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
rs719856	snp	C/T	0.429087	0.174436	utr-variant-3-prime	CD2AP	GRCh38.p7	6:47626986	ACATCAACTGCATTA[C/T]GTAACAGTTATTGAA	23607
rs901186	snp	A/T	0.357238	0.225832	intron-variant	CD2AP	GRCh38.p7	6:47546510	agaacacttgggaaa[A/T]ttatcacaaaaagat	23607
rs901187	snp	A/G	0.243919	0.249926	intron-variant	CD2AP	GRCh38.p7	6:47546543	ttgcctgggcacatt[A/G]tcatcacgttataat	23607
rs923146	snp	A/G	0.498982	0.0225409	intron-variant	CD2AP	GRCh38.p7	6:47607661	TACTGTAATGTTAAT[A/G]TATTAGCTCTTAAAC	23607
rs923149	snp	C/G	0.244205	0.249933	intron-variant	CD2AP	GRCh38.p7	6:47556322	ctcatgaacagaaaa[C/G]caaacactacatgtt	23607
rs923150	snp	A/T	0.498982	0.0225409	intron-variant	CD2AP	GRCh38.p7	6:47553096	CACTTAAAGAAAAAA[A/T]CAATAAGCAGATGGC	23607
rs978448	snp	C/T	0.499	0.0223418	intron-variant	CD2AP	GRCh38.p7	6:47577322	ATTTGTTGTAATTTA[C/T]ATATTGGGAATTATT	23607
rs978449	snp	A/C			intron-variant	CD2AP	GRCh38.p7	6:47577432	CTCTTCCACCTCATT[A/C]TATTTTTTCTCCTGT	23607
rs1004173	snp	C/T	0.305685	0.24372	upstream-variant-2KB	CD2AP	GRCh38.p7	6:47477281	TGCCTAGGTTTCTCC[C/T]TCACCCGACGAAGAC	23607
rs1014001	snp	G/T	0.459016	0.137158	intron-variant	CD2AP	GRCh38.p7	6:47580936	GAATTTTAAAAAATG[G/T]AAAATAGCAAACTGA	23607
rs1043276	snp	C/T	0.498158	0.0302955	utr-variant-3-prime	CD2AP	GRCh38.p7	6:47626266	AGTAACTGAAATACT[C/T]TTACCTTTCTGTCCT	23607
rs1056434	snp	A/C	0.47743	0.103805	utr-variant-5-prime	CD2AP	GRCh38.p7	6:47478053	TTTGCCTCTGCCTCG[A/C]GGGCCGCGCTGAAGA	23607
rs1150807	snp	C/T	0	0	intron-variant	CD2AP	GRCh38.p7	6:47563690	GAGTTAATTTACTCT[C/T]ACATTAGTTTTTAGC	23607
rs1150808	snp	A/C			intron-variant	CD2AP	GRCh38.p7	6:47596405	attccttgaccacat[A/C]ttcccactcccctcc	23607
rs1207257	snp	A/C			intron-variant	CD2AP	GRCh38.p7	6:47543111	agctgagattgcgcc[A/C]ccgcactccagcctg	23607
rs1213124	snp	A/G	0	0	intron-variant	CD2AP	GRCh38.p7	6:47516013	TAAATGCATTTTACA[A/G]AGTTATCTAGAAACC	23607
rs1352027	snp	C/G	0.497641	0.0342639	intron-variant	CD2AP	GRCh38.p7	6:47524386	TAACGGAAAAAACAT[C/G]AGGCTTACATGGGAA	23607
rs1352028	snp	A/G	0.38934	0.207568	intron-variant	CD2AP	GRCh38.p7	6:47524301	AGGCAAGTCGTGCTG[A/G]GTCCAAGGAGCTAGA	23607
rs1352029	snp	G/T	0.498673	0.0257246	intron-variant	CD2AP	GRCh38.p7	6:47581209	ACTAGTTATTCTACC[G/T]TTTCAAATGAAATCC	23607
rs1352030	snp	G/T	0.497641	0.0342639	intron-variant	CD2AP	GRCh38.p7	6:47527988	CTGGGTAGCATGTAT[G/T]TTTAATAGAAACATG	23607
rs1385741	snp	C/T	0.385168	0.210309	intron-variant	CD2AP	GRCh38.p7	6:47519222	TTATCAATGTCATTT[C/T]CCACCTCCCCAAGCA	23607
rs1385742	snp	A/T	0.439224	0.163383	downstream-variant-500B	CD2AP	GRCh38.p7	6:47627419	CCTCCATTTTTTTTT[A/T]AAAAAAAACCTACTC	23607
rs1475763	snp	C/T	0.108402	0.206034	intron-variant	CD2AP	GRCh38.p7	6:47592725	gtgttcacaaaccca[C/T]gagctctctaaactc	23607
rs1485780	snp	A/C	0.357664	0.225629	intron-variant	CD2AP	GRCh38.p7	6:47588894	CTTTTGAGCACATTT[A/C]CCTCTAGACCAATGA	23607
rs1485781	snp	C/T	0.499017	0.0221427	intron-variant	CD2AP	GRCh38.p7	6:47595030	TTATTTTTGTATATA[C/T]GTCTTAAGACACATT	23607
rs1485785	snp	C/T	0.428182	0.17536	intron-variant	CD2AP	GRCh38.p7	6:47600023	ATGTAAAACTTGAAA[C/T]GGAGAACTCTTGATA	23607
rs1485786	snp	C/T	0.430136	0.173352	intron-variant	CD2AP	GRCh38.p7	6:47600454	GGTGACCTTATTCTT[C/T]CCTCTTTCAGTTTGC	23607
rs1485787	snp	C/T	0.24449	0.249939	intron-variant	CD2AP	GRCh38.p7	6:47601274	CTTTGTGGAACAGGG[C/T]GTGAAAACATCTTAT	23607
rs1556624	snp	A/G	0	0	intron-variant	CD2AP	GRCh38.p7	6:47580126	CTCTATGGAAGCTTA[A/G]GCTGTCTGAGGCCTT	23607
rs1564924	snp	A/T	0.384976	0.210431	intron-variant	CD2AP	GRCh38.p7	6:47502145	GGCCTCAGTTTCCTG[A/T]TGTCAGTCAGAGACC	23607
rs1564925	snp	G/T			intron-variant	CD2AP	GRCh38.p7	6:47502297	tacatacAATTCATT[G/T]TCTTTTTCATTATCT	23607
rs1564926	snp	C/T	0.497641	0.0342639	intron-variant	CD2AP	GRCh38.p7	6:47502410	ctgggactacaggtg[C/T]acactgccatgtctg	23607
rs1564927	snp	A/G	0.0898077	0.191933	intron-variant	CD2AP	GRCh38.p7	6:47502555	ctggagtgcagtagc[A/G]cgttcttggctcact	23607
rs1811596	snp	C/T	0.498982	0.0225409	intron-variant	CD2AP	GRCh38.p7	6:47556442	gagaatcgctcctag[C/T]ctgggcaacaagagt	23607
rs1815504	snp	C/T	0.244205	0.249933	intron-variant	CD2AP	GRCh38.p7	6:47482554	CATCTCCACTAAAAA[C/T]ACAAAAAATTAGCCA	23607
rs1825566	snp	C/T	0.40733	0.194287	intron-variant	CD2AP	GRCh38.p7	6:47621897	atcttgggagttcta[C/T]ggccccgcccactgc	23607
rs1843404	snp	C/T	0.154661	0.231107	intron-variant, upstream-variant-2KB	CD2AP	GRCh38.p7	6:47521339	GTCTCAAACTCCTGA[C/T]CTGAGGTGATCTGCC	23607
rs1872505	snp	C/G	0.357238	0.225832	intron-variant	CD2AP	GRCh38.p7	6:47513239	GAAAGTGAGCACCAG[C/G]ATTTAAGAGCCCTCA	23607
rs1931825	snp	C/G/T	0.59801	0.139164	intron-variant	CD2AP	GRCh38.p7	6:47562979	TGGCAAAGAATCTTA[C/G/T]GCCCAGTATGTCATC	23607
rs1948046	snp	C/G	0.498982	0.0225409	intron-variant	CD2AP	GRCh38.p7	6:47618239	TCTGCCTCCTGGGTT[C/G]AAGTGATTCTCATGC	23607
rs1948047	snp	A/G	0.357238	0.225832	intron-variant	CD2AP	GRCh38.p7	6:47618176	TGTACCACCATGCCC[A/G]GCTAATTTTTATATT	23607
rs2039502	snp	A/T	0	0	intron-variant	CD2AP	GRCh38.p7	6:47519333	TGTCTAATTTCAGGG[A/T]TCCTTCTCAAAGGGA	23607
rs2039503	snp	C/T	0.0116283	0.0753586	synonymous-codon	CD2AP	GRCh38.p7	6:47595956	AAAGCCAGTAATTTA[C/T]TGAGATCTTCTGGAA	23607
rs2046464	snp	C/T	0.499017	0.0221427	intron-variant	CD2AP	GRCh38.p7	6:47573645	aggcacctgccacca[C/T]gcccggctaattttt	23607
rs2095386	snp	A/G	0.449218	0.151037	intron-variant	CD2AP	GRCh38.p7	6:47481846	ttcagtggcatgatc[A/G]tagctcactgcagcc	23607
rs2105005	snp	A/G	0.154329	0.23097	intron-variant	CD2AP	GRCh38.p7	6:47494835	TATGTCTGAGTCTTA[A/G]CCCTTCATACGTGTA	23607
rs2151973	snp	A/C	0.243919	0.249926	intron-variant	CD2AP	GRCh38.p7	6:47523496	ATAAATCTTCATTGA[A/C]AATAAGTAAAAATAA	23607
rs2151974	snp	A/G	0.353154	0.227726	intron-variant	CD2AP	GRCh38.p7	6:47547894	aaaccatgcaaatac[A/G]tggaaattaaataac	23607
rs2151975	snp	C/T	0.357451	0.225731	intron-variant	CD2AP	GRCh38.p7	6:47547927	actcctgaatgatca[C/T]tgggtcagaaatgaa	23607
rs2151976	snp	A/G	0.499	0.0223418	intron-variant	CD2AP	GRCh38.p7	6:47547982	ttcttactgaacgac[A/G]atagtgacacacctt	23607
rs2151986	snp	G/T			intron-variant	CD2AP	GRCh38.p7	6:47491593	AGTAAACATTCTGTA[G/T]TCAATGCCCATACAA	23607
rs2152796	snp	C/T	0.110872	0.20771	utr-variant-3-prime	CD2AP	GRCh38.p7	6:47626566	AGTATCATTAATTTC[C/T]GAATTGTATTTCAGT	23607
rs2171086	snp	A/G	0.357664	0.225629	intron-variant	CD2AP	GRCh38.p7	6:47622368	tgtaacaatttgaac[A/G]gggcgagagacctcc	23607
rs2171087	snp	A/C			intron-variant	CD2AP	GRCh38.p7	6:47504922	agccttcagtgagtc[A/C]ccatctttttgctgg	23607
rs2171088	snp	C/T	0.430285	0.173197	intron-variant	CD2AP	GRCh38.p7	6:47535414	GCTATTAATAATTTT[C/T]ATAGAGTCCCCTTAT	23607
rs2171089	snp	A/G	0.305186	0.243833	intron-variant	CD2AP	GRCh38.p7	6:47548075	taaaagtcaacttaa[A/G]agttaaaagttgatg	23607
rs2171090	snp	A/C	0.0901694	0.192235	intron-variant	CD2AP	GRCh38.p7	6:47604899	CACACAAAGAAATTG[A/C]TAGAAAAAATTATCA	23607
rs2184398	snp	C/T	0.243633	0.249919	intron-variant	CD2AP	GRCh38.p7	6:47494879	TTAGAAATAGTTggc[C/T]gggcatggtggctca	23607
rs2184399	snp	C/G	0	0	intron-variant	CD2AP	GRCh38.p7	6:47494921	atctgagtactttgg[C/G]aggccaaattggagg	23607
rs2200440	snp	A/C			intron-variant	CD2AP	GRCh38.p7	6:47553539	acctctactaaaaat[A/C]caaaaaaaaaaaaaa	23607
rs2218356	snp	A/G	0.498982	0.0225409	intron-variant	CD2AP	GRCh38.p7	6:47556953	tggagaaatgggaac[A/G]cctgtacactgttca	23607
rs2275446	snp	A/G	0.498964	0.02274	intron-variant	CD2AP	GRCh38.p7	6:47582147	AAAATCAGTGTAAAT[A/G]ACTCAGTGTGGAGAA	23607
rs2396825	snp	A/G	0.353154	0.227726	intron-variant	CD2AP	GRCh38.p7	6:47600960	GGAGTCCCTTTGGGA[A/G]TTGAAGGAGTAAAAT	23607
rs2629902	snp	C/G	0	0	intron-variant	CD2AP	GRCh38.p7	6:47615002	TCTCTGAGATATGCA[C/G]AAAGAATAATGCAAA	23607
rs2629903	snp	G/T			intron-variant	CD2AP	GRCh38.p7	6:47566554	CAGGTTTGTTACATA[G/T]GTATAAGTGTGCCAT	23607
rs2790310	snp	A/C	0.00716837	0.0594373	intron-variant	CD2AP	GRCh38.p7	6:47588375	CTAATGCGTTACACA[A/C]TAGGTATATAATACA	23607
rs2790311	snp	C/G			intron-variant	CD2AP	GRCh38.p7	6:47614005	gctgcttcgtcacct[C/G]tgttgggccttcaaa	23607
rs2790312	snp	C/G			intron-variant	CD2AP	GRCh38.p7	6:47614091	tacagttggttagat[C/G]tgctatctagaccac	23607
rs2790313	snp	A/C			intron-variant	CD2AP	GRCh38.p7	6:47614098	ggttagatctgctat[A/C]tagaccactcaaact	23607
rs2790314	snp	C/T			intron-variant	CD2AP	GRCh38.p7	6:47614117	ACCACTCAAACTTTC[C/T]TTCATATCAACAATA	23607
rs2790315	snp	C/T			intron-variant	CD2AP	GRCh38.p7	6:47614271	ctgtggctttcaaca[C/T]tgccttcctctctga	23607
rs2894740	snp	A/G	0.38555	0.210062	intron-variant	CD2AP	GRCh38.p7	6:47614105	tctgctatctagacc[A/G]ctcaaactttccttc	23607
rs3756935	snp	A/G	0.000681556	0.0184476	intron-variant	CD2AP	GRCh38.p7	6:47503260	GATTTTAGACATTTC[A/G]TTTTTTCCCCCTTTT	23607
rs3756936	snp	A/G	0.000399281	0.0141238	intron-variant	CD2AP	GRCh38.p7	6:47503557	TGTTTTCTTTGTAAC[A/G]TTTAAGAAAATAGAG	23607
rs3818866	snp	C/T	0.237882	0.249706	intron-variant	CD2AP	GRCh38.p7	6:47581893	CATCAGATGAAACCA[C/T]GGTTTAATAGAAAGA	23607
rs3818867	snp	C/T	0.00318978	0.0398085	intron-variant	CD2AP	GRCh38.p7	6:47581885	GAAACCATGGTTTAA[C/T]AGAAAGAACAATGTA	23607
rs4142970	snp	C/T	0.244205	0.249933	intron-variant	CD2AP	GRCh38.p7	6:47623579	ACTTAATGAAATGAT[C/T]TCCTTCTTCATAAAT	23607
rs4142971	snp	A/C	0.430285	0.173197	intron-variant	CD2AP	GRCh38.p7	6:47623442	AAGCCCTAAATCTTA[A/C]CATGACAAGTCCTGT	23607
rs4495268	snp	A/G	0.389152	0.207694	intron-variant	CD2AP	GRCh38.p7	6:47550735	tagttgcacacacat[A/G]tttatagcagcacag	23607
rs4502933	snp	A/G	0.428182	0.17536	intron-variant	CD2AP	GRCh38.p7	6:47585016	aataaattggaggcc[A/G]ggcgcggtgtcttac	23607
rs4565293	snp	A/G	0.406986	0.194565	intron-variant	CD2AP	GRCh38.p7	6:47504869	AATGTGGATACATTA[A/G]TTTTAAAATATTGGT	23607
rs4601128	snp	C/T	0.0134861	0.0810011	intron-variant	CD2AP	GRCh38.p7	6:47508170	gaagctaggctttga[C/T]ttctttctacttatg	23607
rs4632893	snp	A/G	0.108755	0.206276	intron-variant	CD2AP	GRCh38.p7	6:47508604	agggtggagtgcaat[A/G]gcacgattttggctc	23607
rs4711878	snp	A/G	0.357451	0.225731	intron-variant	CD2AP	GRCh38.p7	6:47488382	ATACTGAGTTGTTAC[A/G]TATGTGTAATTTTAA	23607
rs4711879	snp	C/T	0.108755	0.206276	intron-variant	CD2AP	GRCh38.p7	6:47500823	acaatcttggctcac[C/T]gcaacctccgcctcc	23607
rs4711880	snp	A/G	0.305436	0.243776	intron-variant	CD2AP	GRCh38.p7	6:47512940	GAGATTTCAACATGG[A/G]TACATAATGTAGTTG	23607
rs4711881	snp	A/G	0.497613	0.0344622	intron-variant	CD2AP	GRCh38.p7	6:47525710	TAGATATACCCTTTA[A/G]CTTCCCCCACCATTT	23607
rs4711882	snp	A/G	0.497641	0.0342639	intron-variant	CD2AP	GRCh38.p7	6:47535567	GATTTTATGACACTT[A/G]GACCAATTCTAGGGT	23607
rs4711883	snp	C/T	0.108402	0.206034	intron-variant	CD2AP	GRCh38.p7	6:47558681	tgaagctgacttgat[C/T]gtggtggataagctt	23607
rs4711884	snp	A/G	0.498982	0.0225409	intron-variant	CD2AP	GRCh38.p7	6:47572754	CCTTTGTCCAAGTTT[A/G]TTTATTTGTAAAATG	23607
rs4711885	snp	A/T	0.0170251	0.090679	intron-variant	CD2AP	GRCh38.p7	6:47587771	TCTTATAAAATCACT[A/T]AAATGGTAACTTTTA	23607
rs4711886	snp	A/C	0.499344	0.0250194	intron-variant	CD2AP	GRCh38.p7	6:47587809	TCCTCCTCACTTCCT[A/C]TACACACATACACAG	23607
rs4715019	snp	A/T	0.306182	0.243605	intron-variant	CD2AP	GRCh38.p7	6:47479305	AATAATTCATGTAAT[A/T]AACAAATGATTTAGA	23607
rs4715020	snp	A/T	0.0170251	0.090679	intron-variant	CD2AP	GRCh38.p7	6:47479674	TAATACTAAAGTTAA[A/T]TACACAGTTCTTTTC	23607
rs4715021	snp	A/G	0.497641	0.0342639	intron-variant	CD2AP	GRCh38.p7	6:47480151	TAGAATGTGTTTTGA[A/G]GGTATGTTACTGAGG	23607
rs4715022	snp	A/G	0.497641	0.0342639	intron-variant	CD2AP	GRCh38.p7	6:47488329	TATAAAATCTTTAAG[A/G]TAGGTGTTGTGAAGC	23607
rs4715024	snp	C/T	0.000399281	0.0141238	intron-variant	CD2AP	GRCh38.p7	6:47498201	gtgaaaatgtTATAT[C/T]CTATGCTTGCCTGCT	23607
rs4715025	snp	C/G	0.305436	0.243776	intron-variant	CD2AP	GRCh38.p7	6:47515917	AAGGAAATTCAAAGA[C/G]TAAAGATGGAATGCA	23607
rs4715026	snp	C/T	0.108755	0.206276	intron-variant	CD2AP	GRCh38.p7	6:47517108	tcacttgggatctgg[C/T]tatttaaaagagttt	23607
rs4715027	snp	C/T	0.498982	0.0225409	intron-variant	CD2AP	GRCh38.p7	6:47532420	acacacacacacaca[C/T]aATACTTGCCATATC	23607

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