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
rs2318	snp	C/G	0.360632	0.224189	intron-variant	HERC1	GRCh38.p7	15:63709677	TGAAATGAAAATATA[C/G]AAAGGAGGATGGGTA	8925
rs884495	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63728941	aaagaGCAGGTTTTA[A/T]AAAAAAAAAAAAAGA	8925
rs1039819	snp	G/T	0.29278	0.246313	intron-variant	HERC1	GRCh38.p7	15:63733274	TAGTTTTTATAATTA[G/T]GTACTTCCTGAAGAT	8925
rs1063416	snp	C/T	0	0	synonymous-codon	HERC1	GRCh38.p7	15:63729323	CATCTTCAGCTTTTG[C/T]TGCCTCATGCCACAG	8925
rs1063417	snp	C/T	0	0	synonymous-codon	HERC1	GRCh38.p7	15:63729291	TATTTATTCACGTTC[C/T]GCAAATTTGCTCAAA	8925
rs1063418	snp	C/T	0	0	synonymous-codon	HERC1	GRCh38.p7	15:63729279	TTCTGCAAATTTGCT[C/T]AAAGAAAGTCCTTGG	8925
rs1063419	snp	A/G	0	0	synonymous-codon	HERC1	GRCh38.p7	15:63727783	GATTGTTAACTCCCT[A/G]CTGTTACTCCCTGTG	8925
rs1063420	snp	G/T	0	0	synonymous-codon	HERC1	GRCh38.p7	15:63727771	CCTGCTGTTACTCCC[G/T]GTGTCAGTGGCTCGG	8925
rs1063421	snp	G/T	3.31835e-05	0.00407316	synonymous-codon	HERC1	GRCh38.p7	15:63727756	TGTGTCAGTGGCTCG[G/T]CCTTTATTGAGTTAC	8925
rs1063422	snp	C/T	0	0	synonymous-codon	HERC1	GRCh38.p7	15:63727731	AGTTACCTCCTCGAC[C/T]TGTTGCCACCTCTTG	8925
rs1063423	snp	C/G	0	0	missense	HERC1	GRCh38.p7	15:63727729	TTACCTCCTCGACTT[C/G]TTGCCACCTCTTGAT	8925
rs1063424	snp	A/C	0	0	missense	HERC1	GRCh38.p7	15:63727685	TCCTGCCAGCTGCTG[A/C]TCTTTTAGAAGACCA	8925
rs1065250	snp	A/G	0.262435	0.249691	intron-variant	HERC1	GRCh38.p7	15:63741702	tgtatacccacatgc[A/G]aaagaatgaagttgg	8925
rs1131647	snp	C/T	0.203267	0.245593	utr-variant-3-prime, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63608914	AAAGAAATTAGATGT[C/T]TTTATTTTTCTGTGA	8925
rs1140416	snp	C/T	3.31972e-05	0.004074	synonymous-codon	HERC1	GRCh38.p7	15:63727828	CATAGATGTGATATA[C/T]GTCTCAGCTGCTGGC	8925
rs1140418	snp	A/T			synonymous-codon	HERC1	GRCh38.p7	15:63727816	ATACGTCTCAGCTGC[A/T]GGCAGTATGCTCTGC	8925
rs1140419	snp	A/G			synonymous-codon	HERC1	GRCh38.p7	15:63727669	TCTTTTAGAAGACCA[A/G]GAGTTACAGTGGCCT	8925
rs1140421	snp	A/G			missense	HERC1	GRCh38.p7	15:63630500	TGGCATCAAATGGAG[A/G]TGTGTATGCCTGGGG	8925
rs1140422	snp	C/G	0.235955	0.249605	synonymous-codon	HERC1	GRCh38.p7	15:63626108	TGACACAGTGCCCCC[C/G]CAGTATGGGGCGCTG	8925
rs1142731	snp	A/G	0.262159	0.249704	intron-variant	HERC1	GRCh38.p7	15:63741514	caagaccagcctaac[A/G]tggtgaaaccccgta	8925
rs1396712	snp	C/T	0.0418186	0.138422	intron-variant	HERC1	GRCh38.p7	15:63770043	ATTGCTTCAATAACT[C/T]CACATTACATATGGG	8925
rs1396713	snp	C/T	0.493925	0.054776	intron-variant	HERC1	GRCh38.p7	15:63805739	ACTGCTTGAGGTCAG[C/T]AGTTCAAGACCACCC	8925
rs1470314	snp	C/T	0.446641	0.154377	intron-variant	HERC1	GRCh38.p7	15:63820825	CCAGCTTAACAGAGA[C/T]TTTAAATCAGGAGTT	8925
rs1815128	snp	C/T	0.462472	0.13174	intron-variant	HERC1	GRCh38.p7	15:63643972	GACAGACAGAACCAT[C/T]AGCCAACAAAAAGAG	8925
rs1815129	snp	C/G	0.4628	0.13121	intron-variant	HERC1	GRCh38.p7	15:63639691	TTGAGAGTGTCTACT[C/G]TAGAAACTGTGACAT	8925
rs1815130	snp	C/T	0.462909	0.131034	intron-variant	HERC1	GRCh38.p7	15:63666563	AATTTCCTAGTATTG[C/T]CCAAGTTTAATGAAA	8925
rs1962180	snp	A/G	0.16618	0.23553	intron-variant	HERC1	GRCh38.p7	15:63690353	ATTAAGTTATGGGGT[A/G]TGAGAAGTAGAGGGA	8925
rs1986864	snp	A/G	0.463126	0.13068	intron-variant	HERC1	GRCh38.p7	15:63783806	ggtgcagtggctcac[A/G]cctgtaatcccaaca	8925
rs2053591	snp	A/G	0.46703	0.124089	intron-variant	HERC1	GRCh38.p7	15:63826458	GTACAATGTGAACCA[A/G]TAACTACCATATCAC	8925
rs2053592	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63826479	ACCATATCACATATT[C/T]TAGCCTAAGAAATAT	8925
rs2053593	snp	A/G	0.463018	0.130857	intron-variant	HERC1	GRCh38.p7	15:63826664	ACATGTATGAATGCA[A/G]TATTAGTGGACAATG	8925
rs2063281	snp	A/G	0.445196	0.1562	intron-variant	HERC1	GRCh38.p7	15:63769326	catgaggctgaggca[A/G]ggagaactgcttgaa	8925
rs2089619	snp	C/G	0.478768	0.100824	intron-variant	HERC1	GRCh38.p7	15:63744754	tgggctacaggagaa[C/G]ccactgccctgaagg	8925
rs2099920	snp	A/G	0.462691	0.131387	intron-variant	HERC1	GRCh38.p7	15:63811548	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	8925
rs2099921	snp	A/T	0.462909	0.131034	intron-variant	HERC1	GRCh38.p7	15:63811650	ccgtctctcctaaaa[A/T]tatacaaaattagcc	8925
rs2099922	snp	C/T	0.436834	0.166111	intron-variant	HERC1	GRCh38.p7	15:63812069	CAGATTTGTAACTCT[C/T]GCTCAAAAATGAGCT	8925
rs2165882	snp	A/G	0.366885	0.220993	intron-variant	HERC1	GRCh38.p7	15:63800591	AAGGTATCCCTGACT[A/G]TACCCATGTGAGATT	8925
rs2175087	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63766552	tcattctgtcaccta[A/G]gctggagtgcagtgg	8925
rs2175088	snp	A/G	0.460477	0.134905	intron-variant	HERC1	GRCh38.p7	15:63761494	tgggaggctgaggct[A/G]gaagatcacttgagc	8925
rs2197260	snp	C/T	0.0494327	0.149241	intron-variant	HERC1	GRCh38.p7	15:63816635	ATCCTTTAAATAAAG[C/T]GTATTTATTCAACAT	8925
rs2202867	snp	C/T	0.475877	0.107142	intron-variant	HERC1	GRCh38.p7	15:63711963	CTATCTAGAAGATTG[C/T]TTCTACTTGAGGAAC	8925
rs2228509	snp	C/T	3.31268e-05	0.00406968	synonymous-codon	HERC1	GRCh38.p7	15:63635991	GCGGCCCAGGCAGAT[C/T]GAGGCCTTACAAGGA	8925
rs2228510	snp	A/G	0.49486	0.0504326	missense	HERC1	GRCh38.p7	15:63678257	GCCACTATTCAGCTC[A/G]TCCGTATCCTTCACC	8925
rs2228511	snp	A/G	0.378409	0.214502	synonymous-codon	HERC1	GRCh38.p7	15:63661830	TGGGAGTGGAAATCC[A/G]TACTACCTGTTATGT	8925
rs2228512	snp	A/G/T	0.0478626	0.147113	missense	HERC1	GRCh38.p7	15:63689654	GATTGTATGTGGGAG[A/G/T]CACCCATTGCTCAGG	8925
rs2228513	snp	C/T	0.0772275	0.180692	missense	HERC1	GRCh38.p7	15:63658688	TAGAAAAGAGCTCCT[C/T]TGGGAGAATAACGTT	8925
rs2228514	snp	C/T	0.00461136	0.0477955	synonymous-codon	HERC1	GRCh38.p7	15:63775054	TCTCAGTCTTTGCAA[C/T]GATGTCATTCATACT	8925
rs2228515	snp	A/G	0.0431228	0.140363	synonymous-codon	HERC1	GRCh38.p7	15:63774838	ACGAGGCTCATTGCG[A/G]TATCTTCTTGAATGG	8925
rs2228516	snp	A/G	0.00620554	0.0553558	missense	HERC1	GRCh38.p7	15:63626080	CTGAGAGAAGTCAGC[A/G]TTCACACGGTGCGGG	8925
rs2228517	snp	C/G	0.4903	0.0689643	synonymous-codon	HERC1	GRCh38.p7	15:63640314	CCACCAGAACTGTCT[C/G]CCTGACCCTGCATCC	8925
rs2228518	snp	C/T	0.00594543	0.0541975	synonymous-codon, downstream-variant-500B	HERC1, FBXL22	GRCh38.p7	15:63609108	GAGAAACGTGGACAA[C/T]GCCGAGGGCTCCGAC	8925
rs2228519	snp	C/T	0.00382414	0.0435597	synonymous-codon	HERC1	GRCh38.p7	15:63725295	ATGGACACTCCTCAA[C/T]TGGGTAATGTGCTTC	8925
rs2229748	snp	C/T	0.000827691	0.0203263	synonymous-codon	HERC1	GRCh38.p7	15:63661959	GTGTGAATGCAGCGT[C/T]GTCAGCTTCAATCAG	8925
rs2229749	snp	C/G	0.377861	0.214851	missense	HERC1	GRCh38.p7	15:63645010	AGAAGGATGGTGGGA[C/G]CAGGAATCAAATTGC	8925
rs2255243	snp	C/G	0.375307	0.21634	missense	HERC1	GRCh38.p7	15:63696158	TTGGACACACAGGAG[C/G]CAAGGGAGAGAGTGG	8925
rs2271241	snp	C/T	0.499553	0.0149478	intron-variant	HERC1	GRCh38.p7	15:63756791	ATACTTCTGTGAGTA[C/T]CAAAGTATAATATTT	8925
rs2272209	snp	C/T	0.377072	0.215297	intron-variant	HERC1	GRCh38.p7	15:63660954	GTTTGTTTTGAGAGC[C/T]TCTTTATTTTACATG	8925
rs2414823	snp	A/G	0.463451	0.130149	intron-variant	HERC1	GRCh38.p7	15:63781554	ttggtagagcagtca[A/G]aacacgtaccattta	8925
rs2414824	snp	A/G	0.311369	0.242351	intron-variant	HERC1	GRCh38.p7	15:63703713	ttattttgtagaaac[A/G]gggtttcgccatgtt	8925
rs2414825	snp	A/C	0.462909	0.131034	intron-variant	HERC1	GRCh38.p7	15:63681284	agcccaggaatttga[A/C]gcttcagtgagccat	8925
rs2414826	snp	C/T	0.462144	0.132269	intron-variant	HERC1	GRCh38.p7	15:63679003	TTTTAACATTTACAG[C/T]GTGACTGGCAATGTA	8925
rs2414827	snp	A/G	0.463126	0.13068	intron-variant	HERC1	GRCh38.p7	15:63663872	GATTCAGTAATTTAC[A/G]GGAACAGTGAGAGAA	8925
rs2414828	snp	G/T	0.463018	0.130857	intron-variant	HERC1	GRCh38.p7	15:63663377	GCTATTATTATCCCC[G/T]TTTGCAAGAGAGGAA	8925
rs2899693	snp	A/C	0.0256215	0.110247	intron-variant	HERC1	GRCh38.p7	15:63740966	tcttagctatgacat[A/C]aaaagcacaaacaac	8925
rs2899694	snp	A/G	0.0189856	0.0955633	intron-variant	HERC1	GRCh38.p7	15:63703283	TGTTGAACCACAATT[A/G]CGCCTTTTTCTCCCC	8925
rs2899695	snp	C/T	0.205417	0.245993	intron-variant	HERC1	GRCh38.p7	15:63681169	acaaaacaatacaCC[C/T]AGTCTCAGGCTTAAT	8925
rs3056822	in-del	-/CAAC	0.416992	0.186048	intron-variant	HERC1	GRCh38.p7	15:63800886	ggttgccagagaaac[-/CAAC]caagtgataaaagtg	8925
rs3736570	snp	A/T			intron-variant	HERC1	GRCh38.p7	15:63637801	TTATAGTCATCAAGG[A/T]GTTACGGGACTGCAT	8925
rs3764186	snp	A/G	0.498685	0.0256094	intron-variant	HERC1	GRCh38.p7	15:63764238	CTAATTTTAATGCAT[A/G]TGTCTCTCCCCTTCC	8925
rs3764187	snp	C/T	0.00978769	0.0692679	missense	HERC1	GRCh38.p7	15:63718808	AAACACACAAATTTA[C/T]TTAGTCAAGCATGTG	8925
rs3830606	in-del	-/GTTACGGGACTGCATAGTTATA			intron-variant	HERC1	GRCh38.p7	15:63637779	TATAGTCATCAAGGA[-/GTTACGGGACTGCATAGTTATA]TCAACTCTTCCCTTT	8925
rs4267257	snp	A/G	0.248188	0.249993	intron-variant	HERC1	GRCh38.p7	15:63805938	ACAGAGCAAGACCCT[A/G]TCTCAAAACAAAAAA	8925
rs4283174	snp	A/G	0.465368	0.126951	intron-variant	HERC1	GRCh38.p7	15:63613344	TGGGGAGTGCCAAGT[A/G]GGGTGCAACCAGGGG	8925
rs4332694	snp	C/T	0.00105656	0.02296	intron-variant	HERC1	GRCh38.p7	15:63669740	TAAAAATCCAATTTA[C/T]GAAATAATACATACA	8925
rs4344682	snp	A/G	0.471863	0.115225	intron-variant	HERC1	GRCh38.p7	15:63632111	AACATAACTAAAACT[A/G]AATTCCTTACCCTTC	8925
rs4411464	snp	C/T	0.464096	0.129085	intron-variant	HERC1	GRCh38.p7	15:63703224	ACATATTCACTTTCT[C/T]AGACCAAGGGCTTAG	8925
rs4412925	snp	G/T	0.17654	0.238964	intron-variant	HERC1	GRCh38.p7	15:63613411	AATATTATACAGTAG[G/T]GCATACCCTACACAC	8925
rs4523879	snp	A/G	0.463451	0.130149	intron-variant	HERC1	GRCh38.p7	15:63623180	GTTCAAATCGAATCA[A/G]TAATGATAGCCAACC	8925
rs4536410	snp	C/T	0.477684	0.103247	intron-variant	HERC1	GRCh38.p7	15:63773366	GGAGAATCGCTTGAA[C/T]CCAGGAGGCAGAGGT	8925
rs4577025	snp	A/G	0.439502	0.163061	intron-variant	HERC1	GRCh38.p7	15:63826856	ataaagtatgacaac[A/G]tattctgttggtgct	8925
rs4603505	snp	C/T	0.465578	0.126594	intron-variant	HERC1	GRCh38.p7	15:63623346	ACTTTATTTTTCTAA[C/T]TCCCCTGGAATCTGG	8925
rs4776363	snp	A/G	0.466618	0.124806	intron-variant	HERC1	GRCh38.p7	15:63829801	GCCCCAGAATATAAG[A/G]AAGTGCTTGAAAAAG	8925
rs4776681	snp	A/T	0.463774	0.129618	intron-variant	HERC1	GRCh38.p7	15:63807564	GCTCTCCTTAACCCT[A/T]CCCAAAACTCTACAA	8925
rs4776693	snp	C/T	0.463343	0.130326	intron-variant	HERC1	GRCh38.p7	15:63810313	AAAATGTGGTGTATA[C/T]ACATACACTGAAATA	8925
rs4776937	snp	A/G			intron-variant	HERC1	GRCh38.p7	15:63829561	TGTGTGTGTGTGTGT[A/G]TATATATATATATAT	8925
rs4984252	snp	A/G	0.463126	0.13068	intron-variant	HERC1	GRCh38.p7	15:63609447	TGCCCCGTGGCCCTC[A/G]AGGCTCTGGGTGAAG	8925
rs4984253	snp	A/C	0.476227	0.106402	intron-variant	HERC1	GRCh38.p7	15:63627434	CCCAGCACTTTGGGA[A/C]GCTGAGGCTTGAACT	8925
rs4984304	snp	C/G	0.4628	0.13121	intron-variant	HERC1	GRCh38.p7	15:63622389	CTGGAGTACAGTGGC[C/G]TGATCTCGGCTCACT	8925
rs4984305	snp	C/T	0.441705	0.160466	intron-variant	HERC1	GRCh38.p7	15:63636812	GTGGGAAAACTGAGT[C/T]ACAAAGAGGTCTCGA	8925
rs4984306	snp	C/T			intron-variant	HERC1	GRCh38.p7	15:63646589	ggcggatcatgaagt[C/T]aggaattcgagacca	8925
rs4984307	snp	C/T	0.443464	0.15834	intron-variant	HERC1	GRCh38.p7	15:63657609	ttcaaatcacttttg[C/T]taaacagaggttttc	8925
rs4984310	snp	C/T	0.462363	0.131916	intron-variant	HERC1	GRCh38.p7	15:63667130	tggccataagctcaa[C/T]gttagtgaataaaca	8925
rs4984313	snp	A/G	0.477004	0.104734	intron-variant	HERC1	GRCh38.p7	15:63755579	agctcaggagttcga[A/G]ttcagcctgggcaac	8925
rs4984314	snp	C/T	0.5	0	intron-variant	HERC1	GRCh38.p7	15:63784618	AAATTTTTTTTTTTT[C/T]CCTTTTTGAGACAGA	8925
rs4984315	snp	A/G/T	0.000798403	0.0199641	intron-variant	HERC1	GRCh38.p7	15:63790597	aaaaaTTTTTTTTTT[A/G/T]AAAAGTACTTTTTAA	8925
rs4984317	snp	C/T	0.463989	0.129263	intron-variant	HERC1	GRCh38.p7	15:63792458	AACCCTTTCCAGATA[C/T]AACCCTATCAGCAAA	8925
rs4984318	snp	C/T	0.463989	0.129263	intron-variant	HERC1	GRCh38.p7	15:63792484	GCAAAGCAGAATGAA[C/T]GTGTGCTTCCAGGAG	8925
rs4984319	snp	C/T	0.463343	0.130326	intron-variant	HERC1	GRCh38.p7	15:63697105	ttggtacaatactat[C/T]aactaaacctaaagt	8925
rs6494418	snp	A/G	0.0689305	0.172377	intron-variant	HERC1	GRCh38.p7	15:63632138	CTTCCCCACAAACCA[A/G]CTCATGTCCTCAGTC	8925
rs6494419	snp	G/T	0.463343	0.130326	intron-variant	HERC1	GRCh38.p7	15:63651707	CTAAACTCTTGGGAA[G/T]ACTTCAGAAAAGAAA	8925

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