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
rs6172242	snp	A/T	0.359862	0.224567	intron-variant	Kbtbd12	Mm_Celera	6:88620516	GAATTGTGCCCAGGG[A/T]ATCACAGGTGCTGTT	74589
rs6174943	snp	C/T	0.5	0	intron-variant	Kbtbd12	Mm_Celera	6:88620926	GTTCAAGTTAAATAA[C/T]TAATGGATCTATGTT	74589
rs13478880	snp	G/T	0.447971	0.152668	intron-variant	Kbtbd12	GRCm38.p3	6:88587087	TCTGGCCTTGACTTG[G/T]TTTTGCTGCCTATTT	74589
rs29869230	snp	C/T	0.5	0	intron-variant	Kbtbd12	Mm_Celera	6:88623979	CTAGAATACATGCTG[C/T]ATTCATAATGTGTTT	74589
rs29875293	snp	C/T	0.498615	0.0262793	intron-variant	Kbtbd12	GRCm38.p3	6:88589304	TCAATAAGTCAGCGC[C/T]GTGGCTTTCATTTAT	74589
rs29876985	snp	C/G	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88577537	ATTGGATGTGGGTGG[C/G]TGGGAGGGATGTAGG	74589
rs29882095	snp	G/T	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88577219	TAGGCATCTAGCTTT[G/T]GGTAATGTGTGTTAG	74589
rs29921386	snp	A/G	0.444444	0.157135	intron-variant	Kbtbd12	GRCm38.p3	6:88575760	ACGCTGGGTGTGCAG[A/G]AGTGTATCGGCCTCT	74589
rs29930955	snp	A/G	0.5	0	synonymous-codon	Kbtbd12	GRCm38.p3	6:88586904	CCAGAAGTCCCCATC[A/G]GGGTTGTAGATCTCC	74589
rs29937498	snp	C/T	0.48	0.0979796	intron-variant	Kbtbd12	GRCm38.p3	6:88584369	TTTTATAGCTTCCAC[C/T]GCCCCGCTCTCGATG	74589
rs29967375	snp	A/C	0.444444	0.157135	intron-variant	Kbtbd12	Mm_Celera	6:88597592	CCACCACCACCACCA[A/C]CAACAACAACAACAA	74589
rs30015488	snp	C/T	0.487535	0.077957	intron-variant	Kbtbd12	GRCm38.p3	6:88595212	GTACAGTCACACAAG[C/T]CGCAGGAGAGGCAGA	74589
rs30019951	snp	A/G	0.444444	0.157135	intron-variant	Kbtbd12	GRCm38.p3	6:88578451	CAGGAGCTGGGAATG[A/G]GGAGGATCTGATGCG	74589
rs30022423	snp	C/T	0.49827	0.0293608	intron-variant	Kbtbd12	GRCm38.p3	6:88577344	AATCAAGGCACAGTA[C/T]TGGTTATATATAAAT	74589
rs30028285	snp	A/T	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88557393	CTTTGATCATAAATT[A/T]AAAAAAAATAAAATT	74589
rs30029715	snp	A/T	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88626087	GTAAAGTGAGTAAAT[A/T]AAAAAAAAAAGAGTT	74589
rs30033444	snp	A/G	0.5	0	intron-variant	Kbtbd12	Mm_Celera	6:88586002	AAAGAAAGAAAGAAG[A/G]AAAAAGAAAGAAAGA	74589
rs30062610	snp	C/G	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88579026	AATGGCGGAGCCTTT[C/G]GGGTCTGGGTTTTGA	74589
rs30074031	snp	A/C	0.493827	0.0552116	intron-variant	Kbtbd12	Mm_Celera	6:88590937	GCCTTGGCTTCATAG[A/C]GCTTAGGTTGATGGT	74589
rs30125273	snp	C/T	0.5	0	intron-variant	Kbtbd12	Mm_Celera	6:88592249	AGACCAAACTCCTAC[C/T]GATGCCTCTACAAAG	74589
rs30168129	snp	A/G	0.5	0	intron-variant	Kbtbd12	Mm_Celera	6:88585741	TAATTCACAAAGAAA[A/G]CTGGGCAGTGGTGGC	74589
rs30170054	snp	C/T	0.49827	0.0293608	intron-variant	Kbtbd12	GRCm38.p3	6:88577069	CCATGTGACTCTTCC[C/T]TCTGCATACACTGCC	74589
rs30209980	snp	A/T	0.498615	0.0262793	intron-variant	Kbtbd12	GRCm38.p3	6:88622910	ATCTTTAGCTCTCAA[A/T]TTGACAATAGGTTGA	74589
rs30215676	snp	A/G	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88580242	TAACATGAGTCAACT[A/G]GGTGGTATTAGACAT	74589
rs30218747	snp	A/G	0.444444	0.157135	intron-variant	Kbtbd12	Mm_Celera	6:88596990	TAAGAATAATAATAG[A/G]AATATCCCCAGCTCG	74589
rs30222877	snp	A/G	0.498615	0.0262793	intron-variant	Kbtbd12	GRCm38.p3	6:88621345	GGTGCAACACCCAAG[A/G]GTGTCTATAGCAATG	74589
rs30225945	snp	A/G	0.387812	0.208586	intron-variant	Kbtbd12	GRCm38.p3	6:88549643	CATGTGTTCCTCCAC[A/G]CAGCCATGGTTGAGT	74589
rs30316053	snp	A/G	0.487535	0.077957	intron-variant	Kbtbd12	GRCm38.p3	6:88590155	TGGCTATTTTCTTTC[A/G]TGTTTGAAAGCCACT	74589
rs30316291	snp	C/T	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88566712	TGCCTGCTCGTCGTG[C/T]GATCCAAAGCCACAG	74589
rs30326843	snp	A/G	0.475309	0.108333	intron-variant	Kbtbd12	GRCm38.p3	6:88612319	CAATAGCCTGCTTTC[A/G]TGTGCTGTGTCTGAG	74589
rs30349789	snp	A/T	0.48	0.0979796	intron-variant	Kbtbd12	GRCm38.p3	6:88577572	AAATATGTCAAGATG[A/T]ACGCTTCTTCCTGAT	74589
rs30361465	snp	C/T	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88573653	TAAACTTTAAATCAT[C/T]TTACTAAACTGACTA	74589
rs30367067	snp	A/T	0.493827	0.0552116	intron-variant	Kbtbd12	GRCm38.p3	6:88595373	TTATACATTCCGTGA[A/T]GTTGAAGTGGATTCT	74589
rs30368579	snp	A/G	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88554919	TGTGTGTGCGCGCGC[A/G]CGCACATGCGTGCAC	74589
rs30410781	snp	A/G	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88622226	TTTTAAAACCCGTTC[A/G]TAGCTCATAGACTGT	74589
rs30414613	snp	C/T	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88586325	ATTCAGTAATAAGCA[C/T]ACACACTAGGCATCA	74589
rs30416337	snp	G/T	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88626042	GAGGGAGGGGGGAAA[G/T]ATTGTGGGAGGGGTG	74589
rs30417550	snp	A/G	0.444444	0.157135	intron-variant	Kbtbd12	GRCm38.p3	6:88579677	GCTATGGCAGGGAGA[A/G]AAGAGCAAATTAGAA	74589
rs30426670	snp	A/C	0.444444	0.157135	intron-variant	Kbtbd12	Mm_Celera	6:88595791	AAAAAAACCAACCAA[A/C]CAAACAAACAAACAA	74589
rs30446467	snp	A/G	0.444444	0.157135	intron-variant	Kbtbd12	GRCm38.p3	6:88617007	CCCCATTTTTTTTCC[A/G]TCACAAAGAATTGTA	74589
rs30455600	snp	C/T	0.444444	0.157135	intron-variant	Kbtbd12	GRCm38.p3	6:88580154	AAAAAACAGTGTTTG[C/T]TAAATAAGACATTAA	74589
rs30481317	snp	C/T	0.444444	0.157135	intron-variant	Kbtbd12	GRCm38.p3	6:88586529	ATTTTTTTTTTTCTC[C/T]CCATACTCAACTACT	74589
rs30509036	snp	A/T	0.497041	0.0383476	intron-variant	Kbtbd12	GRCm38.p3	6:88583416	TGGAGGGAATGTTAC[A/T]GTGAAGTGGTAAACC	74589
rs30513373	snp	C/T	0.444444	0.157135	intron-variant	Kbtbd12	GRCm38.p3	6:88607100	CCAGTTCCAGGGCTT[C/T]TGACATTCTGACACA	74589
rs30517214	snp	A/G	0.444444	0.157135	intron-variant	Kbtbd12	Mm_Celera	6:88580126	GAAAACAAAGTTTAT[A/G]AAAGATAGATTTAAA	74589
rs30550310	snp	A/G	0.49827	0.0293608	intron-variant	Kbtbd12	GRCm38.p3	6:88577009	TTTCACAAAACAGAC[A/G]TAAGAGTGAGAATAA	74589
rs30551005	snp	C/T	0.487535	0.077957	intron-variant	Kbtbd12	GRCm38.p3	6:88589397	TACCTTTATAGGTCA[C/T]ACCCAAATACACCCC	74589
rs30557987	snp	C/T	0.492188	0.0620098	intron-variant	Kbtbd12	GRCm38.p3	6:88585587	AGCACAGCCCGAGCA[C/T]GCACTACCCAGCTCT	74589
rs30562256	snp	A/G	0.492188	0.0620098	intron-variant	Kbtbd12	GRCm38.p3	6:88584337	TGGAAGGAGGAACTC[A/G]TGTTGTTTTTTTATG	74589
rs30563215	snp	A/C	0.444444	0.157135	intron-variant	Kbtbd12	Mm_Celera	6:88566464	ATTATATTATAATCT[A/C]AAAAAAATAAAAGAA	74589
rs30617458	snp	A/T	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88576768	AGGTGGAGAGCTTTT[A/T]AAGAAGCGGGGCTTT	74589
rs30659900	snp	C/T	0.5	0	upstream-variant-2KB	Kbtbd12	Mm_Celera	6:88628946	ATATCAATATATAAA[C/T]TATAACTTACTATAG	74589
rs30758242	snp	A/G	0.475309	0.108333	intron-variant	Kbtbd12	GRCm38.p3	6:88608108	GAAGATAGGGTTACT[A/G]TGCTTGCTCCATTTA	74589
rs30765017	snp	A/C	0.5	0	upstream-variant-2KB	Kbtbd12	GRCm38.p3	6:88628672	TAAAGGCAGGGGAAT[A/C]AGGAATTTAAGGGGC	74589
rs30802610	snp	A/G	0.5	0	intron-variant	Kbtbd12	Mm_Celera	6:88585993	GAAAGAAAGAAAGAA[A/G]GAAAGAAGGAAAAAG	74589
rs30806233	snp	A/G	0.484429	0.0868505	intron-variant	Kbtbd12	GRCm38.p3	6:88625696	AGTAAAGGACTTCAT[A/G]TTTTATTCACTTCTC	74589
rs30812446	snp	A/G	0.444444	0.157135	intron-variant	Kbtbd12	Mm_Celera	6:88566497	TTTAAAAGTTAGCGC[A/G]CTTGGGATAGCATTG	74589
rs30850149	snp	A/G	0.465374	0.126941	intron-variant	Kbtbd12	GRCm38.p3	6:88593139	GGAAGACTGGAGTAA[A/G]AAAACATGAATTAGG	74589
rs30860670	snp	C/G	0.475309	0.108333	upstream-variant-2KB	Kbtbd12	Mm_Celera	6:88629131	TGGTTCTCTTCCTCT[C/G]CTACTTCAGTTTGCC	74589
rs30869683	snp	C/T	0.5	0	intron-variant	Kbtbd12	GRCm38.p3	6:88583590	CCCCCGCAAATTTAA[C/T]AGTAACATACAAATA	74589
rs30894814	snp	A/C	0.444444	0.157135	intron-variant	Kbtbd12	Mm_Celera	6:88597595	CCACCACCACCAACA[A/C]CAACAACAACAACAA	74589
rs30899872	snp	C/T	0.48	0.0979796	intron-variant	Kbtbd12	GRCm38.p3	6:88577570	GGAAATATGTCAAGA[C/T]GAACGCTTCTTCCTG	74589
rs30916155	snp	C/T	0.46875	0.121031	intron-variant	Kbtbd12	GRCm38.p3	6:88584551	TGCTACTCCTCAGCT[C/T]GGTGCACAGCAGCTG	74589
rs30957170	snp	A/G	0.49827	0.0293608	intron-variant	Kbtbd12	Mm_Celera	6:88588425	ACGCAGGATGTGCTT[A/G]GCTGCCTTCTCTCCT	74589
rs30987811	snp	C/T	0.497778	0.0332592	intron-variant	Kbtbd12	GRCm38.p3	6:88577835	AAAAAGTATTCCACC[C/T]AAATTCTGCTGAAGC	74589
rs31001079	snp	C/T	0.5	0	intron-variant	Kbtbd12	Mm_Celera	6:88577696	GGATCTGGTCAGAGA[C/T]AATCATCTTGGCCGT	74589
rs36242543	snp	C/T	0.132653	0.220748	intron-variant	Kbtbd12	Mm_Celera	6:88556210	GAATTCAGATTTTAC[C/T]GCAGAAGGACAAACA	74589
rs36243669	snp	A/G	0.231111	0.249285	intron-variant	Kbtbd12	Mm_Celera	6:88619216	CTCAGAGTGAAGGAA[A/G]AAAGAAGTAAAAAGA	74589
rs36266630	snp	C/T	0.124444	0.216185	intron-variant	Kbtbd12	Mm_Celera	6:88612170	ACTTCAAGCTAAGGA[C/T]TGAGGTGTCTCTTGT	74589
rs36268429	snp	G/T	0.231111	0.249285	intron-variant	Kbtbd12	Mm_Celera	6:88594551	CAGTCTCACAATGTC[G/T]GTGTTTCCAAAGTTC	74589
rs36270386	snp	C/T	0.336735	0.234472	upstream-variant-2KB	Kbtbd12	Mm_Celera	6:88628039	CATTTAGAAGCAACT[C/T]ATTGTTTTGAAACCA	74589
rs36272215	snp	G/T	0.124444	0.216185	intron-variant	Kbtbd12	Mm_Celera	6:88602571	TCTGTTGCTATGAAG[G/T]TCCATGCCACTGTGG	74589
rs36272237	snp	C/T	0.336735	0.234472	intron-variant	Kbtbd12	Mm_Celera	6:88550586	ATCTGTGAACTCAAT[C/T]AACCCTGGATGTAAA	74589
rs36277692	snp	C/T	0.124444	0.216185	intron-variant	Kbtbd12	Mm_Celera	6:88554526	GGAGGAAGCTGTTCA[C/T]TTCATGGCAGCTGGG	74589
rs36283645	snp	C/G	0.260355	0.249785	intron-variant	Kbtbd12	Mm_Celera	6:88608476	TTTCACAATGATAAA[C/G]TATTTATTAGACCAG	74589
rs36283901	snp	A/G	0.244898	0.249948	intron-variant	Kbtbd12	Mm_Celera	6:88563228	TTGCCACTTTAAGTG[A/G]AGTATAAGAATCTTT	74589
rs36290052	snp	G/T	0.132653	0.220748	intron-variant	Kbtbd12	Mm_Celera	6:88560289	TGTGATGAAAGGGCA[G/T]GTACCACAAAGTCCA	74589
rs36297888	snp	A/C	0.32	0.24	intron-variant	Kbtbd12	Mm_Celera	6:88563699	TTTGATATCTGTCCT[A/C]TCACACATTATCTGT	74589
rs36299791	snp	A/G	0.244898	0.249948	intron-variant	Kbtbd12	Mm_Celera	6:88557728	GAGGCGTGGCCAACC[A/G]ACAGCAGCCCTGCAC	74589
rs36322967	snp	C/G	0.142012	0.225474	intron-variant	Kbtbd12	Mm_Celera	6:88587086	TTCTGGCCTTGACTT[C/G]TTTTTGCTGCCTATT	74589
rs36337492	snp	A/G	0.142012	0.225474	intron-variant	Kbtbd12	Mm_Celera	6:88579199	TATGGAAGATACCAG[A/G]GCAGCAAACCCTTAG	74589
rs36340203	snp	C/G	0.132653	0.220748	intron-variant	Kbtbd12	Mm_Celera	6:88556851	AGTTGAAAACTGTTT[C/G]TGAGAGTTTCTCTGG	74589
rs36366497	snp	C/T	0.231111	0.249285	intron-variant	Kbtbd12	Mm_Celera	6:88611595	CCCTGAGACTTGGGG[C/T]TGTAAGTACTCTGTC	74589
rs36370673	snp	A/C	0.244898	0.249948	intron-variant	Kbtbd12	Mm_Celera	6:88555895	ATTAGCTGTTGAGAT[A/C]ATGACCTGGTCCTTT	74589
rs36387376	snp	C/T	0.244898	0.249948	intron-variant	Kbtbd12	Mm_Celera	6:88608177	AGTAGATTTTGTCTA[C/T]CATCAATACAGCTAA	74589
rs36390603	snp	C/T	0.142012	0.225474	intron-variant	Kbtbd12	Mm_Celera	6:88587310	TCTTCCGTGACTCAT[C/T]ATGGCAGGCTGGCTT	74589
rs36392144	snp	C/T	0.124444	0.216185	intron-variant	Kbtbd12	Mm_Celera	6:88564149	GTTTCATCCTTAGGG[C/T]CTGCATGGTTAAGGA	74589
rs36392632	snp	G/T	0.375	0.216506	synonymous-codon	Kbtbd12	Mm_Celera	6:88547911	GGAGATAACCTCATG[G/T]CGATCTGAAAGACAG	74589
rs36398320	snp	A/T	0.142012	0.225474	intron-variant	Kbtbd12	Mm_Celera	6:88578732	TTAGGAGAGGCCCAG[A/T]GTGGGACATCAGGCA	74589
rs36408286	snp	A/G	0.260355	0.249785	upstream-variant-2KB	Kbtbd12	Mm_Celera	6:88628015	TTCAGAGATCGCATG[A/G]CCAGTCCACATTTAG	74589
rs36411904	snp	C/T	0.142012	0.225474	intron-variant	Kbtbd12	Mm_Celera	6:88586603	ATCCCACAGAATCCT[C/T]GTCATCTCATAGAGG	74589
rs36412389	snp	A/G	0.336735	0.234472	intron-variant	Kbtbd12	Mm_Celera	6:88559561	AAAACAGTGCCAGCA[A/G]CCGGGGACCAAGTCT	74589
rs36414530	snp	A/C	0.124444	0.216185	intron-variant	Kbtbd12	Mm_Celera	6:88611215	ATACAAGAGGAAGGG[A/C]TCCTTTTGCTTTTGC	74589
rs36417068	snp	A/G	0.142012	0.225474	intron-variant	Kbtbd12	Mm_Celera	6:88587824	AATAAGGAGCAGATA[A/G]AATATGTACAGAGTT	74589
rs36428297	snp	C/T	0.18	0.24	intron-variant	Kbtbd12	Mm_Celera	6:88600403	CTCAATAAATATTAT[C/T]CTGCATGGAAAAAAT	74589
rs36429878	snp	C/T	0.142012	0.225474	intron-variant	Kbtbd12	Mm_Celera	6:88582891	CCTGTAGTGTCATAC[C/T]AATTGGCATAGCAGG	74589
rs36430502	snp	A/G	0.244898	0.249948	intron-variant	Kbtbd12	Mm_Celera	6:88608449	CAATGCAGGTATCCT[A/G]AATACATCTTATTTC	74589
rs36431931	snp	A/T	0.32	0.24	intron-variant	Kbtbd12	Mm_Celera	6:88616742	GCTGCTCCTCCTGAA[A/T]GGTCTTCATATCCAC	74589
rs36432067	snp	C/T	0.231111	0.249285	intron-variant	Kbtbd12	Mm_Celera	6:88614961	GTTTAGAAGGGATCT[C/T]AGATGTGGATCCTTA	74589
rs36434452	snp	C/T	0.124444	0.216185	intron-variant	Kbtbd12	Mm_Celera	6:88611583	AAACGTGCCGAGCCC[C/T]GAGACTTGGGGTTGT	74589

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