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
rs13473711	snp	A/G	0.429688	0.173817	synonymous-codon	Wsb2	GRCm38.p3	5:117370811	GCTGGCCTTCAGCCC[A/G]TGGCCCTCTCCACCC	59043
rs13473713	snp	A/G	0.391111	0.206368	utr-variant-3-prime	Wsb2	Mm_Celera	5:117378271	TGTGCTGTCTGTCAC[A/G]TGTGTTTGTCTCTGC	59043
rs13473714	snp	A/G	0.231111	0.249285	synonymous-codon	Wsb2	Mm_Celera	5:117370862	TCACCATCCCCAGGC[A/G]CCTGATGTTTCTTGC	59043
rs13473715	snp	C/T	0.375	0.216506	synonymous-codon	Wsb2	Mm_Celera	5:117363658	CTGGAAGTCAAGCTG[C/T]GAGACCTGGAGCGTG	59043
rs29522730	snp	C/T	0.444444	0.157135	intron-variant	Wsb2	Mm_Celera	5:117364850	GTCTTTGTTTCCTTT[C/T]TGTTTGTTTTTTTTC	59043
rs29623433	snp	C/T	0.375	0.216506	intron-variant	Wsb2	GRCm38.p3	5:117376254	ATCAGCTTAAAAAGC[C/T]GGTTTTCACGGTGGC	59043
rs29628807	snp	C/T	0.5	0	intron-variant	Wsb2	GRCm38.p3	5:117360282	CGCTCATTAGCTTAA[C/T]TGAGCCCTCCTCTCC	59043
rs29634959	snp	C/T	0.5	0	intron-variant	Wsb2	GRCm38.p3	5:117359625	GACCCCAGATGCATG[C/T]TAACCACAAACTCAA	59043
rs29728111	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Wsb2, LOC105246773	Mm_Celera	5:117358801	AAATATTTCAAGTTT[A/G]ATTTATGCCATGAAA	59043
rs29728654	snp	A/C	0.375	0.216506	intron-variant	Wsb2	GRCm38.p3	5:117371051	AGCTGCTTCCACCTT[A/C]CCCTGACCTCCACCT	59043
rs29774185	snp	C/T	0.375	0.216506	intron-variant	Wsb2	GRCm38.p3	5:117375350	AAAGGAAATCTGATT[C/T]TCATCAAGGTTTACA	59043
rs29777355	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Wsb2, LOC105246773	GRCm38.p3	5:117358412	ACCACCTCCCCCCCC[A/C]CACACACACACTTTT	59043
rs29781652	snp	C/G/T	0.375	0.216506	intron-variant	Wsb2	GRCm38.p3	5:117367080	ACCCCACAACCATAA[C/G/T]ATTATTTTCACTGCT	59043
rs29818358	snp	A/G	0.375	0.216506	intron-variant	Wsb2	Mm_Celera	5:117365059	AGAGAACACAGAAGT[A/G]CATCAGACTTGTTCT	59043
rs29819194	snp	C/T	0.375	0.216506	intron-variant	Wsb2	GRCm38.p3	5:117367046	AACCCTTTAATACAG[C/T]TCCTCATGGCGTGGT	59043
rs33044922	snp	C/T	0.375	0.216506	intron-variant	Wsb2	Mm_Celera	5:117365493	TGTTGTTGTTATTTT[C/T]CTCTAGAGTACTCTT	59043
rs33052078	snp	A/G	0.387812	0.208586	synonymous-codon	Wsb2	GRCm38.p3	5:117371216	TTGGGACCTGAATAA[A/G]CACGGTAGGGGCAGG	59043
rs33055447	snp	A/G	0.375	0.216506	intron-variant	Wsb2	GRCm38.p3	5:117372010	GAAATGGCCTCTCAT[A/G]GGATGCTGGTCAGAA	59043
rs33063188	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Wsb2, LOC105246773	Mm_Celera	5:117358116	ACCAGAGGGCTGGCA[A/G]GGCCGGATGGGGTTG	59043
rs33079941	snp	A/T	0.375	0.216506	intron-variant	Wsb2	Mm_Celera	5:117362253	GTGGGGGCTGAGGGA[A/T]CTTAGGACAACCTGG	59043
rs33080988	snp	A/G	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117365977	GGTGCCGTATTACAC[A/G]AGAGAGGCATGTACA	59043
rs33099855	snp	A/G	0.5	0	intron-variant	Wsb2	GRCm38.p3	5:117359751	ACATGGACACAGAGC[A/G]CTGATTATTATGATG	59043
rs33122204	snp	G/T	0.375	0.216506	downstream-variant-500B	Wsb2, Rfc5	Mm_Celera	5:117378651	GAAGCAAAACAAAAC[G/T]TTTAAACCAAACATA	59043
rs33143804	snp	C/T	0.375	0.216506	intron-variant	Wsb2	Mm_Celera	5:117365017	GTAGTCATTGTACAT[C/T]GTCTTCAGTTGGCAC	59043
rs33158529	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Wsb2, LOC105246773	Mm_Celera	5:117358403	TGTGACCAGACCACC[C/T]CCCCCCCCACACACA	59043
rs33159174	snp	C/T	0.375	0.216506	intron-variant	Wsb2	GRCm38.p3	5:117367033	TTCCTGATGCTGCAA[C/T]CCTTTAATACAGCTC	59043
rs33194792	snp	A/C/T	0.551111	0.120411	intron-variant	Wsb2	GRCm38.p3	5:117376985	GATGCTGTTTTTATC[A/C/T]GGGAAGTCTACAGCT	59043
rs33222389	snp	C/T	0.387812	0.208586	intron-variant	Wsb2	GRCm38.p3	5:117370974	GTGCAGGGCGGTGTG[C/T]GCGTGGCTTGTGGTC	59043
rs33233371	snp	C/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Wsb2, LOC105246773	GRCm38.p3	5:117356605	CAACTACAGGAACTA[C/T]TTAAAACCCCTTTTC	59043
rs33234196	snp	A/G	0.444444	0.157135	intron-variant	Wsb2	GRCm38.p3	5:117371688	ACAGCCTGCATGTGG[A/G]GGCCAGAGGACAGTT	59043
rs33237894	snp	C/T	0.444444	0.157135	intron-variant	Wsb2	GRCm38.p3	5:117360389	GTCCTGACCCAGCCG[C/T]GGCGGGCCATGCAGG	59043
rs33253069	snp	C/T	0.444444	0.157135	intron-variant	Wsb2	Mm_Celera	5:117372798	AGAGATACTGCCCCT[C/T]CCCTGCCCCACAGTG	59043
rs33302924	snp	C/T	0.429688	0.173817	intron-variant	Wsb2	GRCm38.p3	5:117372700	TCCTGTTAATTTTGG[C/T]GATCTCCACAGTCCA	59043
rs33306836	snp	G/T	0.32	0.24	intron-variant	Wsb2	GRCm38.p3	5:117375956	AGTAAGGACCCTGTG[G/T]GGTTATGCGGGTTAC	59043
rs33318618	snp	A/C/T	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117376383	TTGTTTCCCAGTGTG[A/C/T]ACTTGCTACAGTTTT	59043
rs33341300	snp	A/T	0.444444	0.157135	intron-variant	Wsb2	GRCm38.p3	5:117360320	TTGGCTTTCCCACTT[A/T]TCCGTACGTCACGTG	59043
rs33354559	snp	A/T	0.444444	0.157135	intron-variant	Wsb2	Mm_Celera	5:117368093	TGTTTTTCTTTTTTT[A/T]AAAAAAATATTTATT	59043
rs33382668	snp	A/G	0.32	0.24	intron-variant	Wsb2	Mm_Celera	5:117365628	ACCAAAACAAGAAAT[A/G]TATTCACTAGTGTGT	59043
rs33480022	snp	C/T	0.465374	0.126941	intron-variant	Wsb2	GRCm38.p3	5:117372532	GAGCACACTCCAGCC[C/T]GTAGATGGCTATGTC	59043
rs33537422	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Wsb2, LOC105246773	GRCm38.p3	5:117358512	GGCAGAGCTGTTGGG[A/C]GCTACCAAGCTACTG	59043
rs33541787	snp	C/T	0.444444	0.157135	intron-variant	Wsb2	Mm_Celera	5:117364798	TCCTTCAGGGAATTC[C/T]TCCTCCTCCTCCGAT	59043
rs33564658	snp	A/C	0.375	0.216506	intron-variant	Wsb2	Mm_Celera	5:117362331	TCTGGGGGTGGGAAA[A/C]CACACATTTCGTGCA	59043
rs33568973	snp	A/G	0.475309	0.108333	intron-variant	Wsb2	Mm_Celera	5:117367371	GCTGGGCTAGGATGC[A/G]CTTGCCGAGAACTCT	59043
rs33611259	snp	A/T	0.5	0	intron-variant	Wsb2	GRCm38.p3	5:117367235	GAAAACCATTGCTAG[A/T]GCCTCCTGTTCCCTT	59043
rs33621429	snp	C/T	0.444444	0.157135	intron-variant	Wsb2	GRCm38.p3	5:117372596	TTGAATAAAGCACTC[C/T]TCTCATTCTTGAGGG	59043
rs33655429	snp	C/T	0.375	0.216506	intron-variant	Wsb2	GRCm38.p3	5:117375488	TCGTATCTGAGATCT[C/T]CCTCAGCCCTGCTTC	59043
rs33683463	snp	A/G	0.375	0.216506	intron-variant	Wsb2	Mm_Celera	5:117363800	TAGGAGGCCCGTGGC[A/G]GGGAGCTGGGCACTT	59043
rs33716854	snp	A/G	0.375	0.216506	synonymous-codon	Wsb2	Mm_Celera	5:117377537	GAAAGAGTTCCTCAC[A/G]TACAGGACTTTCTAG	59043
rs33726689	snp	C/T	0.432133	0.171253	intron-variant	Wsb2	Mm_Celera	5:117371280	AGGGCTATTTCATGT[C/T]GAGCTGCCTTCCTCC	59043
rs36256421	snp	A/G	0.293367	0.24621	intron-variant	Wsb2	GRCm38.p3	5:117373957	GCTGCTGCCTTCCTA[A/G]GGTGCAGGAGTTTCC	59043
rs36266902	snp	C/G	0.451843	0.147511	intron-variant	Wsb2	Mm_Celera	5:117374045	CTTTTGCCTAGCTGA[C/G]ACCCGGAGGCTTTAC	59043
rs36342988	snp	A/T	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117369877	TCTGCTGGTCAGATA[A/T]ACCTTGAGGAATAGT	59043
rs36372035	snp	A/G	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117372435	GTCTTAGCATTAAGA[A/G]TACTGCTCAGTGCCC	59043
rs36419322	snp	G/T	0.426035	0.177515	intron-variant	Wsb2	Mm_Celera	5:117373781	ATTGTCCTGCTAGCG[G/T]GCTTGAACAGAGTGC	59043
rs36419401	snp	C/T	0.391111	0.206368	intron-variant	Wsb2	GRCm38.p3	5:117367441	TGCTTCAATGCAGGC[C/T]GGTGACACTCAGCCG	59043
rs36439179	snp	A/G	0.32	0.24	intron-variant	Wsb2	GRCm38.p3	5:117370304	GCCGGATAAACAGGG[A/G]AACAGCAGAGTGAAA	59043
rs36456227	snp	C/T	0.391111	0.206368	intron-variant	Wsb2	GRCm38.p3	5:117368787	TCGGTGTCTGCATCC[C/T]GGGATGAGGCTCTTC	59043
rs36460017	snp	A/G	0.366231	0.221338	intron-variant	Wsb2	GRCm38.p3	5:117374091	GAGGCCTGATGAATC[A/G]CCTTCTGTTCTTGTG	59043
rs36530209	snp	A/G	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117372145	AGCCCACATACCCAC[A/G]AACAGACTGCACACA	59043
rs36627311	snp	A/C	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117373708	ACCATACCCTGAGCA[A/C]AGAGCGCAGTGGTTC	59043
rs36701683	snp	A/G	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117369615	ACCAGGTAGGCTAGA[A/G]AGTCCGAGATCTCCA	59043
rs36702980	snp	A/G	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117371016	CTGCCAGTTGGCTGC[A/G]GAGTGGGTGCCAGCC	59043
rs36772592	snp	A/C	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117371997	TCTGGAGAGGTTAGA[A/C]ATGGCCTCTCATGGG	59043
rs36777039	snp	A/T	0.231111	0.249285	upstream-variant-2KB, intron-variant	Wsb2, LOC105246773	Mm_Celera	5:117355971	CACGTTAAAAAGAAC[A/T]GGGAAATAGTGGAAA	59043
rs36819345	snp	C/T	0.132653	0.220748	intron-variant	Wsb2	Mm_Celera	5:117367377	CTAGGATGCACTTGC[C/T]GAGAACTCTGACCTC	59043
rs36875036	snp	C/T	0.32	0.24	intron-variant	Wsb2	GRCm38.p3	5:117367654	ATTAAATGAAACAAG[C/T]GGTACATACTCCTCA	59043
rs36899527	snp	A/G	0.231111	0.249285	upstream-variant-2KB, intron-variant	Wsb2, LOC105246773	Mm_Celera	5:117356348	GGTTCCTACCGTTCC[A/G]GCTCAAAAAACATGG	59043
rs36915432	snp	C/T	0.124444	0.216185	intron-variant	Wsb2	GRCm38.p3	5:117367372	CTGGGCTAGGATGCA[C/T]TTGCCGAGAACTCTG	59043
rs36924546	snp	C/G	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117372049	CGCGGTCCAGCTCAT[C/G]ATCACAGACACCTAG	59043
rs36967950	snp	C/T	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117372860	GCAGATGAAGATGGG[C/T]CTGCTAGCAAGGACC	59043
rs36981807	snp	A/G	0.32	0.24	intron-variant	Wsb2	GRCm38.p3	5:117368871	AGTTATGGCCTCCAG[A/G]GTTCAGTGTGGCCTT	59043
rs37005043	snp	C/T	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117372907	CACCTGACTTAGACA[C/T]ACTACTGCTAAGCTG	59043
rs37059799	snp	A/T	0.391111	0.206368	intron-variant	Wsb2	GRCm38.p3	5:117370412	TTGCTTCTCTCTAGG[A/T]CCAAAACCCAAGAGA	59043
rs37066249	snp	A/G	0.408163	0.193609	intron-variant	Wsb2	GRCm38.p3	5:117368732	TCAGGATCCGTGACA[A/G]AGGCCAGATGATGAT	59043
rs37078265	snp	A/G	0.231111	0.249285	upstream-variant-2KB, intron-variant	Wsb2, LOC105246773	Mm_Celera	5:117356223	CAAAACAGACAACTG[A/G]TAAACCGCGGGTATC	59043
rs37090424	snp	A/G	0.426035	0.177515	intron-variant	Wsb2	Mm_Celera	5:117373313	TCCACATGTACCCAA[A/G]AATCTGCGAGTTCTT	59043
rs37107111	snp	A/G	0.495868	0.0452663	intron-variant	Wsb2	Mm_Celera	5:117370464	CTCCTTGGAGCCTCT[A/G]TGATCTACTTGTCTC	59043
rs37120401	snp	C/T	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117372491	GGCCTTAGCAGCAGA[C/T]CAAAGGAGTAGCACT	59043
rs37156558	snp	C/T	0.391111	0.206368	intron-variant	Wsb2	GRCm38.p3	5:117368928	ACAGCAATCTCTCTC[C/T]AGATAATGGCTTCCG	59043
rs37162385	snp	A/G	0.132653	0.220748	intron-variant	Wsb2	GRCm38.p3	5:117373884	TGTGCACCGAGCTGC[A/G]CACCTTTGCCGTCCT	59043
rs37169406	snp	C/T	0.426035	0.177515	intron-variant	Wsb2	GRCm38.p3	5:117369548	TCAACATATGTTGAC[C/T]TGTAAGCTACGACAA	59043
rs37171602	snp	C/T	0.18	0.24	intron-variant	Wsb2	Mm_Celera	5:117373306	AGTGGGCTCCACATG[C/T]ACCCAAAAATCTGCG	59043
rs37179194	snp	C/T	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117369582	AAAGAATTGTTGGAG[C/T]AAAAACAGAAACAGC	59043
rs37187936	snp	A/G	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117369012	GCACAGAAATGAGAG[A/G]CCAGGATCCCAACAA	59043
rs37277687	snp	A/T	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117372702	CTGTTAATTTTGGCG[A/T]TCTCCACAGTCCATA	59043
rs37316283	snp	C/G	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117370082	CTGTGGTTGGCTGAT[C/G]TGTGGGTTGGTCCCA	59043
rs37390498	snp	A/G	0.391111	0.206368	intron-variant	Wsb2	GRCm38.p3	5:117370485	TACTTGTCTCACAAG[A/G]CAGGTCACCCCATCT	59043
rs37413727	snp	A/T	0.391111	0.206368	intron-variant	Wsb2	GRCm38.p3	5:117367541	GTTTATGTAGGCCAC[A/T]TTAGGATCCCCAAGG	59043
rs37451637	snp	A/G	0.231111	0.249285	synonymous-codon	Wsb2	Mm_Celera	5:117371192	ATCCCGGGATAAGAC[A/G]CTTCGAATTTGGGAC	59043
rs37509029	snp	C/T	0.459184	0.136902	intron-variant	Wsb2	GRCm38.p3	5:117373675	GTCCAGGCCTGACAG[C/T]GTGATGCACAGCCCC	59043
rs37543996	snp	A/G	0.375	0.216506	intron-variant	Wsb2	GRCm38.p3	5:117369495	TCACCCTTTGTCTCT[A/G]TACACCACACATGCA	59043
rs37631215	snp	C/T	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117373721	CAAAGAGCGCAGTGG[C/T]TCTCGCAGCCAGGTT	59043
rs37708334	snp	A/G	0.124444	0.216185	intron-variant	Wsb2	Mm_Celera	5:117370292	AGCTGGAGGCAAGCC[A/G]GATAAACAGGGGAAC	59043
rs37799541	snp	A/G	0.231111	0.249285	intron-variant	Wsb2	Mm_Celera	5:117372766	AGAGTGTTCTCATCC[A/G]AACTCCTCAATCACT	59043
rs37970783	snp	A/G	0.132653	0.220748	intron-variant	Wsb2	Mm_Celera	5:117367403	ACCTCGTGACCCAGC[A/G]GAGTCAATTGTTTTA	59043
rs38057465	snp	A/G	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117373515	CAAGAAGAGAATGCT[A/G]TCCCTCATCTTTCTT	59043
rs38059837	snp	C/G	0.297521	0.245442	intron-variant	Wsb2	Mm_Celera	5:117373681	GCCTGACAGCGTGAT[C/G]CACAGCCCCTGACCA	59043
rs38228543	snp	A/G	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117369844	AATCAACTTAGTCTG[A/G]AAAAGTGGAGCTTGC	59043
rs38229893	snp	C/T	0.48	0.0979796	intron-variant	Wsb2	GRCm38.p3	5:117369655	GCTGCCATTTTAAAA[C/T]GTATTGTCCTATGCA	59043
rs38237254	snp	A/G	0.444444	0.157135	intron-variant	Wsb2	GRCm38.p3	5:117370241	ATGGGCTGTCATGTC[A/G]AGAGAGGGCTCACTG	59043

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