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
rs3692649	snp	A/C	0.290657	0.246672	intron-variant	Rnf212	Mm_Celera	5:108732801	CTGTTGTTGGAGAAG[A/C]CAAGCCTCGGAAGGA	671564
rs3693219	snp	A/G	0.5	0	intron-variant	Rnf212	Mm_Celera	5:108732868	TTCTATACGACCACC[A/G]TAACTAGAACCCTTT	671564
rs6161637	snp	A/G	0.444444	0.157135	downstream-variant-500B, upstream-variant-2KB	Tmed11, Rnf212	Mm_Celera	5:108776852	CAATATTAAAGGCAG[A/G]TTTATTGGGAAGCTG	671564
rs6162623	snp	G/T	0.5	0	downstream-variant-500B, upstream-variant-2KB	Tmed11, Rnf212	Mm_Celera	5:108776987	atagagatagataga[G/T]aGAGAGAGATAAAGA	671564
rs29523509	snp	A/G	0.375	0.216506	intron-variant	Rnf212	GRCm38.p3	5:108739666	GCTACCTATGAGCTG[A/G]CAAGTATTCATGCAA	671564
rs29524388	snp	A/C	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108743879	GGTGTATACTGATGC[A/C]TGGTTGTTTGATCTG	671564
rs29525794	snp	G/T	0.5	0	intron-variant	Rnf212	Mm_Celera	5:108748447	AATATTCTCAATACA[G/T]ATATCTACTCTACAT	671564
rs29545037	snp	A/G	0.188366	0.242283	intron-variant	Rnf212	Mm_Celera	5:108746083	ACACCAGGAGCACAG[A/G]TAATATCACCGTCTT	671564
rs29560272	snp	C/T	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108750521	CCTACACTGGGGCAT[C/T]GAGCCTTCACATGAC	671564
rs29564985	snp	A/G	0.49827	0.0293608	intron-variant	Rnf212	Mm_Celera	5:108759429	AGAGAGACATAGAAA[A/G]AGAGAACACAAAGGA	671564
rs29565498	snp	A/G	0.415225	0.187619	intron-variant	Rnf212	Mm_Celera	5:108731531	TACCTTGGATTAAAA[A/G]CACAATCTATAAAGT	671564
rs29567306	snp	A/G	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108731037	GGCTACATGGTCTAA[A/G]CAATGTGCCTAGTAC	671564
rs29578539	snp	A/G	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108744711	GCTTCTACAGCAAGC[A/G]CTTGATTCACTGAGA	671564
rs29583854	snp	C/T	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108744695	GAACTTAGGTCCTCA[C/T]GCTTCTACAGCAAGC	671564
rs29583921	snp	G/T	0.277778	0.248452	intron-variant	Rnf212	Mm_Celera	5:108749343	CATTAGTGCCTACTT[G/T]TTGTGGCTTACCATC	671564
rs29630134	snp	C/G	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108739652	CTAGAGCCATGCTTG[C/G]TACCTATGAGCTGAC	671564
rs29632535	snp	C/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108743806	GAAGCCCTGCTCTGC[C/T]TTGCCCCAAAATAAA	671564
rs29636631	snp	C/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108738199	GATACAGCCAACCAT[C/T]ATACTGAACATGGGG	671564
rs29684608	snp	C/T	0.265928	0.249492	intron-variant	Rnf212	Mm_Celera	5:108746946	CACTTGGTAATGACC[C/T]AGCCTTGTGAAAGAG	671564
rs29726806	snp	C/T	0.32	0.24	intron-variant	Rnf212	Mm_Celera	5:108745059	CATTATCTTAAGAGT[C/T]TCTCCTAAAATGGTT	671564
rs29730664	snp	C/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108737531	ACAGAAGTGGATGCT[C/T]ACAGCCATCCATTGT	671564
rs29768280	snp	C/T	0.265928	0.249492	downstream-variant-500B	Rnf212	Mm_Celera	5:108727614	ATCTGCTGAATTCCT[C/T]GGCATGGCTTTCAAC	671564
rs29774798	snp	G/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108739647	GCCTGCTAGAGCCAT[G/T]CTTGCTACCTATGAG	671564
rs29778801	snp	A/T	0.455	0.143091	utr-variant-3-prime	Rnf212	Mm_Celera	5:108728665	ACTGGAGTAGTCCAG[A/T]GGGCAGCCTGCCTGC	671564
rs29780229	snp	A/G	0.401235	0.199068	upstream-variant-2KB	Rnf212	Mm_Celera	5:108775944	GGCCCTTAAAAAATT[A/G]GAGGTCCAAATTATG	671564
rs29813001	snp	C/T	0.465374	0.126941	intron-variant	Rnf212	Mm_Celera	5:108730774	AGATACTCAGCAACA[C/T]ACTTGCTCTGTGTGT	671564
rs29825086	snp	A/G	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108749004	AGACTATAACATGGA[A/G]TAATATGATTGTCCA	671564
rs33069806	snp	C/T	0.498615	0.0262793	utr-variant-3-prime	Rnf212	Mm_Celera	5:108728834	TCCTGTGGTGTTGAA[C/T]TCTGAGAGATGCAAG	671564
rs33069833	snp	C/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108749527	CAAAGTATATAAAGG[C/T]TTGGAAATAGTTAAT	671564
rs33139812	snp	C/T	0.455	0.143091	utr-variant-3-prime	Rnf212	Mm_Celera	5:108728569	GAAATGAGGCTTATC[C/T]CTGCTCAGCAGCCCA	671564
rs33145282	snp	G/T	0.5	0	intron-variant	Rnf212	Mm_Celera	5:108746236	TTTCCAGCTGTAAGG[G/T]ATCAGCTGTGACTGT	671564
rs33167470	snp	C/T	0.265928	0.249492	intron-variant	Rnf212	Mm_Celera	5:108750161	ACTTCTGTTCTAAAG[C/T]CATATCCTGGAACCT	671564
rs33184928	snp	A/C	0.290657	0.246672	intron-variant	Rnf212	Mm_Celera	5:108749007	CTATAACATGGAATA[A/C]TATGATTGTCCAGTG	671564
rs33192125	snp	C/T	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108738722	ATGCTAGAAAAAGCC[C/T]TTGAAAAACTCCAAC	671564
rs33193420	snp	C/G	0.32	0.24	utr-variant-5-prime	Rnf212	Mm_Celera	5:108775034	GAGGCCACTGAAGTA[C/G]GAACGCACGGCTCAG	671564
rs33219444	snp	G/T	0.465374	0.126941	intron-variant	Rnf212	Mm_Celera	5:108773243	ATTTAAGAAATTTGT[G/T]TTACCTGAAAAAGTC	671564
rs33221507	snp	C/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108741269	CAGAAAATTGAGACT[C/T]GATCTACCTCAAGAC	671564
rs33266120	snp	C/T	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108746545	GAGAAAGTGAGCATA[C/T]ACAAGAGGCAAGCTG	671564
rs33291154	snp	C/T	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108750533	CATCGAGCCTTCACA[C/T]GACCAAGATACCTCC	671564
rs33299391	snp	C/T	0.277778	0.248452	intron-variant	Rnf212	Mm_Celera	5:108744172	AGCTGTAATAGCAGC[C/T]ACTGTCAAGGGCTGG	671564
rs33302662	snp	G/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108734637	CCTCAAAGATAGAGG[G/T]CTAATGTCCAATGTA	671564
rs33306843	snp	C/G	0.484429	0.0868505	intron-variant	Rnf212	Mm_Celera	5:108731296	GCCAAACCAGTCTGT[C/G]TCTGCTTCTGTGAAG	671564
rs33313542	snp	C/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108744012	GAGAACTCGGCCTTG[C/T]GCCCCCTAGTGTCTA	671564
rs33319338	snp	C/G	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108731921	GGTCCATTAAGTACC[C/G]CAAGCCCATTTGAGT	671564
rs33349669	snp	G/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108737546	TACAGCCATCCATTG[G/T]ACTGAGCACAGGGCC	671564
rs33351395	snp	C/T	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108750480	TCCTCCACCCACCTA[C/T]CCCCTCCCTCCTCCC	671564
rs33358296	snp	C/T	0.48	0.0979796	utr-variant-5-prime	Rnf212	Mm_Celera	5:108775076	AGCTCTGCGCCTGCG[C/T]TCATTCCAGCGCATG	671564
rs33358627	snp	A/G	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108746845	GGTCCTAGAAGTAAC[A/G]CACAATAATGAACTC	671564
rs33361551	snp	C/T	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108758346	TGAAAGAAGCTTTTG[C/T]CCCTCAAAGTCCATC	671564
rs33395470	snp	C/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108749207	GGGTTACTCAATTTT[C/T]ACAAATTCTTACACC	671564
rs33409090	snp	C/T	0.290657	0.246672	intron-variant	Rnf212	Mm_Celera	5:108745576	TAAGTAGGTAAGCAA[C/T]GACAGCTTTGGTGAA	671564
rs33423094	snp	C/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108741163	ACAAGTGACAGCTCA[C/T]GCTGGTAGGATGTGG	671564
rs33469227	snp	C/T	0.444444	0.157135	synonymous-codon	Rnf212	Mm_Celera	5:108729476	CCTAGGGGATGCTGA[C/T]CCTGTGGGAAGCATT	671564
rs33525392	snp	C/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108738774	TAGAGAGATTAGGGA[C/T]AAAAGGGACATACCT	671564
rs33533587	snp	C/G	0.277778	0.248452	intron-variant	Rnf212	Mm_Celera	5:108744923	CTGGAAAGATCACTA[C/G]ACAAGACCCGTCAGG	671564
rs33541655	snp	A/C	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108741240	CAGCCATGAAAATCA[A/C]TATGGCAGTTTCCCA	671564
rs33555012	snp	A/G	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108734770	TGAGGAGCATCTAAA[A/G]AAATGTTCATCAGGG	671564
rs33583257	snp	G/T	0.375	0.216506	intron-variant	Rnf212	Mm_Celera	5:108744655	CACTCTTGTGCCTGG[G/T]TTTCATGTGGGTTTT	671564
rs33600086	snp	C/T	0.444444	0.157135	intron-variant	Rnf212	Mm_Celera	5:108740700	AACAAGTACACTAAA[C/T]CTAATAGAAGAGAAA	671564
rs33608852	snp	A/C	0.48	0.0979796	intron-variant	Rnf212	Mm_Celera	5:108773306	GAACATGGATCATAA[A/C]ATGAGCTAAGTTAAG	671564
rs33638115	snp	A/G	0.444444	0.157135	synonymous-codon	Rnf212	Mm_Celera	5:108747442	AGGAGTCAGGTCAAT[A/G]TCCATTGACTCTATT	671564
rs33649025	snp	C/G	0.32	0.24	intron-variant	Rnf212	Mm_Celera	5:108749876	TAATATCCCTGCTTA[C/G]TGTCTGCTGCATGTT	671564
rs33675311	snp	A/C/T	0.444444	0.157135	intron-variant	Rnf212	GRCm38.p3	5:108746743	ACAAGTGCACACGTT[A/C/T]GTAGCTACCTTGGAT	671564
rs33675474	snp	A/G	0.375	0.216506	upstream-variant-2KB, intron-variant	1700047L14Rik, Rnf212	Mm_Celera	5:108762493	TTATGTTGATTATAT[A/G]CTATTCATGATTTTA	671564
rs33707706	snp	C/G	0.277778	0.248452	intron-variant	Rnf212	Mm_Celera	5:108739921	TGGGGAGCTCCATCT[C/G]CTGTCCTTCCCTCAA	671564
rs33721445	snp	C/T	0.265928	0.249492	intron-variant	Rnf212	Mm_Celera	5:108744255	ACCGATAACAAAGCC[C/T]GAGTCCTGCACTTAA	671564
rs33725433	snp	A/T	0.32	0.24	intron-variant	1700047L14Rik, Rnf212	Mm_Celera	5:108764373	TTTATTTTTATTTTT[A/T]TTTTTGGTACTAAGT	671564
rs33742105	snp	A/G	0.48	0.0979796	intron-variant	Rnf212	Mm_Celera	5:108772727	GCTGGGATTAACAGC[A/G]AAGGTAGTTTGTGCC	671564
rs33745667	snp	A/C	0.455	0.143091	intron-variant	Rnf212	Mm_Celera	5:108729704	GGAGCCAGTACTGGC[A/C]GGAGTGTGAGGTTTC	671564
rs33760444	snp	G/T	0.48	0.0979796	intron-variant	1700047L14Rik, Rnf212	Mm_Celera	5:108765786	ATTTTCTGAGGAACC[G/T]CCAGACTGATTTCCA	671564
rs45657082	snp	C/T	0.260355	0.249785	intron-variant	Rnf212	Mm_Celera	5:108757142	GACAACATATTTCAG[C/T]TGTAGAGGACACAGG	671564
rs45658369	snp	C/T	0.124444	0.216185	intron-variant	Rnf212	Mm_Celera	5:108733574	TCAACATACACCACT[C/T]ACAACTCCAGTATCA	671564
rs45678667	snp	C/T			intron-variant	Rnf212	Mm_Celera	5:108743076	AGCATTTCATGGATG[C/T]CTCGTAGAAAATATA	671564
rs45689966	snp	C/T	0.231111	0.249285	intron-variant	Rnf212	Mm_Celera	5:108756239	TTAGATCTGGTCTTG[C/T]CACAAGGAAATAGGA	671564
rs45712136	snp	C/G/T	0.35503	0.226867	intron-variant	1700047L14Rik, Rnf212	GRCm38.p3	5:108768113	TCTCAAACACACAAA[C/G/T]GTAACAAGGGCACAT	671564
rs45722035	snp	C/T	0.244898	0.249948	nc-transcript-variant, intron-variant	1700047L14Rik, Rnf212	Mm_Celera	5:108763868	AGGTCCTGATGCCAA[C/T]ACTCCTGCTACCTTC	671564
rs45729478	snp	A/G	0.231111	0.249285	intron-variant	Rnf212	Mm_Celera	5:108750078	AGATTAAGATAGTCT[A/G]TGCTTGCAACCAGTC	671564
rs45733971	snp	A/G	0.124444	0.216185	nc-transcript-variant, intron-variant	1700047L14Rik, Rnf212	Mm_Celera	5:108768809	GTGCTGCAGAGGTTT[A/G]TAAACAGTACGATAT	671564
rs45748391	snp	C/T	0.444444	0.157135	downstream-variant-500B	Rnf212	Mm_Celera	5:108727792	CATCTTAGCATTTAG[C/T]CATCAGGTATTTATT	671564
rs45829773	snp	C/T	0.231111	0.249285	intron-variant	1700047L14Rik, Rnf212	Mm_Celera	5:108768209	ATAAAATATCTCAGG[C/T]TAACTTATTCTTTGG	671564
rs45837593	snp	A/G			intron-variant	Rnf212	Mm_Celera	5:108744473	GTGTGTATGTACCTA[A/G]AGCCCAGAGACCTAA	671564
rs45842875	snp	A/G	0.231111	0.249285	upstream-variant-2KB	Rnf212	Mm_Celera	5:108776548	AGGCCCATGTCACAT[A/G]CTCTGCCTGATAGTA	671564
rs45852484	snp	C/T	0.244898	0.249948	intron-variant	Rnf212	Mm_Celera	5:108745569	CAGCCCTTAAGTAGG[C/T]AAGCAATGACAGCTT	671564
rs45863048	snp	A/G	0.244898	0.249948	intron-variant	Rnf212	Mm_Celera	5:108758761	TTTCTGTAGCATTGT[A/G]TCCACACCAATCAGG	671564
rs45914570	snp	C/T			intron-variant	Rnf212	Mm_Celera	5:108733696	CAACAGTCTTGCTGG[C/T]TACAGAGTCCTTATA	671564
rs45918796	snp	A/G	0.244898	0.249948	intron-variant	Rnf212	Mm_Celera	5:108757214	CTTTAAGTGCGGGTC[A/G]CAGCATGTTCTACTT	671564
rs45928960	snp	C/T	0.124444	0.216185	intron-variant	Rnf212	Mm_Celera	5:108756837	AAGGAAAACAAACCT[C/T]CCAGGTGCTGGTAAA	671564
rs45949150	snp	A/G	0.260355	0.249785	intron-variant	Rnf212	Mm_Celera	5:108744933	CACTAGACAAGACCC[A/G]TCAGGGCAATGGACT	671564
rs45962641	snp	C/T	0.124444	0.216185	intron-variant	Rnf212	Mm_Celera	5:108732067	AGAGTTTTAGTCTCA[C/T]GAAGTTGCCCCTGAG	671564
rs45981975	snp	A/C			intron-variant	Rnf212	Mm_Celera	5:108742093	CGTGACACTGCCTGG[A/C]TGACCAGGAATCAGA	671564
rs46036161	snp	A/C/T	0.124444	0.216185	intron-variant	Rnf212	GRCm38.p3	5:108729051	CTATGCCACTGGAGA[A/C/T]TCACAGCACAAGGAA	671564
rs46081173	snp	C/T	0.391111	0.206368	utr-variant-3-prime	Rnf212	Mm_Celera	5:108728442	TGAATGAAAACAACT[C/T]AGAACAGGTATGTTA	671564
rs46142152	snp	A/C	0.231111	0.249285	intron-variant	Rnf212	Mm_Celera	5:108731180	TGGCCTTTGATGCTC[A/C]AAATGTGTGTGAGAG	671564
rs46181531	snp	C/T			intron-variant	Rnf212	Mm_Celera	5:108744638	CTCAGTACCAGGCTG[C/T]GCACTGTTGTGCCTG	671564
rs46217655	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	1700047L14Rik, Rnf212	Mm_Celera	5:108762414	TTTTCAAAAAGGCGA[A/C]TGTATTCTCCACTAC	671564
rs46232570	snp	A/G	0.336735	0.234472	intron-variant	Rnf212	Mm_Celera	5:108757209	AGGAACTTTAAGTGC[A/G]GGTCACAGCATGTTC	671564
rs46275942	snp	C/T	0.132653	0.220748	intron-variant	Rnf212	Mm_Celera	5:108758159	ACCTGAGCTCTGGCT[C/T]TATATTTTTCATGTG	671564
rs46368315	snp	A/C			intron-variant	Rnf212	Mm_Celera	5:108742339	GTTGGGGAAAGAATG[A/C]AGGAGCCAGAGGGAA	671564
rs46381408	snp	C/T			intron-variant	Rnf212	Mm_Celera	5:108733396	ATTTGATTAAGACTC[C/T]TTCCTGGATATCCTG	671564
rs46388378	snp	C/T	0.231111	0.249285	intron-variant	Rnf212	Mm_Celera	5:108748797	AAGGAATAGCCAGAG[C/T]TTCCCAAGGCTGAGT	671564

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