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
rs6186091	snp	A/G	0.375	0.216506	intron-variant	Cfap52	GRCm38.p3	11:67942353	TATTTTTAGCTCTGC[A/G]ATCCAGTATGAGTTC	71860
rs6186143	snp	A/G/T	0.336735	0.234472	intron-variant	Cfap52	Mm_Celera	11:67942395	GTTAAGGTTGGTGTC[A/G/T]GGATCACTGTGAGGG	71860
rs6186204	snp	G/T	0.5	0	intron-variant	Cfap52	Mm_Celera	11:67942430	GGTTTGGGGTACATG[G/T]GTTGAAcatataggt	71860
rs6186642	snp	C/T	0.5	0	intron-variant	Cfap52	Mm_Celera	11:67942447	TTGAAcatataggtg[C/T]ccacttgtaccagca	71860
rs6186749	snp	C/T	0.5	0	intron-variant	Cfap52	Mm_Celera	11:67942508	ggtcgtcttggctcc[C/T]ctgtcagtgttaaga	71860
rs6199546	snp	A/C	0.5	0	intron-variant	Cfap52	Mm_Celera	11:67949213	agaaccgactccaga[A/C]agttgtcctttgacc	71860
rs6199977	snp	C/G	0.5	0	intron-variant	Cfap52	Mm_Celera	11:67949250	tgcttactgtggtgc[C/G]ttgcatggacagatg	71860
rs6200028	snp	A/G	0.5	0	intron-variant	Cfap52	Mm_Celera	11:67949274	acagatgcgcacaGT[A/G]TGTAAATAAATGTAA	71860
rs6200518	snp	G/T	0.5	0	intron-variant	Cfap52	Mm_Celera	11:67949347	TTTTCCTCAACAACA[G/T]TTTTCAAAGAAACAT	71860
rs6350547	snp	C/T	0.5	0	intron-variant	Cfap52	Mm_Celera	11:67942686	gggctgctctggatc[C/T]nttgctgtttttttt	71860
rs6350548	snp	A/G	0.5	0	intron-variant	Cfap52	GRCm38.p3	11:67942686	ggctgctctggatcn[A/G]ttgctgttttttttt	71860
rs13470525	snp	A/G			intron-variant	Cfap52	Mm_Celera	11:67948844	GTATGCTGAGGCACA[A/G]ATGCAGGTTCTGTTC	71860
rs26936046	snp	C/T	0.46281	0.131194	upstream-variant-2KB	Stx8, Cfap52	GRCm38.p3	11:67966214	GCCGGGGTTGACGCG[C/T]TTCCATTCCCTGGGA	71860
rs26936047	snp	C/T	0.32	0.24	upstream-variant-2KB, intron-variant	Stx8, Cfap52	Mm_Celera	11:67965482	AGGTCAGCGTCTCAC[C/T]GTCCCTGAGGCATCA	71860
rs26936048	snp	A/G	0.408163	0.193609	upstream-variant-2KB, intron-variant	Stx8, Cfap52	Mm_Celera	11:67965153	CATTTCTCTCTCAAT[A/G]TTTACCACGACAGTC	71860
rs26936049	snp	A/T	0.21875	0.248039	upstream-variant-2KB, intron-variant	Stx8, Cfap52	Mm_Celera	11:67965031	GCACCGCATCCTTTC[A/T]ACGGTAAAGCTTTCA	71860
rs26936050	snp	A/G	0.231111	0.249285	intron-variant	Cfap52	Mm_Celera	11:67958980	CTAAATGTGAAAAAC[A/G]GGATCTAATGTTTGC	71860
rs26936051	snp	C/T	0.486111	0.0821678	intron-variant	Cfap52	GRCm38.p3	11:67957347	GTAGGAATTACTTCA[C/T]AGGACTCCCATGTAG	71860
rs26936052	snp	C/G	0.244898	0.249948	intron-variant	Cfap52	Mm_Celera	11:67957198	TCATGGTGTCGCTAT[C/G]GCTGGGACAGAAAAC	71860
rs26936053	snp	C/T	0.142012	0.225474	intron-variant	Cfap52	Mm_Celera	11:67955916	CAGAAGTGGGATTGC[C/T]GGGACCACATGGTAG	71860
rs26936054	snp	A/T	0.48	0.0979796	intron-variant	Cfap52	GRCm38.p3	11:67954902	TACTTACGTTAAACA[A/T]TTAAAGACAGAAATT	71860
rs28201368	snp	A/G	0.142012	0.225474	intron-variant	Cfap52	Mm_Celera	11:67954490	ATGTCTGGAAACCTC[A/G]TTTTGGACAGCAAAG	71860
rs28201369	snp	C/T	0.46875	0.121031	intron-variant	Cfap52	GRCm38.p3	11:67952895	GACAGCCAGGTAATG[C/T]CCATGTGGTCTCAGA	71860
rs28201370	snp	A/G	0.429688	0.173817	intron-variant	Cfap52	GRCm38.p3	11:67952870	TGCAGCTGGGCCTTG[A/G]CAGCAGGGAGACAGC	71860
rs28201371	snp	C/T	0.484429	0.0868505	intron-variant	Cfap52	GRCm38.p3	11:67952846	CCAGATCGATCAAAT[C/T]AGACTGTCTGCAGCT	71860
rs28201372	snp	A/G	0.492188	0.0620098	intron-variant	Cfap52	GRCm38.p3	11:67952760	TATTTTCATGCTTGA[A/G]GTCATGATGTCTTTG	71860
rs28201373	snp	C/T	0.142012	0.225474	intron-variant	Cfap52	Mm_Celera	11:67952157	CAAAAATCATGAAAA[C/T]GTTGGCAAATTTCTG	71860
rs28201374	snp	G/T	0.18	0.24	intron-variant	Cfap52	Mm_Celera	11:67951902	CCCAGACAAGGCTCC[G/T]AGCAGAGAGTGGAGG	71860
rs28201375	snp	A/C	0.444444	0.157135	intron-variant	Cfap52	GRCm38.p3	11:67950886	ATGAGACATTTTTGA[A/C]TTGTCAATCCTTTTT	71860
rs28201376	snp	A/G	0.49827	0.0293608	synonymous-codon, intron-variant	Cfap52	GRCm38.p3	11:67949657	CGCCGCGGGGCTGCC[A/G]CAAATGGCATCTCTC	71860
rs28201377	snp	C/G	0.132653	0.220748	intron-variant	Cfap52	Mm_Celera	11:67949443	CAAAAATTACAAAGC[C/G]AGGGGTTCGTTCAGT	71860
rs28201378	snp	A/G	0.497041	0.0383476	intron-variant	Cfap52	GRCm38.p3	11:67948921	CAAGTCATGTCCTGT[A/G]GCTAATAGCTTAAAC	71860
rs28201379	snp	A/G	0.473373	0.11227	intron-variant	Cfap52	GRCm38.p3	11:67948860	ATGCAGGTTCTGTTC[A/G]GATGTTCAAGTCGCT	71860
rs28201380	snp	A/G	0.142012	0.225474	intron-variant	Cfap52	Mm_Celera	11:67948823	ATTGCCAGTTTCTAA[A/G]TTAATGTATGCTGAG	71860
rs28201381	snp	C/G	0.142012	0.225474	intron-variant	Cfap52	Mm_Celera	11:67948764	GGGAAAGGACACTTT[C/G]ATGTCTGTTTCACCT	71860
rs28201382	snp	A/G	0.142012	0.225474	intron-variant	Cfap52	Mm_Celera	11:67948679	AGAGAAATCGCAAAG[A/G]TAGTTTCGCTGAACT	71860
rs28201383	snp	A/G	0.142012	0.225474	intron-variant	Cfap52	Mm_Celera	11:67948627	TCTGGCTGGGGAAGG[A/G]ACGAACAGTCTGTAC	71860
rs28201384	snp	C/T	0.142012	0.225474	intron-variant	Cfap52	Mm_Celera	11:67948295	GAGTTTGCACAAGCA[C/T]TGCCCACAGACATTA	71860
rs28201385	snp	C/T	0.165289	0.235211	intron-variant	Cfap52	Mm_Celera	11:67948045	TGGCCCATGGCCATA[C/T]TGATAGGTATCATGT	71860
rs28201386	snp	A/G	0.124444	0.216185	intron-variant	Cfap52	Mm_Celera	11:67947690	TAATATATGGCCGGT[A/G]CTTCACTACTATATG	71860
rs28201387	snp	C/T	0.260355	0.249785	intron-variant	Cfap52	Mm_Celera	11:67946082	TTTGGTAATGAGTGG[C/T]GAAGGTGCCAGTGAA	71860
rs28201388	snp	G/T	0.42	0.183303	missense	Cfap52	Mm_Celera	11:67945465	AAGCTGTCGTCGTCG[G/T]CCATCTAGGAGATCA	71860
rs28201389	snp	C/T	0.142012	0.225474	synonymous-codon	Cfap52	Mm_Celera	11:67945371	GCTGAATTTGTCCTT[C/T]ACAGGCCCAGTATCT	71860
rs28201390	snp	A/G	0.49827	0.0293608	intron-variant	Cfap52	GRCm38.p3	11:67945083	CTTACAGATCGAAAC[A/G]TACACCTCTCACATA	71860
rs28201391	snp	C/T	0.244898	0.249948	intron-variant	Cfap52	Mm_Celera	11:67944313	AGTGAGAGCAGCCTT[C/T]GGAACTTTCTGGGCA	71860
rs28201392	snp	C/T	0.244898	0.249948	intron-variant	Cfap52	Mm_Celera	11:67943698	TGTAGGATTAACCAA[C/T]GGCCCTGAAATGATC	71860
rs28201393	snp	C/T	0.132653	0.220748	intron-variant	Cfap52	Mm_Celera	11:67941409	AAGGCATTCATTCCA[C/T]GGTGTCTGAGAAGAA	71860
rs28201394	snp	G/T	0.486111	0.0821678	intron-variant	Cfap52	Mm_Celera	11:67941373	GTTTCTTTAAGCTGG[G/T]TTTTGCCTGTTCTGA	71860
rs28201395	snp	C/T	0.336735	0.234472	intron-variant	Cfap52	Mm_Celera	11:67940514	CATAAAGGTTCTAAT[C/T]GAAAATGTGCATGAC	71860
rs28201396	snp	A/G	0.336735	0.234472	intron-variant	Cfap52	Mm_Celera	11:67940474	CAACTATATGGAGGA[A/G]TGATGGCCAGCTCAT	71860
rs28201397	snp	A/G	0.277778	0.248452	intron-variant	Cfap52	Mm_Celera	11:67940404	TCTGAGCTAAGGCAT[A/G]TGGTATACAACCTTA	71860
rs28201398	snp	C/G	0.336735	0.234472	intron-variant	Cfap52	Mm_Celera	11:67940371	TGGGACAGTTCTTAC[C/G]ATTGGGTGATTATAT	71860
rs28201399	snp	C/T	0.244898	0.249948	intron-variant	Cfap52	Mm_Celera	11:67939497	GCTCTGTCATTCCAG[C/T]TATGTACACACTTAG	71860
rs28201400	snp	A/C	0.277778	0.248452	intron-variant	Cfap52	Mm_Celera	11:67939409	TGTACTTATTTATCA[A/C]AAGGGCAGTGTGCCT	71860
rs28201401	snp	A/G	0.244898	0.249948	intron-variant	Cfap52	Mm_Celera	11:67939118	ACAAAAGTGAAGCAG[A/G]GTCATTCAACCAGCA	71860
rs28201402	snp	A/G	0.297521	0.245442	synonymous-codon	Cfap52	Mm_Celera	11:67938931	CAATGGAAAGACAAT[A/G]TCCTGGACAGCTTCA	71860
rs28201403	snp	A/T	0.35503	0.226867	intron-variant	Cfap52	Mm_Celera	11:67938180	AAACAAAATTCAGCC[A/T]GAGAAGAGGTAGTTC	71860
rs28201404	snp	A/G	0.426035	0.177515	intron-variant	Cfap52	Mm_Celera	11:67937994	AGGCTGCTAGATCAG[A/G]GAAACTCAGGGACAC	71860
rs28201405	snp	A/G	0.231111	0.249285	intron-variant	Cfap52	Mm_Celera	11:67937497	TTCTGAAACAGGCTC[A/G]CATCTGAGGAACAAC	71860
rs28201406	snp	A/G	0.244898	0.249948	intron-variant	Cfap52	Mm_Celera	11:67936694	ATAAGTGTAGTCTGG[A/G]AAAGCTGACCTTTAA	71860
rs28201407	snp	A/G	0.35503	0.226867	intron-variant	Cfap52	Mm_Celera	11:67936570	ATTAATTGGTCAGTC[A/G]GGCCACTTGTAAATG	71860
rs29390955	snp	A/T	0.375	0.216506	intron-variant	Cfap52	GRCm38.p3	11:67954991	TGATGGGCACCTTTT[A/T]AAAAGGCTGAATTAC	71860
rs29393014	snp	G/T	0.32	0.24	intron-variant	Cfap52	GRCm38.p3	11:67956724	AGAAACAGAGAGTAG[G/T]ATAGCGCTTGCCAGG	71860
rs29393528	snp	A/T	0.32	0.24	intron-variant	Cfap52	Mm_Celera	11:67927833	TAATTTAAAAAAAAA[A/T]TTTTTTAATAGACTC	71860
rs29397856	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Stx8, Cfap52	Mm_Celera	11:67967750	AGCCCGGTTGTAGAA[C/T]GATTGTTTAGCACAC	71860
rs29403139	snp	C/T	0.444444	0.157135	upstream-variant-2KB, utr-variant-5-prime	Stx8, Cfap52	Mm_Celera	11:67965771	TAGTATGTATTTTAT[C/T]CATTCTGGAAATGTA	71860
rs29403690	snp	A/G	0.375	0.216506	intron-variant	Cfap52	GRCm38.p3	11:67961926	GGACTTTTAAACAGT[A/G]TTGAGACTGTGAACG	71860
rs29412524	snp	G/T	0.444444	0.157135	intron-variant	Cfap52	GRCm38.p3	11:67953055	GAAGACATGTAAGTA[G/T]CTGGGTGGTGGCAGG	71860
rs29414423	snp	A/G	0.444444	0.157135	intron-variant	Cfap52	GRCm38.p3	11:67952902	AGGTAATGTCCATGT[A/G]GTCTCAGAGCTAATG	71860
rs29422324	snp	C/T	0.375	0.216506	intron-variant	Cfap52	GRCm38.p3	11:67961141	AGGGAATCAGTTTTC[C/T]AACAGCTTTAGCCAC	71860
rs29425446	snp	C/T	0.375	0.216506	intron-variant	Cfap52	GRCm38.p3	11:67947289	GAAGACCATGCTAGC[C/T]GGAATGAGCCCATCA	71860
rs29431148	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Stx8, Cfap52	Mm_Celera	11:67967740	TTCAAATTTTAGCCC[A/G]GTTGTAGAACGATTG	71860
rs29444163	snp	C/T	0.444444	0.157135	intron-variant	Cfap52	GRCm38.p3	11:67945891	AATGAATTATGATTC[C/T]GTATATAATCACATC	71860
rs29451713	snp	A/G	0.375	0.216506	intron-variant	Cfap52	GRCm38.p3	11:67962150	TCACTACAGGTTGGT[A/G]GTGAGGTTCAAAAGC	71860
rs29452088	snp	C/G	0.375	0.216506	intron-variant	Cfap52	Mm_Celera	11:67955495	CAGAGGTCCAAAATT[C/G]AATTCCCAAAAAACA	71860
rs29455547	snp	A/G	0.32	0.24	intron-variant	Cfap52	GRCm38.p3	11:67928011	GCTGATTCAGGTCCA[A/G]CCCATCACCTCTCAC	71860
rs29456030	snp	A/G	0.32	0.24	intron-variant	Cfap52	GRCm38.p3	11:67956660	GTCGTGCCAAGCAAA[A/G]TAAGCCAGGCATAGA	71860
rs29458986	snp	A/T	0.375	0.216506	upstream-variant-2KB	Stx8, Cfap52	Mm_Celera	11:67965975	CATGGCATTGATACT[A/T]CTTTTTAAAAGAAAA	71860
rs29472530	snp	C/T	0.375	0.216506	intron-variant	Cfap52	Mm_Celera	11:67961600	ACAGTAGAAAAATTA[C/T]AAAGTAGCAACAAAA	71860
rs29476884	snp	C/T	0.375	0.216506	intron-variant	Cfap52	Mm_Celera	11:67938328	TTTTGCCACAACAGG[C/T]GAGCGGAGGTTGGAG	71860
rs29479282	snp	C/T	0.5	0	intron-variant	Cfap52	Mm_Celera	11:67932761	ACCTGAGATATAGAG[C/T]GTTTGTGGCCTGCCT	71860
rs45716954	snp	A/C			intron-variant	Cfap52	GRCm38.p3	11:67962802	GCCTGTCTCCTTCCC[A/C]GGCCCTCCAGTCCTG	71860
rs45834075	snp	C/T			intron-variant	Cfap52	GRCm38.p3	11:67941188	TTAATGAGCGAGCTT[C/T]GAGGGCTGGGCTTAC	71860
rs47103404	snp	A/G			intron-variant	Cfap52	GRCm38.p3	11:67956929	CTTCAGATTGCATGC[A/G]GTCAAGCTTGTAAGA	71860
rs47211659	snp	A/G			intron-variant	Cfap52	Mm_Celera	11:67950889	AGACATTTTTGAATT[A/G]TCAATCCTTTTTGCA	71860
rs49492908	snp	A/G			intron-variant	Cfap52	GRCm38.p3	11:67962803	CCTGTCTCCTTCCCA[A/G]GCCCTCCAGTCCTGG	71860
rs51885138	snp	C/T			intron-variant	Cfap52	GRCm38.p3	11:67941187	CTTAATGAGCGAGCT[C/T]CGAGGGCTGGGCTTA	71860
rs52052927	snp	A/G			intron-variant	Cfap52	Mm_Celera	11:67944122	GCTTGAATATAAAAT[A/G]ATAATATGATTAAGG	71860
rs52177773	snp	A/G			intron-variant	Cfap52	Mm_Celera	11:67962646	GGTATGTGTGTGCAC[A/G]TGTGCATGTGTGTGT	71860
rs52192776	snp	A/C			intron-variant	Cfap52	GRCm38.p3	11:67962229	TCTCTCTCTCTCTCT[A/C]TCTCTCACTACTGCC	71860
rs52595559	snp	A/G			intron-variant	Cfap52	GRCm38.p3	11:67953391	AGGCTTTCCAAGAAG[A/G]AGGAGGAAGAGGAGG	71860
rs52609122	snp	A/C			intron-variant	Cfap52	Mm_Celera	11:67962634	AAGAGGAGAAGTGGT[A/C]TGTGTGTGCACGTGT	71860
rs52611937	snp	A/G			intron-variant	Cfap52	GRCm38.p3	11:67962621	GCTTCACTCCCTCAA[A/G]AGGAGAAGTGGTATG	71860
rs52622135	snp	C/T			intron-variant	Cfap52	Mm_Celera	11:67958549	ttctttccttccttc[C/T]ttctttctgtctgtc	71860
rs52626758	snp	A/G			intron-variant	Cfap52	GRCm38.p3	11:67937921	GAAAAGAAAGAAAGA[A/G]AGAGAAAGAAAGAAA	71860
rs52640578	snp	A/G			intron-variant	Cfap52	Mm_Celera	11:67937923	AAAGAAAGAAAGAAA[A/G]AGAAAGAAAGAAAGA	71860
rs52641516	snp	C/G			intron-variant	Cfap52	GRCm38.p3	11:67962616	ACAGTGCTTCACTCC[C/G]TCAAGAGGAGAAGTG	71860
rs107903845	snp	G/T			intron-variant	Cfap52	Mm_Celera	11:67955395	GCCTTCTTAGGGTGT[G/T]TCAGTGTACTAATGT	71860
rs107978436	snp	A/C			intron-variant	Cfap52	Mm_Celera	11:67962690	TGTTGTGTAGGCCTG[A/C]GGATAATGTTGGATT	71860
rs108134333	snp	A/G			intron-variant	Cfap52	Mm_Celera	11:67956344	TCTCTCTAGCCCCCA[A/G]TTGCAATCCCTTATA	71860

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