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
rs4229465	snp	C/T	0.287335	0.247197	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84918795	TTGGCCGTTTGGGGC[C/T]GTTCTTCCTCCTAGG	68497
rs4229466	snp	A/G	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84918724	AGGGGGTCAGTGTGT[A/G]TGTGTGACTAGACCT	68497
rs4229467	snp	C/G	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84918689	TTTTAAGCTCTAGTC[C/G]TAGCACTTTTTCAGA	68497
rs4229468	snp	C/T	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Arel1	GRCm38.p3	12:84918559	GGTTTTCTATTCTTC[C/T]AGTTCACTCTCCTGA	68497
rs13467237	snp	A/G	0.32	0.24	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84920064	GACCAGACTGGGTAA[A/G]GCATCACCTCTTCTC	68497
rs13467238	snp	G/T	0.231111	0.249285	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84919850	GATCATTAATCTATA[G/T]GGAATTTGCTAAGCT	68497
rs13467239	snp	A/C	0.231111	0.249285	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84919915	TACAAAAGGATGTCT[A/C]TAAGGTGACAGAACT	68497
rs13467240	snp	C/T	0.32	0.24	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84920135	TTCTGTTGGAAAGCC[C/T]GCATGTGAGACCCTT	68497
rs13467241	snp	A/G			utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84920056	TGGGTAATGCATCAC[A/G]TCTTCTCATCAGTGG	68497
rs13467242	snp	C/G			utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84919739	CGCTTCTCTCGTGGG[C/G]AAGGGCCGTGTCCAG	68497
rs13481567	snp	A/G	0.408163	0.193609	intron-variant	Arel1	GRCm38.p3	12:84923416	TACTTGCTGCTCTAT[A/G]AATTTCAACATTGTA	68497
rs45650444	snp	C/G	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84967493	AAATGTAAACATGTA[C/G]TTTGAGACTAGAAAT	68497
rs45654899	snp	C/T	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84935599	GCCATTGGAATGTGC[C/T]CACACTCATACACAC	68497
rs45661481	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84949648	ACAGTCTATTAGCTC[A/G]GTGTGGAGATCAGGT	68497
rs45681659	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84922840	GACTCTCTTGTTCTC[A/G]ACTCCTAAGGCCTTT	68497
rs45690552	snp	A/G	0.244898	0.249948	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84918860	GCTGAGAGGCAGCAG[A/G]GTAGTGGCTAAATGA	68497
rs45707446	snp	C/T	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84936071	CCCAGAGTCCTGTCC[C/T]TGTGCACGGGTGAGG	68497
rs45714058	snp	C/T	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84960343	TCGTGTGCACATAGC[C/T]GAACATGCATAAATA	68497
rs45760068	snp	A/C	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84939387	GATACTACTTCTCTT[A/C]TTTGGAAAGAACACA	68497
rs45780212	snp	G/T	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84944203	TGTGCGTCAAGGTTT[G/T]AAGAGAGAGAGAGGT	68497
rs45829377	snp	G/T	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84955976	ATTCAGCTGAGACAA[G/T]GTCCTTAGCGTAGAA	68497
rs45841138	snp	C/T	0.152778	0.230321	intron-variant, upstream-variant-2KB	Arel1	Mm_Celera	12:84947674	TCTACTTTCTGTTGG[C/T]CCCACTTTCATACAA	68497
rs45864042	snp	C/T	0.21875	0.248039	intron-variant	Arel1	Mm_Celera	12:84924486	TGGCAGAAGCATCTG[C/T]TCCCACACATTCCTC	68497
rs45867054	snp	C/T	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84958337	AAAGAAAGCTGAGAA[C/T]GGAAATCCCAGACCC	68497
rs45907252	snp	A/C	0.391111	0.206368	intron-variant	Arel1	Mm_Celera	12:84939116	TATCTGGCACAAAGG[A/C]AGGAATCACACATGG	68497
rs45988810	snp	C/T	0.132653	0.220748	intron-variant	Arel1	Mm_Celera	12:84924177	TGTGGTAAAACTGTA[C/T]GCTGTATCAGCCTGA	68497
rs46004732	snp	C/T	0.132653	0.220748	upstream-variant-2KB, intron-variant	Fcf1, Arel1	Mm_Celera	12:84969368	GGTGTCTGGGTAATA[C/T]AGGTGCTGTGATGAT	68497
rs46082628	snp	C/T	0.336735	0.234472	intron-variant, upstream-variant-2KB	Fcf1, Arel1	Mm_Celera	12:84971045	CAGATATAGACTCGG[C/T]GCTTCCTTGTTTGTT	68497
rs46165476	snp	A/G	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84956821	AAAGCTAAAACATGG[A/G]CATGTTCAAACAGTC	68497
rs46184860	snp	C/T	0.231111	0.249285	utr-variant-3-prime, nc-transcript-variant	Arel1	GRCm38.p3	12:84918639	AACCTGGCATGCTAG[C/T]TGCCCCAGCTGGGCT	68497
rs46221596	snp	A/G	0.142012	0.225474	intron-variant	Arel1	Mm_Celera	12:84924895	TCTGTTGAGAATCTT[A/G]CAGGTGAATAACCTG	68497
rs46222386	snp	C/G	0.231111	0.249285	downstream-variant-500B	Arel1	Mm_Celera	12:84918043	ACTCTGTTCACAGCA[C/G]ATTGCTTCCTGCTTC	68497
rs46279685	snp	A/G	0.277778	0.248452	intron-variant, upstream-variant-2KB	Arel1	Mm_Celera	12:84947149	TAGATAGAAACTATA[A/G]TAAATATGAATAAAG	68497
rs46282918	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Arel1	Mm_Celera	12:84947576	AATGTATTCATTAAG[C/T]TCTTTAAGGCCCAAA	68497
rs46380964	snp	C/T	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84918293	CTTGGTACTCATGAC[C/T]GGTCTCCTTCAAGGA	68497
rs46395927	snp	C/T	0.32	0.24	intron-variant	Arel1	Mm_Celera	12:84960498	ATTCAGACCTAACCC[C/T]GACTCTAATTGGAAT	68497
rs46473294	snp	A/T	0.244898	0.249948	intron-variant	Arel1	Mm_Celera	12:84941588	AAGCCTCTCCAGATA[A/T]TAATAATTCCCAAGT	68497
rs46535343	snp	A/G	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Arel1	GRCm38.p3	12:84940356	AACCCGCAGTCCCAC[A/G]GGCCGATGTGCAGGG	68497
rs46670485	snp	C/T	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84924998	TACAAAGACAGAAAA[C/T]GGGCATTCCTAGCCT	68497
rs46681976	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84924554	AGACTTGGGAAGTTG[A/G]CATCAGACACTGCAG	68497
rs46691549	snp	A/G	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84961722	CTGATGGAACCCAAC[A/G]TTTACTTTTATAGTT	68497
rs46700332	snp	A/G	0.375	0.216506	intron-variant	Arel1	Mm_Celera	12:84932985	TGTTATGTAAATGTT[A/G]TCATACACAGTTCCT	68497
rs46713480	snp	C/T	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84934555	AAAAAGACCAAGTCA[C/T]AGCTTTCAACTCACC	68497
rs46718782	snp	A/G	0.391111	0.206368	intron-variant	Arel1	Mm_Celera	12:84962532	CCTAAGCAAGTCCAC[A/G]TCCCTTAAGTCTCTT	68497
rs46746979	snp	A/G	0.244898	0.249948	intron-variant	Arel1	Mm_Celera	12:84944256	GACAGGAAAGTGCCT[A/G]CCTGCCTCTGACAAT	68497
rs46749175	snp	A/T	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84937400	TTCAAACACTCTTCA[A/T]ATGACTTAGTGGAGA	68497
rs46755709	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84959219	ACAGCACCAACTCTG[A/G]GGAGAGGTCATATGC	68497
rs46755958	snp	A/T	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84955160	CTTCCCATTCTACTA[A/T]ACCTCTTCTAAAAAC	68497
rs46791886	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84949004	AAAGCTAAAATCAGG[A/G]CTACAAATTCCTCCA	68497
rs46815474	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Arel1	Mm_Celera	12:84948160	CCAAAAGATAAGCAC[C/T]ATTATTCTCACAGGT	68497
rs46838977	snp	C/T	0.32	0.24	intron-variant	Arel1	Mm_Celera	12:84921991	CTAGTCAGCAGAGGA[C/T]TGCCCAGGGGAAGGG	68497
rs46866198	snp	C/T	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84952454	ACACAAAATGCTAAA[C/T]AAACCAGAACAGAAG	68497
rs46889211	snp	C/T	0.32	0.24	intron-variant	Arel1	Mm_Celera	12:84924213	TCTACAGGCAGTGAC[C/T]GGACTCCCTCAAGTT	68497
rs46892225	snp	A/G	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84919512	CCTTGTCTGTCCCCA[A/G]TGGCTTCACCGCTCC	68497
rs46893973	snp	C/T	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84950100	TTCATCTCTCTCTGT[C/T]CACTCATGTGGATCT	68497
rs46926252	snp	A/G	0.32	0.24	intron-variant	Arel1	Mm_Celera	12:84967405	GTTACTCCATTTAAA[A/G]TCACCAGGTTAGATT	68497
rs46964661	snp	A/T	0.336735	0.234472	intron-variant, upstream-variant-2KB	Fcf1, Arel1	Mm_Celera	12:84971435	TTTTGTTTTGCTTAT[A/T]ATGTCTTAGGTCTGT	68497
rs46971672	snp	A/G	0.32	0.24	intron-variant	Arel1	Mm_Celera	12:84966151	CTGGCCAGAAAGTAC[A/G]ATGAGCACAAAATGC	68497
rs46977075	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84954851	TACAGGGAACCCTTA[A/G]TGCTGCTGGCATCAG	68497
rs46978710	snp	A/C	0.142012	0.225474	intron-variant	Arel1	Mm_Celera	12:84952352	TTTCCCAGTTAACTC[A/C]CAAAAGCAGCAGACA	68497
rs47001244	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84922065	GCTGAACTTTTAACT[A/G]CTTCCCTTTAGCTCT	68497
rs47001891	snp	A/G	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84945377	TGGCACACAGCCTCG[A/G]TGACTGTCATGGGTT	68497
rs47016525	snp	G/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Arel1	Mm_Celera	12:84947768	ACAACTTACTTCCAA[G/T]TTAGCTGACATTCCT	68497
rs47029615	snp	C/T	0.244898	0.249948	intron-variant	Arel1	Mm_Celera	12:84931437	CAGCACACCGGAGAC[C/T]ATGAACAGGCACAGA	68497
rs47035108	snp	A/C	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84919572	CACAGCTGGCAGGCT[A/C]TGTCCCAGTCTGTTG	68497
rs47065178	snp	C/T	0.244898	0.249948	missense, nc-transcript-variant	Arel1	GRCm38.p3	12:84927330	TGTCAGTGAACCGGG[C/T]GAAGAGCTGACTGGT	68497
rs47080019	snp	A/C	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84923945	GTATCCAAGTTAGAG[A/C]CAGACTGCTACTATG	68497
rs47080340	snp	C/T	0.244898	0.249948	intron-variant	Arel1	Mm_Celera	12:84930975	TATAGTCTCAGGAGA[C/T]GGTTCTGCCTTGCTG	68497
rs47092456	snp	A/G	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84943486	AGCCTACCAGCTCTA[A/G]TCTCGTGCCTTAACG	68497
rs47097458	snp	C/T	0.142012	0.225474	intron-variant	Arel1	Mm_Celera	12:84952235	CAGCACAGACTATTA[C/T]CAGCCTTCAGGATTT	68497
rs47111728	snp	C/T	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84956704	ACAGATGACGTGTTC[C/T]TGCAATATCTCTCTT	68497
rs47221476	snp	A/G	0.231111	0.249285	downstream-variant-500B	Arel1	Mm_Celera	12:84918063	CTTCCTGCTTCCAAG[A/G]ACACATAAAGCATCT	68497
rs47299548	snp	A/G	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84924653	GCCACCGAGGGGCAT[A/G]TGAAGAAGTCCCAAA	68497
rs47360836	snp	C/T	0.132653	0.220748	upstream-variant-2KB, intron-variant	Fcf1, Arel1	Mm_Celera	12:84969169	TAGAGACCTGAAAGT[C/T]TAGTAAGAGTTCTGA	68497
rs47367496	snp	A/T	0.391111	0.206368	intron-variant	Arel1	Mm_Celera	12:84961462	GGCTTGCCTCTTGAG[A/T]TCTTGTTTTTAAACT	68497
rs47375800	snp	A/C	0.5	0	intron-variant	Arel1	Mm_Celera	12:84925594	TCAGCGTCACTCAGT[A/C]CTCTGCAGAGTCTTT	68497
rs47396440	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84967719	AGAAGGACTAAAGTA[A/G]TTCTTTCCCTCACGA	68497
rs47400190	snp	C/G	0.32	0.24	intron-variant, upstream-variant-2KB	Arel1	Mm_Celera	12:84947207	TCTGTTCTTTTCTTA[C/G]CTCAGATGCCTAAAG	68497
rs47400230	snp	C/T	0.32	0.24	utr-variant-5-prime, nc-transcript-variant	Arel1	GRCm38.p3	12:84951363	TGAAAGAGGCATCTG[C/T]TCTGGAACCAGGATC	68497
rs47416294	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84961411	TCTTCTTCCTACTGA[A/G]CTCTAGGTCTTTATA	68497
rs47416950	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84943567	CAAATAGACTATGGC[A/G]CTCTGCCTAAGGGCT	68497
rs47419561	snp	C/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84931980	ACACGCCGTCCCAAT[C/G]CTCTAGTCTGACAGT	68497
rs47433953	snp	A/C	0.32	0.24	intron-variant	Arel1	Mm_Celera	12:84961434	TCTTTATAGACTCTA[A/C]ATGGAAGCCCTTGGC	68497
rs47465940	snp	A/G	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84957566	TCCTGCTGAATCCCC[A/G]CTTCTTCCTAGCAAG	68497
rs47496978	snp	A/T	0.244898	0.249948	intron-variant	Arel1	Mm_Celera	12:84922764	TTTCTAACAGGAACG[A/T]TATGAAGAACTTTGA	68497
rs47501314	snp	C/T	0.124444	0.216185	intron-variant	Arel1	Mm_Celera	12:84945185	CTCGTCTTAGAACAT[C/T]TGAGTAAGGCCTGAG	68497
rs47505475	snp	C/T	0.48	0.0979796	intron-variant	Arel1	Mm_Celera	12:84931939	GGTGAAGGTCAATCC[C/T]GACCTGACACCGTGA	68497
rs47509337	snp	G/T	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84944193	TATATCTGATTGTGC[G/T]TCAAGGTTTTAAGAG	68497
rs47510631	snp	A/C	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84940721	CAGCTCTATTCTAGC[A/C]TCAGTGCTAACCCAA	68497
rs47519110	snp	G/T	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Arel1	Mm_Celera	12:84918150	ACTCATTTAGCTCTT[G/T]ATTATTGTAGGCATT	68497
rs47527710	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB	Arel1	Mm_Celera	12:84948131	CACATCTTACCCTAC[A/G]AACCTAACTGTGACC	68497
rs47528088	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84940153	AAGGAATGAACCACG[A/G]ACCTACCAGGCTGAA	68497
rs47530187	snp	A/G	0.21875	0.248039	intron-variant	Arel1	Mm_Celera	12:84924473	ATGCTCTTTCATATG[A/G]CAGAAGCATCTGCTC	68497
rs47566634	snp	A/C/G	0.132653	0.220748	intron-variant	Arel1	GRCm38.p3	12:84945376	CTGGCACACAGCCTC[A/C/G]ATGACTGTCATGGGT	68497
rs47566976	snp	G/T	0.244898	0.249948	synonymous-codon, nc-transcript-variant	Arel1	GRCm38.p3	12:84935101	ATGGCACACAATTTT[G/T]GTTTTGGAAGGAACC	68497
rs47573719	snp	A/G	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84937419	ACTTAGTGGAGAACT[A/G]TGGTTTGGGGCTTTG	68497
rs47591557	snp	C/T	0.32	0.24	intron-variant	Arel1	Mm_Celera	12:84923975	GGCCCCAACGTGTGA[C/T]GCACAAGGAGACGGG	68497
rs47605539	snp	A/T	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84943829	GTCATGCTAGCATCA[A/T]GAAAGCAAAGTGAAC	68497
rs47612852	snp	A/T	0.132653	0.220748	upstream-variant-2KB, intron-variant	Fcf1, Arel1	Mm_Celera	12:84970552	ATGTGCCAGAGGAAA[A/T]CCAGAATGTACTGTC	68497
rs47633677	snp	A/C	0.231111	0.249285	intron-variant	Arel1	Mm_Celera	12:84941150	GTGGGCTTTCCGGCT[A/C]CATTTACTATACTAA	68497

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