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
rs3682238	snp	C/G	0.255	0.24995	intron-variant	Eed	Mm_Celera	7:89958061	CTTAACTGACCGGCT[C/G]GACGAGCAAAGAAGG	13626
rs3682253	snp	A/G	0.415225	0.187619	intron-variant	Eed	GRCm38.p3	7:89958074	CTGGACGAGCAAAGA[A/G]GAGAATCCCCAATCA	13626
rs3682305	snp	A/G	0.42	0.183303	intron-variant	Eed	GRCm38.p3	7:89958099	CAATCAAGACAACCC[A/G]ATAGAATATCATCCA	13626
rs6298169	snp	G/T	0.5	0	intron-variant	Eed	GRCm38.p3	7:89970774	ATGCCTGTGGAAGTA[G/T]TCTACTGCACTGATG	13626
rs6298240	snp	C/G	0.5	0	intron-variant	Eed	Mm_Celera	7:89970814	AACAGCCGGAAACAG[C/G]AGTTGAACATGTAGA	13626
rs6298704	snp	A/G	0.5	0	intron-variant	Eed	Mm_Celera	7:89970852	GTTCTCCAGTAAAAC[A/G]TTATTTATAAAGCTA	13626
rs6298793	snp	A/G	0.5	0	intron-variant	Eed	GRCm38.p3	7:89970896	CAGGTTTGCCTTGCT[A/G]CTGACCCTCTGTCCT	13626
rs13465525	snp	A/G			missense, nc-transcript-variant	Eed	Mm_Celera	7:89976931	GGAAGTCAAAGAAAT[A/G]CAAATATTCTTTCAA	13626
rs13465526	snp	A/G	0.375	0.216506	synonymous-codon, nc-transcript-variant	Eed	GRCm38.p3	7:89976999	AGAACGCCCGGACAC[A/G]CCCACAAATACGCCA	13626
rs13465527	snp	C/T			utr-variant-5-prime, nc-transcript-variant	Eed	GRCm38.p3	7:89980804	CCTCGGTGCAAAGTG[C/T]CGAGAGGGCGGCGGG	13626
rs30674345	snp	A/G	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89976307	GTGTGTGTAAAGGCC[A/G]GCTTACCAGGCACGT	13626
rs30766626	snp	A/G	0.5	0	intron-variant	Eed	GRCm38.p3	7:89976568	ATTTGCTAGGGACCA[A/G]TTAACAGATCACACT	13626
rs30825586	snp	C/T	0.444444	0.157135	intron-variant	Eed	Mm_Celera	7:89975791	CTTCCTGTTATACTG[C/T]ACTCAGTAGGGACAG	13626
rs30971452	snp	C/T	0.5	0	intron-variant	Eed	Mm_Celera	7:89975377	TCTGTTAGGGAGACC[C/T]CCATCTTAAAAAAAC	13626
rs31039311	snp	C/T	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89974499	GTTTCTAAGACTCCA[C/T]ACACTGACGTCCAGT	13626
rs31055914	snp	C/T	0.444444	0.157135	upstream-variant-2KB	Eed	Mm_Celera	7:89981664	AATCAAGGCTATTTA[C/T]TAAAAACCTGTTTGA	13626
rs31099429	snp	C/G	0.375	0.216506	intron-variant	Eed	Mm_Celera	7:89960487	CAGGATAAAGTTTCA[C/G]TACACATCTATTGGA	13626
rs31111529	snp	A/G	0.32	0.24	intron-variant	Eed	GRCm38.p3	7:89968337	CCAGCATCTGTATCG[A/G]GTGGTTCACAATGGT	13626
rs31135477	snp	A/C	0.493827	0.0552116	intron-variant	Eed	Mm_Celera	7:89961422	AAAAAAAATCAAACT[A/C]AGTTCTGCCTAAGAT	13626
rs31145981	snp	A/G	0.375	0.216506	intron-variant	Eed	Mm_Celera	7:89969033	ATCTTTTAATAATAA[A/G]AGTATGGCTCTTCAC	13626
rs31147231	snp	C/T	0.32	0.24	intron-variant	Eed	GRCm38.p3	7:89968173	GGGGTAGGGGTCTGA[C/T]TGAGCAAGAGGACTT	13626
rs31148930	snp	A/C/G/T	0.375	0.216506	intron-variant	Eed	GRCm38.p3	7:89977151	TGAGATTGCTCCGCG[A/C/G/T]GTAAGAGCACTGATT	13626
rs31157670	snp	A/G	0.375	0.216506	intron-variant	Eed	GRCm38.p3	7:89977617	ACTGGTCTACACCAG[A/G]GACACCAATACAATG	13626
rs31180306	snp	C/T	0.432133	0.171253	intron-variant	Eed	GRCm38.p3	7:89972438	GCTCATTCACTACCT[C/T]ATATACTTGGGTGGT	13626
rs31201259	snp	A/G	0.32	0.24	intron-variant	Eed	GRCm38.p3	7:89964324	CCTCCTCAGTGCTGG[A/G]ATTAAAGGTGTTCAC	13626
rs31214498	snp	C/G	0.32	0.24	intron-variant	Eed	GRCm38.p3	7:89968302	GCAATTGCTGCTCTA[C/G]CAGAGGATGAGTCCA	13626
rs31343201	snp	A/G	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89980293	CGCCTGCGTTCTCCC[A/G]AGCGCGGGTGACACC	13626
rs31381671	snp	C/G/T	0.5	0	intron-variant	Eed	GRCm38.p3	7:89966917	AGGCAGGCAGGCAGG[C/G/T]AGGCAAAATGAGTGG	13626
rs31392456	snp	C/T	0.5	0	intron-variant	Eed	GRCm38.p3	7:89961634	TGAAACAGCTTCGCA[C/T]GTGCACATCCTCCCA	13626
rs31402209	snp	A/C	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89969263	AACGGAGCTACTAAA[A/C]ACATCTGAAAAACCT	13626
rs31405924	snp	C/T	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89972788	TTACAAGAGGTGCTA[C/T]GGTCATGGTGTCTCT	13626
rs31473440	snp	A/G	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89974321	GCATGGCTGAATCAC[A/G]TGTCTCTCTGTATCT	13626
rs31487939	snp	C/T	0.375	0.216506	upstream-variant-2KB	Eed	Mm_Celera	7:89982521	ACATTTGCTGGGCAC[C/T]CACTTAATAATAAAA	13626
rs31557945	snp	A/G	0.375	0.216506	intron-variant	Eed	Mm_Celera	7:89969029	CAAAATCTTTTAATA[A/G]TAAGAGTATGGCTCT	13626
rs31598152	snp	A/G	0.5	0	intron-variant	Eed	Mm_Celera	7:89968638	ACCCAGGACTAACTT[A/G]ACAAGTAACTGTTAA	13626
rs31599277	snp	A/G	0.429688	0.173817	intron-variant	Eed	Mm_Celera	7:89972186	CATTTTAGCACTCTA[A/G]TTGTAACAATCAGTA	13626
rs31621269	snp	C/T	0.5	0	intron-variant	Eed	Mm_Celera	7:89978052	CTGCCCAAACAGATA[C/T]AGCTGCAGGAAATAC	13626
rs31640996	snp	C/T	0.444444	0.157135	intron-variant	Eed	Mm_Celera	7:89979001	ACACACACACACACA[C/T]CCTTTGGTGAGGACA	13626
rs31691153	snp	A/G	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89974612	AGAGGCAGAATCTGT[A/G]TTATTTTGATTCCCA	13626
rs31703751	snp	G/T	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89956634	TTAAGTTCAGCTTTG[G/T]ATACGTTCGCATACA	13626
rs31738521	snp	C/T	0.375	0.216506	intron-variant	Eed	Mm_Celera	7:89977174	CACTGATTGTTCTTC[C/T]GAAGGTCCTGAGTTC	13626
rs31790448	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Eed	Mm_Celera	7:89981498	GGCTTAAGTAAGCCT[A/G]TATCTTAAATTACAT	13626
rs31795340	snp	C/T	0.444444	0.157135	intron-variant	Eed	Mm_Celera	7:89979810	AACTTTCAAACTGTT[C/T]CCTCCTTTGCCTTAA	13626
rs31804435	snp	C/G/T	0.5	0	intron-variant	Eed	GRCm38.p3	7:89957254	ACGTTGTTCTCTACC[C/G/T]TCTTCAGATTTAAAA	13626
rs31807551	snp	A/G	0.401235	0.199068	intron-variant	Eed	Mm_Celera	7:89966175	GATGACTCCCATACA[A/G]AGCCTGGTGTAGAAT	13626
rs31834628	snp	G/T	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Eed	GRCm38.p3	7:89981287	CGGAGACGACAGGCC[G/T]CCTCCTGGCCCCTCC	13626
rs31836283	snp	C/T	0.5	0	intron-variant	Eed	Mm_Celera	7:89966948	CCCAGGCTTTATTCT[C/T]ATCACCCAGGAAGCA	13626
rs31860539	snp	A/C	0.48	0.0979796	intron-variant	Eed	GRCm38.p3	7:89964183	TACCTACCTACCTAC[A/C]TACCTACCTATCCAC	13626
rs31874271	snp	A/G	0.5	0	downstream-variant-500B	Eed	Mm_Celera	7:89954364	TTAGAGGCCATAAGA[A/G]GACATTGTGTCCACT	13626
rs31879773	snp	C/T	0.375	0.216506	intron-variant	Eed	Mm_Celera	7:89969045	TAAGAGTATGGCTCT[C/T]CACTGCAGTGCTTCC	13626
rs31896134	snp	A/G	0.444444	0.157135	intron-variant	Eed	Mm_Celera	7:89969103	GTCCTGGGGTGGCCC[A/G]GCATGTGTGTGGAGG	13626
rs31908984	snp	C/T	0.375	0.216506	intron-variant	Eed	Mm_Celera	7:89969059	TTCACTGCAGTGCTT[C/T]CTTTATTATTTTGGG	13626
rs31926222	snp	A/C	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89974625	GTATTATTTTGATTC[A/C]CATATCCTTGGTTGC	13626
rs31928756	snp	G/T	0.32	0.24	intron-variant	Eed	GRCm38.p3	7:89968157	AAGGGACTATCGGGT[G/T]GGGGTAGGGGTCTGA	13626
rs32018029	snp	C/T	0.46875	0.121031	intron-variant	Eed	Mm_Celera	7:89972341	ATAAAATATAAACCA[C/T]GAAAGAAAAATTTAA	13626
rs32024598	snp	A/G	0.492188	0.0620098	intron-variant	Eed	Mm_Celera	7:89971894	GCCTTATAAATCCTC[A/G]CACATTTTATGTAAT	13626
rs32058975	snp	C/T	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Eed	Mm_Celera	7:89981356	ACCGGTTTCTGAAGC[C/T]TCGGGGAGGATTTCA	13626
rs32163733	snp	C/T	0.444444	0.157135	utr-variant-5-prime, nc-transcript-variant	Eed	Mm_Celera	7:89980642	CGCCACCGCCGCCGC[C/T]CCCCCCACTGTCGCA	13626
rs32165409	snp	C/T	0.5	0	intron-variant	Eed	Mm_Celera	7:89961632	CCTGAAACAGCTTCG[C/T]ACGTGCACATCCTCC	13626
rs32224874	snp	C/T	0.375	0.216506	intron-variant	Eed	GRCm38.p3	7:89972754	AAAATGTCAGCACGT[C/T]CCAACTAAATGCGTT	13626
rs32230014	snp	A/G	0.415225	0.187619	intron-variant	Eed	Mm_Celera	7:89967501	TATTCTTCCTCTCAT[A/G]GCACTCATCAGAGTC	13626
rs32269857	snp	A/T	0.5	0	intron-variant	Eed	Mm_Celera	7:89977631	GGGACACCAATACAA[A/T]GCCTCACTCACTCCT	13626
rs32299232	snp	C/T	0.265928	0.249492	intron-variant	Eed	Mm_Celera	7:89960801	GAGTGTGCTGTAGTT[C/T]CAAACTGGAAAAACA	13626
rs32345220	snp	A/G	0.375	0.216506	upstream-variant-2KB	Eed	GRCm38.p3	7:89982610	AATGAGACAATTTAG[A/G]TGAAAAAGTTTAAAT	13626
rs32356524	snp	C/T	0.375	0.216506	intron-variant	Eed	Mm_Celera	7:89972200	AGTTGTAACAATCAG[C/T]ATTGCCAACCTGCCC	13626
rs32389227	snp	C/T	0.375	0.216506	intron-variant	Eed	GRCm38.p3	7:89957489	AGGAATGGCCCGCCT[C/T]CTTTAAGGTGGGATC	13626
rs32406317	snp	C/T	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89974346	GTATCTACATTTCTT[C/T]ACTCAGCTGTTGATG	13626
rs32410399	snp	A/G	0.265928	0.249492	intron-variant	Eed	Mm_Celera	7:89961354	GGAGGGGAAAATGAA[A/G]CCAACAACAGTAAGT	13626
rs32410970	snp	A/G	0.375	0.216506	intron-variant	Eed	GRCm38.p3	7:89972527	TTGAAAGGATGAGGA[A/G]GTGTGGCCTTGTTGG	13626
rs32453068	snp	C/T	0.46875	0.121031	intron-variant	Eed	GRCm38.p3	7:89962545	ACTTGTAAAACTCCA[C/T]AACATAAACTCTGAC	13626
rs32455016	snp	A/G	0.444444	0.157135	intron-variant	Eed	Mm_Celera	7:89980170	AGGGACGATCTGAGC[A/G]GACCTCGCAGACCCT	13626
rs32455633	snp	A/G	0.375	0.216506	intron-variant	Eed	Mm_Celera	7:89959937	AGAAAACCAGCTAAA[A/G]ATTCCAAGAAATATT	13626
rs32469633	snp	G/T	0.48	0.0979796	intron-variant	Eed	Mm_Celera	7:89978252	TAGAGTGAAGCCCAC[G/T]GCTTTTGTGGTCTAA	13626
rs32503923	snp	A/C	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Eed	GRCm38.p3	7:89981280	TGGGTTACGGAGACG[A/C]CAGGCCGCCTCCTGG	13626
rs32522989	snp	A/G	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89972809	TGGTGTCTCTTCATA[A/G]CAATAGAACACTAAG	13626
rs45646063	snp	G/T	0.124444	0.216185	intron-variant	Eed	Mm_Celera	7:89971222	GTTAAGCATTAGAAC[G/T]ATAGTAAAATTGTAA	13626
rs45657463	snp	C/T	0.444444	0.157135	intron-variant	Eed	Mm_Celera	7:89969482	TTCTTTTAATTTAAA[C/T]TATGCATTCTCAGAA	13626
rs45677192	snp	A/G			intron-variant	Eed	GRCm38.p3	7:89975584	CATTGATTTGGGGAA[A/G]GAAAGATGGCTCAGT	13626
rs45724193	snp	C/T	0.297521	0.245442	intron-variant	Eed	Mm_Celera	7:89963549	TTTTAGTCAAATGCA[C/T]ATTATATTACTAGTT	13626
rs45724642	snp	A/T			intron-variant	Eed	Mm_Celera	7:89973171	CTTTTTTTTTTTTTT[A/T]AAAGATTTATTTATT	13626
rs45756058	snp	A/G	0.35503	0.226867	intron-variant	Eed	Mm_Celera	7:89972189	TTTAGCACTCTAGTT[A/G]TAACAATCAGTATTG	13626
rs45782367	snp	C/G	0.32	0.24	intron-variant	Eed	Mm_Celera	7:89965417	AGTGCAAAATGGAAG[C/G]TAAGTTACTTGAGCT	13626
rs45877878	snp	C/T			intron-variant	Eed	Mm_Celera	7:89973571	GCAGAGCTTAGACTA[C/T]GCAGTCGCCAGCAGT	13626
rs45970587	snp	A/G	0.32	0.24	intron-variant	Eed	Mm_Celera	7:89972126	TTTCTTACACAAAGA[A/G]TCATACTGTTAACCC	13626
rs46117693	snp	A/C/G	0.32	0.24	intron-variant	Eed	GRCm38.p3	7:89971323	AATGCTCCTTCTTCC[A/C/G]TCATCTTACCCTACC	13626
rs46432997	snp	C/T	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89969907	GAAAATGGTACCAGT[C/T]AGCCAAGGCTCAGCT	13626
rs46434256	snp	C/T	0.391111	0.206368	intron-variant	Eed	GRCm38.p3	7:89956988	CAATCACTCACTTAG[C/T]CAGTGGTCCACACTA	13626
rs46468726	snp	A/G			utr-variant-5-prime, nc-transcript-variant	Eed	Mm_Celera	7:89980724	GAAAAAGGGGCGCGC[A/G]CGCGCGCGCCCTCCC	13626
rs46501726	snp	A/C			intron-variant	Eed	Mm_Celera	7:89973623	TTAGGGCTTTATTGC[A/C]ATCTCCTGGTATTCA	13626
rs46622132	snp	A/C			intron-variant	Eed	Mm_Celera	7:89979015	ACCCTTTGGTGAGGA[A/C]AGAACCTGTCCCTCC	13626
rs46641819	snp	A/G	0.336735	0.234472	intron-variant	Eed	GRCm38.p3	7:89969891	ACAAAATTATAGGAA[A/G]GAAAATGGTACCAGT	13626
rs46646171	snp	C/T	0.124444	0.216185	intron-variant	Eed	Mm_Celera	7:89956155	AGCAAGTCACAGCAT[C/T]GGGACAACCAAGGTG	13626
rs46799472	snp	A/T	0.124444	0.216185	intron-variant	Eed	Mm_Celera	7:89961514	CATGTTCCATTAACA[A/T]CACCAATCACCCCTC	13626
rs46912410	snp	A/G	0.124444	0.216185	intron-variant	Eed	Mm_Celera	7:89957701	GATTGATAGCCATCA[A/G]ATGACAAATGACAAA	13626
rs46963378	snp	C/T	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89969750	GGGGCAAACCAATAG[C/T]CTAGTACACTCAAGG	13626
rs46998121	snp	A/C/T	0.444444	0.157135	intron-variant	Eed	GRCm38.p3	7:89969359	CAGTAAGAGTCGAGT[A/C/T]GAGGATGACATAATC	13626
rs47107984	snp	A/G	0.391111	0.206368	intron-variant	Eed	GRCm38.p3	7:89972861	ACTTCTGACATTAAA[A/G]CTATAACACCACCCA	13626
rs47353865	snp	A/G	0.391111	0.206368	intron-variant	Eed	GRCm38.p3	7:89962773	TAAAGAACGAAGTGC[A/G]GCCACAAAGCTGCCC	13626
rs47395917	snp	C/T			intron-variant	Eed	GRCm38.p3	7:89969795	TCCAGCCCTGCTGCC[C/T]TCTGCCTCCCAACCC	13626
rs47425578	snp	A/C			intron-variant	Eed	Mm_Celera	7:89965477	ATCTTCCTTAATTTT[A/C]AATTAAATTTTAATT	13626

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