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
rs6186603	snp	A/C/G	0.5	0	intron-variant	Hck	GRCm38.p3	2:153129722	GTGCTAGGTTCCCCC[A/C/G]CCCCTCATGCTCCTG	15162
rs6187150	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153129798	CCACAGCAGGCTGTA[A/G]AAGGTTCCTGTGCCN	15162
rs6187174	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153129813	NAAGGTTCCTGTGCC[A/G]GCTGATCCTCTTCTC	15162
rs6187679	snp	A/C	0.492188	0.0620098	synonymous-codon	Hck	Mm_Celera	2:153129866	GAGTGGTGGAAGGCA[A/C]GGTCCCTGGCTACCA	15162
rs6187791	snp	A/G	0.5	0	synonymous-codon	Hck	Mm_Celera	2:153129937	TAACTCTTTGGAGAC[A/G]GANGAGTAAGTGTTC	15162
rs6187792	snp	A/G	0.492188	0.0620098	synonymous-codon	Hck	Mm_Celera	2:153129940	CTCTTTGGAGACNGA[A/G]GAGTAAGTGTTCCAG	15162
rs6189176	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153130170	ATCCCACAGGCAAAA[A/G]GGGACGTTGCTTTTT	15162
rs6232131	snp	C/T	0.396694	0.202437	intron-variant	Hck	Mm_Celera	2:153144378	AGCAGATTCTGTGGG[C/T]TTCTAATATGTGAGG	15162
rs6232208	snp	A/G	0.46875	0.121031	synonymous-codon	Hck	Mm_Celera	2:153144427	GGTACAGATCTCAGA[A/G]GGCATGGCCTTCATT	15162
rs6232753	snp	A/G	0.459184	0.136902	synonymous-codon	Hck	Mm_Celera	2:153144538	CTTTGGACTGGCACG[A/G]ATCATCGAGGACAAT	15162
rs6233270	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153144632	ACTGACTCttgcatc[A/G]agtcaggaggcagac	15162
rs6329408	snp	A/G	0.396694	0.202437	intron-variant	Hck	Mm_Celera	2:153144288	AGGCAGAACAGTGCC[A/G]GTTGAGAGCCCAGGA	15162
rs13470389	snp	C/T			missense	Hck	Mm_Celera	2:153151100	ACATCCAGAGTGTGC[C/T]GGATGACTTCTACAC	15162
rs27352777	snp	A/C	0.456747	0.140554	utr-variant-3-prime	Hck	Mm_Celera	2:153151355	ATTTGCCTGGAATGA[A/C]TGAATTCAATCTATA	15162
rs27352778	snp	A/G	0.132653	0.220748	utr-variant-3-prime	Hck	Mm_Celera	2:153151200	TCAGTGCCTTGACAC[A/G]CCCAACTTGCTGGGC	15162
rs27352779	snp	G/T	0.48	0.0979796	utr-variant-3-prime	Hck	Mm_Celera	2:153151156	CAGCCTTGACGGCAG[G/T]AAGGACATGAGCAGA	15162
rs27352780	snp	G/T	0.497041	0.0383476	intron-variant	Hck	Mm_Celera	2:153150545	AACAACAGACCAAGA[G/T]ATGCAGAAACAGTAG	15162
rs27352781	snp	A/G	0.486111	0.0821678	intron-variant	Hck	Mm_Celera	2:153149292	TGCACTCAAGCAATC[A/G]AAGTTCAGCTATTTG	15162
rs27352782	snp	A/G	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153149278	TTCCCACACCTTACT[A/G]CACTCAAGCAATCGA	15162
rs27352783	snp	A/G	0.277778	0.248452	intron-variant	Hck	Mm_Celera	2:153149124	CTCCAGCCCAACCTG[A/G]CAATGGCCCATCTCG	15162
rs27352784	snp	A/G	0.345679	0.230967	intron-variant	Hck	Mm_Celera	2:153148850	CATTGCAAGGAAATC[A/G]CTATTTGTAGAGGGC	15162
rs27352785	snp	C/T	0.345679	0.230967	intron-variant	Hck	Mm_Celera	2:153148818	AAGACAAATGTCCCT[C/T]GGTAACATGGGTAAC	15162
rs27352786	snp	A/C	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153147982	AGTGTTCTGATGGTA[A/C]AGACATAGTTGCATT	15162
rs27352787	snp	A/T	0.46875	0.121031	intron-variant	Hck	Mm_Celera	2:153147946	AGCAGAGAGTGATTG[A/T]GAGCCTGGTCATTTA	15162
rs27352788	snp	C/T	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153147835	CCTTCTAGCTCCTTC[C/T]GCCCTACAGCCCTGC	15162
rs27352789	snp	C/G	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153147304	GTGCTCAGGCCTGCG[C/G]TGGGACTTTAACCAT	15162
rs27352790	snp	C/T	0.345679	0.230967	intron-variant	Hck	Mm_Celera	2:153147269	CTAGCATTTTCATCA[C/T]ACAAAGGGGCTAGCT	15162
rs27352791	snp	A/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153147255	GACACCTAAAAGCAC[A/T]AGCATTTTCATCATA	15162
rs27352792	snp	G/T	0.396694	0.202437	intron-variant	Hck	Mm_Celera	2:153147206	TCTTAACTTAGCGGT[G/T]GCTTGGTATATGGTT	15162
rs27352793	snp	C/T	0.152778	0.230321	intron-variant	Hck	Mm_Celera	2:153147158	CGGCCATAATACAAG[C/T]GTCGCCGAATTCCAA	15162
rs27352794	snp	A/G	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153147144	CTTAATCACTTACTC[A/G]GCCATAATACAAGCG	15162
rs27352795	snp	G/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153146348	CATAAAAGAGAAGTA[G/T]GACATAAAGAAAATG	15162
rs27352796	snp	G/T	0.277778	0.248452	intron-variant	Hck	Mm_Celera	2:153145843	GGTACTGCCTCAGAA[G/T]AGCTGGAAGGAGCCT	15162
rs27352797	snp	A/C	0.345679	0.230967	intron-variant	Hck	Mm_Celera	2:153145189	CAGAGTAGATGCCAG[A/C]AGGTTCTACATCATG	15162
rs27352798	snp	C/G	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153145084	CACTGACACAGAAGA[C/G]TATAGACTTCACCCC	15162
rs27352799	snp	C/T	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153144619	AGATCTGTCCTAGAC[C/T]GACTCTTGCATCAAG	15162
rs27352800	snp	C/T	0.42	0.183303	intron-variant	Hck	Mm_Celera	2:153143439	AGTCTGCCATTATCA[C/T]TCTTCATGCTCAGAG	15162
rs27352801	snp	C/T	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153143417	GCTACACTGAAGGGC[C/T]TCGTGAAGTCTGCCA	15162
rs27352802	snp	C/T	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153143347	CTTTCTTCCAGAAGC[C/T]TTAAGAATAAGAATC	15162
rs27352803	snp	C/T	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153143303	ATGGAGCTTTATCTT[C/T]CACCTCTTTTGTCCT	15162
rs27352804	snp	C/T	0.18	0.24	intron-variant	Hck	Mm_Celera	2:153143289	AGGCTTTCTGGGCAA[C/T]GGAGCTTTATCTTTC	15162
rs27352805	snp	A/G	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153143243	AGTCTGCCTTCACAG[A/G]GCTCCAAGGTAGTTC	15162
rs27352806	snp	A/G	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153143061	TTACTGGCCAGCTCT[A/G]TTTTAGGCTGTCTGA	15162
rs27352807	snp	A/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153142713	AGAGGTTGGTAAGAG[A/T]CACATGCTATGCAGC	15162
rs27352808	snp	A/G	0.277778	0.248452	intron-variant	Hck	Mm_Celera	2:153142694	GTGGGAAAGTACTAG[A/G]CACAGAGGTTGGTAA	15162
rs27352809	snp	C/T	0.35503	0.226867	intron-variant	Hck	Mm_Celera	2:153142468	GTGAATACTAGATGG[C/T]AGACACTGTCCTTGC	15162
rs27352810	snp	C/T	0.336735	0.234472	intron-variant	Hck	Mm_Celera	2:153142379	GCAGGGTGTTTGTAT[C/T]AGTCCCAGATCTGCC	15162
rs27352811	snp	A/G/T	0.375	0.216506	intron-variant	Hck	GRCm38.p3	2:153141093	GTGTTATCATTTCAG[A/G/T]ATACTAAGTCTTTAT	15162
rs27352812	snp	A/G	0.42	0.183303	intron-variant	Hck	Mm_Celera	2:153140005	ACGTTGTACAAAGCC[A/G]GCTAACATTCTTTCT	15162
rs27352813	snp	C/T	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153139945	CAAAAATGGTTCAGT[C/T]GTCCAGAGCTTTCCT	15162
rs27352814	snp	C/T	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153139740	TGACAATGGCAAACA[C/T]CACTGGCTTTATGCA	15162
rs27352815	snp	C/G	0.297521	0.245442	intron-variant	Hck	Mm_Celera	2:153139484	CTACAGACCTGAAAT[C/G]GAGGTATGAAGAATT	15162
rs27352816	snp	C/T	0.165289	0.235211	intron-variant	Hck	Mm_Celera	2:153139462	AGGTAATTGTCATTC[C/T]GTCGTCCTACAGACC	15162
rs27352817	snp	C/G	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153137835	ATAAATGCTGGGAGT[C/G]AAGACTAATCTACTA	15162
rs27352818	snp	A/G	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153137526	GTTAGTTTTAGAACA[A/G]CTGGTTTATAGTCAT	15162
rs27352819	snp	A/G	0.297521	0.245442	intron-variant	Hck	Mm_Celera	2:153137096	GCTTCCTTGTGACTC[A/G]TACCTGGGAACCTCA	15162
rs27352820	snp	A/T	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153136892	GGTGCGTGGGCAGGG[A/T]TAGAGTGTGGGCCAA	15162
rs27352821	snp	A/G	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153136562	CCAGAGAAGGTAGGT[A/G]TTTCAGTTGTACTCA	15162
rs27352822	snp	C/T	0.396694	0.202437	intron-variant	Hck	Mm_Celera	2:153136512	GCCCTTCAGTGAGAG[C/T]TTATCCCTTCCACTT	15162
rs27352823	snp	A/G	0.297521	0.245442	intron-variant	Hck	Mm_Celera	2:153136391	GTCATGGGCTGGCCC[A/G]GAGCCTCCAGTCCTC	15162
rs27352824	snp	A/G	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153136163	TGGATGACAAGGACA[A/G]AAAAGTAGGTGTGAT	15162
rs27352825	snp	C/T	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153136133	AGTTTGAGCATGTGT[C/T]GGAGGTGACCTTGGT	15162
rs27352826	snp	C/T	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153135696	GTTAATGTGTAAAAG[C/T]CAGAGTGAGGCCAGA	15162
rs27352827	snp	C/T	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135554	TCCTGGCATCCAAGA[C/T]ACACAGAGAAAGAAA	15162
rs27352828	snp	A/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135331	GATAAAGTGAGTTTT[A/G]AAAGCCTGTGGCTCA	15162
rs27352829	snp	C/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135287	CAGATGGAAAGGACG[C/G]AGCTTGTAGAGATGC	15162
rs27352830	snp	C/T	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135244	GGTCACAATACCTGA[C/T]CCACCATGTTAACAC	15162
rs27352831	snp	G/T	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135204	TGGTCCTTGGCCCAG[G/T]ACCTTGAGAACAGGA	15162
rs27352832	snp	C/T	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153135044	GGCCTCTTGTGATGG[C/T]GAAAATTCATAGTGA	15162
rs27352833	snp	G/T	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153134878	ATAATAACCACAGGA[G/T]GCCACTCCTCAGATA	15162
rs27352834	snp	A/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153134551	GACATGAGGGTGGCG[A/G]TATACAGGTGTCATT	15162
rs27352835	snp	A/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153134471	GTGGCATGCAGCTCT[A/G]CACTCAGACTTCCTG	15162
rs27352836	snp	C/T	0.492188	0.0620098	intron-variant	Hck	Mm_Celera	2:153134331	ACAGCTTTTATTCCT[C/T]AGCACCTTGGCTTTG	15162
rs27352837	snp	A/G	0.49827	0.0293608	intron-variant	Hck	Mm_Celera	2:153134305	GCCAGGCTGTGAAGC[A/G]GTCACTAGCCACAGC	15162
rs27352838	snp	A/C	0.475309	0.108333	synonymous-codon	Hck	Mm_Celera	2:153134173	TTCTACATCTCTCCA[A/C]GGAGCACCTTCAGCA	15162
rs27352839	snp	G/T	0.475309	0.108333	intron-variant	Hck	Mm_Celera	2:153134024	GACATCAGGTAGCAG[G/T]CTTCTAAGGTGCCAT	15162
rs27352840	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153133496	CCTATTTTCACACTT[C/T]AGTAATCAGACCAGA	15162
rs27352841	snp	C/T	0.475309	0.108333	intron-variant	Hck	Mm_Celera	2:153133442	AGCTGCAGGTGTTCA[C/T]ATAAGAGCATCCTGG	15162
rs27352842	snp	A/G	0.475309	0.108333	intron-variant	Hck	Mm_Celera	2:153133385	CTCTGAGTTCCCTGG[A/G]ACACCCCTGGACACT	15162
rs27352843	snp	C/T	0.484429	0.0868505	intron-variant	Hck	Mm_Celera	2:153133056	ACTGCGGCCACAGAT[C/T]GGAATGCTTGTGTAT	15162
rs27352844	snp	A/G	0.408163	0.193609	intron-variant	Hck	Mm_Celera	2:153132793	AAGTGAGGCTGATAC[A/G]TCTATAAAGCATCTG	15162
rs27352845	snp	C/G	0.473373	0.11227	intron-variant	Hck	Mm_Celera	2:153132545	TGGACAGGAAGGTGG[C/G]CTGGACTCGCTTCCA	15162
rs27352846	snp	A/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132521	ACCAACAGCCCAGTG[A/G]CAGACCTGTGGACAG	15162
rs27352847	snp	C/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132465	CTGTGCCTAGAGTAG[C/T]TTAGAGATTGACCTG	15162
rs27352848	snp	C/T	0.473373	0.11227	intron-variant	Hck	Mm_Celera	2:153132253	ATTCCACATGCACAG[C/T]GAGCCTTTGGCTCTT	15162
rs27352849	snp	C/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132229	CACATGCTGTGTGCA[C/T]GATTTCAGATTCCAC	15162
rs27352850	snp	A/C	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132185	CCGACTGGCATTCCC[A/C]TGGGTGAGTTTCCCC	15162
rs27352851	snp	C/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132022	TGGGTGACCAGAGTT[C/T]AAAAATAAAATAAAA	15162
rs27352852	snp	A/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132001	TTGGCAAAGAGTCAT[A/G]TGGAATGGGTGACCA	15162
rs27352853	snp	C/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153131593	TCCCCACTAGATCCT[C/G]GTCTGTTTTAAATAG	15162
rs27352854	snp	A/G	0.35503	0.226867	intron-variant	Hck	Mm_Celera	2:153131490	GGGCCTGGACTAGGT[A/G]GCTTCTTCTAGTTCT	15162
rs27352855	snp	A/G	0.473373	0.11227	intron-variant	Hck	Mm_Celera	2:153131372	GCAAGGCGCCTCTCC[A/G]ACCTTAGGGAAGTCC	15162
rs27352856	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153131193	GTCCATCCTGAGTCT[C/T]ACACTGTCCCTCATT	15162
rs27352857	snp	A/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153130970	CTTGTGAGGATGAAA[A/G]GAACTTCAGCCACTA	15162
rs27352858	snp	C/G	0.456747	0.140554	intron-variant	Hck	Mm_Celera	2:153130939	CCCCATTGTGGTACA[C/G]AGACTGCTCCTTATT	15162
rs27352859	snp	A/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153130892	AACAAAAGTCACCTG[A/G]CAGGCATGCTGATAT	15162
rs27352860	snp	G/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153130856	TCCCTTATTGATAAC[G/T]GAGGCAGCAGAGACC	15162
rs27352861	snp	A/G	0.408163	0.193609	intron-variant	Hck	Mm_Celera	2:153130125	CTCTGTGACTCTCTC[A/G]GAGAGGTGTTTTTAC	15162
rs27352862	snp	C/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153129288	ATAGGACCTACCTCT[C/T]AGTAACAAAACCAGA	15162
rs27352863	snp	G/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153129033	ATCCTGGCATCTCCC[G/T]TCTTGGCAGGCTCTG	15162

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