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
rs3698658	snp	A/G	0.5	0	intron-variant	Epn2	GRCm38.p3	11:61527477	CACCATAGTCTAAAA[A/G]GGTCATATACTGCCC	13855
rs6338513	snp	A/G	0.359862	0.224567	intron-variant	Epn2	GRCm38.p3	11:61528093	ATCTGAGCTCCTAAC[A/G]CACAAGAGCCCTGCC	13855
rs6340658	snp	A/C	0.5	0	intron-variant	Epn2	GRCm38.p3	11:61528509	ggaatgcaatgcctt[A/C]gtctggcttccacag	13855
rs26941068	snp	C/T	0.489796	0.070696	intron-variant	Epn2	GRCm38.p3	11:61543737	TTTTCTACTCCTACA[C/T]TGGGAACAGTGGCTT	13855
rs26941069	snp	C/T	0.336735	0.234472	intron-variant	Epn2	GRCm38.p3	11:61543174	TGTAAAGCTGGTCTT[C/T]CTTACCTTTCCAAAC	13855
rs26941070	snp	C/T	0.408163	0.193609	intron-variant	Epn2	GRCm38.p3	11:61543074	AGAACAGATCCTAAG[C/T]AAGTGGTAGCAAAAT	13855
rs26941071	snp	A/C	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61542549	GGAATTCTCCCAACC[A/C]TTCTCAAGTGCTTCT	13855
rs26941072	snp	A/G	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61541685	CTGGCTTTTATCAGG[A/G]TATAGCAGCAGCTCT	13855
rs26941073	snp	A/G	0.408163	0.193609	intron-variant	Epn2	GRCm38.p3	11:61541523	ACTACCAGCGCTGCC[A/G]TGGTTCCTACACTAC	13855
rs26941074	snp	A/G	0.408163	0.193609	intron-variant	Epn2	GRCm38.p3	11:61541393	AGCTCAAGGATCCCC[A/G]ACATTTTCCTAGGGA	13855
rs26941075	snp	C/T	0.244898	0.249948	intron-variant	Epn2	GRCm38.p3	11:61541277	AAATCCTCTGTGAAG[C/T]GAGCCCAGCAAAGAC	13855
rs26941076	snp	C/T	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61540820	CTTAACCACACTGAC[C/T]TCATTCACCTGCTTT	13855
rs26941077	snp	G/T	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61540264	ATAGATCAGGTTCTA[G/T]GGACCACAAGCCCAG	13855
rs26941078	snp	A/G	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61539275	AGTGAGAGCTGAGCA[A/G]GCTGACTTACCTGGG	13855
rs26941079	snp	G/T	0.142012	0.225474	intron-variant	Epn2	GRCm38.p3	11:61537575	CTTATTTAGAGACAC[G/T]CTAGCCTCAGTGATG	13855
rs26941080	snp	A/T	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61537080	TTGAAAACTGGGGAA[A/T]GAATGGTTAACAAAC	13855
rs26941081	snp	C/G	0.336735	0.234472	intron-variant	Epn2	GRCm38.p3	11:61537006	TAGACATCTCTAGGA[C/G]GCATACATGGGAAAT	13855
rs26941082	snp	C/G	0.35503	0.226867	intron-variant	Epn2	GRCm38.p3	11:61536701	TCCTACCCAATTATA[C/G]TTTTCATTGGACCTC	13855
rs26941083	snp	A/G	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61535777	AGGCATGCTTAGGAA[A/G]AGGAAGCCCACACAG	13855
rs26941084	snp	C/T	0.408163	0.193609	synonymous-codon	Epn2	GRCm38.p3	11:61535367	CTCTAACTCAGAGGA[C/T]ACTCGTGGGGAAGTA	13855
rs26941085	snp	C/T	0.408163	0.193609	intron-variant	Epn2	GRCm38.p3	11:61535056	TCACTCGGAGTTAGC[C/T]GTTTCTCTGGACACT	13855
rs26941086	snp	C/G	0.408163	0.193609	intron-variant	Epn2	GRCm38.p3	11:61535020	TCAGAAGTCCCTGGA[C/G]AGTAAGTCTACATAG	13855
rs26941087	snp	A/G	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61534883	CCACACATCTGCCAC[A/G]GGATATATTGCCCTG	13855
rs26941088	snp	A/G	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61534863	CCTTCTAGCCTTCTA[A/G]TCTCCCACACATCTG	13855
rs26941089	snp	C/T	0.32	0.24	intron-variant	Epn2	GRCm38.p3	11:61533847	TTCCCAGAGGACTCA[C/T]GGAGGTTCCTCCTTC	13855
rs26941090	snp	A/C	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61533168	CACATCAGGTGATAC[A/C]ACTAGTATGCCTGGC	13855
rs26941091	snp	A/G	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61533138	GCAACATCTATCATC[A/G]GGGCCCTGTGGCACC	13855
rs26941092	snp	C/T	0.32	0.24	intron-variant	Epn2	GRCm38.p3	11:61533002	ATCATCATCCCTCTT[C/T]ACCTGCCTTTGGTTT	13855
rs26941093	snp	C/T	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61532825	AACTTGGAAATTGAG[C/T]TGCTCCAATCCCAAA	13855
rs26941094	snp	A/T	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61532813	TAACTCCTGAATAAC[A/T]TGGAAATTGAGCTGC	13855
rs26941095	snp	C/G	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61532776	TAATATTAGTTCTCA[C/G]CACAGCACAGGCCTT	13855
rs26941096	snp	A/G	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61532353	ATTATGACTTCTTGA[A/G]CTTGAGCTGGGTGCA	13855
rs26941097	snp	A/T	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61531921	ACAGAGCCTAGCATT[A/T]GGTATACTTTAACAA	13855
rs26941098	snp	A/C	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61531892	TGGGTGTCCCAGATA[A/C]TTCATATGGGAGGAC	13855
rs26941099	snp	A/G	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61531843	GGTTCACACAGCACT[A/G]CTCGCTGCTACCAGG	13855
rs26941100	snp	A/G	0.32	0.24	intron-variant	Epn2	GRCm38.p3	11:61531797	GATGCTCAACTCACT[A/G]TTCTGATCTGACAAG	13855
rs26941101	snp	C/T	0.132653	0.220748	intron-variant	Epn2	GRCm38.p3	11:61531685	TCTACCTGCTGCCCA[C/T]GTCACAATGCATGGG	13855
rs26941102	snp	C/T	0.32	0.24	intron-variant	Epn2	GRCm38.p3	11:61530882	TGGCAAATTTCATCT[C/T]CATTTGAAGAGCAAG	13855
rs26941103	snp	C/T	0.32	0.24	intron-variant	Epn2	GRCm38.p3	11:61530858	TCCAGTTTTGTTAAA[C/T]AGTCGGAATGGCAAA	13855
rs26941104	snp	C/T	0.32	0.24	intron-variant	Epn2	GRCm38.p3	11:61530789	TCTACCTAGTAACAA[C/T]AGTTATACAGCTCTG	13855
rs26941105	snp	C/T	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61530749	GAGTATGGATTCTTT[C/T]TGGAGTAATGGAAAC	13855
rs26941106	snp	C/T	0.32	0.24	intron-variant	Epn2	GRCm38.p3	11:61530732	GCTGGTGGCTAGGAG[C/T]TGAGTATGGATTCTT	13855
rs26941107	snp	C/T	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61530531	AATGCAAATGTCCAA[C/T]GGGAGGAGAGTGTAC	13855
rs26941108	snp	A/C	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61529464	AGGCCTTCTGAATTA[A/C]CAGGCTGTGAGGCCT	13855
rs26941109	snp	A/G	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61529321	TTCATGTGCACAGCC[A/G]GCAGTCACAGTCCAT	13855
rs26941110	snp	C/T	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61529087	ACGAGGCTGGCCCGC[C/T]GCCCTTAGGAGAGAG	13855
rs26941111	snp	C/T	0.32	0.24	intron-variant	Epn2	GRCm38.p3	11:61528702	CACCACCAGTCTGGA[C/T]ACCTGCAACACTCCT	13855
rs26941112	snp	C/T	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61528617	AAGACAATGCAAAGA[C/T]TAGGAGTCTGAGAGG	13855
rs26941113	snp	A/G	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61528127	GGCCCTCTCAGGCAA[A/G]AGCCACCTAGCTCAA	13855
rs26941114	snp	G/T	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61527884	CTGAGAATCCACACA[G/T]GAAGAACCCCAAGGG	13855
rs26941115	snp	A/G	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61527719	CTAAGTGAAGGTACA[A/G]GCCTCTGGGTAAGTG	13855
rs26941116	snp	A/G	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61527598	CCATGGGGACAGAAC[A/G]CGCAGTTGGCTTTCC	13855
rs26941117	snp	A/G	0.32	0.24	intron-variant	Epn2	GRCm38.p3	11:61527564	CAGGATCTGCAAAGT[A/G]AGCTTCCCTCTCCCT	13855
rs26941118	snp	A/T	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61527446	AATACTCCACCAAAG[A/T]GTTTTCCCCTCACCT	13855
rs26941119	snp	A/G	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61527263	TCTCTCAGCTAGATA[A/G]ATACACTTGAGGGAC	13855
rs26941120	snp	C/T	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61527027	CTACAGGGGTGGTAC[C/T]TCATCAGGCATGGCT	13855
rs26941121	snp	G/T	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61526845	TATTTGGCCTTTCTG[G/T]TTCTAATGCTCCAGA	13855
rs26941122	snp	C/T	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61526737	GGCTTGCTGCAGTGA[C/T]ACACCCAAAAGTTGT	13855
rs26941123	snp	C/G	0.391111	0.206368	intron-variant	Epn2	GRCm38.p3	11:61526606	AAGGCTTACTTGGGT[C/G]CTGCTCAGATATTGC	13855
rs26941124	snp	C/T	0.124444	0.216185	intron-variant	Epn2	GRCm38.p3	11:61526169	ACACAGCTTCCATGC[C/T]TAGCCTGGCCAGACT	13855
rs26941125	snp	A/G	0.32	0.24	intron-variant	Epn2	Mm_Celera	11:61524708	GGTTATCTCTGCCTA[A/G]CTAACCTCAGCAGCA	13855
rs26941126	snp	C/T	0.391111	0.206368	intron-variant	Epn2	Mm_Celera	11:61524589	GTGGTGCATATGAAG[C/T]CTATTTTGCAACCGT	13855
rs26941127	snp	C/T	0.32	0.24	intron-variant	Epn2	Mm_Celera	11:61524570	TTTTTCCATTTGTGT[C/T]GAAGTGGTGCATATG	13855
rs26941128	snp	C/T	0.32	0.24	intron-variant	Epn2	Mm_Celera	11:61524499	TCTAACAGTTTATAA[C/T]CCTCTCAGCAGGTCC	13855
rs26941129	snp	C/T	0.244898	0.249948	intron-variant	Epn2	Mm_Celera	11:61524477	CCAGCACCGTTTCCA[C/T]GCTGGTTCTAACAGT	13855
rs26941130	snp	A/G	0.124444	0.216185	intron-variant	Epn2	Mm_Celera	11:61524202	GAAACAATATGCTGG[A/G]TAGCTATGCCAGATT	13855
rs26941131	snp	A/G	0.132653	0.220748	intron-variant	Epn2	Mm_Celera	11:61524140	ATTTCCAGATCCACC[A/G]CAAAGTGTCCTGAGC	13855
rs26941132	snp	C/T	0.489796	0.070696	intron-variant	Epn2	Mm_Celera	11:61524139	CATTTCCAGATCCAC[C/T]GCAAAGTGTCCTGAG	13855
rs26941133	snp	A/C	0.124444	0.216185	intron-variant	Epn2	Mm_Celera	11:61523798	AATTTTGAGCAACAA[A/C]GGTTAGTCAACTTAG	13855
rs26941134	snp	A/G	0.124444	0.216185	intron-variant	Epn2	Mm_Celera	11:61523545	TTCCCATCACACAAG[A/G]GGCTCACAGGGGTTC	13855
rs26941135	snp	A/G	0.124444	0.216185	intron-variant	Epn2	Mm_Celera	11:61523500	TCTGGCAAGTGCACC[A/G]AGAGGCAAAGCTAAA	13855
rs26941136	snp	C/G	0.124444	0.216185	intron-variant	Epn2	Mm_Celera	11:61523418	CACATATACACAGAG[C/G]ACACCAGTAAGAATA	13855
rs26941137	snp	A/G	0.132653	0.220748	intron-variant	Epn2	Mm_Celera	11:61523214	GAAGTCAGAGTCAAA[A/G]TTCAGAACAGGGGCT	13855
rs26941138	snp	C/T	0.32	0.24	missense	Epn2	GRCm38.p3	11:61523068	CTCCCCAGGCATCTG[C/T]TGTCTTTCCAGCATT	13855
rs26941139	snp	A/C	0.32	0.24	intron-variant	Epn2	Mm_Celera	11:61523000	AGAAGTAGTGAAGCT[A/C]TAGGAACCAGGCTGA	13855
rs26941140	snp	C/T	0.124444	0.216185	intron-variant	Epn2	Mm_Celera	11:61522831	GGTCAGTCTGCCACC[C/T]AGAAAGGAGACCAGA	13855
rs26941141	snp	A/G	0.391111	0.206368	intron-variant	Epn2	Mm_Celera	11:61522761	CAGTGTAGGAAATAC[A/G]TGTTGTTCTGGACAT	13855
rs26941142	snp	A/C	0.391111	0.206368	intron-variant	Epn2	Mm_Celera	11:61522685	GGCAACAGGTGGGAT[A/C]AGAGAACACAAGTGC	13855
rs26941143	snp	A/C	0.32	0.24	intron-variant	Epn2	Mm_Celera	11:61522660	CTTCAGTCACTTGCT[A/C]GACTGGGAAGGCAAC	13855
rs26941144	snp	A/T	0.391111	0.206368	intron-variant	Epn2	Mm_Celera	11:61522608	AGGGGCTTCTCTCCC[A/T]GGTACTCCACATCAT	13855
rs26941145	snp	A/G	0.32	0.24	intron-variant	Epn2	Mm_Celera	11:61522512	GGGGACATACAAGCT[A/G]GTGACTGAAAGCATC	13855
rs26941146	snp	C/T	0.489796	0.070696	intron-variant	Epn2	Mm_Celera	11:61522083	ATTTGGGGTTGGTGG[C/T]AAAGCACAGATGTGT	13855
rs26941147	snp	G/T	0.391111	0.206368	synonymous-codon	Epn2	Mm_Celera	11:61521770	ACTCAGGTGTTTTCC[G/T]GGCACTGCTAGGCTT	13855
rs26941148	snp	C/G	0.124444	0.216185	intron-variant	Epn2	Mm_Celera	11:61520836	GTTGGAGTTGACACT[C/G]CTGGAGATACAGTTC	13855
rs26941149	snp	A/T	0.231111	0.249285	intron-variant	Epn2	Mm_Celera	11:61520530	TTGTAAGCAAGGCCT[A/T]CCACAGTGCTAGACC	13855
rs26941150	snp	C/T	0.32	0.24	intron-variant	Epn2	Mm_Celera	11:61520458	TCTACCCATGTAGCT[C/T]GGATATCTGCCAAAA	13855
rs26941151	snp	A/G	0.391111	0.206368	intron-variant	Epn2	Mm_Celera	11:61520405	ACCCTAGGTTCAAAG[A/G]GGCTGTGTAGCCCCT	13855
rs26941152	snp	A/T	0.124444	0.216185	intron-variant	Epn2	Mm_Celera	11:61519807	CACTTTTGGCATTCC[A/T]GAAGTGATCTGAAGG	13855
rs26941153	snp	C/G	0.124444	0.216185	intron-variant	Epn2	Mm_Celera	11:61519800	CTGCCTCCACTTTTG[C/G]CATTCCAGAAGTGAT	13855
rs26941154	snp	G/T	0.124444	0.216185	missense	Epn2	Mm_Celera	11:61519621	ATGCACTGCTTCCCA[G/T]GACAGGGCTTCCCCG	13855
rs26941155	snp	A/T	0.260355	0.249785	utr-variant-3-prime	Epn2	Mm_Celera	11:61519010	CAAAGGAAAATAAAA[A/T]ATGCACAACCACTTC	13855
rs26941156	snp	A/G	0.497778	0.0332592	utr-variant-3-prime	Epn2	Mm_Celera	11:61518501	CAGAGTCAACTGACT[A/G]ATAATTCATCAAAAG	13855
rs26941157	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Epn2	Mm_Celera	11:61518322	CCAGCCACATTTCTG[A/G]CCTGCAGTAAATGGA	13855
rs26941158	snp	C/T	0.391111	0.206368	utr-variant-3-prime	Epn2	GRCm38.p3	11:61518201	CTGGGCCAGTCTCTG[C/T]CATGACTCAGCTAGG	13855
rs26941159	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Epn2	Mm_Celera	11:61517953	GACACAAACTGCCAG[A/G]ACCAAGAAGGGGCAG	13855
rs26941160	snp	A/G	0.231111	0.249285	utr-variant-3-prime	Epn2	Mm_Celera	11:61517769	GCCTAGGAGCAGCAT[A/G]TAGACTCAGACCCAG	13855
rs26941161	snp	C/T	0.32	0.24	utr-variant-3-prime	Epn2	GRCm38.p3	11:61517686	CCTGAATAGCAGAGC[C/T]CAAACCTTTCCCTCG	13855
rs26941162	snp	A/C	0.391111	0.206368	downstream-variant-500B	Epn2	Mm_Celera	11:61517177	AAGCTGCTTCCCTAG[A/C]CAGCCCTGCCACATC	13855
rs26941163	snp	C/T	0.124444	0.216185	downstream-variant-500B	Epn2	Mm_Celera	11:61517132	CATCAAAAGCAGACC[C/T]GAGCCTGTCCTTGAG	13855
rs26941164	snp	A/G	0.124444	0.216185	downstream-variant-500B	Epn2	Mm_Celera	11:61516885	CTGACAGAGAAATCC[A/G]GTCTGTGGAGAGGTG	13855

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