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
rs14251	snp	A/C	0.483305	0.089826	missense, utr-variant-3-prime	RELL2, FCHSD1	GRCh38.p7	5:141639543	TCTGCAGCCCCTTGC[A/C]TCCATTGCAGCCGCA	89848
rs32955	snp	C/T	0.254105	0.249966	intron-variant, utr-variant-3-prime	RELL2, FCHSD1	GRCh38.p7	5:141639746	CTCTTTCCTCCTGGA[C/T]TGGGAGCTCCGGCAG	89848
rs32956	snp	C/G	0.228529	0.249076	intron-variant, utr-variant-3-prime, missense	RELL2, FCHSD1	GRCh38.p7	5:141640314	GGAAAACACAGCCGG[C/G]ACTGCACTGGGCTGG	89848
rs32957	snp	A/G	0.164387	0.234884	intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641529	GGGTGGCCAGGATCC[A/G]GGGCTTTAGCCGGCG	89848
rs41098	snp	A/C	0.33303	0.235809	intron-variant, utr-variant-3-prime, downstream-variant-500B	RELL2, FCHSD1	GRCh38.p7	5:141640533	GCTCCCTGAACCCCC[A/C]GAGTAAACTGCAGGC	89848
rs173683	snp	C/G	0.494557	0.0518841	intron-variant	FCHSD1	GRCh38.p7	5:141648480	catttcttctctctg[C/G]aatgttcttccccta	89848
rs187515	snp	C/T	0.261056	0.249755	intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641198	GAGGTGGGCCAGAAC[C/T]ACTAGAGACCTTGAT	89848
rs251041	snp	C/G	0.438105	0.164671	intron-variant	FCHSD1	GRCh38.p7	5:141648321	taccatggtccacca[C/G]gttcaatatgagctg	89848
rs251177	snp	C/T	0.320335	0.239902	intron-variant	FCHSD1	GRCh38.p7	5:141647317	GAAGAAAAAGGACAA[C/T]GTGTGAAGCAAAGAG	89848
rs251180	snp	A/G	0.261608	0.24973	intron-variant, utr-variant-3-prime	FCHSD1	GRCh38.p7	5:141642368	ggcaaaggtaggagt[A/G]gaggcaggggcgagg	89848
rs374073	snp	A/G	0.309648	0.24278	intron-variant	FCHSD1	GRCh38.p7	5:141643863	aaaaaaaaaaaaaaa[A/G]aagaaGgctttacct	89848
rs456998	snp	G/T	0.498813	0.0243321	intron-variant, downstream-variant-500B	FCHSD1	GRCh38.p7	5:141645595	GCTCATAATAAAAAT[G/T]TACTGAGGACTCTAT	89848
rs467478	snp	A/G	0.29175	0.246489	intron-variant, downstream-variant-500B	FCHSD1	GRCh38.p7	5:141644166	GGCTTCATTGGGGTG[A/G]GAGGGTCAACCCAGA	89848
rs467677	snp	A/G	0.263535	0.249633	intron-variant	FCHSD1	GRCh38.p7	5:141643714	ttagccgggcgtggc[A/G]gcacgtgcctgtaat	89848
rs468222	snp	C/G	0.367297	0.220775	intron-variant	FCHSD1	GRCh38.p7	5:141647833	GAGCAGAACCAGAGT[C/G]CATGTATGTATCATC	89848
rs468650	snp	C/T	0.261608	0.24973	intron-variant	FCHSD1	GRCh38.p7	5:141643315	gcacttcacgtgtac[C/T]aattcattcaatcct	89848
rs468920	snp	C/T	0.295088	0.245901	intron-variant, downstream-variant-500B	FCHSD1	GRCh38.p7	5:141644156	ATGAATATGAGGCTT[C/T]ATTGGGGTGAGAGGG	89848
rs468968	snp	C/T	0.497749	0.0334707	intron-variant	FCHSD1	GRCh38.p7	5:141647832	GGAGCAGAACCAGAG[C/T]GCATGTATGTATCAT	89848
rs469074	snp	G/T	0.329684	0.23697	intron-variant, downstream-variant-500B	FCHSD1	GRCh38.p7	5:141644569	CAAAATTTCCCTTTC[G/T]TACCTGTGGGCTCTG	89848
rs469522	snp	A/G	0.407538	0.194118	intron-variant, downstream-variant-500B	FCHSD1	GRCh38.p7	5:141644481	AGGGAGGTGGGTAGC[A/G]GTGCCCCAGGACCAT	89848
rs702379	snp	C/T	0.329783	0.236927	intron-variant	FCHSD1	GRCh38.p7	5:141643281	cgcttatgtttacta[C/T]gtctcaagtgttctg	89848
rs702380	snp	A/C/G	0.324643	0.263409	intron-variant	FCHSD1	GRCh38.p7	5:141642977	TCTGTTAGCCTCCCA[A/C/G]GGCTCCCAGTTCCTT	89848
rs1048452	snp	C/T			intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641194	AGGTCTCTAGTAGTT[C/T]TGGCCCACCTCTTTC	89848
rs1048453	snp	A/C			intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641175	CCCACCTCTTTCCCC[A/C]CCCTGGCTCCATGAC	89848
rs1048455	snp	A/C			intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641157	CTGGCTCCATGACCC[A/C]CCCCACTCTGGATGC	89848
rs1048456	snp	A/C			intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641152	TCCATGACCCACCCC[A/C]CTCTGGATGCCAGGG	89848
rs1160948	in-del	-/AGT	0.327568	0.237662	intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641286	AGAAGAGAAGGTAGT[-/AGT]TCCGGTCCTAGAGAT	89848
rs2052455	snp	C/T	0.322483	0.239262	intron-variant	FCHSD1	GRCh38.p7	5:141646014	TACTCCTCTTTCTGA[C/T]GGTGGGAGGAAGGAA	89848
rs2291110	snp	A/C	0.000960249	0.0218907	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141644626	ACTTCCCGGACCTCT[A/C]CCTCCCAGAGAGCAG	89848
rs2306341	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141651453	CAGAGGGCGGGGCCT[G/T]ACCTGGCCTGGGGCG	89848
rs3749760	snp	A/C	0.0373966	0.131529	missense, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141646615	CTACAAGATCCAGAA[A/C]CATGGGCATCGGGTG	89848
rs3763121	snp	C/T	0.462489	0.131713	intron-variant	FCHSD1	GRCh38.p7	5:141647895	CCTGCTTCTTGATCC[C/T]CATGACAGTGGGTGG	89848
rs3830219	in-del	-/A	0.264632	0.249571	intron-variant	FCHSD1	GRCh38.p7	5:141649611	CCCATGGTGTTGGTC[-/A]GGGGGCAGGGGGTGG	89848
rs3833652	in-del	-/TAC	0.336017	0.234736	intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641281	TAGGACCGGAACTAC[-/TAC]CTTCTCTTCTGTCAT	89848
rs3834836	in-del	-/TTATT	0.0473654	0.146421	intron-variant	FCHSD1	GRCh38.p7	5:141642515	TATAGCAGTTTTATT[-/TTATT]ATTTATTTTAGATTC	89848
rs4042097	in-del	-/GTA			intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641284	ACAGAAGAGAAGGTA[-/GTA]GTTCCGGTCCTAGAG	89848
rs4912764	snp	A/C/G	9.9935e-05	0.00706806	intron-variant	FCHSD1	GRCh38.p7	5:141647886	TCCCCTGCACCACCC[A/C/G]CTGTCATGGGGATCA	89848
rs6580193	snp	A/T	0.0310518	0.120672	intron-variant, downstream-variant-500B	FCHSD1	GRCh38.p7	5:141642149	CAGAAAGTTTTAGAA[A/T]AGGCAGGCATTCcac	89848
rs6863184	snp	A/G	0.0310518	0.120672	intron-variant	FCHSD1	GRCh38.p7	5:141649779	GTCAGCTCTACCTAC[A/G]GCTCACGTGCCTTCC	89848
rs6881321	snp	A/G	0.030665	0.119967	intron-variant	FCHSD1	GRCh38.p7	5:141649691	CAGCCCATTAGCTCA[A/G]CCACAAGCCTCACTC	89848
rs6882352	snp	A/C	0.00837292	0.0641588	intron-variant	FCHSD1	GRCh38.p7	5:141649552	CTCCCCAGAGAAGGT[A/C]TGTGTTGAGGAGGAG	89848
rs7711960	snp	A/G	0.40853	0.193309	intron-variant, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141646362	AATTGAAGTCCAGAG[A/G]GGTTAAGTCACTCCC	89848
rs7720458	snp	A/G	0.442926	0.158996	downstream-variant-500B, upstream-variant-2KB	ARAP3, FCHSD1	GRCh38.p7	5:141653036	cgtgccaccacaacc[A/G]gctaattttgtattt	89848
rs7720485	snp	A/G	0.498415	0.0281103	downstream-variant-500B, upstream-variant-2KB	ARAP3, FCHSD1	GRCh38.p7	5:141653094	tgccaggatggtctc[A/G]aactcctgacctcag	89848
rs7735382	snp	C/T	0.01456	0.0840715	intron-variant	FCHSD1	GRCh38.p7	5:141647852	GTATGTATCATCTAC[C/T]CACTCTAAACAGACA	89848
rs10059833	snp	A/G	0.0123036	0.0774623	upstream-variant-2KB	FCHSD1	GRCh38.p7	5:141651987	AGAGCTGGGAGATGC[A/G]CAGGAAGCCCCTGCC	89848
rs10593116	in-del	-/GA			intron-variant	FCHSD1	GRCh38.p7	5:141642548	TAGACATTTAAAAAA[-/GA]AAAAAAGTGGGCATC	89848
rs10699129	in-del	-/GGGG			intron-variant	FCHSD1	GRCh38.p7	5:141643219	ATGCTTGCATTCGGT[-/GGGG]GGGGGGGTGTAGCTG	89848
rs11167754	snp	A/G	0.312593	0.242037	intron-variant, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141646527	ATGACACCCTCAATG[A/G]CTCCAAGATCCCCTC	89848
rs11739451	snp	A/G	0.238666	0.249743	synonymous-codon, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141649505	CGGTGGCATCCAGCA[A/G]GCAGCGCCAGGCACC	89848
rs11741647	snp	C/G	0.245074	0.249964	intron-variant	RELL2, FCHSD1	GRCh38.p7	5:141638887	ATAGCCCCTTGCTCC[C/G]TCTTCTCCAACCTTC	89848
rs11742646	snp	C/G	0.323368	0.238992	missense, utr-variant-3-prime	RELL2, FCHSD1	GRCh38.p7	5:141640263	CAAGAGGCAAATGGG[C/G]AGCCAAGCAAACCAG	89848
rs11948807	snp	A/T	0.0256215	0.110247	intron-variant	FCHSD1	GRCh38.p7	5:141650816	GTTCCTGTGTGTTTA[A/T]GTGGGTGGGAGGGGG	89848
rs12659397	snp	C/T	0.401392	0.198948	intron-variant	FCHSD1	GRCh38.p7	5:141648582	ccccttgttattctt[C/T]atcatagtaccttgt	89848
rs12659410	snp	C/T	0.101301	0.200969	intron-variant	FCHSD1	GRCh38.p7	5:141648644	gctgtctgtctctct[C/T]aaccagactgtgagg	89848
rs17097413	snp	C/T	0.225597	0.248806	upstream-variant-2KB	FCHSD1	GRCh38.p7	5:141651540	GAGAAACTAAACCTG[C/T]TACTGCTGCGAATAC	89848
rs17286989	snp	A/C	0.118184	0.212425	intron-variant	FCHSD1	GRCh38.p7	5:141647245	CCTAGGGGTTGGGAA[A/C]AGTCAAAGTCACTCA	89848
rs17287002	snp	C/T	0.154079	0.230866	synonymous-codon, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141651073	GGTCTGAAGGATGCT[C/T]AGCTGTTCCAGGAAG	89848
rs17855844	snp	C/G	0.324369	0.238682	missense, utr-variant-3-prime	RELL2, FCHSD1	GRCh38.p7	5:141640002	AGGAGCTGGGGCTCT[C/G]GTGGGGGACAGGACC	89848
rs17855845	snp	C/T	0	0	missense, utr-variant-3-prime	RELL2, FCHSD1	GRCh38.p7	5:141639528	ACAGTGCACCTGGGC[C/T]CTGCAGCCCCTTGCC	89848
rs28370911	snp	A/G	0.00597247	0.0543191	intron-variant	FCHSD1	GRCh38.p7	5:141649644	ACAGAGTGCTTTCCC[A/G]TCCTCCCTTGTCTGG	89848
rs34422888	in-del	-/T			intron-variant	RELL2, FCHSD1	GRCh38.p7	5:141639245	TAGTGCCACTCCTTT[-/T]GGGTTAAGCAGTGTT	89848
rs34704377	multinucleotide-polymorphism	CC/TG			intron-variant	FCHSD1	GRCh38.p7	5:141647832	GGAGCAGAACCAGAG[CC/TG]CATGTATGTATCATC	89848
rs34932115	in-del	-/T			upstream-variant-2KB	FCHSD1	GRCh38.p7	5:141651646	TGAGTCAAGACGCCT[-/T]AAGTTCTATTTGTAG	89848
rs35094060	in-del	-/A			intron-variant	FCHSD1	GRCh38.p7	5:141642555	TTAAAAAAGAAAAAA[-/A]GTGGGCATCAGAAAA	89848
rs35340436	in-del	-/A			frameshift-variant, utr-variant-3-prime	RELL2, FCHSD1	GRCh38.p7	5:141640175	CCTCGTGCACTTGAA[-/A]GGGAACCCCAGAGCT	89848
rs35590706	in-del	-/TAG			intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RELL2, FCHSD1	GRCh38.p7	5:141641285	CAGAAGAGAAGGTAG[-/TAG]TTCCGGTCCTAGAGA	89848
rs35869174	in-del	-/A			intron-variant	FCHSD1	GRCh38.p7	5:141643865	AAAAAAAAAAAAGAA[-/A]GAAGGCTTTACCTCG	89848
rs36020673	in-del	-/G			intron-variant	FCHSD1	GRCh38.p7	5:141643130	TCCTGGCATGTGGGG[-/G]AGGTTTTACCAGCTT	89848
rs55691717	snp	C/T	0.0152603	0.0860075	intron-variant	FCHSD1	GRCh38.p7	5:141649837	GTTCCTGGGGCTGAG[C/T]TCCCCATCACTTTTT	89848
rs55741918	in-del	-/C/CAG	0.5	0	intron-variant	FCHSD1	GRCh38.p7	5:141645325	TACTAACAGTAATAG[-/C/CAG]AGTTACAGTAATTGA	89848
rs56017834	snp	A/G			intron-variant, utr-variant-3-prime	RELL2, FCHSD1	GRCh38.p7	5:141639683	GGAAAGGGGGGCTGA[A/G]GTAGGGGGCCCAGTG	89848
rs56206715	in-del	-/A			intron-variant	FCHSD1	GRCh38.p7	5:141643849	CGAAACTCTGTCTCA[-/A]AAAAAAAAAAAAAGA	89848
rs56411617	in-del	-/GGGG/GGGGG	0.5	0	intron-variant	FCHSD1	GRCh38.p7	5:141643226	CATTCGGTGGGGGGG[-/GGGG/GGGGG]TGTAGCTGACAAATA	89848
rs58908491	snp	A/G	0.275999	0.248644	intron-variant	FCHSD1	GRCh38.p7	5:141647659	ATGAGAAAGGCCCTC[A/G]TGTGCAGAGCACTTA	89848
rs60039240	snp	C/G	0.00358779	0.0422022	intron-variant	FCHSD1	GRCh38.p7	5:141649609	CCCCACCCCCTGCCC[C/G]CTGACCAACACCATG	89848
rs61753289	snp	C/T	0.000422744	0.0145325	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141646111	GCGGATGCTCTCTCG[C/T]ACTTCCTGTAACCTC	89848
rs61753290	snp	C/T	0.0253225	0.109636	missense, downstream-variant-500B, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141644430	TGTACAGGGCCTGTG[C/T]CAGGAATGCTACAGA	89848
rs67641160	snp	C/G	0.225893	0.248835	intron-variant	FCHSD1	GRCh38.p7	5:141650886	CTGGAGAGGCCAGGC[C/G]TAGGGTGAGGGCTGT	89848
rs71583662	snp	A/G	0.5	0	intron-variant	FCHSD1	GRCh38.p7	5:141650838	GGGAGGGGGTTGGGA[A/G]GGGTTAGGTGGGGGA	89848
rs71585381	snp	A/G	0.5	0	upstream-variant-2KB	FCHSD1	GRCh38.p7	5:141652443	TTAGACTTCTGGTCT[A/G]ATATCTGATCTCCTT	89848
rs72792345	snp	A/G	0.039522	0.134904	intron-variant	FCHSD1	GRCh38.p7	5:141643741	TAATCCCAGCTACTC[A/G]AGGGGCTGATACAGG	89848
rs72792348	snp	C/G	0.0923359	0.194016	intron-variant	FCHSD1	GRCh38.p7	5:141650848	TGGGAGGGGTTAGGT[C/G]GGGGAGCATTCCTAT	89848
rs73285814	snp	A/G	0.3744	0.216852	intron-variant, utr-variant-3-prime	RELL2, FCHSD1	GRCh38.p7	5:141639757	TGGACTGGGAGCTCC[A/G]GCAGAAGTCAGGCTA	89848
rs73285819	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD1	GRCh38.p7	5:141647577	ACCTCTACTGTAAAA[C/T]AGGCTCGTTCCAGAT	89848
rs73285828	snp	C/G	0.227074	0.248947	intron-variant	FCHSD1	GRCh38.p7	5:141651279	CGTCTCCTACCACAA[C/G]TCGGATGCCCCCTTA	89848
rs73794953	snp	C/G	0.0197687	0.0974348	intron-variant	FCHSD1	GRCh38.p7	5:141642759	TCAATAAGCTAGTAC[C/G]TTTTCCTTACCTCAT	89848
rs73794955	snp	C/T	0.030665	0.119967	intron-variant	FCHSD1	GRCh38.p7	5:141647658	CATGAGAAAGGCCCT[C/T]GTGTGCAGAGCACTT	89848
rs73794956	snp	A/T	0.228842	0.249103	intron-variant	FCHSD1	GRCh38.p7	5:141648224	TGCCTGGCACTACAC[A/T]AAAAATGTTGCATAC	89848
rs73794957	snp	C/T	0.030665	0.119967	intron-variant	FCHSD1	GRCh38.p7	5:141648774	AAAGAAGGGTATTCT[C/T]TCCATTTTATAGAAG	89848
rs73794959	snp	A/C	0.030665	0.119967	intron-variant	FCHSD1	GRCh38.p7	5:141651275	TTCCCGTCTCCTACC[A/C]CAAGTCGGATGCCCC	89848
rs74910284	snp	A/G	0.112754	0.208958	intron-variant, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141646200	GCAGTACCTGGTTGG[A/G]AAGGCAGAGAACAGG	89848
rs75142511	snp	G/T	0	0	missense, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141641739	ATGTCCAGGAACCCA[G/T]GGAAGTCCAGGGCTT	89848
rs75457247	snp	A/C	0.00716266	0.059414	intron-variant	FCHSD1	GRCh38.p7	5:141648174	TGAGAAGCCAGATCC[A/C]GAATGGATTCTCACA	89848
rs75513915	snp	C/T	0.0275645	0.114116	intron-variant	FCHSD1	GRCh38.p7	5:141648278	CTAGTGCCTTCTGCA[C/T]GCATTTAAAATAAAA	89848
rs75791926	snp	A/T	0.0126979	0.078662	intron-variant, downstream-variant-500B	FCHSD1	GRCh38.p7	5:141645407	ATTTAATCTTCATAA[A/T]GACCCAGTGTTAATA	89848
rs76141781	snp	A/G	0.0314385	0.121371	intron-variant	FCHSD1	GRCh38.p7	5:141642927	GGAGAGGACCAGAGC[A/G]TGACCTGGGAGTCCA	89848
rs76634428	snp	C/T	0.107694	0.205546	upstream-variant-2KB	FCHSD1	GRCh38.p7	5:141652673	GTACTCTCCTCCCAC[C/T]GTCTGCTCACTGTGC	89848
rs76846020	snp	A/G	0.00413911	0.0453037	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141648091	CTGGGCTGACTGGGC[A/G]GACAGCTAGGAGGGT	89848
rs77115131	snp	G/T	0.0637582	0.166775	missense, nc-transcript-variant	FCHSD1	GRCh38.p7	5:141646163	CGCTCTGAAGCCTGC[G/T]GCCGCCTCTGCTCCA	89848

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