SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3023311 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Trim17 | Mm_Celera | 11:58970014 | CAGACGCATAAACAG[C/T]ATCACAACACACACA | 56631 |
rs3090225 | snp | G/T | 0.453686 | 0.144955 | intron-variant | Trim17 | GRCm38.p3 | 11:58970090 | ACTGGATTCTAGGGA[G/T]GAGGCGTGGGGAAAG | 56631 |
rs13471087 | snp | A/T | | | synonymous-codon, upstream-variant-2KB | Hist3h2a, Hist3h2bb-ps, Trim17 | GRCm38.p3 | 11:58954845 | GCACCGCCTTCTCCG[A/T]AAGGGTAATTATTCG | 56631 |
rs13471088 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Hist3h2a, Hist3h2bb-ps, Trim17 | GRCm38.p3 | 11:58955103 | GCCCAAGAAGACCGA[A/G]AGCCACCACAAGGCC | 56631 |
rs13474819 | snp | A/G | 0.5 | 0 | synonymous-codon, downstream-variant-500B | Trim17 | GRCm38.p3 | 11:58971532 | GGGGGCTCCCAAGTC[A/G]GGCCAGATGGTCATC | 56631 |
rs13481048 | snp | C/T | 0.49948 | 0.0161206 | upstream-variant-2KB, intron-variant | Trim17 | GRCm38.p3 | 11:58962132 | GGGGCTGTTCGAAGA[C/T]ACGAACCTGTGCGCT | 56631 |
rs26971733 | snp | C/T | 0.489796 | 0.070696 | utr-variant-3-prime | Trim17 | GRCm38.p3 | 11:58971638 | AGGCAGGGTGCTTCA[C/T]CACCGTGGCCACCTA | 56631 |
rs26971734 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Trim17 | GRCm38.p3 | 11:58970930 | GGAAAAGAGCCATTT[A/G]GCCACTGTGTCTGTC | 56631 |
rs26971735 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Trim17 | GRCm38.p3 | 11:58970839 | ATCATCAATATCCAC[C/G]GGGATTTGTAGTGTA | 56631 |
rs26971736 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim17 | GRCm38.p3 | 11:58970759 | GTGTCTCAAACTGTA[C/T]TCACCATCTTTCTAA | 56631 |
rs26971737 | snp | A/G | 0.493827 | 0.0552116 | synonymous-codon, missense | Trim17 | GRCm38.p3 | 11:58970587 | GGTGGTCCTCCCCGC[A/G]GCTATCAAGACCCTG | 56631 |
rs26971738 | snp | A/G | 0.124444 | 0.216185 | missense | Trim17 | Mm_Celera | 11:58970446 | TGAAGGACACCTTGA[A/G]CAGGTACTGTCACCC | 56631 |
rs26971739 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58970358 | ATGTCCCAAAGTAGC[A/G]GGCAACAGAGGTAGC | 56631 |
rs26971740 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Trim17 | GRCm38.p3 | 11:58970148 | GCTTGCTTAGCAGGG[A/G]TTCTGCCCTCTGTCT | 56631 |
rs26971741 | snp | A/G | 0.5 | 0 | intron-variant | Trim17 | GRCm38.p3 | 11:58969944 | TGTGAGCACAAGCTC[A/G]CCATGGTTCACTGTT | 56631 |
rs26971742 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58969909 | CTGTGAGACTCAAGG[A/G]CCAAGGTTGCTTAAT | 56631 |
rs26971743 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58969908 | TCTGTGAGACTCAAG[G/T]GCCAAGGTTGCTTAA | 56631 |
rs26971744 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim17 | GRCm38.p3 | 11:58969774 | CTCTGCAGGTGTGCA[C/T]GAGGAACATTCACAG | 56631 |
rs26971745 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58969390 | TAGGCCAGGGGTGCT[C/T]CTGTAGATTCTGGCT | 56631 |
rs26971746 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58968990 | CAAACAGTCCACATT[A/G]TCCACAGTATACACA | 56631 |
rs26971747 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim17 | GRCm38.p3 | 11:58968961 | TTGTCCCAGCGCTAC[A/G]CGGTGCCTCACAGCA | 56631 |
rs26971748 | snp | C/G | 0.5 | 0 | intron-variant | Trim17 | GRCm38.p3 | 11:58968765 | TTTGGGATTTTCTGT[C/G]TTGCCACAAACCCGT | 56631 |
rs26971749 | snp | A/C/G | 0.244898 | 0.249948 | intron-variant | Trim17 | GRCm38.p3 | 11:58968482 | CCCCCATTCCATTTC[A/C/G]ACAGGAGAGAGTGAA | 56631 |
rs26971750 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Trim17 | GRCm38.p3 | 11:58968457 | TCCATCTCATAGCCA[G/T]TTTGGGGTTCCCCCA | 56631 |
rs26971751 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trim17 | Mm_Celera | 11:58968430 | CCCTGAAGGAAATCC[A/C]TCCTTTCTGAATCCA | 56631 |
rs26971752 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim17 | GRCm38.p3 | 11:58968394 | TAGGTCACCGGTTGT[C/T]CCAGAATTGCTGTGT | 56631 |
rs26971753 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58968236 | TCTTTCTTTGAGGTT[G/T]CATGTTCTAAGCCCA | 56631 |
rs26971754 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim17 | GRCm38.p3 | 11:58968150 | ACAGCTTTAGGGACA[C/T]GGGTAACTCCAAAAT | 56631 |
rs26971755 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Trim17 | GRCm38.p3 | 11:58968096 | TAAGAAGTTTGTCTG[C/T]TGTCTTTGAAACTCT | 56631 |
rs26971756 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim17 | Mm_Celera | 11:58967075 | TAGAACACCTGAAGT[C/T]TGCCAGAGAACAAAA | 56631 |
rs26971757 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58966926 | CCTATCCTCATCTGT[A/G]ACAGGAAAGTGCCTT | 56631 |
rs26971758 | snp | A/G | 0.455 | 0.143091 | intron-variant | Trim17 | GRCm38.p3 | 11:58966700 | TCTGGGGTCGTCAGT[A/G]CAGCTGCAGAGACTG | 56631 |
rs26971759 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58965866 | AATCAAATGAGTTTA[C/T]GAAGTCCAGCAGAAA | 56631 |
rs26971760 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim17 | Mm_Celera | 11:58965825 | ATAGTGAGTAGCAGA[G/T]AGTCAGTACATAGAT | 56631 |
rs26971761 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58965764 | AGGGATGGTCTACAG[A/T]AGCCACGTTTATTAA | 56631 |
rs26971762 | snp | A/G | 0.408163 | 0.193609 | missense | Trim17 | GRCm38.p3 | 11:58965505 | CCAGGAGCACCGGAT[A/G]CACAGGGTGCTGCCT | 56631 |
rs26971763 | snp | A/C | 0.473373 | 0.11227 | synonymous-codon | Trim17 | GRCm38.p3 | 11:58965404 | CCTGGGCTGCAGAAG[A/C]GAGACCTGTGCCAAG | 56631 |
rs26971764 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon | Trim17 | Mm_Celera | 11:58965259 | GAGCTGGGAGAAGGG[C/G]AAGGTCAAGAAAGGG | 56631 |
rs26971765 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim17 | Mm_Celera | 11:58965015 | GGAGGCACTTGTGCT[A/G]TGCTGTACAGGGGCC | 56631 |
rs26971766 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58964978 | GGACAGCAGCTTTTG[C/T]TCCCATCTGTGGATC | 56631 |
rs26971767 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58964915 | GCTTAGCAACTGAGG[G/T]TCAGGGGTCTGGCTA | 56631 |
rs26971768 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Trim17 | GRCm38.p3 | 11:58964869 | CCCAGGAGGGAGCTC[A/G]TAACTAAGCTGACCC | 56631 |
rs26971769 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Trim17 | GRCm38.p3 | 11:58964600 | AGGCCCTGTACTTGC[C/G]TATGAATGTGCTGGT | 56631 |
rs26971770 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Trim17 | GRCm38.p3 | 11:58964477 | ATGCCTGTGTTTGTT[A/G]TGGTGTGTAAGTGGG | 56631 |
rs26971771 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58964302 | CTGAGAGTCGACCTC[A/G]TTCCCAAATTCTCAA | 56631 |
rs26971772 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58964170 | TTGGGTCGGGAGAAG[C/G]TAATGCCCTGTGCTC | 56631 |
rs26971773 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim17 | GRCm38.p3 | 11:58963997 | CCACTCTGATTACGT[A/G]GGTCTCCTGGATGAG | 56631 |
rs26971774 | snp | C/G | 0.497778 | 0.0332592 | intron-variant, utr-variant-5-prime | Trim17 | Mm_Celera | 11:58963895 | ACCGTCCAGAGAATT[C/G]GCTCGCTCACTCACT | 56631 |
rs26971775 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Trim17 | Mm_Celera | 11:58963042 | ATCAGAAATCAAACT[A/G]GGAGGAACCCGAGAT | 56631 |
rs26971776 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Trim17 | GRCm38.p3 | 11:58962937 | ATTCTCTGAGCCTTG[A/G]TTTTTCATACTGTCC | 56631 |
rs26971777 | snp | A/C | 0.459184 | 0.136902 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Trim17 | GRCm38.p3 | 11:58962838 | TCCTGTAGGGTACGA[A/C]AGTCTAGCTGTTGTC | 56631 |
rs26971778 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Trim17 | GRCm38.p3 | 11:58962592 | AAACGCATCTGCTCA[A/G]TAACCAAGTTACTTA | 56631 |
rs26971779 | snp | C/G | 0.18 | 0.24 | upstream-variant-2KB, intron-variant | Trim17 | Mm_Celera | 11:58962494 | TACTACAAGATGATG[C/G]TTGTGTTGCTGACTG | 56631 |
rs26971780 | snp | G/T | 0.484429 | 0.0868505 | upstream-variant-2KB, intron-variant | Trim17 | GRCm38.p3 | 11:58962455 | CCTGCCTTCCCTTGA[G/T]AGGTATAGTGGCCTG | 56631 |
rs26971781 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Trim17 | Mm_Celera | 11:58962114 | CTGCGAGTCGTACCT[C/T]GTGGGGCTGTTCGAA | 56631 |
rs26971782 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Trim17 | Mm_Celera | 11:58961985 | GCGCTACCAGAAGTC[C/G]ACCGAGCTGCTGATT | 56631 |
rs26971783 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Trim17 | Mm_Celera | 11:58961795 | TGAGGAGCAAGGGAG[A/G]CGGACGATTCAGGAA | 56631 |
rs26971784 | snp | A/G | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Trim17 | GRCm38.p3 | 11:58961637 | CCACACCACTCAGAG[A/G]GAATATAAGAGGCAG | 56631 |
rs26971785 | snp | A/G | 0.489796 | 0.070696 | intron-variant, upstream-variant-2KB | Trim17 | Mm_Celera | 11:58960806 | CTAAGCCTCAAAATT[A/G]TTATCCTTCTGATTC | 56631 |
rs26971786 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Trim17 | GRCm38.p3 | 11:58960568 | GGACTCACGTTTTTT[G/T]AAATTATGTGGACGA | 56631 |
rs26971787 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Trim17 | GRCm38.p3 | 11:58960561 | CTTTTCTGGACTCAC[A/G]TTTTTTGAAATTATG | 56631 |
rs26971788 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58960411 | CGCAGGCACGGGCTC[A/G]GGATTCCCCGCTTTG | 56631 |
rs26971789 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim17 | GRCm38.p3 | 11:58960393 | CTACCCGCGACCGCA[C/T]ACCGCAGGCACGGGC | 56631 |
rs26971790 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim17 | GRCm38.p3 | 11:58960132 | TGATCCAATTGGCTG[C/T]GTGAGGTGCAAGATG | 56631 |
rs26971791 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Trim17 | GRCm38.p3 | 11:58960122 | AAGCTCTGACTGATC[C/T]AATTGGCTGTGTGAG | 56631 |
rs26971792 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Trim17 | Mm_Celera | 11:58960043 | TGGAGAAGCGACGCG[C/T]TTTGCCCTCTCCGGC | 56631 |
rs26971793 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58959916 | AACCAACGCGGTGAC[A/G]GCTGTAGTCTGGCCT | 56631 |
rs26971794 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58959530 | CCCTGTCTAAGCTGG[C/T]GATGGGAAGAAATTG | 56631 |
rs26971795 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Trim17 | GRCm38.p3 | 11:58959399 | GGCTACCATCGACGT[C/T]AAAGAGTGCAGAGGC | 56631 |
rs26971796 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58959359 | CTGCTTAGGGATAAA[C/G]TGCAATGTTGTGATC | 56631 |
rs26971797 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58959183 | ACGATCTTTGAAATC[A/G]CTACAGTTGCTGACC | 56631 |
rs26971798 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Trim17 | GRCm38.p3 | 11:58959118 | CAATAGCAAACAGCT[A/C]GAATTTTAAAGCAAA | 56631 |
rs26971799 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58958997 | TATACCTGTTTTAGT[C/T]TTGAGCTGCTACGAC | 56631 |
rs26971800 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Trim17 | GRCm38.p3 | 11:58958826 | GTTTCCACAAATCCG[C/T]AACTCTCCCCAAACT | 56631 |
rs26971801 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Trim17 | Mm_Celera | 11:58958806 | GTGATAGCACCAAAA[C/T]CACCGTTTCCACAAA | 56631 |
rs26971802 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Trim17 | Mm_Celera | 11:58958665 | CAGTTGGACTCAGGC[C/T]GTGTAGACAGCTAAT | 56631 |
rs26971803 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Trim17 | GRCm38.p3 | 11:58958612 | CTTTCCATTCTGTCC[C/T]TCAAGCTAAATTCTG | 56631 |
rs26971804 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim17 | Mm_Celera | 11:58958575 | AGGCTAATGGGGTGC[C/T]TCAAGGACCACAGAG | 56631 |
rs26971805 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Trim17 | GRCm38.p3 | 11:58957800 | GTGTGTGGGAGCTCT[C/T]TGCCTGTCTCCGCAG | 56631 |
rs26971806 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Trim17 | GRCm38.p3 | 11:58957724 | GCTGAAGGCAAGAGA[C/G]AGGGTTCCAGAAGGA | 56631 |
rs26971807 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Trim17 | GRCm38.p3 | 11:58957625 | TGTGTGGAGGTATGG[A/T]GGTCTTTCCCTGGCC | 56631 |
rs26971808 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58956987 | CTTCATGTCCAGAAC[G/T]GGCAAAAGATACAGG | 56631 |
rs26971809 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim17 | GRCm38.p3 | 11:58956944 | ACGGAGCATTAGTCA[A/G]TGAAGGGACTGGACA | 56631 |
rs26971810 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim17 | Mm_Celera | 11:58956672 | TTAAAGGAAGTTCCA[A/G]TCATAGCAGCTGTGA | 56631 |
rs26971811 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Hist3h2bb-ps, Trim17 | GRCm38.p3 | 11:58956386 | TAGGTCATTGTAGCT[A/G]CTCAAACGCTTGAGT | 56631 |
rs26971812 | snp | A/G | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Hist3h2bb-ps, Trim17 | GRCm38.p3 | 11:58955806 | TAAACTAGGTGTGAG[A/G]GTACAGCAGTGTCCT | 56631 |
rs26971813 | snp | C/T | 0.48 | 0.0979796 | downstream-variant-500B, upstream-variant-2KB, intron-variant | Hist3h2a, Hist3h2bb-ps, Trim17 | GRCm38.p3 | 11:58955692 | TTAGTGGTAGGATTA[C/T]AGATGAGCATGGTGG | 56631 |
rs26971814 | snp | A/G | 0.21875 | 0.248039 | downstream-variant-500B, upstream-variant-2KB, intron-variant | Hist3h2a, Hist3h2bb-ps, Trim17 | GRCm38.p3 | 11:58955519 | TGTTCAAGTCTTCCA[A/G]TTAGGACGGGGTTTT | 56631 |
rs26971815 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B, upstream-variant-2KB, utr-variant-5-prime | Hist3h2a, Hist3h2bb-ps, Trim17 | Mm_Celera | 11:58955319 | CAAGGGAGACCAACG[A/G]CTTCATCTGCGGGTG | 56631 |
rs26971816 | snp | A/G | 0.207612 | 0.24638 | synonymous-codon, upstream-variant-2KB | Hist3h2a, Hist3h2bb-ps, Trim17 | Mm_Celera | 11:58955025 | CGAGGAGCTCAACAA[A/G]CTGCTGGGCCGCGTG | 56631 |
rs26971817 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, synonymous-codon | Hist3h2a, Hist3h2bb-ps, Trim17 | GRCm38.p3 | 11:58954441 | CATAATGTCTAGTTG[C/T]ACTACGGAAACGCGG | 56631 |
rs29383406 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim17 | Mm_Celera | 11:58967600 | AGGTGAATGTCTAGG[C/T]GCCCTAAGCCATCTC | 56631 |
rs29383515 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Trim17 | GRCm38.p3 | 11:58970725 | GCCACACAGGACCAG[A/C/T]GCTTCCAACTAGAAA | 56631 |
rs29386375 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Trim17 | GRCm38.p3 | 11:58967866 | CTTCTTCCTCTTCAC[A/G/T]GGAAACGGCCTGCTC | 56631 |
rs29387668 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Trim17, LOC105244174 | Mm_Celera | 11:58972000 | AGACATGAGGGTGGC[A/G]CTGGAGGCTCTGAGC | 56631 |
rs29391052 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim17 | GRCm38.p3 | 11:58967855 | GCAAAGGCTGACTTC[C/T]TCCTCTTCACAGGAA | 56631 |
rs29406898 | snp | C/G | 0.444444 | 0.157135 | synonymous-codon, upstream-variant-2KB | Hist3h2a, Hist3h2bb-ps, Trim17 | Mm_Celera | 11:58954869 | TTATTCGGAGCGGGT[C/G]GGCGCTGGTGCCCCG | 56631 |
rs29414912 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Trim17, LOC105244174 | Mm_Celera | 11:58972039 | GTGCTGCGGGCTATG[A/G]ACACAGAGTAAAAGT | 56631 |
rs29416691 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, synonymous-codon | Hist3h2a, Hist3h2bb-ps, Trim17 | Mm_Celera | 11:58954096 | GGTGCCCTCGGACAC[A/G]GCATGCTTGGCCAGC | 56631 |
rs29420574 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim17 | GRCm38.p3 | 11:58958523 | CAACTGGGAAATCAG[C/T]GGGGGTCAGCTGGAA | 56631 |