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
rs3679467	snp	C/T	0.489796	0.070696	intron-variant	Phf8	Mm_Celera	X:151576826	TCACCAAAAATATTG[C/T]CCCTTCTTTTATATA	320595
rs3714082	snp	A/G	0.495	0.0497494	intron-variant	Phf8	GRCm38.p3	X:151576414	ATGTGCATCAGTTCT[A/G]TGTTATCTGGAAGGA	320595
rs6210851	snp	C/T	0.21875	0.248039	upstream-variant-2KB	Phf8	Mm_Celera	X:151520440	TTTTTTTTCCAACTC[C/T]GTGTTTACCCGGGGT	320595
rs6260901	snp	C/T	0.5	0	intron-variant	Phf8	Mm_Celera	X:151607639	tgtttagtttctgtt[C/T]ctatgatctgtccat	320595
rs6371634	snp	A/G	0.5	0	intron-variant	Phf8	Mm_Celera	X:151607739	taaagtttcttttat[A/G]aatgtacccttgctt	320595
rs6394712	snp	A/T	0.5	0	intron-variant	Phf8	GRCm38.p3	X:151588325	atggacagaagcagc[A/T]gactcctgttgttga	320595
rs6394744	snp	A/G	0.5	0	intron-variant	Phf8	GRCm38.p3	X:151588349	ttgttgaattaagga[A/G]ggctaaaagaagctg	320595
rs6395169	snp	A/G	0.5	0	intron-variant	Phf8	GRCm38.p3	X:151588370	aaagaagctgaggag[A/G]anggtgatcctgtag	320595
rs6395170	snp	A/G	0.5	0	intron-variant	Phf8	GRCm38.p3	X:151588372	agaagctgaggagna[A/G]ggtgatcctgtagaa	320595
rs29293534	snp	A/G	0.244898	0.249948	intron-variant	Phf8	Mm_Celera	X:151566655	AAGGTGAGACTCTGG[A/G]GTAAGAAAGGGGAAA	320595
rs29293535	snp	A/G	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151566607	GGATGGGCAGAACAA[A/G]AGGGTAATGCAATAT	320595
rs29293536	snp	A/C	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151566427	CAGCTGAGTGTGGCC[A/C]AGGACAACAGAAAAT	320595
rs29293537	snp	C/T	0.396694	0.202437	synonymous-codon	Phf8	Mm_Celera	X:151566016	CAAGTTTCCCAACTT[C/T]GAGACCATCTGTTGG	320595
rs29293538	snp	A/C	0.142012	0.225474	intron-variant	Phf8	Mm_Celera	X:151565891	TACATAGCACTGAGA[A/C]TAGCACTTGGTACAT	320595
rs29293539	snp	A/G	0.396694	0.202437	intron-variant	Phf8	Mm_Celera	X:151565752	TGGTTCTTAATGACA[A/G]TTTGACAAGGTTAAC	320595
rs29293540	snp	C/G	0.46875	0.121031	intron-variant	Phf8	Mm_Celera	X:151565682	ATCTGACTGCCTCTG[C/G]ATCCCAAGTTCTGGG	320595
rs29293541	snp	A/G	0.32	0.24	intron-variant	Phf8	Mm_Celera	X:151565639	CCTAGAACTCACCCT[A/G]TAGACTAGGCTGACC	320595
rs29293542	snp	A/C	0.197531	0.244432	intron-variant	Phf8	Mm_Celera	X:151565510	GTCCTTGTGTAAGTC[A/C]CTTGAGTAAAGAATG	320595
rs29293543	snp	C/T	0.165289	0.235211	intron-variant	Phf8	Mm_Celera	X:151564875	TGTGTTTTAGTAGTG[C/T]GCATTTTAGAGTAGT	320595
rs29293684	snp	A/G	0.231111	0.249285	intron-variant	Phf8	Mm_Celera	X:151601274	TTCTTTGTTTTATAT[A/G]TTTTTTGATCCTTTG	320595
rs29293685	snp	C/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151600832	ATTATATACAAGATA[C/T]ATACTGATAGTGTCA	320595
rs29293686	snp	A/T	0.48	0.0979796	intron-variant	Phf8	GRCm38.p3	X:151600616	TCTTTCAACATCAGT[A/T]CATGGAGATCTGCTT	320595
rs29293687	snp	C/T	0.497041	0.0383476	intron-variant	Phf8	GRCm38.p3	X:151600534	TGTTCATACAACTTA[C/T]GTGTAAACATATATA	320595
rs29293688	snp	A/G	0.231111	0.249285	intron-variant	Phf8	Mm_Celera	X:151600095	ATGTATTGAACATGT[A/G]TAGACTCTTCTTTCC	320595
rs29293689	snp	C/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151600036	TGAGCATTCCATATC[C/T]ATTGTTTCATCCATA	320595
rs29293690	snp	A/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151600017	ACCATCAGGTCTCCA[A/T]AGCTGAGCATTCCAT	320595
rs29293691	snp	A/G	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151599943	CTTGCTTATTTGACT[A/G]TTATCATCTGTATTT	320595
rs29293692	snp	C/T	0.32	0.24	intron-variant	Phf8	Mm_Celera	X:151599928	AAACTCATTTCCTCT[C/T]TTGCTTATTTGACTG	320595
rs29293693	snp	C/T	0.124444	0.216185	synonymous-codon	Phf8	Mm_Celera	X:151599343	GGCCAACCTGCAGTC[C/T]TCATCATCCTCACCA	320595
rs29293914	snp	C/T	0.165289	0.235211	intron-variant	Phf8	Mm_Celera	X:151564226	TCCTCTCTGTCACTG[C/T]TACTGGTTGATTTAT	320595
rs29293915	snp	C/T	0.297521	0.245442	intron-variant	Phf8	Mm_Celera	X:151563949	TGACACATTGCATTA[C/T]TCAGACTGTGCTGTC	320595
rs29293916	snp	A/C	0.244898	0.249948	intron-variant	Phf8	Mm_Celera	X:151563662	AAACTTGTGATCTTA[A/C]TGCCTTAAATCTTTT	320595
rs29293917	snp	C/T	0.18	0.24	intron-variant	Phf8	Mm_Celera	X:151563604	TTTTTTCCTTTGTCT[C/T]ACTCAGTCTGTGCTC	320595
rs29293918	snp	A/G	0.375	0.216506	intron-variant	Phf8	Mm_Celera	X:151563504	CCCAGAAAGAGTTGA[A/G]TCTTTTTACATTCTT	320595
rs29293919	snp	C/T	0.375	0.216506	intron-variant	Phf8	Mm_Celera	X:151563459	TGACTTCCTCTCTCA[C/T]AGGAGCTATTAAATT	320595
rs29293920	snp	C/T	0.244898	0.249948	intron-variant	Phf8	Mm_Celera	X:151563418	GGGTCTTTGTGTGCT[C/T]CACTGCGTTTATTTT	320595
rs29293921	snp	A/G	0.21875	0.248039	intron-variant	Phf8	Mm_Celera	X:151562489	CTTTGTGTTTCCCTA[A/G]TGACTATTAATGTTG	320595
rs29293922	snp	A/G	0.408163	0.193609	intron-variant	Phf8	Mm_Celera	X:151562370	CATAGCAATCCTAGT[A/G]TGAGTAAAATAGCAA	320595
rs29293923	snp	A/G	0.297521	0.245442	intron-variant	Phf8	Mm_Celera	X:151561921	GGTATAATAATCTTG[A/G]GGTTCACAGTGTGAT	320595
rs29294024	snp	A/G	0.32	0.24	intron-variant	Phf8	Mm_Celera	X:151599119	AAATTCGCTTTTCAT[A/G]AAAACAGATTTTAGT	320595
rs29294025	snp	A/G	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151598766	ATTTATCCCAGGCTG[A/G]TCTGGAACTCCTAGT	320595
rs29294026	snp	C/T	0.391111	0.206368	intron-variant	Phf8	GRCm38.p3	X:151598655	AGTAATCTTCATTTT[C/T]TAGGCTATCAAAAGA	320595
rs29294027	snp	C/T	0.32	0.24	synonymous-codon	Phf8	Mm_Celera	X:151598571	GAATGGGAGTGGAGC[C/T]GGTGGAATTCTTGAT	320595
rs29294028	snp	C/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151598429	GGATGTTAGGACTCA[C/T]ACTGTCAAACTTGTA	320595
rs29294029	snp	A/G	0.244898	0.249948	intron-variant	Phf8	Mm_Celera	X:151598369	AAGATTTTAAAGATT[A/G]AAATGGAATGATAAA	320595
rs29294030	snp	A/G	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151598061	TAGAAGATAAATACT[A/G]AATGCTAGGGTAGGG	320595
rs29294031	snp	C/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151597288	TTTCGTGGTCTTGTT[C/T]TCATTTTTCTAGTAC	320595
rs29294032	snp	C/T	0.231111	0.249285	intron-variant	Phf8	Mm_Celera	X:151597244	AAGCATGCATTCTAC[C/T]ATTGTTTCATTAGCC	320595
rs29294033	snp	C/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151596927	ACCTAAACATACAAG[C/T]AGCACTATAGCCCTA	320595
rs29294214	snp	A/C	0.5	0	intron-variant	Phf8	Mm_Celera	X:151561546	TCCTTAATCTCCTGG[A/C]TCCTTCTCATTCTCT	320595
rs29294215	snp	C/G	0.165289	0.235211	intron-variant	Phf8	Mm_Celera	X:151561352	TCAATACAATGTTAT[C/G]AGCCTCTGAGATTTA	320595
rs29294216	snp	A/C	0.260355	0.249785	intron-variant	Phf8	Mm_Celera	X:151561328	GCCTACTCCTGGAAG[A/C]TTCTAGCCTCAATAC	320595
rs29294217	snp	A/T	0.197531	0.244432	intron-variant	Phf8	Mm_Celera	X:151561272	ATTCACCCAATGTAA[A/T]CCTCATCTTGGAGGC	320595
rs29294218	snp	C/T	0.197531	0.244432	intron-variant	Phf8	Mm_Celera	X:151561174	GAAATCCTTTGAGAG[C/T]CAAAGCAACTGTGTA	320595
rs29294219	snp	C/G	0.244898	0.249948	intron-variant	Phf8	Mm_Celera	X:151560891	GTTCTGGGAATTGAG[C/G]CCTGGTCTTCTGGAA	320595
rs29294220	snp	A/G	0.152778	0.230321	intron-variant	Phf8	Mm_Celera	X:151560876	TGAGTTGCCAAGTGG[A/G]TTCTGGGAATTGAGG	320595
rs29294221	snp	A/T	0.46875	0.121031	intron-variant	Phf8	Mm_Celera	X:151560871	AGTTGTGAGTTGCCA[A/T]GTGGGTTCTGGGAAT	320595
rs29294222	snp	C/T	0.46875	0.121031	intron-variant	Phf8	Mm_Celera	X:151560865	ACAGATAGTTGTGAG[C/T]TGCCAAGTGGGTTCT	320595
rs29294223	snp	A/G	0.345679	0.230967	intron-variant	Phf8	Mm_Celera	X:151560813	TGTTTCCCCTGGAGG[A/G]CCAAAGATGGCAATT	320595
rs29294464	snp	C/G	0.32	0.24	intron-variant	Phf8	Mm_Celera	X:151596362	TCCACCCAGGGGACA[C/G]TGTCTTAGAACAATG	320595
rs29294465	snp	A/G	0.336735	0.234472	intron-variant	Phf8	Mm_Celera	X:151596246	GACAGTTTCTGTGTA[A/G]CCCTGGTTGTCTTGG	320595
rs29294466	snp	C/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151595540	TTGCCTTGGTACCTT[C/T]GTGAAAAGTAAATTG	320595
rs29294467	snp	A/G	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151594983	AGGATGGGAAACCGG[A/G]TAAGAGGATAACACT	320595
rs29294468	snp	C/G	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151594530	TGGATGCTAAGAAAT[C/G]ATTGCTGAAAGGAGC	320595
rs29294469	snp	C/T	0.444444	0.157135	intron-variant	Phf8	GRCm38.p3	X:151594210	TGACATCTTATTGAC[C/T]CTGCCTTTTGCCTTA	320595
rs29294470	snp	C/T	0.32	0.24	intron-variant	Phf8	Mm_Celera	X:151593981	ACATAGACTCTTTCT[C/T]TGTTACCCTAGGCTA	320595
rs29294471	snp	C/T	0.132653	0.220748	intron-variant	Phf8	Mm_Celera	X:151593746	TCTAGAACTTACTCA[C/T]ACTACATAACTATAA	320595
rs29294472	snp	A/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151592773	tttaattaattttga[A/T]tgaaagtctatttca	320595
rs29294473	snp	A/C	0.475309	0.108333	intron-variant	Phf8	GRCm38.p3	X:151592662	TAATGTTTCTTTTAC[A/C]AATGTGGATGCATTT	320595
rs29294624	snp	C/T	0.18	0.24	intron-variant	Phf8	Mm_Celera	X:151559617	GTCTCATAAAGTTGC[C/T]CAGGTTGGCACCGAG	320595
rs29294625	snp	C/T	0.197531	0.244432	intron-variant	Phf8	Mm_Celera	X:151559540	ATGCTAATTGCTCCA[C/T]CACTGAGCTAGTTCC	320595
rs29294626	snp	A/C	0.132653	0.220748	intron-variant	Phf8	GRCm38.p3	X:151558960	CAGGTTATCTTGTTG[A/C]TCGTTGTTGTGGAGA	320595
rs29294627	snp	C/T	0.244898	0.249948	intron-variant	Phf8	Mm_Celera	X:151558509	CATACATGCTAACGC[C/T]CTTGCCATTTCTACT	320595
rs29294628	snp	A/G	0.345679	0.230967	intron-variant	Phf8	Mm_Celera	X:151558414	TAGCATATATTATCC[A/G]TAAGAGTGGGTCTCT	320595
rs29294629	snp	A/G	0.152778	0.230321	intron-variant	Phf8	Mm_Celera	X:151557795	ACTTCACTTGTATGT[A/G]GATTTTCCTCTTGAG	320595
rs29294630	snp	C/T	0.165289	0.235211	intron-variant	Phf8	Mm_Celera	X:151557615	GTGTTAAGTGTGCCT[C/T]TGTAGAAAATGAGAT	320595
rs29294631	snp	A/T	0.32	0.24	intron-variant	Phf8	Mm_Celera	X:151556700	TTGAATCTTTTATGA[A/T]CAGTCCAATTTAAAT	320595
rs29294632	snp	A/G	0.231111	0.249285	intron-variant	Phf8	Mm_Celera	X:151556655	AACCCTGTTGTCGCA[A/G]TTTGGAGAGAGTTGA	320595
rs29294633	snp	C/T	0.231111	0.249285	intron-variant	Phf8	Mm_Celera	X:151556523	AGTTCATGCCTGGGA[C/T]TTACTTATAGAATTC	320595
rs29294844	snp	A/G	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151592528	TAATTCATAACGTCT[A/G]TAAATTTCATTATTT	320595
rs29294845	snp	C/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151591994	TTACCATCTTTCACT[C/T]TAACTTGGTGACACT	320595
rs29294846	snp	C/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151589073	GAAATTACTTCTTTG[C/T]TGTGTCTTCTTAGTA	320595
rs29294847	snp	A/G	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151588788	ATGTGCTTTGCATCC[A/G]TGATCTCTCCAAGAC	320595
rs29294848	snp	G/T	0.32	0.24	intron-variant	Phf8	Mm_Celera	X:151588011	TGGGTCTCAAGTTGG[G/T]ACAGTCATTGGTTGG	320595
rs29294849	snp	G/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151587997	GACTCTCATTGTTAT[G/T]GGTCTCAAGTTGGTA	320595
rs29294850	snp	C/T	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151587869	GAATGATGGGTGAAG[C/T]TTCTCAGATGAAATC	320595
rs29294851	snp	A/G	0.124444	0.216185	intron-variant	Phf8	Mm_Celera	X:151587736	TCAGTCTGTGTGAGC[A/G]CCTATGGGCCTAGGT	320595
rs29294852	snp	A/G	0.231111	0.249285	intron-variant	Phf8	Mm_Celera	X:151587681	TTACATTTGTGTAGG[A/G]GACCTAGGTCTGTCA	320595
rs29294853	snp	A/T	0.18	0.24	intron-variant	Phf8	Mm_Celera	X:151587257	TTAGGTGTTTTTTTT[A/T]AAATAGTATTTATTA	320595
rs29295034	snp	A/G	0.197531	0.244432	intron-variant	Phf8	Mm_Celera	X:151556471	ATGTTCTAGTCTATA[A/G]CATTGAATGGCCAGA	320595
rs29295035	snp	A/G	0.260355	0.249785	intron-variant	Phf8	Mm_Celera	X:151556292	ACCTCAAGAAAATTT[A/G]TATGTTGGCCAGTAG	320595
rs29295036	snp	C/T	0.336735	0.234472	intron-variant	Phf8	Mm_Celera	X:151555432	GTGGTTCTTTTTCAC[C/T]AAGTTGTCTATCAGA	320595
rs29295037	snp	C/T	0.277778	0.248452	intron-variant	Phf8	Mm_Celera	X:151555055	GTAACATGAGTTTTC[C/T]CTCCCTCAAACTTTA	320595
rs29295038	snp	A/G	0.336735	0.234472	intron-variant	Phf8	Mm_Celera	X:151553906	GTAATAGGAATGGCC[A/G]CTTACTATTGGGGAA	320595
rs29295039	snp	A/G	0.132653	0.220748	intron-variant	Phf8	Mm_Celera	X:151553769	ACTGCCCTCTAGGAG[A/G]TTTTCTGTAATTGTA	320595
rs29295040	snp	A/G	0.132653	0.220748	intron-variant	Phf8	Mm_Celera	X:151553500	CCAGAAAGCCTGTGC[A/G]ATAGCTTGCAGACAT	320595
rs29295041	snp	A/G	0.375	0.216506	intron-variant	Phf8	Mm_Celera	X:151552895	TGATCTTTTCCTAGT[A/G]TTTATATTTTTATTT	320595
rs29295042	snp	C/T	0.444444	0.157135	intron-variant	Phf8	Mm_Celera	X:151552876	GTTCTAGGGCATCTT[C/T]CTTTGATCTTTTCCT	320595
rs29295043	snp	C/T	0.231111	0.249285	intron-variant	Phf8	Mm_Celera	X:151552729	ATTCTAGCAGTTTTG[C/T]TTCTCATTTTGGAGA	320595
rs29295097	snp	C/T	0.231111	0.249285	downstream-variant-500B	Phf8	Mm_Celera	X:151634351	CTCCTGCTAATCTTC[C/T]TCCCAGTCAGTCTCT	320595

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