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
rs26969781	snp	A/G	0.277778	0.248452	intron-variant	Grap	GRCm38.p3	11:61670737	TTATTAGCGCAGCAC[A/G]GTGTTTTGCTTAGAG	71520
rs26969782	snp	C/T	0.35503	0.226867	intron-variant	Grap	GRCm38.p3	11:61659620	ACTTGGTGATGGCAG[C/T]TTCTTCAGCTTGTTT	71520
rs26969783	snp	C/T	0.244898	0.249948	intron-variant	Grap	GRCm38.p3	11:61658200	ACTTCTCCTCAGACC[C/T]GTGGCCTCTTTTCAA	71520
rs26969784	snp	C/G	0.142012	0.225474	intron-variant	Grap	GRCm38.p3	11:61658085	ATGGTACCATGCACC[C/G]TAGCCGCCTGCCCCT	71520
rs26969785	snp	C/T	0.375	0.216506	intron-variant	Grap	GRCm38.p3	11:61657227	GAAAAACTGCACAGA[C/T]AAAAGGGGACATCCT	71520
rs26969786	snp	A/G	0.46875	0.121031	intron-variant	Grap	GRCm38.p3	11:61656629	CTGAATGGGCGTGGT[A/G]GAACAGCCACGATCT	71520
rs26969787	snp	A/G	0.345679	0.230967	intron-variant	Grap	GRCm38.p3	11:61655841	CTTTGCTTTAAAAAC[A/G]ACTTGCTTTTGAAAA	71520
rs26969788	snp	C/T	0.345679	0.230967	intron-variant	Grap	GRCm38.p3	11:61655476	GGAAAGAGGGAGCAC[C/T]GAGTCCAGAAACAGC	71520
rs26969789	snp	A/G	0.46875	0.121031	intron-variant	Grap	GRCm38.p3	11:61655382	CCTGGGTGACAGGGG[A/G]TATCCAGCCCAGAGC	71520
rs26969790	snp	C/T	0.132653	0.220748	intron-variant	Grap	GRCm38.p3	11:61655163	AGAGTGAAGAATTGT[C/T]CTCAAAAGAGGTGTG	71520
rs26969791	snp	A/G	0.375	0.216506	intron-variant	Grap	GRCm38.p3	11:61655013	ATGGGTAGTTGGCAG[A/G]CCTTGGGGTGCAGCT	71520
rs26969792	snp	A/G	0.408163	0.193609	intron-variant	Grap	GRCm38.p3	11:61654977	TTTCAGTGAGGGAGC[A/G]GAAGGAAAGCACAAG	71520
rs26969793	snp	C/T	0.375	0.216506	intron-variant	Grap	GRCm38.p3	11:61654800	GTACAGTCCCTGGGG[C/T]ACCTACTGTGCAGAG	71520
rs26969794	snp	A/G	0.165289	0.235211	intron-variant	Grap	GRCm38.p3	11:61654719	CACTTGAGGCTGGAG[A/G]GTAGCTGGCCTATTA	71520
rs26969795	snp	C/T	0.48	0.0979796	intron-variant	Grap	GRCm38.p3	11:61654310	GTGGAAGACCATGGC[C/T]TGGCTGCAGTGAGCG	71520
rs26969796	snp	C/T	0.277778	0.248452	intron-variant	Grap	GRCm38.p3	11:61653976	CTCACCTGAGCCACT[C/T]TCACTCACAGTGGTT	71520
rs26969797	snp	C/T	0.277778	0.248452	intron-variant	Grap	Mm_Celera	11:61653880	AAAATAAGCAGACAT[C/T]CTAACTTAATTGGGC	71520
rs26969798	snp	C/T	0.132653	0.220748	synonymous-codon	Grap	Mm_Celera	11:61653379	GTACAGCTTCCAGGC[C/T]ACCGAGAGTGACGAG	71520
rs26969799	snp	G/T	0.493827	0.0552116	upstream-variant-2KB	Grap	Mm_Celera	11:61652580	TGAGAGGAGACGGTT[G/T]GAAGTGTCTTGAACG	71520
rs26969800	snp	A/G	0.489796	0.070696	upstream-variant-2KB	Grap	Mm_Celera	11:61652338	CACAGCCTTCCCTTA[A/G]CAATCGCAGAGCTGT	71520
rs26969801	snp	C/T	0.336735	0.234472	upstream-variant-2KB	Grap	Mm_Celera	11:61652194	CACAGCCTGGGTTCT[C/T]TAGCTGTCCCTGTGT	71520
rs30525608	snp	A/G	0.444444	0.157135	intron-variant	Grap	GRCm38.p3	11:61662914	ACACTTTTAATCCAG[A/G]TCTTTGGAACTAGGA	71520
rs45635535	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61654214	CCACCCTGAGCCCTG[A/G]CTCGAAGATTCAAGC	71520
rs45666083	snp	A/T			intron-variant	Grap	GRCm38.p3	11:61656628	CCTGAATGGGCGTGG[A/T]GGAACAGCCACGATC	71520
rs45700728	snp	A/G			intron-variant	Grap	Mm_Celera	11:61665040	GGTCAGGGCCTGGTG[A/G]CATGGCTTAGGACTC	71520
rs45709701	snp	C/G			intron-variant	Grap	Mm_Celera	11:61663998	TTGCCTGGCCTGGTA[C/G]GGACAGCAGGGACAG	71520
rs45724140	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61655656	AATAATATATAAAGA[A/G]CTCTTTTGTCTTGTT	71520
rs45865769	snp	A/T			intron-variant	Grap	GRCm38.p3	11:61666457	GCTCTCTGGAAGACA[A/T]ATTGGTTGGGGACAT	71520
rs45870391	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61669774	AACTCCAGATTTCCC[C/T]CAGATCAGGGTCTGG	71520
rs45886244	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61656383	CGATTGCCTGGACAG[A/G]ATTGGAAATCCTATC	71520
rs45906989	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61670240	GAATGTATGTCTGGG[C/T]GCCTGCTGAGTCCCA	71520
rs45962531	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61669670	AAGGTAAATAAGTTG[C/T]TGGAAGTCACACAGT	71520
rs46001105	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61662151	AACAAACGAACGAAC[A/G]AACAAACAAACAATG	71520
rs46063044	snp	G/T			intron-variant	Grap	Mm_Celera	11:61664614	CTGTTTCCACACAGA[G/T]AAAATAGGTCATTGG	71520
rs46099667	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61666801	CCCTGAGACCCTTCT[C/T]TCATGGCTGATGGGA	71520
rs46128926	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61656590	GGGGGGTGCACAGAG[C/T]ATGAATTAGATACAG	71520
rs46397891	snp	C/T			intron-variant	Grap	Mm_Celera	11:61663099	TGTAGATTTTGGAGC[C/T]ATGTCCAGGCATGGC	71520
rs46421952	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61666558	TGGTCATCCCTCACC[C/T]GTGATGATGAGGTCA	71520
rs46437353	snp	A/G			utr-variant-3-prime, downstream-variant-500B	Slc5a10, Grap	GRCm38.p3	11:61672975	CTGAGAACTTGAAGC[A/G]CCTGTCTTCCCACTG	71520
rs46471614	snp	C/T			intron-variant	Grap	Mm_Celera	11:61665570	AGGATAGCCCAGCCT[C/T]AGTAACTCCTGGAAG	71520
rs46523250	snp	C/G			intron-variant	Grap	Mm_Celera	11:61663226	GGGTCAGTAAGCGAG[C/G]GGCTGGCTGGAAAGG	71520
rs46566879	snp	C/G/T			intron-variant	Grap	GRCm38.p3	11:61666397	GGACCTGAAGGGGAG[C/G/T]CCCCTGTTCAGAGGC	71520
rs46708763	snp	G/T			synonymous-codon	Grap	Mm_Celera	11:61664194	CCACAGGTGGTACTC[G/T]GGCAGGATCTCTCGA	71520
rs46722868	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61667215	ACCTGGCAGGGAACT[A/G]TCTCCCCATCGCCCA	71520
rs46786111	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61661911	GTATGCATCATGTTA[C/T]GAAAGTGGGAGGTAG	71520
rs46843192	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61667097	ATGAGCAGGGCTGGG[C/T]TGCCAGATCCCAGTG	71520
rs46851888	snp	A/G			intron-variant	Grap	Mm_Celera	11:61663638	GAGAACTGACTGGTT[A/G]TCCTCTGGTCTACAT	71520
rs46883631	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61661959	ACTATAGCTGCCCAC[C/T]GCCTGCCTAGGTGGG	71520
rs46929606	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61666825	GATGGGAGATAGATC[C/T]CAATTAAAGTGTCTT	71520
rs47116186	snp	A/T			intron-variant	Grap	GRCm38.p3	11:61656312	TGATCTAAAAAACAA[A/T]TTTTTTTTTTTTTTT	71520
rs47217620	snp	G/T			intron-variant	Grap	GRCm38.p3	11:61655704	ATTTTTCTACATAGG[G/T]TTCCTCCATGTAGCC	71520
rs47230966	snp	A/T			upstream-variant-2KB	Grap	Mm_Celera	11:61651895	TAGAAAACCACCGTC[A/T]TGAAAAAAAAAAAAA	71520
rs47320288	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61670577	TGTGACCCTCAGGGA[C/T]AAGGCCGGGCTGGGC	71520
rs47357905	snp	A/G			intron-variant	Grap	Mm_Celera	11:61663198	CTAGCCTAGGACTCA[A/G]TACAATGCCCTGGGG	71520
rs47472803	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61670129	AGGGCAAGGGGGAAA[A/G]ACAGCATAGAAGGTG	71520
rs47480501	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61662007	TATAGGCTGGGCGGC[A/G]GTGGCACACACCTTT	71520
rs47660284	snp	G/T			intron-variant	Grap	GRCm38.p3	11:61655931	GTGGCAGACAATGAA[G/T]TGACATAATGATCTA	71520
rs47675953	snp	C/T			intron-variant	Grap	Mm_Celera	11:61665913	GGGGTCTGAGGGGTG[C/T]CAGGCACGGGAAACA	71520
rs47705489	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61671167	GCTTCTTCCTTCCTG[A/G]GCTGAGCCCAATAAT	71520
rs47751013	snp	A/G			intron-variant	Grap	Mm_Celera	11:61663205	AGGACTCAATACAAT[A/G]CCCTGGGGTCAGTAA	71520
rs47789171	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61658815	GTTCTCTGGGGAAGG[A/G]GGTCCCACAGCTCCA	71520
rs47858710	snp	C/G			intron-variant	Grap	GRCm38.p3	11:61670331	GGTCTTTCTGTGTGT[C/G]TCTCCCTGGTCTGAA	71520
rs47884472	snp	A/T			intron-variant	Grap	GRCm38.p3	11:61656197	GAATTTAAAAAGCTT[A/T]AAATTTTTGCACTAG	71520
rs47928913	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61670848	GGGGAGGAGGTTCTC[C/T]GACTTCCCACAATCA	71520
rs48178252	snp	C/T			intron-variant	Grap	Mm_Celera	11:61663157	ACCACCACCACCTCC[C/T]AAAGAATCCTTCTAG	71520
rs48181464	snp	C/T			intron-variant	Grap	Mm_Celera	11:61663098	ATGTAGATTTTGGAG[C/T]TATGTCCAGGCATGG	71520
rs48422803	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61667847	GTTGGAAAGTTCTAG[A/G]ACTCCTGGCCCCATG	71520
rs48469719	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61661211	GAGAGAAAAGCATAT[C/T]GTGATGCCTGGGTGC	71520
rs48484106	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61670359	GAAATGCACTGTGTA[A/G]TACAGATGGGCCTTG	71520
rs48503638	snp	C/T			intron-variant	Grap	Mm_Celera	11:61663797	CCTGTAACTCCCTCT[C/T]TGGGAGACCTGACAC	71520
rs48506277	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61669827	GAGGTATTGGGTTTT[C/T]CCCCCCAGTTATGGT	71520
rs48561543	snp	A/C			intron-variant	Grap	Mm_Celera	11:61665854	CACTCCGAGACGAGA[A/C]GGGGCAGCAGAGTCC	71520
rs48767457	snp	A/G			intron-variant	Grap	Mm_Celera	11:61663134	AGCCTCCCGTTCCTG[A/G]GGACCCCACCACCAC	71520
rs48801068	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61653966	TTCATTTGTTCTCAC[C/T]TGAGCCACTTTCACT	71520
rs48801573	snp	C/G			intron-variant	Grap	GRCm38.p3	11:61656296	GAGTTTGAGGTCAGC[C/G]TGATCTAAAAAACAA	71520
rs48880665	snp	C/G/T			intron-variant	Grap	GRCm38.p3	11:61669572	GGGAGGGCTCAGAGG[C/G/T]GCCCAGGGACGATGC	71520
rs48896374	snp	G/T			intron-variant	Grap	GRCm38.p3	11:61656143	TGTTTGACTCATAAA[G/T]GGGCTGTAGCCTACA	71520
rs49003432	snp	A/G			intron-variant	Grap	Mm_Celera	11:61664935	GAAGGGGATGATGAA[A/G]TTCCATCCATAGCAG	71520
rs49017614	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61654216	ACCCTGAGCCCTGGC[C/T]CGAAGATTCAAGCAC	71520
rs49152455	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61655313	AGCCCAGAGCCTGGG[A/G]GAGAGGGAGCACCCA	71520
rs49161900	snp	A/T			intron-variant	Grap	Mm_Celera	11:61663177	AATCCTTCTAGGCCC[A/T]GCGCTCTAGCCTAGG	71520
rs49195722	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61670895	CCTCTTTCTTGATAG[C/T]CTGCTATGTAGCCTG	71520
rs49231558	snp	C/T			intron-variant	Grap	Mm_Celera	11:61664005	GCCTGGTACGGACAG[C/T]AGGGACAGATTGCCT	71520
rs49236193	snp	A/T			intron-variant	Grap	Mm_Celera	11:61663581	CTTCTCACCAAGCCC[A/T]GTGACTTGATTTCAG	71520
rs49279554	snp	A/T			intron-variant	Grap	GRCm38.p3	11:61655097	CATGGGGAGTGAGGC[A/T]GGAGGCTAAGGGTTG	71520
rs49294266	snp	A/C			intron-variant	Grap	Mm_Celera	11:61665692	ACTCCTCTTGAGCTC[A/C]CCACAGACCCAGGCT	71520
rs49305099	snp	C/G			intron-variant	Grap	Mm_Celera	11:61665849	GGACACACTCCGAGA[C/G]GAGACGGGGCAGCAG	71520
rs49540093	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61667086	GGCTGGGGAATATGA[A/G]CAGGGCTGGGCTGCC	71520
rs49690780	snp	C/G			intron-variant	Grap	GRCm38.p3	11:61656587	TCTGGGGGGTGCACA[C/G]AGTATGAATTAGATA	71520
rs49752851	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61671082	GGTTTCTGAGACCCC[A/G]TCTCCCAAACCCCTG	71520
rs49832572	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61656013	CATGTTGTGGTGACC[C/T]CCAACCATGGAATTA	71520
rs49915810	snp	G/T			intron-variant	Grap	GRCm38.p3	11:61669550	GACACTGAAGAGGTG[G/T]GAGAGAGGGAGGGCT	71520
rs50019586	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61670128	CAGGGCAAGGGGGAA[A/G]AACAGCATAGAAGGT	71520
rs50041782	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61660640	ACACAGGGACAGGGG[A/G]TCAGAATAGTGGGAT	71520
rs50045600	snp	G/T			intron-variant	Grap	GRCm38.p3	11:61668586	CTTTCCGACTGGAAG[G/T]CCGAGTGAGATGCTT	71520
rs50111507	snp	A/G			intron-variant, downstream-variant-500B	Slc5a10, Grap	GRCm38.p3	11:61673127	CTAGAGGAGGGTGAA[A/G]TAGGCCAGTGAGGGA	71520
rs50203369	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61656299	TTTGAGGTCAGCCTG[A/G]TCTAAAAAACAATTT	71520
rs50263490	snp	A/G			intron-variant	Grap	GRCm38.p3	11:61670807	TGCTGTGGAGAGGGA[A/G]GGAAGTGTGACTCCA	71520
rs50388019	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61667633	GCCTCTTTTCCAGAA[C/T]TCAGCTCTTGGGTTT	71520
rs50492435	snp	C/T			intron-variant	Grap	GRCm38.p3	11:61659526	GCATTGCCAATGCTC[C/T]ATACCAACTATAGGG	71520

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