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
rs1686	snp	C/T	0.262435	0.249691	intron-variant	CADPS2	GRCh38.p7	7:122729799	ATGGCATGAGTTGCA[C/T]CAACATAATCAGCTC	93664
rs16458	in-del	-/TTCC	0.494442	0.0524218	intron-variant	CADPS2	GRCh38.p7	7:122511273	CTCAAAGTTTTACAA[-/TTCC]ATTCCTTCATTTCCA	93664
rs37888	snp	A/T	0.49681	0.0398085	intron-variant	CADPS2	GRCh38.p7	7:122804099	TCAGTCAGGAACCAG[A/T]GATAAGAGAGCAGTG	93664
rs37889	snp	A/G	0.49681	0.0398085	intron-variant	CADPS2	GRCh38.p7	7:122804082	ATAAGAGAGCAGTGT[A/G]GTAGCTGGGAATGAG	93664
rs37890	snp	G/T	0.5	0	intron-variant	CADPS2	GRCh38.p7	7:122803994	GCTTTGCAGTGTTTT[G/T]TTTTTTTTTTTTTTT	93664
rs37891	snp	A/G	0	0	intron-variant	CADPS2	GRCh38.p7	7:122802504	TAGGGTGTATTATGG[A/G]CCTGTATGTGCTTGC	93664
rs37892	snp	A/G	0.497387	0.0360476	intron-variant	CADPS2	GRCh38.p7	7:122797905	GAGTTAAAATCATAC[A/G]TTCATATGATGAAAT	93664
rs37893	snp	A/G	0.496714	0.0404017	intron-variant	CADPS2	GRCh38.p7	7:122793834	gcaaatgctaaggga[A/G]tccattaccaccaga	93664
rs37894	snp	C/T	0.3512	0.228601	intron-variant	CADPS2	GRCh38.p7	7:122793721	tacatagaccagtga[C/T]gctatgaagcaacca	93664
rs37895	snp	A/C	0.496746	0.040204	intron-variant	CADPS2	GRCh38.p7	7:122793367	attacataattgtta[A/C]agggctcaattcagc	93664
rs37896	snp	A/G	0.497359	0.0362457	intron-variant	CADPS2	GRCh38.p7	7:122792461	GTCCAAGGTCAAGGT[A/G]CTGAAGATTTCACCT	93664
rs37897	snp	G/T	0.497241	0.037038	intron-variant	CADPS2	GRCh38.p7	7:122790367	CTGTCCCCTTGGCTG[G/T]CATGCAGTGACGCAA	93664
rs37898	snp	A/G	0.110167	0.207236	intron-variant	CADPS2	GRCh38.p7	7:122789296	ATAGGATAGGAAGGC[A/G]GTAAGCTTCCTTTCT	93664
rs37899	snp	A/G	0.496905	0.0392151	intron-variant	CADPS2	GRCh38.p7	7:122788328	CATTTCTTTGTGTCA[A/G]AGTAACTTAGATCCT	93664
rs37900	snp	C/T	0.496968	0.0388195	intron-variant	CADPS2	GRCh38.p7	7:122778855	tcattccacccctgg[C/T]ccctcccaagtttca	93664
rs37901	snp	A/G	0.351853	0.228311	intron-variant	CADPS2	GRCh38.p7	7:122777523	ttgggtggggacata[A/G]ccaaactgtatcaGT	93664
rs37902	snp	A/C	0.333261	0.235728	intron-variant	CADPS2	GRCh38.p7	7:122777032	tcgtgagtagctggg[A/C]ctacaggcacacact	93664
rs37903	snp	C/T	0.348794	0.229651	intron-variant	CADPS2	GRCh38.p7	7:122771569	CTACTTATTGCACAT[C/T]ATTTCAATTAATTTC	93664
rs37904	snp	A/G	0.49655	0.04139	intron-variant	CADPS2	GRCh38.p7	7:122771306	TTCCTCATTGCTACC[A/G]GAGTGTTCTCTCTGA	93664
rs37905	snp	G/T	0.331874	0.236213	intron-variant	CADPS2	GRCh38.p7	7:122768393	TTTTGAAACAAAGTA[G/T]GAATACTTTAAAAAT	93664
rs37906	snp	A/G	0.375	0.216506	intron-variant	CADPS2	GRCh38.p7	7:122762031	tgtgtgtgtgtgtgt[A/G]tatatatatatatat	93664
rs37907	snp	A/T			intron-variant	CADPS2	GRCh38.p7	7:122762013	tatatatatatatat[A/T]ttttttttttttttt	93664
rs37908	snp	C/T	0.496483	0.0417852	intron-variant	CADPS2	GRCh38.p7	7:122752843	CGAGGAAAATTATTA[C/T]TTGATGCGTCCTATT	93664
rs37909	snp	A/G	0.349013	0.229557	intron-variant	CADPS2	GRCh38.p7	7:122751131	CAAAGAGAAATGCCT[A/G]TATCTTAAAATATGA	93664
rs37910	snp	C/T	0.348134	0.229934	intron-variant	CADPS2	GRCh38.p7	7:122751042	GCCTGATTTAAAAAT[C/T]GGTTTGAGTTTTATC	93664
rs37911	snp	A/G	0.333491	0.235646	intron-variant	CADPS2	GRCh38.p7	7:122749248	CTTGATTGGTCAGTC[A/G]TGATATTCCATTTCC	93664
rs37912	snp	C/T	0.0869089	0.189476	intron-variant	CADPS2	GRCh38.p7	7:122740447	tatgtagccttttta[C/T]attggctgcttttac	93664
rs37913	snp	G/T	0.497881	0.0324789	intron-variant	CADPS2	GRCh38.p7	7:122740150	ctgttttacaaagta[G/T]ctataccattttgct	93664
rs37914	snp	A/T	0.497907	0.0322805	intron-variant	CADPS2	GRCh38.p7	7:122739569	CCAGGTGACTCTGGC[A/T]TATTTTGTGAACTAT	93664
rs40364	snp	C/T	0.496999	0.0386216	intron-variant	CADPS2	GRCh38.p7	7:122778569	ggtcactgggccagg[C/T]ccacaaaaccatttt	93664
rs702418	snp	A/G	0.484701	0.0861117	intron-variant	CADPS2	GRCh38.p7	7:122342052	AAAGTATCCTTTGAG[A/G]GTCACAAAAGCTAAC	93664
rs702419	snp	A/G	0.231775	0.249335	intron-variant	CADPS2	GRCh38.p7	7:122342149	TATGAGAGAGGAAAT[A/G]AATAAAATCTGCATT	93664
rs702420	snp	C/G	0.231775	0.249335	intron-variant	CADPS2	GRCh38.p7	7:122342749	GCAAGTGAAAACATG[C/G]TTACACACACATTAT	93664
rs702421	snp	C/T	0.348354	0.22984	intron-variant	CADPS2	GRCh38.p7	7:122352935	TTACTCCCTAGTTCC[C/T]GCTCACTACTTAAGA	93664
rs715205	snp	A/G	0.0722614	0.17581	intron-variant	CADPS2	GRCh38.p7	7:122761492	AAAGTGTGCATACAA[A/G]CAAGGATTGTCTGAG	93664
rs718764	snp	A/C	0.385359	0.210185	intron-variant	CADPS2	GRCh38.p7	7:122506983	CTGTGGAATTTTAAA[A/C]ACTGCCTGGTACATG	93664
rs718765	snp	C/T	0.384593	0.210677	intron-variant	CADPS2	GRCh38.p7	7:122506765	TTTCATGATTAAATT[C/T]AGCTCTGGTGTAGTT	93664
rs720941	snp	A/G	0.0182019	0.0936463	intron-variant	CADPS2	GRCh38.p7	7:122852115	AAAATGTTTAACTTC[A/G]TTTTTAATAGAAAAA	93664
rs740812	snp	A/G	0.466308	0.125343	intron-variant	CADPS2, LOC105375481	GRCh38.p7	7:122546920	AGCCTATCTAAATGT[A/G]AAAAAAAAGTGTACA	93664
rs740813	snp	A/G	0.384017	0.211044	intron-variant	CADPS2, LOC105375481	GRCh38.p7	7:122547141	CTTACAAATTAAAAC[A/G]TATTAACCCTGGGGT	93664
rs757428	snp	A/G	0.441568	0.160629	intron-variant	CADPS2	GRCh38.p7	7:122384034	GAATCCTCATTATCC[A/G]TAACTGCACAAAAGC	93664
rs763877	snp	C/T	0.0170251	0.090679	intron-variant	CADPS2	GRCh38.p7	7:122682384	CACATTGAATGAAGG[C/T]GGAAGAGATGGCTTA	93664
rs764510	snp	A/G	0	0	intron-variant	CADPS2	GRCh38.p7	7:122381787	AGAAAATGAGAATGA[A/G]TGAACAAAAACAAAC	93664
rs798677	snp	C/T	0.0107246	0.0724382	intron-variant	CADPS2	GRCh38.p7	7:122350225	ATTTCGAAGACATGT[C/T]ATTTATTGTCTTATA	93664
rs798678	snp	C/T	0.395635	0.2032	intron-variant	CADPS2	GRCh38.p7	7:122350127	AGCAGATAATCATAA[C/T]GCAGGATATTACACT	93664
rs798679	snp	A/G	0.48435	0.0870631	intron-variant	CADPS2	GRCh38.p7	7:122349744	TTCTCTTTAAACAGC[A/G]TGTTCATCTTACTAG	93664
rs798680	snp	A/G	0.269267	0.249256	intron-variant	CADPS2	GRCh38.p7	7:122349668	CCCTTTCTTAAATTC[A/G]TTCACTCACTGATGT	93664
rs798681	snp	A/G	0.48491	0.0855403	intron-variant	CADPS2	GRCh38.p7	7:122348350	AAACTGTAAAGTGTT[A/G]GTTTCAGGTGGTGGA	93664
rs798682	snp	G/T	0.231482	0.249313	intron-variant	CADPS2	GRCh38.p7	7:122347104	AAAGGTTATAAATGC[G/T]TTCTGTGAATACGAA	93664
rs798683	snp	A/T	0.0115144	0.0749975	intron-variant	CADPS2	GRCh38.p7	7:122346996	ATAGATCTACCTATC[A/T]AATTGGTAGCAGATC	93664
rs798684	snp	C/G	0.219648	0.248151	intron-variant	CADPS2	GRCh38.p7	7:122345502	AGTTGAATTTTGATG[C/G]TATGTTTGCAAAGCA	93664
rs798685	snp	A/G	0.309154	0.242901	intron-variant	CADPS2	GRCh38.p7	7:122345487	GTATGTTTGCAAAGC[A/G]TAGTCTCCTTTTTGT	93664
rs798686	snp	C/T	0.484279	0.0872533	intron-variant	CADPS2	GRCh38.p7	7:122345220	AAGAATCGCTTGAGC[C/T]GGGAAGGCAGAGGTT	93664
rs798687	snp	A/G	0.375399	0.216275	intron-variant	CADPS2	GRCh38.p7	7:122361190	GGGAAAGAAAAGGAC[A/G]GTAGAGTTCATGTTC	93664
rs798688	snp	C/T	0.00716266	0.059414	intron-variant	CADPS2	GRCh38.p7	7:122359360	AAAGATTCACTTGGG[C/T]GCTGTTTAATTATTT	93664
rs798689	snp	C/T	0.485933	0.0826777	intron-variant	CADPS2	GRCh38.p7	7:122359155	ATTCACAGGCATATG[C/T]TGTCTGAGGAACGCT	93664
rs798690	snp	A/G	0.486398	0.0813386	intron-variant	CADPS2	GRCh38.p7	7:122354752	GAGAAAGAAAAAGCA[A/G]GACCTGGACTAGGTG	93664
rs798691	snp	A/C	0.0123036	0.0774623	intron-variant	CADPS2	GRCh38.p7	7:122354579	TAACCCCTCCCCCCC[A/C]AAAAAAAAGTTTTGC	93664
rs798692	snp	A/G	0.486332	0.08153	intron-variant	CADPS2	GRCh38.p7	7:122353468	AAGACCAAAACAATG[A/G]GGAAGGAAGAAGAAA	93664
rs798693	snp	C/T	0.368324	0.220226	intron-variant	CADPS2	GRCh38.p7	7:122353404	CCTGATCTTGGTGGT[C/T]TGTCCTAAGATAAAG	93664
rs798694	snp	A/G	0.486398	0.0813386	intron-variant	CADPS2	GRCh38.p7	7:122353246	CACAGACTTGATATG[A/G]GGTCGAGGATCTCCG	93664
rs798695	snp	A/C	0.486464	0.0811471	intron-variant	CADPS2	GRCh38.p7	7:122352235	ATAAGTAGCAATCAT[A/C]ATGATGATGGTTTTA	93664
rs873376	snp	C/G	0.133777	0.221342	intron-variant	CADPS2	GRCh38.p7	7:122343665	GCCATTCTATAAGTA[C/G]ACCATCATAGATAGA	93664
rs873377	snp	A/T	0.212728	0.247206	intron-variant	CADPS2	GRCh38.p7	7:122343653	GTAGACCATCATAGA[A/T]AGATTTGTCAAGGGG	93664
rs873378	snp	C/T	0.212728	0.247206	intron-variant	CADPS2	GRCh38.p7	7:122343463	CTTTCTATGTGGCAA[C/T]GATAACAGACAGAGG	93664
rs886497	snp	A/C	0.266273	0.24947	intron-variant	CADPS2	GRCh38.p7	7:122342855	AAAGATTGAAGAGAA[A/C]AATTTCATTCAGGCA	93664
rs916982	snp	A/G	0.480888	0.0958673	intron-variant	CADPS2	GRCh38.p7	7:122378105	TAATGATAAATGAAG[A/G]GTTTCGTAATATAGT	93664
rs920802	snp	A/G	0.443464	0.15834	intron-variant	CADPS2	GRCh38.p7	7:122330064	GGTGACAAAGAAAAG[A/G]AAAGAAAAAGAACCA	93664
rs920803	snp	A/C	0.32627	0.238082	intron-variant	CADPS2	GRCh38.p7	7:122330265	AAATGAAAGAACAAA[A/C]AATATTTGTTAAATG	93664
rs929295	snp	A/T	0.310632	0.242536	intron-variant	CADPS2	GRCh38.p7	7:122380705	CACTCATCATTATGC[A/T]CTTATATTCACACCC	93664
rs929506	snp	A/G	0.0908922	0.192833	intron-variant	CADPS2, LOC105375481	GRCh38.p7	7:122557709	TAGGTTTAGGAAGAA[A/G]GGCAACAAAACAACT	93664
rs929569	snp	A/G	0.498982	0.0225409	intron-variant	CADPS2	GRCh38.p7	7:122736264	AATATGCGAATATAT[A/G]TTAGACTAATAAACA	93664
rs961628	snp	C/T	0.488363	0.0753851	intron-variant	CADPS2	GRCh38.p7	7:122624357	TTAAAGAAGCAAATA[C/T]TGTTTTTGTGTATAC	93664
rs962335	snp	A/G	0.49655	0.04139	intron-variant	CADPS2	GRCh38.p7	7:122771248	ATTATAAATCCTTCA[A/G]TGACTTTCAACATTC	93664
rs966759	snp	C/T	0	0	intron-variant	CADPS2, LOC105375481	GRCh38.p7	7:122534598	TCCTAACTCAAGACC[C/T]TAATATTTAGAGTTT	93664
rs972621	snp	A/G	0.309401	0.24284	intron-variant	CADPS2	GRCh38.p7	7:122760348	ATATATCTGCTAAAC[A/G]TGAAAAATGAATTAG	93664
rs981321	snp	A/G	0.321769	0.239477	intron-variant	CADPS2	GRCh38.p7	7:122885275	ATGCTTTTTTGGGGA[A/G]CAAAATGCTTATTCT	93664
rs982272	snp	A/C	0.307919	0.243198	intron-variant	CADPS2	GRCh38.p7	7:122805497	ATCTGGACCTAAACT[A/C]TCTAAAATATAAGGG	93664
rs983521	snp	C/T	0.406986	0.194565	intron-variant	CADPS2	GRCh38.p7	7:122434362	TCTTCTATTAAGGGC[C/T]CTATTTCTTTCTTTT	93664
rs986997	snp	G/T	0.483126	0.0902898	intron-variant	CADPS2	GRCh38.p7	7:122669387	ATTTCAGTGTGTGGG[G/T]GTAGTAATTACTTTT	93664
rs986998	snp	A/T	0	0	intron-variant	CADPS2	GRCh38.p7	7:122669340	TATATATATATATAT[A/T]TTTTTTCTTTAGACA	93664
rs986999	snp	G/T	0.287346	0.247195	intron-variant	CADPS2	GRCh38.p7	7:122668971	CAAACAAAACAAAGT[G/T]GCTGCTGAGGTGCTT	93664
rs987000	snp	A/G	0.358515	0.225221	intron-variant	CADPS2	GRCh38.p7	7:122668938	CTTCTGTTTTGATGG[A/G]GGAATGGACAATAAA	93664
rs987227	snp	C/T	0.105214	0.203807	intron-variant	CADPS2	GRCh38.p7	7:122782245	TATCCCTCTTACTAA[C/T]GTGTTATTTTGTCCC	93664
rs990625	snp	C/T	0.308661	0.24302	intron-variant	CADPS2	GRCh38.p7	7:122832418	ACCACATTTTTCTTG[C/T]ACAGTTGATACAAGA	93664
rs995251	snp	A/G	0.203882	0.245709	intron-variant	CADPS2	GRCh38.p7	7:122524920	TCGGAAGGCTGAGGT[A/G]GGCGGATTGTTGAGC	93664
rs996797	snp	A/G	0.29789	0.24537	intron-variant	CADPS2	GRCh38.p7	7:122851515	GTTCATTAAGTCTTA[A/G]CTATTATTTTTAGTA	93664
rs1010496	snp	C/T	0.204496	0.245824	intron-variant	CADPS2	GRCh38.p7	7:122566894	TTAATTGGACATACA[C/T]TGTGAGTCAGAAACT	93664
rs1010497	snp	A/G	0.486595	0.0807641	intron-variant	CADPS2	GRCh38.p7	7:122567064	AAGAGATTGGATTAA[A/G]TGAGCTCCAGTGTCC	93664
rs1010498	snp	A/G	0.39979	0.200158	intron-variant	CADPS2	GRCh38.p7	7:122567133	TAGCCAGAAATAACA[A/G]TTAGTTTTGTTTCTT	93664
rs1017001	snp	A/G	0.491732	0.0637633	intron-variant	CADPS2	GRCh38.p7	7:122469208	TGTTTGAGACTCATT[A/G]TAATGGAAAGTTACT	93664
rs1023535	snp	G/T	0.299411	0.245069	intron-variant	CADPS2	GRCh38.p7	7:122845804	AATAACATGGACAAT[G/T]TATCAAGTTTTCCTG	93664
rs1120018	snp	A/G	0.371177	0.218669	intron-variant	CADPS2	GRCh38.p7	7:122665734	TGCTTATGATTTTTC[A/G]ACTTTACAATGGTAC	93664
rs1120019	snp	A/G	0.0170251	0.090679	intron-variant	CADPS2	GRCh38.p7	7:122665470	CAGGCTTATTAGGAC[A/G]TAACCTCATTGTAGT	93664
rs1154608	snp	C/T	0.48498	0.0853497	intron-variant	CADPS2	GRCh38.p7	7:122340328	GATTTACCAATTAAA[C/T]ATTGTACCCTGATGT	93664
rs1154609	snp	C/T	0.48498	0.0853497	intron-variant	CADPS2	GRCh38.p7	7:122340488	TCAGTCAACTCTCAA[C/T]TGCCTCCACATTTCA	93664
rs1154945	snp	A/G	0.384017	0.211044	intron-variant	CADPS2	GRCh38.p7	7:122332358	ATCCTTGGTTCTTCC[A/G]TAGTAGAACTCTATA	93664
rs1154947	snp	A/C	0.384209	0.210922	intron-variant	CADPS2	GRCh38.p7	7:122332637	CTTTCCTATCTTTGG[A/C]ATTCCATACTTCATC	93664
rs1159907	snp	C/T	0.0948562	0.196037	intron-variant	CADPS2	GRCh38.p7	7:122508944	TTATCCTACACTGAG[C/T]ATGTTCTGGGTTTGT	93664
rs1160020	snp	C/T	0.49168	0.063958	intron-variant	CADPS2	GRCh38.p7	7:122450422	TTAGTTCAACAGAAC[C/T]TAATAATTAAAAACA	93664

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