SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13465281 | snp | A/G | 0.345679 | 0.230967 | utr-variant-3-prime | Enc1 | GRCm38.p3 | 13:97252599 | TCTAGACTCCCGCTC[A/G]TTCAATTGATCTAGG | 13803 |
rs29225400 | snp | C/T | 0.375 | 0.216506 | intron-variant | Enc1 | GRCm38.p3 | 13:97247418 | CTGATCGGCTTCATC[C/T]GGGACCATCCCAGGG | 13803 |
rs29226719 | snp | A/G | 0.32 | 0.24 | intron-variant | Enc1 | Mm_Celera | 13:97247844 | ACAGTTAGGTGTCAC[A/G]TGTGGCTGCTTCGCT | 13803 |
rs29232993 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Enc1 | GRCm38.p3 | 13:97247419 | TGATCGGCTTCATCT[A/C/G]GGACCATCCCAGGGA | 13803 |
rs29238537 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Enc1 | GRCm38.p3 | 13:97240754 | GCGCAGGAAAGCGCC[C/T]AGGGCTGCTTTCCCC | 13803 |
rs29246332 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97240525 | CCACAAGAGTTTGGA[A/G]TCTGGCCTCTTGCCA | 13803 |
rs29249947 | snp | A/G | 0.5 | 0 | utr-variant-5-prime | Enc1 | Mm_Celera | 13:97241494 | ACCGAGGCAAGAACC[A/G]CAGCCGGTTGTGTGC | 13803 |
rs29252100 | snp | G/T | 0.375 | 0.216506 | utr-variant-5-prime | Enc1 | GRCm38.p3 | 13:97241348 | CTGAGACCGAGGTCA[G/T]CTGCCTGCCGAAACC | 13803 |
rs29516210 | snp | A/G | 0.375 | 0.216506 | intron-variant | Enc1 | Mm_Celera | 13:97242730 | AGAAAACACAGCAGC[A/G]TAAACACAGGATGCA | 13803 |
rs29528998 | snp | A/G | 0.197531 | 0.244432 | utr-variant-3-prime | Enc1 | Mm_Celera | 13:97252740 | TTCTTCTTATTTTGT[A/G]AGCCGGTTGCCCTGG | 13803 |
rs29529941 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Enc1 | GRCm38.p3 | 13:97249631 | GGAGATCTGAACTGA[C/T]CCCTGCTGCTCAGTC | 13803 |
rs29534274 | snp | A/C | 0.48 | 0.0979796 | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97240527 | ACAAGAGTTTGGAGT[A/C]TGGCCTCTTGCCAGC | 13803 |
rs29546292 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Enc1 | GRCm38.p3 | 13:97239785 | TCTCAGGAAGCGCCA[C/T]GTGGAGCCTCCTGCG | 13803 |
rs29546301 | snp | G/T | 0.48 | 0.0979796 | upstream-variant-2KB | Enc1 | GRCm38.p3 | 13:97240415 | GAAACACGTGGGCCC[G/T]CAGGACCGAGCTGGG | 13803 |
rs29551125 | snp | A/G | 0.375 | 0.216506 | intron-variant | Enc1 | GRCm38.p3 | 13:97247511 | AAAAACACTGCTCGC[A/G]GCTCCTAGTTTATTG | 13803 |
rs29566610 | snp | C/G | 0.48 | 0.0979796 | upstream-variant-2KB | Enc1 | GRCm38.p3 | 13:97240423 | TGGGCCCGCAGGACC[C/G]AGCTGGGGTTGCTGC | 13803 |
rs29590975 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Enc1 | GRCm38.p3 | 13:97240687 | GAGCGGTGGATCCCC[A/G]GCTTGGCCTTGGCTA | 13803 |
rs29614912 | snp | A/G | 0.375 | 0.216506 | intron-variant | Enc1 | GRCm38.p3 | 13:97242720 | GGGGAGACTTAGAAA[A/G]CACAGCAGCATAAAC | 13803 |
rs29620437 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97240772 | GGCTGCTTTCCCCTG[A/C]GTTGGGTGCCCCAGC | 13803 |
rs29634194 | snp | C/T | 0.375 | 0.216506 | utr-variant-5-prime | Enc1 | GRCm38.p3 | 13:97241380 | GCCCCGGAGCCACTA[C/T]CCCGGACGCTATCGC | 13803 |
rs29676468 | snp | G/T | 0.5 | 0 | utr-variant-5-prime | Enc1 | GRCm38.p3 | 13:97241334 | CGTAGCAGCAGATCC[G/T]GAGACCGAGGTCATC | 13803 |
rs29677076 | snp | A/T | 0.375 | 0.216506 | intron-variant | Enc1 | GRCm38.p3 | 13:97247993 | CCCTCTGACCTGTTA[A/T]CAGGTCACAGCCCAT | 13803 |
rs29684293 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Enc1 | GRCm38.p3 | 13:97239909 | GCCACTACTGAGGCC[C/T]TGCAGGTCTCCAGCC | 13803 |
rs29684585 | snp | C/T | 0.375 | 0.216506 | intron-variant | Enc1 | GRCm38.p3 | 13:97249083 | GAGCCAACTGTATAT[C/T]ACAGGCTTCTCCTGC | 13803 |
rs29714568 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Enc1 | Mm_Celera | 13:97248357 | AGAGAACTTTGGCTC[C/T]GCTTTCCTTACGGTG | 13803 |
rs29725145 | snp | C/T | 0.5 | 0 | utr-variant-5-prime | Enc1 | Mm_Celera | 13:97241499 | GGCAAGAACCGCAGC[C/T]GGTTGTGTGCAGAGG | 13803 |
rs29774460 | snp | C/T | 0.18 | 0.24 | utr-variant-3-prime | Enc1 | Mm_Celera | 13:97250638 | GCTACTGAGACTCCT[C/T]GAATACCATCGGCTG | 13803 |
rs29818538 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Enc1 | GRCm38.p3 | 13:97242475 | TGGAAAGGATGATTC[A/G]TTTTATGTTGAAGGT | 13803 |
rs29831375 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97239747 | GATAAAGGACCAACC[C/G]TGCGGGTTTCAGCAG | 13803 |
rs29859893 | snp | A/G | 0.5 | 0 | intron-variant | Enc1 | GRCm38.p3 | 13:97243310 | AAGTAACATTCCAAA[A/G]CTAAGAGGAAAACAA | 13803 |
rs29864900 | snp | C/T | 0.5 | 0 | intron-variant | Enc1 | GRCm38.p3 | 13:97243189 | TGGGTCCTCTTCATC[C/T]CGCTAGCCACTGGGA | 13803 |
rs29920934 | snp | C/G | 0.48 | 0.0979796 | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97240756 | GCAGGAAAGCGCCCA[C/G]GGCTGCTTTCCCCTG | 13803 |
rs29945732 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97239545 | CCCTCGAGCTTTTTC[C/T]CTGGCTCTGTAAAGC | 13803 |
rs29971633 | snp | A/G | 0.5 | 0 | synonymous-codon | Enc1 | Mm_Celera | 13:97245736 | CATGGAGAACGTGGC[A/G]ATGGAAGAACTCATC | 13803 |
rs30008869 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Enc1 | GRCm38.p3 | 13:97239552 | GCTTTTTCCCTGGCT[C/T]TGTAAAGCAAAATGG | 13803 |
rs30023671 | snp | C/G | 0.5 | 0 | intron-variant | Enc1 | Mm_Celera | 13:97243195 | CTCTTCATCTCGCTA[C/G]CCACTGGGAAGTCCT | 13803 |
rs45829754 | snp | C/T | 0.165289 | 0.235211 | utr-variant-3-prime | Enc1 | Mm_Celera | 13:97250969 | AGCTGCCGTTGGAGA[C/T]GCAAAGCCAAGCAAG | 13803 |
rs45922971 | snp | A/C | | | intron-variant | Enc1 | Mm_Celera | 13:97244126 | AAAAAAAAATTAGCA[A/C]GAAGCTGCCTGCTCA | 13803 |
rs46049168 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Enc1 | Mm_Celera | 13:97246504 | GTTCTCTGCCTGCTC[C/T]GCTTACAAATTCAAT | 13803 |
rs46213944 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97244015 | GTACGTAACAGTCCC[A/G]GTGATGGAGTGTTTA | 13803 |
rs46316674 | snp | C/T | | | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97240219 | GGGTGATGGTTGTTG[C/T]TTTTTTTGGGGGGGG | 13803 |
rs46519330 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97247506 | CTTACAAAAACACTG[C/T]TCGCGGCTCCTAGTT | 13803 |
rs46553944 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Enc1 | Mm_Celera | 13:97250662 | TCGGCTGCACCTTGC[A/G]AACACTCTCAAGTGG | 13803 |
rs46645741 | snp | C/T | | | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97240163 | ATTTAGGATAGAGTT[C/T]CTTCTTTTGCTAGGC | 13803 |
rs46757056 | snp | G/T | 0.124444 | 0.216185 | synonymous-codon | Enc1 | Mm_Celera | 13:97245070 | TAAGTCCTCCTACGC[G/T]GACAGCGTTCTCACT | 13803 |
rs46764859 | snp | A/G | | | upstream-variant-2KB | Enc1 | GRCm38.p3 | 13:97240112 | TGGCCACGTTTGTTT[A/G]TTTATTTATTTATTT | 13803 |
rs46810122 | snp | C/T | | | synonymous-codon | Enc1 | GRCm38.p3 | 13:97246717 | CTCTCTGATCCCTAC[C/T]GCATTCGTCAGCACC | 13803 |
rs46870630 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97246847 | GCTTGAGTGGATGTG[A/G]ACTGAGATGGACTGC | 13803 |
rs46893528 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97249472 | TTACTATACGCAAGA[A/T]GCTGTTAAAAACACT | 13803 |
rs46964808 | snp | G/T | | | synonymous-codon | Enc1 | GRCm38.p3 | 13:97246666 | CTGTTACGACCCAAC[G/T]TTAGATGTGTGGAAC | 13803 |
rs46972509 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Enc1 | Mm_Celera | 13:97245076 | CTCCTACGCGGACAG[C/T]GTTCTCACTCACCTG | 13803 |
rs47014615 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Enc1 | Mm_Celera | 13:97244900 | CTTTGTCTAAGTGAT[C/T]GTTGCTTTTGTGCTA | 13803 |
rs47169126 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Enc1 | Mm_Celera | 13:97250326 | TATGGGCTGACCGTC[A/G]TCATGGCATCAACCT | 13803 |
rs47349243 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97246827 | CTGGAAATTTCAGCC[C/T]GGTAGCTTGAGTGGA | 13803 |
rs47546707 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Enc1 | Mm_Celera | 13:97244291 | ATTCTGTGCATTTAG[A/C]GCTCTGGAGTGGTAG | 13803 |
rs47683478 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Enc1 | Mm_Celera | 13:97245098 | ACTCACCTGAACCTT[C/T]TGCGTCAGCAGCGGC | 13803 |
rs47785153 | snp | C/T | | | synonymous-codon | Enc1 | GRCm38.p3 | 13:97246723 | GATCCCTACTGCATT[C/T]GTCAGCACCTGGAAA | 13803 |
rs47979060 | snp | C/T | | | synonymous-codon | Enc1 | GRCm38.p3 | 13:97246667 | TGTTACGACCCAACT[C/T]TAGATGTGTGGAACA | 13803 |
rs48049889 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Enc1 | Mm_Celera | 13:97244121 | AAGGAAAAAAAAAAT[C/T]AGCACGAAGCTGCCT | 13803 |
rs48107499 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Enc1 | Mm_Celera | 13:97245058 | CTACCTGTTTCATAA[A/G]TCCTCCTACGCGGAC | 13803 |
rs48379610 | snp | A/G | | | utr-variant-3-prime | Enc1 | GRCm38.p3 | 13:97251746 | CACCAGTGGGGGGGA[A/G]AAAACTAAAATGTGT | 13803 |
rs48441730 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Enc1 | Mm_Celera | 13:97250920 | GCAATGGTTGTCAGC[C/T]TCCTCTGAAGACCGA | 13803 |
rs48477097 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Enc1 | Mm_Celera | 13:97249736 | GATGTGGACTTGTTT[A/G]CCTTGTGACTTCTTT | 13803 |
rs48514492 | snp | A/G | | | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97240206 | AGGTGTGTGTGTGGG[A/G]TGATGGTTGTTGTTT | 13803 |
rs48517565 | snp | C/G | | | intron-variant | Enc1 | GRCm38.p3 | 13:97241628 | CATCGAGCCGGCGCC[C/G]GCCACCCTGGCTGAG | 13803 |
rs48547503 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Enc1 | Mm_Celera | 13:97251904 | GAGCTCTTTGGTACA[C/T]GGAAGTGACATCTTT | 13803 |
rs48551544 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97244601 | GGCTGGCCTCCCTCA[A/G]CTTTTGCTGACTTAC | 13803 |
rs48605403 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Enc1 | GRCm38.p3 | 13:97246342 | TTTCGGGGGTACCAG[C/T]GTGAGCCACGACAAG | 13803 |
rs48697057 | snp | A/G | 0.32 | 0.24 | intron-variant | Enc1 | GRCm38.p3 | 13:97246791 | ACGCATGAGGTAAGA[A/G]CCCGTAGCTGGAGGT | 13803 |
rs48825286 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Enc1 | Mm_Celera | 13:97249553 | CCTCCAGCCTGAGTC[C/T]TGATTTCTGAATGCA | 13803 |
rs48977112 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97243622 | CATAAACAACCTCTT[C/T]TGGCAGATTCTTAAG | 13803 |
rs49088954 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Enc1 | Mm_Celera | 13:97244325 | CGTCTAGGTAGAAAC[C/G]GTCTCTTTTACCTTG | 13803 |
rs49107621 | snp | G/T | | | intron-variant | Enc1 | Mm_Celera | 13:97247061 | GGGGGGGGGGGGGGG[G/T]TTGGGGTGGAACCCA | 13803 |
rs49413421 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Enc1 | Mm_Celera | 13:97245196 | GTGCAGCCGCTACTT[C/T]GAAGCCATGTTCAGT | 13803 |
rs49506176 | snp | C/T | 0.459184 | 0.136902 | synonymous-codon | Enc1 | Mm_Celera | 13:97245478 | GTGCACCAAGCTGTA[C/T]GAACTCTCCTGGAGA | 13803 |
rs49648882 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97247534 | GTTTATTGACTCCAG[A/G]GCTGTATAGTCACTT | 13803 |
rs49951794 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Enc1 | GRCm38.p3 | 13:97246872 | GACTGCTTGTTGTCT[C/T]ATCTGAAGTCACACA | 13803 |
rs49972378 | snp | C/G | | | utr-variant-5-prime | Enc1 | GRCm38.p3 | 13:97241369 | TGCCGAAACCAGCCC[C/G]GGAGCCACTACCCCG | 13803 |
rs50001855 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97244641 | AGAACTTCTGGTGTC[C/T]GGAAAGTTGGAAGTT | 13803 |
rs50043652 | snp | C/T | | | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97239385 | TTCCTATCTTCCTCT[C/T]GTCAGAGCCTATCTC | 13803 |
rs50055555 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Enc1 | Mm_Celera | 13:97250362 | GTGTGCACATTTATG[A/G]TTGAACTCAGACTGA | 13803 |
rs50057521 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Enc1 | Mm_Celera | 13:97245955 | AATCATTCCCAAGGC[C/T]GACATTCCCAGCCCG | 13803 |
rs50124325 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Enc1 | Mm_Celera | 13:97249156 | TCCTGGGGACATTCC[A/G]TTCCTTTGATTATCA | 13803 |
rs50134958 | snp | C/T | | | upstream-variant-2KB | Enc1 | Mm_Celera | 13:97240271 | GAACTCCAGACTCCA[C/T]CAACCAACCAAACCC | 13803 |
rs50165323 | snp | C/T | | | intron-variant | Enc1 | Mm_Celera | 13:97247044 | CTCTAGAGACTTTTG[C/T]GGGGGGGGGGGGGGG | 13803 |
rs50455452 | snp | C/T | | | intron-variant | Enc1 | GRCm38.p3 | 13:97246864 | CTGAGATGGACTGCT[C/T]GTTGTCTCATCTGAA | 13803 |
rs50520346 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Enc1 | Mm_Celera | 13:97246762 | TTCCTAATGTAGAGC[A/C]TCCTAAAGAAAGCAC | 13803 |
rs50533097 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Enc1 | Mm_Celera | 13:97244785 | TCTCCTTCCAGGTAG[C/T]TCTCTCCGACTTTGT | 13803 |
rs50568370 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Enc1 | Mm_Celera | 13:97250464 | ATAGCCTGCTTATTA[G/T]CGAATGTCTTAAAAC | 13803 |
rs50690960 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Enc1 | Mm_Celera | 13:97249347 | ACAGGAAAGGCAAGC[A/G]CATAAAAATTGATCT | 13803 |
rs50914168 | snp | A/G | | | intron-variant | Enc1 | Mm_Celera | 13:97244804 | CTCCGACTTTGTTCT[A/G]GAGTGGCCATACCCG | 13803 |
rs50977965 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Enc1 | Mm_Celera | 13:97246159 | GCACTGCCTCTATGT[A/G]GTCGGTGGGCACACA | 13803 |
rs51002164 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Enc1 | Mm_Celera | 13:97252154 | AAGGCAGATAGCCAC[C/T]TTTACATTGTGAGTG | 13803 |
rs51274150 | snp | A/G | | | utr-variant-3-prime | Enc1 | GRCm38.p3 | 13:97251745 | ACACCAGTGGGGGGG[A/G]AAAAACTAAAATGTG | 13803 |
rs51302020 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Enc1 | Mm_Celera | 13:97246597 | CGTGGCGTCCGGGAA[C/T]AAGCTTTACGTAGTT | 13803 |
rs51341332 | snp | C/G/T | 0.244898 | 0.249948 | intron-variant | Enc1 | GRCm38.p3 | 13:97249330 | TCACCTTGGTATCCC[C/G/T]GACAGGAAAGGCAAG | 13803 |
rs51351105 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Enc1 | Mm_Celera | 13:97247536 | TTATTGACTCCAGAG[C/T]TGTATAGTCACTTAT | 13803 |
rs51482664 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Enc1 | GRCm38.p3 | 13:97246806 | GCCCGTAGCTGGAGG[C/T]GCAAGCTGGAAATTT | 13803 |
rs51534342 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Enc1 | Mm_Celera | 13:97252922 | AAGTTAGAAGATGGT[C/T]GGTCATGTCTGTATG | 13803 |
rs51817662 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Enc1 | Mm_Celera | 13:97244014 | GGTACGTAACAGTCC[C/T]GGTGATGGAGTGTTT | 13803 |