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
rs3701869	snp	A/G	0.5	0	intron-variant	Chd4	Mm_Celera	6:125118633	AGGAGTAATTGTGGT[A/G]TACAAACTTACATAT	107932
rs3714944	snp	C/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125114694	TGTTTATTAATCTTA[C/T]TAGTTCTCCATAAAA	107932
rs3715011	snp	C/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125114728	AATTTTTTTTAAAGA[C/T]TTATTTATTATATAT	107932
rs3716297	snp	A/T	0.497778	0.0332592	intron-variant	Chd4	Mm_Celera	6:125114931	AAACGTAGACGAAAC[A/T]ATACATTAAATAACT	107932
rs6270784	snp	G/T	0.444444	0.157135	intron-variant, downstream-variant-500B	Chd4, Mir7045, Gm32616	Mm_Celera	6:125097337	CCAGTGAGGCTGCGT[G/T]CGCGCGCTGCTTGTC	107932
rs13463119	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Nop2, Chd4	Mm_Celera	6:125130499	ttttttttttttttt[C/T]tCAACTTTATTTAGC	107932
rs13463120	snp	A/G	0.475309	0.108333	synonymous-codon	Chd4	Mm_Celera	6:125113968	GTTTGTGACCCGTGC[A/G]TCAGTGGAGGAGCGC	107932
rs13463121	snp	A/T	0.444444	0.157135	missense	Chd4	Mm_Celera	6:125122006	AAGGAAGTTAAATCT[A/T]CAGCCCCTGAGGCGA	107932
rs13463122	snp	A/G	0.5	0	synonymous-codon	Chd4	Mm_Celera	6:125110118	CCTGAAAGAGGGAGG[A/G]CATCGTGTGCTCATC	107932
rs13463123	snp	C/T	0.32	0.24	synonymous-codon	Chd4	Mm_Celera	6:125113986	AGTGGAGGAGCGCAT[C/T]ACGCAGGTGGCAAAG	107932
rs29825573	snp	C/T	0.49827	0.0293608	intron-variant	Chd4	Mm_Celera	6:125104795	CCATAGACACTGATA[C/T]TCATATTCTTTCAGG	107932
rs29833908	snp	C/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125102771	TGGGGTGGGGTAACC[C/T]GAGTCTCTGGTTTTA	107932
rs29869109	snp	C/T	0.33241	0.236027	intron-variant	Chd4	Mm_Celera	6:125121691	CTGCTGGTACGTCTG[C/T]TGTCATGTCATTTCT	107932
rs29874475	snp	C/T	0.444444	0.157135	synonymous-codon, upstream-variant-2KB	Chd4, Gm32616	Mm_Celera	6:125101292	GTTCTCAGAGGAGGA[C/T]TACCGGACCCTCACC	107932
rs29914292	snp	C/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125108516	GAGGAGACTGTTGAG[C/T]GAGTCACTGCTGTTG	107932
rs29920912	snp	C/T	0.33241	0.236027	intron-variant	Chd4	Mm_Celera	6:125121496	GAAGGGAGTCTTGAA[C/T]TTGCTGTTCATTGCT	107932
rs29923991	snp	C/T	0.498615	0.0262793	intron-variant	Chd4	Mm_Celera	6:125106883	AATGGTGCTCTGTGT[C/T]AGGTCTACCTGAAGC	107932
rs29924516	snp	C/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125117611	CCCCACTCCCACCCC[C/T]GGCTTCTTGGGGGCT	107932
rs29967617	snp	A/G/T	0.345679	0.230967	intron-variant	Chd4	GRCm38.p3	6:125103314	CTAGGGCCTGCTGAC[A/G/T]GCATTAGGTTGCTTA	107932
rs29972284	snp	C/T	0.444444	0.157135	intron-variant	Chd4	Mm_Celera	6:125107861	ATAAGTATGGTTGTG[C/T]ACCACCTGTGTGCAG	107932
rs29974106	snp	C/G	0.455	0.143091	intron-variant	Chd4	Mm_Celera	6:125113052	GCTAGATAAAAAGCT[C/G]CTTAGCTGACATTTC	107932
rs29984267	snp	A/T	0.492188	0.0620098	intron-variant	Chd4	Mm_Celera	6:125109665	CGTGGTCGCTGCTTG[A/T]TAGCTTAGCTCCACA	107932
rs30020848	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Chd4, Gm32616	Mm_Celera	6:125100727	CTCAGGACTGTCCTG[A/G]GTGAGCATGTGTGTA	107932
rs30031775	snp	A/G	0.32	0.24	intron-variant	Chd4	Mm_Celera	6:125110244	TAATTAAATTGTTCC[A/G]TTTTACAGATGACCA	107932
rs30072370	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	Chd4, Gm32616	Mm_Celera	6:125099676	TACAAAGAAAGCTGC[C/T]TCCCAGCCTTCTCCC	107932
rs30133357	snp	C/T	0.444444	0.157135	utr-variant-5-prime, upstream-variant-2KB, intron-variant	Chd4, Mir7045, Gm32616	Mm_Celera	6:125096209	GCGGCGAGGAGGAGC[C/T]GGAGCGGGAGTGACA	107932
rs30173456	snp	G/T	0.48	0.0979796	upstream-variant-2KB, downstream-variant-500B	Nop2, Chd4	Mm_Celera	6:125130746	TTTAGCAAACTGTTC[G/T]CAGAGCACTCCTGCA	107932
rs30213549	snp	A/G	0.456747	0.140554	intron-variant	Chd4	Mm_Celera	6:125104852	AATTGAGATTAAGTG[A/G]TGTCTTTTTAACAGT	107932
rs30219394	snp	A/G	0.48	0.0979796	intron-variant	Chd4	Mm_Celera	6:125112587	AGTTCCTGCGTCTGG[A/G]CGTCACAGTGGAAGA	107932
rs30220306	snp	C/T	0.498615	0.0262793	intron-variant	Chd4	Mm_Celera	6:125109655	ATGAGGATGGCGTGG[C/T]CGCTGCTTGTTAGCT	107932
rs30220337	snp	A/G	0.5	0	intron-variant	Chd4	Mm_Celera	6:125125677	AATCTTAGTATTTGC[A/G]TAGTGGAAGCAGGAG	107932
rs30236935	snp	C/T	0.444444	0.157135	intron-variant	Chd4	Mm_Celera	6:125119395	GGGATTAAAGGCGTG[C/T]GCCACCACTGCCGGG	107932
rs30264149	snp	A/G	0.48	0.0979796	intron-variant	Chd4	Mm_Celera	6:125127203	GACCAGGCTGGCCTA[A/G]AACTCAGAAATTGCC	107932
rs30264203	snp	G/T	0.465374	0.126941	intron-variant	Chd4	Mm_Celera	6:125121076	GGTGTTGCTAGCTGC[G/T]GTTGGCAGGTGATGC	107932
rs30264573	snp	A/G	0.33241	0.236027	intron-variant, upstream-variant-2KB	Chd4, Gm32616	Mm_Celera	6:125101055	TTTCTCCCAGATACC[A/G]CCCTGCCCTGTAGCA	107932
rs30278026	snp	C/T	0.487535	0.077957	intron-variant	Chd4	Mm_Celera	6:125117501	GGCTCAAAGCTAGAG[C/T]GCGTCCCATTGGGCC	107932
rs30279940	snp	A/T	0.484429	0.0868505	intron-variant	Chd4	Mm_Celera	6:125109757	CCTCAGTCCAACCGG[A/T]CCTTGTGTCTTGTTC	107932
rs30314437	snp	A/G	0.444444	0.157135	intron-variant	Chd4	Mm_Celera	6:125104144	TGCCTTTCTAGCGCT[A/G]GCATCAAAAACTTGG	107932
rs30317234	snp	A/G	0.456747	0.140554	intron-variant	Chd4	Mm_Celera	6:125118314	CTGTTATGGAGTTAC[A/G]TAATAAGTGGTTTGG	107932
rs30364078	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Chd4, Gm32616	Mm_Celera	6:125099625	GGTGGCTTGGGAAGA[A/G]GGAGAAGGGAACTGG	107932
rs30365166	snp	C/T	0.48	0.0979796	intron-variant	Chd4	Mm_Celera	6:125126875	GCCTCTAGCTTGCAG[C/T]TCTCTTTCTTGCCTC	107932
rs30371834	snp	G/T	0.487535	0.077957	intron-variant	Chd4	Mm_Celera	6:125117527	GGGCCCGCAGCTGGA[G/T]TGCCCAGGTCACACT	107932
rs30379346	snp	A/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125112480	CTCTGACTCTACACG[A/T]ATGTACACACACTTG	107932
rs30407438	snp	A/G	0.5	0	intron-variant	Chd4	Mm_Celera	6:125127321	TAAAGAAACCCAGAT[A/G]ACCTGATTGATTCCA	107932
rs30414412	snp	A/T	0.48	0.0979796	intron-variant	Chd4	Mm_Celera	6:125118957	ACAGCAGTTTTACTC[A/T]GTCATGGTGGGCTTG	107932
rs30420870	snp	C/T	0.487535	0.077957	intron-variant	Chd4	Mm_Celera	6:125127357	CAGGTGACTATGCCA[C/T]TATTAAGAAAAAGCT	107932
rs30446800	snp	A/G	0.5	0	intron-variant	Chd4	Mm_Celera	6:125112392	GGGGCCAGCAGGTGA[A/G]GGTACTTGTCACCCA	107932
rs30456980	snp	G/T	0.484429	0.0868505	intron-variant	Chd4	Mm_Celera	6:125121444	GCCTGTTTTCATTTT[G/T]AAAGTTGAGAAACTG	107932
rs30463814	snp	A/G	0.359862	0.224567	intron-variant	Chd4	Mm_Celera	6:125125388	GTGAGAAAGGTGCTC[A/G]TGTGAGCAGAGAAGC	107932
rs30466515	snp	C/T	0.432133	0.171253	synonymous-codon	Chd4	Mm_Celera	6:125109454	GCGCGTGGAGTTGAG[C/T]CCTATGCAGAAGTGA	107932
rs30508241	snp	A/G	0.5	0	intron-variant	Chd4	Mm_Celera	6:125123113	TGTGTGTGTGTATGT[A/G]TGTGTGTGTGTGTGT	107932
rs30508261	snp	C/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125110903	CAGATGGGGAAGTCA[C/T]GGGAAAGCGTACATG	107932
rs30509590	snp	A/G	0.5	0	intron-variant	Chd4	Mm_Celera	6:125102707	AAACGGGAGCTTTGG[A/G]AAATGTATGTGTAAA	107932
rs30561110	snp	C/G	0.5	0	intron-variant	Chd4	Mm_Celera	6:125110598	TGCCTAGGTACTCTG[C/G]GACTGGAGTGACAGA	107932
rs30561144	snp	G/T	0.493827	0.0552116	synonymous-codon	Chd4	Mm_Celera	6:125109803	CAAGTATATTCTCAC[G/T]CGGAATTTCGAAGCA	107932
rs30565299	snp	A/G	0.375	0.216506	intron-variant	Chd4	Mm_Celera	6:125108813	TGAGGTGTGGGAGGA[A/G]ACGGCCTCCAGTTCT	107932
rs30618367	snp	A/C	0.5	0	missense	Chd4	Mm_Celera	6:125122141	GCACAGCCCCCTGCC[A/C]CTGCCCCTGCCACTG	107932
rs30661215	snp	A/G	0.5	0	intron-variant	Chd4	Mm_Celera	6:125102755	CTGACGTGGGGTGGG[A/G]TGGGGTGGGGTAACC	107932
rs30666174	snp	C/T	0.46875	0.121031	intron-variant	Chd4	Mm_Celera	6:125111795	TAAAATATATTTAGA[C/T]TTTAAAGGTGTGAAC	107932
rs30668821	snp	C/T	0.444444	0.157135	intron-variant	Chd4	Mm_Celera	6:125120806	TTTGGTGAGGAGAGA[C/T]TTGCTTCCTCTCACA	107932
rs30705315	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Chd4, Gm32616	Mm_Celera	6:125099979	GTGGTTCTGAGCAGT[A/G]ATAGTCCCAAAGGGG	107932
rs30711271	snp	C/T	0.277778	0.248452	intron-variant	Chd4	Mm_Celera	6:125120586	ATCTTGCGAGTTGTG[C/T]AGCTGTTGGCATTGT	107932
rs30716592	snp	C/T	0.391111	0.206368	synonymous-codon, upstream-variant-2KB	Chd4, Gm32616	Mm_Celera	6:125101295	CTCAGAGGAGGACTA[C/T]CGGACCCTCACCAAC	107932
rs30754853	snp	A/T	0.48	0.0979796	intron-variant	Chd4	GRCm38.p3	6:125126728	GTGTGTGTGTGTGTG[A/T]GAGAACCTGTGCTCT	107932
rs30763676	snp	C/T	0.444444	0.157135	intron-variant, nc-transcript-variant	Chd4, Gm32616	Mm_Celera	6:125098556	ATGCTGTCTGACCAG[C/T]GTTGCTTCCCATCTT	107932
rs30799485	snp	C/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125109932	ATGGTATGTGCACCT[C/T]CTTGTCTTCTGTGCC	107932
rs30799569	snp	G/T	0.277778	0.248452	intron-variant	Chd4	Mm_Celera	6:125119586	TTCTGAATTGTCAAT[G/T]CGAAAAACTGTAACT	107932
rs30804263	snp	C/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125112401	AGGTGAAGGTACTTG[C/T]CACCCAGCAGTTTAT	107932
rs30806225	snp	C/T	0.465374	0.126941	intron-variant	Chd4	Mm_Celera	6:125121089	GCGGTTGGCAGGTGA[C/T]GCTGTTGTTCCCGAG	107932
rs30841830	snp	C/T	0.444444	0.157135	intron-variant	Chd4	Mm_Celera	6:125120818	AGACTTGCTTCCTCT[C/T]ACAGAGGTTTTTTTT	107932
rs30847307	snp	A/G	0.290657	0.246672	synonymous-codon, upstream-variant-2KB	Chd4, Gm32616	Mm_Celera	6:125101328	CAAGGCCTTCAGCCA[A/G]TTTGTTAGGTAAGTC	107932
rs30851837	snp	C/T	0.444444	0.157135	intron-variant	Chd4	Mm_Celera	6:125104319	GCTGTTATAGGAAGA[C/T]GTACCTGAAAAGAAA	107932
rs30863919	snp	C/T	0.48	0.0979796	intron-variant	Chd4	Mm_Celera	6:125117413	CAACCGGGCCATGTC[C/T]CCAGCCCCTGTAAGT	107932
rs30900563	snp	A/G	0.444444	0.157135	intron-variant	Chd4	Mm_Celera	6:125120800	TTGGTCTTTGGTGAG[A/G]AGAGACTTGCTTCCT	107932
rs30900624	snp	C/T	0.5	0	intron-variant	Chd4	Mm_Celera	6:125112456	GAGAACCAGTTCCTG[C/T]GAGAAGTCCTCTGAC	107932
rs30908637	snp	C/T	0.290657	0.246672	intron-variant	Chd4	Mm_Celera	6:125104752	TGACCTTTGAGTTCA[C/T]GCTCATGCTTGTGCG	107932
rs30934954	snp	C/G	0.345679	0.230967	synonymous-codon, upstream-variant-2KB	Chd4, Gm32616	Mm_Celera	6:125101561	CTTCAAGGGCAGCTC[C/G]GGAGCATCAGTGGCA	107932
rs30948316	snp	A/G	0.375	0.216506	intron-variant	Chd4	Mm_Celera	6:125113188	CTGTACGTGATGTTG[A/G]TATTTGTCCTTTCTA	107932
rs30949066	snp	C/G	0.498615	0.0262793	intron-variant	Chd4	Mm_Celera	6:125107145	TGATGTCTGTCTGTC[C/G]GTTAGGGCCTGGTGG	107932
rs30952151	snp	C/T	0.465374	0.126941	intron-variant	Chd4	Mm_Celera	6:125127885	CTTCGCAGGAATGAT[C/T]ATCTGTGGCGTTATG	107932
rs30962354	snp	A/G	0.5	0	intron-variant	Chd4	Mm_Celera	6:125127269	GTGCCACAACTGCCC[A/G]ACAGCGTTGGGTTTT	107932
rs45697545	snp	A/G	0.124444	0.216185	intron-variant	Chd4	Mm_Celera	6:125118888	AGGCTTGTAGTGAGC[A/G]CCTTTACTCTGTGAG	107932
rs45714474	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Chd4, Gm32616	Mm_Celera	6:125101160	GTTTGACTTCCCAGT[C/T]GGTTGTCTTAGCCAG	107932
rs45750912	snp	A/G	0.32	0.24	intron-variant	Chd4	Mm_Celera	6:125128734	TGGAGGAAGAGATGA[A/G]TCTGTCAGTGAGAAC	107932
rs45761131	snp	C/T	0.124444	0.216185	intron-variant	Chd4	Mm_Celera	6:125118462	GTAGTCTGGACTGCT[C/T]TTTATTGACGTCCTG	107932
rs45807917	snp	C/G	0.124444	0.216185	intron-variant	Chd4	Mm_Celera	6:125121913	GGGCCTTCCTGATTG[C/G]TTGTCTTTTGGTCTG	107932
rs45808661	snp	G/T	0.124444	0.216185	intron-variant	Chd4	Mm_Celera	6:125123711	ACAGATGTGCCCTCA[G/T]TTGGCTCTGAAGGTC	107932
rs45831706	snp	A/T			intron-variant	Chd4	Mm_Celera	6:125117453	GGCTGGCCTTTAACT[A/T]TTTTTTGATTCTCTT	107932
rs46043935	snp	A/G			upstream-variant-2KB, intron-variant	Chd4, Gm32616	Mm_Celera	6:125094169	GGTGATGATGGGGAT[A/G]GGAGGGAAGGGACAG	107932
rs46059651	snp	A/T	0.244898	0.249948	intron-variant	Chd4	Mm_Celera	6:125118003	CGTGCACACTTCAGC[A/T]CTGGAACTTCTTCCC	107932
rs46063157	snp	A/G	0.21875	0.248039	upstream-variant-2KB, intron-variant	Chd4, Gm32616	Mm_Celera	6:125094511	GTTTCTTGAAGGAAG[A/G]CACCTGTGTGTTGGT	107932
rs46074641	snp	C/T	0.408163	0.193609	intron-variant, nc-transcript-variant	Chd4, Gm32616	Mm_Celera	6:125098033	GCTCCCTGGACTGGC[C/T]AAACCCGTATTATTA	107932
rs46097974	snp	A/G			intron-variant	Chd4	Mm_Celera	6:125113203	ATATTTGTCCTTTCT[A/G]GTGATTATTGGTCAC	107932
rs46169042	snp	A/C	0.124444	0.216185	synonymous-codon	Chd4	Mm_Celera	6:125123380	AGAGCGGGCAGCCAC[A/C]GTCACTAAGAAGACT	107932
rs46196659	snp	C/G	0.32	0.24	intron-variant	Chd4	Mm_Celera	6:125106942	ATCCTAGGCCGCATC[C/G]TGCAGTGAGCAGTGA	107932
rs46236331	snp	C/G	0.408163	0.193609	intron-variant	Chd4	Mm_Celera	6:125106753	TGAGTATGGGTGGAA[C/G]AGGAAGGGTGTGTTT	107932
rs46247978	snp	C/T	0.124444	0.216185	intron-variant	Chd4	Mm_Celera	6:125116526	GCATCCGTCCTGTCC[C/T]GATTACTGCCTGAGT	107932
rs46283882	snp	A/G	0.231111	0.249285	intron-variant	Chd4	Mm_Celera	6:125113114	AGTTTCTAGCCAGTT[A/G]TTCCAAGTAGTGTCT	107932
rs46309172	snp	A/G	0.124444	0.216185	intron-variant	Chd4	Mm_Celera	6:125122781	GGGCCCACTGGTTTC[A/G]GATCGCAGCTGACGT	107932
rs46313628	snp	A/G	0.231111	0.249285	intron-variant	Chd4	Mm_Celera	6:125128419	TACATAAAATACAGT[A/G]TTAAAAATGTGGACT	107932

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