SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3024181 | snp | A/G | | | intron-variant | Prex2 | GRCm38.p3 | 1:11297067 | CCCCTTAGTACCACA[A/G]GGACATAGATAATGT | 109294 |
rs3024182 | snp | A/G | | | intron-variant | Prex2 | Mm_Celera | 1:11297149 | CTGCAAGATAGCTAT[A/G]CTAGACAAGGTATTA | 109294 |
rs3024196 | snp | G/T | | | intron-variant | Prex2 | GRCm38.p3 | 1:11036917 | TAAATTTATAATTAC[G/T]GTGGCTAGTTCTTAG | 109294 |
rs3024197 | snp | C/T | | | intron-variant | Prex2 | GRCm38.p3 | 1:11036899 | GGCTAGTTCTTAGAG[C/T]TGTTGAGAAAACTAA | 109294 |
rs3671759 | snp | A/T | 0.455 | 0.143091 | intron-variant | Prex2 | GRCm38.p3 | 1:11182359 | TTTCCCTTTTCTTTT[A/T]ACATATTGCACTTTA | 109294 |
rs3672887 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Prex2 | GRCm38.p3 | 1:11182511 | GCTCCAGGCTTGCAT[C/G]CTTACCATGTAAATT | 109294 |
rs3672901 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11182519 | CTTGCATCCTTACCA[C/T]GTAAATTGTCATCTT | 109294 |
rs3672956 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11182545 | ATCTTCCCTCTGTGG[C/T]TCCTTGTGTGACCTC | 109294 |
rs3674105 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Prex2 | GRCm38.p3 | 1:11182714 | GTTAACATTCAGTAC[C/G]TCTTCCTGCTCAATG | 109294 |
rs3674168 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Prex2 | Mm_Celera | 1:11182754 | AAGAGTTCCATCTCT[A/G]AAAGTGCTTTTTGCT | 109294 |
rs3674698 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Prex2 | Mm_Celera | 1:11182825 | AACTAGTCACATGAA[C/G]TATGTGTGCAGCATC | 109294 |
rs3679024 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Prex2 | Mm_Celera | 1:11055168 | TAATTAAAAAATTGC[A/C]AGCATCTCAGGCTGT | 109294 |
rs3680189 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Prex2 | GRCm38.p3 | 1:11186585 | CTCTAAAGCCAGTGG[C/T]CTTGACTGAGAACCA | 109294 |
rs3681510 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Prex2 | GRCm38.p3 | 1:11186791 | AAGGCAGGGAACATT[C/G]TGATAACGTGGATAC | 109294 |
rs3682122 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Prex2 | GRCm38.p3 | 1:11186867 | TGTAGTGCTTCGTTG[C/G]TATCTGCAGTGATTT | 109294 |
rs3709040 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11224039 | AGATGACCTTGGCCA[A/G]GGGGGCTAAGCAGTT | 109294 |
rs3710150 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Prex2 | Mm_Celera | 1:11118344 | TGGATATAAATAGAT[C/T]GGATAAAAAGCACTG | 109294 |
rs3710796 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11272555 | AGAAAATGTCAGATA[A/G]ATTTCTGGCTATTGT | 109294 |
rs3711521 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11069038 | AGACTTATTTATAGG[A/G]TTTGCCATGAGTTAT | 109294 |
rs3711594 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11069076 | ATGCACTAGCCGGTC[C/T]GGGGCATAAATTCTC | 109294 |
rs3722284 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11269182 | TAGAAGGCCCTCAAC[A/C]CTGGAATTCTTCCTC | 109294 |
rs3722295 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Prex2 | GRCm38.p3 | 1:11269188 | GCCCTCAACCCTGGA[A/C]TTCTTCCTCAGCCTC | 109294 |
rs3722996 | snp | A/C | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11269353 | TTAATGATTATTGTC[A/C]CCCCCTACAGTTGCA | 109294 |
rs3724763 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11269584 | TATTGCTCTTAATTG[A/G]GGGACAATTATATTC | 109294 |
rs6153126 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11093394 | ggcagacagatttct[A/G]agtttgaggccagcc | 109294 |
rs6153707 | snp | A/C | 0.207612 | 0.24638 | intron-variant | Prex2 | Mm_Celera | 1:11093519 | AAGTTAGCTAATGAT[A/C]GACTCTCTCACCTTA | 109294 |
rs6167362 | snp | A/C | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11093694 | tgttcttcttttttc[A/C]cctttcatgtagttc | 109294 |
rs6167480 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11093762 | ggtgtgttcttcata[C/T]tcagtttaacctcca | 109294 |
rs6182992 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11173284 | ttatatccctgtttt[A/G]ttgctaattttgtta | 109294 |
rs6184117 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11173456 | gaccagagtttattt[A/G]tttcttgtcatgtac | 109294 |
rs6185168 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11173625 | cttgttagaactgcc[A/G]ccactgtctccctta | 109294 |
rs6185251 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11173677 | cattttcattcaatt[C/T]tggagggtanttagt | 109294 |
rs6185268 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11173687 | caattntggagggta[C/T]ttagttcttcnctta | 109294 |
rs6185684 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11173698 | ggtanttagttcttc[C/T]cttaatttntgtttg | 109294 |
rs6185698 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11173707 | ttcttcncttaattt[C/T]tgtttgaacccattt | 109294 |
rs6185788 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11173767 | ttaatttgtaagcct[C/T]ctcctgcttatgtag | 109294 |
rs6228078 | snp | A/G | 0.5 | 0 | utr-variant-5-prime | Prex2 | Mm_Celera | 1:10993518 | GCCTCCCCTCGGGCT[A/G]GAGCCGCGTGAGGCC | 109294 |
rs6228152 | snp | C/T | 0.5 | 0 | utr-variant-5-prime | Prex2 | Mm_Celera | 1:10993555 | GCGGGCCGGGCTGGG[C/T]TCCCGCTCTCCGGGG | 109294 |
rs6228328 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11187905 | CCCAATTAATGAATA[A/T]TTTTTAAATGAATGG | 109294 |
rs6242335 | snp | C/G | 0.5 | 0 | missense | Prex2 | Mm_Celera | 1:10993801 | GGCCACCATGAGCGA[C/G]GAAAGCGCCAGGGAA | 109294 |
rs6259073 | snp | A/G | 0.509512 | 0.086336 | intron-variant | Prex2 | GRCm38.p3 | 1:11027020 | ACTAGATCTCTGAAC[A/G]TTTATAAGACAGTCT | 109294 |
rs6260132 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Prex2 | Mm_Celera | 1:11027225 | TAGAGATTGGATTGA[A/G]TGTTTGTCCTTGCCT | 109294 |
rs6260654 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11027324 | AGGAAGGGTGGGTTC[A/G]CTGTAATCCCTGTCC | 109294 |
rs6288198 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Prex2 | GRCm38.p3 | 1:11113153 | GCAGGGTGAATAGAA[C/T]GTAAAACAACAGATG | 109294 |
rs6288746 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Prex2 | GRCm38.p3 | 1:11113269 | GATTCTCATGTGGCT[A/C]TTCTATACTATGAGC | 109294 |
rs6289257 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Prex2 | Mm_Celera | 1:11113363 | AGGACAACACATTGG[A/C]TGTGTATTGAAGGGC | 109294 |
rs6289696 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11113388 | AAGGGCAGGAGAAGA[C/T]GCNTATTTTTACATG | 109294 |
rs6289697 | snp | A/C | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11113391 | GGCAGGAGAAGANGC[A/C]TATTTTTACATGAAG | 109294 |
rs6293530 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11009626 | ctgttctattctatt[C/T]tattctattctattc | 109294 |
rs6297340 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11198111 | CTCTAATTATTCTGT[C/T]GGTGTGGATTTTGGC | 109294 |
rs6297841 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11198157 | AGGACATAGAGAATG[C/T]ACCAGTGACCACATG | 109294 |
rs6297961 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11198220 | agccatcagctaggg[A/G]tatggcatatagagc | 109294 |
rs6298478 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11198282 | agcttaatttttgta[C/T]aggccttgtntatgt | 109294 |
rs6298497 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11198292 | ttgtanaggccttgt[A/G]tatgtattcatagct | 109294 |
rs6298967 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11198337 | ttgcaacaaccgtgt[C/T]atgtccagagaccag | 109294 |
rs6304316 | snp | G/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11113710 | TTGAAGAGTAGGCAT[G/T]GAGCAGTGCTTGTGG | 109294 |
rs6304347 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11113726 | GAGCAGTGCTTGTGG[A/G]NAAAGGTTGGANTTA | 109294 |
rs6304349 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11113727 | AGCAGTGCTTGTGGN[A/G]AAAGGTTGGANTTAC | 109294 |
rs6304364 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Prex2 | GRCm38.p3 | 1:11113738 | TGGNNAAAGGTTGGA[C/T]TTACAACATCGAAAA | 109294 |
rs6304396 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Prex2 | GRCm38.p3 | 1:11113758 | AACATCGAAAACAAG[A/G]AGAAAGTGGTGCTGA | 109294 |
rs6304796 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11113799 | AAAGCTAGAAGATGC[C/T]CAAGTGAAAAGGCAG | 109294 |
rs6307423 | snp | A/C | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11009791 | CATCTGTTTGTAAGT[A/C]CAGTTCTAGGGAGTC | 109294 |
rs6315127 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Prex2 | Mm_Celera | 1:11271434 | CCCATGGAATAAAAG[C/T]TTTACAACTATTGTC | 109294 |
rs6315659 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Prex2 | Mm_Celera | 1:11271526 | GCTTCCTTTTCATAA[C/T]TCAGATGTCAATTTG | 109294 |
rs6315683 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11271543 | CAGATGTCAATTTGT[A/G]TTATGAGTNCTCTTC | 109294 |
rs6315698 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11271552 | ATTTGTNTTATGAGT[C/T]CTCTTCCTTAGAAGT | 109294 |
rs6316095 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11271585 | CTTAAATATTGCAGA[A/C]TTTTCCAATAAGCAA | 109294 |
rs6316157 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Prex2 | Mm_Celera | 1:11271625 | AAAATTTCTGCTGAT[C/T]TGATAAACAGATAAA | 109294 |
rs6316191 | snp | C/T | 0.257117 | 0.249899 | intron-variant | Prex2 | Mm_Celera | 1:11271646 | AACAGATAAATAACA[C/T]AGGTGTATGTAATTT | 109294 |
rs6325251 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11187745 | GAAAGGTTCCCCAGA[A/T]AAGTAACATGTTTTA | 109294 |
rs6325308 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Prex2 | Mm_Celera | 1:11187776 | TTCAATGATGAAATA[C/T]TTTCTTATTTGTAAC | 109294 |
rs6325739 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Prex2 | Mm_Celera | 1:11187796 | TTATTTGTAACTAAA[C/T]TTCTTGGCTATATTT | 109294 |
rs6345992 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Prex2 | Mm_Celera | 1:11083441 | CTAGCAGATAGATGG[C/T]TCAGTTCAGACTTTG | 109294 |
rs6346583 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Prex2 | Mm_Celera | 1:11083520 | TTTAAGGAACCTATT[A/G]TGAATTAGATTTAca | 109294 |
rs6347189 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11083629 | cacagatatttatgt[A/T]ataatttacaacaat | 109294 |
rs6347231 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11083653 | caacaatagtaaaaa[A/T]tagttataaagtaac | 109294 |
rs6357764 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11123496 | TACTGAAATATAACT[A/T]AGCACATTCTAGATT | 109294 |
rs6358124 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11123514 | CACATTCTAGATTTA[C/T]TGCTATTTNAACTTT | 109294 |
rs6358132 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11123523 | GATTTANTGCTATTT[A/G]AACTTTCTGTTTGAA | 109294 |
rs6358714 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Prex2 | Mm_Celera | 1:11123646 | TTCTTCAGTGACTTA[A/G]CTCCTACATTTATCC | 109294 |
rs6359243 | snp | C/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11123780 | TTCTCTTGAGTGATC[C/G]TANCCGTTTCTGATT | 109294 |
rs6359244 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11123783 | TCTTGAGTGATCNTA[C/T]CCGTTTCTGATTTGC | 109294 |
rs6360236 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Prex2 | Mm_Celera | 1:11083825 | AACTGTGAGGGGGCA[A/C]CCAACGGTAGTCTTT | 109294 |
rs6360841 | snp | A/C | 0.30839 | 0.243086 | intron-variant | Prex2 | Mm_Celera | 1:11090509 | ATAAAATCGGCACTT[A/C]TGCTATAAAAATAAG | 109294 |
rs6372231 | snp | A/G | 0.484429 | 0.0868505 | synonymous-codon | Prex2 | Mm_Celera | 1:11123822 | CACACAGGGTGTAAG[A/G]CTCTACTGTCGTCTT | 109294 |
rs6372808 | snp | A/C | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11123938 | AGTCATTTCATTTTA[A/C]GTAATTGTTTATGTC | 109294 |
rs6383525 | snp | A/C | 0.304688 | 0.243945 | intron-variant | Prex2 | Mm_Celera | 1:11045870 | TCCCAGACTGGTCTG[A/C]AACAAACCTTTCTGT | 109294 |
rs6383562 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11045888 | CAAACCTTTCTGTCT[C/T]CACCTCTCAGTGCTG | 109294 |
rs6384765 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11046081 | TCTGTAGCCAGGGAT[A/G]AGCTTGAACTCCTGA | 109294 |
rs6385334 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Prex2 | Mm_Celera | 1:11046163 | CGTCTTCTTGAAGGT[C/G]TTCCTCAAGACACTG | 109294 |
rs13475723 | snp | G/T | 0.5 | 0 | synonymous-codon | Prex2 | GRCm38.p3 | 1:11149879 | TGGACCTTCAGTTGT[G/T]CATGCGGTGGGAAGA | 109294 |
rs30465546 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11285945 | AGATATGCTTTTGTA[A/G]TCATGACCACTTTAT | 109294 |
rs30468596 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Prex2 | GRCm38.p3 | 1:11242221 | CACCCTTGTCTCTGT[G/T]TAGATCCATTTTACT | 109294 |
rs30471054 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11295499 | CTGCTGTATGCTGGG[A/G]ACAGCCTGGGCCAAA | 109294 |
rs30473216 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11076005 | GTTCAAGGCCAGCCT[A/G]GTCTACAAAGTGAGT | 109294 |
rs30474984 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11277829 | GAGCTGGAGATTGAT[A/G]CAATAAGCAAGAGGT | 109294 |
rs30493056 | snp | A/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11244690 | CCCAAATATATTTTT[A/T]ATAATACATAGAAAA | 109294 |
rs30505799 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Prex2 | Mm_Celera | 1:11099895 | AACTAGAAATTCTCA[A/G]CTCCTGAAAAGTGAG | 109294 |
rs30534831 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Prex2 | GRCm38.p3 | 1:11265955 | AGCTAAAATGAAAAG[C/T]GAGGGACACAAAGCT | 109294 |
rs30552273 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11134904 | TAACCAGTATTTGGT[A/G]CCAGCTGTGCTAAAA | 109294 |
rs30561313 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Prex2 | Mm_Celera | 1:11183536 | TTATTACTTTCCAGT[G/T]CTGTGTTACTACTCT | 109294 |
rs30561963 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Prex2 | GRCm38.p3 | 1:11217364 | AAAATCTAGTTGGCC[G/T]GAGATTTACCTCTCC | 109294 |
rs30563881 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11295096 | TAAGTTCTATTCAAC[G/T]TACTGTGCAAACGGT | 109294 |
rs30567311 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11237580 | GCATTCACGTGGAAA[C/T]TGAACAACACTCTAC | 109294 |
rs30569357 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Prex2 | GRCm38.p3 | 1:11273342 | TGAAATAGAAGGAGT[C/G]AAGATTAGTGCGTGT | 109294 |
rs30575400 | snp | C/G | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11045458 | CATGAATATTCAGTT[C/G]TTGACAGGGCAGTAA | 109294 |
rs30591983 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11087675 | TCTACCTTAATCTTT[A/T]GAGCCAAAGTCTCTC | 109294 |
rs30600241 | snp | A/C | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11227688 | CCTTCAAAGGGGTTG[A/C]AGTCTACAGGTTGAG | 109294 |
rs30600855 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:11085667 | ATGTCATCTCCATTC[C/T]TCATGTGGTCATTCA | 109294 |
rs30608843 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Prex2 | Mm_Celera | 1:11145506 | CACTCTCAATATACT[A/G]CTGTGAGCAGCAGAC | 109294 |
rs30618212 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11237565 | AATAATAGAAAGCAA[A/G]CATTCACGTGGAAAC | 109294 |
rs30619489 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11160659 | CTTAGAAACCAGTTT[A/G]TAAATAGATTCACAG | 109294 |
rs30651985 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11275170 | AAGCATTCAACCCTG[A/G]GCTATAACCCCCAAC | 109294 |
rs30652873 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11138460 | CCACACTCAGAATTG[A/G]CCCCAGACCTGGGCT | 109294 |
rs30656018 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11012005 | CCACACTTTAGAATT[G/T]GGACATGTACTTCCT | 109294 |
rs30658884 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11021255 | TTAAAAGATTCTATC[C/T]GTAATTGGTTAAATT | 109294 |
rs30658944 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11065043 | TCTTTTCTCATCACA[A/G]GGAAATAAAACTTAA | 109294 |
rs30664729 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11056598 | ATGGATGGAGACGGG[C/T]AGTCTCCTCTGTCTC | 109294 |
rs30664867 | snp | A/C | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11039749 | CCTTCATCTTCAGCC[A/C]GGAGGCGGAGCTAAG | 109294 |
rs30667635 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11225277 | GGTATAGTCACCCCC[C/T]CCACCCCCCGGGCTG | 109294 |
rs30697902 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Prex2 | Mm_Celera | 1:10992723 | ATTTCAAAACTGAAG[C/T]ATAACTAGCTTCTGT | 109294 |
rs30707561 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11272216 | AGCCACAGCTGGGGC[A/T]GCCCAACCATGTCAG | 109294 |
rs30708233 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11080826 | GCTGAAACAAACCCT[C/T]TCTTCTCCAAATTGC | 109294 |
rs30744307 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11277828 | AGAGCTGGAGATTGA[C/T]GCAATAAGCAAGAGG | 109294 |
rs30755549 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11021321 | TAAGAGACTTCACCT[C/G]CTGATGGTCAACCAT | 109294 |
rs30768053 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Prex2 | GRCm38.p3 | 1:11058927 | GGGATGAGGATTTGG[A/G]AAGTATTCAAGAGAA | 109294 |
rs30771646 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11147702 | GGGAAATTTGCATTT[C/T]TATCACTGATTGCTT | 109294 |
rs30779599 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11073215 | ATCTTCAACAAAATA[A/G]TAGAAGAAAACTTCC | 109294 |
rs30798904 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Prex2 | GRCm38.p3 | 1:11166440 | ATCAAGAAACATCTG[C/G]TCTGGTAAGGCCTGA | 109294 |
rs30800655 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11203321 | AGAATTTTTCTCTTA[A/G]TATAGCACTTGTTTT | 109294 |
rs30807317 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Prex2 | Mm_Celera | 1:11029205 | TGTACCTCAGTGCTC[A/C]CATCTGGAATGGCAT | 109294 |
rs30817359 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Prex2 | GRCm38.p3 | 1:11026864 | GAAGCATTCCTTTCA[A/G]ATGATTTTCTTTGTG | 109294 |
rs30837803 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11222770 | GTCTCTTTGTTTCAA[C/T]TCCTGTGCTAGTACA | 109294 |
rs30852128 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:10998974 | AATTTTATATTTCAT[A/G]TAGTAGCCACCATCA | 109294 |
rs30868536 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11224472 | ATTATTATTGTTGTT[A/G]TTATTATTATTTATT | 109294 |
rs30897875 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:10992380 | TTCATGGAAGTCACA[A/G]TCATATTTTGAAAAG | 109294 |
rs30904378 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Prex2 | GRCm38.p3 | 1:11217503 | TCCCCTCAAGGGCAC[A/G]AGTGACTGGAGCAGT | 109294 |
rs30908076 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Prex2 | GRCm38.p3 | 1:11253312 | GATATTTCATTTCCT[C/T]GGAGCATAGATCTGG | 109294 |
rs30932472 | snp | A/C | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:10996793 | CCCAGAGGCTCCAAA[A/C]TGTTTCCATCACTGT | 109294 |
rs30943807 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Prex2 | GRCm38.p3 | 1:11254002 | ACCATTAGCTTCCTC[C/T]ATAAAATTTGATTAA | 109294 |
rs30944896 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11181678 | TTACTTCTGAGTACT[C/G]AGCAGTAAATCTGAG | 109294 |
rs30982176 | snp | G/T | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11229680 | GCTGTGCCTTCCCTG[G/T]CATGGTAGGAAATCT | 109294 |
rs30996657 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Prex2 | Mm_Celera | 1:11086760 | CCATAGTTGGAGAAG[G/T]CTAGATAAGATACTA | 109294 |
rs31006259 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11021760 | CACCACACTCCCCTC[A/C]TGCCACTTACTGTAT | 109294 |
rs31006535 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Prex2 | Mm_Celera | 1:11028331 | TATCTTTTCTCTCTA[A/G]TCCCTTTTGACAGTA | 109294 |
rs31009947 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Prex2 | GRCm38.p3 | 1:11276073 | ATGATTTTTCAAAAG[A/G]TGTGTATTGAATACC | 109294 |
rs31010118 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11073315 | TCAAAACATCCAGGA[A/T]ATCCAGGACACAATG | 109294 |
rs31013523 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Prex2 | GRCm38.p3 | 1:11106692 | GAAAGGACTGGGATG[G/T]TTTACAGAACACATA | 109294 |
rs31017549 | snp | A/T | 0.401235 | 0.199068 | synonymous-codon | Prex2 | GRCm38.p3 | 1:11208651 | TCCTGTTCTCTTTTC[A/T]CAAGGTGAGCTTTTC | 109294 |
rs31042015 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Prex2 | GRCm38.p3 | 1:11274128 | ATGTGTAGTAATTTT[A/C]TCAAGCATTTCATTT | 109294 |
rs31056197 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11116942 | CAGTCTTGAAATAAA[A/C]TAGTCAATTCATTTT | 109294 |
rs31057844 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11229379 | GGGGGGATCATTACA[A/G]CCTGAGGATCATTTA | 109294 |
rs31057874 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11217829 | AAATTCAGAACTATA[C/T]TTATTGAGAATATTT | 109294 |
rs31081686 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11149702 | CTCAGCTGGAGGAGC[C/T]ACTACCTCCAAATTC | 109294 |
rs31085077 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11155276 | CTAGGGTGAGGGTGA[A/G]AAAGACCTAAAAGAA | 109294 |
rs31095066 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11124832 | TTGTCCTGAATAAAT[A/G]TCTGCTTTAGCAGCA | 109294 |
rs31102920 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Prex2 | Mm_Celera | 1:11036318 | CTTCCAAAGCTGTTT[A/C]TCTGCAAACGTGTTA | 109294 |
rs31102922 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Prex2 | GRCm38.p3 | 1:11253629 | CCAAATTTACTTTTA[A/G]CATAGTTACTTGACT | 109294 |
rs31109309 | snp | C/G | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11297447 | GGAACTGTATTAGCC[C/G]GTTGCAGCATTAGGC | 109294 |
rs31124673 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Prex2 | GRCm38.p3 | 1:11154280 | GATCTGTTAAATACT[A/T]TCAGAAAATGATATA | 109294 |
rs31137526 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11197834 | TACATATTCACTGAT[A/G]GCTAGAAATGTGGCC | 109294 |
rs31139714 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Prex2 | GRCm38.p3 | 1:11277967 | CTTGAGCTGGTTTAA[A/G]CCCATTGTTAGCCCT | 109294 |
rs31140779 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11020838 | AGTCACTCATCAGAT[A/G]CCTAGTCACAGTAGT | 109294 |
rs31141439 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11021917 | TCTAGTATGGCCAGC[C/T]AGCCAACATAAACTT | 109294 |
rs31176959 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11196827 | TACCATACTGCTGTT[C/T]TTCGCTCAGGAATGT | 109294 |
rs31182398 | snp | A/C | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11170426 | GGACAAGTAAATTAA[A/C]TATATTTATAGGCTT | 109294 |
rs31188012 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Prex2 | GRCm38.p3 | 1:11022909 | TTGCTCAATAATATG[G/T]ATTAGTGTTTAGCTC | 109294 |
rs31209525 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11276272 | TCAGGAATCAGCATG[C/T]TGAGGCCGAGTTTGT | 109294 |
rs31210501 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Prex2 | Mm_Celera | 1:11046887 | GCCCCTATATTTCTC[A/G]GGTACATAAATCTCA | 109294 |
rs31232389 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11117984 | GCAAACTGTGCATTG[A/G]TTCACCTTCTTCCCC | 109294 |
rs31235430 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11253148 | TCCTTATCATTTTGA[A/G]GGTCTCGTGCCGCTC | 109294 |
rs31237085 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Prex2 | GRCm38.p3 | 1:11055859 | TCAGGAAGCCTATTG[C/T]GAGGTGAGCGTGCCT | 109294 |
rs31243040 | snp | G/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11015724 | GAGGCAGAGAGAGAG[G/T]CAGAGAGAGAGGCAG | 109294 |
rs31259505 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11223170 | TCACACTACCCAGTA[C/T]CCCAGTAGAATCAAG | 109294 |
rs31270020 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Prex2 | GRCm38.p3 | 1:11217242 | TTATAGGGAGTAAGG[C/T]CCTACCTTATTTATT | 109294 |
rs31278735 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11057024 | ATCTATTTTCATTGA[A/G]TGAGTAATTTTTTCC | 109294 |
rs31312687 | snp | G/T | 0.42 | 0.183303 | intron-variant | Prex2 | GRCm38.p3 | 1:11215358 | ATGAGTATTAGCTCT[G/T]TGTTGGTTAGCTTCA | 109294 |
rs31314367 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Prex2 | GRCm38.p3 | 1:11278265 | TCAGCAGTCCTCTTA[C/T]ATTTTCTATGGTCAC | 109294 |
rs31330191 | snp | A/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11268098 | ATAGCATTGAAAAAT[A/T]TTTTAAAGTATGATT | 109294 |
rs31331558 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Prex2 | GRCm38.p3 | 1:11185024 | GATACCATCTTTTTT[C/G]TAATGTGAGATAAGA | 109294 |
rs31331695 | snp | C/T | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11286792 | ACTCTTTCTTTCGTT[C/T]TTTCTCTCTCTCGCT | 109294 |
rs31331795 | snp | G/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11285370 | AGAATAAAAGGTGGG[G/T]GTTGGGGGGATAGTC | 109294 |
rs31336227 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11115238 | TGGAACAGAGGATAG[C/T]TGTTCATTTCATGGC | 109294 |
rs31344974 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11240458 | TCCACATGTCCCTCA[A/G]CAGAGGAATGGATAC | 109294 |
rs31352012 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11209365 | GGCTAGTCTACTATA[C/T]AGCATAGAAAATGTT | 109294 |
rs31366656 | snp | C/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:10996906 | GGTAGCTGTCATTTA[C/G]TGACAGGCCATTGTA | 109294 |
rs31367023 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11136111 | TTTTTAAATGAATTC[A/G]TAAGACATCAAATAC | 109294 |
rs31382756 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11053577 | CTGTCCTGGAACTCA[C/T]TATGTAGACCAGGCT | 109294 |
rs31392411 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11116925 | GAACCATCTGCTTGA[C/T]CCAGTCTTGAAATAA | 109294 |
rs31394349 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11156900 | TCTATAGTAAGCCCC[C/T]ATGAAAGCAAGGCAG | 109294 |
rs31402983 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Prex2 | GRCm38.p3 | 1:11107000 | GCCCTTCATTTCCCC[A/G]TCTTGGAACCTTTGC | 109294 |
rs31404279 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Prex2 | Mm_Celera | 1:11182175 | AGAAGGACAGCATTG[C/T]TCTCATTAAGGATCC | 109294 |
rs31406688 | snp | C/G | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11244380 | CAAAGATTCTCTTAA[C/G]ATGTGGCTTTGTGTG | 109294 |
rs31408799 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11124753 | TGCATATTGGAATTC[C/T]CTTTTACATCACATA | 109294 |
rs31409933 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Prex2 | GRCm38.p3 | 1:11217786 | ACTACTACCCATATG[A/G]GTCACCAGATGGCGT | 109294 |
rs31419735 | snp | G/T | 0.429688 | 0.173817 | intron-variant | Prex2 | Mm_Celera | 1:11171306 | TCCTAAGAGGGTGTG[G/T]CCATTTCCTTGTTGT | 109294 |
rs31422527 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:10995041 | TTTGAGGTTCACGTG[C/T]TGGGAGAATACCCTG | 109294 |
rs31423133 | snp | C/T | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11286017 | CCCATGGATCTTGTC[C/T]CCAGGATTTCACTAT | 109294 |
rs31426415 | snp | C/G | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:10993931 | AGCCGGCCCCGCGCA[C/G]GGCACCAAGTCTGGA | 109294 |
rs31430530 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11026375 | GGTGAGCCACAATTA[A/G]AAAGTGACGCCTGGT | 109294 |
rs31435325 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Prex2 | GRCm38.p3 | 1:11254063 | TAGTACATTATAAGA[C/T]TATTTTCCGTCCATG | 109294 |
rs31443854 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Prex2 | Mm_Celera | 1:11247868 | TTAGTAGATTTAGCC[C/T]AAGTGACACTGATTT | 109294 |
rs31448607 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11181255 | CCTAACAAAAGCTGC[A/T]TCCATGGAACTCCCC | 109294 |
rs31463544 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Prex2 | GRCm38.p3 | 1:11298804 | TCTTTACAAATAATT[A/G]AAACAGCATCACTGT | 109294 |
rs31468061 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11104546 | GGTAGCGAACCTTTT[C/T]ACCTGCTGAGCCTTC | 109294 |
rs31468625 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11116956 | AATAGTCAATTCATT[C/T]TTATTAAAATTAGTT | 109294 |
rs31472680 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:10996967 | TATGCTAACCTTTGT[C/T]GCTCTTTGGGAACAG | 109294 |
rs31474102 | snp | G/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11019657 | TGAAAGAAGGTTCCT[G/T]GGGCTACAGTTCCCA | 109294 |
rs31485275 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11295330 | TGGAGGTAGGACGTC[A/C]GACATCAGGCTATGA | 109294 |
rs31487323 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Prex2 | Mm_Celera | 1:11026753 | ACAGCAGCTAGACCA[A/G]TGGCCTGGACAAAAC | 109294 |
rs31498136 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11080837 | CCCTCTCTTCTCCAA[A/G]TTGCTTTGATTCTTG | 109294 |
rs31498320 | snp | G/T | 0.375 | 0.216506 | utr-variant-3-prime | Prex2 | GRCm38.p3 | 1:11298420 | TGGACCACTGATGGC[G/T]GTGGGTAGGAAGTTG | 109294 |
rs31499624 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11217015 | TGAAGCAAACCAAAA[C/T]GTAAGTAAATTTACA | 109294 |
rs31501202 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Prex2 | GRCm38.p3 | 1:11117295 | GATTCTATTTCAATG[C/T]AGAGATAGGAACTAG | 109294 |
rs31505059 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11108347 | TCCTGGGACTCGGAA[A/G]TCCCACCTCTATTGA | 109294 |
rs31517249 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11297584 | ATTTTCTACAGTATA[A/G]TCAGTGTAGTGATGG | 109294 |
rs31522944 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11271582 | TAACTTAAATATTGC[A/T]GAATTTTCCAATAAG | 109294 |
rs31524601 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Prex2 | GRCm38.p3 | 1:11274575 | TATCCTCACTACTTG[A/C]TTGCTTTACAATTGA | 109294 |
rs31529936 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Prex2 | GRCm38.p3 | 1:11093031 | CCTGGAACTTGGTGC[A/T]ACTAAATGATCATTT | 109294 |
rs31550893 | snp | C/T | 0.290657 | 0.246672 | intron-variant, upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:11085991 | ACATAACTCTTCTCT[C/T]TCTCCTGATTCTTAC | 109294 |
rs31551464 | snp | A/C/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11020892 | TTTATTCAATAATAC[A/C/G]CCAAAGCACAAGCAT | 109294 |
rs31551696 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11118666 | AGAACAACCCAGTAA[A/G/T]CACCACCCCTCCATG | 109294 |
rs31561703 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Prex2 | GRCm38.p3 | 1:11117166 | TTTGATCAATTATAA[C/T]GTTGTATTTTGAATC | 109294 |
rs31564583 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11170866 | GTTTTTGAAAAATAT[G/T]TTCATTATTGTGAGC | 109294 |
rs31565278 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11095645 | TCGGGTCAGGTGATG[A/G]GGTAGGGCAGGTTCT | 109294 |
rs31566218 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Prex2 | GRCm38.p3 | 1:11140484 | TACCTCTGGGACTGT[A/G]TCTTAGTGATGACTG | 109294 |
rs31566717 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11167148 | TTTTCTGCATGTATT[A/G]CTTGCTGTGGCTTCT | 109294 |
rs31569476 | snp | A/G | 0.255 | 0.24995 | intron-variant | Prex2 | Mm_Celera | 1:11279408 | TGTCCACTGAGAGCA[A/G]AGGAATCCAGTACAG | 109294 |
rs31577106 | snp | C/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11020578 | CCCATCCCAGAAACA[C/G]AGCAGATTTATTTTT | 109294 |
rs31580350 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11269047 | ACGGTCTTAGGAAGA[A/G]TTCAATGTATGCCTG | 109294 |
rs31595016 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11090016 | CATGGGTTGTAGTCA[A/G]CTCAGAAAGTGTCAT | 109294 |
rs31596814 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Prex2 | Mm_Celera | 1:11136553 | TTTTAGATAATGAAA[A/C]AGGAGAAAGCAAATG | 109294 |
rs31607727 | snp | A/C | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11117146 | TTGTTATAGTGCAGT[A/C]AGGATTTGATCAATT | 109294 |
rs31609163 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Prex2 | Mm_Celera | 1:11036133 | TATATCTCAAATGGT[A/G]GAAGTCACCTCAATG | 109294 |
rs31616976 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Prex2 | Mm_Celera | 1:11278460 | GTGGTGTCTCACACC[G/T]ATTAAGAGAACATGT | 109294 |
rs31622769 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Prex2 | GRCm38.p3 | 1:11078092 | GCATGAAGACAATCC[A/G]ATGTGCTGTTTCTGA | 109294 |
rs31623970 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:10992396 | TCATATTTTGAAAAG[A/G]CTTATGGGAAACTGG | 109294 |
rs31625614 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Prex2 | GRCm38.p3 | 1:11286441 | GTGCAGAAGAAGCTC[A/G]GAAATGTTCCTTTAA | 109294 |
rs31627718 | snp | A/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11057372 | ATACGAATGCATGCC[A/T]AGAGCGAAGCCAGGT | 109294 |
rs31642703 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:10998922 | CTTATTCATGGTGTT[C/T]TGTGTGGTCACTCTG | 109294 |
rs31644392 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Prex2 | GRCm38.p3 | 1:11025647 | TGCAATTTTGTAGAG[A/G]TATGTACAGAGCAGG | 109294 |
rs31660786 | snp | A/T | 0.255 | 0.24995 | intron-variant | Prex2 | Mm_Celera | 1:11088341 | TCTTGTCTCACATGT[A/T]AGAGAACAGTTAAGA | 109294 |
rs31670226 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Prex2 | GRCm38.p3 | 1:11270565 | AATACTGAGGGACCT[C/T]ATTCGGCACACATAT | 109294 |
rs31674208 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Prex2 | GRCm38.p3 | 1:10999918 | GGTCTCTGGAGGCCA[A/G]AAGTCTCAGGCTATG | 109294 |
rs31675369 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Prex2 | GRCm38.p3 | 1:11153440 | GGAATGTTTTAGTTA[C/T]GCTTTGAGATGTTTA | 109294 |
rs31676427 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Prex2 | GRCm38.p3 | 1:11218090 | ACATAACTGTTTCCA[C/T]CTGTAAAAAAATTAT | 109294 |
rs31676839 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11164909 | CTTACTAATCAGTGA[A/G]GTGAGATATACTTTC | 109294 |
rs31681189 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11053311 | GGAAAGGGGTCAGGG[A/G]CTGGGGTCAGGGAGA | 109294 |
rs31683720 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11203313 | TTACACATAGAATTT[A/T]TCTCTTAATATAGCA | 109294 |
rs31688153 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Prex2 | GRCm38.p3 | 1:11225108 | AATGAAGAAAAAATA[A/G]CCTTAAATTACTATA | 109294 |
rs31691349 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Prex2 | GRCm38.p3 | 1:11285166 | AGAAAGCAGGTGAGT[C/T]GCTTTCTTTCCAGTC | 109294 |
rs31692721 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Prex2 | GRCm38.p3 | 1:11278628 | CAGCACCAAGAAGCA[A/C]AGACAATTAGCTCCC | 109294 |
rs31697721 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11275114 | TTTCTTCCATTTTTA[C/T]GATACCTTGGACAGA | 109294 |
rs31704917 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11115116 | CTCTTTGCTGTGACC[G/T]AGCATAAGCAATGTA | 109294 |
rs31714596 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11268311 | AGGGCTTAGAGATTT[C/T]TCTCAGTAGGATAAA | 109294 |
rs31715914 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11078310 | TCACATGTCACATGT[A/C]CATGTACCAATGTGC | 109294 |
rs31721125 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Prex2 | GRCm38.p3 | 1:11058109 | ATAGTGCAATCAAAA[C/T]CAGTCTTCTTTCTCA | 109294 |
rs31724608 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Prex2 | GRCm38.p3 | 1:11170949 | AAATGACAATTCATG[A/T]GGATAGGAATATTAA | 109294 |
rs31728414 | snp | C/T | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11268916 | TATGATTAGAAGTGA[C/T]TTAAGCAGTGGACAT | 109294 |
rs31728423 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11007587 | GGAGAATTCTAAATC[A/G]ATCCTCTTTTGGCTG | 109294 |
rs31731422 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11050275 | AGACACTTTAATAAA[A/G]CTCAAAGCACACATT | 109294 |
rs31732113 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Prex2 | GRCm38.p3 | 1:11274610 | CCTGAGTGTGCTTCA[A/T]AACTGGTACCCTTCT | 109294 |
rs31733878 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Prex2 | GRCm38.p3 | 1:11268957 | TCCTCCTTGCGTGTC[C/T]GCTTCTTCCATTGTG | 109294 |
rs31734220 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11235760 | ATGATGCTGATAGAA[A/G]ACATTAGAAGGGCAT | 109294 |
rs31740819 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Prex2 | Mm_Celera | 1:11183689 | TAATGGAGAGTCTTA[A/G]GTGGGCTGGCTCCTG | 109294 |
rs31749863 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11117982 | TAGCAAACTGTGCAT[C/T]GATTCACCTTCTTCC | 109294 |
rs31750397 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11157721 | TTTTTCTTTTTTTTT[A/T]ATGTTTTTTAAAAAT | 109294 |
rs31752078 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11181750 | AAACACAGAAGCCTT[C/T]TGGAAATATTTGTAA | 109294 |
rs31752896 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11020337 | TCTTCTTTTCTATAT[A/T]TTTTTTGGGGTCTCC | 109294 |
rs31765037 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Prex2 | Mm_Celera | 1:11118026 | CCTCTACTTTCTAGA[A/C]GTAATGATTATTGTG | 109294 |
rs31767015 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11286938 | ACAGGGCAGAGAGAG[A/G]GGAAGACCTCATTAT | 109294 |
rs31769133 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:10996423 | GTTGAACAAATTGAC[G/T]GATAAATTCATTGGC | 109294 |
rs31770770 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11081153 | ATATCCACATTCTGG[A/G]GAGGGCACAGAGTTA | 109294 |
rs31774820 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Prex2 | Mm_Celera | 1:11087088 | ACTTTAAATGTAGCT[A/G]TGGTAACCTTCCTGT | 109294 |
rs31782091 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:10995378 | GAGTTCGAGGCCAGC[C/T]TGGTCTACAAAGTGA | 109294 |
rs31790776 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Prex2 | Mm_Celera | 1:11025149 | GATCCAGGTTCAGTT[A/G]TGTTCCATCCTGACA | 109294 |
rs31792734 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Prex2 | GRCm38.p3 | 1:11035570 | TGATGTAAGAGAATA[A/G]GATAAAGTTATGAAA | 109294 |
rs31795542 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:10995552 | CACAGCAGAGGCAGG[C/T]GGATTTCTGAGTTTG | 109294 |
rs31805100 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11291177 | GGGGAGGGAAAAGAG[A/G]AGAGGAAAAGAGAGG | 109294 |
rs31807203 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Prex2 | GRCm38.p3 | 1:11106891 | CTGGGTGTTTTCTTG[C/T]TCATCCACATTGCTC | 109294 |
rs31812994 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11271988 | TACTTTCCATCATTA[A/C]AATAAGAGAAGGCTA | 109294 |
rs31813465 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11271788 | ATTTAAATCTTGATA[A/C]ATTAATACATTAAAT | 109294 |
rs31822147 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11048792 | CATCGTCAGAACCCA[A/G/T]CACTCCCACTTCACC | 109294 |
rs31823705 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Prex2 | GRCm38.p3 | 1:11196346 | TATCTCTAAGTCAGT[A/T]GGATACCCATTGATA | 109294 |
rs31833495 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Prex2 | Mm_Celera | 1:11217682 | TTCTGTGTAAAATGG[C/G]CTTGCATACATAGAG | 109294 |
rs31845944 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Prex2 | GRCm38.p3 | 1:11081243 | TGTAGGAGCACTCAT[A/G]ATAGTCAGATGGCAA | 109294 |
rs31871852 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Prex2 | GRCm38.p3 | 1:11200160 | AGGGAAAAATTTTCC[A/G]TCACCATTTAGGCTT | 109294 |
rs31873002 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11285947 | ATATGCTTTTGTAGT[C/T]ATGACCACTTTATTT | 109294 |
rs31875262 | snp | C/G | 0.207612 | 0.24638 | intron-variant | Prex2 | Mm_Celera | 1:11000333 | TAAGAAGGGCAAACA[C/G]AGTACGGTGGAGAAT | 109294 |
rs31876885 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Prex2 | GRCm38.p3 | 1:11284990 | TTTCTGATAACACTG[A/G]TAGTTCAGATTTCTC | 109294 |
rs31887551 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11042952 | GGTATAGGGAACTTT[C/T]GGGGTAGCATTTGAA | 109294 |
rs31889161 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11056678 | TCACCAGAGAGCGCA[C/T]AGGAGAATCTTTCAG | 109294 |
rs31889908 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Prex2 | Mm_Celera | 1:11207509 | AAGTTATTTGAAAAT[A/G]GTTACAAGAATTTGA | 109294 |
rs31897645 | snp | A/C/T | 0.465374 | 0.126941 | intron-variant | Prex2 | GRCm38.p3 | 1:11200865 | ATGATAGGGTAAGGG[A/C/T]ATTCATCTCAGAATG | 109294 |
rs31911860 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Prex2 | Mm_Celera | 1:11183627 | AAAAGTCATGAAACA[A/G]GTTTTGTCTTTGTCT | 109294 |
rs31914004 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Prex2 | GRCm38.p3 | 1:11000063 | CCATATGGGAGATGG[C/T]TTTCCCAATTTCCCA | 109294 |
rs31914008 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Prex2 | GRCm38.p3 | 1:11000576 | TCTTGGATGAGAAGC[A/G]TACAAGTCTTGGAAG | 109294 |
rs31914011 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Prex2 | GRCm38.p3 | 1:11001539 | CACACATTCGGGTGA[C/G]CCTCTGCACCATTGG | 109294 |
rs31914013 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Prex2 | Mm_Celera | 1:11001872 | TGTTCTAGGATACGG[C/T]GGATGCTGGTGAGGC | 109294 |
rs31915036 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Prex2 | Mm_Celera | 1:11004444 | TACCATGTAGCTCAG[C/T]CTGGTGCTCAAAAGG | 109294 |
rs31915039 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Prex2 | Mm_Celera | 1:11005339 | TGACTGCCTAAACAC[C/T]CATTCTTCTTTTTTT | 109294 |
rs31915042 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Prex2 | GRCm38.p3 | 1:11005743 | AATCATCACATTTGG[A/G]TTCGGAGTTTTCCTT | 109294 |
rs31915130 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Prex2 | GRCm38.p3 | 1:11025654 | TTGTAGAGGTATGTA[A/C]AGAGCAGGGTCAGCT | 109294 |
rs31915133 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11026024 | ATAAAATAAGTAAAT[C/T]TGAAAAAGAATATTA | 109294 |
rs31915875 | snp | A/G/T | 0.297521 | 0.245442 | intron-variant | Prex2 | GRCm38.p3 | 1:11006255 | GTTGAACAGACCAAG[A/G/T]GTGCTTGAAAATGGG | 109294 |
rs31915878 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Prex2 | Mm_Celera | 1:11006743 | GAGTAATCAGATAGC[C/T]TTGTGTCTTGCTAGA | 109294 |
rs31915883 | snp | G/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11007774 | AACCCTCAGGAGCAA[G/T]CGGGTGGCAGCAGCT | 109294 |
rs31916086 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11029341 | TTCTCTTGCCCTGTG[C/T]TCTCTATGTCTTGAG | 109294 |
rs31916089 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11033024 | TGAATCCATGTTGTA[A/G]GATTTAAACCCAGAA | 109294 |
rs31916092 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11033183 | TTCTCTCTCCTGTGT[A/G]TGAGAGAGATTTGAT | 109294 |
rs31916226 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11026248 | AACAAACTTGTCTTT[C/G]AAGAGGAAAATAGAA | 109294 |
rs31916229 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11026573 | CTCACCAGGAGCCCT[A/G]TACCAGGATGTGGCA | 109294 |
rs31916656 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Prex2 | Mm_Celera | 1:11007960 | AAGATTGCTGGTTTC[C/T]GTTGAACTATTCTTA | 109294 |
rs31916659 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11008216 | ATGACCATCATGCCT[C/G]AAAGTGTCCTTTATG | 109294 |
rs31916662 | snp | C/T | 0.42 | 0.183303 | intron-variant | Prex2 | Mm_Celera | 1:11009400 | TCCAAATCAACTCTA[C/T]TGGCTTATGGTGGGA | 109294 |
rs31916925 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11033209 | TTGATCAGAATGTGC[C/T]TGATTAAATAAATAC | 109294 |
rs31916928 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11033233 | TAAATACCCACTGGG[A/G]AGCATTCATTTATTC | 109294 |
rs31916931 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11033280 | TTATAGGAAATGAAC[A/G]TCTCTGAGTTCCTGC | 109294 |
rs31917134 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11026848 | AAGATCGGTGAAAAT[G/T]GAAGCATTCCTTTCA | 109294 |
rs31917139 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11026917 | GAATGAACACCTCTA[C/T]CATGGTTACTTCTCA | 109294 |
rs31917385 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Prex2 | Mm_Celera | 1:11010611 | GTCTCTAGCAAAGTG[A/G]GTATCTCAGCCTTGA | 109294 |
rs31917388 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11011191 | ATTGGTGAGTGATTG[C/T]ACTGATATGGAGTTT | 109294 |
rs31917393 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Prex2 | GRCm38.p3 | 1:11023173 | TAACATTTTCTGCTG[C/T]GAGTGCTCATGGTGG | 109294 |
rs31917504 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11033397 | ATGGGAGCTCAAACA[C/T]GGTATGATGGGAAGT | 109294 |
rs31917507 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11033769 | CAGAACAAATGCCTT[G/T]GGATGTTTGAAGCAA | 109294 |
rs31917510 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11033859 | TAAACACTCACCAGC[A/C]TTTGGTAGGCTTTCC | 109294 |
rs31917513 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11033928 | AATAAAATACTTTTG[A/G]AAATATCCTTGGAAA | 109294 |
rs31917568 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11036335 | CTGCAAACGTGTTAA[A/G]TTCTGCAGTGACTCT | 109294 |
rs31917571 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11036600 | TGCAGCCAGTGAGAA[C/T]AGTGTTTGTTGGTTT | 109294 |
rs31917735 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11059419 | GTTTTGGAGTATTTT[A/G]GCCATTTTTTTCTTA | 109294 |
rs31917738 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11059677 | TTTTCAATACATTAT[A/G]TCTGACTGGGCTTTT | 109294 |
rs31917741 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11059792 | AATGACTATTTTTGT[C/T]AGAATATATTCCTAG | 109294 |
rs31917743 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11060037 | AACTTTTATTTTTTT[A/T]AATGTCATAGTCAGA | 109294 |
rs31917776 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Prex2 | Mm_Celera | 1:11053625 | CCTTAATTATCTTCA[A/T]ATCCAGACATTAGGA | 109294 |
rs31917779 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Prex2 | Mm_Celera | 1:11053838 | GCACTTGATTGTTTA[C/G]ATGTCAGTACAATTT | 109294 |
rs31917782 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11053852 | AGATGTCAGTACAAT[G/T]TAGGCTTTTATCTGA | 109294 |
rs31917896 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Prex2 | GRCm38.p3 | 1:11023201 | TGGGTTCTTCTGTCA[C/T]AGACATGATCAGAAT | 109294 |
rs31917899 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Prex2 | GRCm38.p3 | 1:11023283 | TAGCTTTCATATCAG[A/C]ATATAAACAATTTGA | 109294 |
rs31917902 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11023373 | GCTGCACCTCGTATG[C/T]TCTAACAAAGATCCA | 109294 |
rs31918055 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11034003 | TAGATGAAGTGTTAT[A/G]AATCTTAATTCACTT | 109294 |
rs31918057 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11034139 | TTGATTATTGAACAG[A/G]TGGCTGGCTTTTAAT | 109294 |
rs31918059 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11034157 | GCTGGCTTTTAATCT[A/G]TGTGTCAAGAGCAGA | 109294 |
rs31918062 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11034206 | AATAGACATGAGCAC[C/G]AATAATGAAGCCTGG | 109294 |
rs31918084 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Prex2 | Mm_Celera | 1:11027041 | AAGACAGTCTTGCTC[C/T]TTAAGATCTGCAGGA | 109294 |
rs31918087 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Prex2 | GRCm38.p3 | 1:11027218 | CAGCTACTAGAGATT[G/T]GATTGAATGTTTGTC | 109294 |
rs31918092 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11027434 | CTCCCATTTAAAATC[C/T]GAACAAAAAATAACA | 109294 |
rs31918235 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082943 | CACTGGGGCTTCTCC[A/T]TTCTGATGTCCAGGG | 109294 |
rs31918238 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082976 | GAGGATTGCCGTCAC[A/T]TGCATGATCAAGAGG | 109294 |
rs31918241 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082988 | CACTTGCATGATCAA[A/C/G]AGGATAACATTCTGA | 109294 |
rs31918304 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11066814 | TTTCTTTATCTATAT[A/G]GGATGAACAGGCTCT | 109294 |
rs31918307 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11066869 | ATAATTCTGTCAAAG[A/G]AAAACGTTCCTCAGG | 109294 |
rs31918310 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Prex2 | GRCm38.p3 | 1:11067425 | TTACTGGCAGTTTAA[A/G]CCACTAGAAGATCTT | 109294 |
rs31918313 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11067709 | CCAGAATTGGTTAAC[A/G]TGAAATTCAGGGTTG | 109294 |
rs31918494 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11036765 | ACTACAGGAAAGGAC[A/T]TTCAACTCCACCCTT | 109294 |
rs31918497 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11037040 | AATGCTCCAGTGACT[C/T]ATGATCCTAAACAGA | 109294 |
rs31918500 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11037133 | AACTTCAGTAATTGT[C/T]CCTAGATAGGCATAT | 109294 |
rs31918502 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Prex2 | GRCm38.p3 | 1:11037335 | CAGAGGCACCAAGAA[G/T]GCACCCAAGCAAGGG | 109294 |
rs31918595 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11060146 | AAGGAGTGATGATGC[A/G]CTGGAGAATCTACAA | 109294 |
rs31918598 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11060171 | CTACAATTGAACAAT[A/C]GCCCCACAGGATCTT | 109294 |
rs31918601 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11060416 | CTGAAAGCTTGGTAT[G/T]AAACTCAGGGACTTG | 109294 |
rs31918674 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Prex2 | GRCm38.p3 | 1:11054169 | AAACACATTACCAAC[A/T]ACCTTGGAATGGACA | 109294 |
rs31918677 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Prex2 | GRCm38.p3 | 1:11054190 | GGAATGGACAGCACA[G/T]CTCCCCATAACAAAA | 109294 |
rs31918765 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11023394 | CAAAGATCCAGTTCC[G/T]GAGTGCTCTGCTTCT | 109294 |
rs31918768 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11023478 | TCCGGCTTCATGTCC[A/T]TCATCCCCAGCCTTC | 109294 |
rs31918771 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11023928 | TGTATTTTATAGTGC[A/G]TACATATAGAACTCA | 109294 |
rs31919004 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11083065 | AGGAGGCTTCTTTCC[G/T]TCCATGTGGTTAAAT | 109294 |
rs31919007 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11083093 | AATAGGCATGGGAGA[C/T]AAAAAGGCCATATTT | 109294 |
rs31919010 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11083100 | ATGGGAGACAAAAAG[A/G]CCATATTTGGAATCT | 109294 |
rs31919013 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11083165 | TAGGACAGTTCAAGG[C/T]CTAAAATGATAGCTT | 109294 |
rs31919025 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11034230 | AGCCTGGTTTACTTA[C/T]CTTCTTTTATTACCA | 109294 |
rs31919028 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11034328 | GAGGGCAGCCAAAAG[A/G]AATTTATGACAGTGA | 109294 |
rs31919031 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11034358 | ATTCTCTTCTCTGGA[C/T]GACCAAACAGAGTTT | 109294 |
rs31919055 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11027735 | ATTAAGCTTGCCATA[A/G]TTTAATGCTTTTAAA | 109294 |
rs31919057 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11028014 | CCCTGCTGCAGTATC[C/T]TCACTAAGCCAGCCT | 109294 |
rs31919060 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11028043 | CTAAAATGCTACCCA[C/T]TTAGTACACCTTTTA | 109294 |
rs31919063 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11028118 | TCTTATGGATAACCC[A/C]TTACTTACAGCCTTC | 109294 |
rs31919126 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11068404 | CCCTAGAGATCTGCT[C/T]GCGCCTTAGAGGATT | 109294 |
rs31919129 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11068558 | CACGTTTTGACAGCT[C/T]TGGGGTGTCTTTGTA | 109294 |
rs31919132 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11068676 | TTCTACGTAGCCCTA[C/T]TCCCTCATTTGCTCT | 109294 |
rs31919414 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11037393 | CCATCAACAGTATGT[C/T]CTTGTCCTCACTTGA | 109294 |
rs31919416 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11037409 | CTTGTCCTCACTTGA[G/T]CTTCATCTCTACCCT | 109294 |
rs31919419 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11037477 | GTGGAAAGTGAGGGG[C/T]GAAATAATGTGGGGC | 109294 |
rs31919422 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11037536 | AGGTGCAGAGTATTT[G/T]CCCAGTTCTCTTGTT | 109294 |
rs31919426 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11079105 | CAGGTCTTCCTCTTT[A/G]TACATTTGTTCAGAA | 109294 |
rs31919428 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11079181 | TTCCTGGGGAGCCTC[A/G]TGCCTACTGCCCTGT | 109294 |
rs31919430 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11079347 | ATCACCAGGTTAAAG[C/T]GTTCCAGTTTGGCAA | 109294 |
rs31919433 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11079769 | TGTCTGTTTCTCTAT[A/T]TTTCCTCTCTTTTCC | 109294 |
rs31919441 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11050551 | AAATATTGAAATTGT[C/T]TCATGCATCCTATCA | 109294 |
rs31919484 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11060640 | TAGTGTGCAGATGAT[C/G]TACCTATCTCTCTTT | 109294 |
rs31919487 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | GRCm38.p3 | 1:11060842 | TTAGTTGAAATGTCA[G/T]TTTTCATTCATTGTA | 109294 |
rs31919490 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11061220 | TTTGGAATGCCCAGT[A/G]GTAAGCTTTAGTGTT | 109294 |
rs31919493 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Prex2 | GRCm38.p3 | 1:11061446 | CGGGTATCATGAAGA[C/T]GATGCTGTGATCATC | 109294 |
rs31919574 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11023957 | CAGGGTGAGGATAAG[A/C]GTGTTGCCAGTATCC | 109294 |
rs31919576 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Prex2 | Mm_Celera | 1:11024083 | TTTGGGTTTTATGTA[A/G]ATTTCTCTATTCTAC | 109294 |
rs31919579 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11024132 | CTGGGTCAGAACATG[A/G]GGCTTTATACATGCT | 109294 |
rs31919581 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11024198 | TGATTATACACGGGC[C/T]TTCACATGTTCTTTA | 109294 |
rs31919594 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11056080 | TGTGTGTGTGCAAAT[A/G]TTCAAAACTCTAAAA | 109294 |
rs31919597 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11056197 | TGAGGTGACTTGACT[A/G]TGTGAAATGTGAAAG | 109294 |
rs31919599 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11056352 | ACTGCTCAGGCTCTC[C/T]AGGGACCAAATTTTT | 109294 |
rs31919602 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11056903 | CAAGATTTTGTGTAC[A/G]CTCTCAGAAAAACAA | 109294 |
rs31919844 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11034364 | TTCTCTGGACGACCA[A/G]ACAGAGTTTTTGGTT | 109294 |
rs31919847 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11034431 | GGGTGGTCCTTTGGA[A/G]CGGTTGTTTTATCTG | 109294 |
rs31919849 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11034470 | CGCTTCATCCATGCT[G/T]TCAAGCAGTGGTACC | 109294 |
rs31919851 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11034560 | TTCGAGCAGGGCACC[C/T]AGTTCTGGCAGAGGT | 109294 |
rs31919906 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11083230 | TATTGAGCCTGATTC[C/T]GGCACTTTGAAGTCA | 109294 |
rs31919909 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11083279 | GCATGTCAGATTAAT[C/T]TTTCATTCATGAAGG | 109294 |
rs31919912 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11083314 | ACCCTCTGAATAGAA[A/G]ACCAAGTTAGGGTTT | 109294 |
rs31919975 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11068774 | TTATTATATAGGGCA[C/G]AGTATCCTCAAATTT | 109294 |
rs31919978 | snp | A/C | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11068783 | AGGGCAGAGTATCCT[A/C]AAATTTGTAACCCCT | 109294 |
rs31919980 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Prex2 | Mm_Celera | 1:11068845 | AGTGATCAGATTTCA[A/T]GTTTTTGGAGACTTT | 109294 |
rs31919983 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Prex2 | Mm_Celera | 1:11074421 | CTACCTAAATTCAGG[C/T]AGTTTATTGCTCTTT | 109294 |
rs31920095 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11028145 | CTTCCATCATCTTCA[C/T]TTGTCTTGCTGATTA | 109294 |
rs31920098 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11028214 | ACATCACCTTCCCTT[A/C]CTGTCCCACGTGGAG | 109294 |
rs31920101 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11028223 | TCCCTTACTGTCCCA[C/G]GTGGAGATTTTTTGG | 109294 |
rs31920103 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11028249 | TTTGGAATGATTATG[C/T]TTAAGAAAGCTAGGA | 109294 |
rs31920166 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11085773 | TCATTGCTGCTTAAA[C/G]AGCTCAATCTAACAT | 109294 |
rs31920169 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11085832 | TGTTTTTAATAGCAT[C/T]ATTACATCTCTCCAA | 109294 |
rs31920172 | snp | A/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11085990 | AACATAACTCTTCTC[A/T]CTCTCCTGATTCTTA | 109294 |
rs31920265 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11061488 | CAGGGCTCTTCAATT[C/T]AGTGTCAGCTCCACT | 109294 |
rs31920268 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Prex2 | GRCm38.p3 | 1:11061641 | AACCATTTGAAAAGA[G/T]GAAGAAAAATAAGAA | 109294 |
rs31920271 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Prex2 | GRCm38.p3 | 1:11061740 | CAAGAAGGCAAGAAA[C/T]GGGGAAATGGGAATT | 109294 |
rs31920273 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11061826 | AAGATTGTAGTACCC[A/C]AACACAAAAGTAATA | 109294 |
rs31920404 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11037685 | TCAGGACTTCCTCAT[G/T]TAATAATCTCTGACG | 109294 |
rs31920407 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11037863 | TTTCAGGCTCCTGAT[A/G]CAGGCTGCAATGTGA | 109294 |
rs31920410 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11038000 | GCTCATTTTCCATAG[C/T]GGCATGTTCCATGGC | 109294 |
rs31920413 | snp | A/T | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11038063 | ATATAATAGGAGCTG[A/T]CTTTTTGTTGAAGGA | 109294 |
rs31920435 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11057124 | ATAGCCACATTTCCA[A/G]GATGATCAAAAGATG | 109294 |
rs31920438 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11057147 | AAAAGATGCTGAGAT[A/T]TGTCTATATGTGAAA | 109294 |
rs31920441 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11057231 | GACATCGAGTGGCTA[A/G]AATCTAACTTGTAAA | 109294 |
rs31920455 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11079804 | TCTACTTAAACCCTT[A/C]CTCTTCATGCTTGCT | 109294 |
rs31920458 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11079904 | TAGGTCTTGACTGAA[C/T]CTTGTAACATGGTAT | 109294 |
rs31920461 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11080017 | TTATGTTTATTTACC[C/T]TGCAGAACTGCATGC | 109294 |
rs31920514 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11024224 | CTTTACCATTTCTTC[A/G]TAACATTGAGTGTAT | 109294 |
rs31920517 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11024376 | ACATTCGTAGTGTTT[C/T]GGTGAACACTTGCAC | 109294 |
rs31920520 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Prex2 | Mm_Celera | 1:11024490 | TAGATTCTACTTGCT[A/T]GCTTGCATATGTTTC | 109294 |
rs31920522 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11024838 | TCTAATAGCCCATTG[A/G]AGTTTCTATGCACAT | 109294 |
rs31920771 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11083918 | CCATGGCTACCTGAT[A/G]TAATTCCTTAGCTAT | 109294 |
rs31920804 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11035092 | GCCAGGTCATACAGA[C/G]GAAAATGCTGTGGTT | 109294 |
rs31920807 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11035161 | TTTTAACTCCTATTG[C/T]GTTCCCAGAAGGTAG | 109294 |
rs31920810 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11035438 | CTTGAGTTTTCCAAT[A/G]TTTTAAGAGCAAACC | 109294 |
rs31920813 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11035484 | GTTCATCAGCCACTG[C/T]GTTGTTACCTTTGCT | 109294 |
rs31920855 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11074533 | TGTTGGTCACAGAGG[G/T]AAAGCTTTGTAAGCT | 109294 |
rs31920861 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Prex2 | Mm_Celera | 1:11074873 | TAGCTCATTTTTTTT[A/T]AATATTGGAAGCTAT | 109294 |
rs31920977 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11086208 | TTCTTGGGTGAAGGT[C/T]TTTCTTCTAATTTCT | 109294 |
rs31920980 | snp | A/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11086388 | TGCTTTATGTACCAT[A/G]AAGGTAGTCTCCAGA | 109294 |
rs31920983 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11086478 | GTACAATAGTAAGAG[C/G]AACTAGCTATACTCT | 109294 |
rs31921058 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11028416 | TTTAAACAGCAATAT[G/T]GGCTGCTAAAATTTT | 109294 |
rs31921061 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11028512 | ATTTGGTATCTGCAT[C/T]GTATTTGGTATCTGC | 109294 |
rs31921174 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Prex2 | GRCm38.p3 | 1:11057295 | TAGGTCTAGTTGGTG[A/T]AAATAATAGGAACGG | 109294 |
rs31921177 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Prex2 | GRCm38.p3 | 1:11057334 | GAGCTTGGGGAGGTG[C/T]GTTAGAGCCTTGAAA | 109294 |
rs31921180 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11057581 | TCGCTTATAGTTAGA[A/C]TAAAACAACACGGAA | 109294 |
rs31921183 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11057606 | ACGGAAAGATACAGA[G/T]AAAATGAAGCATGTG | 109294 |
rs31921206 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Prex2 | GRCm38.p3 | 1:11061869 | CTTGTAAAACATAGG[A/G]AAGGGGTCCAGGGAT | 109294 |
rs31921209 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11061885 | AAGGGGTCCAGGGAT[A/G]GAGCTTAGTGGTGGT | 109294 |
rs31921256 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11038332 | TTCTGGTTATAGTTA[A/G]AATCAAACTTCAGAA | 109294 |
rs31921259 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11038426 | TTCAAGGTGGGTGTT[C/T]TGTCTAGGAGTTCGA | 109294 |
rs31921262 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11038642 | GCATATAAGAGAAGA[A/C]AACTTGCAATAGTTC | 109294 |
rs31921405 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11024971 | TACTTATATGAGGCA[G/T]GTGTTACCTTGTATA | 109294 |
rs31921444 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11080150 | TATGTATAGAGTTTG[C/T]TATTACCTTAATATT | 109294 |
rs31921447 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11080269 | GCTGTTTTGTCATAA[A/G]TTCCTGTCTTGAATA | 109294 |
rs31921450 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11080281 | TAAATTCCTGTCTTG[A/T]ATAGGAAACAAACCT | 109294 |
rs31921452 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Prex2 | Mm_Celera | 1:11080319 | AAAGAGCATTAAAGG[A/C]TGCTCTTAGTGCTCT | 109294 |
rs31921648 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | GRCm38.p3 | 1:11035621 | AAAACTTCATTAAAA[A/G]CAGCCATGTTAAGAT | 109294 |
rs31921651 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11035779 | CATGAGTAAAGGAAA[A/T]ACCAGATTATTAAGG | 109294 |
rs31921784 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11075206 | CTTGGTGTTTGAAAT[C/T]CACTCTTTATCTCTT | 109294 |
rs31921786 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11075225 | TCTTTATCTCTTATT[A/G]AGCAACTGTTTATAA | 109294 |
rs31921788 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11075261 | TAAATGCTGTGGTAT[A/G]CAGCACATAGCCAGA | 109294 |
rs31921791 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11076391 | CCACATCAGTGTTTT[C/T]TCCTGTTGCCTTGGA | 109294 |
rs31921793 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11076462 | CTCTGTTCTTCACAT[C/T]GGATGATTTATGTGA | 109294 |
rs31921814 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11084126 | GAAAGAGCTAAGACA[A/T]ATAAGGAAGACTGTC | 109294 |
rs31921817 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11084226 | TAAAAACTGGTTATT[A/G]GATGACTTGAGGTAT | 109294 |
rs31921820 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11084478 | AGGATTTTTAGGGGA[A/G]TCTGGCTAAGGAGAG | 109294 |
rs31921823 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Prex2 | GRCm38.p3 | 1:11084495 | CTGGCTAAGGAGAGT[A/G]TGAGAATTAGGAACA | 109294 |
rs31921836 | snp | A/C | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:11086502 | ATACTCTAGTCCCAA[A/C]TCTCTGGAAGGGTAG | 109294 |
rs31921839 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Prex2 | Mm_Celera | 1:11086537 | TAGAATCCAGATTAT[A/G]TAACAGTCCAATAAG | 109294 |
rs31921842 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Prex2 | Mm_Celera | 1:11086589 | GCTCCTTATATTCTG[A/G]CCTAGGAGAGGGGAG | 109294 |
rs31921954 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11028513 | TTTGGTATCTGCATC[A/G/T]TATTTGGTATCTGCT | 109294 |
rs31921957 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11028703 | CTCTCCATCCTCTCT[C/G]TTACTAGTTTGTGCT | 109294 |
rs31921959 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11028997 | CATCTCTCTTCTCTA[C/T]GGGTTTTGACCACAT | 109294 |
rs31921961 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11029092 | TCCATTTGTTCACTC[A/G]TCCTCAGAAAGCATG | 109294 |
rs31921986 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11057725 | TGTGCTGACACACCC[G/T]TGAGCTGCAGGGTCC | 109294 |
rs31921989 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11057800 | TCTATCTTGTCTGAA[C/T]ACCTGCTTACATTCC | 109294 |
rs31921992 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11057895 | TCTAAGTTGCTGGGT[A/C/G]AAGGGGTCACACACA | 109294 |
rs31922015 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11039241 | ATATCTTTAAAGGGT[A/G]TGCCCTCTGCTTGGA | 109294 |
rs31922017 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11039443 | CAGCTCCCTGAGTGG[G/T]CTTGGAAATTTAGAC | 109294 |
rs31922020 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11043068 | TTTAAATTGAACAAA[A/G]TAACGTTTTCGTTCT | 109294 |
rs31922022 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11043275 | TCCTTGCAGAGCAGC[A/G]ATTCTATCAAGCAGC | 109294 |
rs31922047 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11064520 | AGATTGTTTGGTGAT[A/G]TGAGGGACATTCAAG | 109294 |
rs31922155 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11093000 | TTTCAATAAATTCTC[C/T]CAAATAATTTTCCTA | 109294 |
rs31922159 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11093137 | ATGGCTTTTGAGGAG[A/C]CTTGATGTTTAGTCT | 109294 |
rs31922162 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11093225 | GTAGATAGTGTGGAT[G/T]ATTTCAAGAATTTAA | 109294 |
rs31922305 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11080398 | CTTTAGAAGAGACCC[C/T]ACTAAATCATTATGA | 109294 |
rs31922308 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11080424 | TATGATTGGCTTCTA[C/T]AGCACTTTAGCTATA | 109294 |
rs31922311 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11080929 | TGTATGGTGTAGACC[A/T]CATGGAACCAGAGAT | 109294 |
rs31922313 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11081068 | GTAGTGTGGTTTCAT[A/G]TTCCTGTTACTTTCT | 109294 |
rs31922424 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11035887 | CTTGGTAAGTACTTG[A/C]GATGGTTATCCAGGG | 109294 |
rs31922427 | snp | A/C | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11035949 | AAAATAATACTTTTA[A/C]AATAATACTGCTTTG | 109294 |
rs31922430 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Prex2 | Mm_Celera | 1:11035984 | TCATGGTGACTTTGT[C/T]ATTTTTAAATAAAAA | 109294 |
rs31922433 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11036082 | TTACCCCATGTATCA[C/T]TGCTAATGTCAGGAT | 109294 |
rs31922565 | snp | G/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11084542 | CCACTCTGTAACTGA[G/T]CATACAGAAACCTTG | 109294 |
rs31922568 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11084753 | CAAAAGTTGCCATTT[C/T]AGTCTTCTCTATAGT | 109294 |
rs31922571 | snp | A/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11084850 | CTGCCCTGGAGGGAT[A/T]GACCTTAAGTCTAGA | 109294 |
rs31922585 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11086690 | AGAAGACTACATAAG[A/G]CTAACAAGATCCTAT | 109294 |
rs31922588 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11086706 | CTAACAAGATCCTAT[A/G]TAGCCAGAGAATACT | 109294 |
rs31922591 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11086718 | TATGTAGCCAGAGAA[G/T]ACTAGATAGGATGCC | 109294 |
rs31922655 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Prex2 | Mm_Celera | 1:11057954 | TAAAAGATGGAATGA[A/G]AGAATCTGTCTTGCC | 109294 |
rs31922658 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11057978 | TCTTGCCACTGCAGT[C/T]CACTTGATAAAACTT | 109294 |
rs31922661 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11058055 | CTATCAGAAGGTAGG[C/T]TCTGGATCTGATTTA | 109294 |
rs31922674 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Prex2 | Mm_Celera | 1:11098546 | AAATATTCAAGAACG[A/G]GTGTTTTTTCTTTTT | 109294 |
rs31922677 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon | Prex2 | Mm_Celera | 1:11098573 | TTTTGATAATCTTTT[A/G]GTATACTGCAAAAGA | 109294 |
rs31922679 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Prex2 | GRCm38.p3 | 1:11098612 | GTAAGCTTATAAAAA[G/T]TCACATTTTGGAATT | 109294 |
rs31922682 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Prex2 | GRCm38.p3 | 1:11098663 | TCCCCACAGGAATCC[C/T]AGAACTCATCTCACT | 109294 |
rs31922798 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11065167 | ACCTTCTAGATTATA[C/T]ATTTAACTTGCAGGC | 109294 |
rs31922801 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11065408 | TATGACTTCTACACA[C/T]AAGCACCTGAGAGAA | 109294 |
rs31922816 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11089426 | AAATCAGATTTATAA[A/G]AGCTAGGATGTGGTC | 109294 |
rs31922819 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11089502 | TCTAAAATACAGGTA[A/G]GTTTGAGGAAAAACA | 109294 |
rs31922822 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11089653 | TGTAGTTTTCATTTC[C/G]TGGTCAGCCTGCTGT | 109294 |
rs31922834 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11029111 | TCAGAAAGCATGTCC[C/T]GATTCTGATTCATAA | 109294 |
rs31922837 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11029127 | GATTCTGATTCATAA[C/T]GTGAGCTCTGCATCC | 109294 |
rs31922840 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11029139 | TAACGTGAGCTCTGC[A/T]TCCAGGTGAGCAGGG | 109294 |
rs31922906 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11076513 | AGTTCTCTTTTCATT[C/T]GATGTCTGTTTGATT | 109294 |
rs31922909 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11076568 | AGGGTTCCTGTTCCC[G/T]GCTCACCCTTCAGTT | 109294 |
rs31922911 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11077152 | TTGTCAAAGATATTC[A/C]TTCTCTCAGGAAAAT | 109294 |
rs31922913 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11077548 | CTTAGTTTAGTTTGC[C/T]TAGTGACTATAGGTC | 109294 |
rs31923025 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11093278 | AATATCATGAAAGTT[A/C]TGCAAACATGAAGCA | 109294 |
rs31923028 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Prex2 | Mm_Celera | 1:11093345 | TCTTTAAGAATCTCC[G/T]ATGATACTTTAATCC | 109294 |
rs31923031 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Prex2 | GRCm38.p3 | 1:11093493 | AGAATTTCCGATTTG[C/T]AGAGTGTATGAAGTT | 109294 |
rs31923084 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11043287 | AGCAATTCTATCAAG[C/G]AGCTCGTGAGATACA | 109294 |
rs31923087 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11043385 | CAGGAAAGTTTGCTA[A/G]ACTCTTGGCTTGAGC | 109294 |
rs31923090 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11043444 | ATGATATTTAATTAT[G/T]TGGCTGCTTGGATTA | 109294 |
rs31923093 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11044583 | AATTCCTAAGATGGC[A/C]AAAGATCATTGAGGT | 109294 |
rs31923175 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11102427 | ATTAAAAAAGAAAAG[A/G]TTTGCCTTTGAAATT | 109294 |
rs31923178 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11102636 | TAAGGATGAACAAGA[C/T]CTTGAAGACAAGCAA | 109294 |
rs31923181 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11102876 | TTCATCAGCTTTTTC[A/C]CTTTCTTACTTCCCT | 109294 |
rs31923245 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11081198 | GCAAAATCCACAAAA[A/G]TCCTTCAAGAAAAAT | 109294 |
rs31923248 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11081228 | TGATACTGTAGCCTA[C/T]GTAGGAGCACTCATA | 109294 |
rs31923252 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11081404 | CCAGAAGCAGCTGAG[A/G]GCTGACACAAGTCTG | 109294 |
rs31923266 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11058450 | TCCTGTTGATCTACA[A/G]GACAGAAGACTTAAA | 109294 |
rs31923269 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11058613 | AGTACGTTCCCCAAT[A/G]TCATGCAGGACTGAA | 109294 |
rs31923272 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11058643 | AGATAGAAATGTCAA[A/T]TGGCTAGGTGGTATA | 109294 |
rs31923284 | snp | A/C | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11084916 | GTATAAGGAACTATT[A/C]AAAAGAAATGACAAA | 109294 |
rs31923286 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:11084995 | GGGGCTGGTCTAATG[C/T]ACCTGGAATTGTTGT | 109294 |
rs31923288 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11085117 | AAGATTGTTGATCAC[A/G]ATAGAAGCCAGTATG | 109294 |
rs31923290 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11085162 | GCCAGACCTGTCATT[A/G]TGGGGAATAAAGGTC | 109294 |
rs31923292 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11085174 | ATTGTGGGGAATAAA[A/G]GTCAACTAGGCTGGA | 109294 |
rs31923466 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11087012 | GTGCTAAATCTGAAA[A/G]TGAACCCTCCTTATC | 109294 |
rs31923471 | snp | G/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11087092 | TAAATGTAGCTATGG[G/T]AACCTTCCTGTTCCA | 109294 |
rs31923524 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11065613 | CATAGTGTATTCATC[C/G]CCAGAGTTTTGTGGG | 109294 |
rs31923527 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11065679 | GTGGGAGTAAGAGAT[A/G]CCGTGATGTAGCGCT | 109294 |
rs31923529 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | GRCm38.p3 | 1:11065692 | ATGCCGTGATGTAGC[A/G/T]CTCTGTCTAGGATGC | 109294 |
rs31923532 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11065744 | ATTTAATTTTTCAAA[G/T]TTGCTTCACAACTAC | 109294 |
rs31923535 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Prex2 | Mm_Celera | 1:11089661 | TCATTTCCTGGTCAG[C/T]CTGCTGTACCGGAGC | 109294 |
rs31923538 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11089671 | GTCAGCCTGCTGTAC[C/T]GGAGCACTGGAGATC | 109294 |
rs31923541 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11089932 | TGTGGCTTCTCCTCA[A/G]TGCACGGAACCCTGT | 109294 |
rs31923685 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11044698 | GTAACTGAAGTGGAT[G/T]GTGTAATGTGGTCAT | 109294 |
rs31923690 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11045905 | ACCTCTCAGTGCTGG[C/G]ATTGCAGGTAGTTGT | 109294 |
rs31923795 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11077790 | AGTTTCTAGTTTGGG[A/T]TGATGATGGTACTAT | 109294 |
rs31923797 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11077813 | GGTACTATCTTGGGC[C/T]TTTGCTGATGCTGTT | 109294 |
rs31923800 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11078065 | CAGCTAGGGCAAGTA[C/T]GTTCTGTGCATGCAT | 109294 |
rs31923894 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Prex2 | GRCm38.p3 | 1:11093495 | AATTTCCGATTTGTA[G/T]AGTGTATGAAGTTAG | 109294 |
rs31923899 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11094802 | CAGATAACCAATAGA[A/C]ACAGTGTGAAACTTG | 109294 |
rs31923902 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Prex2 | GRCm38.p3 | 1:11094960 | ACTGTAATAATCTTA[C/T]TTGAGTTAATTTGGC | 109294 |
rs31923914 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11098694 | AATAACCCATTTCAG[C/T]CCAGCCTGCTTGCTT | 109294 |
rs31923917 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Prex2 | Mm_Celera | 1:11098740 | TGGGTAATCATGGCC[A/T]ATGACTCAGTATCTC | 109294 |
rs31923919 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11098745 | AATCATGGCCAATGA[C/T]TCAGTATCTCTTGTG | 109294 |
rs31923922 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11098851 | GCTTCTGAGCCATTT[C/T]TTCCTGTATCTGTAG | 109294 |
rs31923945 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11058715 | TCAGTTTTACAACTT[C/T]CAGGATTTCATTTAG | 109294 |
rs31923948 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11058752 | AAGAGTGCGCTGGGT[C/T]CTGTTTATGAAGAAA | 109294 |
rs31923951 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11058905 | CAAAAAAGCCGAGGA[C/T]CCTGCTGGGATGAGG | 109294 |
rs31924055 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11106103 | CAAATGATATATGTG[C/T]AGCCCTTGGTGTGTT | 109294 |
rs31924058 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11106237 | AGTGTTTCTCATGTA[A/G]GTTGAATATAGCTAT | 109294 |
rs31924061 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11106313 | GGATCTTTTAAACAA[A/T]GGAGCAAGGTTCACA | 109294 |
rs31924284 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11102956 | TTAAATGAAAACCTA[G/T]GATTCTGGAAGATCT | 109294 |
rs31924287 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11102985 | CTGGGCCTGACTGAC[A/T]ATGTCCACTGCCTAG | 109294 |
rs31924290 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11102998 | ACTATGTCCACTGCC[A/T]AGTACTCTCTCTGTC | 109294 |
rs31924293 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11103052 | GGAACATATCTGTTT[A/C]TCTTATCTGCTTATC | 109294 |
rs31924364 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11087213 | TGCTCATCAGAAGGA[G/T]TCACAAGAAGTCTTT | 109294 |
rs31924367 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11087219 | TCAGAAGGATTCACA[A/G]GAAGTCTTTCAAAAA | 109294 |
rs31924370 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11087262 | GTCAGGGAGGTTCTC[A/C]GTCACAGCAGGCACC | 109294 |
rs31924373 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11087357 | AGAAACCAGATCTTC[A/T]GGGAGGGCTTGAAGT | 109294 |
rs31924385 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11066456 | TCAGAAGTTTGTTTG[C/T]GGTGCTGTGGAAAGA | 109294 |
rs31924388 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11066549 | CAGGGTAGCTGGAAT[A/T]ATGTAATCAATTTGC | 109294 |
rs31924391 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11066756 | GTATTATATCCCAAA[A/T]GAAGCTTTGAGTATG | 109294 |
rs31924395 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11081425 | CACAAGTCTGTTGGA[A/G]CCATGTGTCTGGTCC | 109294 |
rs31924398 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11081448 | TCTGGTCCTCTGACT[C/G]CAACTGCTTTGAGGG | 109294 |
rs31924401 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11081502 | CTCTACCAAAGGAAG[C/T]GGACAAGGCTTTTGA | 109294 |
rs31924444 | snp | C/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11085235 | TAGATAGGACAGGGT[C/T]TGAGAGGTCTCTGAG | 109294 |
rs31924446 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11085264 | AGAGCATTCCCAACA[A/G]GAAGTGGCCTTCTTG | 109294 |
rs31924449 | snp | A/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:11085336 | GGACATTTATTTAGT[A/T]GGCTCTTGTAGTGAT | 109294 |
rs31924452 | snp | A/C | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:11085413 | AAGACTGAGTTTATG[A/C]CCTGGACAAATAAAA | 109294 |
rs31924456 | snp | C/T | 0.455 | 0.143091 | intron-variant | Prex2 | GRCm38.p3 | 1:11090107 | AATACCATGTGCCTC[C/T]AAGCTCTGGCCCTTC | 109294 |
rs31924459 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Prex2 | Mm_Celera | 1:11090380 | AGTTTTATGAGTCAT[C/T]AAAGAAAGTTTTTTA | 109294 |
rs31924484 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11108158 | TAGACAGATAACTCA[A/C]TGTCTGGGTGAAGAA | 109294 |
rs31924487 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Prex2 | GRCm38.p3 | 1:11108354 | ACTCGGAAATCCCAC[C/G]TCTATTGACACACTC | 109294 |
rs31924489 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11108367 | ACGTCTATTGACACA[A/C]TCAAGAACCAATTAG | 109294 |
rs31924492 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Prex2 | Mm_Celera | 1:11108424 | GTAATTGGCACATTA[A/C]AATGAAAATAAAACC | 109294 |
rs31924725 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Prex2 | GRCm38.p3 | 1:11046518 | CCACTGATTGGAAAT[A/G]CTTCCTTTCAGATAC | 109294 |
rs31924730 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Prex2 | GRCm38.p3 | 1:11048021 | AAACATTGGTGGGAT[A/G]GAGAGTATTGATCTT | 109294 |
rs31924795 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11095135 | CTCAAGTCTCTAGAG[C/T]TTCCGGGCAGACGAC | 109294 |
rs31924798 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11095143 | TCTAGAGCTTCCGGG[C/T]AGACGACAGAACATC | 109294 |
rs31924801 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11095180 | GTTCATGAGAAGAGC[C/T]AACTCACTTATAGAA | 109294 |
rs31924864 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11098903 | CTGTTCATATGTTTT[C/T]CCAATTGATCACTCA | 109294 |
rs31924867 | snp | C/G | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11098983 | CTGTCATCATCCAGG[C/G]TATTTTCAAAATTCC | 109294 |
rs31924870 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Prex2 | GRCm38.p3 | 1:11099071 | CCACCAGTCCTATGC[C/T]GGTACCTGAAGCTTG | 109294 |
rs31924873 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11099132 | CACTTTAATCATCCC[A/G]TCCTGAAAGCTAGTG | 109294 |
rs31924924 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11106330 | GAGCAAGGTTCACAT[C/G]TAAGGATCTTATCAG | 109294 |
rs31924926 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11106559 | TTAAATAAAAATAGC[A/G]AGTCCCCTAAGCTCC | 109294 |
rs31924929 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Prex2 | Mm_Celera | 1:11106580 | CCTAAGCTCCTTTTA[C/T]AAGTTTGAGGTTCTG | 109294 |
rs31924932 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Prex2 | GRCm38.p3 | 1:11106671 | TGGGATAATGTGACT[A/G]GTGCAGAAAGGACTG | 109294 |
rs31925034 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11059073 | CCAAAAGCTATAAAG[A/T]GGTTGAAAAATTATA | 109294 |
rs31925066 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11103115 | CAACTCAGCAGCTAT[A/G]CTTTATCTTGATCAA | 109294 |
rs31925068 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11103154 | GAGTTGAGGATATCT[A/G]GAATTTATGATGGAA | 109294 |
rs31925071 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11103338 | TTATTCTGGTGGAAA[A/G]TTACTTAGCCTTCAG | 109294 |
rs31925094 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11078307 | GTGTCACATGTCACA[A/T]GTCCATGTACCAATG | 109294 |
rs31925097 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11078673 | GGAAAGAGGGTTACC[A/G]CAGCTGCTAACATAT | 109294 |
rs31925099 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11078729 | TCGTGGAATAGTATA[A/T]GATGTAAATAATCGT | 109294 |
rs31925102 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11078806 | TCTTGGCTGCTCTGT[C/G]TGTTGTGAAGTCCAG | 109294 |
rs31925254 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11066783 | TATGTTTTCCATGTC[A/G]TCATTTATCTTGTAG | 109294 |
rs31925336 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11087370 | TCAGGGAGGGCTTGA[A/T]GTTTTTAATTGTTTT | 109294 |
rs31925339 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11087888 | TGAGTCACCTCTGAA[A/G]CTTGTAAGAACCTTA | 109294 |
rs31925342 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11088068 | TGGCTCTGTATGTTC[G/T]GATGTTCTGAGAGTC | 109294 |
rs31925344 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11081522 | AAGGCTTTTGATTGG[A/C]CCCTGATGTCTTGAT | 109294 |
rs31925347 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11081547 | CTTGATTAGTATGAA[C/G]TATACTGGACAGAAA | 109294 |
rs31925349 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11081696 | TCATTGGTGAGGAAA[G/T]ATTTACTGTACAGGG | 109294 |
rs31925352 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082075 | TCTAGTCTAAGTTCT[G/T]CCATGAGTCCTGTTA | 109294 |
rs31925425 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11108501 | GTTGCTTTTTCAGTT[A/G]GTTCAGATTTGAAAG | 109294 |
rs31925428 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11108536 | TTTTACATCTTTGAA[C/T]GTTACTTTTCCACCT | 109294 |
rs31925431 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11108595 | CAGATATAGTCATCC[A/G]GTGCATTGCAATATC | 109294 |
rs31925444 | snp | C/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:11085473 | GGCTGCTATCAGTGT[C/T]TGGAGCTTTTTATGA | 109294 |
rs31925445 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Prex2 | Mm_Celera | 1:11085505 | TGTCTGAAGTTGGCT[A/G]AGTTAAGAGAGTGGC | 109294 |
rs31925448 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Prex2 | GRCm38.p3 | 1:11085579 | TTCTTGTCTTCTTGA[A/G]GTATATAACAGGGAC | 109294 |
rs31925464 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Prex2 | Mm_Celera | 1:11090575 | TAATATGATCTTCGG[G/T]CTAGCAGAATTTTTT | 109294 |
rs31925467 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Prex2 | Mm_Celera | 1:11090586 | TCGGTCTAGCAGAAT[G/T]TTTTTTTCATGTGAT | 109294 |
rs31925470 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11090666 | TATAGCCAAGTACAA[A/C]TCAAGCCAATACACA | 109294 |
rs31925473 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Prex2 | Mm_Celera | 1:11090920 | TGCAGCAAGAATCCT[G/T]CCTCTTTTAATCAGA | 109294 |
rs31925664 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Prex2 | GRCm38.p3 | 1:11095197 | ACTCACTTATAGAAG[G/T]TAGAAGTAACCAGGC | 109294 |
rs31925667 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11095830 | GAACATTTTACTGAA[A/G]TTATGTTAGGATAAT | 109294 |
rs31925670 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11096156 | ATACAGCCAGAAAGT[A/G]AAGAGTTTCAGAGTA | 109294 |
rs31925673 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11096389 | ACATGACACTGTTTA[A/G]TAATTAAGCTTAAAG | 109294 |
rs31925756 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Prex2 | GRCm38.p3 | 1:11099168 | ATCATCAAATCCAGA[A/G]CTTTTGCAAAATTAT | 109294 |
rs31925759 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Prex2 | Mm_Celera | 1:11099233 | ACCCAGAAAATTACT[A/G]AAAGGTTATATTGAA | 109294 |
rs31925762 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11099540 | AACCACTGAACTAGA[C/T]TGAGGTGTCCTTTCT | 109294 |
rs31925776 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11106741 | GAATACATTCTGGGG[A/G]TCAGCCAATTAACAG | 109294 |
rs31925779 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Prex2 | GRCm38.p3 | 1:11106763 | AATTAACAGAAGATA[A/C]CATGTTGTTTTGGCA | 109294 |
rs31925856 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Prex2 | GRCm38.p3 | 1:11109813 | CTGCCATACCCACTA[C/G]AGCACCTGGATACTT | 109294 |
rs31925859 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11109972 | TTGACTGAGCCTTTC[C/T]AGTAATATGGTTTCC | 109294 |
rs31925862 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11110030 | TGCTAATTTCATTTA[A/C]TCCTCTTCCTCTTGC | 109294 |
rs31925914 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11103375 | CATAAAATATAACTC[A/G]ATTATTCTCACAAGC | 109294 |
rs31925916 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11103441 | CTGAACTCTAGCCCC[C/T]CAGTAAATAATTATG | 109294 |
rs31925919 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11103600 | GTGTAGCCAGATTGC[C/T]ATTCACTCATTATCT | 109294 |
rs31925922 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11103660 | TTAGTTTCTCTTCAG[G/T]GGTTATTGCTGCAGA | 109294 |
rs31926065 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11078819 | GTGTGTTGTGAAGTC[C/T]AGATGAAGTGATCAT | 109294 |
rs31926067 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11078856 | CTAAGTACACATATC[A/G]GCACTGAGGCTTCGG | 109294 |
rs31926069 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11078961 | TCATATGGAATGTTA[G/T]TATAAAACTGTGACA | 109294 |
rs31926194 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11108612 | TGCATTGCAATATCA[C/T]GGGACCTCCAAGGAA | 109294 |
rs31926197 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11108637 | AAGGAATGCTCTCTA[C/T]GTTTTTATAGCACAT | 109294 |
rs31926200 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11108684 | AATAGGTAAGCTTTA[C/T]AATTCAGATTAAAGC | 109294 |
rs31926203 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Prex2 | Mm_Celera | 1:11108756 | TCATTGAATACAATG[C/T]AATGTCACCAATAAG | 109294 |
rs31926225 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11088128 | GGGCTTATGTACCCA[C/T]AGGTATCCTGATCCC | 109294 |
rs31926229 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11088384 | AACTTAGCTCCTTTT[C/T]CTTTGTGGGAAGATT | 109294 |
rs31926232 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11088490 | TGAAAAATTATGCTT[A/T]TATTGTCTTTGAGTG | 109294 |
rs31926315 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082203 | CTATCTTCCTTATCC[A/G]CCTTTGCTATAGGCC | 109294 |
rs31926318 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Prex2 | GRCm38.p3 | 1:11082264 | AATCAGAAGGTGAGA[A/G]AGGGAGTGTTTAGAA | 109294 |
rs31926320 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082298 | ATGATGTAGCCATAT[A/G]AATAACAATACCAAA | 109294 |
rs31926323 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082325 | CAAAGTCTGTCTGCA[C/T]TCAACTCTCTGTTGC | 109294 |
rs31926356 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | GRCm38.p3 | 1:11096460 | TTTAACTGTGGTTAT[C/G]CCCAAAATAAGGAAT | 109294 |
rs31926359 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11096500 | ACAAGGAAGTAATAA[A/G]CAATCATGCTACTGT | 109294 |
rs31926362 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Prex2 | Mm_Celera | 1:11096665 | TTTCCTAAAACAAAA[A/T]ATGTTTGGAATATAG | 109294 |
rs31926426 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Prex2 | GRCm38.p3 | 1:11090986 | GATAATTCCTTTCCT[A/G]CGGAGCAGTTGTCCT | 109294 |
rs31926429 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11091184 | GTTGTAATTTGGTTC[C/T]GTTCTAGTATGTAGC | 109294 |
rs31926432 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11091258 | AATATTGCTTTTTTG[C/T]ATAGCCATGGATTGC | 109294 |
rs31926454 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11099591 | GAATAATTCCTTCAA[C/G]CAGAAACAACCCAGA | 109294 |
rs31926457 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11099737 | ATTCATCTTCATGCC[A/C]TAGGACTTATTTTTG | 109294 |
rs31926460 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11099763 | TTTTGCATCTGAGTA[C/T]TGCTCTACATATGAG | 109294 |
rs31926463 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11099812 | CTCTGAAGATGAATC[A/G]GAAGAACTAATTGAC | 109294 |
rs31926514 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11114424 | GTAACGTTCTCTGCG[A/C]ACAATGCTCATTCTC | 109294 |
rs31926517 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11114533 | TGGAGTTTTGAATTT[A/G]CAATTAGTGTGTGTG | 109294 |
rs31926519 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11114769 | GTTATTTATTATCTC[A/G]TTGTCTCTTTTACCC | 109294 |
rs31926522 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11114828 | AATGTTAGCACACAA[G/T]CCTTTGTTATATACC | 109294 |
rs31926526 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11118169 | TATTCAAGGCAATGC[A/G]TAAGCTCTTCAGATT | 109294 |
rs31926529 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11118188 | GCTCTTCAGATTGCC[C/T]CAAGGTTATGAAGAT | 109294 |
rs31926532 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11118233 | CCTAACTGATTAACA[C/T]GGCCTTGTTTTGGTG | 109294 |
rs31926644 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11112158 | TCTTAACAAATATTT[C/T]TTTAACTAACCAACA | 109294 |
rs31926646 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11112183 | CCAACATACTTGTAG[A/T]GTTCTGTGTTCTTAT | 109294 |
rs31926649 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11112209 | CTTATTTGATAGAAA[G/T]TATTTGTTACCTGTG | 109294 |
rs31926652 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11112253 | AGAATGGTTTGGTAT[C/T]GGCCATAGCTTCAAT | 109294 |
rs31926704 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Prex2 | GRCm38.p3 | 1:11110078 | AGGCACAGCTGTACA[A/G]AGTTACCTTGTACAC | 109294 |
rs31926707 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11110109 | TGGGGCTATGGCCTT[C/G]CCAGTCTCACTAGGA | 109294 |
rs31926710 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11110195 | TTCTGGTTGATGGTG[A/G]CTTCAGCAATGAGAG | 109294 |
rs31926713 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Prex2 | GRCm38.p3 | 1:11110224 | AGCTTGCTAAATGAA[A/G]GTGTCAATGAATAAA | 109294 |
rs31926754 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11106911 | CCACATTGCTCTGTA[C/T]TGGCTACGGCTGCCT | 109294 |
rs31926757 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11106919 | CTCTGTACTGGCTAC[G/T]GCTGCCTAATGCCTT | 109294 |
rs31926760 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Prex2 | GRCm38.p3 | 1:11106967 | TCCCTTTGGTTGGTG[C/T]TGATGCTGATTCAGG | 109294 |
rs31926785 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11104096 | GAACCATCTTAAGGT[A/G]TTGAACATATTACTG | 109294 |
rs31926788 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11104171 | TTCATGTAATTTTTA[A/G]ATGTTGAAAAATACA | 109294 |
rs31926791 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11104685 | AGAAATTTGAGTGTC[A/C/G]AAAAAAACGTAAGAG | 109294 |
rs31926827 | snp | C/T | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11123743 | AAAGAGTTGATTTAG[C/T]ATTCTGAATCTTCAG | 109294 |
rs31926831 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11132230 | CACTGGCTGGCTGAA[A/G]GCTCACTGGTAGACT | 109294 |
rs31926916 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11108784 | AAGTAGCTTGTCTCT[A/G]TGAGATATCCTGTTT | 109294 |
rs31926919 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Prex2 | Mm_Celera | 1:11109051 | AATACTGTGAGGTAC[C/T]TGGAATCCTAGGAAG | 109294 |
rs31926922 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Prex2 | GRCm38.p3 | 1:11109211 | ATCCACTGATTGTGA[A/G]TGGTCTCAGGATTTC | 109294 |
rs31927055 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Prex2 | Mm_Celera | 1:11097194 | TTATGGAAATATGAG[A/G]CTATGCTTAATGTTT | 109294 |
rs31927058 | snp | C/T | 0.32 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11097299 | AAGAAAGCAGGCACA[C/T]TTAAAGCTGAAATAT | 109294 |
rs31927061 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11097344 | CCAGCTGAAAGTTTG[A/C]ATTCTTTTATTTGTC | 109294 |
rs31927225 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11088500 | TGCTTATATTGTCTT[G/T]GAGTGGTTTTATTTA | 109294 |
rs31927228 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11088565 | TATGAGTAACCATTA[A/G]AATTATATTTGATTT | 109294 |
rs31927231 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11089144 | CACATTACATTTTTC[C/G]CAAGATGAAGCTGAA | 109294 |
rs31927238 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11099975 | CATCTGTCGTGTAGG[A/C]TTGACCGTGTGAAGT | 109294 |
rs31927241 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11099980 | GTCGTGTAGGCTTGA[C/T]CGTGTGAAGTCTGAC | 109294 |
rs31927256 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082412 | AATCACCTCAACATA[C/T]TGTCATTCTGGAAAC | 109294 |
rs31927259 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082760 | ATCAGTGATTAGGTG[G/T]TAGCTCCCATCCTTC | 109294 |
rs31927260 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11082821 | TTTCTCAAAGGATTT[A/G]TTGGCTCTTTCTCAA | 109294 |
rs31927275 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11091300 | AGTAGATCACACAGA[A/G]GATGTATCCATTAGG | 109294 |
rs31927278 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11091311 | CAGAGGATGTATCCA[G/T]TAGGCCAGTTGCTAA | 109294 |
rs31927281 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11091486 | GATATTTAGATGTTG[C/T]GACCTTCCTGTTTCT | 109294 |
rs31927297 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11119066 | GGCTCACCAAATGCT[A/G]TTACTTTTGACAGAA | 109294 |
rs31927300 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Prex2 | Mm_Celera | 1:11119164 | CTTTGTAGCACATGA[C/T]CTATCCTGAGTATGT | 109294 |
rs31927303 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11120354 | TTGATTTCATTCTCA[A/G]ATGCAGATTTGTACA | 109294 |
rs31927495 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Prex2 | Mm_Celera | 1:11114895 | CTCAGTAAACACATG[A/C]TAACTGAGTAAGAAA | 109294 |
rs31927497 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11114954 | TTGATTCATTAATAG[G/T]AAAACATCTAATAAA | 109294 |
rs31927500 | snp | G/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11115038 | TAATAGTAAAACATC[G/T]AAAGCATCATATCAT | 109294 |
rs31927503 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11115058 | CATCATATCATACAC[A/G]TGTATTTAGCACTGT | 109294 |
rs31927515 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11112291 | GCTGTGTGCAAGTAA[C/T]GAAAACGATTCTGAA | 109294 |
rs31927518 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11112325 | CATTCATCAGTTTGT[A/G]TAAATATTCAAGTGT | 109294 |
rs31927521 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11112337 | TGTGTAAATATTCAA[C/G]TGTTAGATCTTTGTA | 109294 |
rs31927536 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon | Prex2 | GRCm38.p3 | 1:11110325 | CTGGGTAATGATCTC[C/T]GAGCAGGGTGAGAAA | 109294 |
rs31927538 | snp | A/C/T | 0.46875 | 0.121031 | intron-variant | Prex2 | GRCm38.p3 | 1:11110438 | GAAGGTAAGCTTGGT[A/C/T]TCTTGGGTGTATCAT | 109294 |
rs31927541 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11110456 | TTGGGTGTATCATCT[A/G]TCTTATATGGTTTGT | 109294 |
rs31927605 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11107018 | TTGGAACCTTTGCTT[A/G]CTGAGCATGACTGAG | 109294 |
rs31927608 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11107040 | ATGACTGAGTAGTAG[A/G]GACAGATTCTGTTAT | 109294 |
rs31927611 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11107157 | TTACTTTTGCACACC[A/T]TTCTTTTCTGCTGAC | 109294 |
rs31927664 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11104763 | AAGTCCTGTCCTGTG[A/T]TGTGTTGGATGCTAG | 109294 |
rs31927667 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11104892 | CTTTTAGAACTGATA[C/T]ATTCACTGTTGATCA | 109294 |
rs31927670 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11104935 | CTGAATGCACTATGG[A/G]GATATCATTAATATT | 109294 |
rs31927673 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11104983 | ATTTTGGTGGTTTCT[G/T]CTTTTGTAGCATGAG | 109294 |
rs31927705 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Prex2 | Mm_Celera | 1:11109213 | CCACTGATTGTGAGT[A/G]GTCTCAGGATTTCAT | 109294 |
rs31927708 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11109247 | TGAATCTGGCTCCTG[C/T]TCCCTATGTTCTTTG | 109294 |
rs31927711 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Prex2 | GRCm38.p3 | 1:11109263 | TCCCTATGTTCTTTG[A/C]TTGGCTTATCTGTTC | 109294 |
rs31927834 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11097439 | GTGCTAGCAGGAAGT[A/G]AGCCAGACACTGTAG | 109294 |
rs31927837 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11097475 | CAGTGGAGGTGTTGA[A/G]AGCGGTGTGTTCAGC | 109294 |
rs31927840 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | GRCm38.p3 | 1:11098194 | TGTCTCTGGGTAAAC[A/C/G]TAGATTCTCTATGCA | 109294 |
rs31927843 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11098206 | AACGTAGATTCTCTA[A/T]GCAGACTGGGACGGA | 109294 |
rs31927974 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Prex2 | Mm_Celera | 1:11132244 | AGGCTCACTGGTAGA[C/T]TTTCCTCTGCACACT | 109294 |
rs31927977 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon | Prex2 | Mm_Celera | 1:11132377 | TTACAAATCTGTTGT[A/C]ATGGCCAACAAATTG | 109294 |
rs31927980 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Prex2 | Mm_Celera | 1:11132407 | GATAGACTGGTTAAT[C/T]GCACAGGTAAGAAGA | 109294 |
rs31927983 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11132441 | ATAGATGTTGCCCCG[A/C]TTCCTTCTTTCTCAT | 109294 |
rs31928074 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11089191 | CCCAAATCTTAAGAC[A/G]GACATACAACACCAG | 109294 |
rs31928076 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11089417 | TTTGAACAGAAATCA[A/G]ATTTATAAAAGCTAG | 109294 |
rs31928094 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Prex2 | GRCm38.p3 | 1:11100909 | CCTCCTTCCAGCCTG[C/T]GCCACAACCCACCAG | 109294 |
rs31928097 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11100992 | CTAAGCAGTTTGAGA[C/G]ATTTTTCCCAATGAA | 109294 |
rs31928100 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Prex2 | Mm_Celera | 1:11101049 | ACAAAGGCTTTGTGG[G/T]TTTTTTTTTTTAAGA | 109294 |
rs31928103 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Prex2 | Mm_Celera | 1:11101076 | AAGACGGCTGAAGAA[C/T]AGTAAGGCATCCACA | 109294 |
rs31928104 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Prex2 | Mm_Celera | 1:11091496 | TGTTGTGACCTTCCT[A/G]TTTCTCTCTTATATT | 109294 |
rs31928107 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11091951 | ACATACTATCTCACC[A/C]GAGATCAAAGCAATG | 109294 |
rs31928110 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Prex2 | GRCm38.p3 | 1:11092189 | AGGGCTCAACTGTGT[A/C]ACACAGGGCAGTTGA | 109294 |
rs31928113 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11092228 | ATACCCTCTGTTCTT[A/G]AGAAGATTTAGAAGA | 109294 |
rs31928186 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Prex2 | Mm_Celera | 1:11120375 | GATTTGTACATTTAC[C/T]AAAGCAAGTTATTCA | 109294 |
rs31928189 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Prex2 | Mm_Celera | 1:11120405 | ATTTTTTTAAAAAAG[A/G]GATTTATGTGCATAG | 109294 |
rs31928192 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11120462 | TTCATTTCTTTTCCT[A/G]TTGGAGTCTCATGAG | 109294 |
rs31928314 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Prex2 | Mm_Celera | 1:11112400 | ATTTGTATTTATTGA[A/G]TATTTATCTCAGTGA | 109294 |
rs31928317 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Prex2 | Mm_Celera | 1:11112455 | GGGAGAGTGTCATCT[C/T]TTAACTAAATCTTCT | 109294 |
rs31928320 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11112523 | CAGTTATTTAGTGGG[C/T]ACAGCATCAGAGAGC | 109294 |
rs31928322 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | GRCm38.p3 | 1:11112588 | TCTCTGGTTATGAGC[C/T]CTACGCATGTGAAAA | 109294 |
rs31928364 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Prex2 | GRCm38.p3 | 1:11110520 | CCTGTCTCTTAATAC[A/T]TGTTTTCTGGGTGGT | 109294 |
rs31928367 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11110555 | ATATGAGGTAATGGA[C/T]AAAGATGCAGTCATG | 109294 |
rs31928369 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Prex2 | GRCm38.p3 | 1:11110620 | TCTCCATAATTGCTG[A/G]CATGCCTGTTGTCAT | 109294 |
rs31928371 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11110717 | GATAGGTGTGATATG[A/G]ACATGTTCTGGATCT | 109294 |
rs31928406 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11115487 | TAGTCTTTCACATTT[C/T]CTAACTCAAGTTCAT | 109294 |
rs31928409 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11115721 | AAGTAGGTGGCACAA[A/C]ATTGTGGTCAACCAG | 109294 |
rs31928412 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11115768 | TCATTTAGACTTCTA[C/T]ATCCAGAGACACTTC | 109294 |
rs31928426 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11105033 | GTCTATCTTACTAAA[A/C]TACAATATGGTGTAA | 109294 |
rs31928429 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11105057 | GGTGTAAATGGCTAC[A/C]AGTGTCTCCACTGAG | 109294 |
rs31928432 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11105104 | TTAGGAAGAACTCCA[C/T]TCCTGTCAGTGGAAG | 109294 |
rs31928434 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11107234 | AGTAAGATTGTCTTT[C/T]TTCTGAAATCTAGAG | 109294 |
rs31928437 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Prex2 | Mm_Celera | 1:11107472 | AGTATATCTACCATG[C/T]AAATATTTCCTTAAT | 109294 |
rs31928440 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11107515 | TGTATATGAGTTATC[A/G]TGAGTGCATCATGAA | 109294 |
rs31928443 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11107560 | TCAATTGATGTAATA[C/T]GTATTGCTCTGCAGT | 109294 |
rs31928514 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11109280 | TGGCTTATCTGTTCT[C/T]ATTAGAGTGACTTCT | 109294 |
rs31928516 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Prex2 | GRCm38.p3 | 1:11109311 | GTTCTGACACTTGTG[A/T]ACTTCTTTGTGGCCA | 109294 |
rs31928519 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11109340 | CAGCCTCTCTTCTTT[C/T]TTGGGCTTTGTACTA | 109294 |
rs31928522 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Prex2 | GRCm38.p3 | 1:11109378 | ATGCTGACCTCTGGA[C/T]CACTTGACATTGTCA | 109294 |
rs31928686 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11132466 | TCTCATGTAAGTGTG[A/G]GATGTGAACTTGCTG | 109294 |
rs31928689 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11132639 | AACATGAGCTGAGTT[A/T]CATCAAACAAACAAA | 109294 |
rs31928692 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11132716 | TATCAGTGAAGAATA[A/G]CTATGTTCAGTCACT | 109294 |
rs31928746 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Prex2 | Mm_Celera | 1:11098218 | CTATGCAGACTGGGA[A/C]GGAGACAGCATTCAG | 109294 |
rs31928748 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Prex2 | Mm_Celera | 1:11098243 | ATTCAGTGTAACCAC[C/T]TTGACTGTGTACATG | 109294 |
rs31928750 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Prex2 | Mm_Celera | 1:11098325 | TAATTGCATACAAAA[A/T]GTCAGGCAGGACTTG | 109294 |
rs31928752 | snp | A/G | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11098421 | TATAAAGATAATAAT[A/G]TTAGGCAATCAGACA | 109294 |
rs31928826 | snp | C/T | 0.124444 | 0.216185 | missense | Prex2 | Mm_Celera | 1:11101098 | GCATCCACAGATGGG[C/T]ATCGGTATGTCTTTC | 109294 |
rs31928828 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11101196 | TGATGGAATAATTTG[C/T]CTTCAATGTATCAGA | 109294 |
rs31928831 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11101231 | AGCGGTGGCTTGCTA[A/G]GTATAACAGGGGTGT | 109294 |
rs31928846 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Prex2 | GRCm38.p3 | 1:11092310 | AGCTTAGATGAGCCA[A/G]CTACTAGATAACTCA | 109294 |
rs31928849 | snp | A/G | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11092474 | CCTGAGAGAGAACAG[A/G]AATGGGTTAAAGAGT | 109294 |
rs31928852 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11092574 | TTGATGTAGATGGTA[C/T]AATGATATTCACAGA | 109294 |
rs31928954 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11112643 | AAAATGATGCTTTGT[A/G]TATTTAAGATTCCTT | 109294 |
rs31928956 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11112661 | TTTAAGATTCCTTTC[A/G]TAGCTTTTTTATGAT | 109294 |
rs31928958 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11112675 | CGTAGCTTTTTTATG[A/G]TGTGTGGACCAGACA | 109294 |
rs31928960 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11112677 | TAGCTTTTTTATGAT[A/G]TGTGGACCAGACACA | 109294 |
rs31928963 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Prex2 | GRCm38.p3 | 1:11112788 | AGAGATTCACAGGCC[C/T]GAAGAAGGTGTTCAC | 109294 |
rs31928994 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11134990 | TCACCTCATCCTACA[A/G]TAGCTATTTGTGGCT | 109294 |
rs31928997 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11135055 | TACTGGTCAATGTGT[A/T]CGGTTAAGGCAGACT | 109294 |
rs31929000 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11135091 | GCTCTTAATACTGAG[C/T]TTCAAGATCATGGGT | 109294 |
rs31929002 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11135173 | ACAAAATAGGGCTCG[C/T]TTTCCACCTAGACTT | 109294 |
rs31929056 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11107599 | TTCACTTGTTACTTT[C/T]CAGCTGATTTTCACA | 109294 |
rs31929059 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Prex2 | Mm_Celera | 1:11107688 | GTTTGTATGCATGGC[G/T]AAAAGCCCTGAAGAA | 109294 |
rs31929062 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Prex2 | Mm_Celera | 1:11107712 | TGAAGAAAAGCATGA[A/G]TGGTTTGAAGCTATT | 109294 |
rs31929105 | snp | A/C/T | 0.426035 | 0.177515 | intron-variant | Prex2 | GRCm38.p3 | 1:11120571 | AAAAAATGGTGTTTC[A/C/T]TGTAACGAAGGGGAG | 109294 |
rs31929108 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11120708 | GCATTCCTAAACATG[C/G]TCGTGTAATCAAGGT | 109294 |
rs31929111 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11120752 | ACATCACACGGTTTT[A/T]AATGGCCGATGAGGA | 109294 |
rs31929195 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11105142 | AATCAATGTAAGGAA[C/T]TCTCAGATCACATGG | 109294 |
rs31929198 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11105197 | TGGGTTTGACCTTCA[A/G]ATATTTCTGATTTTA | 109294 |
rs31929200 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11105297 | CTCTCCTTTGCACAT[C/G]TATAAAATTCATCTT | 109294 |
rs31929202 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11105432 | TCTCAGTAATAGGAT[A/G]ACTGCTGAGCTCTGG | 109294 |
rs31929204 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11110757 | AGTTGGGCATGAGTC[C/T]ACAGAGTGAAGGGAT | 109294 |
rs31929206 | snp | A/C/G | 0.497041 | 0.0383476 | intron-variant | Prex2 | GRCm38.p3 | 1:11110779 | TGAAGGGATATTAGA[A/C/G]CTGAGAGAAAACAAT | 109294 |
rs31929208 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11110807 | AATTTAAATAAAGGA[G/T]TGTATGTAGATTAAG | 109294 |
rs31929211 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11110838 | AGTCCAGTAGATTAT[C/T]TTCCAAGGGGCCTAG | 109294 |
rs31929315 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11141940 | CCTTGTCATCTTTCC[A/G]AGTGTTGCATTAGGT | 109294 |
rs31929317 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11141984 | GTTGGACTGTACTTG[C/G]TTAGATCCCTTGACA | 109294 |
rs31929319 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Prex2 | Mm_Celera | 1:11142290 | CTTTCTATCTATCAA[C/T]CTATCTACCTCAGTT | 109294 |
rs31929322 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11142376 | CAATAACAAGAGAGA[A/G]CCAAAGATGCATACA | 109294 |
rs31929345 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Prex2 | GRCm38.p3 | 1:11116181 | TAATTAAGACAATTA[A/C]CTACTAAACAAAAAG | 109294 |
rs31929348 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Prex2 | GRCm38.p3 | 1:11116225 | TGCAATCAGGCCACT[A/G]TTGTACTAGTAGCCA | 109294 |
rs31929350 | snp | A/C | 0.32 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11116231 | CAGGCCACTGTTGTA[A/C]TAGTAGCCATATCTT | 109294 |
rs31929353 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11116287 | GTATTGTTCACATCA[A/G]GGTGATATTGCTGAA | 109294 |
rs31929475 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Prex2 | Mm_Celera | 1:11132795 | ATTAGTCCTCACAAA[C/T]AATTCAACTCTTCCA | 109294 |
rs31929478 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Prex2 | Mm_Celera | 1:11132814 | TCAACTCTTCCATGT[C/T]ATTTTGTTTTATACC | 109294 |
rs31929481 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Prex2 | Mm_Celera | 1:11132822 | TCCATGTCATTTTGT[C/T]TTATACCAGCCTGGC | 109294 |
rs31929515 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11092618 | TGAAGTGTTTTTTGT[A/G]GTTAGGAAATTGGGG | 109294 |
rs31929518 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11092711 | ATAAGCATTCTTGCA[C/T]CAGTCACTAAAATGA | 109294 |
rs31929521 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Prex2 | GRCm38.p3 | 1:11092726 | TCAGTCACTAAAATG[A/C]TGTTGAATAGCACCA | 109294 |
rs31929564 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11109404 | TGTCAGGACTTCTTT[C/G]TCCTCCACAGTTTGC | 109294 |
rs31929567 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Prex2 | GRCm38.p3 | 1:11109433 | GCCTGGAAAGCAACT[C/T]CACTTCCCCTTTTCT | 109294 |
rs31929570 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11109442 | GCAACTCCACTTCCC[C/T]TTTTCTCTTGCAACC | 109294 |
rs31929573 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Prex2 | Mm_Celera | 1:11109537 | TATCACCTCCTGCTT[A/C]TTTCTCAGCATCTTC | 109294 |
rs31929586 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11113024 | ATTCTATAAAATGTT[C/T]AGCATCTGCACAGGC | 109294 |
rs31929588 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11113122 | CAAGGGGGCAGTGGC[A/G]TTGGAGATGGACATC | 109294 |
rs31929593 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11113219 | TCAGCTATAGTAGTA[A/G]GAATTTCATGGTAGC | 109294 |
rs31929654 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11101278 | TGAGATGCAGACCTG[C/T]AGGACCCTTGTTTAA | 109294 |
rs31929657 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11101435 | ATACATGTGCAGAAA[A/G]TGTCTAATGAGTGAG | 109294 |
rs31929660 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11101576 | GGCTTGACTTGCAGA[A/G]GGAAACTGTGGAGAT | 109294 |
rs31929662 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11101589 | GAGGGAAACTGTGGA[A/G]ATGATCTTTGTGCTT | 109294 |
rs31929783 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11162623 | TTCTTTTTCACATAT[C/T]TTATGGTCTCCAGTG | 109294 |
rs31929784 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Prex2 | GRCm38.p3 | 1:11120779 | AGGAATATCCCACAG[C/T]AAAGAATTTAACATC | 109294 |
rs31929787 | snp | A/C/G | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11120870 | GCTTTGACAGAGGAG[A/C/G]ACTAAAGTTTATCTC | 109294 |
rs31929790 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11121069 | TGGCCTCTGTCAAGT[A/G]TGCATGTCCAGGTAG | 109294 |
rs31929793 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11121636 | AAAGTCTTACAAACA[C/T]GATGTTCTGATGAGG | 109294 |
rs31929805 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Prex2 | Mm_Celera | 1:11107739 | TATTTTGAAAGAAAG[A/G]GAACGTCGGAAAGGT | 109294 |
rs31929808 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11107775 | CATAAAGTAGGAGCT[A/G]TTGTGCTTTGTGAAC | 109294 |
rs31929810 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11107817 | GTATGAGTGCAGAGA[A/G]TGGGAAAAATTTATG | 109294 |
rs31929813 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11107830 | GAATGGGAAAAATTT[A/T]TGAGAACGTGTTGAG | 109294 |
rs31929816 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11136693 | GGAGATGTTCCTTAA[A/C]CTATAATTCAGGTGC | 109294 |
rs31929819 | snp | C/T | 0.32 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11136738 | TTGCCTGTCACCATG[C/T]GCAGTGATTTATTTT | 109294 |
rs31929822 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11136753 | TGCAGTGATTTATTT[C/T]TTGGTTAACAGGGTG | 109294 |
rs31929955 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon | Prex2 | Mm_Celera | 1:11098477 | GGGGTCCAACATTAC[C/T]GACACCTGTACTGAG | 109294 |
rs31929965 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Prex2 | Mm_Celera | 1:11135213 | TTAATCTGCATACTA[A/C]TCAGTACTGACTGGA | 109294 |
rs31929968 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11135238 | ACTGGATTTGGACAG[C/G]ATGATTGGGCAGTTG | 109294 |
rs31929971 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Prex2 | Mm_Celera | 1:11135280 | GCTACAGTGCAGCAG[G/T]CCATAGGCTGTTGTG | 109294 |
rs31929973 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11135291 | GCAGGCCATAGGCTG[A/T]TGTGAGATATCTCTG | 109294 |
rs31930085 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11105569 | TTATGAATAAGTTTT[C/T]TAATGGGATTATTTT | 109294 |
rs31930088 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11105588 | TGGGATTATTTTGAA[A/C]AATGTGCTGTCGTTA | 109294 |
rs31930091 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Prex2 | Mm_Celera | 1:11105630 | ACAGAGTGTTGCATT[A/T]TAAAGTAAATCAGGA | 109294 |
rs31930126 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Prex2 | Mm_Celera | 1:11116721 | CCAGTTTGTAGGCAC[C/T]GCCTGGATCAGTAGC | 109294 |
rs31930129 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11116753 | CAGTCTCTTTTAAAA[A/G]CGCTTTCATACTAAT | 109294 |
rs31930132 | snp | C/G | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11116817 | TTGGCAGTTAGATGG[C/G]ATCTTTTGGAAATCT | 109294 |
rs31930154 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11110879 | TGTATGTCATCTGGG[C/T]GCATGAGATTCCCTG | 109294 |
rs31930157 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Prex2 | GRCm38.p3 | 1:11110922 | AGCTACTTCAGCTGG[A/G]TCTTCATAGGCCAGG | 109294 |
rs31930159 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11110943 | ATAGGCCAGGCTCTG[A/G]TGTCTTTCTGTATGT | 109294 |
rs31930161 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Prex2 | GRCm38.p3 | 1:11111077 | TGGATGCTGAAGTCC[A/G]TCTACAAAAGTTACC | 109294 |
rs31930163 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Prex2 | GRCm38.p3 | 1:11111094 | CTACAAAAGTTACCT[A/G]GAGTCATGTCAAAGA | 109294 |
rs31930284 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11092743 | GTTGAATAGCACCAA[A/T]GTCTTTTAAGTGATG | 109294 |
rs31930287 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11092775 | ATATGCACTAATTCT[A/C]ATTTGGGGTGAAAAT | 109294 |
rs31930290 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Prex2 | GRCm38.p3 | 1:11092801 | AAAATTCTTCTCATT[C/T]AATTATCCAGGGTCC | 109294 |
rs31930395 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11101953 | CATTCTAAATTACAA[G/T]AATCCCTTATCAGTA | 109294 |
rs31930410 | snp | A/T | 0.375 | 0.216506 | utr-variant-3-prime | Prex2 | GRCm38.p3 | 1:11298541 | ATATGAAGTCTTACT[A/T]TGAAATGTCAGACTG | 109294 |
rs31930414 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11132846 | GCCTGGCATGTATAA[C/T]ATAAGCTTTAATGTC | 109294 |
rs31930417 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Prex2 | Mm_Celera | 1:11132875 | TCTGTGAAGTGCAGA[C/G]AGTATATTCATTGTT | 109294 |
rs31930420 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11133071 | ATAGGTCAACTAATA[A/G]GTGCTTGGATATATT | 109294 |
rs31930423 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11133092 | TGGATATATTCTGTT[A/G]ACTAAACTCAAGACA | 109294 |
rs31930466 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Prex2 | GRCm38.p3 | 1:11109541 | ACCTCCTGCTTATTT[C/T]TCAGCATCTTCCTCA | 109294 |
rs31930469 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11109568 | CTCATTTTGTAATTC[A/G]TCTTGTTTACAAAGG | 109294 |
rs31930472 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Prex2 | GRCm38.p3 | 1:11109581 | TCATCTTGTTTACAA[A/G]GGCTTTGGCTTGCTT | 109294 |
rs31930536 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11121790 | CTACTTTTAACCCAT[C/T]GATTGGTGAGACTAG | 109294 |
rs31930539 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Prex2 | Mm_Celera | 1:11121875 | TTGGTCCCACACAGA[A/G]GTATGCAAGAAATTG | 109294 |
rs31930542 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Prex2 | Mm_Celera | 1:11122310 | AGAAATAAGTAACAT[G/T]TAAAAAATAGCGCTA | 109294 |
rs31930544 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11142377 | AATAACAAGAGAGAA[A/C]CAAAGATGCATACAG | 109294 |
rs31930546 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11142495 | GTATTATTATAATTG[C/T]TAACCCTCGTCATAG | 109294 |
rs31930549 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11142531 | TTGTATAAGGCTGCT[A/G]TAGATGTGTTTTCAT | 109294 |
rs31930552 | snp | A/G | 0.18 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11142557 | TTCATGTCCAAATGT[A/G]GACATGCTGAGCCTC | 109294 |
rs31930659 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11113504 | CCGCCAGAGGTCTGA[A/G]CTTGACCTAGAAGTA | 109294 |
rs31930705 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Prex2 | Mm_Celera | 1:11136924 | TCTCAGTGATCCACT[A/G]AGGTCAAGACAACCT | 109294 |
rs31930708 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11136951 | ACCTATCTGGGTCTC[A/G]CCATGGGTCCCAGAT | 109294 |
rs31930711 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11137021 | TTTTTGTAGCACATT[A/G]TCTACCAGTTTTTCT | 109294 |
rs31930712 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11137075 | TTGTGTTGACTCCAA[A/G]AGAGCCAGAACATGA | 109294 |
rs31930726 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11107838 | AAAATTTATGAGAAC[A/G]TGTTGAGGCATGATG | 109294 |
rs31930729 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Prex2 | Mm_Celera | 1:11107933 | CTCTCTTCCTTCCCT[A/C]GTGGCTAGGCTCAGA | 109294 |
rs31930732 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11107963 | AGATCAGCCACCGCA[A/G]GTCTCACTCAACTCC | 109294 |
rs31930755 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11135414 | GATGCTTTTATTCCA[A/G]TGGCTTATAACCAAA | 109294 |
rs31930758 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Prex2 | Mm_Celera | 1:11135440 | CCAAATACCTTATTC[C/T]TCACTGGATAAGTAT | 109294 |
rs31930761 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11135493 | ATGTGATTTGCTTAT[A/G]TGTGATGTGCAGGAA | 109294 |
rs31930804 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11105828 | ATTACCATTATTCTT[C/T]CATTTGAAATCATAT | 109294 |
rs31930807 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11106058 | TACACACTAATTTAT[G/T]TCAATTCCTATGATA | 109294 |
rs31931014 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11116882 | GAGCTCACGTTTTTG[C/G]CTTTGCCAGGAGATA | 109294 |
rs31931019 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Prex2 | GRCm38.p3 | 1:11117017 | ACTTAAATTAGGAGA[A/G]TTAAAAACTGTTTTG | 109294 |
rs31931022 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Prex2 | GRCm38.p3 | 1:11117049 | ATATTTATAGCCTTG[C/T]TAATTCTTCTTACTG | 109294 |
rs31931195 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Prex2 | Mm_Celera | 1:11109582 | CATCTTGTTTACAAA[A/G]GCTTTGGCTTGCTTG | 109294 |
rs31931198 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11109616 | TTTCTCAGCTTTCCT[C/T]CAAATGGTTTCCTCT | 109294 |
rs31931201 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Prex2 | GRCm38.p3 | 1:11109660 | TTCTTTAATTTACTC[C/T]ATACCTGGTCCTCTA | 109294 |
rs31931203 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Prex2 | GRCm38.p3 | 1:11109684 | TCCTCTAAGCTACAT[A/C]TAAAGTGATAGAACC | 109294 |
rs31931226 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11111121 | AAGATCAGTCTGTAA[C/T]CATCCATCTTTGTTC | 109294 |
rs31931228 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11111243 | CAGGATATCCTTTAA[C/G]TAGCTACCAGAAAAT | 109294 |
rs31931231 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11111262 | CTACCAGAAAATAGC[A/T]CATGGCCACCTCTGA | 109294 |
rs31931233 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11111291 | GAACTGTAGGCCAGG[A/G]AACCTCAGACTGAAG | 109294 |
rs31931286 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | GRCm38.p3 | 1:11133197 | TATTTGAGTCAATTT[C/T]ATAAGCAGCCTTACT | 109294 |
rs31931289 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Prex2 | GRCm38.p3 | 1:11133209 | TTTCATAAGCAGCCT[C/T]ACTATTTTGTTTGTA | 109294 |
rs31931292 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Prex2 | Mm_Celera | 1:11133382 | TCAAATGTCATCCAG[C/T]CTTTTCTTACCTGTC | 109294 |
rs31931405 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11122440 | TGGTGTATGTGTGGT[A/C]TTGGCACCATCAGTA | 109294 |
rs31931407 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Prex2 | Mm_Celera | 1:11122471 | TATGGTAAAATAGTT[A/T]CAAGCAAATATGCAC | 109294 |
rs31931410 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Prex2 | Mm_Celera | 1:11122596 | TTTAAATTAAAATGT[A/C]TTCTATTTTGTGAGG | 109294 |
rs31931413 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11122784 | GGGTGTTTGTTCTTT[C/G]ATGTTCAGTTCAGTC | 109294 |
rs31931434 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11135513 | ATGTGCAGGAAACAT[A/T]TATATTTTTTTAACT | 109294 |
rs31931436 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Prex2 | Mm_Celera | 1:11135696 | ATTAGTCCAGTAAAT[A/G]AAACATTTAAATAAT | 109294 |
rs31931439 | snp | A/C | 0.32 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11135734 | ACCAAAGCTTTCAGC[A/C]TAACCCTTTAAATAG | 109294 |
rs31931442 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11135786 | ACACATGCAGGCAAG[G/T]TCCTACCTTTCAGAA | 109294 |
rs31931475 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11142581 | GAGCCTCCTCTGATT[C/T]AGTTTTGTGAAAATA | 109294 |
rs31931478 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Prex2 | Mm_Celera | 1:11142726 | ACCTTTTCCTGAAGT[C/T]GATTGCTTCCTGAAA | 109294 |
rs31931481 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Prex2 | Mm_Celera | 1:11142795 | GAGCACAAAGCCAAG[A/G]GAGTAAGTGACATAG | 109294 |
rs31931525 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Prex2 | GRCm38.p3 | 1:11107989 | ACTCCGCCAAAGACC[A/G]GTTGGCCATTTTCCT | 109294 |
rs31931636 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11113887 | TCCTAATAGGCAGTG[A/G]TGCACAAAGAAAGCA | 109294 |
rs31931639 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11113961 | GCCTGGTATCATCCT[C/T]TACCTTGTTGGGCAT | 109294 |
rs31931642 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Prex2 | GRCm38.p3 | 1:11114018 | CCCTCCGAGAATTGG[C/T]ACTTCTGCAATCTCT | 109294 |
rs31931724 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11137196 | ATAGGGGGATGCATA[A/G]ATAAGAGCATGTATG | 109294 |
rs31931727 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11137239 | TGTTCATTTTAGGAC[A/G]TCATACTCAAAATCG | 109294 |
rs31931728 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11137331 | GATGCCTTCAAATAT[C/T]ATTACACATTAGTGG | 109294 |
rs31931731 | snp | A/C | 0.32 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11137571 | TTTTAATTTTAATTT[A/C]TCCATTTATCAAAGT | 109294 |
rs31931732 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11137676 | CGTGCTTCTCAACAT[C/G]TGGCTGATATAGCAC | 109294 |
rs31931754 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11147537 | TAATCATTCGATGTT[C/T]AAATGAAATGGACAC | 109294 |
rs31931759 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11147817 | CAGGGTCTTCTGTGA[A/G]CTGCCTCCAATAGAT | 109294 |
rs31931762 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11147895 | TTTGCTTTATAACTA[A/T]CTCATCCTTTTCTGA | 109294 |
rs31931897 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Prex2 | GRCm38.p3 | 1:11117257 | GTGAGAAATCTTATT[A/T]TGCAATTTTATATTA | 109294 |
rs31931902 | snp | C/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11117314 | GATAGGAACTAGATT[C/T]TATGGGTATTGAGTC | 109294 |
rs31931946 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11109712 | ACCTTCTTTCCCATC[A/T]TACTCAACTTTTTCA | 109294 |
rs31931948 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Prex2 | GRCm38.p3 | 1:11109755 | AATATGTTGCTATTT[C/T]CCCAGTACCCAAGGA | 109294 |
rs31931965 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11133392 | TCCAGTCTTTTCTTA[C/G]CTGTCCTTGGTTTAA | 109294 |
rs31931968 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11133423 | AGACACAGTCATTGA[C/T]AACTTCTAAGTTCTT | 109294 |
rs31931971 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11133867 | CTTCAATTTACTTGA[G/T]GGACTCTTCTTCAAT | 109294 |
rs31932076 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11152520 | GTACATTTCCATAGG[C/T]ACACAGTTATGCACC | 109294 |
rs31932079 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11153253 | AAAGTTAGATTGACT[A/C]GACATAAGAAAGGGA | 109294 |
rs31932082 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11153382 | ATCACTGGTAAAGAA[C/T]TGGTAGGAGTGAGGG | 109294 |
rs31932085 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Prex2 | Mm_Celera | 1:11164195 | GCTCATAGATAGGCC[A/T]CTGCAAAGAATTAGT | 109294 |
rs31932088 | snp | A/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11164317 | CAATTTTTTTTTCTA[A/T]GATAGGCCAGGAAGG | 109294 |
rs31932091 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Prex2 | Mm_Celera | 1:11164412 | ATTCCTGTCCTCTCA[A/C]ACTTAGCACCTAATT | 109294 |
rs31932236 | snp | G/T | 0.375 | 0.216506 | intron-variant | Prex2 | GRCm38.p3 | 1:11111319 | AAGGCCAGTCTGAGG[G/T]AGTGGTACTCATAGT | 109294 |
rs31932239 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11111423 | CTAGTACAAAGGAAA[A/G]CAGATCTAGTTCCAC | 109294 |
rs31932241 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11111539 | AGATAAGTCTACTTG[C/T]TGGTAAGTCACTGAA | 109294 |
rs31932243 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11111651 | ACTTACTCTGGCCTC[A/T]CTCCCACATTAAAAC | 109294 |
rs31932265 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11135821 | GTACTCATTTGGGCT[C/T]ATTTTTAATCTTTTG | 109294 |
rs31932268 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11135869 | ATCTTCCACAGAAGT[A/C]CTCATGGATCCTCCA | 109294 |
rs31932271 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11135916 | TCTCTGTACACCAGA[A/G]TCAGGCTGACTAAGA | 109294 |
rs31932273 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11135932 | TCAGGCTGACTAAGA[A/T]TCTTAACTGAATTGG | 109294 |
rs31932296 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Prex2 | Mm_Celera | 1:11122828 | AAGAAATAGGAAGCA[A/T]GAGTCTGCATTTCCT | 109294 |
rs31932299 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11122857 | CTGTCAGTACATAGT[C/G]TATGGCATACATACT | 109294 |
rs31932301 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11122937 | TAACCTCAATCAATT[C/T]TTCAGATCATATGGG | 109294 |
rs31932303 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11122972 | TTCCTTGTTGTAAAG[A/T]ACAAAACCTTACAAA | 109294 |
rs31932304 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11142811 | GAGTAAGTGACATAG[C/T]GGAAGGAACAGGGAT | 109294 |
rs31932307 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11142919 | GCATGGTAGGAGCAG[A/G]TCTATGAGTGAGAGA | 109294 |
rs31932310 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11142973 | AAGGTGCTCACTCCT[C/G]AATTAAATGGTGTTT | 109294 |
rs31932313 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11143298 | AGTAAAGACTAATTT[A/C]GTGGAACACCTTTAA | 109294 |
rs31932415 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11114085 | CCTATGTAACAGATA[A/G]AAGCTGACGGCACTC | 109294 |
rs31932418 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11114131 | TATTCCTGGCTTCTT[A/T]TCAGCTCAAGTCCAG | 109294 |
rs31932421 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Prex2 | GRCm38.p3 | 1:11114207 | TACAGTGCAGTACTT[A/G]ATTTGGGCTCTCAGG | 109294 |
rs31932665 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11148173 | CAAATTCATTTGGTG[C/T]GAGTTCTTTGGCAAT | 109294 |
rs31932668 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Prex2 | Mm_Celera | 1:11148290 | AGGATACGATGTAGT[A/G]TTAGACAGCTCTGTC | 109294 |
rs31932671 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11148358 | TGCAAGAGTAGAAGT[A/G]TATTTCCTGTATGTG | 109294 |
rs31932673 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11148369 | AAGTATATTTCCTGT[A/T]TGTGATAGTAAGCCA | 109294 |
rs31932744 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Prex2 | Mm_Celera | 1:11169954 | CCCAACCAACTGCCA[C/T]GTCAATGTGATGGAA | 109294 |
rs31932746 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11170158 | TAGATTCCCAGTGTG[C/G]AAGGAAACCAATGTT | 109294 |
rs31932750 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Prex2 | Mm_Celera | 1:11170196 | GGAAAGGATTTCGGG[A/C]TATACTTGCTTAGAT | 109294 |
rs31932751 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11170269 | TTCCCTTGAAGAAGG[C/G]CAATTGCTTTTGCTT | 109294 |
rs31932754 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Prex2 | Mm_Celera | 1:11175953 | TGTGCTCACTGGAAA[A/G]GCAACAAGAAATACA | 109294 |
rs31932757 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Prex2 | Mm_Celera | 1:11175984 | CAATAGCTAGAGAAG[C/T]GAATTTGGTCTTCTC | 109294 |
rs31932760 | snp | C/T | 0.5 | 0 | intron-variant | Prex2 | Mm_Celera | 1:11176019 | AACACCATGTAATTT[C/T]ATTCTAAATATAAAC | 109294 |
rs31932763 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Prex2 | Mm_Celera | 1:11176036 | TTCTAAATATAAACA[C/T]TTTCCACATAATTTG | 109294 |
rs31932785 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11137739 | TATCAACAACTGAGT[A/C]AAAAGGGAGCACCAG | 109294 |
rs31932787 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11137832 | CACCAGGAGTGTTAA[A/G]TTAAAGAAATATTGG | 109294 |
rs31932789 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11138006 | TTTCCAAAGTACTAA[A/G]TGACAGCAAAAGTTC | 109294 |
rs31932792 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Prex2 | Mm_Celera | 1:11138097 | TGTTGTGATCTTCCA[A/G]AAAACAGATAGATCA | 109294 |
rs31932805 | snp | A/T | 0.375 | 0.216506 | intron-variant | Prex2 | Mm_Celera | 1:11117368 | AAAAACAGAATTTCT[A/T]AAAATAGAATTGAAT | 109294 |
rs31932808 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | GRCm38.p3 | 1:11117560 | TCCTATGAACTCGTA[A/G]GTAGGGATAAAATAG | 109294 |
rs31932811 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Prex2 | Mm_Celera | 1:11117703 | TTTGTATAAGCTTCT[A/G]AGTGCTGGTAATCAA | 109294 |
rs31932813 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Prex2 | GRCm38.p3 | 1:11117789 | TAACTAGGCATATAA[G/T]GCACAGAATGATGGG | 109294 |
rs31932894 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Prex2 | GRCm38.p3 | 1:11134004 | TTCTGACTTCATAAT[C/T]AAGACAAGCCTTTAA | 109294 |
rs31932897 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Prex2 | Mm_Celera | 1:11134028 | CCTTTAAAAAAAGGA[A/G]TATTCATCTACTGCA | 109294 |
rs31932900 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Prex2 | Mm_Celera | 1:11134067 | ATAAGATAAACTGTA[G/T]ATGATATTGCTAGAA | 109294 |
rs31932903 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Prex2 | Mm_Celera | 1:11134190 | TTTATTTTTTGCACC[C/T]GTTCAACTGGCCTTT | 109294 |
rs31932914 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Prex2 | Mm_Celera | 1:11165896 | AAATGCTGCTAGTCT[C/T]TTCCGTGTGCATAGA | 109294 |
rs31932916 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | Mm_Celera | 1:11166018 | GCGTATAATGACTTG[A/G]TTATGGAGGATTGAG | 109294 |
rs31932918 | snp | A/G | 0.32 | 0.24 | intron-variant | Prex2 | Mm_Celera | 1:11166168 | TGGTGTGTTTAAAGT[A/G]TATTGCCTTTATATA | 109294 |
rs31932920 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Prex2 | Mm_Celera | 1:11166281 | TTCAATTATAGACTG[C/T]ATTGTGGTATGTGTC | 109294 |
rs31933024 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Prex2 | GRCm38.p3 | 1:11153430 | AGATTCATCAGGAAT[A/G]TTTTAGTTATGCTTT | 109294 |