SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3723096 | snp | A/G | 0.362812 | 0.2231 | intron-variant | Ube2e3 | Mm_Celera | 2:78901723 | TTGTCTTCAGGATAA[A/G]GATGCAGGTCCATTT | 22193 |
rs6306601 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Ube2e3 | Mm_Celera | 2:78873904 | AGATCAGAGAAAAAA[A/T]TTCTGCAATTTAAAA | 22193 |
rs6308275 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e3 | Mm_Celera | 2:78874225 | AAGTGAGGCTTGGCT[C/G]GTGCTTGTAGCCAGC | 22193 |
rs6308721 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2e3 | Mm_Celera | 2:78874301 | GCAGGCCATGCCGGT[C/T]AGTTCTCTGCATAAG | 22193 |
rs6381009 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Ube2e3 | Mm_Celera | 2:78878474 | GCTGAAGGATGGCGC[C/G]TAGCAGTTCAGTAAC | 22193 |
rs6394738 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78878702 | ATCTGATGAAAAGTA[C/T]TCAGAGTTTGAGAGT | 22193 |
rs6394801 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e3 | Mm_Celera | 2:78878741 | GTGTGTTTATTGTAA[A/G]TGTATTCCTTTGCTC | 22193 |
rs6395314 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e3 | Mm_Celera | 2:78878818 | TCCCAAAGTGAGCTT[A/C]AAGTGGTTAAGTTGG | 22193 |
rs27936011 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78919735 | AATGTAAATATAGTC[A/G]TGTAGGATTCTCAAA | 22193 |
rs27936012 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78919426 | CTCAGACTTTCATAG[C/T]TGAATAAAGTGTCAA | 22193 |
rs27936013 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ube2e3 | Mm_Celera | 2:78919326 | GTTACTTCATGACTG[G/T]CAGGGATCGTTTCAT | 22193 |
rs27936014 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78919122 | TGAGTTCTGAGTCTC[A/G]GGCATCCAGAAGGGA | 22193 |
rs27936015 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e3 | Mm_Celera | 2:78919005 | TTTAATAGTATGTCG[G/T]AATACAGGGACCTTG | 22193 |
rs27936016 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78918892 | TAATGTTGGTCAAGA[A/C]ATAAATGTTACTATT | 22193 |
rs27936017 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78918563 | ACTACTTAACTGTTA[C/T]TACATCCAATGTAAG | 22193 |
rs27936018 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78918074 | CCTAACCTTTCAAGA[A/G]TCATTTATCTTCGTA | 22193 |
rs27936019 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78917990 | CTTCCTCCCAGTCCT[A/T]CACTTTATTCTGACA | 22193 |
rs27936020 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78917960 | AAGGACAGTAACACA[A/G]ATGATGGCCGCAGCC | 22193 |
rs27936021 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78917804 | CAAGTCCAAGTGATG[A/T]GTTTACTCTCTCAAC | 22193 |
rs27936022 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78917732 | TTCCTGTCCCCTGAT[A/G]CTCCTTTGAAGCTCA | 22193 |
rs27936023 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78917714 | AAGCACTTTTGGGTA[A/T]TCTTCCTGTCCCCTG | 22193 |
rs27936024 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78917612 | ATCATGATATCATCT[A/G]TAGCCCCTATTAAGC | 22193 |
rs27936025 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78916788 | ATTTTTCTTAGCACT[A/G]TTCATGGAAATAGAA | 22193 |
rs27936026 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ube2e3 | Mm_Celera | 2:78916782 | TCTTACATTTTTCTT[A/G]GCACTGTTCATGGAA | 22193 |
rs27936027 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78916454 | ATCTTAGAAGCTCTT[A/G]AAGTCTCCATGTTCC | 22193 |
rs27936028 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78916418 | CAGTGTGACCCATTA[A/G]AATCTAAGATCCTAA | 22193 |
rs27936029 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78916405 | TTTAAGTGTTATACA[C/G]TGTGACCCATTAGAA | 22193 |
rs27936030 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78914846 | TGTGAAAAATGCTTC[C/T]CATTTCAAATCCTGA | 22193 |
rs27936031 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78914384 | ACCCTAGAGCTTAGT[C/T]TGTATATCTGAGTTT | 22193 |
rs27936032 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Ube2e3 | GRCm38.p3 | 2:78914318 | TGCAAAGCCTAAACA[C/G/T]GATACTTATTTGAAG | 22193 |
rs27936033 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Ube2e3 | Mm_Celera | 2:78914230 | ACTGACGAGTGGCAG[A/G]CTCACTTGTACTTTC | 22193 |
rs27936034 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78914199 | ATTTTGTGCCTTCTT[A/G]TGAGTGTGATACAAA | 22193 |
rs27936035 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e3 | Mm_Celera | 2:78913551 | TATACATGTGTGCAG[A/G]AACATGTTGGTCTTA | 22193 |
rs27936036 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78912160 | TGTGAAAATGCATTC[C/T]AAACAGAGGAAAATG | 22193 |
rs27936037 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78911804 | TTTTACAATGTCAGT[C/T]TTGCAGAATTAATAA | 22193 |
rs27936038 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ube2e3 | Mm_Celera | 2:78911308 | CTCTCCATATTCTAA[A/G]TGATGCTGTAAAGGA | 22193 |
rs27936039 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78910652 | TTATTTTTTAAATTT[A/G]CAACAGCTTTTCCAT | 22193 |
rs27936040 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78910353 | GAATTGACAAGTCTC[C/G]CTACAAACTTGATAT | 22193 |
rs27936041 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78910134 | AGTTGTATTGCAAGT[C/T]TTCAATTTGGGCAAT | 22193 |
rs27936042 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78908848 | AATGCTTCCATAGTT[C/G]AGGACACCTAGTTTC | 22193 |
rs27936043 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78908679 | AACTGAGGTAGTATG[A/G]TTAATGTAGCTTTAA | 22193 |
rs27936044 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2e3 | Mm_Celera | 2:78908629 | GGCCAGAGTGAATAC[C/T]TGCCAACTACATGAA | 22193 |
rs27936045 | snp | G/T | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78908594 | GGGGTGTCAAGTTGT[G/T]TTTGTAAGGATAGGA | 22193 |
rs27936046 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78907204 | TCCTGTCTCACCTTT[A/C]CTTGGATTCTTTCCT | 22193 |
rs27936047 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78906863 | AGAAACTTAAAAAAA[A/G]TCTGGAAATGGTCTG | 22193 |
rs27936048 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78906569 | GCTAAGTGGTGTTTG[C/T]CTCCTGTGGGAACAT | 22193 |
rs27936049 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ube2e3 | Mm_Celera | 2:78906543 | TCTCTTTCTTTCCTT[C/T]TGTAATTCATGCTAA | 22193 |
rs27936050 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2e3 | Mm_Celera | 2:78906330 | ATGCATTTCTTTTTG[A/G]TATGCAAGTTTATTC | 22193 |
rs27936051 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2e3 | Mm_Celera | 2:78906120 | CAGTGGTTACCTTGG[A/G]TATGTGTACATATGA | 22193 |
rs27936052 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78906119 | CCAGTGGTTACCTTG[C/G]ATATGTGTACATATG | 22193 |
rs27936053 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78904047 | TAATTTACAAAAAAG[A/G]TTGGAGATTACACAG | 22193 |
rs27936054 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78904000 | GAGATTAAGTCCCCC[A/C]AAAAAACATAACTAC | 22193 |
rs27936055 | snp | G/T | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78903955 | AAAGAGGAAAGCAGT[G/T]TATGTGCCTCATTCC | 22193 |
rs27936056 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78903947 | CTGAGAAAAAAGAGG[A/G]AAGCAGTGTATGTGC | 22193 |
rs27936057 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2e3 | Mm_Celera | 2:78903925 | ACATTGTACAACATT[A/G]TCAGGGCTGAGAAAA | 22193 |
rs27936058 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78903709 | AGAAGAAAGGTTTGA[A/C]TATTTGGAACATCTT | 22193 |
rs27936059 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2e3 | Mm_Celera | 2:78903161 | GTTAATGTAATCTGT[C/T]TTACATGTTAGGAAT | 22193 |
rs27936060 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78901932 | TGCTTCCTTCTGGTC[A/G]TTACTTTTGTTGTTT | 22193 |
rs27936061 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78901910 | CTCAGTTATCTTCCC[C/T]AGGCACTGCTTCCTT | 22193 |
rs27936062 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e3 | Mm_Celera | 2:78901758 | CATTGGTTACTTCCT[C/T]ATAAGCTCAACTCTT | 22193 |
rs27936063 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ube2e3 | Mm_Celera | 2:78901479 | CCTTGTAAGAAAGTT[A/G]TGAAGTCATTATCTT | 22193 |
rs27936064 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Ube2e3 | Mm_Celera | 2:78901260 | TCCCAAACCTGTTAA[A/T]ACCTTAAATCCTTTC | 22193 |
rs27936065 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ube2e3 | Mm_Celera | 2:78900767 | GAATTCCTTGGATAT[C/T]TTAAAGGCTTTTTAG | 22193 |
rs27936066 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Ube2e3 | Mm_Celera | 2:78900643 | AAGGCAGTCTCATTC[C/G]ACCTTTAGGACTCTT | 22193 |
rs27936067 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Ube2e3 | Mm_Celera | 2:78900402 | ACCTTGTATGAGTTG[G/T]ATGATCCTTTCCTCT | 22193 |
rs27936068 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ube2e3 | Mm_Celera | 2:78898453 | GCTATTTCTCACCAT[A/G]GCTTTTTGAGGTTAT | 22193 |
rs27936069 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ube2e3 | Mm_Celera | 2:78898047 | TTTATCTTGACCAAT[A/G]TGTTAAATGTTTATT | 22193 |
rs27936070 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ube2e3 | Mm_Celera | 2:78897383 | TTTTTATTATGAGAT[C/T]CATTAACCATCTTCT | 22193 |
rs27936071 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2e3 | Mm_Celera | 2:78894056 | AAATAGTTCCACAAC[A/G]CCCAAACTAGTCTAG | 22193 |
rs27936072 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Ube2e3 | Mm_Celera | 2:78893943 | TATTATGAACAACTC[C/G]AGCTTTATCTAAGCC | 22193 |
rs27936073 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78893714 | GTTCGTTACCTGACT[C/T]TATTCTATGTGCACT | 22193 |
rs27936074 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78892846 | CAGGGCTGTGTTCAT[A/C]CTGGACAAGCTTGTT | 22193 |
rs27936075 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e3 | Mm_Celera | 2:78892797 | GAGGAAGCTGCAGTG[A/G]TTTGGTTTGGTTTAT | 22193 |
rs27936076 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Ube2e3 | Mm_Celera | 2:78892771 | CCTGGGAAAACAAAT[A/C]TTGTCTTGCAGAGGA | 22193 |
rs27936077 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78892537 | GCTAATTTAATTCAG[C/G]CTTTTCAGTAAAATT | 22193 |
rs27936078 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78892348 | AAAATCTAATGAGAA[A/G]TTCCACAGACTAAGA | 22193 |
rs27936079 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ube2e3 | Mm_Celera | 2:78892056 | ATCTTTACAGGCTAA[C/T]TTAATTCAAGCTTCT | 22193 |
rs27936080 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2e3 | Mm_Celera | 2:78891892 | ACTAGAATGTGTAAT[A/G]TTTAAGTGAAATAAC | 22193 |
rs27936081 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Ube2e3 | Mm_Celera | 2:78891099 | CTGTGTATTTTGTCA[A/G]GGATGAATCTAGGGT | 22193 |
rs27936082 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78890942 | TATGTGTTAATTACA[C/T]TGAAAGCATGTGGTT | 22193 |
rs27936083 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ube2e3 | Mm_Celera | 2:78890905 | ACAGATCCATTCAAG[A/T]GTAATCAATGATGAG | 22193 |
rs27936084 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e3 | Mm_Celera | 2:78890131 | CCTGAATACTTGCCC[C/T]GTTTACTAGACTAGA | 22193 |
rs27936085 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e3 | Mm_Celera | 2:78890101 | CAAAAGCGTGTGCAC[C/T]GTGGCTTCAGTAAAC | 22193 |
rs27936086 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78890039 | TCATTAAATACCATG[C/T]TTAGTTCTCTGTACA | 22193 |
rs27936087 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2e3 | Mm_Celera | 2:78889568 | ACATATGATATGTGT[C/T]TTATGGTTACATACA | 22193 |
rs27936088 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Ube2e3 | Mm_Celera | 2:78888589 | ACCATAAAGACATTT[A/G]GGTATGAATCTCTGA | 22193 |
rs27936089 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ube2e3 | Mm_Celera | 2:78888464 | TGTAAGTTTAATGAA[A/G]GAAATAGCATAGCAG | 22193 |
rs27936090 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Ube2e3 | Mm_Celera | 2:78888388 | GGTTTGTGCTGCAGC[C/T]GTTGCTTGTCCCTGA | 22193 |
rs27936091 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ube2e3 | Mm_Celera | 2:78888331 | ACCTATCAGGCATTC[A/G]TTTGCTGTGGGATGA | 22193 |
rs27936092 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e3 | Mm_Celera | 2:78886301 | TAGGGCTACATGTAT[A/G]AGAGAGAAGATAGAT | 22193 |
rs27936093 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2e3 | Mm_Celera | 2:78886212 | TCTTCCCTTGGTCTT[C/T]TTTCCAACTTTTAGA | 22193 |
rs27936094 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ube2e3 | Mm_Celera | 2:78886203 | TCCTCAGTATCTTCC[C/T]TTGGTCTTTTTTCCA | 22193 |
rs27936095 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e3 | Mm_Celera | 2:78886117 | ATACAAAAAAAGAAC[C/T]TTTGGAATGAAAAAT | 22193 |
rs27936096 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78886022 | ACCACCTCAAAGGGA[G/T]AACATGCTGGATTCA | 22193 |
rs27936097 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e3 | Mm_Celera | 2:78885478 | GAGTACATCCATGGG[C/T]CACCTGCCATGTGCT | 22193 |
rs27936098 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78885467 | TTCTTTACACTGAGT[A/C]CATCCATGGGTCACC | 22193 |
rs27936099 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Ube2e3 | Mm_Celera | 2:78884945 | TTTAAAAATAGCATG[A/T]CTATATCAAGTCAGT | 22193 |
rs27936100 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2e3 | Mm_Celera | 2:78884779 | TTTGCTTCCACCTTC[A/G]CGTGGGTTCTGGGGA | 22193 |
rs27936101 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2e3 | Mm_Celera | 2:78884696 | TGTGACTGTATGTGG[A/G]TGTGAGTGTGTGTGT | 22193 |
rs27936102 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Ube2e3 | Mm_Celera | 2:78884543 | TGAAATCACTACACA[G/T]ATTGGCATTGTGAAT | 22193 |