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
rs13465077	snp	A/G	0.444444	0.157135	missense, intron-variant	Cblc, Gm34744	GRCm38.p3	7:19785287	GGACTGCTGCAGATG[A/G]CTCAAGAGACAACTG	80794
rs13465078	snp	C/T			missense	Cblc	GRCm38.p3	7:19792876	CCTGCTGGGAAGTAC[C/T]GTGGGCACCTGTACC	80794
rs13465079	snp	G/T			intron-variant, missense	Cblc, Gm34744	Mm_Celera	7:19786194	TGCAGCTGCTGCCTG[G/T]CTGCCTGGCAGGACT	80794
rs31089813	snp	C/T	0.444444	0.157135	intron-variant	Cblc	GRCm38.p3	7:19792005	AGGAACCTCAATTCT[C/T]AGCCTCTCAGAAGTT	80794
rs31097598	snp	C/T	0.444444	0.157135	intron-variant	Cblc, Gm34744	Mm_Celera	7:19784476	GCTACACGTTCACGG[C/T]GCACAGAAATACATG	80794
rs31111851	snp	A/C	0.444444	0.157135	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19788100	GCTAGATGTCGGTAG[A/C]ACTCTCTGTACATAT	80794
rs31177924	snp	C/T	0.49827	0.0293608	intron-variant	Cblc, Gm34744	Mm_Celera	7:19784708	GGGATGGCATCTTAA[C/T]ATTGGTGCTGAGTAT	80794
rs31209875	snp	A/C	0.444444	0.157135	intron-variant, nc-transcript-variant	Cblc, Gm34744	Mm_Celera	7:19790082	AGGCAGCTGAGGTTA[A/C]AGGTGGAAAACCACT	80794
rs31233612	snp	A/C	0.375	0.216506	intron-variant	Cblc, Gm34744	Mm_Celera	7:19783425	CCTAAAACTAACTAA[A/C]TAAATATGATGATGA	80794
rs31326534	snp	A/T	0.444444	0.157135	intron-variant	Cblc	GRCm38.p3	7:19791493	CAAAACCATTTTTTT[A/T]AAAGATTTATTTATT	80794
rs31473674	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Cblc, Gm34744	GRCm38.p3	7:19790222	TGCAGCCGCTGCCTG[A/G]CTGCAGACATTCCCC	80794
rs31476459	snp	C/T	0.444444	0.157135	intron-variant, nc-transcript-variant	Cblc, Gm34744	GRCm38.p3	7:19789952	TAGCATCTGGCCTAG[C/T]TAGGAAGCATCCCCA	80794
rs31502315	snp	A/G	0.375	0.216506	intron-variant	Cblc, Gm34744	Mm_Celera	7:19788563	TGAGGGGCTGGGGGC[A/G]TGGCTCAGTGGGAGA	80794
rs31505568	snp	A/G	0.375	0.216506	intron-variant	Cblc, Gm34744	Mm_Celera	7:19784207	GGAAGGAAAAGGAGG[A/G]GAGGGGGAGGGGAAG	80794
rs31544246	snp	C/G	0.444444	0.157135	intron-variant	Cblc	Mm_Celera	7:19794154	ATTCCACAATTAAAG[C/G]ACCTGCTGCTGTTTC	80794
rs31594579	snp	A/G	0.444444	0.157135	intron-variant	Cblc, Gm34744	Mm_Celera	7:19784560	GTGTGGTGTGGTGGC[A/G]CACGCCTTTAATCCC	80794
rs31598144	snp	A/G	0.48	0.0979796	intron-variant	Cblc, Gm34744	Mm_Celera	7:19785007	GTCTCCCCTCAGGTC[A/G]GACTGCCAGGCAAAG	80794
rs31709937	snp	C/T	0.375	0.216506	intron-variant	Cblc	GRCm38.p3	7:19790956	CAAGGACATTGTCAC[C/T]GAGCAGCGTCTGGTA	80794
rs31734704	snp	G/T	0.444444	0.157135	intron-variant	Cblc, Gm34744	Mm_Celera	7:19788921	AGCACCACATCCCCA[G/T]ATCTCCGAGATGAGT	80794
rs31752668	snp	C/T	0.375	0.216506	intron-variant	Cblc, Gm34744	Mm_Celera	7:19783526	AAGGACCTAACAATG[C/T]CAAGAACATTTGAAC	80794
rs31796593	snp	C/T	0.32	0.24	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19789362	TAAACCTCTGTCCTT[C/T]CAGGATCCGTGTTCT	80794
rs31828455	snp	A/C/T	0.444444	0.157135	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19787933	GAAGTTAGGAGGCAG[A/C/T]GGCAGATGGAGTTTA	80794
rs31851187	snp	C/T	0.48	0.0979796	intron-variant	Cblc	Mm_Celera	7:19796139	CTTCTAGGAGAGACA[C/T]ACGCCTGCACCCCAG	80794
rs31894628	snp	C/T	0.375	0.216506	intron-variant	Cblc	Mm_Celera	7:19793146	AGCTAAAGTCCAAAC[C/T]GGCCTCCAGCCAGCA	80794
rs31961669	snp	G/T	0.207612	0.24638	intron-variant	Cblc	GRCm38.p3	7:19791709	CAGGTTTATAGCATA[G/T]CCTCTAACTTGTCAA	80794
rs31970687	snp	A/G	0.21875	0.248039	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19788885	AGCAAGGGTTGGCTC[A/G]TATGTACACGGCTCC	80794
rs31999348	snp	A/C	0.375	0.216506	intron-variant	Cblc	GRCm38.p3	7:19795806	CTATGCAGTTGTCCC[A/C]CAAGCCAGAGGGCAG	80794
rs32003050	snp	C/T	0.444444	0.157135	intron-variant	Cblc, Gm34744	Mm_Celera	7:19789878	TGAGAAGCAACAGGT[C/T]TGTGCACCTGTCCCT	80794
rs32004548	snp	C/G	0.5	0	intron-variant	Cblc, Gm34744	Mm_Celera	7:19789803	TCCTTGAGAGTAACA[C/G]TGTTGTTTGTAATGA	80794
rs32119882	snp	A/G	0.375	0.216506	intron-variant	Cblc, Gm34744	Mm_Celera	7:19788467	GGGGCGTGGCTCAGT[A/G]GTAGAGCCCCTGCCT	80794
rs32121120	snp	A/G	0.375	0.216506	intron-variant	Cblc	GRCm38.p3	7:19791935	ACCTCCCAAGTGCTG[A/G]AATTACGGGAAAACC	80794
rs32136445	snp	C/T	0.5	0	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19785069	TAACATCTAAGCATC[C/T]TGTTCTAGACCCTCC	80794
rs32143022	snp	C/T	0.48	0.0979796	intron-variant	Cblc	Mm_Celera	7:19795613	TATTTTCATTATATA[C/T]ACACACACACATACA	80794
rs32155580	snp	C/T	0.46281	0.131194	intron-variant	Cblc, Gm34744	Mm_Celera	7:19789762	GGTATAAAATGGGAT[C/T]ATGAAGGCGACATAA	80794
rs32217502	snp	C/T	0.375	0.216506	intron-variant	Cblc, Gm34744	Mm_Celera	7:19788825	TTGGCGAGGAGGCTG[C/T]AGAGGCGACAGTTCC	80794
rs32247020	snp	C/T	0.5	0	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19789253	CCCAGAGCAAGTGTA[C/T]TCTCCAATCCCTGGG	80794
rs32263030	snp	C/T	0.444444	0.157135	intron-variant	Cblc, Gm34744	Mm_Celera	7:19784376	ACCCAGGTTCGATTC[C/T]CAGCTCCCACATGGC	80794
rs32266034	snp	C/T	0.5	0	intron-variant	Cblc	Mm_Celera	7:19794633	CTAGAGCAGAAAGCC[C/T]TCTGCCTCTAAGCCA	80794
rs32276576	snp	A/C	0.444444	0.157135	intron-variant	Cblc, Gm34744	Mm_Celera	7:19784541	AAAATTAAAAATAGG[A/C]CAGGTGTGGTGTGGT	80794
rs32297840	snp	A/G	0.444444	0.157135	intron-variant	Cblc, Gm34744	Mm_Celera	7:19784345	TAATTAAGAGCACTG[A/G]CTGCTTTTGCAAAGG	80794
rs32298538	snp	A/G	0.375	0.216506	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19788460	GGAGCTGGGGGCGTG[A/G]CTCAGTGGTAGAGCC	80794
rs32332564	snp	G/T	0.444444	0.157135	upstream-variant-2KB	Cblc	GRCm38.p3	7:19797911	AGCCTGGTCTACACA[G/T]TGAGAGTTCCAGGTA	80794
rs32371462	snp	A/G	0.21875	0.248039	intron-variant, downstream-variant-500B	Cblc, Gm34744	GRCm38.p3	7:19790760	GAATGAGCCTAATAC[A/G]GGAAAAAACGGAAGC	80794
rs32423936	snp	A/G	0.497778	0.0332592	downstream-variant-500B, intron-variant	Cblc, Gm34744	Mm_Celera	7:19779229	CTAGGTGCATGGTAC[A/G]AGTGGCCTGGTGGAC	80794
rs32423938	snp	A/G	0.345679	0.230967	downstream-variant-500B, intron-variant	Cblc, Gm34744	GRCm38.p3	7:19779269	GAGAGAGAGGGTGTG[A/G]AAGCCATGGGCTGGT	80794
rs32423940	snp	G/T	0.35503	0.226867	downstream-variant-500B, intron-variant	Cblc, Gm34744	Mm_Celera	7:19779381	GTGGTTACATTATTT[G/T]TTGAGAAAGGGTGAG	80794
rs32423942	snp	A/G	0.5	0	downstream-variant-500B, intron-variant	Cblc, Gm34744	Mm_Celera	7:19779492	TCAGGGCTGGTGACC[A/G]GATGGTGGGCAGGGC	80794
rs32424714	snp	A/C	0.48	0.0979796	downstream-variant-500B, intron-variant	Cblc, Gm34744	Mm_Celera	7:19779530	GTGCGTGCGTGCGTG[A/C]TGACCTGAGAACTGT	80794
rs32424716	snp	A/C	0.277778	0.248452	utr-variant-3-prime, intron-variant	Cblc, Gm34744	GRCm38.p3	7:19779781	CCCAAGGCTCCCTTC[A/C]TCCAGTCCAGGTGCC	80794
rs32424718	snp	A/G	0.391111	0.206368	intron-variant	Cblc, Gm34744	Mm_Celera	7:19780858	AGCTTCTGCCATGGA[A/G]AGAGTCACCAGGTGG	80794
rs32424720	snp	A/G	0.497041	0.0383476	intron-variant	Cblc, Gm34744	Mm_Celera	7:19781859	GGAAGTTGCTCAGGT[A/G]TTCCTAGTCCTTTCA	80794
rs32424722	snp	A/G	0.473373	0.11227	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19781918	CAGACAGCTGCAAAG[A/G]CCTCTGGGTAACTGG	80794
rs32425454	snp	A/G	0.297521	0.245442	intron-variant	Cblc, Gm34744	Mm_Celera	7:19782323	GAAGCAAGAAAATCC[A/G]GAGTTCAGGCACAGC	80794
rs32425456	snp	A/G	0.486111	0.0821678	intron-variant	Cblc, Gm34744	Mm_Celera	7:19782374	TCCTGCCAGGAAAGC[A/G]CACACGCAGGACTGT	80794
rs32425458	snp	C/T	0.142012	0.225474	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19782478	TTCCCAGGTCTAAAT[C/T]CCCTATGCTCGTGGT	80794
rs32425461	snp	C/T	0.18	0.24	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19783535	ACAATGCCAAGAACA[C/T]TTGAACTGCTCTCAA	80794
rs32425463	snp	A/G	0.142012	0.225474	intron-variant	Cblc, Gm34744	GRCm38.p3	7:19783558	GCTCTCAAAAGTACA[A/G]TCACCTTTCTGGTAA	80794
rs32426225	snp	C/T	0.48	0.0979796	intron-variant	Cblc, Gm34744	Mm_Celera	7:19783675	AAGTCTCATGCCAGG[C/T]AGAGGGCACGGCCTA	80794
rs32426228	snp	C/T	0.165289	0.235211	intron-variant	Cblc, Gm34744	Mm_Celera	7:19785148	ATGTATTGAGTCTAG[C/T]CTCCTCCCTCAGATC	80794
rs32426231	snp	A/C	0.444444	0.157135	intron-variant	Cblc, Gm34744	Mm_Celera	7:19785418	GGGACAAAGAGGAAA[A/C]ATGTCACTCACCTTG	80794
rs32426233	snp	A/G	0.495868	0.0452663	intron-variant	Cblc, Gm34744	Mm_Celera	7:19785668	TGCACTACGGATGAT[A/G]GTATCTTATGTTCTA	80794
rs32427155	snp	A/T	0.444444	0.157135	intron-variant	Cblc, Gm34744	Mm_Celera	7:19787307	GGTGCGTTTTAGCTA[A/T]TTAGTTTTAAATAAG	80794
rs32427157	snp	C/T	0.197531	0.244432	intron-variant	Cblc, Gm34744	Mm_Celera	7:19788254	CTGCCCAGTCCTTTA[C/T]AGTATAGTCAATAAA	80794
rs32427160	snp	A/G	0.5	0	intron-variant	Cblc, Gm34744	Mm_Celera	7:19789324	AACTGTTGGCCTCCA[A/G]CCTGAGAATCAAGAA	80794
rs32428185	snp	A/G	0.408163	0.193609	intron-variant, nc-transcript-variant	Cblc, Gm34744	Mm_Celera	7:19790191	AAGCCCAGTCTGCCG[A/G]AGGGATTTTGCACTT	80794
rs32428187	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	Cblc, Gm34744	Mm_Celera	7:19790285	GCTCGTGGCGTTGCA[A/G]CTTGGTGTGCTGGCT	80794
rs32428189	snp	C/T	0.21875	0.248039	intron-variant, nc-transcript-variant	Cblc, Gm34744	Mm_Celera	7:19790336	AAGCCAAACGCATGA[C/T]TTGTGCTAAATCTCT	80794
rs32428191	snp	A/G	0.408163	0.193609	intron-variant, downstream-variant-500B	Cblc, Gm34744	Mm_Celera	7:19790711	TCTGTGGCTTTAGCT[A/G]CCATTGCCCACCATA	80794
rs32429134	snp	A/C/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Cblc, Gm34744	GRCm38.p3	7:19790787	AAGCAAGTTACACTC[A/C/G]GGCATGACCTCCGAT	80794
rs45759301	snp	A/G			intron-variant	Cblc, Gm34744	Mm_Celera	7:19780580	TTACAGACCCTTGTC[A/G]CTACTCAGTTTACAA	80794
rs45814097	snp	A/G			intron-variant	Cblc, Gm34744	Mm_Celera	7:19780225	TCTCTCCCAAACCTC[A/G]TTTGTTGTTTAGAAA	80794
rs45990479	snp	A/T			intron-variant	Cblc	Mm_Celera	7:19793580	CCCCCAGTGAGGGGC[A/T]GGGGGCGTGGCTCAG	80794
rs46004975	snp	A/G			upstream-variant-2KB	Cblc	Mm_Celera	7:19798056	GAACAAAGATGTTGA[A/G]TTATGGTCCAGCCTG	80794
rs46061762	snp	A/G			intron-variant	Cblc, Gm34744	Mm_Celera	7:19780563	TCTCCTAAGTGCTGT[A/G]ATTACAGACCCTTGT	80794
rs46087479	snp	A/C			intron-variant	Cblc, Gm34744	Mm_Celera	7:19786493	CTACCGCCAGCCCCA[A/C]ATAAACTGGATGTGC	80794
rs46127423	snp	A/C			downstream-variant-500B, intron-variant	Cblc, Gm34744	GRCm38.p3	7:19779287	GCCATGGGCTGGTTG[A/C]ATCTAAAATAAATGG	80794
rs46334159	snp	C/T			intron-variant	Cblc	Mm_Celera	7:19793133	AAGGAAGTGTGGAAG[C/T]TAAAGTCCAAACTGG	80794
rs46343723	snp	A/G			intron-variant	Cblc, Gm34744	GRCm38.p3	7:19779879	TTTATCTGCTTTTTG[A/G]TACAGGGTTTCCCTG	80794
rs46678538	snp	A/G			intron-variant	Cblc	GRCm38.p3	7:19796000	AGACAGGGTTTCTCT[A/G]TGTAGCCCTGGCTGT	80794
rs46804624	snp	A/C			intron-variant	Cblc	GRCm38.p3	7:19793533	GTGAGGGGCAGGGGG[A/C]GTGGCTCAGTGGTAG	80794
rs47068748	snp	A/G			intron-variant	Cblc, Gm34744	Mm_Celera	7:19780609	AAAATGCCAAGGACC[A/G]ACCCCGGAACTTTGA	80794
rs47165153	snp	A/G			intron-variant	Cblc, Gm34744	Mm_Celera	7:19782581	GTGAGGAAGCCATGA[A/G]ACTCCTTTAAAAAGG	80794
rs47399448	snp	C/T			intron-variant	Cblc, Gm34744	Mm_Celera	7:19780212	aactgttgggttctc[C/T]ctccCAAACCTCATT	80794
rs47497735	snp	A/C			intron-variant	Cblc, Gm34744	GRCm38.p3	7:19788541	GCCCCTGCCTAGAAT[A/C]CCCCAGTGAGGGGCT	80794
rs47535307	snp	A/G			intron-variant	Cblc, Gm34744	GRCm38.p3	7:19781965	GGGGGGAGGGGGAGC[A/G]CCAAGCTAGAAGGGG	80794
rs47635961	snp	C/T			intron-variant	Cblc, Gm34744	Mm_Celera	7:19782637	GTGGCCCGGAGGCCA[C/T]CAGAGAAGGGCTAGG	80794
rs47732551	snp	G/T			intron-variant	Cblc	Mm_Celera	7:19793546	GGAGTGGCTCAGTGG[G/T]AGAGCCCCTGCCTAG	80794
rs48132526	snp	A/G			downstream-variant-500B, intron-variant	Cblc, Gm34744	Mm_Celera	7:19779449	CTGAAAACATCCAGA[A/G]GGATTTCTAGGTTTA	80794
rs48378045	snp	A/G			intron-variant	Cblc, Gm34744	Mm_Celera	7:19786439	GCTGGGGATTAGCAC[A/G]GTTGGCAGGTTTGCC	80794
rs48392650	snp	A/T			intron-variant	Cblc, Gm34744	Mm_Celera	7:19785774	TTTTTTATATTTTTT[A/T]AAGATTTATTTATTT	80794
rs48524643	snp	C/T			intron-variant	Cblc, Gm34744	GRCm38.p3	7:19782936	CGTAAATGTAAAATG[C/T]CAGACATGATGGCAC	80794
rs48879637	snp	A/G			intron-variant	Cblc, Gm34744	GRCm38.p3	7:19781215	ACTTAACTCCTACAA[A/G]TTGTCTTCTGACCCC	80794
rs48927130	snp	A/G			intron-variant	Cblc, Gm34744	GRCm38.p3	7:19780006	CATCACCCTGCTTAT[A/G]TATGTTTAATAATAC	80794
rs49077832	snp	A/G			intron-variant	Cblc, Gm34744	GRCm38.p3	7:19781240	GACCCCTACAAATGT[A/G]CCGAGACAGAAGCAA	80794
rs49192300	snp	A/T			intron-variant	Cblc, Gm34744	Mm_Celera	7:19780297	CCTGACGACTTGAGA[A/T]CCAGTCTCATGGTGG	80794
rs49227731	snp	A/C			intron-variant	Cblc, Gm34744	Mm_Celera	7:19786043	CGGCAGCAGGGTGGA[A/C]AGCCCCACCCACCAG	80794
rs49683284	snp	C/T			intron-variant	Cblc, Gm34744	Mm_Celera	7:19786094	CCTGCTTCCTCAATG[C/T]TCAATGAGGTCCCTG	80794
rs49834372	snp	G/T			downstream-variant-500B, intron-variant	Cblc, Gm34744	Mm_Celera	7:19779450	TGAAAACATCCAGAG[G/T]GATTTCTAGGTTTAG	80794
rs49922556	snp	G/T			intron-variant	Cblc, Gm34744	Mm_Celera	7:19780082	TGTAATGCCTGAGGA[G/T]GCCAGAAGGGGGCGA	80794
rs49991296	snp	A/C/G			intron-variant	Cblc, Gm34744	GRCm38.p3	7:19786027	GACTGAGACGGCTAA[A/C/G]CGGCAGCAGGGTGGA	80794

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