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
rs3706576	snp	A/G	0.387812	0.208586	intron-variant	Rnf2	GRCm38.p3	1:151475755	CACAGAGCTCACTAC[A/G]AACTTCCAAAGGGGC	19821
rs3707084	snp	A/T	0.401235	0.199068	intron-variant	Rnf2	GRCm38.p3	1:151475821	CAGATGGAGAGACAA[A/T]CCTCTCAAAGGTATG	19821
rs3716514	snp	A/G	0.48	0.0979796	upstream-variant-2KB	Rnf2, Gm36527	GRCm38.p3	1:151501497	TAGCCATAGATAGTT[A/G]TCATTACCACCACCA	19821
rs6263578	snp	C/G	0.5	0	intron-variant	Rnf2	GRCm38.p3	1:151496845	CTCTAAGTCAGTCCC[C/G]GGCTGAGGGGGCAGT	19821
rs13465911	snp	A/G			missense	Rnf2	Mm_Celera	1:151471372	GTTTGTTCACTTTCC[A/G]GTATTTCTCACTGAC	19821
rs13465912	snp	A/G	0.42	0.183303	utr-variant-3-prime	Rnf2	GRCm38.p3	1:151470740	TCTATACAAACTGTA[A/G]TATCTTCATGAAGAC	19821
rs30472091	snp	G/T	0.375	0.216506	intron-variant	Rnf2	GRCm38.p3	1:151494030	AAGTAATGGGGCTAG[G/T]GGCTGGGTAACAGGC	19821
rs30497655	snp	C/G	0.375	0.216506	intron-variant	Rnf2	GRCm38.p3	1:151484093	TGATCCCTGCATTGG[C/G]GAAGACAGAGGCAGG	19821
rs30754287	snp	A/G	0.49827	0.0293608	intron-variant	Rnf2	GRCm38.p3	1:151473677	ACGAGTAAATTTGGT[A/G]AAATACATTGTCACT	19821
rs30802204	snp	C/T	0.444444	0.157135	intron-variant	Rnf2	Mm_Celera	1:151490211	CTTCCAAAGCTTTAC[C/T]GCCCAGCATTAACTT	19821
rs30870258	snp	A/G	0.375	0.216506	intron-variant	Rnf2	GRCm38.p3	1:151472381	GCCGGGCGTGGTGGC[A/G]CACGCCTTTAGTCCC	19821
rs30992484	snp	A/G	0.493827	0.0552116	intron-variant	Rnf2	GRCm38.p3	1:151488636	CCTTTAAAATGGACT[A/G]GATCTGGGTAAATGA	19821
rs30993819	snp	C/T	0.33241	0.236027	intron-variant	Rnf2	Mm_Celera	1:151478692	GTATCAATGTATATG[C/T]ATTCCTCAAACTGGT	19821
rs31138012	snp	A/G	0.375	0.216506	intron-variant, utr-variant-3-prime	Rnf2, Gm36527	GRCm38.p3	1:151499234	TTAGATGTTACCATC[A/G]AGTCTTTAAAAAAGG	19821
rs31288766	snp	C/T	0.32	0.24	intron-variant	Rnf2	GRCm38.p3	1:151497103	GGTTGTGAACCACCA[C/T]GTAGTCGATGGGAAC	19821
rs31322119	snp	A/G	0.444444	0.157135	intron-variant, missense	Rnf2, Gm36527	Mm_Celera	1:151499877	GGCATACAAACTTCC[A/G]ACAGCTTCTTTAAAA	19821
rs31338308	snp	C/T	0.444444	0.157135	intron-variant	Rnf2	Mm_Celera	1:151492821	GAATTTGCCTCAGTC[C/T]CCTTAGCTAAGATAT	19821
rs31549935	snp	A/G	0.444444	0.157135	intron-variant	Rnf2	GRCm38.p3	1:151494831	GTTGGTGGTACTGCT[A/G]CAGGGGACAGAACAA	19821
rs31552386	snp	C/T	0.32	0.24	intron-variant	Rnf2	GRCm38.p3	1:151495259	CTAGACAACATTTGG[C/T]TGAGTTCCAAGACAG	19821
rs31600592	snp	A/G	0.33241	0.236027	intron-variant	Rnf2	GRCm38.p3	1:151487198	ACAGAAACTAATCTC[A/G]AGTAAGGACAGTGAA	19821
rs31731476	snp	C/T	0.465374	0.126941	intron-variant	Rnf2	GRCm38.p3	1:151478194	ATTGAGTTGTTTGGT[C/T]TCTTAAATATTTTGC	19821
rs31732775	snp	A/C	0.345679	0.230967	intron-variant	Rnf2	GRCm38.p3	1:151495132	TTCATGCAAAGGGGG[A/C]GAGCATCACACCCAG	19821
rs31771533	snp	G/T	0.375	0.216506	intron-variant	Rnf2	Mm_Celera	1:151477798	CACCTTTGAACCTCA[G/T]AAAGTCTAATTCTAC	19821
rs31819741	snp	C/G/T	0.375	0.216506	intron-variant	Rnf2	GRCm38.p3	1:151472475	GTTCCAGGACAGCCA[C/G/T]GGCTACACAGAGAAA	19821
rs32039057	snp	A/G	0.5	0	intron-variant, missense	Rnf2, Gm36527	GRCm38.p3	1:151500294	TCCCGAGCCCACCCC[A/G]GTGCCAGGTCCCAAA	19821
rs32054360	snp	A/G	0.498615	0.0262793	intron-variant	Rnf2	GRCm38.p3	1:151491277	GGACAAGATGTGGCT[A/G]CATTAGAGATATTAG	19821
rs32103388	snp	A/G	0.375	0.216506	intron-variant	Rnf2	GRCm38.p3	1:151493971	GTCACCAGGCAAGAT[A/G]AGGATAGATGAGGCA	19821
rs32105398	snp	A/G	0.444444	0.157135	intron-variant	Rnf2	Mm_Celera	1:151486595	TGTATTTAAAGGGTC[A/G]CTGCAGCATTAGAAA	19821
rs32185058	snp	A/T	0.484429	0.0868505	intron-variant	Rnf2	GRCm38.p3	1:151494390	AGTTAAAATTTACTG[A/T]TAAAAAAGTCATATT	19821
rs32215800	snp	C/T	0.359862	0.224567	intron-variant	Rnf2	GRCm38.p3	1:151475239	CTCATGATTGTGCTA[C/T]ACTCTAAAAAGAAGT	19821
rs32219639	snp	A/G	0.32	0.24	intron-variant	Rnf2	Mm_Celera	1:151477605	AAACAGAAATGAAAC[A/G]CAGGACCACAGCTGT	19821
rs32225135	snp	A/G	0.375	0.216506	intron-variant	Rnf2	GRCm38.p3	1:151489152	CTCAGGCCCACCTGC[A/G]TAATTCAGTACAATC	19821
rs32241680	snp	C/T	0.444444	0.157135	intron-variant, utr-variant-5-prime	Rnf2	GRCm38.p3	1:151483825	GGACAGCCTTGTCTA[C/T]ACAGCAAGTTCCAGG	19821
rs32254634	snp	C/T	0.5	0	intron-variant	Rnf2	Mm_Celera	1:151471580	CAGGGCTCCCCCCCC[C/T]ACCAGACCCACCCAG	19821
rs32329765	snp	A/G	0.375	0.216506	intron-variant	Rnf2	Mm_Celera	1:151494681	AGAAATTTTATAAAG[A/G]TAAAATGATGTAGAA	19821
rs32380772	snp	A/C/G	0.444444	0.157135	intron-variant	Rnf2	GRCm38.p3	1:151495068	AGTCTCTCCCCCCAC[A/C/G]GTCTTTTTCTAAGTG	19821
rs32451993	snp	C/T	0.375	0.216506	intron-variant	Rnf2	GRCm38.p3	1:151487852	CCCACACCAAGACCC[C/T]GAGCTCTAAGAAAAG	19821
rs32457363	snp	C/T	0.375	0.216506	intron-variant	Rnf2	GRCm38.p3	1:151496113	ATGCTGGTGCTCTAA[C/T]TACTTCACTTAACCA	19821
rs32490619	snp	C/G	0.444444	0.157135	upstream-variant-2KB	Rnf2, Gm36527	GRCm38.p3	1:151501124	GCAGCCCCCAGCCAA[C/G]GCCTGCTGACTTGGG	19821
rs32491601	snp	A/G	0.444444	0.157135	intron-variant	Rnf2	GRCm38.p3	1:151474357	ATTAAAATTGTGCCC[A/G]AATGTGGTGGCTTAT	19821
rs32578800	snp	A/T	0.375	0.216506	intron-variant	Rnf2	GRCm38.p3	1:151496496	CACACCATACAGTAG[A/T]TTGTGTCGTGCCCAC	19821
rs32580688	snp	G/T	0.498615	0.0262793	intron-variant	Rnf2	GRCm38.p3	1:151493440	GTACCTCATGTCATA[G/T]CGAGAAAAGCTGGCT	19821
rs45640770	snp	C/T	0.375	0.216506	intron-variant	Rnf2	Mm_Celera	1:151474094	ACACAGTTAACATAC[C/T]TTGTTAGATATTTAC	19821
rs45687556	snp	C/G	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151475314	AATTCACAAATGGAA[C/G]TCATCTTTTAACCTT	19821
rs45713938	snp	C/T	0.336735	0.234472	intron-variant	Rnf2	Mm_Celera	1:151484706	GCCATCAATTCTTCC[C/T]TCAGGATATCAAGAA	19821
rs45809250	snp	A/G	0.391111	0.206368	intron-variant	Rnf2	Mm_Celera	1:151488644	ATGGACTGGATCTGG[A/G]TAAATGAGGTTACTA	19821
rs45822602	snp	A/G	0.391111	0.206368	intron-variant	Rnf2	Mm_Celera	1:151489883	CAGGGGAAAATAAGA[A/G]ATTTAGAGTAGGCAA	19821
rs45832846	snp	A/G	0.152778	0.230321	intron-variant	Rnf2	Mm_Celera	1:151473388	CATTATCTTTAAGGC[A/G]TCAAACTTGAAACCA	19821
rs45836615	snp	C/T	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151489917	AAACTGCCATCTTTA[C/T]CCTGCCTCCAGGCAG	19821
rs45856053	snp	C/T	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151489996	CGTCTGTAAACAGGG[C/T]GCCCGCCAACCTCTG	19821
rs45923423	snp	A/G	0.132653	0.220748	intron-variant	Rnf2	Mm_Celera	1:151477163	CTCATAGCCAATGTT[A/G]TCCTAGCTAAAATAT	19821
rs46127561	snp	A/G	0.142012	0.225474	intron-variant	Rnf2	Mm_Celera	1:151488008	AGCCGCACGTGGCTT[A/G]ATACTAACTGTAACT	19821
rs46191220	snp	C/T	0.375	0.216506	intron-variant	Rnf2	Mm_Celera	1:151488000	ACGGTAACAGCCGCA[C/T]GTGGCTTGATACTAA	19821
rs46193765	snp	A/G	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151493596	TAACCATAGGTAGGC[A/G]ATACCCAGATCCACC	19821
rs46254560	snp	G/T			intron-variant	Rnf2	Mm_Celera	1:151486327	AGGGCTGGGGGGGGG[G/T]GGAGGAGACAGGAGA	19821
rs46297480	snp	A/G	0.391111	0.206368	intron-variant	Rnf2	Mm_Celera	1:151490491	CCTAGTGATCTCAGC[A/G]GCAATCTGATTTTAT	19821
rs46327676	snp	C/T	0.152778	0.230321	intron-variant	Rnf2	Mm_Celera	1:151478282	ATGTGTTTATAAAAC[C/T]TCTCTGTATAATTAG	19821
rs46402174	snp	A/C	0.408163	0.193609	intron-variant	Rnf2	Mm_Celera	1:151490939	GGCCAGGCCAAGAGC[A/C]AGCATGAGCAGCACT	19821
rs46439064	snp	A/G	0.260355	0.249785	intron-variant	Rnf2	Mm_Celera	1:151484761	AAACAGGTAGAATGC[A/G]AAATAAAGAAAGTAC	19821
rs46511121	snp	C/G	0.391111	0.206368	intron-variant	Rnf2	Mm_Celera	1:151485736	GACAAAGGGAACTAA[C/G]TGAGCATTGCTGCAA	19821
rs46542059	snp	C/T	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151491408	GTGACTGCATAGATG[C/T]TGATGCTAAGGAGTA	19821
rs46648657	snp	A/G	0.142012	0.225474	intron-variant	Rnf2	Mm_Celera	1:151481120	AGCATATAAAAACAG[A/G]ATAGATCCAAAACTA	19821
rs46675574	snp	C/T	0.426035	0.177515	intron-variant	Rnf2	Mm_Celera	1:151486906	CTCTCCAGTCCTCTA[C/T]ATATTCATTTTATAA	19821
rs46739726	snp	C/T	0.391111	0.206368	intron-variant	Rnf2	Mm_Celera	1:151490781	TAATGGACAGACAAC[C/T]CCAATATATGCTTTC	19821
rs46743933	snp	C/T	0.244898	0.249948	intron-variant	Rnf2	Mm_Celera	1:151472763	ACAAATATCTGATGT[C/T]TAGCTGCACTCCTGA	19821
rs46832232	snp	A/C	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151488042	AGAAAGTTAAAAGGG[A/C]GCAGAAGTGCACTAG	19821
rs46850043	snp	A/G	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151481000	AATTTAGAGCCAGAG[A/G]AATAATTCACAGTTG	19821
rs46857988	snp	C/T	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151491021	CCAGTGCTTGGGAGG[C/T]CACACTTACCTCAGA	19821
rs46889226	snp	A/C	0.152778	0.230321	intron-variant	Rnf2	Mm_Celera	1:151476745	CTCCAATAACTAAAA[A/C]CTAGAATCTACACCT	19821
rs46893410	snp	C/G	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151484982	TGACAAGCACACTGG[C/G]AATTAGTGATAACAA	19821
rs46978547	snp	A/G	0.391111	0.206368	intron-variant	Rnf2	Mm_Celera	1:151488875	AATCCACACTGGTGA[A/G]CTGCAGGACTGAGTT	19821
rs46994253	snp	A/G	0.32	0.24	intron-variant	Rnf2	Mm_Celera	1:151476777	TTAGGAAGGGCTCCA[A/G]TTCTGAAATACTTAG	19821
rs47077769	snp	A/G	0.132653	0.220748	intron-variant	Rnf2	Mm_Celera	1:151483532	ATAATCAAAAGTGAC[A/G]GGGTTGAGAGGCTCC	19821
rs47079301	snp	A/G	0.375	0.216506	utr-variant-3-prime	Rnf2	GRCm38.p3	1:151470553	ATTCGACTTTTCCCC[A/G]TGACCTGAAATTCTA	19821
rs47134426	snp	C/T	0.391111	0.206368	intron-variant	Rnf2	Mm_Celera	1:151495092	CTAAGTGCTGGCTGG[C/T]GACTGAGCCTAGGGC	19821
rs47252134	snp	A/G	0.408163	0.193609	intron-variant	Rnf2	Mm_Celera	1:151479619	GCAATGCTAACATGA[A/G]CCAGGCAGTGCAGCA	19821
rs47257370	snp	A/C	0.336735	0.234472	intron-variant	Rnf2	Mm_Celera	1:151475609	CCTTACACTGATACG[A/C]TAATTCTGAAACACT	19821
rs47264361	snp	A/G	0.277778	0.248452	intron-variant	Rnf2	Mm_Celera	1:151482803	CCTAGAAGGCTATGT[A/G]TGTGATCAATTTGTG	19821
rs47356479	snp	C/T	0.132653	0.220748	intron-variant	Rnf2	Mm_Celera	1:151488210	GAACCAGAGGGCCTT[C/T]GTCCTTTAGTCAAAT	19821
rs47410937	snp	A/G	0.32	0.24	intron-variant	Rnf2	Mm_Celera	1:151475377	AATCACTTAGAACCT[A/G]AGAACAGTATATGGA	19821
rs47431087	snp	C/T			intron-variant	Rnf2	Mm_Celera	1:151495487	CTGGGTAACAGTTAT[C/T]AATACAATAAGGGAA	19821
rs47472845	snp	A/G	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151485066	ACCACTGCTGTTACC[A/G]AAACGACCGTGTCGA	19821
rs47510548	snp	A/G	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151489835	TGCTTGCTTACAGGA[A/G]AGAGAGGTTAGATTT	19821
rs47659269	snp	C/T	0.142012	0.225474	intron-variant	Rnf2	Mm_Celera	1:151484492	GAGGAATAGGGGAGT[C/T]AAGAAAGCATGGATG	19821
rs47712375	snp	G/T	0.260355	0.249785	intron-variant	Rnf2	Mm_Celera	1:151481502	GAGTACCTCAGAAAC[G/T]GACCAGGTAGTTCCC	19821
rs47713201	snp	C/G	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151477258	GACACACAGGAGAGA[C/G]TATTAGTAGGAAGTC	19821
rs47714696	snp	C/T	0.244898	0.249948	intron-variant	Rnf2	Mm_Celera	1:151474309	GTCCTGATGGCAGGG[C/T]TTTACAATTAGCATA	19821
rs47825242	snp	A/G	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151479655	CATGACAACTCAGAT[A/G]GAAATACACAGTCCC	19821
rs47855815	snp	C/T	0.459184	0.136902	intron-variant	Rnf2	Mm_Celera	1:151486929	TTTTATAATACCAGG[C/T]AAACAGAAAAATATA	19821
rs47862542	snp	A/T	0.444444	0.157135	intron-variant	Rnf2	Mm_Celera	1:151490944	GGCCAAGAGCAAGCA[A/T]GAGCAGCACTCAGTG	19821
rs47869990	snp	A/C	0.124444	0.216185	synonymous-codon	Rnf2	Mm_Celera	1:151476901	TGTGATAATACAATC[A/C]GCGCAAAACCGATGT	19821
rs47911624	snp	C/T	0.152778	0.230321	intron-variant	Rnf2	Mm_Celera	1:151493347	CTCTTTACCCTGATA[C/T]TCTACCTCTAGCTCT	19821
rs48012027	snp	A/G	0.277778	0.248452	intron-variant	Rnf2	Mm_Celera	1:151485306	AACTCTCTAGAGATG[A/G]AATGCCAGACTACAC	19821
rs48022353	snp	G/T	0.375	0.216506	intron-variant	Rnf2	Mm_Celera	1:151479778	TAACTACCTAGTCTT[G/T]CCTGACTCCAGTGCT	19821
rs48057893	snp	C/T	0.124444	0.216185	intron-variant	Rnf2	Mm_Celera	1:151494772	ATTTGTGATGCCTAC[C/T]AAAGCAAAGCTCTGT	19821
rs48066108	snp	C/T	0.152778	0.230321	synonymous-codon	Rnf2	GRCm38.p3	1:151473074	CGCCCACGCTTACCT[C/T]GTCTGTGCGCTGTCG	19821
rs48172945	snp	A/G	0.459184	0.136902	intron-variant	Rnf2	Mm_Celera	1:151481658	TCGGAGGCCACTTGT[A/G]ACCATGGTCTAAGGC	19821
rs48243816	snp	A/G	0.408163	0.193609	intron-variant	Rnf2	Mm_Celera	1:151493206	GGTATCCTTAGTGCT[A/G]CAGACCTTATAGGGT	19821
rs48382835	snp	A/G	0.408163	0.193609	intron-variant	Rnf2	Mm_Celera	1:151494376	GGAAAGCAGCTAGTA[A/G]TTAAAATTTACTGAT	19821
rs48585268	snp	C/T	0.132653	0.220748	intron-variant	Rnf2	Mm_Celera	1:151479801	CCAGTGCTGGAGGGA[C/T]CTGAAATACTCCTCC	19821

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