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
rs13464397	snp	C/G	0.2952	0.24588	missense, intron-variant	Rnf34	GRCm38.p3	5:122861852	CAGCAGCTACTGAAG[C/G]ACCCAATATAGTTTG	80751
rs13464398	snp	A/C	0.231111	0.249285	synonymous-codon	Rnf34	Mm_Celera	5:122868164	CAAGTGTGGCAAGCG[A/C]ATGAGTGAGTGTCCC	80751
rs29515957	snp	C/T	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122861389	TTAACTCACAGAGAT[C/T]TGCCTGCCTTTGTCT	80751
rs29523659	snp	C/T	0.5	0	upstream-variant-2KB, nc-transcript-variant, intron-variant	Rnf34, Gm33044	Mm_Celera	5:122849879	AGGGAAGCTATCCAC[C/T]CAAAATAGGAAGCCA	80751
rs29528954	snp	A/G	0.5	0	intron-variant	Rnf34	Mm_Celera	5:122857823	CTCTTTCTGGAGGAT[A/G]TAAAAGAAATTCTTG	80751
rs29543939	snp	C/T	0.5	0	intron-variant	Rnf34	Mm_Celera	5:122852527	AAATCATCATCTTTG[C/T]TGTGAGATCCAAAAC	80751
rs29543985	snp	A/C	0.498615	0.0262793	intron-variant	Rnf34	GRCm38.p3	5:122863398	GATTTTACATAAAGC[A/C]CTTACGCTAACACTT	80751
rs29565678	snp	A/C	0.5	0	intron-variant	Rnf34	Mm_Celera	5:122860530	AATTTCAAATATAAC[A/C]TGAAATTTTAAAATT	80751
rs29578150	snp	A/T	0.48	0.0979796	downstream-variant-500B	Rnf34	Mm_Celera	5:122869218	TCTTCTTTTTTAGTT[A/T]TATGACACATATGTA	80751
rs29582381	snp	C/T	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122860565	GCACGTCTCTCTTGG[C/T]CTCCCACTGAATTGC	80751
rs29677928	snp	A/G	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122860197	AGGACAACCAATGTT[A/G]TATCAGGAGTCTGCA	80751
rs29678031	snp	A/C	0.444444	0.157135	intron-variant, upstream-variant-2KB	Rnf34, Gm33044	GRCm38.p3	5:122851483	TGGAAAACCAACCAA[A/C]AACAATCCCCTGAGA	80751
rs29728441	snp	A/G	0.5	0	intron-variant	Rnf34	Mm_Celera	5:122852469	ATGTCACTGCAACTT[A/G]AGAATACTTTATTAA	80751
rs29771598	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Rnf34, Gm33044	GRCm38.p3	5:122851801	GTTTTGAGATAGGGT[C/T]TCACTGTCAATCCCT	80751
rs29776535	snp	C/T	0.432133	0.171253	synonymous-codon	Rnf34	GRCm38.p3	5:122866885	TGAAGATGACGACGA[C/T]GAACAAGAGGAGGAG	80751
rs33065685	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Rnf34, Gm33044	Mm_Celera	5:122851297	CAGCAGCTTCACTGC[C/T]TTAGTCAAGATGGGG	80751
rs33072984	snp	C/T	0.375	0.216506	intron-variant	Rnf34	GRCm38.p3	5:122862923	GAGCCTATAGGCATT[C/T]GTGACCTATCAGACA	80751
rs33079748	snp	A/C	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122862755	GGGTTTAGAACCAAA[A/C]AAAGGCTCTCCAAGA	80751
rs33127337	snp	G/T	0.5	0	intron-variant	Rnf34	Mm_Celera	5:122861964	CAGGGGGGGAAAATA[G/T]ATCATAATTCTTTTT	80751
rs33151036	snp	A/C	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122862706	TAGAGGGTGTTGAGT[A/C]CCCTGGATCTGGCAG	80751
rs33156153	snp	C/G	0.48	0.0979796	downstream-variant-500B	Rnf34	Mm_Celera	5:122869224	TTTTTAGTTTTATGA[C/G]ACATATGTAGCCCTG	80751
rs33167648	snp	C/T	0.426035	0.177515	intron-variant	Rnf34	GRCm38.p3	5:122856341	GTCAGTCTCACAGGT[C/T]GAGGCAATTACTTAG	80751
rs33217313	snp	C/T	0.5	0	intron-variant	Rnf34	Mm_Celera	5:122865445	GTAGATATGGGCTCA[C/T]TAATGGGAGCACTGG	80751
rs33276019	snp	C/T	0.444444	0.157135	intron-variant	Rnf34	Mm_Celera	5:122855587	AAACTAAAACCAAAA[C/T]AAAACAATAATTAAG	80751
rs33298853	snp	C/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Rnf34, Gm33044	GRCm38.p3	5:122851287	GTGTTTTGCCCAGCA[C/G]CTTCACTGCCTTAGT	80751
rs33306141	snp	A/C	0.48	0.0979796	intron-variant	Rnf34	GRCm38.p3	5:122865016	GGTTGTCTGCCTAAC[A/C]GGGATCAACAGTGTG	80751
rs33308486	snp	A/C	0.444444	0.157135	intron-variant	Rnf34	GRCm38.p3	5:122861091	GCATTGTGTTGTTCA[A/C]GATAAAGATACTTAC	80751
rs33314553	snp	A/G	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122861534	AGGCCAGAAGAGAGC[A/G]TCGGGGACTGGAGTT	80751
rs33316991	snp	G/T	0.432133	0.171253	intron-variant	Rnf34	Mm_Celera	5:122862168	TTGATTGTTTGTAGT[G/T]CATTTAATAAAAAAT	80751
rs33344727	snp	C/T	0.375	0.216506	downstream-variant-500B	Rnf34	GRCm38.p3	5:122869296	GGGATTAAAGGTGTG[C/T]GCCACCACGCCCGGC	80751
rs33353280	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Rnf34, Gm33044	GRCm38.p3	5:122851872	GAATTTGGATTACAA[A/G]TGTAGGATCTGGAAT	80751
rs33368438	snp	C/G	0.5	0	intron-variant	Rnf34	Mm_Celera	5:122862044	GGCTGTTCTAGAACT[C/G]GCTTTGTAGACCAGA	80751
rs33381649	snp	A/G	0.48	0.0979796	intron-variant	Rnf34	GRCm38.p3	5:122865041	AGTGTGCATCATGCC[A/G]GGCATGGTGGCGCAC	80751
rs33381768	snp	C/T	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122867806	GTCAGGTGAACTAGA[C/T]AAACAATTGCTGAGT	80751
rs33398425	snp	G/T	0.375	0.216506	intron-variant	Rnf34	Mm_Celera	5:122863058	TGAATACACTGTAGC[G/T]GTCTTCAGACACAAC	80751
rs33403333	snp	A/G	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122861468	ATTTTCTGTTTGGAT[A/G]TTGTGCTTGCATGTA	80751
rs33454473	snp	A/G	0.375	0.216506	downstream-variant-500B	Rnf34	GRCm38.p3	5:122869297	GGATTAAAGGTGTGT[A/G]CCACCACGCCCGGCA	80751
rs33467496	snp	C/T	0.375	0.216506	downstream-variant-500B	Rnf34	Mm_Celera	5:122869105	TTAGCTATATATTTA[C/T]ATATTGGAGTAAGGG	80751
rs33493234	snp	C/T	0.444444	0.157135	intron-variant	Rnf34	Mm_Celera	5:122856621	TTGGTTTGCCCTTCC[C/T]GTGCTGCCAAGAGTG	80751
rs33519461	snp	C/T	0.444444	0.157135	intron-variant	Rnf34	Mm_Celera	5:122855558	ACACAGAAACCCTGT[C/T]TCGAAAAAACAAAAA	80751
rs33565515	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Rnf34, Gm33044	GRCm38.p3	5:122850419	GACCACGTAGCGGGG[C/T]GCCCGGCCCGAAGTG	80751
rs33585335	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Rnf34, Gm33044	GRCm38.p3	5:122850404	GGCTTCGTGAGAGAC[C/G]ACCACGTAGCGGGGT	80751
rs33586014	snp	A/G	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122861955	ATAACACAGGGGGGG[A/G]AAATATATCATAATT	80751
rs33599378	snp	A/G	0.432133	0.171253	intron-variant	Rnf34	GRCm38.p3	5:122866772	AAAAACTTGATCACT[A/G]ATATAATTGGATCTG	80751
rs33622685	snp	C/T	0.5	0	intron-variant	Rnf34	GRCm38.p3	5:122858967	GAAGACTTTTCATAA[C/T]GAACGATCACTGGTA	80751
rs33652102	snp	C/G	0.455	0.143091	intron-variant	Rnf34	GRCm38.p3	5:122864398	GTCCTGGCACAGGTA[C/G]GGTGGTGTGATTGTT	80751
rs36248961	snp	C/T	0.297521	0.245442	intron-variant	Rnf34	Mm_Celera	5:122852970	TGTTAGCCTAGTCTA[C/T]TTTGATATGTTAAGG	80751
rs36355826	snp	C/G	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122865278	ACTTTGTATACTAAG[C/G]CAACACTCACAACAA	80751
rs36454005	snp	C/G	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122863549	CTTAGAGTGTAATCA[C/G]GGCTATGCTGGCTAC	80751
rs36508498	snp	A/G	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122865914	ACATTGTGTCCTGTG[A/G]TCAAAAGATGTCATT	80751
rs36527489	snp	C/T	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122867828	TTGCTGAGTATAGAT[C/T]CCTTGCTTATAACAA	80751
rs36720266	snp	C/T	0.297521	0.245442	intron-variant	Rnf34	Mm_Celera	5:122860133	AGTAACATCTCTAGG[C/T]TGCCAGTGTGGTATA	80751
rs36830045	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Rnf34	Mm_Celera	5:122868407	AGTGCCATGACCCAT[C/T]TCCCTGTGGACACAC	80751
rs36853439	snp	A/G	0.124444	0.216185	intron-variant	Rnf34	Mm_Celera	5:122867956	TCCCTGTAATAATCT[A/G]GAGGCTTCTGTGAGA	80751
rs36984006	snp	A/G	0.165289	0.235211	intron-variant	Rnf34	Mm_Celera	5:122853446	TGACTTAGTAAAAAA[A/G]CTCTTGCTGTGCAAG	80751
rs37093505	snp	C/G	0.124444	0.216185	intron-variant	Rnf34	Mm_Celera	5:122864533	GGCATCTCACACCTG[C/G]CTGATGCTTAGGTGC	80751
rs37138556	snp	A/G	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122865778	CGAATTTGCATAATC[A/G]TATAAACAGATACAC	80751
rs37146877	snp	G/T	0.260355	0.249785	intron-variant, upstream-variant-2KB	Rnf34, Gm33044	Mm_Celera	5:122851130	GAAGGTGGTGATGTC[G/T]TCCCTCACGGTGTTG	80751
rs37192525	snp	A/G	0.231111	0.249285	utr-variant-3-prime	Rnf34	Mm_Celera	5:122868401	CTGGCCAGTGCCATG[A/G]CCCATCTCCCTGTGG	80751
rs37316120	snp	C/T	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122865403	GAGATGAAATTTTTT[C/T]CCCTTTGAGGAAAGT	80751
rs37421846	snp	A/G	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122864610	TATTAAATAACTTAT[A/G]ATTGTCGAAGTAATA	80751
rs37442695	snp	C/T	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122865895	GATAGTGGAAGCAAC[C/T]TCGACATTGTGTCCT	80751
rs37530552	snp	C/T	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122863886	AAATAGGCTGCTGCT[C/T]GGGTGCTTCATATAA	80751
rs37578287	snp	A/G	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122864450	CCATGTGTGGTCAGG[A/G]TCTTTGAATGCTAGG	80751
rs37688959	snp	A/C	0.231111	0.249285	utr-variant-3-prime	Rnf34	Mm_Celera	5:122868266	ACTCACATGACATTA[A/C]CCCAAACATTTCAGT	80751
rs37797752	snp	C/G	0.297521	0.245442	intron-variant	Rnf34	Mm_Celera	5:122860497	CAGTGCATGTCTAGG[C/G]TTAACAGGAAATATC	80751
rs37809905	snp	A/T	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122867093	TTTGGGCTTGTGGGA[A/T]CAAGGTAACAGATAC	80751
rs37917164	snp	C/T	0.32	0.24	utr-variant-3-prime	Rnf34	Mm_Celera	5:122868534	CCCTTACTTTACCTT[C/T]ATCCTGTGTTTGTTC	80751
rs37941730	snp	A/G	0.142012	0.225474	utr-variant-3-prime	Rnf34	Mm_Celera	5:122868712	TAAACATAATTGGGA[A/G]ACAACTGACATTCTA	80751
rs38054742	snp	C/G	0.497778	0.0332592	intron-variant	Rnf34	GRCm38.p3	5:122865855	TGGCACAGTGCTGCT[C/G]TGTGGCACCTGGTGG	80751
rs38267564	snp	A/C	0.297521	0.245442	intron-variant, upstream-variant-2KB	Rnf34, Gm33044	Mm_Celera	5:122851376	GTTAAAAGAAAAGAG[A/C]CCCTTAAGCATGGTG	80751
rs38289422	snp	C/G	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122865253	AGGTAGTGCCAGGGA[C/G]TGAATCAAGACTTTG	80751
rs38304436	snp	G/T	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122863581	GATTTCTGTACTAGT[G/T]GGATCTTCTCTGTCC	80751
rs38559697	snp	G/T	0.391111	0.206368	intron-variant	Rnf34	GRCm38.p3	5:122865747	AAGACCAGAGTTTTA[G/T]GATTTTTCTCAAATG	80751
rs38713828	snp	A/G	0.32	0.24	intron-variant	Rnf34	Mm_Celera	5:122863420	CTAACACTTTAATGG[A/G]GCATCTTGTAGTTTG	80751
rs38761995	snp	A/G	0.297521	0.245442	intron-variant	Rnf34	Mm_Celera	5:122860100	GGAGAATTCAAGAGG[A/G]AACTATCTGTGAGAT	80751
rs38838290	snp	A/C	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122867011	AGATGTAGTAAAACG[A/C]ACTTCAGGCAGCTCA	80751
rs39282945	snp	A/T	0.297521	0.245442	intron-variant	Rnf34	GRCm38.p3	5:122853955	AGATGGGTTCTTTGA[A/T]GAAGCTTTCACTAGT	80751
rs39372895	snp	A/T	0.231111	0.249285	intron-variant	Rnf34	Mm_Celera	5:122867687	ATGAATAGATTTTTT[A/T]AAGAAAAGCATTATA	80751
rs39835448	snp	A/G	0.231111	0.249285	utr-variant-3-prime	Rnf34	Mm_Celera	5:122868423	TCCCTGTGGACACAC[A/G]GCTTTCCCAGGTTCT	80751
rs46115688	snp	C/G			intron-variant	Rnf34	Mm_Celera	5:122856933	CTGTTATGATCTGTG[C/G]CTGAAAATAGTAATA	80751
rs46478501	snp	G/T			intron-variant	Rnf34	GRCm38.p3	5:122853735	AGTAGCCTTTTCTTT[G/T]CACATTTCTTAAGTA	80751
rs46502786	snp	C/G			upstream-variant-2KB, nc-transcript-variant	Rnf34, Gm33044	Mm_Celera	5:122849630	GAACGACAAAGAATT[C/G]GAATTGGACAGCCTT	80751
rs47517143	snp	G/T			upstream-variant-2KB, intron-variant	Rnf34, Gm33044	GRCm38.p3	5:122848760	TGCACCCAGCTGTAT[G/T]CGTGTTCTGTCAAAA	80751
rs47891217	snp	A/G			upstream-variant-2KB, intron-variant	Rnf34, Gm33044	GRCm38.p3	5:122848603	TAGAGCCTGAAGAAA[A/G]ATAGGCTTGACATAG	80751
rs47899253	snp	A/G			intron-variant	Rnf34	Mm_Celera	5:122855430	AATTAAGTTTGGGCT[A/G]GGCATGGTGGCGCAT	80751
rs48230997	snp	C/T			intron-variant, upstream-variant-2KB	Rnf34, Gm33044	Mm_Celera	5:122852118	TAGACCCCCCTGGAA[C/T]TGGAGTTACTAATGG	80751
rs48612277	snp	A/G			intron-variant	Rnf34	GRCm38.p3	5:122854024	TAATCCTAGCACTTG[A/G]GAGGCAGAGACAGTG	80751
rs48875859	snp	A/G			intron-variant	Rnf34	Mm_Celera	5:122853505	CCCTTGTAAATGTGG[A/G]AAGAGAACCAGCTTC	80751
rs49075752	snp	C/T			intron-variant	Rnf34	Mm_Celera	5:122864713	ATTGTTCTGATTTGG[C/T]TTTATTTATTTTGAG	80751
rs49367540	snp	A/G			upstream-variant-2KB, intron-variant	Rnf34, Gm33044	GRCm38.p3	5:122848775	TCGTGTTCTGTCAAA[A/G]AGTTCATCTAAGCAG	80751
rs50810328	snp	A/T			intron-variant	Rnf34	GRCm38.p3	5:122854107	TAGAACTATGTAGAC[A/T]CTGTCTCAAACACCA	80751
rs51475336	snp	A/G			intron-variant	Rnf34	GRCm38.p3	5:122863013	TTACCTTGCCCTGGG[A/G]TTTTTTGTTTTGTTT	80751
rs51886760	snp	G/T			intron-variant	Rnf34	Mm_Celera	5:122864456	GTGGTCAGGATCTTT[G/T]AATGCTAGGTGACTG	80751
rs52439755	snp	A/G			intron-variant	Rnf34	Mm_Celera	5:122865172	AGAAACCCTGTCTCG[A/G]AAAAAAAAAAAAAAA	80751
rs108530729	snp	G/T			intron-variant	Rnf34	Mm_Celera	5:122856682	TTTCTTTTTTTTTTG[G/T]TTTTTTTTTTTCGAG	80751
rs211738544	in-del	-/GGGG			intron-variant	Rnf34	Mm_Celera	5:122854697	TTTCTTTCTTTTTTT[-/GGGG]GGGGGGGGCATTTTT	80751
rs211747869	in-del	-/T			downstream-variant-500B	Rnf34	Mm_Celera	5:122869014	GAACAGGTGCCTCTC[-/T]TCAGAAGAGCATCTC	80751
rs211968338	in-del	-/C			intron-variant, upstream-variant-2KB	Rnf34, Gm33044	Mm_Celera	5:122852107	AGAGGTGGCATTAGA[-/C]CCCCCTGGAACTGGA	80751
rs212109825	snp	A/G			intron-variant	Rnf34	Mm_Celera	5:122859265	AAGTGGAACTGTGGT[A/G]TTTATTATCTGGTGT	80751

Full records

It may take some time, please wait.