SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6157807 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73553419 | GGCTTGTCCCATGCA[C/T]GGGGTCACCCCATTC | 105841 |
rs6158472 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73553572 | gcttggggtgtagct[C/T]agtggaagaatattt | 105841 |
rs6159005 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73553663 | TTAAAATACATATTG[C/T]TCAACTACTTTGACT | 105841 |
rs6218142 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73522005 | tttccactttagtta[C/T]tgagacactcactgt | 105841 |
rs6233051 | snp | C/T | 0.46875 | 0.121031 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Dennd3 | Mm_Celera | 15:73522349 | GGCCAGCTGTGCTCT[C/T]GGCAAAGGCAGGAGG | 105841 |
rs6369525 | snp | A/G | 0.32 | 0.24 | intron-variant | Dennd3 | Mm_Celera | 15:73515496 | CTGTGAACTCATCCA[A/G]GAGTGGGTGGCGGTG | 105841 |
rs6370165 | snp | A/C/T | 0.5 | 0 | intron-variant | Dennd3 | GRCm38.p3 | 15:73515649 | AGCCAAACATGGCCA[A/C/T]CGAACCCTGGAAGAA | 105841 |
rs6370195 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73515670 | CCTGGAAGAATGGCT[C/T]GTGTGTTGGGGAACA | 105841 |
rs6370601 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73515686 | GTGTGTTGGGGAACA[C/T]TGGATTTTACantta | 105841 |
rs6370617 | snp | A/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73515698 | ACANTGGATTTTACa[A/T]ttaattaattaatta | 105841 |
rs6371168 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73515813 | aagagggcatcagct[C/T]tcattatagatggtt | 105841 |
rs6404792 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73553145 | TCCCTGGCTCTTTCA[C/T]TCTCTCNGGCACTGG | 105841 |
rs6404804 | snp | A/G | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73553152 | CTCTTTCANTCTCTC[A/G]GGCACTGGCGTGGTC | 105841 |
rs6404891 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Dennd3 | Mm_Celera | 15:73553210 | TCTTCCTGCACCACA[C/T]NTAACTGAAAGACCT | 105841 |
rs6405294 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Dennd3 | Mm_Celera | 15:73553211 | CTTCCTGCACCACAN[A/G]TAACTGAAAGACCTC | 105841 |
rs6405368 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Dennd3 | Mm_Celera | 15:73553269 | GTGCTTATGGTTCGT[C/T]TGAGCTCTGTTAGTC | 105841 |
rs6405418 | snp | A/G | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73553293 | GTTAGTCTGCACCCC[A/G]GGNCCCCAGTAGGCT | 105841 |
rs6405419 | snp | A/G | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73553296 | AGTCTGCACCCCNGG[A/G]CCCCAGTAGGCTGTT | 105841 |
rs13460525 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Dennd3 | Mm_Celera | 15:73571639 | ACGTGTGGACACAAC[A/G]CCTCTATTGAACTGT | 105841 |
rs13460526 | snp | G/T | 0.42 | 0.183303 | utr-variant-3-prime, nc-transcript-variant | Dennd3 | Mm_Celera | 15:73571172 | GAAGTCAGCACCTGA[G/T]CTGCCAACTCAGCTG | 105841 |
rs13460527 | snp | C/T | 0.387812 | 0.208586 | utr-variant-3-prime, nc-transcript-variant | Dennd3 | Mm_Celera | 15:73571849 | TCAAGATTCCATGTC[C/T]GCCATTGGAGAGGCG | 105841 |
rs31554784 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73519669 | AAGGGGAGCAGGTGG[A/T]GGGTGGATCGTGTCT | 105841 |
rs31556689 | snp | A/G | 0.48 | 0.0979796 | downstream-variant-500B | Dennd3 | Mm_Celera | 15:73572635 | ATTTGTGGTGATTTT[A/G]ATTTGTACGACCTCA | 105841 |
rs31556701 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dennd3 | Mm_Celera | 15:73551479 | GGTGAGATCCAAGTG[C/T]ACACATGAGGACTGG | 105841 |
rs31569771 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Dennd3 | Mm_Celera | 15:73550705 | CTTTTCCTCTTCCCA[A/G]TGTGTGACCTCATAA | 105841 |
rs31570571 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Dennd3 | Mm_Celera | 15:73521368 | ATGTGAGTGACAACT[C/T]GGGGTGCCTGAATCT | 105841 |
rs31572621 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | Dennd3 | Mm_Celera | 15:73512112 | TCTTCCAGGTACCCA[A/C]AGGGTCTACTTCCCG | 105841 |
rs31597527 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Dennd3 | Mm_Celera | 15:73534629 | TGGATCCAGGGTAGA[C/T]GGGTCCAACCGTCAG | 105841 |
rs31600680 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Dennd3 | Mm_Celera | 15:73512255 | GGATGACGTGGCTGG[G/T]CACCTGGGGATGCCG | 105841 |
rs31617497 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73570337 | GCCTTCAGCCTGCAG[C/T]AGCCAAGGACACTCC | 105841 |
rs31622804 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73538575 | ATGTTTAGGTACATG[C/T]AGGTATTCAGACTTT | 105841 |
rs31622814 | snp | A/G | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73524288 | GTAAGTTGGGGCCAG[A/G]GTTGTTAGTAAGAGC | 105841 |
rs31625415 | snp | A/G | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73569574 | TCTGGAGATCCCCAG[A/G]TAGCTCTCTCTGCTC | 105841 |
rs31629986 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Dennd3 | Mm_Celera | 15:73536488 | ACTTGCTGTCCCAGA[C/T]AAGACTTTAGAAGTC | 105841 |
rs31634348 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73514942 | GCCGGGTGTGGTGGC[A/G]CACGCCTTTAATCCC | 105841 |
rs31640201 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73568543 | ACTCCAGGCCTGTGT[A/G]CACAAGTCCGGCCTT | 105841 |
rs31671045 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73539589 | GTAGGGGAGTCCCTG[A/G]TGTTCTGTCCCTCCT | 105841 |
rs31684301 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Dennd3 | Mm_Celera | 15:73542291 | CCATACCCTGCAGGC[C/T]GTCGAGTATTTATAG | 105841 |
rs31687646 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Dennd3 | Mm_Celera | 15:73569179 | TGACTTCTTGGGAGA[C/T]AATACTCACAACACG | 105841 |
rs31687859 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73530961 | AATAATACAACTGAA[A/G]CCCAGCTATCATTTT | 105841 |
rs31688610 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Dennd3 | Mm_Celera | 15:73521753 | GAGTCTTAAAGGACA[G/T]GGTTCCTCTGCCAAA | 105841 |
rs31696453 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73569972 | CTTTGCTCACCACTC[C/G]CTAAGTCTCTTTCTC | 105841 |
rs31700693 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Dennd3 | Mm_Celera | 15:73521822 | AAGCCCACCTAGAAA[G/T]GGTGTCATGAATGAG | 105841 |
rs31727239 | snp | C/T | 0.455 | 0.143091 | intron-variant | Dennd3 | Mm_Celera | 15:73569147 | CTTTCCAAATCATTT[C/T]GCTTTCTGAAAGGGT | 105841 |
rs31728893 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73546923 | CTAACTCGGAAGTCC[C/T]TACTCGCCCAGTGAT | 105841 |
rs31732912 | snp | A/G | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73520956 | GCCTGTGTCAAGTTG[A/G]CACACAAGACCAGCC | 105841 |
rs31734653 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | Dennd3 | Mm_Celera | 15:73567157 | CTGCACAACGACCGC[A/G]TATGGTGTTGTAAGT | 105841 |
rs31740079 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Dennd3 | Mm_Celera | 15:73551386 | TGACATACCTACTCT[A/C]ACAAGGCCACACATC | 105841 |
rs31761704 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73518786 | ACACTGGAGTGTGGC[A/G]CAGGGACAGATAGGG | 105841 |
rs31762226 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73514779 | TAGAGTGAGTTCTAG[A/G]TAGGTCAACCTGGGC | 105841 |
rs31791060 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Dennd3 | Mm_Celera | 15:73531010 | ATAGGAAGATAAACT[C/T]GACACAGGGACAAGC | 105841 |
rs31798749 | snp | G/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73519012 | GCAGTCGTGGTGGCG[G/T]CATGATGGCTGTGAG | 105841 |
rs31801541 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73560745 | GGTCTCAGGTTGGGG[C/T]AGTCATTGTTTGGCT | 105841 |
rs31815197 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73519631 | CCTGGTGTAGGGGCA[C/T]TTCCCTCTGTCATTG | 105841 |
rs31817366 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73565353 | AGCGGTTTTGGCTCT[C/T]TGCCTTACAGCCAAG | 105841 |
rs31818791 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Dennd3 | Mm_Celera | 15:73541244 | GAGCCCCGGGGCGTC[A/G]GCTAAGTAGTCAAGT | 105841 |
rs31840419 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73560910 | ATCTGTAGTGGACAC[G/T]TAAGTTGGATCTGCC | 105841 |
rs31850380 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73569820 | AAGATCTGCCTGCCT[C/T]GGTTAAGATAGCTAG | 105841 |
rs31850607 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73520784 | CCTGGCTTACTCAGC[C/T]TGCTTTCTTATAGAA | 105841 |
rs31863836 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73520725 | TCAGGAAGCAGGAGC[C/T]GATGCAGAGGCCATG | 105841 |
rs31864267 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73560777 | CTCCCTCGATCTCTG[C/T]TCCATCTTTATCCCT | 105841 |
rs31864979 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73547757 | GCTGTGTCCTCACTG[A/G]ACATGGACACTGAAC | 105841 |
rs31876404 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Dennd3 | Mm_Celera | 15:73533112 | GCTTAGACCCGACAC[G/T]TAATGCAGCAGTGTC | 105841 |
rs31905404 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73562537 | CCGGGCGTGGTGGCG[A/C]ACGCCTTTAATCCCA | 105841 |
rs31912274 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73546680 | CCCAGACGAGCCACC[A/G/T]CCGTGAAGAAAGACA | 105841 |
rs31913911 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dennd3 | Mm_Celera | 15:73569096 | TGTTTCCCAAAGCCC[C/T]GGGCCACTGCAGCTG | 105841 |
rs31915490 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73515590 | CAAAACTTCCTGGAC[C/T]GTGACAGTGTTCTCC | 105841 |
rs31919568 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Dennd3 | Mm_Celera | 15:73540644 | GAACTGTCTACCTGG[C/T]CTCTGCCCACGTCAC | 105841 |
rs31926950 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73518416 | GAGACCCTGAAGCAG[A/T]GGATGATCCTGGAGG | 105841 |
rs31933865 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73521585 | TTGCTTCCAGCAGCT[C/T]GGGGCAGAGCTGGCT | 105841 |
rs31934474 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73570470 | AGTCAGCTGTCAGCT[C/G]TTCTGCAGTGTGGAC | 105841 |
rs31950094 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73533011 | GGGGGTGGGGAACTG[G/T]CCTCAGCCTCTGGGT | 105841 |
rs31953237 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73551026 | TGCACCTGGGCATCT[G/T]TTGTTCTGTAGTTGT | 105841 |
rs31955252 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73548774 | AGATCAGCCTGCTGC[C/T]GCCTCTTAAGTCGTG | 105841 |
rs31963852 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Dennd3 | Mm_Celera | 15:73521308 | ATTATCAAGGCCTTG[C/T]CCATTCCTCTGCTTA | 105841 |
rs31966371 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Dennd3 | Mm_Celera | 15:73568842 | TTCCTTCCCGCCTTA[A/G]TGGGAATGAGTGGGA | 105841 |
rs31975845 | snp | G/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73560754 | TTGGGGTAGTCATTG[G/T]TTGGCTGCTCCCTCG | 105841 |
rs31976503 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Dennd3 | Mm_Celera | 15:73550636 | TATGCGTGTGCTACT[A/G]TGTGAAGGGAGACAA | 105841 |
rs31976717 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73542225 | TGTAAGACTCTAGAT[A/G]AGTGTGTCTTCTCTC | 105841 |
rs31983183 | snp | A/G | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73538631 | AAGCTGGGTTCTTTG[A/G]TCTGTGGTGGGGTTA | 105841 |
rs31990486 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | Dennd3 | Mm_Celera | 15:73511232 | ACTGGCCTGAAATTC[A/C]TTTATGATCCTCTGC | 105841 |
rs32002972 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73551022 | GAGTTGCACCTGGGC[A/G]TCTTTTGTTCTGTAG | 105841 |
rs32003115 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73532337 | ATGGTTATGAGCCAC[C/T]GTGTGGCTTCTTGGA | 105841 |
rs32005069 | snp | A/G | 0.49827 | 0.0293608 | intron-variant, upstream-variant-2KB | Dennd3 | Mm_Celera | 15:73524112 | AGCAGAGGAGGTGAC[A/G]ACGTGTCTTTGTTGC | 105841 |
rs32006369 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73521590 | TCCAGCAGCTCGGGG[C/T]AGAGCTGGCTGGCAT | 105841 |
rs32008894 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Dennd3 | Mm_Celera | 15:73534314 | AGGCATCCACTGGTC[C/G]TGGTGTTTGCCCTGT | 105841 |
rs32030475 | snp | C/T | 0.32 | 0.24 | intron-variant | Dennd3 | Mm_Celera | 15:73540054 | GGGCCTCTGCCTGGT[C/T]CATACTCACAGTCTG | 105841 |
rs32041697 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73546975 | AATTGGTTCACAAGA[A/G]CAGCACCAGGCCCAT | 105841 |
rs32048348 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73566921 | TGATGTGTCCCTGGT[A/G]TGTCCCACTTATCAT | 105841 |
rs32053971 | snp | C/G | 0.42 | 0.183303 | intron-variant | Dennd3 | Mm_Celera | 15:73518503 | ATAGCTTACCTTCTG[C/G]CTCCTGTCTGGTAAA | 105841 |
rs32054929 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dennd3 | Mm_Celera | 15:73520256 | TTTTAATTCTTTTTT[A/T]AAATTTATTTATTTA | 105841 |
rs32059174 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Dennd3 | Mm_Celera | 15:73521117 | GACATACTATACCCG[C/T]TTTCCTTTGTTTTGC | 105841 |
rs32069488 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Dennd3 | Mm_Celera | 15:73521055 | TTTTGGGACGGTGCA[A/G]GCCTCCTTCTTCCCA | 105841 |
rs32070515 | snp | C/T | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73567240 | CCCCTTTCCCTTCAC[C/T]GTCCCTGTTTCCAGC | 105841 |
rs32071566 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73524885 | TACAAAGTGAGTTCC[A/G]GGACAGCCAGGGCTA | 105841 |
rs32077911 | snp | A/G | 0.5 | 0 | intron-variant | Dennd3 | Mm_Celera | 15:73524813 | AGCAATAAGATAAAT[A/G]CCCAGCACTCAGGGG | 105841 |
rs32081843 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Dennd3 | Mm_Celera | 15:73569091 | CTCTGTGTTTCCCAA[A/G]GCCCTGGGCCACTGC | 105841 |
rs32082011 | snp | A/G | 0.415225 | 0.187619 | synonymous-codon, nc-transcript-variant | Dennd3 | Mm_Celera | 15:73567111 | GATCAGCCGGTTCCA[A/G]CTGTCATACGGTGAC | 105841 |
rs32082046 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Dennd3 | Mm_Celera | 15:73570431 | ACTAACAGGTGGCAA[A/G]GTGTGGTCCCACTGT | 105841 |
rs32082604 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dennd3 | Mm_Celera | 15:73513228 | GATGGGTTCTGTACT[C/T]CGTGCCGAATAGTGA | 105841 |