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
rs702965	snp	A/G	0.327445	0.237702	utr-variant-3-prime	PHRF1	GRCh38.p7	11:611868	CCCGGGCATGGCCCC[A/G]ATTCCCGCCACTCCC	57661
rs702966	snp	C/G	0.398894	0.200825	utr-variant-3-prime	PHRF1	GRCh38.p7	11:611919	CCGACGGCAGGCATG[C/G]TGATGCCCCCCATTT	57661
rs936468	snp	C/T	0.295923	0.245746	synonymous-codon	PHRF1	GRCh38.p7	11:607175	TGGCCTGTTTCCTGA[C/T]GGGCCTTGGGCCGGG	57661
rs936469	snp	C/T	0.304937	0.243889	intron-variant	PHRF1	GRCh38.p7	11:606749	AACTGAGAAACTGCT[C/T]AAGAAGGGAAATCAA	57661
rs936470	snp	C/G	0.302936	0.244331	intron-variant	PHRF1	GRCh38.p7	11:606656	TGGGCTGAGTGCTTG[C/G]GAACAGCCTGAGGAC	57661
rs936471	snp	C/T	0.0146672	0.084371	intron-variant	PHRF1	GRCh38.p7	11:594264	AGGTCTATCATGCCA[C/T]GGTCTCTCAGGCCGT	57661
rs936472	snp	A/G	0.470618	0.117591	intron-variant	PHRF1	GRCh38.p7	11:593453	CTTCACCAGGAGCCC[A/G]TCCTCGGTGCGGCTC	57661
rs1055382	snp	C/T	0.399073	0.200692	utr-variant-3-prime, downstream-variant-500B	PHRF1, IRF7	GRCh38.p7	11:612182	AGCTGCTGTGTACCT[C/T]TGGCTCTGAATTAGG	57661
rs1802427	snp	A/G	1.65996e-05	0.00288089	downstream-variant-500B, missense	PHRF1, IRF7	GRCh38.p7	11:612686	AACAGCCTCTATGAC[A/G]ACATCGAGTGCTTCC	57661
rs2396545	snp	A/G	0.359998	0.2245	intron-variant	PHRF1	GRCh38.p7	11:601785	GAGGGTGCCAAGGCC[A/G]GCGGGAGGCTTAGGC	57661
rs3740648	snp	A/C	0.161596	0.233848	intron-variant	PHRF1	GRCh38.p7	11:596672	CAGGTGAGGTCACAG[A/C]GGGGAGGCGGCCGTC	57661
rs3740649	snp	C/T	0.0166325	0.0896639	intron-variant	PHRF1	GRCh38.p7	11:592825	TGTAACAGGAAGGCC[C/T]GCAGGACTGAACCGC	57661
rs3832719	in-del	-/G			intron-variant	PHRF1	GRCh38.p7	11:596638	AAGTCAGGAAGGGGG[-/G]CCTCCCCAGGAACCA	57661
rs4623937	snp	A/G	0.302184	0.244493	intron-variant	PHRF1	GRCh38.p7	11:605856	GGCCGACTGATGAGC[A/G]TGACAGCTGAGGGGA	57661
rs4963128	snp	A/G	0.415727	0.187175	intron-variant	PHRF1	GRCh38.p7	11:589564	CCCCCGAGTGTGTCC[A/G]GGCCTCTTCTAAGCC	57661
rs4963140	snp	C/T	0.499265	0.0191552	intron-variant	PHRF1	GRCh38.p7	11:588654	AAACTGCTGGGATTA[C/T]AGGCGTGAGCCACCA	57661
rs4963177	snp	A/T	0.000399281	0.0141238	intron-variant	PHRF1	GRCh38.p7	11:596194	TCCCAAAGACCCCAG[A/T]CAGCCCTGAGTAAGG	57661
rs4963178	snp	A/G	0.0803491	0.183626	intron-variant	PHRF1	GRCh38.p7	11:593098	CAGGGAGAGCAGCAG[A/G]TGCAGCATAACTGGA	57661
rs6598010	snp	C/T	0.00914312	0.0669923	intron-variant	PHRF1	GRCh38.p7	11:597318	TCCCCCTGTGGCTGC[C/T]GGCCAAGTAGCAGCC	57661
rs6598011	snp	A/G	0.426966	0.176587	intron-variant, upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:577809	AAAAGGGCCTCTGGT[A/G]TCCGGGGTGCCTGCA	57661
rs7101726	snp	A/G	0.399611	0.200291	intron-variant	PHRF1	GRCh38.p7	11:599313	cagtgagccaagatc[A/G]tgccactgcactcca	57661
rs7103762	snp	A/G	0.0715223	0.175059	intron-variant	PHRF1	GRCh38.p7	11:589589	ACCTGCCCCACAGGC[A/G]CCTCCTGCCCCCCCG	57661
rs7107379	snp	A/G	0.0894459	0.191631	intron-variant	PHRF1	GRCh38.p7	11:589076	caatctcagctcact[A/G]caacctccaactccc	57661
rs7112149	snp	C/T	0.305436	0.243776	intron-variant	PHRF1	GRCh38.p7	11:595890	AGCAGAGGGGGGCGG[C/T]GGGTGGGGGCACTCC	57661
rs7113728	snp	A/C	0.0279526	0.114869	intron-variant	PHRF1	GRCh38.p7	11:578078	CTTCCCTTCCCCATA[A/C]CCACCTCTGCCATGT	57661
rs7113872	snp	C/G	0.151668	0.229849	intron-variant	PHRF1	GRCh38.p7	11:577908	GATTAAAGAGGAAAA[C/G]AAAAAACTGGAAAGG	57661
rs7115784	snp	A/C	0.0733688	0.176922	intron-variant	PHRF1	GRCh38.p7	11:589647	AGTCCGAGATCTTGA[A/C]TCCGTCCGGCATCGT	57661
rs7115912	snp	C/T	0.0858192	0.188533	intron-variant	PHRF1	GRCh38.p7	11:589597	CCCAGCTGACCTGCC[C/T]CACAGGCGCCTCCTG	57661
rs7116027	snp	G/T	0.00653559	0.0567898	missense	PHRF1	GRCh38.p7	11:609148	TCGGCCGTAGCCACC[G/T]CCGGCGAGACATGTG	57661
rs7116322	snp	C/T	0.0744748	0.178019	intron-variant	PHRF1	GRCh38.p7	11:589246	TGTCTTACACGTCTC[C/T]TTATGACTTATTTCT	57661
rs7116433	snp	C/T	0.0894459	0.191631	intron-variant	PHRF1	GRCh38.p7	11:589162	ATTTTAACAGTTCAT[C/T]TGTAAGAGTTCTCCt	57661
rs7117022	snp	A/G	0.333722	0.235565	intron-variant	PHRF1	GRCh38.p7	11:583787	TGGCAACAGGGGACA[A/G]GGAAGGAGGTACCAC	57661
rs7118452	snp	C/T	0.0894459	0.191631	intron-variant	PHRF1	GRCh38.p7	11:596309	TTCTATCGAGCCTTC[C/T]GGGAAGGTAGTTTGG	57661
rs7118859	snp	C/T	0.0894459	0.191631	intron-variant	PHRF1	GRCh38.p7	11:596005	CTATGAGAAGGTGTC[C/T]GCTGTGTGGCCCTTG	57661
rs7119844	snp	A/G	0.151668	0.229849	intron-variant	PHRF1	GRCh38.p7	11:577915	TTTGGGGGATTAAAG[A/G]GGAAAACAAAAAACT	57661
rs7119851	snp	A/C	0.151668	0.229849	intron-variant	PHRF1	GRCh38.p7	11:577903	AAGAGGAAAACAAAA[A/C]ACTGGAAAGGCTATT	57661
rs7120313	snp	C/T	0.498871	0.0237351	intron-variant	PHRF1	GRCh38.p7	11:584112	AACTCTGGAAGGACA[C/T]GGCCAACACACATTG	57661
rs7121828	snp	A/T	0.0850919	0.187897	intron-variant	PHRF1	GRCh38.p7	11:589595	CAGCTGACCTGCCCC[A/T]CAGGCGCCTCCTGTC	57661
rs7122021	snp	C/T	0.305685	0.24372	intron-variant	PHRF1	GRCh38.p7	11:595810	GGACAAAGGCAAGGA[C/T]GAGCAGTACCTTCTT	57661
rs7123948	snp	A/G	0.139932	0.224466	missense	PHRF1	GRCh38.p7	11:609577	TGTACCCTCCCACTC[A/G]CAGAGGGGCTGTCTT	57661
rs7124881	snp	A/C	0.0279272	0.11482	intron-variant	PHRF1	GRCh38.p7	11:587238	GAGGAAACATGCCAG[A/C]TGGTGCAAGCAGGAT	57661
rs7926440	snp	A/G	0.283947	0.247685	intron-variant	PHRF1	GRCh38.p7	11:589819	CTCAGGCTGAGCCCC[A/G]CACGCTCTGTGCCCG	57661
rs7928902	snp	C/T	0.36377	0.222613	synonymous-codon	PHRF1	GRCh38.p7	11:609068	CCCCTGTGCAAGGGG[C/T]GCTGGGGAAGCCTCC	57661
rs7929316	snp	A/G	0.134508	0.221724	intron-variant	PHRF1	GRCh38.p7	11:606399	GTCACTGCCTCCCAC[A/G]GCCTGAGGGCCCGCA	57661
rs7929655	snp	A/G	0.089084	0.191327	intron-variant	PHRF1	GRCh38.p7	11:606156	CCAACTCCACCAACA[A/G]GTGGGAGGGGGCAGA	57661
rs7931013	snp	A/T	0.0232847	0.105357	intron-variant	PHRF1	GRCh38.p7	11:586334	GAGGCAGCAGAAGAG[A/T]TTTAAGTTCCCATCT	57661
rs7932229	snp	C/T	0.499218	0.0197529	intron-variant	PHRF1	GRCh38.p7	11:578759	GTTATGAGACCAGCC[C/T]GGGCAACATGGCAAA	57661
rs7935737	snp	A/G	0.0894459	0.191631	intron-variant	PHRF1	GRCh38.p7	11:592406	CTCCACGTGTACACA[A/G]GGATTTTTATGTTTT	57661
rs7935754	snp	A/G	0.0894459	0.191631	intron-variant	PHRF1	GRCh38.p7	11:592377	TTCTACCATCTCAGG[A/G]TGGTGATCTAAGAGG	57661
rs7936397	snp	C/T	0.370568	0.219005	intron-variant, upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:577534	CATGATGCTGAGGTG[C/T]CATCCATCCACTAGC	57661
rs7936642	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:577357	GCTGTTCTGCTGTTG[C/T]CGAAACAAGTAAAGC	57661
rs7938382	snp	A/C			missense	PHRF1	GRCh38.p7	11:608151	TGGACATGGCGGAGG[A/C]CGGTCCGAGAGGGGG	57661
rs7938821	snp	A/G	0.0894459	0.191631	intron-variant	PHRF1	GRCh38.p7	11:586417	TGTTATCTGGCAAAG[A/G]GAAAGACACACCCAG	57661
rs7940747	snp	C/G	0.170084	0.236883	intron-variant	PHRF1	GRCh38.p7	11:606224	CTCGCAGCTCTGGCC[C/G]CAGGGAAACCAGGCG	57661
rs7941547	snp	C/T	0.397271	0.202018	intron-variant	PHRF1	GRCh38.p7	11:611503	CAGCACGCAGACAGA[C/T]GGCGGCAGAGGCCGC	57661
rs7943546	snp	A/G	0.346811	0.230494	utr-variant-3-prime, downstream-variant-500B	PHRF1, IRF7	GRCh38.p7	11:612148	GGCGGGAGGCCACCT[A/G]GAGATTTATCAAGGA	57661
rs7943961	snp	C/T	0.0905309	0.192535	intron-variant	PHRF1	GRCh38.p7	11:605857	GGGCCGACTGATGAG[C/T]GTGACAGCTGAGGGG	57661
rs7947833	snp	A/G	0.0894459	0.191631	intron-variant	PHRF1	GRCh38.p7	11:588289	CAGACTTTGGGTGAC[A/G]TCACAGCCTGCCACC	57661
rs7949750	snp	C/G	0.0894459	0.191631	intron-variant	PHRF1	GRCh38.p7	11:586635	TTCAACACGGCAGAG[C/G]CCATACGTGCACTGC	57661
rs7952542	snp	A/G	0.0240604	0.107011	intron-variant	PHRF1	GRCh38.p7	11:592510	ACCCAAACTCCCCGC[A/G]GTCACTTCCCAGCGT	57661
rs9666658	snp	A/G	0.0803491	0.183626	intron-variant	PHRF1	GRCh38.p7	11:599471	ggccaggctggtctt[A/G]aactcccgacctcag	57661
rs10736899	snp	A/C	0.199873	0.244923	intron-variant	PHRF1	GRCh38.p7	11:579256	CCCAGCCCTGCTCCT[A/C]CCCCCAGCCCTGCTC	57661
rs10902175	snp	C/T	0.33693	0.2344	intron-variant	PHRF1	GRCh38.p7	11:578996	AGGTGCACGCCGCCA[C/T]GCCCGGCTCATTTTT	57661
rs10902176	snp	A/C	0.00438332	0.0466095	intron-variant	PHRF1	GRCh38.p7	11:585026	gacaggcatgagcca[A/C]cgcgcctggccAGGA	57661
rs10902177	snp	A/G	0.294576	0.245994	intron-variant	PHRF1	GRCh38.p7	11:591083	GACTTGAACAGGCTC[A/G]CCGCAGAGGGGCCTG	57661
rs11246193	snp	A/G			upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:576031	cagacgtgggggcgg[A/G]gctgcgggcgcgagg	57661
rs11246194	snp	A/G	0.147656	0.228091	intron-variant, upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:577309	ATGCTCCTTTTGACG[A/G]GGCTTGTGTTGCCCC	57661
rs11246195	snp	C/T	0.118235	0.212457	intron-variant, upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:577354	TGTGCTTTACTTGTT[C/T]CGACAACAGCAGAAC	57661
rs11246196	snp	C/T	0.147321	0.227941	intron-variant, upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:577442	CGAGCTGAGGTTTGA[C/T]TTCGGGTTTGGCATA	57661
rs11246197	snp	C/T	0.119978	0.213528	intron-variant, upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:577454	TGACTTCGGGTTTGG[C/T]ATAGTTGATCTCTCT	57661
rs11246198	snp	C/G	0.118933	0.212888	intron-variant, upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:577670	TTTGAGTTCTCCTAG[C/G]TGATACAGCAGATGG	57661
rs11246199	snp	A/G	0.136506	0.222754	intron-variant, upstream-variant-2KB	PHRF1, LOC143666	GRCh38.p7	11:577684	GCTGATACAGCAGAT[A/G]GTGAATACAAGAATA	57661
rs11246200	snp	A/G	0.183886	0.241099	intron-variant	PHRF1	GRCh38.p7	11:583107	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAG	57661
rs11246201	snp	C/G	0.117537	0.212022	intron-variant	PHRF1	GRCh38.p7	11:583122	GAGGCGGGCGGATCA[C/G]GAGGTCAGGAGATCG	57661
rs11246202	snp	C/T	0.0693013	0.172766	intron-variant	PHRF1	GRCh38.p7	11:584769	tgagaccgagtttca[C/T]tcttgttgcccaggc	57661
rs11246203	snp	C/G	0.198014	0.244535	intron-variant	PHRF1	GRCh38.p7	11:590605	TTGTGTATGGTGTAC[C/G]TTAATAAAGCCAACA	57661
rs11246204	snp	A/T	0.139903	0.224452	intron-variant	PHRF1	GRCh38.p7	11:595168	TCTCTACTAAAAATA[A/T]AAAAATTGGCCGGGC	57661
rs11246205	snp	G/T			intron-variant	PHRF1	GRCh38.p7	11:599753	GACTCAGTGTCTGTG[G/T]GTCTGGTGCAGGGTC	57661
rs11246206	snp	G/T	0.00914312	0.0669923	intron-variant	PHRF1	GRCh38.p7	11:599774	GTGCAGGGTCCTGGG[G/T]CTCCAGAGGACTCGG	57661
rs11246207	snp	A/G	0.00914312	0.0669923	intron-variant	PHRF1	GRCh38.p7	11:599781	GTCCTGGGTCTCCAG[A/G]GGACTCGGCGTCTGT	57661
rs11246208	snp	A/G	0.00716266	0.059414	intron-variant	PHRF1	GRCh38.p7	11:599788	GTCTCCAGAGGACTC[A/G]GCGTCTGTGGGTCTG	57661
rs11246209	snp	C/T	0.00716266	0.059414	intron-variant	PHRF1	GRCh38.p7	11:599790	CTCCAGAGGACTCGG[C/T]GTCTGTGGGTCTGGT	57661
rs11246210	snp	A/G	0.103082	0.202275	intron-variant	PHRF1	GRCh38.p7	11:600474	AGCCTGGGTGACAGA[A/G]TGAGACTCTGTCTCC	57661
rs11246211	snp	C/T	0.118235	0.212457	intron-variant	PHRF1	GRCh38.p7	11:606294	GAGCACCTCTTAGAA[C/T]AGCAGCCGGAGCCAG	57661
rs11246212	snp	C/T	0.250934	0.249998	missense	PHRF1	GRCh38.p7	11:610277	CAGGGGTCAGGCAGG[C/T]GTTCTCCGAGCTGCC	57661
rs11539530	snp	A/G	0.318158	0.240538	synonymous-codon	PHRF1	GRCh38.p7	11:609353	CACAGACTCTTCCCC[A/G]GAGCGAGACTTCCCA	57661
rs11539531	snp	A/G			synonymous-codon	PHRF1	GRCh38.p7	11:608987	ACGGGAGCACAGGCG[A/G]CCTCGGTCCCGTGAG	57661
rs11539532	snp	C/G			missense	PHRF1	GRCh38.p7	11:607969	CCGACCCCACCGGCT[C/G]CGACTCCAGCGCCCC	57661
rs11604252	snp	C/T			intron-variant	PHRF1	GRCh38.p7	11:602894	cagcctcctgagtcg[C/T]tgggattataggcgt	57661
rs11825714	snp	A/C	0.0205511	0.0992634	intron-variant	PHRF1	GRCh38.p7	11:603413	tcctggctcactgca[A/C]ccgccttgacctccc	57661
rs11826379	snp	G/T	0.5	0	intron-variant	PHRF1	GRCh38.p7	11:603730	CCATATTTAAGTTTG[G/T]TTTTTTTTTTTTTTT	57661
rs12226533	snp	A/G	0.00755907	0.0610114	intron-variant	PHRF1	GRCh38.p7	11:592106	atttttagtagagac[A/G]gggtttcactgtgtt	57661
rs12272314	snp	A/G	0.354019	0.227333	intron-variant	PHRF1	GRCh38.p7	11:590648	GTGGGTCAGAACACT[A/G]TTAATAAAGGCAAAA	57661
rs12281144	snp	A/G			intron-variant	PHRF1	GRCh38.p7	11:599435	tttgtatttttagta[A/G]agatggggcttcacc	57661
rs12283876	snp	A/G	0	0	intron-variant	PHRF1	GRCh38.p7	11:581659	GGAGCAGGGTGCCTG[A/G]TGTTTCCCTTTGGAG	57661
rs12285890	snp	C/T	0.0876345	0.190099	upstream-variant-2KB, nc-transcript-variant	PHRF1, LOC143666	GRCh38.p7	11:574754	CCCTGGCCCCAGCGC[C/T]GCTGGCCCTCGGTGA	57661
rs12285942	snp	A/C	0.287346	0.247195	upstream-variant-2KB, nc-transcript-variant	PHRF1, LOC143666	GRCh38.p7	11:574813	GGCTCCCTCCCCCGC[A/C]TGTGTGTGCACGCCC	57661
rs12293073	snp	C/T	0	0	intron-variant	PHRF1	GRCh38.p7	11:581279	ACCCTTCACGTGCTG[C/T]GGCGGTGGATGTGAC	57661
rs12293369	snp	C/T	0.0696718	0.173152	intron-variant	PHRF1	GRCh38.p7	11:581803	TTGAACGAAAGGATG[C/T]TCCCTTTCCTTGCTT	57661
rs12293832	snp	C/T	0.106382	0.204631	intron-variant	PHRF1	GRCh38.p7	11:606607	GGCGGGTGAGTGCCT[C/T]CCCTGCCACGGCCCC	57661

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