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
rs6152772	snp	A/T	0.49827	0.0293608	intron-variant	Dcaf17	Mm_Celera	2:71096634	TGTCTTCTTGACTAA[A/T]AATGTTTTTATTAAA	75763
rs6168080	snp	A/G	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71097143	tgttgaaggacattg[A/G]ggttctttatattcc	75763
rs6168147	snp	A/G	0.444444	0.157135	intron-variant	Dcaf17	Mm_Celera	2:71097180	GTCTTGAATAGAGCA[A/G]CAGTATGGCTGAATG	75763
rs6169828	snp	C/G	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71097452	ctgcctctacctccc[C/G]aatgctgggattatg	75763
rs6169924	snp	C/T	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71097503	atttctgcttattct[C/T]ttgagaagtctgttc	75763
rs6184186	snp	A/G	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71097795	cacacctccacaccc[A/G]tgtcatgttgggtac	75763
rs6400729	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Dcaf17, Mettl8	Mm_Celera	2:71054779	TTCCATTTAAAACAA[C/T]AAAATGAAACGGNTA	75763
rs6400763	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Dcaf17, Mettl8	Mm_Celera	2:71054792	AANAAAATGAAACGG[C/T]TAACGTTTGATCCAG	75763
rs6401211	snp	A/C	0.456747	0.140554	upstream-variant-2KB, intron-variant	Dcaf17, Mettl8	Mm_Celera	2:71054854	CAGAAAGCTGGTGTG[A/C]TTACTGACTTTTTCT	75763
rs6401865	snp	G/T	0.49827	0.0293608	upstream-variant-2KB, intron-variant	Dcaf17, Mettl8	Mm_Celera	2:71055021	AGTAATTTTGAACAC[G/T]CAGGCTGAGCTAGTT	75763
rs6402365	snp	C/T	0.456747	0.140554	upstream-variant-2KB, intron-variant	Dcaf17, Mettl8	Mm_Celera	2:71055092	ATTATCTTAGGCAGT[C/T]CAATAAGAATGCAAA	75763
rs6402844	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Dcaf17, Mettl8	Mm_Celera	2:71055136	ATTCCCTATAAGGGG[A/G]AAAAATGGAAGGAGG	75763
rs6403489	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	Dcaf17, Mettl8	Mm_Celera	2:71055270	CAGCAACTTTCACCA[A/C]TAATTACCATACAAA	75763
rs6412540	snp	C/T	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71096377	catgaccaccggagc[C/T]ngaccaagtggcact	75763
rs6412542	snp	G/T	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71096378	atgaccaccggagcn[G/T]gaccaagtggcacta	75763
rs13472434	snp	C/T	0.456747	0.140554	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	Dcaf17, Mettl8	Mm_Celera	2:71055911	CCGCGTCAGCCTTCC[C/T]TTGAGGTTCGCAGGT	75763
rs13472435	snp	A/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	Dcaf17	Mm_Celera	2:71090479	AACAAAACATAAAGA[A/T]ATACTATATACTCTA	75763
rs27971666	snp	C/G	0.401235	0.199068	downstream-variant-500B	Dcaf17	Mm_Celera	2:71114613	CACAATAAGGCAAAA[C/G]GTGAGCCATCCATTA	75763
rs27971667	snp	C/T	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71114273	GAAAGTGTAGTCTAC[C/T]CATTAGCAGGGTTCT	75763
rs27971668	snp	A/G	0.497041	0.0383476	intron-variant	Dcaf17	Mm_Celera	2:71113920	ATAGCCCGGTTCCTT[A/G]CACTGTTTAATGTCC	75763
rs27971669	snp	A/T	0.35503	0.226867	intron-variant	Dcaf17	Mm_Celera	2:71113753	AAACGATTTCTGAGG[A/T]CTTGTTGCCTATGAA	75763
rs27971670	snp	C/T	0.497041	0.0383476	intron-variant	Dcaf17	Mm_Celera	2:71113690	CATGCTTACACAATC[C/T]TTTCACACTTCAATA	75763
rs27971671	snp	C/T	0.244898	0.249948	intron-variant	Dcaf17	Mm_Celera	2:71113292	AGAGATATGGTTTAG[C/T]CTTCCCATGATCCAG	75763
rs27971672	snp	C/T	0.336735	0.234472	intron-variant	Dcaf17	Mm_Celera	2:71112227	GTGGCTCGTCCCAAA[C/T]TTCTTCCTGTTGTCT	75763
rs27971673	snp	A/G	0.375	0.216506	intron-variant	Dcaf17	Mm_Celera	2:71112162	ACTTCTCCTGCTCCT[A/G]GTTAACAAATTACAG	75763
rs27971674	snp	A/G	0.336735	0.234472	intron-variant	Dcaf17	Mm_Celera	2:71111402	ATCAGAATGGTAACC[A/G]GACTTTGTAAGACAG	75763
rs27971675	snp	A/G	0.336735	0.234472	intron-variant	Dcaf17	Mm_Celera	2:71111387	ATATACTCCTGTCAC[A/G]TCAGAATGGTAACCG	75763
rs27971676	snp	A/G	0.46875	0.121031	intron-variant	Dcaf17	Mm_Celera	2:71111205	TGCATGCCAATCACC[A/G]TCCATAAACAAAAAC	75763
rs27971677	snp	A/G	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71111187	CAGGCCCTGAGTGCC[A/G]ACTGCATGCCAATCA	75763
rs27971678	snp	C/T	0.132653	0.220748	intron-variant	Dcaf17	Mm_Celera	2:71111093	CCTCATCTGGGGCTT[C/T]GGCAAGGAGGTATTA	75763
rs27971679	snp	A/G	0.336735	0.234472	intron-variant	Dcaf17	Mm_Celera	2:71111036	GCATGAGAGCCATGC[A/G]TCGTGCTGTATTAGT	75763
rs27971680	snp	C/G	0.336735	0.234472	intron-variant	Dcaf17	Mm_Celera	2:71110942	AGCATTAAACCGACG[C/G]AAACATGCATCTGAT	75763
rs27971681	snp	C/T	0.46875	0.121031	intron-variant	Dcaf17	Mm_Celera	2:71110382	TGTTTCTGATAAGGA[C/T]ATAACAAGGCCGATT	75763
rs27971682	snp	A/C	0.375	0.216506	intron-variant	Dcaf17	Mm_Celera	2:71110290	GGAAGCTCACAGGAC[A/C]GTGGGCCTTAGACAT	75763
rs27971683	snp	G/T	0.48	0.0979796	intron-variant	Dcaf17	Mm_Celera	2:71110226	TCCCTCAGGCAGTAA[G/T]GGCTGCTCTGTATCT	75763
rs27971684	snp	A/G	0.48	0.0979796	intron-variant	Dcaf17	Mm_Celera	2:71110224	GTTCCCTCAGGCAGT[A/G]AGGGCTGCTCTGTAT	75763
rs27971685	snp	C/T	0.244898	0.249948	intron-variant	Dcaf17	Mm_Celera	2:71110008	TAAACTGGTCCTCCT[C/T]TCCTacacacacaca	75763
rs27971686	snp	C/T	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71109967	AGACTCTGACATGAG[C/T]CTATGTAAATGCTGC	75763
rs27971687	snp	A/T	0.444444	0.157135	intron-variant	Dcaf17	Mm_Celera	2:71108745	GATCTCGTTCCTTTC[A/T]TGACCTGAGACAGAT	75763
rs27971688	snp	A/G	0.49827	0.0293608	intron-variant, nc-transcript-variant	Dcaf17	Mm_Celera	2:71107585	GAACCCAGTCGAGTC[A/G]CCCATTGCTGACATC	75763
rs27971689	snp	C/T	0.244898	0.249948	intron-variant	Dcaf17	Mm_Celera	2:71107423	TGCTTCTAGTACCTT[C/T]TAACCAATAACAGCT	75763
rs27971690	snp	A/G	0.132653	0.220748	intron-variant	Dcaf17	Mm_Celera	2:71107218	CTCCAGCAGTCATCC[A/G]GGAATTTTAAAAAGC	75763
rs27971691	snp	A/G	0.489796	0.070696	intron-variant, utr-variant-3-prime, nc-transcript-variant	Dcaf17	Mm_Celera	2:71106219	CAGGACATGCCAAGC[A/G]AGCCCAGTGCTACTG	75763
rs27971692	snp	A/G	0.48	0.0979796	intron-variant, utr-variant-3-prime, nc-transcript-variant	Dcaf17	Mm_Celera	2:71106190	TTTTTCAGTTGGAGT[A/G]CTGGGATCCAACCCA	75763
rs27971693	snp	A/G	0.489796	0.070696	intron-variant	Dcaf17	Mm_Celera	2:71105636	CTCACCAGCTGTTCA[A/G]TCTTTCCTGTTTGTG	75763
rs27971694	snp	A/T	0.48	0.0979796	intron-variant	Dcaf17	Mm_Celera	2:71105517	TCACAGAATTGCCAA[A/T]GTCGGGAAGGCAAAT	75763
rs27971695	snp	G/T	0.152778	0.230321	intron-variant	Dcaf17	Mm_Celera	2:71104997	CCTGGGAGAGAAGAG[G/T]CCAAGGCTGTGATCT	75763
rs27971696	snp	C/T	0.124444	0.216185	intron-variant	Dcaf17	Mm_Celera	2:71104936	AGGCCCACAGCAAAT[C/T]GGAGAAACCCATGCT	75763
rs27971697	snp	A/G	0.473373	0.11227	intron-variant	Dcaf17	Mm_Celera	2:71104756	TTAGCTTAGAACATC[A/G]TGTAGTTAAAGATTC	75763
rs27971698	snp	A/G	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71104615	GGTTACTCTAATTTT[A/G]CATATAGCTGGCCCT	75763
rs27971699	snp	A/G	0.444444	0.157135	intron-variant	Dcaf17	Mm_Celera	2:71104284	CTGGCACCTAGCCCA[A/G]CATCCTTTGGAGATT	75763
rs27971700	snp	C/T	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71104254	CCTTTACATATATCA[C/T]AACTGACTTGAAGTC	75763
rs27971701	snp	A/C	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71104169	TAGTACAGTAGATGC[A/C]TTACAGGGATCTCTT	75763
rs27971702	snp	C/G	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71104140	AAGGTGGTCAGTTCC[C/G]TGTTGGGGTCCTATA	75763
rs27971703	snp	C/T	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71104034	AGATGGGATATGTAG[C/T]CCTTAGAACTTTAAA	75763
rs27971704	snp	C/T	0.473373	0.11227	intron-variant	Dcaf17	Mm_Celera	2:71103926	GTGTTTGAATTGGCA[C/T]TAAATGAAGAGAAGC	75763
rs27971705	snp	A/G	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71103889	TCAGCATTCCAGCAG[A/G]AGGGAGAAGTCATGT	75763
rs27971706	snp	C/T	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71103661	TCCAATCTAGGGTTT[C/T]TGAGTCCTCTGTCTT	75763
rs27971707	snp	A/G	0.473373	0.11227	intron-variant	Dcaf17	Mm_Celera	2:71103609	ATAAAGGCTAAAACA[A/G]TTACTCTCTTGTCTT	75763
rs27971708	snp	C/T	0.473373	0.11227	intron-variant	Dcaf17	Mm_Celera	2:71103541	CGACAGCTGCATTTG[C/T]GCCACACTGAGAGCT	75763
rs27971709	snp	A/G	0.486111	0.0821678	intron-variant	Dcaf17	Mm_Celera	2:71103521	TGTACCTCTGATTGT[A/G]CTGTCGACAGCTGCA	75763
rs27971710	snp	C/T	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71103499	GCCTGTTTGAGGAAG[C/T]GAAATTTGTACCTCT	75763
rs27971711	snp	A/T	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71103437	AGGGAGGCCAAGATC[A/T]TACAGCGAAGGCTGT	75763
rs27971712	snp	C/T	0.444444	0.157135	intron-variant	Dcaf17	Mm_Celera	2:71103409	ATGAAGGCTCTGAGG[C/T]ATAGGCTCATACAGG	75763
rs27971713	snp	A/G	0.473373	0.11227	intron-variant	Dcaf17	Mm_Celera	2:71103370	TTGTTAAAGAATTGA[A/G]ACCCAGTTTAAGTCT	75763
rs27971714	snp	A/C	0.444444	0.157135	intron-variant	Dcaf17	Mm_Celera	2:71103333	ATAGTAACCAATGGG[A/C]TGAAATTGTAGAACC	75763
rs27971715	snp	A/T	0.495868	0.0452663	intron-variant	Dcaf17	Mm_Celera	2:71103311	TATTCTGCCTAGAAG[A/T]GTGGAGATAGTAACC	75763
rs27971716	snp	A/C	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71103254	AGTGAGAAGGTTTGC[A/C]GTGTTTCAGAAATCA	75763
rs27971717	snp	A/G	0.132653	0.220748	intron-variant	Dcaf17	Mm_Celera	2:71103240	CTGAGATGCTCTGAA[A/G]TGAGAAGGTTTGCAG	75763
rs27971718	snp	C/T	0.244898	0.249948	intron-variant	Dcaf17	Mm_Celera	2:71103006	AGAAACAGTCTCCAT[C/T]TTCCTCCCAGGTGGT	75763
rs27971719	snp	A/G	0.493827	0.0552116	intron-variant	Dcaf17	Mm_Celera	2:71102983	AACCATGCTGTGGGC[A/G]TTCCTACAGAAACAG	75763
rs27971720	snp	A/G	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71102974	TACTTAGTAAACCAT[A/G]CTGTGGGCATTCCTA	75763
rs27971721	snp	A/G	0.124444	0.216185	intron-variant	Dcaf17	Mm_Celera	2:71101648	AACGGGCAGAGTGGT[A/G]TTAGTCCAGGACCCA	75763
rs27971722	snp	A/G	0.46875	0.121031	intron-variant	Dcaf17	Mm_Celera	2:71101424	CATCACATGGAAATC[A/G]GCTTCAAGGCAGAAG	75763
rs27971723	snp	C/T	0.489796	0.070696	intron-variant	Dcaf17	Mm_Celera	2:71101382	AAAAGGAGAGATGGT[C/T]CTACTGTATCAGTGA	75763
rs27971724	snp	A/G	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71101291	TCTTGGATGAGGCCT[A/G]AGAAAATCTGTTTGG	75763
rs27971725	snp	A/G	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71101211	GTGCGCAAGACCTGA[A/G]CTTCATCCCAGTAGT	75763
rs27971726	snp	A/G	0.124444	0.216185	intron-variant	Dcaf17	Mm_Celera	2:71101200	AGATGCATACTGTGC[A/G]CAAGACCTGAGCTTC	75763
rs27971727	snp	G/T	0.486111	0.0821678	intron-variant	Dcaf17	Mm_Celera	2:71101165	CAGGATGTGGACCCA[G/T]GGATGAGACTCTGTT	75763
rs27971728	snp	A/T	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71100871	GTTTTCATCACACAT[A/T]GCTTGGTTGAAGGCT	75763
rs27971729	snp	A/T	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71100840	TGGACACTATGTAGC[A/T]GGGAGAAAGCTTAGT	75763
rs27971730	snp	A/G	0.444444	0.157135	intron-variant	Dcaf17	Mm_Celera	2:71100748	TGCTCCTGCAGTAGT[A/G]TAGGCACCCATGGAT	75763
rs27971731	snp	C/T	0.495868	0.0452663	intron-variant	Dcaf17	Mm_Celera	2:71100692	CACCATGGACACGCA[C/T]CATGGGACCCTACAT	75763
rs27971732	snp	A/T	0.277778	0.248452	intron-variant	Dcaf17	Mm_Celera	2:71100633	GGAAGCTCAAAACCA[A/T]TTAAGACTGGTGGTT	75763
rs27971733	snp	C/T	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71100630	TGAGGAAGCTCAAAA[C/T]CAATTAAGACTGGTG	75763
rs27971734	snp	A/C	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71100600	ATGGAGACATGGCTG[A/C]TACTGCCTGCTGAAT	75763
rs27971735	snp	C/G	0.124444	0.216185	intron-variant	Dcaf17	Mm_Celera	2:71100559	AAGGCTGAGCCAACT[C/G]GCTGACTGGAAGAAG	75763
rs27971736	snp	C/T	0.473373	0.11227	intron-variant	Dcaf17	Mm_Celera	2:71100293	TTCAGTCCCACATAT[C/T]CATTCATTATGTATC	75763
rs27971737	snp	A/G	0.132653	0.220748	intron-variant	Dcaf17	Mm_Celera	2:71100123	CTGCATGTACAAAAC[A/G]TGTGAGACATATGCT	75763
rs27971738	snp	C/T	0.498615	0.0262793	intron-variant	Dcaf17	Mm_Celera	2:71099977	GCCTGAGCTACATGG[C/T]GACACCTCATCTAGA	75763
rs27971739	snp	A/G	0.124444	0.216185	intron-variant	Dcaf17	Mm_Celera	2:71099936	GCATGTTGCAATCCT[A/G]ACACTGAGTCATGAG	75763
rs27971740	snp	A/G	0.124444	0.216185	intron-variant	Dcaf17	Mm_Celera	2:71099931	GTGAGGCATGTTGCA[A/G]TCCTAACACTGAGTC	75763
rs27971741	snp	C/T	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71099759	AGGATATCCACAGTC[C/T]ATAAGTTAGTGACTC	75763
rs27971742	snp	C/T	0.132653	0.220748	intron-variant	Dcaf17	Mm_Celera	2:71099729	CTTCCTCTGCAGGGA[C/T]CAGGTGACCTAGCCA	75763
rs27971743	snp	A/G	0.459184	0.136902	intron-variant	Dcaf17	Mm_Celera	2:71098679	CTTTGCCATGTATCC[A/G]GGTTCCTCTGTTGGA	75763
rs27971744	snp	C/T	0.486111	0.0821678	intron-variant	Dcaf17	Mm_Celera	2:71098600	GTTATAGAAACATTT[C/T]CTCCTAAGTTAGATT	75763
rs27971745	snp	C/T	0.489796	0.070696	intron-variant	Dcaf17	Mm_Celera	2:71098473	AAAAGTTTACAAAAG[C/T]TCACATTGTTCTCAA	75763
rs27971746	snp	C/T	0.493827	0.0552116	intron-variant	Dcaf17	Mm_Celera	2:71098392	AGTAAGTTAACCTAT[C/T]ATTAGATTGTAACAT	75763
rs27971747	snp	G/T	0.493827	0.0552116	intron-variant	Dcaf17	Mm_Celera	2:71098347	CTTATCACATTAAAA[G/T]TCCAATGTTAAAAAT	75763
rs27971748	snp	A/G	0.5	0	intron-variant	Dcaf17	Mm_Celera	2:71098264	TCTAAGTGCTCCACA[A/G]TAGCAATATTCGCAG	75763

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