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
rs6157685	snp	A/C/G	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105247606	TAGAGGGGTCTGCCC[A/C/G]CAGGGACAGTGCAGT	71816
rs6159285	snp	C/T	0.207612	0.24638	intron-variant	Rnf180	Mm_Celera	13:105247865	AATGAGTTGTTTGGA[C/T]GGATGTCACTACTCA	71816
rs6277139	snp	C/T	0.290657	0.246672	intron-variant	Rnf180	Mm_Celera	13:105266733	AGCATAACAGGTCAT[C/T]TCCTTGCCAATAGGG	71816
rs6277538	snp	C/T	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105266757	AATAGGGAACTTACA[C/T]GCTAGACAAGGCTAT	71816
rs6317918	snp	A/G	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105159170	ATATGGAGCTTCTTT[A/G]TATTTTTCTATGGTG	71816
rs6317964	snp	A/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105159195	ATGGTGAGGAGATTT[A/T]AATACAAATNATCAG	71816
rs6317978	snp	G/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105159205	GATTTNAATACAAAT[G/T]ATCAGATAGCTTCCA	71816
rs6318471	snp	G/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105159300	CACACATATACGAGT[G/T]GGTTCTNGAGGACTA	71816
rs6318487	snp	G/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105159307	ATACGAGTNGGTTCT[G/T]GAGGACTAGNTTAAT	71816
rs6318501	snp	C/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105159317	GTTCTNGAGGACTAG[C/T]TTAATATGACTGAAA	71816
rs6318551	snp	G/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105159345	AAAACCTTGTCAGTT[G/T]GACACTATTAAGGTG	71816
rs6318996	snp	C/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105159366	TATTAAGGTGGAACA[C/T]TATAAAGGANACTAT	71816
rs6319015	snp	A/C	0.42	0.183303	intron-variant	Rnf180	Mm_Celera	13:105159376	GAACANTATAAAGGA[A/C]ACTATTGCCTAGAAA	71816
rs6384347	snp	A/G	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105245911	CAATCGACCAGTCAC[A/G]GGTGGGAGGAGCCAC	71816
rs6385443	snp	A/C	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105246075	CTTGCCAGTTTTCTA[A/C]GTTAGGCTGAGAAGA	71816
rs6385500	snp	C/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105246109	GCCTAGCTTCTGTTC[C/T]CCACCTACTTCTTCT	71816
rs6385575	snp	C/T	0.290657	0.246672	intron-variant	Rnf180	Mm_Celera	13:105246148	GCTTCCTGACACTTC[C/T]GGCTTTTCCTTCTTT	71816
rs6399070	snp	A/G	0.359862	0.224567	intron-variant	Rnf180	Mm_Celera	13:105246269	ATTGTCCTCAGGCTT[A/G]TAGAGAAATGCACAA	71816
rs6399103	snp	C/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105246294	GCACAAATGAACATA[C/T]NTCAACANGTGTGAA	71816
rs6399104	snp	A/C	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105246295	CACAAATGAACATAN[A/C]TCAACANGTGTGAAG	71816
rs6399118	snp	A/C	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105246302	GAACATANNTCAACA[A/C]GTGTGAAGAAGACGC	71816
rs6399222	snp	A/G	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105246352	GACTTACTGAAAATT[A/G]GCTGTANTCTCTCTT	71816
rs6399606	snp	A/G	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105246359	TGAAAATTNGCTGTA[A/G]TCTCTCTTTGCTACT	71816
rs6408929	snp	A/G	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105164450	ataataaaCCAAACT[A/G]CAGAACTTCNGGTGA	71816
rs6409358	snp	C/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105164460	AAACTNCAGAACTTC[C/T]GGTGAGAATTTACTT	71816
rs6410441	snp	C/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105164664	TATGACCCAGGAAAA[C/T]GTAGGCATTTATAGC	71816
rs6411078	snp	A/G	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105164796	GCTCTTTACTGAAAT[A/G]GATCAATTTCAGAAA	71816
rs6411162	snp	C/T	0.5	0	intron-variant	Rnf180	Mm_Celera	13:105164836	GAGTGACAAAGCAAG[C/T]TTAGAATATACATAT	71816
rs29226507	snp	A/G	0.415225	0.187619	intron-variant	Rnf180	Mm_Celera	13:105153431	ATATTTGCTGTTCCC[A/G]TTCTCCACTGCCTTT	71816
rs29226789	snp	C/T	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105170810	TTTGACCCAGAATTG[C/T]TCCTGTCTAAAAGAA	71816
rs29228793	snp	G/T	0.492188	0.0620098	intron-variant	Rnf180	GRCm38.p3	13:105215074	GCAGGGAGTTCCACT[G/T]GGGCATCTTCTTTTG	71816
rs29228966	snp	A/T	0.415225	0.187619	intron-variant	Rnf180	GRCm38.p3	13:105216934	ATCCCAGAGAGTTGA[A/T]GGCTAGTGTTGGCTA	71816
rs29229081	snp	C/G	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105166545	TCAACCATACAAACT[C/G]TGCATGCATATGTCC	71816
rs29232988	snp	C/G	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105200867	AAGGTGAGTGCCCTT[C/G]CATTTGGAGCACAGA	71816
rs29234261	snp	A/G	0.33241	0.236027	intron-variant	Rnf180	Mm_Celera	13:105195529	GGTTGCTTAAACGAT[A/G]CAATAGAATTTTAAC	71816
rs29234297	snp	A/G	0.444444	0.157135	intron-variant	Rnf180	GRCm38.p3	13:105197866	TACATGTCTGTATGT[A/G]TATATGTCACATGTG	71816
rs29235514	snp	A/G	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105208204	TCCACATTTCCTCCC[A/G]TGAGTATTTTGAAAA	71816
rs29237487	snp	C/T	0.429688	0.173817	intron-variant	Rnf180	Mm_Celera	13:105206293	ATTATAAAAAGAACA[C/T]TGCAAAATGCCAGAG	71816
rs29239788	snp	C/G	0.444444	0.157135	intron-variant	Rnf180	GRCm38.p3	13:105223111	TCTCAGGAGTGCTAT[C/G]CCCTGCTTCTGAATT	71816
rs29240512	snp	A/G/T	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105218927	AACAACAGACAAGCC[A/G/T]ACAAGCTGTGCAATA	71816
rs29240801	snp	A/G	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105207743	AAACTAGGGCATTGA[A/G]CCTTCACAGAACCAA	71816
rs29242011	snp	C/T	0.32	0.24	intron-variant	Rnf180	GRCm38.p3	13:105182822	TCAGTGAGGATTGCA[C/T]TGCTTCACCTGACAC	71816
rs29242499	snp	A/G/T	0.336735	0.234472	intron-variant	Rnf180	GRCm38.p3	13:105216266	GGGGCCTTTTCTTTC[A/G/T]GAATATATTTATATA	71816
rs29244507	snp	A/C	0.444444	0.157135	intron-variant	Rnf180	Mm_Celera	13:105174570	TATAACAAAATATAA[A/C]ATACACACCCCCCCC	71816
rs29244590	snp	C/T	0.444444	0.157135	intron-variant	Rnf180	Mm_Celera	13:105221282	AAGATTTTCAATGGT[C/T]TTGACGTTCTTTTTA	71816
rs29245540	snp	A/T	0.456747	0.140554	intron-variant	Rnf180	Mm_Celera	13:105206554	CTTCAAAAGGGCTAA[A/T]GGTAGATGCCCTAAG	71816
rs29245684	snp	G/T	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105220113	AAATAAACATCATTA[G/T]TGGGCACTGATCTAA	71816
rs29246961	snp	A/T	0.444444	0.157135	intron-variant	Rnf180	Mm_Celera	13:105190019	AAAGAGGTTCCAGAA[A/T]GTCATCTGCACTCTA	71816
rs29247620	snp	A/G	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105182019	CAGAATGTTGCCATG[A/G]CATCAGTCTCTCTTC	71816
rs29250703	snp	A/G	0.290657	0.246672	intron-variant	Rnf180	Mm_Celera	13:105177598	AGGATGTTTGTAAAA[A/G]GATCCTCACTTTGTT	71816
rs29493555	snp	G/T	0.32	0.24	intron-variant	Rnf180	GRCm38.p3	13:105182823	CAGTGAGGATTGCAT[G/T]GCTTCACCTGACACT	71816
rs29493595	snp	A/G	0.492188	0.0620098	intron-variant	Rnf180	GRCm38.p3	13:105215106	TTTCCTCTAGTCTTC[A/G]CAAAATGACCTTTGG	71816
rs29493636	snp	C/T	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105195168	AGGTTTGGCCTCCAT[C/T]GACTCCTGTGTTTGA	71816
rs29493827	snp	C/T	0.32	0.24	intron-variant	Rnf180	Mm_Celera	13:105170328	CATTATTGAAGGGTG[C/T]TATTATCCTATAGAT	71816
rs29494191	snp	A/G	0.32	0.24	intron-variant	Rnf180	Mm_Celera	13:105183126	TGAACCTCATTATTC[A/G]TTGGTCCTGAGTAAT	71816
rs29495487	snp	C/T	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105203621	CCTAACTAGACTGCC[C/T]TGTCTGGCTTCAGTG	71816
rs29496553	snp	A/G	0.408163	0.193609	intron-variant	Rnf180	Mm_Celera	13:105194535	AATTTTAGAATTTAA[A/G]GATTCACTTAGATGG	71816
rs29496835	snp	C/T	0.32	0.24	intron-variant	Rnf180	GRCm38.p3	13:105206060	TACTTTGTTTTATGC[C/T]TAAAGGTTGCCATAC	71816
rs29508685	snp	C/T	0.32	0.24	intron-variant	Rnf180	GRCm38.p3	13:105182945	GTTGCAGTACCAAGA[C/T]CTGGTGGTTTGTGCT	71816
rs29509285	snp	C/T	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105208203	CTCCACATTTCCTCC[C/T]ATGAGTATTTTGAAA	71816
rs29509713	snp	A/T	0.444444	0.157135	intron-variant	Rnf180	GRCm38.p3	13:105206494	CTTTCATCTTTATCT[A/T]GTTACCAGATCTCAG	71816
rs29510863	snp	C/G	0.484429	0.0868505	intron-variant	Rnf180	GRCm38.p3	13:105204278	CAACCTCAGCCTATT[C/G]TGTCAGGCTCTGCCT	71816
rs29514175	snp	A/C	0.290657	0.246672	intron-variant	Rnf180	GRCm38.p3	13:105182321	CCAGGTGATCCACTG[A/C]AAACACTTAGCTCAA	71816
rs29514595	snp	A/G	0.46875	0.121031	intron-variant	Rnf180	Mm_Celera	13:105217459	TTGTTACACTAGTAC[A/G]TTTATTTGGTCTCTA	71816
rs29515950	snp	A/G	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105144911	AGTTCACAACTTGTG[A/G]GCTGTGCCCCCTTGG	71816
rs29517474	snp	A/G	0.32	0.24	intron-variant	Rnf180	Mm_Celera	13:105181803	CTGTTTCTGTAACAC[A/G]TTCCAAGTGATATAA	71816
rs29526561	snp	A/G	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105190249	ACATACATTATACAT[A/G]ATTTTATATATACAT	71816
rs29528340	snp	A/G	0.484429	0.0868505	intron-variant	Rnf180	GRCm38.p3	13:105204446	TGTATACGTCTCCAT[A/G]CATGCCCCAGTCCAC	71816
rs29528985	snp	A/G	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105170761	GATGGGACATTAAGT[A/G]GAGGAATAGGGCTGC	71816
rs29530190	snp	A/G	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105211130	AAATATAAGATATAT[A/G]AAGATCTTATACTTT	71816
rs29533954	snp	C/T	0.484429	0.0868505	intron-variant	Rnf180	GRCm38.p3	13:105208259	TCTGATGTATTGTCA[C/T]TTTCTAATGCTTTCC	71816
rs29534475	snp	A/G	0.444444	0.157135	intron-variant	Rnf180	GRCm38.p3	13:105222205	CTGTGCAGGTGAGGT[A/G]CAGGGCCTGCTCCTA	71816
rs29534818	snp	A/G	0.336735	0.234472	intron-variant	Rnf180	Mm_Celera	13:105251436	ATACTATTTTATTTA[A/G]TACTACTGAGAGGAA	71816
rs29546049	snp	A/C	0.32	0.24	intron-variant	Rnf180	Mm_Celera	13:105172000	TGGTTCCTATGGGCT[A/C]ATATATTTGAGTACT	71816
rs29546929	snp	C/T	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105200892	CACAGATGCTCAGAA[C/T]TAAGAATTCATCTTG	71816
rs29551192	snp	G/T	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105171737	GATGGCCCCGGATGT[G/T]TACTTCCTATTACAA	71816
rs29573910	snp	A/G	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105197901	TGTGCCCAAGTGGGC[A/G]AGAAGGTGCTAGATC	71816
rs29584878	snp	A/G	0.487535	0.077957	intron-variant	Rnf180	GRCm38.p3	13:105208216	CCCATGAGTATTTTG[A/G]AAAGCTTTTAAGGCC	71816
rs29589036	snp	A/G	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105219839	TGCCCATTTGGGGAC[A/G]AGCTACGGTGGAAGC	71816
rs29590016	snp	C/G	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105221324	TTTAATACCAGTGTG[C/G]GCATATGCGAGTGGG	71816
rs29620659	snp	A/G	0.33241	0.236027	intron-variant	Rnf180	Mm_Celera	13:105190050	GTGTCCATTATTGGG[A/G]CTGTGGGCTAAATTA	71816
rs29638873	snp	A/G	0.32	0.24	intron-variant	Rnf180	GRCm38.p3	13:105185302	AGTCTACCTCTTACC[A/G]TGATATATTAATCAA	71816
rs29639669	snp	A/C/T	0.426035	0.177515	intron-variant	Rnf180	GRCm38.p3	13:105214492	GAAGTGTCAGAAGTG[A/C/T]GTGCTGCCTAGCACT	71816
rs29665165	snp	A/G	0.444444	0.157135	intron-variant	Rnf180	Mm_Celera	13:105191546	GGCTACATAGCTCAA[A/G]CTGGTCTTGACTTGC	71816
rs29676236	snp	C/T	0.408163	0.193609	intron-variant	Rnf180	GRCm38.p3	13:105187223	AGAAAGTGTATCATA[C/T]CATGCGACCCAGAAA	71816
rs29679204	snp	A/G	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105198270	ACAATATACTCAAGG[A/G]AAGTAAAGGATGGGA	71816
rs29682018	snp	C/T	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105172089	AGGTGGGGGGGGGGG[C/T]GCTTTGAGATTTCAA	71816
rs29710382	snp	A/G	0.32	0.24	intron-variant	Rnf180	Mm_Celera	13:105182516	ATGAGATCAGTGAGT[A/G]AGATTTGAAAGGACT	71816
rs29734770	snp	A/G	0.465374	0.126941	intron-variant	Rnf180	Mm_Celera	13:105206373	AAAAACGACGACCTT[A/G]AGTAAACAGTTCCTG	71816
rs29755934	snp	C/T	0.32	0.24	intron-variant	Rnf180	GRCm38.p3	13:105190413	CTGTCCTCAAACTCA[C/T]AGAGATGCACCTGTT	71816
rs29757792	snp	C/T	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105172119	AAAGCCCATACCATT[C/T]TCAGTTAGCTCTCTT	71816
rs29763642	snp	G/T	0.32	0.24	intron-variant	Rnf180	Mm_Celera	13:105172087	GGAGGTGGGGGGGGG[G/T]GTGCTTTGAGATTTC	71816
rs29777384	snp	A/G	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105170766	GACATTAAGTAGAGG[A/G]ATAGGGCTGCCATCC	71816
rs29779487	snp	A/G	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105190530	AGTGTTTAAGCCTGG[A/G]TTGCACATGTGTATG	71816
rs29781053	snp	A/G	0.375	0.216506	intron-variant	Rnf180	GRCm38.p3	13:105207969	TAACTCCTCCATTAG[A/G]AACCCCATGCTCAGT	71816
rs29783619	snp	C/T	0.32	0.24	utr-variant-3-prime, intron-variant	Rnf180	Mm_Celera	13:105148844	AGTATATGTACTAAA[C/T]TGTAATTTGGGAGAT	71816
rs29834280	snp	C/T	0.375	0.216506	intron-variant	Rnf180	Mm_Celera	13:105214048	CTTCGTAATTTTGCT[C/T]CTGTCATGAACTGTA	71816
rs29853132	snp	C/T	0.444444	0.157135	intron-variant	Rnf180	GRCm38.p3	13:105203042	TCCTGACAAACCATG[C/T]TCACATGCAATTGTG	71816
rs29856291	snp	C/T	0.290657	0.246672	intron-variant	Rnf180	Mm_Celera	13:105190125	AACTCTAAAATAAGT[C/T]CTTCATTATTCCTGT	71816
rs29864903	snp	C/T	0.375	0.216506	upstream-variant-2KB, intron-variant	Rnf180	Mm_Celera	13:105293552	TACATCAGGCAAGTT[C/T]TAATACCAGCTTCCA	71816

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