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
rs6178928	snp	A/G	0.46875	0.121031	intron-variant	Phip	GRCm38.p3	9:82947959	TTTTACAACAGAAAC[A/G]CTATTCTAGGACTCA	83946
rs6179383	snp	C/G	0.46875	0.121031	intron-variant	Phip	GRCm38.p3	9:82948020	ACTGTAACATCTATC[C/G]ATCCTACTATACCTT	83946
rs6208037	snp	C/G	0.5	0	intron-variant	Phip	Mm_Celera	9:82955295	TTTATAAAAACTCTC[C/G]GAAGGGTTGGCTCAG	83946
rs6208078	snp	A/G	0.396694	0.202437	intron-variant	Phip	Mm_Celera	9:82955325	GTGAGTTAAGTGTCA[A/G]AGATAGTTCTATTAA	83946
rs6209196	snp	A/T	0.5	0	intron-variant	Phip	GRCm38.p3	9:82955540	AGAAGGACAATCCCA[A/T]AATCATTTAATAATC	83946
rs6210165	snp	G/T	0.5	0	intron-variant	Phip	GRCm38.p3	9:82955682	ATGTGCAGATTTGTT[G/T]TTTAGTTGTTCTACT	83946
rs6210302	snp	A/G	0.391111	0.206368	intron-variant	Phip	GRCm38.p3	9:82955766	AGAAGCAAAGCAGCT[A/G]AAATTTCAGACAGGA	83946
rs6213853	snp	A/G	0.5	0	intron-variant	Phip	Mm_Celera	9:82949858	ACCTTTAATTTCTGT[A/G]CCAGAATGACAAAAC	83946
rs6303689	snp	A/G	0.5	0	intron-variant	Phip	Mm_Celera	9:82928047	AGGTCATTCCCATCT[A/G]Caaattataatatta	83946
rs6316826	snp	A/G	0.5	0	intron-variant, utr-variant-5-prime	Phip	Mm_Celera	9:82928248	GGGGGAAGATCAGAG[A/G]CTCTATCAAAATGTA	83946
rs6317246	snp	A/C	0.5	0	intron-variant, utr-variant-5-prime	Phip	GRCm38.p3	9:82928307	CATCTTTATTTACAA[A/C]GTATTCTAATACAGC	83946
rs6317282	snp	G/T	0.5	0	intron-variant, utr-variant-5-prime	Phip	GRCm38.p3	9:82928324	TATTCTAATACAGCA[G/T]AAATAGTTNCCTAAG	83946
rs6317298	snp	A/C	0.5	0	intron-variant, utr-variant-5-prime	Phip	GRCm38.p3	9:82928333	ACAGCANAAATAGTT[A/C]CCTAAGTCTCTATAA	83946
rs6317828	snp	G/T	0.456747	0.140554	intron-variant, utr-variant-5-prime	Phip	GRCm38.p3	9:82928440	TCAAAATGCCTGAAG[G/T]TCACTTGACAAACAG	83946
rs6319001	snp	A/C	0.444444	0.157135	intron-variant, upstream-variant-2KB	Phip, LOC105243467	GRCm38.p3	9:82967747	GGTTTACTCATGTCA[A/C]CAAAATATTCTCTCA	83946
rs6323465	snp	A/G	0.5	0	intron-variant	Phip	Mm_Celera	9:82896199	AGGAAATAAATCTGT[A/G]CAAAAATTTTACTCT	83946
rs6323931	snp	C/T	0.5	0	intron-variant	Phip	Mm_Celera	9:82896228	CTCCAGTATTAAAAC[C/T]TTTTACTAGAAAAGC	83946
rs6337766	snp	C/G	0.5	0	intron-variant	Phip	GRCm38.p3	9:82896479	AGCAATACTAACTAA[C/G]TAAGACTCTATCCTA	83946
rs6338327	snp	C/G	0.304688	0.243945	intron-variant	Phip	GRCm38.p3	9:82896582	TAAACAACCTAACAA[C/G]AGTCTCATTCATTCA	83946
rs13464262	snp	C/T			utr-variant-3-prime	Phip	GRCm38.p3	9:82866861	AACTACTTAATCCCA[C/T]CATGGGATATTTAGA	83946
rs13464263	snp	A/G	0.408163	0.193609	utr-variant-3-prime	Phip	Mm_Celera	9:82867668	TTTTAATATTTTGTT[A/G]GCGTGAAGTTTATTT	83946
rs13464264	snp	A/G			utr-variant-3-prime	Phip	GRCm38.p3	9:82867444	AGGTTAAAAATTGGG[A/G]AAAGTACACCTTTTG	83946
rs29793861	snp	A/C	0.375	0.216506	intron-variant	Phip	Mm_Celera	9:82894652	AGTGTACCCCCCCCC[A/C]CCCACACACACACAA	83946
rs29931655	snp	A/G	0.32	0.24	intron-variant	Phip	Mm_Celera	9:82917203	GCATCCTCTCTCTCA[A/G]AAATCTCGCATTGCA	83946
rs29938732	snp	C/T	0.375	0.216506	intron-variant	Phip	Mm_Celera	9:82973243	AGTTCAAATTTCAAT[C/T]ACTTTGGACCAAGTA	83946
rs30334702	snp	A/C	0.375	0.216506	intron-variant	Phip	Mm_Celera	9:82894654	TGTACCCCCCCCCCC[A/C]CACACACACACAAAT	83946
rs33702150	snp	G/T	0.444444	0.157135	intron-variant	Phip	Mm_Celera	9:82956018	AATGTTATAACTTTT[G/T]GTTGGTGCTAACAGA	83946
rs45649862	snp	A/G			intron-variant	Phip	GRCm38.p3	9:82946108	AAATAAACAATACAA[A/G]TAATTAAGTTCCTTG	83946
rs45664061	snp	A/C	0.391111	0.206368	intron-variant	Phip	Mm_Celera	9:82942679	TAAAGTAGAGATTGG[A/C]AAAAGATTCAAATTT	83946
rs45669734	snp	C/T	0.244898	0.249948	intron-variant	Phip	Mm_Celera	9:82917077	AGAAGACAAAGACTT[C/T]ATAACTGCTTCTAGA	83946
rs45674220	snp	A/T	0.21875	0.248039	intron-variant	Phip	Mm_Celera	9:82904674	GATAGTTGTTTTTGT[A/T]CTTCATTTTTTTTCT	83946
rs45688394	snp	C/G	0.142012	0.225474	intron-variant	Phip	Mm_Celera	9:82886792	ATTTTAAGATTCACT[C/G]GTACATTAGGATGAA	83946
rs45714856	snp	A/G			intron-variant	Phip	GRCm38.p3	9:82972286	TCTGCTCATATTACT[A/G]TCCAGTTTATCAGTT	83946
rs45730935	snp	C/T	0.375	0.216506	intron-variant	Phip	GRCm38.p3	9:82889629	GCTATAGGCTCCAGA[C/T]AGACAAGGACTGTCA	83946
rs45739587	snp	C/T	0.336735	0.234472	intron-variant	Phip	GRCm38.p3	9:82914791	CACAAGTTACAAATG[C/T]AAATCTAGATTGTTC	83946
rs45741183	snp	C/T	0.473373	0.11227	intron-variant	Phip	GRCm38.p3	9:82953072	ACAGCTGAGCCAAAG[C/T]TTCAAGACCAATGAT	83946
rs45749951	snp	A/G	0.244898	0.249948	intron-variant	Phip	GRCm38.p3	9:82947029	ATTCCATAATCTAAC[A/G]CCTGAAACCTCTGAG	83946
rs45755140	snp	C/T	0.42	0.183303	intron-variant	Phip	GRCm38.p3	9:82946493	CATCTAACTAAATTA[C/T]TACTGTACTTACTTT	83946
rs45756347	snp	A/T			intron-variant	Phip	GRCm38.p3	9:82972366	CCAAATAATTTTAAA[A/T]TAATTCTTGTTAATT	83946
rs45776001	snp	C/T	0.132653	0.220748	missense	Phip	Mm_Celera	9:82880216	TCCATGCCTGAATAT[C/T]GTAAGACTGAGCTCT	83946
rs45788551	snp	C/T	0.391111	0.206368	intron-variant	Phip	GRCm38.p3	9:82940163	CACTTGCCTGACATG[C/T]ATAAGGCCACTTCAG	83946
rs45793615	snp	C/G	0.375	0.216506	intron-variant	Phip	GRCm38.p3	9:82968233	TCTGAGAATCCTGAA[C/G]TGCACATAACTGTTC	83946
rs45820911	snp	C/T			intron-variant	Phip	Mm_Celera	9:82923227	GGTATTATTAAAATA[C/T]TGTCTCTAAATATAC	83946
rs45851513	snp	A/C	0.336735	0.234472	intron-variant	Phip	GRCm38.p3	9:82941688	TTAAGCTCTCTTCAT[A/C]TGTAATGTTGTTTTC	83946
rs45858975	snp	C/G	0.35503	0.226867	intron-variant	Phip	GRCm38.p3	9:82885879	TTTCAGTGCTATATC[C/G]AAGGCTCTAATTCAC	83946
rs45899484	snp	C/G	0.375	0.216506	intron-variant	Phip	Mm_Celera	9:82892757	TTTGCCAAAATTAAT[C/G]AAGAAAAGCAACATG	83946
rs45906847	snp	C/T	0.426035	0.177515	utr-variant-3-prime	Phip	GRCm38.p3	9:82867337	TTTTCATTTGGATCA[C/T]TTTGATAATTATAAT	83946
rs45924118	snp	A/G			intron-variant	Phip	GRCm38.p3	9:82957340	AATGCGTAAGTAATT[A/G]AACAGAGGCGAGAGG	83946
rs45931947	snp	A/G			intron-variant	Phip	GRCm38.p3	9:82957483	GCCTCTTACAGAGCC[A/G]CTATGGAATGCAAAG	83946
rs45946438	snp	C/T	0.426035	0.177515	intron-variant	Phip	GRCm38.p3	9:82902992	AGATATAGTTGTAAT[C/T]TTTTCCCATAAAGAC	83946
rs45959334	snp	C/T	0.48	0.0979796	intron-variant	Phip	GRCm38.p3	9:82896806	TGACTCATTTATGCT[C/T]GTCCCAAAACAACAC	83946
rs45989337	snp	C/T	0.142012	0.225474	intron-variant	Phip	Mm_Celera	9:82949915	TTCCCAAGGATTCGT[C/T]TATTTATCTACTTAC	83946
rs45990758	snp	C/T	0.459184	0.136902	intron-variant	Phip	GRCm38.p3	9:82933775	ATGATCCGAGGAGTT[C/T]AGAACACCAGTATTT	83946
rs45998373	snp	A/G	0.32	0.24	intron-variant	Phip	Mm_Celera	9:82921155	TTTATGCCAACAAAT[A/G]AAAGAGATGAAAGAA	83946
rs46069467	snp	C/T			intron-variant	Phip	GRCm38.p3	9:82957201	TCAGAAAACTGAGTA[C/T]CTGATTTCAAATTCA	83946
rs46095271	snp	C/T	0.336735	0.234472	intron-variant	Phip	GRCm38.p3	9:82910094	TGATGAGAAGGAGTG[C/T]GTATTTTGTGCTTAT	83946
rs46116477	snp	C/T	0.297521	0.245442	intron-variant	Phip	GRCm38.p3	9:82890819	CATCAAGATTTCAGA[C/T]TGATCATCTCCATCA	83946
rs46138548	snp	A/T	0.426035	0.177515	intron-variant	Phip	GRCm38.p3	9:82936030	CAGTCCTAAGGGATC[A/T]GACACCCTTCTAAGC	83946
rs46172342	snp	A/G	0.391111	0.206368	intron-variant	Phip	GRCm38.p3	9:82909745	TTCTCCAGTGCTGGT[A/G]ATTAGGACGACCTGA	83946
rs46222404	snp	C/T	0.336735	0.234472	intron-variant, upstream-variant-2KB	Phip	GRCm38.p3	9:82930748	GCAAAGCAGGTTGTA[C/T]GTTATCAGTATATAG	83946
rs46272729	snp	C/T	0.375	0.216506	intron-variant	Phip	GRCm38.p3	9:82884660	GAAAGGCAAGACTTA[C/T]ATTTTTTTCTTTACA	83946
rs46276391	snp	A/G	0.391111	0.206368	synonymous-codon	Phip	GRCm38.p3	9:82896109	CTCTTCTAACGTTAG[A/G]CCATTCTCAGTTAGT	83946
rs46281608	snp	A/G	0.336735	0.234472	utr-variant-3-prime	Phip	GRCm38.p3	9:82867007	GAAAGTAATCAGCAT[A/G]TGTATCTGCATGTAA	83946
rs46284023	snp	A/G	0.473373	0.11227	intron-variant	Phip	Mm_Celera	9:82920640	TATATATTACAATCT[A/G]TTAAAAACTTCCTAC	83946
rs46296733	snp	C/G	0.124444	0.216185	intron-variant	Phip	Mm_Celera	9:82872763	CTGCCATAGCTTTGA[C/G]ATGCCTTACCTAGTC	83946
rs46301810	snp	A/T	0.5	0	intron-variant	Phip	Mm_Celera	9:82901190	CCTAAAGAACCAGCA[A/T]GCATGTACCACAATA	83946
rs46308089	snp	G/T	0.231111	0.249285	intron-variant	Phip	Mm_Celera	9:82923927	CAGAGTATGCATTTG[G/T]ATTCCTCAAAGCTTT	83946
rs46310748	snp	G/T	0.48	0.0979796	intron-variant	Phip	GRCm38.p3	9:82911895	CAGTCTGGATTTGTA[G/T]TACTCTTGAAATTCG	83946
rs46325512	snp	C/T	0.35503	0.226867	intron-variant	Phip	GRCm38.p3	9:82883447	AGCAAAAGTTGAATA[C/T]TGCATCTGGCTTCAA	83946
rs46411348	snp	A/G	0.336735	0.234472	intron-variant	Phip	Mm_Celera	9:82925040	CAAACTTACCTGATG[A/G]GAGAAAATTCCGAAT	83946
rs46440736	snp	C/T	0.459184	0.136902	intron-variant	Phip	GRCm38.p3	9:82955215	ACAACAAAAGAATTT[C/T]ACCCATCACAGAGTC	83946
rs46447984	snp	A/C	0.336735	0.234472	intron-variant	Phip	GRCm38.p3	9:82890501	GAACCAGCCTGTCTC[A/C]TCCATCAAATTGGTA	83946
rs46465116	snp	A/G	0.391111	0.206368	intron-variant	Phip	GRCm38.p3	9:82912146	GGTATTTTTCAGGGA[A/G]GATGAAGGTATCTAG	83946
rs46467228	snp	A/G	0.391111	0.206368	intron-variant	Phip	GRCm38.p3	9:82915726	ATAACTGAACCATAC[A/G]TTCCATCTATTTCCA	83946
rs46469536	snp	G/T	0.231111	0.249285	intron-variant	Phip	Mm_Celera	9:82915765	TGCCCTTTCTGTAAA[G/T]GCTAAGAACATAGAG	83946
rs46475869	snp	A/G	0.21875	0.248039	intron-variant	Phip	GRCm38.p3	9:82958719	ACAAGAGAGTAACAA[A/G]CTACATCAAAAAGTC	83946
rs46498771	snp	C/T	0.391111	0.206368	intron-variant	Phip	GRCm38.p3	9:82925902	AGAGGAGGACACATA[C/T]CACTTAATAAGCTGT	83946
rs46502410	snp	A/T			intron-variant	Phip	Mm_Celera	9:82943243	AAAACTTCACTTACC[A/T]ATTACAAGGATTTCC	83946
rs46519416	snp	A/G	0.408163	0.193609	intron-variant	Phip	GRCm38.p3	9:82922480	TAAAGCTACAATGAT[A/G]CTTTCTTCATGCCAA	83946
rs46544113	snp	A/C	0.336735	0.234472	intron-variant	Phip	GRCm38.p3	9:82899959	CAGAGACATATATGC[A/C]TTTACCTCAGAGGAA	83946
rs46621171	snp	A/T	0.32	0.24	intron-variant	Phip	Mm_Celera	9:82920788	AAACCTGGATCATCC[A/T]GCCTGAACTGACTGA	83946
rs46642056	snp	A/G	0.408163	0.193609	intron-variant	Phip	Mm_Celera	9:82903588	AAATTAATGATGGAC[A/G]ACAAACTCTATAGTT	83946
rs46647288	snp	A/C/G	0.35503	0.226867	intron-variant	Phip	GRCm38.p3	9:82895313	AGGTTCAAGCGTCAG[A/C/G]GCCTAAAGACGAGCC	83946
rs46647394	snp	C/G	0.277778	0.248452	intron-variant	Phip	GRCm38.p3	9:82889821	ACTTCTTGCCTTTGC[C/G]TCAAAAATGCTAGGA	83946
rs46694091	snp	A/C	0.124444	0.216185	intron-variant	Phip	Mm_Celera	9:82941622	ACCAAGAAGCAGAGG[A/C]AACAGCTTTGCCAGT	83946
rs46718593	snp	A/G			intron-variant	Phip	Mm_Celera	9:82876640	GCAATATAGGGAATA[A/G]TAAAGGAAGCATTAA	83946
rs46727548	snp	A/G	0.132653	0.220748	intron-variant	Phip	Mm_Celera	9:82935926	CGGAGCTCAAGACAC[A/G]ACTCAGCAGTTGACA	83946
rs46751480	snp	C/T	0.48	0.0979796	intron-variant	Phip	GRCm38.p3	9:82938814	TCAATCATTGTACAA[C/T]AAAAATTTGTAGACT	83946
rs46757282	snp	C/T	0.336735	0.234472	intron-variant	Phip	Mm_Celera	9:82889214	ATGCCACTTACAAAC[C/T]TTTTGGGCATGGATA	83946
rs46759430	snp	G/T	0.497778	0.0332592	intron-variant	Phip	GRCm38.p3	9:82920686	TTTATTTTGTTCATA[G/T]TGTTCCTCTTAATAT	83946
rs46788864	snp	A/G	0.408163	0.193609	intron-variant	Phip	Mm_Celera	9:82905195	AGCCAGACCATCATA[A/G]GAGCAATTTAATAAC	83946
rs46795180	snp	C/T			intron-variant	Phip	GRCm38.p3	9:82948807	GAAAACCCATTTTGA[C/T]TGTGGATGGGACCAT	83946
rs46855891	snp	A/T	0.132653	0.220748	intron-variant	Phip	Mm_Celera	9:82935721	TAGAAGACCAAGCAA[A/T]GCTTTGAACCACTGA	83946
rs46870162	snp	C/T	0.132653	0.220748	utr-variant-3-prime	Phip	Mm_Celera	9:82869754	CCACAGCAGTACATA[C/T]AGAAATACATTCCCC	83946
rs46881630	snp	C/T	0.231111	0.249285	intron-variant	Phip	Mm_Celera	9:82922525	AGTAAGCTTGCTAAA[C/T]TATACACACTGTGTG	83946
rs46884319	snp	C/T	0.426035	0.177515	intron-variant	Phip	GRCm38.p3	9:82907907	AACTGGCATAATGAG[C/T]CATTTAAAAAAAAAG	83946
rs46928938	snp	C/T	0.231111	0.249285	intron-variant	Phip	Mm_Celera	9:82913678	GACTCCTGTGAAACC[C/T]GAGGCCTACCTGAAG	83946
rs46946447	snp	C/T	0.426035	0.177515	intron-variant	Phip	GRCm38.p3	9:82968726	ACCTCCTTCACACTA[C/T]GTAAATGCCCAGCCA	83946
rs46957479	snp	G/T	0.459184	0.136902	intron-variant	Phip	GRCm38.p3	9:82898678	GTAAATCACAAATGT[G/T]TATCAATAAATTAGA	83946
rs46966610	snp	A/G	0.408163	0.193609	intron-variant	Phip	GRCm38.p3	9:82916167	CACATCTAGGGACTG[A/G]TTTTCAGAAACGTCT	83946

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