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
rs745800	snp	C/G/T	0	0	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095793	GATATCTTAACTTTT[C/G/T]GTGCTTAGCAGAAGA	54778
rs877269	snp	A/T	0.413083	0.189483	intron-variant	RNF111	GRCh38.p7	15:59081595	CTGGGTGAGGCTCAT[A/T]CCCGTAATCCCCAGT	54778
rs935363	snp	C/T	0.159622	0.233092	intron-variant	RNF111	GRCh38.p7	15:59069478	AAGTTGTATACATAA[C/T]TGATGTCTCAAACTA	54778
rs935364	snp	A/G	0.0271762	0.113356	intron-variant	RNF111	GRCh38.p7	15:59010046	CACAAAGCTAAAAAA[A/G]AATTGCATATAAACT	54778
rs1014443	snp	C/T	0.171704	0.237423	intron-variant	RNF111	GRCh38.p7	15:59045598	TGGGCATTACCAATT[C/T]GACATGGAGAAAAGT	54778
rs1044673	snp	A/G	0.124144	0.21601	utr-variant-3-prime	RNF111	GRCh38.p7	15:59097267	AACTAAAATTCTTTT[A/G]TTAGCAAGTCCTTAT	54778
rs1044674	snp	C/T	0	0	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095832	TTGATTTTGTAGACA[C/T]ATTAAGTCAAGATTT	54778
rs1074701	snp	A/G	0.489608	0.0713316	intron-variant	RNF111	GRCh38.p7	15:59073862	tgtatttctttaata[A/G]taagacttgaaagtt	54778
rs1074702	snp	G/T	0.415399	0.187465	intron-variant	RNF111	GRCh38.p7	15:59073900	ctccttgattcatag[G/T]ctgcagactggatgt	54778
rs1345116	snp	A/G	0.471292	0.116318	intron-variant	RNF111	GRCh38.p7	15:59038714	GAAATGATGCCATAT[A/G]TAAAAAAGAATTAAA	54778
rs1374155	snp	C/T	0.426201	0.177351	intron-variant	RNF111	GRCh38.p7	15:59030630	TCTTATAAAACGTTT[C/T]TCTCTGGTCACTCTA	54778
rs1374156	snp	A/G	0.495671	0.0463237	intron-variant	RNF111	GRCh38.p7	15:59046746	tgtcttttgaagcac[A/G]aaagtctctaatttt	54778
rs1446237	snp	A/G	0.424348	0.179172	intron-variant	RNF111	GRCh38.p7	15:59052603	TTTTGGTAAGAGATA[A/G]AATATTGCTATGTTA	54778
rs1446238	snp	A/G	0.424037	0.179474	intron-variant	RNF111	GRCh38.p7	15:59055558	ATGATTTTTAATTAC[A/G]ATTATTTCTTTGGAG	54778
rs1446239	snp	A/C	0.475496	0.107942	synonymous-codon	RNF111	GRCh38.p7	15:59055730	TTGGAGCCAGGGTTC[A/C]AGTTCTCATGCAAGT	54778
rs1446240	snp	A/C	0.42574	0.177808	intron-variant	RNF111	GRCh38.p7	15:59004292	AACAGCAAGTTCCTT[A/C]TGTTGGAGATAATAA	54778
rs1613602	snp	A/C	0.103689	0.203589	intron-variant	RNF111	GRCh38.p7	15:59002418	TATTAGAACATTCTT[A/C]TGTGAGGGACAAGTT	54778
rs1665049	snp	A/G	0.463666	0.129795	intron-variant	RNF111	GRCh38.p7	15:58998453	cccctcattgtgtcc[A/G]tatgttcttgggaag	54778
rs1665050	snp	A/G	0.481087	0.0953875	intron-variant	RNF111	GRCh38.p7	15:59001406	TCTACTTTGCCTGCT[A/G]TTAGTTCCTATTTTT	54778
rs1665051	snp	C/T	0.488786	0.0740357	intron-variant	RNF111	GRCh38.p7	15:59003025	TCATTATGTTGCCAG[C/T]GCGGGATTGCAGTTG	54778
rs1665053	snp	C/T	0.451234	0.14834	intron-variant	RNF111	GRCh38.p7	15:58990275	CGACAAACACAACAA[C/T]GAATACCAAAAACCT	54778
rs1693532	snp	C/T	0.481165	0.0951993	intron-variant	RNF111	GRCh38.p7	15:58993820	AACTAAGATGCTAAT[C/T]GTGTATGCCCTCAGG	54778
rs1693534	snp	A/C	0.461813	0.132798	intron-variant	RNF111	GRCh38.p7	15:58989763	CTGCACCTTAGCTTT[A/C]TACAAGCAAGGTGCT	54778
rs1693535	snp	C/T	0.0283406	0.115616	intron-variant	RNF111	GRCh38.p7	15:58998706	aagtttgaattttat[C/T]ttggcaataaattct	54778
rs1693536	snp	C/T	0.0279526	0.114869	intron-variant	RNF111	GRCh38.p7	15:59004938	TTTTGCTGCTCTCCA[C/T]TGGGTCTCACTTCCC	54778
rs1867757	snp	A/G	0.492533	0.0606443	intron-variant	RNF111	GRCh38.p7	15:59072315	ttctatgggtaaaac[A/G]ccattaaacagcatc	54778
rs1867758	snp	G/T	0.418653	0.184544	intron-variant	RNF111	GRCh38.p7	15:59072270	aatctttcatgaaag[G/T]aacagtcaatcaatg	54778
rs1965171	snp	A/G	0.0592355	0.161582	intron-variant	RNF111	GRCh38.p7	15:59019763	caggaattcgagacc[A/G]gcctggccaacgtgg	54778
rs1968605	snp	G/T	0.0329836	0.124112	intron-variant	RNF111	GRCh38.p7	15:59019818	acaaaaattagccag[G/T]tgtggtggtgtgtgc	54778
rs1968606	snp	C/T	0.424659	0.17887	intron-variant	RNF111	GRCh38.p7	15:59019875	gaggcagcaaaattg[C/T]ttgaacctgggagat	54778
rs1968607	snp	C/T	0.424968	0.178567	intron-variant	RNF111	GRCh38.p7	15:59019925	gatcgtgccactgca[C/T]ttcagcctgggtgac	54778
rs1971181	snp	A/G	0.41023	0.191902	intron-variant	RNF111	GRCh38.p7	15:59069005	CTCACTGCAATCTCC[A/G]CCTCCCACGTTCAAT	54778
rs1975534	snp	C/T	0.416871	0.186156	intron-variant	RNF111	GRCh38.p7	15:59044043	aactctgtctccccc[C/T]accagaaaaaaaaaG	54778
rs2121236	snp	A/G	0.492435	0.0610346	intron-variant	RNF111	GRCh38.p7	15:59091923	TCCTGTCAGATCAGC[A/G]GCAGCGATAGATTCT	54778
rs2121237	snp	C/T	0.444666	0.15686	intron-variant	RNF111	GRCh38.p7	15:59091888	GAAGCGTGAACCCTA[C/T]TGTAAACTGTGCATG	54778
rs2289895	snp	A/T	0.414245	0.188477	intron-variant	RNF111	GRCh38.p7	15:59089570	CTCAATGTTTTCAAT[A/T]CAACTGCTCATAAAA	54778
rs2414618	snp	C/T	0.420892	0.182472	intron-variant	RNF111	GRCh38.p7	15:59019684	AGTATTTAAGCCAGG[C/T]GTGGTGGCTTATGCC	54778
rs2592092	snp	A/C	0.426047	0.177503			GRCh38.p7	15:59003608	ggttttgccgtgttg[A/C]ccaggctggtcttga	54778
rs2874741	snp	A/G			intron-variant	RNF111	GRCh38.p7	15:59086159	gagtctcactctgtc[A/G]cccaggctggagtgc	54778
rs2899640	snp	A/G	0.438526	0.164189	intron-variant	RNF111	GRCh38.p7	15:59060281	TATATACAATAACAT[A/G]TAAGATACCCAAGTA	54778
rs2899641	snp	C/T	0.00755907	0.0610114	intron-variant	RNF111	GRCh38.p7	15:59052552	CACTAATCTGATATA[C/T]GCATACTCAAACTGG	54778
rs2899642	snp	C/G	0.464087	0.129169	missense	RNF111	GRCh38.p7	15:59030849	GACTCCTGAATATAA[C/G]GAGCTCTACACCTTA	54778
rs2935478	snp	C/T	0.303438	0.244222	intron-variant	RNF111	GRCh38.p7	15:58990648	GACAGAGCGAGACTG[C/T]TTCTCAAAACAAACA	54778
rs2955703	snp	C/T	0.0275645	0.114116	intron-variant	RNF111	GRCh38.p7	15:59003384	ttatgggattacagg[C/T]gtgagccgccacacc	54778
rs2955704	snp	A/G	0.498982	0.0225409	intron-variant	RNF111	GRCh38.p7	15:58990372	AAAACCTGTCATGAA[A/G]CTGTGGGCCAGGCGT	54778
rs3052989	in-del	-/AAT	0.373196	0.217538	intron-variant	RNF111	GRCh38.p7	15:59060785	aataataataataat[-/AAT]GCTACATAAAGCTAC	54778
rs3052991	in-del	-/TA	0.420415	0.182917	intron-variant	RNF111	GRCh38.p7	15:59023535	AGTGTTATTTTTATT[-/TA]TATATTTTTGGTAAA	54778
rs3751539	snp	A/G	0.0166325	0.0896639	utr-variant-3-prime, downstream-variant-500B	RNF111	GRCh38.p7	15:59096014	TAATTTGTGCCTCAC[A/G]GTATCTGCAGATTTA	54778
rs3809531	snp	G/T	0.210301	0.246828	intron-variant	RNF111	GRCh38.p7	15:59085254	CTTGGTTGTTGACAT[G/T]AAGGACGATTAGAAT	54778
rs3809532	snp	A/C	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59085126	ATGTTCTGCCTCAAA[A/C]GTCATTGTGGTTCAA	54778
rs4145892	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime	RNF111	GRCh38.p7	15:59095278	AAGCCTTGATAATTA[C/T]GAATTTTTTATCCAT	54778
rs4531678	snp	G/T	0.377385	0.215112	intron-variant	RNF111	GRCh38.p7	15:58995754	CAGGCATGAGATGCC[G/T]TGCCCCGGCCTTTTT	54778
rs4531679	snp	A/G	0.492679	0.0600586	intron-variant	RNF111	GRCh38.p7	15:59083246	GTAAACTGGGATGCA[A/G]AATAAAGAGTATGAA	54778
rs4774320	snp	C/T	0.436408	0.16659	intron-variant	RNF111	GRCh38.p7	15:59033234	TAGTCTACTTTTGGA[C/T]GTGCCATTTCTTCTT	54778
rs4774321	snp	C/T	0.462582	0.131564	intron-variant	RNF111	GRCh38.p7	15:59033264	TCTCTTCTTCTTCTT[C/T]ATGAGTCCCTTTCTT	54778
rs4775110	snp	C/G	0.439224	0.163383	intron-variant	RNF111	GRCh38.p7	15:59023685	CCCTTGTTTAAATGA[C/G]TTTACTAGCCTTTCC	54778
rs4775111	snp	C/T	0.44768	0.153045	intron-variant	RNF111	GRCh38.p7	15:59033591	AGCTCAGTTTGTGCT[C/T]GAAGTCAGTGAGACA	54778
rs4775112	snp	A/G	0.0329836	0.124112	intron-variant	RNF111	GRCh38.p7	15:59034356	AAAATGTTGTTGGCT[A/G]TTGTTACCAGAATGC	54778
rs4775114	snp	A/G	0.427727	0.175821	intron-variant	RNF111	GRCh38.p7	15:59059635	CCGTTGCCTAATCCA[A/G]GGTCACAAAAATTTA	54778
rs4775115	snp	G/T	0.433527	0.169758	intron-variant	RNF111	GRCh38.p7	15:59076311	TCCCAGTTCTTAAAT[G/T]TTTAGTATTTACTTG	54778
rs5812958	in-del	-/T	0.0659589	0.169201	intron-variant	RNF111	GRCh38.p7	15:59019547	TGTTTTTCATATGGG[-/T]TTATACACCATTCTT	54778
rs5812960	in-del	-/T	0.49681	0.0398085	intron-variant	RNF111	GRCh38.p7	15:59045168	ACAGTTTTTTTTTTT[-/T]AAGTGTTTCCTCTTT	54778
rs5812961	in-del	-/A/ATT			intron-variant	RNF111	GRCh38.p7	15:59060809	ATTATTATTATTATT[-/A/ATT]TTTTTTTTTGTGAGA	54778
rs6145580	in-del	-/GTTCTTGTCAGGCT			intron-variant	RNF111	GRCh38.p7	15:59019570	CATTCTTGTCAGGCT[-/GTTCTTGTCAGGCT]TAATACCTTGGAATA	54778
rs6145581	in-del	-/AGTTGGTGATTCATTCAGCAA	0.493293	0.0575177	intron-variant	RNF111	GRCh38.p7	15:59055523	ATTCTTAGGTCAATT[-/AGTTGGTGATTCATTCAGCAA]AGTTTACCGAGTGCC	54778
rs6494052	snp	A/G	0.0648419	0.167978	intron-variant	RNF111	GRCh38.p7	15:59003726	AATAGCACGTGTTTC[A/G]CTCTAAAATTATCTT	54778
rs6494054	snp	A/G	0.497881	0.0324789	intron-variant	RNF111	GRCh38.p7	15:59014581	AGAAAGCTTCAGAAG[A/G]AATGTATACTTGTTT	54778
rs6494058	snp	C/T	0.0637235	0.166737	intron-variant	RNF111	GRCh38.p7	15:59035203	ccacctggccctgtc[C/T]atgacacgtgggaat	54778
rs6494064	snp	C/T	0.495596	0.0467178	intron-variant	RNF111	GRCh38.p7	15:59053192	TCTGAACTAACACAT[C/T]AATGAAACATCCTTA	54778
rs6494065	snp	A/G	0.493293	0.0575177	intron-variant	RNF111	GRCh38.p7	15:59053249	ACATTGCCCTATTGC[A/G]GAATCACTTTGACTC	54778
rs6494066	snp	A/G	0.201418	0.245234	intron-variant	RNF111	GRCh38.p7	15:59059622	catatctaagaaacc[A/G]ttgcctaatccaggg	54778
rs6494067	snp	C/G	0.0930568	0.194599	intron-variant	RNF111	GRCh38.p7	15:59067809	TTCCCCTTTTACCTC[C/G]TACTGTAGAGTTCAC	54778
rs6494069	snp	C/T	0.491936	0.0629843	intron-variant	RNF111	GRCh38.p7	15:59094151	ACATCTCCTTTTAAC[C/T]TACCTGTTAAACAGT	54778
rs7163736	snp	A/G	0.138886	0.22395	intron-variant	RNF111	GRCh38.p7	15:59034341	AGGGTATATGCATTG[A/G]AAATGTTGTTGGCTG	54778
rs7164061	snp	A/G	0.0637235	0.166737	intron-variant	RNF111	GRCh38.p7	15:59034271	CAACATTGTGCTTGC[A/G]TTTTATACACCTATG	54778
rs7164205	snp	C/T	0.0115144	0.0749975	intron-variant	RNF111	GRCh38.p7	15:59056171	AAAGTAGAAGCAGTA[C/T]TTTTTAAATATAAAC	54778
rs7165028	snp	A/T	0.489318	0.0722982	intron-variant	RNF111	GRCh38.p7	15:59078703	GTCTCTACTAAAAAT[A/T]CAAAAACTAGCCGGG	54778
rs7168102	snp	C/G	0.438526	0.164189	intron-variant	RNF111	GRCh38.p7	15:59023115	taactgggcatggtg[C/G]tgcgtgtctgtaatc	54778
rs7169181	snp	A/G	0.35445	0.227135	intron-variant	RNF111	GRCh38.p7	15:59032154	ATGTTGAACAGGCTA[A/G]TCTTGAGCTCCTGAT	54778
rs7170844	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF111	GRCh38.p7	15:59009201	tgacctcaggtgatc[A/C/T]gcccaccttggcctt	54778
rs7171252	snp	A/G	0.0379877	0.132479	intron-variant	RNF111	GRCh38.p7	15:59050166	gcctcctgagttcca[A/G]cgattttcctgcctc	54778
rs7171621	snp	A/T	0	0	intron-variant	RNF111	GRCh38.p7	15:59007750	taatttgcattcctc[A/T]ggtgactaaagatat	54778
rs7171680	snp	A/G	0.0486741	0.148216	intron-variant	RNF111	GRCh38.p7	15:59016768	cctattaggaactag[A/G]ccatgtaccagtagg	54778
rs7173135	snp	G/T	0.488485	0.0749998	intron-variant	RNF111	GRCh38.p7	15:59016939	AGGGATCTAGGTTGC[G/T]TGCTCCTTACGAGAA	54778
rs7174057	snp	C/T	0.00676609	0.0577691	intron-variant	RNF111	GRCh38.p7	15:59032562	AAGTAGCTGGGACTA[C/T]AGGCCCACACCACCA	54778
rs7175215	snp	C/G	0.484632	0.086302	intron-variant	RNF111	GRCh38.p7	15:59041399	tctctaccaaaaata[C/G]aaaaattagccgggt	54778
rs7175246	snp	A/G	0.491421	0.0649309	intron-variant	RNF111	GRCh38.p7	15:59014054	ccatggcctcccaac[A/G]tgctaggattacagg	54778
rs7175490	snp	C/T	0.487049	0.0794222	intron-variant	RNF111	GRCh38.p7	15:59041735	gtgattgtaaccatt[C/T]tgaatgctcaccggc	54778
rs7176281	snp	A/G	0.468249	0.121932	intron-variant	RNF111	GRCh38.p7	15:59036230	gcccagctaatcttt[A/G]tatttttattagaga	54778
rs7176576	snp	C/T	0.491368	0.0651254	intron-variant	RNF111	GRCh38.p7	15:59013949	acacgccaccacgcc[C/T]ggctaatttttgtat	54778
rs7177112	snp	A/C/G	0.039737	0.135242	intron-variant	RNF111	GRCh38.p7	15:59089648	AAATTGATTTAGCCT[A/C/G]TCTCTTCTGTTGAAA	54778
rs7178935	snp	A/G	0.445773	0.155477	synonymous-codon	RNF111	GRCh38.p7	15:59075968	GCAGGCATTGCCAGT[A/G]GACCTGAGCAACAGT	54778
rs7180666	snp	A/G	0.105569	0.204058	intron-variant	RNF111	GRCh38.p7	15:59072352	tcagaattggaatca[A/G]tcctttcaaactttg	54778
rs7181728	snp	A/C	0.0368353	0.130617	intron-variant	RNF111	GRCh38.p7	15:59081389	gtggcatgcacttgt[A/C]gtcacagctccttgg	54778
rs7181747	snp	A/G	0.136166	0.22258	intron-variant	RNF111	GRCh38.p7	15:59034131	AAGGATAAATAATGT[A/G]GCTCTTTTTATATCA	54778
rs7183794	snp	A/G	0.0275645	0.114116	intron-variant	RNF111	GRCh38.p7	15:59052098	AGAGGAAGTAAACAT[A/G]CAAAGAAGTGTAGAT	54778
rs7183822	snp	A/T	0.5	0	intron-variant	RNF111	GRCh38.p7	15:59060807	attattattattatt[A/T]tttttttttttgtga	54778
rs8024187	snp	A/G	0.0126979	0.078662	intron-variant	RNF111	GRCh38.p7	15:59006231	taatttatatacaat[A/G]tgaggcacacgtttt	54778
rs8025246	snp	G/T	0.494187	0.0535994	intron-variant	RNF111	GRCh38.p7	15:59025814	CGGCTCACCGCAACC[G/T]CTGCCTTGCGGATTC	54778
rs8025439	snp	C/G	0.0134861	0.0810011	intron-variant	RNF111	GRCh38.p7	15:59025945	atgttggtcaggctg[C/G]tctcgaactcccaac	54778

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