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
rs1894	snp	A/G	0.314787	0.241459	utr-variant-3-prime	PCGF3	GRCh38.p7	4:768062	TACAAAGTTACAAAT[A/G]TATATTATGAGATTA	10336
rs7336	snp	G/T	0.429987	0.173507	utr-variant-3-prime, upstream-variant-2KB	PCGF3, LOC107986211	GRCh38.p7	4:766470	CATGATAAGCCTCAA[G/T]TGTAGTTGGACTTTT	10336
rs747504	snp	A/G	0.490287	0.0690083	intron-variant, nc-transcript-variant	PCGF3, LOC107986246	GRCh38.p7	4:740889	CTGCCGGTGGCTTTG[A/G]GCAGCCCTCTGCACC	10336
rs899389	snp	C/G	0.332106	0.236133	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:752183	GGAAACTGGCGAAGC[C/G]GCCTCTTCCACTGCC	10336
rs899390	snp	G/T	0.3746	0.216737	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:752650	GACTCGGGGGTGGGG[G/T]GCCATGCAGTCTTGG	10336
rs899391	snp	C/T	0.323671	0.238899	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:764212	GCAGGGTGTTGgtgg[C/T]aggggggttccaagg	10336
rs899392	snp	C/T	0.440609	0.161766	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:764433	GGGGCTGGTGTGGAC[C/T]GGGCCTGGGTGGGAT	10336
rs899393	snp	C/T	0.321769	0.239477	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:764578	TCCCGTTGCTCAGTA[C/T]GGCAGGTGTGGTAGA	10336
rs1026740	snp	A/G	0.255224	0.249945	utr-variant-3-prime	PCGF3	GRCh38.p7	4:769175	AGGCTGCCCCTGGGC[A/G]GGGCCATGTGGCCTC	10336
rs1026741	snp	C/T	0.147656	0.228091	utr-variant-3-prime	PCGF3	GRCh38.p7	4:769619	ACGTGGCCAAGGCCC[C/T]GCAGGAACGCGCCGA	10336
rs1044147	snp	A/G	0.106987	0.205054	utr-variant-3-prime	PCGF3	GRCh38.p7	4:769289	AACAGCAACAGAACA[A/G]TGTTCACAGCGATTC	10336
rs1044180	snp	C/T	0.107694	0.205546	utr-variant-3-prime	PCGF3	GRCh38.p7	4:769842	TTTACCAGCAGCGTA[C/T]GGCAGACGAAGGCAG	10336
rs1531583	snp	G/T	0.204803	0.245881	intron-variant	PCGF3	GRCh38.p7	4:751184	ATTCCGTGTCCGTTT[G/T]TGGGATTATCCGCGT	10336
rs1531584	snp	C/G	0.324145	0.238752	intron-variant, downstream-variant-500B	PCGF3, LOC107986211	GRCh38.p7	4:751657	AGCACCTGCCACCCA[C/G]GCCCATGTTTCTGCT	10336
rs1811560	snp	C/T	0.146314	0.227484	utr-variant-3-prime	PCGF3	GRCh38.p7	4:769441	AACATCCAATTTCTC[C/T]GTTTCCTCAGGAAGT	10336
rs2242233	snp	A/G	0.377561	0.215008	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:761237	CCAGAACCGTCCGGG[A/G]GAACCCTCCTGCTGC	10336
rs2242234	snp	C/T	0.117766	0.212165	synonymous-codon, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:761341	GCGGAAGTGGATCCG[C/T]TGCTCAGCCCAGGCG	10336
rs2242235	snp	A/G	0.162495	0.234186	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:761422	CTTTAACGAGGTAAC[A/G]GTTGATCCCTAAGTA	10336
rs2279174	snp	C/T	0.146985	0.227789	intron-variant	PCGF3	GRCh38.p7	4:743808	GGGAGAGCAGGAGGG[C/T]CCCCCGAGAGTGTCT	10336
rs2291056	snp	C/T			intron-variant	PCGF3	GRCh38.p7	4:751309	TTTATTTCACACTAA[C/T]TTTATTCTAGGAATC	10336
rs2306243	snp	A/C	0.00953873	0.0683987	intron-variant	PCGF3	GRCh38.p7	4:743382	AACTTCATAATGCAA[A/C]TCCCTAATTTTCTTT	10336
rs2335171	snp	A/G	0.34526	0.23114	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:756075	catgccaccataccc[A/G]gctaattttttgtat	10336
rs3214921	in-del	-/T	0.314057	0.241654	intron-variant	PCGF3	GRCh38.p7	4:751051	GAGAATACATTTTTT[-/T]CCCCTCTCCATGAGG	10336
rs3755966	snp	A/G	0.0818113	0.184966	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:764656	GTGGGCTCCCATCCC[A/G]CCCCTATCTGGCCTG	10336
rs3834219	in-del	-/G	0.172997	0.237846	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:764848	TGGGGTGGGGGGGGC[-/G]CTGGTTCATGTATTC	10336
rs4076064	snp	C/T	0.417683	0.185425	intron-variant	PCGF3	GRCh38.p7	4:718433	TCTGGGGTCCCACCT[C/T]AGTGAATGTACCTTA	10336
rs4077049	snp	A/C	0.0023933	0.0345097	intron-variant	PCGF3	GRCh38.p7	4:724811	tcaCACACACACACA[A/C]aaaattagttgggtg	10336
rs4234853	snp	A/G	0.312837	0.241974	intron-variant, nc-transcript-variant	PCGF3, LOC107986246	GRCh38.p7	4:741362	TCAGGCTGGACTGCC[A/G]CAGCTCAAGAGCAAT	10336
rs4234854	snp	C/G	0.410568	0.191619	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:762483	TGGGAGTTAGGGCCT[C/G]GGGGAGGCGCTCAGG	10336
rs4317149	snp	C/T	0.405776	0.195535	intron-variant	PCGF3	GRCh38.p7	4:730093	TGTCCTCATCCCCAC[C/T]GAGCCCAACACCAGG	10336
rs4521289	snp	C/T	0.0189856	0.0955633	intron-variant	PCGF3	GRCh38.p7	4:731377	TTCCCGGCGTGTCGC[C/T]GAGGAGCAGTGCTGC	10336
rs4525922	snp	A/G	0	0	intron-variant	PCGF3	GRCh38.p7	4:716633	GTGCTGGGACCCTGT[A/G]GACACTGAGTGTGAG	10336
rs4549331	snp	A/G	0.0748431	0.178382	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:752692	CTCTACATGGACTTC[A/G]ACCCCTGTGTGTGCA	10336
rs4690186	snp	A/G	0.364401	0.222289	intron-variant	PCGF3	GRCh38.p7	4:709818	CTCAGTGTCAGCCAC[A/G]TCGTGTCCCTGCGTG	10336
rs4690187	snp	C/T	0.3742	0.216966	intron-variant	PCGF3	GRCh38.p7	4:710024	CTGTACTGTCTGGTT[C/T]CCAGGCTTTTAGAGG	10336
rs4690188	snp	C/G	0.354881	0.226936	intron-variant	PCGF3	GRCh38.p7	4:710141	TTAAACCAACAGTCC[C/G]ATGATAACTTACTGT	10336
rs4690189	snp	G/T	0.390277	0.206936	intron-variant, upstream-variant-2KB	PCGF3, LOC107986246	GRCh38.p7	4:739111	ATACCTTGATAATGT[G/T]TAGGAAAATAGTAGA	10336
rs4690190	snp	A/G	0.153332	0.230554	intron-variant	PCGF3	GRCh38.p7	4:748677	TCACCTTCTTCTTTC[A/G]TGACCCCGGTTTCAC	10336
rs4690191	snp	C/T	0.329084	0.237162	intron-variant	PCGF3	GRCh38.p7	4:748917	CAGTTTTGGGGTCTG[C/T]TGGGTGGGCTGGTGT	10336
rs4690192	snp	A/G	0.313082	0.241911	intron-variant	PCGF3	GRCh38.p7	4:749882	GAGTGCAATGGTGCA[A/G]TCACAGCTCCCTGTA	10336
rs4690193	snp	C/T	0.302184	0.244493	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:753804	ATACAAAAAATTAGC[C/T]GGGCATGGTGGTGGG	10336
rs4690194	snp	C/T	0.322007	0.239405	utr-variant-3-prime, upstream-variant-2KB	PCGF3, LOC107986211	GRCh38.p7	4:767031	TGGTGGCTTCGGGCT[C/T]ATGCCCAGACACACT	10336
rs4690281	snp	A/G	0.384976	0.210431	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:760156	TGACTGCACCGTGTC[A/G]GAGTGGGTATTTCTT	10336
rs4690282	snp	C/T	0.323434	0.238972	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:760696	GGGGGCCAAGCCGGC[C/T]GGGCCCTTGGGTGAA	10336
rs4690291	snp	C/T	0.49753	0.0350569	intron-variant	PCGF3	GRCh38.p7	4:707599	CCTGGGGGTCGGGAC[C/T]CTGGGACAGCTCTGT	10336
rs4690292	snp	A/G	0.353587	0.22753	intron-variant	PCGF3	GRCh38.p7	4:709923	ATTTGCTCTTTTGAC[A/G]TATCCTTTACTGTTT	10336
rs4690293	snp	A/G	0.362732	0.22314	intron-variant	PCGF3	GRCh38.p7	4:712312	TTTGTAGAATTATCC[A/G]CTGAGTTAAGCAAAA	10336
rs4690294	snp	A/G	0.354235	0.227234	intron-variant	PCGF3	GRCh38.p7	4:725871	ACGGAGCCTCCTGGA[A/G]CCGCCTCAGTTTCCC	10336
rs4690295	snp	A/G	0.354235	0.227234	intron-variant	PCGF3	GRCh38.p7	4:725926	CATTTCAGGAGCCCC[A/G]GGGCCACTCTCCGCC	10336
rs4690296	snp	A/G	0.151001	0.229563	intron-variant, upstream-variant-2KB	PCGF3, LOC107986246	GRCh38.p7	4:738473	TTAAGAAACGTTTGC[A/G]CCGAGTGTTTCAGAC	10336
rs4690297	snp	A/G	0.150333	0.229274	intron-variant, upstream-variant-2KB	PCGF3, LOC107986246	GRCh38.p7	4:738511	AGTGGGCGGGATCGG[A/G]GCGGGACCCCAAGTT	10336
rs4690299	snp	C/T	0.473543	0.111932	intron-variant	PCGF3	GRCh38.p7	4:747685	GCTGCAGTGTTAGTG[C/T]TCGCCGTGGAGGCGT	10336
rs4690300	snp	A/G	0.148661	0.22854	intron-variant	PCGF3	GRCh38.p7	4:747691	GTGTTAGTGCTCGCC[A/G]TGGAGGCGTGAGCAG	10336
rs4690301	snp	C/T	0.329317	0.237084	intron-variant	PCGF3	GRCh38.p7	4:748784	CTGTTTTTCTGTCTC[C/T]GGTGTTGGTCTCGTC	10336
rs4690303	snp	A/G	0.244776	0.249945	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:754476	AGAGCCCACCCATCC[A/G]GGCCAGAGCCCCTGG	10336
rs4690304	snp	A/G	0.479258	0.0997024	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:754659	GGACCTTGGGGGCCT[A/G]TGGCGAGAACTTGCT	10336
rs4690305	snp	C/T	0.499816	0.0095829	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:754663	CTTGGGGGCCTGTGG[C/T]GAGAACTTGCTGTTC	10336
rs4690306	snp	A/C	0.0197687	0.0974348	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:756835	GGGGCCTGCCGGGGG[A/C]TCTGAGGTGATGGAA	10336
rs4690307	snp	A/G	0.323671	0.238899	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:761961	AGGAGCATGGGTCTG[A/G]TGTCGTTTTTGAAAA	10336
rs4690308	snp	A/G	0.434543	0.168653	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:762353	AGGCAGCCTCGAGGC[A/G]AGCCAGGGAGCCCCT	10336
rs4690309	snp	C/T	0.449345	0.150869	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:762589	TCCCCAACATGAGGA[C/T]GCAGCAGAAGGCCTT	10336
rs4690310	snp	A/G	0.324619	0.238604	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:764736	CCCCCTAACTGGCAC[A/G]GGCCTGCCCTGTAAT	10336
rs5024302	snp	A/G	0.407502	0.194147	intron-variant	PCGF3	GRCh38.p7	4:732159	TCCCCTCCCCTCGTG[A/G]GTGGGCGTGGTCCTC	10336
rs6599374	snp	G/T	0.350109	0.229081	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:756424	cactatgttggcccg[G/T]ctggcctcgaactcc	10336
rs6599375	snp	C/T	0.135143	0.222054	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:756789	aacactcactcccca[C/T]cccgctcccccAGCA	10336
rs6810428	snp	A/G	0.46014	0.13543	intron-variant, upstream-variant-2KB	PCGF3, LOC107986211	GRCh38.p7	4:765921	TCTGTGCAGCCCTGC[A/G]TGTGGACTGTGCCTC	10336
rs6813457	snp	A/G	0.0197687	0.0974348	intron-variant	PCGF3, LOC107986211	GRCh38.p7	4:754163	CCCAGCACCAGAAAC[A/G]GGGGAAATGGCTCCT	10336
rs6815857	snp	C/T	0.0588605	0.161139	intron-variant, upstream-variant-2KB	PCGF3, LOC107986211	GRCh38.p7	4:765586	TGCTGAGGCCATGAG[C/T]GCCATGAGCAGAGGG	10336
rs6816483	snp	C/T	0.442249	0.159814	intron-variant, upstream-variant-2KB	PCGF3, LOC107986211	GRCh38.p7	4:765945	GTGCCTCACGGGACG[C/T]GATTCCTCAGCACCC	10336
rs6821861	snp	C/G	0.314301	0.241589	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:761958	GGCAGGAGCATGGGT[C/G]TGGTGTCGTTTTTGA	10336
rs6823290	snp	C/T	0.444444	0.157135	intron-variant, synonymous-codon	PCGF3, LOC107986211	GRCh38.p7	4:759715	CCCGAGTTCTTCTCC[C/T]TCCGGACTCTGGGTC	10336
rs6823299	snp	C/T	0.5	0	intron-variant, missense	PCGF3, LOC107986211	GRCh38.p7	4:759725	TCTCCTTCCGGACTC[C/T]GGGTCTTTCTCCCCG	10336
rs6823876	snp	C/T	0.325799	0.238232	intron-variant, missense	PCGF3, LOC107986211	GRCh38.p7	4:760019	ACATTGTCCCTCTCC[C/T]GTGATGCTTGCAGGC	10336
rs6829951	snp	A/G	0.31357	0.241783	intron-variant, upstream-variant-2KB	PCGF3, LOC107986211	GRCh38.p7	4:765852	ATGTCTTCCTAGCCC[A/G]TCTTCCCCCAGCAAC	10336
rs6835343	snp	A/G	0.0267878	0.112589	intron-variant	PCGF3	GRCh38.p7	4:744438	TGGGGAGACCCCTGC[A/G]GACACTTTGCGGACG	10336
rs6837071	snp	G/T			intron-variant, synonymous-codon	PCGF3, LOC107986211	GRCh38.p7	4:759687	CGGGTCTTTCTCCCC[G/T]CGCGGCCCCTCTCCC	10336
rs6837180	snp	A/G	0.452965	0.145963	upstream-variant-2KB	PCGF3	GRCh38.p7	4:704503	ACTCCCTCAGCCACC[A/G]CCTCTCCAGACGGGA	10336
rs6837284	snp	C/G	0.5	0	intron-variant, missense	PCGF3, LOC107986211	GRCh38.p7	4:759814	CCCCTCTCCCGAGTT[C/G]TTCTCCTTCCGGACT	10336
rs6838241	snp	A/C	0.40086	0.199352	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:762898	GGTGATGCAGAGAAA[A/C]GGAAGGGGTCAGGAA	10336
rs6841958	snp	C/T	0.317909	0.2406	intron-variant	PCGF3	GRCh38.p7	4:744724	GCTGCAGTGTTAGTG[C/T]TCGCCGTGGAGGCGT	10336
rs6842189	snp	C/T	0.499839	0.00898417	intron-variant	PCGF3	GRCh38.p7	4:744838	GCTGCAGTGTTAGTG[C/T]TCGCCGTGGAGGCGT	10336
rs6844082	snp	A/T	0.00993419	0.0697739	upstream-variant-2KB	PCGF3	GRCh38.p7	4:704910	CCCTGTCCGTCCTGA[A/T]GCTGAACATAACCTA	10336
rs6845891	snp	C/T	0.313814	0.241719	intron-variant	PCGF3	GRCh38.p7	4:750445	GTTTGCTGGTTGGTG[C/T]GGTGGGTAAACAAGC	10336
rs6848678	snp	A/C	0.0166325	0.0896639	intron-variant, upstream-variant-2KB	PCGF3, LOC107986211	GRCh38.p7	4:765613	AGGGTCCCCTGGGGC[A/C]TTTGGGCCCCTCTGA	10336
rs6856224	snp	C/G	0	0	intron-variant, missense	PCGF3, LOC107986211	GRCh38.p7	4:759714	TCCCGAGTTCTTCTC[C/G]TTCCGGACTCTGGGT	10336
rs6856650	snp	C/G	0.173965	0.238157	intron-variant, missense	PCGF3, LOC107986211	GRCh38.p7	4:759920	CCCCTCTCCCGAGTT[C/G]TTCTCCTTCCGGACT	10336
rs6856839	snp	C/T	0.00953873	0.0683987	intron-variant, synonymous-codon	PCGF3, LOC107986211	GRCh38.p7	4:759991	TCCAGACTCCCGGAT[C/T]TTCTTCCCGCTCACA	10336
rs6856848	snp	C/G	0.0217236	0.101931	intron-variant, missense	PCGF3, LOC107986211	GRCh38.p7	4:760001	CGGATCTTCTTCCCG[C/G]TCACATTGTCCCTCT	10336
rs6857306	snp	C/T	0.00993419	0.0697739	intron-variant, utr-variant-5-prime	PCGF3, LOC107986211	GRCh38.p7	4:760212	AATCTGAGGACTGCC[C/T]TTCACTGTTGTGGGA	10336
rs6858101	snp	A/G	0.444799	0.156695	intron-variant, upstream-variant-2KB	PCGF3, LOC107986211	GRCh38.p7	4:765547	CCAGCTGAGCTGCGA[A/G]GGGCACAGGCCCTGG	10336
rs7376232	snp	C/T			intron-variant	PCGF3	GRCh38.p7	4:747571	GCTGCAGTGTTAGTG[C/T]TCGCCGTGGAGGCGT	10336
rs7376288	snp	C/T	0.454784	0.1434	intron-variant	PCGF3	GRCh38.p7	4:747954	AACATGGCAGGTCAG[C/T]GGCCGGCTCTGGCCT	10336
rs7376403	snp	A/T	0.359998	0.2245	intron-variant	PCGF3	GRCh38.p7	4:749337	gcctggctaattttg[A/T]atttttagtagagat	10336
rs7377200	snp	C/T	0.451483	0.148002	intron-variant	PCGF3	GRCh38.p7	4:749731	acctcgtgatccacc[C/T]gcctcggcttcccaa	10336
rs7378489	snp	C/G	0.46875	0.121031	intron-variant	PCGF3	GRCh38.p7	4:747663	AGGTGGGCGGGGCCC[C/G]GGGGTCGCTGCAGTG	10336
rs7438761	snp	C/G	0.422	0.181428	intron-variant	PCGF3	GRCh38.p7	4:726719	TGCAATACAAGCTGA[C/G]AGTTTGGCTTTTTTT	10336
rs7663064	snp	C/T			intron-variant	PCGF3	GRCh38.p7	4:713402	GGTCCTGTGTGGCCT[C/T]GTGGGGGCTGTGGCC	10336
rs7663102	snp	C/T	0.0733688	0.176922	intron-variant	PCGF3	GRCh38.p7	4:709054	TGAGGTATTCAGAAG[C/T]GAGCGGTCTATGCTG	10336
rs7663343	snp	C/T	0.482384	0.0921818	intron-variant	PCGF3	GRCh38.p7	4:706243	GCTGGGACTCCAGCC[C/T]AGGCAGGACGCAGGG	10336
rs7663801	snp	C/T			intron-variant	PCGF3	GRCh38.p7	4:737029	TGAGCGCACGGGACG[C/T]GGGGAACCTGGGGTG	10336

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