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
rs6280170	snp	A/G	0.485582	0.0836725	intron-variant	Hgs	GRCm38.p3	11:120479308	CAGGCGTAGGTGCCC[A/G]CCCTCCGGGGTCCCG	15239
rs6281276	snp	C/T	0.5	0	intron-variant	Hgs	Mm_Celera	11:120479500	GAACAGAGGCCCACA[C/T]CACCTAGGCTCTCAG	15239
rs13466219	snp	C/T	0.456747	0.140554	synonymous-codon, upstream-variant-2KB	Hgs, Mrpl12	GRCm38.p3	11:120483493	CCAGCTCATCTCCTT[C/T]GACTGACCTTGAGTC	15239
rs13466220	snp	A/T			missense, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469038	CAGCTTCTGTTGGAG[A/T]CAGACTGGGAGTCCA	15239
rs13466221	snp	A/G	0.244898	0.249948	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483654	CTCTTCCCTGTCCTC[A/G]GTGGTCTGGCTCCTA	15239
rs26981053	snp	G/T	0.124444	0.216185	downstream-variant-500B, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120484027	GGTTGGACCAACAAT[G/T]TAATAGTCTGCATCT	15239
rs26981054	snp	C/T	0.124444	0.216185	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483901	CAGCAAGGGTAGAAG[C/T]TTTAGGTATCTCTGT	15239
rs26981055	snp	C/T	0.231111	0.249285	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483886	CATGTGGCTCCTGCA[C/T]AGCAAGGGTAGAAGC	15239
rs26981056	snp	C/G	0.124444	0.216185	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483772	GCCCGGCTGTGTTGG[C/G]TGCCACAGGTGAATG	15239
rs26981057	snp	A/G	0.408163	0.193609	utr-variant-3-prime, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483688	CTGGTTCCCTGCTTC[A/G]GTCCTGATGCCGTCT	15239
rs26981058	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483336	AGCTTGTTCTAAGCC[A/G]AAGGTTTTGTTTGTG	15239
rs26981059	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483294	TGCCATATTGGTAAC[A/G]ACCTGATCTACTATG	15239
rs26981060	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483272	TACAAGAGATCACAC[A/G]TGCCATTGCCATATT	15239
rs26981061	snp	C/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483201	CAGACAGAATCATGA[C/G]ATGCCATTAAGTGCA	15239
rs26981062	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483139	GCCCTTGGACTTCTG[A/G]GCTTCCTTTGATCCC	15239
rs26981063	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120483109	ACCAGCAGGTGAGCC[A/G]TCTCCCAGCGGCCTG	15239
rs26981064	snp	A/G	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120480803	TTCCTGCCAGTTAGT[A/G]TCGTCAGCCTCCCTC	15239
rs26981065	snp	A/G	0.408163	0.193609	intron-variant	Hgs	Mm_Celera	11:120480759	CACCTCAGGACTGCA[A/G]GTGTCTTGGCTCAGA	15239
rs26981066	snp	A/G	0.197531	0.244432	intron-variant	Hgs	Mm_Celera	11:120480750	CTTAGAAAGCACCTC[A/G]GGACTGCAGGTGTCT	15239
rs26981067	snp	C/T	0.489796	0.070696	intron-variant	Hgs	Mm_Celera	11:120480610	TCAATTTGTTTTGTC[C/T]GGTGGTTCTACTTCC	15239
rs26981068	snp	C/G	0.396694	0.202437	intron-variant	Hgs	Mm_Celera	11:120480560	GTGCCTATAGTGTGG[C/G]CTTGAACCATTGTAC	15239
rs26981069	snp	C/T	0.152778	0.230321	intron-variant	Hgs	Mm_Celera	11:120479035	GCTTCCTGAGCTTAA[C/T]GGGCATAGCGTTCAC	15239
rs26981070	snp	A/G	0.165289	0.235211	intron-variant	Hgs	Mm_Celera	11:120479006	ATCTACCTGCCTAGC[A/G]CCTTTGCGAGGATGC	15239
rs26981071	snp	C/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120478983	GAAGGACACAGTGGG[C/T]AGCGCCTATCTACCT	15239
rs26981072	snp	C/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120478905	AGTCATGCCCAGTCA[C/T]AGGTGGAAGAGGGCC	15239
rs26981073	snp	C/T	0.42	0.183303	intron-variant	Hgs	Mm_Celera	11:120478885	CAACTGCTGAGGTGC[C/T]TGCCAGTCATGCCCA	15239
rs26981074	snp	C/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120478637	CTCTCTTGACTGTCG[C/T]TCCTAGGGCAAGGTC	15239
rs26981075	snp	C/T	0.375	0.216506	intron-variant	Hgs	Mm_Celera	11:120478276	AAGATTGCTTGGGAT[C/T]ACTTGATCACTTGAT	15239
rs26981076	snp	G/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120478043	TAGATAGTCAAGTTA[G/T]TGTGGCCACTGCTGC	15239
rs26981077	snp	A/C/T	0.32	0.24	intron-variant	Hgs	Mm_Celera	11:120477902	GCCACAGATGGGACC[A/C/T]GGAGCTAGAAACAGC	15239
rs26981078	snp	C/T	0.277778	0.248452	intron-variant	Hgs	Mm_Celera	11:120477650	TGGCTGCTCATTTTC[C/T]AGGGATCACCACAGG	15239
rs26981079	snp	A/G	0.18	0.24	intron-variant	Hgs	Mm_Celera	11:120477001	GCTGGCTGAGGCACC[A/G]AGGTCCCTTCTGCCA	15239
rs26981080	snp	C/G	0.277778	0.248452	intron-variant	Hgs	Mm_Celera	11:120476868	ACACTGTCCTTTCTG[C/G]CACCTTCTGAAGGGA	15239
rs26981081	snp	C/T	0.42	0.183303	intron-variant	Hgs	Mm_Celera	11:120476104	TTCTCTTGGATTTCT[C/T]AACTGTGGTTTGTGT	15239
rs26981082	snp	G/T	0.18	0.24	intron-variant	Hgs	Mm_Celera	11:120475281	CGGACTCTGTGATGC[G/T]TCAGAACTGCAGGCC	15239
rs26981083	snp	C/T	0.165289	0.235211	intron-variant	Hgs	Mm_Celera	11:120475104	TTCACTGGGCCTGTC[C/T]TGCTCTGTCTCACAG	15239
rs26981084	snp	A/G	0.277778	0.248452	intron-variant	Hgs	Mm_Celera	11:120474682	ATAGCTTCCCATCTC[A/G]CTTCCCGCCTGACAG	15239
rs26981085	snp	C/T	0.375	0.216506	intron-variant	Hgs	Mm_Celera	11:120474437	CTAACCTGATGGTTT[C/T]GGAACCACATTCATC	15239
rs26981086	snp	C/T	0.297521	0.245442	intron-variant	Hgs	Mm_Celera	11:120474146	GCCATGTGGTTTAGG[C/T]CACAGAATTCGATGG	15239
rs26981087	snp	A/G	0.426035	0.177515	intron-variant	Hgs	Mm_Celera	11:120472941	GAAAAGCAGCCGTTA[A/G]CCCCAGGTCAAGTTG	15239
rs26981088	snp	C/T	0.396694	0.202437	synonymous-codon	Hgs	Mm_Celera	11:120472643	AAGTGATGCCATGTT[C/T]GCTGCTGAAAGAGTG	15239
rs26981089	snp	C/T	0.444444	0.157135	intron-variant	Hgs	Mm_Celera	11:120472513	TATCCTTTCCTAGTC[C/T]TGACAGTTTTGTCTG	15239
rs26981090	snp	G/T	0.345679	0.230967	intron-variant	Hgs	Mm_Celera	11:120472290	TGCAAGGCTACAAGA[G/T]TGGCTCATGCCAGCA	15239
rs26981091	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120471820	TTGCACCTTACACAT[C/T]TACCCCACAGGGAGG	15239
rs26981092	snp	A/G	0.32	0.24	intron-variant	Hgs	Mm_Celera	11:120471783	AGAGCTCCGTAGAGA[A/G]AGGCCAGGCTCTGAC	15239
rs26981093	snp	A/G	0.132653	0.220748	intron-variant	Hgs	Mm_Celera	11:120471732	GGTCTTCCCTGAGTG[A/G]TTGGGAGTGAGGAGG	15239
rs26981094	snp	A/G	0.260355	0.249785	intron-variant	Hgs	Mm_Celera	11:120471712	GGGACAAGGGAGGGC[A/G]GACTGGTCTTCCCTG	15239
rs26981095	snp	G/T	0.336735	0.234472	intron-variant	Hgs	Mm_Celera	11:120471449	CACCTGGAGTCTCCT[G/T]AGCCCTCCCCACTTT	15239
rs26981096	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120471371	CTCCCCTACCTTTGC[A/G]CTAATCGTCTCTGCT	15239
rs26981097	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120471309	GCAAGCATAGACCCA[A/G]GAGAGTCGCTTCTGT	15239
rs26981098	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120471200	ATCCCCTGGAGAGAT[A/G]GAAGGAGGCATGGTT	15239
rs26981099	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120471131	GGTCCTGTCTTCCTC[A/G]TGCTTTTTGGAGAGT	15239
rs26981100	snp	A/G	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120471005	TCATCCCAACATAAT[A/G]TGTCACAGCCTCCCT	15239
rs26981101	snp	A/G/T	0.260355	0.249785	intron-variant	Hgs	Mm_Celera	11:120470925	TGCTCCTCTCCTGGA[A/G/T]GGAACCCTTAGAGGG	15239
rs26981102	snp	C/T	0.231111	0.249285	intron-variant	Hgs	Mm_Celera	11:120470900	TGCTGCAAGGGGCAG[C/T]AGGCTGGCTTGCTCC	15239
rs26981103	snp	C/T	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120470705	CCCCATTTCATGGGA[C/T]CCAGCATCAGGGTTT	15239
rs26981104	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120470648	ACCTAAGGATTGTGA[C/T]GTGGATGGTGATACA	15239
rs26981105	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120470467	AGACATTCAGAGCAG[C/T]ACATTCAGGGATGGG	15239
rs26981106	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120470448	ATATGTGTGAGCTTG[A/G]GGAAGACATTCAGAG	15239
rs26981107	snp	A/G	0.391111	0.206368	intron-variant	Hgs	Mm_Celera	11:120470213	CAGAATACAGCAGGA[A/G]GAGCAGTGGGTGTGT	15239
rs26981108	snp	A/C	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120470202	CTGTTTGTGGGCAGA[A/C]TACAGCAGGAAGAGC	15239
rs26981109	snp	C/G	0.152778	0.230321	intron-variant	Hgs	Mm_Celera	11:120469985	GCAAGAGGGGCTCTT[C/G]CCTCTTCCCTGAACA	15239
rs26981110	snp	C/G	0.142012	0.225474	intron-variant	Hgs	Mm_Celera	11:120469950	TAACAAGTTAGGTGG[C/G]TTCAGAGACCTGTCT	15239
rs26981111	snp	A/G	0.336735	0.234472	intron-variant	Hgs	Mm_Celera	11:120469944	GGTTTCTAACAAGTT[A/G]GGTGGGTTCAGAGAC	15239
rs26981112	snp	C/G	0.32	0.24	intron-variant	Hgs	Mm_Celera	11:120469911	GGGCCTGGAACCCGA[C/G]TTTGAGCTGCTGCTT	15239
rs26981113	snp	A/G	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120469909	CAGGGCCTGGAACCC[A/G]ACTTTGAGCTGCTGC	15239
rs26981114	snp	A/G	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120469805	GTGAGCTCGGCCACT[A/G]AGCCTGGCTGCTCTC	15239
rs26981115	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120469781	AGACCTTTAGCACTT[C/T]GTACAGTTGTGAGCT	15239
rs26981116	snp	C/T	0.124444	0.216185	intron-variant	Hgs	Mm_Celera	11:120469692	TAACTAGAGCGCTGT[C/T]GCAGTTGTTTCTCTC	15239
rs26981117	snp	C/T	0.152778	0.230321	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469546	CCCATCCTTTTCTCT[C/T]TCTGCTGTTACTAAT	15239
rs26981118	snp	C/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469520	GCTTTCCTAACCATA[C/G]TGAGGGCTTTCCCAT	15239
rs26981119	snp	A/G	0.391111	0.206368	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469257	TTGAGGAGGTCTGTC[A/G]GGCTAAACTCATGGT	15239
rs26981120	snp	A/G/T	0.152778	0.230321	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469204	TGGGACAATTAAAAC[A/G/T]GCACAATTTGGAGAT	15239
rs26981121	snp	A/G	0.152778	0.230321	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120469136	AAGATTAAATGGGCA[A/G]CATGAGTTTTTTGTT	15239
rs26981122	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468955	TGACTTTTGACGGGC[C/T]GGCTCGGAAACATAG	15239
rs26981123	snp	C/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468826	CTGATAGGGACTAAG[C/T]ATCATTTCCACATTA	15239
rs26981124	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468795	GAACTGAGTGAAGCC[A/G]AGCTTGAGCTGACAG	15239
rs26981125	snp	A/C	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468697	CATTTTAAAGTGCCC[A/C]GCAAGCTGTGACAAA	15239
rs26981126	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468677	TGAGAAGCAGCAGGG[C/T]ATGCCATTTTAAAGT	15239
rs26981127	snp	C/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468365	CTTGCTCCTTTTTGA[C/G]CTAAGGTTTTCAAAG	15239
rs26981128	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468320	CCTCAATAAATGTGT[C/T]CAGGAGCAGGCCCCA	15239
rs26981129	snp	C/T	0.165289	0.235211	upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120467634	GGCGTTGCGCGTGCG[C/T]GAGCAGAAAAAGAAA	15239
rs26981130	snp	A/G/T	0.426035	0.177515	upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	GRCm38.p3	11:120467592	AGCGCAAGTCTCGCC[A/G/T]TGGAGCAGGACTCGG	15239
rs26981131	snp	C/T	0.35503	0.226867	upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	Mm_Celera	11:120467481	AATGAGGCCCGCCTC[C/T]GCTTAGCTTTCATTG	15239
rs26981132	snp	A/C	0.277778	0.248452	upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	Mm_Celera	11:120467466	TCCGAGCTACCACGC[A/C]ATGAGGCCCGCCTCC	15239
rs26981133	snp	A/T	0.408163	0.193609	upstream-variant-2KB, utr-variant-5-prime	Hgs, Arl16	Mm_Celera	11:120467435	ACATCCCTTCCTCGG[A/T]TAACGCGCTTGTACC	15239
rs26981134	snp	C/T	0.132653	0.220748	upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120467093	ACCCAACCTACTGAC[C/T]ACAGGCACCGCGGCT	15239
rs26981135	snp	C/T	0.260355	0.249785	upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120466952	CGTCAACCATAGAGA[C/T]GGGCCTTGAGAGTGA	15239
rs26981136	snp	C/T	0.165289	0.235211	upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120465871	TCGCCACAAAGTTGT[C/T]CTACCCACAGCTGCA	15239
rs46890120	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120471135	CTGTCTTCCTCATGC[C/T]TTTTGGAGAGTTTAG	15239
rs211711843	in-del	-/GAAAAGTT			intron-variant, upstream-variant-2KB	Hgs, Mrpl12	Mm_Celera	11:120482671	CTACCAGGTATGTGG[-/GAAAAGTT]GCACCCAGCATCTAC	15239
rs211731773	snp	C/G			intron-variant	Hgs	Mm_Celera	11:120481001	AGTGCTGGGATTAAA[C/G]GCAGGCACCACATTC	15239
rs212196577	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120471077	TGAGCCCCTGGAGAA[A/G]CATCTGAAGAGGATA	15239
rs212261854	snp	A/G			intron-variant	Hgs	Mm_Celera	11:120478810	GTAAGGAGGCTCCAG[A/G]CTCCAGCTGCTCTGT	15239
rs212327077	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120477684	CTGTTGATTCAGGAC[G/T]TCACTGTGGCGTATT	15239
rs212825440	snp	C/T			intron-variant	Hgs	Mm_Celera	11:120476568	CTGGATGCTGTTATG[C/T]TCCCACCTTGGTGAT	15239
rs212886351	snp	A/T			intron-variant	Hgs	Mm_Celera	11:120475694	ATGAAGTTTACAAGC[A/T]GAGAATAGTGGTGCA	15239
rs213171728	snp	G/T			intron-variant, upstream-variant-2KB	Hgs, Arl16	Mm_Celera	11:120468503	CTTGGGATAGCTCAC[G/T]TTCGTAAGGGAGGGG	15239
rs213246372	snp	C/T			upstream-variant-2KB, intron-variant	Hgs, Arl16	Mm_Celera	11:120467099	CCTACTGACCACAGG[C/T]ACCGCGGCTTCCATT	15239
rs213318379	snp	G/T			intron-variant	Hgs	Mm_Celera	11:120474451	TCGGAACCACATTCA[G/T]CTCAGAATTGTGTGG	15239

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