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
rs13471568	snp	A/T			synonymous-codon	Rnf135	Mm_Celera	11:80198721	TTCTCAGGCCCTCTC[A/T]TCTGGACAGAAGTAC	71956
rs28227521	snp	A/G	0.297521	0.245442	intron-variant	Rnf135	GRCm38.p3	11:80192620	AAATCATCACCCTCT[A/G]GGAGAGAAGCCTTCA	71956
rs28227522	snp	C/T	0.165289	0.235211	intron-variant	Rnf135	Mm_Celera	11:80192428	CATGTGTGATCTGAA[C/T]TGTGGCAGTGTCTGT	71956
rs28227523	snp	A/G	0.197531	0.244432	intron-variant	Rnf135	GRCm38.p3	11:80192341	CATAGATAGCATTTT[A/G]ATGAACTTCTTTCTC	71956
rs28227524	snp	C/T	0.197531	0.244432	intron-variant	Rnf135	GRCm38.p3	11:80192164	AGATTTGTGGTATCG[C/T]CTGCTCTCACAGCCA	71956
rs28227525	snp	C/T	0.165289	0.235211	intron-variant	Rnf135	GRCm38.p3	11:80192139	GAATAGCCGTAATCC[C/T]GTGGAACCGAGATTT	71956
rs28227526	snp	C/T	0.165289	0.235211	intron-variant	Rnf135	GRCm38.p3	11:80191931	GGTCTTAAGACACTC[C/T]TGGCTGGCCAGTGGT	71956
rs28227527	snp	A/G	0.165289	0.235211	intron-variant	Rnf135	GRCm38.p3	11:80191572	ATTTTAGGCCAGCAC[A/G]TACAGGAGCCCAGTG	71956
rs28227528	snp	A/G	0.165289	0.235211	intron-variant	Rnf135	Mm_Celera	11:80191456	CACTCTATTTTAGTT[A/G]GCTCCCTTCACACAA	71956
rs28227529	snp	A/G	0.165289	0.235211	intron-variant	Rnf135	GRCm38.p3	11:80191311	CCTTACCTGCCTAGC[A/G]GTGCATGGTAGCTCC	71956
rs28227530	snp	C/G/T	0.18	0.24	intron-variant	Rnf135	GRCm38.p3	11:80190676	TTTCAGTATGTAATT[C/G/T]GAGCTGCCTTTGAAC	71956
rs28227531	snp	C/T	0.444444	0.157135	intron-variant	Rnf135	Mm_Celera	11:80190251	TCTTCACTGCCAAGC[C/T]AACTCTCCAGCCTCA	71956
rs28227532	snp	C/T	0.18	0.24	intron-variant	Rnf135	GRCm38.p3	11:80187082	CTGGCCTTTTGCAAG[C/T]TGGGTAAGGGTCCCT	71956
rs28227533	snp	A/G	0.18	0.24	intron-variant	Rnf135	GRCm38.p3	11:80186846	TCCATCGGGAAGGAA[A/G]GACCCTGACTGAATT	71956
rs28227534	snp	A/G	0.18	0.24	intron-variant	Rnf135	GRCm38.p3	11:80185466	ACTACTTTCAGTTTC[A/G]TATTTTCAGGGCTGC	71956
rs28227535	snp	A/C	0.18	0.24	intron-variant	Rnf135	Mm_Celera	11:80185011	TTAGGTCAGAAAGCG[A/C]CGCACTGAGACCACC	71956
rs28227536	snp	C/T	0.18	0.24	missense	Rnf135	GRCm38.p3	11:80184128	GTCGGAAGGGTCCCT[C/T]GACAAAGCCCAAGCT	71956
rs28227537	snp	C/T	0.18	0.24	utr-variant-5-prime	Rnf135	GRCm38.p3	11:80183915	CTGGCTGTCGCCTAA[C/T]TATGGCGGCCGTTTG	71956
rs28227538	snp	C/T	0.165289	0.235211	upstream-variant-2KB	Rnf135	Mm_Celera	11:80182598	GAGTGGGTCATAACA[C/T]CTTTGGCAAACTCCT	71956
rs28227539	snp	C/T	0.18	0.24	upstream-variant-2KB	Rnf135	Mm_Celera	11:80182560	TGACTGCTGAGGTAC[C/T]TGCTAGAGCAGTGAT	71956
rs28227540	snp	A/G	0.21875	0.248039	upstream-variant-2KB	Rnf135	GRCm38.p3	11:80182408	GTGCCTTCATGCCTG[A/G]TGAGGTCCTCTGAAT	71956
rs28227541	snp	A/C	0.32	0.24	upstream-variant-2KB	Rnf135	GRCm38.p3	11:80181831	CCCAAGGTACTTGTT[A/C]GGTGCTTCTTTGTTT	71956
rs211877884	snp	A/T			intron-variant	Rnf135	Mm_Celera	11:80198509	AAGCATACAGACATA[A/T]AAATTAAAGAAGTAA	71956
rs211892556	snp	C/T			utr-variant-3-prime	Rnf135	Mm_Celera	11:80199565	AAAAGTCTAGCCCAA[C/T]AGTATAGCTGGGTGA	71956
rs212081963	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80190889	GTTAGCAGTTGAGTC[C/T]TGTAGCAAACCCCAG	71956
rs212103915	snp	G/T			intron-variant	Rnf135	GRCm38.p3	11:80185707	AGGGCAGGAGAGTTC[G/T]ACCCTGAGCAGTAAC	71956
rs212254645	snp	C/T			upstream-variant-2KB	Rnf135	Mm_Celera	11:80183573	ACCAGAAGAGGGCAT[C/T]AGATCCCATTTTTGT	71956
rs212532709	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80186315	CCCTTACATAGACAT[A/G]CATGTAGTCAAAACA	71956
rs212857816	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80196114	GTTAGCAAGGAGTTT[C/T]GGGTTCTGTAGGGGA	71956
rs212914727	snp	G/T			intron-variant	Rnf135	Mm_Celera	11:80189046	GTATTTGCATCTACC[G/T]ATGGAGTGCTGGGAT	71956
rs213608436	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80196274	TGGATGCTGAAGTGG[A/G]CATTTCTGGTTTCTT	71956
rs213666628	snp	C/G			intron-variant	Rnf135	Mm_Celera	11:80197043	GGTGGGTTCCCCCAG[C/G]ACTGCATAAACCAGG	71956
rs213681442	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80198232	GATTTATTGGTAAAT[A/G]TCACACCAAAAAATG	71956
rs213818618	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80189868	TAGGCTGGAGAGATG[A/G]CTCAGCGGTTAAGAG	71956
rs213992318	snp	A/G			intron-variant	Rnf135	GRCm38.p3	11:80190179	CTATAGATGGGTGTG[A/G]CCCATCATGTGGGTA	71956
rs214300959	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80190421	TCTCTTTGTCCATTG[C/T]AGGTTCCAGGAATCT	71956
rs214409469	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80193248	GTGAGTTTGAGTCCA[A/G]TTTGGGCTACAAAGC	71956
rs214558501	snp	A/G			synonymous-codon	Rnf135	Mm_Celera	11:80184237	TGAACCCGCCCCCGC[A/G]CCGCGTTCTGCGCCC	71956
rs214617635	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80194433	ATCATCATCGGTGTT[A/G]CAATCCAGCAGCAAC	71956
rs214627933	snp	A/T			intron-variant	Rnf135	Mm_Celera	11:80194849	CAGCGTCGTCCACTG[A/T]CTGCTGGGTAATATT	71956
rs214705323	snp	A/C			intron-variant	Rnf135	Mm_Celera	11:80192660	TCTTAAGATTTCATA[A/C]GCCTTGTGTGTTTTA	71956
rs214820071	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80194256	GAATCAGCAGTGGCC[A/G]CTCAGATTCACTCAC	71956
rs214825662	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80184420	TTTTGGAGTGGCTTG[C/T]CCCACAGGGCCAGAG	71956
rs214865749	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80185644	CTGATGCAAACTGCA[A/G]GAGGTTTTATTATCA	71956
rs215079728	snp	A/T			intron-variant	Rnf135	GRCm38.p3	11:80186480	CCTCTGCCTCCCAAG[A/T]GCTGGGATTAAAGGC	71956
rs215346395	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80195053	TGATTGTGTCAGCTG[A/G]GTAGGGGCGAGCTGA	71956
rs215402470	snp	G/T			intron-variant	Rnf135	Mm_Celera	11:80195993	GTTCTGGATTTGAGG[G/T]TGCCGCAATCCCCTG	71956
rs215537075	in-del	-/AC			upstream-variant-2KB	Rnf135	Mm_Celera	11:80181923	AAGAGATTCCACATA[-/AC]ACACATGCACACACA	71956
rs215720921	snp	A/G			intron-variant	Rnf135	GRCm38.p3	11:80194162	AGCCCACCACCCACC[A/G]GAGGTAGTGGAAAGG	71956
rs215756219	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80190978	ACCAAATGGCCTGAG[A/G]CCGCAGCAGCAGCAA	71956
rs215765514	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80191878	TCTGGAGAATCTGAA[C/T]TTGGTGCTATGTGAG	71956
rs216145964	in-del	-/AA			intron-variant	Rnf135	Mm_Celera	11:80193595	AAAACAAACACAAAC[-/AA]ACAAACAAAAAACCC	71956
rs216263629	in-del	-/AAAA			intron-variant	Rnf135	Mm_Celera	11:80193065	AAAAAAACATAAAAT[-/AAAA]AGGATCTTATAGACT	71956
rs216331700	snp	C/G			intron-variant	Rnf135	Mm_Celera	11:80193388	TTTCTAGAAGAACTG[C/G]GGTTGATCTTCAATA	71956
rs216546415	snp	A/T			upstream-variant-2KB	Rnf135	Mm_Celera	11:80183448	TTGAACTTCAGACCT[A/T]CGGAAGAGCAGTTGG	71956
rs216708731	snp	A/T			upstream-variant-2KB	Rnf135	Mm_Celera	11:80183201	TTCCAATTTTTTGTT[A/T]GGTATTTTCTTCATT	71956
rs216780112	in-del	-/TTTTTTTTTT			upstream-variant-2KB	Rnf135	Mm_Celera	11:80183306	AAGACTGAGGCTGTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTA	71956
rs217047332	snp	C/T			upstream-variant-2KB	Rnf135	Mm_Celera	11:80182593	TCAATGAGTGGGTCA[C/T]AACACCTTTGGCAAA	71956
rs217052589	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80185685	GATGAACTCCTCAAC[A/G]CCCTGCAGGGCAGGA	71956
rs217289970	snp	A/G			upstream-variant-2KB	Rnf135	GRCm38.p3	11:80182882	GCTATCTTCAGACAC[A/G]CCAGAAGAAGGCATC	71956
rs217410865	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80190556	TAGCCTTCAACGTGA[A/G]CTCCTCCTAGCCTCC	71956
rs217721160	snp	C/G			intron-variant	Rnf135	Mm_Celera	11:80192540	GTCCCTGTGGCATGT[C/G]TGTGTTTTCCCACTA	71956
rs217723971	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80191989	GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCG	71956
rs218321564	snp	C/T			synonymous-codon	Rnf135	Mm_Celera	11:80199045	CGCCTTCTGGCTGTA[C/T]GGCTTAAGTCCTGGA	71956
rs218386343	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80193470	CTGCCTGGATGTGAT[A/G]GTGAATGCCTTTAAT	71956
rs218448520	snp	C/G			intron-variant	Rnf135	Mm_Celera	11:80194409	GCAGTGTCAGAATAG[C/G]AAACACAAATCATCA	71956
rs218537356	snp	A/G			intron-variant	Rnf135	GRCm38.p3	11:80186954	CCAGGGGGTATCTGG[A/G]TGATGCTATGATTGG	71956
rs218591501	snp	C/T			intron-variant	Rnf135	GRCm38.p3	11:80190531	TGGAATTTTGTTGTG[C/T]TGTCCAGTCTAGCCT	71956
rs218654596	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80184908	GACCTCTGTACCCAC[C/T]CACTAAGCAATAACA	71956
rs218936733	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80197560	AAGGCTAAGAGGGTT[C/T]AGAGTCCTAGATTCT	71956
rs218959476	in-del	-/T			upstream-variant-2KB	Rnf135	Mm_Celera	11:80182820	AAGAGTAGTTGGTTA[-/T]TTTTTTTTTAAAGAT	71956
rs218961938	snp	G/T			intron-variant	Rnf135	Mm_Celera	11:80186046	AGTCGGGGTCCCACA[G/T]ATATATATCACTTTC	71956
rs219002714	snp	A/G			intron-variant	Rnf135	GRCm38.p3	11:80196360	TTTGCTGAGGCAGAC[A/G]CTTGAGAAAGCCAGC	71956
rs219046946	snp	A/C			intron-variant	Rnf135	Mm_Celera	11:80198401	CCCTCTCGGTGCCTC[A/C]CAATGTTCTGGAATT	71956
rs219378049	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80194654	AACATCACGTATCTT[C/T]TCGTGGGTCTTGCAT	71956
rs219433056	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80195366	GAGTTGGCAACAGGT[A/G]CCTTTAACCATTGAA	71956
rs219446488	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80189600	GAAGACAGCTTTCAG[C/T]TAGAGCTGTATGGGA	71956
rs219629819	snp	A/G			intron-variant	Rnf135	GRCm38.p3	11:80194765	AAGTGGCAGGAAGCC[A/G]CTCAACACCACCAGG	71956
rs219704498	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80197773	ATTAGTTACCTCTTA[A/G]GGCTTGGTTCTCCTA	71956
rs219795561	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80197674	GTATATATATACTGT[A/G]TTAGCCCAGGCTAGG	71956
rs219859225	snp	C/G			intron-variant	Rnf135	Mm_Celera	11:80189951	AGTTCACAACCATTC[C/G]TAATGAGATCAGATG	71956
rs219860023	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80196438	TCTCTTGTTTTGCTA[C/T]GTCATGCAGTACTTT	71956
rs220171263	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80193637	AATAAAACAAAGCCT[A/G]TTTATACTTCATTTA	71956
rs220527792	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80191096	GATGGTTGTGAGCCA[C/T]CATGTGGTTGCTGGG	71956
rs220740590	snp	G/T			intron-variant	Rnf135	Mm_Celera	11:80193718	CAGGAGGCAGAGGCA[G/T]GCGGATTTCTGAGTT	71956
rs220774837	snp	A/T			intron-variant	Rnf135	Mm_Celera	11:80185328	GATTATTAACAGCCC[A/T]TTGTCTCAATCTGCT	71956
rs220798026	snp	G/T			intron-variant	Rnf135	Mm_Celera	11:80194480	AATCAGCACGAGTCA[G/T]CAGGAGCAACCGTGG	71956
rs220866015	in-del	-/A			synonymous-codon	Rnf135	Mm_Celera	11:80199092	GCAGCTAAACACATG[-/A]AGCTTCCCTCGGGGT	71956
rs221104308	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80195146	CTCCTATTTTTAAGA[C/T]ATGTGATCCCTAATC	71956
rs221152362	snp	C/T			intron-variant	Rnf135	GRCm38.p3	11:80186745	GTGTTAGGGTTAGAA[C/T]TGCTGAAGAATGATA	71956
rs221260466	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80190595	CTTGAGTTCCCCTGT[A/G]CTCTCCAGGTTGCCT	71956
rs221442584	snp	C/G			intron-variant	Rnf135	Mm_Celera	11:80194562	AAGATCAGTGAAGAC[C/G]CAAGACCACCAAAGC	71956
rs221458564	in-del	-/T			intron-variant	Rnf135	Mm_Celera	11:80194863	GTCTGCTGGGTAATA[-/T]TTATTTCCCTTCTGA	71956
rs221498866	in-del	-/AAT			intron-variant	Rnf135	Mm_Celera	11:80190036	ATAAATCTTTAAAAA[-/AAT]AAAAGATGTATTTAT	71956
rs221521082	in-del	-/AAAAAA			intron-variant	Rnf135	GRCm38.p3	11:80186692	GAGAAACCCTGTCTC[-/AAAAAA]AAAAAAAAAAAATTC	71956
rs221541999	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80186002	TGGGGAACGTCCAGG[A/G]GCTTTACCTTCTAGG	71956
rs221720721	snp	A/G			intron-variant	Rnf135	Mm_Celera	11:80191013	CTGCAGGAACAGGGA[A/G]AACACTTTGTGTGAG	71956
rs221753100	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80184345	GAACCTTAAAAAGTT[C/T]ATAGCTGTATAAAGA	71956
rs221890925	in-del	-/CTC			downstream-variant-500B	Rnf135	Mm_Celera	11:80199914	ACTGCTCTTCCAGAT[-/CTC]CTGAATTCAAGTCCC	71956
rs222121173	snp	C/T			intron-variant	Rnf135	Mm_Celera	11:80189175	GAGGGAGCTATATTC[C/T]GGGGTCCAAGTTTTT	71956

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