SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13470953 | snp | A/G | | | utr-variant-5-prime | Epn3 | GRCm38.p3 | 11:94496580 | CGGCCCTCTACCTCC[A/G]ACGGGGGCGGGGGCC | 71889 |
rs27059702 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Epn3, Mycbpap | GRCm38.p3 | 11:94501934 | CATCAAACAGAACTT[A/C]TGGTCAAATGAGACC | 71889 |
rs27059703 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Epn3, Mycbpap | GRCm38.p3 | 11:94501767 | AGCTTCCAAGACTGA[A/G]CCCTCTACTGCAGCT | 71889 |
rs27059704 | snp | C/T | 0.429688 | 0.173817 | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | GRCm38.p3 | 11:94501152 | GCTATGAAAGGCCAT[C/T]TTGTCCTGTCACCTG | 71889 |
rs27059705 | snp | C/G | 0.46875 | 0.121031 | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | GRCm38.p3 | 11:94501031 | GTGCTGAAGTAGAAG[C/G]CTTCAGACAGTCAGG | 71889 |
rs27059706 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Epn3 | GRCm38.p3 | 11:94500527 | TCTGAGCAGGCAGTG[C/T]GTGCTTTCCCAGCTG | 71889 |
rs27059707 | snp | A/G | 0.197531 | 0.244432 | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500079 | GCCTGTTTGTCAGCC[A/G]GTGACCCCAGAGGTT | 71889 |
rs27059708 | snp | A/G | 0.336735 | 0.234472 | utr-variant-5-prime, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499831 | GCTCTACCTTGGACC[A/G]AAAGGCACAGAGCTC | 71889 |
rs27059709 | snp | C/G | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499558 | AGGTTAGAAGCCTCC[C/G]GGTACTCCACAGCCC | 71889 |
rs27059710 | snp | A/G | 0.197531 | 0.244432 | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498539 | AGGTGGACATTGTGG[A/G]CACACCTTTGCTGGA | 71889 |
rs27059711 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498442 | CTTCCTACTTTGCCA[A/G]GGTGAATACAGCCAG | 71889 |
rs27059712 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Epn3 | Mm_Celera | 11:94498040 | ACAAGTGAAAGATCA[A/G]CTCAGTTCAAAGTAC | 71889 |
rs27059713 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Epn3 | GRCm38.p3 | 11:94497702 | CAGGAGAATCAGTCA[C/T]ATGTCTTTCCACAGC | 71889 |
rs27059714 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Epn3 | Mm_Celera | 11:94497685 | CCTAATGGAGGCCGA[C/G]TCAGGAGAATCAGTC | 71889 |
rs27059715 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Epn3 | Mm_Celera | 11:94497324 | AGAAGATGTAGGGGA[C/G]CAGCAAGGCCAGGAA | 71889 |
rs27059716 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Epn3 | GRCm38.p3 | 11:94497293 | GCACTCGAGGGAAGC[A/G]CAACAGGGAAAATCA | 71889 |
rs27059717 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Epn3 | GRCm38.p3 | 11:94496870 | AAAACCATCAGACCA[A/C]GATGCTGAAATCCCT | 71889 |
rs27059718 | snp | A/G | 0.375 | 0.216506 | intron-variant | Epn3 | GRCm38.p3 | 11:94496817 | CTTATTGCACTCACT[A/G]TCCAATGGACACGCT | 71889 |
rs27059719 | snp | A/C | 0.387812 | 0.208586 | synonymous-codon | Epn3 | GRCm38.p3 | 11:94496120 | ATGGGTTCGCTCTTG[A/C]CGCAGGCGCTCCTCA | 71889 |
rs27059720 | snp | A/G | 0.484429 | 0.0868505 | synonymous-codon | Epn3 | Mm_Celera | 11:94496060 | CAGCTGCCCGCTGCC[A/G]ATACCCATGCCTTCC | 71889 |
rs27059721 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Epn3 | Mm_Celera | 11:94495931 | TCCTGGGTGGAGAGC[C/T]ATGACTGTGGCTGGC | 71889 |
rs27059722 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Epn3 | GRCm38.p3 | 11:94495447 | ATGGAAGGAGGGCCT[G/T]TCTGTTCCTCAGGTC | 71889 |
rs27059723 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Epn3 | Mm_Celera | 11:94495319 | CTGACTTCAGCTCTT[A/G]AACTCTTCAATAGGA | 71889 |
rs27059724 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn3 | Mm_Celera | 11:94495273 | CGAAGGGGGCTGGCA[A/G]TAGTCCTAAGTCAGG | 71889 |
rs27059725 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Epn3 | GRCm38.p3 | 11:94494749 | CACTGCCCTTTCTGG[A/G]TCCCGCAGGAGAACA | 71889 |
rs27059726 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Epn3 | Mm_Celera | 11:94494458 | TTTCTTCTGGGTACC[C/T]TGAGAACTTCCCTAG | 71889 |
rs27059727 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Epn3 | Mm_Celera | 11:94493983 | GGCACCCAGGTTAGC[A/G]CAGCTGAGAGAGAAG | 71889 |
rs27059728 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Epn3 | GRCm38.p3 | 11:94493909 | GATCTCACCCCCTGC[A/G]GAATGACAGGTAGGG | 71889 |
rs27059729 | snp | A/C | 0.124444 | 0.216185 | missense | Epn3 | Mm_Celera | 11:94493829 | TCTCAGGCTCCCTGT[A/C]CCGTTGACGACGTTG | 71889 |
rs27059730 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Epn3 | Mm_Celera | 11:94493576 | AAAGGGGAAACTGAG[A/G]CCAGTAGTATTCCAA | 71889 |
rs27059731 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Epn3 | Mm_Celera | 11:94492811 | GTGGCTGGAAGGAAG[C/G]AGGGCTCTTAGGGGC | 71889 |
rs27059732 | snp | A/G | 0.375 | 0.216506 | intron-variant | Epn3 | GRCm38.p3 | 11:94492526 | CCCAGCCCAGGTTGG[A/G]TGATGTGCCCACTTC | 71889 |
rs27059733 | snp | C/T | 0.345679 | 0.230967 | synonymous-codon | Epn3 | GRCm38.p3 | 11:94492194 | GGTCTCCATAGAGGC[C/T]CCCCAAGGGTCTGCT | 71889 |
rs27059734 | snp | A/G | 0.475309 | 0.108333 | missense | Epn3 | GRCm38.p3 | 11:94491470 | TTGGTTGGGGACGGA[A/G]CACCCAGACCTGCGG | 71889 |
rs27059735 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94491100 | TCAGTGCTCAACCTG[A/C]ACGATCCGCCCTCGA | 71889 |
rs27059736 | snp | A/G | 0.401235 | 0.199068 | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94491020 | TATTAGGCGGGTGTA[A/G]TCTTCGTCCCCAAGA | 71889 |
rs27059737 | snp | C/G | 0.429688 | 0.173817 | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490644 | TGGACAGAGAGTACT[C/G]CATATCCAGCTTAGG | 71889 |
rs27059738 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94490266 | GACAGTCAGTGTTTG[C/T]TGTATTAAACCTGAT | 71889 |
rs27059739 | snp | A/G | 0.489796 | 0.070696 | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94490029 | GTCCAGACCTCAGAT[A/G]GTCAAGGTGGCTCTC | 71889 |
rs27059740 | snp | C/T | 0.18 | 0.24 | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94489851 | GGCTGAGGAAGTCCA[C/T]GTGCTCTCGGTGACC | 71889 |
rs27059741 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94489629 | TCATTTACTCAAGAG[C/T]GACTTAACCACTCAT | 71889 |
rs27059742 | snp | C/G | 0.132653 | 0.220748 | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489300 | CCATGAGGAAAGCAT[C/G]CTGGGAATGGGGAGT | 71889 |
rs27059743 | snp | A/G | 0.486111 | 0.0821678 | downstream-variant-500B | Epn3 | GRCm38.p3 | 11:94489230 | GAGACATGAATGAAG[A/G]TGGATGAGAGGTCCA | 71889 |
rs27059744 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489149 | ATGCTCCGGTGCCAA[A/G]AGAGTAGTTCCCAGG | 71889 |
rs29393573 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Epn3 | GRCm38.p3 | 11:94492461 | GAGGGAGATAGCACA[C/T]ATATTATCCCAACAC | 71889 |
rs29399722 | snp | A/T | 0.5 | 0 | missense | Epn3 | GRCm38.p3 | 11:94491194 | GGGGGCAGCGGCCCC[A/T]TTGGGCCGGACGTGG | 71889 |
rs29400527 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94490364 | GAACATGTCACTGTA[C/T]TTCTCGAAAGCCTCT | 71889 |
rs29403226 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Epn3 | GRCm38.p3 | 11:94500230 | ACCCTCCTAGCCGGA[C/G]GACATTAAAGCAGAA | 71889 |
rs29405050 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Epn3 | GRCm38.p3 | 11:94498117 | TGTGGAAATCAGATC[C/T]CCACTGGCCCATAGT | 71889 |
rs29411377 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94489929 | TGGGTCCTGAGCGCA[C/T]GTGGGTAGCCATGGT | 71889 |
rs29419765 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490555 | TCCTCTTACCTCCAC[C/T]CCCTTAAGTACTGGG | 71889 |
rs29433001 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490565 | TCCACTCCCTTAAGT[A/G]CTGGGATTACTCGTA | 71889 |
rs29434808 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Epn3, Mycbpap | GRCm38.p3 | 11:94501619 | GATGGAGAGAGAAAC[A/G]CCAAAGTTGCTCCGA | 71889 |
rs29437296 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Epn3 | GRCm38.p3 | 11:94500479 | CAGCCTAACCAGTTG[C/T]TTACAGTCGTTTCAA | 71889 |
rs29439033 | snp | A/G | 0.375 | 0.216506 | intron-variant | Epn3 | GRCm38.p3 | 11:94494263 | CCCAGGCATGGCATG[A/G]TGATGGAAAAGCCCC | 71889 |
rs29444218 | snp | A/G | 0.375 | 0.216506 | intron-variant | Epn3 | GRCm38.p3 | 11:94495068 | CTGCAACAAGGGTGG[A/G]GCCCGTGAGCACAAC | 71889 |
rs29444912 | snp | C/T | 0.5 | 0 | intron-variant | Epn3 | Mm_Celera | 11:94494254 | ACAATCCTGCCCAGG[C/T]ATGGCATGATGATGG | 71889 |
rs29444968 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Epn3 | GRCm38.p3 | 11:94493015 | GAGGGGAGGTCTGAC[C/T]GGTGGCCAGAAGCCA | 71889 |
rs29445026 | snp | A/G | 0.5 | 0 | synonymous-codon | Epn3 | GRCm38.p3 | 11:94496189 | AACATTGACGCCCTG[A/G]TCCTTGCCATCTCGG | 71889 |
rs29448771 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Epn3 | GRCm38.p3 | 11:94493123 | AAACATTTCCTCATC[C/T]GTCTAGTGCCCCATT | 71889 |
rs29451149 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94490376 | GTATTTCTCGAAAGC[C/T]TCTGTTGGCTATTAA | 71889 |
rs29468906 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | Epn3, Mycbpap | GRCm38.p3 | 11:94501389 | ACTTTTTTCAAACCA[C/T]CTTCCCAGGAGGAAG | 71889 |
rs29469945 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Epn3 | Mm_Celera | 11:94493151 | ATTTCATAACATCCC[C/T]GTGAGGTAGGTAATG | 71889 |
rs29470164 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Epn3 | GRCm38.p3 | 11:94492570 | TGACTTGGAGCAAGC[A/T]GCTCTCTCAAGTCCA | 71889 |
rs29472458 | snp | A/G | 0.375 | 0.216506 | utr-variant-5-prime, upstream-variant-2KB | Epn3 | GRCm38.p3 | 11:94499960 | TTGTTCAGCTGGCCA[A/G]GCAGGTCTGCCTCAG | 71889 |
rs29479864 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94490001 | TCCTAAGCCCTGCAA[C/T]AACCTTGCAGAGGTC | 71889 |
rs29480813 | snp | A/T | 0.375 | 0.216506 | intron-variant | Epn3 | GRCm38.p3 | 11:94495169 | CTCTTCAGGCACTTG[A/T]GAGCCAGACAGTACA | 71889 |
rs29481331 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490395 | GTTGGCTATTAAATA[A/G]GACTAGTAAGAAAGA | 71889 |
rs29481849 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94489926 | CCCTGGGTCCTGAGC[A/G]CATGTGGGTAGCCAT | 71889 |
rs29482520 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Epn3 | GRCm38.p3 | 11:94493016 | AGGGGAGGTCTGACT[A/G]GTGGCCAGAAGCCAG | 71889 |
rs29484294 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | GRCm38.p3 | 11:94501231 | TTAATCATCACCTCT[C/T]TGGTGTGTGTGGCTC | 71889 |
rs46156896 | snp | C/G | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499112 | CAAATCCAGAAGGGT[C/G]CCAGAGTGGGGGATG | 71889 |
rs46180387 | snp | C/G | | | intron-variant | Epn3 | Mm_Celera | 11:94496967 | GAGCCGCTAAGTGTG[C/G]ACATTCCTCCCCCCA | 71889 |
rs46184841 | snp | C/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497176 | GGAGTCCTTTCCGAC[C/T]CCCACCATCTGCTTG | 71889 |
rs46760372 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94496921 | GGTGGGACTCGGGCA[A/G]TCAATCGGTCAGCGA | 71889 |
rs47822916 | snp | G/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94496854 | GGCACGCTCATTCCA[G/T]AAAACCATCAGACCA | 71889 |
rs47960202 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94496905 | GGTCACAAATGGGGA[C/T]GGTGGGACTCGGGCA | 71889 |
rs48228481 | snp | C/G | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497417 | ACTCAGCCACCACCC[C/G]CTGGCCTACACACAG | 71889 |
rs48781197 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94496956 | CTGAGGTCACAGAGC[C/T]GCTAAGTGTGCACAT | 71889 |
rs49123343 | snp | C/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497353 | AATCTGTCACCTGAT[C/T]AGACAGCCAGGGGAA | 71889 |
rs49170265 | snp | A/C | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497426 | CCACCCGCTGGCCTA[A/C]ACACAGGGCTGCTGT | 71889 |
rs49841793 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94497460 | CCGCCTATGTCACAG[A/G]CCATGTAGGTGGCAG | 71889 |
rs50090873 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94496916 | GGGACGGTGGGACTC[A/G]GGCAGTCAATCGGTC | 71889 |
rs50934276 | snp | A/C | | | intron-variant | Epn3 | Mm_Celera | 11:94497427 | CACCCGCTGGCCTAC[A/C]CACAGGGCTGCTGTG | 71889 |
rs51608544 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94496946 | CAGCGATGCTCTGAG[A/G]TCACAGAGCCGCTAA | 71889 |
rs108368783 | snp | C/T | | | downstream-variant-500B | Epn3 | GRCm38.p3 | 11:94489333 | CTGCCCCAGACAGGG[C/T]AGAGCAGAGCAGAGT | 71889 |
rs211903744 | snp | A/T | | | upstream-variant-2KB, intron-variant | Epn3, Mycbpap | Mm_Celera | 11:94501573 | CTCGGTTTTGCAGGC[A/T]CCAATGTATCAGTCT | 71889 |
rs212111524 | snp | C/G | | | intron-variant | Epn3 | Mm_Celera | 11:94493753 | CCTGGTCAGCTCACA[C/G]TCCCCAGCCCTCTCT | 71889 |
rs212235000 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94494869 | GGTGAAAAGCCCAAA[C/T]GGGGACTAGTGAACA | 71889 |
rs212525744 | snp | A/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497851 | ATACACACACACACA[A/T]AGAAGCTGGATCAGC | 71889 |
rs212642529 | snp | G/T | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499008 | AGGCTAGTCAGGAAG[G/T]GGGGGGGGGGCGGGG | 71889 |
rs212915704 | in-del | -/C | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500666 | CCCACCCCGACATTG[-/C]GCAGGCTGGCCTCAG | 71889 |
rs213055242 | snp | A/C | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500559 | TACCCTTCACCTACT[A/C]CACAGTCCCACATTC | 71889 |
rs213982928 | snp | A/C/G | | | intron-variant | Epn3 | Mm_Celera | 11:94495968 | CCCCCCACTTGCCCC[A/C/G]CCCCCACAAGCCATA | 71889 |
rs214246698 | snp | G/T | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499272 | CCCTCCCCATCTTCT[G/T]TCCCCATCAGCTCCA | 71889 |
rs214341375 | snp | C/T | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490318 | TCTGACTCTGAATCC[C/T]AGCCCCACGTCACTC | 71889 |
rs214355483 | snp | A/G | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500505 | TTCAACAGAAACCCC[A/G]GGATGATCTGAGCAG | 71889 |
rs215008739 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94493684 | TTCCCATTTAGTGCT[C/T]GGAGCGAGCTCTGCT | 71889 |
rs215172456 | snp | C/T | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489523 | GATAGGGATGAATGG[C/T]CAACTGCCACGGGAG | 71889 |
rs215338734 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94492560 | AGTGGGATGCTGACT[C/T]GGAGCAAGCAGCTCT | 71889 |
rs215394956 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94497172 | TCTGGGAGTCCTTTC[C/T]GACCCCCACCATCTG | 71889 |
rs215951831 | snp | C/G | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497746 | GAAGAGTAATACCCC[C/G]CCACCCCCGTGGGAC | 71889 |
rs216197796 | snp | C/T | | | downstream-variant-500B | Epn3 | GRCm38.p3 | 11:94489571 | CACAAAGAAGGAACT[C/T]TTGCAAAGAAGGAAA | 71889 |
rs216439953 | snp | A/G | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489500 | GGGTTTCGATGGGGC[A/G]GAAGACAGATAGGGA | 71889 |
rs216506821 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499627 | TGAGCCCACTCTAGC[-/T]CCCCACCCCCACCCC | 71889 |
rs217214411 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94495913 | TAGGAACTATCTCAT[A/G]GCTCCTGGGTGGAGA | 71889 |
rs217426245 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94495078 | GGTGGGGCCCGTGAG[C/T]ACAACAGTACCTGGG | 71889 |
rs217465652 | snp | G/T | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500366 | CCTGCCCTGAAGCTC[G/T]TTCCATAGCTTACAT | 71889 |
rs218136398 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499020 | AAGTGGGGGGGGGGC[C/G/T]GGGGGGGCTAGAGTG | 71889 |
rs218280753 | snp | A/C | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94491131 | GGAGGCGGGGCTTCG[A/C]GCGCAGGCGCTAAAG | 71889 |
rs218291203 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94492585 | AGCTCTCTCAAGTCC[A/G]TGGTTAACAAGCCCA | 71889 |
rs218628754 | snp | C/G | | | synonymous-codon | Epn3 | Mm_Celera | 11:94496435 | TGACATGAGAGAACT[C/G]GGTGGGCCCCAGGGG | 71889 |
rs218954512 | snp | G/T | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498529 | CCTAGGAGCAAGGTG[G/T]ACATTGTGGACACAC | 71889 |
rs218971717 | in-del | -/AACC | | | intron-variant | Epn3 | Mm_Celera | 11:94493184 | CCTATTTTACAGATG[-/AACC]AACTAGTTGAAGCCC | 71889 |
rs219013550 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499723 | CCTCGCCCCAGCCCC[A/C]GCAGCCTCTGCAGTG | 71889 |
rs219022200 | snp | C/G | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489159 | GCCAAAAGAGTAGTT[C/G]CCAGGGGAGACCGAG | 71889 |
rs219100965 | in-del | -/CAGGG | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489327 | AGTGGCTGCCCCAGA[-/CAGGG]CAGGGCAGAGCAGAG | 71889 |
rs220370141 | snp | A/C | | | upstream-variant-2KB, intron-variant | Epn3, Mycbpap | Mm_Celera | 11:94501942 | AGAACTTCTGGTCAA[A/C]TGAGACCTGAGGGTA | 71889 |
rs220672867 | in-del | -/CCTC | | | intron-variant | Epn3 | Mm_Celera | 11:94497037 | GGGCTGCCACTCTCT[-/CCTC]CCCCTCGTGCTCATC | 71889 |
rs223229540 | snp | C/G | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499018 | GGAAGTGGGGGGGGG[C/G]CGGGGGGGGCTAGAG | 71889 |
rs223300707 | snp | A/G | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489434 | CAGGGGAGGAGGGGC[A/G]GAGAGGTATGGGGCA | 71889 |
rs223695470 | snp | A/G | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490079 | GCTGGGGCAGAGTTG[A/G]ATTTTGGATGACCAA | 71889 |
rs223724674 | snp | C/T | | | synonymous-codon | Epn3 | Mm_Celera | 11:94496267 | GCGGCACTGGTGGGC[C/T]ACACGTTCTGAGCCC | 71889 |
rs224252952 | snp | G/T | | | intron-variant | Epn3 | Mm_Celera | 11:94495581 | TGTCAGGTGTCTGAG[G/T]AAAAAGGCCAAGGGC | 71889 |
rs224306759 | in-del | -/A | | | intron-variant | Epn3 | Mm_Celera | 11:94497314 | GGGAAAATCAAGAAG[-/A]TGTAGGGGACCAGCA | 71889 |
rs224427525 | snp | A/G | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498279 | GGGCGGGCTGGCAGC[A/G]GCAGAGTCAAGACGG | 71889 |
rs224623542 | in-del | -/TCATAATAATAATAATAATAA | | | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94490466 | TCTTCTCCTGCCTTG[-/TCATAATAATAATAATAATAA]TAATAATAATAATAA | 71889 |
rs224918517 | in-del | -/TAATAATAATAATAA | | | cds-indel | Epn3 | Mm_Celera | 11:94490467 | TCTTCTCCTGCCTTG[-/TAATAATAATAATAA]TAATAATAATAATAA | 71889 |
rs225346480 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94497648 | CTACCAAGACCTCAG[A/G]CATACACAAGACCTC | 71889 |
rs225511879 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94494797 | GGACTGGGACTGACC[A/G]GGAACACCAAGAGGC | 71889 |
rs225635020 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94493917 | CCCCTGCAGAATGAC[A/G]GGTAGGGCATGAGCA | 71889 |
rs225691611 | snp | A/T | | | upstream-variant-2KB, missense, nc-transcript-variant | Epn3, Mycbpap | Mm_Celera | 11:94501480 | AGCTCATCAGCCAGG[A/T]CCATCACATCTGTCA | 71889 |
rs225799538 | snp | A/G | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500667 | CCACCCCGACATTGC[A/G]CAGGCTGGCCTCAGA | 71889 |
rs225893166 | snp | A/G | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498966 | AGAAATGGAAAGAAG[A/G]CAGGAGGGTACTCCA | 71889 |
rs226353532 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn3 | GRCm38.p3 | 11:94499517 | GCGCCCCTTTTCTGG[A/G]GGTAACAGGAAGGTA | 71889 |
rs226654819 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499854 | CAGAGCTCTCTCTCG[C/G]AAGGACCGCAGGGTC | 71889 |
rs229128341 | snp | C/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497740 | ACCAAAGAAGAGTAA[C/T]ACCCCCCCACCCCCG | 71889 |
rs229204157 | snp | A/G | | | synonymous-codon | Epn3 | Mm_Celera | 11:94492280 | GGGGTCCAGAAGGTA[A/G]CACTGGGGTCCTGCC | 71889 |
rs229211417 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94493509 | TAGGCCACACAGCAT[C/T]GTATGATTCTATAAG | 71889 |
rs229327149 | snp | C/T | | | synonymous-codon | Epn3 | Mm_Celera | 11:94495009 | AGAAGTCTGAGGCCG[C/T]GCCTGCTCCAGGTCT | 71889 |
rs229937978 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94497298 | CGAGGGAAGCGCAAC[A/G]GGGAAAATCAAGAAG | 71889 |
rs229990119 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94497948 | CAGATCACCCTCCAG[C/T]CCCTACTGTTGGGCC | 71889 |
rs230056369 | snp | C/T | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94489706 | GGCTCGGCTTCTAAG[C/T]AGCTGCTCTTGCCCC | 71889 |
rs230417666 | snp | A/C | | | intron-variant | Epn3 | Mm_Celera | 11:94495185 | GAGCCAGACAGTACA[A/C]TGGACACCCCTTTGT | 71889 |
rs230635403 | snp | C/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94496750 | CAGTCAAGAGTGGCA[C/T]GGCCAGAGTGTCCCT | 71889 |
rs231038614 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94495979 | CCCCGCCCCCACAAG[C/T]CATACCATCAGGGCC | 71889 |
rs231256925 | snp | A/C | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489385 | GATCCTTGTAGCTTC[A/C]GGAAGCAAGGCCACC | 71889 |
rs231529160 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94493718 | CACACTGCGCAGATG[C/T]CAATTCAGTCATGCC | 71889 |
rs231564934 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94493611 | CTAAGTGGCAGGAGG[A/G]CCCAGGAGTCTCCAT | 71889 |
rs231745708 | in-del | -/GG | | | intron-variant | Epn3 | Mm_Celera | 11:94497432 | GCTGGCCTACACACA[-/GG]GCTGCTGTGACCCGC | 71889 |
rs231891282 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94497784 | AAACCCAAAGTGGGA[A/G]CCCTCTGCCAGCACA | 71889 |
rs232009337 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94495927 | TAGCTCCTGGGTGGA[A/G]AGCTATGACTGTGGC | 71889 |
rs232075244 | in-del | -/CC | | | intron-variant | Epn3 | Mm_Celera | 11:94497741 | CAAAGAAGAGTAATA[-/CC]CCCCCCCACCCCCGT | 71889 |
rs232089918 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94494722 | CATTGCCCTTTCTGG[C/T]CCCCAACTACACACT | 71889 |
rs232114716 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | Mm_Celera | 11:94501296 | AGGTCCTAGACCTTC[A/G]CCTGATGCCGTTGAG | 71889 |
rs232169989 | snp | C/T | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490247 | AGCCCAGCATTTCAT[C/T]CAAGACAGTCAGTGT | 71889 |
rs232256731 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499574 | GGTACTCCACAGCCC[-/T]TGCCTTACTCTCTAG | 71889 |
rs232820091 | snp | C/T | | | missense | Epn3 | Mm_Celera | 11:94491195 | GGGGCAGCGGCCCCA[C/T]TGGGCCGGACGTGGG | 71889 |
rs233092217 | snp | C/T | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500433 | CCTGGCTACTGGCTT[C/T]CCTCACTCCTCCACT | 71889 |
rs233463108 | snp | A/G | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498676 | GGAGGAAGAAAGCCA[A/G]GGTGAGGTCCCAGAG | 71889 |
rs233749582 | in-del | -/AT | | | intron-variant | Epn3 | Mm_Celera | 11:94497220 | TCCAAGAGAAAGGAC[-/AT]AGATACATAAGGAAG | 71889 |
rs234811636 | snp | G/T | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500629 | TTGTTGTTTTGAAAC[G/T]TTGTGGTCCCTCCTT | 71889 |
rs235151611 | snp | A/C | | | intron-variant | Epn3 | Mm_Celera | 11:94495886 | ATGGATCCTCCCAAT[A/C]ACCTTTTGAGGTAGG | 71889 |
rs235343999 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | GRCm38.p3 | 11:94501075 | GCTTCTCTCCCTAGT[C/T]CCTCACTTGAGTTGG | 71889 |
rs235476788 | snp | A/T | | | intron-variant | Epn3 | Mm_Celera | 11:94492699 | CTCCCATGAGCTAAG[A/T]TCTGCAGGTGTGCGC | 71889 |
rs235598015 | in-del | -/AC | | | intron-variant | Epn3 | Mm_Celera | 11:94497424 | ACCACCCGCTGGCCT[-/AC]ACACACAGGGCTGCT | 71889 |
rs235750062 | snp | A/C | | | intron-variant | Epn3 | Mm_Celera | 11:94495653 | AGGGAGGGAGGTGTA[A/C]CTCTGTTTTACAGAG | 71889 |
rs235788317 | snp | C/T | | | synonymous-codon | Epn3 | Mm_Celera | 11:94496528 | CACCTGGCGGCGGAG[C/T]GCAGAGGTTGTCATA | 71889 |
rs236437224 | in-del | -/ATAC | | | intron-variant | Epn3 | Mm_Celera | 11:94497836 | CATGAATACATTTGT[-/ATAC]ACACACACACATAGA | 71889 |
rs236503147 | snp | C/T | | | upstream-variant-2KB, intron-variant | Epn3, Mycbpap | Mm_Celera | 11:94501587 | CTCCAATGTATCAGT[C/T]TTGCTAAGAGAGACG | 71889 |
rs237332049 | snp | C/T | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489171 | GTTCCCAGGGGAGAC[C/T]GAGAGCCCTGTTGTG | 71889 |
rs237845102 | snp | C/T | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500061 | CTTCAGGGGAGGAGG[C/T]TGGCCTGTTTGTCAG | 71889 |
rs237907112 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | Mm_Celera | 11:94501104 | GGCTTCAGGAAGCAC[A/G]GCCCTGAAAGTCTAG | 71889 |
rs237981786 | snp | A/T | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94491057 | CAGTCCCTAGTTGGG[A/T]TTCAGGATGTGTCAG | 71889 |
rs238197526 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94494012 | AGCGATTAGTGCCCC[C/T]TTAGACCTGCCACCA | 71889 |
rs238612607 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499083 | GATTCGGAGCAGTGG[A/G]ATCTCTCAGGACACA | 71889 |
rs238749356 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94497173 | CTGGGAGTCCTTTCC[A/G]ACCCCCACCATCTGC | 71889 |
rs238800594 | snp | A/G | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490847 | GGGAGGCACCAGGCC[A/G]AGAGGAAAGGGGAAT | 71889 |
rs239284841 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94497078 | CCACGTGTGTTGCAG[C/T]CTTACCAATTTAGCC | 71889 |
rs239856648 | snp | A/G | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498423 | TGGGCCTGGCTTCCT[A/G]GGCCTTCCTACTTTG | 71889 |
rs240341397 | in-del | -/CT | | | intron-variant | Epn3 | Mm_Celera | 11:94496883 | ACGATGCTGAAATCC[-/CT]CTCTCTGGTCACAAA | 71889 |
rs240383114 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94495090 | GAGCACAACAGTACC[C/T]GGGGTCCCCACACTC | 71889 |
rs240624297 | snp | C/T | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489510 | GGGGCAGAAGACAGA[C/T]AGGGATGAATGGCCA | 71889 |
rs240925887 | snp | C/T | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498166 | TTCTGTCTTTCTGTC[C/T]GGCTGGCCTTCTGTG | 71889 |
rs241137239 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | Mm_Celera | 11:94500862 | AATGAATGGGAAGAG[A/G]AAAACTGTACTTGTG | 71889 |
rs241767181 | snp | A/G | | | synonymous-codon | Epn3 | Mm_Celera | 11:94496135 | CCGCAGGCGCTCCTC[A/G]TCCTTGAGAAGGGCC | 71889 |
rs241803435 | snp | A/G | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490197 | CCTAGCTCCTGGAAG[A/G]TGGGGGTTCAGCCAT | 71889 |
rs241858749 | snp | C/T | | | synonymous-codon | Epn3 | Mm_Celera | 11:94491178 | ATTAGTGCCAGCCTG[C/T]GGGGGCAGCGGCCCC | 71889 |
rs241924581 | snp | A/G | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497690 | TGGAGGCCGACTCAG[A/G]AGAATCAGTCACATG | 71889 |
rs243088672 | in-del | -/CACT | | | intron-variant | Epn3 | Mm_Celera | 11:94496731 | GGCCTCCTTGCTGTC[-/CACT]CAGTCAAGAGTGGCA | 71889 |
rs243156433 | snp | A/C | | | intron-variant | Epn3 | Mm_Celera | 11:94493729 | GATGTCAATTCAGTC[A/C]TGCCCAGTCCTGGTC | 71889 |
rs243206368 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94494802 | GGGACTGACCGGGAA[C/T]ACCAAGAGGCCCTGT | 71889 |
rs243527164 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94497818 | CACTAATATAGTTTT[A/G]CACATGAATACATTT | 71889 |
rs243587723 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499002 | GTGCACAGGCTAGTC[A/G]GGAAGTGGGGGGGGG | 71889 |
rs243709105 | snp | C/T | | | synonymous-codon | Epn3 | Mm_Celera | 11:94496276 | GTGGGCCACACGTTC[C/T]GAGCCCGTCTTGAGC | 71889 |
rs243962048 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94491855 | GAAGAGGGCAGAGGC[A/G]CCCCTGGAGTCTCTC | 71889 |
rs244166143 | snp | C/G | | | upstream-variant-2KB, missense, nc-transcript-variant | Epn3, Mycbpap | Mm_Celera | 11:94501513 | AGGTTGTCCAGCAAC[C/G]CATAGACCTGGAAGA | 71889 |
rs244868702 | snp | A/G | | | missense | Epn3 | Mm_Celera | 11:94491318 | GCACGCTGCTGAGCG[A/G]AAGGGGCAGAGAGGC | 71889 |
rs245450599 | in-del | -/T | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500610 | GAATTCTTCAAGCTG[-/T]TTTTTGTTGTTTTGA | 71889 |
rs246231391 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94497364 | TGATCAGACAGCCAG[A/G]GGAAGGAGCATGCCT | 71889 |
rs246639401 | in-del | -/TTC | | | intron-variant | Epn3 | Mm_Celera | 11:94497109 | CTTCATCCTTTTTTT[-/TTC]CTCAGATGACCAACT | 71889 |
rs246803107 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94495468 | TCCTCAGGTCAAAAA[A/G]GCCTCCACCACTTTG | 71889 |
rs246829432 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499898 | GCCGCTCAGACTCTC[C/G]CGGCTGCCTCCTCGA | 71889 |
rs247192523 | snp | C/T | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489441 | GGAGGGGCGGAGAGG[C/T]ATGGGGCAGCAGAGC | 71889 |
rs247865811 | in-del | -/TCCC | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500432 | CCCTGGCTACTGGCT[-/TCCC]TCACTCCTCCACTGC | 71889 |
rs247883995 | snp | G/T | | | missense | Epn3 | Mm_Celera | 11:94492340 | GCAAATCCCAAGGCT[G/T]GCTTCGGGACAGGGC | 71889 |
rs247947508 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94493529 | GATTCTATAAGGCGA[A/G]AGCTGGGACTGTCCA | 71889 |
rs247986771 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499009 | GCTAGTCAGGAAGTG[-/T]GGGGGGGGGCGGGGG | 71889 |
rs248106247 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | Mm_Celera | 11:94501239 | CACCTCTCTGGTGTG[G/T]GTGGCTCTGAGAACT | 71889 |
rs248982843 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94492582 | AGCAGCTCTCTCAAG[C/T]CCATGGTTAACAAGC | 71889 |
rs249409390 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94495266 | ACATGATCGAAGGGG[A/G]CTGGCAGTAGTCCTA | 71889 |
rs249474931 | snp | C/T | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498737 | AAGGCGGGAGGCGGG[C/T]GCGGCTGGGAGCCCT | 71889 |
rs249700575 | snp | A/G | | | synonymous-codon | Epn3 | Mm_Celera | 11:94496399 | AAAGGCCACCGTGTT[A/G]AAGGTCAGGTCAGCA | 71889 |
rs249725163 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94494478 | AACTTCCCTAGGTCA[C/T]CCATTGTAAGAGGCA | 71889 |
rs249895859 | in-del | -/C | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94489825 | GGCCACCTCTGACTA[-/C]TGGTGCTTCAGGCTG | 71889 |
rs250302279 | snp | C/G | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500546 | CTTTCCCAGCTGTTA[C/G]CCTTCACCTACTACA | 71889 |
rs250338739 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94496752 | GTCAAGAGTGGCACG[A/G]CCAGAGTGTCCCTGC | 71889 |
rs251376334 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499019 | GAAGTGGGGGGGGGG[-/C]GGGGGGGGCTAGAGT | 71889 |
rs251393880 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94494723 | ATTGCCCTTTCTGGT[C/T]CCCAACTACACACTG | 71889 |
rs251404876 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499711 | CAGAGTGGGCTCCCT[C/T]GCCCCAGCCCCCGCA | 71889 |
rs251948853 | snp | A/G | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489512 | GGCAGAAGACAGATA[A/G]GGATGAATGGCCAAC | 71889 |
rs252423242 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94492531 | CCCAGGTTGGGTGAT[A/G]TGCCCACTTCACAAG | 71889 |
rs253204913 | in-del | -/CCA | | | cds-indel | Epn3 | Mm_Celera | 11:94490323 | CTCTGAATCCTAGCC[-/CCA]CGTCACTCCAGCTTT | 71889 |
rs253987858 | in-del | -/C | | | intron-variant | Epn3 | Mm_Celera | 11:94496938 | AATCGGTCAGCGATG[-/C]CTCTGAGGTCACAGA | 71889 |
rs253990756 | snp | G/T | | | intron-variant | Epn3 | Mm_Celera | 11:94495897 | CAATCACCTTTTGAG[G/T]TAGGAACTATCTCAT | 71889 |
rs254089601 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94495691 | CCCAAGCCACTCAGC[C/T]TGGAGGGAACAGAAT | 71889 |
rs254378054 | snp | C/G | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499019 | GAAGTGGGGGGGGGG[C/G]GGGGGGGGCTAGAGT | 71889 |
rs254468738 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499011 | TAGTCAGGAAGTGGG[-/GT]GGGGGGGCGGGGGGG | 71889 |
rs254818471 | in-del | -/TAGG | | | intron-variant | Epn3 | Mm_Celera | 11:94497915 | CCTGTCAGCCATAGA[-/TAGG]TATGATACCTTCCCC | 71889 |
rs254822371 | snp | A/G | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489421 | GTTCTTCGGGGCTCA[A/G]GGGAGGAGGGGCGGA | 71889 |
rs254884824 | snp | C/G | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490070 | GTGAAAGGAGCTGGG[C/G]CAGAGTTGAATTTTG | 71889 |
rs254901321 | snp | A/G | | | upstream-variant-2KB, intron-variant | Epn3, Mycbpap | Mm_Celera | 11:94501610 | GAGAGACGAGATGGA[A/G]AGAGAAACGCCAAAG | 71889 |
rs255273902 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94495578 | GGATGTCAGGTGTCT[A/G]AGTAAAAAGGCCAAG | 71889 |
rs255571943 | snp | A/G | | | downstream-variant-500B | Epn3 | GRCm38.p3 | 11:94489546 | CACGGGAGCTTCCAC[A/G]TAGCAACCCCACAAA | 71889 |
rs255668422 | snp | A/G | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489413 | ACCAACCTGTTCTTC[A/G]GGGCTCAGGGGAGGA | 71889 |
rs255682004 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94493236 | GTCTGAAGTTCTATA[A/G]CCAGGAAAAGACAGA | 71889 |
rs255740322 | snp | C/G | | | intron-variant | Epn3 | Mm_Celera | 11:94494435 | CAGTCTCAGCTCTCA[C/G]CTATCTTTTTCTTCT | 71889 |
rs256116302 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94493640 | ATGGTGACCCTGATC[C/T]GTCACCAGCCCCTGC | 71889 |
rs256379131 | in-del | -/GCAC | | | intron-variant | Epn3 | Mm_Celera | 11:94496840 | GACACGCTTTGCTTG[-/GCAC]GCTCATTCCAGAAAA | 71889 |
rs256502713 | in-del | -/AG | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490634 | AACCCAGTTTTGGAC[-/AG]AGAGTACTGCATATC | 71889 |
rs257997037 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94497111 | TCATCCTTTTTTTTT[C/T]CTCAGATGACCAACT | 71889 |
rs258136336 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94495133 | AAGCTGGGGCTCACA[C/T]AGTGAGCCAGAGAAA | 71889 |
rs258345675 | in-del | -/C | | | intron-variant | Epn3 | Mm_Celera | 11:94495950 | CTGTGGCTGGCCTAA[-/C]CCCCCCCCACTTGCC | 71889 |
rs258354324 | snp | A/G | | | upstream-variant-2KB, missense, nc-transcript-variant | Epn3, Mycbpap | Mm_Celera | 11:94501439 | TGCAAAAACGTAAAG[A/G]CTCTTCAACATTCTT | 71889 |
rs258523634 | snp | C/T | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498278 | AGGGCGGGCTGGCAG[C/T]AGCAGAGTCAAGACG | 71889 |
rs258550493 | in-del | -/C | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498758 | TGGGAGCCCTGCCAG[-/C]GGTGTTACAAGCAGA | 71889 |
rs258717491 | snp | C/T | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94489998 | GTTTCCTAAGCCCTG[C/T]AACAACCTTGCAGAG | 71889 |
rs258772944 | snp | C/G | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490213 | TGGGGGTTCAGCCAT[C/G]CTGGGTTCCTCCTGG | 71889 |
rs259785687 | snp | A/C | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500249 | ATTAAAGCAGAAGAC[A/C]GAACATTCCCTGGGG | 71889 |
rs260634151 | in-del | -/TTTG | | | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | Mm_Celera | 11:94500910 | GCAAAGAGTTATGCC[-/TTTG]TTTGTGTTTCTTCAG | 71889 |
rs260906606 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499853 | ACAGAGCTCTCTCTC[G/T]GAAGGACCGCAGGGT | 71889 |
rs261337162 | snp | A/G | | | downstream-variant-500B | Epn3 | Mm_Celera | 11:94489181 | GAGACCGAGAGCCCT[A/G]TTGTGAGTGCCAAGG | 71889 |
rs262045544 | in-del | -/CCCCCCG | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497746 | AAGAGTAATACCCCC[-/CCCCCCG]CCACCCCCGTGGGAC | 71889 |
rs262603943 | snp | C/T | | | intron-variant | Epn3 | Mm_Celera | 11:94494078 | ATGGCCTAGGTGACT[C/T]GGCCCCTATACTACC | 71889 |
rs262615306 | in-del | -/T | | | intron-variant | Epn3 | Mm_Celera | 11:94497102 | TTTAGCCCTTCATCC[-/T]TTTTTTTTCCTCAGA | 71889 |
rs262947087 | snp | C/T | | | utr-variant-3-prime | Epn3 | Mm_Celera | 11:94490989 | GGTAAGAGCTGAGGA[C/T]GTAGATTCCAGTCTT | 71889 |
rs263139502 | snp | A/T | | | intron-variant | Epn3 | Mm_Celera | 11:94495423 | CCCAAGCAGGCCATC[A/T]TAGACTTTATGGAAG | 71889 |
rs263294964 | snp | A/G | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498958 | GCTGCTTCAGAAATG[A/G]AAAGAAGGCAGGAGG | 71889 |
rs263579159 | snp | C/G | | | intron-variant | Epn3 | Mm_Celera | 11:94494572 | AGAGGTGTTGTCCCT[C/G]TCCTTCCAAAAGGAC | 71889 |
rs263636567 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499008 | GGCTAGTCAGGAAGT[-/GG]GGGGGGGGGGCGGGG | 71889 |
rs263929500 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94492792 | GGAGGTATTTTGCCA[A/G]CAAGTGGCTGGAAGG | 71889 |
rs264270878 | snp | C/T | | | upstream-variant-2KB | Epn3 | Mm_Celera | 11:94500644 | GTTGTGGTCCCTCCT[C/T]CCCTTCCCCACCCCG | 71889 |
rs264593339 | snp | A/G | | | intron-variant | Epn3 | Mm_Celera | 11:94497692 | GAGGCCGACTCAGGA[A/G]AATCAGTCACATGTC | 71889 |
rs265203151 | snp | A/G | | | synonymous-codon | Epn3 | Mm_Celera | 11:94491439 | CGGCCTGCCCTGATC[A/G]CCCGCGCCAAACGGG | 71889 |
rs265582564 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Epn3 | Mm_Celera | 11:94499899 | CCGCTCAGACTCTCG[C/T]GGCTGCCTCCTCGAC | 71889 |
rs265845101 | in-del | -/C | | | intron-variant | Epn3 | Mm_Celera | 11:94495154 | GCCAGAGAAAATTGG[-/C]TCTTCAGGCACTTGT | 71889 |
rs265858413 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | Mm_Celera | 11:94501271 | CACATGTGAGCAGGT[A/G]GGATACAGGAGGTCC | 71889 |
rs266254532 | snp | C/G | | | intron-variant, utr-variant-5-prime | Epn3 | Mm_Celera | 11:94498630 | CCTGTCATAGACTCT[C/G]ATGGTGTTTCACCCA | 71889 |
rs387178762 | snp | C/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497588 | TTGGAACCACCTTTT[C/T]GGGCAGAATGGAAGT | 71889 |
rs387476016 | snp | C/T | | | intron-variant, utr-variant-5-prime | Epn3 | GRCm38.p3 | 11:94498396 | ACATCCTGACTCCAC[C/T]AGAGCCCTACCTGGG | 71889 |
rs387662929 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | GRCm38.p3 | 11:94501226 | ATCCCTTAATCATCA[C/T]CTCTCTGGTGTGTGT | 71889 |
rs578914805 | snp | A/G | | | intron-variant | Epn3 | GRCm38.p3 | 11:94495963 | TAACCCCCCCCACTT[A/G]CCCCGCCCCCACAAG | 71889 |
rs579708280 | snp | A/G | | | intron-variant | Epn3 | GRCm38.p3 | 11:94496830 | CTGTCCAATGGACAC[A/G]CTTTGCTTGGCACGC | 71889 |
rs580068830 | snp | C/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497928 | GATAGGTATGATACC[C/T]TCCCCAGATCACCCT | 71889 |
rs581002382 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn3 | GRCm38.p3 | 11:94499593 | CTTACTCTCTAGAGG[C/T]TGGGAAAGAGACTAA | 71889 |
rs582281943 | snp | C/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497225 | GAGAAAGGACATAGA[C/T]ACATAAGGAAGGCAC | 71889 |
rs583991504 | snp | C/T | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497751 | GTAATACCCCCCCAC[C/T]CCCGTGGGACTTACC | 71889 |
rs584687295 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Epn3, Mycbpap | GRCm38.p3 | 11:94500906 | GTACAGCAAAGAGTT[A/G]TGCCTTTGTGTTTCT | 71889 |
rs585294497 | snp | A/C | | | utr-variant-3-prime | Epn3 | GRCm38.p3 | 11:94490468 | CTTCTCCTGCCTTGT[A/C]ATAATAATAATAATA | 71889 |
rs585456001 | snp | A/G | | | intron-variant | Epn3 | GRCm38.p3 | 11:94497322 | CAAGAAGATGTAGGG[A/G]ACCAGCAAGGCCAGG | 71889 |
rs586833562 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn3 | GRCm38.p3 | 11:94499015 | TCAGGAAGTGGGGGG[A/G]GGGCGGGGGGGGCTA | 71889 |