SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3673417 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxw11 | Mm_Celera | 11:32649598 | AGCTGTACATATGGA[A/T]ACCTGGAGAGCCTTC | 103583 |
rs3719109 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw11 | Mm_Celera | 11:32697733 | TTTTTTTTCTTTTTA[C/T]CATTTTCTTTCTTAT | 103583 |
rs6190386 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32712465 | GCACACATGTGCGCA[C/T]GCGCGCACACACACA | 103583 |
rs6196269 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Fbxw11 | Mm_Celera | 11:32746239 | AGGGGGAGGGGAAGA[A/G]GTGAGTTCTGCACAG | 103583 |
rs6252070 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw11 | Mm_Celera | 11:32650364 | TTCTGATTAATGTTT[C/T]ATTGTTTTAGGGTGT | 103583 |
rs6252110 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw11 | Mm_Celera | 11:32643831 | ACACCCCTAACCCGT[C/T]TCTGACCTCAGACTT | 103583 |
rs6252480 | snp | C/G | 0.5 | 0 | intron-variant | Fbxw11 | Mm_Celera | 11:32643847 | TCTGACCTCAGACTT[C/G]GTGCTAGAAAGGTTT | 103583 |
rs6252600 | snp | A/G | 0.5 | 0 | intron-variant | Fbxw11 | Mm_Celera | 11:32650493 | AATTAGTTGACAGTG[A/G]GGGAAAACCTGTTGG | 103583 |
rs6265923 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxw11 | Mm_Celera | 11:32650688 | GTTTTGTGATGTCAG[C/T]AGGAAGATTGCTTAG | 103583 |
rs6280308 | snp | A/G/T | 0.294052 | 0.246088 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32717589 | GCTCACGAAGGTGTC[A/G/T]GGACTTTGGAGAATG | 103583 |
rs6319541 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32732793 | CTGCAGTGGGCGTGG[A/G]TAAGCTGCAGGGTGC | 103583 |
rs6333546 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32733035 | GCCCGCTCTGTCATC[G/T]CATGACCTGTTTCAA | 103583 |
rs6333960 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw11 | Mm_Celera | 11:32733054 | GACCTGTTTCAATTC[C/T]TAAGTGCTTAGTTTG | 103583 |
rs6408720 | snp | C/T | 0.5 | 0 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32665172 | TACCCACAGATGCTT[C/T]AGTTTGGGAGTTAAC | 103583 |
rs6408722 | snp | G/T | 0.5 | 0 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32665175 | CCACAGATGCTTTAG[G/T]TTGGGAGTTAACCTT | 103583 |
rs13460205 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Fbxw11 | GRCm38.p3 | 11:32745442 | TTTATTTGTTGTGTG[A/G]CATCTGCAGTGGGCA | 103583 |
rs26824723 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Fbxw11 | GRCm38.p3 | 11:32746997 | CCCTGCAGGTCCGTG[C/T]CTCAGGTGAGCGTGA | 103583 |
rs26824724 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32743958 | CATGTCACTGTGGCA[G/T]AGTTGAGGAGCTGGG | 103583 |
rs26824725 | snp | C/T | 0.42 | 0.183303 | intron-variant | Fbxw11 | Mm_Celera | 11:32743757 | GGGCTTAACACACTG[C/T]AGCCAAGCATTGAAT | 103583 |
rs26824726 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Fbxw11 | Mm_Celera | 11:32743325 | TCCTACCTGGAAGAT[A/T]TGCCGGGATCCATTA | 103583 |
rs26824727 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Fbxw11 | Mm_Celera | 11:32743132 | CTTAATTATGCTGTG[C/T]ATTCTTCATGGTGAG | 103583 |
rs26824728 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Fbxw11 | Mm_Celera | 11:32743041 | TGCCCATGCATGCGC[A/G]CACACAGGACCATCC | 103583 |
rs26824729 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32742969 | GCAGAAATCAACCTT[C/T]TTACCTGGTCTTTCA | 103583 |
rs26824730 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32742907 | AGTTCCTTCATGATC[A/G]TAGCCATTTAACACC | 103583 |
rs26824731 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Fbxw11 | Mm_Celera | 11:32742772 | AAAGCATCTACCAGA[A/C]TAGCAGGTAAGGTCT | 103583 |
rs26824732 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32742450 | GTTAACCAAGCCGCT[C/T]TTCCATAGGAACACT | 103583 |
rs26824733 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32742448 | ATGTTAACCAAGCCG[C/T]TTTTCCATAGGAACA | 103583 |
rs26824734 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32741947 | TACAGTATATCCTGA[A/G]TGGGTATTACTCTGA | 103583 |
rs26824735 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32741673 | ACTGCTATGACTTAA[C/T]ACAGATGTTCTTGGT | 103583 |
rs26824736 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxw11 | Mm_Celera | 11:32741586 | GCTCTCTAGGCCCAG[C/G]AGTTGTATCTGCATT | 103583 |
rs26824737 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32741381 | GACACACACCTCTAA[A/T]CTTCACAGATAAATC | 103583 |
rs26824738 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Fbxw11 | Mm_Celera | 11:32741079 | GGTCAGTGTCTGCCC[A/G]TGTCTGCTTTATTAT | 103583 |
rs26824739 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32741078 | GGGTCAGTGTCTGCC[C/T]GTGTCTGCTTTATTA | 103583 |
rs26824740 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxw11 | Mm_Celera | 11:32740341 | AGGTATTTTTGGCCA[A/G]CCAGAACATAGTTCA | 103583 |
rs26824741 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Fbxw11 | Mm_Celera | 11:32740108 | TAGACCTTTCAAGTG[A/T]ACTGTTTTGTCATGG | 103583 |
rs26824742 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw11 | Mm_Celera | 11:32740013 | CTGAGAGGGGTTAGG[C/T]TCTTTTTCTAAAATC | 103583 |
rs26824743 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Fbxw11 | Mm_Celera | 11:32739416 | AAGCTGAAGTAAAGC[A/C]TGCCTCAATCGTGTT | 103583 |
rs26824744 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32739361 | TCTATGAGAAAGATC[C/T]GTCATAGCAGTGGGT | 103583 |
rs26824745 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Fbxw11 | Mm_Celera | 11:32739331 | GTGTATTAAACAGCA[A/G]TGTGAATGCAGAACT | 103583 |
rs26824746 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32739119 | GCGTGAGTCATGTGA[A/G]AGAATTTGTTTCATA | 103583 |
rs26824747 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Fbxw11 | Mm_Celera | 11:32738799 | CTCATGTCCACATCT[C/T]CAGAAAAACTTTTCC | 103583 |
rs26824748 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32738359 | ACTGCTGCCTTCCTG[C/T]AGGTGTGGAGCACGA | 103583 |
rs26824749 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fbxw11 | Mm_Celera | 11:32738332 | GCTCTCTGAAGGTGT[C/T]GTCCTAACTGCACTG | 103583 |
rs26824750 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32738196 | CAGTGGCCAACTTCC[A/G]TTCAGCCTATCATTA | 103583 |
rs26824751 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32737924 | GACTCACAAGAGGAG[A/G]CTGTTTAAATCCTGT | 103583 |
rs26824752 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Fbxw11 | Mm_Celera | 11:32737825 | GCTGCTGTCGCTCTC[A/G]CTCGGGACTCTGGCC | 103583 |
rs26824753 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Fbxw11 | Mm_Celera | 11:32737478 | TATACACTATGGATA[A/T]GAGGCCCTTAATCAG | 103583 |
rs26824754 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Fbxw11 | Mm_Celera | 11:32736616 | GGAGATTGCTCCACT[C/G/T]GCCACCTGTCCACAC | 103583 |
rs26824755 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Fbxw11 | Mm_Celera | 11:32736541 | CCATATGCCAAGAGT[C/G]AGCACAAGATCAGCC | 103583 |
rs26824756 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Fbxw11 | Mm_Celera | 11:32736479 | TATATCACATGAAAC[C/T]GGAGGTGTCTGAGAG | 103583 |
rs26824757 | snp | A/C | 0.18 | 0.24 | intron-variant | Fbxw11 | Mm_Celera | 11:32735871 | TTGTAGACTAAGATA[A/C]CCTGCAGCACCGGTG | 103583 |
rs26824758 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32735631 | TGTATAGGAGTTTTA[A/T]ACAGGTCATCTCATC | 103583 |
rs26824759 | snp | C/T | 0.473373 | 0.11227 | synonymous-codon | Fbxw11 | Mm_Celera | 11:32735258 | GGACCGTTCCATTGC[C/T]GTGTGGGACATGGCT | 103583 |
rs26824760 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon | Fbxw11 | Mm_Celera | 11:32735246 | GACTTGTTCCAAGGA[C/T]CGTTCCATTGCCGTG | 103583 |
rs26824761 | snp | C/G | 0.18 | 0.24 | intron-variant | Fbxw11 | Mm_Celera | 11:32735046 | GCCAGGGATCTGCTG[C/G]TGCTACCACACACCT | 103583 |
rs26824762 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32734787 | GTGCTCTGACAAAAT[A/G]CCACAGCTTAGTTTG | 103583 |
rs26824763 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw11 | Mm_Celera | 11:32734521 | CAGGACATAGGATAG[C/T]TGCTCATTCTACCTC | 103583 |
rs26824764 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32734471 | AAGCAGCAAATCTTA[C/T]GTGATTCAGATGCTT | 103583 |
rs26824765 | snp | C/G | 0.375 | 0.216506 | intron-variant | Fbxw11 | Mm_Celera | 11:32734288 | CTAGTAGTTGGGTAT[C/G]AAAGATTAAAAAGGG | 103583 |
rs26824766 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Fbxw11 | Mm_Celera | 11:32734232 | TTTTTAGTTGTCAAC[C/T]CAGGATAGAGTGGAG | 103583 |
rs26824767 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Fbxw11 | Mm_Celera | 11:32734164 | TGAGCCTTGAGTTTA[A/G]GTAACCTGTGACTGT | 103583 |
rs26824768 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32733940 | CAGAGGGGAAGAAGT[C/T]CGCTGTTGTTGAAGT | 103583 |
rs26824769 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Fbxw11 | Mm_Celera | 11:32733665 | GAGGAGACAAGGATG[C/T]GTACCCTCTTCAGAG | 103583 |
rs26824770 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Fbxw11 | Mm_Celera | 11:32732967 | AGGAAGAGCTCAGGC[C/G]TGAGAGGAGCCGTTT | 103583 |
rs26824771 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Fbxw11 | Mm_Celera | 11:32732909 | GATTGGTTCAGTGTG[A/T]GCTGTTCTGAAAGAG | 103583 |
rs26824772 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Fbxw11 | Mm_Celera | 11:32731757 | CCTCATACCCAGGAA[C/T]CCAGTGGCCTTCCCA | 103583 |
rs26824773 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxw11 | Mm_Celera | 11:32731332 | TCTTGCCTCCTTTCT[C/T]CAGACCATAGAATCC | 103583 |
rs26824774 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Fbxw11 | Mm_Celera | 11:32730545 | GAATATGCTAACAGC[C/T]CATTAAACAACACAT | 103583 |
rs26824775 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxw11 | Mm_Celera | 11:32729835 | TGTTCTGTGTTCTCT[A/G]CCTAAGAGCTAAGAC | 103583 |
rs26824776 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32729714 | ACTTCCTCATTGAAC[C/T]GGGCCATGGTCTCAG | 103583 |
rs26824777 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxw11 | Mm_Celera | 11:32728545 | GGCATGTGCCATCCC[A/G]CTTGTTGATTGTTCA | 103583 |
rs26824778 | snp | C/G | 0.18 | 0.24 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32728526 | CTGTTGTCTCTAAGG[C/G]TTGGGCATGTGCCAT | 103583 |
rs26824779 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32728222 | AATATCTGGCTTCCT[A/T]AGTCAGCATTTCCCT | 103583 |
rs26824780 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32727858 | TTAAAAATCATGGCC[A/G]GCTCACCCATTCTAG | 103583 |
rs26824781 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Fbxw11 | Mm_Celera | 11:32727813 | TCCTCTTCCTCATCC[A/G]TTCTCTGTGTCCTAG | 103583 |
rs26824782 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Fbxw11 | Mm_Celera | 11:32727812 | CTCCTCTTCCTCATC[C/T]GTTCTCTGTGTCCTA | 103583 |
rs26824783 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32727215 | GCTGTTCTGCTCAGC[C/T]ACACCATTGGCCGAG | 103583 |
rs26824784 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw11 | Mm_Celera | 11:32726966 | AGTAGCTGAGTTCCA[C/T]GTGAAGGCTGAGCAC | 103583 |
rs26824785 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Fbxw11 | Mm_Celera | 11:32726934 | TGTGACTGGCCTCGA[C/T]GCGGCCTCACTGGGG | 103583 |
rs26824786 | snp | A/G | 0.18 | 0.24 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32726891 | ACCTTACGGCATGGT[A/G]CGGCAGGTATTAGAG | 103583 |
rs26824788 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32725479 | CTCTACTGAATGAAA[A/C]CCTCTACAGTAGCTG | 103583 |
rs26824789 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxw11 | Mm_Celera | 11:32725435 | CAGTGTTTTGAGATT[C/T]TGCGAAGGGTAAGGC | 103583 |
rs26824790 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32724983 | CCACAAGGGACTTGG[C/T]TAGGTGGCCTCCAGG | 103583 |
rs26824791 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxw11 | Mm_Celera | 11:32724916 | AAGAGGGCAGCCACA[C/G]TTTCCTAGAGTCCTT | 103583 |
rs26824792 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Fbxw11 | Mm_Celera | 11:32724774 | GAGAATCAGAGTCTG[A/T]GGAGAATAGTTCACA | 103583 |
rs26824793 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Fbxw11 | Mm_Celera | 11:32724730 | TGGTTTTGTGTGGCT[A/T]GTTCCTGCTGTTCAG | 103583 |
rs26824794 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxw11 | Mm_Celera | 11:32724604 | CTCCTCAAGTACAAC[A/G]CTCTCAGCTTGGGCT | 103583 |
rs26824795 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Fbxw11 | Mm_Celera | 11:32724587 | CCTTGACAGCTTGCT[A/G]ACTCCTCAAGTACAA | 103583 |
rs26824796 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Fbxw11 | Mm_Celera | 11:32724539 | CCCACAGATCGGCTC[C/T]TCCTCGATCCCACTC | 103583 |
rs26824797 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Fbxw11 | Mm_Celera | 11:32724503 | CTCCCTGGCCTGCAC[A/G]CAGCTCCGTCTGTTC | 103583 |
rs26824798 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Fbxw11 | Mm_Celera | 11:32724479 | AGGAACACGAGAGAG[A/T]GTCCTGGCCTCCCTG | 103583 |
rs26824799 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxw11 | Mm_Celera | 11:32724410 | CGGGCCTTGCTTTAG[C/T]TCTGTTAGGGAAAAG | 103583 |
rs26824800 | snp | C/T | 0.42 | 0.183303 | intron-variant | Fbxw11 | Mm_Celera | 11:32724387 | CCTTGACTGTTCAGA[C/T]GAGATCCCGGGCCTT | 103583 |
rs26824801 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxw11 | Mm_Celera | 11:32724371 | ATGTGGACACTCAGC[A/G]CCTTGACTGTTCAGA | 103583 |
rs26824802 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Fbxw11 | Mm_Celera | 11:32724330 | AAAGGCATGCTTTAT[C/T]CCTGTAGACTTGTCT | 103583 |
rs26824803 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32724322 | TGAAGGAGAAAGGCA[C/T]GCTTTATTCCTGTAG | 103583 |
rs26824804 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Fbxw11 | GRCm38.p3 | 11:32724299 | TCCAAAGTAGAAAGT[C/G/T]GAGGAAGTGAAGGAG | 103583 |
rs26824805 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Fbxw11 | Mm_Celera | 11:32724005 | CTCTCATGGTCACGT[G/T]ATCGAGTGGTACAGT | 103583 |
rs26824806 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Fbxw11 | Mm_Celera | 11:32723743 | AGTTTCTTAGTATGA[A/G]GGATGACGCTTATAC | 103583 |
rs26824807 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Fbxw11 | Mm_Celera | 11:32723657 | ATGGTGGTCTTCCCC[A/G]TGGTTCTTAAAGTGT | 103583 |