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
rs3715103	snp	C/T	0.444444	0.157135	upstream-variant-2KB	Rnf123, Mst1, Mir7088	GRCm38.p3	9:108080055	GACTACTGTGATGGG[C/T]ACCACACCTCTACAG	84585
rs4227915	snp	C/G	0.48	0.0979796	intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108052431	TGACCTGACCCACCC[C/G]CTGGTTCACTTACAA	84585
rs4227916	snp	A/G	0.436656	0.166311	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	Rnf123, Amigo3	Mm_Celera	9:108052494	AGGCAAGGTAGTGCC[A/G]GGTGCTAGGGGCTCT	84585
rs8240616	in-del	-/A	0.375	0.216506	upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079564	TACCTTGCCTGGAGG[-/A]NNCCTGACCCACATG	84585
rs8240617	in-del	-/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079565	ACCTTGCCTGGAGGN[-/G]NCCTGACCCACATGC	84585
rs8240618	in-del	-/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108079566	CCTTGCCTGGAGGNN[-/G]CCTGACCCACATGCA	84585
rs13470922	snp	C/T	0.231111	0.249285	synonymous-codon, downstream-variant-500B, nc-transcript-variant	Rnf123, Amigo3	GRCm38.p3	9:108056048	CCTCCTGGTGCACGG[C/T]CCAACCTCAGAGTGA	84585
rs29590617	snp	A/C	0.484429	0.0868505	intron-variant	Rnf123	GRCm38.p3	9:108064093	CACAGGGGAACGGAT[A/C]TGAGTGGTGATGACA	84585
rs29591029	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Rnf123, Amigo3	Mm_Celera	9:108053108	AGCCAATGGGAACTT[A/G]GGTCCCCGCCCCTGA	84585
rs29600065	snp	C/T	0.432133	0.171253	intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055441	AGCTACAGGCAGACC[C/T]AATCCCTAAGGCTCA	84585
rs29602266	snp	A/C	0.444444	0.157135	intron-variant, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108056139	AAGGGGAGGGAAGGA[A/C]GATGAAGTGGTTCCA	84585
rs29603889	snp	C/T	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime, intron-variant	Rnf123, Mst1	GRCm38.p3	9:108079352	GGCCAAACCGCGTGC[C/T]CGCTCGAGCGCTGCT	84585
rs29694349	snp	A/G	0.49827	0.0293608	intron-variant	Rnf123	GRCm38.p3	9:108056720	TGAATCTAAACCACC[A/G]GCAGGTAGCCAGGAA	84585
rs29736527	snp	C/T	0.48	0.0979796	upstream-variant-2KB, intron-variant	Rnf123, Mst1, Mir7088	Mm_Celera	9:108081125	GTTAAAGTACTAATG[C/T]GCTCATGCTCACCAC	84585
rs29741418	snp	C/T	0.465374	0.126941	intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054366	TCAGGATGGTAGCAT[C/T]GCTGTGTTGGCTGAT	84585
rs29743766	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108058496	CGGGGTATGTATCCC[C/T]CAAGCTACTTACTGT	84585
rs29791847	snp	G/T	0.375	0.216506	synonymous-codon, downstream-variant-500B, upstream-variant-2KB, utr-variant-5-prime	Mst1, Mir7088, Rnf123	Mm_Celera	9:108081591	GCTTCCAGATTATGT[G/T]CGGACCTGCATTATG	84585
rs29795241	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108060439	TCTCAGAGTCTCTAC[C/T]AGGATTAAGTGATGG	84585
rs29825851	snp	G/T	0.5	0	intron-variant	Rnf123	Mm_Celera	9:108063781	GGACGGGGCAGGGGG[G/T]GTCATGCCTCCATCC	84585
rs29830998	snp	A/G	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108064955	GCTGGGATTAAAGGC[A/G]TGAGCCACCACGCCT	84585
rs29841586	snp	A/C	0.497778	0.0332592	intron-variant	Rnf123	Mm_Celera	9:108065527	AGTCTCTTGTGCCCG[A/C]GGAAGGCACTGCTGG	84585
rs29880471	snp	C/T	0.459184	0.136902	intron-variant	Rnf123	GRCm38.p3	9:108059059	GATTAAGGCATAGAT[C/T]CACTGTGGGGATTGG	84585
rs29894165	snp	A/G	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108077254	ACAGCTGGGAGCCTA[A/G]TGAGAATAGGACACC	84585
rs29930943	snp	C/T	0.429688	0.173817	intron-variant	Rnf123	GRCm38.p3	9:108058123	GGGCTACCAGCCTCT[C/T]TGGAGCCATCACCAG	84585
rs29933460	snp	A/G	0.5	0	intron-variant	Rnf123	GRCm38.p3	9:108075866	AGACTTAAAACTACT[A/G]CCTGTGGAGCTAACA	84585
rs29946565	snp	A/C	0.48	0.0979796	intron-variant	Rnf123	Mm_Celera	9:108059339	GTCTTGCTACAATGG[A/C]AAGCTACTCTGCCTG	84585
rs29982935	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108067244	TTTCCTAGGAACTGA[C/T]TTACACAGGACTACT	84585
rs29983208	snp	C/T	0.48	0.0979796	intron-variant, utr-variant-5-prime, nc-transcript-variant	Rnf123	GRCm38.p3	9:108078327	ATTAGTTTTCTTGCA[C/T]GCGTGCACGCGCTCA	84585
rs29986886	snp	C/T	0.484429	0.0868505	intron-variant, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108056016	CCAGTTCCCAGGAGG[C/T]CAGCAGTCCCCAACA	84585
rs30029385	snp	C/T	0.375	0.216506	intron-variant	Rnf123	Mm_Celera	9:108061265	ACGTTGTTGAAGAAA[C/T]GGAGAACCGGGACTA	84585
rs30037645	snp	A/G	0.465374	0.126941	intron-variant, utr-variant-5-prime	Rnf123, Amigo3	Mm_Celera	9:108053268	AGCGTTGTGCCTCTC[A/G]AGCCATGGGCCATAG	84585
rs30124349	snp	A/G	0.375	0.216506	intron-variant	Rnf123	Mm_Celera	9:108077468	AGAGAAAAAAGGCAC[A/G]TGGTCAGAGCAGCTC	84585
rs30135775	snp	A/T	0.391111	0.206368	intron-variant	Rnf123	Mm_Celera	9:108056343	GCTGAGGTGCGGGAC[A/T]TCTAGATCCTTACCA	84585
rs30178216	snp	A/G	0.375	0.216506	intron-variant, downstream-variant-500B, upstream-variant-2KB	Mst1, Mir7088, Rnf123	Mm_Celera	9:108081762	CCCAGTGTGCACTGT[A/G]GTAAGAATCTTTGTC	84585
rs30180698	snp	A/G	0.48	0.0979796	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108054471	GCACCACAACCAGAC[A/G]CTTGAGTACAATGTG	84585
rs30217128	snp	C/T	0.375	0.216506	missense, nc-transcript-variant	Rnf123	Mm_Celera	9:108066317	CGGGGGTTGGAAGCT[C/T]TGTATTCATCCCAAT	84585
rs30223385	snp	C/G	0.32	0.24	intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	Mm_Celera	9:108055394	GCATACACACCTACA[C/G]GACCCTCCTACAGAG	84585
rs30227658	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108060954	CTATTCAACATAGCA[C/T]TGGGGATCACAGCCA	84585
rs30277324	snp	A/G	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108064936	CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA	84585
rs30278931	snp	A/G	0.498615	0.0262793	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108053412	ATCAGGTATACTACT[A/G]TGCATGTTGGGTGCT	84585
rs30282838	snp	A/G	0.277778	0.248452	intron-variant	Rnf123	Mm_Celera	9:108066556	GCAGGCTGAGGTGGC[A/G]GATGCCCAGGCTGCA	84585
rs30326944	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108059656	AGATCGTGAATGGCC[C/T]CATCACCTGGGAGTT	84585
rs30333350	snp	C/T	0.5	0	intron-variant	Rnf123	Mm_Celera	9:108071359	CCTCACCCACCCCAC[C/T]CCTGAGAACACCTCC	84585
rs30380920	snp	A/C	0.498615	0.0262793	intron-variant	Rnf123	GRCm38.p3	9:108057039	GCATTAAGAATGCAG[A/C]GACGCCTGCCTAAGA	84585
rs30382918	snp	A/C/T	0.375	0.216506	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108054507	GCAAAAGGCTCGCCC[A/C/T]GAGCCAGAGACTTTC	84585
rs30427123	snp	A/T	0.48	0.0979796	intron-variant	Rnf123	GRCm38.p3	9:108071778	TAAATAAGTCTTTTT[A/T]AAAAATGATTGCTAC	84585
rs30468021	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	GRCm38.p3	9:108062504	TCCCTCCCAGTATAC[C/T]TAGGACCCTGTGCAA	84585
rs30524227	snp	C/T	0.375	0.216506	intron-variant, nc-transcript-variant, upstream-variant-2KB	Mst1, Mir7088, Rnf123	Mm_Celera	9:108081543	GAGTAACAGGGGCCA[C/T]GAGGCCTCAGGCCCT	84585
rs33279253	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB, synonymous-codon, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108051215	TGAGTCATGCATCGT[A/G]GGCTGGCGCTGCCGT	84585
rs33280265	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108051482	AGGGCTGGCCAAGCA[C/T]CCACTTTGCCATCAG	84585
rs33280267	snp	C/T	0.231111	0.249285	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108051805	TGGGTAAACAGGGCC[C/T]GGTCTGCGGCTGATG	84585
rs33280269	snp	A/G	0.124444	0.216185	missense, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108051865	GAGGACATGGCGCTT[A/G]TGTTGGCTGCCTTGT	84585
rs33280271	snp	C/T	0.132653	0.220748	intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108051995	GAGTGCTACCTCGTG[C/T]GTCCTAATTTGCCTC	84585
rs33280273	snp	A/G	0.124444	0.216185	synonymous-codon, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	Mm_Celera	9:108052112	GCAGAGGTCCTCTTC[A/G]TTGGTGGGCTACAGG	84585
rs33281005	snp	C/G	0.142012	0.225474	intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108052166	GATCCTTACCCCTGT[C/G]CTGGTGTTTACAGAT	84585
rs33281007	snp	C/G	0.231111	0.249285	intron-variant, upstream-variant-2KB, downstream-variant-500B	Rnf123, Amigo3, Gmppb	GRCm38.p3	9:108052343	CATCAGGGCCCCTGT[C/G]GTCTGAGAACTCAGT	84585
rs33281009	snp	A/C	0.124444	0.216185	intron-variant, upstream-variant-2KB	Rnf123, Amigo3	Mm_Celera	9:108052840	CCCCAGAACCTCACA[A/C]GTCGTCGTCCGACGT	84585
rs33281011	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Rnf123, Amigo3	GRCm38.p3	9:108053010	GCTTCCAGCCAAGCA[A/G]ACTGGGACACTGGGG	84585
rs33281216	snp	C/T	0.124444	0.216185	intron-variant	Rnf123	Mm_Celera	9:108058152	AGGGCTGGTCTAACC[C/T]GAACACTCACTTTGG	84585
rs33281218	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108058883	GGGCAATGAAGACTG[C/T]GGCCGGGAATAAAGG	84585
rs33281220	snp	A/G	0.465374	0.126941	intron-variant	Rnf123	Mm_Celera	9:108059117	GCTCTAACTCATTCT[A/G]GAACATGCCTGGTGA	84585
rs33281222	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108059219	AGGCACAAGACAAGT[A/G]AGGGCCCGCCAGCTT	84585
rs33282025	snp	C/T	0.231111	0.249285	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108053526	GTTGAGCTGTGCGGG[C/T]CGTGGGTTACAGGAC	84585
rs33282027	snp	C/T	0.124444	0.216185	intron-variant, missense	Rnf123, Amigo3	Mm_Celera	9:108053690	TCCTGGGCCATGGTG[C/T]GTTCACCAATGCCAG	84585
rs33282029	snp	C/T	0.475309	0.108333	intron-variant, synonymous-codon	Rnf123, Amigo3	GRCm38.p3	9:108054168	GTCCCGAGTGCGCTT[C/T]TTTGAGCACAGCCGG	84585
rs33282031	snp	A/G	0.124444	0.216185	intron-variant, synonymous-codon	Rnf123, Amigo3	Mm_Celera	9:108054342	TGAGCTGCTTGTGGC[A/G]CCAGCCTCTCAGGAT	84585
rs33282405	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Rnf123	Mm_Celera	9:108059802	CTCAATGGTCCGTAG[A/G]CAGACACGCAGTAAC	84585
rs33282407	snp	C/G	0.165289	0.235211	intron-variant	Rnf123	Mm_Celera	9:108059853	CTCCTGCAGGAGGCA[C/G]AGAGGAGGCATTTAC	84585
rs33282409	snp	A/G	0.260355	0.249785	intron-variant	Rnf123	GRCm38.p3	9:108059923	AAAGGCCTACCCAGG[A/G]CAGTGGCCTCACAAC	84585
rs33282410	snp	A/G	0.124444	0.216185	intron-variant	Rnf123	Mm_Celera	9:108060236	TTTCTGAAGCTGAAG[A/G]TCATGGAGCAGAGAC	84585
rs33282412	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108060725	GGCAGCTGTAGTCCA[A/G]GAAAGCACTCACACT	84585
rs33282413	snp	A/G	0.345679	0.230967	intron-variant	Rnf123	GRCm38.p3	9:108061909	TATGGCCTCATGGCC[A/G]TATCTCTCACCTGAC	84585
rs33282965	snp	A/G	0.142012	0.225474	intron-variant, missense	Rnf123, Amigo3	Mm_Celera	9:108054895	GGCTCAGAGGGTCTC[A/G]TGATGAGCTAGACTG	84585
rs33282967	snp	C/T	0.486111	0.0821678	intron-variant, utr-variant-3-prime, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055157	CCTGGCATCAGAGTC[C/T]GGGGACCACCCCCAG	84585
rs33282970	snp	A/G	0.244898	0.249948	intron-variant, utr-variant-3-prime	Rnf123, Amigo3	GRCm38.p3	9:108055696	TAAAAGTGGTACATG[A/G]TCATCGCTGGGCCTT	84585
rs33282971	snp	C/T	0.32	0.24	intron-variant, downstream-variant-500B	Rnf123, Amigo3	GRCm38.p3	9:108055895	TTTACACATCACCAG[C/T]TACTCTTTGCCTCAG	84585
rs33283375	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108062002	TCGTTTCTGCCAGTG[C/T]TGACCAGTGGTGACC	84585
rs33283377	snp	A/G	0.32	0.24	intron-variant	Rnf123	Mm_Celera	9:108062087	GGGGTCTGAGCTAGT[A/G]TGAGCATCCAGGACA	84585
rs33283379	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108062139	ATAGCTGGCTAGGCC[C/T]GAGGCTTTGGTGACA	84585
rs33283380	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108062401	TCAGCCAGCCTTGCT[C/T]TTAACACTCAGTGCA	84585
rs33283382	snp	C/T	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Rnf123	GRCm38.p3	9:108062574	TACCCTCTTAGGGCA[C/T]CGACGGAGCTTGTCC	84585
rs33283966	snp	C/T	0.142012	0.225474	synonymous-codon, downstream-variant-500B, nc-transcript-variant	Rnf123, Amigo3	Mm_Celera	9:108056054	TGAGGTTGGGCCGTG[C/T]ACCAGGAGGCGTACC	84585
rs33283971	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108057225	AGTTCTGAGTCACAT[A/G]CCTGTCGGGCAGATG	84585
rs33283973	snp	A/T	0.336735	0.234472	intron-variant, downstream-variant-500B	Rnf123	GRCm38.p3	9:108057562	AAGGAAGAACTTGCT[A/T]TGTGAATCTACACAA	84585
rs33284124	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108063024	GCCCTCAACTGGGGA[A/G]CACAACACGGCATGA	84585
rs33284126	snp	C/G	0.132653	0.220748	intron-variant	Rnf123	Mm_Celera	9:108063352	TCTTATCCTCAGACT[C/G]TGCTTCCTGTGCCCT	84585
rs33284129	snp	C/T	0.260355	0.249785	intron-variant	Rnf123	Mm_Celera	9:108064126	GGCAGGCTGGGCAGG[C/T]GGGCTTGCACAGCTT	84585
rs33284131	snp	C/T	0.142012	0.225474	intron-variant	Rnf123	GRCm38.p3	9:108064434	CCTTGCCATCTCAGC[C/T]TCCGGCAGCCCCTCG	84585
rs33284945	snp	G/T	0.244898	0.249948	intron-variant, downstream-variant-500B	Rnf123	GRCm38.p3	9:108057682	CCCTCTCTGCAAGCT[G/T]CACAGCCCAAGGTCT	84585
rs33284964	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108065548	GCACTGCTGGCTAAA[C/T]AGGAGATCAGATACA	84585
rs33284966	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	Mm_Celera	9:108065573	GATACAGCCTAGCAG[A/G]TCACCCTGTCTCAAC	84585
rs33284968	snp	C/T	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108065609	AGAGAGTCTTGGGCA[C/T]CCTCTGGTGGACACA	84585
rs33284972	snp	A/G	0.426035	0.177515	intron-variant	Rnf123	GRCm38.p3	9:108067311	ACCAGGGCAGAAGAG[A/G]CCCCAGGTGCCCGGT	84585
rs33285884	snp	C/T	0.132653	0.220748	intron-variant	Rnf123	Mm_Celera	9:108067793	GAGAGAGACCAGCTT[C/T]GGCCTCCTGGTCAGT	84585
rs33285886	snp	A/G	0.231111	0.249285	intron-variant, synonymous-codon	Rnf123	Mm_Celera	9:108068100	AGGTATTACATGGCA[A/G]ATCTGTCTGGCAACA	84585
rs33285888	snp	C/T	0.444444	0.157135	intron-variant	Rnf123	Mm_Celera	9:108068605	GTATACCTTGCGCTG[C/T]GGCAAAGGGCAGGCA	84585
rs33285890	snp	A/G	0.231111	0.249285	intron-variant	Rnf123	GRCm38.p3	9:108068613	TGCGCTGCGGCAAAG[A/G]GCAGGCACTAGTAAA	84585
rs33285892	snp	G/T	0.32	0.24	intron-variant	Rnf123	GRCm38.p3	9:108068905	GGCAGGTAACACGCT[G/T]AGCACCCGAGGCCCC	84585
rs33285893	snp	C/T	0.124444	0.216185	intron-variant	Rnf123	Mm_Celera	9:108069487	CATTTTTATGCTTAC[C/T]TGCTCAATGGAGACA	84585
rs33286795	snp	A/G	0.32	0.24	intron-variant	Rnf123	GRCm38.p3	9:108069580	TGTGTACACACCACA[A/G]CAGCTAGGCCTGCCA	84585

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