SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4224440 | snp | A/T | 0.21875 | 0.248039 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41291441 | ACAAGAGTTTTGTTT[A/T]CTTAAACACACAAGT | 68970 |
rs4224441 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41291501 | ACTAAGACATCTACA[A/G]CCTGTAGTTTAAGAA | 68970 |
rs4224442 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41291601 | TTTCTCTAGATTATA[A/G]GATGATTATTCTAAA | 68970 |
rs4224443 | snp | A/C | 0.21875 | 0.248039 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41291625 | TTCTAAAACCTGTGG[A/C]GGATGCTGTGTCCTA | 68970 |
rs4224444 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41291626 | TCTAAAACCTGTGGA[A/G]GATGCTGTGTCCTAC | 68970 |
rs4224445 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41291658 | GTGGGCCTGCCGCTT[C/T]CCTCCCCAGCAGCCC | 68970 |
rs4224446 | snp | G/T | 0.21875 | 0.248039 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41291741 | GAGCAACTGAGAAAC[G/T]GGGTGCAGGTGTATG | 68970 |
rs13473869 | snp | A/C | 0.32 | 0.24 | missense, utr-variant-5-prime | Dcaf12 | GRCm38.p3 | 4:41313412 | CCCCCCAGTGAAGAG[A/C]TCCCTAGTGTACTAC | 68970 |
rs28303122 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Dcaf12 | Mm_Celera | 4:41318662 | AGGAAGCCGAGCAAA[C/T]GAAACAAACAATGAA | 68970 |
rs28303123 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, utr-variant-5-prime | Dcaf12 | Mm_Celera | 4:41316703 | TTAACACATTGTGAG[C/T]GGGCAGGACTGTGGC | 68970 |
rs28303124 | snp | A/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Dcaf12 | Mm_Celera | 4:41315772 | CAGTATGGTCAGATT[A/T]TTGCCACATCAAAGT | 68970 |
rs28303125 | snp | C/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Dcaf12 | GRCm38.p3 | 4:41315465 | GATAAGAGAATGTCC[C/G]GTCGTTGTTCTTTCC | 68970 |
rs28303126 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | Dcaf12 | Mm_Celera | 4:41315010 | CCTCTTGCCAATGGC[A/G]GTTAAGCTGTGGCCA | 68970 |
rs28303127 | snp | A/C | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | Dcaf12 | Mm_Celera | 4:41314902 | TGCGCAGCCGCACAT[A/C]GCAGCACGTCGCCAC | 68970 |
rs28303128 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41312860 | CACTACAGTTTACTC[A/T]TTCCTTGAGCACTTC | 68970 |
rs28303129 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41312784 | GGACAAGGTCACCAA[C/T]GAAGGAGGAGGGAGA | 68970 |
rs28303130 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41311928 | AGGGTCAGTTTACTC[A/G]CCATTCTAACATTAC | 68970 |
rs28303131 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcaf12 | Mm_Celera | 4:41311460 | CACTACCAGTACTTA[C/T]GGTCTCTGGCAGTTT | 68970 |
rs28303132 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41309209 | TTCTTGGTTCCCAGA[A/T]TTGGTTCTAAAAGCT | 68970 |
rs28303133 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41308700 | ACAGTCTAACCTATT[C/T]CAACTCTCTAGATAC | 68970 |
rs28303134 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Dcaf12 | Mm_Celera | 4:41308567 | TGTCATTTAGATTTA[G/T]CCCATTATCTCTCAC | 68970 |
rs28303135 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Dcaf12 | GRCm38.p3 | 4:41308121 | GAAAACTAGGAACTG[A/C/G]CCCATGTCCTGCCCA | 68970 |
rs28303136 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41307963 | ACTTTCTTGGTTTCT[C/T]CTGGTCTCCTCGTTT | 68970 |
rs28303137 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41307330 | GGCTGCCTCACCATT[A/G]CTACTCACAGCTTTA | 68970 |
rs28303138 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41307060 | GTCTCCCTCCTATCT[A/G]ACAACCAATTGCAGT | 68970 |
rs28303139 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41306723 | GAAATAAAGGGCTCA[C/T]ACATTTCAACTATGC | 68970 |
rs28303140 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41306600 | CACCCAACAGTAATC[A/C]TGGTACTGACTGTAA | 68970 |
rs28303141 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41306248 | CTGTGTGTACACTTC[A/G]GGATAGTCCTGGATG | 68970 |
rs28303142 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41304945 | CAGTGATTACACTCC[A/G]TCAAACGTGATACCC | 68970 |
rs28303143 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41304829 | ATACTTATTTGTGGG[C/T]GTGTTTATGCGTACA | 68970 |
rs28303144 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41304161 | ACAAGAAGATAAACA[A/C]CTCTGGGCCAGCAGG | 68970 |
rs28303145 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41304131 | AAGGAGAGCAAATTT[A/C]AGCTGGTTTTCCAGA | 68970 |
rs28303146 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41303714 | GAAATGTAGAGTGCT[C/T]AGGCAATCAAAATCA | 68970 |
rs28303147 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41302177 | CACAGTTCCTTTAAG[C/G]GGCCCTGGTCACATG | 68970 |
rs28303148 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41301892 | AATACGCCTGGCAGT[C/T]GTGCAGACAGGAAGA | 68970 |
rs28303149 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41301829 | ACGTGGGCCTCTGAT[A/G]ATCTTGTGAGGTCAG | 68970 |
rs28303150 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41301493 | TTCTGAAAAGCGTGC[C/T]GGTCTGACTGAAAAT | 68970 |
rs28303151 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, utr-variant-5-prime | Dcaf12 | GRCm38.p3 | 4:41301362 | AGTATCGTTGATCCA[C/T]GCAATAGAAAAGATC | 68970 |
rs28303152 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41300506 | TTCTAGAGGCCCTGC[A/G]CAGCGCTGAGTCCAT | 68970 |
rs28303153 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Dcaf12 | Mm_Celera | 4:41299452 | CACCTTGCAGTTGTC[C/T]GGGTTTGTATCCTCC | 68970 |
rs28303154 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41299332 | TAAAACCAAGTTACA[C/G]AGCAAGCACTGCCTT | 68970 |
rs28303155 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41298700 | TGGGCCCTTGTGTAT[A/G]TGATGCACATACACC | 68970 |
rs28303156 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dcaf12 | Mm_Celera | 4:41298581 | CCTTTCTGCGCTCCT[C/T]ATCTTCCTGACATCC | 68970 |
rs28303157 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Dcaf12 | Mm_Celera | 4:41298563 | ATCTGTGGGTAAAAC[A/C]GTCCTTTCTGCGCTC | 68970 |
rs28303158 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41298507 | ACACCCACGTGCCGC[A/C]GTTACACAGTATATG | 68970 |
rs28303159 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41298414 | GAAGCACCAGACTAC[A/G]CAGGGGAAGAAGCTG | 68970 |
rs28303160 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41298190 | CCCCAGACCTTGGGC[A/G]AAAGGTGTTTTGGGC | 68970 |
rs28303161 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41297787 | TAGAGGATCAGGCGT[C/T]CTGGGTTAGTGCATT | 68970 |
rs28303162 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41297660 | ACAGTCACTCTACAA[A/G]CCAGTGCTTAAATAT | 68970 |
rs28303163 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41297547 | CCACTCCATTTTCTC[A/T]TCATCTAACAAGATT | 68970 |
rs28303164 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41296902 | TAGCACAGGCAAGAC[A/G]TGAAGAAGACTTTAC | 68970 |
rs28303165 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41296685 | TGTAGTTTATTTCTA[G/T]GACTGAGCCCTCTGT | 68970 |
rs28303166 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41296580 | ACCTAAGTCAGGGAC[A/T]AGACAAAGCCTAGTA | 68970 |
rs28303167 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41295844 | TTAGAATACGAAATC[C/T]GGGCAGAGGCTGGGA | 68970 |
rs28303168 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41295824 | AGGAAGGTGAGCGAC[A/G]GCCCTTAGAATACGA | 68970 |
rs28303169 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41295795 | GAGACAACAGCAGCA[C/T]AAGTCTTCCACAGAG | 68970 |
rs28303170 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41295747 | CTTGGAGGGAGAAAA[C/T]GAGTCATCAGAACAA | 68970 |
rs28303171 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41295458 | GCAACTTTAGATTGG[A/C]CGGTCTTCAGACCTT | 68970 |
rs28303172 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41295139 | CAAACACTGCCGCCA[C/T]CAACAAACCCAAAAA | 68970 |
rs28303173 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41295104 | TGGTACCCGCCTTCC[A/C]TAGCAATACTCGGGG | 68970 |
rs28303174 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41294449 | CTGTACCTGTGGATT[A/G]AGTACAATGGATACA | 68970 |
rs28303175 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41294227 | TACTGGGAAAATCTA[C/T]ATTGTTTTGTGCCAA | 68970 |
rs28303176 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41293751 | GAGCCGAGATTACAA[A/G]CATCTGCCCCACCAC | 68970 |
rs28303177 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dcaf12 | Mm_Celera | 4:41293690 | GCACCAGCATATTTT[C/T]CTAGGCCTTTCACTT | 68970 |
rs28303178 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Dcaf12 | Mm_Celera | 4:41293302 | TGCCAAAGGCAGGAG[G/T]TCTATCACCCGCCAT | 68970 |
rs28303179 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dcaf12 | Mm_Celera | 4:41293235 | GGAAGATGAGGAGAC[A/G]GTTAGTACCTCTAGG | 68970 |
rs28303180 | snp | A/G | 0.165289 | 0.235211 | utr-variant-3-prime | Dcaf12 | GRCm38.p3 | 4:41292942 | AACTGCCTGACCCAC[A/G]AGCAAACTCTGTTTG | 68970 |
rs28303181 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Dcaf12 | GRCm38.p3 | 4:41292805 | CTTTAAAAAGCAGAA[A/G]AGGGAAAAGTAAAAT | 68970 |
rs28303182 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41292246 | TTATCTAGGCTGTGA[C/T]GTGGCCTGCAGTCCC | 68970 |
rs28303183 | snp | A/G | 0.18 | 0.24 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41292168 | AGCACACAAGCTCGA[A/G]ACTGCCTGCTCTCGG | 68970 |
rs28303184 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Dcaf12 | GRCm38.p3 | 4:41292006 | CAGAGCAGGACAGTG[A/G]CTTCCAACACTAAGC | 68970 |
rs28303185 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41291402 | CATCACAGGAGACGG[A/T]CTGGCAATGGCACAA | 68970 |
rs28303186 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Dcaf12 | Mm_Celera | 4:41291284 | CATCTTTGCCATATA[C/T]AGTCACTCAAACAGC | 68970 |
rs28303187 | snp | C/G | 0.124444 | 0.216185 | downstream-variant-500B | Dcaf12 | Mm_Celera | 4:41290972 | TGGAAAGCCTTGGTC[C/G]TGTGACTTAGCAGTC | 68970 |
rs28303188 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Dcaf12 | Mm_Celera | 4:41290963 | TGCTTGCCCTGGAAA[A/G]CCTTGGTCGTGTGAC | 68970 |
rs211952307 | snp | A/T | | | intron-variant | Dcaf12 | Mm_Celera | 4:41312519 | ATTTGGATTCTAATA[A/T]ATGAAAAAGTATTTG | 68970 |
rs212002124 | snp | A/G | | | intron-variant | Dcaf12 | Mm_Celera | 4:41311512 | TAAACACTTTTATTT[A/G]TATGTGGTAGTGGGC | 68970 |
rs212074196 | snp | C/T | | | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41291947 | CACTGTCACATGCAG[C/T]GATGCTGGCACAGCC | 68970 |
rs212082069 | snp | A/G | | | intron-variant | Dcaf12 | Mm_Celera | 4:41303462 | CCTAGAGAGAGCCCA[A/G]TGGTTAGGAACATGT | 68970 |
rs212144728 | snp | C/T | | | intron-variant | Dcaf12 | Mm_Celera | 4:41293387 | TACATGAGCTCTTGC[C/T]TTCTTGCTCCCCCTC | 68970 |
rs212278384 | in-del | -/T | | | intron-variant | Dcaf12 | Mm_Celera | 4:41308216 | GTGTCTTTTCTTTCA[-/T]AGTAACACAGCAATT | 68970 |
rs212420523 | in-del | -/GGCGT | | | intron-variant | Dcaf12 | Mm_Celera | 4:41297853 | GCCTTTGCTTGCTTA[-/GGCGT]GGCGGTGGCTGTCAG | 68970 |
rs212456447 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dcaf12 | Mm_Celera | 4:41315374 | GCGACCACACCTTGC[C/T]GACGACTGCTTACTT | 68970 |
rs212512940 | snp | A/G | | | intron-variant | Dcaf12 | Mm_Celera | 4:41305997 | CAGCCATCCTGCCTT[A/G]GCCTCCTGAGTGCTG | 68970 |
rs212622119 | in-del | -/C | | | intron-variant | Dcaf12 | Mm_Celera | 4:41304019 | GTGAGGGTGTGATGA[-/C]CGTATAAATGCACAC | 68970 |
rs212676564 | snp | C/G | | | intron-variant | Dcaf12 | Mm_Celera | 4:41295678 | TGCACTCAGGGCCTC[C/G]GAGTCAGCAGTCTTA | 68970 |
rs212785710 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Dcaf12 | Mm_Celera | 4:41314817 | GCTTTCCTACCGCCG[G/T]GTCTGGAAAGGACGG | 68970 |
rs212792229 | snp | C/T | | | intron-variant | Dcaf12 | Mm_Celera | 4:41305079 | GCATACTCAGTTACA[C/T]TCTCTGGGCCTGGCC | 68970 |
rs212964877 | in-del | -/AA | | | intron-variant | Dcaf12 | Mm_Celera | 4:41308384 | AAAAAACCAAAAACC[-/AA]AAACCAAACCAAAAC | 68970 |
rs213036777 | snp | C/T | | | upstream-variant-2KB | Dcaf12 | Mm_Celera | 4:41316878 | CCATGTCAGGACACA[C/T]AGGACACTGGTGCAG | 68970 |
rs213099892 | snp | G/T | | | upstream-variant-2KB | Dcaf12 | Mm_Celera | 4:41317898 | GAAGTACTGTTTTTA[G/T]TTCCCAAGCTAGCTT | 68970 |
rs213124669 | snp | A/G | | | intron-variant | Dcaf12 | Mm_Celera | 4:41298511 | CCACGTGCCGCCGTT[A/G]CACAGTATATGCAAT | 68970 |
rs213422836 | snp | A/G | | | intron-variant | Dcaf12 | Mm_Celera | 4:41304402 | TGCAGATCTGAGTTA[A/G]AAGTCAGCCTGGTTC | 68970 |
rs213459887 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Dcaf12 | GRCm38.p3 | 4:41314651 | CATGAACCGGGCCCT[A/G]GGGCCGCGCGCTTTC | 68970 |
rs213481347 | snp | A/G | | | intron-variant | Dcaf12 | Mm_Celera | 4:41304850 | TATGCGTACAAGCAC[A/G]CAGTTACGTAGTGTG | 68970 |
rs213494956 | snp | A/G | | | intron-variant | Dcaf12 | Mm_Celera | 4:41305829 | CTGCCTCCAGAGTAC[A/G]TGTGCCACCACTACC | 68970 |
rs213495000 | snp | A/C | | | intron-variant | Dcaf12 | Mm_Celera | 4:41294800 | ACATCTCTGTGAATT[A/C]AAGGCTAGTCTGGTC | 68970 |
rs213550774 | snp | G/T | | | intron-variant | Dcaf12 | Mm_Celera | 4:41295542 | ACAGCCCTGTTTGAT[G/T]AGCCTGGAATTTACT | 68970 |
rs213729725 | in-del | -/CAAAAGAC | | | utr-variant-3-prime | Dcaf12 | Mm_Celera | 4:41292991 | CACAGCTAGGGAAAT[-/CAAAAGAC]CAAACAAGGAAACTG | 68970 |
rs213734804 | snp | A/T | | | intron-variant | Dcaf12 | Mm_Celera | 4:41299387 | GGACAGGCTGCTGGA[A/T]TCCCTTGGCGAGTTC | 68970 |