 66840 |
rs27000809 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121340360 | GCTTTTACATCAGGC[C/T]TGAGCTATTCCACTT | 66840 |
rs27000810 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Wdr45b | Mm_Celera | 11:121338717 | ATAGCACTACCACCT[G/T]ATTGATGAGGCCAAG | 66840 |
rs27000811 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr45b | Mm_Celera | 11:121338676 | GTGCACGTGGTGTCA[C/T]AAGTGGCCCACAGAC | 66840 |
rs27000812 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121338296 | GTTCTCCTCTCCTTT[C/T]AGCATGGGAACACCC | 66840 |
rs27000813 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Wdr45b | Mm_Celera | 11:121338104 | TAAGCACCACCCTAA[G/T]GAACCTACTCTACAG | 66840 |
rs27000814 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr45b | Mm_Celera | 11:121336894 | AGAGCCAGAGCTGCT[C/T]ACAAAGGACACGCTG | 66840 |
rs27000815 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr45b | Mm_Celera | 11:121336892 | ACAGAGCCAGAGCTG[C/T]TCACAAAGGACACGC | 66840 |
rs27000816 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr45b | Mm_Celera | 11:121336813 | CTGTGGCAAGGTGGT[A/G]GCTTCCCAACTCTCA | 66840 |
rs27000817 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr45b | Mm_Celera | 11:121336756 | GGCTAGTGATGCTCG[A/C]GACTGCTGGGGAGGA | 66840 |
rs27000818 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr45b | Mm_Celera | 11:121336582 | AATACAGGGAACAAC[C/G]AGTGCGGTGAGCAAT | 66840 |
rs27000819 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121336445 | ACTAGTGTGCCAGCT[A/C]CTCTGGAGTAGCTAC | 66840 |
rs27000820 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr45b | Mm_Celera | 11:121336198 | CTGGAAAATGGAAAG[A/G]CCAAAAGACTTTTGA | 66840 |
rs27000821 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Wdr45b | Mm_Celera | 11:121335691 | AACCACTCGTGGAGC[A/G]AATTTACCTTCGAAT | 66840 |
rs27000822 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Wdr45b | Mm_Celera | 11:121335656 | ATGTCCTTCCTGCCC[G/T]CAATCCTCAGTCACA | 66840 |
rs27000823 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr45b | Mm_Celera | 11:121335373 | GACTCACATAGATGG[C/T]CTGAACTTACTTTTT | 66840 |
rs27000824 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr45b | Mm_Celera | 11:121335251 | ACTATACCTAGGTTA[G/T]CGTTCGTTCTATCTT | 66840 |
rs27000825 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121335154 | GAAAGATACTTCTGA[A/C]GTGTCATCAGACAAC | 66840 |
rs27000826 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Wdr45b | Mm_Celera | 11:121334717 | AGACAAAATGAGGAT[A/G]ACATAGTTATAGGGG | 66840 |
rs27000827 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121334253 | CACAGGCTCTCCAGC[A/G]CCTGAGCTGCACTTG | 66840 |
rs27000828 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121334208 | GGTTCTAGGAGGCCG[A/C]GAAGCGCAGAACTTC | 66840 |
rs27000829 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr45b | Mm_Celera | 11:121331946 | AGACTCGGTCAACAT[A/G]GTTCAAGTGTGGGAC | 66840 |
rs27000830 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdr45b | Mm_Celera | 11:121331916 | GCACACACTGATCCC[C/T]GTCTCTTGATAAAAA | 66840 |
rs27000831 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr45b | Mm_Celera | 11:121331827 | GTAAGACTCTCAAAA[C/T]CAAACAACATGCTCC | 66840 |
rs27000832 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121331794 | AGACAAGTTCATGGC[A/G]TGCCAGGGTTATACT | 66840 |
rs27000833 | snp | G/T | 0.124444 | 0.216185 | intron-variant, missense | Wdr45b | Mm_Celera | 11:121331091 | GACACCGACATGGCT[G/T]TAAGGACCAAGTAAA | 66840 |
rs27000834 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant, missense | Wdr45b | Mm_Celera | 11:121331053 | TTCACTTGATGCACC[C/G/T]GGCCACCACACTGCT | 66840 |
rs27000835 | snp | C/T | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime | Wdr45b | Mm_Celera | 11:121330684 | TTTGCTGGAGCAATG[C/T]TATCTCAGACAAGAA | 66840 |
rs27000836 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-3-prime | Wdr45b | Mm_Celera | 11:121330306 | AAATGATTTATATTA[C/T]AACCCACTGGCCCCA | 66840 |
rs27000837 | snp | C/T | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Wdr45b | Mm_Celera | 11:121329976 | AGAATGTGGCAAACA[C/T]ATCCATGCTGCAACA | 66840 |
rs27000838 | snp | A/C | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Wdr45b | Mm_Celera | 11:121329880 | CTTGAAACCAACAGT[A/C]TACAATAATTACAGA | 66840 |
rs27000839 | snp | A/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Wdr45b | Mm_Celera | 11:121329784 | CCAAATTTGGCTCAA[A/T]ACCCACAGGCCTGGG | 66840 |
rs27000840 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr45b | Mm_Celera | 11:121329601 | TCTGTTCACCAGGAC[C/T]CCATAGGCACAATGG | 66840 |
rs27000841 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr45b | Mm_Celera | 11:121329568 | AGCCAGGATCCAAGC[C/T]AAAAGTCCAGGCAAC | 66840 |
rs27000842 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr45b | Mm_Celera | 11:121329534 | TCCCTGGTCTCACGA[C/T]TTTAAGCATCTGTTG | 66840 |
rs27000843 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr45b | Mm_Celera | 11:121329531 | TCATCCCTGGTCTCA[C/T]GACTTTAAGCATCTG | 66840 |
rs27000844 | snp | C/T | 0.455 | 0.143091 | intron-variant | Wdr45b | Mm_Celera | 11:121329489 | CATCTAACTCTCTTG[C/T]CCTCAACATACACAA | 66840 |
rs27000845 | snp | A/G | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Wdr45b | Mm_Celera | 11:121329292 | TAACCCTGATTTGGG[A/G]CTGTCCCCTGCTTAC | 66840 |
rs27000846 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Wdr45b | Mm_Celera | 11:121328978 | ACACAGAAGTCAATG[A/G]CTTAATTCCAGAGTG | 66840 |
rs27000847 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr45b | Mm_Celera | 11:121328746 | ATCTGGGAAGTTGGT[A/G]CAGCCTGGACCACAT | 66840 |
rs27000848 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wdr45b | Mm_Celera | 11:121328714 | GACCCAGCCCAGTTA[A/C]AGAAGGAAGAAAGGG | 66840 |
rs27000849 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr45b | Mm_Celera | 11:121328639 | CTGCTCTCAAAGCAT[C/T]CCTGGGAACCTGGCA | 66840 |
rs27000850 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr45b | Mm_Celera | 11:121328556 | GCCACACCAAGCCAA[A/G]GCTCATGCTTATCCA | 66840 |
rs27000851 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Wdr45b | GRCm38.p3 | 11:121328018 | CATCCTACAAGCTTC[C/T]GCTGATTCGTGCTTG | 66840 |
rs27000852 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Wdr45b | Mm_Celera | 11:121327994 | CTAGTATTTAAGCCC[C/T]GACACACTCATCCTA | 66840 |
rs27000853 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Wdr45b | GRCm38.p3 | 11:121327919 | TCTGAACAGTGCTCC[C/T]CATGTGAGGCAGGGG | 66840 |
rs27000854 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Wdr45b | GRCm38.p3 | 11:121327868 | CTGGGATGTGACTCA[C/T]TCTAATGGCCAAAGT | 66840 |
rs27000855 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Wdr45b | Mm_Celera | 11:121327132 | GGTCAACAGCCTACA[A/G]GTCTGTCCTGCAGCA | 66840 |
rs27000856 | snp | C/G | 0.32 | 0.24 | downstream-variant-500B | Wdr45b | Mm_Celera | 11:121326969 | CACACAGCACTGGCA[C/G]GGCACAGGGCAGAGA | 66840 |
rs27000857 | snp | C/G | 0.244898 | 0.249948 | downstream-variant-500B | Wdr45b | Mm_Celera | 11:121326813 | TTAGGGTACCTTCAG[C/G]AACACAAGCTAGAAA | 66840 |
rs27000858 | snp | G/T | 0.142012 | 0.225474 | downstream-variant-500B | Wdr45b | Mm_Celera | 11:121326802 | TATGGATTCTCTTAG[G/T]GTACCTTCAGGAACA | 66840 |
rs29396486 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr45b | GRCm38.p3 | 11:121353474 | AAGGGAAGTTAGCTG[A/G]CATAGTGGCACACTC | 66840 |
rs29404294 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr45b | Mm_Celera | 11:121335801 | CAATTTACTACCCAA[A/C]TTATTTATCAAGTGC | 66840 |
rs29411538 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Wdr45b | Mm_Celera | 11:121333423 | TTATGTCCCACGTTT[G/T]TTTGTTTGTTTGTTT | 66840 |
rs29414204 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr45b | Mm_Celera | 11:121345402 | CATGTGCCACCACAC[C/T]TGGCAAGAATTGTGT | 66840 |
rs29425771 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wdr45b | Mm_Celera | 11:121329569 | GCCAGGATCCAAGCC[A/T]AAAGTCCAGGCAACA | 66840 |
rs29426953 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr45b | Mm_Celera | 11:121333349 | TCTACACATCAGACT[A/G]GTCAAGAATTGATCC | 66840 |
rs29431910 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr45b | Mm_Celera | 11:121344890 | CATTCCCAGCTAAGC[A/T]TTCAGCCCTTGCCTC | 66840 |
rs29448942 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr45b | Mm_Celera | 11:121347879 | TACATATCCTCACCT[A/G]GCCTGCAATTCACTA | 66840 |
rs29450886 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr45b | Mm_Celera | 11:121347182 | CAGGAGTTGGCAGCT[A/G]CACAGCTCAGTTTGG | 66840 |
rs29459392 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdr45b | Mm_Celera | 11:121333835 | TCTATCTGCCTCTGC[A/C]GCTAAGTGGTGGGAC | 66840 |
rs29469567 | snp | G/T | 0.48 | 0.0979796 | upstream-variant-2KB, downstream-variant-500B | Wdr45b, Rab40b | Mm_Celera | 11:121355698 | TTGTTTTGGTTTTTG[G/T]TTTTTGTTTTTTTGT | 66840 |
rs29471834 | snp | G/T | 0.48 | 0.0979796 | upstream-variant-2KB, downstream-variant-500B | Wdr45b, Rab40b | Mm_Celera | 11:121355691 | GGTGGCTTTGTTTTG[G/T]TTTTTGGTTTTTGTT | 66840 |
rs29477654 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr45b | Mm_Celera | 11:121346758 | CTGTGCCTGGGGTAC[A/G]TAAGCCTTTCCTCCC | 66840 |
rs29478821 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr45b | Mm_Celera | 11:121332427 | TACTGTGTTTTGCTC[A/G]CATGTCTGTCTGTAC | 66840 |
rs29479421 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr45b | Mm_Celera | 11:121348950 | AAATAAATAAATCTT[A/T]AAAAAAAAAAAAAAA | 66840 |
rs29480024 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr45b | Mm_Celera | 11:121334836 | AGGAGACAGAATCTT[C/G]CTTGAGGAAGTACTA | 66840 |
rs29487243 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr45b | Mm_Celera | 11:121337266 | CAGCTACCTTTAGCC[C/T]CAAACTTGCAATGAA | 66840 |
rs45808656 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | Wdr45b, Rab40b | Mm_Celera | 11:121355968 | GACATACAGCACTAC[G/T]TGTTTTCTCTGCATT | 66840 |
rs47173890 | snp | C/T | | | intron-variant | Wdr45b | Mm_Celera | 11:121333234 | TTGAAAATGGAGAAT[C/T]TAAGGAAAAAAAGGA | 66840 |
rs47580062 | snp | A/G | | | intron-variant | Wdr45b | Mm_Celera | 11:121339860 | GGAAAGGCAAGGCTC[A/G]GCCAGTAACTGCCAC | 66840 |
rs48928420 | snp | G/T | | | intron-variant | Wdr45b | Mm_Celera | 11:121342682 | CAAGCAAGAAAAACC[G/T]AATCCATCAATCCTG | 66840 |
rs51324251 | snp | A/C | | | intron-variant | Wdr45b | Mm_Celera | 11:121333006 | GACCTCAAAGCCTGC[A/C]TACACAATGACACTC | 66840 |
rs212034720 | snp | A/G | | | intron-variant | Wdr45b | Mm_Celera | 11:121345543 | CGAACTCAGAAATCC[A/G]CCTGCCTCTGCCTCC | 66840 |
rs212068776 | in-del | -/T | | | intron-variant | Wdr45b | Mm_Celera | 11:121344933 | TCTCTACTGCCTTCC[-/T]TAAAACACTGGTGAG | 66840 |