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
rs4163487	snp	A/G	0.274723	0.248775	intron-variant, missense	Bfar, 3110001I22Rik	Mm_Celera	16:13677895	TTCAGTTTGCGCTCC[A/G]GCAGAATTTACATGA	67118
rs4163488	snp	A/T	0.375	0.216506	intron-variant	Bfar	Mm_Celera	16:13696705	CCTTTATTCACTGAG[A/T]TATCTTGCCTAAGCT	67118
rs6389023	snp	G/T	0.244898	0.249948	intron-variant	Bfar	Mm_Celera	16:13690920	CACCATACATGGATG[G/T]TTTTAACAGTGAGTT	67118
rs6389537	snp	G/T	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691008	GTTTTCTTTCTTTTA[G/T]AGATANNTATTTTTT	67118
rs6389550	snp	A/G	0.5	0	intron-variant	Bfar	GRCm38.p3	16:13691014	TTTCTTTTANAGATA[A/G]NTATTTTTTAAAATT	67118
rs6389551	snp	A/C	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691015	TTCTTTTANAGATAN[A/C]TATTTTTTAAAATTT	67118
rs6389570	snp	C/T	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691031	TATTTTTTAAAATTT[C/T]Atctatttttatatg	67118
rs6403876	snp	C/T	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691299	ATCTCAGTACAATCA[C/T]TGTTTTGGGGTAttt	67118
rs6403919	snp	A/G	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691321	GGGGTAttttttgaa[A/G]tggagatcttgatat	67118
rs13471626	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13703498	gaaggagagagtcag[A/G]gagaCTTGGTAATTC	67118
rs13471627	snp	A/T			missense	Bfar	Mm_Celera	16:13702238	AGGAAGTCCGACGGC[A/T]GGAAACCCAAGTGTT	67118
rs45670848	snp	A/G	0.277778	0.248452	intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678565	AATCCCAGCATCAAA[A/G]TGAATATTTTAAACC	67118
rs45799154	snp	C/T	0.277778	0.248452	intron-variant	Bfar	GRCm38.p3	16:13684562	TCCCCAAGCTCTTGT[C/T]GTCGTGGCCGCTGTG	67118
rs45928616	snp	C/G	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13701272	TTCCATGGCCAAGCT[C/G]AAGGTATAAAGCATA	67118
rs45977180	snp	A/G	0.493827	0.0552116	intron-variant	Bfar	GRCm38.p3	16:13679171	CCGGTTTGATTGTGA[A/G]TGTTCTCTGTGGAAC	67118
rs45990034	snp	A/G	0.391111	0.206368	intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678243	TGTATGGCTCAGTGT[A/G]CTTTACAGTTAGATT	67118
rs46017551	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13690344	GGTAAACCTGGGTTA[A/T]ACATCACACCCTGTC	67118
rs46019810	snp	A/G	0.142012	0.225474	intron-variant	Bfar	Mm_Celera	16:13690894	ATTCTCTACCACTGA[A/G]CTGTGTCTCCCACCA	67118
rs46027378	snp	A/G	0.489796	0.070696	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13675033	ATGGTGAATGAGGGG[A/G]AAAATTCAGTTCAAT	67118
rs46044794	snp	A/C	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13694051	CAGGTCACAAATAAT[A/C]CACAGCTTCATCTTT	67118
rs46109823	snp	C/G	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13694103	TCATTGTGACGGTAT[C/G]AGTTGATTCTCCCCC	67118
rs46147051	snp	C/T	0.142012	0.225474	intron-variant, missense	Bfar	Mm_Celera	16:13688838	TAGATAAGTGGACGA[C/T]GGAAGAAGTTGTCCT	67118
rs46149705	snp	A/G	0.231111	0.249285	intron-variant	Bfar	Mm_Celera	16:13697851	TCACGGTAGTAAGCC[A/G]TGGCCCAGGATGTGA	67118
rs46245581	snp	A/G	0.32	0.24	intron-variant	Bfar	Mm_Celera	16:13693410	AAGTTGCTTGAGAGA[A/G]GTCTTGTTGTCTTTG	67118
rs46250200	snp	C/T	0.124444	0.216185	upstream-variant-2KB	Bfar, 3110001I22Rik, Parn	GRCm38.p3	16:13670047	ACTATGCATATCTAT[C/T]TCCCTTCTTGCTTAA	67118
rs46281976	snp	C/T	0.165289	0.235211	upstream-variant-2KB	Bfar, 3110001I22Rik	GRCm38.p3	16:13671104	GCCTCTGCTGGCTTA[C/T]AGGAGATAAGAGTTT	67118
rs46343127	snp	C/T	0.459184	0.136902	intron-variant, utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13676937	ACATCTCCTAGAGTC[C/T]AGCCTATCTAGTGTG	67118
rs46548249	snp	C/T	0.152778	0.230321	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674625	TTTAGTCTTATTTTC[C/T]TTTTCCATAGCAGGG	67118
rs46571207	snp	A/T	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13680165	GGCTATGGAACCTAC[A/T]TGTTTCCACCTGTCA	67118
rs46605412	snp	C/G	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13700103	AGTAGACCAAGGTCA[C/G]AAAATGCTAGGACTA	67118
rs46616049	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13690480	TCTCTACCATTGAAA[C/T]CCTCCCCAGCCCTAG	67118
rs46637094	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13699165	CTGGCATGGGGGATG[A/G]GGTTGCCTAGCGCCC	67118
rs46701843	snp	C/T	0.426035	0.177515	intron-variant	Bfar	Mm_Celera	16:13693950	TAATTTTAATGGTTA[C/T]AACAAATCATGCTGC	67118
rs46869703	snp	A/G	0.489796	0.070696	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673706	TTAATCATCAAAGAC[A/G]GTTTGGATCTTGTGA	67118
rs46969771	snp	A/G	0.132653	0.220748	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13676557	TGATATAACCAGCAC[A/G]GTATTGCTCTGGAGG	67118
rs47037279	snp	C/T	0.244898	0.249948	intron-variant	Bfar	Mm_Celera	16:13688473	CTTAAGTCCAGTCCT[C/T]TGAAGTTCTTAATGT	67118
rs47081610	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690163	GTGAAACCCTGTCTC[A/G]AGGGGAAAATAATAA	67118
rs47177442	snp	A/T	0.277778	0.248452	intron-variant	Bfar	GRCm38.p3	16:13684481	TAGCGGGTCTCATGC[A/T]GGAGGTGGTGTGCTT	67118
rs47227380	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13699221	AACCTCAGAGCATCT[A/G]GCATCCTCTTCTGGC	67118
rs47236061	snp	A/T	0.142012	0.225474	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676289	AACCATTGTTCTAGT[A/T]CCTTAATAGGCAAAA	67118
rs47385146	snp	A/G	0.132653	0.220748	intron-variant, utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13676864	CCTCTAACTGCTCCT[A/G]TGGCAGCCTGCGTAC	67118
rs47452457	snp	C/T	0.244898	0.249948	utr-variant-5-prime	Bfar	Mm_Celera	16:13685119	CTATGTGTATGGATC[C/T]CAGAATTTGCTGAGA	67118
rs47468544	snp	C/T	0.231111	0.249285	intron-variant	Bfar	Mm_Celera	16:13698313	TGTATATGAATGTGA[C/T]ATTGGTGCATATGTG	67118
rs47501759	snp	A/G	0.132653	0.220748	utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13672059	GCGGTGACAGAGTGG[A/G]TACCAGGACTAGTGG	67118
rs47544365	snp	C/T	0.152778	0.230321	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670637	ATAGCTAAGTCTCCA[C/T]AGTCTTAAACTTTTT	67118
rs47564034	snp	A/C	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13698751	TTTGAAGGCAGCTAG[A/C]TATAACCAGGTGTTG	67118
rs47623983	snp	C/T	0.260355	0.249785	intron-variant	Bfar	Mm_Celera	16:13684329	CCAGGAGTGAATACA[C/T]GTGGCTTGTTATATC	67118
rs47737883	snp	A/G	0.244898	0.249948	intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678815	CCCAACACAGCTTAA[A/G]GCAATCTGTTCAGAC	67118
rs47755656	snp	A/G	0.497778	0.0332592	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13675375	TAAGAGATGACTAAA[A/G]GAGCCTGGTGGTGGT	67118
rs47781943	snp	C/T	0.132653	0.220748	intron-variant	Bfar	Mm_Celera	16:13678952	TGGAAATGCTTTCTG[C/T]CTTATTAATGGAAGA	67118
rs47788856	snp	A/T			intron-variant	Bfar	GRCm38.p3	16:13695617	CACCATGCTGCTAGG[A/T]CTACACGCCTTCCTC	67118
rs47809744	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13689920	CCCAGCAGCCACATG[G/T]TGGCTTACAACCATC	67118
rs47860036	snp	A/G	0.32	0.24	intron-variant	Bfar	Mm_Celera	16:13691657	AATAGTGTTCAGTTG[A/G]ATTTCCTTCTAGTTT	67118
rs47972379	snp	G/T	0.32	0.24	intron-variant	Bfar	Mm_Celera	16:13684424	ATTTTGTTGTATAGC[G/T]CTCCTAAGTAATTTA	67118
rs48005213	snp	C/T	0.244898	0.249948	intron-variant	Bfar	GRCm38.p3	16:13687336	CTGGTGGGTGTAGTC[C/T]CTGAATGCTATATCT	67118
rs48199348	snp	A/G	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13700464	ATAACTTCCAGATTA[A/G]TGTAGGATGAGAACA	67118
rs48243762	snp	A/G	0.277778	0.248452	downstream-variant-500B	Bfar	Mm_Celera	16:13703631	TTATAGAGAAATCTG[A/G]TTGCTAAGGAAATAG	67118
rs48253436	snp	A/G	0.132653	0.220748	intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678772	GACAGGCTTAGCCTA[A/G]TGCCCTTCTCAGCCT	67118
rs48290907	snp	A/C	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13679212	CTAACAGTTGGAGTT[A/C]ATGTCCCAGATAGTA	67118
rs48298575	snp	G/T	0.244898	0.249948	intron-variant	Bfar	Mm_Celera	16:13692306	ATTCATCAACACAGC[G/T]TTTAATGTTCAGCCT	67118
rs48304681	snp	C/T	0.142012	0.225474	utr-variant-5-prime	Bfar	Mm_Celera	16:13685075	AGACTTTATGATGCA[C/T]TGCAGCAGTGTCCTG	67118
rs48344242	snp	C/T	0.444444	0.157135	intron-variant	Bfar	GRCm38.p3	16:13698806	AAACGTAAAGCTCAT[C/T]CATCGACATTACTTG	67118
rs48371934	snp	C/T	0.336735	0.234472	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673972	ATCAGAGTAAACTTT[C/T]ATTCCTGGCAGGGCA	67118
rs48405547	snp	A/G	0.231111	0.249285	intron-variant	Bfar	Mm_Celera	16:13681933	TCCCATTAAGAGCAA[A/G]ACCTGAGAACTCCTG	67118
rs48483996	snp	C/T	0.132653	0.220748	intron-variant, missense	Bfar, 3110001I22Rik	GRCm38.p3	16:13677415	CAGAGCTTAGGAAGT[C/T]CGAGCATGCTCATTC	67118
rs48585717	snp	A/G	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13681337	ACCAGACAACTTAGA[A/G]CAGGAATGGACAAGT	67118
rs48602962	snp	C/T	0.142012	0.225474	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671652	ACCCCAAATTCCGAC[C/T]CTATAAATAAAACTT	67118
rs48605896	snp	A/G	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13679958	AAGAGAGGATTGAAA[A/G]AAAAAGTTTTAGGCT	67118
rs48611555	snp	A/G	0.124444	0.216185	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13675600	GAAAGTCCCGGAGGA[A/G]ACACCAAAGGAGGAC	67118
rs48665769	snp	A/G	0.336735	0.234472	intron-variant, missense	Bfar, 3110001I22Rik	Mm_Celera	16:13677565	GTTTAAACAAACTCA[A/G]AAGGCTTGATGAAAA	67118
rs48668766	snp	A/G	0.375	0.216506	intron-variant	Bfar	Mm_Celera	16:13679378	TATTTTATGTGTATT[A/G]AGATTTTTATTTTAG	67118
rs48722655	snp	A/G	0.297521	0.245442	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13676636	CTATTGAGGGACAAG[A/G]CCAACCTGGGAGGGT	67118
rs48842361	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670572	TTTACCAACTTGAAA[A/G]GAACACTCTCATTTA	67118
rs48877736	snp	A/T	0.18	0.24	utr-variant-3-prime	Bfar	Mm_Celera	16:13703007	GAGAAAACTTCAGGC[A/T]AAGAGACAGTGCTGC	67118
rs48917079	snp	A/G	0.132653	0.220748	intron-variant	Bfar	Mm_Celera	16:13695064	AGATAACTGACACAT[A/G]TACACAAACACCCAC	67118
rs49044297	snp	A/G	0.260355	0.249785	intron-variant	Bfar	Mm_Celera	16:13700476	TTAATGTAGGATGAG[A/G]ACATTGGGCTACCTA	67118
rs49090431	snp	C/T	0.391111	0.206368	downstream-variant-500B	Bfar	Mm_Celera	16:13703745	GCTTAGAGATTTCTA[C/T]AGGAAGGGACGAGTC	67118
rs49096758	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13690353	GGGTTATACATCACA[C/T]CCTGTCTCAAAAAAA	67118
rs49161310	snp	A/G	0.152778	0.230321	intron-variant	Bfar	Mm_Celera	16:13692378	AGTGTGTAAGCACGC[A/G]TTGTCTGCATCCTGT	67118
rs49277348	snp	C/T	0.124444	0.216185	intron-variant	Bfar	Mm_Celera	16:13698293	CTTATTTTTGACTTT[C/T]TGTGTGTATATGAAT	67118
rs49383365	snp	C/T	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13697781	AGATTTGGCAGAACC[C/T]CTAAAGAGTAGTAGT	67118
rs49492871	snp	C/T	0.336735	0.234472	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673529	AACTGAGTCTAGAAA[C/T]CTGGACTTATGCAAA	67118
rs49551488	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695630	GGACTACACGCCTTC[C/T]TCACCATGCTGCTAG	67118
rs49571937	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13689976	TAGCTACATAGTATG[C/T]TCATATACGTAAAAT	67118
rs49644714	snp	A/G	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13701010	CCCAGAGATGCAAAT[A/G]CTCTCCTCGGGGCTG	67118
rs49819365	snp	C/T	0.408163	0.193609	downstream-variant-500B	Bfar	Mm_Celera	16:13704093	TAGCTTCCGTTAGAG[C/T]GGGCATGCTCAGATC	67118
rs49876216	snp	A/G	0.124444	0.216185	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676331	CTAGGTCACGTGTAT[A/G]ATTCAAGATTGGTTA	67118
rs49886524	snp	A/C	0.391111	0.206368	synonymous-codon	Bfar	Mm_Celera	16:13697386	TCTCAAGAGCTCACC[A/C]AGACTTGGCTTGCTA	67118
rs49946225	snp	A/C/T	0.277778	0.248452	intron-variant	Bfar	Mm_Celera	16:13679903	GTCATCTCTTCAGAC[A/C/T]CAAAGTGGGGTTGTT	67118
rs50068107	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690164	TGAAACCCTGTCTCG[A/G]GGGGAAAATAATAAT	67118
rs50119351	snp	C/T	0.124444	0.216185	intron-variant	Bfar	GRCm38.p3	16:13699501	TTAGGTTTCTAATGC[C/T]GTGCTAAAACACTGT	67118
rs50128825	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13690173	GTCTCGAGGGGAAAA[A/T]AATAATAATAATAGT	67118
rs50363818	snp	G/T	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13698237	AATCTTCCACAACTC[G/T]ACAATAAACATCTCA	67118
rs50432716	snp	C/G	0.391111	0.206368	synonymous-codon	Bfar	Mm_Celera	16:13698950	GTACCAGCTGATCGC[C/G]GAGTTTGCCTGGGAC	67118
rs50538488	snp	A/G	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13693472	CCTGGAGCTACCACT[A/G]TAAAGGTAAAATGGC	67118
rs50599551	snp	A/G	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13693196	TTCCTGTTGATAGTC[A/G]CAATTTTTCTGTTGT	67118
rs50616396	snp	C/G	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13700400	AGGCCAGAGAGACAT[C/G]ATGTGAATTTTATAG	67118
rs50637453	snp	C/T	0.408163	0.193609	utr-variant-3-prime	Bfar	Mm_Celera	16:13703115	ACCAGGCCGAGTCTT[C/T]TTAGATGACTGAGCA	67118
rs50823047	snp	C/T	0.260355	0.249785	intron-variant	Bfar	Mm_Celera	16:13681800	GCAAGACCTAAGCTA[C/T]CATTTTCTCAACCTG	67118
rs50892295	snp	C/T	0.493827	0.0552116	intron-variant	Bfar	Mm_Celera	16:13693134	CTCTAGTTCATTCCA[C/T]CTTTTTGATGGAATT	67118

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