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
rs901954	snp	A/T	0.494896	0.0502606	intron-variant	NSMAF	GRCh38.p7	8:58613180	ttaaaaatactaaaa[A/T]atatttttaatactt	8439
rs931396	snp	A/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58587448	TTAGGTTTCCAAGTC[A/T]ACTTTGTTTTGTTTT	8439
rs973807	snp	C/T	0.499713	0.0119774	intron-variant	NSMAF	GRCh38.p7	8:58658728	TGTCACCAAAAATGC[C/T]CTGGGAACTATACAT	8439
rs1050488	snp	C/T	0.393987	0.204372	utr-variant-3-prime	NSMAF	GRCh38.p7	8:58583931	AAAGCCATTAGTTGC[C/T]ATTCTCTTAGGGCAG	8439
rs1050504	snp	A/G	0.3744	0.216852	utr-variant-3-prime	NSMAF	GRCh38.p7	8:58583857	CAGATGATCGTCCCC[A/G]TATGATGATTGTCAG	8439
rs1352496	snp	C/G	0.368119	0.220336	intron-variant	NSMAF	GRCh38.p7	8:58636433	GTACCCGTGTACTAC[C/G]TCTGAAAGTATTCTT	8439
rs1387222	snp	A/T	0.435407	0.167703	intron-variant	NSMAF	GRCh38.p7	8:58643172	TGTTTGTTAAATTCA[A/T]GAATGGAAAAGCTTT	8439
rs2054900	snp	A/G	0.147991	0.228242	intron-variant	NSMAF	GRCh38.p7	8:58601976	TTCCCCTAAGCCTTG[A/G]AGAAACGAATTTCCT	8439
rs2130072	snp	C/T	0.372592	0.217879	intron-variant	NSMAF	GRCh38.p7	8:58614140	tcacaacatatgagg[C/T]gggaaattaaagaaa	8439
rs2228505	snp	A/G/T	0.0621084	0.164914	missense	NSMAF	GRCh38.p7	8:58595575	AGTTACACGAGCACT[A/G/T]TAAAATCCACAAAGA	8439
rs2228506	snp	A/G/T	0.000164786	0.00907584	synonymous-codon	NSMAF	GRCh38.p7	8:58597514	GGTAGCCATGCTTAC[A/G/T]CAAATCTTGGAATTT	8439
rs2229740	snp	A/G/T	0.00694917	0.0585432	synonymous-codon	NSMAF	GRCh38.p7	8:58589470	GCTATATTCTGCATC[A/G/T]TGGGACTCTACAGTG	8439
rs2242344	snp	G/T	0.486595	0.0807641	intron-variant	NSMAF	GRCh38.p7	8:58658989	GAATCAGGCCTTTCC[G/T]GCGGCCCCCCTCCCA	8439
rs2255834	snp	A/G	0.496783	0.0399767	intron-variant	NSMAF	GRCh38.p7	8:58603197	TGGTCAGAATTCCAC[A/G]TGTGGCAGTTACCTA	8439
rs2279459	snp	C/G	0.152001	0.229992	intron-variant	NSMAF	GRCh38.p7	8:58595874	AAGTATAAAAAGATT[C/G]TAGTATTATTCAAAG	8439
rs2279460	snp	A/G	0.491783	0.0635686	intron-variant	NSMAF	GRCh38.p7	8:58595816	TTTTCCTTGACTAAC[A/G]TGGAACCATCTAACA	8439
rs2279462	snp	G/T	0.491421	0.0649309	intron-variant	NSMAF	GRCh38.p7	8:58595391	ATCTCCACCTGAGGT[G/T]GATGTAGTAGGGAAA	8439
rs2326129	snp	C/T	0.499539	0.0151687	intron-variant	NSMAF	GRCh38.p7	8:58611978	TCTCTGCTCCCAGTT[C/T]GTGGCACAGAGCTCC	8439
rs2634488	snp	C/T	0.499999	0.000798721	intron-variant	NSMAF	GRCh38.p7	8:58598751	ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCCCTGG	8439
rs2634489	snp	C/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58598498	tcttttttttttttt[C/T]tttttttgtttgaga	8439
rs2634527	snp	A/G	0.483995	0.0880135	intron-variant	NSMAF	GRCh38.p7	8:58586830	CTTTAGCAATACTTC[A/G]TTTCTTCTTGTATTC	8439
rs2634529	snp	A/G	0.188946	0.24243	intron-variant	NSMAF	GRCh38.p7	8:58602953	TAATGATAACCCTGG[A/G]TTAAAATCATGCCCA	8439
rs2634530	snp	A/C	0.495135	0.0490805	intron-variant	NSMAF	GRCh38.p7	8:58603597	AAATTATTAAATACA[A/C]TGAGCTATTACACTA	8439
rs2634531	snp	C/T	0.497586	0.0346604	intron-variant	NSMAF	GRCh38.p7	8:58604499	AGCTTAATGTATGAA[C/T]AAAATACTAGCTATA	8439
rs2634532	snp	A/G	0.121717	0.214577	intron-variant	NSMAF	GRCh38.p7	8:58606960	AGCTCTATACCCAAA[A/G]GAGGAGATTTTTAAT	8439
rs2634533	snp	C/G	0.118933	0.212888	intron-variant	NSMAF	GRCh38.p7	8:58623063	AGGAGAACTCTCTAG[C/G]GCTTCCTCAACTCTT	8439
rs2634534	snp	C/T	0.494484	0.0522255	intron-variant	NSMAF	GRCh38.p7	8:58614479	AGGTTATAGGATAAG[C/T]CTGTGCCTAGGCAAA	8439
rs2680896	snp	A/G	0.16618	0.23553	intron-variant	NSMAF	GRCh38.p7	8:58603922	AAGAAGAAAACAGGC[A/G]TTTGGCAGGAGGACC	8439
rs2680897	snp	A/G	0.494143	0.0537956	intron-variant	NSMAF	GRCh38.p7	8:58607078	CAAATTAAAAGCACA[A/G]AAATAAGAATTAAAA	8439
rs2680898	snp	A/G	0.121717	0.214577	intron-variant	NSMAF	GRCh38.p7	8:58607232	AGTAAGACATGTGTC[A/G]GAAATAGGACCTAAG	8439
rs2680899	snp	C/T	0.494774	0.0508504	intron-variant	NSMAF	GRCh38.p7	8:58609475	ATACACAGATGCTGC[C/T]TGTGAAGGGGGTGGG	8439
rs2680900	snp	A/G	0.122064	0.214785	intron-variant	NSMAF	GRCh38.p7	8:58609976	AGCCATGACAGACAA[A/G]TAAATAATACCAAAT	8439
rs2680901	snp	C/T	0.49533	0.0480965	intron-variant	NSMAF	GRCh38.p7	8:58610885	CTGTGGAAGAGAAAG[C/T]CTTTATCACTCCCTC	8439
rs2680903	snp	C/T	0.128684	0.218592	synonymous-codon	NSMAF	GRCh38.p7	8:58599775	ACAGATGGTTGACGA[C/T]GTGGAGCTTCCCCCT	8439
rs2680904	snp	C/T	0.162253	0.234095	intron-variant	NSMAF	GRCh38.p7	8:58598687	CTTTTGCCCAAATAA[C/T]ACCAAATTCATCCTG	8439
rs2946577	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58600619	agagcaagactttgt[C/T]tcaaaaaaaaaaaaa	8439
rs2946578	snp	C/T	0.493837	0.055168	intron-variant	NSMAF	GRCh38.p7	8:58602515	GTGAATATTATTATT[C/T]TTCAATATTAGCCTA	8439
rs2969915	snp	A/T	0.147991	0.228242	intron-variant	NSMAF	GRCh38.p7	8:58602569	CTAGAAATATGATAA[A/T]GTATTTCTCTGAAAA	8439
rs2969916	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58600615	tttttttttgagaca[A/G]agtcttgctctgtcg	8439
rs3736236	snp	C/T	0.046008	0.144524	intron-variant	NSMAF	GRCh38.p7	8:58589976	CCCTGCTCTGTGATT[C/T]GACGTGCAGAATAGC	8439
rs3739327	snp	A/G	0.498034	0.0312882	downstream-variant-500B	NSMAF	GRCh38.p7	8:58583493	AGTTACTTAAATAAA[A/G]TGAAAACAGCTTTCT	8439
rs3816846	snp	C/T	0.381891	0.212379	intron-variant	NSMAF	GRCh38.p7	8:58586678	GACTACATATTTGAA[C/T]CAGACTAGAGAAACA	8439
rs3816847	snp	A/G	0.186737	0.241863	intron-variant	NSMAF	GRCh38.p7	8:58603551	AGTATTTGTTCAGCT[A/G]TGTATAAACAGTTCC	8439
rs3837194	in-del	-/T	0.498392	0.028309	downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583149	AATATTTAATAACAC[-/T]TGAAACTGACTTTGG	8439
rs4266636	snp	A/G	0.419936	0.183362	intron-variant	NSMAF	GRCh38.p7	8:58619986	AAGGTATAATAATTA[A/G]CTTAGTGGTACCAGA	8439
rs4421339	snp	A/G	0.0901694	0.192235	intron-variant	NSMAF	GRCh38.p7	8:58630098	CAATCATGTGGTGCT[A/G]TGTGGGACAGAGGAT	8439
rs4598239	snp	G/T	0.411746	0.190626	intron-variant	NSMAF	GRCh38.p7	8:58620148	AAACCATTAGAACAG[G/T]AGAAGTGTACTCTCT	8439
rs4737504	snp	A/G	0.493969	0.05458	intron-variant	NSMAF	GRCh38.p7	8:58628020	ccaaaatagcatggg[A/G]ctagtataacaacag	8439
rs4737505	snp	A/G	0.214843	0.247516	intron-variant	NSMAF	GRCh38.p7	8:58644964	CGGGGACCTGTTGGC[A/G]GGGTGGGGAGCTAGA	8439
rs4738695	snp	C/G	0.183886	0.241099	intron-variant	NSMAF	GRCh38.p7	8:58609412	AACAGATCAGAAGAA[C/G]TCAAACTTCAGAGAC	8439
rs4738696	snp	C/T	0.305436	0.243776	intron-variant	NSMAF	GRCh38.p7	8:58611577	GTTTCAGCAGAGAAA[C/T]AGAAACTATGAAAAA	8439
rs4738697	snp	C/T	0.0349115	0.127424	intron-variant	NSMAF	GRCh38.p7	8:58620467	CCATGTTAAGGTGTT[C/T]AGGCTTTATCCTGAA	8439
rs4738699	snp	C/T	0.490287	0.0690083	intron-variant	NSMAF	GRCh38.p7	8:58654830	ATCTAAATTTCTTTT[C/T]TATTATGTATTTATT	8439
rs5891688	in-del	-/TGAT	0.383053	0.211653	downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583103	ACTCATTGAGGCTAC[-/TGAT]TGATTGTCCCTAGCA	8439
rs5891689	in-del	-/ATTG			downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583109	TGAGGCTACTGATTG[-/ATTG]TCCCTAGCAATACCT	8439
rs5891691	in-del	-/A	0.365024	0.221967	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660100	GTGTCCTCCATTGTG[-/A]AAAAAAAAAAAAGAC	8439
rs6471732	snp	C/T	0.419296	0.183954	intron-variant	NSMAF	GRCh38.p7	8:58626583	attccatggtgtata[C/T]atataggactttttc	8439
rs6985007	snp	G/T	0.499954	0.00479211	intron-variant	NSMAF	GRCh38.p7	8:58649186	tcataggagattatt[G/T]tggagttttaagatt	8439
rs6985643	snp	A/G	0.499839	0.00898417	intron-variant	NSMAF	GRCh38.p7	8:58649528	atgtttgtcccctcc[A/G]aatctcatgttaata	8439
rs6991020	snp	A/G	0.497959	0.0318836	intron-variant	NSMAF	GRCh38.p7	8:58592819	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	8439
rs6991479	snp	C/T	0.305186	0.243833	intron-variant	NSMAF	GRCh38.p7	8:58610191	AATACATTTGAGTAA[C/T]TGTATATTCCTTTGT	8439
rs6991644	snp	A/G	0.307671	0.243257	intron-variant	NSMAF	GRCh38.p7	8:58610347	GAAAAAATAAGGGAA[A/G]ACAACCAAATCATCA	8439
rs6994461	snp	C/T	0.17332	0.23795	intron-variant	NSMAF	GRCh38.p7	8:58654609	AATATTATACACTCA[C/T]GGAATGTCTGAAACA	8439
rs6994565	snp	C/T	0.130351	0.219509	intron-variant	NSMAF	GRCh38.p7	8:58598854	atggtgaaaccgtca[C/T]gaccaaaaaaaatac	8439
rs6994622	snp	C/G/T	0.0209503	0.100241	intron-variant	NSMAF	GRCh38.p7	8:58656488	ataaaaatatcatat[C/G/T]cccagttacatttga	8439
rs6995115	snp	A/G	0.498369	0.0285077	intron-variant	NSMAF	GRCh38.p7	8:58586055	CAGAATGTGGTTTAC[A/G]TTATTCTGGATTTTA	8439
rs6998210	snp	C/T	0.418007	0.185132	intron-variant	NSMAF	GRCh38.p7	8:58625691	ccgaaaatgagtctc[C/T]tgcagatggcatata	8439
rs7001188	snp	C/T	0.111224	0.207945	intron-variant	NSMAF	GRCh38.p7	8:58645004	gcattaggagaaata[C/T]ctaatgtagatgatg	8439
rs7006797	snp	A/G	0.496999	0.0386216	intron-variant	NSMAF	GRCh38.p7	8:58588588	AAGCAAATAGGCATC[A/G]AAGATGCTCGCTTCA	8439
rs7006937	snp	C/G	0.414905	0.187899	intron-variant	NSMAF	GRCh38.p7	8:58618624	taacacacacacaca[C/G]aGAGCAACAATGTGA	8439
rs7008292	snp	C/T	0.130351	0.219509	intron-variant	NSMAF	GRCh38.p7	8:58597156	GCCAACTTTCACTCA[C/T]ATTCAATTGCCAGAA	8439
rs7011033	snp	C/T	0.0325976	0.123435	intron-variant	NSMAF	GRCh38.p7	8:58618909	TTTCATTTCATATGG[C/T]AAAAATCCCTTCCCC	8439
rs7011066	snp	C/G	0.412082	0.190341	intron-variant	NSMAF	GRCh38.p7	8:58618972	ATACATTAAAACGTT[C/G]ACAGTGAACTATTTT	8439
rs7014666	snp	C/G	0	0	intron-variant	NSMAF	GRCh38.p7	8:58632073	CCTGTACTTTCCTCA[C/G]TGCTTTTCCTCCTGC	8439
rs7015319	snp	A/G	0.26326	0.249648	intron-variant	NSMAF	GRCh38.p7	8:58594912	CATGACCTGTATGCC[A/G]GAGGGGCTGTCTGTC	8439
rs7015870	snp	G/T	0.0952156	0.196321	intron-variant	NSMAF	GRCh38.p7	8:58625386	tatgtctgtatatat[G/T]tatatgcatatgtat	8439
rs7465261	snp	C/T			upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660356	ggagggtgggggatt[C/T]ttgctaaactgccgt	8439
rs7816499	snp	C/T	0.305436	0.243776	intron-variant	NSMAF	GRCh38.p7	8:58612566	ctaaggaatgtgttg[C/T]gggaatctctgattt	8439
rs7820921	snp	A/C	0.493386	0.0571263	intron-variant	NSMAF	GRCh38.p7	8:58650097	AAGCACTTGGGTACC[A/C]TTTGCATCTTCACCC	8439
rs7825739	snp	C/T	0.418814	0.184396	intron-variant	NSMAF	GRCh38.p7	8:58606917	AAAGCACTTAATCAA[C/T]GTTAATTTCTTCTCT	8439
rs7826122	snp	A/G	0.499502	0.0157669	intron-variant	NSMAF	GRCh38.p7	8:58593570	CCCTTCCATCTCTGC[A/G]TCTTCCAGAGTGCCA	8439
rs7826603	snp	A/G	0.499527	0.0153681	intron-variant	NSMAF	GRCh38.p7	8:58593628	AAGACATACTTTAAT[A/G]AATAATATATAATGC	8439
rs7830228	snp	A/C	0.498611	0.0263212	intron-variant	NSMAF	GRCh38.p7	8:58657617	GATTCCAGTGCATAC[A/C]TGATGTGAGACAGAT	8439
rs7831185	snp	A/G	0.121717	0.214577	intron-variant	NSMAF	GRCh38.p7	8:58617494	acccatcaaaaagtg[A/G]gcaaaggatatgaac	8439
rs7833097	snp	A/G	0.110519	0.207473	intron-variant	NSMAF	GRCh38.p7	8:58635709	ATTAACTGGTAAAAC[A/G]AAACACAGAATAGTG	8439
rs7833791	snp	C/T	0.409382	0.192607	intron-variant	NSMAF	GRCh38.p7	8:58630142	cacaaatttttatac[C/T]ggctttgatgtggtt	8439
rs7836960	snp	C/T	0.493793	0.055364	intron-variant	NSMAF	GRCh38.p7	8:58634011	ATGAAAACCCTATCT[C/T]CAAGTCAAAAAGTAC	8439
rs7840932	snp	A/G	0.498369	0.0285077	intron-variant	NSMAF	GRCh38.p7	8:58589256	AGATATATTTTATAT[A/G]TATTTTTTAAACACA	8439
rs7841618	snp	C/T	0.305685	0.24372	intron-variant	NSMAF	GRCh38.p7	8:58610835	TAAAGCACAAAGATA[C/T]CTCTAGAATCCTTCA	8439
rs7844231	snp	G/T	0.49949	0.0159663	intron-variant	NSMAF	GRCh38.p7	8:58593473	ATGATAAAGACTAAA[G/T]AACGAGTAGCCTTAC	8439
rs10086028	snp	G/T	0.370974	0.218781	intron-variant	NSMAF	GRCh38.p7	8:58612325	actatgaggctggga[G/T]agcttctgggttgct	8439
rs10086130	snp	A/G	0.192088	0.2432	intron-variant	NSMAF	GRCh38.p7	8:58605399	CTCATAAACTAATAT[A/G]AGACCTGACTGAACA	8439
rs10086457	snp	C/G	0.293294	0.246223	intron-variant	NSMAF	GRCh38.p7	8:58605629	AAAGAGGCGATTCTA[C/G]AAATAGCATTTTTCT	8439
rs10087843	snp	C/T	0.413748	0.188909	intron-variant	NSMAF	GRCh38.p7	8:58621783	gcatgtatgtctttt[C/T]ttgaaaagtgtctgt	8439
rs10088312	snp	A/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58639015	aatgggtgggtgtgg[A/T]ggctcacgcctgtaa	8439
rs10088541	snp	A/G	0.411914	0.190483	intron-variant	NSMAF	GRCh38.p7	8:58618348	TAATATGAAGCTATA[A/G]GATGatattatgatt	8439
rs10090212	snp	A/G	0.43309	0.17023	intron-variant	NSMAF	GRCh38.p7	8:58643597	GAGTAAAATGGCGCA[A/G]TCTCAGCTCAAGTAA	8439
rs10090837	snp	G/T	0.417683	0.185425	intron-variant	NSMAF	GRCh38.p7	8:58621978	ctttagtttaattag[G/T]tctcatttgtcaatt	8439
rs10091952	snp	A/G	0.37138	0.218556	intron-variant	NSMAF	GRCh38.p7	8:58631854	GCAGACAGGGAAGGA[A/G]GCTAATCCAAGTGCT	8439
rs10093782	snp	A/G	0.191147	0.242974	intron-variant	NSMAF	GRCh38.p7	8:58607161	AAAAAATGAATTTCT[A/G]TTGGTGTCGAATTAA	8439

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