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
rs3674805	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108426732	CACACCAAAAAGTAT[C/T]CATAGTAACCATTAG	68519
rs3683974	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108516767	ATTTACAAGTAAAAT[A/G]AGAGAATTTGAAGCT	68519
rs3683977	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108516769	TTACAAGTAAAATAA[A/G]AGAATTTGAAGCTAC	68519
rs3683995	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108516784	GAGAATTTGAAGCTA[C/T]CCAACACTTCCTGTT	68519
rs3685901	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108517122	ACCAGCGTGGGGATA[C/T]CACTCCATCCCCAGC	68519
rs3685943	snp	C/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108517142	CCATCCCCAGCTATG[C/G]AGGATGGAGGATTTC	68519
rs3693681	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521188	TGCACAGTAAGTTCA[A/G]GGCTAGCCTGGACTA	68519
rs3707852	snp	A/C	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521261	CCCAAAAAAGCCAAA[A/C]ACCAATTGAATGAAA	68519
rs3709227	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521495	CCCGTTAATATGGAC[A/G]CGTGTGAGTTTCCCA	68519
rs3709266	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521519	TTTCCCAGTGTGGTG[A/G]CCTCCTGCTTCAGTT	68519
rs3709283	snp	G/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521534	ACCTCCTGCTTCAGT[G/T]CGGTGTTCTGTGGCA	68519
rs3709399	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108426355	GCCCTAGCATGTACA[C/T]GTGTGCTCAGGCCAG	68519
rs3709760	snp	C/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521557	CTGTGGCATGATTAA[C/G]CTTGAGAGGAAAGAG	68519
rs3709797	snp	A/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521574	TTGAGAGGAAAGAGC[A/T]CATGAGACGGTCCTT	68519
rs3709814	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521582	AAAGAGCTCATGAGA[C/T]GGTCCTTCGGGGGTG	68519
rs3719674	snp	A/G	0.5	0	upstream-variant-2KB	Eml1	Mm_Celera	12:108370181	ATGTCAAGCCTGCTC[A/G]CTCAGTCCCTGCTTG	68519
rs4136848	snp	C/G	0.429688	0.173817	intron-variant	Eml1	GRCm38.p3	12:108431525	AACTGAGAAAGACCC[C/G]GGATCTCTGCTCCAG	68519
rs4136915	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521607	GGGGTGCCGTTGTGA[C/T]GGTGGGATCTCAGAG	68519
rs4139205	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108516868	AACCTCTAGAATCCA[A/G]CATGCTTCGTGCACA	68519
rs4229553	snp	C/T	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539302	CTGGGGACTGTATCT[C/T]GGATCTTTAAATAGA	68519
rs4229554	snp	C/G	0.21875	0.248039	utr-variant-3-prime, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539377	GTAAACTCGTTTAAG[C/G]GAGTGAGTGAGTTGA	68519
rs4229555	snp	C/T	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108539408	GTTACCTGAACTCTG[C/T]AGCACTGGTTGTTCA	68519
rs4229556	snp	C/T	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108539424	AGCACTGGTTGTTCA[C/T]AGTGATGAAGGACAG	68519
rs4229557	snp	A/G	0.48	0.0979796	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	GRCm38.p3	12:108539438	ATAGTGATGAAGGAC[A/G]GCACTGCAGACATCT	68519
rs4229558	snp	A/G	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108539439	TAGTGATGAAGGACA[A/G]CACTGCAGACATCTC	68519
rs4229559	snp	A/C	0.375	0.216506	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	GRCm38.p3	12:108539445	TGAAGGACAGCACTG[A/C]AGACATCTCCCTTGC	68519
rs4229560	snp	A/G	0.277778	0.248452	downstream-variant-500B, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539582	TTCTTATTGACCTAC[A/G]TTTCTGAAAGTATGT	68519
rs4229561	snp	A/T	0.252401	0.249988	downstream-variant-500B, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539583	TCTTATTGACCTACG[A/T]TTCTGAAAGTATGTG	68519
rs4229562	snp	A/G	0.375	0.216506	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539598	TTTCTGAAAGTATGT[A/G]AATTAAAGAATTTAA	68519
rs4229563	snp	C/T	0.21875	0.248039	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539601	CTGAAAGTATGTGAA[C/T]TAAAGAATTTAAAAT	68519
rs4229564	snp	C/G	0.30839	0.243086	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539627	AAAATTAGATGGGGT[C/G]CACACTACATCCTGT	68519
rs4229565	snp	A/G	0.21875	0.248039	downstream-variant-500B, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539631	TTAGATGGGGTCCAC[A/G]CTACATCCTGTTCCC	68519
rs4229566	snp	A/G	0.4992	0.019984	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539683	GGATCCCTTGCACAC[A/G]GAGTTCTGTTCTGCA	68519
rs6153877	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108534200	TTATCAATTTAGGGC[C/T]CAATGGTTAAGAGCA	68519
rs6153878	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108534203	TCAATTTAGGGCCCA[A/G]TGGTTAAGAGCACTA	68519
rs6153945	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108534243	ACAAAGGATCTGGGC[C/T]CAATTCCCAGCACCC	68519
rs6239767	snp	A/C	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533097	GGTTTATTTATGTTG[A/C]GTTCCTGCTTTTCCA	68519
rs6239832	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533147	GTTATTTATGGGATA[A/G]CCTTCTTTCCTGGTA	68519
rs6239861	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108506449	GGAGCGCCCCGAGGC[A/G]TGTCACTGACACCTT	68519
rs6239906	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533196	AACCCCCCCACTCCC[C/T]GCCTGAGCCCNGTCT	68519
rs6240304	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533207	TCCCNGCCTGAGCCC[C/T]GTCTCAGACATTTGA	68519
rs6240371	snp	C/T	0.492188	0.0620098	intron-variant	Eml1	GRCm38.p3	12:108533247	TCAGCTCGCAGACGC[C/T]TCCCAGTTCCCCACG	68519
rs6240406	snp	C/T	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108533274	CACGTGCATTCTCTG[C/T]TCTCANCTTTGTATT	68519
rs6240423	snp	A/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533280	CATTCTCTGNTCTCA[A/T]CTTTGTATTGATTCT	68519
rs6240517	snp	C/T	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108506620	GGGTGTATCCTTTAC[C/T]GGCCAACCAGACTGT	68519
rs6240887	snp	C/T	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108533345	AACAGATGAAGTTAG[C/T]GCAGGGACACGTCCT	68519
rs6241375	snp	A/G	0.426035	0.177515	intron-variant	Eml1	GRCm38.p3	12:108533407	CAGAGGCAGCAGGGT[A/G]GATGTTCTTCCCAGC	68519
rs6241420	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533437	CACCCCAGCTTCTGT[A/G]GTATCCNTCCCCCAG	68519
rs6241424	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533444	GCTTCTGTNGTATCC[C/T]TCCCCCAGAAAATAT	68519
rs6243578	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108533873	ATGCTGGCAGTTTTT[A/G]GACTAGTCTCCAGGC	68519
rs6244188	snp	A/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533973	GTCTAGCATTTCAGC[A/T]CCAGCACTACCACCC	68519
rs6244638	snp	C/G	0.396694	0.202437	intron-variant	Eml1	GRCm38.p3	12:108534007	AGCCCAGACTTCCTT[C/G]ACACAGGAGGCTCCA	68519
rs6244699	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108534043	GTGGACCCCCCAGGA[A/G]GATATGGGAAAGCCT	68519
rs13474898	snp	A/G			utr-variant-3-prime, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108538797	TACTACAGAACCCCC[A/G]AGCTGCTGTGGGTCC	68519
rs13474899	snp	A/G	0.486111	0.0821678	utr-variant-3-prime, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539171	CTGACTCTCGTGCAC[A/G]GACAGCATGCAGCAT	68519
rs13481641	snp	C/T	0.491278	0.0654592	intron-variant	Eml1	GRCm38.p3	12:108371681	AGTGGGTGCAGGGTG[C/T]ATGACCTTTGACACC	68519
rs29124775	snp	C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108433004	TATGCTCTTCCCAGT[C/T]TGGTTCTCTGGGTCT	68519
rs29125627	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108373516	GAGATGAAGTCCAGC[A/G]GGCAGATGACATGCC	68519
rs29125630	snp	A/C	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108461322	GTTTTAAAACAGTTC[A/C]GACAGTATTCTGGAA	68519
rs29126227	snp	C/T	0.188366	0.242283	intron-variant	Eml1	Mm_Celera	12:108389430	GGAGAATGCTTTGTG[C/T]ACTCAGGAACACCTT	68519
rs29126556	snp	A/T	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108510113	TTATGTTTAAACTTT[A/T]GGAAGATTGTAGAAG	68519
rs29126641	snp	C/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108435092	GGTATGTCTTGGTAA[C/G]AGAAAACCAGTGAAG	68519
rs29127529	snp	G/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108433103	GTCTTACTGTGAGAC[G/T]CGAGATCCTGTACAC	68519
rs29128166	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108515693	CGCATGCGCACAGAT[C/T]AGACCTTTTTTTTTT	68519
rs29128195	snp	C/G	0.444444	0.157135	upstream-variant-2KB	Eml1	Mm_Celera	12:108369434	ACCTGGCATAGGACA[C/G]GACATGGGCCAGGCC	68519
rs29128306	snp	A/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108509431	CAGATTATCTGAGGG[A/T]AAAAGCTTCAGGAAG	68519
rs29128751	snp	C/T	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108372769	TGACAAGAGACCCTG[C/T]GCAAGCTCTTGGAAT	68519
rs29128933	snp	A/C	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108513318	TAACAAACCCAGGAA[A/C]CCACTATGTGCTGGG	68519
rs29129879	snp	A/G	0.415225	0.187619	intron-variant	Eml1	GRCm38.p3	12:108389345	CAGATAAGTTACAGG[A/G]ACTGTTTTACATGAG	68519
rs29131598	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108528333	CAAGAAAGGAGGCCC[C/T]CTTTCTCAGCTAGAG	68519
rs29131651	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108374893	AGACCTCGGAGGACA[A/G]ACCTGACAGCTGTCT	68519
rs29131881	snp	G/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108382326	CCAGGCATGTGCCTG[G/T]GACCCCAACATTGTG	68519
rs29132320	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108470672	CCTGACTACAATCAC[C/T]GGAGAGGACAGCTTC	68519
rs29133349	snp	A/G	0.375	0.216506	intron-variant	Eml1, Gm33385	Mm_Celera	12:108407769	TAGTTAACTTGGTTG[A/G]ACAGAAACTTCAGAC	68519
rs29133944	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108506006	AGAAGGGCAACAGAT[C/T]TCTTGGAGTATTGTG	68519
rs29134853	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108502672	ACTTCTCAGGAAAGA[C/T]GCCCTTTGCCTGTAG	68519
rs29136747	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108515732	TTTGGTTTTTTGAGA[C/T]AGGGTTTCTCAGTAT	68519
rs29136871	snp	A/G	0.48	0.0979796	intron-variant	Eml1	Mm_Celera	12:108371901	GATGTGTGTAGGATT[A/G]GCTACCTGAAATAGT	68519
rs29137688	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108532038	AGAGTCTGGAACTCA[C/T]TAACCTTCTTCTGAC	68519
rs29138318	snp	C/T	0.465374	0.126941	intron-variant	Eml1	GRCm38.p3	12:108396515	AGGGAATAGGGCATC[C/T]GAGATGCTGAAGTCT	68519
rs29138546	snp	C/T	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108526105	TCCCTCTCTGGAGTT[C/T]GGTGGCAAAGACATC	68519
rs29138815	snp	A/C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108437615	AACATTCGGCCACTG[A/C/T]GGCTTTTATCTTGTG	68519
rs29139004	snp	G/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108387438	TGGGGTTGGAGCCCA[G/T]AGAACCCAGAAGAAG	68519
rs29139323	snp	C/T	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108447868	TTGGAGGCTTCTCAT[C/T]ACCAGGTGCCCTGCG	68519
rs29139647	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108531057	ATGTATGTATGTGTG[A/G]TTTATGAGTGTATAA	68519
rs29140024	snp	A/G	0.49827	0.0293608	intron-variant	Eml1	GRCm38.p3	12:108530962	CCCAGCCCTTTTGAT[A/G]AGTTTATTCTTCTAG	68519
rs29141037	snp	A/G	0.387812	0.208586	intron-variant	Eml1	Mm_Celera	12:108420736	AACTCACACTTTCCC[A/G]TGTCTGTGCCCCATC	68519
rs29141754	snp	C/T	0.484429	0.0868505	intron-variant, nc-transcript-variant	Eml1, Gm16596	GRCm38.p3	12:108537139	AGCTGTTAGAAGAGA[C/T]GCAGGGCTTCTCAGG	68519
rs29142954	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108512584	AATACTGGCCTTCCA[A/G]AGGACTCGGGATCGA	68519
rs29143185	snp	A/G	0.475309	0.108333	intron-variant	Eml1	GRCm38.p3	12:108428529	GTGCTCTCTCAAAGG[A/G]CAACCCAATATAACC	68519
rs29143692	snp	A/C	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108431555	GCCCCACACATGCAC[A/C]GACACAGACACGTAC	68519
rs29143792	snp	C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108432987	AGGTGCCCTGCCTGA[C/T]TTATGCTCTTCCCAG	68519
rs29144148	snp	C/T	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108503895	TCACTTTGAACTCCA[C/T]CATTCCCGCTTCCCT	68519
rs29145047	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108391442	GCTGGGCTGCGGCCC[A/G]TGTTAAATGAAGAAA	68519
rs29146868	snp	C/T	0.375	0.216506	intron-variant	Eml1, Gm33385	Mm_Celera	12:108407160	TTTTATACTTCTTGG[C/T]TGAGATGTGTTATCT	68519
rs29147133	snp	C/G	0.401235	0.199068	intron-variant	Eml1	Mm_Celera	12:108376546	CTCTCCTCCACTTCT[C/G]TATTCTCTCATTCAT	68519
rs29147196	snp	A/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108472225	AGTAGTATGGGGTAA[A/G]TATTTTTGCTTACCG	68519
rs29147218	snp	C/G/T	0.444444	0.157135	utr-variant-3-prime, nc-transcript-variant, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539255	CGAGAAGGCCTTACC[C/G/T]GTGGTGTGACAGATT	68519
rs29149162	snp	G/T	0.5	0	missense	Eml1	GRCm38.p3	12:108471939	AGTGCCTCCCTCCCG[G/T]CACCCTCCGGGGCCA	68519
rs29149683	snp	C/T	0.375	0.216506	upstream-variant-2KB	Eml1	Mm_Celera	12:108369232	AGGGTTGGTAGAGTT[C/T]AGGAGCAGGAGCAGT	68519

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