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
rs15150	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570302	TTTATTTTGTGTTTT[C/G/T]TTTTCTCCTTTTTGG	1108
rs1057510	snp	A/G	0.448708	0.151707	intron-variant	CHD4	GRCh38.p7	12:6574121	AGCAACTTTTCTAAT[A/G]TAGTAATACTGTGGC	1108
rs1639122	snp	A/C	0.484446	0.0868443	missense	CHD4	GRCh38.p7	12:6601981	ATCATCATCATCATC[A/C]TCCTCCTCCTCCTCC	1108
rs1639123	snp	C/T	0.449853	0.150196	intron-variant	CHD4	GRCh38.p7	12:6605502	AAAACACAGATAGCG[C/T]AACCCCTAGCACACC	1108
rs1734114	snp	A/G	0.437683	0.165152	intron-variant	CHD4	GRCh38.p7	12:6604284	ATCTCAAAAATAAAA[A/G]AGAAAATAATATCCC	1108
rs1734115	snp	C/G	0.0448719	0.142907	intron-variant	CHD4	GRCh38.p7	12:6605873	CAGCAACCACAGGAT[C/G]CTACTAGCACAGATG	1108
rs1734116	snp	A/G	0.434831	0.168337	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606427	CCTGCCGGCGGCCTG[A/G]GGACCTCTACACTGG	1108
rs2267968	snp	A/G	0.148996	0.228688	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570577	GGAAGATGGGCAGAA[A/G]GAAGGTGAGGGTCTC	1108
rs2267969	snp	A/C	0.251887	0.249993	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581020	AAACAAACAAACAAA[A/C]AAAAAAAATGTGGAT	1108
rs2267970	snp	A/G	0.150333	0.229274	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582393	TGGCTCCACCTTGAG[A/G]TAAAGCCCACCACTG	1108
rs2267971	snp	C/T	0.0418186	0.138422	intron-variant	CHD4	GRCh38.p7	12:6600150	TTTCCATCCAGGCCC[C/T]GAAGAGCTTTACTGT	1108
rs2267972	snp	A/G	0.0558544	0.157504	intron-variant	CHD4	GRCh38.p7	12:6604925	ACTACTGTTTCTCAT[A/G]CCCCTCTCAGAAGGA	1108
rs2267973	snp	A/G	0.164219	0.234823	intron-variant	CHD4	GRCh38.p7	12:6604940	GCCCCTCTCAGAAGG[A/G]CAGGGTCCCCTTACC	1108
rs2267974	snp	A/G	0.0905955	0.192588	synonymous-codon	CHD4	GRCh38.p7	12:6606361	GGGACGGGGAGCCCA[A/G]GCCCGACGCCATCCC	1108
rs2284324	snp	A/T	0	0	intron-variant	CHD4	GRCh38.p7	12:6579230	CAAGGTGGGTGGATC[A/T]CCTGAGGTGAGGAGT	1108
rs2284325	snp	A/T	0.423726	0.179776	intron-variant	CHD4	GRCh38.p7	12:6595047	ATTAAGCCAGATTCC[A/T]ATGTAAGTGCATAAA	1108
rs3831756	in-del	-/A			intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581019	aaacaaacaaacaaa[-/A]caaAAAAAATGTGGA	1108
rs3834496	in-del	-/C			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608045	ATAGTCAGAAACTCA[-/C]CCCCCCCCATACTAC	1108
rs4764608	snp	A/G	0.0614824	0.164198	intron-variant	CHD4	GRCh38.p7	12:6596998	aaataggccgagtgc[A/G]gcggctcacgcctgt	1108
rs5796243	in-del	-/G			intron-variant	CHD4	GRCh38.p7	12:6573460	TTTCCCTTTTTCAAT[-/G]TCCTCATTTTTAAAA	1108
rs6489723	snp	C/G/T	0.276123	0.248631	intron-variant	CHD4	GRCh38.p7	12:6574654	TTCTGATCCCACTAG[C/G/T]GTATGGTGATGGGGG	1108
rs7132970	snp	C/T	0.228105	0.249039	intron-variant	CHD4	GRCh38.p7	12:6599732	ACATAGAAAAGACTA[C/T]ACTTTCCCATTTTTT	1108
rs7294416	snp	A/T	0.212122	0.247114	intron-variant	CHD4	GRCh38.p7	12:6580520	gagactggcctgacc[A/T]atatggagaaacccc	1108
rs7303171	snp	C/T	0.330016	0.236849	intron-variant	CHD4	GRCh38.p7	12:6576439	ctcattgcagcctcc[C/T]aagtagctggaacta	1108
rs7303399	snp	A/T	0.131381	0.220067	intron-variant	CHD4	GRCh38.p7	12:6599647	CAACACTATAGGATG[A/T]AGGAGAATACCTTTC	1108
rs7305251	snp	A/G	0.423726	0.179776	intron-variant	CHD4	GRCh38.p7	12:6597315	TAAAGATAATAACAT[A/G]AAGTgtcaggcgcag	1108
rs7305490	snp	C/T	0.0418186	0.138422	intron-variant	CHD4	GRCh38.p7	12:6596778	gcactccagcctggg[C/T]gacagaacgagactc	1108
rs7307709	snp	A/G	0.329783	0.236927	intron-variant	CHD4	GRCh38.p7	12:6580043	cctgggcgacaaagc[A/G]agactccgtctcaaa	1108
rs7308584	snp	A/G	0.426354	0.177198	intron-variant	CHD4	GRCh38.p7	12:6597578	agaccagcctggcca[A/G]cagaatgaaaaccct	1108
rs7309207	snp	A/C	0.212122	0.247114	intron-variant	CHD4	GRCh38.p7	12:6580519	ggagactggcctgac[A/C]aatatggagaaaccc	1108
rs7310535	snp	C/G/T	0.0151661	0.0857571	intron-variant	CHD4	GRCh38.p7	12:6598463	AATCTCAAATCATAA[C/G/T]CATGGGAGGAGAAGG	1108
rs7311397	snp	A/G	0.329084	0.237162	intron-variant	CHD4	GRCh38.p7	12:6580639	ttgaactcaggaggc[A/G]gaggttgcagtaagc	1108
rs7316626	snp	A/G	0.277213	0.248515	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582286	AGACATATGCCCTGT[A/G]TAAAGAAGTAGAGAA	1108
rs7487055	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6586027	attgcttgaacccag[A/G]aagtggaggttgcag	1108
rs7965883	snp	A/G	0.424503	0.179021	intron-variant	CHD4	GRCh38.p7	12:6586621	tcactcttcagccca[A/G]gagtttaaggttgca	1108
rs7969177	snp	A/G	0.248471	0.249995	intron-variant	CHD4	GRCh38.p7	12:6603814	GGACTTGTGGTCAGC[A/G]CATACAACCTTCTCC	1108
rs7973027	snp	A/C	0.3744	0.216852	intron-variant	CHD4	GRCh38.p7	12:6579807	cacgcctgtaatccc[A/C]gcactttgggaggcc	1108
rs7974020	snp	A/G	0.424348	0.179172	intron-variant	CHD4	GRCh38.p7	12:6588676	ccagctactcaggag[A/G]ctgaggcaggagaac	1108
rs9630275	snp	C/T	0	0	intron-variant	CHD4	GRCh38.p7	12:6592108	AGAGCCTTTCAATGA[C/T]TAATAATGCAGTGCC	1108
rs9888313	snp	A/G	0.430136	0.173352	intron-variant	CHD4	GRCh38.p7	12:6573845	CCTGGCCAACATGAC[A/G]AAACCCCGTCTCTAC	1108
rs10437832	snp	A/G	0.115088	0.210473	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581984	atttttgtattttta[A/G]tagagatggggtttc	1108
rs10774438	snp	C/T	0.423881	0.179625	intron-variant	CHD4	GRCh38.p7	12:6590699	AGTGGATCAAGCCTA[C/T]AGCCCCAGCTAGTTG	1108
rs10849491	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6591143	AAAAAAAAAAAAAAA[A/C]AAAAAAAACCTAGTA	1108
rs11064256	snp	C/T	0.0509478	0.151255	intron-variant	CHD4	GRCh38.p7	12:6571372	CCTTATTTCACCCTC[C/T]GCCTCCTCATAACCT	1108
rs11064258	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6572397	CACCACTGCACTCCA[A/G]CCTGGGCAACAGAGC	1108
rs11064259	snp	C/T	0.115788	0.21092	intron-variant	CHD4	GRCh38.p7	12:6575957	TTCTACCAAAAAAAT[C/T]TCCGTCGCATTCTTC	1108
rs11064260	snp	A/T	0.418974	0.184249	intron-variant	CHD4	GRCh38.p7	12:6576103	gtggctcacgcctgt[A/T]atctcagcactttgg	1108
rs11064261	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6580122	AATCCCAGCTACTCA[A/G]AGGCTGAGGCAGGAG	1108
rs11064262	snp	A/C	0.362313	0.223351	intron-variant	CHD4	GRCh38.p7	12:6580232	ACTCCATCTCGAAAA[A/C]AACAACAACAACAAC	1108
rs11064263	snp	A/C	0	0	intron-variant	CHD4	GRCh38.p7	12:6585015	AAATCACAGGTAAGC[A/C]TCAGGGAAACACAGC	1108
rs11064264	snp	A/C	0	0	intron-variant	CHD4	GRCh38.p7	12:6585026	AAGCATCAGGGAAAC[A/C]CAGCAAGGGGGATGG	1108
rs11064265	snp	A/C	0.141934	0.225437	intron-variant	CHD4	GRCh38.p7	12:6585138	ACAGAGGACAAGAAA[A/C]AGGAAATTTTATTTT	1108
rs11064266	snp	A/G	0.335559	0.234904	intron-variant	CHD4	GRCh38.p7	12:6585489	GGGTTTCATCGTGTT[A/G]GCCAGGATGGGCTCG	1108
rs11064267	snp	A/G	0.0209421	0.100162	intron-variant	CHD4	GRCh38.p7	12:6585967	TAGCCGGGCATGGTG[A/G]TGCATACCTGTAATC	1108
rs11064268	snp	C/T	0.424659	0.17887	intron-variant	CHD4	GRCh38.p7	12:6586112	ATCAAAAAAAAAATA[C/T]ATAAGGCCAGGGGCA	1108
rs11064269	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6586816	AATTCTCCTGCCTCA[A/G]CCTCCCGAACACCTG	1108
rs11064270	snp	C/T	0.148996	0.228688	intron-variant	CHD4	GRCh38.p7	12:6586822	CCTGCCTCAGCCTCC[C/T]GAACACCTGGGACTA	1108
rs11064271	snp	A/G	0.115788	0.21092	intron-variant	CHD4	GRCh38.p7	12:6590488	gcaacttttttctaa[A/G]tctaaaattaaaata	1108
rs11064272	snp	A/G	0.332337	0.236052	intron-variant	CHD4	GRCh38.p7	12:6590980	ATACAAAAATTAGCT[A/G]GGCGTGGTGGCACAC	1108
rs11064273	snp	A/C	0.0452528	0.143452	intron-variant	CHD4	GRCh38.p7	12:6594381	TTTTTTTATTCCCTT[A/C]TCTCTCTACTCAGTG	1108
rs11064274	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6595670	gcagacgcctgtaat[C/T]tcagctactcgggag	1108
rs11064275	snp	G/T	0.226188	0.248863	intron-variant	CHD4	GRCh38.p7	12:6596771	CGCCACTGCACTCCA[G/T]CCTGGGCGACAGAAC	1108
rs11064276	snp	A/G	0.162581	0.234218	intron-variant	CHD4	GRCh38.p7	12:6597816	CAAGTCTAAGTTACT[A/G]GTGACAGCCATTTTC	1108
rs11064278	snp	C/G/T	1.64749e-05	0.00287005	intron-variant	CHD4	GRCh38.p7	12:6602336	TCAGAGCTCCTCCCT[C/G/T]CTTCCTCTGATTCCC	1108
rs11064279	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6603776	TTTCAATCATCAGAG[C/T]TGAGATTTAACAAAG	1108
rs11064280	snp	C/T	0.0023933	0.0345097	intron-variant	CHD4	GRCh38.p7	12:6604900	GTGGAACCCAGAATG[C/T]TTAGGCAGCACTACT	1108
rs11539542	snp	C/T	0.224741	0.248721	synonymous-codon	CHD4	GRCh38.p7	12:6599893	GGAATTCTGTCGGGT[C/T]TGCAAGGATGGTGGG	1108
rs11539543	snp	C/T	0.225314	0.248778	synonymous-codon	CHD4	GRCh38.p7	12:6598360	TCAGCCACCATCTCC[C/T]ACACCAGTGCCTCGG	1108
rs11830845	snp	C/G	0	0	upstream-variant-2KB	CHD4	GRCh38.p7	12:6607598	GCCCCCTTCGCAGCG[C/G]GCGCGCGCGCGTCAC	1108
rs11833125	snp	A/G	0.00755907	0.0610114	intron-variant	CHD4	GRCh38.p7	12:6576220	aaattagctgggcgt[A/G]gtggcacacgcctgt	1108
rs11833796	snp	C/T	0.340108	0.233197	intron-variant	CHD4	GRCh38.p7	12:6590381	taccaatgttaattt[C/T]ctagttttgatcatt	1108
rs11834945	snp	A/G	0.162581	0.234218	intron-variant	CHD4	GRCh38.p7	12:6584547	TGAGCAACCACACTC[A/G]GCTAATGTTTTTATT	1108
rs12099908	snp	A/C	0.336245	0.234652	intron-variant	CHD4	GRCh38.p7	12:6604470	GACCAGGCACAAGAA[A/C]GCCCCTCCCATTCCC	1108
rs12301764	snp	A/G	0.0479149	0.147179	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608544	CCCCCATCTCCAGGC[A/G]CTGTCAGTCTATTCT	1108
rs12310569	snp	A/G	0.227074	0.248947	intron-variant	CHD4	GRCh38.p7	12:6588187	ACACAAAAAGAATCT[A/G]TTGTTTCTCACTTAA	1108
rs12312677	snp	A/G	0.0475351	0.146656	intron-variant	CHD4	GRCh38.p7	12:6589507	ggcgtggtggctcac[A/G]cctgtaatcccagca	1108
rs12315480	snp	C/G	0.0479149	0.147179	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608265	TATCAAAAAGATAAC[C/G]CATAATGATCAACAG	1108
rs12321714	snp	C/T	0.0126979	0.078662	intron-variant	CHD4	GRCh38.p7	12:6576096	gggcacagtggctca[C/T]gcctgttatctcagc	1108
rs12322604	snp	A/G	0.334182	0.235401	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608479	CATCTCCACTCTACC[A/G]CCCCTATACCCTTCG	1108
rs12812446	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6600436	GTTATTGGAAAAAAA[C/T]TACCTCCCCCCACCC	1108
rs12813188	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6600435	AGTTATTGGAAAAAA[A/C]CTACCTCCCCCCACC	1108
rs12813401	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6586121	aaaaTATATAAggcc[A/G]ggggcagtggctcac	1108
rs12816349	snp	A/G	0.297128	0.245518	intron-variant	CHD4	GRCh38.p7	12:6600779	ATCCCAGCAAGCACC[A/G]TTATACAGGGAGCCT	1108
rs12818623	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6601194	TCCTCCCTCCTATCT[C/T]CTACCTTAGGGCTGA	1108
rs12818651	snp	C/T	1.67402e-05	0.00289306	intron-variant	CHD4	GRCh38.p7	12:6601241	TGCTGTCTTTGACAT[C/T]TTAAGCCCACACTAG	1108
rs12824453	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6601231	AGCATTCCCATGCTG[G/T]CTTTGACATCTTAAG	1108
rs16927894	in-del	-/GAA			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607849	ATTAGGTCCAAGAGT[-/GAA]GAAGAAGTTGGCAAA	1108
rs16928087	snp	G/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607894	GCCATGGGGAGGGAG[G/T]GGTGATGAATTATTA	1108
rs16932768	snp	C/T	0.00743484	0.0605156	missense	CHD4	GRCh38.p7	12:6578864	TGTCTTCTACCACAA[C/T]AGGGGTCAGATCTAT	1108
rs17726105	snp	A/G	1.6588e-05	0.00287988	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582761	TACCTAGGGGAAGAA[A/G]AAACCCAGGTGAGAG	1108
rs17788043	snp	C/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583506	TACTTGGTGTGCCTG[C/T]TTGGACCTAAGAACT	1108
rs17788055	snp	A/T	0.0283406	0.115616	intron-variant	CHD4	GRCh38.p7	12:6583846	ACTGTCTGCAGAACG[A/T]AAAGAATTCTATATA	1108
rs17790300	snp	A/G	0.148996	0.228688	intron-variant	CHD4	GRCh38.p7	12:6576022	CCATTTGTGAGTTCC[A/G]TCCCTACTCCAATTC	1108
rs28866502	snp	C/T	0.448323	0.15221	intron-variant	CHD4	GRCh38.p7	12:6572043	AGGCAGGAGAATCAC[C/T]TGAACACAGGAGGCG	1108
rs34219949	in-del	-/T	0.0244538	0.107838	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608484	CCACTCTACCACCCC[-/T]ATACCCTTCGAGCCA	1108
rs34224003	in-del	-/A			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582951	GCTGCAAGAAGAAAA[-/A]GATGAATGAGTGACA	1108
rs34260297	in-del	-/A			upstream-variant-2KB	CHD4	GRCh38.p7	12:6609011	TGGGGATGGACATCC[-/A]CATCACGATGTGAAC	1108
rs34287606	in-del	-/C			upstream-variant-2KB	CHD4	GRCh38.p7	12:6609134	CCTAGCAAGGCCGAG[-/C]TCCGCACCATGGAGA	1108
rs34509399	snp	C/T	0.00267675	0.0364858	synonymous-codon	CHD4	GRCh38.p7	12:6578040	CTACTGGCTGCTAGC[C/T]GGCATTATAAAGTAT	1108
rs34659145	in-del	-/G			intron-variant	CHD4	GRCh38.p7	12:6595199	TGTGGAGAAGTGGGG[-/G]AAGCCGACTTTGTGA	1108

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