SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4165057 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ppil2 | Mm_Celera | 16:17098163 | ATCTAGATAAGACTT[C/T]TAAAAAATCTGTTAA | 66053 |
rs6392982 | snp | A/C | 0.32 | 0.24 | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086326 | AATGGATATAAACAA[A/C]CCATTTATCAAGGTT | 66053 |
rs6393577 | snp | A/G | 0.359862 | 0.224567 | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086437 | AGACCACAACCAGGC[A/G]TGCTGGTAAACCNCT | 66053 |
rs6393589 | snp | A/G | 0.21875 | 0.248039 | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086450 | GCNTGCTGGTAAACC[A/G]CTGAATGTCTCACCT | 66053 |
rs13470670 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086998 | CAGACACGCCACAGA[C/T]GGCTGACAGCTTTGG | 66053 |
rs32777920 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17087089 | GGTGGGGGCGGCGGC[A/G]AGCCACGTTCGTTCC | 66053 |
rs45676136 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Ppil2 | Mm_Celera | 16:17096472 | TCCTAACACCTAAGA[C/G]AGTTATGAGGCAAGT | 66053 |
rs45708448 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17095693 | TCACCTGCAGCCCTG[C/T]CACTGTACCCTGGAA | 66053 |
rs45715282 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17092971 | ACTTGCTACAATGTG[A/G]GTTCTGTCCCAGGGA | 66053 |
rs45746610 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17091658 | GGTAGGACCCTGAGG[A/C]TTAGGAAAGAGGCCC | 66053 |
rs45875036 | snp | C/T | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17092502 | ATTTGCACATAGATA[C/T]ACTTACCAAGCAGCT | 66053 |
rs46196142 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17090052 | CATGTCTGGGGAAAG[A/G]CAGTGAAGGCCCACA | 66053 |
rs46201998 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17104757 | AGCATGCACGATGGC[A/G]GTAAGCCAAGTGTGG | 66053 |
rs46288071 | snp | C/T | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17096608 | GTGTTATGGTACAGG[C/T]GACCACCAAGCCTGG | 66053 |
rs46389995 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17087881 | CCCAGGGAGCAAAGC[A/G]CTGTGACGAGCAGGT | 66053 |
rs46550925 | snp | C/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17097111 | GGTCCATGCTGAAGA[C/G]AGGGTAATACTTTCC | 66053 |
rs46646492 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17089558 | CAGTGGGCAGTTGTG[C/T]TTTGTTCTCCCTAGG | 66053 |
rs46677755 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17101243 | CTTGCCCACAGATGA[A/G]GAGTGCCAAGAAAGA | 66053 |
rs46686709 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17090039 | GAGGGATAATAGCCA[G/T]GTCTGGGGAAAGGCA | 66053 |
rs46997030 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113092 | CTGGGTAGAAACACC[C/T]ATCAAACTAGGCCTG | 66053 |
rs47047717 | snp | A/T | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17110504 | AGATCATTCGCAGAT[A/T]AAATTACTAAGCGCC | 66053 |
rs47138892 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17095366 | CAGCCTTTTCACAAT[G/T]ATGTTTTGCTTTTGT | 66053 |
rs47195015 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17091708 | AGGGGCATGCACAAG[A/G]TAGGCCACAAGGCCA | 66053 |
rs47196082 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111833 | TAGAGGAGTGTGCCA[C/T]CATGCCCGGCCCCAA | 66053 |
rs47212748 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17099860 | AGAAGTCATGTGACA[C/T]CTGGAAAAGCAAAAG | 66053 |
rs47218918 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17097954 | CACCTTCTCCTCTCA[A/T]AAGCCATGCCAGACA | 66053 |
rs47309424 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17096332 | CAAGCTTCAGTAACA[A/G]CCACAGAGTCGTTTA | 66053 |
rs47468528 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17089132 | GGAGATGCTGCCCAT[C/T]AGTCACACTCACGTG | 66053 |
rs47468575 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17090308 | TGTCTCTGCTAAGGC[C/T]ACAGAGGTAAATCCA | 66053 |
rs47495640 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17094640 | CCTGTGTCAGGGCCA[A/G]TAGCATAAGGCAGCC | 66053 |
rs47631434 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17110936 | GACTAGAGCCAGGAC[A/G]AAGCGGACAACCAAC | 66053 |
rs47718190 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17095616 | CAGTGTGGTCAATGG[C/T]GTGGACCAAGCACAG | 66053 |
rs47749839 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17107157 | AAAGCCAAGGGAAAA[C/G]AGAAGGATTTGAAGC | 66053 |
rs47820554 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086113 | CAAGGGAGACAGACC[C/T]GAGTACGTCCTTATA | 66053 |
rs47944082 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | GRCm38.p3 | 16:17086956 | AAGCTCGAGCAAACA[A/G]AGCGCCTTGGCCTCC | 66053 |
rs48073251 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111336 | TGCAGGCACCGTGCT[A/G]GGCTGAAGCTTGCTA | 66053 |
rs48136896 | snp | G/T | 0.231111 | 0.249285 | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112497 | AAGGCAGTCATCCTG[G/T]CAGCTTCTTACTTCA | 66053 |
rs48199182 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17093194 | AAACTGAGAGCTGGC[A/G]AAGACCAGATGACCA | 66053 |
rs48252015 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111880 | TGTGTGTGTGGTTAA[A/G]TAGTGGCCATGCCAC | 66053 |
rs48387325 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17096477 | ACACCTAAGAGAGTT[A/G]TGAGGCAAGTGTAGC | 66053 |
rs48401968 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ppil2 | Mm_Celera | 16:17087562 | TCAAGAACAGCCATG[G/T]GTGAACAGCAGTCAT | 66053 |
rs48461401 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17098995 | CACCAATCATCTTTC[A/G]TCTAGATTCTGCCCA | 66053 |
rs48468963 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17112914 | CCCAAGTGAGGTATG[A/G]TCAACCATGACTCAA | 66053 |
rs48688742 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17095725 | GAACAGTGGCCAACG[A/G]CAATCCAGAAAGCAC | 66053 |
rs48770704 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17104323 | TACAGACAGGAAGAG[C/T]AGCTTAAAGAAGGGG | 66053 |
rs48904480 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17097891 | ACAAGACCACATTCC[C/T]GCCGCCTTTCTCAGA | 66053 |
rs48952452 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ppil2 | Mm_Celera | 16:17089827 | CAGAAATGAGCAGCA[C/T]ACCACACCCAGCCAG | 66053 |
rs48984355 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17109612 | CTGGATCACAGGAGA[C/T]AGCATTCTTCAGGAC | 66053 |
rs49080981 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17106160 | TGTCCCTGACACCAC[A/G]TCATAAGGATAAGCT | 66053 |
rs49107826 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17109590 | AATGTCAGTGTTCTG[G/T]ATAGCTCTGGATCAC | 66053 |
rs49108891 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17090589 | GGAGCACCTGCAATC[C/G]TAGCAGGAGGCTGAG | 66053 |
rs49118843 | snp | A/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111924 | AGAGGACAAGTGAGG[A/G]GTTGGTTCTCTTTGC | 66053 |
rs49157833 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B, intron-variant, missense | Ppil2, Ypel1 | Mm_Celera | 16:17087204 | CACCTTGTAGTAGCT[C/T]GTGAGTGGCCTGAGA | 66053 |
rs49163524 | snp | A/C | 0.260355 | 0.249785 | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086615 | ATACATAGTATTTTT[A/C]TACCTTAATGCTTAT | 66053 |
rs49199876 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17090894 | GGAACCAAGGATGCC[A/G]GAGCTGACTGTTGCC | 66053 |
rs49251054 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17104617 | TTCCCCTGAGCTACA[C/T]TTGGCGTCTGCAGAA | 66053 |
rs49251668 | snp | A/G | 0.32 | 0.24 | utr-variant-5-prime | Ppil2 | GRCm38.p3 | 16:17111184 | CCCCATGGTGGCAAC[A/G]AACCGAAGAGACCAC | 66053 |
rs49347668 | snp | G/T | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17092571 | TCAGGGCCCTTTTGA[G/T]TCTCAGGGGCAGTCA | 66053 |
rs49429032 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17089407 | CTAACAAGGCCATGA[C/T]TTGCTTGGCACCTTC | 66053 |
rs49429426 | snp | C/T | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17101480 | AAGTCACAGAGATCA[C/T]GAGGACAACTGTAGA | 66053 |
rs49532127 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17089376 | GATACAGAGCCTCCA[G/T]TGTGCCCTCCTGCTC | 66053 |
rs49590532 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17089714 | CAGAGAGAGGCATCA[C/T]GGCAGAGCTGAGACA | 66053 |
rs49622702 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17096800 | GCTCCACTGCCTAGA[C/G]CAGTACAGAGATATC | 66053 |
rs49667182 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ppil2 | Mm_Celera | 16:17095666 | CCTAGACAAGTCTCA[C/T]GTCACCCAGTCTCAC | 66053 |
rs49704180 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ppil2 | Mm_Celera | 16:17095646 | GGAAGCAGGAAGGTC[A/C]GGGCCCTAGACAAGT | 66053 |
rs49710349 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086985 | CCCTGTCTCCTAGCC[A/C]AAGCTGTCAGCCCTC | 66053 |
rs49946371 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111836 | AGGAGTGTGCCACCA[C/T]GCCCGGCCCCAAGTT | 66053 |
rs50025840 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17103441 | ACACTTGTAGAAAGC[A/G]CAGGACTGTCACTCC | 66053 |
rs50035948 | snp | C/T | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17089094 | TTGCTGGCTTGGTAA[C/T]CATGAAGCACTATGA | 66053 |
rs50113161 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17087319 | TTTTCTTTTTTTAAG[A/T]CAAGGTCTCATAACC | 66053 |
rs50126901 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17094793 | CCAACAGCACTGGGA[A/G]GGTCCCTGCCACCAT | 66053 |
rs50190160 | snp | A/C/T | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | GRCm38.p3 | 16:17113171 | GAAAGTGAAGCCCTA[A/C/T]GGGGTCTGAACCACT | 66053 |
rs50405187 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon, utr-variant-5-prime, intron-variant | Ppil2 | GRCm38.p3 | 16:17107199 | GTGGTCAAAAGGTAA[G/T]CGGCGAAAACTTGTC | 66053 |
rs50431564 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17099425 | GGACTCAGAGTAGGA[A/G]GCTCCAAGTGGGGCA | 66053 |
rs50431673 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ppil2 | Mm_Celera | 16:17096646 | AGCTGGGGGGCAGAG[C/T]GCAGAGCAGAGGGCA | 66053 |
rs50535819 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17099647 | ATCTTGAGTAGGAAA[C/T]GCCTCCCTACCACCA | 66053 |
rs50783486 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17109722 | GAGCATGTGTTACTG[A/G]GTCCTGCCACGGACA | 66053 |
rs50820676 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17092831 | ACTTGCCCTGCACCC[A/G]AGATACCTCCTCCAT | 66053 |
rs50862395 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17096957 | AGTTCCAACATGGGC[C/T]CTCCTGTATCATGCC | 66053 |
rs51035980 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17089880 | GGATGAGCCACAATC[C/T]GTGTTTCCATACTTC | 66053 |
rs51075978 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17095279 | GGAGCACACAGAAGA[C/T]GCTGTCATGGTGAGT | 66053 |
rs51135068 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17101417 | GATTGCAAACCTAAG[A/G]TGCATCCAGGGGTAA | 66053 |
rs51137633 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17090269 | CTTGGAGCTTCCTTG[A/G]ACCCGTGTATGCTGC | 66053 |
rs51196327 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ppil2 | Mm_Celera | 16:17091067 | GGCTTCATCTAGGTT[A/G]CTTTGATTGGATTTA | 66053 |
rs51197103 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17091026 | ATTCAACCCGCTGAC[C/T]TGGGCTCCTTTATTG | 66053 |
rs51236177 | snp | A/G | 0.32 | 0.24 | intron-variant | Ppil2 | Mm_Celera | 16:17096087 | GGTGGGGTCCTGTGA[A/G]AAGAAGAGAACACTC | 66053 |
rs51251544 | snp | C/T | | | upstream-variant-2KB | Ppil2 | GRCm38.p3 | 16:17111997 | TAAGCTGGGTTTTTG[C/T]TTGTTTTTGTTTTTT | 66053 |
rs51274376 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ppil2 | Mm_Celera | 16:17101024 | GGTGTTTATCACTGA[A/G]CCTGGCCTAACAGAG | 66053 |
rs51314537 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17100629 | GAATAAAGACTGCTG[G/T]GTATTTCTACAAGGT | 66053 |
rs51393646 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111797 | GAAATCCGCCTGCCT[C/T]TGCCTCCCGAGTGCT | 66053 |
rs51495997 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17095319 | CCTGAAGGGATGTGG[A/G]AGTCACCCTGTTTCC | 66053 |
rs51524095 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113117 | GGCCTGTGTTTGGAG[A/G]TTACATGCAGGAACA | 66053 |
rs51527899 | snp | C/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088206 | CACATACTAACTGGG[C/T]TCAGCAGGTCACCAT | 66053 |
rs51543644 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17095744 | TCCAGAAAGCACAGT[C/T]CCACCAGAGCTAGGG | 66053 |
rs51624545 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ppil2 | Mm_Celera | 16:17097933 | CTCCAGACTGGCTCA[A/G]GTAGCCACCTTCTCC | 66053 |
rs51643897 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ppil2 | Mm_Celera | 16:17090338 | AGACCTCTGGCTCTC[C/T]GGAGAAAGCCGGAGT | 66053 |
rs51645485 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17096453 | CTGAAAAGCAGCCTA[A/C]GTGTCCTAACACCTA | 66053 |
rs51680193 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086399 | AGAACTGACCATGAG[C/T]TGGCTTCAGGGTAAG | 66053 |
rs51723988 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | GRCm38.p3 | 16:17087012 | CCTCTGTGGCGTGTC[C/T]GTGGGAGGTATAAAA | 66053 |
rs51749879 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ppil2 | Mm_Celera | 16:17098849 | CACCTCTGCTGGAAT[A/G]TTCTTCCCACACCTT | 66053 |
rs51984948 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ppil2 | Mm_Celera | 16:17109207 | TTCCTCCTATAAAGA[A/C]TAAGGTTGCTGGGCA | 66053 |
rs52149706 | snp | A/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111728 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 66053 |
rs211699562 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109947 | GGGGAAGCCCTTTAC[A/T]GGAATAACACTTACT | 66053 |
rs211700952 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17099322 | AGACCACAAAGGGTT[A/C]ACAAAAGATCAATCA | 66053 |
rs211787633 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100111 | TGATGTCCTCTTCTG[C/G]TGTGTCAGCAACAAG | 66053 |
rs211910400 | snp | C/T | | | synonymous-codon | Ppil2 | GRCm38.p3 | 16:17091183 | GACTCACAACTGAGA[C/T]TTGTTGGTGTTGGGC | 66053 |
rs212023388 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17090350 | CTCCGGAGAAAGCCG[A/G]AGTTTGGTTGCCAGA | 66053 |
rs212224148 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17087538 | ATAGTGTACCGGGCT[A/G]GGGAAGTGTCAAGAA | 66053 |
rs212227010 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17097743 | AGAGGAGGAAAAAAA[A/G]AGACGGAGGAACCAG | 66053 |
rs212507923 | in-del | -/CT | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113215 | GGATTTCCCACCCCA[-/CT]CTCTCAAGCACAACA | 66053 |
rs212634397 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17098004 | TTTCGACCTCTTCTC[-/A]ATCTTTATCTCCTGG | 66053 |
rs212744103 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17106515 | GGTCTCAAGCCTTTA[A/G]TTCTAGTGTTCTCGA | 66053 |
rs212760373 | in-del | -/CTCTGGGT | | | intron-variant | Ppil2 | Mm_Celera | 16:17095480 | TTCCCTAGGCCTGGC[-/CTCTGGGT]CTCCTGAGCGCAGTT | 66053 |
rs212791253 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17096666 | AGCAGAGGGCAGAGC[C/G]GAGGGTCAAGGCAAG | 66053 |
rs212917387 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103071 | ACTACTGGGCTATAG[C/T]CCCAAGCCAAGGGCT | 66053 |
rs213006182 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103467 | ACTCCCAGGTTCTGT[A/G]AGGTGAGCAGTTCTC | 66053 |
rs213022979 | snp | A/C | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112669 | AAAAGCAAATCAAAA[A/C]TAAACAAAACTACCA | 66053 |
rs213040821 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17105398 | ACTTAGTGGATAAAG[G/T]ACTTTCTCCACAGCA | 66053 |
rs213083971 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086095 | TCCCCAGTGGGAAGG[C/T]GGCAAGGGAGACAGA | 66053 |
rs213216906 | in-del | -/AGG | | | intron-variant | Ppil2 | Mm_Celera | 16:17103123 | CAGGCTGAGAAGTGA[-/AGG]AGAAGTTTTATCTGC | 66053 |
rs213243743 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094832 | ATGCATCTAGGCCCC[C/G]TGAGCACCTCCCCTG | 66053 |
rs213308312 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113231 | TCTCTCAAGCACAAC[A/G]GAATTGCTTGTTACA | 66053 |
rs213313060 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17092917 | GAGAAGAATGCAGGA[A/G]CCAATGCAGATGCGG | 66053 |
rs213426579 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101743 | CTCCTGACATCCTGG[C/T]TAGACTCCACCCCCA | 66053 |
rs213607363 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086683 | AATGAGATTTTTTTT[C/T]CCCTCAAAAGTCCTT | 66053 |
rs213910518 | in-del | -/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17108967 | TAAAAGAGAAAAAAA[-/T]ATATATATATTTATG | 66053 |
rs213958576 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17101197 | GTGCTTCACATGGGT[A/C]AGGACCTAGGTACAG | 66053 |
rs214124802 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17109057 | ACCCACAGGGCAGCT[C/G]ACAGCCATCTGTAAC | 66053 |
rs214239672 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17100043 | CTTCCAGAGGTCGTT[G/T]AGTTCAATTCCCAGC | 66053 |
rs214364221 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17099213 | CTGCTCCTCCCTATG[A/C]TTGCAACATTTCCCT | 66053 |
rs214552660 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17105206 | CTGCCTGAGGCCTGG[C/T]GGTCCCTCCCAGTTA | 66053 |
rs214568248 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111448 | GTCTGGCTACTTGTT[C/T]AGTCCATGCTATGCT | 66053 |
rs214918236 | in-del | -/CTT | | | intron-variant | Ppil2 | Mm_Celera | 16:17090629 | CCTGAGCTACAAGAC[-/CTT]CTCTCTGAATAAATC | 66053 |
rs214923103 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17095813 | TCTGACAGACATGGT[A/T]GTGTACGCTTGTAAT | 66053 |
rs215107547 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104574 | TGCTGGCGAGTGAAC[A/G]AAGGCTTGTGTACTC | 66053 |
rs215177091 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17087983 | TCAAAAGTCAAAAGC[C/T]AGGCATGGTGGTGAC | 66053 |
rs215196983 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17096550 | TGGTGGCTGTAGGGG[A/G]AGGGGGTGGCACTAA | 66053 |
rs215221581 | snp | A/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111775 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCGC | 66053 |
rs215240236 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17087384 | CAGGATCTTGCTGTG[C/G]GGCCTTAACGATCCT | 66053 |
rs215426373 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103415 | CATCCTCATCCGTGT[A/G]CACACAGGCAACACT | 66053 |
rs215537135 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103026 | GTAATCCAAAGCCTT[C/G]TGAAAGCAAATGAGC | 66053 |
rs215678933 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110881 | GAGCACGACCCGCCT[A/G]TCTTCAACTTGAAGG | 66053 |
rs216001581 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094267 | TAGCTGTGTTCAGCT[A/T]GGGAAATTATAGATG | 66053 |
rs216073339 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17089312 | ATGTCTGATAAAGAA[C/T]CCAAGGGCTGGCTCT | 66053 |
rs216197941 | in-del | -/AC | | | intron-variant, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17087231 | GAGAAGAGTGTGAGA[-/AC]ACAGTTAGGCACCAG | 66053 |
rs216234591 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110043 | GTACGTAGCAGCAGA[A/G]AAAGACACAGAAGCA | 66053 |
rs216250127 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101052 | GAGGAGAGAGAGAAC[C/T]CCCACAGCTGCACCC | 66053 |
rs216298871 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17091497 | GGGTCCAAGTCATAG[C/T]TGGCCCATGGAGTTG | 66053 |
rs216311383 | in-del | -/CGCGCGCATG | | | intron-variant | Ppil2 | Mm_Celera | 16:17105917 | CTGGGTGGGCAGGCA[-/CGCGCGCATG]CACACACACACACAC | 66053 |
rs216517849 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094756 | TGTTTGGGGCCCAGT[C/T]ACCCCAGCAGCCCTG | 66053 |
rs216574333 | snp | A/G | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088317 | TGGAAGTGGTGTCAA[A/G]GTAAGACCATAAGAC | 66053 |
rs216879557 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17100241 | CCTGGAGCTGTGTCC[A/T]AAAGGGATCCTCACC | 66053 |
rs216894597 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17087100 | CGGCGAGCCACGTTC[G/T]TTCCTGCAGCATCCA | 66053 |
rs216999999 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086736 | GCAGTTTTCAAAATC[C/T]AAGTGTCTTTACTGT | 66053 |
rs217112965 | in-del | -/A | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112784 | CAGTGAGACCAAAAC[-/A]AAAACAAAACAAAAA | 66053 |
rs217118310 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17092645 | AGGCAGGACTAGCCT[A/G]TGGCCCCAGGAACCA | 66053 |
rs217188559 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094161 | TTTTTATATACAACA[G/T]TACATGGAATAAAAG | 66053 |
rs217643861 | snp | A/G | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088462 | ATATAGCCAGGGTTG[A/G]TCTTGGTATTCTGAA | 66053 |
rs217727623 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17092986 | AGTTCTGTCCCAGGG[A/C]ACAAGAGGCAGAGGC | 66053 |
rs217775550 | in-del | -/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17099614 | GGCGTGAGCCACCAC[-/T]ACCCGGCTGACAGTC | 66053 |
rs217783566 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17098364 | ACACATGCTCACACA[C/T]GTATACAAACATACA | 66053 |
rs217790149 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17109002 | TGGAGATAACAGTTA[A/C]GAGCACTGGCTGCTA | 66053 |
rs217849209 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17099057 | GCATGCACGCACACA[C/T]GCACTGCCACACATG | 66053 |
rs218064605 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17106998 | AATAAATAAATCTTT[A/T]TAAAAAATCTATGCA | 66053 |
rs218160680 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17104480 | CCCTGTCTCGATAAA[C/T]AAACAAACAAACAAA | 66053 |
rs218228159 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17097308 | CTCAGCCAGGCACAC[A/G]TTCGGGCCCAACATT | 66053 |
rs218252229 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103566 | CACGGAGCTCTGCAT[A/G]AGCACCTACCTCTCC | 66053 |
rs218599383 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103719 | TTGCACAGGGCCTGA[A/G]CTCCCAGCACCCACA | 66053 |
rs218693586 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17093662 | CCATGTGCATGTCTA[G/T]TGCTCTTAAAGATCA | 66053 |
rs218713046 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17095898 | ATCTATACAGCAAAT[G/T]TCATGATAGTCAAAA | 66053 |
rs218768615 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094391 | CTTGGGAGAAAGACA[G/T]CACCTATCGGCTAAA | 66053 |
rs218798344 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086927 | GGGAGTTCACCAAGA[A/G]CAGCAGGACCAGCAA | 66053 |
rs218833078 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17102344 | CTTCAGCTGGGATTC[C/T]ATGGCTTCCCACAGC | 66053 |
rs218860376 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17095268 | AGGGGGTTGGTGGAG[C/T]ACACAGAAGACGCTG | 66053 |
rs219106991 | in-del | -/AAACAAAC | | | intron-variant | Ppil2 | Mm_Celera | 16:17104476 | AAACCCTGTCTCGAT[-/AAACAAAC]AAACAAACAAACAAA | 66053 |
rs219159439 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17105628 | ACAAACAAACTAACT[-/A]AAAAAAAAAACCAAA | 66053 |
rs219240710 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17111018 | GTTAGTTAGTCCGGC[C/G]GTAGAACGCCCTGGC | 66053 |
rs219298311 | in-del | -/GT | | | intron-variant | Ppil2 | Mm_Celera | 16:17106359 | AATGAGGCCCCTGTG[-/GT]GTACTGTCTGTACAC | 66053 |
rs219386349 | snp | A/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112414 | AAAATGCAACCAAAA[A/T]ATCTGGGTCACTGGT | 66053 |
rs219495773 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102886 | GTCTCAGACTGCCAC[C/G]AGAGCCAGAAAGACT | 66053 |
rs219545912 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101995 | TTCTACAATAAAGAC[G/T]GTCTTTGCTCATCAA | 66053 |
rs219658453 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109472 | GGCCTGAACTTGAAA[G/T]AGTTATATTTTTAAG | 66053 |
rs219699178 | in-del | -/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094367 | TCAGGCTCTCCAGAC[-/T]TCAGTCTACTTGGGA | 66053 |
rs219748129 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17097116 | ATGCTGAAGAGAGGG[C/T]AATACTTTCCAGGCT | 66053 |
rs219765087 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100452 | AGATCTCTCTGGGAA[C/G]TCTCCAAGACACAGC | 66053 |
rs219785037 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111680 | GAATGGGTCCCAAGT[C/T]TCCTTTTTTTTTTTT | 66053 |
rs219827636 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17098112 | GTCCCAATAGACAAT[A/G]GGGTGGGAGAGCAAA | 66053 |
rs219883621 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17105670 | TAAAGAAAAAGAAAG[A/C]CAGCTAAAGACAGCA | 66053 |
rs219899363 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17110441 | AAGGAAACACCCCCG[A/T]GGTCTGGGACAAGGG | 66053 |
rs219900839 | in-del | -/CA | | | intron-variant | Ppil2 | Mm_Celera | 16:17098173 | ACTTCTAAAAAATCT[-/CA]GTTAAAAAAAAAAAA | 66053 |
rs220301033 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17104787 | GTGTAAGCTTAGCTA[C/T]TTGGGAGATGTATGA | 66053 |
rs220379581 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17105813 | AAAAAATAAGATGAA[G/T]AACAACAGAGAAAGC | 66053 |
rs220684607 | in-del | -/AAG | | | intron-variant | Ppil2 | Mm_Celera | 16:17109821 | CATTGTGTGGCACAT[-/AAG]AAGGACAAAAGATGG | 66053 |
rs220719117 | in-del | -/CT | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112714 | AGGCTGGTAAGTTCT[-/CT]GTAAGTTCAAGTCCT | 66053 |
rs220748512 | snp | G/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17112947 | TGTATATCCACTAAT[G/T]TCCAGTAATGATTGA | 66053 |
rs220820788 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17107541 | TTTCGAGAAAGAAGA[A/G]TGTATTATGTGTTAC | 66053 |
rs220875140 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103632 | GAACAATGTTCCTGA[A/T]GGGAAGAGAGAACAA | 66053 |
rs220938053 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17111046 | GGCCCGCGTAGGCTG[A/C]ACTGAGGGACGAGAC | 66053 |
rs221010017 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17103273 | AATCTAAATGATAAA[A/C]ACATAATTATTTTCT | 66053 |
rs221209157 | snp | C/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113031 | CACAGTTTTGAAACT[C/T]GGGCAAGTAACAAGC | 66053 |
rs221320892 | in-del | -/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17087745 | ATTCAAGGTTTAGGG[-/T]TAAAAGGTCAAGCCT | 66053 |
rs221376285 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17110719 | GCTACTTTTGGAAAG[G/T]GAAGAAGCCCAAGGA | 66053 |
rs221509860 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104644 | AGAAGTTTTACTGCA[A/G]TTACATATCAATAAG | 66053 |
rs222014917 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086138 | CTTATAGATGCCTCA[C/G]TAAAGCTGAAGAGTC | 66053 |
rs222079934 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094474 | AGCATGCTCGTCCCC[A/G]GTAGGGCCCAGGTAA | 66053 |
rs222102102 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109331 | CCAGGACATCCAAGG[C/T]TACACAGAGAAATTC | 66053 |
rs222245361 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17107849 | AGGCAGTTAAGAATA[C/T]ATTCTGCTCTTATAC | 66053 |
rs222417688 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17089956 | CCTGGGTGTCTCCTC[C/T]TCTTGGCCCCACAGG | 66053 |
rs222438773 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111252 | ACTTCCGGAGATCGA[A/C]GCACTGGATCCCGGA | 66053 |
rs222507918 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17087556 | GAAGTGTCAAGAACA[A/G]CCATGGGTGAACAGC | 66053 |
rs222599692 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17093898 | GTGCTGGGATTAAAG[A/G]CGTACGCCACCATGC | 66053 |
rs222624426 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086966 | AAACAGAGCGCCTTG[C/G]CCTCCCTGTCTCCTA | 66053 |
rs222808372 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17087783 | AATGTAGTGTGGCAT[A/T]CTCTAAGGACAGTGC | 66053 |
rs222877584 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090732 | GCAGCCTTCCCCTGA[C/T]AGCCACATCTAGTGA | 66053 |
rs223309840 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17087927 | GGACACGTGGGCCCC[A/C]CGAGGCCTTTTCAGC | 66053 |
rs223321991 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086315 | TATTGGGGAGTAATG[A/G]ATATAAACAAACCAT | 66053 |
rs223348335 | snp | A/G | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088455 | GCTCCCTATATAGCC[A/G]GGGTTGGTCTTGGTA | 66053 |
rs223459364 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | GRCm38.p3 | 16:17086871 | CTGGGGACAGGTGTC[A/G]GCTGCTGAGCAAGGC | 66053 |
rs223682700 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17096394 | ATTCACACACCACCA[C/T]GGGGACAACTGTGTA | 66053 |
rs223683444 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17091769 | GAAAGATTATATACC[C/T]AGAACTTAAAACCCA | 66053 |
rs223689714 | in-del | -/AT | | | intron-variant | Ppil2 | Mm_Celera | 16:17108415 | CACGTAGACAAATAC[-/AT]ACACACACACATACA | 66053 |
rs223773913 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17087084 | GTGGAGGTGGGGGCG[A/G]CGGCGAGCCACGTTC | 66053 |
rs223831576 | in-del | -/TA | | | intron-variant | Ppil2 | Mm_Celera | 16:17104964 | AGTATTTTTTTATTT[-/TA]TTTTATTTTTATTTT | 66053 |
rs224040603 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094497 | CCAGGTAAGGGCTGA[A/G]ACCTTAGTAGCTATA | 66053 |
rs224092781 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17095161 | ATGAGAAGAAGCCAC[A/G]GGTGAGTTGATTAGG | 66053 |
rs224234870 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101444 | GTAACAGAAAAACAA[C/T]ATCCAGCAGAAAAGA | 66053 |
rs224289477 | in-del | -/TA | | | intron-variant | Ppil2 | Mm_Celera | 16:17100154 | CATTAAATAAATATT[-/TA]AAAAAAAAAGAGAGA | 66053 |
rs224319447 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17092041 | GGTCTTCCTGGATGA[A/G]CACTGAAGGGCCAGC | 66053 |
rs224335982 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17102203 | GGACCCCATTTTGTT[C/T]TCAGCTCTTCTGCCG | 66053 |
rs224447036 | in-del | -/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100163 | ATATTTAAAAAAAAA[-/G]AGAGAGAGAAGAAAG | 66053 |
rs224612095 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17092118 | ACACATGGCCTGGAA[C/T]GAGGTATCTGGAACC | 66053 |
rs224660855 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103324 | GACAAGAAAAAGTAT[A/G]TCACCTTCCACAAAT | 66053 |
rs224662222 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17093983 | TTGTTTGTTTGTTTT[G/T]GTTTGGTTTTGGTTT | 66053 |
rs224701109 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17094601 | TTGGAACACCAAAGA[A/C]AGCGGGAACATTGGT | 66053 |
rs224739911 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17090666 | AAAGCAGGAAGTATG[A/C]TATCCCTACCCAGAG | 66053 |
rs224767593 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102733 | GCCTCTACCCCACAC[A/G]GCCGAAGAGAAGCTC | 66053 |
rs225147169 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17100707 | GTTAAGTGTGTGCTC[G/T]ACCACTGAGCTTCAT | 66053 |
rs225188048 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17091111 | ACAACTTTTAGGGAG[A/C]CCTCTTAGGTCCTTT | 66053 |
rs225218248 | in-del | -/AAAAAC | | | intron-variant | Ppil2 | Mm_Celera | 16:17110638 | AGAAACCCTATCTTG[-/AAAAAC]AAAAACAAAAACAAA | 66053 |
rs225230211 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109889 | AGGAAATGAACTGGA[C/T]TTATAGACTATCTGA | 66053 |
rs225251569 | in-del | -/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17102132 | GGGAACCACCCAGCA[-/C]CCCCTCTCCCTGCCC | 66053 |
rs225273880 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100059 | AGTTCAATTCCCAGC[A/G]ACTACATGGAGGTTC | 66053 |
rs225276670 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17099533 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 66053 |
rs225469227 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17098733 | GGCCTTGAAAACACC[A/G]AGATCCACCTGTCTC | 66053 |
rs225490897 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17105483 | TGAGGCTGAAGAGAT[A/G]GCTCAATGGTTAAAA | 66053 |
rs225556569 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17103976 | CAGCAACCACATGGT[A/C]ACTCACAACCAACCG | 66053 |
rs225559972 | in-del | -/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17102601 | AAACGATGTTGTCAT[-/C]CCAGCCTGGACCCTT | 66053 |
rs225710430 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17096929 | CCAAACCAACCTGGC[C/T]GCTTCTGGCAAGAGT | 66053 |
rs225729237 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17104705 | GTGAGTATATCTATA[C/T]ACAAAATACTGGGTC | 66053 |
rs225794906 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094872 | TCGGTCAGGCAGAGT[G/T]CCCCACTCACCGCAT | 66053 |
rs225830776 | in-del | -/TG | | | intron-variant | Ppil2 | Mm_Celera | 16:17099476 | CTTTTTTGTTGTTGT[-/TG]TTTTTTTTTCGAGAC | 66053 |
rs225832040 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17108342 | AGAAGACCAGAGCTT[C/T]GTTCCCAGCACCCAC | 66053 |
rs225837369 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17096113 | CACTCAGAAGTACAA[C/T]GGACTGTGTCAAGCA | 66053 |
rs225838121 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17097723 | GGAGACAGGGAGGAC[A/G]GGACAGAGGAGGAAA | 66053 |
rs225883914 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17098919 | CTGCTGCCCTCAGTG[G/T]GTGTCCTACTGGTCC | 66053 |
rs225930523 | in-del | -/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100581 | AATATCACTATGTAA[-/G]GGGTAGTCACTGGGC | 66053 |
rs225958633 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17106333 | CGGGGCATCCTCCCC[A/G]TCCCAGGGTTTAATG | 66053 |
rs226350340 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104282 | AGCTCCGACCCGGCG[A/G]GAGTGGAGGGCAGGC | 66053 |
rs226415130 | snp | C/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113182 | CCTAAGGGGTCTGAA[C/T]CACTAAAGGGAAGAA | 66053 |
rs226443774 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103440 | AACACTTGTAGAAAG[C/T]ACAGGACTGTCACTC | 66053 |
rs226513434 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102391 | GCCGCAAGGAAAGGC[A/G]TCCGCCTGCCCAGAG | 66053 |
rs226740081 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17110520 | AAATTACTAAGCGCC[A/C]AGCCTTTAATCCTAG | 66053 |
rs226814684 | in-del | -/TGAC | | | intron-variant | Ppil2 | Mm_Celera | 16:17087818 | TGACAGAGAACATAG[-/TGAC]TGACACGACACTGCC | 66053 |
rs226841924 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100535 | TGTAAGCCCCAGGCT[A/G]TGAGCAGATCCTCAG | 66053 |
rs226945485 | snp | A/C | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112801 | AAACAAAACAAAAAA[A/C]CACTTTCTTGGCCAC | 66053 |
rs227029440 | snp | G/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112015 | GTTTTTGTTTTTTGA[G/T]ACAGGGTTTCTCTGT | 66053 |
rs227040413 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101721 | GTCACACAGACAATG[C/T]CCCAAGCTCCTGACA | 66053 |
rs227053050 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103180 | CCAGTCTCATAAAAC[A/T]CTGTAGCATTTGACC | 66053 |
rs227067201 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17102427 | GAAGTCTTGACAGGA[C/T]GAGGGTTTTCTCCCA | 66053 |
rs227075509 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17109353 | GAGAAATTCTGCCTC[-/A]AAAAAAAACAAAAAA | 66053 |
rs227134069 | snp | A/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111422 | AGCCCTCAAAAACTT[A/T]TCTATGCACTGTCTG | 66053 |
rs227540279 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17108805 | TAGCTCTGGCTGTCC[A/T]GGAATTAAAAGCATG | 66053 |
rs227547097 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109032 | ATTCCAGAGGACCCA[G/T]GTTCCCAACACCCAC | 66053 |
rs227600843 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17101388 | TTGATATCCCAAAGA[A/G]CACCTGTGATGCAGA | 66053 |
rs227776732 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17087949 | CTTTTCAGCTGATAC[A/C]CTGACAACTGTCCTA | 66053 |
rs227915469 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17087110 | CGTTCGTTCCTGCAG[C/G]ATCCACTAGGAGCAA | 66053 |
rs227985320 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17106541 | CTCGAGGCAGAGGCA[C/G]GTCAGTCTTTTTAAG | 66053 |
rs228177992 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104861 | ACTCCCCCACCCTCT[A/G]CACTCACCAAAGAAA | 66053 |
rs228344514 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104386 | AGCACTCAGGAGGCA[A/G]AGGCAGGCAGATTTC | 66053 |
rs228851745 | snp | G/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112432 | CTGGGTCACTGGTCT[G/T]ATTCTCATTTGGCAG | 66053 |
rs228927420 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112292 | TACATAAACATAAAA[C/T]ATTAGAAACCCCCTA | 66053 |
rs228942448 | in-del | -/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17101033 | ACTGAACCTGGCCTA[-/C]ACAGAGGAGAGAGAG | 66053 |
rs229003951 | in-del | -/TGGA | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086077 | TGAGGCATGGGCGGC[-/TGGA]TTTCCCCAGTGGGAA | 66053 |
rs229148719 | snp | A/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111479 | AGGCAGACTCACTCA[A/G]ACTCACCTCCTTTGT | 66053 |
rs229226999 | snp | C/T | | | synonymous-codon | Ppil2 | Mm_Celera | 16:17091255 | AAGGTTGGGACGGAA[C/T]TCATCTTTGAAAGGC | 66053 |
rs229252816 | snp | G/T | | | synonymous-codon | Ppil2 | Mm_Celera | 16:17089192 | CTGGCGGTATGTCTG[G/T]GGTCCCTGGTTTCCA | 66053 |
rs229334824 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17090057 | CTGGGGAAAGGCAGT[A/G]AAGGCCCACACTGCA | 66053 |
rs229399176 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17098996 | ACCAATCATCTTTCA[C/T]CTAGATTCTGCCCAC | 66053 |
rs229633725 | in-del | -/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102987 | TTTTTGGTTGGGGGA[-/G]GGGGGTTGGCAGAGT | 66053 |
rs229690965 | in-del | -/TC | | | intron-variant | Ppil2 | Mm_Celera | 16:17101946 | TGGCCATGGCTGGCT[-/TC]TCTCTTTCTACCTTC | 66053 |
rs229801004 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | Ppil2 | GRCm38.p3 | 16:17096744 | GGAAAAGGGCTCATC[A/G]GTCAACAGATCCCGC | 66053 |
rs229824133 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17087540 | AGTGTACCGGGCTGG[A/G]GAAGTGTCAAGAACA | 66053 |
rs230053988 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094399 | AAAGACAGCACCTAT[C/T]GGCTAAATGTGCTAA | 66053 |
rs230090401 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094842 | GCCCCGTGAGCACCT[C/T]CCCTGGGATCTTTCT | 66053 |
rs230157212 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103072 | CTACTGGGCTATAGC[C/T]CCAAGCCAAGGGCTC | 66053 |
rs230181838 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110753 | AAAAGCTGGATACTA[A/G]ATCTGGCAATACAGA | 66053 |
rs230202505 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086686 | GAGATTTTTTTTCCC[C/T]TCAAAAGTCCTTTAT | 66053 |
rs230341532 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17087995 | AGCTAGGCATGGTGG[C/T]GACTGCCTTTAATCC | 66053 |
rs230410162 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17092957 | AAGCAGGAAGCCCCA[C/G]TTGCTACAATGTGAG | 66053 |
rs230460453 | in-del | -/AAAG | | | intron-variant | Ppil2 | Mm_Celera | 16:17109391 | AAAACAAAAAACAAA[-/AAAG]AAAGAAAGAAAGAAA | 66053 |
rs230511147 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17088995 | AGTGCTGCTCCCACA[C/T]AGCCCAGCCAGTAAG | 66053 |
rs230708897 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17096311 | TGGACTGGGAAGCCA[C/T]TGGACCAAGCTTCAG | 66053 |
rs230925014 | in-del | -/GTGCCG | | | intron-variant | Ppil2 | Mm_Celera | 16:17091065 | AGGCTTCATCTAGGT[-/GTGCCG]TACTTTGATTGGATT | 66053 |
rs230934147 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086596 | CTTGTTGTCTTGTTA[C/G]TGTATACATAGTATT | 66053 |
rs231000770 | in-del | -/TAAGC | | | intron-variant | Ppil2 | Mm_Celera | 16:17092419 | CTGACTTCTAAGAGT[-/TAAGC]TAAGCTACAGAGTCC | 66053 |
rs231032049 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101826 | AGCAAGATAGCCCAA[C/T]CAACTATAAAAGGGG | 66053 |
rs231115107 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109075 | AGCCATCTGTAACTC[C/T]AGTTCCAGGGGATCT | 66053 |
rs231125711 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17098116 | CAATAGACAATGGGG[G/T]GGGAGAGCAAACAGT | 66053 |
rs231219921 | in-del | -/CACA | | | intron-variant | Ppil2 | Mm_Celera | 16:17105916 | ACCTGGGTGGGCAGG[-/CACA]CACACACACACACAC | 66053 |
rs231225721 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17107168 | AAAACAGAAGGATTT[A/G]AAGCTCTCACCTGCA | 66053 |
rs231370730 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17099275 | TCGCCCATGTCACTT[A/G]CACCAGAGTAAAAAG | 66053 |
rs231391648 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17092821 | TGAGCTCTGCACTTG[C/G]CCTGCACCCGAGATA | 66053 |
rs231494369 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17104991 | TTTTGCAAATTTTAG[-/A]AAAAAATGTAGGATG | 66053 |
rs231540761 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17095455 | GGCTGTAACTTACTG[A/G]GCAGTGAGCTTCCCT | 66053 |
rs231831217 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090203 | AGCAGGCTGTCCCAA[C/T]AGTGTGCTCTAGGCT | 66053 |
rs231930833 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17105209 | CCTGAGGCCTGGTGG[C/T]CCCTCCCAGTTACCA | 66053 |
rs231937667 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17095819 | AGACATGGTTGTGTA[C/T]GCTTGTAATGCCAGC | 66053 |
rs232023465 | in-del | -/TCA | | | intron-variant | Ppil2 | Mm_Celera | 16:17105748 | CCGGGAGCCTGCTGG[-/TCA]GCCAGTCTTGCTGAC | 66053 |
rs232067292 | in-del | -/GGAAGTGGAGAG | | | intron-variant | Ppil2 | Mm_Celera | 16:17087602 | CATGCAACAGCAGCT[-/GGAAGTGGAGAG]GGAGGGCAGTAGAGC | 66053 |
rs232068158 | in-del | -/GAGA | | | intron-variant | Ppil2 | Mm_Celera | 16:17090442 | GGAAGGAAATGGAGT[-/GAGA]GACTCAAGCCCATCA | 66053 |
rs232096964 | in-del | -/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104347 | AAGGGGAGCAGGGCA[-/G]CGGTGGCGCACGCCT | 66053 |
rs232127047 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17093937 | GTCAAGTGTTCTTAA[A/C]AACAGATCCATTTCT | 66053 |
rs232165034 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090967 | ACCTACCTAGAGAGG[A/T]CTTTGGTGCCTATCT | 66053 |
rs232180881 | in-del | -/TTT | | | intron-variant | Ppil2 | Mm_Celera | 16:17103344 | TTCCACAAATACTTC[-/TTT]ATGAGCATAGCTGAC | 66053 |
rs232183059 | snp | A/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112515 | GCTTCTTACTTCATA[A/G]CTTCTGCCTTCCAAA | 66053 |
rs232186012 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17088094 | AGGACAGCCAAGGGT[-/A]ATGCAGACAGACTGT | 66053 |
rs232186604 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102230 | GCCGTGTCCAGCAGT[C/G]TCTGGGATGCCCGAG | 66053 |
rs232233965 | in-del | -/TT | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111683 | GGGTCCCAAGTCTCC[-/TT]TTTTTTTTTTTTTTT | 66053 |
rs232292331 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100018 | TCAGTGGTTAAGAGC[A/G]CTGTCTGCTCTTCCA | 66053 |
rs232363038 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100587 | ACTATGTAAGGGGTA[C/G]TCACTGGGCTGAATA | 66053 |
rs232402855 | in-del | -/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111990 | CCACCCTAAGCTGGG[-/T]TTTTTGTTTGTTTTT | 66053 |
rs232440000 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103044 | AAAGCAAATGAGCAA[G/T]GCTAGTACTCTACTA | 66053 |
rs232565411 | in-del | -/T | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086338 | AAACCATTTATCAAG[-/T]GTTTTTTTGGATTTT | 66053 |
rs232615206 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17104615 | CTTTCCCCTGAGCTA[C/T]ATTTGGCGTCTGCAG | 66053 |
rs232736362 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17097534 | TTAACTGTAGCTACC[C/T]AGGAAACTAAGGCAG | 66053 |
rs232778388 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17095332 | GGGAGTCACCCTGTT[C/T]CCTGTATTACCTCTA | 66053 |
rs232933712 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17099077 | TGCCACACATGCGTG[A/C]ACACACACCTCACTC | 66053 |
rs233191181 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17098311 | AGAAACCCTGTCTCG[-/A]AAAAAAAAAAAAATT | 66053 |
rs233196460 | snp | C/G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17105075 | GCAGGGGACTCTGCA[C/G/T]CTCTCACCATGCAGA | 66053 |
rs233263893 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17105497 | TGGCTCAATGGTTAA[A/G]AGCAATGACTGCTCT | 66053 |
rs233368215 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103000 | GGAGGGGGTTGGCAG[A/G]GTGCCAGAATGTAAT | 66053 |
rs233490230 | snp | A/C | | | intron-variant, utr-variant-3-prime | Ppil2 | Mm_Celera | 16:17088715 | AAAGCTCAGGGACAG[A/C]CCCAGAAGCCCACAG | 66053 |
rs233519438 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17106999 | ATAAATAAATCTTTT[A/T]AAAAAATCTATGCAA | 66053 |
rs233556157 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17110827 | GAAGAGACAACAGAA[A/T]ACAGAAAGTACAGCA | 66053 |
rs233560143 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17110891 | CGCCTATCTTCAACT[C/T]GAAGGCTGTCGCCTG | 66053 |
rs233583907 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101003 | AAAACAGGCTCAGCA[A/T]GTGAAGGTGTTTATC | 66053 |
rs233639810 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086208 | CTTTATGCTCTGGGC[A/G]TGCTATCTGCCCCTC | 66053 |
rs233664415 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086783 | TAAGCTATAGACAAC[C/T]GACCCATGGAAATGC | 66053 |
rs233683320 | in-del | -/GAGTT | | | intron-variant | Ppil2 | Mm_Celera | 16:17092415 | CAGTCTGACTTCTAA[-/GAGTT]AAGCTAAGCTACAGA | 66053 |
rs233870155 | in-del | -/GGAA | | | intron-variant | Ppil2 | Mm_Celera | 16:17098560 | AGGGTGAGGGGGGGG[-/GGAA]TAGGGGCTTGGGGGG | 66053 |
rs234003022 | in-del | -/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102931 | CCACCCAGTAGGTTA[-/G]AGTCTTAAACGCTTT | 66053 |
rs234029185 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17110665 | AAAACAAAAACAAAC[-/A]AAAAAAAACTACTAA | 66053 |
rs234238717 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17110098 | AGTCAAAGATCAAGG[A/C]GAGTACTCTCTATTT | 66053 |
rs234398954 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109334 | GGACATCCAAGGCTA[C/T]ACAGAGAAATTCTGC | 66053 |
rs234420653 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17103378 | AATCAAGAACATGGA[A/C]TCTGCACGAGTGCCA | 66053 |
rs234505085 | in-del | -/AAGT | | | intron-variant | Ppil2 | Mm_Celera | 16:17092938 | GCAGATGCGGATGAG[-/AAGT]AAGCAGGAAGCCCCA | 66053 |
rs234634441 | snp | C/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111331 | CTGGGTGCAGGCACC[C/G]TGCTAGGCTGAAGCT | 66053 |
rs234658629 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17105399 | CTTAGTGGATAAAGG[A/G]CTTTCTCCACAGCAC | 66053 |
rs234704691 | in-del | -/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17091519 | TGGAGTTGGAGGCTT[-/G]GGGGAAGATTGCTGT | 66053 |
rs234720834 | snp | A/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111705 | TTTTTTTTTTTTGGT[A/T]TTTCGAAACAGGGTT | 66053 |
rs234746942 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103496 | TCCCCTGCTGAAAGC[A/G]TGAGAGCTGCACAAA | 66053 |
rs234840571 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17089755 | AGGACTGGCAGACAG[G/T]GCAGAGCCTCAGAAA | 66053 |
rs234863193 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | 2610318N02Rik, Ppil2 | Mm_Celera | 16:17113253 | CTTGTTACAGTGCAC[A/G]TGAGGGGCCATTGCA | 66053 |
rs234878688 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17090538 | CAGTCTGTAAACAGG[A/G]GAGAGCAAAAGGCTG | 66053 |
rs234977172 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17101622 | GAGGCTTGTTCTGTC[A/G]ACCCACTAGAAACAG | 66053 |
rs235022741 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17099740 | ACAGCCCACGGCCTC[C/G]GCCAGGTACAGCTCA | 66053 |
rs235545981 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112821 | TTCTTGGCCACCCCA[C/T]TCACCTCTCTCATAG | 66053 |
rs235645193 | in-del | -/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17098824 | TGCCATGCATGGACA[-/C]CCTCTAGCACACCTC | 66053 |
rs235752659 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17110469 | GGGGAGGGGAAGCCC[A/C]GCAAAGAGGAATGAA | 66053 |
rs235808896 | snp | A/G | | | synonymous-codon | Ppil2 | Mm_Celera | 16:17093045 | GGGCACCATGGCAGT[A/G]GAGGTGAAGGATGCA | 66053 |
rs236020102 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102376 | AGACACCCACCAGGG[A/G]CCGCAAGGAAAGGCG | 66053 |
rs236037802 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17093705 | AGATCCCCTAGATAG[C/T]TGTGAGCTGCTATGT | 66053 |
rs236162664 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104684 | TGGGCAAAAGGGCAA[A/G]CAAATGTGAGTATAT | 66053 |
rs236276294 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17087501 | AGTCTGGCATGTGAA[C/T]TGCCATCCCAGGCAG | 66053 |
rs236443261 | snp | A/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112733 | AGTTCAAGTCCTCCT[A/G]GTCTACATATTGAGT | 66053 |
rs236508073 | in-del | -/AG | | | intron-variant | Ppil2 | Mm_Celera | 16:17090801 | CCTCACCCAGCAAAC[-/AG]GGGCATTTCTGAGGC | 66053 |
rs236544482 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17101520 | GAGGCAGCAGCTTGG[A/G]AACGGAAGTGGCAGA | 66053 |
rs236585216 | snp | A/G | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088243 | TGCAGAAAGGTAGGC[A/G]ACAGAGTAGACAGGA | 66053 |
rs236627545 | in-del | -/CAG | | | intron-variant | Ppil2 | Mm_Celera | 16:17105181 | TGCAACAGCATCTGC[-/CAG]CAGCTAGTGCTGCCT | 66053 |
rs237059106 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086951 | CCAGCAAGCTCGAGC[A/G]AACAGAGCGCCTTGG | 66053 |
rs237172000 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17095963 | AGGAAGGACTTGCCC[A/G]AGAACATGTAGTCAC | 66053 |
rs237251469 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17105688 | GCTAAAGACAGCACC[C/T]ATCTGTAACTTTAGT | 66053 |
rs237287882 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17097166 | GCAGCCCAAACTGCC[A/G]GCCTGGGTTTGAGGT | 66053 |
rs237352711 | in-del | -/GGACCAAG | | | intron-variant | Ppil2 | Mm_Celera | 16:17102094 | GGCCATCCTGAGTAC[-/GGACCAAG]GGCTCTCACCCACAT | 66053 |
rs237542498 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17110944 | CCAGGACGAAGCGGA[C/T]AACCAACTCAGGGGC | 66053 |
rs237624237 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17100249 | TGTGTCCTAAAGGGA[G/T]CCTCACCTTCGCTGT | 66053 |
rs237630784 | in-del | -/AGTAAA | | | intron-variant | Ppil2 | Mm_Celera | 16:17098607 | ATGAAGAAAATATCT[-/AGTAAA]AATAAGTGGAAAAAA | 66053 |
rs237662016 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090682 | TATCCCTACCCAGAG[C/T]GGCAAGAGGACAGTC | 66053 |
rs237840874 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104854 | CAGTGAGACTCCCCC[A/G]CCCTCTGCACTCACC | 66053 |
rs238306477 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086887 | GCTGCTGAGCAAGGC[A/T]GACTGCAGTGCTGTG | 66053 |
rs238338342 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090820 | GCATTTCTGAGGCCA[C/T]CAAGCACACACTGTG | 66053 |
rs238412744 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17099657 | GGAAATGCCTCCCTA[A/C]CACCACAACCACAGT | 66053 |
rs238449986 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100479 | CAGCCAGGACTCCTG[A/G]GGCTTCTAGGATATT | 66053 |
rs238498845 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17111102 | AGATGATAGCCTTCA[G/T]CACGGCGACGAGCTG | 66053 |
rs238500888 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17100606 | CTGGGCTGAATAAGG[A/C]GGGTGTGGAATAAAG | 66053 |
rs238556669 | snp | A/G | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088336 | AGACCATAAGACCCC[A/G]TCACAATAGCCTGGG | 66053 |
rs238600519 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17101445 | TAACAGAAAAACAAC[A/G]TCCAGCAGAAAAGAG | 66053 |
rs238653120 | in-del | -/ATAT | | | intron-variant | Ppil2 | Mm_Celera | 16:17108966 | TTAAAAGAGAAAAAA[-/ATAT]ATATATATTTATGGG | 66053 |
rs238670774 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17097978 | CCAGACAGAGACCCC[A/G]TCTCCACCACTTTCG | 66053 |
rs238842981 | snp | A/G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17104540 | GTTTTCAAATACATC[A/G/T]GGGTGAGAGTTTTTC | 66053 |
rs239005735 | in-del | -/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17099295 | AGAGTAAAAAGGAGA[-/C]CCCCTTAGCCAAGAC | 66053 |
rs239121456 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17110725 | TTTGGAAAGGGAAGA[A/T]GCCCAAGGACTGAAA | 66053 |
rs239364947 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102493 | AGGGAGCTGCAGGGT[A/G]ACATTCCTAGGTTGA | 66053 |
rs239364970 | snp | A/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17112958 | TAATGTCCAGTAATG[A/T]TTGACATCTTACATG | 66053 |
rs239405603 | in-del | -/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17098552 | TGGGGAGCAGGGTGA[-/G]GGGGGGGGTAGGGGC | 66053 |
rs239452973 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094296 | TGAACTTTGGTTTTC[C/T]ACATTTTCCTAGAAA | 66053 |
rs239531043 | snp | A/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112140 | GTGTGTGCCACCACC[A/G]CCTGGCTGATCAAAG | 66053 |
rs239552838 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17111034 | GTAGAACGCCCTGGC[C/T]CGCGTAGGCTGCACT | 66053 |
rs239565321 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17091541 | GATTGCTGTGCTCTG[C/T]AGGAGCAATGGGGGC | 66053 |
rs239613690 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17093483 | CCAACACAGTTGTTT[-/A]AAAAAAAAAAGATGA | 66053 |
rs239658919 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103291 | ATAATTATTTTCTGA[A/T]ACTGCTTAGCAAACA | 66053 |
rs239702653 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101085 | ACACACACACCCTAG[C/T]GAGAGCATCTACATA | 66053 |
rs239730437 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103633 | AACAATGTTCCTGAT[G/T]GGAAGAGAGAACAAA | 66053 |
rs239800522 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094253 | ACCCAGAAGTGCAAT[A/G]GCTGTGTTCAGCTTG | 66053 |
rs240055049 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17109234 | GGCAGTGGCAGTGCA[C/G]GCCTTTAATCCCAGC | 66053 |
rs240430861 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17101496 | AGGACAACTGTAGAC[-/A]AGGTAGCAGAGGCAG | 66053 |
rs240612349 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17106314 | GTCAGACTAAGCTTC[A/G]CCCCGGGGCATCCTC | 66053 |
rs240634989 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17108493 | TTAAGATGGATTATC[-/A]ATGAGGACAACACAC | 66053 |
rs240794465 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103780 | CAGTTCCAGAGGATC[C/T]GTGTCCTCTCCCAGC | 66053 |
rs240842376 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17107952 | CCTCTGGCCTCTAAG[A/G]GCAGGTATCTATTCA | 66053 |
rs240915990 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17089327 | CCCAAGGGCTGGCTC[C/T]TCTCACCCCCAGCTA | 66053 |
rs241274159 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, intron-variant | Ppil2 | Mm_Celera | 16:17103594 | TCCAGTGCTGGGATT[C/T]GTCCCATACTTCTTA | 66053 |
rs241309379 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17087929 | ACACGTGGGCCCCCC[A/G]AGGCCTTTTCAGCTG | 66053 |
rs241325052 | snp | C/T | | | missense | Ppil2 | Mm_Celera | 16:17094959 | TCTCCTTTGAACTCT[C/T]TGTAGAGCTCCTGTA | 66053 |
rs241344210 | snp | C/T | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088480 | TTGGTATTCTGAATG[C/T]TGGGACTACAGGAGC | 66053 |
rs241795720 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17097316 | GGCACACGTTCGGGC[C/T]CAACATTAGATAGTC | 66053 |
rs241930672 | snp | A/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111947 | CTCTTTGCCAGACTT[A/G]CACAGCTCTTATTTG | 66053 |
rs242030494 | snp | G/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111877 | AATTGTGTGTGTGGT[G/T]AAATAGTGGCCATGC | 66053 |
rs242337324 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090959 | TCTGCCTGACCTACC[C/T]AGAGAGGACTTTGGT | 66053 |
rs242365521 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17091828 | ACATTTATTATTCCA[A/T]CAGAACAAGGCTGGC | 66053 |
rs242441475 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17108780 | TTTTTTGAGATGGTA[C/T]TTCTCTGTATAGCTC | 66053 |
rs242542826 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17102097 | CATCCTGAGTACGGA[C/T]CAAGGGCTCTCACCC | 66053 |
rs242637010 | in-del | -/A | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17093455 | CTCAGCACTTGGATT[-/A]AAGGTGTTTGTCACC | 66053 |
rs242657079 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100125 | GCTGTGTCAGCAACA[A/G]GATGCTCATACAACA | 66053 |
rs242740294 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17087869 | TGTGGAAAGGTTCCC[A/T]GGGAGCAAAGCACTG | 66053 |
rs242804690 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17109948 | GGGAAGCCCTTTACA[A/G]GAATAACACTTACTG | 66053 |
rs242937496 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17091128 | CTCTTAGGTCCTTTG[A/G]ATATCACCCCCAGCA | 66053 |
rs242948994 | in-del | -/AAC | | | intron-variant | Ppil2 | Mm_Celera | 16:17105637 | ACTAACTAAAAAAAA[-/AAC]CAAAAAACAAAAAAC | 66053 |
rs243003463 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17100062 | TCAATTCCCAGCGAC[C/T]ACATGGAGGTTCACA | 66053 |
rs243070544 | in-del | -/AAA | | | intron-variant | Ppil2 | Mm_Celera | 16:17104195 | TAATAAATAAATCTT[-/AAA]AAAAAAAAAAAAGGA | 66053 |
rs243084219 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090349 | TCTCCGGAGAAAGCC[G/T]GAGTTTGGTTGCCAG | 66053 |
rs243086183 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17100792 | ATTGAGATGGCATTC[A/T]ATATCACACAAGCCT | 66053 |
rs243188035 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094605 | AACACCAAAGAAAGC[A/G]GGAACATTGGTCACT | 66053 |
rs243321577 | in-del | -/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17102324 | CCCCAACCCCTCCCA[-/C]CCCCCTTCAGCTGGG | 66053 |
rs243350361 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094131 | CGTGTGCCACCACCG[C/T]CTGGTCCCAGGTTAT | 66053 |
rs243686937 | snp | C/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113078 | CACTCATTTCTCCTC[C/T]GGGTAGAAACACCTA | 66053 |
rs243690379 | in-del | -/TGCC | | | intron-variant | Ppil2 | Mm_Celera | 16:17093263 | ATAGGTAAAAAGTGT[-/TGCC]TGCCACACTTGCACT | 66053 |
rs243786792 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103359 | CATGAGCATAGCTGA[C/T]TGAAATCAAGAACAT | 66053 |
rs243946537 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17095176 | AGGTGAGTTGATTAG[A/G]GCAGGGTTCGCTGGT | 66053 |
rs244058336 | in-del | -/CAGT | | | intron-variant | Ppil2 | Mm_Celera | 16:17089374 | CTGATACAGAGCCTC[-/CAGT]GTGCCCTCCTGCTCC | 66053 |
rs244064693 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17095534 | TAGCTGGCTCCTTGG[C/T]ATGGCACAAGTGAGC | 66053 |
rs244219173 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094831 | AATGCATCTAGGCCC[C/T]GTGAGCACCTCCCCT | 66053 |
rs244223003 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104291 | CCGGCGAGAGTGGAG[A/G]GCAGGCGGCACCTTA | 66053 |
rs244331650 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17098971 | CTAAAACAGAGAAGA[C/T]ATCTGATGCACCAAT | 66053 |
rs244409759 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17106466 | TGTGTCTGCAGCTGT[A/G]AGCTGCCTGGGCCAC | 66053 |
rs244456662 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17109547 | TGTCCTCTTTTTATC[-/A]ACTATGGACCGTCTC | 66053 |
rs244485433 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17097726 | GACAGGGAGGACGGG[A/T]CAGAGGAGGAAAAAA | 66053 |
rs244568327 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17093256 | CCTACTCTATAGGTA[A/G]AAAGTGTTGCCACAC | 66053 |
rs244872375 | in-del | -/TATCCAGA | | | intron-variant | Ppil2 | Mm_Celera | 16:17099379 | TAGCTGTAGCTACAT[-/TATCCAGA]TATCCAGATAGGCAA | 66053 |
rs244896593 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17105377 | ATATAGAGTGCTGGG[A/G]AGACAACTTAGTGGA | 66053 |
rs245056276 | snp | G/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111322 | GTCCAGGTGCTGGGT[G/T]CAGGCACCGTGCTAG | 66053 |
rs245103799 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109498 | TTAAGTATTCTCCTC[G/T]AAGATGGAAGTATAC | 66053 |
rs245204559 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17109033 | TTCCAGAGGACCCAT[A/G]TTCCCAACACCCACA | 66053 |
rs245269468 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17109812 | AAACATCTGCATTGT[C/G]TGGCACATAAGAAGG | 66053 |
rs245427376 | in-del | -/AGC | | | intron-variant | Ppil2 | Mm_Celera | 16:17104096 | GGGCCAACCAGAGTG[-/AGC]AGAGGTCCAAAATTC | 66053 |
rs245486109 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17101142 | TTGTAAAAGGAAACA[A/C]AGCACTGAAAGTGGA | 66053 |
rs245488963 | snp | A/C/T | | | upstream-variant-2KB | Ppil2 | GRCm38.p3 | 16:17111424 | CCCTCAAAAACTTTT[A/C/T]TATGCACTGTCTGGC | 66053 |
rs245560720 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101738 | CCAAGCTCCTGACAT[C/T]CTGGTTAGACTCCAC | 66053 |
rs245618703 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17088889 | GTGAAGAAAAATACT[C/G]CAGTTGCCACAAAAG | 66053 |
rs245619391 | snp | A/G | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088458 | CCCTATATAGCCAGG[A/G]TTGGTCTTGGTATTC | 66053 |
rs245646596 | in-del | -/TTTTT | | | intron-variant | Ppil2 | Mm_Celera | 16:17093765 | CAAAGTCAAGTGGGG[-/TTTTT]TTTTGTTTGTTTGTT | 66053 |
rs245881226 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17098773 | AGTGCCCAGCCTCTA[C/T]CCCTGGCTGAGATGG | 66053 |
rs245936778 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17096148 | ACCCACCTGTGCCAG[A/G]TGTTGAAGGCTGGAA | 66053 |
rs245997595 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110922 | TGTGTAGGCTCTCAG[A/G]CTAGAGCCAGGACGA | 66053 |
rs246309060 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112442 | GGTCTGATTCTCATT[C/T]GGCAGGATTAACAAG | 66053 |
rs246410540 | in-del | -/TTG | | | intron-variant | Ppil2 | Mm_Celera | 16:17099466 | CAGTCTGATCCTTTT[-/TTG]TTGTTGTTGTTTTTT | 66053 |
rs246597559 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094478 | TGCTCGTCCCCGGTA[A/G]GGCCCAGGTAAGGGC | 66053 |
rs246644799 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17091370 | GCCGTGTCCTTGAGG[C/T]AGCCTCCCTGATTAC | 66053 |
rs246664185 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104563 | AGTTTTTCTGGTGCT[A/G]GCGAGTGAACAAAGG | 66053 |
rs246704582 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17105105 | AGACCATCCAGCACA[C/T]CTCTACTGCACATCT | 66053 |
rs246868891 | in-del | -/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17091962 | CCCTGCCGACTAACT[-/G]GGACAGGCTTCCCAC | 66053 |
rs246895878 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094508 | CTGAGACCTTAGTAG[C/G]TATAGCAACCCTAGC | 66053 |
rs246938210 | in-del | -/A | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17093416 | ACTGGCCTTGAACTC[-/A]AGAGATCTGCCTTCC | 66053 |
rs246939468 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17092051 | GATGAGCACTGAAGG[A/G]CCAGCTATAAGATCC | 66053 |
rs246940372 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086503 | ATTCTGTGACTATTT[A/T]AAAGAGGTTTCCTCA | 66053 |
rs247263911 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103237 | CATTAAGCCATCTCC[A/T]GATTGCCTGCTACCT | 66053 |
rs247496660 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17089918 | CAGTTTGCTAAGGCA[A/G]GATCTTGTATGAACT | 66053 |
rs247544917 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17089930 | GCAGGATCTTGTATG[-/A]ACTATGGCTGCCTGG | 66053 |
rs247696588 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17087088 | AGGTGGGGGCGGCGG[C/T]GAGCCACGTTCGTTC | 66053 |
rs247718001 | in-del | -/A | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112330 | AGTTTGGGGGATATT[-/A]AAAAAAAAAATTCTC | 66053 |
rs247726949 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17099835 | CTTACTTAAACCACC[G/T]GGACCTTTGAGAAGT | 66053 |
rs247813056 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110873 | GGAACATGGAGCACG[A/G]CCCGCCTATCTTCAA | 66053 |
rs247827993 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086715 | ATTTTCTGATGAGCT[C/T]ATCAGGCAGTTTTCA | 66053 |
rs247946354 | in-del | -/TT | | | intron-variant | Ppil2 | Mm_Celera | 16:17104966 | GTATTTTTTTATTTT[-/TT]TATTTTTATTTTGCA | 66053 |
rs248077747 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17090078 | CCACACTGCAATCCA[A/C]ATATTTACAGCATCT | 66053 |
rs248223529 | snp | A/G | | | synonymous-codon | Ppil2 | Mm_Celera | 16:17089252 | CTCTGGATCCACCTG[A/G]TGCTGTGTCTTCTTC | 66053 |
rs248247511 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17099553 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCAC | 66053 |
rs248327820 | in-del | -/CAGTC | | | intron-variant | Ppil2 | Mm_Celera | 16:17089774 | GAGCCTCAGAAAGGT[-/CAGTC]CAGTCACCAGGCAGG | 66053 |
rs248338722 | in-del | -/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17108473 | TAGTATGAAAACAGA[-/T]TTTTTTAAGATGGAT | 66053 |
rs248585101 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17104154 | CAACCATCTGTACAG[C/T]TACAGTGTGTACTCA | 66053 |
rs248631501 | snp | A/G | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088461 | TATATAGCCAGGGTT[A/G]GTCTTGGTATTCTGA | 66053 |
rs248632560 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17099276 | CGCCCATGTCACTTA[C/T]ACCAGAGTAAAAAGG | 66053 |
rs248674608 | in-del | -/AA | | | intron-variant | Ppil2 | Mm_Celera | 16:17104196 | TAATAAATAAATCTT[-/AA]AAAAAAAAAAGGAAA | 66053 |
rs248718479 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17098128 | GGGTGGGAGAGCAAA[C/T]AGTCATATTACCTAC | 66053 |
rs248806518 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17105861 | TGGCTTCCACATATA[A/C]ATGTATCTGAACACA | 66053 |
rs248846393 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17089664 | CAACCCTGCAGCAGA[G/T]TGACAGAGTTGACTG | 66053 |
rs248919260 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17102836 | GGCTGGTAGCATGTG[C/T]GTCTACACTGGAGAG | 66053 |
rs248938676 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17087567 | AACAGCCATGGGTGA[A/G]CAGCAGTCATCCCTG | 66053 |
rs249387317 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112387 | CTTTAGGGAGATAAC[C/T]CTGTCTAACTGAAAA | 66053 |
rs249435504 | in-del | -/AG | | | intron-variant | Ppil2 | Mm_Celera | 16:17096877 | GGGCCACTCTGGGGT[-/AG]AGTCTCAAGAGTTCT | 66053 |
rs249796698 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103063 | AGTACTCTACTACTG[G/T]GCTATAGCCCCAAGC | 66053 |
rs249829129 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17110769 | ATCTGGCAATACAGA[A/T]GTCAAAGATATCCTT | 66053 |
rs249888738 | in-del | -/CT | | | intron-variant | Ppil2 | Mm_Celera | 16:17093122 | TACACCCTACAACCC[-/CT]GTCCTCAGTGCAGCC | 66053 |
rs249901423 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17102272 | GTTATCTCTGGTCTC[C/T]GTGAGGCCCAGAGAC | 66053 |
rs249922499 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17091716 | GCACAAGGTAGGCCA[C/G]AAGGCCAGCCACTGA | 66053 |
rs249943482 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17088019 | TTAATCCTACTTGGG[A/G]AGGTAGAGGCAGGTG | 66053 |
rs249965496 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17093902 | TGGGATTAAAGGCGT[A/G]CGCCACCATGCCCGG | 66053 |
rs249999260 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100517 | TGGTTGCACTGATGT[A/G]TCTGTAAGCCCCAGG | 66053 |
rs250038574 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101266 | AAGAAAGAACACACC[C/T]CCATGGGGTTCCATG | 66053 |
rs250182865 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17102394 | GCAAGGAAAGGCGTC[C/T]GCCTGCCCAGAGCAC | 66053 |
rs250239467 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17100544 | CAGGCTGTGAGCAGA[C/T]CCTCAGATTTATAAA | 66053 |
rs250422795 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110584 | TTCGAGGCCAGCCTG[A/G]TCTACAAAGTGAGTT | 66053 |
rs250725713 | in-del | -/A | | | intron-variant | Ppil2 | Mm_Celera | 16:17107795 | TCTTGGAGAAAAAAG[-/A]AAAAAAAAAATCTTC | 66053 |
rs250804702 | snp | C/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113210 | GAACGGGATTTCCCA[C/T]CCCACTCTCTCAAGC | 66053 |
rs250856780 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17098475 | GTATATATTTGATGT[C/G]ACCAGGGAATTCCTG | 66053 |
rs250901544 | in-del | -/TT | | | intron-variant | Ppil2 | Mm_Celera | 16:17094014 | TCAAGACAGGGTTTC[-/TT]TCTGTGTAGCCTTGG | 66053 |
rs250950281 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17107107 | AGCTGCAGTTAAAAC[A/G]CACACACCTGTTTTG | 66053 |
rs251054085 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17105602 | CTACAGCTAGTGTAC[G/T]TAAATAAACAAACAA | 66053 |
rs251123635 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17095849 | CACTTAGAAGGGAAA[A/C]ACAGGAGGATGCTGC | 66053 |
rs251194183 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103707 | CACTTGGTGCTCTTG[C/T]ACAGGGCCTGAACTC | 66053 |
rs251219723 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17095234 | TGATCATCTGGCAGG[A/G]GCTCTAGTAGGTGCA | 66053 |
rs251429421 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086269 | AGCTCTGACTGGAAC[A/G]TTTTTGCTAGTACTC | 66053 |
rs251457806 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17093938 | TCAAGTGTTCTTAAA[A/C]ACAGATCCATTTCTC | 66053 |
rs251725974 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17107729 | GCATTCAAGGCCAGC[A/C]TGGTATACAATGCAA | 66053 |
rs251981404 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17111040 | CGCCCTGGCCCGCGT[A/T]GGCTGCACTGAGGGA | 66053 |
rs252248810 | in-del | -/AG | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112708 | AGGCAGAGGCTGGTA[-/AG]AGTTCTGTAAGTTCA | 66053 |
rs252289334 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17099085 | ATGCGTGAACACACA[C/T]CTCACTCCCACCTGC | 66053 |
rs252331069 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | Ppil2 | Mm_Celera | 16:17100272 | TTCGCTGTTCTTTGC[A/G]AAGTTCAGCTTGATC | 66053 |
rs252359071 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17096487 | GAGTTATGAGGCAAG[C/T]GTAGCCCTCATACAG | 66053 |
rs252407483 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109344 | GGCTACACAGAGAAA[C/T]TCTGCCTCAAAAAAA | 66053 |
rs252433302 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17099602 | TGCTGGGATTAAAGG[C/T]GTGAGCCACCACACC | 66053 |
rs252441539 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110142 | GGGAAGCTGGTGGGT[A/G]ATTTTGAGCAGGACC | 66053 |
rs252872339 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17094691 | TTGCCATGGGACCCC[A/C]GCTTGTCAACCATTC | 66053 |
rs253225949 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17101828 | CAAGATAGCCCAACC[A/C]ACTATAAAAGGGGCT | 66053 |
rs253275873 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094859 | CCTGGGATCTTTCTC[A/G]GTCAGGCAGAGTGCC | 66053 |
rs253376075 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094414 | CGGCTAAATGTGCTA[A/G]AGAAATTCCAGCACC | 66053 |
rs253434364 | snp | C/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111512 | CTAAAGATCTTCAAC[C/G]TTTTTCACCTTCTCT | 66053 |
rs253441588 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103400 | CGAGTGCCAACTGTA[C/T]ATCCTCATCCGTGTG | 66053 |
rs253485878 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086120 | GACAGACCCGAGTAC[A/G]TCCTTATAGATGCCT | 66053 |
rs253511580 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103630 | GGGAACAATGTTCCT[A/G]ATGGGAAGAGAGAAC | 66053 |
rs253616290 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109921 | AGGAAGAGCTAGGCA[C/T]ACAAAGCTCTGGGGA | 66053 |
rs253711586 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17109967 | TAACACTTACTGAGG[C/T]TGGAACAGGACAAGC | 66053 |
rs253798261 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17092517 | CACTTACCAAGCAGC[C/T]AAGGAGGTATGTTGC | 66053 |
rs253854722 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17101646 | GAAACAGTGAGCCAC[A/G]TTCCCAGTGACAGGT | 66053 |
rs253937567 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17092644 | AAGGCAGGACTAGCC[C/T]GTGGCCCCAGGAACC | 66053 |
rs254023038 | in-del | -/CTGGAACGAGGTAT | | | intron-variant | Ppil2 | Mm_Celera | 16:17092112 | CTGGCCACACATGGC[-/CTGGAACGAGGTAT]CTGGAACCGGGAAGG | 66053 |
rs254434170 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17097197 | CCAAAGGCCACTAGA[A/G]TCACCTGACCTTTAT | 66053 |
rs254563290 | snp | A/G | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088269 | CAGGACAATAAACAC[A/G]CTTGTCCCAAGCAAG | 66053 |
rs254625607 | in-del | -/TT | | | intron-variant | Ppil2 | Mm_Celera | 16:17100151 | AACATTAAATAAATA[-/TT]TTTAAAAAAAAAAGA | 66053 |
rs254714788 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17106898 | AATCCCAGCAACCAC[A/G]TGGTGGCTCACAACC | 66053 |
rs254789240 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104403 | GGCAGGCAGATTTCT[A/G]AGTTCGAGGCCAGCT | 66053 |
rs254829945 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17104858 | GAGACTCCCCCACCC[C/T]CTGCACTCACCAAAG | 66053 |
rs254879313 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17096381 | CTCCCTCGAGGCCAT[C/T]CACACACCACCACGG | 66053 |
rs254969522 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17087040 | AAATAAAGCTCCTGT[C/T]GTCACACAGCAAGGT | 66053 |
rs255169094 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17087555 | GGAAGTGTCAAGAAC[A/G]GCCATGGGTGAACAG | 66053 |
rs255384257 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112744 | TCCTAGTCTACATAT[C/T]GAGTTACAGGTCAAC | 66053 |
rs255530719 | snp | A/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112570 | TAGCCCAGTATGGTG[A/G]TGTACACTTGGGAGG | 66053 |
rs255583074 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17101466 | CAGAAAAGAGGCAGA[A/G]GTCACAGAGATCATG | 66053 |
rs255843752 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110992 | AGGCTAGGGGTAGGG[A/G]AATCCCGGAAGTTAG | 66053 |
rs256085820 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17109096 | CAGGGGATCTAACAC[A/C]CTCACACAAACATAC | 66053 |
rs256110920 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17099734 | TCATGAACAGCCCAC[A/G]GCCTCGGCCAGGTAC | 66053 |
rs256134126 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110742 | CCCAAGGACTGAAAA[A/G]CTGGATACTAGATCT | 66053 |
rs256178197 | in-del | -/TTTTTT | | | intron-variant | Ppil2 | Mm_Celera | 16:17108558 | TTTGTTGTTGTTTGC[-/TTTTTT]TTTTTTTTTTTTTTT | 66053 |
rs256261947 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17109840 | AGGACAAAAGATGGA[A/G]AGATAAAGAAACATC | 66053 |
rs256409738 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17086906 | TGCAGTGCTGTGGAA[C/G]CCACAGGGAGTTCAC | 66053 |
rs256411661 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090821 | CATTTCTGAGGCCAC[C/T]AAGCACACACTGTGT | 66053 |
rs256566381 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17105735 | GAAACAGGTGGAACC[A/G]GGAGCCTGCTGGTCA | 66053 |
rs256586977 | in-del | -/AAAAA | | | intron-variant | Ppil2 | Mm_Celera | 16:17098610 | AAGAAAATATCTAAT[-/AAAAA]AAGTGGAAAAAAAAG | 66053 |
rs256966380 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17104781 | AGTGTGGTGTAAGCT[C/T]AGCTACTTGGGAGAT | 66053 |
rs257122530 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100040 | GCTCTTCCAGAGGTC[C/G]TTTAGTTCAATTCCC | 66053 |
rs257193552 | in-del | -/AC | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111547 | CATGTCCATGTGTAT[-/AC]ACTCAACTCTTCTCT | 66053 |
rs257194190 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102523 | AACAGCAGCAGAGGT[C/G]AGCAAAGCAGAGCAC | 66053 |
rs257241121 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17093978 | TCTGTTTGTTTGTTT[A/G]TTTTTGTTTGGTTTT | 66053 |
rs257241215 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17103305 | AAACTGCTTAGCAAA[A/C]AATGACAAGAAAAAG | 66053 |
rs257401551 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094368 | CAGGCTCTCCAGACT[A/T]CAGTCTACTTGGGAG | 66053 |
rs257507207 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094546 | GCCATCACAGATCTG[C/T]ACACCCTCCTATCTC | 66053 |
rs257549663 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104251 | TAGCTGGCAGTGGCA[A/G]TCCCTGAGGCCTTAG | 66053 |
rs257673562 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17097615 | AGTGGAATTCTAAAA[A/G]GGAGTGGCAGCAGGG | 66053 |
rs257685598 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17091637 | TTCACCTCCCTGTCT[C/T]GTTATGGTAGGACCC | 66053 |
rs257793542 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17087959 | GATACCCTGACAACT[A/G]TCCTAGAATCAAAAG | 66053 |
rs258255635 | in-del | -/AACT | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112667 | TCAAAAGCAAATCAA[-/AACT]AAACAAAACTACCAG | 66053 |
rs258284192 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110681 | AAAAAAAACTACTAA[A/G]CGCATGTAAGATCTC | 66053 |
rs258379905 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17106319 | ACTAAGCTTCGCCCC[A/G]GGGCATCCTCCCCGT | 66053 |
rs258413945 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17108326 | CACTTGATGCTATTG[C/T]AGAAGACCAGAGCTT | 66053 |
rs258509255 | in-del | -/TGTGCCCCAACCCAGTG | | | intron-variant | Ppil2 | Mm_Celera | 16:17096176 | GAAGGAGGCCAAGGC[-/TGTGCCCCAACCCAGTG]ACAAGCAAGATGGCA | 66053 |
rs258579799 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17087699 | CAGGTACTAGCTACA[C/T]CCCAGAACCAAGAAC | 66053 |
rs258633615 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17094264 | CAATAGCTGTGTTCA[A/G]CTTGGGAAATTATAG | 66053 |
rs258713388 | snp | C/T | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088489 | TGAATGTTGGGACTA[C/T]AGGAGCCCCTTGAAA | 66053 |
rs258764450 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103012 | CAGAGTGCCAGAATG[C/T]AATCCAAAGCCTTCT | 66053 |
rs258770641 | snp | C/T | | | synonymous-codon | Ppil2 | Mm_Celera | 16:17094991 | CGTCTCTCTCGTCTC[C/T]GAATTTGTGTTTTTC | 66053 |
rs258855676 | snp | A/G | | | synonymous-codon, intron-variant | Ppil2 | GRCm38.p3 | 16:17109673 | ACCATAGAAATGAGT[A/G]TACTCAGCACAAGTG | 66053 |
rs259323141 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17099053 | ACATGCATGCACGCA[C/T]ACATGCACTGCCACA | 66053 |
rs259338072 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17087946 | GGCCTTTTCAGCTGA[C/T]ACCCTGACAACTGTC | 66053 |
rs259367039 | in-del | -/AG | | | intron-variant | Ppil2 | Mm_Celera | 16:17093349 | TTGGTTTTTGAGGTA[-/AG]AGTTTCTTTCTGTGC | 66053 |
rs259563635 | snp | C/G | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111404 | ACTGCGTTGCCTCCC[C/G]CAAGCCCTCAAAAAC | 66053 |
rs259832529 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102167 | CTCCCTTTGGCCCCG[A/G]GACTGACCAAGGTGC | 66053 |
rs259870216 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17093139 | GTCCTCAGTGCAGCC[G/T]CCCTGACCACCACTC | 66053 |
rs260041543 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17108808 | CTCTGGCTGTCCAGG[A/G]ATTAAAAGCATGCAC | 66053 |
rs260047719 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17093893 | CCTGAGTGCTGGGAT[C/T]AAAGGCGTACGCCAC | 66053 |
rs260072483 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100196 | AAGGAAGTTGCTGAG[A/G]GTAAGAGCTCGGGGT | 66053 |
rs260459840 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17107777 | GCTACACAGAGAAAC[C/T]CTATCTTGGAGAAAA | 66053 |
rs260511602 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17104923 | GATCCTGGACAGTGA[C/T]GTCATTGGGGTAAAT | 66053 |
rs260637791 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104686 | GGCAAAAGGGCAAGC[A/G]AATGTGAGTATATCT | 66053 |
rs260991894 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094607 | CACCAAAGAAAGCGG[G/T]AACATTGGTCACTGA | 66053 |
rs261013842 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103096 | AGGGCTCTTGCCAAG[A/G]GAATGCCAACTGCAG | 66053 |
rs261247875 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086449 | GGCATGCTGGTAAAC[C/T]ACTGAATGTCTCACC | 66053 |
rs261382493 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101620 | ATGAGGCTTGTTCTG[G/T]CGACCCACTAGAAAC | 66053 |
rs261467645 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17111327 | GGTGCTGGGTGCAGG[C/T]ACCGTGCTAGGCTGA | 66053 |
rs261535058 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17109562 | AACTATGGACCGTCT[A/C]GTTATCTACTATAAT | 66053 |
rs261546093 | in-del | -/AAG | | | intron-variant | Ppil2 | Mm_Celera | 16:17097775 | AGTGGTCAGAAAAGA[-/AAG]AAGGCAATACCTTAG | 66053 |
rs261681992 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17087533 | TGGCTATAGTGTACC[A/G]GGCTGGGGAAGTGTC | 66053 |
rs261828141 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | Mm_Celera | 16:17087048 | CTCCTGTCGTCACAC[A/C]GCAAGGTTCCCAGGG | 66053 |
rs262067501 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17093372 | TTCTGTGCATCCCTG[A/G]CTGTCCTAGAACTCA | 66053 |
rs262243197 | snp | C/T | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112143 | TGTGCCACCACCGCC[C/T]GGCTGATCAAAGAAT | 66053 |
rs262298827 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090715 | ACAGGGCCAACAGGA[C/T]AGCAGCCTTCCCCTG | 66053 |
rs262476839 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17092059 | CTGAAGGGCCAGCTA[A/T]AAGATCCCTGGCACA | 66053 |
rs262485456 | in-del | -/CTC | | | intron-variant | Ppil2 | Mm_Celera | 16:17090230 | GGCTAGTAATGACTG[-/CTC]CTCAATAGAAGCCCT | 66053 |
rs262815259 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17097682 | AGTACCACAGGAGAG[G/T]AGAGAGGGAAGAAGG | 66053 |
rs262863669 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17098077 | ATGATCTACCATCCA[A/G]CAGGGACCTTGTCTA | 66053 |
rs262872206 | in-del | -/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17098046 | TAGCTCTCCACCCAG[-/C]TAGCCAGCCCGATAG | 66053 |
rs262893044 | in-del | -/TT | | | intron-variant | Ppil2 | Mm_Celera | 16:17095772 | GGAAAGGTAGGTGTC[-/TT]TGTGTTTCAGCTGCT | 66053 |
rs262910766 | snp | C/T | | | intron-variant, downstream-variant-500B | Ppil2 | Mm_Celera | 16:17088391 | CAGACTAGGTAGGGT[C/T]TGAGTGAGGACCATT | 66053 |
rs262920794 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17089944 | GAACTATGGCTGCCT[A/G]GGTGTCTCCTCCTCT | 66053 |
rs262953598 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Ppil2, Ypel1 | GRCm38.p3 | 16:17086840 | TGGAGGACAGGAGAG[A/G]ACACAGCTGCCTGCC | 66053 |
rs263061076 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17095391 | TTTTGTGAATTTAAA[C/T]GTGTTTATTTCAAGG | 66053 |
rs263080460 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086531 | TCAGAACAGTGGGAG[A/G]TGATACCAGGTCATG | 66053 |
rs263262304 | in-del | -/ACAG | | | intron-variant | Ppil2 | Mm_Celera | 16:17102642 | CCTGGAACTTCATGA[-/ACAG]CAAGCAGCCACACTC | 66053 |
rs263353838 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103244 | CCATCTCCAGATTGC[C/T]TGCTACCTACCATAA | 66053 |
rs263368342 | in-del | -/TAAA | | | intron-variant | Ppil2 | Mm_Celera | 16:17108451 | CATACATATAAGTCT[-/TAAA]TAAAAAATAGTATGA | 66053 |
rs263401947 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17101419 | TTGCAAACCTAAGAT[A/G]CATCCAGGGGTAACA | 66053 |
rs263557288 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17102395 | CAAGGAAAGGCGTCC[A/G]CCTGCCCAGAGCACC | 66053 |
rs263564811 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17091939 | TGATGATGCTGATCA[C/T]CCCACACACCCTGCC | 66053 |
rs263576117 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17093911 | AGGCGTACGCCACCA[C/T]GCCCGGCCAAGTCAA | 66053 |
rs263614178 | snp | G/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17090961 | TGCCTGACCTACCTA[G/T]AGAGGACTTTGGTGC | 66053 |
rs263657489 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17099451 | GGGCAGAGGTGATGA[C/T]AGTCTGATCCTTTTT | 66053 |
rs263733084 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17100556 | AGATCCTCAGATTTA[C/T]AAACACACAAATATC | 66053 |
rs263924546 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17109330 | TCCAGGACATCCAAG[A/G]CTACACAGAGAAATT | 66053 |
rs264080924 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17104932 | CAGTGACGTCATTGG[A/G]GTAAATTGTTCTATT | 66053 |
rs264165091 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17098665 | TTGCTTTGTTTCATG[C/T]CAGGGTTTCTGAGTA | 66053 |
rs264198833 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17105408 | TAAAGGACTTTCTCC[A/G]CAGCACAAAAGCCTG | 66053 |
rs264299848 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17103364 | GCATAGCTGACTGAA[A/T]TCAAGAACATGGACT | 66053 |
rs264330224 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17103502 | GCTGAAAGCGTGAGA[A/G]CTGCACAAACAAAGC | 66053 |
rs264459324 | in-del | -/TG | | | intron-variant | Ppil2 | Mm_Celera | 16:17098472 | TGGGTATATATTTGA[-/TG]TCACCAGGGAATTCC | 66053 |
rs264514192 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17110795 | TCCTTGCAAGCAGCT[A/G]GGGGCGGGGAGCATC | 66053 |
rs264561096 | in-del | -/AT | | | upstream-variant-2KB | Ppil2 | Mm_Celera | 16:17112710 | GCAGAGGCTGGTAAG[-/AT]TTCTGTAAGTTCAAG | 66053 |
rs264579365 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113079 | ACTCATTTCTCCTCT[A/G]GGTAGAAACACCTAT | 66053 |
rs264606956 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17102378 | ACACCCACCAGGGGC[C/T]GCAAGGAAAGGCGTC | 66053 |
rs264640833 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17100980 | GTCTAACACTAGTAG[A/G]AAGCCCCAAAACAGG | 66053 |
rs264691916 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17108793 | TACTTCTCTGTATAG[C/T]TCTGGCTGTCCAGGA | 66053 |
rs264978334 | snp | C/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ppil2, 2610318N02Rik | Mm_Celera | 16:17113016 | GGTGACAATGAGAAT[C/T]ACAGTTTTGAAACTC | 66053 |
rs265042136 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | Ppil2, Ypel1 | Mm_Celera | 16:17086371 | GTTGGCCTTCTGTGA[A/C]ATATAAACCAAAAGA | 66053 |
rs265115122 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17091100 | TTAGGCTGAGCACAA[C/T]TTTTAGGGAGACCTC | 66053 |
rs265397394 | snp | C/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17088981 | AAGCCCCCCTCCACA[C/G]TGCTGCTCCCACACA | 66053 |
rs265451537 | snp | A/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17096155 | TGTGCCAGATGTTGA[A/T]GGCTGGAAGGAGGCC | 66053 |
rs265630576 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17101671 | ACAGGTGCCTGACAC[C/T]ACAGAACCCCAACTC | 66053 |
rs265686506 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094494 | GGCCCAGGTAAGGGC[C/T]GAGACCTTAGTAGCT | 66053 |
rs265767553 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17090184 | TACAGGGAGATGAGG[A/G]AGCAGCAGGCTGTCC | 66053 |
rs265771429 | in-del | -/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17094180 | ATGGAATAAAAGTAC[-/T]TTTTTCATCATATAG | 66053 |
rs265989519 | snp | C/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17097513 | ACAATCATGATAGTA[C/T]ATATTTTAACTGTAG | 66053 |
rs266018805 | snp | A/G | | | intron-variant | Ppil2 | Mm_Celera | 16:17106089 | CCTCGTCAGCTTCTA[A/G]GCACACTGAGCATGC | 66053 |
rs266041562 | snp | A/C | | | intron-variant | Ppil2 | Mm_Celera | 16:17103968 | TCAAATCCCAGCAAC[A/C]ACATGGTAACTCACA | 66053 |
rs266256707 | in-del | -/T | | | intron-variant | Ppil2 | Mm_Celera | 16:17097143 | GGCTACAAGGAATCC[-/T]TGCTTAGGCAGCCCA | 66053 |
rs578336314 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17104394 | GGAGGCAAAGGCAGG[C/T]AGATTTCTGAGTTCG | 66053 |
rs578398346 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17091740 | CCACTGAATGGCCAG[C/T]CACCCCCAAGTTTGA | 66053 |
rs578589458 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17099304 | AGGAGACCCCCTTAG[C/T]CAAGACCACAAAGGG | 66053 |
rs578620696 | snp | A/G | | | upstream-variant-2KB | Ppil2 | GRCm38.p3 | 16:17112112 | CTCTGCCTCCCAAGT[A/G]CTGGGATTAAAGGTG | 66053 |
rs578709595 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17105753 | AGCCTGCTGGTCAGC[C/T]AGTCTTGCTGACAGT | 66053 |
rs578729862 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17090616 | TGAGCTCGGCCCAGC[C/T]TGAGCTACAAGACCT | 66053 |
rs578949076 | snp | G/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17097805 | TAGGCCAGCTGCCAA[G/T]ACCTGGGAAGGCCAG | 66053 |
rs579325268 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17098253 | CAGGTGGATTTCTGA[A/G]TTTGAGGCAGCCTGG | 66053 |
rs579563886 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17108640 | ACACTCCAGAAGAGG[A/G]AGTCAGATCTCATTA | 66053 |
rs579605744 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17102114 | AAGGGCTCTCACCCA[C/T]ATGGGAACCACCCAG | 66053 |
rs579860955 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17109433 | GAAAGAAAGAAAGAA[A/G]GCTATAGCACTTCCT | 66053 |
rs580114003 | snp | A/C | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17099606 | GGGATTAAAGGCGTG[A/C]GCCACCACACCCGGC | 66053 |
rs580182660 | snp | G/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17093496 | TTTAAAAAAAAAAGA[G/T]GATGTCACGGAGTAG | 66053 |
rs580593957 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17100568 | TTATAAACACACAAA[C/T]ATCACTATGTAAGGG | 66053 |
rs580704238 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17094120 | GGGATCAAAGGCGTG[C/T]GCCACCACCGTCTGG | 66053 |
rs581158841 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17095493 | GCCTCTGGGTCTCCT[A/G]AGCGCAGTTATCCCT | 66053 |
rs581185423 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17104342 | TTAAAGAAGGGGAGC[A/G]GGGCACGGTGGCGCA | 66053 |
rs581268965 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17090816 | AGGGGCATTTCTGAG[A/G]CCACCAAGCACACAC | 66053 |
rs581357587 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17097993 | ATCTCCACCACTTTC[A/G]ACCTCTTCTCAATCT | 66053 |
rs581429767 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17110674 | AACAAACAAAAAAAA[C/T]TACTAAGCGCATGTA | 66053 |
rs581654162 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17087757 | AGGGTAAAAGGTCAA[A/G]CCTAAGTTACAATGT | 66053 |
rs581703297 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17104358 | GGGCACGGTGGCGCA[C/T]GCCTTTAATCCCAGC | 66053 |
rs581815612 | snp | A/C | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17098276 | CAGCCTGGTCTACAG[A/C]GTGAGTTCCAGGACA | 66053 |
rs581902815 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17104455 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 66053 |
rs582029874 | snp | A/G | | | upstream-variant-2KB | Ppil2 | GRCm38.p3 | 16:17112715 | AGGCTGGTAAGTTCT[A/G]TAAGTTCAAGTCCTC | 66053 |
rs582075126 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17091745 | GAATGGCCAGCCACC[C/T]CCAAGTTTGAAAGAT | 66053 |
rs582139193 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17099366 | GAGCAAGGCAGCTGT[A/G]GCTGTAGCTACATTA | 66053 |
rs582377291 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17099621 | AGCCACCACACCCGG[C/T]TGACAGTCTGATCTT | 66053 |
rs582381298 | snp | A/C | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17090431 | AGACTCTTTGGAGGA[A/C]GGAAATGGAGTGACT | 66053 |
rs582412010 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17105958 | ACACACACACACACA[C/T]AAAAAGAAATTTAAA | 66053 |
rs582740053 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17091528 | GAGGCTTGGGGAAGA[C/T]TGCTGTGCTCTGCAG | 66053 |
rs582811113 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17088086 | TAACTTCTAGGACAG[C/T]CAAGGGTAATGCAGA | 66053 |
rs582938192 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17108763 | CCAGCCCTGTTGTTT[A/G]CTTTTTTGAGATGGT | 66053 |
rs583056521 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17101042 | TGGCCTAACAGAGGA[A/G]AGAGAGAACCCCCAC | 66053 |
rs583160651 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17094121 | GGATCAAAGGCGTGT[A/G]CCACCACCGTCTGGT | 66053 |
rs583367241 | snp | G/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17102143 | AGCACCCCCTCTCCC[G/T]GCCCTCTCCTCCCTT | 66053 |
rs583391742 | snp | C/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17091747 | ATGGCCAGCCACCCC[C/G]AAGTTTGAAAGATTA | 66053 |
rs583952988 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17093863 | TCGAACACAGAAATC[C/T]GCCTGCCTCTGCCTC | 66053 |
rs584427335 | snp | A/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17105620 | AATAAACAAACAAAC[A/T]AACTAACTAAAAAAA | 66053 |
rs584606239 | snp | C/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17090450 | AATGGAGTGACTCAA[C/G]CCCATCATGAGCCCT | 66053 |
rs584721947 | snp | A/C | | | upstream-variant-2KB | Ppil2 | GRCm38.p3 | 16:17112794 | CAAAACAAAACAAAA[A/C]AAAAAAACACTTTCT | 66053 |
rs584903199 | snp | A/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17091070 | TTCATCTAGGTTACT[A/T]TGATTGGATTTAACT | 66053 |
rs584954301 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17104354 | AGCAGGGCACGGTGG[C/T]GCACGCCTTTAATCC | 66053 |
rs585108311 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17098038 | TCCTCACCTAGCTCT[C/T]CACCCAGCTAGCCAG | 66053 |
rs585344716 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17104359 | GGCACGGTGGCGCAC[A/G]CCTTTAATCCCAGCA | 66053 |
rs585556914 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17099506 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 66053 |
rs585622278 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17098550 | TCATGGGGAGCAGGG[C/T]GAGGGGGGGGTAGGG | 66053 |
rs585738396 | snp | C/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17091746 | AATGGCCAGCCACCC[C/G]CAAGTTTGAAAGATT | 66053 |
rs586052824 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17091531 | GCTTGGGGAAGATTG[C/T]TGTGCTCTGCAGGAG | 66053 |
rs586072988 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17093257 | CTACTCTATAGGTAA[A/G]AAGTGTTGCCACACT | 66053 |
rs586139543 | snp | A/C | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17105960 | ACACACACACACATA[A/C]AAAGAAATTTAAAAA | 66053 |
rs586248191 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17100567 | TTTATAAACACACAA[A/G]TATCACTATGTAAGG | 66053 |
rs586496132 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17108557 | TTTTTGTTGTTGTTT[A/G]CTTTTTTTTTTTTTT | 66053 |
rs586578296 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17090427 | CATTAGACTCTTTGG[A/G]GGAAGGAAATGGAGT | 66053 |
rs586602556 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17102078 | TAACCTCCCACCAGA[A/G]GGCCATCCTGAGTAC | 66053 |
rs586657481 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17102633 | GAAAAAGCTCCTGGA[A/G]CTTCATGAACAGCAA | 66053 |
rs586798279 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17109421 | GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAGGCT | 66053 |
rs586862590 | snp | C/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17094166 | ATATACAACAGTACA[C/T]GGAATAAAAGTACTT | 66053 |
rs586961615 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17087622 | TGGAGAGGGAGGGCA[A/G]TAGAGCAAGGCAGAC | 66053 |
rs587144983 | snp | A/C | | | utr-variant-5-prime | Ppil2 | GRCm38.p3 | 16:17111187 | CATGGTGGCAACAAA[A/C]CGAAGAGACCACAGC | 66053 |
rs587292574 | snp | A/C | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17110586 | CGAGGCCAGCCTGAT[A/C]TACAAAGTGAGTTCC | 66053 |
rs587492325 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17104355 | GCAGGGCACGGTGGC[A/G]CACGCCTTTAATCCC | 66053 |
rs587522558 | snp | A/G | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17093874 | AATCTGCCTGCCTCT[A/G]CCTCCTGAGTGCTGG | 66053 |
rs864264526 | snp | A/G/T | | | upstream-variant-2KB | Ppil2 | GRCm38.p3 | 16:17111712 | TTTTTGGTATTTCGA[A/G/T]ACAGGGTTTCTCTGT | 66053 |
rs864271322 | snp | A/T | | | intron-variant | Ppil2 | GRCm38.p3 | 16:17088079 | TACATAGTAACTTCT[A/T]GGACAGCCAAGGGTA | 66053 |