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
rs725303	snp	C/T	0.0387552	0.1337	intron-variant	RNF2	GRCh38.p7	1:185054536	CTTCTCCATTACGAG[C/T]GCTCTTCCTGAGAGC	6045
rs1008502	snp	C/G	0.245346	0.249957	intron-variant	RNF2	GRCh38.p7	1:185049554	GAAGCAACAAGATAT[C/G]TGAGAGCAGTTAGAA	6045
rs1046592	snp	A/G	0.311369	0.242351	utr-variant-3-prime	RNF2	GRCh38.p7	1:185100429	TTTCTGAGCCAGACT[A/G]GTTTACGCTATTCAA	6045
rs1884447	snp	A/G	0.499846	0.00878459	intron-variant	RNF2	GRCh38.p7	1:185052278	Aacacacaggttcct[A/G]gcaccgctattcatg	6045
rs2057222	snp	C/T	0.499693	0.0123764	intron-variant	RNF2	GRCh38.p7	1:185098673	tctccagcacactgc[C/T]tgctgttgagtacag	6045
rs2144664	snp	A/G	0.102014	0.201495	upstream-variant-2KB	RNF2	GRCh38.p7	1:185044217	AGTTATAGATAGTAG[A/G]CAAAAGCTTTCAAGC	6045
rs2281482	snp	A/G	0.0248432	0.108648	utr-variant-5-prime, upstream-variant-2KB	RNF2	GRCh38.p7	1:185045588	GCCGGCGTCCGCGGC[A/G]GCTGATACCAGAGTC	6045
rs2378957	snp	A/G	0.405429	0.195811	intron-variant, upstream-variant-2KB	RNF2	GRCh38.p7	1:185070933	TGAGCCACTGCACCC[A/G]GCCAGACTGCAGTAT	6045
rs2378958	snp	G/T	0.277867	0.248442	intron-variant	RNF2	GRCh38.p7	1:185073268	CCCTGTGTGAGAATT[G/T]GTGCTGGGTAAATTT	6045
rs3036553	in-del	-/TTTT			intron-variant	RNF2	GRCh38.p7	1:185082364	TTTTTTTTTTTTTTT[-/TTTT]GAAGACAGAGTCTTG	6045
rs3753570	snp	G/T	0	0	intron-variant	RNF2	GRCh38.p7	1:185067036	CTCCATTATCCGGTC[G/T]TAAGTTTTTGAATAC	6045
rs3753571	snp	A/C	0.0471551	0.14613	intron-variant	RNF2	GRCh38.p7	1:185048475	TATGATAAATGGCAA[A/C]CATGTTAATTCTCAA	6045
rs3753572	snp	A/G	0.000798403	0.0199641	intron-variant	RNF2	GRCh38.p7	1:185047471	CACAGACGTGACACC[A/G]CAAACTGTAGGTCAC	6045
rs3753573	snp	C/T	0.0513262	0.151752	upstream-variant-2KB	RNF2	GRCh38.p7	1:185044870	CCCCTTCCAGTGTTA[C/T]CTTCTGAACTTGAGG	6045
rs3766720	snp	G/T	0.244205	0.249933	intron-variant	RNF2	GRCh38.p7	1:185086134	GTTAAGGAGGCTTTG[G/T]TAGAGATGAAATAAA	6045
rs3766721	snp	C/T	0	0	intron-variant	RNF2	GRCh38.p7	1:185054240	AAAAAGAATGAATGA[C/T]AATGTCCAGTTTAGT	6045
rs3766723	snp	G/T	0.267636	0.249377	intron-variant	RNF2	GRCh38.p7	1:185046402	GGCTCCCGGCAAAAG[G/T]GGGTACTAGCATCTC	6045
rs3820183	snp	C/G	0.407502	0.194147	intron-variant	RNF2	GRCh38.p7	1:185067375	ATTTACTCAAGACTA[C/G]GCAAATAATAAATTG	6045
rs3820184	snp	C/T	0.046775	0.145601	intron-variant	RNF2	GRCh38.p7	1:185053946	CTGCTACATTCAATC[C/T]GGGTTACTAACATCC	6045
rs3835513	in-del	-/TT	0.00716266	0.059414	intron-variant	RNF2	GRCh38.p7	1:185062477	AGTTTCCCAACATCA[-/TT]GTTTAGTTCTCTCTT	6045
rs3841690	in-del	-/C			intron-variant	RNF2	GRCh38.p7	1:185099490	GTTCCTTTTTTTCCC[-/C]TTAGTACTTTGTGTA	6045
rs4651247	snp	A/G	0.405603	0.195673	intron-variant	RNF2	GRCh38.p7	1:185079623	tgttgtccaattcca[A/G]gagcccaaataaaag	6045
rs5779238	in-del	-/C	0	0	upstream-variant-2KB	RNF2	GRCh38.p7	1:185045374	GCGGCGCACCCTCCC[-/C]TCGCGCCGCGGGCCT	6045
rs5779240	in-del	-/T	0.499087	0.0213463	intron-variant	RNF2	GRCh38.p7	1:185073060	TGCTCTACGACTTGC[-/T]TTTTTTTTTTTTTTT	6045
rs6674345	snp	G/T	0.00835141	0.0640778	utr-variant-3-prime	RNF2	GRCh38.p7	1:185102002	TGATAAAACTGCTTA[G/T]ATTTTGTTGATGACA	6045
rs6677056	snp	A/G	0.417521	0.185571	intron-variant	RNF2	GRCh38.p7	1:185085555	TACAGGTTTTTAACA[A/G]CTTTCTCTCACTGAT	6045
rs6679466	snp	A/G	0.0581099	0.160244	intron-variant	RNF2	GRCh38.p7	1:185061372	ATCTCTTAAAAGGGG[A/G]AAAAAAAAGGGAAAC	6045
rs6684195	snp	A/G	0.42263	0.180829	intron-variant	RNF2	GRCh38.p7	1:185057681	TTTTAGGTAGTGCAG[A/G]GCATATGTTCTTGAC	6045
rs7519019	snp	C/T	0.499987	0.00259581	intron-variant	RNF2	GRCh38.p7	1:185068972	TTGCTCAAAATGTTA[C/T]ATTTAAAGTTCCTTT	6045
rs7541639	snp	C/T	0.444444	0.157135	intron-variant	RNF2	GRCh38.p7	1:185076206	TATGAACCTTTCAGT[C/T]TTCTGGGTATTGTAT	6045
rs7541641	snp	C/T	0.444444	0.157135	intron-variant	RNF2	GRCh38.p7	1:185076209	GAACCTTTCAGTCTT[C/T]TGGGTATTGTATCTT	6045
rs9628633	snp	C/T			intron-variant	RNF2	GRCh38.p7	1:185075583	gtacaggaagcatgg[C/T]tgggggaggcctcag	6045
rs10911671	snp	A/G	0.0189856	0.0955633	intron-variant	RNF2	GRCh38.p7	1:185054915	atgttgcccaggctg[A/G]tctggaactcctgag	6045
rs10911672	snp	C/T	0.0256215	0.110247	intron-variant	RNF2	GRCh38.p7	1:185055309	tctttttagcatgat[C/T]ttttgagcatcatgt	6045
rs10911673	snp	C/G	0.309154	0.242901	intron-variant	RNF2	GRCh38.p7	1:185065370	agctggccaccgaag[C/G]ccccagtggcagcct	6045
rs10911674	snp	G/T	0.278399	0.248382	intron-variant	RNF2	GRCh38.p7	1:185077442	TAACATTGATTGTTT[G/T]GGGACTTCCGGTAGA	6045
rs10911675	snp	A/G	0.401747	0.198678	intron-variant	RNF2	GRCh38.p7	1:185079943	CAGAAAAAAAAAAAA[A/G]CCAATTGTGTCTTTA	6045
rs10911676	snp	C/T	0.321769	0.239477	downstream-variant-500B	RNF2	GRCh38.p7	1:185102699	TATTTTCAAGGTTCA[C/T]GTGATAGCATATATC	6045
rs11334881	in-del	-/T			intron-variant	RNF2	GRCh38.p7	1:185081396	GCCTAATTCCATCAA[-/T]TTTTTTTTTTTTTTG	6045
rs11432393	in-del	-/T	0.375	0.216506	utr-variant-3-prime	RNF2	GRCh38.p7	1:185100543	CTGAAGTTTCTTGTG[-/T]TTTTTTTTTTTCCCC	6045
rs11808499	snp	A/G	0.00318978	0.0398085	intron-variant	RNF2	GRCh38.p7	1:185085539	CACATAGTTAATATC[A/G]TACAGGTTTTTAACA	6045
rs12030761	snp	A/G	0.278664	0.248351	intron-variant	RNF2	GRCh38.p7	1:185061253	ctgcctcagcctccc[A/G]agtagctgggactac	6045
rs12038919	snp	A/G	0.2776	0.248472	intron-variant	RNF2	GRCh38.p7	1:185072498	AGATAAAGAATTACA[A/G]GGTTAGAATTTCTTT	6045
rs12038977	snp	A/G	0.0763149	0.179815	intron-variant	RNF2	GRCh38.p7	1:185072685	ACAGCTCATGCCTGT[A/G]ATCCCAGCACTTTGG	6045
rs12039657	snp	A/T	0.277067	0.24853	intron-variant	RNF2	GRCh38.p7	1:185076676	TATTTGAAAAGGGTT[A/T]AAATTTTTTTTTTGT	6045
rs12043617	snp	A/G	0.244205	0.249933	intron-variant	RNF2	GRCh38.p7	1:185087813	ACAAATAATCTGAAT[A/G]CTCTATACAAGCTTT	6045
rs12044161	snp	C/T	0.124144	0.21601	intron-variant	RNF2	GRCh38.p7	1:185097326	ATCGCCTTAGCTGAC[C/T]TGGCGGAAGGTCAGC	6045
rs12044346	snp	C/T			intron-variant	RNF2	GRCh38.p7	1:185066236	CCTTTGTATTGCATA[C/T]TAGGCCTCACTGATC	6045
rs12044997	snp	A/T	0.245631	0.249962	intron-variant	RNF2	GRCh38.p7	1:185097520	GTCAATTAATTCTTA[A/T]AGTCTTTTGTTTAAT	6045
rs12046202	snp	C/T	0.255503	0.249939	intron-variant	RNF2	GRCh38.p7	1:185099120	ACAGTGGCACAATCT[C/T]GGCTGACTGCAACCT	6045
rs12049293	snp	C/T	0.245061	0.249951	intron-variant, upstream-variant-2KB	RNF2	GRCh38.p7	1:185070798	TGCCCGCCACCTCGC[C/T]GGCTCATTTTTTTAT	6045
rs12059402	snp	G/T	0.0260105	0.111035	intron-variant	RNF2	GRCh38.p7	1:185048040	CCAGATATCCTGACT[G/T]TTTGCCTACTGGTCT	6045
rs12062374	snp	A/G	0.0244538	0.107838	intron-variant	RNF2	GRCh38.p7	1:185050099	atctggACGAATAGT[A/G]TAGGTTAAGATGTAG	6045
rs12070618	snp	A/G	0.00874735	0.0655527	intron-variant	RNF2	GRCh38.p7	1:185060620	GGACTGAGAGCCTGG[A/G]TTATGCCAAAGTCTG	6045
rs12077730	snp	G/T	0.0123036	0.0774623	intron-variant	RNF2	GRCh38.p7	1:185083041	ATGGTTCACCTCAAA[G/T]TCAACAACTAGAGTC	6045
rs12080414	snp	A/G	0.00835141	0.0640778	intron-variant	RNF2	GRCh38.p7	1:185066228	TCTTGATACCTTTGT[A/G]TTGCATACTAGGCCT	6045
rs12081098	snp	C/G	0.498503	0.0273153	intron-variant	RNF2	GRCh38.p7	1:185089147	atgcagtctagatcc[C/G]ttgcatgtgcagttc	6045
rs12091158	snp	G/T			intron-variant	RNF2	GRCh38.p7	1:185082367	ttttttttttttttt[G/T]gaagacagagtcttg	6045
rs12092074	snp	G/T			utr-variant-3-prime	RNF2	GRCh38.p7	1:185101832	ATCTGTTTTTACAGG[G/T]ttttttttttttttt	6045
rs12126822	snp	C/G	0.00953873	0.0683987	intron-variant	RNF2	GRCh38.p7	1:185066848	AGGGGTAGTAGTAGT[C/G]TTAGAGGAGATGAGA	6045
rs12127009	snp	A/G	0.161267	0.233723	intron-variant	RNF2	GRCh38.p7	1:185061415	TTCTGATCTCAGGCA[A/G]AAACCAACCCACCAA	6045
rs12145600	snp	C/T	0.5	0	intron-variant	RNF2	GRCh38.p7	1:185076247	GGCTGCCCTTCTTTT[C/T]TTCTAGATCTTTTAT	6045
rs12408074	snp	A/G	0.398354	0.201224	intron-variant	RNF2	GRCh38.p7	1:185091886	AATGGCACGATCTTG[A/G]CTCACTGCAACCTCT	6045
rs12408279	snp	A/G	0.244776	0.249945	intron-variant, upstream-variant-2KB	RNF2	GRCh38.p7	1:185070091	TCTCCCTGGTCTTTT[A/G]CATGTTAGGGGACTA	6045
rs12409926	snp	C/T	0.245631	0.249962	intron-variant	RNF2	GRCh38.p7	1:185083295	TATTTTGTCAGTTTT[C/T]TCAGGTTCTTTGAAT	6045
rs12563135	snp	C/T	0.418169	0.184985	intron-variant	RNF2	GRCh38.p7	1:185092013	TATTTTTAGTAGAGA[C/T]GGGGTTTCAACTTGT	6045
rs12749846	snp	C/T			intron-variant	RNF2	GRCh38.p7	1:185056602	tctcaaactcctggc[C/T]tcaagtgatcctccc	6045
rs16865296	snp	A/T	0.245061	0.249951	utr-variant-3-prime	RNF2	GRCh38.p7	1:185100711	TGTATTCTGACTTTT[A/T]TTTTCCCCCGGAGTC	6045
rs17314171	snp	C/T	0.0629771	0.165899	intron-variant	RNF2	GRCh38.p7	1:185073437	CTGTTATTCTTTTAT[C/T]CAGCCAAAGAGCAGA	6045
rs17379801	snp	C/T	0.0460142	0.144533	intron-variant, upstream-variant-2KB	RNF2	GRCh38.p7	1:185071326	TTCCGGGCTAGTTTA[C/T]AGGGAAGATATGTAT	6045
rs28609768	snp	A/C	0.435837	0.167226	intron-variant	RNF2	GRCh38.p7	1:185064348	AGAATCCTACAGAAT[A/C]GGTACTTTATTTCAA	6045
rs28690032	snp	A/C	0.498133	0.030494	intron-variant	RNF2	GRCh38.p7	1:185062820	AGACCTCCCCCCCCC[A/C]AAAAAAAGGCCAATA	6045
rs34086865	in-del	-/A			intron-variant	RNF2	GRCh38.p7	1:185078684	GAGGCCGAGGTGGGC[-/A]GGATCACCTGAGGTT	6045
rs34143770	in-del	-/T	0.418169	0.184985	intron-variant	RNF2	GRCh38.p7	1:185051735	CTCCTTAACTAATTC[-/T]TTTTTTTTTTTCATC	6045
rs34216534	in-del	-/T	0.154661	0.231107	intron-variant	RNF2	GRCh38.p7	1:185068009	CCACAGCGCCCGGCC[-/T]TTTTTTTTTTTAGAG	6045
rs34284435	in-del	-/T	0.499396	0.0173617	intron-variant	RNF2	GRCh38.p7	1:185061129	CTATTTCTCTCTCTC[-/T]TTTTTTTTTTTTTTT	6045
rs34348424	snp	A/C	0	0	utr-variant-3-prime, downstream-variant-500B	RNF2	GRCh38.p7	1:185101591	CCAACTTTATATATC[A/C]CAGTATTTAAAAAGA	6045
rs34494448	in-del	-/T			intron-variant	RNF2	GRCh38.p7	1:185058046	GGAACATCACCGGAG[-/T]CCTGGGAGGGTTGAG	6045
rs34522033	in-del	-/T			intron-variant	RNF2	GRCh38.p7	1:185051907	AAAAAGTCGTATTTG[-/T]ATTTATACATATATT	6045
rs34763973	in-del	-/G			intron-variant	RNF2	GRCh38.p7	1:185079900	CGCCACTGCACTCTA[-/G]GCCTGGGCAACAAGA	6045
rs34784535	in-del	-/T	0.00953873	0.0683987	intron-variant	RNF2	GRCh38.p7	1:185062651	TATAAAAGATAAAAG[-/T]TATGTACTGAAGAAG	6045
rs34810150	in-del	-/T			intron-variant	RNF2	GRCh38.p7	1:185057344	TAAATATAATTAACA[-/T]TTTTCTGTGCCATAG	6045
rs34969721	snp	A/G	0.379158	0.214052	intron-variant	RNF2	GRCh38.p7	1:185096042	AGTTACATTAATATA[A/G]CTCTGTCACATCAAT	6045
rs34982714	in-del	-/C			utr-variant-3-prime, downstream-variant-500B	RNF2	GRCh38.p7	1:185102603	TTCTCTTCTTCTTAA[-/C]CCCCTAGCAACCTCT	6045
rs35117337	in-del	-/G			intron-variant	RNF2	GRCh38.p7	1:185047854	GTTATTGCACACACT[-/G]GTAGAAGACATTGTC	6045
rs35163206	in-del	-/G			intron-variant	RNF2	GRCh38.p7	1:185087912	TGAAAAAGTACATAT[-/G]CTATAAAATTCACAT	6045
rs35163800	in-del	-/T			intron-variant	RNF2	GRCh38.p7	1:185075566	AAGGTTCTGCAAGGC[-/T]TGTACAGGAAGCATG	6045
rs35165842	in-del	-/G			intron-variant	RNF2	GRCh38.p7	1:185087242	ACAGTTCTGGAGACT[-/G]GGGAATTCCAAGATC	6045
rs35280730	in-del	-/A	0.499863	0.00828277	intron-variant	RNF2	GRCh38.p7	1:185059228	ATCCCAGTCTGGATT[-/A]AAAAAAAAAAAACCT	6045
rs35586940	in-del	-/A	0.5	0	intron-variant	RNF2	GRCh38.p7	1:185088556	TCAAAAAAAAAAAAA[-/A]GCTAAAGGAAGTATT	6045
rs36053005	snp	C/T	0.0486741	0.148216	intron-variant	RNF2	GRCh38.p7	1:185075871	CTAAATATTAGTCAT[C/T]TTAATCTTTGTCAAT	6045
rs36086867	in-del	-/T			intron-variant	RNF2	GRCh38.p7	1:185048834	TAAGTTCAGCTAAGC[-/T]TTTGGTGTTGGAACA	6045
rs41529047	snp	C/T	0.0345262	0.126772	intron-variant, utr-variant-5-prime	RNF2	GRCh38.p7	1:185071657	AAAGAACTGGGTGAC[C/T]ATGTTCAACTTGTCC	6045
rs55738529	snp	C/T	0.0883596	0.190715	intron-variant	RNF2	GRCh38.p7	1:185082807	TTGTTTTTTGTCTAA[C/T]AACATTTCCATAGTC	6045
rs55743893	snp	A/G	0.0228947	0.104514	intron-variant	RNF2	GRCh38.p7	1:185077452	TGTTTTGGGACTTCC[A/G]GTAGATTTTTCATGA	6045
rs55756628	snp	C/T	0.0287284	0.116357	intron-variant	RNF2	GRCh38.p7	1:185074690	ATTAGGGAAAAAAAA[C/T]GGTATGGTTGCATCT	6045
rs56048451	snp	C/T			utr-variant-3-prime	RNF2	GRCh38.p7	1:185100881	AGTTCTTTATGAACT[C/T]AGTGTCCATTGTCAT	6045
rs56098414	in-del	-/A			intron-variant	RNF2	GRCh38.p7	1:185068721	GTTATAAGCCTTCAA[-/A]TTTGTGATAATGTTA	6045
rs56110440	snp	C/T	0.0232847	0.105357	intron-variant	RNF2	GRCh38.p7	1:185067744	GAGACGGAGTCTTGC[C/T]CTGTTGCCCAGGCTG	6045
rs56121579	snp	A/G			missense	RNF2	GRCh38.p7	1:185098130	GCAGAAGATAATGGT[A/G]ACAGTTCACACTGCA	6045

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