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
rs3688850	snp	C/T	0.48	0.0979796	intron-variant	Nol10	GRCm38.p3	12:17360249	ATCTGTATCAGCTAA[C/T]AGTGACAGCAGGGTC	217431
rs3698784	snp	A/G	0.444444	0.157135	intron-variant	Nol10	Mm_Celera	12:17407844	GTTAGCACAGTATTA[A/G]TATTGTCCCGAGTTG	217431
rs3699424	snp	C/G	0.5	0	intron-variant	Nol10	Mm_Celera	12:17407972	CCAAACCCTTGCCCA[C/G]CAGAAGAGCATGCAG	217431
rs3699893	snp	A/G	0.465374	0.126941	intron-variant	Nol10	GRCm38.p3	12:17407986	ACCAGAAGAGCATGC[A/G]GGACCTGGAGTCAGG	217431
rs3699933	snp	G/T	0.408163	0.193609	intron-variant	Nol10	Mm_Celera	12:17408012	TCAGGGCCTAACCTT[G/T]TGGCCTTGGGCCCTG	217431
rs3715155	snp	C/T	0.444444	0.157135	intron-variant	Nol10	Mm_Celera	12:17408218	ATCTTACTGCTGTCA[C/T]TTCTGTGGTGTTCCG	217431
rs3720255	snp	C/T	0.444444	0.157135	intron-variant	Nol10	Mm_Celera	12:17409036	ATTTTCTCTCCCTCC[C/T]CAGTGCTGAGATTAT	217431
rs6239445	snp	A/G	0.207612	0.24638	intron-variant	Nol10	Mm_Celera	12:17379550	GAACTTAAAACTATC[A/G]ACTAAGCAGAAATCT	217431
rs6239912	snp	A/G	0.5	0	intron-variant	Nol10	Mm_Celera	12:17379617	ccttcctaatgctgc[A/G]accctttaatacagt	217431
rs6240033	snp	C/T	0.5	0	intron-variant	Nol10	Mm_Celera	12:17379692	cttcataactataat[C/T]ttgntactgttatcg	217431
rs6240043	snp	C/G	0.48	0.0979796	intron-variant	Nol10	Mm_Celera	12:17379696	ATAACTATAATTTTG[C/G]TACTGTTATCGTAAT	217431
rs6254382	snp	A/G	0.21875	0.248039	intron-variant	Nol10	Mm_Celera	12:17380043	TTAGTCAGTAAGGCA[A/G]CCTTCATGTAGAGCT	217431
rs6254912	snp	C/T	0.5	0	intron-variant	Nol10	Mm_Celera	12:17380120	GGGCTCTCACTGCTG[C/T]CAGCCTCCCATCATG	217431
rs6275937	snp	A/G	0.444444	0.157135	intron-variant	Nol10	GRCm38.p3	12:17408896	GTGTGTTGGGGAAAG[A/G]GTCTTGGTGTGTGTT	217431
rs13472642	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Nol10	Mm_Celera	12:17429335	ATGTGTGTGCATGGT[A/G]CTGGTGGTCTGACTG	217431
rs13472643	snp	A/G	0.290657	0.246672	utr-variant-3-prime	Nol10	Mm_Celera	12:17429531	CACCCTACTGGAAAC[A/G]GGACATTATCATGCT	217431
rs13472644	snp	A/G			utr-variant-3-prime	Nol10	Mm_Celera	12:17429601	gcctttgatcccagc[A/G]cttgggaggcagagg	217431
rs13472645	snp	G/T	0.277778	0.248452	missense	Nol10	Mm_Celera	12:17429174	TCAGGAAAGGAAAAA[G/T]CTGCGCAGGTCGGCC	217431
rs29123191	snp	A/G	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17371908	ACAACACTAATACAC[A/G]TAAAATAAAAATAAG	217431
rs29123304	snp	A/G	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17384501	CCTGTCCCGCTTACA[A/G]GTAGTATGCAAATAC	217431
rs29123569	snp	A/T	0.375	0.216506	intron-variant	Nol10	GRCm38.p3	12:17386337	AGTAGAAAGCAAACC[A/T]TGACACCCAGGGATT	217431
rs29124635	snp	A/G	0.265928	0.249492	intron-variant	Nol10	Mm_Celera	12:17392047	TTTGTTATACCTGCT[A/G]ACAAATTCCTTATTT	217431
rs29125898	snp	A/G	0.426035	0.177515	intron-variant	Nol10	Mm_Celera	12:17394785	GCCACTGTAGCGCTT[A/G]GGGCTGCTTCTGAGC	217431
rs29126552	snp	A/G	0.277778	0.248452	intron-variant	Nol10	Mm_Celera	12:17369862	GGAGGGCTTGGACTC[A/G]GGTCATCAGGCTGGT	217431
rs29127750	snp	A/T	0.444444	0.157135	intron-variant	Nol10	Mm_Celera	12:17368743	TGCATGCAAAGAGCC[A/T]TTTTTTTTCTTTTTC	217431
rs29128267	snp	C/T	0.401235	0.199068	intron-variant	Nol10	GRCm38.p3	12:17360898	TTTCAGAAGGAGGGC[C/T]TCTCTTGTCTGGCAT	217431
rs29128312	snp	A/G	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17410409	TTGTTAATAAAATGG[A/G]CCCTGACTTGCTTTT	217431
rs29128775	snp	C/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17427932	CATGCATGTGGAGGT[C/T]AGAGGGCAACTTGAG	217431
rs29128948	snp	A/T	0.444444	0.157135	upstream-variant-2KB	Nol10	Mm_Celera	12:17347817	TCCGGGGACTGTGCC[A/T]ACACTACTTGATAGA	217431
rs29129102	snp	A/G	0.444444	0.157135	intron-variant	Nol10	Mm_Celera	12:17400401	TGGTGTTTTTCAGTG[A/G]TGGGGATTAAACCTA	217431
rs29132349	snp	A/G	0.32	0.24	intron-variant	Nol10	Mm_Celera	12:17409986	AGCATTGAAAGACAC[A/G]CCATGGTGGCTGCTG	217431
rs29132621	snp	A/T	0.444444	0.157135	intron-variant	Nol10	Mm_Celera	12:17412921	TTGGCAAATACATCA[A/T]GATGTTAATTTTTTC	217431
rs29133318	snp	C/T	0.277778	0.248452	intron-variant, upstream-variant-2KB	Nol10, Mir3066	Mm_Celera	12:17353478	TGAGATGTTTGGACA[C/T]AGTTACTGAGAGCTG	217431
rs29133691	snp	C/T	0.444444	0.157135	intron-variant	Nol10	GRCm38.p3	12:17362527	TGAGCTTTGATTCTG[C/T]ATGCTGGTAAATGTT	217431
rs29134351	snp	C/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17419748	GAAGGCTCACAGCCA[C/T]GTGTAAGTCCAGCTC	217431
rs29136005	snp	C/T	0.415225	0.187619	intron-variant	Nol10	Mm_Celera	12:17424201	AAAAACTAAAGGTGT[C/T]AGAGACCCCCTGTGA	217431
rs29136268	snp	C/T	0.277778	0.248452	intron-variant	Nol10	Mm_Celera	12:17360783	GCTTTGTTTGCACAT[C/T]CAGGTCTTGAGGTTG	217431
rs29136581	snp	G/T	0.375	0.216506	intron-variant	Nol10	GRCm38.p3	12:17364977	TTTTGTACTGATTTT[G/T]TTGTTGTTGTTGTTG	217431
rs29137573	snp	G/T	0.387812	0.208586	upstream-variant-2KB	Nol10	Mm_Celera	12:17346783	AACAAAATGGCCTAG[G/T]ATCTTTAACCACATT	217431
rs29137765	snp	A/G	0.277778	0.248452	intron-variant	Nol10	Mm_Celera	12:17396754	AACCCCTATCGCTCA[A/G]TCCCTGCTTGCTCTG	217431
rs29138683	snp	C/G	0.375	0.216506	intron-variant	Nol10	GRCm38.p3	12:17377225	ACACATGTGTGAGTC[C/G]CACCCCAGCCTGTTA	217431
rs29138912	snp	C/T	0.304688	0.243945	intron-variant	Nol10	Mm_Celera	12:17396521	CTTGCGTAGACCAGC[C/T]GACAGGGAGAGAGCA	217431
rs29139180	snp	C/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17427525	AGGGCAGAATATGCT[C/T]CCCCCTCTTCTGCCC	217431
rs29139263	snp	C/T	0.32	0.24	intron-variant	Nol10	Mm_Celera	12:17428878	ACACTTCCCGGTGTG[C/T]GGACAGACACTTCCC	217431
rs29139283	snp	A/G	0.345679	0.230967	intron-variant	Nol10	Mm_Celera	12:17369085	AGGCTCTGACTAAGT[A/G]TGTTTGTCATGTTCA	217431
rs29139503	snp	A/G	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17374227	CAGTCACGGAATGGG[A/G]TTGGAGTGGCTTTGT	217431
rs29139563	snp	C/T	0.359862	0.224567	intron-variant	Nol10	Mm_Celera	12:17401750	GTATGTTAGAGCATA[C/T]TTATGATACTAAATA	217431
rs29139819	snp	C/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17421045	AGATAGAGCTGTCCC[C/T]CATACCCAGAAAGGT	217431
rs29139854	snp	G/T	0.391111	0.206368	intron-variant	Nol10	GRCm38.p3	12:17427665	GGGCAGTGTAGTCCC[G/T]AGGTTCCAGAGTCTC	217431
rs29140394	snp	A/G	0.359862	0.224567	intron-variant	Nol10	GRCm38.p3	12:17400598	CTGTGTTGTTTTGCT[A/G]TCCTATACATGACAG	217431
rs29141487	snp	G/T	0.444444	0.157135	intron-variant	Nol10	Mm_Celera	12:17353278	GCAGTAGCATGTAAG[G/T]TTAATGTGTGTATGC	217431
rs29142046	snp	A/G/T	0.290657	0.246672	intron-variant	Nol10	GRCm38.p3	12:17423009	CTTCCAGTTTGTCAT[A/G/T]TGGAAGCTTGTCACT	217431
rs29143780	snp	C/G	0.387812	0.208586	intron-variant	Nol10	Mm_Celera	12:17393605	CTAGGAAATACTCTG[C/G]AATTCAAGTGCAGTA	217431
rs29144822	snp	A/G	0.290657	0.246672	intron-variant	Nol10	Mm_Celera	12:17357536	TTCTTGTAACTCATC[A/G]AGAGGGTGTAGTGTG	217431
rs29145002	snp	A/T	0.444444	0.157135	intron-variant	Nol10	Mm_Celera	12:17419837	TTGTTCCGGTAATTT[A/T]AAAAATTTTAAGAGT	217431
rs29145783	snp	C/T	0.33241	0.236027	intron-variant	Nol10	Mm_Celera	12:17427583	ACAAACGCAGAGCCT[C/T]ATTCATCAGAATTAA	217431
rs29145886	snp	C/T	0.5	0	intron-variant	Nol10	Mm_Celera	12:17349787	TGTGTTCAGCCTGGG[C/T]GACAGAGCTTACATT	217431
rs29146948	snp	A/T	0.33241	0.236027	intron-variant	Nol10	Mm_Celera	12:17367146	GCTGCTCAGTGCAGC[A/T]CCAGGCTAAGGCTGT	217431
rs29147266	snp	A/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17391069	TTTATTTATTTAAAA[A/T]TTTAAAGGCAGAGGG	217431
rs29147956	snp	C/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17421290	AGCATAGAGCTGGAA[C/T]TGCAGCTTGTGTTCA	217431
rs29148521	snp	C/T	0.207612	0.24638	intron-variant	Nol10	Mm_Celera	12:17383610	CCCCTGCATCCGGAG[C/T]TGCCTGCATATTCCA	217431
rs29149319	snp	A/C	0.473373	0.11227	intron-variant	Nol10	Mm_Celera	12:17349956	AAAACAGATGCTTTA[A/C]AATTGTTTAGTATAT	217431
rs29150901	snp	G/T	0.207612	0.24638	intron-variant	Nol10	Mm_Celera	12:17406508	CCAGCTTTCTAGGGA[G/T]CTGGGAAGGCAGTAT	217431
rs29151151	snp	A/G	0.33241	0.236027	synonymous-codon	Nol10	Mm_Celera	12:17369531	CCAGTATGGGCTGCC[A/G]ATTAAGTCAGTTCAT	217431
rs29152393	snp	C/G	0.290657	0.246672	intron-variant	Nol10	Mm_Celera	12:17371980	GAAGTGGTGACCTTA[C/G]TTTATTCCTTTGGCT	217431
rs29153221	snp	A/C	0.444444	0.157135	intron-variant	Nol10	Mm_Celera	12:17395284	ATCAGCAAGTCTCTC[A/C]GCCTGTATCAGAGTG	217431
rs29153811	snp	A/G	0.32	0.24	intron-variant	Nol10	Mm_Celera	12:17361863	AAATTATGAACATTA[A/G]GACACTTCATGCCTA	217431
rs29154129	snp	A/G	0.277778	0.248452	synonymous-codon	Nol10	Mm_Celera	12:17416956	CACCAAGCAGAGACT[A/G]ATGAAGTGAGTAGCC	217431
rs29155171	snp	A/G	0.33241	0.236027	intron-variant	Nol10	Mm_Celera	12:17349256	ACTGCCTTGGCGTAT[A/G]CTTAGGGTCTAGGGA	217431
rs29155320	snp	A/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17370743	AAAGTTTTTTTTTTT[A/T]AAGATTTATTTATTT	217431
rs29155627	snp	A/G	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17368199	TGGGATTACATTTGT[A/G]TGGGAAATGTCTTTT	217431
rs29155773	snp	A/G	0.290657	0.246672	intron-variant	Nol10	Mm_Celera	12:17392729	TTCTTCACAGCCATG[A/G]TAATGGTTAGGTTTT	217431
rs29156597	snp	A/G	0.207612	0.24638	intron-variant	Nol10	Mm_Celera	12:17408557	CGTCCTCCCCAGAGC[A/G]TTCACATTGGTCTTG	217431
rs29156827	snp	C/T	0.345679	0.230967	intron-variant	Nol10	Mm_Celera	12:17389588	CTTAAAGGCAGTGTG[C/T]GTAAGGTGAGGCAAC	217431
rs29156915	snp	A/C	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17362229	AAAGTAAAAAGTAAT[A/C]CAGATTAAAGAAAAG	217431
rs29157439	snp	G/T	0.387812	0.208586	intron-variant	Nol10	Mm_Celera	12:17420929	GCAGAAGAGGCCCCT[G/T]TTCAGAAACCCATGG	217431
rs29157678	snp	C/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17385810	GGTTTGTTAGCTTGA[C/T]ACAAGCTAGAATAAT	217431
rs29157679	snp	C/T	0.265928	0.249492	intron-variant	Nol10	Mm_Celera	12:17374501	GGTAGTGATAGTTTG[C/T]CACAGTTCAACACCT	217431
rs29158402	snp	A/T	0.345679	0.230967	intron-variant	Nol10	GRCm38.p3	12:17357454	TTCTGATTACTGATG[A/T]TAGCCTAGGCATGTT	217431
rs29158625	snp	A/G	0.497778	0.0332592	intron-variant	Nol10	Mm_Celera	12:17366730	TGTGTTATTTAGTAA[A/G]TTTAGTAATTTTAGT	217431
rs29159901	snp	A/C	0.32	0.24	intron-variant	Nol10	Mm_Celera	12:17393568	CTCAGCATCTTGTTA[A/C]TGCAGTCTTTGGGCA	217431
rs29160165	snp	A/G	0.33241	0.236027	missense	Nol10	Mm_Celera	12:17416714	TATTTTTGATTTCAG[A/G]AAGAGGAGGAAGAAC	217431
rs29160201	snp	A/C	0.197531	0.244432	intron-variant	Nol10	Mm_Celera	12:17380186	TTGGTTTTCACCAGC[A/C]TCCACCTGCTGCTGA	217431
rs29160293	snp	A/G	0.5	0	synonymous-codon	Nol10	Mm_Celera	12:17416923	TGGCGAAGAGTTCAG[A/G]AGCTTCAAAGAGTCT	217431
rs29160429	snp	G/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17367544	TGTGTGCCCATGAGT[G/T]CAGGTGCCTGCAGAG	217431
rs29161340	snp	G/T	0.375	0.216506	intron-variant	Nol10	GRCm38.p3	12:17386338	GTAGAAAGCAAACCT[G/T]GACACCCAGGGATTA	217431
rs29161991	snp	A/G	0.5	0	intron-variant	Nol10	Mm_Celera	12:17413557	CTCTTTCTCTGAATA[A/G]TGGCTCCCCCCAAGT	217431
rs29162167	snp	A/G	0.32	0.24	intron-variant	Nol10	GRCm38.p3	12:17361290	TGCTTATATAGAGAT[A/G]AGAAGACAACTTACT	217431
rs29162622	snp	A/C/T	0.277778	0.248452	intron-variant	Nol10	GRCm38.p3	12:17398777	TGATACGTTAATATG[A/C/T]AGTCATTGTAAATAT	217431
rs29163014	snp	A/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17420472	TCATGCTTTACACGT[A/T]GCTAACTGTGTTTGT	217431
rs29164658	snp	A/T	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17370732	TTCATGTATGTAAAG[A/T]TTTTTTTTTTTAAGA	217431
rs29164694	snp	C/G	0.487535	0.077957	intron-variant	Nol10	GRCm38.p3	12:17386924	ACCAGGGGCCTGTGA[C/G]GACCAGCTACCTGTT	217431
rs29165237	snp	A/G	0.5	0	intron-variant	Nol10	Mm_Celera	12:17362061	AAAAATAAGGTAGGC[A/G]TGGTGAAGCACGCCT	217431
rs29166694	snp	A/G	0.265928	0.249492	intron-variant	Nol10	GRCm38.p3	12:17367193	TTGCTAGTGCTCCGG[A/G]CATGGTCTGGCCTTG	217431
rs29166885	snp	C/T	0.255	0.24995	intron-variant	Nol10	Mm_Celera	12:17428165	GGCTGCCACCTGAAT[C/T]GGAAGGGCATACTGG	217431
rs29167052	snp	G/T	0.33241	0.236027	intron-variant	Nol10	Mm_Celera	12:17393361	CAACCAAGGACAGCA[G/T]CCTAAGCCATCCGTG	217431
rs29167090	snp	A/G	0.277778	0.248452	intron-variant	Nol10	Mm_Celera	12:17373387	TCATTTCTAAAACAA[A/G]GCCGTCTGATATGCT	217431
rs29167295	snp	A/G	0.197531	0.244432	intron-variant	Nol10	Mm_Celera	12:17376769	GACTTAGAGAAGTAC[A/G]CCAGGCAGGCCAATA	217431
rs29167727	snp	C/T	0.33241	0.236027	intron-variant	Nol10	Mm_Celera	12:17410983	GTATAGGCGCCTGTA[C/T]CCCATTTGGCTTTTA	217431
rs29167965	snp	C/G	0.375	0.216506	intron-variant	Nol10	Mm_Celera	12:17409466	GGACCCAGTGTTTTC[C/G]TTTGCCCTAATAAAT	217431

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