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
rs3692334	snp	C/T	0.336735	0.234472	intron-variant	Grb2	GRCm38.p3	11:115675907	TTCTGTCCTGTCCTG[C/T]GGTCCTCAAGCATCT	14784
rs3693512	snp	C/T	0.5	0	intron-variant	Grb2	GRCm38.p3	11:115676070	TATAACCCCAGTACT[C/T]AGCAAGGGAAGTCAG	14784
rs6219508	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Grb2	Mm_Celera	11:115699811	CCTGTCAGAATCCAC[A/G]CAGGACTTGGGTCTC	14784
rs6221522	snp	G/T	0.5	0	upstream-variant-2KB, intron-variant	Grb2	Mm_Celera	11:115700141	CACAAGAGCATGGCT[G/T]AAGTTCTCATTTATA	14784
rs6221664	snp	G/T	0.5	0	upstream-variant-2KB, intron-variant	Grb2	Mm_Celera	11:115700233	gtagcctagaactcc[G/T]tataagtacaccaga	14784
rs6297198	snp	C/T	0.5	0	upstream-variant-2KB	Grb2	Mm_Celera	11:115710299	AATGACAATATACCA[C/T]CCAAATACCAGAGTC	14784
rs6298428	snp	A/G	0.5	0	upstream-variant-2KB	Grb2	Mm_Celera	11:115710507	aaagacccaggcttc[A/G]ttcccagcatcttca	14784
rs6298883	snp	C/T	0.5	0	upstream-variant-2KB	Grb2	Mm_Celera	11:115710540	gcactaacgatcatc[C/T]ataactccagttcnt	14784
rs6298898	snp	C/T	0.5	0	upstream-variant-2KB	Grb2	Mm_Celera	11:115710554	cnataactccagttc[C/T]tgggaatccaaggtc	14784
rs13471888	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Grb2	GRCm38.p3	11:115644519	CTTGTCTTCTGTGAG[C/T]TTTCCGTCCTCTGTA	14784
rs13471889	snp	A/C			utr-variant-5-prime	Grb2	Mm_Celera	11:115699239	TGCTGAGCACTGAGC[A/C]GCGCTCAGAATGGAA	14784
rs13471890	snp	A/G			utr-variant-5-prime	Grb2	GRCm38.p3	11:115708475	GCGGGCGCCGCAGTC[A/G]GGGAGCAGCAGCGAG	14784
rs13471891	snp	A/G			missense	Grb2	Mm_Celera	11:115645907	TGACCCCCAGGAGGA[A/G]GGCGAGCTGGGCTTT	14784
rs27015950	snp	C/T	0.142012	0.225474	upstream-variant-2KB, intron-variant	Grb2	Mm_Celera	11:115700927	CTTAGTTAGTCTATG[C/T]GGTGCCACCTCTCAA	14784
rs27015951	snp	A/G	0.260355	0.249785	upstream-variant-2KB, intron-variant	Grb2	Mm_Celera	11:115700369	ATACAGGCTGGTGCC[A/G]GACAGTCAGACCCCA	14784
rs27015952	snp	A/G	0.260355	0.249785	intron-variant	Grb2	Mm_Celera	11:115698966	AAGGCAGTTAAGGAC[A/G]ACACATCACAGCGAC	14784
rs27015953	snp	C/T	0.260355	0.249785	intron-variant	Grb2	Mm_Celera	11:115698411	AAGGAAACCGTCATC[C/T]GGAAGGGCGAGCTGC	14784
rs27015954	snp	A/T	0.429688	0.173817	intron-variant	Grb2	GRCm38.p3	11:115698163	TCCATCACTTTGAGC[A/T]CTGAGGGCAAACGTT	14784
rs27015955	snp	C/T	0.290657	0.246672	intron-variant	Grb2	GRCm38.p3	11:115697813	GGTTGAGTCCAGACC[C/T]GTTGCCTGGAAGAGG	14784
rs27015956	snp	A/G	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115696203	CACACTCAGTGCAAA[A/G]GCGTGAAGCTTGCAG	14784
rs27015957	snp	A/G	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115695497	CTTGCCACGACACTG[A/G]TTAAGCTGAGCTGGA	14784
rs27015958	snp	C/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115694061	AAACCAGCACGGGCA[C/T]TCCTTTAAAAGCTAA	14784
rs27015959	snp	C/G/T	0.297521	0.245442	intron-variant	Grb2	Mm_Celera	11:115693210	GCAGGAGGGCTTGCC[C/G/T]GAGTTTGAGGCCAGA	14784
rs27015960	snp	A/G	0.260355	0.249785	intron-variant	Grb2	Mm_Celera	11:115692737	GCTTTGCTCTTATTA[A/G]CGTGGCCTGCTCTCC	14784
rs27015961	snp	C/T	0.260355	0.249785	intron-variant	Grb2	Mm_Celera	11:115692330	GTCTATGGATGTCAG[C/T]CATTGCTTTGAGCAC	14784
rs27015962	snp	A/G	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115690935	CAGAGCTATGAGGAT[A/G]AATAATCACCTTAAA	14784
rs27015963	snp	A/G	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115688030	TACAGGCTCTGGGGT[A/G]CAGTCCATTTTCATC	14784
rs27015964	snp	A/T	0.277778	0.248452	intron-variant	Grb2	GRCm38.p3	11:115686933	CGTCTGTAGCAGACC[A/T]CACTCAACACCAAAC	14784
rs27015965	snp	A/G	0.231111	0.249285	intron-variant	Grb2	Mm_Celera	11:115686923	GAAGTTCAGTCGTCT[A/G]TAGCAGACCTCACTC	14784
rs27015966	snp	C/T	0.32	0.24	intron-variant	Grb2	GRCm38.p3	11:115686584	CACCAAATACACTTC[C/T]CCGAGACAATTTCAA	14784
rs27015967	snp	C/G	0.124444	0.216185	intron-variant	Grb2	Mm_Celera	11:115684888	CAGAATGGAAGTAAC[C/G]AGCTGTGGATGGACA	14784
rs27015968	snp	C/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115684704	GAGGGCTAGGGACAA[C/T]GAGGCAGAAACAGAC	14784
rs27015969	snp	A/C	0.231111	0.249285	intron-variant	Grb2	Mm_Celera	11:115683897	TCAGTGAAGTGCGTG[A/C]GACAAGCAGAAGGAC	14784
rs27015970	snp	A/G	0.231111	0.249285	intron-variant	Grb2	Mm_Celera	11:115683672	GACACTTGGAAATGG[A/G]AAGACTGAGCAGTGG	14784
rs27015971	snp	A/C	0.231111	0.249285	intron-variant	Grb2	GRCm38.p3	11:115683604	ACACACAGCATTTCA[A/C]GCCTAAATGCACAGC	14784
rs27015972	snp	C/T	0.124444	0.216185	intron-variant	Grb2	Mm_Celera	11:115682819	AATGTCCAAACCAGT[C/T]TTGAATAGGCCCCAG	14784
rs27015973	snp	A/G	0.231111	0.249285	intron-variant	Grb2	Mm_Celera	11:115682424	AACTATAGTCACTCT[A/G]GGCGAGAATACGAAA	14784
rs27015974	snp	G/T	0.290657	0.246672	intron-variant	Grb2	GRCm38.p3	11:115682277	GTACAGGCAAAAAGA[G/T]CAATATGGCTGAAGA	14784
rs27015975	snp	A/G	0.231111	0.249285	intron-variant	Grb2	Mm_Celera	11:115680232	CTCACTTAAAGCAGC[A/G]AGGTAAGCAACAGAG	14784
rs27015976	snp	A/G	0.231111	0.249285	intron-variant	Grb2	Mm_Celera	11:115680159	CTGTCAACTAGCCTC[A/G]GCACTCTGGCAAGGC	14784
rs27015977	snp	C/G	0.231111	0.249285	intron-variant	Grb2	Mm_Celera	11:115680106	AGAGGTCAAAGAGCA[C/G]CCGTGCAAATACAGG	14784
rs27015978	snp	C/T	0.5	0	intron-variant	Grb2	GRCm38.p3	11:115680080	GCACCACAGACCAAG[C/T]CACACCAGGAAGAGG	14784
rs27015979	snp	C/G/T	0.391111	0.206368	intron-variant	Grb2	GRCm38.p3	11:115679991	CCAAGACACAATGTA[C/G/T]GCTACCTGTCCTTTC	14784
rs27015980	snp	C/T	0.231111	0.249285	intron-variant	Grb2	GRCm38.p3	11:115679967	TCACTGAAGCTGCCC[C/T]GAGGCTGACCAAGAC	14784
rs27015981	snp	C/T	0.231111	0.249285	intron-variant	Grb2	Mm_Celera	11:115679872	CAGTATCCTGTGGCC[C/T]GAAACCTGTCTGGGG	14784
rs27015982	snp	A/G	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115679635	GGTCAAGGTCAGCCT[A/G]GCACCACAGACAGAG	14784
rs27015983	snp	A/G	0.277778	0.248452	intron-variant	Grb2	GRCm38.p3	11:115679532	AAAAAAGTACAACTC[A/G]AGGTTTCTTTGTATC	14784
rs27015984	snp	A/G	0.473373	0.11227	intron-variant	Grb2	GRCm38.p3	11:115679465	GCACAGAATCTCAGC[A/G]TACATCAAGGCTAAG	14784
rs27015985	snp	A/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115679363	GACCCATCTGAGAAG[A/T]GGTGATGCCATACCT	14784
rs27015986	snp	A/G	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115679102	AAGCTAAAGCCTCAC[A/G]TGACACGAAATCTGT	14784
rs27015987	snp	C/T	0.277778	0.248452	intron-variant	Grb2	GRCm38.p3	11:115678455	AGAAGACATTTTGAA[C/T]CAGACAGCTTGGAGA	14784
rs27015988	snp	C/T	0.46875	0.121031	intron-variant	Grb2	Mm_Celera	11:115677456	TGTGCCGCGTGTGCA[C/T]CTGGGCATGTGCACA	14784
rs27015989	snp	C/T	0.375	0.216506	intron-variant	Grb2	GRCm38.p3	11:115677448	CTTATGAGTGTGCCG[C/T]GTGTGCACCTGGGCA	14784
rs27015990	snp	C/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115673593	GTCTATCGGCTCCCT[C/T]GCAACTAGAACTGCA	14784
rs27015991	snp	C/G	0.290657	0.246672	intron-variant	Grb2	GRCm38.p3	11:115673223	AGATGATCCGAGTTC[C/G]GGACTGGTGAGATGA	14784
rs27015992	snp	A/C	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115673205	CAAGCAATCTACCTA[A/C]AAAGATGATCCGAGT	14784
rs27015993	snp	G/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115671117	TTTTTAGGAGCCTTC[G/T]TTCACTTTTCATCAT	14784
rs27015994	snp	C/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115671067	TTTGTAATCCTTCCT[C/T]CACACAGAAGAGGGT	14784
rs27015995	snp	C/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115670782	GAGAAGACAAGGATC[C/T]GAAACACTAATAACA	14784
rs27015996	snp	C/G	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115670535	GTAAAGGCAGTCCTG[C/G]TAATTACCACATTTA	14784
rs27015997	snp	A/G	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115670386	TGCAAGACCATGAGC[A/G]CATACCCTTTCATGA	14784
rs27015998	snp	A/G	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115670119	GGAGGTCAAATAAGG[A/G]CAACAGAGCCTCTGG	14784
rs27015999	snp	A/G	0.304688	0.243945	intron-variant	Grb2	GRCm38.p3	11:115668005	AAATGATCAATTGGT[A/G]ATGTCACTCCATTGC	14784
rs27016000	snp	A/G	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115667411	CAGAGCAAGACAAGG[A/G]CAGAGCGGCCCAATG	14784
rs27016001	snp	A/G	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115667130	TTAAGGGACTGCTAC[A/G]GTATGTTACAACTAC	14784
rs27016002	snp	A/G	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115667106	TGGAAAGTGTAACCC[A/G]GCCGGCTATTAAGGG	14784
rs27016003	snp	G/T	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115666840	CACTGTAGCTAAGCA[G/T]GGCGGCTCCTTGGGT	14784
rs27016004	snp	C/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115666757	AAGCCATCCTCAGGC[C/T]TCATTCTCCTGAGCA	14784
rs27016005	snp	A/G	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115666345	GTGCCCTGGGTCTAT[A/G]TGAACCACCAACAGG	14784
rs27016006	snp	C/G	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115665453	GTGAGGTTAACATCT[C/G]GGCACTATAGTTACA	14784
rs27016007	snp	A/G	0.359862	0.224567	intron-variant	Grb2	GRCm38.p3	11:115665146	CCACCCAGGAACCGG[A/G]ACCAAAGCTGTAAAT	14784
rs27016008	snp	C/T	0.152778	0.230321	intron-variant	Grb2	Mm_Celera	11:115664491	GCCTCACCAAGAAAG[C/T]CCATCCCAAACGTCA	14784
rs27016009	snp	C/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115664433	TCTAGACTCCCATGC[C/T]GTCAGGTGTCCCAGG	14784
rs27016010	snp	A/G	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115664054	AGCCCAAATGCTCAG[A/G]CACCACAGAACAGAC	14784
rs27016011	snp	C/T	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115663256	GGAGAGCAGGCCCTG[C/T]CCAGAGTCCACTATC	14784
rs27016012	snp	C/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115662928	ATGCAGAGATAAACG[C/T]GCTTCGGATACCCAA	14784
rs27016013	snp	A/G	0.375	0.216506	intron-variant	Grb2	GRCm38.p3	11:115662927	GATGCAGAGATAAAC[A/G]CGCTTCGGATACCCA	14784
rs27016014	snp	C/T	0.142012	0.225474	intron-variant	Grb2	Mm_Celera	11:115662926	TGATGCAGAGATAAA[C/T]GCGCTTCGGATACCC	14784
rs27016015	snp	C/T	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115662492	CCATGTACCTCAAAG[C/T]GGGAAGGCGCAGAAT	14784
rs27016016	snp	A/G	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115660948	CTGCTTCCTACACAC[A/G]CAAAGGTCGACACCT	14784
rs27016017	snp	C/T	0.244898	0.249948	intron-variant	Grb2	GRCm38.p3	11:115660500	GTTACACAGGAACGA[C/T]GGAGTGCTCACCAAG	14784
rs27016018	snp	A/G	0.244898	0.249948	intron-variant	Grb2	Mm_Celera	11:115659877	CTCACTGTAACGGAA[A/G]TGTACCATCTTAGCT	14784
rs27016019	snp	A/G	0.165289	0.235211	intron-variant	Grb2	GRCm38.p3	11:115659128	CTATCCTCAGGACCC[A/G]CACGGTAGAAAGAAA	14784
rs27016020	snp	G/T	0.231111	0.249285	intron-variant	Grb2	Mm_Celera	11:115658989	GAACTGGGTATGTTG[G/T]TTGTGGAAATTCAGT	14784
rs27016021	snp	G/T	0.277778	0.248452	intron-variant	Grb2	GRCm38.p3	11:115658675	TAGCCTCTGTACTGC[G/T]TAGACTTATGACTCA	14784
rs27016022	snp	C/G	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115658537	ACTGTCTCTCCTACC[C/G]TTTCTTTCTCTGCAG	14784
rs27016023	snp	C/T	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115658466	AGAGAGCGCCCTGAA[C/T]GCTCACAGCCCTTAT	14784
rs27016024	snp	A/G	0.297521	0.245442	intron-variant	Grb2	GRCm38.p3	11:115658337	TATAAAGTGAACATG[A/G]GTTTCAAGTATCGTG	14784
rs27016025	snp	A/G	0.165289	0.235211	intron-variant	Grb2	Mm_Celera	11:115658019	AGGGAGTTGTGGAGT[A/G]CAGTGGGTCAAACTG	14784
rs27016026	snp	C/T	0.165289	0.235211	intron-variant	Grb2	Mm_Celera	11:115657995	CGCATCTTCCAGAGC[C/T]GGAGTTACAGGGAGT	14784
rs27016027	snp	C/T	0.165289	0.235211	intron-variant	Grb2	Mm_Celera	11:115657918	AGTGCTCATCTTTTT[C/T]GATATGTGGGTATGT	14784
rs27016028	snp	A/G	0.165289	0.235211	intron-variant	Grb2	Mm_Celera	11:115657793	GTTCTAAGAGAGCCA[A/G]TGCTGCCTTCTAGAG	14784
rs27016029	snp	A/G	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115656917	GACGGCAGGGAATAC[A/G]ATGCCTGGCGCCAAG	14784
rs27016030	snp	C/T	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115656889	ACTTGGTGTATTATA[C/T]CTCTGTCGCCCAGAC	14784
rs27016031	snp	C/T	0.375	0.216506	intron-variant	Grb2	GRCm38.p3	11:115656833	TCCCAGACCTGGAGA[C/T]GCTTTACAGCATGGT	14784
rs27016032	snp	C/T	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115656808	TTAAAGCAGGAGGTA[C/T]CAAGGCAACTCCCAG	14784
rs27016033	snp	A/G	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115656768	CAAGCTAGAGAAGCC[A/G]TGTCCCCTCAAAAGT	14784
rs27016034	snp	A/G	0.375	0.216506	intron-variant	Grb2	GRCm38.p3	11:115656733	AGTCCCCAAAGCTGC[A/G]TGTTCTTACTGCCAA	14784
rs27016035	snp	C/T	0.277778	0.248452	intron-variant	Grb2	Mm_Celera	11:115655322	GAGACAAGCAGGTGA[C/T]CTCTTTGCTTAGGGG	14784
rs27016036	snp	C/T	0.260355	0.249785	intron-variant	Grb2	Mm_Celera	11:115654992	TTTGTGTATCCTTGG[C/T]TGCCGCCAGAGCACT	14784

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