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
rs173355	snp	C/T	0.363985	0.222503	intron-variant	HCK	GRCh38.p7	20:32078334	acaggtgtgagccac[C/T]gcgcccagccGGGGG	3055
rs242598	snp	C/T	0.499984	0.00279548	intron-variant	HCK	GRCh38.p7	20:32076386	GGGGGCTCTTAGCTG[C/T]TTCTCTCTCCTTCTT	3055
rs242599	snp	A/G	0.306431	0.243548	intron-variant	HCK	GRCh38.p7	20:32076571	AAAACGCAGGGTGTA[A/G]ACAACATGAATGGGG	3055
rs242600	snp	A/G	0.405603	0.195673	intron-variant	HCK	GRCh38.p7	20:32077760	CGAACTCCTGAACTC[A/G]TGATCCTCCTGCCTT	3055
rs242601	snp	G/T	0.491834	0.0633738	intron-variant	HCK	GRCh38.p7	20:32078031	CAGTTGGTttttttt[G/T]tttgtttgtttgttt	3055
rs242602	snp	C/T	0.496034	0.0443518	intron-variant	HCK	GRCh38.p7	20:32079145	CCAAATATCTCAATA[C/T]TCAGGAAGAATGAAG	3055
rs242603	snp	C/T	0.499831	0.00918375	intron-variant	HCK	GRCh38.p7	20:32079256	ATTCAACTCCATATA[C/T]GCGGAGGAGGATTGG	3055
rs242604	snp	C/T	0.499839	0.00898417	intron-variant	HCK	GRCh38.p7	20:32080448	gcgatccacccctct[C/T]gccctcccaaagtgc	3055
rs242605	snp	C/G	0.318415	0.240457	intron-variant	HCK	GRCh38.p7	20:32080741	ggcctcgaacttctg[C/G]actcaagcaatctgc	3055
rs242606	snp	A/G	0.499913	0.00658888	intron-variant	HCK	GRCh38.p7	20:32080830	TTTTTTTAAATACCC[A/G]TAACAGACCAAGTAG	3055
rs242607	snp	C/T	0.36928	0.219709	intron-variant	HCK	GRCh38.p7	20:32084072	CAGGGGTGACATCCC[C/T]ACCACGATGGGCCCA	3055
rs242608	snp	C/T	0.392881	0.205147	intron-variant	HCK	GRCh38.p7	20:32085033	AACTTAAGAACAACA[C/T]TGCCTGCTTTGCAGG	3055
rs242609	snp	C/T	0.299158	0.245119	intron-variant	HCK	GRCh38.p7	20:32085621	AAATATCATATAAGA[C/T]GCTAGACTCCTACTA	3055
rs242610	snp	C/T	0.4628	0.13121	intron-variant	HCK	GRCh38.p7	20:32085889	gtggacgaggctggg[C/T]catgtagggcctggg	3055
rs242611	snp	A/G	0.499693	0.0123764	intron-variant	HCK	GRCh38.p7	20:32086175	caggcgcccacaact[A/G]cgcctggctaatttt	3055
rs242612	snp	A/T	0.493827	0.0552116	intron-variant	HCK	GRCh38.p7	20:32087646	taatttctaaaaaaa[A/T]tttttttttttttga	3055
rs242613	snp	A/G	0.499866	0.0081858	intron-variant	HCK	GRCh38.p7	20:32087728	ctcaatgcaagctcc[A/G]cctaccaggttcacg	3055
rs242614	snp	A/G	0.302936	0.244331	intron-variant	HCK	GRCh38.p7	20:32087873	ggtctcaatctcctg[A/G]ccttgtgatccgccc	3055
rs242615	snp	C/G	0.499908	0.00678851	intron-variant	HCK	GRCh38.p7	20:32088011	aactcctgggttcaa[C/G]tgatcctcccaaagc	3055
rs381619	snp	C/T	0.274929	0.248754	intron-variant	HCK	GRCh38.p7	20:32076080	gtaatcccagcactt[C/T]gggaggccaaggcac	3055
rs442268	snp	A/T	0.391954	0.205789	intron-variant	HCK	GRCh38.p7	20:32076078	ctgtaatcccagcac[A/T]tcgggaggccaaggc	3055
rs885495	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32059297	TCCTTCCTTCCTTCC[C/T]TCCCTCCCTCCTTTC	3055
rs910185	snp	A/G	0.0856613	0.188395	intron-variant	HCK	GRCh38.p7	20:32086815	GGCCAAAGGTGCTGC[A/G]TGCTGGGGCTGGGGG	3055
rs926687	snp	G/T	0.499713	0.0119774	intron-variant	HCK	GRCh38.p7	20:32092422	GGTTCATCTTCAACC[G/T]CTTTTGTCCAAACCC	3055
rs926688	snp	G/T	0.499703	0.0121769	intron-variant	HCK	GRCh38.p7	20:32092535	CCACGCAGTCTGTTA[G/T]TCACTCAGCAGCCAT	3055
rs980367	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32093508	gtgtgtgtgtgtgtg[G/T]gtgtgtgtgtgtgtg	3055
rs980368	snp	A/G	0.499928	0.00598999	intron-variant	HCK	GRCh38.p7	20:32093740	GCCCTCCCGACACAA[A/G]AGGGAGGGCTGGTGC	3055
rs1004910	snp	A/C	0.205417	0.245993	upstream-variant-2KB	HCK	GRCh38.p7	20:32051627	CCCAGGGGTCTATAC[A/C]GCCGGTCCAAAGATT	3055
rs1883882	snp	C/T	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32082498	AATACAAAAATTAGC[C/T]GGGCGTAGTGGCGGG	3055
rs1987960	snp	C/T	0.0134861	0.0810011	intron-variant	HCK	GRCh38.p7	20:32062031	tgcaacctctgactc[C/T]ggggttcaagcgatt	3055
rs2001413	snp	C/G	0.334147	0.239924	intron-variant	HCK	GRCh38.p7	20:32061199	GTCAGGAGTTCAAGA[C/G]CAGCCTGGCCAACAT	3055
rs2223785	snp	C/T	0.122064	0.214785	intron-variant	HCK	GRCh38.p7	20:32088513	CAAAAGTAATTGTGG[C/T]TTTTGCCATTAAATA	3055
rs2227967	snp	C/T	0.00186575	0.030486	synonymous-codon	HCK	GRCh38.p7	20:32073771	CGAGGCCATTCACCA[C/T]GAAGACCTCAGCTTC	3055
rs2269052	snp	A/G	0.117188	0.211804	intron-variant	HCK	GRCh38.p7	20:32091179	CATCCCTGCCCCATC[A/G]AGCTCCTGTGAAAAT	3055
rs2297303	snp	A/T	0.0652144	0.168387	intron-variant	HCK	GRCh38.p7	20:32073449	GAGGCATAAATCCCA[A/T]ACAGTCAAACCCCTG	3055
rs2297304	snp	A/G	0.455144	0.142885	intron-variant	HCK	GRCh38.p7	20:32073494	AATTTCCTCTGAAGT[A/G]CTTTGCGCAGGCTAT	3055
rs2297305	snp	A/G	0.222035	0.248431	intron-variant	HCK	GRCh38.p7	20:32073501	TCTGAAGTGCTTTGC[A/G]CAGGCTATTGTGTTT	3055
rs3073296	in-del	-/CTTT/TT	0	0	intron-variant	HCK	GRCh38.p7	20:32059420	TCTCTTTCTTTCTTT[-/CTTT/TT]TTTCTTTCTTTCTTT	3055
rs3073297	in-del	-/GT			intron-variant	HCK	GRCh38.p7	20:32093491	AGTATCCTAGGGTTC[-/GT]GTGTGTGTGTGTGTG	3055
rs3746601	snp	A/C	0.499885	0.00758699	intron-variant	HCK	GRCh38.p7	20:32075002	CTTTGGTTGGTTACA[A/C]GTGCATTCTCTGCCT	3055
rs3746602	snp	A/G	0.495407	0.0477027	intron-variant	HCK	GRCh38.p7	20:32075034	CCCTGCAAGGAAGAG[A/G]GCTGGTGAGAGCGGG	3055
rs3746603	snp	A/G	0.0617873	0.164548	intron-variant	HCK	GRCh38.p7	20:32079887	CTAAAGGTGACACCA[A/G]CCCTCCCCACCTTGT	3055
rs3787366	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062683	AAAGTTTTGAGCTCT[A/G]TGAGAAAGAAGCTGA	3055
rs3787367	snp	A/G	0.332337	0.236052	intron-variant	HCK	GRCh38.p7	20:32064574	gttgagacttgccta[A/G]catcacacaatgagc	3055
rs3833316	in-del	-/A	0.146314	0.227484	intron-variant	HCK	GRCh38.p7	20:32058231	TCAGTTCCCAAATCC[-/A]AAAAAAAAATGGAAC	3055
rs3833317	in-del	-/G	0.112983	0.209108	intron-variant	HCK	GRCh38.p7	20:32098879	GGAGGCCACGTATCA[-/G]GGAAATTGCAGGTCT	3055
rs3838038	in-del	-/TAAAAAAAA			intron-variant	HCK	GRCh38.p7	20:32072563	GAGACCCTGTCTCTT[-/TAAAAAAAA]AAAAAAAAAAAAAAA	3055
rs4359727	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32054716	GAGGCTGAGGCAGGA[A/G]AATGGCGTGAACCCT	3055
rs4911541	snp	C/T	0.489608	0.0713316	intron-variant	HCK	GRCh38.p7	20:32060775	agactcccatagcat[C/T]aaatgtgcaagaaat	3055
rs4911542	snp	C/T	0.484421	0.0868729	intron-variant	HCK	GRCh38.p7	20:32061022	agagtcttgctctgt[C/T]gcccaggctggagtg	3055
rs5841096	in-del	-/A	0.499527	0.0153681	intron-variant	HCK	GRCh38.p7	20:32091810	GACCTCTTCTCTATT[-/A]AAAAAAAAAAAAATT	3055
rs5841098	in-del	-/T	0.491421	0.0649309	intron-variant	HCK	GRCh38.p7	20:32099903	TGTCCTTTCTCCACC[-/T]TTTTTTTTTTTTTTA	3055
rs6058519	snp	A/C			upstream-variant-2KB	HCK	GRCh38.p7	20:32050638	gtctgatcttggaag[A/C]taagcaggatcaagc	3055
rs6058520	snp	C/T	0.00953873	0.0683987	intron-variant	HCK	GRCh38.p7	20:32054898	ATTTGCCCCATCTTA[C/T]CATTAAGTTGTCAAA	3055
rs6058522	snp	C/T	0.318656	0.240388	intron-variant	HCK	GRCh38.p7	20:32058156	GACcccgagtctgag[C/T]gccagctctgccaaa	3055
rs6058523	snp	A/G	0.301177	0.244706	intron-variant	HCK	GRCh38.p7	20:32062500	GGCATCTCAGAGCCA[A/G]CCCTATGGCTCAGCC	3055
rs6058524	snp	C/T	0	0	synonymous-codon	HCK	GRCh38.p7	20:32084006	ATCCCCCCGAAGCAC[C/T]TTCAGCACTCTGCAG	3055
rs6058525	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32094751	AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAGGA	3055
rs6061134	snp	C/G	0.5	0	intron-variant	HCK	GRCh38.p7	20:32052792	CTTCTTGGGGGGGGG[C/G]GGGGatttttttttt	3055
rs6061135	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32054625	TCCTGGCTAACACGG[G/T]GAAACCCCGTCTCTA	3055
rs6061136	snp	G/T	0.15665	0.231917	intron-variant	HCK	GRCh38.p7	20:32056662	gtttatattttatta[G/T]tattattattaccat	3055
rs6061137	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057308	CTTTTTTATAGAAAA[A/G]GAACATGAAGggctg	3055
rs6061138	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057391	gatcatctgagctca[A/G]gagttcgagaccagc	3055
rs6061139	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057503	tactcaggaggctga[A/G]gtgggaggatcgtct	3055
rs6061140	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32057535	agcacagaaggtgaa[A/G]gttgcagtgatctga	3055
rs6061141	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32057993	CTAGGACGTGCGCTC[C/T]TGACTCTCCCTTCGA	3055
rs6061142	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32058386	aaaatgcaaaaatta[G/T]ccgggcgtggtggcg	3055
rs6061143	snp	C/T	0.0452528	0.143452	intron-variant	HCK	GRCh38.p7	20:32059584	gcagtgatgctatca[C/T]ggctcatgcagcccc	3055
rs6061144	snp	A/G	0.00477324	0.0486193	intron-variant	HCK	GRCh38.p7	20:32060120	AAACTTCCACTCAGC[A/G]GCAGCCAAGGAAAGA	3055
rs6061145	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32063918	TGCCTTGCTGCTGCA[A/G]GCCTTTTTTTCCAGC	3055
rs6061146	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32065835	agtgggagaaagctg[A/G]ttctccaaaggaaaa	3055
rs6061147	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32066330	TTTTTTTTTTTTTTT[G/T]TGACAGAGTCTTGCT	3055
rs6061148	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32066331	TTTTTTTTTTTTTTT[A/T]GACAGAGTCTTGCTC	3055
rs6061151	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32071533	TGCATGGAGCTGGCA[A/G]GGGAGTTAAGACCGG	3055
rs6061152	snp	C/T	0.292523	0.246357	intron-variant	HCK	GRCh38.p7	20:32072818	GACCGAAGGCCGAGG[C/T]CACAGCTCAAGAAAC	3055
rs6061153	snp	G/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32074444	GCACAGCAGGAACTG[G/T]TGTAAGGATCCCTAC	3055
rs6061154	snp	C/G	0.311859	0.242226	intron-variant	HCK	GRCh38.p7	20:32074471	CTACCCTAATCATGG[C/G]CACATGCTGGGGCTG	3055
rs6061156	snp	C/T	0	0	synonymous-codon	HCK	GRCh38.p7	20:32086632	TCCCCCTCCAGCCAC[C/T]TACAACAAGCACACC	3055
rs6087815	snp	A/G	0.396694	0.202437	intron-variant	HCK	GRCh38.p7	20:32078880	AAAAAAAAAAAAAAA[A/G]GGGGGGAATGATAAA	3055
rs6087816	snp	A/G	0.220843	0.248294	intron-variant	HCK	GRCh38.p7	20:32101041	agagatgaagggtgc[A/G]ttctccaaagactct	3055
rs6089157	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059513	tctctctctctctct[C/T]ttttttttctttttc	3055
rs6089158	snp	A/T	0.235854	0.249599	intron-variant	HCK	GRCh38.p7	20:32063767	GGGCAAGACTCTTTG[A/T]TGTTTAAAGGGAAAT	3055
rs6089159	snp	G/T	0.360632	0.224189	intron-variant	HCK	GRCh38.p7	20:32064035	TTGAGATAGAGTCTC[G/T]CTCTGTCACCCAGGC	3055
rs6089160	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32066031	cccctgtgaggttga[A/G]gctgctggttctcac	3055
rs6089161	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32066108	ACCACTTTGTCACAA[A/G]GCACTCTGCAGAGAG	3055
rs6089162	snp	C/G	0	0	intron-variant	HCK	GRCh38.p7	20:32066148	TACATAAACCTCTTT[C/G]TTCCACCATTCTCTC	3055
rs6089163	snp	C/T	0.384976	0.210431	intron-variant	HCK	GRCh38.p7	20:32068260	tggagatggcaccac[C/T]gtactccagcctggg	3055
rs6089164	snp	A/G	0.332337	0.236052	intron-variant	HCK	GRCh38.p7	20:32069816	CATCTAAGCCTAGGA[A/G]TTTGGGGTTTTTTTC	3055
rs6089165	snp	C/T	1.64846e-05	0.0028709	missense	HCK	GRCh38.p7	20:32071718	ATACATTCTCAAAAA[C/T]TGAAACCAGCGCCAG	3055
rs6089166	snp	G/T	0.010341	0.0711587	missense	HCK	GRCh38.p7	20:32073782	ACCACGAAGACCTCA[G/T]CTTCCAGAAGGGGGA	3055
rs6089167	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32075080	tgcatcctcggcaca[G/T]gctggcatgcagtca	3055
rs6089168	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32076273	agaggttgcagtgag[C/T]tgaaatatcatgcca	3055
rs6089170	snp	C/T	0.499853	0.008585	intron-variant	HCK	GRCh38.p7	20:32089405	GTTAAGTGGCTTGCA[C/T]AAGTTACTGTGCTAA	3055
rs6089171	snp	C/T	0.282632	0.247861	intron-variant	HCK	GRCh38.p7	20:32094968	GATGCCACTTGGTTT[C/T]GTTTTTGTGAAATTC	3055
rs6089174	snp	A/T	0.499703	0.0121769	intron-variant	HCK	GRCh38.p7	20:32096985	acgttataactcgat[A/T]aaaaaaAATTTAgac	3055
rs6089175	snp	A/T	0.499703	0.0121769	intron-variant	HCK	GRCh38.p7	20:32097026	ggctcatgactataa[A/T]cctagcactttggga	3055
rs6089177	snp	C/T	0.0912534	0.193131	intron-variant	HCK	GRCh38.p7	20:32100937	TCAGCAACTCAGCAG[C/T]TGTCAGGACTCTGGG	3055
rs6119756	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059419	CTTCTTTCTCTCTCT[C/T]TCTTTCTTTCTTTTT	3055
rs6119757	snp	C/T	0.0107246	0.0724382	intron-variant	HCK	GRCh38.p7	20:32061453	gcacagcagctgagc[C/T]gctgatcaatttctc	3055
rs6119758	snp	A/G	0.290718	0.246662	intron-variant	HCK	GRCh38.p7	20:32061858	ttacccaccttggag[A/G]ggacttgggctttta	3055

Full records

It may take some time, please wait.