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 |