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
rs14218	snp	A/G/T	0.00310999	0.0393106	synonymous-codon	RNF126	GRCh38.p7	19:648224	ACAGAACACGGCCAC[A/G/T]AACCCCCCTGGCCTC	55658
rs757331	snp	A/G	0.409212	0.192748	downstream-variant-500B	RNF126	GRCh38.p7	19:647251	GGCTGAGGTGTGACC[A/G]AAGCGTGGGGCAGAG	55658
rs916904	snp	A/G	0.490727	0.0674567	upstream-variant-2KB	RNF126	GRCh38.p7	19:663929	TCTCGGGTGCGGAGA[A/G]GGCAGGAAACCTAAC	55658
rs929263	snp	C/T	0.243919	0.249926	upstream-variant-2KB	RNF126	GRCh38.p7	19:663373	GGGCGGGGCTTCCGG[C/T]GGGGGCGGGGCCAAA	55658
rs1009628	snp	A/G	0.189576	0.242588	intron-variant	RNF126	GRCh38.p7	19:658013	ACCTTCTCCGGGGGC[A/G]GCACGCACTGGGGGC	55658
rs1009629	snp	C/T	0.317692	0.240661	intron-variant	RNF126	GRCh38.p7	19:660913	AGGCACAAGCAGATG[C/T]CCTTGGGATCACCCG	55658
rs1859224	snp	A/G	0.490943	0.0666801	upstream-variant-2KB	RNF126	GRCh38.p7	19:663485	TTCGTGTCCCTCAGT[A/G]CTTCCCTACCTCATC	55658
rs2040736	snp	C/G	0.178785	0.239642	intron-variant	RNF126	GRCh38.p7	19:649110	CCTTGGAGCCCGCCC[C/G]GGGTCGGAGATCACT	55658
rs2040737	snp	A/G	0.114036	0.209795	intron-variant	RNF126	GRCh38.p7	19:649139	CTGTGGAGCCCACGC[A/G]GCCCCCCCGCTCCTG	55658
rs2040738	snp	A/G	0.238171	0.24972	intron-variant	RNF126	GRCh38.p7	19:650931	atggggcctccctac[A/G]ttgctcaggctggtc	55658
rs2040739	snp	A/G	0.190371	0.242785	intron-variant	RNF126	GRCh38.p7	19:658368	TGACTGACAGTGACC[A/G]GGGCAGGCAGGCCCC	55658
rs2072104	snp	C/G	0.100773	0.200577	synonymous-codon	RNF126	GRCh38.p7	19:648173	GGGCGAGCTGGAGGA[C/G]GACGATGACGACGAG	55658
rs2074460	snp	C/T	0.187685	0.242109	downstream-variant-500B	RNF126	GRCh38.p7	19:647039	CTCCTCTCCGTTAGC[C/T]GTCTCCATCGTCTGA	55658
rs2285751	snp	C/T	0.114459	0.210068	missense	RNF126	GRCh38.p7	19:651852	ACAGGTGCTGGTCCA[C/T]GTGCTGGGGAGAGGA	55658
rs2285752	snp	C/T	0.000654046	0.0180719	intron-variant	RNF126	GRCh38.p7	19:651874	GGGAGAGGAGGGGGG[C/T]GTGACCTCGGGGGCT	55658
rs3077449	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655014	CCTGGGCTTTTTTTT[C/T]TTTCTTTCTTTCTTT	55658
rs3170527	snp	C/T	0.0663309	0.169604	utr-variant-3-prime	RNF126	GRCh38.p7	19:648014	TTGGCTGGTCAGCGC[C/T]GCAGGTCCCGCCTGT	55658
rs3179858	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647530	TACACTACTTACAAA[A/G]AGAAGCCGGTGCTGT	55658
rs3180572	snp	A/G			utr-variant-3-prime	RNF126	GRCh38.p7	19:647528	CACTACTTACAAAGA[A/G]AAGCCGGTGCTGTGG	55658
rs3787004	snp	C/T	0.377582	0.214995	intron-variant	RNF126	GRCh38.p7	19:657666	CTCATATCTGAAATC[C/T]GGGTGCCATCGAGGA	55658
rs3787005	snp	A/G	0.367503	0.220665	intron-variant	RNF126	GRCh38.p7	19:658983	CAGCCGGCCAGAGAG[A/G]GCAGCCGACATCCAC	55658
rs3787006	snp	A/C	0.0170251	0.090679	intron-variant	RNF126	GRCh38.p7	19:659328	CTGGCCGTAGCAGCC[A/C]TCACTTCCTGGTGGC	55658
rs3787007	snp	A/G	0.0640965	0.167152	intron-variant	RNF126	GRCh38.p7	19:660657	CGTTTTTGAGACAGC[A/G]TCTTGCTTGTCACCC	55658
rs3787008	snp	A/G	0.000798403	0.0199641	intron-variant	RNF126	GRCh38.p7	19:660872	TGCCATGCTGTCTAC[A/G]GGCGCCTTGTTGCGT	55658
rs3787010	snp	A/G	0.000399281	0.0141238	intron-variant	RNF126	GRCh38.p7	19:661031	CAATCACTGTTCCAT[A/G]CTGGCTCCCTGGCCA	55658
rs3787011	snp	A/G	0.200492	0.245049	intron-variant	RNF126	GRCh38.p7	19:661080	GGCAAAGACCACAGC[A/G]GCCTGTCACCACAGA	55658
rs3787012	snp	C/T	0.499776	0.0105807	intron-variant	RNF126	GRCh38.p7	19:661781	AGCCGGGCGGCTACG[C/T]ACACAGCACAGTAAA	55658
rs3826951	snp	C/T	0.285519	0.247464	intron-variant	RNF126	GRCh38.p7	19:658092	ATCCATTCACCTCTC[C/T]GTCAGAGAACAGATG	55658
rs3826952	snp	A/C	0.314544	0.241524	intron-variant	RNF126	GRCh38.p7	19:661958	GTTTCCCCATCTATA[A/C]AGCACGGGTGGCTCG	55658
rs4594371	snp	A/G	0.474	0.111014	intron-variant	RNF126	GRCh38.p7	19:654968	gtgagactccgtatc[A/G]ggaaaaaaaaaaGTG	55658
rs4919820	snp	G/T	0.172997	0.237846	intron-variant	RNF126	GRCh38.p7	19:657588	CGCCCACCCTAGGGG[G/T]TTCAAAGGTCACCTC	55658
rs4919879	snp	A/C	0.486332	0.08153	intron-variant	RNF126	GRCh38.p7	19:651280	CACCAGGAGTGGGGC[A/C]CTGCGACGGCTCCCC	55658
rs4919880	snp	C/T	0.353587	0.22753	intron-variant	RNF126	GRCh38.p7	19:653830	GAAAATGGCCTCACA[C/T]GGCACGTGTCATCAC	55658
rs4919881	snp	C/T	0.166832	0.235761	intron-variant	RNF126	GRCh38.p7	19:656701	GCCAACGACCACCAC[C/T]GTGGCCCTGAGCTTA	55658
rs4919882	snp	C/T	0.16846	0.236329	intron-variant	RNF126	GRCh38.p7	19:662431	GAGGAACGCAGGCTC[C/T]GCTCACAAAGCCCCG	55658
rs4919883	snp	C/T	0.256897	0.249905	upstream-variant-2KB	RNF126	GRCh38.p7	19:664278	TTGAACTCCTGACCT[C/T]GTGATCCGCCCGCCT	55658
rs6510868	snp	C/T	0.453209	0.145623	intron-variant	RNF126	GRCh38.p7	19:655608	CCAGCCAGGACGAGA[C/T]GCAAGACCCCGTCAG	55658
rs6510873	snp	A/G	0.489083	0.0730708	upstream-variant-2KB	RNF126	GRCh38.p7	19:664931	CAGGCGTAAGCCACC[A/G]CGCCCGGCCTGCATT	55658
rs7245869	snp	C/T	0.286303	0.24735	intron-variant	RNF126	GRCh38.p7	19:659658	CTGGGTCTGCGCAGC[C/T]GCCTGTGGCCTGAGC	55658
rs7254550	snp	C/G/T	0.0225671	0.103817	intron-variant	RNF126	GRCh38.p7	19:648345	ggccgcggtcggggt[C/G/T]ggggggcgggtgggc	55658
rs7255896	snp	A/C	0.486984	0.079614	upstream-variant-2KB	RNF126	GRCh38.p7	19:663956	TAACCCCTGCTTCCA[A/C]ATTTAATCAGTAGAA	55658
rs7257070	snp	C/T	0.415727	0.187175	downstream-variant-500B	RNF126	GRCh38.p7	19:647486	CCCAGCTTGGCCTTT[C/T]CCTGACGCACGGGCG	55658
rs8100039	snp	C/G	0.0475351	0.146656	intron-variant	RNF126	GRCh38.p7	19:659469	TGGGGGGTCGGCAGG[C/G]AGAGCTGGAACCACC	55658
rs8102953	snp	A/G	0.0442142	0.141958	intron-variant	RNF126	GRCh38.p7	19:652206	AAGGCTGACACGATC[A/G]GGAAGCACGAGGGGC	55658
rs8113363	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	RNF126	GRCh38.p7	19:664841	agacggggtttcact[A/G]tgttggccaggctgg	55658
rs10153505	snp	G/T	0.106633	0.204807	intron-variant	RNF126	GRCh38.p7	19:652948	GCAAACCCCCCCAAG[G/T]GTGAGGACAGAGGGG	55658
rs10401924	snp	C/T	0.0547245	0.156101	intron-variant	RNF126	GRCh38.p7	19:659623	CAGCTCCAGTCAGTG[C/T]CTCCTCAGCAGGCTC	55658
rs10408182	snp	G/T	0.0475351	0.146656	intron-variant	RNF126	GRCh38.p7	19:659907	tcactgggactacag[G/T]tgcctgccaccacgc	55658
rs10418071	snp	A/G	0.0887219	0.191022	intron-variant	RNF126	GRCh38.p7	19:648823	aaaatacaagtatga[A/G]ccaggcgtggcggcg	55658
rs10426061	snp	A/G	0.11968	0.213514	intron-variant	RNF126	GRCh38.p7	19:651343	CGTTTGACGACACGC[A/G]TGTGGACAGCAGTCT	55658
rs10601849	in-del	-/CT	0.157311	0.232183	intron-variant	RNF126	GRCh38.p7	19:660488	GCAGCAGTGCCGCCC[-/CT]GACTCAGCCGCCGGG	55658
rs11292816	in-del	-/A	0.28578	0.247426	intron-variant	RNF126	GRCh38.p7	19:655656	AAGTCCCCCAGATGG[-/A]ACTACCCCATGACCC	55658
rs11554788	snp	C/T	0.467539	0.123193	synonymous-codon	RNF126	GRCh38.p7	19:652238	CAGAGCCGGCCACCG[C/T]TGGAGGTGAGTCGCC	55658
rs11554790	snp	A/G/T	1.90984e-05	0.00309012	missense	RNF126	GRCh38.p7	19:651735	GCTGACGACGGCAGG[A/G/T]ACCCTGAGAGCCGGC	55658
rs12973146	snp	C/G	0.442385	0.15965	intron-variant	RNF126	GRCh38.p7	19:652739	CGGCCCCACACTCGG[C/G]GGGGCGGACGCCAGC	55658
rs12974698	snp	A/T			intron-variant	RNF126	GRCh38.p7	19:649829	ACTCACCAGGGGCCC[A/T]GGCTGGGGATGGGGA	55658
rs12976320	snp	C/G	0.486	0.0824865	intron-variant	RNF126	GRCh38.p7	19:649239	GGGGGGGGCCGCGCT[C/G]CTGAGTGCCCTGACG	55658
rs12981407	snp	C/G	0.317451	0.240729	intron-variant	RNF126	GRCh38.p7	19:653624	TGGATGGCTGGGCCC[C/G]TGGTGATGGCGGAGC	55658
rs12982248	snp	A/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:649856	GGGACAGGCACCCCC[A/T]CCTACTCACCAGGGA	55658
rs12982249	snp	C/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:649859	ACAGGCACCCCCTCC[C/T]ACTCACCAGGGACCC	55658
rs12984279	snp	A/G			intron-variant	RNF126	GRCh38.p7	19:649825	CCCCACTCACCAGGG[A/G]CCCAGGCTGGGGATG	55658
rs17604088	snp	A/G	0.209693	0.246729	upstream-variant-2KB	RNF126	GRCh38.p7	19:665186	GGTTCAAACGACGCC[A/G]AACCACGAACTGGCT	55658
rs28418740	snp	C/T	0.0603597	0.1629	intron-variant	RNF126	GRCh38.p7	19:656990	AGGGGTAGCTCAGGG[C/T]TCAGGCTCTCCCTGC	55658
rs34088660	in-del	-/TT			intron-variant	RNF126	GRCh38.p7	19:655021	GCACCTGGCCTGGGC[-/TT]TTTTTTCTTTCTTTC	55658
rs34210228	in-del	-/C			intron-variant	RNF126	GRCh38.p7	19:659507	CCTTGCCCCTGACCT[-/C]CCCCGTCTCTGGGTG	55658
rs34323762	snp	A/G	0.304937	0.243889	intron-variant	RNF126	GRCh38.p7	19:658420	GCACAGCTTCCCGAG[A/G]GCCCTGCCACCCACA	55658
rs34495183	in-del	-/A			intron-variant	RNF126	GRCh38.p7	19:650609	GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	55658
rs34538684	snp	A/G	0.296873	0.245566	intron-variant	RNF126	GRCh38.p7	19:653468	GCTGGGGAACTGTGA[A/G]CGTGGTTTTGGGACT	55658
rs34540044	in-del	-/A			downstream-variant-500B	RNF126	GRCh38.p7	19:647387	CCAGGGCCGGCTAGC[-/A]AAAACTGCTCTCCCG	55658
rs34930504	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:659702	CAGAGTGGGGCGTGT[-/G]GCGGCAGGAACCAGA	55658
rs35085693	snp	A/G	0.285519	0.247464	intron-variant	RNF126	GRCh38.p7	19:655434	CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC	55658
rs35233618	snp	A/G	0.362732	0.22314	intron-variant	RNF126	GRCh38.p7	19:654224	CCTCACGGTGGGTTC[A/G]TGTGCATCTGGCATC	55658
rs35641190	in-del	-/A			intron-variant	RNF126	GRCh38.p7	19:659782	AGCAAGACTCCTTCC[-/A]AAAAAAAAAAAAAAA	55658
rs35688047	in-del	-/G			intron-variant	RNF126	GRCh38.p7	19:657581	CCTTTGAACCCCCTA[-/G]GGTGGGCGTTCCAGC	55658
rs35831797	snp	G/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:659830	GTTGCAGTGAGCCGA[G/T]ATTGTGCCACTGCAG	55658
rs35891903	snp	A/C	0.0644444	0.167538	synonymous-codon	RNF126	GRCh38.p7	19:648943	AAACACAGGCCCCCC[A/C]CCGGCAGATAAAGAG	55658
rs35953948	in-del	-/C			intron-variant	RNF126	GRCh38.p7	19:651530	AATCCAGCACGGGTT[-/C]CCACGGAAACGTGGC	55658
rs55925830	snp	A/G	0.0792508	0.182605	intron-variant	RNF126	GRCh38.p7	19:649148	CCACGCGGCCCCCCC[A/G]CTCCTGGGTCCCCTG	55658
rs56044504	snp	C/G	0.0637235	0.166737	intron-variant	RNF126	GRCh38.p7	19:661726	AACTGCACTGCTTCT[C/G]GGGGGCTTGGACTTC	55658
rs56141012	in-del	-/AAAAAAAAAAA			intron-variant	RNF126	GRCh38.p7	19:654669	AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]GTGCTGGCCGGGCGC	55658
rs56334730	in-del	-/GA	0.37778	0.214877	upstream-variant-2KB	RNF126	GRCh38.p7	19:664592	ATGAGGCATTGGAGC[-/GA]GACTGTTGAGGAATT	55658
rs56376239	snp	A/G	0.0733688	0.176922	downstream-variant-500B	RNF126	GRCh38.p7	19:647455	AGGACCGGACTCTGC[A/G]GAGCCCGACCAGCCT	55658
rs57115154	snp	A/G	0.108755	0.206276	upstream-variant-2KB	RNF126	GRCh38.p7	19:664210	CCACCACACCGGCTA[A/G]TTTTTGTATTTTTAG	55658
rs57869478	in-del	-/G	0.498016	0.0314335	intron-variant	RNF126	GRCh38.p7	19:658368	GACTGACAGTGACCA[-/G]GGGCAGGCAGGCCCC	55658
rs59145335	snp	A/G	0.0372196	0.131242	intron-variant	RNF126	GRCh38.p7	19:649268	CGGCGGAATGGGGGG[A/G]CCGTGCTCCGGCTGG	55658
rs59297411	snp	A/G	0.125528	0.21681	intron-variant	RNF126	GRCh38.p7	19:657397	GCACTGCCGGCTCAC[A/G]ACAGCCCGACCTGGC	55658
rs60101917	snp	A/G	0.367297	0.220775	intron-variant	RNF126	GRCh38.p7	19:658272	GCCCCTTCATCCACG[A/G]GGCCTGCACGGGGCG	55658
rs60873291	snp	A/G	0.084728	0.187577	intron-variant	RNF126	GRCh38.p7	19:652544	GTGGGTAGGGCCCCC[A/G]TGGCCCCTTCCCCGG	55658
rs61754469	snp	C/T	0.0390187	0.134115	missense, intron-variant	RNF126	GRCh38.p7	19:651684	CGCGGGGCTGTCGGG[C/T]GCCGTACCGGTGCCG	55658
rs62134273	snp	C/T	0.0162398	0.0886349	downstream-variant-500B	RNF126	GRCh38.p7	19:647445	CCCTGGAGACAGGAC[C/T]GGACTCTGCAGAGCC	55658
rs62134274	snp	C/T			intron-variant	RNF126	GRCh38.p7	19:655636	CAGGCCTGCTGGGAG[C/T]CCAGAAGTCCCCCAG	55658
rs62134275	snp	C/G	0.5	0	intron-variant	RNF126	GRCh38.p7	19:656089	GGGTTCTTTTTGCAG[C/G]TGTGAGAATGCTGTG	55658
rs62134276	snp	A/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:660641	CCCAGCATAAAAAAT[A/T]CGTTTTTGAGACAGC	55658
rs67039359	in-del	-/GG	0	0	intron-variant	RNF126	GRCh38.p7	19:649221	GAATGGGGGGGGGGG[-/GG]CCGCGCTGCTGAGTG	55658
rs71335262	snp	C/T	0.5	0	intron-variant	RNF126	GRCh38.p7	19:654476	GGTGAAACTCTGTCT[C/T]TACTAAAAATACAAA	55658
rs71335263	snp	C/G	0.5	0	intron-variant	RNF126	GRCh38.p7	19:657272	TGGCACAGCGCTCGG[C/G]CGCTCTGGTCCCCAT	55658
rs72974187	snp	C/T	0.0554543	0.157009	intron-variant	RNF126	GRCh38.p7	19:652888	ACAGATATAATCCTG[C/T]AGGAGAGAACAGGAG	55658
rs72974191	snp	A/G	0.0581099	0.160244	intron-variant	RNF126	GRCh38.p7	19:653805	CTCAAGTGCTCCATC[A/G]CAGCAACGTGAAAAT	55658
rs72974194	snp	A/C	0.00119737	0.0244387	intron-variant	RNF126	GRCh38.p7	19:655798	ATCATCGTCGTCGGC[A/C]GATGCAAACAGCTCC	55658
rs72974200	snp	A/G	0.0663309	0.169604	intron-variant	RNF126	GRCh38.p7	19:662140	CCTGGGCAACACAGG[A/G]AGACCCCATTCCTAA	55658

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