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
rs12448	snp	A/G	0.324382	0.238678	utr-variant-3-prime	RNF141	GRCh38.p7	11:10512405	AGCTCCAAGACACTT[A/G]CTGATCTACTGTGAA	50862
rs1043778	snp	A/G	0	0	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513267	AAATCAATTTCAAGG[A/G]AAAACATCTGGCCAG	50862
rs1047730	snp	A/G	0.367913	0.220446	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514751	AAAAATAAACTTCCC[A/G]TGTCTTCCATTTGTG	50862
rs1065052	snp	C/T	0.48196	0.0932449	synonymous-codon	RNF141	GRCh38.p7	11:10534042	TTATGAAGAATTTCT[C/T]GGGAGAGTAGCTGAG	50862
rs1074375	snp	A/G	0.497803	0.033074	intron-variant	RNF141	GRCh38.p7	11:10517312	GAGATAGCAATAGTA[A/G]CTATCCAGGATGAAA	50862
rs1074376	snp	C/G	0.0263992	0.111815	intron-variant	RNF141	GRCh38.p7	11:10517332	CCAGGATGAAACCCA[C/G]AGAAAGACTCAAAAA	50862
rs1074377	snp	A/G	0.493154	0.0581045	intron-variant	RNF141	GRCh38.p7	11:10517727	CATACTGAAAGAAAA[A/G]ATACTCTCAAGTCTA	50862
rs1350991	snp	C/T	0.378174	0.214642	intron-variant	RNF141	GRCh38.p7	11:10533083	TAAGAGGTGACTCCA[C/T]AGGTTCTAATTATAC	50862
rs1462940	snp	G/T	0.16846	0.236329	upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541389	AGTCTCGCCTGTCAC[G/T]CTCCCGGAGCAGGGG	50862
rs1462941	snp	G/T	0.317933	0.240593	upstream-variant-2KB, splice-donor-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541543	CAGTTGGGCTCCAAG[G/T]TACCACTTCCCAGAC	50862
rs1462942	snp	C/G	0.0126979	0.078662	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541578	AGCCTCCCCACTGAT[C/G]ATAGATACACAAAGG	50862
rs1531479	snp	C/T	0.465788	0.126237	intron-variant	RNF141	GRCh38.p7	11:10535383	CAAAAAACAACAGTT[C/T]TGAATCTGAGCCTAC	50862
rs1841811	snp	A/G	0.416218	0.186739	intron-variant	RNF141	GRCh38.p7	11:10524333	CTGCCTCCCGGGTTC[A/G]CGCCATTCTCCTGCC	50862
rs1979367	snp	A/T	0.130351	0.219509	upstream-variant-2KB, nc-transcript-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541509	ACCAAGGCCGCACTG[A/T]GAGCCCTGGTTTGGT	50862
rs1993817	snp	C/T	0.497722	0.0336691	intron-variant	RNF141	GRCh38.p7	11:10518592	AATACATGTAGTTTA[C/T]TGTATGTATTTTATA	50862
rs1993818	snp	A/C	0.497695	0.0338674	intron-variant	RNF141	GRCh38.p7	11:10518784	TTTGATTTTAGACTT[A/C]AGTCAGGCACAAATT	50862
rs1993819	snp	A/G	0.497359	0.0362457	intron-variant	RNF141	GRCh38.p7	11:10518796	CTTAAGTCAGGCACA[A/G]ATTTTCATACAGCAA	50862
rs1993820	snp	A/G	0.00795532	0.062565	intron-variant	RNF141	GRCh38.p7	11:10535720	TTATAAGTTCTTTTT[A/G]AGATTTTTGTTAAGT	50862
rs2054390	snp	C/T	0.367708	0.220556	intron-variant	RNF141	GRCh38.p7	11:10528704	ATAAACAAGGAAAGC[C/T]TCAACCTATCCCAGT	50862
rs2054391	snp	A/C	0.370365	0.219117	intron-variant	RNF141	GRCh38.p7	11:10535961	ATTCAACAAGTAGCA[A/C]gtgcctggtgcttat	50862
rs2054392	snp	C/G	0.473081	0.112848	intron-variant	RNF141	GRCh38.p7	11:10537052	AGTTTGTTTAAATAT[C/G]TGAGGAGCTGTCATG	50862
rs3074399	in-del	-/CA			intron-variant	RNF141	GRCh38.p7	11:10534501	acacacacacacaca[-/CA]CGCATTCAAGTAATT	50862
rs3075189	in-del	-/AA			upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542808	AAAAAAAAAAAAAAA[-/AA]GCAGCAAATTTGGGA	50862
rs3177103	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513278	AAATAAAATTCAAAT[C/T]AATTTCAAGGAAAAA	50862
rs3781862	snp	A/G	0.399611	0.200291	intron-variant	RNF141	GRCh38.p7	11:10538802	ATTAATTTAATGACA[A/G]ATTTTCACAGTTTTA	50862
rs3781863	snp	C/T	0.477515	0.103619	intron-variant	RNF141	GRCh38.p7	11:10538561	CTCACTAGAGGGAAA[C/T]GGCCAAGTGACTTAA	50862
rs3943326	snp	A/G	0.0023933	0.0345097	intron-variant	RNF141	GRCh38.p7	11:10517968	tatgaaatacttggg[A/G]atagatgtcaaagat	50862
rs4146830	snp	C/T	0.406986	0.194565	utr-variant-3-prime	RNF141	GRCh38.p7	11:10514569	GAGTATTCTGGAATC[C/T]TTTTACTTAGATATA	50862
rs4243915	snp	A/G	0.422473	0.180978	intron-variant	RNF141	GRCh38.p7	11:10523857	CCACTATTCTGGAGA[A/G]AAGAAAAGCAGAAAA	50862
rs4909936	snp	A/C	0	0	intron-variant	RNF141	GRCh38.p7	11:10518164	gtaaaatggcacaag[A/C]ctgctttggaaaata	50862
rs4909937	snp	C/T	0.0142736	0.0832652	intron-variant	RNF141	GRCh38.p7	11:10518339	gataaatatggaaaa[C/T]aatctaatttccctc	50862
rs4909938	snp	C/T	0.367091	0.220884	intron-variant	RNF141	GRCh38.p7	11:10520066	gggctgcatgcagcc[C/T]gtgggccgtgagttg	50862
rs4909939	snp	C/T	0.0154538	0.0865337	intron-variant	RNF141	GRCh38.p7	11:10520428	acagcgtcaggatca[C/T]caccatcactgtctt	50862
rs4909940	snp	C/T	0.365232	0.22186	intron-variant	RNF141	GRCh38.p7	11:10521749	TTCTAGGTGCATAAA[C/T]AAAGTTGTAGAGGTA	50862
rs4909941	snp	C/T	0.35445	0.227135	intron-variant	RNF141	GRCh38.p7	11:10536978	ACATATTCATGGGCA[C/T]AGAAAAAAAAAGAGG	50862
rs4909942	snp	G/T	0.327914	0.237549	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10540593	GCCTAAGCCAATTCA[G/T]AAGTGTGGGGCTGGC	50862
rs4910149	snp	A/C	0.367913	0.220446	downstream-variant-500B	RNF141	GRCh38.p7	11:10511509	GGGTGAATAGACATA[A/C]GAACAAATGAGTCTG	50862
rs4910150	snp	C/T	0.367913	0.220446	downstream-variant-500B	RNF141	GRCh38.p7	11:10511626	TAGTTTTCTTATTCC[C/T]GGATAGACTAAGCTT	50862
rs4910151	snp	A/G	0.365439	0.221752	intron-variant	RNF141	GRCh38.p7	11:10524272	TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC	50862
rs4910152	snp	C/G	0.416055	0.186885	intron-variant	RNF141	GRCh38.p7	11:10530475	AGCAATTAGACAACT[C/G]TAAGATTCAAACAGC	50862
rs4910153	snp	C/T	0.499908	0.00678851	intron-variant	RNF141	GRCh38.p7	11:10531808	ATAAAATGAGGCCAT[C/T]GAAAGTTAAGCAACT	50862
rs4910154	snp	C/T	0.378174	0.214642	intron-variant	RNF141	GRCh38.p7	11:10532125	TGCTAAAGGGCAAAA[C/T]TTCATACAATAGACA	50862
rs4910155	snp	C/T	0.00795532	0.062565	intron-variant	RNF141	GRCh38.p7	11:10532128	TAAAGGGCAAAACTT[C/T]ATACAATAGACAGGG	50862
rs6484344	snp	C/T	0.498459	0.0277128	intron-variant	RNF141	GRCh38.p7	11:10515177	AATAGCATAGAAATA[C/T]ATAGTGAAAAATAAA	50862
rs7112744	snp	A/T	0.181022	0.240296	intron-variant	RNF141	GRCh38.p7	11:10536324	TTGAGGTAATTTTTA[A/T]AAAGGCCACAAGGAC	50862
rs7115413	snp	A/G	0.00953873	0.0683987	intron-variant	RNF141	GRCh38.p7	11:10515388	gcacctgttagagct[A/G]tttattctttttaac	50862
rs7123581	snp	A/C	0.365853	0.221536	intron-variant	RNF141	GRCh38.p7	11:10522377	CCAGTGGAACCAGTA[A/C]AAAGTTCTCTTAACT	50862
rs7126551	snp	G/T	0.370772	0.218893	intron-variant	RNF141	GRCh38.p7	11:10536336	TTAAAAAGGCCACAA[G/T]GACTAAAGCAGAGAG	50862
rs7128848	snp	A/G	0.358515	0.225221	intron-variant	RNF141	GRCh38.p7	11:10538236	TCACTAACTCCTTGC[A/G]TTAAAATGCAACAGT	50862
rs7129207	snp	A/C	0.304937	0.243889	intron-variant	RNF141	GRCh38.p7	11:10532537	CACACACACACACAC[A/C]CCCCACAACTATATA	50862
rs7131507	snp	A/T	0.239037	0.24976	intron-variant	RNF141	GRCh38.p7	11:10537801	CTAGGAAGATAAGGG[A/T]TACTTTAAGAAGGCT	50862
rs7929890	snp	A/G	0.375	0.216506	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513802	CTGCCTCAGCCTCCC[A/G]AGTAGCTGAGATTAC	50862
rs7934688	snp	A/C	0.123452	0.215605	intron-variant	RNF141	GRCh38.p7	11:10528863	tgccctcaggagctt[A/C]ctctctaaaggggag	50862
rs7936626	snp	C/T	0.367297	0.220775	intron-variant	RNF141	GRCh38.p7	11:10533337	TTAACAAATAGAAGA[C/T]TAAGTTGTATTAGGT	50862
rs7938430	snp	A/G	0.000399281	0.0141238	intron-variant	RNF141	GRCh38.p7	11:10536878	GCAGCCTACTAGTCC[A/G]TTATGCTTTGCAATG	50862
rs7938782	snp	A/G	0.354235	0.227234	intron-variant	RNF141	GRCh38.p7	11:10537230	AGTATGGAAGTGTTT[A/G]GGTAAAGATTAGAAG	50862
rs7949992	snp	A/G	0.130351	0.219509	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541723	TAGATATGATGATGA[A/G]CACATGTTAGTGATA	50862
rs7950829	snp	C/G	0.130351	0.219509	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10541726	ATATGATGATGAGCA[C/G]ATGTTAGTGATATTA	50862
rs7951653	snp	A/T	0.498503	0.0273153	intron-variant	RNF141	GRCh38.p7	11:10520154	atgaacactgtacat[A/T]taggctatacgaaat	50862
rs9300104	snp	C/T	0.416055	0.186885	intron-variant	RNF141	GRCh38.p7	11:10529559	TAGTTTGGAGTCATA[C/T]TGTAGGAGTTGGGAC	50862
rs9665807	snp	C/T			intron-variant	RNF141	GRCh38.p7	11:10537533	ggagatagaatttct[C/T]tccctctgctctctg	50862
rs10458930	snp	C/G	0.416708	0.186302	intron-variant	RNF141	GRCh38.p7	11:10527921	tcacttacagattgt[C/G]aggtgtgagagacaa	50862
rs10458931	snp	A/G	0.416708	0.186302	intron-variant	RNF141	GRCh38.p7	11:10527926	tacagattgtcaggt[A/G]tgagagacaaagaaa	50862
rs10500725	snp	A/G	0.421051	0.182323	intron-variant	RNF141	GRCh38.p7	11:10516174	TCTAGTTCTTCAGAG[A/G]TATTTTACAAGATAA	50862
rs10500726	snp	A/T	0.496937	0.0390173	intron-variant	RNF141	GRCh38.p7	11:10528900	ACCTAAACAACTTTT[A/T]TCGTAATGCAGTATT	50862
rs10500727	snp	C/T	0.18134	0.240387	intron-variant	RNF141	GRCh38.p7	11:10531777	AGTGGGGATATCACA[C/T]TCAACTAACAGCTAA	50862
rs10524171	in-del	-/T/TATATATATATAT/TATATATATATATATATATAT	0.5	0	intron-variant, upstream-variant-2KB	RNF141, MRVI1-AS1	GRCh38.p7	11:10539701	TATATATATATATTA[lengthTooLong]GAGAGAGAAGGAGAG	50862
rs10559393	in-del	-/CA			intron-variant	RNF141	GRCh38.p7	11:10532498	TTTCTACACACACAC[-/CA]ACACACACACACACA	50862
rs10602390	in-del	-/TGAA	0.357664	0.225629	intron-variant	RNF141	GRCh38.p7	11:10518467	CCAAGGTAATTAGAC[-/TGAA]TGAAAGAAGCCAGAC	50862
rs10664382	in-del	-/A/AA/AAA	0.625	0.125	intron-variant	RNF141	GRCh38.p7	11:10531388	CAAAAAAAAAAAAAA[-/A/AA/AAA]GGTTAGCTAGTGTCA	50862
rs10743143	snp	C/T	0.0134861	0.0810011	intron-variant	RNF141	GRCh38.p7	11:10523305	TAGGTTAGAGCACAG[C/T]TGTACTGCCAGACAG	50862
rs10770123	snp	C/T	0.498568	0.0267188	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513319	TAAAATCCTACTATC[C/T]AGAAATTCTGTCATC	50862
rs10770124	snp	A/G	0.354665	0.227036	intron-variant	RNF141	GRCh38.p7	11:10538943	AATTCAACAAAAGAT[A/G]AATTTCTGGTCAAGA	50862
rs10840432	snp	A/G	0.323197	0.239044	intron-variant	RNF141	GRCh38.p7	11:10524166	atgcctgtaatccca[A/G]cactctgggaggccg	50862
rs10840433	snp	C/G	0.416218	0.186739	intron-variant	RNF141	GRCh38.p7	11:10525627	TTAATTAGGCATTAT[C/G]CTGTTGATGGGTAAG	50862
rs10840434	snp	A/T	0.416382	0.186593	intron-variant	RNF141	GRCh38.p7	11:10534894	TTAAAAATATATAAA[A/T]AGACTTGTGGCTTGA	50862
rs10840435	snp	C/G	0.482083	0.0929373	intron-variant	RNF141	GRCh38.p7	11:10536299	TGAGACAGGAAGCAG[C/G]ACGGTGACTTTGAGG	50862
rs10840436	snp	C/T	0.498568	0.0267188	intron-variant	RNF141	GRCh38.p7	11:10536403	TGTTTAACATTTTTG[C/T]TGATGACCTGAAGAC	50862
rs10840437	snp	C/T	0.355954	0.226437	intron-variant	RNF141	GRCh38.p7	11:10538348	GAAAACCATAAAATA[C/T]TGATAAATATTAACA	50862
rs11042866	snp	C/G	0.312593	0.242037	downstream-variant-500B	RNF141	GRCh38.p7	11:10511606	TAACTTCCCTCATCT[C/G]CAAGTAGTTTTCTTA	50862
rs11042867	snp	A/G	0	0	utr-variant-3-prime	RNF141	GRCh38.p7	11:10512934	ACTTTTATATAGTGG[A/G]GTATAGGGTATGTGT	50862
rs11042868	snp	A/C	0.305436	0.243776	intron-variant	RNF141	GRCh38.p7	11:10516781	CTCTAAAGGGTCTTG[A/C]TATTAGTGGGACATA	50862
rs11042869	snp	G/T	0	0	intron-variant	RNF141	GRCh38.p7	11:10518227	ATACCATATGATCTA[G/T]CCATTCCATGTCTAG	50862
rs11042870	snp	C/T	0	0	intron-variant	RNF141	GRCh38.p7	11:10525103	AAAAGATTTAAGATG[C/T]TACAATGAGCAACAG	50862
rs11042871	snp	A/G	0.416055	0.186885	intron-variant	RNF141	GRCh38.p7	11:10531204	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	50862
rs11042872	snp	C/T	0.415235	0.18761	intron-variant	RNF141	GRCh38.p7	11:10531243	AGCCGGGCGTGGTGG[C/T]GTACACCTGTAATCC	50862
rs11042873	snp	A/C			intron-variant	RNF141	GRCh38.p7	11:10535616	GCTGAATTTCAAAGA[A/C]TAGTAAAATCTCAAA	50862
rs11300664	in-del	-/T	0.499053	0.0217445	utr-variant-3-prime	RNF141	GRCh38.p7	11:10513688	CTCTATTTTCTTGTG[-/T]TTTTTTTTTGATTAG	50862
rs11397587	in-del	-/A/AT			intron-variant	RNF141	GRCh38.p7	11:10533540	ACACAGTAAAAAAAA[-/A/AT]GTATATATATATATG	50862
rs11553579	snp	A/G	0.0205511	0.0992634	utr-variant-3-prime	RNF141	GRCh38.p7	11:10512250	CATTTCATCCATTAA[A/G]CAAATTTACAACTTT	50862
rs11602469	snp	C/T	0.24019	0.249807	intron-variant	RNF141	GRCh38.p7	11:10517269	taatggcaagttaga[C/T]attgaagaaaaatgg	50862
rs11604691	snp	C/T	0.242488	0.249887	intron-variant	RNF141	GRCh38.p7	11:10526501	CAAGAATGAGTCATG[C/T]GGCCAGGCACGGTGG	50862
rs11607008	snp	C/G	0.36606	0.221428	intron-variant	RNF141	GRCh38.p7	11:10517559	aaaaactactctaag[C/G]cacatcataatcaaa	50862
rs12099382	snp	A/T	0.0832709	0.186283	downstream-variant-500B	RNF141	GRCh38.p7	11:10511375	ctaactaatgcctga[A/T]gatctgaggtggaaa	50862
rs12225339	snp	C/G	0	0	intron-variant	RNF141	GRCh38.p7	11:10516489	tgagctgaacacaca[C/G]agctgagaatcttgg	50862
rs12225816	snp	A/G	0	0	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542119	gcaatcctgtgagta[A/G]gtattattaatacct	50862
rs12275930	snp	C/T	0.365232	0.22186	intron-variant	RNF141	GRCh38.p7	11:10531155	GCCAAGGCAGGCAGA[C/T]CACGAGGTCAGGAGT	50862
rs12277871	snp	C/G	0.497473	0.0354532	intron-variant	RNF141	GRCh38.p7	11:10534714	GGTGATTTATCTAAA[C/G]TTACACAGCTGTAAG	50862
rs12278433	snp	C/T	0.2776	0.248472	upstream-variant-2KB, intron-variant	RNF141, MRVI1-AS1	GRCh38.p7	11:10542276	actgCCTCGGTAGTA[C/T]GGTAAGACTTCATTA	50862
rs12279850	snp	C/T	0.497695	0.0338674	intron-variant	RNF141	GRCh38.p7	11:10518383	ACAAGCTATGGTATC[C/T]ACATAACAGACATTA	50862

Full records

It may take some time, please wait.