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
rs14819	snp	A/G	0	0	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922094	GTTTCTTAAATTCAA[A/G]GAAATAGCTCTAAAG	26091
rs14840	snp	C/T	0.00975586	0.0691575	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922874	ACTATTTGTGTTTTT[C/T]TTGTGGTGATGAATT	26091
rs471341	snp	A/G	0.475525	0.107882	intron-variant	HERC4	GRCh38.p7	10:68068453	gttacccaggctggc[A/G]tgcagtggtgtgatc	26091
rs474391	snp	G/T	0.141934	0.225437	intron-variant	HERC4	GRCh38.p7	10:67963972	GGTTCTCTAAAGGAA[G/T]AGTTTGAGAAGCTTT	26091
rs482806	snp	C/G	0.499722	0.0117779	intron-variant	HERC4	GRCh38.p7	10:68032181	TAATTATCTGGTAAA[C/G]GTTAACTGAATGCTT	26091
rs483507	snp	A/C	0.0182019	0.0936463	intron-variant	HERC4	GRCh38.p7	10:67967825	TTAAATAAACATCAC[A/C]ATGAGGAAACAATCA	26091
rs497849	snp	A/G	0.115788	0.21092	intron-variant	HERC4	GRCh38.p7	10:67993863	TAAGGAATGGGAATA[A/G]GATAACAGGGATAGA	26091
rs499092	snp	A/G			intron-variant, upstream-variant-2KB	HERC4	GRCh38.p7	10:68075120	TCCCAGGGGCCGGGG[A/G]GGGGAGCAGCGGACC	26091
rs501169	snp	C/T	0.0733688	0.176922	intron-variant	HERC4	GRCh38.p7	10:68023747	ataaatagtcaatta[C/T]cctagcaccattAAA	26091
rs503677	snp	A/G	0.438666	0.164028	intron-variant	HERC4	GRCh38.p7	10:68067255	ATACATTTCTCTAAC[A/G]GTAGTCATCTGTTTG	26091
rs506460	snp	G/T	0.0966517	0.197444	intron-variant	HERC4	GRCh38.p7	10:68066938	TGTGCACTAGTATTT[G/T]ACCTGCCTCAAACAG	26091
rs507160	snp	C/G	0.02016	0.0983543	intron-variant	HERC4	GRCh38.p7	10:68034694	AGGATGCCCCAGACT[C/G]AATTCATGACCCCCA	26091
rs515489	snp	A/G	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:68004027	aaatggcttttatct[A/G]aaagagggcaataac	26091
rs519204	snp	A/G	0.02016	0.0983543	intron-variant	HERC4	GRCh38.p7	10:68041316	AATTTTGAAAAATTT[A/G]TCTCAGAATAGGGGA	26091
rs521935	snp	C/T	0.483491	0.0893421	intron-variant	HERC4	GRCh38.p7	10:68041027	TCTGCTAAAGCATAT[C/T]AATTATGGAATATGT	26091
rs524256	snp	A/G	0.444666	0.15686	intron-variant	HERC4	GRCh38.p7	10:67993276	CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	26091
rs526333	snp	C/T	0.480618	0.0965156	intron-variant	HERC4	GRCh38.p7	10:67993002	TAGCTTTTGTTCTAT[C/T]TTTTTTAAATCATCT	26091
rs534251	snp	C/T	0.0741063	0.177655	intron-variant	HERC4	GRCh38.p7	10:68007125	gatctagaaaatagc[C/T]tcaaaagggcaaatc	26091
rs534611	snp	G/T	0.438526	0.164189	intron-variant	HERC4	GRCh38.p7	10:68073590	AGTTGGCTAAATTTT[G/T]CACTGTGTATATTTG	26091
rs540894	snp	A/G	0.0193772	0.0965046	intron-variant	HERC4	GRCh38.p7	10:68021093	cgtagaattcattgg[A/G]gcttatggatgttta	26091
rs542411	snp	G/T	0.438526	0.164189	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012803	ATTTTTgatactgaa[G/T]ttttacaaattgaag	26091
rs542704	snp	C/T	0.0737376	0.17729	intron-variant	HERC4	GRCh38.p7	10:68030203	atctgcccgcctctg[C/T]ctcccagaatgctgg	26091
rs544425	snp	A/G	0.499218	0.0197529	intron-variant	HERC4	GRCh38.p7	10:68020717	cagtggcgcgatctc[A/G]gctcattgcaagctc	26091
rs544508	snp	A/G	0.49925	0.0193545	intron-variant	HERC4	GRCh38.p7	10:68020693	caagctccgcctccc[A/G]ggttcacgccattct	26091
rs545435	snp	C/G	0.400147	0.19989	intron-variant	HERC4	GRCh38.p7	10:68028445	ttgttcttctgagag[C/G]accgtagtaatcttt	26091
rs548787	snp	C/T	0.437824	0.164991	intron-variant	HERC4	GRCh38.p7	10:68052573	aacaagaacctggac[C/T]tgtctatcctgtatg	26091
rs560523	snp	C/T	0.438246	0.16451	intron-variant	HERC4	GRCh38.p7	10:68047287	GAAACAGAAATGGCC[C/T]GTGGAGAAATGCAAA	26091
rs562961	snp	C/T	0.483708	0.088773	intron-variant	HERC4	GRCh38.p7	10:68033196	ACTTCATGATAGTTA[C/T]ACCCACAGGAGCCTA	26091
rs562994	snp	G/T	0	0	intron-variant	HERC4	GRCh38.p7	10:68049583	tttttttgggggcag[G/T]gtctcactctgtcac	26091
rs565447	snp	C/T	0.0659589	0.169201	intron-variant	HERC4	GRCh38.p7	10:67967008	TACAAGCACCCGCCA[C/T]CATGACCGGCTAATT	26091
rs566192	snp	C/T	0.471673	0.115589	intron-variant	HERC4	GRCh38.p7	10:67967054	AGAGACGGAGTTTCA[C/T]CGTGTTAGCCAGGAT	26091
rs567987	snp	C/T	0.438526	0.164189	intron-variant	HERC4	GRCh38.p7	10:68005773	gaggctgcagtgagc[C/T]atgattgtgccactg	26091
rs568006	snp	C/T	0.02016	0.0983543	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012327	tatcaaaagcccaga[C/T]aggctgaaagcaagg	26091
rs574391	snp	A/G	0.437824	0.164991	intron-variant	HERC4	GRCh38.p7	10:68052137	TGAAAAATGAATTCA[A/G]AAGGCAATTTTTTCC	26091
rs584613	snp	C/G	0.480697	0.0963277	intron-variant	HERC4	GRCh38.p7	10:68002880	GCTGGGATTACAAGC[C/G]TGAGCCACCGTGCCT	26091
rs586540	snp	A/G	0.483636	0.0889627	intron-variant	HERC4	GRCh38.p7	10:68034450	ATCACATAACAAGGA[A/G]TAATCTCATTTCCTT	26091
rs592114	snp	G/T	0.0103295	0.0711199	intron-variant	HERC4	GRCh38.p7	10:68047939	tttttgttttttttt[G/T]tgtgagacagggtct	26091
rs593024	snp	C/T	0.438526	0.164189	intron-variant	HERC4	GRCh38.p7	10:68048150	tcatgaactcctggg[C/T]tcaagtgctcctccc	26091
rs596682	snp	C/T	0.0970103	0.197722	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075936	ATGAATCAGGGACTG[C/T]AGCCAATGTGTAATT	26091
rs597889	snp	A/G	0.480775	0.0961398	intron-variant	HERC4	GRCh38.p7	10:67964676	aaatccaaattccta[A/G]tcctagtttactaaa	26091
rs599870	snp	C/T	0.02016	0.0983543	intron-variant	HERC4	GRCh38.p7	10:68003939	ccatactgttctcca[C/T]agtggctatactaat	26091
rs608300	snp	A/G	0.47614	0.106587	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069640	CTAATAAGGAATGAA[A/G]GAGAAAGAGGTAGCC	26091
rs612131	snp	A/G	0.0741063	0.177655	intron-variant	HERC4	GRCh38.p7	10:67965580	GCAACCTGATTCCGG[A/G]AGGTGGGAGTATCCT	26091
rs619973	snp	A/T	0.0737376	0.17729	intron-variant	HERC4	GRCh38.p7	10:67991463	CTTAATTTTTAAAAT[A/T]CCATGTTTTAAAGCA	26091
rs623494	snp	A/G	0.438526	0.164189	intron-variant	HERC4	GRCh38.p7	10:68050291	CAAGCTTCTCAATGT[A/G]TATTTAAATTGCTTT	26091
rs625576	snp	A/C	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011582	gcagtattttgaaag[A/C]aatctttttactgag	26091
rs631322	snp	C/T	0.0737376	0.17729	intron-variant	HERC4	GRCh38.p7	10:68037535	AATATGATGTTTAGC[C/T]TTCTTTATTTCTATG	26091
rs634546	snp	C/T	0.437824	0.164991	intron-variant	HERC4	GRCh38.p7	10:68056952	TTTAAGGTCTGAACC[C/T]AAGTAAGTGCAAGCA	26091
rs636550	snp	C/T	0	0	intron-variant	HERC4	GRCh38.p7	10:68018329	attaaaaacttaaca[C/T]ccattcacaataaaa	26091
rs655017	snp	C/T	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:68007004	ccttgcacttgaata[C/T]tgatatttttcttta	26091
rs659082	snp	C/T	0	0	intron-variant	HERC4	GRCh38.p7	10:68045669	GTCAGGTTTTTTTAC[C/T]AGTATCACAAGTTTT	26091
rs659420	snp	C/T	0.438526	0.164189	intron-variant	HERC4	GRCh38.p7	10:67974631	GCACTTTAAAAGGAT[C/T]GGTCTATATCTGTTG	26091
rs660640	snp	A/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68000408	GTATTTTTTGTAGAG[A/T]TGGGGTTTTACCATG	26091
rs669322	snp	A/T	0.0970103	0.197722	intron-variant	HERC4	GRCh38.p7	10:68052130	TGAATTCAGAAGGCA[A/T]TTTTTTCCACTTGTG	26091
rs669794	snp	A/T	0.499218	0.0197529	intron-variant	HERC4	GRCh38.p7	10:67969257	aacagggtaccagaa[A/T]tggctcatttgtggc	26091
rs672383	snp	A/G	0.439085	0.163545	intron-variant	HERC4	GRCh38.p7	10:67981733	gaggccaaggcgggt[A/G]gattacttgaggcca	26091
rs674486	snp	C/T	0.474272	0.110462	intron-variant	HERC4	GRCh38.p7	10:68060160	GCACAGTACCTGGCA[C/T]ATAATGGAGGTTTAC	26091
rs679645	snp	A/C	0.0193772	0.0965046	intron-variant	HERC4	GRCh38.p7	10:68021045	gaagaagtaatagcc[A/C]aaaactcccaaatat	26091
rs684284	snp	A/C	0.481087	0.0953875	intron-variant	HERC4	GRCh38.p7	10:67982091	ataccaatgacattg[A/C]tcacagaaataggaa	26091
rs685634	snp	A/G	0.437542	0.165312	intron-variant	HERC4	GRCh38.p7	10:68053428	tggtcccagctactc[A/G]ggaggctgaagcagg	26091
rs689211	snp	A/C	0.480697	0.0963277	intron-variant	HERC4	GRCh38.p7	10:68047843	cttacaaaagtaaat[A/C]tactcttaccatatg	26091
rs747024	snp	C/T	0.152001	0.229992	intron-variant	HERC4	GRCh38.p7	10:68042943	GCAGAAATACCTTAA[C/T]ATACAGCTTAAAGTT	26091
rs863110	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67972252	aaaggccaggcacgg[G/T]ggctcacaccggtaa	26091
rs863874	snp	C/T	0.438666	0.164028	intron-variant	HERC4	GRCh38.p7	10:68036577	GCCCTTTATAACAGA[C/T]TTCTCTTTTTATTTC	26091
rs865248	snp	A/G	0	0	intron-variant	HERC4	GRCh38.p7	10:68062068	TTACTTAACAGGTTA[A/G]AACTGGGAGAAGTCT	26091
rs866255	snp	A/G	0.489684	0.0710729	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68014084	TTTTACAGTAAAGGG[A/G]CTTTTCCTGTTGCTT	26091
rs1097165	snp	C/T	0.1472	0.227886	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075226	cgcttgcctcccgtt[C/T]ttccccgcccgctcc	26091
rs1104020	snp	C/T	0.0582	0.160352	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075239	gtgctctccgccccg[C/T]ttgcctcccgttctt	26091
rs1149674	snp	G/T	0.0248432	0.108648	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069866	tttagtagggacggg[G/T]tttcaccgtgttagc	26091
rs1191993	snp	A/C	0.482905	0.0908579	intron-variant	HERC4	GRCh38.p7	10:68028134	cattatttttcctag[A/C]gttatgagctggaat	26091
rs1204083	snp	C/G	0.47743	0.103805	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075440	GGCGCCTGTGGCCAG[C/G]CACCCCCCCCCCCCC	26091
rs1209191	snp	A/G	0.0741063	0.177655	intron-variant	HERC4	GRCh38.p7	10:68029662	TCAATTTTTAAGGAC[A/G]Aatatttatataatt	26091
rs1210158	snp	A/C	0	0	intron-variant	HERC4	GRCh38.p7	10:68049589	gagtgagacactgcc[A/C]caaaaaaaaaaaaaa	26091
rs1211222	snp	A/G	0	0	intron-variant	HERC4	GRCh38.p7	10:68030196	cgcctctgcctccca[A/G]aatgctgggattaca	26091
rs1490008	snp	C/T	0.271702	0.249056	intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68074698	GCCGGCCTCTGAAGC[C/T]GTTGCGAGCGGCCGG	26091
rs1812671	snp	C/T	0.188631	0.242351	intron-variant	HERC4	GRCh38.p7	10:67973425	CAAGGCCCAATCCCG[C/T]AGGAATTAGAATAAG	26091
rs1906722	snp	A/G	0	0	intron-variant	HERC4	GRCh38.p7	10:68048953	ACTGTTTTGTTTTTA[A/G]ACTAACAGTATACAA	26091
rs1981180	snp	C/T	0.27393	0.248852	intron-variant, missense	HERC4	GRCh38.p7	10:68070509	aagcaattctcctgc[C/T]tcagcctcccgaata	26091
rs1981181	snp	A/C	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:68068953	TACAACATTCTttca[A/C]atggagtatctcatt	26091
rs2007505	snp	C/T	0.0788843	0.182262	intron-variant	HERC4	GRCh38.p7	10:68004328	CAGAATGGGAGAAAA[C/T]ATTTGCAAACTACCC	26091
rs2029474	snp	C/T	0.152334	0.230133	intron-variant	HERC4	GRCh38.p7	10:67992056	atacaattagctggg[C/T]gtggtggtgcacacc	26091
rs2039700	snp	C/T	0.252983	0.249982	intron-variant	HERC4	GRCh38.p7	10:67955376	TAGAGTAAGCCAGTA[C/T]AGAACGGTAGTAATA	26091
rs2176102	snp	G/T	0	0	intron-variant	HERC4	GRCh38.p7	10:68050626	ATAGCTGACTTTTTA[G/T]ACATCAAATACACAA	26091
rs2308195	in-del	-/ATAG	0.0252325	0.109451	intron-variant	HERC4	GRCh38.p7	10:67995355	TAAGATAACTATATA[-/ATAG]ATAGGGAGAAACTAA	26091
rs2451402	snp	A/G	0	0	intron-variant	HERC4	GRCh38.p7	10:68062077	AGGTTAAAACTGGGA[A/G]AAGTCTACAGTTGGA	26091
rs2451403	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68061880	ttttttttttttttt[A/T]aaatggagtctcgct	26091
rs2459115	snp	C/G	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:68031180	TACAAAAGATTAAGA[C/G]AATTAGCATTTCTTA	26091
rs2485677	snp	C/T	0.499722	0.0117779	intron-variant	HERC4	GRCh38.p7	10:68031401	GTAAAATTTAAGACT[C/T]GCCAACAGGAATAAA	26091
rs2485679	snp	G/T	0.185788	0.241613	intron-variant	HERC4	GRCh38.p7	10:68051522	gctagtttttttttg[G/T]ttttttttttgtatt	26091
rs2485680	snp	A/G	0.474634	0.109726	intron-variant	HERC4	GRCh38.p7	10:68060108	AAAAGTCTTGTATCT[A/G]TCCTGCAAAAGTATG	26091
rs2485681	snp	A/G	0.0112482	0.0741458	intron-variant	HERC4	GRCh38.p7	10:68062239	AAATTCACCTTACCA[A/G]AATCTTTTAACTTGC	26091
rs2932413	snp	C/T	0.5	0	intron-variant	HERC4	GRCh38.p7	10:67974075	AAAAAAATTACTGTA[C/T]ACACACACACACACA	26091
rs2943770	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68061852	gtgccctgcactcca[A/G]cctgggcgacagagt	26091
rs3740055	snp	C/T	0.252702	0.249985	intron-variant	HERC4	GRCh38.p7	10:68033887	TACATTTCTCTCTTA[C/T]ACTAAGAATCACTGA	26091
rs3758392	snp	C/T	0.499339	0.0181672	intron-variant	HERC4	GRCh38.p7	10:67932573	CTTTCCATTTAACAA[C/T]ATCAGAGATTAGTTT	26091
rs3758393	snp	C/T	0.178144	0.239451	intron-variant	HERC4	GRCh38.p7	10:68032964	AGCTCAGTAGATAGT[C/T]GTGACTAAATAATTT	26091
rs3814178	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68044745	ACTATTCAACAAATA[C/T]GTTCCAAACGTAATT	26091
rs3832649	in-del	-/A	0.319616	0.240112	intron-variant	HERC4	GRCh38.p7	10:68073904	ATAATTATAATACAG[-/A]AAAAAAAACATGCAA	26091
rs3834396	in-del	-/A	3.81003e-05	0.00436448	splice-acceptor-variant	HERC4	GRCh38.p7	10:68025678	ACACTCCACCTTCCT[-/A]AAAAAAAGACAAAAC	26091
rs3891387	snp	C/G	0.144296	0.226554	intron-variant	HERC4	GRCh38.p7	10:68008151	GAGAGAGAGTGAGAG[C/G]GAAACTTCATTTGTT	26091

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