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
rs1133216	snp	A/G	0.470424	0.117954	intron-variant	RNF152	GRCh38.p7	18:61886127	TGACCAGGCTGCAGT[A/G]CGTATACCAATGTTT	220441
rs1135529	snp	C/T	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61808353	AGATAAATGAGCTGC[C/T]GGGCTGTGTAGAAAA	220441
rs1142939	snp	C/T	0	0	utr-variant-3-prime	RNF152	GRCh38.p7	18:61815385	Ctttatttttttttt[C/T]tttttattGAAACCC	220441
rs4072460	snp	A/G	0.433673	0.1696	intron-variant	RNF152	GRCh38.p7	18:61867925	TAAATTTACATAATA[A/G]TAAAGTTGTATTTTT	220441
rs4073064	snp	A/G	0.0588605	0.161139	intron-variant	RNF152	GRCh38.p7	18:61865494	AACCAGGTTTGTCAC[A/G]TGGATTAGTAATTTA	220441
rs4075336	snp	C/T	0.34659	0.230587	intron-variant	RNF152	GRCh38.p7	18:61867335	CATGCTCCTGTAGTC[C/T]CAGCTACTCGGGAGG	220441
rs4076952	snp	C/G/T	0.251014	0.249998	intron-variant	RNF152	GRCh38.p7	18:61829504	GAGAGGGGAGAGAGA[C/G/T]ATATATATATATCAG	220441
rs4078129	snp	C/T	0.483923	0.0882034	intron-variant	RNF152	GRCh38.p7	18:61884637	AATCTCAGCTCACTG[C/T]AACCTCCACCTCTCA	220441
rs4083955	snp	A/T	0.482979	0.0906686	intron-variant	RNF152	GRCh38.p7	18:61838564	CTAGAATGAACAGTC[A/T]TCATTCCTCTGAAGT	220441
rs4129490	snp	C/T	0.474992	0.108989	intron-variant	RNF152	GRCh38.p7	18:61833955	TCCTTTAATTATGTG[C/T]GGTTAGCAAAAGCTA	220441
rs4129491	snp	C/T	0.474903	0.109173	intron-variant	RNF152	GRCh38.p7	18:61834114	ATCTTATTTTTGTTA[C/T]GTCCTGGCTTGAATC	220441
rs4131216	snp	C/T	0.48692	0.0798058	intron-variant	RNF152	GRCh38.p7	18:61838115	TTGGGAATTGTTTCA[C/T]AGGGACTGATAAAGG	220441
rs4131217	snp	A/G			intron-variant	RNF152	GRCh38.p7	18:61838062	AACCTCTACCTTTGT[A/G]TGTGGGGACGGGAAG	220441
rs4280353	snp	C/T	0.480775	0.0961398	intron-variant	RNF152	GRCh38.p7	18:61847750	CCGGTCTCCCTCCCA[C/T]CCACTTCCCAAACCT	220441
rs4293482	snp	C/T	0.483923	0.0882034	intron-variant	RNF152	GRCh38.p7	18:61884906	GCCTAATAAGTGGTT[C/T]AAATACCTGATGCTC	220441
rs4294914	snp	A/G	0.482309	0.0923707	intron-variant	RNF152	GRCh38.p7	18:61841642	CCTCTACCTCTGAGT[A/G]GGTAGAGATGCAGAA	220441
rs4297789	snp	A/C	0.486984	0.079614	intron-variant	RNF152	GRCh38.p7	18:61837327	TGGGGAAAATGCCCA[A/C]AGTGATACAAGGCAT	220441
rs4319862	snp	G/T	0.331874	0.236213	intron-variant	RNF152	GRCh38.p7	18:61826101	CAAGGAATGAGCAAG[G/T]CTATGTTCTGTGGGG	220441
rs4358044	snp	G/T	0.431325	0.172108	intron-variant	RNF152	GRCh38.p7	18:61880545	TAAAGCACTTTAAAC[G/T]GAAAGCACCCAAGCG	220441
rs4362478	snp	A/G	0.0901274	0.1922	synonymous-codon	RNF152	GRCh38.p7	18:61816077	GGTCACCACGGTGAC[A/G]GACTTCTGCTGGCTC	220441
rs4381693	snp	C/T	0.482234	0.0925596	intron-variant	RNF152	GRCh38.p7	18:61841947	CAGCCATTGACAATA[C/T]GTAACAAATGGACAT	220441
rs4389228	snp	C/T	0.42666	0.176893	intron-variant	RNF152	GRCh38.p7	18:61841922	TCAACTCTACCACTG[C/T]AACAGAAAGCAGCCA	220441
rs4398187	snp	C/T	0.021333	0.101051	intron-variant	RNF152	GRCh38.p7	18:61833899	TAAAAAAAAAAGTTT[C/T]ATCCACAAGATAAAA	220441
rs4398188	snp	C/T	0.27008	0.249192	intron-variant	RNF152	GRCh38.p7	18:61862195	TCCATCCTGACCCCC[C/T]TATCTCCTCTCTGCC	220441
rs4424997	snp	C/T	0.0722614	0.17581	intron-variant	RNF152	GRCh38.p7	18:61837426	GATTATGTAAGAGAA[C/T]GTCCTTATTATCAGG	220441
rs4432347	snp	G/T	0.205723	0.246048	intron-variant	RNF152	GRCh38.p7	18:61825836	ACATTTTAATAAAAT[G/T]AACTACACATGTTCC	220441
rs4445995	snp	A/T	0.427119	0.176434	intron-variant	RNF152	GRCh38.p7	18:61841575	TAGTCTAGGGATTCT[A/T]AACTTTGGGGGGTTA	220441
rs4459645	snp	A/G	0.482309	0.0923707	intron-variant	RNF152	GRCh38.p7	18:61841471	TGAATAAATGAACTT[A/G]AGCTGGATCTATTTT	220441
rs4473290	snp	A/G	0.00318978	0.0398085	intron-variant	RNF152	GRCh38.p7	18:61844798	ATTTATCAAGGGAAG[A/G]TGCAAAATGCATTTT	220441
rs4476269	snp	C/T	0.474903	0.109173	intron-variant	RNF152	GRCh38.p7	18:61832747	GCCAGCAAATAAAAT[C/T]GACAGGATTTTAAAA	220441
rs4517883	snp	A/T	0.475525	0.107882	intron-variant	RNF152	GRCh38.p7	18:61888323	GAGTCAATTAGAAAT[A/T]GAAAATCCCTAAGCA	220441
rs4520933	snp	C/T	0.497722	0.0336691	utr-variant-3-prime	RNF152	GRCh38.p7	18:61813848	GTCAGACATGCATTA[C/T]GGCAGCCTGGGAGAG	220441
rs4538107	snp	C/G	0.0891305	0.191366	synonymous-codon	RNF152	GRCh38.p7	18:61815969	GCACACCCCCGACCA[C/G]GTGGAGCTTTTCACC	220441
rs4550566	snp	A/G	0.204803	0.245881	intron-variant	RNF152	GRCh38.p7	18:61827536	TCCTCAAATTACCCA[A/G]AGAACATTCTATATT	220441
rs4555248	snp	A/G	0.340784	0.232934	intron-variant	RNF152	GRCh38.p7	18:61834519	TGATGGACTCTATTG[A/G]CCTTTATTTACCTTC	220441
rs4616381	snp	C/T	0.487746	0.0773096	intron-variant	RNF152	GRCh38.p7	18:61824944	AAAGATGCTGACAGA[C/T]AGACAGACAGGCAGG	220441
rs4940528	snp	G/T	0.487241	0.0788465	intron-variant	RNF152	GRCh38.p7	18:61818021	CACTCCTTCACATTT[G/T]TCTTAAAAGTGACCC	220441
rs4940529	snp	C/T	0.0722614	0.17581	intron-variant	RNF152	GRCh38.p7	18:61830114	gcaaccttcacttca[C/T]gggttccagggattc	220441
rs4940530	snp	C/T	0.00755907	0.0610114	intron-variant	RNF152	GRCh38.p7	18:61830146	cctgcctcagactcc[C/T]gggtagctgggacta	220441
rs4940531	snp	G/T	0.49121	0.0657086	intron-variant	RNF152	GRCh38.p7	18:61852256	AGTCTCAAGGGACTT[G/T]CCCATTTGAGGAAAA	220441
rs4940532	snp	C/T	0.273856	0.248859	intron-variant	RNF152	GRCh38.p7	18:61852553	AAAAGAACATCTAGA[C/T]TGTCAGTCTTCAAAG	220441
rs4940533	snp	A/G	0.431769	0.17164	intron-variant	RNF152	GRCh38.p7	18:61860558	gctgccggttgcata[A/G]gagtctagcacacac	220441
rs4940534	snp	A/G	0.442791	0.15916	intron-variant, utr-variant-5-prime	RNF152	GRCh38.p7	18:61868195	TTCGGGTGTTGCTGT[A/G]GACTTACAGCATATA	220441
rs4941060	snp	A/T	0.335101	0.23507	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810026	TGCCCCACCTGCTTA[A/T]GTTCTTCAATGATTA	220441
rs4941061	snp	A/C	0.0633504	0.166319	utr-variant-3-prime	RNF152	GRCh38.p7	18:61810243	AACAGTTTTTTACTG[A/C]ATTTTAACTCCAATT	220441
rs4941062	snp	A/G	0.481087	0.0953875	intron-variant	RNF152	GRCh38.p7	18:61817851	TCCACTGGCATTTCA[A/G]TAAGGGCTGCCTGAC	220441
rs4941063	snp	A/C	0.0581099	0.160244	intron-variant	RNF152	GRCh38.p7	18:61817874	TGCCTGACTCAGTTT[A/C]CCATTGAAAGCATCC	220441
rs4941064	snp	A/C	0	0	intron-variant	RNF152	GRCh38.p7	18:61820330	AGAGACTCCGTCTCA[A/C]CAAAAAAAAAAAAAA	220441
rs4941065	snp	A/G	0.0626037	0.165477	intron-variant	RNF152	GRCh38.p7	18:61823488	ATTTTTAGTAGAGAT[A/G]GGGTTTCGCCATATT	220441
rs4941066	snp	C/G	0.417359	0.185718	intron-variant	RNF152	GRCh38.p7	18:61833028	ATACATTAATTCAGT[C/G]ACTGTGCCAGTTAAG	220441
rs4941067	snp	C/T	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61833076	CTTCCATTCCTCAGC[C/T]GTATCTACTAAAATT	220441
rs4941068	snp	A/C	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61833408	AAAGAATCCAAATTT[A/C]AGGTGATTCACAATG	220441
rs4941069	snp	A/G	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61833514	TCGAAACTCCTCTGC[A/G]TTTCCCTCTAATGGA	220441
rs4941070	snp	A/C	0.0718919	0.175435	intron-variant	RNF152	GRCh38.p7	18:61838326	AGACTCCTCTTTTGG[A/C]TTTTCATTTGCTTTG	220441
rs4941071	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61861312	acaatatttttattg[C/T]atctcttccatgttt	220441
rs4941072	snp	A/G	0.121369	0.214369	intron-variant	RNF152	GRCh38.p7	18:61866687	GCTGTGTGCTCCTAC[A/G]GTGACATGTTCATCC	220441
rs4941073	snp	C/G	0.42803	0.175514	intron-variant	RNF152	GRCh38.p7	18:61870879	ATCACACACATTGCA[C/G]CCATGATTCCATCCC	220441
rs4941074	snp	A/C	0.440609	0.161766	intron-variant	RNF152	GRCh38.p7	18:61870880	TCACACACATTGCAC[A/C]CATGATTCCATCCCC	220441
rs4941075	snp	A/G	0.0622301	0.165053	intron-variant	RNF152	GRCh38.p7	18:61875135	AGAGTTTGAATAGAA[A/G]GATAGAGGAAGAAAG	220441
rs4941076	snp	C/T	0.0618563	0.164627	intron-variant	RNF152	GRCh38.p7	18:61879521	CTATGCTGTGTTTTG[C/T]GGGAGGGCAGAGAGG	220441
rs4941077	snp	A/G	0.0626037	0.165477	intron-variant	RNF152	GRCh38.p7	18:61879561	GAGAAAGCGTGTTCC[A/G]GGGAAAGGGAACTAC	220441
rs4941078	snp	A/G	0.477004	0.104734	intron-variant	RNF152	GRCh38.p7	18:61879793	ACACGGAGAAACCCC[A/G]TCTCTACTGAAAAAA	220441
rs4941079	snp	G/T	0.470618	0.117591	intron-variant	RNF152	GRCh38.p7	18:61879992	AAAAATTTTTTTTGT[G/T]CACAGCTTTTTAGTA	220441
rs4941080	snp	A/G	0.470521	0.117772	intron-variant	RNF152	GRCh38.p7	18:61886641	GCAGGTCCAGGGTGA[A/G]TGATAACTGGAAGGG	220441
rs4941081	snp	A/G	0.483199	0.0901004	intron-variant	RNF152	GRCh38.p7	18:61890690	TAATATGGAAAAGCA[A/G]CATTTGTTTCAAAAT	220441
rs4941082	snp	C/T	0.492087	0.0623997	intron-variant	RNF152	GRCh38.p7	18:61890819	AATGACCCTCAACAA[C/T]GTAAGGACCGAACTG	220441
rs4941083	snp	C/T	0.483491	0.0893421	intron-variant	RNF152	GRCh38.p7	18:61890827	TCAACAATGTAAGGA[C/T]CGAACTGTATGGAAT	220441
rs5016055	snp	G/T	0.204803	0.245881	intron-variant	RNF152	GRCh38.p7	18:61827597	CCAGTGGGTTTTATA[G/T]ATATCTCTTTAAGTA	220441
rs5825462	in-del	-/ATAT			intron-variant	RNF152	GRCh38.p7	18:61827601	GGGTTTTATAGATAT[-/ATAT]CTCTTTAAGTAAGTC	220441
rs5825463	in-del	-/A	0.475702	0.107512	intron-variant	RNF152	GRCh38.p7	18:61833885	TGCCATTTGAGCTTT[-/A]AAAAAAAAAGTTTCA	220441
rs5825464	in-del	-/T	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61834680	ACTGAAATTAGGCCA[-/T]TTTTAAAAAAAATTA	220441
rs5825466	in-del	-/AC	0.327445	0.237702	intron-variant	RNF152	GRCh38.p7	18:61838018	CAGTCTTTTGAAGAA[-/AC]ACACACATGGTTCCT	220441
rs5825467	in-del	-/CA			intron-variant	RNF152	GRCh38.p7	18:61838025	TTGAAGAAACACACA[-/CA]TGGTTCCTCTGACTT	220441
rs6567245	snp	C/T	0.495999	0.0445491	intron-variant	RNF152	GRCh38.p7	18:61828295	TTGCCCAAGCTAGTA[C/T]GGTGACTATTCACAA	220441
rs6567246	snp	C/G	0.404733	0.196361	intron-variant	RNF152	GRCh38.p7	18:61828373	CTTCCTGCCTTAGCC[C/G]CCCGAGTAGCTGGGA	220441
rs6567248	snp	A/G	0.349671	0.229272	intron-variant	RNF152	GRCh38.p7	18:61883209	ATGCAGCTTTCAAAA[A/G]TATTTCTGAAGAATA	220441
rs7227060	snp	A/G	0.476918	0.104919	intron-variant	RNF152	GRCh38.p7	18:61865417	GAGAATTTGAAAGGA[A/G]ATTGCTTCCAGGATA	220441
rs7228799	snp	A/T			intron-variant	RNF152	GRCh38.p7	18:61851938	ACGACATCTGCACAG[A/T]ACCTTGTGGCTCATT	220441
rs7229409	snp	C/T	0.427423	0.176128	intron-variant	RNF152	GRCh38.p7	18:61840405	TCTATCTTTTCTTTA[C/T]AACCCAGAACCCCAA	220441
rs7229834	snp	C/T	0.48955	0.071525	intron-variant	RNF152	GRCh38.p7	18:61853127	TTtattagtttccta[C/T]tgccactgtaacaaa	220441
rs7230629	snp	A/C	0.00119737	0.0244387	intron-variant	RNF152	GRCh38.p7	18:61844873	GGCCTTTTAAAACAA[A/C]AAAAAAAAAGCATTT	220441
rs7230956	snp	A/G	0.322245	0.239334	intron-variant	RNF152	GRCh38.p7	18:61857028	AAGTAGTAAAACAAG[A/G]AGAAACCAGCATTAT	220441
rs7231456	snp	A/G	0.320814	0.239761	intron-variant	RNF152	GRCh38.p7	18:61857410	CAAATATTTTGCCTT[A/G]GAACTGCTTTAGAAC	220441
rs7232949	snp	C/T	0	0	intron-variant	RNF152	GRCh38.p7	18:61857575	AATTTTTCTTCAAAC[C/T]TACTGTTACTTCCTT	220441
rs7233207	snp	C/T	0.430732	0.172731	intron-variant	RNF152	GRCh38.p7	18:61843967	attttatgttatgtg[C/T]attttaccacagtaa	220441
rs7234737	snp	C/G	0.406123	0.195258	intron-variant	RNF152	GRCh38.p7	18:61826238	AAAGCAGAAACTTCT[C/G]AGAAATGAGAACTGC	220441
rs7235368	snp	A/G	0.406123	0.195258	intron-variant	RNF152	GRCh38.p7	18:61826272	AAATACCTTCTTTAG[A/G]GCAGGTCTATTTCCA	220441
rs7236480	snp	A/G	0.450231	0.149691	intron-variant	RNF152	GRCh38.p7	18:61842474	CGAGTTGTCACAGGG[A/G]CTTTGTTTCCCTGGA	220441
rs7237239	snp	A/G	0.179105	0.239737	intron-variant	RNF152	GRCh38.p7	18:61871989	gactgggtaatttat[A/G]aagaaaagaggctta	220441
rs7237854	snp	A/G	0.480302	0.0972668	intron-variant	RNF152	GRCh38.p7	18:61839756	AAAAAATTGCTGGGC[A/G]TGGTGGTGGGTGCCT	220441
rs7238578	snp	C/T	0.0711525	0.174681	intron-variant	RNF152	GRCh38.p7	18:61875022	CCATCCCCTGGGATA[C/T]GCCATGGTCTGCAAG	220441
rs7238823	snp	C/T	0.419135	0.184101	intron-variant	RNF152	GRCh38.p7	18:61839714	TCCTGGCTAACACAG[C/T]GACACCCTGTCTCTA	220441
rs7240831	snp	G/T	0.474813	0.109357	intron-variant	RNF152	GRCh38.p7	18:61835612	tcaaaaataataaat[G/T]aaaaaggataaacaa	220441
rs7241508	snp	A/T	0.230896	0.249269	intron-variant	RNF152	GRCh38.p7	18:61872118	aaatgggaacaggca[A/T]cttacatggcaggac	220441
rs7242295	snp	C/T	0.254385	0.249962	intron-variant	RNF152	GRCh38.p7	18:61823273	TGATGAAGCAAAGAA[C/T]CCAGAAAGTGAAAAT	220441
rs7243378	snp	C/T	0.0360663	0.129354	intron-variant	RNF152	GRCh38.p7	18:61817925	GAGCCATGATGACTC[C/T]AGAAAGAATTACTCA	220441
rs7244472	snp	A/G	0.334642	0.235236	intron-variant	RNF152	GRCh38.p7	18:61819842	cctagtcaacataac[A/G]agactctgtctctac	220441
rs7244703	snp	A/G	0.332799	0.23589	intron-variant	RNF152	GRCh38.p7	18:61828448	TTTTTTTGTAGAGAC[A/G]GGATCTTGCCATGTT	220441
rs7359752	snp	C/T	0.18134	0.240387	intron-variant	RNF152	GRCh38.p7	18:61861444	tagcctatatgtgta[C/T]tgggctacaccacct	220441
rs7505697	snp	A/G	0.48435	0.0870631	intron-variant	RNF152	GRCh38.p7	18:61888172	CCCTCACAACTCCAC[A/G]AAGAACGTAGTCCAG	220441

Full records

It may take some time, please wait.