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
rs8645	snp	A/C	0.241914	0.249869	utr-variant-3-prime	SUMO3	GRCh38.p7	21:44806651	CATTTTTTTAACCCC[A/C]AAATTATAGCCTGAA	6612
rs180313	snp	C/T	0.0678174	0.1712	intron-variant	SUMO3	GRCh38.p7	21:44807883	CTGCTCAGCTGCTCT[C/T]AGCAGCTTCTCCCTG	6612
rs235292	snp	G/T	0.106633	0.204807	utr-variant-3-prime	SUMO3	GRCh38.p7	21:44805750	AGGAAATGAGAACAT[G/T]TCAGCAAGATTTCAA	6612
rs235293	snp	C/T	0.0654584	0.168655	intron-variant	SUMO3	GRCh38.p7	21:44809015	GCACAAATCGGAAGT[C/T]GCCCTGGAACCACGC	6612
rs235334	snp	A/G	0.486332	0.08153	intron-variant	SUMO3	GRCh38.p7	21:44815259	GGGAAGCAAGCATGG[A/G]TGCAGTCCCTGGGTT	6612
rs235335	snp	C/G	0.0655868	0.168795	intron-variant	SUMO3	GRCh38.p7	21:44815992	AGGGGAAGAGGTGGA[C/G]TCTGGGGCCCGGTGG	6612
rs235336	snp	A/G	0.0547245	0.156101	intron-variant	SUMO3	GRCh38.p7	21:44816508	GACCACCCTCCCTTT[A/G]CAGATGAGGGTGGAG	6612
rs235337	snp	C/T	0.3742	0.216966	intron-variant	SUMO3	GRCh38.p7	21:44817356	CACTTCTCCGCATCG[C/T]GTCCCGGCCATCGCG	6612
rs663223	snp	G/T	0.0119091	0.0762411	upstream-variant-2KB	SUMO3	GRCh38.p7	21:44818236	TCCCGCGCGACCCCG[G/T]CGGGCGCGGAAGCCC	6612
rs873301	snp	C/T	0.118584	0.212673	intron-variant	SUMO3	GRCh38.p7	21:44808833	GCCCAGCACTTGGCT[C/T]CATCTCCAAACAGCA	6612
rs1051306	snp	A/C			utr-variant-5-prime	SUMO3	GRCh38.p7	21:44817973	CCCGCGCCGCTCGCG[A/C]AGCCATGTCCGAGGA	6612
rs1051311	snp	C/T	0	0	missense	SUMO3	GRCh38.p7	21:44814014	ATCAAGAGGCACACG[C/T]CGCTGAGCAAGCTGA	6612
rs1051331	snp	C/T	0.285298	0.247496	utr-variant-3-prime	SUMO3	GRCh38.p7	21:44806871	TGCCGACCACAAAGG[C/T]GTCTGCGGAAACTCG	6612
rs1555002	snp	C/T	0.0185938	0.0946107	intron-variant	SUMO3	GRCh38.p7	21:44814948	ACTGGGAGCCAACTT[C/T]GGGGCAGCTCAGTCT	6612
rs1555003	snp	C/T	0.0146672	0.084371	intron-variant	SUMO3	GRCh38.p7	21:44814982	CCGAAAAGTGGGGCA[C/T]CCCTCTGCCGGCCTG	6612
rs2016874	snp	A/G	0.0279526	0.114869	intron-variant	SUMO3	GRCh38.p7	21:44809258	CGGCTTAATTCAAAA[A/G]CCAAATATTTTAATC	6612
rs2017089	snp	A/G	0.117886	0.21224	intron-variant	SUMO3	GRCh38.p7	21:44809478	AACTGCCACTGGTTT[A/G]GCTTTAAGAAGTTCC	6612
rs2329902	snp	A/G	0.324382	0.238678	intron-variant	SUMO3	GRCh38.p7	21:44807248	AGCCCTTACGGTTCA[A/G]CAAGCTTCCCCTAAC	6612
rs2838692	snp	C/T	0.23031	0.249223	downstream-variant-500B	SUMO3	GRCh38.p7	21:44805481	AAATGAGCTGCCAGG[C/T]GAATACTAACCTTCC	6612
rs2838693	snp	A/C	0.41441	0.188333	intron-variant	SUMO3	GRCh38.p7	21:44807957	TTCCTCAAGTAGGTA[A/C]AAATGGATACTTGTT	6612
rs2838694	snp	C/G	0.127944	0.218179	intron-variant	SUMO3	GRCh38.p7	21:44810229	TGAAATGAAGTAAAT[C/G]AAAAAGGCACAAACA	6612
rs2838695	snp	C/T	0.320575	0.239832	intron-variant	SUMO3	GRCh38.p7	21:44810837	CACTGTGCAGCAGCC[C/T]AGAGAGGAGGGGAGG	6612
rs2838696	snp	C/T	0.125874	0.217008	intron-variant	SUMO3	GRCh38.p7	21:44813315	CTGGTGGGCAAAGCC[C/T]ATAAAAGTGGCCTAG	6612
rs2838697	snp	A/C	0.325459	0.238349	missense, intron-variant	SUMO3	GRCh38.p7	21:44813921	TGGGGATGCCTGGAA[A/C]GCACAGGACCAGTGC	6612
rs2838698	snp	C/T	0.471958	0.115042	intron-variant	SUMO3	GRCh38.p7	21:44814326	GTAAAACAATGCAAG[C/T]CTAGGGTCCTCTGAC	6612
rs2838699	snp	C/T	0.249038	0.249998	intron-variant	SUMO3	GRCh38.p7	21:44814650	GTGACTCAGAGGAAC[C/T]CTATGGGACATTCAA	6612
rs2838700	snp	C/T	0.471004	0.116864	intron-variant	SUMO3	GRCh38.p7	21:44815998	GGCCCCAGAGTCCAC[C/T]TCTTCCCCTTCGTCA	6612
rs3746969	snp	A/G	1.64776e-05	0.00287028	intron-variant	SUMO3	GRCh38.p7	21:44809121	TCATTGACAAGCCCT[A/G]GAAAGGAAAAGCAGT	6612
rs3827259	snp	C/T	0.067446	0.170804	intron-variant	SUMO3	GRCh38.p7	21:44809509	CAGTTTCAAAGCAGA[C/T]AGGTAAGTGGTCCAT	6612
rs4437050	snp	A/C	0.00345393	0.041413	intron-variant	SUMO3	GRCh38.p7	21:44807059	TCATGGTTGTCACAA[A/C]AGGCACAGCGAGAGA	6612
rs4818977	snp	C/T	0.422944	0.180528	intron-variant	SUMO3	GRCh38.p7	21:44809891	TGTCCTGGGTCATCC[C/T]TCCCATCTTTCCAGA	6612
rs4818978	snp	C/T			intron-variant	SUMO3	GRCh38.p7	21:44811175	GCACACACCCACACA[C/T]ACACACACATGCACA	6612
rs7282882	snp	G/T	0.418653	0.184544	intron-variant	SUMO3	GRCh38.p7	21:44817494	CCGAGCCGACTCCGT[G/T]CACTCGACACAGGAT	6612
rs7283053	snp	A/G/T	0.0267878	0.112589	intron-variant	SUMO3	GRCh38.p7	21:44817603	CGGGGACACTGCTGG[A/G/T]GCGGGATCCGAGGGC	6612
rs7283639	snp	C/T	0.130694	0.219696	intron-variant	SUMO3	GRCh38.p7	21:44808250	GGGCGCGTTGGCTCA[C/T]GCCTTTAATCCCAGC	6612
rs9306115	snp	A/G	0.422944	0.180528	intron-variant	SUMO3	GRCh38.p7	21:44813156	AAAATCCACAGGCAA[A/G]AGAGTAAAATAAAAG	6612
rs9306116	snp	A/T	0.471958	0.115042	intron-variant	SUMO3	GRCh38.p7	21:44814164	TAACCGCGACTTGAA[A/T]GGGCAAGTCTTTAGG	6612
rs9306117	snp	A/C/T	0.138488	0.231878	intron-variant	SUMO3	GRCh38.p7	21:44816666	ATGAACACTGGAGAA[A/C/T]GCGACTACAGACCCT	6612
rs9637164	snp	C/G			utr-variant-3-prime	SUMO3	GRCh38.p7	21:44805925	ACTGAAATCACCAGA[C/G]TAATGCATAAATTCA	6612
rs9637189	snp	A/G	0.327445	0.237702	intron-variant	SUMO3	GRCh38.p7	21:44814522	TCTGGGCAACAGAGC[A/G]AGACCCCATCTCTTT	6612
rs9975507	snp	A/G	0.157642	0.232314	intron-variant	SUMO3	GRCh38.p7	21:44812774	GCCCCCCCCACATGT[A/G]CACGGCCCCACACGC	6612
rs9975777	snp	C/G	0.133435	0.221162	intron-variant	SUMO3	GRCh38.p7	21:44816635	ACACCAAGGGCTTCG[C/G]AAAGGTTCTCTTTTT	6612
rs9976897	snp	A/G	0.0520825	0.152737	upstream-variant-2KB	SUMO3	GRCh38.p7	21:44818970	GCGTCCCTCAGGAGT[A/G]CCCGGGTGGTGCCAG	6612
rs9977439	snp	A/G	0.104504	0.2033	intron-variant	SUMO3	GRCh38.p7	21:44813600	CAGGGTGACAGCGGC[A/G]TGGGGCACACGCCAC	6612
rs9977465	snp	A/T	0.422944	0.180528	intron-variant	SUMO3	GRCh38.p7	21:44812352	cccaaagtgctggga[A/T]tacaggcataagcca	6612
rs9979741	snp	C/T	0.135484	0.22223	intron-variant	SUMO3	GRCh38.p7	21:44817151	ATGGGGAGGAGTGGG[C/T]ACACACCATGGGGGG	6612
rs9981327	snp	C/T	0.0513938	0.151841	missense, intron-variant	SUMO3	GRCh38.p7	21:44813951	CGCACACGGGGAGGC[C/T]CTGCGGGGGAGCAAG	6612
rs9984357	snp	C/T	0.362104	0.223456	intron-variant	SUMO3	GRCh38.p7	21:44807688	CAGCAAGGCTGGAAG[C/T]AGTCATGCTCCCAGA	6612
rs10483079	snp	C/G	0.0252325	0.109451	utr-variant-3-prime	SUMO3	GRCh38.p7	21:44806623	AGATCCCTGGCCAGA[C/G]TAAAAGCGAACATTC	6612
rs10658457	snp	C/T			intron-variant	SUMO3	GRCh38.p7	21:44812053	cactgaacttctcac[C/T]ttttttttttttttt	6612
rs11545089	snp	C/G	0.00597247	0.0543191	utr-variant-3-prime	SUMO3	GRCh38.p7	21:44806362	GGTTAAAAAATAACC[C/G]AGTCTTTTGGTAATT	6612
rs11545091	snp	C/G			utr-variant-5-prime	SUMO3	GRCh38.p7	21:44818002	GCTCCGCGCTGCTTC[C/G]CCCGCGCCGCCTCCC	6612
rs11545092	snp	A/G/T	9.92185e-05	0.00704276	synonymous-codon	SUMO3	GRCh38.p7	21:44814012	CAAGAGGCACACGCC[A/G/T]CTGAGCAAGCTGATG	6612
rs11701732	snp	C/T	0.426354	0.177198	upstream-variant-2KB	SUMO3	GRCh38.p7	21:44819512	TCGACTCCAAGACAC[C/T]GTTAATCATAAAACA	6612
rs11702064	snp	C/T	0.248755	0.249997	intron-variant	SUMO3	GRCh38.p7	21:44815048	TGAGGCAGGGCCCTC[C/T]GGCTCACTCTGAAAG	6612
rs11911014	snp	C/T	0.0970103	0.197722	intron-variant	SUMO3	GRCh38.p7	21:44814968	CAGCTCAGTCTGAGC[C/T]GAAAAGTGGGGCACC	6612
rs13046717	snp	C/T			intron-variant	SUMO3	GRCh38.p7	21:44810993	acacccatgcacaca[C/T]ccacacaTGcacaca	6612
rs13046718	snp	A/C			intron-variant	SUMO3	GRCh38.p7	21:44810994	CACCCATGCACACAC[A/C]CACACATGCACACAC	6612
rs13049657	snp	A/G	0.248471	0.249995	intron-variant	SUMO3	GRCh38.p7	21:44811835	ggaacagagtctgga[A/G]aaggatacaaattat	6612
rs13050872	snp	C/G	0.367922	0.220441	missense, intron-variant	SUMO3	GRCh38.p7	21:44813948	GTGCGCACACGGGGA[C/G]GCTCTGCGGGGGAGC	6612
rs17217834	snp	A/G	0.117537	0.212022	intron-variant	SUMO3	GRCh38.p7	21:44813057	AGGGGCTGCTTGCCA[A/G]TAAAGAATGCAAGGC	6612
rs17526563	snp	C/T	0.127944	0.218179	upstream-variant-2KB	SUMO3	GRCh38.p7	21:44818544	GGCGGGTGGCGCCCC[C/T]AATCGTCTAGGGTGC	6612
rs17526570	snp	C/G			upstream-variant-2KB	SUMO3	GRCh38.p7	21:44818207	GACCCGCCCCGTGAC[C/G]CATCTCCAACCGCCC	6612
rs35209448	in-del	-/CA			intron-variant	SUMO3	GRCh38.p7	21:44813395	ACAGACACACACACA[-/CA]CCACGTCACAAACAG	6612
rs35934209	snp	A/G	0.0966517	0.197444	intron-variant	SUMO3	GRCh38.p7	21:44815397	AAGGTGCGTGTCCTG[A/G]GGCGGCACTCACCCC	6612
rs56230948	snp	A/G	0.000399281	0.0141238	intron-variant	SUMO3	GRCh38.p7	21:44811708	TTGAAATGACCTCCC[A/G]GAAAGAAGCCCAAAT	6612
rs56656758	snp	C/T			intron-variant	SUMO3	GRCh38.p7	21:44808072	ACATTCCAGTGGATT[C/T]TCACAACATTGAAAG	6612
rs57205597	snp	A/G	0.133435	0.221162	intron-variant	SUMO3	GRCh38.p7	21:44816760	GAGGCACACCCCAGC[A/G]TGGCAATGGGGGAGA	6612
rs57451321	snp	C/G			intron-variant	SUMO3	GRCh38.p7	21:44808367	AATACAAAAAAATTA[C/G]CCGGGAGTGGTGGTG	6612
rs59498244	snp	A/G	0.0221141	0.102801	intron-variant	SUMO3	GRCh38.p7	21:44807963	AAGTAGGTACAAATG[A/G]ATACTTGTTGCAAAG	6612
rs59528804	in-del	-/CCACATATGCACACAC			intron-variant	SUMO3	GRCh38.p7	21:44811010	CACACATGCACACAC[-/CCACATATGCACACAC]GCACACACCCACATA	6612
rs59575993	in-del	-/AT	0.426047	0.177503	intron-variant	SUMO3	GRCh38.p7	21:44810497	CCCACGGCAGCACAC[-/AT]GAGATGTGCTTTCTG	6612
rs59687051	snp	C/G	0.0785177	0.181917	upstream-variant-2KB	SUMO3	GRCh38.p7	21:44819563	GACACACTAAACTCC[C/G]GCAGGCTGTGGATGA	6612
rs59713448	in-del	-/TGGACACCAGGA	0	0	intron-variant	SUMO3	GRCh38.p7	21:44815801	TCTGCTCCAAACAGA[-/TGGACACCAGGA]ATGACGATCTGTCCC	6612
rs60007138	snp	C/G	0.0115144	0.0749975	intron-variant	SUMO3	GRCh38.p7	21:44816455	ACCATGGTTCCTGAC[C/G]GTTCCATCCCACTTC	6612
rs60685574	snp	G/T	0.141934	0.225437	intron-variant	SUMO3	GRCh38.p7	21:44811159	ACACATACACACACA[G/T]GCACACACCCACACA	6612
rs61602523	snp	G/T	0.146314	0.227484	upstream-variant-2KB	SUMO3	GRCh38.p7	21:44819532	ATCATAAAACAACAC[G/T]ACCGTAGGTAGCACA	6612
rs62220110	snp	A/G			intron-variant	SUMO3	GRCh38.p7	21:44809990	AGGTTGTGTGCCAAT[A/G]AGGGACAGATAAGAA	6612
rs67264081	in-del	-/GATGGACACCAG			intron-variant	SUMO3	GRCh38.p7	21:44815800	CTCTGCTCCAAACAG[-/GATGGACACCAG]AATGACGATCTGTCC	6612
rs67879920	in-del	-/GAGGACAGGGTGACAGCGGCG	0.355096	0.226837	intron-variant	SUMO3	GRCh38.p7	21:44813580	GGCCAGCTCATACGC[-/GAGGACAGGGTGACAGCGGCG]TGGGGCACACGCCAC	6612
rs71199631	in-del	-/AC	0.35445	0.227135	intron-variant	SUMO3	GRCh38.p7	21:44813384	TACCAAGAACAACAG[-/AC]ACACACACACACCAC	6612
rs71199633	in-del	-/G	0	0	intron-variant	SUMO3	GRCh38.p7	21:44815711	ACGTCCCCCACAGGG[-/G]TAATGGCTGCAGCCC	6612
rs71322592	snp	C/G	0.248188	0.249993	intron-variant	SUMO3	GRCh38.p7	21:44817206	ACCGGGGGGCGCGAT[C/G]GGGAGGGGTGGGCGC	6612
rs72613649	snp	A/G	0.424348	0.179172	intron-variant	SUMO3	GRCh38.p7	21:44817645	CAGGAGCAGCAGCGC[A/G]GGGCCCGACACCGGG	6612
rs73232962	snp	A/G	0.106278	0.204558	intron-variant	SUMO3	GRCh38.p7	21:44807449	TTTATACCAAGTGCG[A/G]GGGACCATGCCATGA	6612
rs73232964	snp	C/T	0.5	0	intron-variant	SUMO3	GRCh38.p7	21:44812054	ACTGAACTTCTCACC[C/T]TTTTTTTTTTTTTTT	6612
rs73232966	snp	C/T	0.127599	0.217986	upstream-variant-2KB	SUMO3	GRCh38.p7	21:44819390	CAGCTCAGACGGTCC[C/T]GGGAGGGGGCTCCGC	6612
rs73372511	snp	C/T	0.148661	0.22854	intron-variant	SUMO3	GRCh38.p7	21:44811495	GAGGATCACTTGAGC[C/T]CCAGGGCTCAAGGCT	6612
rs73372522	snp	C/G	0.00199481	0.0315187	intron-variant	SUMO3	GRCh38.p7	21:44815659	TCTTTAGGGAAGGAA[C/G]GTATGAGTGTGTTCA	6612
rs73906926	snp	A/G	0.0119091	0.0762411	upstream-variant-2KB	SUMO3	GRCh38.p7	21:44820013	GGGTAAAGAACCCAA[A/G]TGGCCAGAGCCCCTC	6612
rs74706647	snp	A/G	0.0437281	0.141251	intron-variant	SUMO3	GRCh38.p7	21:44809412	ATCTTCTCTCTGATG[A/G]GCTAAAACGGCTCAT	6612
rs74881430	snp	A/C	0.0130921	0.0798413	intron-variant	SUMO3	GRCh38.p7	21:44809263	TAATTCAAAAACCAA[A/C]TATTTTAATCCAAGT	6612
rs75760356	snp	C/G	0.5	0	intron-variant	SUMO3	GRCh38.p7	21:44807793	CAGGCAGGGCTCCCT[C/G]TGCCTCTCGGTCCAC	6612
rs76003441	snp	G/T			intron-variant	SUMO3	GRCh38.p7	21:44808722	CCAGCTGGCCCCTAA[G/T]CTGCACACGGGCTAC	6612
rs76299308	snp	C/G	0.130351	0.219509	intron-variant	SUMO3	GRCh38.p7	21:44815493	TGAGTGGTGAGCTGG[C/G]ACACCCCCATCTCCC	6612
rs76430289	snp	G/T	0.00636936	0.0560724	intron-variant	SUMO3	GRCh38.p7	21:44811768	GAAAAATTATCAAAT[G/T]TAAAATATCTAGGAC	6612
rs76455805	snp	C/T	0.130351	0.219509	downstream-variant-500B	SUMO3, LINC01424	GRCh38.p7	21:44805152	GGTTTTGTTACACCA[C/T]TGCACACTGGGAAAT	6612
rs76559724	in-del	-/CGAGGACAGGGTGACAGCGGCG			intron-variant	SUMO3	GRCh38.p7	21:44813579	AGGCCAGCTCATACG[-/CGAGGACAGGGTGACAGCGGCG]TGGGGCACACGCCAC	6612
rs76675574	snp	A/G	0.0193772	0.0965046	intron-variant	SUMO3	GRCh38.p7	21:44815005	CCGGCCTGCACTGCT[A/G]GGATAAAGTCGTTTG	6612
rs77015779	snp	C/T	0.0134861	0.0810011	intron-variant	SUMO3	GRCh38.p7	21:44815499	GTGAGCTGGCACACC[C/T]CCATCTCCCCATCCC	6612

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