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
rs6190059	snp	A/G	0.5	0	intron-variant	Hdac4	Mm_Celera	1:92172252	CATCCTACAGATGGC[A/G]TGAGATGAACCAAGA	208727
rs6190698	snp	C/T	0.5	0	intron-variant	Hdac4	Mm_Celera	1:92172405	TATTCCCCAGGCAGA[C/T]AGTGCCAAAATCAGC	208727
rs6284237	snp	C/T	0.5	0	intron-variant	Hdac4	Mm_Celera	1:91955391	CCCTGTGCCCACCTG[C/T]GGCCACAAGGAGAGA	208727
rs6284354	snp	C/T	0.359862	0.224567	intron-variant	Hdac4	Mm_Celera	1:91955463	TTGAACTAGGGTGGA[C/T]TGGACTGGCGTGCCC	208727
rs6285286	snp	C/T	0.231111	0.249285	intron-variant	Hdac4	Mm_Celera	1:91955614	TGAACTAGGAGGAAT[C/T]ACTGAAAGACAAAAG	208727
rs6352576	snp	C/T	0.207612	0.24638	intron-variant	Hdac4	Mm_Celera	1:92044192	GCTGGAGTCCCTCAC[C/T]AGCTCCAATCTGCTG	208727
rs6353056	snp	C/T	0.5	0	intron-variant	Hdac4	Mm_Celera	1:92044269	AACACAGGATTGAAT[C/T]CTCAGCANTAGGCTG	208727
rs6353068	snp	C/G	0.5	0	intron-variant	Hdac4	Mm_Celera	1:92044277	ATTGAATNCTCAGCA[C/G]TAGGCTGCAGTGTAG	208727
rs6353499	snp	A/G	0.21875	0.248039	intron-variant	Hdac4	Mm_Celera	1:92044321	GCTCTCCCAGCAGCA[A/G]CAAAGCCCAGAGGTT	208727
rs6353587	snp	A/C	0.5	0	intron-variant	Hdac4	Mm_Celera	1:92044366	CAAATTTTAAATCAT[A/C]ATCATTAAATTAAAC	208727
rs6356589	snp	A/G	0.5	0	intron-variant	Hdac4	Mm_Celera	1:92038322	agagtaaactgactt[A/G]cacccagaggcatnt	208727
rs6356608	snp	A/G	0.5	0	intron-variant	Hdac4	Mm_Celera	1:92038336	tncacccagaggcat[A/G]taggctagcacacat	208727
rs6356671	snp	A/G	0.5	0	intron-variant	Hdac4	Mm_Celera	1:92038374	agcacacaagcgcgc[A/G]cncacacacacacac	208727
rs6356673	snp	A/G	0.5	0	intron-variant	Hdac4	Mm_Celera	1:92038376	cacacaagcgcgcnc[A/G]cacacacacacacac	208727
rs6358171	snp	A/C	0.5	0	utr-variant-3-prime	Hdac4	GRCm38.p3	1:91933058	AAGCTTCTTCCTTCG[A/C]GGCTTCCCAGGGGGA	208727
rs6358662	snp	A/C	0.207612	0.24638	utr-variant-3-prime	Hdac4	GRCm38.p3	1:91933132	CCCGTGTGTTGCGCG[A/C]TGTCCTGTGTTCCAT	208727
rs6359127	snp	C/T	0.498615	0.0262793	utr-variant-3-prime	Hdac4	GRCm38.p3	1:91933213	GGGCGGCAGAAAGGC[C/T]TCCCGTTGCTGCTGC	208727
rs6359582	snp	A/G	0.207612	0.24638	utr-variant-3-prime	Hdac4	GRCm38.p3	1:91933286	ACGCAGGAGTGATAC[A/G]GGTAAGTTTCTTGGC	208727
rs6366413	snp	C/T	0.304688	0.243945	intron-variant	Hdac4	Mm_Celera	1:92044486	ATACTATCCCCAGAC[C/T]CTGTATCTTCAGATC	208727
rs6367471	snp	C/T	0.304688	0.243945	intron-variant	Hdac4	Mm_Celera	1:92044651	GGCATGTAAGGGCTG[C/T]TTGATCCACAGAGGC	208727
rs6367521	snp	G/T	0.304688	0.243945	intron-variant	Hdac4	Mm_Celera	1:92044678	AGGCTCCAATCTGCA[G/T]CTCCAGCCATTGTTC	208727
rs6370212	snp	A/G	0.207612	0.24638	intron-variant	Hdac4	Mm_Celera	1:92038574	ATTTTATCCATACAT[A/G]CCGGACAAATGTCTC	208727
rs6370722	snp	C/T	0.207612	0.24638	intron-variant	Hdac4	Mm_Celera	1:92038660	AGAATTCCACGCTAT[C/T]AAGTGACTAGAAAGT	208727
rs6370776	snp	C/T	0.35503	0.226867	intron-variant	Hdac4	Mm_Celera	1:92038694	CCCACTTTTTAGTCT[C/T]AAAAATGGATTTTAT	208727
rs13474690	snp	A/G			utr-variant-3-prime	Hdac4	GRCm38.p3	1:91929568	TCTGGCAAGCTGGCT[A/G]GGGGCATTTTCTTTT	208727
rs13474691	snp	C/T	0.391111	0.206368	utr-variant-3-prime	Hdac4	GRCm38.p3	1:91929519	TTTTCTCTCCCCACA[C/T]AGGGCCAGGTGCACC	208727
rs13475981	snp	C/T	0.477291	0.104109	intron-variant	Hdac4	Mm_Celera	1:92035888	TGGAGGGGCTGAAAA[C/T]TCCTCCATAGGCTGT	208727
rs30463752	snp	A/G	0.492188	0.0620098	intron-variant	Hdac4	GRCm38.p3	1:92060967	TCCTGAGTTAAGGAT[A/G]TATGTGTTGTATGTG	208727
rs30468291	snp	C/T	0.5	0	utr-variant-3-prime	Hdac4	GRCm38.p3	1:91933054	CCACAAGCTTCTTCC[C/T]TCGAGGCTTCCCAGG	208727
rs30472740	snp	C/G	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:92023377	CCTCAGGTCACAGTA[C/G]TGAGTAAAGTAACTA	208727
rs30494535	snp	C/T	0.432133	0.171253	intron-variant	Hdac4	GRCm38.p3	1:92033184	ACGACAGGCCAATCA[C/T]CCCTGCCAGTGAACC	208727
rs30496007	snp	A/G	0.487535	0.077957	intron-variant	Hdac4	GRCm38.p3	1:91933830	ACTCAGTGACTCCCC[A/G]CTTCTGCAGGTTAAT	208727
rs30498501	snp	A/G	0.375	0.216506	intron-variant	Hdac4	Mm_Celera	1:91988011	TTGTTTTTTTTTTTA[A/G]CTTCGAAAGGTCAAA	208727
rs30505246	snp	A/T	0.391111	0.206368	intron-variant	Hdac4	GRCm38.p3	1:92011423	GCTAGAGAGATCCCC[A/T]TCCACTACAGAGCTG	208727
rs30512724	snp	C/T	0.5	0	intron-variant	Hdac4	GRCm38.p3	1:91984839	CCAATACAAGCAGCA[C/T]ACCCAGGGCTGCAAG	208727
rs30524049	snp	A/T	0.444444	0.157135	intron-variant	Hdac4	Mm_Celera	1:92101211	TTGTTTGTTTGTTTT[A/T]AAAAAAAAAAAAAAA	208727
rs30528203	snp	A/G	0.444444	0.157135	intron-variant	Hdac4	Mm_Celera	1:91936329	AGAGCAAGGGCCCCC[A/G]TGAAGCACTGGTGAC	208727
rs30550725	snp	C/T	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:91939333	AATGGTTTCCCTTCC[C/T]CTGTTACATCCTGCT	208727
rs30558969	snp	C/T	0.5	0	intron-variant	Hdac4	GRCm38.p3	1:91984879	AGCATGAGGTGCTGA[C/T]GTGTGGTTGCCTGGT	208727
rs30565856	snp	A/G	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:92019338	GCAAGCCAGTAAGCA[A/G]CACCCTTCCATGGCG	208727
rs30565861	snp	A/G	0.444444	0.157135	utr-variant-3-prime	Hdac4	Mm_Celera	1:91932721	CAGGCTCACATTTCT[A/G]TTCTGTCCAGTTTTT	208727
rs30566253	snp	C/T	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:91956546	GCAACCCCTTTGGGG[C/T]TGCATATCAGAGTTC	208727
rs30572404	snp	C/T	0.456747	0.140554	intron-variant	Hdac4	GRCm38.p3	1:91977984	ATGTGAACAGCTGAG[C/T]CTCATGATGCTCACA	208727
rs30593351	snp	C/T	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:92019582	CTCAGATTACTTTCT[C/T]TTTTTCATTCAGTCC	208727
rs30611750	snp	C/T	0.495	0.0497494	intron-variant	Hdac4	GRCm38.p3	1:92001065	TTCCATGTAAATAAA[C/T]GGGCCACTTTAGTGG	208727
rs30618645	snp	C/G	0.49827	0.0293608	intron-variant	Hdac4	GRCm38.p3	1:91990570	AGAGTAAGCAGGAGA[C/G]AACTGCATGAAAAGG	208727
rs30659397	snp	C/T	0.5	0	intron-variant	Hdac4	GRCm38.p3	1:92072780	ACAGACAATAGAGTG[C/T]CTCATAGAAATGTTG	208727
rs30660551	snp	A/G	0.465374	0.126941	intron-variant	Hdac4	Mm_Celera	1:92027309	ATCTAGAAATATGGA[A/G]TAGTGGGGCGTGCTG	208727
rs30660786	snp	C/T	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:91993963	GGCAGCTGCGCTCTG[C/T]GCATGAGAAAGGTCA	208727
rs30660946	snp	G/T	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:92149893	TATGTCAACTGATCT[G/T]CACTCAATAACACCA	208727
rs30702728	snp	C/T	0.432133	0.171253	intron-variant	Hdac4	GRCm38.p3	1:92027261	AGGCCAGCCCTGAAG[C/T]TAGATTTCTGGGCCT	208727
rs30704064	snp	A/G	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:92032427	AAATGAAACAAGATG[A/G]AAAAGTTATCAGGCC	208727
rs30711918	snp	A/C	0.375	0.216506	missense	Hdac4	GRCm38.p3	1:91975501	CTGTCTCTCGAGTGG[A/C]CTCCGCTTCTTCCTC	208727
rs30714536	snp	A/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Hdac4, LOC105246664	GRCm38.p3	1:92181466	GAGTTAGAAAGCTTC[A/G]TTCACTGGGAGAAAT	208727
rs30752356	snp	C/T	0.49827	0.0293608	intron-variant	Hdac4	GRCm38.p3	1:92011560	CCAGCTTCCCTTTCA[C/T]TCTTTGTTGTCATAG	208727
rs30761657	snp	A/C	0.49827	0.0293608	intron-variant	Hdac4	Mm_Celera	1:92026797	CAATTCTGGCTAATG[A/C]CACAGCACCCCCTCT	208727
rs30766209	snp	C/G	0.432133	0.171253	intron-variant	Hdac4	GRCm38.p3	1:92005402	ATCTTTTGATAAACA[C/G]CCACTATTTCCCCTA	208727
rs30796840	snp	C/T	0.387812	0.208586	intron-variant	Hdac4	GRCm38.p3	1:91935750	TGGAACTGCTGATAA[C/T]TCCAGAGGGCAGAGC	208727
rs30811262	snp	A/G	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:91967043	GCAGGACAGTGGGCT[A/G]TAGAGGGCAAAACAA	208727
rs30821156	snp	A/C	0.498615	0.0262793	intron-variant	Hdac4	GRCm38.p3	1:92029160	AGGCCTCAGATGCGA[A/C]TAGCATGACCAACAT	208727
rs30836730	snp	G/T	0.456747	0.140554	intron-variant	Hdac4	GRCm38.p3	1:92026223	ACCTCCCTTCCAGCC[G/T]CTCAGGATGCATCTA	208727
rs30853111	snp	A/G	0.375	0.216506	utr-variant-3-prime	Hdac4	GRCm38.p3	1:91931490	TACTAGCGGTGTTGC[A/G]GGGCAGAAGCCCCTG	208727
rs30870176	snp	A/G	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:91958918	TGCGCGCGCGCACAC[A/G]CACACACACACACAC	208727
rs30884356	snp	C/T	0.495	0.0497494	intron-variant	Hdac4	GRCm38.p3	1:92011323	AGCACAGGCAAAGGC[C/T]TGACTGAACACTCTC	208727
rs30895093	snp	C/T	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:92005774	GCCAGATCGGCTGGC[C/T]GGAGAGTGATACATG	208727
rs30896987	snp	A/G	0.375	0.216506	intron-variant	Hdac4	Mm_Celera	1:92123799	AGGACACCCTGCTGA[A/G]GTTCTATCACCTAGA	208727
rs30944960	snp	C/T	0.475309	0.108333	intron-variant	Hdac4	Mm_Celera	1:92032628	TCCCCCTATTTTGAG[C/T]TCACATATACGATCC	208727
rs30955801	snp	C/G	0.375	0.216506	intron-variant	Hdac4	Mm_Celera	1:92023721	GATAACACAAGTAAC[C/G]ACCCCCCTCAAAAAT	208727
rs30957942	snp	A/G	0.432133	0.171253	intron-variant	Hdac4	Mm_Celera	1:91997159	AGAATGGACTGAAGG[A/G]ACTCTCAGACACATC	208727
rs31009217	snp	C/T	0.42	0.183303	intron-variant	Hdac4	GRCm38.p3	1:91999241	TGCCCTACCTGTCTG[C/T]GAAGGGAGAGCCCTG	208727
rs31033254	snp	A/G	0.455	0.143091	intron-variant	Hdac4	Mm_Celera	1:92001308	TCTACAGCACACCAC[A/G]AACAGCCCATGTTGG	208727
rs31045861	snp	C/G	0.42	0.183303	intron-variant	Hdac4	GRCm38.p3	1:91987704	CATTGGGTAGACTCA[C/G]AGAGCCCTACTGCCT	208727
rs31052514	snp	A/G	0.5	0	intron-variant	Hdac4	GRCm38.p3	1:92017306	TCAGGAGCATGGAGT[A/G]GGTCATTGATGAAGA	208727
rs31058838	snp	A/T	0.255	0.24995	intron-variant	Hdac4	GRCm38.p3	1:92129155	ACAGACCCAAGACTT[A/T]CCCAGGCTCAAGGAA	208727
rs31099961	snp	C/T	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:92002314	GAGGAGGAAGCAGTA[C/T]GGAGCAGGCAGTATG	208727
rs31137204	snp	C/T	0.493827	0.0552116	intron-variant	Hdac4	GRCm38.p3	1:92032205	ATGAGCTAATCTCTC[C/T]TACCACACATAGTAG	208727
rs31140504	snp	C/T	0.49827	0.0293608	intron-variant	Hdac4	GRCm38.p3	1:92015170	TTTATGGAAGACAAA[C/T]AGATGTACCCAGAGA	208727
rs31148914	snp	A/G	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:91958916	CATGCGCGCGCGCAC[A/G]CACACACACACACAC	208727
rs31153584	snp	G/T	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:92035849	CGTCAGAACAATAAT[G/T]CCTGTATGCTCAGGA	208727
rs31163257	snp	A/T	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:91984143	AGCTGTAGGGAAACC[A/T]ATCAGTGGGAGAGCA	208727
rs31185137	snp	A/G	0.487535	0.077957	intron-variant	Hdac4	Mm_Celera	1:92023654	GTTAAAAGAGCTGAG[A/G]AAATTTCAGTTAATT	208727
rs31188852	snp	A/T	0.387812	0.208586	intron-variant	Hdac4	GRCm38.p3	1:91956491	GGGTTGGCTACTTAC[A/T]GGCACGTCACAAAGG	208727
rs31218975	snp	C/T	0.42	0.183303	intron-variant	Hdac4	GRCm38.p3	1:91987508	TACAAGGCAGGTATG[C/T]GGGGTGCTTGGCCTA	208727
rs31247451	snp	A/G	0.498615	0.0262793	intron-variant	Hdac4	GRCm38.p3	1:91944297	AGCAGGGTTTCTCTT[A/G]TAATAGTGTCCACAG	208727
rs31261304	snp	C/T	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:92027551	ACAACGTTGACTATT[C/T]ACTATACCTGCTAGA	208727
rs31265040	snp	G/T	0.387812	0.208586	intron-variant	Hdac4	GRCm38.p3	1:92048699	TTTAAAAATAGATGC[G/T]TATTGCATGGGGTGG	208727
rs31284498	snp	A/G	0.42	0.183303	intron-variant	Hdac4	GRCm38.p3	1:91983604	CTGAGTGTAGGGAGC[A/G]GTCCATGGTCACTGA	208727
rs31286515	snp	C/T	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:92023362	CCTAAACTTGCTGTT[C/T]CTCAGGTCACAGTAC	208727
rs31318047	snp	A/T	0.48	0.0979796	intron-variant	Hdac4	Mm_Celera	1:92020171	AGCCATTTTTTTCAA[A/T]GAAAGCTGGTTCCTG	208727
rs31327036	snp	G/T	0.375	0.216506	intron-variant	Hdac4	Mm_Celera	1:92035103	TGTGTGGACTACAGC[G/T]CTCCAGAGGGTACCT	208727
rs31356893	snp	A/G	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:92092299	GGAGTGTATGGTTTA[A/G]AGTAAACCCACTGAG	208727
rs31372649	snp	A/G	0.498615	0.0262793	intron-variant	Hdac4	GRCm38.p3	1:91950825	CAGTGGCTTCTCTGC[A/G]GGTGAGCACAGCATA	208727
rs31374183	snp	C/T	0.375	0.216506	utr-variant-3-prime	Hdac4	GRCm38.p3	1:91931475	CTGCCCGCCCTGTAA[C/T]ACTAGCGGTGTTGCA	208727
rs31374412	snp	A/C	0.444444	0.157135	intron-variant	Hdac4	Mm_Celera	1:91964604	AAAAACCAAAAAAAA[A/C]CAAAAACGCTCTCAG	208727
rs31374952	snp	C/T	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:92032400	GCCTTGCCTTTTTAA[C/T]CTCTTATTACAAAAT	208727
rs31380367	snp	C/T	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:91989735	CAGCATGAACTTCAT[C/T]CCAGCTGGGAAGAGT	208727
rs31380476	snp	C/T	0.444444	0.157135	intron-variant	Hdac4	GRCm38.p3	1:91972236	AAACTAAAGTGGCAC[C/T]GAGACACTACTTCCA	208727
rs31403786	snp	C/T	0.5	0	intron-variant	Hdac4	GRCm38.p3	1:91970426	GGAGAAGAGGCTAGA[C/T]ACCCAATATGGTAGT	208727
rs31421674	snp	G/T	0.375	0.216506	intron-variant	Hdac4	GRCm38.p3	1:91995778	TAGAACTAACCTACT[G/T]CTCTGGACTGTAGAG	208727
rs31424621	snp	C/G	0.387812	0.208586	intron-variant	Hdac4	GRCm38.p3	1:92011431	GATCCCCTTCCACTA[C/G]AGAGCTGGGACTGAG	208727

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