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
rs3717575	snp	A/G	0.444444	0.157135	missense	Arnt	GRCm38.p3	3:95489687	TAGAGATGGGTACAG[A/G]GCAGCTGCCATCCAG	11863
rs6303140	snp	C/T	0.290657	0.246672	intron-variant	Arnt	Mm_Celera	3:95480957	TGTGCTTAAGAATAA[C/T]TCAAAAGATAGATAG	11863
rs6304219	snp	A/G	0.5	0	intron-variant	Arnt	Mm_Celera	3:95481131	cctggctgctttgga[A/G]ctgactttgtagacc	11863
rs6412915	snp	A/G	0.290657	0.246672	intron-variant	Arnt	Mm_Celera	3:95460668	AACTGTAGACTTCTT[A/G]GGCATATTATATTTG	11863
rs8251882	snp	A/G	0.244898	0.249948	intron-variant	Arnt	GRCm38.p3	3:95448844	ctgtagctgtcttca[A/G]acanaccagacgagg	11863
rs8251883	snp	C/T	0.21875	0.248039	intron-variant	Arnt	GRCm38.p3	3:95448840	agctgtcttcanaca[C/T]accagacgagggcat	11863
rs8251884	snp	C/T	0.21875	0.248039	intron-variant	Arnt	GRCm38.p3	3:95448770	gctgggaattgaact[C/T]aggacctcagtgctc	11863
rs8251885	in-del	-/A	0.18	0.24	intron-variant	Arnt	Mm_Celera	3:95448686	atattcaaattatac[-/A]aaaaaaattaaagaa	11863
rs8251886	snp	A/G	0.197531	0.244432	intron-variant	Arnt	GRCm38.p3	3:95448637	GCCTGGATAAGGAAT[A/G]ATCCAGGGACTAAGA	11863
rs8251887	snp	C/T	0.21875	0.248039	missense	Arnt	GRCm38.p3	3:95448467	CTGACCGTCGCTTAA[C/T]AGCCCTCTGTACAAC	11863
rs8251888	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Arnt	GRCm38.p3	3:95450923	AAGCAAACACTATTT[A/G]AAATGTGTTTTTAAT	11863
rs8251889	snp	A/G	0.297521	0.245442	intron-variant, upstream-variant-2KB	Arnt	GRCm38.p3	3:95450861	atgattttattttat[A/G]atgtgtctgtatagg	11863
rs8251890	snp	A/C	0.277778	0.248452	intron-variant, upstream-variant-2KB	Arnt	GRCm38.p3	3:95450765	gatgtgagtcactga[A/C]atgggttctaggacc	11863
rs8251891	in-del	-/A/AG/G	0.31405	0.280505	intron-variant, upstream-variant-2KB	Arnt	Mm_Celera	3:95450697	Tgggctggagaaaag[-/A/AG/G]ntcagagattgagag	11863
rs8251893	snp	G/T	0.426035	0.177515	intron-variant	Arnt	GRCm38.p3	3:95462427	TTTATCTATAAAAAC[G/T]GTATAATCTATANAA	11863
rs8251894	snp	C/T	0.35503	0.226867	intron-variant	Arnt	GRCm38.p3	3:95462414	ACNGTATAATCTATA[C/T]AAACACATAATTAAA	11863
rs8251895	snp	C/T	0.132653	0.220748	intron-variant	Arnt	GRCm38.p3	3:95462384	AAATGAAATAGATCA[C/T]TTTTAAAGTAATCAA	11863
rs8251896	snp	C/T	0.32	0.24	intron-variant	Arnt	GRCm38.p3	3:95462324	AATTTTTGAGAGGAT[C/T]ACAAACTCAATTTTA	11863
rs8251897	snp	C/T	0.124444	0.216185	intron-variant	Arnt	GRCm38.p3	3:95462253	GGGAAAGTTAAAAGG[C/T]NNCCTCAGATGTTGN	11863
rs8251898	snp	A/G	0.32	0.24	intron-variant	Arnt	GRCm38.p3	3:95462252	GGAAAGTTAAAAGGN[A/G]NCCTCAGATGTTGNT	11863
rs8251899	snp	A/C/G	0.32	0.24	intron-variant	Arnt	GRCm38.p3	3:95462251	GAAAGTTAAAAGGNN[A/C/G]CCTCAGATGTTGNTC	11863
rs8251900	snp	C/T	0.285375	0.247485	intron-variant	Arnt	GRCm38.p3	3:95462238	NNNCCTCAGATGTTG[C/T]TCGATGCCTTCCACN	11863
rs8251901	in-del	-/T	0.32	0.24	intron-variant	Arnt	Mm_Celera	3:95462223	NTCGATGCCTTCCAC[-/T]TNNNNNGAGACAGAC	11863
rs8251902	in-del	-/A	0.32	0.24	intron-variant	Arnt	Mm_Celera	3:95462221	CGATGCCTTCCACNT[-/A]NNNNGAGACAGACAC	11863
rs8251903	in-del	-/G	0.32	0.24	intron-variant	Arnt	Mm_Celera	3:95462220	GATGCCTTCCACNTN[-/G]NNNGAGACAGACACT	11863
rs8251904	in-del	-/T	0.32	0.24	intron-variant	Arnt	Mm_Celera	3:95462219	ATGCCTTCCACNTNN[-/T]NNGAGACAGACACTC	11863
rs8251905	in-del	-/C	0.336735	0.234472	intron-variant	Arnt	Mm_Celera	3:95462218	TGCCTTCCACNTNNN[-/C]NGAGACAGACACTCT	11863
rs8251906	in-del	-/T	0.336735	0.234472	intron-variant	Arnt	Mm_Celera	3:95462217	GCCTTCCACNTNNNN[-/T]GAGACAGACACTCTt	11863
rs8251907	snp	C/T	0.32	0.24	intron-variant	Arnt	GRCm38.p3	3:95462201	GAGACAGACACTCTt[C/T]ttttttaagtttttt	11863
rs8251908	snp	C/T	0.336735	0.234472	intron-variant	Arnt	GRCm38.p3	3:95462133	ctgtcttcagacaca[C/T]cagaagagggcatca	11863
rs8251909	in-del	-/T	0.124444	0.216185	intron-variant	Arnt	Mm_Celera	3:95462108	gcatcagatcccatt[-/T]cagatggttgtgagc	11863
rs8251910	snp	A/G	0.231111	0.249285	intron-variant	Arnt	GRCm38.p3	3:95462080	agccaccatgtggtc[A/G]ctggnaattgaactc	11863
rs8251911	snp	G/T	0.32	0.24	intron-variant	Arnt	GRCm38.p3	3:95462075	ccatgtggtcnctgg[G/T]aattgaactcaggac	11863
rs8251912	snp	A/C	0.124444	0.216185	intron-variant	Arnt	GRCm38.p3	3:95462059	aattgaactcaggac[A/C]tctagaagagcantc	11863
rs8251913	snp	G/T	0.124444	0.216185	intron-variant	Arnt	GRCm38.p3	3:95462046	acntctagaagagca[G/T]tcttcaccactgcgc	11863
rs8251914	snp	C/T	0.132653	0.220748	intron-variant	Arnt	GRCm38.p3	3:95461988	TTGTTCACTGCTGCA[C/T]ACACCAAGTTAGCTG	11863
rs8251915	snp	C/T	0.132653	0.220748	intron-variant	Arnt	GRCm38.p3	3:95461933	ATCTCTGTCTTCTAT[C/T]GCNCAATAAAGACTC	11863
rs8251916	snp	A/C	0.142012	0.225474	intron-variant	Arnt	GRCm38.p3	3:95461930	TCTGTCTTCTATNGC[A/C]CAATAAAGACTCACT	11863
rs8251917	snp	C/T	0.18	0.24	intron-variant	Arnt	Mm_Celera	3:95465476	gtttctctggaggag[C/T]agccagtgttcctta	11863
rs8251918	snp	C/T	0.310651	0.242531	intron-variant	Arnt	Mm_Celera	3:95465602	CTCTCTTAAAATGAG[C/T]ACTTATAATACTGAG	11863
rs8251919	in-del	-/G/T/TT	0.392337	0.26022	intron-variant	Arnt	Mm_Celera	3:95465646	gttttggtttgtttg[-/G/T/TT]nnncgtttttgtgta	11863
rs8251923	snp	C/T	0.260355	0.249785	intron-variant	Arnt	Mm_Celera	3:95465732	cctgcctctgcctcc[C/T]aantgctgggattaa	11863
rs8251924	snp	A/G	0.345679	0.230967	intron-variant	Arnt	Mm_Celera	3:95465816	CCTTTTTGTGCGGTG[A/G]GTATTGAGCCAGTCC	11863
rs8251925	snp	C/G	0.260355	0.249785	intron-variant	Arnt	GRCm38.p3	3:95465855	TGCCCTGGTTATCCT[C/G]GAACTNTCTATCTCT	11863
rs8251926	snp	C/T	0.142012	0.225474	intron-variant	Arnt	Mm_Celera	3:95465861	GGTTATCCTNGAACT[C/T]TCTATCTCTGTGTGT	11863
rs8251927	snp	C/T	0.287335	0.247197	intron-variant	Arnt	Mm_Celera	3:95465918	TGCTAGGATCGGAGG[C/T]ACCACCACCATGCCT	11863
rs8251928	snp	G/T	0.345679	0.230967	intron-variant	Arnt	GRCm38.p3	3:95468800	ACAGAATTGGGGTAT[G/T]TTGGAATTTTATTTG	11863
rs8251929	snp	C/T	0.345679	0.230967	intron-variant	Arnt	GRCm38.p3	3:95468784	TTGGAATTTTATTTG[C/T]TATACTAATGCACAA	11863
rs8251930	snp	A/G	0.375	0.216506	intron-variant	Arnt	GRCm38.p3	3:95468544	AAGAGTTTACAAATG[A/G]ACTCTTTGGGGTCTC	11863
rs8251931	snp	C/T	0.375	0.216506	intron-variant	Arnt	GRCm38.p3	3:95468519	GGTCTCCCACGAGGA[C/T]GCCTCGAAGGAACAG	11863
rs8251932	snp	C/T	0.152778	0.230321	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95469642	TCAAAAGTTGGTCAT[C/T]TTATTTTATAGCCTT	11863
rs8251933	snp	C/G	0.142012	0.225474	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95469707	AGCTGAGATTTATCC[C/G]CTTAGGAACTTAAAT	11863
rs8251934	snp	C/G	0.142012	0.225474	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95469954	TTAATGGAAGTGGTT[C/G]NCTGGAGAGGCNNTN	11863
rs8251935	snp	A/C	0.142012	0.225474	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95469955	TAATGGAAGTGGTTN[A/C]CTGGAGAGGCNNTNT	11863
rs8251936	snp	A/G	0.290657	0.246672	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95469966	GTTNNCTGGAGAGGC[A/G]NTNTGTACTTGTTCT	11863
rs8251937	snp	A/G	0.359862	0.224567	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95469967	TTNNCTGGAGAGGCN[A/G]TNTGTACTTGTTCTT	11863
rs8251938	snp	A/G	0.290657	0.246672	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95469969	NNCTGGAGAGGCNNT[A/G]TGTACTTGTTCTTTG	11863
rs8251939	snp	G/T	0.152778	0.230321	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95470050	CTTGGCTTCTGAGAT[G/T]TGAACATCATCAGAC	11863
rs8251940	snp	A/C	0.152778	0.230321	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95470081	CTAAGTTACTGCATC[A/C]NNCAGCAGCTGACCA	11863
rs8251941	snp	G/T	0.165289	0.235211	intron-variant, upstream-variant-2KB	Arnt, Gm36887	GRCm38.p3	3:95470081	TAAGTTACTGCATCN[G/T]NCAGCAGCTGACCAG	11863
rs8251942	in-del	-/T	0.165289	0.235211	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95470083	AAGTTACTGCATCNN[-/T]CAGCAGCTGACCAGG	11863
rs8251943	snp	C/T	0.165289	0.235211	intron-variant, upstream-variant-2KB	Arnt, Gm36887	Mm_Celera	3:95470105	CTGACCAGGTATCCA[C/T]ATCACTCTCCTGATA	11863
rs8251944	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Arnt, Gm36887	GRCm38.p3	3:95470565	ATGTCTCCTGAAGAA[C/T]CACTCTCCTGAAGCT	11863
rs8251945	snp	A/G	0.21875	0.248039	intron-variant, upstream-variant-2KB	Arnt, Gm36887	GRCm38.p3	3:95470555	AAGAANCACTCTCCT[A/G]AAGCTGGACATGGTG	11863
rs8251946	snp	A/G	0.297521	0.245442	intron-variant, upstream-variant-2KB	Arnt, Gm36887	GRCm38.p3	3:95470466	AAAAAAACCAAGCAA[A/G]CAACCAAACAAAACC	11863
rs8251947	snp	A/C	0.21875	0.248039	intron-variant, upstream-variant-2KB	Arnt, Gm36887	GRCm38.p3	3:95470426	GTCCAAAACTTTCAA[A/C]AGATATACCCAGAGT	11863
rs8251948	snp	C/T	0.277778	0.248452	intron-variant	Arnt	Mm_Celera	3:95477838	attgcttgtcttaaa[C/T]catagtnctcaggag	11863
rs8251949	snp	A/G	0.277778	0.248452	intron-variant	Arnt	Mm_Celera	3:95477845	gtcttaaancatagt[A/G]ctcaggaggcagagg	11863
rs8251950	snp	A/C	0.244898	0.249948	intron-variant	Arnt	Mm_Celera	3:95477862	tcaggaggcagaggc[A/C]ggcatatgtgagtga	11863
rs8251951	snp	A/G	0.244898	0.249948	intron-variant	Arnt	Mm_Celera	3:95477900	ggttctcgagatcac[A/G]agactgatagagaat	11863
rs8251952	snp	A/T	0.32	0.24	intron-variant	Arnt	Mm_Celera	3:95478125	TGTTGGTTCTTTCCT[A/T]CAACACTGTGGGTTG	11863
rs8251953	in-del	-/A	0.152778	0.230321	intron-variant	Arnt	Mm_Celera	3:95480037	TTGTTGTtttgttta[-/A]tttgaggcagcacnt	11863
rs8251954	snp	C/T	0.132653	0.220748	intron-variant	Arnt	GRCm38.p3	3:95480023	antttgaggcagcac[C/T]ttcaggcttaggctg	11863
rs8251955	snp	C/T	0.124444	0.216185	intron-variant	Arnt	GRCm38.p3	3:95479951	tgaccctttgatcaa[C/T]agcacctgagtgatg	11863
rs8251956	snp	A/G	0.124444	0.216185	intron-variant	Arnt	GRCm38.p3	3:95479927	agtgatggcactaca[A/G]gcaggtancaacata	11863
rs8251957	snp	C/T	0.124444	0.216185	intron-variant	Arnt	GRCm38.p3	3:95479919	cactacangcaggta[C/T]caacataccagtcnn	11863
rs8251958	in-del	-/A/T/TTATAT	0.12642	0.223592	intron-variant	Arnt	Mm_Celera	3:95479905	ancaacataccagtc[-/A/T/TTATAT]nnnnnggtgttaggt	11863
rs8251964	snp	A/G	0.132653	0.220748	intron-variant	Arnt	GRCm38.p3	3:95479824	atattcccgaccctg[A/G]ctgattgtgtgtctg	11863
rs8251965	snp	C/G	0.124444	0.216185	intron-variant	Arnt	Mm_Celera	3:95479803	tgtgtgtctgtctgt[C/G]tgtntgtctgtctgn	11863
rs8251966	in-del	-/T	0.124444	0.216185	intron-variant	Arnt	Mm_Celera	3:95479788	ntgtntgtctgtctg[-/T]nnnnnnnnnnnnnnn	11863
rs8251967	in-del	-/C	0.231111	0.249285	intron-variant	Arnt	Mm_Celera	3:95479783	tgtctgtctgnnnnn[-/C]nnnnnnnnnnnctgt	11863
rs8251968	in-del	-/T	0.244898	0.249948	intron-variant	Arnt	Mm_Celera	3:95479782	gtctgtctgnnnnnn[-/T]nnnnnnnnnnctgtc	11863
rs8251969	in-del	-/G	0.244898	0.249948	intron-variant	Arnt	Mm_Celera	3:95479781	tctgtctgnnnnnnn[-/G]nnnnnnnnnctgtct	11863
rs8251970	in-del	-/T	0.244898	0.249948	intron-variant	Arnt	Mm_Celera	3:95479780	ctgtctgnnnnnnnn[-/T]nnnnnnnnctgtctg	11863
rs8251971	in-del	-/C	0.231111	0.249285	intron-variant	Arnt	Mm_Celera	3:95479779	tgtctgnnnnnnnnn[-/C]nnnnnnnctgtctgt	11863
rs8251972	in-del	-/T	0.231111	0.249285	intron-variant	Arnt	Mm_Celera	3:95479778	gtctgnnnnnnnnnn[-/T]nnnnnnctgtctgtc	11863
rs8251973	in-del	-/G	0.231111	0.249285	intron-variant	Arnt	Mm_Celera	3:95479777	tctgnnnnnnnnnnn[-/G]nnnnnctgtctgtcn	11863
rs8251975	snp	G/T	0.124444	0.216185	intron-variant	Arnt	GRCm38.p3	3:95479765	nnnnnnctgtctgtc[G/T]ntctctctctctgtc	11863
rs8251976	snp	C/G	0.124444	0.216185	intron-variant	Arnt	Mm_Celera	3:95479765	nnnnnctgtctgtcn[C/G]tctctctctctgtct	11863
rs8251977	snp	C/G	0.132653	0.220748	intron-variant	Arnt	GRCm38.p3	3:95479737	tgtctCTGTCtctnt[C/G]nntnncnnatgnagg	11863
rs8251978	snp	C/T	0.132653	0.220748	intron-variant	Arnt	GRCm38.p3	3:95479738	gtctCTGTCtctntn[C/T]ntnncnnatgnaggt	11863
rs8251979	snp	A/C	0.132653	0.220748	intron-variant	Arnt	Mm_Celera	3:95479737	tctCTGTCtctntnn[A/C]tnncnnatgnaggtt	11863
rs8251980	snp	C/G	0.132653	0.220748	intron-variant	Arnt	GRCm38.p3	3:95479734	tCTGTCtctntnnnt[C/G]ncnnatgnaggttcc	11863
rs8251981	snp	C/T	0.132653	0.220748	intron-variant	Arnt	Mm_Celera	3:95479734	CTGTCtctntnnntn[C/T]cnnatgnaggttcca	11863
rs8251982	snp	C/T	0.132653	0.220748	intron-variant	Arnt	GRCm38.p3	3:95479731	GTCtctntnnntnnc[C/T]natgnaggttccagt	11863
rs8251983	snp	C/T	0.124444	0.216185	intron-variant	Arnt	Mm_Celera	3:95479731	TCtctntnnntnncn[C/T]atgnaggttccagta	11863
rs8251984	snp	G/T	0.124444	0.216185	intron-variant	Arnt	Mm_Celera	3:95479727	tntnnntnncnnatg[G/T]aggttccagtaatca	11863
rs8251985	snp	A/G	0.185493	0.241534	intron-variant	Arnt	GRCm38.p3	3:95479708	ttccagtaatcaacc[A/G]tgtattatcaggctt	11863
rs8251986	snp	C/T	0.142012	0.225474	intron-variant	Arnt	GRCm38.p3	3:95479560	ccaagtaatgagata[C/T]agaaagtaccaccag	11863
rs8251987	snp	A/G	0.244898	0.249948	intron-variant	Arnt	Mm_Celera	3:95481416	ggttcctgtacttat[A/G]ttgtgtccataaatt	11863

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