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
rs892752	snp	C/T	0.0923359	0.194016	intron-variant	TRIM4	GRCh38.p7	7:99899044	cttgaatggccccca[C/T]attcttatcacgtca	89122
rs1048705	snp	A/T	0.487684	0.0775019	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891317	CAGTGAGATGGAAAG[A/T]CAAATCCTATTTGTA	89122
rs1138665	snp	A/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99896239	ggaccatagggtcat[A/T]gttagggtatgcttg	89122
rs1865472	snp	A/T	0.436265	0.166749	intron-variant	TRIM4	GRCh38.p7	7:99913940	gtcttcattttatag[A/T]taaggaagccttgat	89122
rs2247761	snp	C/T	0.491465	0.0647671	synonymous-codon	TRIM4	GRCh38.p7	7:99903288	GGATGTGAACTATTC[C/T]CTTGAAGCTGTAAAG	89122
rs2247762	snp	A/G	0.484539	0.0865542	synonymous-codon	TRIM4	GRCh38.p7	7:99903276	TTCTCTTGAAGCTGT[A/G]AAGGTGAAGACAGTG	89122
rs2527909	snp	A/C	0.487684	0.0775019	intron-variant	TRIM4	GRCh38.p7	7:99914601	gggaaaggtggcatg[A/C]gatgtgaaacgagat	89122
rs2527911	snp	C/T	0.483636	0.0889627	intron-variant	TRIM4	GRCh38.p7	7:99906002	gtgtgccaccacacc[C/T]ggctaatttttctat	89122
rs2527912	snp	A/C	0.436408	0.16659	intron-variant	TRIM4	GRCh38.p7	7:99902419	tctctactaaaatac[A/C]aaaattagctgagca	89122
rs2527913	snp	A/T	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99902249	aaaaaacaaacaaac[A/T]aaaaagaaCCATGTT	89122
rs2527914	snp	C/T	0.483345	0.0897213	intron-variant	TRIM4	GRCh38.p7	7:99900522	GAAATGGTAATGACA[C/T]GAATAAATATATATT	89122
rs2527915	snp	G/T	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99900395	attttgggtgttttt[G/T]tgagggtgattttgg	89122
rs2527916	snp	A/T	0.499587	0.0143711	intron-variant	TRIM4	GRCh38.p7	7:99900334	tgtagactgcccttc[A/T]taatgtgggtgggcc	89122
rs2527918	snp	A/C	0.450105	0.149859	intron-variant	TRIM4	GRCh38.p7	7:99897849	CATTCTGAGAGCACC[A/C]CCCCTGGCAGTGGCC	89122
rs2527919	snp	A/G	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99896890	CAGTCAGGACTGGCC[A/G]GCCAACTGCAGCTGC	89122
rs2527920	snp	C/G	0.449853	0.150196	intron-variant	TRIM4	GRCh38.p7	7:99896257	tgaacccacattcta[C/G]ttggaccatagggtc	89122
rs2527921	snp	C/G	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99895647	tcacaattacgtttg[C/G]agttttcagtacctt	89122
rs2527922	snp	C/T	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99895133	tccaccttaagacac[C/T]agagaaagaggagca	89122
rs2571994	snp	G/T	0.488545	0.074807			GRCh38.p7	7:99920648	ATTATAGGAAAGGCA[G/T]TATTTGATATTGGGA	89122
rs2571995	snp	C/G	0.43655	0.16643			GRCh38.p7	7:99920468	GTTTCAGCCAATCAC[C/G]GCCGAGCTTCAGCAA	89122
rs2571996	snp	A/G	0.483418	0.0895317			GRCh38.p7	7:99917477	ccaccttggcctccc[A/G]aagtgctgggattac	89122
rs2571997	snp	G/T	0.487684	0.0775019			GRCh38.p7	7:99916794	GGAATGATATGATCG[G/T]TTTTTTTGTTTTAGA	89122
rs2571998	snp	C/T	0.487621	0.0776941			GRCh38.p7	7:99913749	GTTTTCATATACGTA[C/T]AATTTTCTGGTGCTA	89122
rs2571999	snp	A/T	0.487558	0.0778863			GRCh38.p7	7:99913227	CCAGTTTAGATTCCA[A/T]CTGTGGCCAGATTGA	89122
rs2572000	snp	A/G	0.436123	0.166908			GRCh38.p7	7:99911701	ggtagcatttcattc[A/G]cctgctaatgttgtg	89122
rs2572001	snp	A/C	0.297521	0.245442			GRCh38.p7	7:99909730	AAAAAAAAAAAAAAA[A/C]CAAAAAGAAAAAAGA	89122
rs2572002	snp	C/T	0.437118	0.165792			GRCh38.p7	7:99907431	GCAAAGTTAGGGAAA[C/T]GATTAAAAAAGATGA	89122
rs2572003	snp	A/T	0.487621	0.0776941			GRCh38.p7	7:99903690	TGTGACATGAGCAAA[A/T]GCAACCGTCAGAAAA	89122
rs2572004	snp	G/T	0.00874735	0.0655527			GRCh38.p7	7:99902889	AAATTCAGAGGAAGG[G/T]CTCTGTTGGGGGCGA	89122
rs2572005	snp	C/T	0.487621	0.0776941			GRCh38.p7	7:99896407	aacctccatttaacc[C/T]gaatcaaagggcctt	89122
rs2572006	snp	C/T	0.487558	0.0778863			GRCh38.p7	7:99896188	tctgccatacGatac[C/T]ataaaccttaaacca	89122
rs2572007	snp	G/T	0.165289	0.235211			GRCh38.p7	7:99894673	ttttctttttttttt[G/T]gggggggggatggag	89122
rs2572008	snp	A/T	0.487746	0.0773096			GRCh38.p7	7:99893333	CCAAATTTTAGGCTG[A/T]TTGTGAAAACTTGGG	89122
rs2572009	snp	C/T	0.483563	0.0891524			GRCh38.p7	7:99891382	AACGCTTGTTAAATA[C/T]CTTTTGCTAGCCTCT	89122
rs2572010	snp	A/G	0.488606	0.0746142			GRCh38.p7	7:99890920	TCTCCCAGATTTTCA[A/G]TAAAGACTTTCAGGC	89122
rs2897031	snp	A/G	0.0584853	0.160693	intron-variant	TRIM4	GRCh38.p7	7:99898554	TCGTCTTCACCTGCC[A/G]GACACATTCTGTCCC	89122
rs3220811	microsatellite	(CA)22/23/24/25/26	0.593066	0.127205	intron-variant	TRIM4	GRCh38.p7	7:99909127	ACAGATGAATGGATG[(CA)22/23/24/25/26]CTCCTAAAGATTTGG	89122
rs4727439	snp	A/C	0.450105	0.149859	intron-variant	TRIM4	GRCh38.p7	7:99912611	TTTGTTTGCAATTGA[A/C]TTTTAAAAGCATCAA	89122
rs6957718	snp	A/T	0.281841	0.247964	intron-variant	TRIM4	GRCh38.p7	7:99892878	CCACTGCTGCCCAAC[A/T]GATCCTCAGCCAGGC	89122
rs7781442	snp	A/G	0.434976	0.168179	intron-variant	TRIM4	GRCh38.p7	7:99907600	TATGTACTTGCAACT[A/G]CATTGCTTAAGCATG	89122
rs7787525	snp	A/G	0.281841	0.247964	intron-variant	TRIM4	GRCh38.p7	7:99896037	ttattagtatgatta[A/G]atttgtgtctattat	89122
rs7801568	snp	A/G	0.0551013	0.156571	intron-variant	TRIM4	GRCh38.p7	7:99904488	gaaaataaaatgaat[A/G]ctaggtaaaaactga	89122
rs7809747	snp	C/G	0.483418	0.0895317	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918359	atcacttgaggtcag[C/G]agttcgagaccagcc	89122
rs9690545	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914807	CTTTTTCtttttttc[C/T]ttttttctttttttt	89122
rs10236432	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914808	tttttctttttttct[C/T]tttttcttttttttt	89122
rs10245980	snp	A/G	0	0	intron-variant	TRIM4	GRCh38.p7	7:99896657	cagcaggaggttgga[A/G]aaaattccacgagtg	89122
rs10246091	snp	A/G	0	0	intron-variant	TRIM4	GRCh38.p7	7:99896749	atgtggggcccaata[A/G]ccactatccttgatg	89122
rs10271594	snp	C/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99912986	TTCAATTATAACTGC[C/T]GCTTTGTGGTCACTG	89122
rs10464605	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99913234	GGCCACAGTTGGAAT[A/C]TAAACTGGGAGGTGA	89122
rs10808114	snp	A/T	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99900876	AAGATTTTCTTTTTA[A/T]CACTGGTTTCCAGCA	89122
rs11539679	snp	C/T			missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919151	TGGGCCCCGTGCCCC[C/T]GGGCCTGTGCGGCCG	89122
rs11539682	snp	C/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890979	ACTTTAATTTTTATA[C/T]TTTTTGCATCTTACA	89122
rs11980179	snp	C/T	0.283158	0.247791	intron-variant	TRIM4	GRCh38.p7	7:99905919	cgaagccaaggcagg[C/T]ggatcactcgaggtc	89122
rs12536945	snp	C/T	0.0248432	0.108648	intron-variant	TRIM4	GRCh38.p7	7:99895849	TACTAATATACCCAC[C/T]CCAGATCTATtaaca	89122
rs12537676	snp	C/T	0.0356815	0.128715	intron-variant	TRIM4	GRCh38.p7	7:99896972	acttacaagatgagc[C/T]gcaactagggagata	89122
rs12666007	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891346	TGAGTTGTGATGAGA[A/G]TCATATGCAACAGCA	89122
rs12667341	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918188	tagccatacaagcac[C/T]tgaaacgtggatatt	89122
rs12670351	snp	C/G	0.0209421	0.100162	intron-variant	TRIM4	GRCh38.p7	7:99898532	gggctggtagatgca[C/G]ctggggtcgtcttca	89122
rs13232037	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99906699	TTTAAAaaaaaacag[C/T]tgggggcggtggctc	89122
rs13232044	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99906706	aaaaacagctggggg[C/G]ggtggctcacacctg	89122
rs13235389	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99907232	aagtgattctcctgc[A/C]tcagcctcccaagta	89122
rs13246364	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99906700	TTAAAaaaaaacagc[G/T]gggggcggtggctca	89122
rs13310326	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99893370	ATTAACAAATTCTCA[C/T]GTTGAATCAAAACTA	89122
rs17277546	snp	A/G	0.0333695	0.124785	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891948	TCCCAAAAGCGTCTT[A/G]GAAAATTTCCTGTCC	89122
rs28360802	snp	C/T	0.00358779	0.0422022	intron-variant	TRIM4	GRCh38.p7	7:99894430	CAATGCTTTGGGAGG[C/T]CAAGGCAGTGGATTA	89122
rs28477519	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906427	AAACTCCTGAGCTCA[A/G]GAGATCCTCCCATCT	89122
rs28548943	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99909728	CTTCTTTTTTCTTTT[G/T]GTTTTTTTTTTTTTT	89122
rs28847643	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99905036	ACGCTGTCTAAAAAA[A/T]AAAAAATAAAAATTA	89122
rs33998596	snp	C/G	0.113619	0.209524	missense	TRIM4	GRCh38.p7	7:99892245	ACACCTTTTCTTGTT[C/G]TTCTGTCTCACGCCT	89122
rs34083877	in-del	-/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891828	ACGGCAACAAAAACT[-/G]CTGTTTCTTCTACCT	89122
rs34275396	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99905239	GCAACTGGAACTCTT[-/A]ATTTTACACACTGGT	89122
rs34277597	snp	A/T	0.486398	0.0813386	intron-variant	TRIM4	GRCh38.p7	7:99912544	ATTAAAAAAAAAAAA[A/T]AATACCATAAACAAA	89122
rs34293437	snp	A/G	0	0	intron-variant	TRIM4	GRCh38.p7	7:99911819	AAACATGTACCCATA[A/G]ATAGACCTGTACAAG	89122
rs34360797	in-del	-/T	0.450357	0.149522	intron-variant	TRIM4	GRCh38.p7	7:99900709	TGTTTTTGAAGGATA[-/T]TTTTTTGCCAGTTCT	89122
rs34395561	snp	C/G	0.0240643	0.107019	intron-variant	TRIM4	GRCh38.p7	7:99908525	ACATTCAGCTCTAAA[C/G]ACAAGAGAGAGTTCA	89122
rs34402397	snp	C/T	0.00143823	0.0267777	synonymous-codon	TRIM4	GRCh38.p7	7:99892700	TCCCAAACTCGTCTT[C/T]TCCCAGGAAGGGAGA	89122
rs34698695	in-del	-/C			intron-variant	TRIM4	GRCh38.p7	7:99916154	TTTAAGGGCTATGTT[-/C]CCCCTTTCATACCCA	89122
rs34914690	in-del	-/A	0.495407	0.0477027	intron-variant	TRIM4	GRCh38.p7	7:99912531	ATTAAAAAAAAAAAA[-/A]TAATACCATAAACAA	89122
rs34997124	in-del	-/C			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921463	AGTAGCACCTAGTGT[-/C]CCCTGCACCACCGTT	89122
rs35432946	snp	C/T	0.113882	0.209695	missense	TRIM4	GRCh38.p7	7:99892567	AGATTTCAGCACTTA[C/T]CCTGTGTTCTGGGAA	89122
rs35520899	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99916284	GTTTCCCAAGCTTCT[-/A]CTTTGTGCCTTTTTT	89122
rs35926610	in-del	-/A			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920281	GCAGCACTCAGAACC[-/A]AAAAGAGGTTCAGAG	89122
rs35959826	in-del	-/C			intron-variant	TRIM4	GRCh38.p7	7:99901828	CTGATCAGAACTCTG[-/C]CCAAACAACTAGGAA	89122
rs35997738	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99895932	TGTTTCTTTTCCAGT[-/A]AAAAATTGGGTCTTA	89122
rs36063762	in-del	-/G			intron-variant	TRIM4	GRCh38.p7	7:99911571	TAACAATTACTAATA[-/G]GGTATAACTTTTCAT	89122
rs41280953	snp	A/G	0.0923359	0.194016	intron-variant	TRIM4	GRCh38.p7	7:99902974	GAGTGCTGTGTGTCT[A/G]TCTCTCCAATGTGCT	89122
rs56337108	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99897913	CCTTTCTTGTACCCA[C/T]TAAACATCTCACCTG	89122
rs56337765	snp	C/G	0.00557542	0.0525036	intron-variant	TRIM4	GRCh38.p7	7:99893172	CTGGGGAGGCTGAGG[C/G]AGAAGAATCACTTAA	89122
rs57028043	snp	A/G	0.0337553	0.125452	intron-variant	TRIM4	GRCh38.p7	7:99898208	TCCACCTAGTATGGG[A/G]GCAGGTTAGTGCTAC	89122
rs57128906	snp	A/T	0.0391387	0.134304	intron-variant	TRIM4	GRCh38.p7	7:99904351	AAATACCTGACCAAC[A/T]CTCCTCAAAACTTTC	89122
rs57799977	in-del	-/TAAA/TAAATAAA			intron-variant	TRIM4	GRCh38.p7	7:99913697	AAATAAATAAATAAA[-/TAAA/TAAATAAA]AATAATAATTTTTTT	89122
rs57960671	in-del	-/TGTGTG/TGTGTGTG	0	0	intron-variant	TRIM4	GRCh38.p7	7:99909158	GTGTGTGTGTGTGTG[-/TGTGTG/TGTGTGTG]CGTGTGTGTGTGCAT	89122
rs58242927	in-del	-/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99909750	TTTTTTTTTTTTTTT[-/T]GAGACAAAGTCTCAC	89122
rs58730747	snp	C/T	0.0391387	0.134304	intron-variant	TRIM4	GRCh38.p7	7:99914405	AAGCAATCCTCCTGC[C/T]TCAGCCTCCCAAAGT	89122
rs58750403	snp	C/T	0.0333695	0.124785	intron-variant	TRIM4	GRCh38.p7	7:99908282	ATTGTTTAATAATTA[C/T]AAATGTACACATAAG	89122
rs59409421	in-del	-/A	0.5	0	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918574	GAAAAAAAAAAAAAA[-/A]TCTCATTGATAATTT	89122
rs59996356	snp	C/T	0.0629771	0.165899	intron-variant	TRIM4	GRCh38.p7	7:99896882	AAGCTGTGGCAGCTG[C/T]AGTTGGCCGGCCAGT	89122
rs60305755	snp	A/T	0.0391387	0.134304	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890994	CTTTTTGCATCTTAC[A/T]AACTTTCTACAATAA	89122
rs61742750	snp	G/T	0.00972114	0.0690367	missense	TRIM4	GRCh38.p7	7:99903241	CGCTTTAGCATTTCC[G/T]TCATCAATGGTATCT	89122
rs66953435	snp	G/T	0.0240643	0.107019	intron-variant	TRIM4	GRCh38.p7	7:99909177	GTGTGTGTGCATCCA[G/T]TCATCTGTTTCTTTC	89122

Full records

It may take some time, please wait.