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
rs3690140	snp	A/G	0.492188	0.0620098	intron-variant	Trim67	GRCm38.p3	8:124805572	CAGGTGAAGGACTCA[A/G]ATACAGGGTGATGGG	330863
rs30679502	snp	C/T	0.444444	0.157135	intron-variant	Trim67	GRCm38.p3	8:124819094	CCAGCTCATTAGGCA[C/T]GGACTGTATTCCCAC	330863
rs30925505	snp	C/G	0.32	0.24	intron-variant	Trim67	GRCm38.p3	8:124819218	ATGACCATGTTTCTA[C/G]GAATGCATGTCCTCT	330863
rs31915332	snp	A/G	0.290657	0.246672	intron-variant	Trim67	GRCm38.p3	8:124797161	CGTCTGTGTGCCATG[A/G]TGCGAGTGTGTTGGC	330863
rs31916115	snp	A/G	0.408163	0.193609	intron-variant	Trim67	GRCm38.p3	8:124797383	CATGCATGTGCACAT[A/G]TGTATAGGTACACAC	330863
rs31916118	snp	A/G	0.297521	0.245442	intron-variant	Trim67	Mm_Celera	8:124797471	TCCACCTCACATTCT[A/G]AGACAAGGTCTTTTA	330863
rs31916121	snp	A/G	0.32	0.24	intron-variant	Trim67	GRCm38.p3	8:124797617	CTATAAAGGTTCTGG[A/G]GATTTTGCCTGGGTA	330863
rs31916864	snp	A/C	0.142012	0.225474	intron-variant	Trim67	Mm_Celera	8:124808935	GTGGTCTAGCTATGG[A/C]TAAGGTTGAGATTCT	330863
rs31916867	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809070	CATTTTCACTTTGCT[C/T]TACCATTGTTCGAAT	330863
rs31916870	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809100	TATTCTCAAGGTCTC[C/T]AGTGGGCATTTATTT	330863
rs31916873	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809109	GGTCTCCAGTGGGCA[C/T]TTATTTTAACACTAG	330863
rs31916894	snp	C/T	0.277778	0.248452	intron-variant	Trim67	Mm_Celera	8:124797861	AGCTGTTTAGAACAC[C/T]TGTTGCTCTTGCAGA	330863
rs31916897	snp	C/G	0.444444	0.157135	intron-variant	Trim67	GRCm38.p3	8:124798003	AGCACCCATATCAGT[C/G]TCCAGCTCCTGGGAA	330863
rs31916900	snp	C/T	0.18	0.24	intron-variant	Trim67	GRCm38.p3	8:124798206	AAGACTAATTTGGGG[C/T]CCTGTTACCCAAACA	330863
rs31916903	snp	G/T	0.244898	0.249948	intron-variant	Trim67	GRCm38.p3	8:124798330	TGATAATGGGCTAAG[G/T]TGTCAGGGTCCAAGG	330863
rs31917556	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809171	TTAGACTCTTATTAT[C/T]CGCACCTGTCGATGA	330863
rs31917559	snp	A/C/G	0.132653	0.220748	intron-variant	Trim67	GRCm38.p3	8:124809182	TTATTCGCACCTGTC[A/C/G]ATGATGCCACACAGC	330863
rs31917562	snp	C/T	0.244898	0.249948	intron-variant	Trim67	Mm_Celera	8:124809197	GATGATGCCACACAG[C/T]TAACAGAACCTGGCA	330863
rs31917816	snp	A/G	0.124444	0.216185	intron-variant	Trim67	Mm_Celera	8:124798354	TCCAAGGTCATGCAG[A/G]GAAAAATCAGCAGTC	330863
rs31917819	snp	C/T	0.244898	0.249948	intron-variant	Trim67	GRCm38.p3	8:124798413	AATAAATGCCTCTCT[C/T]GTCAACCTCAATGGC	330863
rs31917822	snp	A/G	0.142012	0.225474	intron-variant	Trim67	GRCm38.p3	8:124798537	GAGTTTGAATCTTGT[A/G]TCTAGTGCTCCAGCC	330863
rs31918185	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809264	ACACGTAAATAACAG[C/T]GTAACTCAAGAATCC	330863
rs31918188	snp	A/C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809295	TGTGAGCAAGGATTA[A/C/T]GCCTTACTGTGTTTT	330863
rs31918191	snp	A/G	0.152778	0.230321	intron-variant	Trim67	Mm_Celera	8:124809345	GGGCAGCCAGCACTC[A/G]GGAGACCTCGAGAAC	330863
rs31918355	snp	G/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124813568	AGCTGCATGGTCTGG[G/T]AAATCTCAGGCAGCA	330863
rs31918357	snp	A/G	0.244898	0.249948	intron-variant	Trim67	GRCm38.p3	8:124813693	CTAAGGAAGTTCCTG[A/G]ATGCTGATCCTCTGT	330863
rs31918360	snp	A/G	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124813712	CTGATCCTCTGTGCA[A/G]GGTCCTACATGGACT	330863
rs31918362	snp	C/T	0.132653	0.220748	intron-variant	Trim67	GRCm38.p3	8:124813715	ATCCTCTGTGCAGGG[C/T]CCTACATGGACTGCC	330863
rs31918654	snp	G/T	0.244898	0.249948	intron-variant	Trim67	GRCm38.p3	8:124798753	TCAAAGTGCTTGCCT[G/T]GAGACTATGAGGCCT	330863
rs31918656	snp	C/T	0.152778	0.230321	intron-variant	Trim67	Mm_Celera	8:124798781	CCTGGATTTGATCCC[C/T]GGCATCCAACATAAA	330863
rs31918658	snp	C/T	0.152778	0.230321	intron-variant	Trim67	Mm_Celera	8:124799199	TTAAAAAAAGAAAGA[C/T]GCACAGCAGCAGACA	330863
rs31918661	snp	C/T	0.165289	0.235211	intron-variant	Trim67	Mm_Celera	8:124799221	CAGCAGACACCTGTA[C/T]TCTCTGCACTAGGAA	330863
rs31918974	snp	A/G	0.497041	0.0383476	intron-variant	Trim67	Mm_Celera	8:124809355	CACTCGGGAGACCTC[A/G]AGAACCTTTATTGAG	330863
rs31918977	snp	C/T	0.165289	0.235211	intron-variant	Trim67	Mm_Celera	8:124809360	GGGAGACCTCGAGAA[C/T]CTTTATTGAGTGGTG	330863
rs31918980	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809385	GTGGTGAATAAGATG[C/T]TACCCTGGAATGTAT	330863
rs31918983	snp	A/G	0.231111	0.249285	intron-variant	Trim67	Mm_Celera	8:124809411	TGTATGCTAATGTCA[A/G]TACCATAGATTATTA	330863
rs31919344	snp	A/C	0.497041	0.0383476	intron-variant	Trim67	GRCm38.p3	8:124813813	CTGTGCGTCTAGTCT[A/C]GGGCACCCTCGGAGG	330863
rs31919347	snp	A/G	0.132653	0.220748	intron-variant	Trim67	GRCm38.p3	8:124814046	TTACTTTGAAAAAAT[A/G]TGACTCAAGTTAAAT	330863
rs31919349	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124814395	CAACTTGACACACCT[C/T]GTATCACCCAGGAAG	330863
rs31919352	snp	G/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124814396	AACTTGACACACCTC[G/T]TATCACCCAGGAAGA	330863
rs31919524	snp	A/G	0.152778	0.230321	intron-variant	Trim67	Mm_Celera	8:124799565	CTTCTGACTCCCACT[A/G]TGGTGTAAGTTTCCC	330863
rs31919607	snp	C/G	0.244898	0.249948	intron-variant	Trim67	GRCm38.p3	8:124819836	GTTTACATGTCTGAA[C/G]CCACCATGACTTCAT	330863
rs31919610	snp	A/G	0.21875	0.248039	synonymous-codon	Trim67	GRCm38.p3	8:124820298	TCTGGACAGCGAGCC[A/G]CTGCTGCAAGCCATC	330863
rs31919613	snp	G/T	0.165289	0.235211	intron-variant	Trim67	GRCm38.p3	8:124820419	AAGGGCAGCTGGATG[G/T]TGGTGACAGAGGCCG	330863
rs31919806	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809455	ACTATTAGCTGCTCA[C/T]TGACTCACAGAACAG	330863
rs31919809	snp	A/G	0.497041	0.0383476	intron-variant	Trim67	Mm_Celera	8:124809797	CACCAGAGGACAGGA[A/G]CCAGCTGAGAAATGC	330863
rs31919812	snp	A/G	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809872	GTAAGTTTGTGTACT[A/G]GAATGCCCCATGGAT	330863
rs31920054	snp	C/T	0.49827	0.0293608	utr-variant-3-prime	Trim67	Mm_Celera	8:124832644	ACCATTTGGGGGTCC[C/T]AAGAACACATCACAG	330863
rs31920057	snp	C/G	0.456747	0.140554	utr-variant-3-prime	Trim67	GRCm38.p3	8:124833345	CTGGCTTTGGTGTTG[C/G]CTCATGGCATGTGTG	330863
rs31920060	snp	C/T	0.21875	0.248039	utr-variant-3-prime	Trim67	GRCm38.p3	8:124833554	TTCCCGTAAGCTCCC[C/T]GTGACCAGGGCAGCA	330863
rs31920063	snp	A/G	0.304688	0.243945	utr-variant-3-prime	Trim67	GRCm38.p3	8:124833675	CCAGGGCCTTGACCA[A/G]GCCAAACCCTGAGTG	330863
rs31920275	snp	C/T	0.244898	0.249948	intron-variant	Trim67	GRCm38.p3	8:124814530	TGGAGAGAGTTAGTC[C/T]ACTGTGCGTGGCACC	330863
rs31920278	snp	C/T	0.260355	0.249785	intron-variant	Trim67	GRCm38.p3	8:124814668	TGGTGTTCTGAGTTC[C/T]TGCCTAGTTCCCCAT	330863
rs31920281	snp	A/G	0.152778	0.230321	intron-variant	Trim67	Mm_Celera	8:124814702	AACTAACAGGTTGTA[A/G]CCTGGAATTGCCAAA	330863
rs31920342	snp	C/T	0.48	0.0979796	intron-variant	Trim67	Mm_Celera	8:124800600	GCCTTGTGAGTGCTT[C/T]CAGGCCTCTCGGCCT	330863
rs31920446	snp	C/T	0.297521	0.245442	intron-variant	Trim67	GRCm38.p3	8:124821197	CAAGGTCATTGATGT[C/T]CCAGCAACTTGGCTA	330863
rs31920449	snp	A/G	0.277778	0.248452	intron-variant	Trim67	GRCm38.p3	8:124821230	CTAGAGCTTACAAAG[A/G]ATGGCCAGAACTGGG	330863
rs31920452	snp	A/G	0.18	0.24	intron-variant	Trim67	GRCm38.p3	8:124821871	GCTCAGAGCATGCCC[A/G]ATTCAGTTCCTGGGT	330863
rs31920665	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124809980	ATGTGTTTTTTCTTG[C/T]CTGAGCTTGCGCACC	330863
rs31920668	snp	A/G	0.244898	0.249948	intron-variant	Trim67	Mm_Celera	8:124810591	TTTTGTTGCTACTTC[A/G]TTTTGCTACTGTTAT	330863
rs31920671	snp	G/T	0.244898	0.249948	intron-variant	Trim67	Mm_Celera	8:124810618	TTATGGATCGTAATG[G/T]AAGTATCTGTGTTTT	330863
rs31920956	snp	C/T	0.5	0	utr-variant-3-prime	Trim67	GRCm38.p3	8:124833897	AGGGGATGGCTGGTC[C/T]CAAGTGAATTTTAGA	330863
rs31920959	snp	A/G	0.46875	0.121031	utr-variant-3-prime	Trim67	GRCm38.p3	8:124834086	TCAACTCGGCTCTGG[A/G]AAAGTTCCCAGAGTT	330863
rs31920962	snp	A/G	0.391111	0.206368	utr-variant-3-prime	Trim67	Mm_Celera	8:124834179	TGGCCCGCGGTGGCC[A/G]TTCCAAGCCCCAGGA	330863
rs31921014	snp	A/G	0.207612	0.24638	intron-variant	Trim67	GRCm38.p3	8:124815295	CTGTCTGGTTGTACC[A/G]TTGTGGGTGCTGAAG	330863
rs31921017	snp	C/T	0.207612	0.24638	intron-variant	Trim67	GRCm38.p3	8:124815372	AGGCAGGCCTGTGTA[C/T]TCAAATCAAAATATA	330863
rs31921020	snp	A/G	0.207612	0.24638	intron-variant	Trim67	GRCm38.p3	8:124815460	GAGCCCAACAAACAC[A/G]GAAATCAGTGAATCT	330863
rs31921023	snp	A/G	0.489796	0.070696	intron-variant, missense	Trim67	Mm_Celera	8:124815921	AGAGATGGAGCAGAC[A/G]CAGCAACGGAAACGG	330863
rs31921045	snp	G/T	0.48	0.0979796	intron-variant	Trim67	GRCm38.p3	8:124800640	ACTTCACTAGAGTGT[G/T]CGTAGCAAGCCTTGG	330863
rs31921048	snp	A/C/G/T	0.486111	0.0821678	intron-variant	Trim67	GRCm38.p3	8:124800693	TGTCTAAACATCGCA[A/C/G/T]AATCCATGTCCCAGC	330863
rs31921051	snp	C/T	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124800945	ACCTGTAGGTCTTGT[C/T]GAAACACATTTTTAT	330863
rs31921053	snp	C/T	0.152778	0.230321	intron-variant	Trim67	Mm_Celera	8:124801034	ACGGAGGGCTGCTGA[C/T]CTTCAGTCTATTAGA	330863
rs31921185	snp	C/T	0.152778	0.230321	intron-variant	Trim67	GRCm38.p3	8:124822037	ACCTGATATTTCTGT[C/T]ACACCTGAGATGATC	330863
rs31921188	snp	C/T	0.489796	0.070696	intron-variant	Trim67	GRCm38.p3	8:124822647	GCAGCCAAGATGGAA[C/T]GTGGAAATTGGTAAG	330863
rs31921191	snp	C/T	0.493827	0.0552116	intron-variant	Trim67	GRCm38.p3	8:124822694	TTGTTGGGAGAGAGA[C/T]TCTGACAGCATGGTC	330863
rs31921564	snp	A/G	0.244898	0.249948	intron-variant	Trim67	Mm_Celera	8:124810731	AATGGAAACAGTATC[A/G]GACCCAAAAGATCTG	330863
rs31921566	snp	A/G	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124810800	CTCTGTGTGCCTCAG[A/G]AAAGGCTAGTGTGTG	330863
rs31921568	snp	C/G	0.244898	0.249948	intron-variant	Trim67	Mm_Celera	8:124810845	AGTTGGCAGGGTGCC[C/G]TCAAAGGTGCTAACA	330863
rs31921571	snp	A/G	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124810889	TCCTCTGGAAAGCTC[A/G]ATGTCTGTTTGTGTT	330863
rs31921795	snp	C/T	0.498615	0.0262793	utr-variant-3-prime	Trim67	GRCm38.p3	8:124834258	GGGTGTAGACACAAC[C/T]GAAAACGTGAATGCA	330863
rs31921798	snp	A/G	0.493827	0.0552116	utr-variant-3-prime	Trim67	GRCm38.p3	8:124834464	GGTTGGTATTTGGTG[A/G]CAGCTCTTGGTTCTG	330863
rs31921801	snp	G/T	0.124444	0.216185	utr-variant-3-prime	Trim67	Mm_Celera	8:124834569	TAGCTATCCACAAGC[G/T]TTTGTATTTTTTGAA	330863
rs31921856	snp	A/G	0.33241	0.236027	intron-variant, missense	Trim67	GRCm38.p3	8:124815929	AGCAGACGCAGCAAC[A/G]GAAACGGATTCAGTT	330863
rs31921859	snp	C/T	0.18	0.24	intron-variant, utr-variant-3-prime	Trim67	Mm_Celera	8:124816221	TTAACCAGAAGCCGT[C/T]ACCTACCCAGATCCC	330863
rs31921862	snp	C/T	0.5	0	intron-variant, utr-variant-3-prime	Trim67	Mm_Celera	8:124816223	AACCAGAAGCCGTTA[C/T]CTACCCAGATCCCAG	330863
rs31921965	snp	A/G	0.152778	0.230321	intron-variant	Trim67	GRCm38.p3	8:124801211	ACACTGGATGGATGT[A/G]ACAGGGTGCAGTGTC	330863
rs31921968	snp	A/G	0.142012	0.225474	intron-variant	Trim67	Mm_Celera	8:124801568	TGAGCACCACACAGC[A/G]GGTCATGTTAATGCA	330863
rs31921971	snp	A/T	0.124444	0.216185	intron-variant	Trim67	GRCm38.p3	8:124801767	AGCCGCAGGACAGAA[A/T]TGCAACAGGGAACAC	330863
rs31922024	snp	C/T	0.48	0.0979796	intron-variant	Trim67	GRCm38.p3	8:124822886	CACTTGGTTTCCTGC[C/T]GTCTGCCATCTGAGC	330863
rs31922027	snp	A/G	0.48	0.0979796	intron-variant	Trim67	GRCm38.p3	8:124822964	CTGAGGTCACTTGGT[A/G]TGCCACATGACTTGG	330863
rs31922030	snp	A/G	0.21875	0.248039	intron-variant	Trim67	GRCm38.p3	8:124823018	GCAGACGGAAAAGAG[A/G]ACTTCCTTCCTTGTG	330863
rs31922033	snp	A/G	0.408163	0.193609	intron-variant	Trim67	GRCm38.p3	8:124823917	TTCAAAACATGGCAA[A/G]CTTCTGGTTCATGAA	330863
rs31922384	snp	A/G	0.132653	0.220748	intron-variant	Trim67	Mm_Celera	8:124811153	AGAAAGTGCTTGCTG[A/G]CGGGAACCTGATATA	330863
rs31922390	snp	A/G	0.244898	0.249948	intron-variant	Trim67	GRCm38.p3	8:124812572	TCAAGACCAAACAAT[A/G]TAGTCACAGGAAAAG	330863
rs31922393	snp	C/T	0.489796	0.070696	intron-variant	Trim67	GRCm38.p3	8:124812879	GCATTGAACTCACAG[C/T]TATTCTCCTGTCTCA	330863
rs31922574	snp	A/C	0.231111	0.249285	utr-variant-3-prime	Trim67	Mm_Celera	8:124834697	ATAAATTCTTTTGAC[A/C]CTGCCAACAACTGGA	330863
rs31922577	snp	A/C	0.48	0.0979796	downstream-variant-500B	Trim67	GRCm38.p3	8:124834848	CAAAGCACAACTTCT[A/C]CAGTGAAATTATAGC	330863
rs31922605	snp	A/G	0.5	0	intron-variant, downstream-variant-500B	Trim67	GRCm38.p3	8:124816788	CTGCCTCAGGCTCTC[A/G]GGTGCTGGGATGACA	330863
rs31922608	snp	A/G	0.489796	0.070696	intron-variant, downstream-variant-500B	Trim67	Mm_Celera	8:124816869	CCACTTTCCCATGGC[A/G]TTCAGCATTCTATGA	330863
rs31922611	snp	A/G	0.188366	0.242283	intron-variant, downstream-variant-500B	Trim67	GRCm38.p3	8:124816912	CGTGCCACGGTTCCC[A/G]GAAGCTTCCTTGGTA	330863

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