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
rs12558	snp	A/C/T	1.65721e-05	0.0028785	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423397	CTCTGCCCGAGCCTT[A/C/T]TAGGCTCAGATCCCA	79004
rs1044476	snp	C/T	0.188828	0.242401	synonymous-codon	CUEDC2	GRCh38.p7	10:102424324	GCCCCTGCAGCGGCC[C/T]GAAATGCTCAAAGAA	79004
rs1409312	snp	A/G	0.217851	0.247924	intron-variant	CUEDC2	GRCh38.p7	10:102432043	GCTTCACAGGGGCTG[A/G]GAGAAGCAGTGAAGA	79004
rs1409313	snp	A/G	0.21725	0.247846	intron-variant	CUEDC2	GRCh38.p7	10:102431844	GTCCACAGTGTCTCT[A/G]TCTAGCATCTGGAGG	79004
rs1572530	snp	C/T	0.438666	0.164028	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434077	AGCATAGTATCTTGG[C/T]ACTGCCTTAGTCCCT	79004
rs1572531	snp	A/G	0.198324	0.244601	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433976	CCCAGCACCCCACGA[A/G]GGAACTAGCACTAAA	79004
rs2902543	snp	A/C	0.00993419	0.0697739	intron-variant	CUEDC2	GRCh38.p7	10:102427676	ctcttgcctgcaaga[A/C]cttcctaacccttct	79004
rs3210927	snp	C/T	0.00865784	0.0652224	synonymous-codon	CUEDC2	GRCh38.p7	10:102423806	GCTGAAGTCCTTCAT[C/T]CTGCAGAAGTACATG	79004
rs3837341	in-del	-/C			intron-variant	CUEDC2	GRCh38.p7	10:102432428	CACGGTACCCCCCCC[-/C]GGGGCCCGTCGGACC	79004
rs6584498	snp	A/G	0.00993419	0.0697739	intron-variant	CUEDC2	GRCh38.p7	10:102428478	GAGCACCTAGCCAGC[A/G]CGGGCATTTTTCTAG	79004
rs6584499	snp	G/T	0.419616	0.183658	intron-variant	CUEDC2	GRCh38.p7	10:102428502	TTTCTAGGTGCTAGG[G/T]TACACAAACTATTTC	79004
rs7074566	snp	A/G	0.0345262	0.126772	intron-variant	CUEDC2	GRCh38.p7	10:102430047	tcaggtgatctgccc[A/G]ccttggcctcccaaa	79004
rs7081280	snp	G/T	0.00358779	0.0422022	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432731	TATGGACGGGCTCCC[G/T]TGGCGGCCAGTTTTG	79004
rs7894593	snp	A/G	0.109108	0.206518	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434324	AGGCTGCAGTAAGCC[A/G]TGATTGTGCTACTGC	79004
rs7921010	snp	G/T	0.318174	0.240525	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433069	tagctgggattacag[G/T]cgcgcgccaccacgc	79004
rs9665587	snp	A/C	0.438946	0.163706	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432810	TCGAAGTGGGTAGGA[A/C]TGCATCCCCGTCTTG	79004
rs10654228	in-del	-/T/TT	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102430144	TCTTTTTTTTTTTTT[-/T/TT]AATTTTATTTATTTA	79004
rs11352968	in-del	-/A	0.425894	0.177655	intron-variant	CUEDC2	GRCh38.p7	10:102429022	GTGAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAA	79004
rs11398443	in-del	-/CCT/T	0.499121	0.020948	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432910	CTCTCTCTCTCTCAC[-/CCT/T]TTTTTTTTCCTTTTC	79004
rs11440410	in-del	-/C	0.222035	0.248431	intron-variant	CUEDC2	GRCh38.p7	10:102430646	ACATCCTCCCTCCCT[-/C]CCTCCTGTTTTTGGT	79004
rs11550025	snp	C/T	0.000415769	0.0144122	missense	CUEDC2	GRCh38.p7	10:102424286	GGTCTTCGGCTGCTG[C/T]TGCTGCAGACACCCA	79004
rs11592718	snp	C/T	0.283158	0.247791	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432934	CCTTTTCTTCTTCTT[C/T]TTTTTTTTTGGGAGG	79004
rs11593146	snp	A/G	0.450022	0.149989	intron-variant	CUEDC2	GRCh38.p7	10:102425224	ACAGACAGGATGGCC[A/G]GGCCTTCTTCTGCCT	79004
rs11594302	snp	A/G	0.190205	0.242744	intron-variant	CUEDC2	GRCh38.p7	10:102427072	gatctacaaaaaaaa[A/G]ggggggaatttctca	79004
rs11595402	snp	A/G	0.5	0	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434396	AAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAAAGA	79004
rs11597439	snp	C/G	0.450872	0.14883	utr-variant-5-prime	CUEDC2	GRCh38.p7	10:102425196	AGCTCCATGCTCTCT[C/G]TTCTGAAGGGACACA	79004
rs12360467	snp	C/G			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434038	TCACAGTCCAAGAGA[C/G]AAGTCCCATCTTTCC	79004
rs12415921	snp	G/T	0.196149	0.244131	intron-variant	CUEDC2	GRCh38.p7	10:102432012	AGGGAGGCAGCAAGG[G/T]GTCTAGCATGGAAGG	79004
rs12569389	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102428806	agggggttggatcac[C/G]aggtcaggagatcaa	79004
rs12778231	snp	C/T	0.237905	0.249707	intron-variant	CUEDC2	GRCh38.p7	10:102424432	CAGGTTTGCCAAGGC[C/T]CTGGGGAGCAGGCAG	79004
rs17855346	snp	A/C			stop-gained	CUEDC2	GRCh38.p7	10:102423695	GAATCTTCTGATCCT[A/C]TGCGCTATCCACCAT	79004
rs28686884	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430254	GCTCACCGCAACCTC[A/C]ACCTCCTGGGTTCAA	79004
rs34608648	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102429997	TAGAGACGGGGTTTC[A/C]CCATGTTGGCCAGGC	79004
rs35950389	in-del	-/C			intron-variant	CUEDC2	GRCh38.p7	10:102430766	CTAATACTTCTCCCC[-/C]GCATAGCCCCTGAGT	79004
rs41287462	snp	A/G	0.36075	0.22413	intron-variant	CUEDC2	GRCh38.p7	10:102424456	CAGGCAGTTGGGGGA[A/G]CGGGATTATGAATCA	79004
rs55659266	in-del	-/T	0.114036	0.209795	intron-variant	CUEDC2	GRCh38.p7	10:102429822	AGCCCAGTTTCTTTC[-/T]TTTTTTTTTTTTTTG	79004
rs55824105	in-del	-/A			intron-variant	CUEDC2	GRCh38.p7	10:102429037	AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAATATT	79004
rs57965979	in-del	-/AAAAA	0	0	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434398	AAAAAAAAAAAAAAA[-/AAAAA]GAAGAAGAAAAGAAG	79004
rs59973108	in-del	-/G			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434396	AAAAAAAAAAAAAAA[-/G]AAGAAGAAGAAAAGA	79004
rs60025237	snp	C/G/T	0.0017033	0.0291338	downstream-variant-500B, synonymous-codon, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422808	TCCTCCCTCAGGACA[C/G/T]TGGCCGAGTACTGCC	79004
rs60312809	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434147	TGAGGTGGGAGGATC[A/G]CTTGAGCCCAGGAAT	79004
rs61031688	in-del	-/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433471	TTTTTTTTTTTTTTT[-/T]GTAGAGACAGGGTTT	79004
rs61873665	snp	A/G	0.109461	0.206758	intron-variant	CUEDC2	GRCh38.p7	10:102430095	ATGAGCCACCTGTGT[A/G]GTGGTGACTGAAACT	79004
rs71016379	in-del	-/T	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102429037	AATATTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	79004
rs71016380	in-del	-/TAAA	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102430167	AGTAAAATAAATAAA[-/TAAA]TAAATAAATAAATAA	79004
rs71948033	in-del	-/TTTA			intron-variant	CUEDC2	GRCh38.p7	10:102430168	TATTTATTTATTTAT[-/TTTA]TTATTTATTTTACTT	79004
rs72845696	snp	C/T	0.28578	0.247426	intron-variant	CUEDC2	GRCh38.p7	10:102427647	TCTCCATCTCTACTC[C/T]CACTTTTCTCCATCT	79004
rs74608233	snp	A/C	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102429023	TGAGACTTTGTCTCA[A/C]AAAAAAAAAAAAAAG	79004
rs75659956	in-del	-/C	0.0603597	0.1629	intron-variant	CUEDC2	GRCh38.p7	10:102432014	GAGGCAGCAAGGGGT[-/C]CTAGCATGGAAGGTC	79004
rs76297957	snp	C/G	0.0248432	0.108648	intron-variant	CUEDC2	GRCh38.p7	10:102426407	TCATAGACTACTGAT[C/G]TGCGCACATCCCCCT	79004
rs76691226	snp	G/T	0.5	0	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433984	TAGTTCCTTCGTGGG[G/T]TGCTGGGGACCCGGA	79004
rs76802044	snp	G/T	0.5	0	intron-variant	CUEDC2	GRCh38.p7	10:102429834	TTCTTTTTTTTTTTT[G/T]TTGAGACGGAGTTTC	79004
rs77579852	snp	C/G	0.0248432	0.108648	intron-variant	CUEDC2	GRCh38.p7	10:102425637	AAGCACAGCCCTTCC[C/G]CCACCCAGAACAGGC	79004
rs78678650	snp	A/G	0.0991586	0.199366	intron-variant	CUEDC2	GRCh38.p7	10:102430767	CTAATACTTCTCCCC[A/G]CATAGCCCCTGAGTT	79004
rs79317042	snp	A/C	0	0	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434374	AGCAAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA	79004
rs80152299	snp	A/G	0.030665	0.119967	intron-variant	CUEDC2	GRCh38.p7	10:102430746	ATCCTTCCTGCTCAG[A/G]GGCTCCTAATACTTC	79004
rs80160917	snp	A/G	0.0310518	0.120672	intron-variant	CUEDC2	GRCh38.p7	10:102431856	AGATAGAGACACTGT[A/G]GACAAATTTAAGTGA	79004
rs111910906	snp	C/G/T	0	0	splice-acceptor-variant	CUEDC2	GRCh38.p7	10:102423718	TCCACCATCATGTAC[C/G/T]TGTCAAAAACTGGCT	79004
rs112673733	snp	G/T	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102430208	AGTTTCACTCTTGTT[G/T]CCCAGGCTAGAGTGC	79004
rs114399613	snp	C/T	0.0248432	0.108648	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433847	ATTCCCGGTGCTGCC[C/T]TGTGGGGAAGCCCCA	79004
rs114489414	snp	C/T	0.00755907	0.0610114	intron-variant	CUEDC2	GRCh38.p7	10:102432051	GCTTCTCCCAGCCCC[C/T]GTGAAGCCCGGTTCC	79004
rs114914917	snp	A/T	0.0248432	0.108648	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433495	AGGGTTTTTGCCACG[A/T]GGCCCAGGCTGGTCT	79004
rs117106761	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430458	ATAGGCGTGAGCCAC[C/T]GTGCCCGGCCTGAGA	79004
rs117107179	snp	C/T	0.00199481	0.0315187	intron-variant	CUEDC2	GRCh38.p7	10:102425937	CCTGCGGGACATCCA[C/T]GGCTCGTCCAGTCAC	79004
rs117878070	snp	A/T	0.013466	0.0809424	intron-variant, utr-variant-3-prime	CUEDC2, FBXL15	GRCh38.p7	10:102423004	TCTGACCCGCCTGCC[A/T]ATCGGAGCACAGCTG	79004
rs138190749	snp	C/T	6.62427e-05	0.00575473	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423632	CCACCCATTCCGCAT[C/T]CCCAGCAACCCTTAA	79004
rs138763107	snp	A/G	0.0107246	0.0724382	intron-variant	CUEDC2	GRCh38.p7	10:102426953	CAGCCATGAGTCACC[A/G]TGCCCGGCCTCAAAA	79004
rs138779369	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433366	GGCTCACTGCAGCCC[C/T]GACCTCCTGGGTTCA	79004
rs139005407	snp	C/T	0.0023933	0.0345097	intron-variant	CUEDC2	GRCh38.p7	10:102428767	GGAGGCTCATGCCTG[C/T]AATCCCAGCACTTTG	79004
rs139747085	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102429741	GGGTTACATCACCCT[C/T]GAATCCTGGGCTGTC	79004
rs140083599	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430943	AGAGATCATTGGTTG[A/G]TGGTGTCTACCAAAT	79004
rs140462766	snp	A/C	0.00517822	0.0506191	intron-variant	CUEDC2	GRCh38.p7	10:102431343	GAGACGGGGTTTCAC[A/C]ATGTTGGCCAGACTG	79004
rs141067478	snp	G/T	0.000102513	0.00715862	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422865	CACTGCCACCATGTG[G/T]CGGAGTCCAGCCTGA	79004
rs141182150	snp	C/G	0.00597247	0.0543191	intron-variant	CUEDC2	GRCh38.p7	10:102428333	ATCATCTGAGTGGGA[C/G]AATGAGCTGCCATTT	79004
rs141221578	in-del	-/CTTT			intron-variant	CUEDC2	GRCh38.p7	10:102427191	ATTTCTTCGAAGGCC[-/CTTT]CTTTCTCTGTCCCCT	79004
rs142262811	snp	A/G	0.00279162	0.0372561	intron-variant	CUEDC2	GRCh38.p7	10:102432207	AGCACAAACAGGGAG[A/G]GCGAGCACAGGAAGT	79004
rs142302379	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431191	GCCATCCAGGCTGGA[A/G]TGCAGTGGTGCGATC	79004
rs142869292	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430249	TCTTGGCTCACCGCA[A/C]CCTCCACCTCCTGGG	79004
rs143090336	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430211	TTCACTCTTGTTGCC[A/C]AGGCTAGAGTGCAAT	79004
rs143479353	snp	A/C	0.0134861	0.0810011	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434511	TCCTTCCTCTTCTGG[A/C]CTCAGAGACAGCAAG	79004
rs143589722	snp	A/G	0.00352149	0.0418132	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423628	AGTCCCACCCATTCC[A/G]CATCCCCAGCAACCC	79004
rs143655912	snp	C/G	0.00165683	0.0287345	intron-variant	CUEDC2	GRCh38.p7	10:102424594	TGAGAGGATGACTCT[C/G]CCCACCCCATAATCA	79004
rs144013189	in-del	-/CT			intron-variant	CUEDC2	GRCh38.p7	10:102427273	CTTCTCACTGCAGCG[-/CT]CTCTCTCTCTCTGGA	79004
rs144450686	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102429944	GCTGGGATTACAGGC[A/G]CCTGCCACAACGCCC	79004
rs145290548	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430180	TTATTTATTTATTTT[A/C]CTTTTGAGACAGAGT	79004
rs145311924	in-del	-/G			downstream-variant-500B, frameshift-variant	CUEDC2, FBXL15	GRCh38.p7	10:102422959	GCTGCAGGATATGGC[-/G]GGGCTTCGCACCTTT	79004
rs145688904	snp	A/G	4.71242e-05	0.00485385	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422904	CGGAAGCGCGGCGTG[A/G]ACATCGACGTGGAGC	79004
rs145943166	snp	A/C	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426514	TTTGCCCTCTTTCAC[A/C]CCTACCAGTCAATCA	79004
rs146403832	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429701	CCTCAGGGTAGAACC[A/G]CCTCCAGGGACCTAC	79004
rs147214320	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430212	TCACTCTTGTTGCCC[A/C]GGCTAGAGTGCAATG	79004
rs147652970	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102432076	GGTTCCTGAGGCCCT[A/G]GACCCATAACGCAGG	79004
rs148003733	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434549	CTGCTTGGGGGAGGT[A/G]GCAGGGAAGGAAGGG	79004
rs148221748	in-del	-/ATTTT	0.039522	0.134904	intron-variant	CUEDC2	GRCh38.p7	10:102431121	ACTGTTATTCTCCCC[-/ATTTT]ATTTTATTTATTTTA	79004
rs148855837	snp	C/T	0.0115144	0.0749975	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434323	AAGGCTGCAGTAAGC[C/T]GTGATTGTGCTACTG	79004
rs148904455	snp	A/G	0.000976845	0.0220787	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423419	CGGGCAGAGTCCGGC[A/G]AGTGCCTCAATGGAA	79004
rs149435454	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429612	ATTCATACCACCTGC[A/G]CCAGAGCCCTCATGG	79004
rs149977211	snp	G/T	0.00478085	0.0486577	intron-variant	CUEDC2	GRCh38.p7	10:102431380	AACTCCTGACCTCAG[G/T]CAATCCACCCGCCTC	79004
rs150719622	snp	A/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428400	ATGCTCCTGACTCCC[A/T]AACAGACTTTTGGGA	79004
rs151012832	snp	C/G	0.000153988	0.00877328	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422824	TGGCCGAGTACTGCC[C/G]CGTGCTGCGTTCGCT	79004
rs151254319	snp	C/G	0.00279162	0.0372561	intron-variant	CUEDC2	GRCh38.p7	10:102431298	TCGCATGCCACCATG[C/G]CTGGCAAATTTATTT	79004

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