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
rs13470953	snp	A/G			utr-variant-5-prime	Epn3	GRCm38.p3	11:94496580	CGGCCCTCTACCTCC[A/G]ACGGGGGCGGGGGCC	71889
rs27059702	snp	A/C	0.444444	0.157135	upstream-variant-2KB, intron-variant	Epn3, Mycbpap	GRCm38.p3	11:94501934	CATCAAACAGAACTT[A/C]TGGTCAAATGAGACC	71889
rs27059703	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Epn3, Mycbpap	GRCm38.p3	11:94501767	AGCTTCCAAGACTGA[A/G]CCCTCTACTGCAGCT	71889
rs27059704	snp	C/T	0.429688	0.173817	upstream-variant-2KB, downstream-variant-500B	Epn3, Mycbpap	GRCm38.p3	11:94501152	GCTATGAAAGGCCAT[C/T]TTGTCCTGTCACCTG	71889
rs27059705	snp	C/G	0.46875	0.121031	upstream-variant-2KB, downstream-variant-500B	Epn3, Mycbpap	GRCm38.p3	11:94501031	GTGCTGAAGTAGAAG[C/G]CTTCAGACAGTCAGG	71889
rs27059706	snp	C/T	0.48	0.0979796	upstream-variant-2KB	Epn3	GRCm38.p3	11:94500527	TCTGAGCAGGCAGTG[C/T]GTGCTTTCCCAGCTG	71889
rs27059707	snp	A/G	0.197531	0.244432	upstream-variant-2KB	Epn3	Mm_Celera	11:94500079	GCCTGTTTGTCAGCC[A/G]GTGACCCCAGAGGTT	71889
rs27059708	snp	A/G	0.336735	0.234472	utr-variant-5-prime, upstream-variant-2KB	Epn3	Mm_Celera	11:94499831	GCTCTACCTTGGACC[A/G]AAAGGCACAGAGCTC	71889
rs27059709	snp	C/G	0.197531	0.244432	intron-variant, upstream-variant-2KB	Epn3	Mm_Celera	11:94499558	AGGTTAGAAGCCTCC[C/G]GGTACTCCACAGCCC	71889
rs27059710	snp	A/G	0.197531	0.244432	intron-variant, utr-variant-5-prime	Epn3	Mm_Celera	11:94498539	AGGTGGACATTGTGG[A/G]CACACCTTTGCTGGA	71889
rs27059711	snp	A/G	0.124444	0.216185	intron-variant, utr-variant-5-prime	Epn3	Mm_Celera	11:94498442	CTTCCTACTTTGCCA[A/G]GGTGAATACAGCCAG	71889
rs27059712	snp	A/G	0.132653	0.220748	intron-variant	Epn3	Mm_Celera	11:94498040	ACAAGTGAAAGATCA[A/G]CTCAGTTCAAAGTAC	71889
rs27059713	snp	C/T	0.46281	0.131194	intron-variant	Epn3	GRCm38.p3	11:94497702	CAGGAGAATCAGTCA[C/T]ATGTCTTTCCACAGC	71889
rs27059714	snp	C/G	0.495868	0.0452663	intron-variant	Epn3	Mm_Celera	11:94497685	CCTAATGGAGGCCGA[C/G]TCAGGAGAATCAGTC	71889
rs27059715	snp	C/G	0.21875	0.248039	intron-variant	Epn3	Mm_Celera	11:94497324	AGAAGATGTAGGGGA[C/G]CAGCAAGGCCAGGAA	71889
rs27059716	snp	A/G	0.48	0.0979796	intron-variant	Epn3	GRCm38.p3	11:94497293	GCACTCGAGGGAAGC[A/G]CAACAGGGAAAATCA	71889
rs27059717	snp	A/C	0.497041	0.0383476	intron-variant	Epn3	GRCm38.p3	11:94496870	AAAACCATCAGACCA[A/C]GATGCTGAAATCCCT	71889
rs27059718	snp	A/G	0.375	0.216506	intron-variant	Epn3	GRCm38.p3	11:94496817	CTTATTGCACTCACT[A/G]TCCAATGGACACGCT	71889
rs27059719	snp	A/C	0.387812	0.208586	synonymous-codon	Epn3	GRCm38.p3	11:94496120	ATGGGTTCGCTCTTG[A/C]CGCAGGCGCTCCTCA	71889
rs27059720	snp	A/G	0.484429	0.0868505	synonymous-codon	Epn3	Mm_Celera	11:94496060	CAGCTGCCCGCTGCC[A/G]ATACCCATGCCTTCC	71889
rs27059721	snp	C/T	0.401235	0.199068	intron-variant	Epn3	Mm_Celera	11:94495931	TCCTGGGTGGAGAGC[C/T]ATGACTGTGGCTGGC	71889
rs27059722	snp	G/T	0.444444	0.157135	intron-variant	Epn3	GRCm38.p3	11:94495447	ATGGAAGGAGGGCCT[G/T]TCTGTTCCTCAGGTC	71889
rs27059723	snp	A/G	0.484429	0.0868505	intron-variant	Epn3	Mm_Celera	11:94495319	CTGACTTCAGCTCTT[A/G]AACTCTTCAATAGGA	71889
rs27059724	snp	A/G	0.124444	0.216185	intron-variant	Epn3	Mm_Celera	11:94495273	CGAAGGGGGCTGGCA[A/G]TAGTCCTAAGTCAGG	71889
rs27059725	snp	A/G	0.444444	0.157135	intron-variant	Epn3	GRCm38.p3	11:94494749	CACTGCCCTTTCTGG[A/G]TCCCGCAGGAGAACA	71889
rs27059726	snp	C/T	0.475309	0.108333	intron-variant	Epn3	Mm_Celera	11:94494458	TTTCTTCTGGGTACC[C/T]TGAGAACTTCCCTAG	71889
rs27059727	snp	A/G	0.231111	0.249285	intron-variant	Epn3	Mm_Celera	11:94493983	GGCACCCAGGTTAGC[A/G]CAGCTGAGAGAGAAG	71889
rs27059728	snp	A/G	0.48	0.0979796	intron-variant	Epn3	GRCm38.p3	11:94493909	GATCTCACCCCCTGC[A/G]GAATGACAGGTAGGG	71889
rs27059729	snp	A/C	0.124444	0.216185	missense	Epn3	Mm_Celera	11:94493829	TCTCAGGCTCCCTGT[A/C]CCGTTGACGACGTTG	71889
rs27059730	snp	A/G	0.465374	0.126941	intron-variant	Epn3	Mm_Celera	11:94493576	AAAGGGGAAACTGAG[A/G]CCAGTAGTATTCCAA	71889
rs27059731	snp	C/G	0.465374	0.126941	intron-variant	Epn3	Mm_Celera	11:94492811	GTGGCTGGAAGGAAG[C/G]AGGGCTCTTAGGGGC	71889
rs27059732	snp	A/G	0.375	0.216506	intron-variant	Epn3	GRCm38.p3	11:94492526	CCCAGCCCAGGTTGG[A/G]TGATGTGCCCACTTC	71889
rs27059733	snp	C/T	0.345679	0.230967	synonymous-codon	Epn3	GRCm38.p3	11:94492194	GGTCTCCATAGAGGC[C/T]CCCCAAGGGTCTGCT	71889
rs27059734	snp	A/G	0.475309	0.108333	missense	Epn3	GRCm38.p3	11:94491470	TTGGTTGGGGACGGA[A/G]CACCCAGACCTGCGG	71889
rs27059735	snp	A/C	0.444444	0.157135	utr-variant-3-prime	Epn3	GRCm38.p3	11:94491100	TCAGTGCTCAACCTG[A/C]ACGATCCGCCCTCGA	71889
rs27059736	snp	A/G	0.401235	0.199068	utr-variant-3-prime	Epn3	GRCm38.p3	11:94491020	TATTAGGCGGGTGTA[A/G]TCTTCGTCCCCAAGA	71889
rs27059737	snp	C/G	0.429688	0.173817	utr-variant-3-prime	Epn3	Mm_Celera	11:94490644	TGGACAGAGAGTACT[C/G]CATATCCAGCTTAGG	71889
rs27059738	snp	C/T	0.336735	0.234472	utr-variant-3-prime	Epn3	GRCm38.p3	11:94490266	GACAGTCAGTGTTTG[C/T]TGTATTAAACCTGAT	71889
rs27059739	snp	A/G	0.489796	0.070696	utr-variant-3-prime	Epn3	GRCm38.p3	11:94490029	GTCCAGACCTCAGAT[A/G]GTCAAGGTGGCTCTC	71889
rs27059740	snp	C/T	0.18	0.24	utr-variant-3-prime	Epn3	Mm_Celera	11:94489851	GGCTGAGGAAGTCCA[C/T]GTGCTCTCGGTGACC	71889
rs27059741	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Epn3	GRCm38.p3	11:94489629	TCATTTACTCAAGAG[C/T]GACTTAACCACTCAT	71889
rs27059742	snp	C/G	0.132653	0.220748	downstream-variant-500B	Epn3	Mm_Celera	11:94489300	CCATGAGGAAAGCAT[C/G]CTGGGAATGGGGAGT	71889
rs27059743	snp	A/G	0.486111	0.0821678	downstream-variant-500B	Epn3	GRCm38.p3	11:94489230	GAGACATGAATGAAG[A/G]TGGATGAGAGGTCCA	71889
rs27059744	snp	A/G	0.444444	0.157135	downstream-variant-500B	Epn3	Mm_Celera	11:94489149	ATGCTCCGGTGCCAA[A/G]AGAGTAGTTCCCAGG	71889
rs29393573	snp	C/T	0.444444	0.157135	intron-variant	Epn3	GRCm38.p3	11:94492461	GAGGGAGATAGCACA[C/T]ATATTATCCCAACAC	71889
rs29399722	snp	A/T	0.5	0	missense	Epn3	GRCm38.p3	11:94491194	GGGGGCAGCGGCCCC[A/T]TTGGGCCGGACGTGG	71889
rs29400527	snp	C/T	0.5	0	utr-variant-3-prime	Epn3	GRCm38.p3	11:94490364	GAACATGTCACTGTA[C/T]TTCTCGAAAGCCTCT	71889
rs29403226	snp	C/G	0.375	0.216506	upstream-variant-2KB	Epn3	GRCm38.p3	11:94500230	ACCCTCCTAGCCGGA[C/G]GACATTAAAGCAGAA	71889
rs29405050	snp	C/T	0.444444	0.157135	intron-variant	Epn3	GRCm38.p3	11:94498117	TGTGGAAATCAGATC[C/T]CCACTGGCCCATAGT	71889
rs29411377	snp	C/T	0.375	0.216506	utr-variant-3-prime	Epn3	GRCm38.p3	11:94489929	TGGGTCCTGAGCGCA[C/T]GTGGGTAGCCATGGT	71889
rs29419765	snp	C/T	0.5	0	utr-variant-3-prime	Epn3	Mm_Celera	11:94490555	TCCTCTTACCTCCAC[C/T]CCCTTAAGTACTGGG	71889
rs29433001	snp	A/G	0.5	0	utr-variant-3-prime	Epn3	Mm_Celera	11:94490565	TCCACTCCCTTAAGT[A/G]CTGGGATTACTCGTA	71889
rs29434808	snp	A/G	0.48	0.0979796	upstream-variant-2KB, intron-variant	Epn3, Mycbpap	GRCm38.p3	11:94501619	GATGGAGAGAGAAAC[A/G]CCAAAGTTGCTCCGA	71889
rs29437296	snp	C/T	0.48	0.0979796	upstream-variant-2KB	Epn3	GRCm38.p3	11:94500479	CAGCCTAACCAGTTG[C/T]TTACAGTCGTTTCAA	71889
rs29439033	snp	A/G	0.375	0.216506	intron-variant	Epn3	GRCm38.p3	11:94494263	CCCAGGCATGGCATG[A/G]TGATGGAAAAGCCCC	71889
rs29444218	snp	A/G	0.375	0.216506	intron-variant	Epn3	GRCm38.p3	11:94495068	CTGCAACAAGGGTGG[A/G]GCCCGTGAGCACAAC	71889
rs29444912	snp	C/T	0.5	0	intron-variant	Epn3	Mm_Celera	11:94494254	ACAATCCTGCCCAGG[C/T]ATGGCATGATGATGG	71889
rs29444968	snp	C/T	0.48	0.0979796	intron-variant	Epn3	GRCm38.p3	11:94493015	GAGGGGAGGTCTGAC[C/T]GGTGGCCAGAAGCCA	71889
rs29445026	snp	A/G	0.5	0	synonymous-codon	Epn3	GRCm38.p3	11:94496189	AACATTGACGCCCTG[A/G]TCCTTGCCATCTCGG	71889
rs29448771	snp	C/T	0.48	0.0979796	intron-variant	Epn3	GRCm38.p3	11:94493123	AAACATTTCCTCATC[C/T]GTCTAGTGCCCCATT	71889
rs29451149	snp	C/T	0.5	0	utr-variant-3-prime	Epn3	GRCm38.p3	11:94490376	GTATTTCTCGAAAGC[C/T]TCTGTTGGCTATTAA	71889
rs29468906	snp	C/T	0.48	0.0979796	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	Epn3, Mycbpap	GRCm38.p3	11:94501389	ACTTTTTTCAAACCA[C/T]CTTCCCAGGAGGAAG	71889
rs29469945	snp	C/T	0.48	0.0979796	intron-variant	Epn3	Mm_Celera	11:94493151	ATTTCATAACATCCC[C/T]GTGAGGTAGGTAATG	71889
rs29470164	snp	A/T	0.48	0.0979796	intron-variant	Epn3	GRCm38.p3	11:94492570	TGACTTGGAGCAAGC[A/T]GCTCTCTCAAGTCCA	71889
rs29472458	snp	A/G	0.375	0.216506	utr-variant-5-prime, upstream-variant-2KB	Epn3	GRCm38.p3	11:94499960	TTGTTCAGCTGGCCA[A/G]GCAGGTCTGCCTCAG	71889
rs29479864	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Epn3	GRCm38.p3	11:94490001	TCCTAAGCCCTGCAA[C/T]AACCTTGCAGAGGTC	71889
rs29480813	snp	A/T	0.375	0.216506	intron-variant	Epn3	GRCm38.p3	11:94495169	CTCTTCAGGCACTTG[A/T]GAGCCAGACAGTACA	71889
rs29481331	snp	A/G	0.5	0	utr-variant-3-prime	Epn3	Mm_Celera	11:94490395	GTTGGCTATTAAATA[A/G]GACTAGTAAGAAAGA	71889
rs29481849	snp	A/G	0.375	0.216506	utr-variant-3-prime	Epn3	Mm_Celera	11:94489926	CCCTGGGTCCTGAGC[A/G]CATGTGGGTAGCCAT	71889
rs29482520	snp	A/G	0.48	0.0979796	intron-variant	Epn3	GRCm38.p3	11:94493016	AGGGGAGGTCTGACT[A/G]GTGGCCAGAAGCCAG	71889
rs29484294	snp	C/T	0.375	0.216506	upstream-variant-2KB, downstream-variant-500B	Epn3, Mycbpap	GRCm38.p3	11:94501231	TTAATCATCACCTCT[C/T]TGGTGTGTGTGGCTC	71889
rs46156896	snp	C/G			intron-variant, upstream-variant-2KB	Epn3	Mm_Celera	11:94499112	CAAATCCAGAAGGGT[C/G]CCAGAGTGGGGGATG	71889
rs46180387	snp	C/G			intron-variant	Epn3	Mm_Celera	11:94496967	GAGCCGCTAAGTGTG[C/G]ACATTCCTCCCCCCA	71889
rs46184841	snp	C/T			intron-variant	Epn3	GRCm38.p3	11:94497176	GGAGTCCTTTCCGAC[C/T]CCCACCATCTGCTTG	71889
rs46760372	snp	A/G			intron-variant	Epn3	Mm_Celera	11:94496921	GGTGGGACTCGGGCA[A/G]TCAATCGGTCAGCGA	71889
rs47822916	snp	G/T			intron-variant	Epn3	GRCm38.p3	11:94496854	GGCACGCTCATTCCA[G/T]AAAACCATCAGACCA	71889
rs47960202	snp	C/T			intron-variant	Epn3	Mm_Celera	11:94496905	GGTCACAAATGGGGA[C/T]GGTGGGACTCGGGCA	71889
rs48228481	snp	C/G			intron-variant	Epn3	GRCm38.p3	11:94497417	ACTCAGCCACCACCC[C/G]CTGGCCTACACACAG	71889
rs48781197	snp	C/T			intron-variant	Epn3	Mm_Celera	11:94496956	CTGAGGTCACAGAGC[C/T]GCTAAGTGTGCACAT	71889
rs49123343	snp	C/T			intron-variant	Epn3	GRCm38.p3	11:94497353	AATCTGTCACCTGAT[C/T]AGACAGCCAGGGGAA	71889
rs49170265	snp	A/C			intron-variant	Epn3	GRCm38.p3	11:94497426	CCACCCGCTGGCCTA[A/C]ACACAGGGCTGCTGT	71889
rs49841793	snp	A/G			intron-variant	Epn3	Mm_Celera	11:94497460	CCGCCTATGTCACAG[A/G]CCATGTAGGTGGCAG	71889
rs50090873	snp	A/G			intron-variant	Epn3	Mm_Celera	11:94496916	GGGACGGTGGGACTC[A/G]GGCAGTCAATCGGTC	71889
rs50934276	snp	A/C			intron-variant	Epn3	Mm_Celera	11:94497427	CACCCGCTGGCCTAC[A/C]CACAGGGCTGCTGTG	71889
rs51608544	snp	A/G			intron-variant	Epn3	Mm_Celera	11:94496946	CAGCGATGCTCTGAG[A/G]TCACAGAGCCGCTAA	71889
rs108368783	snp	C/T			downstream-variant-500B	Epn3	GRCm38.p3	11:94489333	CTGCCCCAGACAGGG[C/T]AGAGCAGAGCAGAGT	71889
rs211903744	snp	A/T			upstream-variant-2KB, intron-variant	Epn3, Mycbpap	Mm_Celera	11:94501573	CTCGGTTTTGCAGGC[A/T]CCAATGTATCAGTCT	71889
rs212111524	snp	C/G			intron-variant	Epn3	Mm_Celera	11:94493753	CCTGGTCAGCTCACA[C/G]TCCCCAGCCCTCTCT	71889
rs212235000	snp	C/T			intron-variant	Epn3	Mm_Celera	11:94494869	GGTGAAAAGCCCAAA[C/T]GGGGACTAGTGAACA	71889
rs212525744	snp	A/T			intron-variant	Epn3	GRCm38.p3	11:94497851	ATACACACACACACA[A/T]AGAAGCTGGATCAGC	71889
rs212642529	snp	G/T			intron-variant, upstream-variant-2KB	Epn3	Mm_Celera	11:94499008	AGGCTAGTCAGGAAG[G/T]GGGGGGGGGGCGGGG	71889
rs212915704	in-del	-/C			upstream-variant-2KB	Epn3	Mm_Celera	11:94500666	CCCACCCCGACATTG[-/C]GCAGGCTGGCCTCAG	71889
rs213055242	snp	A/C			upstream-variant-2KB	Epn3	Mm_Celera	11:94500559	TACCCTTCACCTACT[A/C]CACAGTCCCACATTC	71889
rs213982928	snp	A/C/G			intron-variant	Epn3	Mm_Celera	11:94495968	CCCCCCACTTGCCCC[A/C/G]CCCCCACAAGCCATA	71889
rs214246698	snp	G/T			intron-variant, upstream-variant-2KB	Epn3	Mm_Celera	11:94499272	CCCTCCCCATCTTCT[G/T]TCCCCATCAGCTCCA	71889
rs214341375	snp	C/T			utr-variant-3-prime	Epn3	Mm_Celera	11:94490318	TCTGACTCTGAATCC[C/T]AGCCCCACGTCACTC	71889
rs214355483	snp	A/G			upstream-variant-2KB	Epn3	Mm_Celera	11:94500505	TTCAACAGAAACCCC[A/G]GGATGATCTGAGCAG	71889
rs215008739	snp	C/T			intron-variant	Epn3	Mm_Celera	11:94493684	TTCCCATTTAGTGCT[C/T]GGAGCGAGCTCTGCT	71889
rs215172456	snp	C/T			downstream-variant-500B	Epn3	Mm_Celera	11:94489523	GATAGGGATGAATGG[C/T]CAACTGCCACGGGAG	71889
rs215338734	snp	C/T			intron-variant	Epn3	Mm_Celera	11:94492560	AGTGGGATGCTGACT[C/T]GGAGCAAGCAGCTCT	71889

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