SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3709329 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Ubr4 | Mm_Celera | 4:139422666 | GCAGTGAGTCATAAG[A/C]ATGCAGAACCTAGAA | 69116 |
rs3710710 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139422960 | GCCTGAGTTGAAGAC[A/C]GCTTTCCTTCAGTTA | 69116 |
rs3711278 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubr4 | Mm_Celera | 4:139423036 | GAACAGGAGTGTGCG[C/T]GTGTGAATTTAGAAG | 69116 |
rs3715512 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139426513 | GAGGCATATGTCTTC[A/G]TTAGCAACTTTAGTC | 69116 |
rs3716198 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139426641 | GTCTTCTATAACGTC[C/T]GTGTATCACGCTCGC | 69116 |
rs3716221 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139426642 | TCTTCTATAACGTCT[G/T]TGTATCACGCTCGCT | 69116 |
rs3716861 | snp | A/G | 0.5 | 0 | intron-variant | Ubr4 | Mm_Celera | 4:139487967 | TCCCTTCCCATTGCT[A/G]TCAGGTAAGGCCATC | 69116 |
rs6224472 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Ubr4 | Mm_Celera | 4:139449984 | gctgaatgtctaggt[G/T]tttctcccggtgttc | 69116 |
rs6224533 | snp | A/G | 0.5 | 0 | intron-variant | Ubr4 | Mm_Celera | 4:139450030 | agtcacttacaaagc[A/G]attacaccatagcct | 69116 |
rs6225018 | snp | C/T | 0.5 | 0 | intron-variant | Ubr4 | Mm_Celera | 4:139450079 | agatgatttaatgct[C/T]gaagngtgtgcaggg | 69116 |
rs6225028 | snp | A/G | 0.5 | 0 | intron-variant | Ubr4 | Mm_Celera | 4:139450084 | atttaatgctngaag[A/G]gtgtgcagggtatcg | 69116 |
rs6239420 | snp | A/G | 0.5 | 0 | synonymous-codon | Ubr4 | Mm_Celera | 4:139450416 | ACAGCTCCGAGACCT[A/G]CACACCCTGGACTCC | 69116 |
rs6239968 | snp | A/G | 0.5 | 0 | synonymous-codon | Ubr4 | Mm_Celera | 4:139450530 | TTTGCAGTATGACAC[A/G]CTCATCAGCCTGGTA | 69116 |
rs13463280 | snp | A/G | | | synonymous-codon | Ubr4 | Mm_Celera | 4:139476157 | AACGGACTCCATCAC[A/G]AGCCTGCATAAGCTG | 69116 |
rs13463281 | snp | A/G | 0.475309 | 0.108333 | synonymous-codon | Ubr4 | Mm_Celera | 4:139473200 | GAAGGGAATCACCCA[A/G]AATGCCCTGGACTAC | 69116 |
rs27552695 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Ubr4 | Mm_Celera | 4:139489905 | GCCTCTGAACTTAGT[A/G]TCTGGACCTCTGAGA | 69116 |
rs27552696 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139489058 | TCCATTGCTGGAATC[A/C]CATCAGAGCATGCTG | 69116 |
rs27552697 | snp | A/G | 0.32 | 0.24 | intron-variant | Ubr4 | Mm_Celera | 4:139488242 | GGCCAAGGACTTGAT[A/G]TAGAGAGTGCACTGG | 69116 |
rs27552698 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ubr4 | Mm_Celera | 4:139487435 | GTCTCTGGGTCTGCC[C/T]TGCTGTCTGAGCTGC | 69116 |
rs27552699 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ubr4 | Mm_Celera | 4:139487258 | GGGAATTGTATACGG[A/G]CAAGGGAGAAATCCC | 69116 |
rs27552700 | snp | A/G | 0.32 | 0.24 | intron-variant | Ubr4 | Mm_Celera | 4:139486981 | GGAGTTGGACTCTCA[A/G]ATGCAGGCGCTTTAA | 69116 |
rs27552701 | snp | A/G | 0.32 | 0.24 | intron-variant | Ubr4 | Mm_Celera | 4:139486950 | AGTCCATGCTCTCCC[A/G]TACAAACTCTTTGTG | 69116 |
rs27552702 | snp | C/T | 0.32 | 0.24 | intron-variant | Ubr4 | Mm_Celera | 4:139486694 | GCTCGACCACTGGCA[C/T]GGGAGTCCAGCATTC | 69116 |
rs27552703 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ubr4 | Mm_Celera | 4:139486670 | CAGCATGCCCTGTCC[A/G]TTGCCTCAGCTCGAC | 69116 |
rs27552704 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ubr4 | Mm_Celera | 4:139486544 | GGAACTTGCTTTTAG[C/T]GGCTGTGCATCTCTG | 69116 |
rs27552705 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ubr4 | Mm_Celera | 4:139486462 | ACAGAGCAGAAGTAG[G/T]CGCACACTAACCCCC | 69116 |
rs27552706 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ubr4 | Mm_Celera | 4:139485806 | TGAGATCATGTAGAA[C/T]GTTGCATAAGCAAAG | 69116 |
rs27552707 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ubr4 | Mm_Celera | 4:139485773 | ATGCAGGTGTGGGGC[C/T]GTCCCATGTTGAAAC | 69116 |
rs27552708 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Ubr4 | Mm_Celera | 4:139485674 | GCCCCTACCGGCGAT[A/C]TGCCTGGACCCACAC | 69116 |
rs27552709 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ubr4 | Mm_Celera | 4:139473064 | CTGAGACTTTATGCT[C/T]TCCTAGGTACGATGA | 69116 |
rs27552710 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubr4 | Mm_Celera | 4:139472943 | AGCCTAGACGCAGGG[C/T]GGGCAAGAGGAGACG | 69116 |
rs27552711 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139472894 | AGGTGCGCGGAGCTG[C/T]GTTTGCAAAAGCCTG | 69116 |
rs27552712 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139472831 | TCACCAAACCCTAGT[A/G]TAATGAAGCAGTGGT | 69116 |
rs27552713 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139472745 | GAGGCTGAACAGGGC[C/T]GCCTGGGGTTTTGTT | 69116 |
rs27552714 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ubr4 | Mm_Celera | 4:139472446 | GCTACAGCCACCATC[C/T]TTATTCCCACCCTTT | 69116 |
rs27552715 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ubr4 | Mm_Celera | 4:139472440 | TTCTTGGCTACAGCC[A/G]CCATCTTTATTCCCA | 69116 |
rs27552716 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ubr4 | Mm_Celera | 4:139471980 | AGTTTCTACTTAGGG[C/T]TATATCATTGCGCTG | 69116 |
rs27552717 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139471705 | TCACTCACAAGTGAC[C/T]GACTGTGCCCTGGCT | 69116 |
rs27552718 | snp | C/T | 0.5 | 0 | intron-variant | Ubr4 | Mm_Celera | 4:139471646 | ACTTACATGCATGGG[C/T]GCACATGCAGCCCCT | 69116 |
rs27552719 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Ubr4 | Mm_Celera | 4:139471549 | CCTGCCCCTGTGCTG[A/G]GTGTAGACTCAAGAC | 69116 |
rs27552720 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Ubr4 | Mm_Celera | 4:139471482 | TTGCAGTACCAAGCC[G/T]GCTCCTTCAGCTCAC | 69116 |
rs27552721 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Ubr4 | Mm_Celera | 4:139471455 | ACAGGGAGCTTTGGC[G/T]CCAATGAGAGATTGC | 69116 |
rs27552722 | snp | C/G | 0.5 | 0 | intron-variant | Ubr4 | Mm_Celera | 4:139470978 | CCTGCTAATTGAGAA[C/G]TCACTTAGAGCAGTG | 69116 |
rs27552723 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139470918 | TAAGATGGTGACCTG[A/G]AATGAGAGCCCAGGA | 69116 |
rs27552724 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139470717 | TAATGTCTACCTTGT[A/G]AGCTTTACAAGGACA | 69116 |
rs27552725 | snp | A/G | 0.5 | 0 | intron-variant | Ubr4 | Mm_Celera | 4:139470498 | GCTCCCTTAGATCTG[A/G]GCTGTGGCGGTCTTC | 69116 |
rs27552726 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ubr4 | Mm_Celera | 4:139470382 | GAAGCTGAGGTCATT[A/G]AGCCACTTGACACTA | 69116 |
rs27552727 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubr4 | Mm_Celera | 4:139470026 | ACTGTAGTTGACTTA[A/G]GCCTTGAGCAAGGCC | 69116 |
rs27552728 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Ubr4 | Mm_Celera | 4:139469987 | TCAGTGGTATTTGCT[A/T]GGGCTTTGCTGTAAT | 69116 |
rs27552729 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139469910 | ATTGGGATGAAACCG[C/T]TCAGGCTGTCGGAAA | 69116 |
rs27552730 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139469802 | GCTGCATATTGGACT[A/C]AGGCCAGAGCAAGCA | 69116 |
rs27552731 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139469672 | CCAACTTTTCTCTGC[G/T]TAGGGAGAGCCCATG | 69116 |
rs27552732 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139469517 | GTGAGTCTCTTCCAC[A/G]TGTGAATTACAGCCT | 69116 |
rs27552733 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ubr4 | Mm_Celera | 4:139469267 | CCTGAAATGTGTACT[A/G]CATTCTTTGGTTCAG | 69116 |
rs27552734 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139469213 | TCTCTGTGATGAAGA[A/G]AGAGCCTGCTGTCTG | 69116 |
rs27552735 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ubr4 | Mm_Celera | 4:139469126 | GATGCCTGGCATAGG[C/T]AGCCTCTCCCAGCAG | 69116 |
rs27552736 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139468595 | TTTTTCTGGTGCTCA[A/G]GGTGAAAGGTCTTCA | 69116 |
rs27552737 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ubr4 | Mm_Celera | 4:139468552 | TTGAGTCTGGTGTTA[C/T]CACCCATATGACTCA | 69116 |
rs27552738 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139468506 | GAGTACTGGTCATAG[A/C]CCCTGTTAATACCAG | 69116 |
rs27552739 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139468348 | CGAGGGTTGTGACCG[G/T]TCCTGCCATGGAACA | 69116 |
rs27552740 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139467924 | GGTTACCATGTTTAA[C/T]GTGTGGGCATGGTAC | 69116 |
rs27552741 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Ubr4 | Mm_Celera | 4:139467848 | ACCTGTGAGGAGTGC[A/G]TGATCTTCAGGCTGC | 69116 |
rs27552742 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Ubr4 | Mm_Celera | 4:139467401 | CTCCCACATGGAGGA[C/T]AATTTAGTATTTTTA | 69116 |
rs27552743 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139466450 | AGGCCCCATGCAAGC[C/T]GGTCTTCTCCGCTCG | 69116 |
rs27552744 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Ubr4 | Mm_Celera | 4:139465891 | TTCCTAGGGCCCATT[C/T]ATGTTTTCTAGTTCC | 69116 |
rs27552745 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ubr4 | Mm_Celera | 4:139465853 | GTGCCTGATCCATCA[C/T]TCTGTTACTCTAAAG | 69116 |
rs27552746 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ubr4 | Mm_Celera | 4:139465569 | CTCAGGTGTGGGAGA[A/G]GAGTCTGTCTCAAGA | 69116 |
rs27552747 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139464825 | TCCAGCAATACTTGA[A/G]CCTCTTTAGCCTCTT | 69116 |
rs27552748 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ubr4 | Mm_Celera | 4:139464805 | CTGTTTTGGGGTAAA[C/T]GGTCTCCAGCAATAC | 69116 |
rs27552749 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139464521 | TCTCTAAGGGTGTCC[A/G]TCTCCGTCCGTCCAC | 69116 |
rs27552750 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ubr4 | Mm_Celera | 4:139464236 | GCCACAGAAGCCAGC[A/G]CTTTAGGGTATTAGT | 69116 |
rs27552751 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Ubr4 | Mm_Celera | 4:139464188 | AGGGCTGGGAGGTAC[C/G]CCAGGTGGTATATAA | 69116 |
rs27552752 | snp | C/T | 0.5 | 0 | intron-variant | Ubr4 | Mm_Celera | 4:139464185 | GTCAGGGCTGGGAGG[C/T]ACCCCAGGTGGTATA | 69116 |
rs27552753 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ubr4 | Mm_Celera | 4:139463883 | CCCTTTGCCTGGACA[C/T]ATTTCCAGAATTCTG | 69116 |
rs27552754 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139463815 | CCTCAAACGAGCAAA[C/T]TAGAGCATGTCATAG | 69116 |
rs27552755 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Ubr4 | Mm_Celera | 4:139463556 | CCGTCTCTACTTGAC[C/T]GAGAAGTACGTGTGG | 69116 |
rs27552756 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Ubr4 | Mm_Celera | 4:139463460 | CTGCTTCCCCCAGGC[C/T]TTGACACTTACCCCT | 69116 |
rs27552757 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ubr4 | Mm_Celera | 4:139463416 | CTATCCGAGGTGTGC[C/T]TCTTCCCTCCCGCCA | 69116 |
rs27552758 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139463197 | GCATGGTGTTTTTTA[C/T]GTCACTCCTGGAGTG | 69116 |
rs27552759 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ubr4 | Mm_Celera | 4:139463159 | GTGCAGATAGCGAGA[G/T]TCCCTATTGGGCCAT | 69116 |
rs27552760 | snp | A/G | 0.493827 | 0.0552116 | synonymous-codon | Ubr4 | Mm_Celera | 4:139460232 | CAATCCAGCCCTGCG[A/G]CACATCCTCGTCTCC | 69116 |
rs27552761 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ubr4 | Mm_Celera | 4:139458493 | CCTTTGTCCCATGGT[C/T]AGCCTCAGCAGAGAA | 69116 |
rs27552762 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ubr4 | Mm_Celera | 4:139456601 | TGCTGGCCACCTTAG[C/T]GGACTTTATATGGCT | 69116 |
rs27552763 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139456089 | GCTCAAGCGCTGCTA[C/T]GGCCACAGAAGGAGC | 69116 |
rs27552764 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139454572 | TTAACTTTGTGGTTT[C/T]TCATGTGCATTTGTG | 69116 |
rs27552765 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139454147 | TTGTGTATGCTGGAG[C/T]GCTCATGAATTCAGT | 69116 |
rs27552766 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Ubr4 | Mm_Celera | 4:139454022 | GAGGACTCAGAACCA[C/T]ATCCTCACCAATCAC | 69116 |
rs27552767 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ubr4 | Mm_Celera | 4:139453931 | CATCTTGCGAGCCCA[G/T]GACTCGGGTTTTTAG | 69116 |
rs27567768 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139453496 | CACAGCAAGTGGCTG[A/G]CAGAGATGTGGGCCG | 69116 |
rs27567769 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ubr4 | Mm_Celera | 4:139453055 | GCATGGGAGAAGACA[A/G]TGCAGACATAGTTTC | 69116 |
rs27567770 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ubr4 | Mm_Celera | 4:139452972 | CTGCTCTGGAGTAAG[A/G]TGGGGTGCCAACAGT | 69116 |
rs27567771 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ubr4 | Mm_Celera | 4:139452234 | TCCTTCGCTTTCTCT[A/G]CTTCTCATGGTCCTC | 69116 |
rs27567772 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Ubr4 | Mm_Celera | 4:139452225 | CCTTCCTTCTCCTTC[A/G]CTTTCTCTACTTCTC | 69116 |
rs27567773 | snp | A/G | 0.5 | 0 | intron-variant | Ubr4 | Mm_Celera | 4:139451993 | GATCCTGTGCTAGGC[A/G]CTCAGCCCCGTGAGT | 69116 |
rs27567774 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139451606 | GATCACTCCATGGCT[C/T]CTGCCGATCTGCTCC | 69116 |
rs27567775 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139451130 | GTCCATCAGCCAACT[C/T]GGGGACACCTGCCTC | 69116 |
rs27567776 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubr4 | Mm_Celera | 4:139450962 | AGGTTGTAGCTTCTG[A/G]GTGCATGGCCTTCCC | 69116 |
rs27567777 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ubr4 | GRCm38.p3 | 4:139450797 | CACTTTGGATTTTGT[C/T]CTTAAGTACTAAAGC | 69116 |
rs27567778 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubr4 | Mm_Celera | 4:139450763 | ATTTGTTACACATAG[G/T]ATCCACCTGAGATTG | 69116 |
rs27567779 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ubr4 | Mm_Celera | 4:139450703 | GAGTTGAATTTAGGG[C/T]TCCTTACCTGTGAAG | 69116 |