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
rs6171719	snp	A/T	0.387812	0.208586	intron-variant	Rnf41	Mm_Celera	10:128435869	ATTTCCTGTCTGTGA[A/T]GTGGGAAGTATTAAA	67588
rs6171784	snp	A/G	0.493827	0.0552116	intron-variant	Rnf41	Mm_Celera	10:128435912	CCTTTGAGCAGCGAT[A/G]TAGGCCTCCTNATAA	67588
rs6171798	snp	A/C	0.32	0.24	intron-variant	Rnf41	Mm_Celera	10:128435923	CGATNTAGGCCTCCT[A/C]ATAAAGGAATGTGTG	67588
rs6172862	snp	C/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128436082	tgctgccagctcagt[C/T]ggcagagtgctttcc	67588
rs6273500	snp	A/C	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128420516	caatagtaactgtaa[A/C]caaganagaaatagg	67588
rs6273505	snp	C/G	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128420522	taactgtaancaaga[C/G]agaaataggtagcag	67588
rs6343610	snp	C/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128436341	TAAAGAAAGGGAGGC[C/T]TGGAAAGATTGTTAG	67588
rs13471487	snp	C/T	0.444444	0.157135	utr-variant-3-prime, intron-variant, nc-transcript-variant	Rnf41	Mm_Celera	10:128439039	GCACAGGGTGGGTTG[C/T]TGAAATGTTGCTGAA	67588
rs13471488	snp	A/G	0.375	0.216506	utr-variant-3-prime, intron-variant, nc-transcript-variant	Rnf41	Mm_Celera	10:128438767	CTAGAGGATCAGGGT[A/G]GAGTGAGGCATTTCT	67588
rs13480826	snp	C/T	0.265928	0.249492	synonymous-codon, nc-transcript-variant	Rnf41	Mm_Celera	10:128437400	GACAATCGAATACAA[C/T]GAGATCCTCGAGTGA	67588
rs29315989	snp	A/G	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128414414	TAAAGAAGTATATAT[A/G]TGGGGCTGGAGAGAT	67588
rs29317345	snp	C/T	0.5	0	utr-variant-3-prime, nc-transcript-variant	Rnf41	Mm_Celera	10:128439990	TCTGGGAGTTCCACT[C/T]CAGGCTAGCCTGCTG	67588
rs29319370	snp	G/T	0.484429	0.0868505	upstream-variant-2KB, intron-variant, utr-variant-5-prime	Rnf41, Nabp2	Mm_Celera	10:128410474	GGTTCGGCTCAGGGC[G/T]CTGGGACAAGCAGCA	67588
rs29319432	snp	A/C	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128414504	ACCCACTAAGCAGTT[A/C]ACAACTGTCTAACTC	67588
rs29320009	snp	G/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128429910	CTCTCAGTAACTGCA[G/T]CTTTAAGGAGATCCG	67588
rs29321266	snp	C/T	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128435166	TGAAAATGCTCTGCC[C/T]AAAAAGATCTGTCCT	67588
rs29322839	snp	A/G/T	0.429688	0.173817	upstream-variant-2KB, intron-variant	Rnf41, Nabp2	GRCm38.p3	10:128409890	AAGGTCCGATCTGCC[A/G/T]CCCAAAGCGCCCCAC	67588
rs29323312	snp	G/T	0.444444	0.157135	utr-variant-3-prime, intron-variant, nc-transcript-variant	Rnf41	Mm_Celera	10:128439189	TCAAGAGGGTGTCTG[G/T]GTTGCCTCGGTGGCC	67588
rs29323478	snp	C/T	0.359862	0.224567	intron-variant	Rnf41	Mm_Celera	10:128435063	GTGTCCTGTGAGTCT[C/T]TTACTGTTACAGAAC	67588
rs29324020	snp	C/T	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128434355	TTCTGTTAACTGTCT[C/T]GCCAGCCCCTGTTTG	67588
rs29324799	snp	A/G	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128419107	TTGTAAACCAGGTTG[A/G]CTTCGAACTCAGAAA	67588
rs29326538	snp	C/G	0.345679	0.230967	intron-variant	Rnf41	Mm_Celera	10:128437556	GTTTGTCCAGAACTA[C/G]CTGGGGACCACCATG	67588
rs29327142	snp	A/G	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128430168	TCTCTGTGAGTTCAC[A/G]TTGTCACTTGAACGT	67588
rs29328310	snp	C/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128435961	ACGCCAAAAGAGGAG[C/T]CTGAGAGACATACAA	67588
rs29330406	snp	G/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128429883	ACAGCAACCACATCT[G/T]TGCTACAGTGGCTCT	67588
rs29331680	snp	C/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128417959	ATCTCTATGCCAAGG[C/T]CCAGGTCAGAAACTT	67588
rs29332858	snp	C/G	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128416205	AGACAGCCAGGCCTA[C/G]ATAGTGAGGTCCCTT	67588
rs29332912	snp	C/T	0.48	0.0979796	intron-variant	Rnf41	Mm_Celera	10:128428920	ATTTCAAGGTCTGTG[C/T]TCTGTCTGTGACGGA	67588
rs29334535	snp	A/G	0.391111	0.206368	utr-variant-3-prime, nc-transcript-variant	Rnf41	Mm_Celera	10:128439861	GCTGCTGGGTCCCCC[A/G]TGGTGGCTAGTAGAG	67588
rs29336106	snp	G/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128436014	TGGCTCCTAAGATGA[G/T]GGCTGGCTCTTAAAG	67588
rs29338004	snp	C/T	0.408163	0.193609	intron-variant	Rnf41	Mm_Celera	10:128415521	TGAAGACGGTGATTG[C/T]GTTCCTCTTTATTCT	67588
rs29338337	snp	A/T	0.304688	0.243945	intron-variant	Rnf41	GRCm38.p3	10:128430680	TGACCGGGTTGCTCA[A/T]AGCTCTGTCTAGCAA	67588
rs29338911	snp	A/G	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128427498	GTTTTTATTTGAGGC[A/G]GGGCTTCACTGTCTG	67588
rs29342330	snp	A/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128418206	TATTTTAAACTGATT[A/T]AGTAACACTGAATTA	67588
rs29345964	snp	C/T	0.497778	0.0332592	intron-variant	Rnf41	Mm_Celera	10:128422653	TGAGTAACCGCAGAG[C/T]TGTTCCAGGCTTGGT	67588
rs29346314	snp	A/G	0.408163	0.193609	intron-variant	Rnf41	Mm_Celera	10:128437872	ACCATGCATGCATTG[A/G]GACTTGAAAGAATAA	67588
rs29346747	snp	A/G	0.359862	0.224567	intron-variant	Rnf41	Mm_Celera	10:128435607	TCCTCCTTCCACTCC[A/G]TTCAGACATGGGCCT	67588
rs29347227	snp	A/G	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128426696	TTTTTTTTTTAAACT[A/G]TTATTTTCATTGTGT	67588
rs29349747	snp	A/C	0.49827	0.0293608	intron-variant	Rnf41	Mm_Celera	10:128437167	CACTGCCCAGCGTGG[A/C]GTGCTGTCTTCATGA	67588
rs29349846	snp	C/G	0.415225	0.187619	intron-variant	Rnf41	Mm_Celera	10:128435631	TGGGCCTTCCTGGCT[C/G]CACTCCTGTAGGCAA	67588
rs29350208	snp	C/T	0.465374	0.126941	intron-variant	Rnf41	Mm_Celera	10:128429371	CGGGCACCTTTCAGA[C/T]TTTGATTCTTTCTAG	67588
rs29351120	snp	A/G	0.336735	0.234472	intron-variant	Rnf41	Mm_Celera	10:128436644	ATGTTCTCCTGGTAA[A/G]GGATCTCCTGCCAGT	67588
rs29351424	snp	C/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128413800	TACCGTACCTGCCTT[C/T]GTTCTTCCTGTTTAT	67588
rs29351716	snp	A/G	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128414238	GGAATGCAGGCATGG[A/G]CTGTCCTCCCTGGCC	67588
rs29352387	snp	A/C/T	0.444444	0.157135	intron-variant	Rnf41	GRCm38.p3	10:128419161	TGCTGGGATTAAAGG[A/C/T]GTGCACCACCATGCC	67588
rs29352649	snp	C/T	0.48	0.0979796	intron-variant	Rnf41	Mm_Celera	10:128437632	GGGTAGCTTAGCACG[C/T]GGAGGAGAGGGCAGA	67588
rs29354681	snp	A/G	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128418031	CAATTGTGGATTGTA[A/G]TTCAATCCAGATATA	67588
rs29359146	snp	C/T	0.345679	0.230967	intron-variant	Rnf41	Mm_Celera	10:128437716	GGAAGTGTAAGACCA[C/T]GTAAGACCCTGTCTA	67588
rs29359347	snp	A/G	0.492188	0.0620098	intron-variant	Rnf41	Mm_Celera	10:128435158	ACCTGACCTGAAAAT[A/G]CTCTGCCCAAAAAGA	67588
rs29360309	snp	A/G	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128435904	ACACTGATCCTTTGA[A/G]CAGTGATGTAGGCCT	67588
rs29360836	snp	C/T	0.492188	0.0620098	intron-variant	Rnf41	Mm_Celera	10:128416815	GTGTTAGCACCAAGG[C/T]TCAGATTCAGAAGTG	67588
rs29361943	snp	A/G	0.497778	0.0332592	intron-variant	Rnf41	Mm_Celera	10:128434941	GTGGTCGCCCTTGCC[A/G]GCAGGGCTCACCTTC	67588
rs29363785	snp	A/G	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128418173	TAAAGAAAACAAACA[A/G]ATGAAATACAGACTG	67588
rs29363965	snp	C/T	0.415225	0.187619	intron-variant	Rnf41	Mm_Celera	10:128414044	TCTGACTTTTTCCAG[C/T]CCTGGCACTATAGGC	67588
rs29364686	snp	C/T	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128418015	TGGCTGGTGAGTCTT[C/T]CAATTGTGGATTGTA	67588
rs29364939	snp	C/T	0.49827	0.0293608	intron-variant	Rnf41	Mm_Celera	10:128437614	GTACTCAGGAGCAAA[C/T]GGGGGTAGCTTAGCA	67588
rs29365035	snp	A/G	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128413995	GCTTACATCCCTGCC[A/G]GGAATGATCTAAAGC	67588
rs29367379	snp	A/G	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128414006	TGCCGGGAATGATCT[A/G]AAGCCCTGCTTTCTC	67588
rs29374566	snp	A/G	0.345679	0.230967	intron-variant	Rnf41	GRCm38.p3	10:128426600	TTTATTTTTTTCAGT[A/G]TCGGGGTTGAGTCCA	67588
rs29374973	snp	C/T	0.489796	0.070696	intron-variant	Rnf41	Mm_Celera	10:128418266	AATGCAAGGGAATGT[C/T]ACTTCTCTCTCTTTT	67588
rs29376261	snp	C/T	0.48	0.0979796	intron-variant	Rnf41	Mm_Celera	10:128437424	CGAGTGAGTGTCACT[C/T]GGTGTGGAGTCAGGG	67588
rs29376734	snp	C/T	0.497778	0.0332592	intron-variant	Rnf41	Mm_Celera	10:128435908	TGATCCTTTGAACAG[C/T]GATGTAGGCCTCCTC	67588
rs29379061	snp	C/T	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128414523	ACTGTCTAACTCCAA[C/T]ACCAGGGAATCCACT	67588
rs29379322	snp	G/T	0.391111	0.206368	intron-variant	Rnf41	Mm_Celera	10:128415558	CTCTGTTGGCAAGAA[G/T]ATTGTATGTTAGGAT	67588
rs29381889	snp	C/G	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128434403	AGGGACTGTTCTTTT[C/G]TTGAGACAAGGTCTT	67588
rs29382878	snp	G/T	0.48	0.0979796	utr-variant-3-prime, nc-transcript-variant	Rnf41	Mm_Celera	10:128440249	GAGGCTGAAGTTTGC[G/T]TGCCCTTTGCACCAG	67588
rs29382915	snp	A/G	0.5	0	intron-variant	Rnf41	Mm_Celera	10:128437846	AGTCTGGCAGTTGCT[A/G]TGTGGTAGGCACCAT	67588
rs33880955	snp	C/T	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128434507	GTGCACCAGCCTGCC[C/T]GGATTTTTTTTTTCT	67588
rs33880974	snp	A/G	0.444444	0.157135	intron-variant	Rnf41	Mm_Celera	10:128434439	GTAGACCATGCTGGC[A/G]TGGGACTTAGAGACC	67588
rs33881241	snp	C/G	0.444444	0.157135	intron-variant	Rnf41	GRCm38.p3	10:128434542	TTGCTTATTTTGTGT[C/G]TGTGTGTGTGTGTGT	67588
rs36257932	snp	A/G	0.459184	0.136902	upstream-variant-2KB, intron-variant, utr-variant-5-prime	Rnf41, Nabp2	Mm_Celera	10:128410450	CACATCATCTTTAAT[A/G]TACCGAACGGTTCGG	67588
rs36258589	snp	A/G	0.375	0.216506	intron-variant	Rnf41	Mm_Celera	10:128425243	AATAAGAAGTTGAAG[A/G]TGATCTCTAGAGCCA	67588
rs36270348	snp	A/G	0.244898	0.249948	intron-variant	Rnf41	Mm_Celera	10:128427544	tcttgaagtcaaagg[A/G]attaaaaggcttggg	67588
rs36271752	snp	C/G	0.165289	0.235211	intron-variant	Rnf41	Mm_Celera	10:128416868	TTAGTTTGTACATGT[C/G]GAGGTGGCCTGGGAC	67588
rs36274950	snp	A/G	0.35503	0.226867	intron-variant	Rnf41	Mm_Celera	10:128427162	GATAAAATTAGGTGG[A/G]CAGATTCTAAACTCC	67588
rs36313384	snp	A/G	0.142012	0.225474	intron-variant	Rnf41	Mm_Celera	10:128437829	ATTTCTTCCTTCAGG[A/G]CAGTCTGGCAGTTGC	67588
rs36348654	snp	C/T	0.336735	0.234472	intron-variant	Rnf41	Mm_Celera	10:128437977	TTTTCTGGACCAATG[C/T]TAGTAAGAAAGTCAG	67588
rs36356806	snp	C/G/T	0.459184	0.136902	upstream-variant-2KB, utr-variant-5-prime	Rnf41, Nabp2	Mm_Celera	10:128411116	TTTGAAGAGCCATCA[C/G/T]GAATACTACAAGAGT	67588
rs36367891	snp	C/T	0.42	0.183303	utr-variant-3-prime, intron-variant, nc-transcript-variant	Rnf41	Mm_Celera	10:128439121	GAGCACTGGTGTTCG[C/T]ACACTCAGCAGGAAG	67588
rs36370384	snp	A/G	0.132653	0.220748	intron-variant	Rnf41	Mm_Celera	10:128426987	ATGAACCCTGACGGC[A/G]TGTGCATGTGTGTGA	67588
rs36379393	snp	C/G	0.142012	0.225474	intron-variant	Rnf41	Mm_Celera	10:128426471	gtagtctagaactta[C/G]tatatagctcaggct	67588
rs36407710	snp	A/G	0.35503	0.226867	utr-variant-3-prime, intron-variant, nc-transcript-variant	Rnf41	Mm_Celera	10:128438856	GCTTGCTGAAGTCAC[A/G]CAGCATTGAGAGCTG	67588
rs36457765	snp	A/T	0.336735	0.234472	intron-variant	Rnf41	Mm_Celera	10:128426325	CTTGCACTTGTGTTG[A/T]CTCGTCAGTGAGTTC	67588
rs36470660	snp	A/G	0.132653	0.220748	intron-variant	Rnf41	Mm_Celera	10:128433662	CCCAGTTCTGGGCAC[A/G]TGTAATAAATGCAAA	67588
rs36494069	snp	A/G	0.46281	0.131194	intron-variant	Rnf41	Mm_Celera	10:128418564	TTACCTTTACCTGCC[A/G]GGACTTGTAAACCCT	67588
rs36519327	snp	C/T	0.132653	0.220748	intron-variant	Rnf41	Mm_Celera	10:128428473	TATTCCTCACATAAC[C/T]AGATTCTCAATCAAT	67588
rs36524070	snp	C/T	0.336735	0.234472	intron-variant	Rnf41	Mm_Celera	10:128429075	TCTATTGAAAAAGTT[C/T]GATGTAGCCATGCAC	67588
rs36573073	snp	A/G	0.426035	0.177515	intron-variant	Rnf41	Mm_Celera	10:128428359	ACCACTGTTCTTTCA[A/G]CCTGGATCAGGAGTC	67588
rs36601015	snp	C/T	0.165289	0.235211	intron-variant	Rnf41	Mm_Celera	10:128426864	GTTAAACAGTGAAAC[C/T]CTCACTTGAATAGTA	67588
rs36689511	snp	C/T	0.297521	0.245442	intron-variant	Rnf41	Mm_Celera	10:128428932	GTGTTCTGTCTGTGA[C/T]GGACCTTCTAGACCT	67588
rs36690886	snp	G/T	0.375	0.216506	intron-variant	Rnf41	Mm_Celera	10:128427138	TCCAGCATGGCCCCC[G/T]TTCAGAAAGATAAAA	67588
rs36722747	snp	C/T	0.277778	0.248452	intron-variant	Rnf41	Mm_Celera	10:128426962	GACAAACACTGCTCC[C/T]GAGCTGAGCATGAAC	67588
rs36723631	snp	A/G	0.18	0.24	intron-variant	Rnf41	Mm_Celera	10:128424968	GGTTTATAGAGCATT[A/G]CTTGTTGTATGTGAG	67588
rs36726530	snp	A/G	0.124444	0.216185	intron-variant	Rnf41	Mm_Celera	10:128426203	ATCAGTAGTGGATGA[A/G]AAACCACCCACAAAA	67588
rs36731101	snp	A/G	0.132653	0.220748	intron-variant	Rnf41	Mm_Celera	10:128436047	ACAAGAGGAGAATCC[A/G]TGGCAGGGTGCTGGG	67588
rs36737915	snp	C/T	0.396694	0.202437	utr-variant-3-prime, nc-transcript-variant	Rnf41	Mm_Celera	10:128439757	CAGCCAAGTGGGATA[C/T]AAATCAGATGTCTCC	67588
rs36751974	snp	C/T	0.260355	0.249785	intron-variant	Rnf41	Mm_Celera	10:128429202	AGCTGTAAGGTAAAC[C/T]GCTGACAGCAACATT	67588
rs36767117	snp	C/T	0.336735	0.234472	intron-variant	Rnf41	Mm_Celera	10:128426403	CAGATATTTACTGTG[C/T]GTGTTATAGGTTAGG	67588
rs36769146	snp	C/T	0.244898	0.249948	downstream-variant-500B	Rnf41	Mm_Celera	10:128441492	TCACTGATCGCACAG[C/T]GGAAGCCACCTGCTG	67588
rs36791503	snp	C/T	0.152778	0.230321	intron-variant	Rnf41	Mm_Celera	10:128430627	AGAGGATCTCAAGTT[C/T]AAGGTTAACCTGGAC	67588

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