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
rs6175057	snp	G/T	0.5	0	upstream-variant-2KB	Ccdc12, Nbeal2	GRCm38.p3	9:110655500	gtgccgggattaaag[G/T]cgtgcgccaccacgc	235627
rs6189046	snp	A/G	0.5	0	upstream-variant-2KB	Ccdc12, Nbeal2	GRCm38.p3	9:110655778	ATTTGCTTTTAAGCA[A/G]GTAAGGTAGCCTGAC	235627
rs29593654	snp	A/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Nbeal2, Mir8107	Mm_Celera	9:110635748	AGAAAGCTTCTTCAC[A/G]CCCTCCAGGGCAGGG	235627
rs29595119	snp	C/G	0.32	0.24	intron-variant	Nbeal2	GRCm38.p3	9:110652146	GGAGGGGCCACCTGC[C/G]CTGCTGGCTGGTTGG	235627
rs29843569	snp	A/G	0.375	0.216506	intron-variant	Nbeal2	Mm_Celera	9:110651116	TGTGTGTGTGTGTGC[A/G]CGTGCGTGCACTGCT	235627
rs29890894	snp	A/C/G	0.32	0.24	intron-variant	Nbeal2	GRCm38.p3	9:110649429	AGCTCCAGTCTGTCC[A/C/G]GGCATTTTAGGACAA	235627
rs29986349	snp	A/G	0.375	0.216506	stop-gained	Nbeal2	Mm_Celera	9:110641482	GGGGCGCCCGGGCCT[A/G]CAGGTAAAGCTGTGG	235627
rs30042960	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Nbeal2, Mir8107	GRCm38.p3	9:110638061	ATGCTCTCACCCCAC[A/C]CTGGGCCACATGAGA	235627
rs30126001	snp	A/G	0.415225	0.187619	synonymous-codon, downstream-variant-500B	Nbeal2, Mir8107	GRCm38.p3	9:110635946	GAGGAGGGGCCCACC[A/G]CCATCAGCAGCCGCC	235627
rs30179325	snp	A/T	0.375	0.216506	upstream-variant-2KB	Ccdc12, Nbeal2	Mm_Celera	9:110655996	TGACCTCAGAGTGAG[A/T]TGGGAATGAGAGTGG	235627
rs30374967	snp	G/T	0.277778	0.248452	synonymous-codon	Nbeal2	Mm_Celera	9:110638628	GGGCCGTAGTGACAC[G/T]CGACCCAGAGCTTGC	235627
rs33289864	snp	A/G	0.132653	0.220748	intron-variant	Nbeal2	Mm_Celera	9:110631167	ATGGGCCAGCAAAAC[A/G]TTACAGAGCCCCCAC	235627
rs33289865	snp	A/G	0.260355	0.249785	intron-variant	Nbeal2	GRCm38.p3	9:110632205	CCTGGGCATGCAGCT[A/G]TAGGTGCAAGGCAAT	235627
rs33289866	snp	A/G	0.124444	0.216185	synonymous-codon	Nbeal2	Mm_Celera	9:110632365	CCGGAGATCTGCTGT[A/G]CTATTGGCGAGATGT	235627
rs33289868	snp	A/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110632547	CAAGGTCACTCACTG[A/T]AAGGTATACCCAGCC	235627
rs33289870	snp	C/T	0.32	0.24	intron-variant	Nbeal2	GRCm38.p3	9:110632589	CTGCCATCCATTGAA[C/T]GCTTGGCCTGACTAA	235627
rs33289872	snp	C/T	0.244898	0.249948	synonymous-codon	Nbeal2	GRCm38.p3	9:110633057	GAAGACCTGGCCACG[C/T]TCCCGCCAGGCGGCC	235627
rs33290904	snp	C/T	0.391111	0.206368	intron-variant	Nbeal2	GRCm38.p3	9:110633260	AAGAGAGGCAGCATT[C/T]GGCAAACAGCCAGAC	235627
rs33290906	snp	C/T	0.142012	0.225474	intron-variant	Nbeal2	Mm_Celera	9:110633375	CAGAGAGGAGATATT[C/T]ACAAAGGCCTTACTC	235627
rs33290908	snp	C/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110633507	TCCTATCTGTAGGCC[C/T]TACAAAGCCTGGGCC	235627
rs33290910	snp	C/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110633580	CGTGACAGTACCAGC[C/T]CTGGTATTAGACCGC	235627
rs33290912	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110633620	AAGACCACACTGCCA[A/G]CTCTCCATTCCTGAG	235627
rs33291794	snp	A/G	0.124444	0.216185	synonymous-codon	Nbeal2	Mm_Celera	9:110633754	GCCATCTTCCAGCAC[A/G]TTGGAGAGACTGGAG	235627
rs33291796	snp	G/T	0.391111	0.206368	synonymous-codon	Nbeal2	Mm_Celera	9:110633877	GCTGCCGCCACCAGC[G/T]GTATTGCCCGAGCCA	235627
rs33291798	snp	A/G	0.32	0.24	intron-variant	Nbeal2	GRCm38.p3	9:110634216	CCAAACCAGGGGACA[A/G]CAAATAAGAGGTCAT	235627
rs33291800	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110634954	TGTGTGGCTCCAGAA[A/G]AGGCCTGTGAAAGTG	235627
rs33291802	snp	C/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110635003	CTTCTAGCCGGCGGC[C/T]TCAGTAAATGGGATT	235627
rs33292544	snp	C/T	0.124444	0.216185	synonymous-codon	Nbeal2	Mm_Celera	9:110635157	CAAGGGGTCTTGCAC[C/T]GGAGAACCCTGAAGC	235627
rs33292546	snp	A/G	0.231111	0.249285	synonymous-codon	Nbeal2	GRCm38.p3	9:110635307	GCCTACCTGGCCATC[A/G]TCACCGGTAGCTGCC	235627
rs33292548	snp	A/C	0.231111	0.249285	intron-variant, downstream-variant-500B	Nbeal2, Mir8107	GRCm38.p3	9:110635611	AGGGCCCGCCAGCCT[A/C]ACCTGTAGTGCGTGC	235627
rs33292550	snp	A/G	0.408163	0.193609	synonymous-codon, downstream-variant-500B	Nbeal2, Mir8107	GRCm38.p3	9:110635943	GTAGAGGAGGGGCCC[A/G]CCGCCATCAGCAGCC	235627
rs33292553	snp	A/T	0.231111	0.249285	missense, nc-transcript-variant	Nbeal2, Mir8107	GRCm38.p3	9:110636011	TCATATCCATGGCCG[A/T]ACTGGGGACCTGAGG	235627
rs33293385	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Nbeal2, Mir8107	GRCm38.p3	9:110636133	CTGCTCACAGCTTTT[C/T]AGGGCCGCTGCCATC	235627
rs33293387	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Nbeal2, Mir8107	Mm_Celera	9:110636473	GGTCAAGGGTGTGCC[A/G]GAAGCCACTACCTCA	235627
rs33293388	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Nbeal2, Mir8107	Mm_Celera	9:110636810	AGCCTGGACTCTCTC[A/G]AACTGGTCTCCCAAA	235627
rs33293389	snp	A/G	0.231111	0.249285	missense, upstream-variant-2KB	Nbeal2, Mir8107	GRCm38.p3	9:110637103	TGGAGGAGCAACTTG[A/G]TGCCAAACTCATGTA	235627
rs33293391	snp	C/T	0.124444	0.216185	synonymous-codon, upstream-variant-2KB	Nbeal2, Mir8107	Mm_Celera	9:110637117	GGTGCCAAACTCATG[C/T]AGTTCACCCTCAGGC	235627
rs33293392	snp	A/G	0.124444	0.216185	synonymous-codon, upstream-variant-2KB	Nbeal2, Mir8107	Mm_Celera	9:110637623	GACTGATGACGCGGG[A/G]AGCCCTGTGGTGGTT	235627
rs33293914	snp	C/T	0.124444	0.216185	missense	Nbeal2	Mm_Celera	9:110642402	TTCCTCCTGCAAGGA[C/T]GGCACCAAAGAGGTG	235627
rs33293915	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110642540	AAGGACTGCACAAGA[A/G]GTGGGATATCCCAGC	235627
rs33293916	snp	G/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110642600	GTACGCTAGAGGGAT[G/T]TCAGTGGTGCTTGAG	235627
rs33293917	snp	C/T	0.231111	0.249285	intron-variant	Nbeal2	GRCm38.p3	9:110642667	CCTAGATCCTTATGT[C/T]CAAAAAGGAGGGCTT	235627
rs33293918	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110642792	GTGGGAGTTCCTGGC[A/G]CTCTGACCTGGGGAC	235627
rs33293919	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110643001	ATGAGCATCAGTCCT[A/G]AGGATGTCAGGCTAC	235627
rs33293920	snp	A/G	0.35503	0.226867	intron-variant	Nbeal2	Mm_Celera	9:110643063	AATCTAGATGGTTCT[A/G]GGAGTGCCTAGGCTG	235627
rs33293922	snp	C/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110643322	GCCAGGGAGAACAAA[C/T]GGCCAGAAGGGCTTC	235627
rs33294404	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Nbeal2, Mir8107	GRCm38.p3	9:110637800	AGAGCAGTACAGGCT[A/G]AAGATACACAGGGTT	235627
rs33294405	snp	A/G	0.473373	0.11227	synonymous-codon	Nbeal2	GRCm38.p3	9:110638119	CGCGAAGGACACTTC[A/G]GGCAAGTTCACGGTC	235627
rs33294407	snp	C/T	0.142012	0.225474	missense	Nbeal2	GRCm38.p3	9:110638126	GACACTTCGGGCAAG[C/T]TCACGGTCACGTACT	235627
rs33294409	snp	C/T	0.132653	0.220748	missense	Nbeal2	GRCm38.p3	9:110638130	CTTCGGGCAAGTTCA[C/T]GGTCACGTACTCCTT	235627
rs33294411	snp	A/G	0.124444	0.216185	missense	Nbeal2	Mm_Celera	9:110638537	CGGCGCCTGCATGGC[A/G]AGCCTTCTGAGATTC	235627
rs33295074	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110643357	CTTCACTCCTCCAGG[A/G]ATACGGAAGCAGAGG	235627
rs33295076	snp	A/T	0.124444	0.216185	synonymous-codon	Nbeal2	Mm_Celera	9:110644491	CAGCTGCTCCGCTAG[A/T]GCATGTAGAGCATCT	235627
rs33295078	snp	G/T	0.231111	0.249285	intron-variant	Nbeal2	GRCm38.p3	9:110644900	AACCAGAGGACTGTG[G/T]TGTGGACAGGTCACC	235627
rs33295080	snp	A/G	0.391111	0.206368	intron-variant	Nbeal2	GRCm38.p3	9:110644978	CAGAGACCTGACACA[A/G]GCAGAGGAGGAGCTT	235627
rs33295082	snp	A/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110645592	TTCAAAGTACCCACA[A/T]TTCCTGACGTGGCTT	235627
rs33295454	snp	A/C	0.142012	0.225474	synonymous-codon	Nbeal2	Mm_Celera	9:110638655	TTGCAGCAAGGCTAA[A/C]AGCTGCTCCTGGCAG	235627
rs33295456	snp	A/G	0.32	0.24	synonymous-codon	Nbeal2	GRCm38.p3	9:110638748	CACACAGGTGGTGCG[A/G]CTGGCAGGGCAGCTG	235627
rs33295458	snp	G/T	0.165289	0.235211	synonymous-codon	Nbeal2	Mm_Celera	9:110638823	AGCTGTGGGCAGTGC[G/T]GGTAGCCACTGCATC	235627
rs33295460	snp	C/T	0.32	0.24	intron-variant	Nbeal2	GRCm38.p3	9:110638923	TGTAGGTGGAAAGAA[C/T]GTGACAATCCCGGTC	235627
rs33295462	snp	C/T	0.231111	0.249285	intron-variant	Nbeal2	GRCm38.p3	9:110639089	TCCATGCTTTTGGCT[C/T]GTAGCCTAGTATGGC	235627
rs33295794	snp	G/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110646711	CCTGCACGGTTACCC[G/T]GAAGGCAATGCAAAG	235627
rs33295796	snp	A/G	0.244898	0.249948	intron-variant	Nbeal2	GRCm38.p3	9:110646997	ATTATCCATTGATAG[A/G]TTTGTGATCTGGGCT	235627
rs33295798	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	GRCm38.p3	9:110647359	AACCCGCTACGGGAC[A/G]TGGAAAGCCTCAGAA	235627
rs33295800	snp	C/T	0.336735	0.234472	intron-variant	Nbeal2	GRCm38.p3	9:110647821	GATCCCGGATCTGTG[C/T]TTCTCAGAATCTGGG	235627
rs33295802	snp	G/T	0.132653	0.220748	intron-variant	Nbeal2	Mm_Celera	9:110648444	CTCTGAAGGGGACTC[G/T]AAGGACAGACGAGGA	235627
rs33296334	snp	A/C	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110639437	TATGGGTGCTGTGGG[A/C]AACTTGCACTCCCTT	235627
rs33296336	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110639502	GTCACAGTGCAGAAA[A/G]AACAAGGACAACAGA	235627
rs33296338	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110639588	GTGTCCTTTCTCTAC[A/G]TGGCCGGGACCCAGG	235627
rs33296340	snp	C/T	0.231111	0.249285	intron-variant	Nbeal2	GRCm38.p3	9:110639599	CTACATGGCCGGGAC[C/T]CAGGACACCCAACTC	235627
rs33296342	snp	C/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110639651	ACCCACCAAGCCTAT[C/T]GAACCACACCCCAGC	235627
rs33296520	snp	C/T	0.32	0.24	missense	Nbeal2	Mm_Celera	9:110626573	ATGCACGTGGTATCC[C/T]GGGAGCCGGAGATGA	235627
rs33296522	snp	C/T	0.197531	0.244432	synonymous-codon	Nbeal2	GRCm38.p3	9:110629857	TAGGCGCAGAAGCAA[C/T]GAGTACACCTGGTTC	235627
rs33296523	snp	C/T	0.21875	0.248039	synonymous-codon	Nbeal2	GRCm38.p3	9:110630007	GAAGAAGAGTTCGAG[C/T]GCCGAACGCCGCAGG	235627
rs33296704	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110648516	AGGAGGAAGTACTTG[A/G]ACCTTGCTACAGGGG	235627
rs33296706	snp	G/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110648662	ATAGTTCCTGCTTGG[G/T]CATGCAACTGCCATT	235627
rs33297094	snp	A/G	0.132653	0.220748	intron-variant	Nbeal2	Mm_Celera	9:110640747	CAGGGGAGTCACCTA[A/G]CTCTGCCTGACTTGA	235627
rs33297096	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110640802	AGAAAGTCACACTGG[A/G]CAATAAGCACGGGAG	235627
rs33297098	snp	A/G	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110640879	CCAGGTGTGAAGCCT[A/G]TAGTCCTCTTCCATC	235627
rs33297100	snp	C/T	0.124444	0.216185	intron-variant	Nbeal2	Mm_Celera	9:110640900	CTCTTCCATCAGGTG[C/T]TGGGCCAGGGCACAG	235627
rs33297102	snp	A/G	0.124444	0.216185	synonymous-codon	Nbeal2	Mm_Celera	9:110642147	GGGTGGTGCTCGGCT[A/G]GCATGCAGAACGTGC	235627
rs33297524	snp	C/T	0.375	0.216506	synonymous-codon	Nbeal2	GRCm38.p3	9:110631083	TCGCATACGGGAGTA[C/T]GTCTCTGCACTAGAC	235627
rs33298044	snp	A/C	0.124444	0.216185	missense	Nbeal2	Mm_Celera	9:110642269	CCTGCACAGAGCCAG[A/C]ACTCACAGCCATCTG	235627
rs33629139	snp	A/G	0.444444	0.157135	intron-variant	Nbeal2	Mm_Celera	9:110653221	TGCAAGGAGGGAGGC[A/G]TAACCCCGGGATCAC	235627
rs33707247	snp	C/T	0.32	0.24	intron-variant	Nbeal2	GRCm38.p3	9:110652351	CGCCCTTGCCTTACA[C/T]ACCCCGTGACACACA	235627
rs46515230	snp	A/G			synonymous-codon	Nbeal2	Mm_Celera	9:110644463	GCAGGGCTTGATCCA[A/G]GTCGTCCTGGTCCAG	235627
rs211984744	snp	A/G			intron-variant	Nbeal2	Mm_Celera	9:110634553	ATCCTGACAGATGCT[A/G]CTGCTCCCTCTACTG	235627
rs212085426	snp	A/G			intron-variant, upstream-variant-2KB	Nbeal2, Mir8107	GRCm38.p3	9:110636254	CCCACCGTCCAGAAG[A/G]CCTCCCCTGTCTCTC	235627
rs212162598	snp	C/G			upstream-variant-2KB, downstream-variant-500B	Nradd, Nbeal2	Mm_Celera	9:110624563	GAAGCCGACACCAGC[C/G]TGCCTGGCAGAGCAG	235627
rs212231463	snp	A/G			intron-variant	Nbeal2	Mm_Celera	9:110647018	GATCTGGGCTACTGG[A/G]AAGGGGAGGAAGTGC	235627
rs212278467	snp	G/T			intron-variant	Nbeal2	Mm_Celera	9:110647696	AGGTGTAGTGAGAGA[G/T]CCTGTCTCAGACAAT	235627
rs212342832	snp	C/T			intron-variant, upstream-variant-2KB	Nbeal2, Mir8107	GRCm38.p3	9:110637313	CTGATGCCCTGGAAT[C/T]AGGACAATGGGGTAG	235627
rs212507518	snp	A/G			upstream-variant-2KB, synonymous-codon	Nradd, Nbeal2	GRCm38.p3	9:110626331	CCCTGCTGACAGACC[A/G]CTCTGTGGGAAGGCA	235627
rs212721298	snp	C/T			intron-variant	Nbeal2	Mm_Celera	9:110640639	GCCATGGTTGAGCCC[C/T]CTGGGCCCTCTGCAC	235627
rs212845506	snp	C/T			intron-variant	Nbeal2	Mm_Celera	9:110648798	AGCTATGTGAAGAAG[C/T]TCACGCCCAGTACAG	235627
rs212847994	snp	C/T			missense	Nbeal2	Mm_Celera	9:110638536	ACGGCGCCTGCATGG[C/T]GAGCCTTCTGAGATT	235627
rs212905548	snp	A/G			intron-variant	Nbeal2	Mm_Celera	9:110649514	AACTTGCTGCCTTAG[A/G]CAGGGAAGAGCTCCA	235627
rs213041537	snp	C/T			intron-variant	Nbeal2	Mm_Celera	9:110639459	CACTCCCTTCGGCTG[C/T]GGAACACCTTCGCTA	235627
rs213057893	snp	G/T			intron-variant	Nbeal2	GRCm38.p3	9:110629487	CACATCTTAGTCGCA[G/T]GTAAACTACTCAGGG	235627
rs213114987	snp	C/T			missense	Nbeal2	Mm_Celera	9:110628401	CTCCTCACCAGAGCC[C/T]GGCGGTGTTTCTGGA	235627

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