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
rs3702238	snp	C/T	0.444444	0.157135	intron-variant	Scap	Mm_Celera	9:110338881	AGCTGCAGTGACTTT[C/T]CACCCTAGTCCAAAA	235623
rs6155736	snp	A/T	0.5	0	intron-variant	Scap	GRCm38.p3	9:110353420	CTACGGGTTGTCTCA[A/T]ATGCTTGCTTCTCTT	235623
rs6155819	snp	G/T	0.231111	0.249285	intron-variant	Scap	GRCm38.p3	9:110353472	CCCTTGTTACTTGCC[G/T]GCTGTGTGGCAAGGT	235623
rs6156279	snp	C/T	0.5	0	intron-variant	Scap	GRCm38.p3	9:110353523	ACTTGTGTTTCTTTT[C/T]TTTCACAGGCCTCAT	235623
rs6156841	snp	A/G	0.5	0	intron-variant	Scap	Mm_Celera	9:110353625	AACATTTTCAGCTAT[A/G]TGAAGAACCCACCTT	235623
rs6156864	snp	A/G	0.5	0	intron-variant	Scap	Mm_Celera	9:110353641	TGAAGAACCCACCTT[A/G]ATATAATTTTCTCTA	235623
rs6305329	snp	C/T	0.5	0	downstream-variant-500B, utr-variant-3-prime	Scap, Ptpn23	Mm_Celera	9:110385185	GCCTGCAGTGCATCT[C/T]CATCTGGCAGAGCTG	235623
rs6312216	snp	G/T	0.5	0	intron-variant	Scap	GRCm38.p3	9:110341475	ctgtgctgaggattt[G/T]gggtgggaacaagga	235623
rs6312761	snp	A/G	0.5	0	intron-variant	Scap	GRCm38.p3	9:110341570	ccaggcctgatgcag[A/G]cttatattcccatct	235623
rs6312793	snp	A/C	0.5	0	intron-variant	Scap	GRCm38.p3	9:110341586	cttatattcccatct[A/C]ccaaggaagactgag	235623
rs6312824	snp	A/G	0.5	0	intron-variant	Scap	GRCm38.p3	9:110341607	gaagactgaggcagg[A/G]ggatggcaagttcat	235623
rs6313694	snp	C/T	0.5	0	intron-variant	Scap	GRCm38.p3	9:110341733	TTCCTAGGTTCCCTC[C/T]TTTTACCAGAAGAAA	235623
rs6314230	snp	A/G	0.5	0	intron-variant	Scap	Mm_Celera	9:110341823	TGGTAGATTAGTggt[A/G]ggagatgtaactcan	235623
rs6314254	snp	A/G	0.5	0	intron-variant	Scap	GRCm38.p3	9:110341838	nggagatgtaactca[A/G]cttgttgaatacttg	235623
rs6402747	snp	C/T	0.5	0	intron-variant	Scap	GRCm38.p3	9:110353181	TATGCTTTCAGTTTG[C/T]CCCTTACGTGGTAGA	235623
rs13480416	snp	A/G	0.232988	0.249421	intron-variant	Scap	Mm_Celera	9:110362838	GATCCTAGGTAGTCA[A/G]AACAGCAGAGCATCC	235623
rs29940312	snp	C/G/T	0.444444	0.157135	intron-variant	Scap	GRCm38.p3	9:110334838	GGGGGGGGGGGCGGG[C/G/T]GGGAAGTACCTCTCC	235623
rs30183695	snp	C/T	0.375	0.216506	intron-variant	Scap	GRCm38.p3	9:110335812	AATGATTAAATAGAG[C/T]AGTCAGGGATATTAA	235623
rs30378282	snp	A/G	0.21875	0.248039	intron-variant	Scap	Mm_Celera	9:110352518	ACAAATGAGGAACTT[A/G]CAGTTTTCACCGTGA	235623
rs33720744	snp	C/T	0.387812	0.208586	intron-variant, upstream-variant-2KB	Scap	GRCm38.p3	9:110343696	AGCATGTGGTTGGGG[C/T]CTTTCCTAGACTTTT	235623
rs45651261	snp	C/T	0.152778	0.230321	intron-variant	Scap	Mm_Celera	9:110368049	TTACTGTTCCTTCCC[C/T]GGAGGATCTCTGGTA	235623
rs45746742	snp	C/T	0.142012	0.225474	intron-variant	Scap	GRCm38.p3	9:110352642	ATTTGAGACTCGCAT[C/T]TCCAGACTCTACATA	235623
rs45748598	snp	A/G	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110367696	TATGAACACTTCTGC[A/G]TCCATTGTCACTCAT	235623
rs45795246	snp	C/T	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110370199	GCTCTGGGAGTGAGA[C/T]GGCTACACACCAAGT	235623
rs45808482	snp	C/T	0.132653	0.220748	synonymous-codon	Scap	GRCm38.p3	9:110373073	CCCGAACATGGCTGC[C/T]TGCTGCTGTCCCCTG	235623
rs45827705	snp	G/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110346895	CAAAATAAAAATCAC[G/T]CCCTCAAGACCCAGG	235623
rs45839061	snp	A/C	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110345099	GCAGTCGTATGGAGA[A/C]CATGTGGTCAGGAGA	235623
rs45907580	snp	A/G	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110372121	AGGGCGTATTTTCCC[A/G]ACACCTAACTCATTA	235623
rs45943287	snp	G/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110350467	CAATGTGGAACAGAC[G/T]TGAACTTGAACCTTA	235623
rs46024287	snp	C/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110346083	GAGGCCAGGGTCCCA[C/T]GATCTCCTTCAAGAA	235623
rs46039577	snp	C/T			intron-variant	Scap	GRCm38.p3	9:110335209	TGGTTTTCATTCTCT[C/T]TCCCGTGGAACCAGT	235623
rs46076395	snp	A/G	0.165289	0.235211	downstream-variant-500B, utr-variant-3-prime	Scap, Ptpn23	Mm_Celera	9:110385123	ATTTCAGCAGCCCAG[A/G]GCTGGAAAAATGTCA	235623
rs46185206	snp	C/T	0.244898	0.249948	intron-variant	Scap	GRCm38.p3	9:110368957	TCCTTTGCTGAAATA[C/T]AGGCCCAAGCCAGGC	235623
rs46192516	snp	A/G	0.231111	0.249285	intron-variant	Scap	GRCm38.p3	9:110366739	ACTTCTAAGCCAGCA[A/G]TGTAGTGTTTGTGGT	235623
rs46195213	snp	A/G	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110373507	CCAAGTAAGGTGCTC[A/G]GGTTCTCGTACTCTG	235623
rs46251390	snp	A/G	0.142012	0.225474	intron-variant	Scap	Mm_Celera	9:110364567	CGTGGCGGCAGCAGA[A/G]TGTGGTGGAAGAGCC	235623
rs46255109	snp	C/T			intron-variant	Scap	GRCm38.p3	9:110335323	GGAACTTACCACTGT[C/T]CTGAGTTGGCTAAAG	235623
rs46263239	snp	A/C	0.142012	0.225474	intron-variant	Scap	GRCm38.p3	9:110351202	TGCACAGAAGAGGAC[A/C]GGGAGGATGTTCAGA	235623
rs46345198	snp	A/G	0.489796	0.070696	intron-variant	Scap	GRCm38.p3	9:110365185	CAGGGCCCTGTGCTA[A/G]CTGCCTTCCGCATGA	235623
rs46422739	snp	A/G	0.132653	0.220748	intron-variant	Scap	Mm_Celera	9:110370068	TAGGAATGTTCCATG[A/G]CATGGCACGTGAATG	235623
rs46506713	snp	C/T	0.32	0.24	intron-variant	Scap	Mm_Celera	9:110350731	GCCATCTCTGTGGGG[C/T]GAATAGGAACTACCG	235623
rs46595807	snp	C/T	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110372168	CGTGCTCAGTGTTTC[C/T]TTTCTACCCCGTCCT	235623
rs46694853	snp	A/T			intron-variant	Scap	Mm_Celera	9:110346697	GTTTTGACCTAGCTA[A/T]TGGGATGAACCAAGA	235623
rs46716848	snp	C/T	0.132653	0.220748	intron-variant	Scap	Mm_Celera	9:110365110	TGCTTGGACTGCTTG[C/T]AAGGTCACTAGGTAT	235623
rs46729447	snp	C/T	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110345579	TAACTCGAGATTGGC[C/T]TGACGTGAATTATTA	235623
rs46874185	snp	A/G	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110349955	CTAAAGCTTGGGTTT[A/G]TTTTCCATATGCTCT	235623
rs46956800	snp	C/G	0.132653	0.220748	intron-variant	Scap	Mm_Celera	9:110365284	CCAATGTTTTACGCA[C/G]CACAGATGCCCAAGA	235623
rs46991972	snp	A/C	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110348461	GGATGGTATGTTGTT[A/C]TGTTGCTCAGGCTGG	235623
rs47055089	snp	A/C	0.152778	0.230321	intron-variant	Scap	Mm_Celera	9:110360079	TCTAGCACTTATGTA[A/C]GAGGTTCCAATATTA	235623
rs47069852	snp	C/T	0.244898	0.249948	intron-variant	Scap	GRCm38.p3	9:110365224	CTGGGCCTCTGCTTG[C/T]ATTGCCGTGCTGTGA	235623
rs47103671	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Scap	Mm_Celera	9:110342224	TACTCAGAGAGAAAG[C/T]AGGAAAGCCTGGCAG	235623
rs47268749	snp	C/G	0.32	0.24	synonymous-codon	Scap	GRCm38.p3	9:110374081	GAACCTGGTCCACGT[C/G]CACTTCAAAGAGGAG	235623
rs47288960	snp	A/G			intron-variant	Scap	GRCm38.p3	9:110334593	CTAGGGCATTGGTCT[A/G]CCACTGAGTAACACC	235623
rs47406480	snp	C/T	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110368145	AATATGGAGTCCCTC[C/T]GCTCTACTTGCTCAG	235623
rs47601225	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Scap	Mm_Celera	9:110342301	GCATAGCAGTAGCAA[A/G]GGCGCATTGAGAACG	235623
rs47662119	snp	C/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110350076	GGCCCCACAGTTGAA[C/T]GGGTCCTCTTGCTGG	235623
rs47679629	snp	A/G	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110369156	GGAATTTAGGCCCAC[A/G]TGATTCTGGGTGTGA	235623
rs47700755	snp	A/G	0.32	0.24	synonymous-codon	Scap	GRCm38.p3	9:110373156	TGGGACCATCCATCA[A/G]CATGAGCCCAAAACT	235623
rs47789946	snp	A/G	0.132653	0.220748	intron-variant	Scap	Mm_Celera	9:110356364	TCCCTTTCTATCCAC[A/G]TCTCAGGTTGTTCTA	235623
rs48138925	snp	C/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110350375	GTCATCCTTATAGCC[C/T]GGTTGTCATCAGGGA	235623
rs48205826	snp	C/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110346338	CCAAATACAGTGAGA[C/T]GGGACTGTCTGTAGT	235623
rs48261791	snp	C/T	0.132653	0.220748	intron-variant	Scap	GRCm38.p3	9:110366012	GCTCTGCTAGGTAGT[C/T]CATGGATGTGAAGCA	235623
rs48291752	snp	C/T	0.142012	0.225474	intron-variant	Scap	Mm_Celera	9:110366556	GAAAAGCCCGAGGGC[C/T]TCAGCACTTGCATGC	235623
rs48316206	snp	G/T	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110372948	ATGCTGGCAGAAACA[G/T]CAGCGGCTTCCTCCG	235623
rs48377822	snp	C/G/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110350577	AAAATTAGCAGCAAA[C/G/T]AGCAAATTAACTTTA	235623
rs48394054	snp	A/C	0.444444	0.157135	intron-variant	Scap	GRCm38.p3	9:110346824	TTTACTGCTGTTGTT[A/C]TACTGTTGCTACTGT	235623
rs48479277	snp	A/G	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110366602	TGTCTTGGTGACTGG[A/G]ACCTGACTACTTACG	235623
rs48496868	snp	C/T	0.32	0.24	synonymous-codon	Scap	Mm_Celera	9:110377727	CACCCTCGTGCCTGC[C/T]ATCCAGGTAATGCTC	235623
rs48505171	snp	A/G	0.244898	0.249948	intron-variant	Scap	GRCm38.p3	9:110350989	TGTGAACCAAGAACA[A/G]AGGCTGTAAGCCAGT	235623
rs48539703	snp	C/T			synonymous-codon	Scap	GRCm38.p3	9:110362412	CCCGCTGCTGAAGCT[C/T]CCCTTGCCTGGAACG	235623
rs48602337	snp	A/G	0.260355	0.249785	intron-variant	Scap	Mm_Celera	9:110375887	TCTCAGGCAGACATA[A/G]GAAAAACCACTTTGC	235623
rs48633719	snp	C/T	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110367730	GGCTACCATTCCTAT[C/T]TGCGTCCATACCTCT	235623
rs48912083	snp	A/G	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110346524	ATGGTATTAAACTAG[A/G]AGAGGGACTAAGATT	235623
rs49140330	snp	A/G	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110348437	CAGCCAGCTTGCTGG[A/G]AGGCGGCAGGATGGT	235623
rs49154889	snp	A/C			intron-variant	Scap	GRCm38.p3	9:110334606	CTGCCACTGAGTAAC[A/C]CCTGTGGCTTTTTAT	235623
rs49190158	snp	A/T			intron-variant	Scap	Mm_Celera	9:110360658	TACACTTATTTAAAA[A/T]TTTTTTATTTTTATA	235623
rs49340130	snp	A/G	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110372897	TTTAGGAACTCGATG[A/G]CAGATGATTCCCCAT	235623
rs49380162	snp	C/T	0.231111	0.249285	intron-variant	Scap	GRCm38.p3	9:110373778	CCTCTGTCTTCTGAG[C/T]AGGCCACTGCAGGCA	235623
rs49400336	snp	A/G	0.32	0.24	intron-variant	Scap	Mm_Celera	9:110341099	TATTTTGTCACAACC[A/G]CATTTCTCTGGGACC	235623
rs49494681	snp	C/T			intron-variant	Scap	GRCm38.p3	9:110337352	CAGATATTTTCTCCC[C/T]TTTTTTTTTTTTTTT	235623
rs49550351	snp	A/G	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110345977	CAGTTGAGTTGCTTT[A/G]TGGCCTGCAGAGAGG	235623
rs49605821	snp	A/C	0.124444	0.216185	intron-variant	Scap	GRCm38.p3	9:110346477	AGTGTGTGTGAGGTT[A/C]CATAGCTGAAATGCT	235623
rs49607661	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Scap	Mm_Celera	9:110342272	GTTAAGGAAGCCAGA[C/T]GTAATACTCTGCAGC	235623
rs49650856	snp	A/C	0.231111	0.249285	intron-variant, upstream-variant-2KB	Scap	Mm_Celera	9:110342332	TCTCAGAAATCGGCC[A/C]GCTTCTGCCTATAGC	235623
rs49698091	snp	C/T			intron-variant	Scap	GRCm38.p3	9:110335349	TAAAGAAACAAGATC[C/T]GGGTGACTTTAGCCA	235623
rs49729803	snp	A/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110346866	CTTTGGGAAGAAGAT[A/T]TGGACTCAAGACACA	235623
rs49918931	snp	C/T	0.142012	0.225474	intron-variant	Scap	Mm_Celera	9:110357525	TGTTAGAGCAGTAAA[C/T]ATAAACAGAGCACTC	235623
rs49935160	snp	A/G	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110370356	AAAATTCCATCTCTG[A/G]GGTGCGAGTGGGCAG	235623
rs49954998	snp	A/G	0.124444	0.216185	intron-variant	Scap	Mm_Celera	9:110369411	AATGTGTGCCAAGTC[A/G]GCAAATCGCCACAGG	235623
rs50314758	snp	C/T	0.244898	0.249948	intron-variant	Scap	GRCm38.p3	9:110345630	GAGCAGTTTTAGTAG[C/T]GTGGTGATTGGTGGT	235623
rs50326735	snp	C/T	0.165289	0.235211	synonymous-codon	Scap	GRCm38.p3	9:110377706	CATCATCCTCATTGG[C/T]TACTTCACCCTCGTG	235623
rs50444395	snp	A/G	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110346391	TCTGCTATTCATTGG[A/G]TTCTGTAGGGTTCTG	235623
rs50590281	snp	C/G	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110346910	TCCCTCAAGACCCAG[C/G]AATAAAGCCTGTCTA	235623
rs50630456	snp	C/G	0.231111	0.249285	intron-variant	Scap	GRCm38.p3	9:110373854	CTTCTGGGCCTCTGG[C/G]ACCTGGAACCAGGTG	235623
rs50811071	snp	G/T	0.32	0.24	intron-variant, upstream-variant-2KB	Scap	GRCm38.p3	9:110343182	GCCCTCCTCCTTTCC[G/T]GTACCACAGTTTATC	235623
rs50872561	snp	A/C			intron-variant	Scap	Mm_Celera	9:110358192	AGACAGACTGACTGA[A/C]TAAGGTGCCTCTGGA	235623
rs50915840	snp	C/T	0.231111	0.249285	intron-variant	Scap	GRCm38.p3	9:110369390	CCCTTGTCCTTCACC[C/T]AGGCTAATGTGTGCC	235623
rs50947869	snp	G/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110373560	TTGCTTCTCTGACCA[G/T]CATGGCCCCAGGCCT	235623
rs51002194	snp	C/T	0.32	0.24	intron-variant	Scap	GRCm38.p3	9:110349281	TCTCTGCTCTACTCA[C/T]GCCCTTATCCTTTCA	235623
rs51061866	snp	A/G	0.142012	0.225474	intron-variant	Scap	GRCm38.p3	9:110358083	GCATGCGCTTAACAC[A/G]CCGGAGATAATAAAA	235623

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