iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

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

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