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
rs14987	snp	G/T			utr-variant-3-prime	HERC5	GRCh38.p7	4:88506082	ATaggggtatccaag[G/T]gagagaatacagtca	51191
rs2629564	snp	C/G			intron-variant	HERC5	GRCh38.p7	4:88499704	AACAAGAGCTGTGAA[C/G]CAGGCAGGCAGCCTG	51191
rs2629565	snp	C/G			intron-variant	HERC5	GRCh38.p7	4:88499705	ACAAGAGCTGTGAAG[C/G]AGGCAGGCAGCCTGC	51191
rs2717532	snp	A/G	0.0596104	0.162024	intron-variant	HERC5	GRCh38.p7	4:88502800	gatatccaaacagcc[A/G]ataagcatataaagt	51191
rs3733446	snp	G/T	0.164546	0.234942	intron-variant	HERC5	GRCh38.p7	4:88499805	CGCAGAGAAAGAGGT[G/T]CTGTGAACTATACCT	51191
rs4132726	snp	C/G			intron-variant	HERC5	GRCh38.p7	4:88481117	tgcagtgagccgaga[C/G]tgcgccactgcactc	51191
rs4544677	snp	A/G	0.0116955	0.0755709	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88461048	GTAGGGTAATAGAGG[A/G]GAATTCGAAGTCAAG	51191
rs4585264	snp	A/C	0.472522	0.113946	intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88468489	AGGGTTCTAGTATCC[A/C]AGTTTGGTGAATTCC	51191
rs6816627	snp	A/C/G/T	0.0547245	0.156101	intron-variant	HERC5	GRCh38.p7	4:88471284	GTAGAAAACAATGTA[A/C/G/T]AAACAATATGATCCa	51191
rs6826311	snp	A/T	0.105569	0.204058	intron-variant	HERC5	GRCh38.p7	4:88488155	TTCTCTCCTGATTTT[A/T]AACAAGGTTCCAGAG	51191
rs6832416	snp	C/T	0.00874735	0.0655527	intron-variant	HERC5	GRCh38.p7	4:88501886	tcactgcaacctccg[C/T]ctcccgggttcaagc	51191
rs6847262	snp	A/G	0.00480766	0.0487926	upstream-variant-2KB, nc-transcript-variant, intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88456407	gtaggggtggggggg[A/G]gggtAGCTGCCTGCA	51191
rs6857425	snp	C/T	0.00236951	0.0343386	synonymous-codon	HERC5	GRCh38.p7	4:88494245	CAATGTTGCCAACCT[C/T]CCTTTCCCACTGGCA	51191
rs7437274	snp	A/T	0	0	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88461056	ATAGAGGGGAATTCG[A/T]AGTCAAGGGAATTTT	51191
rs7663568	snp	C/T	0.0225045	0.103662	intron-variant	HERC5	GRCh38.p7	4:88487451	AGTTGGCAGTGGCAG[C/T]CTGTAGTCTTCTGAA	51191
rs7667551	snp	A/G	0.217851	0.247924	intron-variant	HERC5	GRCh38.p7	4:88472755	CACATATATGCATAC[A/G]CATTCGTAGAGGGAA	51191
rs7681411	snp	C/T	0.388775	0.207946	intron-variant	HERC5	GRCh38.p7	4:88495492	ttgagctcaggaggt[C/T]gaagctgcagtgagc	51191
rs7687886	snp	C/T	0.0803491	0.183626	intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88468747	CTTTGCAGGCCAGTA[C/T]TAAGAAAGACACCAA	51191
rs7688056	snp	A/G	0.02016	0.0983543	intron-variant	HERC5	GRCh38.p7	4:88503591	CCTGGTATATGACTC[A/G]GTTGTCATTAGTAAA	51191
rs7699006	snp	A/G	0.492876	0.0592575	missense	HERC5	GRCh38.p7	4:88475940	CTCCCAGAATGTCCT[A/G]TGATGCATATTTCCA	51191
rs9784397	snp	A/G	0.497445	0.0356514	upstream-variant-2KB, nc-transcript-variant, intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88455565	gcacaaaagcttgtg[A/G]ggcaggtcagagatt	51191
rs10049671	snp	A/T	0.00358779	0.0422022	intron-variant	HERC5	GRCh38.p7	4:88498385	aaacttaggagccca[A/T]ccccaaacccagtgt	51191
rs10516808	snp	A/G	0.170408	0.236992	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88462511	AGAATCAGTCCAAGA[A/G]GCATACATAGTGTGG	51191
rs10516809	snp	A/G	0.140899	0.224938	synonymous-codon	HERC5	GRCh38.p7	4:88499935	CCTTAGGAATTTGCA[A/G]ACACTTCTGGATGAT	51191
rs11722508	snp	A/C	0.164873	0.23506	intron-variant	HERC5	GRCh38.p7	4:88496349	agaatagccagaaat[A/C]attcttaaggcaaat	51191
rs11946864	snp	A/T	0	0	intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88458021	GCGTTCTTTAAAATT[A/T]TGCCCATCTGTGGAG	51191
rs11947119	snp	G/T	0.0543475	0.155628	intron-variant	HERC5	GRCh38.p7	4:88482751	GGTCCTAGGGCTGTA[G/T]tcccaagtacctggg	51191
rs12331773	snp	C/T	0.493107	0.0583	intron-variant	HERC5	GRCh38.p7	4:88489975	GATCATGCCACTGCA[C/T]TCCGGCCTGGGTGAC	51191
rs12505811	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88468006	TTATAGCCAGCAGTC[A/G]TTGCTTAAATCTTGA	51191
rs13119367	snp	A/T			intron-variant	HERC5	GRCh38.p7	4:88482231	aggagagtcgcttga[A/T]tccaggaggcagagg	51191
rs13146052	snp	A/G	0.0186899	0.0948454	intron-variant	HERC5	GRCh38.p7	4:88474000	GAGGTTCTGCGATAC[A/G]GACTCTCAGACCTTT	51191
rs13147515	snp	G/T			intron-variant	HERC5	GRCh38.p7	4:88475342	ttttttttttttttt[G/T]gagatggagtcttgc	51191
rs13148298	snp	A/C	0	0	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88462031	CATCAGTGCAAAGGT[A/C]CAATATTGTGATATT	51191
rs13152493	snp	G/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88458391	CATTTTTGTAGTAAT[G/T]TTAAGGTTTTTTTTT	51191
rs17014143	snp	A/G/T	0.0131427	0.0799923	missense, intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88463975	AGAGTGACTCAGATA[A/G/T]CATGTGGAAGGTAAG	51191
rs17014146	snp	A/T	0.214239	0.247429	intron-variant, nc-transcript-variant	HERC5, LOC102723458	GRCh38.p7	4:88467923	ACGAACAGAGTTATT[A/T]CCTTAAGCAGCATGT	51191
rs17014147	snp	G/T	0.0464069	0.145088	intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88468323	GACTTTCTAAAACTC[G/T]TACTCTTTGTGCATC	51191
rs17014153	snp	C/G	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88469986	CATTAGTTTGTGTAC[C/G]TGTTATTCTTAGCTG	51191
rs17014156	snp	G/T	0.125182	0.216612	intron-variant	HERC5	GRCh38.p7	4:88473813	GTCTGTGAAGGGAAG[G/T]GATTGGATCAGTTCA	51191
rs28410134	snp	G/T	0.492287	0.0616198	intron-variant	HERC5	GRCh38.p7	4:88482047	GGTGTGGTGGCTCAT[G/T]CCTGTAATCCCAGCA	51191
rs28441580	snp	C/G			intron-variant	HERC5	GRCh38.p7	4:88475390	GTGACACAATCTCGG[C/G]TCACTGCAACCTCTG	51191
rs28517536	snp	C/T	0.0023933	0.0345097	intron-variant	HERC5	GRCh38.p7	4:88486360	TCCTCAAAATCTATG[C/T]AATTTTGCAGTCAGA	51191
rs28569005	snp	A/G			intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88469526	AAAATCTGTAGGGCA[A/G]GCCAGCAGGCTGGAG	51191
rs34100798	in-del	-/T			intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88458530	AATACTTCCTTTTTT[-/T]CAACTGATTTGAAAT	51191
rs34182426	in-del	-/C			intron-variant	HERC5	GRCh38.p7	4:88470116	ATGGCTTTCTAATTC[-/C]TGGAAAATGATTGTA	51191
rs34457268	in-del	-/C			frameshift-variant	HERC5	GRCh38.p7	4:88494216	TTCTATGTGGACTTT[-/C]CCCTGTTCAATTGCA	51191
rs34778861	snp	A/G			intron-variant	HERC5	GRCh38.p7	4:88488254	TTTTTTTTTTTGAGA[A/G]AGAGTCTCCCTCTGT	51191
rs34823613	snp	A/G	0.0076247	0.0612716	synonymous-codon	HERC5	GRCh38.p7	4:88472445	TGTTTATTTGGACTT[A/G]AATAAAGCAAGAAAC	51191
rs34840817	snp	A/G	0.00557542	0.0525036	intron-variant	HERC5	GRCh38.p7	4:88500359	ATTCTCCAATAGGCT[A/G]GCTGAGGCTTTTGAA	51191
rs34980419	in-del	-/C			upstream-variant-2KB, frameshift-variant, intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88457079	GCAGGCCCCGCCCCC[-/C]AAACAGCACGTGGGG	51191
rs35087151	in-del	-/T			utr-variant-3-prime	HERC5	GRCh38.p7	4:88506077	CCCGTGACTGTATTC[-/T]TCTCCCTTGGATACC	51191
rs35414633	in-del	-/T			intron-variant	HERC5	GRCh38.p7	4:88503253	GAACCTATAGATCAA[-/T]TTTTTGAAAAAATTG	51191
rs35420686	snp	A/G			intron-variant	HERC5	GRCh38.p7	4:88488256	TTTTTTTTTGAGAGA[A/G]AGTCTCCCTCTGTTG	51191
rs35438949	in-del	-/T	0	0	intron-variant	HERC5	GRCh38.p7	4:88477080	TTTTTTTTTTTTTTT[-/T]AAGAATCTCATTTGA	51191
rs35511740	in-del	-/T			intron-variant	HERC5	GRCh38.p7	4:88472790	TCAACTCAGGGCTTT[-/T]AGGAAGATGATTAAG	51191
rs35749883	in-del	-/C			intron-variant	HERC5	GRCh38.p7	4:88474929	CAAATGATTACTGTG[-/C]ATCTAAGCACACATA	51191
rs35999083	in-del	-/G			intron-variant	HERC5	GRCh38.p7	4:88502221	TGTTGGTATGTAACT[-/G]GGGAGAAGTGCTTGG	51191
rs36021764	in-del	-/C			intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88460610	ATTCAAGGATCTCCC[-/C]TAGCCCTGTAGTATT	51191
rs55816888	snp	A/G			upstream-variant-2KB, nc-transcript-variant, intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88455249	AATTTTTGCTCCTTA[A/G]CTCAGCTAAAATCCA	51191
rs55990584	snp	C/T	0.0233443	0.105486	synonymous-codon	HERC5	GRCh38.p7	4:88470620	CTAATATAGGGAAAT[C/T]CAAGAGATATTTTCA	51191
rs56006160	snp	A/G	0.021333	0.101051	intron-variant	HERC5	GRCh38.p7	4:88471190	GGCCAGGCTGGTCTC[A/G]AACTCCTGAGCTCAG	51191
rs57966410	snp	A/G	0.0209421	0.100162	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88466439	ATTGCCCGGATAGTT[A/G]AACTTAATCTCCAGC	51191
rs58490237	in-del	-/GTT			utr-variant-3-prime	HERC5	GRCh38.p7	4:88505946	GTTGTTGTTGTTGTT[-/GTT]TCTCTACTTTGTTTT	51191
rs58497654	snp	A/T	0.0166325	0.0896639	intron-variant	HERC5	GRCh38.p7	4:88501590	CTGGCCTACATCACA[A/T]CTTTTTCCACGATTT	51191
rs58577205	in-del	-/A			intron-variant	HERC5	GRCh38.p7	4:88480085	AAAAAAAAAAAAAAA[-/A]GAAATAACCTGTGTG	51191
rs59412540	snp	A/G	0.0217236	0.101931	intron-variant	HERC5	GRCh38.p7	4:88483408	AGACAGGGCCTAACT[A/G]TGTTGCTCAGGCTGG	51191
rs59421640	snp	C/T	0.0205511	0.0992634	intron-variant	HERC5	GRCh38.p7	4:88472934	TTCTTTTTTTTTTTT[C/T]TTTTCCATTCTACTT	51191
rs60661158	snp	A/G	0.125874	0.217008	intron-variant	HERC5	GRCh38.p7	4:88502577	TTGGAGGCGAAAGGG[A/G]AAAAAGGAGGAGTGG	51191
rs61337796	in-del	-/TT			intron-variant	HERC5	GRCh38.p7	4:88502910	CTAGATGCAAGTCTT[-/TT]GTTGGTTATATGTAC	51191
rs61755702	snp	A/G	0.000286149	0.0119579	synonymous-codon, intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88462157	GCTTTTTGCCTGGGG[A/G]CAGAACCTGCATGGG	51191
rs62308681	snp	G/T	0.5	0	intron-variant	HERC5	GRCh38.p7	4:88476297	AAATTTCACAGAGAA[G/T]TTGAAAGAATAGTAT	51191
rs62308682	snp	A/C			intron-variant	HERC5	GRCh38.p7	4:88483034	TTTCTTTTTCCAGTC[A/C]ATATACGTTTTATTA	51191
rs62308683	snp	A/G	0.0463947	0.145069	intron-variant	HERC5	GRCh38.p7	4:88502649	ACACTTTCATCAGTA[A/G]GGTACGACAGTTCTA	51191
rs66502916	snp	C/T	0.390277	0.206936	intron-variant	HERC5	GRCh38.p7	4:88502093	GTGAGCCACTGCGCC[C/T]GGCCTATCTGTAGTA	51191
rs71609527	snp	A/T	0.5	0	intron-variant	HERC5	GRCh38.p7	4:88501650	AAGTATAACCTATAT[A/T]ACAGAATTTTGCACA	51191
rs72879395	snp	A/G	0.00809425	0.0631	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88459319	ATAATCAAAGTGACA[A/G]TAGTTCCTGGTTGGA	51191
rs72881108	snp	A/G	0.0244538	0.107838	intron-variant	HERC5	GRCh38.p7	4:88478286	TTGTAATTATAATAT[A/G]TACTAAAATATTTTG	51191
rs72881116	snp	G/T	0.0217236	0.101931	intron-variant	HERC5	GRCh38.p7	4:88498318	CACTAATGTGTGAGA[G/T]CCTCTAGGGGTGGGC	51191
rs73841943	snp	A/G	0.021333	0.101051	intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88457992	TCTCATCGAAGTGGG[A/G]GAAATAGTTGCCCGC	51191
rs73841944	snp	A/C	0.0221141	0.102801	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88467417	TTCAGATTAGGATTA[A/C]TGTGAATTTAAATGA	51191
rs73841945	snp	A/G	0.0221141	0.102801	intron-variant	HERC5	GRCh38.p7	4:88472757	CATATATGCATACAC[A/G]TTCGTAGAGGGAAGT	51191
rs73841946	snp	G/T	0.00639822	0.0561976	intron-variant	HERC5	GRCh38.p7	4:88479534	TTTAGAAACCTCTGT[G/T]TTTTTATCTAGCTGT	51191
rs73841947	snp	A/G	0.5	0	intron-variant	HERC5	GRCh38.p7	4:88496746	GACATGCAGTGTACC[A/G]ACAGTAAAGAAAAGA	51191
rs73841948	snp	A/G	0.0197687	0.0974348	intron-variant	HERC5	GRCh38.p7	4:88497717	GTAAAGAATGCAAAC[A/G]TGTTTGGAAGAGAGC	51191
rs74374958	snp	A/T	0.0134861	0.0810011	intron-variant	HERC5	GRCh38.p7	4:88497160	TAAATGGACTAAGGG[A/T]AATTGCTACCAAGAA	51191
rs74581848	snp	A/G	0.0236746	0.106192	intron-variant	HERC5	GRCh38.p7	4:88492099	ACCTTCATCTCCCGG[A/G]TTCAAGTGAGTCTCC	51191
rs74632998	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	HERC5, LOC102723458	GRCh38.p7	4:88458422	TTAAGTTAAAATTTT[A/T]CGTACGCTTGGAATT	51191
rs74658427	snp	C/T	0.216649	0.247765	intron-variant	HERC5	GRCh38.p7	4:88499388	GAAATAATTTAAAAA[C/T]TGGTTACTGTCCATT	51191
rs74782314	snp	A/G	0.0166325	0.0896639	intron-variant	HERC5	GRCh38.p7	4:88478058	CAAGTTTGTAGTTGT[A/G]TTAACTGTAAAGGAA	51191
rs74876955	snp	C/T	0.0158469	0.0875917	intron-variant	HERC5	GRCh38.p7	4:88494400	ATATTTAAGTACACA[C/T]GCTTCATAATATTTC	51191
rs74945477	snp	A/T	0.5	0	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88459156	TTCTAATTAAAAAAA[A/T]TCTATGTCAAGACCG	51191
rs74958280	snp	A/G	0.0168055	0.0901129	intron-variant	HERC5	GRCh38.p7	4:88484910	AATGCCTTTAAACAT[A/G]TTTGTTACAGCTTTT	51191
rs75070724	snp	A/G	0.00640729	0.0562369	missense, intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88459389	AGATACATTCCGTGG[A/G]CCAAGGAGCAGAGCA	51191
rs75121676	snp	C/T	0.0142736	0.0832652	intron-variant	HERC5	GRCh38.p7	4:88495541	CTCCAGCCTGGGCGA[C/T]AGTAGAAGACCCTGT	51191
rs75124661	snp	A/G	0.00438332	0.0466095	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88462570	CAGGGCTGTGTGTGA[A/G]ACGGGAAAGGGCATT	51191
rs75362741	snp	C/T	0	0	intron-variant	HERC5	GRCh38.p7	4:88471984	CTTCCCTTCCTTCTT[C/T]CTTTTCTTTTTTTCT	51191
rs75376862	snp	A/G	0.00478085	0.0486577	intron-variant	HERC5	GRCh38.p7	4:88501123	AAGTTGGTGTGTGTT[A/G]TATGTGTTTTGACAT	51191
rs75842378	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88464728	GGAATAGCTAGGATT[A/G/T]CAGGCGTGCACTGCC	51191
rs76041741	snp	A/C/T			intron-variant	HERC5, LOC102723458	GRCh38.p7	4:88464726	CTGGAATAGCTAGGA[A/C/T]TACAGGCGTGCACTG	51191
rs76095623	snp	C/T	0.0142736	0.0832652	intron-variant	HERC5	GRCh38.p7	4:88501126	TTGGTGTGTGTTGTA[C/T]GTGTTTTGACATATA	51191

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