SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6381669 | snp | A/G | 0.5 | 0 | intron-variant | Epn1 | Mm_Celera | 7:5091009 | GTGAGGACACCGTGG[A/G]ACNTGCTCAGGTGGA | 13854 |
rs6382045 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Epn1 | Mm_Celera | 7:5091012 | AGGACACCGTGGNAC[G/T]TGCTCAGGTGGACCT | 13854 |
rs6384218 | snp | G/T | 0.5 | 0 | intron-variant | Epn1 | Mm_Celera | 7:5085018 | TTCACCTGTTGTTTT[G/T]ATATAGAGTTTTGCT | 13854 |
rs6384973 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Epn1 | Mm_Celera | 7:5085203 | TTTTATTTTTCTGGT[C/G]CTGGAGTTGCTGGGC | 13854 |
rs13473772 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon | Epn1 | Mm_Celera | 7:5097693 | AGCGCCACCCACCTA[C/T]ATCTCTCCTCTTGGT | 13854 |
rs13473773 | snp | A/G | | | utr-variant-3-prime | Epn1 | Mm_Celera | 7:5097993 | GAGGGGAGCCGGCCA[A/G]AGGAGGACCCTTTTC | 13854 |
rs31230666 | snp | C/G | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5080078 | CTTGGACCTTTACGC[C/G]TCTCCACTGCTGCGT | 13854 |
rs31417679 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Epn1 | Mm_Celera | 7:5096768 | TGCGTTTCCATTGGT[G/T]CATTCCTAGAGGGAA | 13854 |
rs31467388 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5096105 | TGAGTCAAGTGCAGC[C/T]TCCCTTCTTCACAGA | 13854 |
rs31723015 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Epn1 | Mm_Celera | 7:5088874 | TTTCACTTTATGTGT[A/G]TGATTGTTTGCCTGT | 13854 |
rs31828550 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5096262 | TCTTCTGTTTAACCG[C/T]GTGAGGCCCTGGAAC | 13854 |
rs31912323 | snp | C/T | 0.375 | 0.216506 | intron-variant | Epn1 | Mm_Celera | 7:5089142 | TTTCTCTTAAGTACT[C/T]TAATTTCATCTTGCT | 13854 |
rs32246310 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5079946 | TTACTTTATGGATCC[C/T]CATCTGTGTCCAGTG | 13854 |
rs32291999 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB, utr-variant-5-prime | U2af2, Epn1 | Mm_Celera | 7:5080215 | AGGGCGGGGCACGTG[A/G]GTTCATTTCCGCTTC | 13854 |
rs32308419 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5096408 | GCTTACCTTTGGTCA[C/T]TGTTTGTTTTGAGAT | 13854 |
rs32348822 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083230 | CTGGTGAGGAAGGAG[C/G]AAGAGTTTGTTAGCA | 13854 |
rs32391756 | snp | C/T | 0.375 | 0.216506 | intron-variant | Epn1 | Mm_Celera | 7:5093061 | ACTCCTCTCCCTGCT[C/T]CTGCTGTCTCTCTGT | 13854 |
rs33894318 | snp | C/T | 0.375 | 0.216506 | intron-variant | Epn1 | Mm_Celera | 7:5095340 | CGCAGAGTAAGGGGT[C/T]GTGAGATGGCCAAGG | 13854 |
rs33894842 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078329 | TTTTAACAGATTTTT[A/T]AAAAAGATTTATTTA | 13854 |
rs45648575 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5081544 | GTCACAGGGTTGTTT[C/T]GCTGGTTGCTTATGT | 13854 |
rs45734141 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5093515 | GGACACTGGCTAGAT[C/G]TGCTCCAGACCTGGG | 13854 |
rs45737008 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5092644 | CTTCAGCACACTGGT[C/T]GTCCCTTAGCAGCAG | 13854 |
rs45812928 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5081580 | GGATTTGAGTGCAAA[C/T]TTTGTGTTCTTTTAA | 13854 |
rs45862554 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5087545 | AGATGTGAAGATGGT[A/G]ACCCTCTTTTAAATG | 13854 |
rs46006859 | snp | A/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082785 | TCCCTACCATTTTTT[A/T]AAATCCCATCATTGG | 13854 |
rs46037867 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5092193 | TGCTATAGTGTATGG[A/G]CCTTCTCTGGGTCAC | 13854 |
rs46164984 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5087078 | TCTCCCAATTCTGAT[C/T]GTGTGATGCCCTTGG | 13854 |
rs46255124 | snp | A/G | 0.336735 | 0.234472 | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098664 | TTTCATTACTCCCCA[A/G]GACAGATCCTGACTG | 13854 |
rs46296871 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5085847 | ATTGATTCAGTTCCT[C/T]ACTGGACTTGGAGCC | 13854 |
rs46349092 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5085252 | GAAAGGTTGGTAAGT[G/T]TGGTCTGGTTGCATA | 13854 |
rs46351396 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5090572 | AATCACAGAGGAGGC[C/T]AGCATCGTGCCGACA | 13854 |
rs46374432 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5090548 | CCCTCTAGCTAAAGG[A/G]TGCTGTTAAATCACA | 13854 |
rs46379597 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Epn1 | Mm_Celera | 7:5094980 | GGATCTTGCTGATGT[C/T]TTCACAACCCCAGCG | 13854 |
rs46619260 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5087951 | TCTCTGCTTCTGTGT[C/T]GCACATAGCAGTTGT | 13854 |
rs46676394 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Epn1 | Mm_Celera | 7:5097514 | CCCACCTGGGTGTGT[A/G]TCCAAGACTTGGACG | 13854 |
rs46679970 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5089869 | CCCAGACGCTTCCTC[A/G]GTCTCTAGTCCCTTT | 13854 |
rs46819013 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5086765 | ATAGCCTCCAGAAGA[C/T]AGAAAAGACTTCCTA | 13854 |
rs46828263 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5090584 | GGCCAGCATCGTGCC[A/G]ACAGGACAGGCTGTG | 13854 |
rs46850851 | snp | A/T | 0.124444 | 0.216185 | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098405 | TCCTACACAGGCATC[A/T]CTAATTCATCCAGCT | 13854 |
rs46901778 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5089499 | TAGAGCTCTCATGTA[C/T]AGTCGTCAGCTTTTT | 13854 |
rs46910733 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5088509 | GTCTGTATAGGAAAT[A/C]ACTGTGTCTCTGTCC | 13854 |
rs47275866 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5092297 | AGGGCATGGTGCAGG[A/G]CTGAAGGAGGTGGTG | 13854 |
rs47290200 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5085806 | CATCACAACACACCA[A/C]GATTGGTCCTGAGTT | 13854 |
rs47445789 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Epn1 | Mm_Celera | 7:5095551 | AGTGAGGCTAGTCGT[C/T]TGTTTGGGTGATTTG | 13854 |
rs47526444 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5096997 | CACAGTAAGATCCTC[G/T]CGGTTTTTAGTCCAA | 13854 |
rs47622534 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5097447 | TCCTGTGTCTTTGGT[A/G]TCTTCTGTGGTCCCT | 13854 |
rs47697653 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Epn1 | Mm_Celera | 7:5093575 | AGCAGCAGGCCAGGG[C/T]GAGAGGCCTCCTCCT | 13854 |
rs47810242 | snp | A/G | 0.142012 | 0.225474 | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098459 | CTGCTGGCTAAACCC[A/G]GTGGACCGCCAGATG | 13854 |
rs47836967 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5086888 | GCCTCAGACTTGTGC[C/G]CCACCAAGGCTTGGA | 13854 |
rs47936841 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5090954 | GACCCTGGTTCTAAC[C/T]GTAGGCCTCTGTCTA | 13854 |
rs48007369 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083568 | TTGCTTTCCCCTCAA[A/G]GGTGGTGGAAAACCT | 13854 |
rs48077795 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5088811 | GGTCTTGACTTAGAT[C/T]TTTCCTTGGGTTGGT | 13854 |
rs48105477 | snp | A/G | 0.35503 | 0.226867 | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098494 | CTCTAGGCCATTGCT[A/G]TGTGTTTTTATCATG | 13854 |
rs48170730 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083383 | TGTTAAGATGTGGCT[A/G]AGTTAGAGTATGGAC | 13854 |
rs48334504 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5085787 | CTGAGGACTGTTTCA[C/T]GCCCATCACAACACA | 13854 |
rs48459785 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Epn1 | GRCm38.p3 | 7:5093509 | CACCCAGGACACTGG[A/C/G]TAGATCTGCTCCAGA | 13854 |
rs48641210 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5085142 | TAGGCCGTGGCAGTG[C/T]TTTGTTCTTTTAAGC | 13854 |
rs48643737 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5087338 | TATGTGCTGAGAGGA[C/T]ACAGGTCTCAGTTGC | 13854 |
rs48747220 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5085832 | GAGTTGTATTTAATC[A/C]TTGATTCAGTTCCTC | 13854 |
rs48831844 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087924 | CTCTGCTTACCAGGC[C/T]TGGGGCCATGATCTC | 13854 |
rs48845353 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5086795 | AAAAGAGGCTGCCAC[A/G]GGTAGATTACAAATG | 13854 |
rs48958754 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089368 | TTAATTTGGCTCTGT[C/T]GCTTCAGATTTTGCC | 13854 |
rs49002948 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5093465 | CTGAGTACAGGAGTA[A/C/T]TCACTTTCAGCATCT | 13854 |
rs49172171 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5088076 | GTTTCCTGCTTCATA[A/G]CCTTAGCTGCAGTTC | 13854 |
rs49218512 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5084059 | CCTAGTTTCTCAAGA[A/G]GGGGAAGGTTGAAGA | 13854 |
rs49293337 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Epn1 | Mm_Celera | 7:5096143 | AACAATGGATATCCT[A/C]TCCACACTCCTGTCT | 13854 |
rs49318620 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5088808 | ACAGGTCTTGACTTA[A/G]ATCTTTCCTTGGGTT | 13854 |
rs49368633 | snp | A/C | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5092133 | TGAGGATGTTCCAGG[A/C]TCTATCTTAGGATGA | 13854 |
rs49380221 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082552 | CTTTTGCATTTATGA[A/T]ATGACCTTGACCAAG | 13854 |
rs49425274 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Epn1 | Mm_Celera | 7:5093574 | CAGCAGCAGGCCAGG[A/G]TGAGAGGCCTCCTCC | 13854 |
rs49482140 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5084988 | TTTATTGTTTACATC[C/G]TCAACATTGAATTTT | 13854 |
rs49491907 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Epn1 | Mm_Celera | 7:5087547 | ATGTGAAGATGGTAA[C/G]CCTCTTTTAAATGTT | 13854 |
rs49503114 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Epn1 | Mm_Celera | 7:5096515 | CTCCCCGGTACCTTT[A/T]CTTGTTATACTGGAA | 13854 |
rs49519235 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5094923 | CTGTCTCTAGTTCTC[C/G]GCTCACATCCCTTCT | 13854 |
rs49655098 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Epn1 | Mm_Celera | 7:5091159 | CTTTGTGGAGGGTGT[A/G]TGGTGTGCATGCCTA | 13854 |
rs49757752 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5086711 | AGGCAAGTAGTTGTG[A/G]TTGGCCAGTTGTATT | 13854 |
rs49957003 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Epn1 | Mm_Celera | 7:5095298 | AAGCCCCCAGGGGAA[A/G]CCATCTCTTTAGGAA | 13854 |
rs50029144 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5085277 | TGCATACATGACCCA[G/T]CGAGGTTCTCAGATT | 13854 |
rs50069905 | snp | C/G | 0.124444 | 0.216185 | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098479 | ACCGCCAGATGGCAT[C/G]TCTAGGCCATTGCTA | 13854 |
rs50231119 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5089183 | TTTGTTTTCATATTA[C/T]AAAATAGAGATACCA | 13854 |
rs50268870 | snp | A/C | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5085742 | TCAAGATAAGGAGAC[A/C]TAGTAACATCTATGC | 13854 |
rs50405118 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5090308 | GACTCTGAAATTTTG[C/T]AGAATGCCTCCTTTG | 13854 |
rs50435342 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094094 | CAGCTCCAGCCCCAG[C/T]CCCAATGTGACTTTC | 13854 |
rs50511597 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5084782 | GGGATGTCAGACTTG[A/C]TGATATTTATTGATG | 13854 |
rs50588678 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084463 | CTGGGATTGTGTCAG[C/T]ACCCAGACATATATT | 13854 |
rs50738476 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Epn1 | Mm_Celera | 7:5095512 | CTAAGTCATGCTAAC[A/T]TGTTTGTAGTAGAAG | 13854 |
rs51009146 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Epn1 | Mm_Celera | 7:5093540 | CCTGGGGGTACAAGT[A/G]TCACTAGGTCATGCA | 13854 |
rs51060388 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083313 | TAGTAGACCCTTATC[A/G]CATGTGCAACACTTC | 13854 |
rs51246281 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Epn1 | Mm_Celera | 7:5095973 | CTCTGGGAGCAGCAC[A/G]GGTGAGTCACCGCTC | 13854 |
rs51247145 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Epn1 | Mm_Celera | 7:5087116 | CCTGGGATGCTGGGC[A/G]TGGCTTTGAGTGCTT | 13854 |
rs51328913 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Epn1 | Mm_Celera | 7:5080937 | GCTTTTGCTTAGGAT[A/G]TGCTTCCCAGGTTTC | 13854 |
rs51376128 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5091530 | CCTGTCCACACACAC[A/G]TGAGCTGGGTCACAG | 13854 |
rs51428631 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5090782 | TTTCATGCTGAGGGA[C/T]CATGGCAGGGGAAGC | 13854 |
rs51456860 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5088798 | TGCTCTGGAAACAGG[C/T]CTTGACTTAGATCTT | 13854 |
rs51515220 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5089555 | GTATAGTCCGTGCTG[A/G]TGTCACACCCTGGCT | 13854 |
rs51548232 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Epn1 | Mm_Celera | 7:5081246 | GTACTGTTTAATAAG[A/C]AATTCTAAATTAACT | 13854 |
rs51603106 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Epn1 | Mm_Celera | 7:5092215 | CTGGGTCACTGCTGG[A/T]GCAGTGGTTAGAAAC | 13854 |
rs51657294 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5088192 | TACTGTGCTCCTGTC[C/G]CGTGTTGCATGGCTG | 13854 |
rs51739584 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5088039 | TTTTGTGTGCATGGC[A/T]CTATGCCTGGGCATT | 13854 |
rs51800750 | snp | A/T | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5092714 | GGACTCTGGCTCCAT[A/T]ACTTTCTCTCCCAGT | 13854 |
rs51847966 | snp | A/G | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5085568 | CTGACTGCCCCAGAT[A/G]GGGGGAGTGTATCTG | 13854 |
rs51929702 | snp | C/T | 0.32 | 0.24 | intron-variant | Epn1 | Mm_Celera | 7:5092014 | CATTTCCTTGTAAGG[C/T]TTGAAGTGGGGCCTT | 13854 |
rs52032357 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Epn1 | Mm_Celera | 7:5088694 | TCCACGGAGTCTTTG[C/T]AGCCATTGCATAAAG | 13854 |
rs52087735 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Epn1 | Mm_Celera | 7:5084659 | CATCAGTTCCCAGCC[A/G]CTGAAGGCTGTCTTT | 13854 |
rs52423441 | snp | A/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094369 | TGAGTGTGAGTATAC[A/T]CAAGCGCTCGCTCTC | 13854 |
rs108174744 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082846 | TGTTTGCttctctct[C/T]tctttctttctttct | 13854 |
rs108901282 | snp | A/G | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078410 | ATCCCATTAGAGATG[A/G]TTGTGAGCCACTGTG | 13854 |
rs211778259 | in-del | -/TA | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098493 | TCTCTAGGCCATTGC[-/TA]TGTGTTTTTATCATG | 13854 |
rs212068362 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5092526 | CTGTTCCTGCCAGGG[C/T]TGCAATCCTGCCTGG | 13854 |
rs212206181 | snp | A/C | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083655 | TTTCCAACCCCCCAA[A/C]CCCCCAGATGTGGTG | 13854 |
rs212249485 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5090550 | CTCTAGCTAAAGGGT[A/G]CTGTTAAATCACAGA | 13854 |
rs212311822 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091190 | TGTGTGTGTGGGGTG[C/T]GCATGTGAACAGATG | 13854 |
rs212525393 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094555 | CATGGTGTGCACTGC[A/G]GGGCAGTGATGTGGC | 13854 |
rs212528564 | snp | G/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078997 | TTTCTGTGATGTCTC[G/T]CTTCTGTGCCTTGTT | 13854 |
rs212656562 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086283 | TCTCTGGGAGCTCCC[A/G]GGGGTCCAGCTTAGT | 13854 |
rs212691096 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5095321 | TTTAGGAAGGAAGGC[C/T]TTACGCAGAGTAAGG | 13854 |
rs212861673 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084819 | AAGGCAGAGCCTTGG[G/T]GGCAGGTGACAGACT | 13854 |
rs212873842 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5094435 | GGTTATCTCCACTGT[A/C]ACATCAGGGCTTTGG | 13854 |
rs213882230 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5097463 | TCTTCTGTGGTCCCT[A/G]CAGGGTAGAAGTTTC | 13854 |
rs213997882 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078835 | TGAGCTTTCCTTACC[-/CA]TTGTCTGTGGGGAGA | 13854 |
rs214020049 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5088302 | GATTCCAAAACATAA[C/G]GACCTACCACCTACC | 13854 |
rs214292674 | snp | G/T | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098612 | TTTGCCAACAGTGTC[G/T]TCCCATGCTTCCTGG | 13854 |
rs214368331 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5085685 | GCACTGTCCTGAACT[A/C]TCTGAGAGACTTCCT | 13854 |
rs214511302 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5078876 | GTGGCTTGGGGAACA[-/CT]CTGTAGGGTGCATGA | 13854 |
rs214609839 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091353 | GTCTCTGTCTCCCTA[A/G]GCTGGAATTACTAGT | 13854 |
rs214625943 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083294 | GCTTCTACTGCAACC[C/T]GTGTAGTAGACCCTT | 13854 |
rs214854215 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086468 | CCTGCATCTGGAGTG[A/G]CCCTGGAATCCGCTC | 13854 |
rs214941060 | in-del | -/TCTG | | | intron-variant | Epn1 | Mm_Celera | 7:5090505 | TTACTTCTGATGGAG[-/TCTG]CTGCTAGTCTGGCTT | 13854 |
rs215159861 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094449 | TCACATCAGGGCTTT[A/G]GTTGGCTGCTTTTAT | 13854 |
rs215308432 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5095421 | GAAGGCTGTAGAGGG[C/G]AAGTGGTGGGAAAGT | 13854 |
rs215350298 | in-del | -/ACATCCTCA | | | intron-variant | Epn1 | Mm_Celera | 7:5084983 | AACGCTTTATTGTTT[-/ACATCCTCA]ACATTGAATTTTTCA | 13854 |
rs215735551 | snp | A/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096219 | TGGAGAAATGTGGGC[A/T]CCCCCTTGGGCTGGG | 13854 |
rs215883403 | in-del | -/AC | | | intron-variant | Epn1 | Mm_Celera | 7:5091488 | CCTTGAACTTTGCTG[-/AC]ACAGGAGACTGAGGG | 13854 |
rs216287518 | snp | A/C | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078738 | TAATCATTTCCTTTA[A/C]GGTGATTGAGTGGTT | 13854 |
rs216480636 | in-del | -/G | | | intron-variant | Epn1 | Mm_Celera | 7:5092097 | TTGGCAGTGGGGCGT[-/G]GGTTGCCGGCACTGA | 13854 |
rs216712412 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5081937 | TCTTTGCCTAGTTAT[A/G]CCTGTTTGCAGGTGC | 13854 |
rs216772689 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082919 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 13854 |
rs217160256 | in-del | -/G | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098556 | GTCCTTGAGTGGCCT[-/G]GGTGGGTAGGTGCTC | 13854 |
rs217461521 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089354 | AGACTTCCTGCACTT[G/T]AATTTGGCTCTGTCG | 13854 |
rs217497322 | snp | G/T | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098629 | CCCATGCTTCCTGGG[G/T]TTTCCTTCTAGGTGG | 13854 |
rs217677725 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094524 | ATGGACGGGCAGTCA[C/T]AGGCAGGCAGCGCTG | 13854 |
rs217757517 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5085762 | AACATCTATGCATTG[A/C]AGCAGAGACCTGAGG | 13854 |
rs217771767 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5097097 | TCCTCCCTCCCTGCT[C/T]CCCCCAACTCAGGCT | 13854 |
rs217807002 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5096339 | ACTGCAAATACCCCA[A/C]GAGTGGGCCTGCGTC | 13854 |
rs217924924 | snp | A/G | | | missense | Epn1 | Mm_Celera | 7:5095065 | CCTGTGGCTGCTGCC[A/G]CTTCAGACCCTTGGG | 13854 |
rs218010771 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091551 | TGGGTCACAGGCTTC[G/T]CACGCTCCTGTTGTG | 13854 |
rs218028234 | snp | A/G | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098327 | CCTGATTCAGTTCCT[A/G]GAGCTGGGCTGGCTG | 13854 |
rs218046700 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5090876 | TATGGGGATGGGAAG[A/G]CAGTGCTGTCCTGGG | 13854 |
rs218080860 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5092444 | GCCCCTCTGACGCCA[A/C]TGGCTCTTGTTCCCA | 13854 |
rs218119211 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086231 | ATGTGCAGGGGCCTC[C/G]GTCCAGCCCATGTAT | 13854 |
rs218206117 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091509 | GAGACTGAGGGGATA[G/T]GTCACCCTGTCCACA | 13854 |
rs218325713 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083390 | ATGTGGCTAAGTTAG[A/G]GTATGGACTCAGGGT | 13854 |
rs218349754 | snp | A/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085229 | TGGGCCAGAGGGCAC[A/T]TGAGTGTGAAAGGTT | 13854 |
rs218381990 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5093651 | CAGGCATCCTTTCCA[C/T]AGCACCCTACACACA | 13854 |
rs218488347 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085784 | GACCTGAGGACTGTT[C/T]CATGCCCATCACAAC | 13854 |
rs218620311 | in-del | -/TTTG | | | intron-variant | Epn1 | Mm_Celera | 7:5089111 | TTTTTTTTTTTTTTT[-/TTTG]TTGTTGTTCTGTTTT | 13854 |
rs218816228 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5085391 | GGGGTTGTGCCAGTG[C/G]CCCCCCCCCCCCCCC | 13854 |
rs219390453 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5088849 | TTTCATTTGCTTAAG[A/G]TTTATTTAATTTCAC | 13854 |
rs219742586 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5087536 | TTTCTCTCCAGATGT[A/G]AAGATGGTAACCCTC | 13854 |
rs219755086 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5095549 | AGAGTGAGGCTAGTC[A/G]TTTGTTTGGGTGATT | 13854 |
rs219776071 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087607 | GAACTGGTTTAAAAT[G/T]TTACAAGCTCCATGG | 13854 |
rs219811910 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5086631 | CTGAGGCCAGGTGAG[C/T]TGGCCTGAGGGAGCG | 13854 |
rs219860558 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096795 | GGAAAAGGTTTGTCC[C/T]CCAGCCCTTAGATGT | 13854 |
rs220100373 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089436 | GCCCTGATTGGCTAT[C/T]TTGGTGGTTGCCATC | 13854 |
rs220115242 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091946 | AAGGGCTGGAGGCCA[C/T]AGGGAGCCTGAAGTT | 13854 |
rs220135100 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5084012 | GTGGTCCCTTGGGGC[A/C]GTAGAACGGGAACAT | 13854 |
rs220177594 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082698 | GAGCTTCCCTCCCTA[C/T]CCTCTGGACACCTAG | 13854 |
rs220215338 | snp | C/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5079139 | ATGCTGAGTAGATGC[C/T]AGGAGCCAACCTTGT | 13854 |
rs220686141 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089417 | TTTTGTGGTCCTACA[G/T]GGTGCCCTGATTGGC | 13854 |
rs220722316 | in-del | -/TTTCAGTAAGGTCCAAATCCTGATTT | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078274 | CTCTAAAATGTCTTG[-/TTTCAGTAAGGTCCAAATCCTGATTT]TGGTTGCAGTTTCTT | 13854 |
rs220916777 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5081165 | TCTAGTTACTAGAGA[-/T]TTTTGTCTCGCTTAG | 13854 |
rs221129472 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085286 | GACCCAGCGAGGTTC[C/T]CAGATTTCCGGCATT | 13854 |
rs221199755 | in-del | -/TGGAGCAG | | | intron-variant | Epn1 | Mm_Celera | 7:5092212 | TCTCTGGGTCACTGC[-/TGGAGCAG]TGGTTAGAAACCTGC | 13854 |
rs221435258 | snp | A/G | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078384 | CCAGACCCACCTGAA[A/G]ACGTCATCGGATCCC | 13854 |
rs221551314 | in-del | -/TTTTTTTTTT | | | intron-variant | Epn1 | Mm_Celera | 7:5086812 | TAGATTACAAATGAA[-/TTTTTTTTTT]TTTTTTTTTTTTTTA | 13854 |
rs221675364 | in-del | -/CTCG | | | intron-variant | Epn1 | Mm_Celera | 7:5096014 | CTGGGAAGCCCCGTA[-/CTCG]GTTGCTTCTTGTCTC | 13854 |
rs221943355 | snp | A/C | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098369 | GACCTGGGCTGTGGT[A/C]CTGAGTCCTGCATCA | 13854 |
rs222018205 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5080005 | GTGGAGGGTGGCACC[C/T]AGGGAAGGAGGCAGG | 13854 |
rs222102545 | in-del | -/AG | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098589 | TCAGCTTGCATATAC[-/AG]AGAGGCATTTGCCAA | 13854 |
rs222345563 | in-del | -/A | | | intron-variant | Epn1 | Mm_Celera | 7:5092172 | TGGGGACAGGGGCAG[-/A]CAGCTTGCTATAGTG | 13854 |
rs222418245 | in-del | -/TTTCCAGTGGAG | | | intron-variant | Epn1 | Mm_Celera | 7:5089882 | CGGTCTCTAGTCCCT[-/TTTCCAGTGGAG]TTCAGTGTCAGTGAC | 13854 |
rs223006984 | snp | C/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5092661 | TCCCTTAGCAGCAGC[C/T]GTTGTGTTGAGGGTG | 13854 |
rs223455000 | in-del | -/C | | | intron-variant | Epn1 | Mm_Celera | 7:5092267 | GGAGCCACCATGGAG[-/C]CTGTAGACAGTGCCA | 13854 |
rs223683394 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5095510 | AGCTAAGTCATGCTA[A/G]CTTGTTTGTAGTAGA | 13854 |
rs223716724 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094653 | GGCTAGATCGTCTTA[A/G]AGATCCAGCCAAAGC | 13854 |
rs223933720 | snp | A/G | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098514 | TTTTTATCATGTGCT[A/G]GACCACCTGTGATTA | 13854 |
rs224058378 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089578 | CCCTGGCTGGAGGAT[A/G]AACTTCTCTTTGACC | 13854 |
rs224446043 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5093758 | CTCCATACATTGTTC[A/G]CATTCCATTTTAATT | 13854 |
rs224534241 | snp | G/T | | | missense | Epn1 | Mm_Celera | 7:5097201 | GCTCGCAGCCCTGGG[G/T]CATTCGACATGAGTG | 13854 |
rs224714660 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094647 | GGGTTGGGCTAGATC[A/G]TCTTAGAGATCCAGC | 13854 |
rs224727791 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091225 | TGTACTTGCAGCCAC[A/G]TGTATGGAGGCCAGC | 13854 |
rs224993191 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5096189 | CTGGATCATTTATTA[A/C]GTGGGGATAGGAATT | 13854 |
rs224996946 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089545 | TTGGCATCTGGTATA[A/G]TCCGTGCTGGTGTCA | 13854 |
rs224999494 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5090727 | GTGGCATGCTCAGTG[C/G]CACGTGTGGGGTCCA | 13854 |
rs225068744 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5095611 | TCCGAGCAGGAGATG[C/T]TATTAACTCATATAT | 13854 |
rs225176525 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5087258 | GGGTCTAATTAACCC[A/G]TGGGGAATGTGCTTT | 13854 |
rs225247923 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5088587 | TTATAGCAAATTTCG[A/C]TGTGTAGATAGTGCT | 13854 |
rs225398044 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | Epn1 | Mm_Celera | 7:5092875 | CTCTGGACCACCTCC[C/T]GAGGCGGAGCAGGCA | 13854 |
rs225466223 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087716 | TGAAGGAAGCCTGAG[C/T]ATTTAACCTGATGAG | 13854 |
rs225560856 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084173 | CACTTGACCGGAGTC[G/T]GATGATGGTCAAGTA | 13854 |
rs225780774 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5092040 | GCCTTCAGTGTCACT[A/G]TATGCAACCTGGGTG | 13854 |
rs225824251 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5085595 | TCTGTCTGGGTTGGG[A/G]GCTGGCGAATAGGTA | 13854 |
rs225828199 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094763 | CAGGGGTTGTACAGG[C/G]AATAGACAAGGGCCA | 13854 |
rs225922114 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5085067 | TCTGACTTGCTGTAG[A/G]CCTTGAGTTTGTGGG | 13854 |
rs225963628 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5093555 | ATCACTAGGTCATGC[A/G]CCTCAGCAGCAGGCC | 13854 |
rs225997547 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5085893 | TGTTGAGAACTGGGA[A/G]AAGGCCCAGTGTCAC | 13854 |
rs226172887 | in-del | -/A | | | intron-variant | Epn1 | Mm_Celera | 7:5085568 | CTGACTGCCCCAGAT[-/A]GGGGGAGTGTATCTG | 13854 |
rs226230922 | in-del | -/ACTGA | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5079050 | GGTAAACACCCTCAT[-/ACTGA]ACTGAAGTCCTCTGT | 13854 |
rs226235239 | snp | A/G | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078659 | TCCACTCTCTTCTGA[A/G]GTCAACTGGTTTGTT | 13854 |
rs226278746 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089860 | GCCCCAGGGCCCAGA[C/T]GCTTCCTCGGTCTCT | 13854 |
rs226993222 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085872 | GGAGCCAGGTGGCAT[G/T]TGCTCTGTTGAGAAC | 13854 |
rs227074507 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084622 | TTTGTTTTGTTTTTT[G/T]TTGTTGTTGTTTTTG | 13854 |
rs227512823 | snp | A/G | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078593 | ATGCCGGAATTGTAG[A/G]GCCATTTTGCTGGCC | 13854 |
rs227653157 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5086498 | CCTGCTCAGTGGCTG[A/C]GATTATGCTGCCAGG | 13854 |
rs227738318 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5087858 | CATCTGTACATCTGT[C/G]AGAACTTCTTAGGTA | 13854 |
rs227784011 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078488 | CTTAACTGTTGAGCC[-/CT]CTCTCTCTCCAGCCC | 13854 |
rs227849645 | in-del | -/TGGGTTGCAGCCCACATC | | | intron-variant | Epn1 | Mm_Celera | 7:5092776 | ATCTGTGCTGGGTTT[-/TGGGTTGCAGCCCACATC]TGGCTGTGGGTCCCC | 13854 |
rs227869126 | in-del | -/CCCG | | | intron-variant | Epn1 | Mm_Celera | 7:5093430 | TTTCCTTACTCCTTC[-/CCCG]CCCGTCCTGAGCTGT | 13854 |
rs227950915 | in-del | -/CGCCCC | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082468 | AGAGAGATGTTGTGT[-/CGCCCC]CACCCCCTCCCCCCA | 13854 |
rs228136641 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5086176 | GGGGTTAGGTGCATC[A/C]TCTTCCACTGAGGCC | 13854 |
rs228407545 | in-del | -/GTGTGTGTGTGTGA | | | intron-variant | Epn1 | GRCm38.p3 | 7:5094329 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGA]GTGTGAGTGTGTGAG | 13854 |
rs228855787 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084294 | AAATGGTGTATAACA[G/T]AGTGTCTGTCATACT | 13854 |
rs229122321 | in-del | -/TTTT | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5081905 | TTGGGACCCAGCTGC[-/TTTT]TTTTTTTTTTTTTTT | 13854 |
rs229136473 | snp | C/T | | | missense | Epn1 | Mm_Celera | 7:5095093 | GGGGGGGACCTGCTG[C/T]CCCTCCAGCTGCTGA | 13854 |
rs229272619 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091209 | TGTGAACAGATGGCT[C/G]TGTACTTGCAGCCAC | 13854 |
rs229364399 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082792 | CATTTTTTTAAATCC[C/T]ATCATTGGCCTCTTT | 13854 |
rs229416305 | in-del | -/TGCT | | | intron-variant | Epn1 | Mm_Celera | 7:5096860 | GTTTCTGCGCTGAAG[-/TGCT]TGCTCATTTGAGACT | 13854 |
rs229804830 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5096830 | ACCTGTCCCAGGGCT[A/G]TGGGTGTCTGCTTGG | 13854 |
rs230123948 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096347 | TACCCCAAGAGTGGG[C/T]CTGCGTCTCCTTGTC | 13854 |
rs230476498 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5092528 | GTTCCTGCCAGGGTT[A/G]CAATCCTGCCTGGAA | 13854 |
rs230538603 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083742 | CAGCCCCTTGACACC[A/G]CTACTGGGCACAATG | 13854 |
rs230538695 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5093483 | ACTTTCAGCATCTTT[A/C]GCTGGAGAGACACCC | 13854 |
rs230785530 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089431 | ATGGTGCCCTGATTG[A/G]CTATTTTGGTGGTTG | 13854 |
rs230827278 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5081906 | TTGGGACCCAGCTGC[-/TT]TTTTTTTTTTTTTTT | 13854 |
rs230841885 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5090569 | TTAAATCACAGAGGA[G/T]GCCAGCATCGTGCCG | 13854 |
rs231126011 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5095326 | GAAGGAAGGCCTTAC[G/T]CAGAGTAAGGGGTTG | 13854 |
rs231160208 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094602 | AGTGGAGTGACCTGG[C/T]AGGAGCTCAGGGAAG | 13854 |
rs231183926 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5086360 | TCTTCTGTAGGGGTC[C/T]CGACCTCAGTCCAGT | 13854 |
rs231493262 | snp | C/T | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098614 | TGCCAACAGTGTCGT[C/T]CCATGCTTCCTGGGG | 13854 |
rs231518410 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094487 | CCCTCAGAATACCAG[A/G]GCATTACTTTAGTGT | 13854 |
rs231777239 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5092335 | TATAGGAACTGGGGT[C/G]TCTTGGTCCTCCTCT | 13854 |
rs231860377 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5084821 | GGCAGAGCCTTGGGG[A/G]CAGGTGACAGACTAG | 13854 |
rs232151620 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094897 | AGCCACCTGTGGGTG[C/G]CATCCTGAATCTGTC | 13854 |
rs232208451 | snp | A/T | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098483 | CCAGATGGCATCTCT[A/T]GGCCATTGCTATGTG | 13854 |
rs232259993 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089047 | AAGTACTTTTAACCA[C/T]GGAGCCAGCTCTCTG | 13854 |
rs232436598 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086729 | GGCCAGTTGTATTTG[A/G]AGGGGCTGGTGACAG | 13854 |
rs232474532 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5093174 | TCTGCCCATCTTTAT[C/T]GGTCTGGGAGAACCA | 13854 |
rs232562116 | in-del | -/AGAGAGAGAGAG | | | intron-variant | Epn1 | Mm_Celera | 7:5095356 | TGAGATGGCCAAGGC[-/AGAGAGAGAGAG]AGAGAGAGGCGTGGG | 13854 |
rs232667768 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089114 | TTTTTTTTTTTTTTT[G/T]TTGTTGTTCTGTTTT | 13854 |
rs232687868 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5096999 | CAGTAAGATCCTCGC[A/G]GTTTTTAGTCCAAGC | 13854 |
rs232820566 | snp | A/G | | | intron-variant, utr-variant-5-prime | Epn1 | Mm_Celera | 7:5080971 | GTCTCTGGTGTTCTG[A/G]CAAGAGCTCTGGCTG | 13854 |
rs232899469 | snp | C/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5079164 | CCTTGTTCACAGATA[C/T]GCCTCTTGTTCCTAC | 13854 |
rs232934176 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5090642 | TGTTGTAAGTGGTGA[A/G]TTCAAGTTTGCTGAT | 13854 |
rs232961638 | snp | A/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5094342 | gtgtgtgtgtgtgtg[A/T]gtgtgagtgtgtgag | 13854 |
rs233045446 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5081628 | CCCCCCCCAGCCCTG[C/G]GTGTCATGTGTGTGT | 13854 |
rs233281335 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089333 | CAGGCCATCTCTTTA[G/T]CCTTAAGACTTCCTG | 13854 |
rs233325534 | in-del | -/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5084577 | CTGATCCTTCAGGTA[-/T]TTTTATTTATTTATT | 13854 |
rs233372577 | in-del | -/TTTATTTATTTA | | | intron-variant | Epn1 | GRCm38.p3 | 7:5084578 | GATCCTTCAGGTATT[-/TTTATTTATTTA]TTTATTTATTTATTT | 13854 |
rs233501322 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091156 | TCGCTTTGTGGAGGG[C/T]GTGTGGTGTGCATGC | 13854 |
rs233522857 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5081308 | GTGAGATTTAGTATG[-/T]TTTTTTTGAACATGC | 13854 |
rs233638231 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082732 | CCTGGGCACCCCCAC[C/T]CCCCAGTCTCCCACT | 13854 |
rs233721987 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5086260 | ATGCTCTTTAGTTGG[C/T]AGCTTAGTCTCTGGG | 13854 |
rs233919327 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5093409 | TGGCCTCCCTCCCCT[C/G]TAGGGTTTTCCTTAC | 13854 |
rs233943582 | in-del | -/TCA | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5082985 | TTCTTTCTTTCTTTC[-/TCA]ATTTCCTTCCTGCAC | 13854 |
rs234077207 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5084704 | GTGTGTACTTCTGAT[C/G]CACAGATGGCTCTGG | 13854 |
rs234343708 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5088247 | ATTCTCAGGTGTGTC[C/T]CTGTGCAGTGTCTTC | 13854 |
rs234385220 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5090432 | TCTTGTTAGATTGCT[G/T]GAGGTTTGGAACTCC | 13854 |
rs234905140 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094531 | GGCAGTCATAGGCAG[A/G]CAGCGCTGCATGGTG | 13854 |
rs235080559 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5086907 | CAAGGCTTGGAAAGA[-/T]TTTTTTTTTTAATGC | 13854 |
rs235207487 | in-del | -/G | | | intron-variant | Epn1 | Mm_Celera | 7:5096093 | CACATGATAGAGTGA[-/G]TCAAGTGCAGCTTCC | 13854 |
rs235301157 | in-del | -/CC | | | intron-variant | Epn1 | GRCm38.p3 | 7:5081611 | TTATATCTCTTCCCA[-/CC]CCCCCCCCCAGCCCT | 13854 |
rs235363615 | in-del | -/A | | | intron-variant | Epn1 | Mm_Celera | 7:5094684 | ACATAGTGGGTGGGG[-/A]AGGCCTTATAGCTTG | 13854 |
rs235691701 | snp | A/C | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5079029 | TTGGGTACTGGAGAA[A/C]GTTTGGGTAAACACC | 13854 |
rs235801607 | snp | C/G | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098340 | CTGGAGCTGGGCTGG[C/G]TGAGGATGGGGAGGA | 13854 |
rs235807686 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087911 | TTGGGGTCTCTTGCT[C/T]TGCTTACCAGGCTTG | 13854 |
rs235837085 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096823 | TGTCATGACCTGTCC[C/T]AGGGCTGTGGGTGTC | 13854 |
rs236369071 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085170 | GCAAGACTGATGCTG[-/T]GAATATCCTGGTGTG | 13854 |
rs236393875 | in-del | -/TC | | | intron-variant | Epn1 | Mm_Celera | 7:5087943 | GCCATGATCTCTGCT[-/TC]TCTGTGTCGCACATA | 13854 |
rs236486786 | in-del | -/ACTC | | | intron-variant | Epn1 | Mm_Celera | 7:5091449 | GCAGCAAGTATGTTA[-/ACTC]ACTAGGCCATTTTCC | 13854 |
rs236806793 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5088804 | GGAAACAGGTCTTGA[C/G]TTAGATCTTTCCTTG | 13854 |
rs237013609 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091803 | TGTCTTGACATGTTC[-/T]TTTCATTTTCTTTCT | 13854 |
rs237051841 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082180 | TGTGTAAAGTGGCTG[-/T]TGAGTCATGGATTTG | 13854 |
rs237074283 | in-del | -/TTTTTG | | | intron-variant | Epn1 | Mm_Celera | 7:5085934 | TTGGTTTGTTTTTGT[-/TTTTTG]TTTTTTTTTCTCGAG | 13854 |
rs237314746 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5097499 | GCAGGCATGCTTCTC[C/T]CCACCTGGGTGTGTA | 13854 |
rs237355557 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094700 | AGGCCTTATAGCTTG[A/G]CTGGTTGCAGGGAGG | 13854 |
rs237408990 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094199 | GCTGTAGGAGGCTCA[C/T]TTGTTTCTGCCTCTG | 13854 |
rs237461017 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5081491 | AGCAAGCTTGCCGGG[C/T]AGCACCCCTCCCTTT | 13854 |
rs237849390 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089705 | AGCACACATTGTGTG[A/G]CCTTTGTCCCTGGCC | 13854 |
rs237850027 | in-del | -/CG | | | intron-variant | Epn1 | Mm_Celera | 7:5092661 | TCCCTTAGCAGCAGC[-/CG]TTGTGTTGAGGGTGG | 13854 |
rs237928031 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5093691 | CTCTGGACCACACCA[A/C]GCTCCAAGCCTCCTG | 13854 |
rs237966265 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5093109 | CTTTAGCTTTTCTCC[C/T]GGGAAGCTGTGCTGC | 13854 |
rs237976490 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091658 | TCTTGTGTAGTCCTG[A/G]CTGTCCTGGAACTCA | 13854 |
rs238309592 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089446 | GCTATTTTGGTGGTT[A/G]CCATCTTGTCTTCTG | 13854 |
rs238332691 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087424 | GTCCTGTGCACTGCC[C/T]GCTTTGTAAGTAAAG | 13854 |
rs238351649 | in-del | -/TTGT | | | intron-variant | Epn1 | Mm_Celera | 7:5096408 | GCTTACCTTTGGTCA[-/TTGT]TTGTTTTGAGATGAG | 13854 |
rs238374553 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5096229 | TGGGCACCCCCTTGG[A/G]CTGGGTGCGGTGGGT | 13854 |
rs238654386 | in-del | -/CAAACCCTC | | | intron-variant | Epn1 | Mm_Celera | 7:5086382 | CAGTCCAGTGCTAAG[-/CAAACCCTC]CTGGAGGGTGAGGAG | 13854 |
rs239128871 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5096436 | GATGAGACATTGCTA[C/G]GTTGCTAGCTTGTTA | 13854 |
rs239418780 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091517 | GGGGATAGGTCACCC[G/T]GTCCACACACACGTG | 13854 |
rs239667843 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082850 | TGCttctctctttct[C/T]tctttctttctttct | 13854 |
rs239820960 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094791 | CCAGAGACTGCGTAG[C/G]TAAATTGGGGCCCTC | 13854 |
rs239845183 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5086667 | CTTGATTTCCAGGTT[C/T]ATTTCTGCTTCCAGC | 13854 |
rs240031008 | snp | A/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087609 | ACTGGTTTAAAATTT[A/T]ACAAGCTCCATGGCT | 13854 |
rs240041134 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091496 | TTTGCTGACACAGGA[C/G]ACTGAGGGGATAGGT | 13854 |
rs240250170 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082702 | TTCCCTCCCTACCCT[C/T]TGGACACCTAGTCCC | 13854 |
rs240303322 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085381 | TTAGGGAGTGGGGGT[G/T]GTGCCAGTGCCCCCC | 13854 |
rs240407935 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082515 | GTTTATACAGGTAAT[A/G]TGGGTTTGATTGTTG | 13854 |
rs240415825 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084037 | GAACATATCAGGGTA[C/T]GCCTTGCCTAGTTTC | 13854 |
rs240550009 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5093620 | CTGCTTCCTAAGCTG[-/T]TTTTACAGCCAGGTT | 13854 |
rs240598325 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086480 | GTGGCCCTGGAATCC[C/G]CTCCTGCTCAGTGGC | 13854 |
rs241184847 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5081277 | TGGAAAATGGCCCCA[-/T]TTTTCAGCAGCATTT | 13854 |
rs241247015 | in-del | -/G | | | intron-variant | Epn1 | Mm_Celera | 7:5087177 | GGTCCTGCTTGCTTT[-/G]ACTCTGTGGTTTCTC | 13854 |
rs241514194 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5095483 | GCGTAGGGCCTAGCC[C/T]GCCCCTTGACTAGCT | 13854 |
rs241536509 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086545 | GTGACCTTAGCTAGG[C/G]CTGGGGAGTTCTGGA | 13854 |
rs241756018 | in-del | -/G | | | intron-variant | Epn1 | Mm_Celera | 7:5088950 | TAGAAGAAGGTGTTA[-/G]ATCCCTGAAACTAGA | 13854 |
rs241800922 | snp | A/T | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098504 | TTGCTATGTGTTTTT[A/T]TCATGTGCTAGACCA | 13854 |
rs242086391 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5080186 | GGAAGTGGAGGCTGC[C/T]GGGCGAAGTGCAGAG | 13854 |
rs242168525 | snp | A/G | | | synonymous-codon | Epn1 | Mm_Celera | 7:5097723 | TGGAGGCCCTGGCCT[A/G]CCCCCCATGATGCCC | 13854 |
rs242239935 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096142 | TAACAATGGATATCC[C/T]CTCCACACTCCTGTC | 13854 |
rs242248471 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5088683 | TTTGGGGGGGCTCCA[C/T]GGAGTCTTTGTAGCC | 13854 |
rs242432170 | in-del | -/CA | | | downstream-variant-500B, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5079957 | ATCCTCATCTGTGTC[-/CA]GTGTGTCCGCCCGTC | 13854 |
rs242506076 | in-del | -/C | | | intron-variant | Epn1 | Mm_Celera | 7:5096493 | GAAGTATGGTGCATT[-/C]CCCATACTCCCCGGT | 13854 |
rs242597870 | snp | A/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078931 | CTGGGGTCTTGCCTC[A/T]GGCCACTGCCCCGTG | 13854 |
rs242920649 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5085771 | GCATTGCAGCAGAGA[A/C]CTGAGGACTGTTTCA | 13854 |
rs243159817 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5092480 | GGTCTCCATAGTCTG[A/G]ACAGATACTGCCTTC | 13854 |
rs243636339 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5093456 | GCTGTCTCCCTGAGT[A/C]CAGGAGTAATCACTT | 13854 |
rs243851505 | in-del | -/TTATTTATTTA | | | intron-variant | Epn1 | Mm_Celera | 7:5084591 | TTTTTATTTATTTAT[-/TTATTTATTTA]TTTTTGTTTCTTTGT | 13854 |
rs243963704 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091338 | CGTGCGCTGGCCCCT[G/T]TCTCTGTCTCCCTAG | 13854 |
rs244008310 | snp | C/T | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098458 | TCTGCTGGCTAAACC[C/T]AGTGGACCGCCAGAT | 13854 |
rs244015777 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089171 | CTGAAAATGGAATTT[A/G]TTTTCATATTACAAA | 13854 |
rs244075467 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5083067 | ACAAATATCCTTTCT[A/G]TCACTGTGGGTCTTA | 13854 |
rs244314867 | in-del | -/TTTT | | | intron-variant | Epn1 | Mm_Celera | 7:5091586 | TGAAATTGGAATTGA[-/TTTT]TTTTTTTTTTTTTTT | 13854 |
rs244336731 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087309 | GTGGAGACCTGTAAT[C/T]CACCCCTTTGATTTA | 13854 |
rs244402679 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5085874 | AGCCAGGTGGCATGT[A/G]CTCTGTTGAGAACTG | 13854 |
rs244479797 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5087970 | CATAGCAGTTGTGTC[A/G]CTGATACTCTGACAC | 13854 |
rs244589233 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5088248 | TTCTCAGGTGTGTCT[C/T]TGTGCAGTGTCTTCC | 13854 |
rs244605427 | snp | C/G | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098517 | TTATCATGTGCTAGA[C/G]CACCTGTGATTACTA | 13854 |
rs244825806 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091094 | ATGCAGGACTGGGCC[A/G]GGCTGGGGAGGGATG | 13854 |
rs244945963 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5084913 | GTCATGGAGACTGTT[A/G]TATGGTGTTGCTTGT | 13854 |
rs244951359 | snp | A/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094414 | GTGCTCGTGCGTGCC[A/T]CTGTGGGTTATCTCC | 13854 |
rs244984588 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5093497 | TAGCTGGAGAGACAC[C/T]CAGGACACTGGCTAG | 13854 |
rs245789948 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085966 | CGAGACAGGGTTTCT[C/T]TGTGTAGCCCTGGCT | 13854 |
rs245819157 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085655 | ATCTACTCTCATGGT[C/T]CCAGTTTAAAGTCTG | 13854 |
rs246155180 | snp | A/G | | | intron-variant, utr-variant-5-prime | Epn1 | Mm_Celera | 7:5080740 | GTACAAAAGGGCTTG[A/G]AGATCCGAGTGCTGT | 13854 |
rs246187451 | snp | C/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078684 | TTTGTTAAAGTAGTG[C/T]GGTAGTCATGCAGTT | 13854 |
rs246252440 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084632 | TTTTTGTTGTTGTTG[C/T]TTTTGTTTTTGCATC | 13854 |
rs246610781 | in-del | -/TCCAGT | | | intron-variant | Epn1 | Mm_Celera | 7:5094076 | AAGTACTCTACCAGC[-/TCCAGT]TCCAGCTCCAGCCCC | 13854 |
rs246719886 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094648 | GGTTGGGCTAGATCG[C/T]CTTAGAGATCCAGCC | 13854 |
rs246864558 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089348 | GCCTTAAGACTTCCT[G/T]CACTTTAATTTGGCT | 13854 |
rs247398434 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091947 | AGGGCTGGAGGCCAC[A/G]GGGAGCCTGAAGTTG | 13854 |
rs247516822 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5087717 | GAAGGAAGCCTGAGC[A/G]TTTAACCTGATGAGT | 13854 |
rs247553816 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096560 | TTCCTTACCATTGAG[C/T]TCCAGCTTTTTCCAT | 13854 |
rs247810030 | in-del | -/GCC | | | intron-variant | Epn1 | Mm_Celera | 7:5081607 | TAAGTTATATCTCTT[-/GCC]CCCACCCCCCCCCAG | 13854 |
rs247906640 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5093594 | AGGCCTCCTCCTCTT[C/G]CTCGGTCCCACTGCT | 13854 |
rs247982911 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094542 | GCAGGCAGCGCTGCA[C/T]GGTGTGCACTGCAGG | 13854 |
rs248076591 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082733 | CTGGGCACCCCCACT[C/T]CCCAGTCTCCCACTG | 13854 |
rs248183444 | in-del | -/GTGTGTGTGTGTGTGA | | | intron-variant | Epn1 | GRCm38.p3 | 7:5094327 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGA]GTGTGAGTGTGTGAG | 13854 |
rs248554935 | snp | A/G | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5078278 | AAAATGTCTTGTTTC[A/G]GTAAGGTCCAAATCC | 13854 |
rs248761621 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5092490 | GTCTGGACAGATACT[G/T]CCTTCCCTCGTAAGT | 13854 |
rs248910996 | snp | A/G | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098351 | CTGGCTGAGGATGGG[A/G]AGGACCTGGGCTGTG | 13854 |
rs249233278 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085585 | GGGGAGTGTATCTGT[C/T]TGGGTTGGGGGCTGG | 13854 |
rs249355039 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082624 | GATGATATGTGCCTC[A/G]TGGCACAGTTGGTAT | 13854 |
rs249429087 | in-del | -/TTC | | | intron-variant | Epn1 | Mm_Celera | 7:5084078 | GAAGGTTGAAGACTA[-/TTC]TTTTATTTTTTATGT | 13854 |
rs249510078 | snp | A/T | | | synonymous-codon | Epn1 | Mm_Celera | 7:5093916 | AGAGCGGATCCGTCG[A/T]GGGGATGACCTGAGG | 13854 |
rs249748122 | in-del | -/TT | | | intron-variant | Epn1 | Mm_Celera | 7:5085014 | ATTTTTCACCTGTTG[-/TT]TTGATATAGAGTTTT | 13854 |
rs249812287 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089435 | TGCCCTGATTGGCTA[C/T]TTTGGTGGTTGCCAT | 13854 |
rs249812417 | in-del | -/AT | | | intron-variant | Epn1 | Mm_Celera | 7:5081215 | AGTCCCCCTTGGGGA[-/AT]CTCACTATATTGTTT | 13854 |
rs249954119 | in-del | -/C | | | intron-variant | Epn1 | Mm_Celera | 7:5091056 | CAGTAGAGGGAGGAG[-/C]CTGGGGAAGAGAGGA | 13854 |
rs249971626 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5090756 | CAGGATTTATATAGG[A/G]GTTTCATTTTTTTCA | 13854 |
rs250048263 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5080042 | GGTCCCGCGAGGGTA[G/T]CCACAGTGGAGGCTT | 13854 |
rs250212604 | in-del | -/C | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5078486 | CTCTTAACTGTTGAG[-/C]CCCTCTCTCTCCAGC | 13854 |
rs250215377 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5085798 | TTCATGCCCATCACA[A/G]CACACCAAGATTGGT | 13854 |
rs250270530 | snp | A/T | | | intron-variant | Epn1 | Mm_Celera | 7:5086363 | TCTGTAGGGGTCCCG[A/T]CCTCAGTCCAGTGCT | 13854 |
rs250597594 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5095525 | ACTTGTTTGTAGTAG[A/G]AGGACCTGAGAGTGA | 13854 |
rs250752543 | in-del | -/TT | | | intron-variant | Epn1 | Mm_Celera | 7:5086813 | TAGATTACAAATGAA[-/TT]TTTTTTTTTTTTAAA | 13854 |
rs250758721 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084237 | CCAGCGGACGTCTTC[C/T]CGTGTCTTTCTCTTT | 13854 |
rs250766411 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086581 | CTGTTCTAGTGGCTG[C/G]AGATGGCAGGGGAGT | 13854 |
rs250768484 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5096366 | CGTCTCCTTGTCAGT[A/G]CCTTACCCACAGCCA | 13854 |
rs250807033 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | Epn1 | Mm_Celera | 7:5092881 | ACCACCTCCCGAGGC[A/G]GAGCAGGCATGGCCA | 13854 |
rs250833199 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5087598 | TTCTTGGTGGAACTG[A/G]TTTAAAATTTTACAA | 13854 |
rs250864318 | in-del | -/G | | | intron-variant | Epn1 | Mm_Celera | 7:5087926 | CTGCTTACCAGGCTT[-/G]GGGCCATGATCTCTG | 13854 |
rs250910148 | in-del | -/TTTTTTTTGTTG | | | intron-variant | Epn1 | Mm_Celera | 7:5089106 | TTTTTTTTTTTTTTT[-/TTTTTTTTGTTG]TTGTTCTGTTTTCTC | 13854 |
rs250992788 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091926 | AGGAGTTGGAGAGGG[C/T]TGCAAAGGGCTGGAG | 13854 |
rs251120172 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5081988 | CAAGGTAAAGAGCAG[-/C]CTTTCCTATTCTCCT | 13854 |
rs251149473 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082678 | TCTTATCTCTCTGCT[C/T]CCTTGAGCTTCCCTC | 13854 |
rs251196070 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084001 | AGCACCTGGGTGTGG[G/T]CCCTTGGGGCAGTAG | 13854 |
rs251293769 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096213 | AGGAATTGGAGAAAT[G/T]TGGGCACCCCCTTGG | 13854 |
rs251366690 | in-del | -/TG | | | intron-variant | Epn1 | Mm_Celera | 7:5094395 | CTCTCTTGCGTGCTC[-/TG]GTGTGCTCGTGCGTG | 13854 |
rs252105550 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5081715 | CTTTCTTTTTGCCCG[A/C]GTTTTGGTGTGTCTC | 13854 |
rs252450564 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086261 | TGCTCTTTAGTTGGC[A/G]GCTTAGTCTCTGGGA | 13854 |
rs252625109 | snp | A/G | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098628 | TCCCATGCTTCCTGG[A/G]GTTTCCTTCTAGGTG | 13854 |
rs252686829 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082416 | GGAGGGACACATGGA[-/T]TTTAGCTCTTCAAGT | 13854 |
rs252739591 | in-del | -/TTGTC | | | intron-variant | Epn1 | Mm_Celera | 7:5085935 | GGTTTGTTTTTGTTT[-/TTGTC]TTTGTTTTTTTTTCT | 13854 |
rs253004381 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5087688 | GCTTTTCATTGAGGT[A/G]TATGGGAGCAACTGA | 13854 |
rs253112569 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086189 | TCATCTTCCACTGAG[A/G]CCAGACAAGGCAGTC | 13854 |
rs253135390 | in-del | -/GC | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078873 | GTTGTGGCTTGGGGA[-/GC]ACACTGTAGGGTGCA | 13854 |
rs253156806 | snp | C/T | | | missense | Epn1 | Mm_Celera | 7:5095048 | CTGTGCCTACTGCTG[C/T]CCCTGTGGCTGCTGC | 13854 |
rs253170627 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5088535 | TGTCCTGTCCTCCCC[A/G]CCCCATTACAGAACT | 13854 |
rs253206276 | in-del | -/GCTTGACTTGGGT | | | intron-variant | Epn1 | Mm_Celera | 7:5089255 | TTCCTGTGGTGTCTG[-/GCTTGACTTGGGT]GCTTGGCTTCCTGAG | 13854 |
rs253214867 | snp | C/T | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098218 | CCACGGTTCAGATGT[C/T]CTGAGAAGCCCCTCT | 13854 |
rs253269546 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091328 | cttgagccagcgtgc[A/G]ctggcccctgtctct | 13854 |
rs253299508 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5093194 | TGGGAGAACCAGTGT[C/T]TCCTCCTTCCCTGAT | 13854 |
rs253591472 | in-del | -/G | | | utr-variant-3-prime | Epn1 | Mm_Celera | 7:5097865 | GAGTGCATGTGAAAT[-/G]GGGGGGCCCTCCCCC | 13854 |
rs253674695 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5097059 | CCCACCGCCTCCCCC[A/C]ACCCCCACCCCCCAC | 13854 |
rs253694484 | snp | C/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078645 | TATCTCATATTCTCT[C/T]CACTCTCTTCTGAAG | 13854 |
rs254201693 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087389 | TAACCAGAAGTCAGC[-/T]GAGGGCAGGCTCTGG | 13854 |
rs254227439 | snp | C/G | | | intron-variant | Epn1 | Mm_Celera | 7:5092999 | GGTGAGGGCCGACTT[C/G]TGTTCTGCCATCCTG | 13854 |
rs254255896 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5092150 | CTATCTTAGGATGAA[A/G]GTGCTTTGGGGACAG | 13854 |
rs254338102 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5081922 | TTTTTTTTTTTTTTT[-/T]CTTTGCCTAGTTATG | 13854 |
rs254473785 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096828 | TGACCTGTCCCAGGG[C/T]TGTGGGTGTCTGCTT | 13854 |
rs254726817 | in-del | -/TTTTTTTTTGTTG | | | intron-variant | Epn1 | Mm_Celera | 7:5089105 | TTTTTTTTTTTTTTT[-/TTTTTTTTTGTTG]TTGTTCTGTTTTCTC | 13854 |
rs254792869 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091607 | TTTTTTTTTTTTTTT[-/T]GTTCATTTGTATTTT | 13854 |
rs255080336 | snp | C/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078943 | CTCTGGCCACTGCCC[C/T]GTGTACTTAAGTGAC | 13854 |
rs255267982 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5085778 | AGCAGAGACCTGAGG[A/G]CTGTTTCATGCCCAT | 13854 |
rs255417411 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085590 | GTGTATCTGTCTGGG[-/T]TGGGGGCTGGCGAAT | 13854 |
rs255612455 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083623 | TGGGTGCTGGTTGCC[C/T]CCACATCTCTTTTGT | 13854 |
rs255857179 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091208 | ATGTGAACAGATGGC[C/T]GTGTACTTGCAGCCA | 13854 |
rs255958022 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096853 | CTGCTTGGTTTCTGC[G/T]CTGAAGTGCTTGCTC | 13854 |
rs256501168 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5092311 | GGCTGAAGGAGGTGG[C/T]GAGAAGACTATAGGA | 13854 |
rs256576289 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5093125 | GGGAAGCTGTGCTGC[A/G]CTTTGACAGTTAGGC | 13854 |
rs256580843 | in-del | -/C | | | intron-variant | Epn1 | GRCm38.p3 | 7:5081683 | TGTCCTCCCTGTCCT[-/C]CTGCCTCGCTGTATT | 13854 |
rs256768981 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084534 | TAGGGTCTTAAGGAG[C/T]CCAGGCTAGCTTTGT | 13854 |
rs256808730 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094272 | CTGGCTGTTTTGTCT[C/T]TCTGACTGTTTGCCT | 13854 |
rs256959865 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094705 | TTATAGCTTGACTGG[C/T]TGCAGGGAGGAGGGC | 13854 |
rs257176795 | snp | A/C | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078330 | TTTAACAGATTTTTT[A/C]AAAAGATTTATTTAA | 13854 |
rs257185898 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089858 | CTGCCCCAGGGCCCA[A/G]ACGCTTCCTCGGTCT | 13854 |
rs257250002 | snp | C/G | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078234 | TGGTGTCTAGTCTAC[C/G]TAAGTTCTGTTTAAA | 13854 |
rs257305896 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5080196 | GCTGCCGGGCGAAGT[A/G]CAGAGGGCGGGGCAC | 13854 |
rs257340371 | snp | C/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078652 | TATTCTCTCCACTCT[C/T]TTCTGAAGTCAACTG | 13854 |
rs257497057 | in-del | -/AG | | | intron-variant | Epn1 | Mm_Celera | 7:5096117 | GCTTCCCTTCTTCAC[-/AG]AGAGATGTGTAACAA | 13854 |
rs257593954 | in-del | -/TGTG | | | intron-variant | Epn1 | Mm_Celera | 7:5088869 | TTTAATTTCACTTTA[-/TGTG]TGTGATTGTTTGCCT | 13854 |
rs257598349 | in-del | -/CTGCTGGAGCAGTGGTTAGAAAC | | | intron-variant | Epn1 | Mm_Celera | 7:5092208 | ACCTTCTCTGGGTCA[-/CTGCTGGAGCAGTGGTTAGAAAC]CTGCCCTCTGTCAGG | 13854 |
rs257786686 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082354 | TATTTAGGTTAATTT[-/A]AAAGCATGAGTTTAA | 13854 |
rs258060708 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083420 | TGTCTGACCTACCAC[-/T]TACATGTTCTGCCTT | 13854 |
rs258133923 | in-del | -/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086437 | GGCTTGAATGGGGAT[-/G]GATGGACAGGGAGGC | 13854 |
rs258156073 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094493 | GAATACCAGAGCATT[A/G]CTTTAGTGTCTGCAT | 13854 |
rs258202257 | snp | A/T | | | intron-variant | Epn1 | Mm_Celera | 7:5094616 | GTAGGAGCTCAGGGA[A/T]GGCTTGATGTGGTGA | 13854 |
rs258232221 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085746 | GATAAGGAGACATAG[G/T]AACATCTATGCATTG | 13854 |
rs258399425 | snp | A/G | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5083084 | CACTGTGGGTCTTAG[A/G]TCAACCATAGTTTCC | 13854 |
rs258477608 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5092359 | CTCCTCTTGGCACCA[C/T]CTACCCCTCCCTTGT | 13854 |
rs258829353 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5096464 | TTATCCTTCTGCCTT[A/G]GTTTGAGTGTCTGGA | 13854 |
rs258922806 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089048 | AGTACTTTTAACCAC[G/T]GAGCCAGCTCTCTGG | 13854 |
rs258973759 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096755 | TGTGGCATAGAGATG[C/T]GTTTCCATTGGTTCA | 13854 |
rs259017799 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5096056 | TCCAGGTGGTGCCTG[C/T]TCTACTTGAGGGGGT | 13854 |
rs259124257 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5086171 | GGACGGGGGTTAGGT[A/G]CATCATCTTCCACTG | 13854 |
rs259190404 | in-del | -/G | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098378 | GTGGTACTGAGTCCT[-/G]GCATCACTGAGTCCT | 13854 |
rs259386406 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085059 | GGCTTGTCTCTGACT[C/T]GCTGTAGGCCTTGAG | 13854 |
rs259580989 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091497 | TTGCTGACACAGGAG[A/G]CTGAGGGGATAGGTC | 13854 |
rs259704452 | snp | G/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082703 | TCCCTCCCTACCCTC[G/T]GGACACCTAGTCCCC | 13854 |
rs260020263 | in-del | -/ACACA | | | intron-variant | Epn1 | Mm_Celera | 7:5085411 | CCCCCCCCCCCCCCC[-/ACACA]CACACACACACCTTG | 13854 |
rs260025343 | in-del | -/CCCCCCACCCCCA | | | intron-variant | Epn1 | Mm_Celera | 7:5097054 | GACCTCCCACCGCCT[-/CCCCCCACCCCCA]CCCCCCACCCCCACG | 13854 |
rs260526822 | snp | A/G | | | intron-variant, utr-variant-5-prime | Epn1 | Mm_Celera | 7:5080974 | TCTGGTGTTCTGACA[A/G]GAGCTCTGGCTGTGG | 13854 |
rs260539579 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5086487 | TGGAATCCGCTCCTG[C/T]TCAGTGGCTGAGATT | 13854 |
rs260574988 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5095505 | TGACTAGCTAAGTCA[C/T]GCTAACTTGTTTGTA | 13854 |
rs260771194 | snp | A/T | | | intron-variant | Epn1 | Mm_Celera | 7:5088852 | CATTTGCTTAAGGTT[A/T]Atttaatttcacttt | 13854 |
rs260978009 | snp | A/G | | | downstream-variant-500B | Epn1 | Mm_Celera | 7:5098511 | GTGTTTTTATCATGT[A/G]CTAGACCACCTGTGA | 13854 |
rs261282735 | snp | A/T | | | intron-variant | Epn1 | Mm_Celera | 7:5084289 | AATGCAAATGGTGTA[A/T]AACATAGTGTCTGTC | 13854 |
rs261633457 | in-del | -/A | | | intron-variant | Epn1 | Mm_Celera | 7:5087659 | AGTTGTCTGCATTAG[-/A]AAAATATATCCAGGC | 13854 |
rs262020209 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5085892 | CTGTTGAGAACTGGG[A/G]AAAGGCCCAGTGTCA | 13854 |
rs262096267 | snp | C/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5079076 | GTCCTCTGTGCAGTG[C/T]GGTGAGGTGTTCTCT | 13854 |
rs262148748 | in-del | -/TG | | | intron-variant | Epn1 | Mm_Celera | 7:5086604 | GGGGAGTGCAAGACA[-/TG]TGGATGGGCTTCTGA | 13854 |
rs262405522 | in-del | -/CTCCCAA | | | intron-variant | Epn1 | Mm_Celera | 7:5091721 | TCCGCCTGCCTCTGC[-/CTCCCAA]GTGCTAGGATTAAAG | 13854 |
rs262669503 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5093743 | CCATTCCCACCCCCA[C/T]TCCATACATTGTTCG | 13854 |
rs262732683 | in-del | -/CCACACA | | | intron-variant | Epn1 | Mm_Celera | 7:5085409 | CCCCCCCCCCCCCCC[-/CCACACA]CACACACACACCTTG | 13854 |
rs262764201 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5094878 | GTTGAGGAGAAGGAG[A/G]TACAGCCACCTGTGG | 13854 |
rs262860244 | in-del | -/TGT | | | intron-variant | Epn1 | Mm_Celera | 7:5090624 | TTTGAAGTCTTAGAA[-/TGT]TGTTGTAAGTGGTGA | 13854 |
rs262880168 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5090703 | AAGAGAGAGCGTGTC[C/T]CATGTCCAGTGGCAT | 13854 |
rs263063054 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5088014 | GTGGCCCCAGTGCAT[C/T]TGCAACAGTTTTTGT | 13854 |
rs263232331 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5092760 | CATTTGGGGGGAAGG[A/G]GATCTGTGCTGGGTT | 13854 |
rs263641849 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087474 | GGCCCCTGCAGCTAC[C/T]ACTTTGGAGTAGTTG | 13854 |
rs263896171 | snp | A/C | | | intron-variant | Epn1 | Mm_Celera | 7:5094652 | GGGCTAGATCGTCTT[A/C]GAGATCCAGCCAAAG | 13854 |
rs264106781 | snp | A/G | | | synonymous-codon | Epn1 | Mm_Celera | 7:5093979 | GACTGGGGGCAAGGA[A/G]GAGGTGAGCGCCTGT | 13854 |
rs264119167 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5093533 | CTCCAGACCTGGGGG[-/T]ACAAGTATCACTAGG | 13854 |
rs264195868 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | Mm_Celera | 7:5082541 | TGTTGAGTCTGCTTT[C/T]GCATTTATGATATGA | 13854 |
rs264311790 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089414 | ATGTTTTGTGGTCCT[A/G]CATGGTGCCCTGATT | 13854 |
rs264321497 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5089131 | TGTTGTTCTGTTTTC[C/T]CTTAAGTACTCTAAT | 13854 |
rs264426409 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5080054 | GTAGCCACAGTGGAG[C/G]CTTCAAGGCTTGGAC | 13854 |
rs264556036 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5091722 | tccgcctgcctctgc[A/G]tgctaggattaaagg | 13854 |
rs264767946 | in-del | -/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085932 | CTTGGTTTGTTTTTG[-/T]TTTTTTGTTTTTTTT | 13854 |
rs264910280 | snp | G/T | | | intron-variant | Epn1 | Mm_Celera | 7:5085589 | AGTGTATCTGTCTGG[G/T]TTGGGGGCTGGCGAA | 13854 |
rs265459117 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089017 | AATGGAACTGGGGTC[A/G]TCTGCAAGAGCAACA | 13854 |
rs265513115 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5095588 | GACAGATTGAGAGGC[A/G]GCAGCTTTCCGAGCA | 13854 |
rs265810274 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5091142 | GCCTGGTCGGCTGCT[C/T]GCTTTGTGGAGGGTG | 13854 |
rs265979604 | snp | C/T | | | missense, intron-variant | Epn1 | Mm_Celera | 7:5093316 | CTCTCCGCCAGCCCC[C/T]GTCCTGCGGCCCTGA | 13854 |
rs266076955 | snp | A/G | | | intron-variant | Epn1 | Mm_Celera | 7:5089574 | CACACCCTGGCTGGA[A/G]GATGAACTTCTCTTT | 13854 |
rs266094127 | snp | C/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078422 | ATGGTTGTGAGCCAC[C/T]GTGTGGTTGCTGTGA | 13854 |
rs266148995 | snp | C/T | | | intron-variant | Epn1 | Mm_Celera | 7:5087765 | GGCTGGAGGCTCCTC[C/T]CGGAGGGAGGTGGAG | 13854 |
rs386923357 | in-del | -/C | | | intron-variant | Epn1 | Mm_Celera | 7:5081684 | GTCCTCCCTGTCCTC[-/C]TGCCTCGCTGTATTG | 13854 |
rs387046804 | in-del | -/TGTT | | | intron-variant | Epn1 | Mm_Celera | 7:5089113 | TTTTTTTTTTTTTTT[-/TGTT]GTTGTTCTGTTTTCT | 13854 |
rs387274648 | in-del | -/C | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078489 | TTAACTGTTGAGCCC[-/C]TCTCTCTCCAGCCCC | 13854 |
rs387382660 | in-del | -/ATTTATTTATTTATTTATTT | | | intron-variant | Epn1 | Mm_Celera | 7:5084593 | TTTATTTATTTATTT[-/ATTTATTTATTTATTTATTT]TTTGTTTCTTTGTTT | 13854 |
rs387809464 | in-del | -/TTT | | | intron-variant | Epn1 | Mm_Celera | 7:5086826 | ATTTTTTTTTTTTTT[-/TTT]AAATGTAGTCTTGGC | 13854 |
rs387834826 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | Mm_Celera | 7:5078878 | GGCTTGGGGAACACT[-/CT]GTAGGGTGCATGATG | 13854 |
rs578266741 | snp | C/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5087653 | TCATTCAGTTGTCTG[C/T]ATTAGAAAAATATAT | 13854 |
rs578442400 | snp | C/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5081728 | CGAGTTTTGGTGTGT[C/T]TCTTCTCTTCTCTTC | 13854 |
rs578453167 | snp | C/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5094678 | CAAAGCACATAGTGG[C/G]TGGGGAAGGCCTTAT | 13854 |
rs578786384 | snp | A/T | | | downstream-variant-500B | Epn1 | GRCm38.p3 | 7:5098505 | TGCTATGTGTTTTTA[A/T]CATGTGCTAGACCAC | 13854 |
rs578821774 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5079787 | GGCTTCTGGTCCTTC[C/T]TGTTCTCCACCCTGG | 13854 |
rs579001978 | snp | G/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5096087 | AGAGTGCACATGATA[G/T]AGTGAGTCAAGTGCA | 13854 |
rs579027444 | snp | A/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5094409 | CTGGTGTGCTCGTGC[A/G]TGCCTCTGTGGGTTA | 13854 |
rs579038607 | snp | A/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5092162 | GAAAGTGCTTTGGGG[A/G]CAGGGGCAGACAGCT | 13854 |
rs579390538 | snp | C/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5091051 | TGAGCACAGTAGAGG[C/G]AGGAGCTGGGGAAGA | 13854 |
rs579589168 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5082974 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTCAAT | 13854 |
rs579792635 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5082923 | CTTCCTTCCTTTCTT[C/T]CTTTCTTTCTTTCTT | 13854 |
rs580074385 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5082858 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTCCTTCCT | 13854 |
rs580340396 | snp | C/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5092205 | TGGACCTTCTCTGGG[C/T]CACTGCTGGAGCAGT | 13854 |
rs580945518 | snp | A/C | | | intron-variant | Epn1 | GRCm38.p3 | 7:5087931 | TACCAGGCTTGGGGC[A/C]ATGATCTCTGCTTCT | 13854 |
rs581008053 | snp | C/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5086344 | CAGTCCTTCCCCTAA[C/G]TCTTCTGTAGGGGTC | 13854 |
rs581183919 | snp | C/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5084601 | ATTTATTTTTTGTTT[C/G]TTTGTTTTGTTTTGT | 13854 |
rs581426716 | snp | A/C | | | intron-variant | Epn1 | GRCm38.p3 | 7:5093423 | TCTAGGGTTTTCCTT[A/C]CTCCTTCCCCGTCCT | 13854 |
rs581479488 | snp | G/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5094693 | GTGGGGAAGGCCTTA[G/T]AGCTTGACTGGTTGC | 13854 |
rs581554227 | snp | A/T | | | intron-variant, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5078848 | ACCTTGTCTGTGGGG[A/T]GAACATGACAGTTGT | 13854 |
rs581814927 | snp | C/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5091482 | CTAGTGCCTTGAACT[C/T]TGCTGACACAGGAGA | 13854 |
rs581935046 | snp | G/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5081200 | TGATACCAGGTTTTT[G/T]AGTCCCCCTTGGGGA | 13854 |
rs582119943 | snp | A/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5092167 | TGCTTTGGGGACAGG[A/G]GCAGACAGCTTGCTA | 13854 |
rs582127303 | snp | A/G | | | downstream-variant-500B | Epn1 | GRCm38.p3 | 7:5098542 | TTACTATGTCAGTGA[A/G]TCCTTGAGTGGCCTG | 13854 |
rs582596617 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5082862 | TCTTTCTTTCTTTCT[C/T]TCTTCCTTCCTTCCT | 13854 |
rs582676089 | snp | A/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5097050 | CTGAGACCTCCCACC[A/G]CCTCCCCCCACCCCC | 13854 |
rs582698937 | snp | A/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5091479 | TTCCTAGTGCCTTGA[A/G]CTTTGCTGACACAGG | 13854 |
rs582741032 | snp | A/C | | | intron-variant | Epn1 | GRCm38.p3 | 7:5081787 | TCTCTTCTCTCTCTC[A/C]CCCCCTCCCTCTTTC | 13854 |
rs583179313 | snp | C/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5092192 | TTGCTATAGTGTATG[C/G]ACCTTCTCTGGGTCA | 13854 |
rs583509811 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5082966 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 13854 |
rs584169442 | snp | A/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5094673 | CCAGCCAAAGCACAT[A/G]GTGGGTGGGGAAGGC | 13854 |
rs584247164 | snp | A/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5081611 | GTTATATCTCTTCCC[A/T]CCCCCCCCCAGCCCT | 13854 |
rs584289117 | snp | A/T | | | utr-variant-3-prime, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5079761 | TTGCAGGACCACAGC[A/T]CCCGTCCTTTGGCTT | 13854 |
rs584654284 | snp | C/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5086897 | TTGTGCCCCACCAAG[C/G]CTTGGAAAGATTTTT | 13854 |
rs584840034 | snp | C/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5089252 | GTCATTCCTGTGGTG[C/T]CTGGCTTGGCTTCCT | 13854 |
rs584888529 | snp | A/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5096081 | GGGGGTAGAGTGCAC[A/G]TGATAGAGTGAGTCA | 13854 |
rs584918168 | snp | G/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5084619 | TGTTTTGTTTTGTTT[G/T]TTGTTGTTGTTGTTT | 13854 |
rs585066538 | snp | A/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5092182 | GGCAGACAGCTTGCT[A/G]TAGTGTATGGACCTT | 13854 |
rs585282000 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5079588 | TGTGTGCACAGCAGG[A/G]CGGGTAGGACCTCCA | 13854 |
rs585324723 | snp | A/T | | | downstream-variant-500B | Epn1 | GRCm38.p3 | 7:5098596 | TGCATATACAGAGGC[A/T]TTTGCCAACAGTGTC | 13854 |
rs585810465 | snp | C/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5097065 | GCCTCCCCCCACCCC[C/T]ACCCCCCACCCCCAC | 13854 |
rs585917499 | snp | A/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5092204 | ATGGACCTTCTCTGG[A/G]TCACTGCTGGAGCAG | 13854 |
rs586335041 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5082854 | TCTCTCTTTCTTTCT[C/T]TCTTTCTTTCTTCCT | 13854 |
rs586627110 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5082915 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 13854 |
rs586637892 | snp | C/T | | | intron-variant, upstream-variant-2KB | Epn1 | GRCm38.p3 | 7:5082970 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 13854 |
rs586697085 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5079589 | GTGTGCACAGCAGGG[C/T]GGGTAGGACCTCCAC | 13854 |
rs586874908 | snp | C/G | | | intron-variant | Epn1 | GRCm38.p3 | 7:5085922 | ACAAGCAAACCCTTG[C/G]TTTGTTTTTGTTTTT | 13854 |
rs587038000 | snp | C/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5093539 | ACCTGGGGGTACAAG[C/T]ATCACTAGGTCATGC | 13854 |
rs587106388 | snp | G/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5092667 | AGCAGCAGCCGTTGT[G/T]TTGAGGGTGGGGCTG | 13854 |
rs587548442 | snp | G/T | | | intron-variant | Epn1 | GRCm38.p3 | 7:5084593 | TTTTATTTATTTATT[G/T]TTTGTTTCTTTGTTT | 13854 |
rs864272601 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5079455 | AACTGGAATGGCAGC[A/G]ATTAAGGGGGGTGGG | 13854 |
rs864281642 | snp | A/T | | | utr-variant-3-prime, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5079883 | CCCTCTCTGTGGCAG[A/T]TTCATATTTGCTAAT | 13854 |
rs864287247 | snp | A/C | | | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | U2af2, Epn1 | GRCm38.p3 | 7:5079934 | TTTTGTTGTATTTTA[A/C]TTTATGGATCCTCAT | 13854 |
rs864299100 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | U2af2, Epn1 | GRCm38.p3 | 7:5079881 | CCCCCTCTCTGTGGC[A/G]GTTTCATATTTGCTA | 13854 |