SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3710725 | snp | C/T | 0.5 | 0 | intron-variant | Cfap44 | Mm_Celera | 16:44476611 | GAAGTATGATCAGCA[C/T]ATTACAAGGCTGTCT | 212517 |
rs4179717 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Cfap44 | Mm_Celera | 16:44393696 | TGTTTCCAACTTTAA[C/T]CTGTTACAAATAAAC | 212517 |
rs4179718 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Cfap44 | Mm_Celera | 16:44393996 | TGTTCATTGGTATTT[G/T]TATGCCTTCTTTCAT | 212517 |
rs4179719 | snp | C/T | 0.362812 | 0.2231 | upstream-variant-2KB | Cfap44 | Mm_Celera | 16:44394588 | CATCTGGTTCATAAA[C/T]TGTTGGAATGCTGGG | 212517 |
rs4179720 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Cfap44 | Mm_Celera | 16:44394770 | CCAGCAGGCGGAGGG[A/G]CGTTGCTATGGCAAC | 212517 |
rs4179721 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44398097 | CAGAAAGCATTGTGA[C/T]GCTTTTGTCCTTGTA | 212517 |
rs4179722 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44398365 | GCATTATCAAGATAG[A/C]GAGCGAGAGACACCC | 212517 |
rs4179723 | snp | A/G | 0.32 | 0.24 | intron-variant | Cfap44 | Mm_Celera | 16:44399367 | ACCCACCCAAGAGCA[A/G]CTTCCCAATCAACCT | 212517 |
rs4179724 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44399787 | ATGGAGAAAGGGAGC[A/G]GCTTATACGTAGTTG | 212517 |
rs4179725 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44399885 | TGACATGCTAATCCA[C/T]CTACTCTTCATACAT | 212517 |
rs4179726 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44400978 | TTGATCAAAAACCAA[C/T]TGGGGACAAGGACCT | 212517 |
rs4179727 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44404411 | GTCCCCTGTTGGAAG[C/T]GTGGCCAGCACGCGC | 212517 |
rs4179728 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Cfap44 | Mm_Celera | 16:44404645 | TGAAGTTAAGGAAGA[A/G]CCAGAAGCCGACGTA | 212517 |
rs4179729 | snp | C/T | 0.265928 | 0.249492 | synonymous-codon, nc-transcript-variant | Cfap44 | Mm_Celera | 16:44404720 | TGTTTCCATACCATA[C/T]GTGTCTTCGGAAGAG | 212517 |
rs4179730 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44404805 | AACGCGGGAGGGTTT[C/T]GTTTCCTAGGTCAGG | 212517 |
rs4179731 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44407670 | GAAGCCCAAGCTGGC[C/T]TTAAAGTCAGTACAG | 212517 |
rs4179733 | snp | A/G | 0.32 | 0.24 | intron-variant | Cfap44 | Mm_Celera | 16:44408653 | CTTCATTATCACTAC[A/G]AATTTAATACTCATA | 212517 |
rs4179734 | snp | A/T | 0.32 | 0.24 | intron-variant | Cfap44 | GRCm38.p3 | 16:44410589 | AAGATATAAAGATAA[A/T]TTTTACTATCATTAA | 212517 |
rs4179735 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44411550 | GCACGCCTGCGGTTC[C/T]TCAGTCACCCGGACT | 212517 |
rs4179736 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44412019 | GTTTGCTTCTTTGTT[A/T]TTTTTTTTTTTTCCT | 212517 |
rs4179737 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44412375 | ACCTCTGGCCTCCAC[A/G]GAAGAACTAAGTTCT | 212517 |
rs4179738 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Cfap44 | Mm_Celera | 16:44414321 | ACCTTGTGCTGGGGA[A/G]CTCAGAGATTTCACT | 212517 |
rs4179739 | snp | G/T | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Cfap44 | Mm_Celera | 16:44414564 | ATGTACACATTTATC[G/T]TCTTTCTTTCTTTCT | 212517 |
rs4179740 | snp | C/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44415554 | TTGGTTGTGAGCCTA[C/G]CCTTTAACAACTGAG | 212517 |
rs4179741 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44415563 | AGCCTAGCCTTTAAC[A/G]ACTGAGCCATCTCTC | 212517 |
rs4179742 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44415564 | GCCTAGCCTTTAACA[A/G]CTGAGCCATCTCTCC | 212517 |
rs4179743 | snp | A/G | 0.32 | 0.24 | intron-variant | Cfap44 | Mm_Celera | 16:44415639 | GGATGAAGCTTCCAG[A/G]TCTTCACCAACGTGA | 212517 |
rs4179744 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap44 | Mm_Celera | 16:44415650 | CCAGATCTTCACCAA[C/T]GTGATTTTGCCATGT | 212517 |
rs4179745 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44416414 | GTAAGTGCCCGTTTT[C/T]CTTATTTTCTCCTAA | 212517 |
rs4179746 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Cfap44 | Mm_Celera | 16:44416547 | TCCTAAACACAGGGA[A/G]TCTTCATTTCTATTA | 212517 |
rs4179747 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Cfap44 | Mm_Celera | 16:44416651 | TCATTAACTTCAGAG[C/T]CAGGACTCCATCTGG | 212517 |
rs4179748 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Cfap44 | Mm_Celera | 16:44416747 | TTTTATTTATTGTCT[A/C]TAAGGTTGACTTTAA | 212517 |
rs4179749 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44416773 | TTTAATTATATATGA[C/T]GCTGTCTTTGAGATC | 212517 |
rs4179750 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44417116 | GGTGTTCTGATGTAT[A/G]TGTGTGTATAATATC | 212517 |
rs4179751 | snp | C/T | 0.5 | 0 | intron-variant | Cfap44 | Mm_Celera | 16:44417128 | TATGTGTGTGTATAA[C/T]ATCAGGAATCTTTCT | 212517 |
rs4179752 | snp | C/T | 0.5 | 0 | intron-variant | Cfap44 | Mm_Celera | 16:44417141 | AATATCAGGAATCTT[C/T]CTCCACTGCTTTGCA | 212517 |
rs4179753 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44417238 | GGCAGCTCCAGGGAT[C/T]CTCTGTCTCTGCCTT | 212517 |
rs4179754 | snp | A/G | 0.499055 | 0.0217186 | intron-variant | Cfap44 | Mm_Celera | 16:44417421 | ATGCAAACTGAAAAC[A/G]TGTGGCTATTAGAGG | 212517 |
rs4179755 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Cfap44 | Mm_Celera | 16:44417725 | GGCCCTTGAGATCAG[G/T]GGAAGGAGGCTCTCA | 212517 |
rs4179756 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44417849 | GAGAGAGGCAGGCAG[A/G]CAGTGTTTGTGCAGG | 212517 |
rs4179757 | snp | G/T | 0.495 | 0.0497494 | intron-variant | Cfap44 | Mm_Celera | 16:44417914 | CGCCGCAAGGAAATC[G/T]GTTACCATGCATGCT | 212517 |
rs4179758 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cfap44 | Mm_Celera | 16:44418557 | TGGATAAAGACTACC[C/T]TCAATGTACCGTGGT | 212517 |
rs4179759 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cfap44 | Mm_Celera | 16:44419827 | TATATACAGAAATAC[A/G]TATGTATAGACACAT | 212517 |
rs4179760 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44420507 | CAAAGCTTCATGCCT[C/T]CCTATCCTGCCTTCA | 212517 |
rs4179761 | snp | A/G | 0.32 | 0.24 | intron-variant | Cfap44 | Mm_Celera | 16:44420552 | AGAGACGGGGTTAGG[A/G]TGCATTGTCAGGAAT | 212517 |
rs4179762 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cfap44 | Mm_Celera | 16:44420783 | GCTCCTTGGAACTCA[C/T]TCTGTAGACCAGGCT | 212517 |
rs4179763 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cfap44 | Mm_Celera | 16:44420859 | GGATTAAAGGCATGC[A/G]CCACCACTCCCCAGC | 212517 |
rs4179764 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Cfap44 | Mm_Celera | 16:44420924 | AATCTAATTTTAGTC[A/T]TCAGGTTAGTAATGA | 212517 |
rs4179765 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44421104 | TTCCTTCTTTCCTTT[A/C]TTTTTTTCCTTTTTT | 212517 |
rs4179766 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44424527 | CAACTATAGTTAGCA[C/T]TTCAAAATGATCATG | 212517 |
rs4179767 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cfap44 | GRCm38.p3 | 16:44426141 | AGAAAATCTTTTGTT[A/G]AAAATAAAAATCTTC | 212517 |
rs4179768 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cfap44 | Mm_Celera | 16:44426206 | TCATTTCCTCCCAGA[C/T]ACTCTCTACCTCCCG | 212517 |
rs4179769 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44426612 | TGGACATAGCTTCTT[A/G]ATTAGTAGTCGAGCT | 212517 |
rs4179770 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44426701 | CCAACCGCAGACAGC[C/T]GTCAGTCTACTCCCT | 212517 |
rs4179771 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44426791 | GTTCTCCAGGTTCAT[C/T]CATTCCACAGAGTAT | 212517 |
rs4179772 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44426909 | AACACATAGATCATG[C/T]CTACCCTTTGGCTGA | 212517 |
rs4179773 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44426935 | GCTGATGGGAATAAC[A/G]CTTTGTACACATGGG | 212517 |
rs4179774 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Cfap44 | Mm_Celera | 16:44427997 | TTACTATTACCTCCT[A/T]AAGATTTCTCTTTGC | 212517 |
rs4179775 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | GRCm38.p3 | 16:44428803 | AGTACAAAAGTAACT[C/T]GTCTCTGGGTATTCA | 212517 |
rs4179776 | snp | C/T | 0.35124 | 0.228584 | intron-variant | Cfap44 | Mm_Celera | 16:44429023 | CAAGGAGCTGCAGGT[C/T]GACTCTTTCAGCTTC | 212517 |
rs4179777 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44429051 | TTCTTTGTCTCTGTA[C/T]CCATCACCAATTTAT | 212517 |
rs4179778 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44429176 | TGTTATTTTCTTCCC[C/T]GATTATCCCCAGTGG | 212517 |
rs4179779 | snp | A/G | 0.362812 | 0.2231 | intron-variant | Cfap44 | Mm_Celera | 16:44429312 | TCATTTATTTCATGT[A/G]TAGATGTCCAGGCAT | 212517 |
rs4179780 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44430186 | TATAAATGAGTGTTC[A/G]GCTGCTCTTGTCTTT | 212517 |
rs4179781 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44430285 | TTAAAGTAATGGAGA[A/G]AATTCCTTACAGGCG | 212517 |
rs4179782 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Cfap44 | Mm_Celera | 16:44430360 | TGATAAGAGTACCGG[C/T]CATAACTGGAATTGT | 212517 |
rs4179783 | snp | C/T | 0.340265 | 0.233136 | intron-variant | Cfap44 | Mm_Celera | 16:44430516 | TATGGCAGTTTCTGT[C/T]TATCACATAAATCTG | 212517 |
rs4179784 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44430995 | TGGATTAGGATTTCT[C/T]GTTATGCTCTCATCT | 212517 |
rs4179785 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44431212 | ACCAGGCTGGCCTCG[A/G]ACTCAGAAATCTGCC | 212517 |
rs4179786 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Cfap44 | Mm_Celera | 16:44431569 | TGCTACCCAGCAGAC[G/T]TGGAACATCCGCGTG | 212517 |
rs4179787 | snp | A/C/G | 0.375 | 0.216506 | synonymous-codon, nc-transcript-variant | Cfap44 | GRCm38.p3 | 16:44432196 | AGCCAAAGTACCATC[A/C/G]CCCAGGGTATGTAAG | 212517 |
rs4179788 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Cfap44 | Mm_Celera | 16:44432319 | GACTAAGTTATATAT[A/G]TTAACCTCATAATGT | 212517 |
rs4179789 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Cfap44 | Mm_Celera | 16:44432530 | GACAAAGTTTCTTTT[A/T]CTTCTTCAAAATGGG | 212517 |
rs4179790 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44432549 | CTTCAAAATGGGCAA[A/T]ATTTTTCAGATCTAT | 212517 |
rs4179791 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44432666 | AGAGTTGTTCTGACA[C/T]ACATCTTAAGAACTC | 212517 |
rs4179792 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Cfap44 | Mm_Celera | 16:44433001 | GGCTTCTCTTTTAAA[A/G]TTTAAGGATGTTCTC | 212517 |
rs4179793 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44434422 | GACTCGGCTACTTCT[A/C]TGATGTGCTTTTTCT | 212517 |
rs4179794 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44435038 | GAATTTTAGTTCAAT[C/T]CCCAGTAGTCTCATA | 212517 |
rs4179795 | snp | A/G | 0.5 | 0 | intron-variant | Cfap44 | Mm_Celera | 16:44435064 | TCATAAGAAGCAGGC[A/G]TGGTGGAGCGTGCTA | 212517 |
rs4179796 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44435154 | CTTGTAAGACAGCCA[C/T]CCTGGCCTAACTGGC | 212517 |
rs4179797 | snp | C/T | 0.5 | 0 | intron-variant | Cfap44 | Mm_Celera | 16:44436821 | GCATAGGGCAGTAGA[C/T]TACACATATTCAGAG | 212517 |
rs4179798 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | GRCm38.p3 | 16:44437908 | ATTACTTAAGGGCAT[A/C/T]CTGTAAGGAGCTGGT | 212517 |
rs4179799 | snp | A/G | 0.329861 | 0.236901 | intron-variant | Cfap44 | Mm_Celera | 16:44438570 | ACTCTGTAACAGTGT[A/G]TAAGCATACCCACCT | 212517 |
rs4179802 | snp | A/G | 0.5 | 0 | intron-variant | Cfap44 | Mm_Celera | 16:44442201 | ACTTCCCAAACATAA[A/G]GAAAGAGATGCCCAT | 212517 |
rs4179807 | snp | A/T | 0.5 | 0 | intron-variant | Cfap44 | Mm_Celera | 16:44447094 | TTGTTGTTGTTGTTG[A/T]TTGTTGTTTTTTAAA | 212517 |
rs4179808 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44447328 | TGATATCCTTTCTTG[C/T]CTTGTTTTAGCATTA | 212517 |
rs4179809 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Cfap44 | GRCm38.p3 | 16:44447344 | CTTGTTTTAGCATTA[A/G/T]TTGGGTGTTTCTTTC | 212517 |
rs4179810 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44447555 | TCTGTTTCATTTAAA[C/T]GTGTGCTGCTTAGTT | 212517 |
rs4179811 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cfap44 | Mm_Celera | 16:44447633 | TTTCATTTCTTATTA[C/T]CATAGAAAGCAATTA | 212517 |
rs4179812 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap44 | Mm_Celera | 16:44448017 | TCTCCTCAACTAGTG[A/G]GCTTGCTGGGTTACG | 212517 |
rs4179813 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cfap44 | Mm_Celera | 16:44448129 | TTTGCTTGAATTCTC[C/T]GAAGAGTTGGTTTCC | 212517 |
rs4179814 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cfap44 | Mm_Celera | 16:44448132 | GCTTGAATTCTCTGA[A/G]GAGTTGGTTTCCTAT | 212517 |
rs4179815 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44448185 | TGATGCTTGCATGTC[C/T]GAGTGTAGCCATCTC | 212517 |
rs4179816 | snp | C/T | 0.2688 | 0.249292 | intron-variant | Cfap44 | Mm_Celera | 16:44451020 | GTAAACAGTAAACAG[C/T]AAACAGTGGCAAAGA | 212517 |
rs4179817 | snp | A/T | 0.32 | 0.24 | intron-variant | Cfap44 | Mm_Celera | 16:44451066 | GGAGGACTTATAGTT[A/T]GGACATAGATGGGCA | 212517 |
rs4179818 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Cfap44 | Mm_Celera | 16:44451308 | GACCCCCGAAAGCCA[A/G]AGGAAAGCATAATTG | 212517 |
rs4179819 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44451405 | CGTTCCAGACCACCC[C/T]GTGTGAGTAGGCTGT | 212517 |
rs4179820 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44451411 | AGACCACCCCGTGTG[A/G]GTAGGCTGTGCTGTT | 212517 |
rs4179821 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Cfap44 | Mm_Celera | 16:44452383 | cctctgtgtttctgt[C/G]tttctgtctctTTGG | 212517 |
rs4179822 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cfap44 | Mm_Celera | 16:44453177 | CTGTTTCCCGCATGG[C/T]GTCTAGCCGTAAGGC | 212517 |