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
rs13467329	snp	C/T	0.444444	0.157135	missense	Chd3	Mm_Celera	11:69345208	GGGGCAGCCTTCAGC[C/T]CCGCACCCGTAGGGG	216848
rs13467330	snp	C/T			utr-variant-3-prime	Chd3	GRCm38.p3	11:69344066	TGCCCCACCACCAAA[C/T]ATACACAGCTTCCCA	216848
rs13474982	snp	A/G			utr-variant-3-prime	Chd3	GRCm38.p3	11:69343473	CTTGCCTGTGGGACC[A/G]AGCAACACAGTGGAT	216848
rs26922758	snp	A/G	0.465374	0.126941	intron-variant, upstream-variant-2KB	Chd3	Mm_Celera	11:69366769	CTGCACATGCGTACT[A/G]AATGCAGGAGGTGGG	216848
rs26922759	snp	C/G	0.277778	0.248452	intron-variant, utr-variant-5-prime	Chd3	Mm_Celera	11:69366452	GACGTCGGTGGCCAG[C/G]AGAGGGAAAGAATGG	216848
rs26922760	snp	C/T	0.207612	0.24638	intron-variant	Chd3	Mm_Celera	11:69365853	TAAGCCCTAATGCCA[C/T]ATAGAAACGGCCGTG	216848
rs26922761	snp	C/T	0.244898	0.249948	intron-variant	Chd3	Mm_Celera	11:69365572	CACCTCTAAATCTGT[C/T]CCAGACATGCTGACA	216848
rs26922762	snp	G/T	0.277778	0.248452	intron-variant	Chd3	Mm_Celera	11:69364916	ATAACTCCTCTAAAT[G/T]TCGCTGCCCCTCAAC	216848
rs26922763	snp	A/G	0.124444	0.216185	intron-variant	Chd3	Mm_Celera	11:69364846	ATCTAAACTTGGAGC[A/G]TCCTTCGTTGTCCCC	216848
rs26922764	snp	A/G	0.396694	0.202437	intron-variant	Chd3	Mm_Celera	11:69363042	TCTGTTTTTACTAGG[A/G]CTTAAGAAAGGGTCC	216848
rs26922765	snp	G/T	0.231111	0.249285	intron-variant	Chd3	Mm_Celera	11:69362909	TTGTGTTAAACCTCA[G/T]CATGTACATCCATGG	216848
rs26922766	snp	A/G	0.132653	0.220748	intron-variant	Chd3	Mm_Celera	11:69362888	TGAAACTAGGGCACT[A/G]AACTGTTGTGTTAAA	216848
rs26922767	snp	A/G	0.142012	0.225474	intron-variant	Chd3	GRCm38.p3	11:69362747	ATCCCTTGAGGCTAC[A/G]CACCAACATTCCTGA	216848
rs26938068	snp	C/T	0.497778	0.0332592	intron-variant	Chd3	Mm_Celera	11:69362746	TATCCCTTGAGGCTA[C/T]GCACCAACATTCCTG	216848
rs26938069	snp	A/G	0.132653	0.220748	intron-variant	Chd3	Mm_Celera	11:69361644	CCCTTGGCACTCTGC[A/G]TTGGGCAGACGAGCA	216848
rs26938070	snp	C/T	0.396694	0.202437	intron-variant	Chd3	Mm_Celera	11:69361376	GCTCACACAAGGGGA[C/T]GTCCTCACCCTTCTT	216848
rs26938071	snp	G/T	0.244898	0.249948	synonymous-codon	Chd3	Mm_Celera	11:69360668	GCCGTCCTTGCACAC[G/T]CGGCAGTACTCCATG	216848
rs26938072	snp	A/G	0.260355	0.249785	intron-variant	Chd3	Mm_Celera	11:69360489	GACGAGCTGGTTGGT[A/G]TCTGGGCCTCAGAAA	216848
rs26938073	snp	C/T	0.124444	0.216185	synonymous-codon	Chd3	Mm_Celera	11:69359910	CATCTCCGCATAGTG[C/T]GGGTCCTTCACCTTG	216848
rs26938074	snp	C/T	0.345679	0.230967	intron-variant	Chd3	Mm_Celera	11:69359526	AACTGTCAAATGTCC[C/T]GGCTAATTGCTCACA	216848
rs26938075	snp	A/G	0.408163	0.193609	intron-variant	Chd3	Mm_Celera	11:69359495	CTGGATCGAGGCACT[A/G]GGCTGAGCAGGAGTG	216848
rs26938076	snp	A/G	0.290657	0.246672	intron-variant	Chd3	Mm_Celera	11:69359316	AATAATATGGATCAT[A/G]CGTTGCACAAAGTTC	216848
rs26938077	snp	C/T	0.265928	0.249492	synonymous-codon	Chd3	GRCm38.p3	11:69359192	CTCATCCTCCTCCCA[C/T]GTGGACTGGTCGTAA	216848
rs26938078	snp	A/G	0.197531	0.244432	synonymous-codon	Chd3	GRCm38.p3	11:69359156	GCTCTGCTTATGGTC[A/G]TCGTACTCTGGGATG	216848
rs26938079	snp	C/T	0.473373	0.11227	intron-variant	Chd3	GRCm38.p3	11:69357325	AGGACAAAGAAATGG[C/T]AGATCTGAGGGTCTC	216848
rs26938080	snp	C/T	0.265928	0.249492	intron-variant	Chd3	Mm_Celera	11:69354850	ATTCGCGAATAAGGC[C/T]GGTAACTGGTACGAG	216848
rs26938081	snp	C/T	0.426035	0.177515	intron-variant	Chd3	GRCm38.p3	11:69354801	GGTGTATATACCTTT[C/T]ATCAGAATCCTAAAG	216848
rs26938082	snp	C/T	0.473373	0.11227	intron-variant	Chd3	GRCm38.p3	11:69353557	GGAAGAAGGGATTTG[C/T]CCTTTACAGGCTGAG	216848
rs26938083	snp	A/G	0.260355	0.249785	synonymous-codon	Chd3	Mm_Celera	11:69352683	GTAGTCAGGATCCAC[A/G]TTCTCCTCCTGCTTG	216848
rs26938084	snp	C/T	0.408163	0.193609	intron-variant	Chd3	Mm_Celera	11:69351538	TTGTGTTGGTCAAGA[C/T]GCCAACCCCTGGACT	216848
rs26938085	snp	A/T	0.5	0	intron-variant	Chd3	Mm_Celera	11:69347934	ACACATACAGCTGAG[A/T]AAGGACGAGGACTAA	216848
rs26938086	snp	C/T	0.396694	0.202437	intron-variant	Chd3	GRCm38.p3	11:69347237	ATCAAGGAATTTAAC[C/T]TCATGGACTTGACTG	216848
rs26938087	snp	A/G	0.152778	0.230321	intron-variant	Chd3	Mm_Celera	11:69346991	TACCTCAACTCTCAC[A/G]ACGCTAACATTCTTT	216848
rs29383007	snp	A/G	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69354211	GAGAAGTAAGAGGCC[A/G]AGTTTACCCCTGGTT	216848
rs29384625	snp	A/G	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69364589	CACATGAGAGAGGGG[A/G]TAAAGTCTCTTGACC	216848
rs29389652	snp	A/G	0.375	0.216506	intron-variant	Chd3	Mm_Celera	11:69350010	ATGTAGGAAGCTCTA[A/G]TTTCCTCTCTCACAC	216848
rs29389759	snp	C/T	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69346336	CAACAGGTGTCACCA[C/T]GTGGTCCCACTCACA	216848
rs29392280	snp	A/G	0.375	0.216506	intron-variant	Chd3	Mm_Celera	11:69354285	GTTTCCAGCGTCCCC[A/G]CCCCGTCTCCCATCC	216848
rs29394778	snp	A/G	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69345376	AGACCGTGGGGAGCA[A/G]GCTGCTTCCCTCCAC	216848
rs29397045	snp	C/T	0.375	0.216506	synonymous-codon	Chd3	GRCm38.p3	11:69357843	CTGATACATGTGCAG[C/T]GTGCCGCCCGTGGCT	216848
rs29401042	snp	A/G	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69345420	ATGGAAGGTTTGTGT[A/G]TATGTACAACGGGCA	216848
rs29402989	snp	A/G	0.444444	0.157135	upstream-variant-2KB, nc-transcript-variant	Chd3, Gm32483	Mm_Celera	11:69371145	AAGCCAAGCAAGAAG[A/G]GCAGATAGCCTGGCT	216848
rs29404964	snp	G/T	0.444444	0.157135	intron-variant, utr-variant-5-prime	Chd3	Mm_Celera	11:69366389	GGCGAGGAAGCCCGT[G/T]AACTCTACTTCCCAC	216848
rs29405715	snp	A/G	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69345717	GACAGTCAGATGGAC[A/G]AGTACAGTCAGGAAG	216848
rs29406023	snp	C/T	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69355613	GCCACACCATCTGTC[C/T]CCGCTCACTGTCCCT	216848
rs29407780	snp	A/G	0.375	0.216506	upstream-variant-2KB, nc-transcript-variant	Chd3, Gm32483	Mm_Celera	11:69371306	TCATGGGGACCCTGA[A/G]GGGAAGGTGGGCAAC	216848
rs29414255	snp	C/T	0.32	0.24	synonymous-codon	Chd3	GRCm38.p3	11:69349192	CTCCATCTTTTCCCC[C/T]ACTTTGCTGTTCTTC	216848
rs29419672	snp	A/G	0.375	0.216506	intron-variant	Chd3	Mm_Celera	11:69354605	GTCACCCTGCTGCCC[A/G]CTCCCATGTCTACTC	216848
rs29420008	snp	C/T	0.444444	0.157135	intron-variant	Chd3	GRCm38.p3	11:69357615	TCAAGGGTGTGCACA[C/T]CAGTCTGCCTGCTGC	216848
rs29423170	snp	C/T	0.375	0.216506	upstream-variant-2KB, nc-transcript-variant	Chd3, Gm32483	Mm_Celera	11:69370978	CTCAGGCCTTTTCAC[C/T]GAACCGGCTGACCTG	216848
rs29424458	snp	C/T	0.375	0.216506	intron-variant	Chd3	Mm_Celera	11:69365798	CCTGACCCCTGCCAG[C/T]CTGCTTAAGGTTTGG	216848
rs29425958	snp	C/T	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69364447	AGGCTCTGAGCTCCT[C/T]CCTCAGTAGACAGTG	216848
rs29429936	snp	A/G	0.444444	0.157135	missense	Chd3	GRCm38.p3	11:69361451	CAGGGCCATCAGGCC[A/G]GCCTGAGGCACTATG	216848
rs29436929	snp	A/G	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69346021	TTAATACATGTTGGC[A/G]AGGGAGTTAAAGAGT	216848
rs29437017	snp	C/G	0.5	0	intron-variant	Chd3	GRCm38.p3	11:69354902	GAGCCAGCCATGCCA[C/G]GCCTTTTATTTTTAA	216848
rs29439893	snp	A/G	0.5	0	utr-variant-3-prime	Chd3	Mm_Celera	11:69343307	TATGTACAACCGATA[A/G]CCTGATACAGAAGAA	216848
rs29440172	snp	C/T	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69345381	GTGGGGAGCAGGCTG[C/T]TTCCCTCCACGTGCA	216848
rs29441844	snp	A/G	0.375	0.216506	synonymous-codon	Chd3	GRCm38.p3	11:69356364	CGGCAAACTCCTCCA[A/G]GAAGCCCTCCAAGTT	216848
rs29444756	snp	C/T	0.375	0.216506	synonymous-codon	Chd3	GRCm38.p3	11:69350185	CCGAGGGACCCCATC[C/T]GCAAACGTTTCGGAG	216848
rs29447512	snp	A/G	0.5	0	intron-variant	Chd3	Mm_Celera	11:69352070	AAGTGAAGTGAGAGA[A/G]TAGAGACAGAAAGTC	216848
rs29447983	snp	A/G	0.32	0.24	intron-variant	Chd3	Mm_Celera	11:69349437	AGGTGGGGCTTAAAG[A/G]AGATAACCAGGGCTA	216848
rs29448156	snp	A/G	0.444444	0.157135	intron-variant	Chd3	GRCm38.p3	11:69345767	GGACCACAGGCCAAG[A/G]ACAAAATGGCAGAGA	216848
rs29453726	snp	A/G	0.375	0.216506	intron-variant	Chd3	Mm_Celera	11:69352730	TCTCCTCAATCTGAG[A/G]GGCAGCAGAGGGAAG	216848
rs29458170	snp	C/T	0.375	0.216506	intron-variant	Chd3	Mm_Celera	11:69353431	ATGGGTGAGATGCCT[C/T]TCCTTCTCCCTCACT	216848
rs29463949	snp	G/T	0.32	0.24	intron-variant	Chd3	Mm_Celera	11:69348907	CCCCATCATCAGTGG[G/T]ATAATACACCCACCA	216848
rs29464020	snp	C/G	0.48	0.0979796	intron-variant	Chd3	Mm_Celera	11:69358024	TCTAGTCTTCAGTCT[C/G]CTTCCGCCCCCGGTC	216848
rs29464463	snp	C/T	0.32	0.24	intron-variant	Chd3	Mm_Celera	11:69349368	CATGTTGAAACTTAA[C/T]GCCCAGGGTAAAGTA	216848
rs29465061	snp	A/G	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69360121	CCCAGAGGACAGAGC[A/G]GGTGCCTGGGAGCTG	216848
rs29466939	snp	A/G	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69346349	CACGTGGTCCCACTC[A/G]CAGGGATCATGTCCC	216848
rs29469089	snp	C/T	0.375	0.216506	upstream-variant-2KB, nc-transcript-variant	Chd3, Gm32483	Mm_Celera	11:69371415	CAGTCCCCCACCCCA[C/T]CCCCACTACACTTTA	216848
rs29470305	snp	C/T	0.5	0	intron-variant	Chd3	GRCm38.p3	11:69348669	TTCCACCTCCCCAGA[C/T]ACCCTCAGGGACTCA	216848
rs29472521	snp	A/G	0.444444	0.157135	intron-variant	Chd3	GRCm38.p3	11:69354038	TGCTGAATGTTACAG[A/G]GGATGCAGGATGCAG	216848
rs29474336	snp	C/T	0.444444	0.157135	intron-variant	Chd3	Mm_Celera	11:69355604	CGAGAAGCAGCCACA[C/T]CATCTGTCCCCGCTC	216848
rs29482040	snp	C/T	0.5	0	intron-variant	Chd3	GRCm38.p3	11:69361379	CACACAAGGGGATGT[C/T]CTCACCCTTCTTCTT	216848
rs29486461	snp	A/C	0.32	0.24	intron-variant, upstream-variant-2KB	Chd3, Gm32483	Mm_Celera	11:69368021	AGAAGGGTCTGTCCC[A/C]AGCACAGCTGGACGT	216848
rs45687933	snp	C/T			intron-variant	Chd3	Mm_Celera	11:69363134	TCAATTCCCAGCACC[C/T]ACATGGTAGCTCATC	216848
rs45743593	snp	C/T			intron-variant	Chd3	Mm_Celera	11:69348009	CAAAGGAGCAGACTT[C/T]GGTTCACAGCCCCAA	216848
rs45747090	snp	A/G			intron-variant	Chd3	GRCm38.p3	11:69349337	GGCTGTGACCTAAGT[A/G]CTCTCTAAAGGGTCA	216848
rs46067963	snp	C/T			intron-variant	Chd3	GRCm38.p3	11:69357676	GCTAGACCTCAGTCC[C/T]CCCGGGAGGCCTAGA	216848
rs46230493	snp	A/G			synonymous-codon	Chd3	Mm_Celera	11:69362267	TCCACTTGGCCCCCA[A/G]GATGGTCATCATCTT	216848
rs46362274	snp	C/G			intron-variant	Chd3	Mm_Celera	11:69348001	GGCTCACGCAAAGGA[C/G]CAGACTTCGGTTCAC	216848
rs46442324	snp	A/G			intron-variant	Chd3	Mm_Celera	11:69362570	AATTATATGGAACCT[A/G]AAGAAAGTTTCCCTT	216848
rs46581793	snp	C/T			intron-variant	Chd3	Mm_Celera	11:69362867	AATTAAGTACCTTGC[C/T]CAAGATGAAACTAGG	216848
rs46639427	snp	A/G			intron-variant	Chd3	Mm_Celera	11:69362989	TAGTCTCTGCTTGGA[A/G]AGTCCCACAGCTGAA	216848
rs46675427	snp	C/T			intron-variant	Chd3	Mm_Celera	11:69349730	AAGCAGAGATTTTTC[C/T]ACCCTGACATCTGGC	216848
rs46745294	snp	A/T			intron-variant, upstream-variant-2KB	Chd3, Gm32483	Mm_Celera	11:69367521	CCAGATCCGGAGTTC[A/T]GAACAGTTAGGCGAG	216848
rs46823845	snp	A/G			intron-variant	Chd3	Mm_Celera	11:69363335	CTGGCAGAGGAGAAG[A/G]TTCAATCCTTCCTGT	216848
rs47302071	snp	A/G			synonymous-codon	Chd3	GRCm38.p3	11:69360632	GGAGGAGATGCAAGC[A/G]TCACAGCACAGGAGC	216848
rs47368910	snp	C/T			intron-variant	Chd3	GRCm38.p3	11:69347965	AGGCTCCTCAGGAAC[C/T]GTGGGAGGGGCTGCA	216848
rs47495940	snp	A/C			intron-variant	Chd3	Mm_Celera	11:69347866	TGTGTGCAGCTCTGC[A/C]GAGAACAGAAGAGTC	216848
rs48074166	snp	C/G			intron-variant	Chd3	GRCm38.p3	11:69346396	GGTACTCTACTGGTC[C/G]CTGGTGTGAACCGTA	216848
rs48180074	snp	A/T			intron-variant	Chd3	GRCm38.p3	11:69355935	TCCCAAGTGCTGAGA[A/T]TAAAAGTGTGGGCAG	216848
rs48547070	snp	A/G			intron-variant	Chd3	Mm_Celera	11:69362458	AAAATATTAATTTAA[A/G]TAATGAGAGAAGTAA	216848
rs48642069	snp	A/G			intron-variant	Chd3	Mm_Celera	11:69345971	ATGGGGAGGAAATAG[A/G]AGGCGTGCGGACAGT	216848
rs48660592	snp	A/G			intron-variant	Chd3	Mm_Celera	11:69347978	ACCGTGGGAGGGGCT[A/G]CAGGGGTGGCTCACG	216848
rs48782683	snp	C/T			intron-variant	Chd3	GRCm38.p3	11:69357678	TAGACCTCAGTCCTC[C/T]CGGGAGGCCTAGAAT	216848
rs48911047	snp	A/G			intron-variant	Chd3	Mm_Celera	11:69347389	TGCCTTCATAAGGTC[A/G]GGCTGTAGGCAAACC	216848
rs48961341	snp	C/T			intron-variant	Chd3	Mm_Celera	11:69364296	TTTTTCAGAGGAAAC[C/T]GAGGCACAGGGAGTC	216848
rs49049580	snp	A/G			intron-variant	Chd3	GRCm38.p3	11:69348061	GTAACTCCACTTATA[A/G]GGGATACAGTACTGT	216848
rs49169688	snp	C/G			intron-variant	Chd3	Mm_Celera	11:69363329	ACAGAGCTGGCAGAG[C/G]AGAAGATTCAATCCT	216848

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