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
rs3673876	snp	A/G	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105295555	AGCCTTCAGAAAAAG[A/G]TGTAAAACTCTCAAC	320311
rs3681551	snp	A/G	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105325071	TGGGAGGAGTGGGGC[A/G]CTATTAGAAAGAACT	320311
rs3681582	snp	C/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105325088	TATTAGAAAGAACTG[C/T]CTAGCTTATGGGCCT	320311
rs3696200	snp	A/T	0.231111	0.249285	intron-variant	Rnf152	Mm_Celera	1:105345427	ATAACATTGGGTATG[A/T]TCCAGAAACATCTAA	320311
rs3705237	snp	C/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105320080	GCCCTGGACAGCTCT[C/T]CACCCTACCCTACCT	320311
rs3705297	snp	C/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105320117	GGGGGTTGGGGTGAA[C/T]TGGCACATAGTCAAC	320311
rs3706859	snp	C/T	0.32	0.24	intron-variant	Rnf152	Mm_Celera	1:105320331	AATTAGGTCCACCTG[C/T]AGGAATGCTGGTGTC	320311
rs3707424	snp	C/T	0.459184	0.136902	intron-variant	Rnf152	Mm_Celera	1:105320422	GCATTTACATAGAGG[C/T]AGACCCACTGTTCCT	320311
rs6179013	snp	C/T	0.207612	0.24638	downstream-variant-500B	Rnf152	Mm_Celera	1:105276756	TCACTACAAACCCAT[C/T]CTCGGGCATCTCAAA	320311
rs30494232	snp	C/T	0.493827	0.0552116	intron-variant	Rnf152	Mm_Celera	1:105327481	AGAGCAGCTGTGACC[C/T]CCTGTCCACGCCTCT	320311
rs30494961	snp	C/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105351401	GATGAGAAGGGTGGC[C/T]TCCACATCATTAGGC	320311
rs30503453	snp	A/G	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105323865	GTGTAATTTGTTGCA[A/G]AAAGACCCACCCTAA	320311
rs30556488	snp	A/G	0.465374	0.126941	intron-variant	Rnf152	Mm_Celera	1:105293236	TTTGTGCCCATTCAA[A/G]GAATGCATCCAGCTA	320311
rs30556949	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105351753	TAATGGAAACATGAA[C/T]GCACTGGAACACTCT	320311
rs30603083	snp	A/G	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105286690	AAAACAAGAGAGACC[A/G]AGACAGGAGAAGCCT	320311
rs30611284	snp	G/T	0.497778	0.0332592	intron-variant	Rnf152	Mm_Celera	1:105339368	TCCTTAAGGAGATTT[G/T]AAACTAGGTAGAAAT	320311
rs30618380	snp	C/T	0.432133	0.171253	intron-variant	Rnf152	Mm_Celera	1:105290410	TATGGTATTACAGTT[C/T]GTTTTCTGGAACATG	320311
rs30694899	snp	A/G	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105343407	CAATGCTGGGGACCT[A/G]GCAATAAGGTAATTA	320311
rs30743234	snp	A/G	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105348014	CTTGCAACAAAGGCC[A/G]AATCCTCCAAAGCAC	320311
rs30808916	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105317967	CATGGATCTTGTTCC[C/T]CTTCATGTATCTGTC	320311
rs30844345	snp	C/T	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105322322	GTAGCTAGTGCTCTG[C/T]ACCCCTGGCTAGAAT	320311
rs30851712	snp	C/T	0.32	0.24	intron-variant	Rnf152	Mm_Celera	1:105352091	GAGGTAACTACTAAC[C/T]TATCCCTGCAGAGTA	320311
rs30856664	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105347291	AAGCATAGCAACTAT[C/T]GTTATTTAGGGGTGG	320311
rs30856855	snp	A/T	0.244898	0.249948	intron-variant	Rnf152	Mm_Celera	1:105339785	AGAAAATATTTTAAG[A/T]AGTTTAAATCCAGAA	320311
rs30888373	snp	C/T	0.5	0	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Rnf152, Gm17634	Mm_Celera	1:105356227	ACCTCCAGTTATATC[C/T]CAGGCTACCGTTGCC	320311
rs30905431	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105326819	TAAATGGCATTTTAG[C/T]CATAAAGCGATAAGC	320311
rs30911297	snp	C/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105323965	AGGCAGAAATGCATT[C/T]ACTCCCCTGCATTCT	320311
rs30959900	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105318057	CTTTCATAAAAAATA[C/T]ATACCACAGTTCCTG	320311
rs30985278	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Rnf152, Gm17634	Mm_Celera	1:105354564	TGAAAAGATGGGAGA[A/G]AAACAGTCCTTCTTC	320311
rs30994592	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105314930	ATAGCTTTCTATGCT[C/T]TACCACACCAGCAAA	320311
rs31007039	snp	A/G	0.444444	0.157135	upstream-variant-2KB, nc-transcript-variant	Rnf152, Gm17634	Mm_Celera	1:105356955	CGACTGGGACTGGCC[A/G]AGGTGGTGACCCAGC	320311
rs31013477	snp	C/T	0.432133	0.171253	intron-variant	Rnf152	Mm_Celera	1:105294589	AAGTGCACAGTGAGG[C/T]CCTGCCATTCCTCAT	320311
rs31055447	snp	A/G	0.401235	0.199068	intron-variant	Rnf152	Mm_Celera	1:105347827	GTGGCTGATCCACTG[A/G]TGCTCAATGTTTCAA	320311
rs31078123	snp	A/C	0.42	0.183303	intron-variant	Rnf152	Mm_Celera	1:105310248	CTGACCTTCCTCAAC[A/C]GCGCTATTTTTATTG	320311
rs31081741	snp	C/T	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105342269	AGTCCATTACAGAGC[C/T]TGTCAGCTGGGAGTA	320311
rs31145644	snp	G/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Rnf152, Gm17634	Mm_Celera	1:105354474	GTCTCTTCTATGTTC[G/T]TTCTGCTCCTACCCA	320311
rs31156238	snp	A/G	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105343092	GATGGCCCTTTAATC[A/G]ACAGCAGAGAGATGA	320311
rs31202079	snp	C/T	0.32	0.24	intron-variant	Rnf152	Mm_Celera	1:105293623	GATAAAAGATGCTGG[C/T]CCCAGAATGAGTGAA	320311
rs31207676	snp	A/G	0.401235	0.199068	intron-variant	Rnf152	Mm_Celera	1:105296958	AATTGCTCTTGATAT[A/G]GACAAAAATCCTTCA	320311
rs31293681	snp	A/G	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105286241	ATTGAAATGAGGTTC[A/G]AGGGCTGCCCTTTCT	320311
rs31327456	snp	C/G	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105317927	TGAGTTATTACGCTA[C/G]CTGGGAATTTTGACA	320311
rs31338163	snp	A/G	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105333721	CTGACAGGCCAGTGC[A/G]TCTTGATGCCCCTCT	320311
rs31368173	snp	A/G	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105322567	CTATGTGGGTTGCAG[A/G]TTGGATGTCAGGACA	320311
rs31378585	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105319548	AGCCTGAGAGGCTGG[C/T]TTCAACCTTTACAGT	320311
rs31378625	snp	C/T	0.49827	0.0293608	intron-variant	Rnf152	Mm_Celera	1:105331082	GTCTTTCTCAGTCAA[C/T]TTTGGATCCTCAAAG	320311
rs31385471	snp	C/G	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105346065	AGCTTGTTAAGTGCC[C/G]CACAGTGTCTGCTAC	320311
rs31398851	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Rnf152	Mm_Celera	1:105279160	GAGAGTTAGTTGTAG[C/T]AAGTCATTTCTATCA	320311
rs31403531	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105341861	GAATCCCTACTTCCC[C/T]TCATACCTGAAACGC	320311
rs31422686	snp	A/G	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105340829	TAACCTCTATACCCA[A/G]CTTTCCTCATCTGTA	320311
rs31447323	snp	C/T	0.484429	0.0868505	intron-variant	Rnf152	Mm_Celera	1:105331213	CACTGTCTCCAAAAA[C/T]AACGTTGGTGGTACA	320311
rs31474430	snp	G/T	0.487535	0.077957	intron-variant	Rnf152	Mm_Celera	1:105331144	ACAGCCAGACCTCTG[G/T]GGATCATGGCCATCT	320311
rs31476063	snp	C/T	0.429688	0.173817	intron-variant	Rnf152	Mm_Celera	1:105340207	AAAACTCCATTCAAC[C/T]GCTTCATACCATTGG	320311
rs31517180	snp	C/T	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105296121	CTCTCACTCCAAGTC[C/T]TAAGGTAGAAGGTGA	320311
rs31529593	snp	A/T	0.429688	0.173817	intron-variant	Rnf152	Mm_Celera	1:105340884	CTGCCTATCCCTTAT[A/T]GGACTGTTGTGAAGG	320311
rs31567876	snp	A/C	0.497778	0.0332592	intron-variant	Rnf152	Mm_Celera	1:105341902	GCTTCAGCTAGGTCC[A/C]TTCATCCCAAGTGTC	320311
rs31570670	snp	A/G	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105319516	GATGGGCAGAGCACA[A/G]CATCAGCACTGCGTG	320311
rs31574072	snp	A/C/T	0.375	0.216506	intron-variant	Rnf152	GRCm38.p3	1:105323893	TAAACTGAGTGGCAC[A/C/T]ATTGACTGGGATTTA	320311
rs31591743	snp	C/T	0.48	0.0979796	intron-variant	Rnf152	Mm_Celera	1:105293631	ATGCTGGTCCCAGAA[C/T]GAGTGAAAAAGAATT	320311
rs31593214	snp	C/G	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105294835	AGACTGGCATACACC[C/G]TCAAGTTGAGTACAA	320311
rs31594608	snp	A/G	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105339704	AGTTTGTGTGGAAAG[A/G]GTCCTTCCACCAGAT	320311
rs31656688	snp	A/T	0.401235	0.199068	intron-variant	Rnf152	Mm_Celera	1:105294709	AAATAGTGGCTTTAC[A/T]ATGGCATCCTTGGTA	320311
rs31682834	snp	G/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105342007	GTTTATCTCTTCCCA[G/T]CATTGCATTCTAAGC	320311
rs31690368	snp	A/T	0.444444	0.157135	utr-variant-3-prime	Rnf152	Mm_Celera	1:105279150	GAGAGAGAGAGAGAG[A/T]TAGTTGTAGCAAGTC	320311
rs31693543	snp	A/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105291091	ATGCAGGTGTGGTGA[A/T]ATACTTGAATAAATG	320311
rs31713633	snp	A/G	0.497778	0.0332592	intron-variant	Rnf152	Mm_Celera	1:105339433	GTTATGGCCAGGAAT[A/G]TGCAGATGTATCAGC	320311
rs31728547	snp	A/G	0.32	0.24	utr-variant-3-prime	Rnf152	Mm_Celera	1:105282140	CATAACATCCTTTAC[A/G]CAACATTTTTGTCTA	320311
rs31732805	snp	C/G	0.487535	0.077957	intron-variant	Rnf152	Mm_Celera	1:105331465	CCTACAGCTAAGTTT[C/G]CAGCACACATACCCC	320311
rs31744970	snp	A/G	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105311078	ATACCAAGTCTGACC[A/G]CCTCTGAGGGGGAGT	320311
rs31759714	snp	C/T	0.32	0.24	intron-variant	Rnf152	Mm_Celera	1:105352558	TGCTTGCACGGCAAG[C/T]GCTTTACTCACTGAG	320311
rs31765418	snp	A/G	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105314047	TGTATATATATATAT[A/G]TATACATATATACAT	320311
rs31787124	snp	A/G	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105317767	TAGGATTTCCTCCGT[A/G]CTAAGAAGGTACTCC	320311
rs31799869	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Rnf152, Gm17634	Mm_Celera	1:105354498	CTACCCAGCAGCCCT[C/T]TCTGCTACCTGCCAG	320311
rs31804998	snp	G/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105318956	TCTGTTCATCCACAA[G/T]TTTCTAACCATTAAG	320311
rs31844304	snp	C/T	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105333847	GCATAGCAAGCACTT[C/T]ACTACTGAGTCACTT	320311
rs31874838	snp	C/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105305503	GGTTAAAACAGATGA[C/T]TTTTTTAATCCCACT	320311
rs31911191	snp	A/G	0.492188	0.0620098	intron-variant	Rnf152	Mm_Celera	1:105319172	CATTTAACAACCTTA[A/G]AAGACAACTGAAAAA	320311
rs31921306	snp	A/G	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105293081	AACACTGTAAACTTC[A/G]CCGTGCCATCCCTAG	320311
rs31928216	snp	A/T	0.498615	0.0262793	intron-variant	Rnf152	Mm_Celera	1:105347007	GCATCTCTAACAAGA[A/T]CATTCTGGGGTGTCC	320311
rs31935542	snp	C/T	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105352905	GGGCCTGAGCAACTA[C/T]AGCGAGCCTGGCCTT	320311
rs31960817	snp	A/G	0.207612	0.24638	intron-variant	Rnf152	Mm_Celera	1:105340126	TCCAAGGTCAGCACT[A/G]ATTTCTCTAAATCTG	320311
rs31970935	snp	A/T	0.444444	0.157135	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Rnf152, Gm17634	Mm_Celera	1:105356108	CCCAACTCAAAGCAA[A/T]GCCCGAGGAAAACCC	320311
rs31970936	snp	C/G	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105319535	CAGCACTGCGTGCAG[C/G]CTGAGAGGCTGGTTT	320311
rs31975745	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105342441	TGACTTCAGTGGGCG[C/T]CTCAGCAGTGTCTGC	320311
rs31975750	snp	C/G/T	0.5	0	intron-variant	Rnf152	GRCm38.p3	1:105324054	GAGTGAAACCTAGAA[C/G/T]GGAAAACCAAATAAA	320311
rs32004843	snp	A/C	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105306967	TTCCTTAAGGAATCA[A/C]AGGAAAATACAATTA	320311
rs32011503	snp	C/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105351863	CTAAGTCTGTCCGTA[C/T]CGTTCTCCTCTGCTG	320311
rs32036584	snp	C/T	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105341901	TGCTTCAGCTAGGTC[C/T]ATTCATCCCAAGTGT	320311
rs32054311	snp	C/T	0.46875	0.121031	intron-variant	Rnf152	Mm_Celera	1:105322483	CTGCAGTGGGCCAGA[C/T]TTAGTAGAGCCACCT	320311
rs32085422	snp	C/T	0.32	0.24	intron-variant	Rnf152	Mm_Celera	1:105342477	TCACACACACGCCCA[C/T]ACCCAAGTTCATCAT	320311
rs32090599	snp	C/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105290670	ATTTGAGTTTGGCAT[C/T]GCCTTCCTTGAGAGC	320311
rs32106646	snp	G/T	0.32	0.24	intron-variant	Rnf152	Mm_Celera	1:105331421	GACCAGACATACATG[G/T]CTTGTCACAATATCA	320311
rs32109883	snp	A/G	0.456747	0.140554	intron-variant	Rnf152	Mm_Celera	1:105326885	CCCAGAGTTGCTGCA[A/G]TGCTTCCTCTGAAAT	320311
rs32114840	snp	A/G	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105292631	GATATAATTCTACTC[A/G]TAAACAGCAAGTTAC	320311
rs32118721	snp	A/G	0.48	0.0979796	intron-variant	Rnf152	Mm_Celera	1:105323713	CTTGCCTCTGTTCAC[A/G]CTGTACCCTCCTATC	320311
rs32130110	snp	C/T	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105317591	ATGTCTCAAAGTTGA[C/T]GTGTCTGAAGCAGAA	320311
rs32130992	snp	A/C	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105318663	TAATGGGAACATTGC[A/C]AAGCATCCCTTGTCC	320311
rs32146382	snp	A/G	0.375	0.216506	intron-variant	Rnf152	Mm_Celera	1:105348088	GGTTGGTTTGATCGT[A/G]TTGCTTTTGTTGTAG	320311
rs32164833	snp	C/T	0.5	0	intron-variant	Rnf152	Mm_Celera	1:105322250	AAGCAGATAGTGTCA[C/T]CTATTGTCAAAGGCA	320311
rs32201400	snp	A/T	0.444444	0.157135	intron-variant	Rnf152	Mm_Celera	1:105318292	GCCCTGTAGTGGTTT[A/T]AATGAGCCACCATCA	320311
rs32203432	snp	A/C/G	0.375	0.216506	intron-variant	Rnf152	GRCm38.p3	1:105308213	GCTCCAAATGCAAGG[A/C/G]CACCCACATTCATAA	320311

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