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
rs4227859	snp	G/T	0.375	0.216506	intron-variant	Copb2	Mm_Celera	9:98587712	TCAGCAAGGGAT[G/T]	50797
rs4227860	snp	A/T	0.375	0.216506	intron-variant	Copb2	Mm_Celera	9:98587710	AGCAAGGGAT[A/T]	50797
rs4227861	snp	A/G	0.375	0.216506	intron-variant	Copb2	Mm_Celera	9:98587709	GCAAGGGAT[A/G]	50797
rs4227862	snp	A/G	0.21875	0.248039	intron-variant	Copb2	GRCm38.p3	9:98587682	CAGAGGGAGCTCAGG[A/G]TTAGGAAGTGGCTTT	50797
rs4227863	snp	A/T	0.21875	0.248039	intron-variant	Copb2	Mm_Celera	9:98587450	TGCAGCACATTTCAA[A/T]CTTGGACTTGTGAAT	50797
rs4227864	snp	C/T	0.21875	0.248039	intron-variant	Copb2	GRCm38.p3	9:98587448	CAGCACATTTCAAAC[C/T]TGGACTTGTGAATGT	50797
rs13466556	snp	C/T	0.391111	0.206368	synonymous-codon	Copb2	Mm_Celera	9:98588137	AGATATTCTGGATGA[C/T]TAAAGTTTGCCATTT	50797
rs13480365	snp	A/G	0.498047	0.0311889	intron-variant	Copb2	Mm_Celera	9:98579312	ATGACGTGATGCTTG[A/G]GTTTAAGGCAAAGTA	50797
rs30283520	snp	G/T	0.401235	0.199068	intron-variant	Copb2	Mm_Celera	9:98579781	GTGTGCTGAGTAGTA[G/T]TCCATTGAATGGATG	50797
rs33164971	snp	A/G	0.124444	0.216185	upstream-variant-2KB	Copb2	Mm_Celera	9:98561871	TGGGATGAAGCAGCC[A/G]TCCTAGAGATTGACC	50797
rs33164972	snp	A/G	0.132653	0.220748	upstream-variant-2KB, downstream-variant-500B	Copb2, 4930579K19Rik	Mm_Celera	9:98562014	TCCACATGCCTCTAA[A/G]CCAGAGTAAACAAGA	50797
rs33164973	snp	A/G	0.391111	0.206368	upstream-variant-2KB, downstream-variant-500B	Copb2, 4930579K19Rik	Mm_Celera	9:98562263	GTATTGAACTCGCAG[A/G]TCTTCAAGGTTTGTG	50797
rs33165794	snp	A/T	0.391111	0.206368	upstream-variant-2KB, nc-transcript-variant	Copb2, 4930579K19Rik	Mm_Celera	9:98562588	TATAGTTCACATTTT[A/T]AAAAGTTTCAACTAA	50797
rs33165795	snp	A/G	0.391111	0.206368	upstream-variant-2KB, nc-transcript-variant	Copb2, 4930579K19Rik	Mm_Celera	9:98562621	CTTGCAATTGGTTGC[A/G]CTACAGTATGCGATT	50797
rs33165796	snp	C/T	0.391111	0.206368	upstream-variant-2KB, nc-transcript-variant	Copb2, 4930579K19Rik	Mm_Celera	9:98562754	TTTGTATATGAAAAA[C/T]TGAGGCCTATAAATC	50797
rs33165797	snp	C/T	0.391111	0.206368	upstream-variant-2KB, nc-transcript-variant	Copb2, 4930579K19Rik	Mm_Celera	9:98562836	CTATACAATTCCTTT[C/T]TGGAAACCTAGGCTT	50797
rs33165798	snp	C/T	0.391111	0.206368	upstream-variant-2KB, nc-transcript-variant	Copb2, 4930579K19Rik	Mm_Celera	9:98562909	TTTGTTTCATAGCAT[C/T]ATCTTTTTAAAAGGT	50797
rs33165799	snp	A/G	0.336735	0.234472	upstream-variant-2KB, nc-transcript-variant	Copb2, 4930579K19Rik	Mm_Celera	9:98562936	AGGTGTGTGAAATCG[A/G]TACACAATGTATTTG	50797
rs33165800	snp	C/T	0.336735	0.234472	upstream-variant-2KB, nc-transcript-variant	Copb2, 4930579K19Rik	GRCm38.p3	9:98563227	ATGCTCTTTGAAGGG[C/T]AATCACCCGACTGCC	50797
rs33165801	snp	C/G	0.231111	0.249285	upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98563689	CAGGCGCAGAGCCTG[C/G]CTCCGAGTACCGCGA	50797
rs33165802	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98564022	ACAGTAGTGTAACTG[A/G]GTACCCGCGAAGGAG	50797
rs33165803	snp	G/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98564126	AAGTAAATGCTAGAG[G/T]CAGGACTCGGATGCC	50797
rs33166634	snp	G/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98564245	TGTGCAGGCACCACA[G/T]TGCAAACTTAAGCAG	50797
rs33166635	snp	A/G	0.391111	0.206368	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98564525	CTTTCGGTGGAAGAC[A/G]TTTGAGGAAAACTGT	50797
rs33166636	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98564539	CATTTGAGGAAAACT[A/G]TTGTGTGAACATGTG	50797
rs33166637	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98564891	GTGGTTACTATAAGC[C/T]GTGCTCTGCTCTAAC	50797
rs33166638	snp	G/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98565056	AGACTGTGGACCTCA[G/T]CTATACTACCTGTTC	50797
rs33166639	snp	A/C/G	0.152778	0.230321	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	GRCm38.p3	9:98565077	CTACCTGTTCCTCCC[A/C/G]TATTCCCAAATACAT	50797
rs33166640	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98565205	ATCCTCTGGCTAGGC[C/T]AATCAGAAAGGGCAT	50797
rs33166641	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98565218	GCTAATCAGAAAGGG[C/T]ATAATGGTGGCAGTG	50797
rs33166642	snp	A/C	0.231111	0.249285	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98565411	GGTATGTGCAGCTAT[A/C]TACTAGGTAGTTCAG	50797
rs33166643	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98565574	GAAGATCCCACTATG[A/G]CTCCTGGCATAACAT	50797
rs33167414	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Copb2, 4930579K19Rik	Mm_Celera	9:98565590	CTCCTGGCATAACAT[A/G]CTTCCTGCTTGTTGT	50797
rs33167415	snp	C/G	0.124444	0.216185	intron-variant	Copb2	Mm_Celera	9:98565748	GTTAGAGATGGGCAG[C/G]GCTGCATGACAGTGG	50797
rs33167416	snp	C/T	0.391111	0.206368	intron-variant	Copb2	Mm_Celera	9:98566118	GAAGAAGAGAGAGTG[C/T]TCCAGGACTTCACTG	50797
rs33167417	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98566143	TCACTGTGGAATGAA[C/T]TAACTTTTCTTCTGG	50797
rs33167418	snp	A/G	0.391111	0.206368	intron-variant	Copb2	Mm_Celera	9:98566255	TGGTCTGACTGGAGA[A/G]GGACAGTTTTAAACT	50797
rs33167419	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98566324	TGTTTTTCAGTATGT[A/G]TCTGTAAATTCAAAA	50797
rs33167420	snp	C/T	0.336735	0.234472	intron-variant	Copb2	Mm_Celera	9:98566542	GATTTAGCTGATGTT[C/T]TAAATTTATTTACCT	50797
rs33167421	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98566857	ACCACATCCGACCTG[A/G]TAACATGTTCTGATT	50797
rs33167422	snp	A/G	0.124444	0.216185	intron-variant	Copb2	Mm_Celera	9:98566961	GCTGTCAATCTCAAC[A/G]CCTCAGGAGGCATCT	50797
rs33167423	snp	C/T	0.391111	0.206368	intron-variant	Copb2	Mm_Celera	9:98567332	AATAAAATTTGTTAT[C/T]TGTGTGGATCTGTGT	50797
rs33168164	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98567354	GATCTGTGTAACTCA[A/G]TGAACCATCCTGTCC	50797
rs33168165	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98567409	AAAAACCAAGCAGGA[A/G]CTAAGACTCTGCAGA	50797
rs33168166	snp	C/T	0.132653	0.220748	intron-variant	Copb2	Mm_Celera	9:98567470	GCCAAGTGTAAATAG[C/T]TACTTCTAGGCTTCA	50797
rs33168167	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98567634	TTTTGTTATGCCTCA[A/G]CCAGAACCGTATACT	50797
rs33168168	snp	C/T	0.336735	0.234472	intron-variant	Copb2	Mm_Celera	9:98567878	CTGTAGAATTGATAC[C/T]ATTCACAATTTAGGA	50797
rs33168169	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98568200	AATAATGAAAGAGCC[A/G]CCAGAGGCCAAGCAG	50797
rs33168170	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98568239	GTGCTGCTGCTCAAA[A/G]TAGGATGGAGTGTTT	50797
rs33168171	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98568288	TGTGTGGGTGTTGCC[C/T]GTGGAAGAAGTTCTG	50797
rs33168172	snp	C/T	0.391111	0.206368	intron-variant	Copb2	Mm_Celera	9:98568614	CTAGCCACACTGAGC[C/T]TTGATTTACTACTCT	50797
rs33168173	snp	A/G	0.391111	0.206368	intron-variant	Copb2	Mm_Celera	9:98568675	TGAAGAAAGAACGTG[A/G]AATAAAATGTTAGGC	50797
rs33168864	snp	A/G	0.132653	0.220748	intron-variant	Copb2	Mm_Celera	9:98568721	ACAAAGAACCATCTT[A/G]GTGTTAGCTGTTGCT	50797
rs33168865	snp	C/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98569087	TGTTGGTTTTCCAGT[C/G]TACCTTGGTAAATGA	50797
rs33168866	snp	A/G	0.244898	0.249948	intron-variant	Copb2	Mm_Celera	9:98569451	CCCCACCTTGAATCC[A/G]TGTAGATGATCCACT	50797
rs33168867	snp	C/T	0.297521	0.245442	intron-variant	Copb2	Mm_Celera	9:98569603	TCATTTCTATGGGTT[C/T]CATtttatttattta	50797
rs33168868	snp	A/G	0.244898	0.249948	intron-variant	Copb2	Mm_Celera	9:98569921	CTGCCCTTGGAGAGC[A/G]CAGTGGGAAGAGTGA	50797
rs33168869	snp	C/T	0.165289	0.235211	intron-variant	Copb2	Mm_Celera	9:98569992	GAGTAAAGCTTCCTC[C/T]CTGGGTAGGTTTCCA	50797
rs33168870	snp	A/G	0.408163	0.193609	intron-variant	Copb2	Mm_Celera	9:98570086	CCCGTCTGTCTGTCC[A/G]TCCTATGACCGTCTG	50797
rs33168871	snp	A/G	0.336735	0.234472	intron-variant	Copb2	GRCm38.p3	9:98570185	CTTTAATGCTGAGCT[A/G]TCATACACTTGTTTT	50797
rs33168872	snp	A/G	0.132653	0.220748	synonymous-codon	Copb2	Mm_Celera	9:98570651	GTTTGAAGCACACTC[A/G]GATTACATTCGTTGT	50797
rs33168873	snp	C/T	0.124444	0.216185	intron-variant	Copb2	Mm_Celera	9:98570748	ATGTGCACTGAGTGA[C/T]GATTTGTTCCCACGA	50797
rs33169664	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98571293	TAGTAGCTGTCCATA[C/T]GCACTTTGTCTGCAC	50797
rs33169665	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98571323	CTGTTCTGTAGTTAG[A/G]AATGCTCTGAGGGCA	50797
rs33169666	snp	A/G	0.260355	0.249785	intron-variant	Copb2	Mm_Celera	9:98571405	GGATGTGTGAACTGT[A/G]CTACATTTGTTGCCT	50797
rs33169667	snp	A/C	0.260355	0.249785	intron-variant	Copb2	Mm_Celera	9:98571430	TTGCCTTAAAGGACA[A/C]CAAGCCTGTCTTACT	50797
rs33169668	snp	A/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98571661	AGTGTCCACTGTTGG[A/T]GCTTTACTATGACTG	50797
rs33169669	snp	C/T	0.132653	0.220748	intron-variant	Copb2	Mm_Celera	9:98571844	GTCTGTCTGTCCGTC[C/T]GTTAGTCATTCTTGA	50797
rs33169670	snp	A/G	0.244898	0.249948	intron-variant	Copb2	Mm_Celera	9:98572271	GAGTGTGTGTCACTC[A/G]CTTTAGATTTTGTTT	50797
rs33169671	snp	A/C/G	0.32	0.24	intron-variant	Copb2	Mm_Celera	9:98572383	GGAGCTCTGTCTTCC[A/C/G]TTGCACAGCCCCAGG	50797
rs33169672	snp	C/T	0.142012	0.225474	intron-variant	Copb2	Mm_Celera	9:98572423	GAGAGTAGCACAGTG[C/T]GTTGGCTGTACTGGG	50797
rs33169673	snp	C/T	0.124444	0.216185	intron-variant	Copb2	Mm_Celera	9:98572536	TTGTTGAATTGCCCT[C/T]GCTTTTGACATAGGT	50797
rs33170224	snp	A/G	0.231111	0.249285	synonymous-codon	Copb2	Mm_Celera	9:98581182	TATCGCCACCGAGGA[A/G]TCATTTTTTATTCTT	50797
rs33170225	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98581294	GTGAGTGTCTGAGTC[C/T]AGCTTAGGGCATTGA	50797
rs33170226	snp	A/G	0.124444	0.216185	intron-variant	Copb2	Mm_Celera	9:98582042	ACATTCCAGTTTCAT[A/G]TGTTGCAGTTTAGAT	50797
rs33170227	snp	A/T	0.260355	0.249785	intron-variant	Copb2	Mm_Celera	9:98582131	TATTCATTGAAAACT[A/T]TTTTTTAAGACAAAA	50797
rs33170228	snp	C/T	0.124444	0.216185	intron-variant	Copb2	Mm_Celera	9:98582453	CTAAATTTGAAAGTG[C/T]TTTATGAACCAAATG	50797
rs33170229	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98582504	GTGATGGGTTAATTT[C/T]CCCCCATTAGTTTTA	50797
rs33170230	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98583073	TCTTGCTTCTTTAGG[C/T]GTAGGAACCTCAGTG	50797
rs33170231	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98583121	GCTGATTTTATCACT[C/T]TTCTTACATCCCCTT	50797
rs33170232	snp	A/C	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98583814	GAGTTTATGCCCCCC[A/C]AACACAAAAACTACC	50797
rs33170233	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98583881	AAAGCAAGGACATGT[C/T]GCCCTCTTCCTCTGT	50797
rs33170374	snp	A/C	0.244898	0.249948	intron-variant	Copb2	Mm_Celera	9:98572734	CCTCTCTCCCTGGCA[A/C]GTGTTCTTTCATTTT	50797
rs33170375	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98572830	GTTAATTGTAGATTC[A/G]TGCACTTCATCTGTA	50797
rs33170376	snp	A/G	0.152778	0.230321	intron-variant	Copb2	Mm_Celera	9:98572910	AAAGCAATTTGGCAA[A/G]GAAAGGGTTTATTTC	50797
rs33170377	snp	A/G	0.142012	0.225474	intron-variant	Copb2	Mm_Celera	9:98573053	ATTGGCTTGCTCTTC[A/G]TGAGTTGCTCAGCCT	50797
rs33170378	snp	C/T	0.132653	0.220748	intron-variant	Copb2	Mm_Celera	9:98573285	GGCACCTTCAGAGAG[C/T]AGTGATTCTGCTTCC	50797
rs33170379	snp	A/G	0.152778	0.230321	intron-variant	Copb2	Mm_Celera	9:98573335	AGCAGATATCCTTGA[A/G]CACACTGTGTGTTGG	50797
rs33170380	snp	A/G	0.244898	0.249948	intron-variant	Copb2	Mm_Celera	9:98573371	GGTGTTGGATGTCTT[A/G]TGTTAAAAGTGAGTT	50797
rs33170381	snp	C/T	0.132653	0.220748	synonymous-codon	Copb2	Mm_Celera	9:98573452	GTGGCAGCTGGGCTC[C/T]TCATCACCAAACTTC	50797
rs33170382	snp	C/T	0.231111	0.249285	synonymous-codon	Copb2	Mm_Celera	9:98573560	TGCAGATGACCGGCT[C/T]GTTAAAATATGGGAT	50797
rs33170383	snp	C/T	0.260355	0.249785	synonymous-codon	Copb2	Mm_Celera	9:98574164	CACAGGGTCAGAAGA[C/T]GGTAAGTTAGAGGCT	50797
rs33171004	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98583928	CTGACCAGTTCCAAA[C/T]ATCTGCTGTTCACTC	50797
rs33171005	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98584092	CTCTGAATGTTGTCC[A/G]GCTTCTCTGTCCTGA	50797
rs33171006	snp	A/G	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98584856	CCATTTGGTCCTCTG[A/G]AATAGATGGCTATGG	50797
rs33171007	snp	G/T	0.391111	0.206368	intron-variant	Copb2	Mm_Celera	9:98584912	GAGAAATAATTTGTT[G/T]TGTGCATACTATATG	50797
rs33171008	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98585213	CTGTTGTATCTTTGG[C/T]CTTTTTAAAGGTGCA	50797
rs33171009	snp	C/T	0.231111	0.249285	intron-variant	Copb2	Mm_Celera	9:98585494	ATTAGCTGTCAAGAT[C/T]ATTTAAATGTGCATT	50797
rs33171010	snp	A/C	0.231111	0.249285	synonymous-codon	Copb2	Mm_Celera	9:98585994	TCAGTTCAGCCTAGC[A/C]CAGGAGTGTCTGCAC	50797
rs33171011	snp	C/T	0.231111	0.249285	synonymous-codon	Copb2	Mm_Celera	9:98586102	AGGTGCGGAGAGAGA[C/T]GGCAAAAATAACGTG	50797

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