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
rs3683	snp	A/C	0.0391999	0.1344	utr-variant-3-prime	HDAC4	GRCh38.p7	2:239048749	GGCCGAGCTAAGAAC[A/C]CGCTCAGCTTCGTTA	9759
rs169731	snp	C/T	0.454061	0.144427	intron-variant, utr-variant-5-prime	HDAC4	GRCh38.p7	2:239230401	aaaaaGCAAAGCAGG[C/T]GACATGTTCCGTGGC	9759
rs172365	snp	C/T	0.476833	0.105105	intron-variant, utr-variant-5-prime	HDAC4	GRCh38.p7	2:239230446	TGGCCAATCCTTGCC[C/T]GTGGCTGGCAAGCTG	9759
rs291329	snp	C/T	0.499759	0.0109798	intron-variant	HDAC4	GRCh38.p7	2:239222726	CAATGCAAAAGCAAT[C/T]GAATAGAAACAATAA	9759
rs291330	snp	A/G	0.49998	0.00319482	intron-variant	HDAC4	GRCh38.p7	2:239223207	CCTAACAGCTGGGCC[A/G]AAGTAGGAACCACTA	9759
rs291331	snp	A/C	0.163892	0.234703	intron-variant	HDAC4	GRCh38.p7	2:239223262	ATTTAAAAATAGAAA[A/C]CATTGGAGAAGAAGA	9759
rs291332	snp	C/T	0.130694	0.219696	intron-variant	HDAC4	GRCh38.p7	2:239223609	TGAACACACGGTACG[C/T]AGCTGAGTGACAGAT	9759
rs291333	snp	G/T	0.323197	0.239044	intron-variant	HDAC4	GRCh38.p7	2:239223680	CATCATTGCTGTAAT[G/T]AGGAGCAACCACGAG	9759
rs291334	snp	A/G	0.36955	0.219562	intron-variant	HDAC4	GRCh38.p7	2:239224582	CCCCTCCACTCCCGA[A/G]CCCTGCTCTGCCTTC	9759
rs291335	snp	A/G	0.499961	0.0043928	intron-variant, utr-variant-5-prime	HDAC4	GRCh38.p7	2:239226151	AGCCTTAAAGCACAC[A/G]AAGCTGGTAATAAAA	9759
rs291336	snp	A/G	0.0614824	0.164198	intron-variant, utr-variant-5-prime	HDAC4	GRCh38.p7	2:239226343	CACTGAGTATCTCTC[A/G]GGGAGGATTCCACAG	9759
rs291337	snp	A/G	0.499968	0.00399348	intron-variant, utr-variant-5-prime	HDAC4	GRCh38.p7	2:239227891	GCAGCTGGGAGACCT[A/G]GCAGAGGGCCCGGGC	9759
rs291338	snp	A/G	0.131723	0.220251	intron-variant, utr-variant-5-prime	HDAC4	GRCh38.p7	2:239228266	GGAGGCCATGTGGCC[A/G]AAGGGAGACAGGAAG	9759
rs291339	snp	C/T	0.4776	0.103433	intron-variant, utr-variant-5-prime	HDAC4	GRCh38.p7	2:239230476	GCCGAGTCCGTGGGC[C/T]GGAGGGCATTGATTC	9759
rs484661	snp	C/T	0.168135	0.236216	intron-variant	HDAC4	GRCh38.p7	2:239201514	CCTGTAATTACTATT[C/T]GCTGAGAGCCTACAG	9759
rs486396	snp	C/T	0.233527	0.249457	intron-variant	HDAC4	GRCh38.p7	2:239201668	GCCCCACCTCCCTTC[C/T]CAACAGCACCAGAAA	9759
rs489806	snp	A/C	0.499879	0.0077866	intron-variant	HDAC4	GRCh38.p7	2:239177760	TGAGAACATGACAGG[A/C]AGCCCACTAAAACGT	9759
rs496316	snp	A/G	0.142272	0.225598	intron-variant	HDAC4	GRCh38.p7	2:239233535	GCTTTGGGAAAGTCT[A/G]TACAGGTTGAGTATC	9759
rs506324	snp	C/T	0.379746	0.213696	intron-variant	HDAC4	GRCh38.p7	2:239182650	ATTTATAACAGATTA[C/T]CTGTAGAGCAAAGCC	9759
rs507159	snp	C/G	0.499722	0.0117779	intron-variant	HDAC4	GRCh38.p7	2:239198786	AATATATATTTTTAT[C/G]TTTCATGAGAAATTC	9759
rs518274	snp	A/G	0.499977	0.00339449	intron-variant	HDAC4	GRCh38.p7	2:239209462	acaaacacttatcct[A/G]ctattctacggggaa	9759
rs519165	snp	A/G	0.366473	0.221211	intron-variant	HDAC4	GRCh38.p7	2:239219687	AGGCTCAGATTAGAC[A/G]GGTAAAAAGCCCCAA	9759
rs522916	snp	C/G	0.49998	0.00319482	intron-variant	HDAC4	GRCh38.p7	2:239209980	GGGTGGAGAGGCAGG[C/G]AGCGGGGGCGTGGGA	9759
rs528213	snp	G/T	0.499853	0.008585	intron-variant	HDAC4	GRCh38.p7	2:239205380	ACGTTATCCAACAAA[G/T]GAAATGCAGTCACAG	9759
rs530689	snp	A/G	0.499987	0.00259581	intron-variant	HDAC4	GRCh38.p7	2:239216970	GGCGTGAATGCAGTC[A/G]CCTGTCTTTTGCTAC	9759
rs531993	snp	A/T	0.492435	0.0610346	intron-variant	HDAC4	GRCh38.p7	2:239189781	GCTGGAGTCACCGGG[A/T]GTTGAGGGTGCCGGA	9759
rs541417	snp	C/T	0.492435	0.0610346	intron-variant	HDAC4	GRCh38.p7	2:239203043	GCTGGCAGCGCTGAG[C/T]GGAGCCTCAGCCCTA	9759
rs548717	snp	G/T	0.167158	0.235875	intron-variant	HDAC4	GRCh38.p7	2:239203849	AATTATCAGCTTCAA[G/T]GGATTCGAGTAGGAC	9759
rs549639	snp	C/G	0.499995	0.00159744	intron-variant	HDAC4	GRCh38.p7	2:239212043	GAGCAAAGTCTTCAA[C/G]AGCATTTTTCACTTA	9759
rs551326	snp	C/T	0.267091	0.249415	intron-variant	HDAC4	GRCh38.p7	2:239179915	ACATCAACGTGCTTG[C/T]GCACCCAAGTGTGCG	9759
rs552298	snp	C/G	0.375	0.216506	intron-variant, upstream-variant-2KB	HDAC4	GRCh38.p7	2:239232003	AGCCTCGATTGAGGA[C/G]AGGGGCGCTTCGGGG	9759
rs552356	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	HDAC4	GRCh38.p7	2:239231982	CGCTTCGGGGAGGAC[A/G]CCTACCTCAGGCATC	9759
rs552954	snp	A/G	0.498611	0.0263212	intron-variant	HDAC4	GRCh38.p7	2:239173484	accccgagcaaacaa[A/G]gaatggaagggaaac	9759
rs554946	snp	A/C	0.499992	0.00199679	intron-variant	HDAC4	GRCh38.p7	2:239218088	tttttgttttttgag[A/C]tggggcctcactctg	9759
rs555834	snp	C/T	0.463559	0.129972	intron-variant, upstream-variant-2KB	HDAC4	GRCh38.p7	2:239231427	CTGGGACAGCGGCCA[C/T]GGGATCTGAGGCTCT	9759
rs563856	snp	C/T	0.236144	0.249616	intron-variant	HDAC4	GRCh38.p7	2:239200386	GGGGAGGGGCACGCA[C/T]GCAAAGTAGAGACGA	9759
rs566435	snp	G/T	0.499918	0.00638925	intron-variant	HDAC4	GRCh38.p7	2:239200648	AAGAAGAAGGTGCTT[G/T]GTATTGCTTTCCATT	9759
rs574636	snp	C/T	0.176219	0.238865	intron-variant	HDAC4	GRCh38.p7	2:239221070	GTGAGGCCTCTGTGC[C/T]TCACTCAGCGGGTCA	9759
rs577090	snp	A/G	0.495252	0.0484902	intron-variant	HDAC4	GRCh38.p7	2:239187239	CAATGGCCGACGGGG[A/G]CTTCTGAGAGGCACA	9759
rs581362	snp	A/G	0.499977	0.00339449	intron-variant	HDAC4	GRCh38.p7	2:239210389	TGGATTTGCTTTTCC[A/G]AGCTTTTAATAATCG	9759
rs583445	snp	C/G	0.49925	0.0193545	intron-variant	HDAC4	GRCh38.p7	2:239199266	AGGCAGCTTAGACTT[C/G]CCAGCAAGGCCTAAG	9759
rs584293	snp	A/C	0.493703	0.0557558	intron-variant	HDAC4	GRCh38.p7	2:239199421	agcaggaccatttct[A/C]taacgggaaggaatc	9759
rs589712	snp	A/G	0.235564	0.249583	intron-variant	HDAC4	GRCh38.p7	2:239200756	TGTGTGGGGCTGGGC[A/G]GGAGAGAGACGCGTC	9759
rs592695	snp	A/C	0.265727	0.249505	intron-variant	HDAC4	GRCh38.p7	2:239180244	GCACACACACCTTTC[A/C]AACCCCTAGGCTTCT	9759
rs593337	snp	A/G	0.499996	0.00139776	intron-variant	HDAC4	GRCh38.p7	2:239205720	GGGAGGACGAGGAGG[A/G]AGGGAGAAGAACAAA	9759
rs598377	snp	C/G	0.159622	0.233092	intron-variant	HDAC4	GRCh38.p7	2:239200265	AAGCTGACATTCAAA[C/G]GCCTGAACGGTCATA	9759
rs604067	snp	A/G	0.447291	0.153545	intron-variant	HDAC4	GRCh38.p7	2:239201630	GCTCAAGGCCGAGAC[A/G]ACAGCCCCAGAGGCA	9759
rs604433	snp	A/G	0.168785	0.236441	intron-variant	HDAC4	GRCh38.p7	2:239220468	GATCCGCAATCTGTC[A/G]GATTTCTTTCATCTT	9759
rs604827	snp	C/G	0.165527	0.235296	intron-variant	HDAC4	GRCh38.p7	2:239220527	ACTGTCTTCCCCTAC[C/G]AAGCACAAACTGTCC	9759
rs605614	snp	C/T	0.499984	0.00279548	intron-variant	HDAC4	GRCh38.p7	2:239212747	CCAGAGAGGACCCTC[C/T]CAGCTCCTCCCTGGA	9759
rs606531	snp	A/G	0.166832	0.235761	intron-variant	HDAC4	GRCh38.p7	2:239220422	CTTTTTCAGTGCACA[A/G]TGTATGCTTTAATTT	9759
rs607835	snp	C/T	0.499998	0.000998401	intron-variant	HDAC4	GRCh38.p7	2:239213222	GCCCCTCCCTGGCCC[C/T]TACTTTGCTGTTATG	9759
rs608911	snp	A/G	0.267908	0.249358	intron-variant	HDAC4	GRCh38.p7	2:239181595	AAGCAAGCTCTTGCC[A/G]TGTCCTTCATCAGGG	9759
rs614200	snp	C/T	0.375	0.216506	intron-variant	HDAC4	GRCh38.p7	2:239184817	GTCCCTCAGTGTCTG[C/T]CCTGGAGACTGTGTC	9759
rs614588	snp	C/T			intron-variant	HDAC4	GRCh38.p7	2:239184860	GTCCCTCAGTGTCTG[C/T]CCTGGAGGATGTATC	9759
rs615994	snp	A/G	0.0387552	0.1337	intron-variant	HDAC4	GRCh38.p7	2:239213956	atgtgacctaggcag[A/G]tttctctacctccct	9759
rs617829	snp	A/G	0.491783	0.0635686	intron-variant	HDAC4	GRCh38.p7	2:239221168	ATTCGCAAGAACACT[A/G]ATACCATCTGACAGG	9759
rs618655	snp	A/G	0.273318	0.24891	intron-variant	HDAC4	GRCh38.p7	2:239179190	TGTGCTCCATGAGTG[A/G]CTGCGCTGGCACAGC	9759
rs621578	snp	C/T	0.171704	0.237423	intron-variant	HDAC4	GRCh38.p7	2:239182089	TCTGCCCTGGGGACC[C/T]GGAGCTGTGTACACA	9759
rs625839	snp	A/G	0.444133	0.157519	intron-variant, nc-transcript-variant	HDAC4, MGC16025	GRCh38.p7	2:239194472	GTGTGCCTGTGAGGC[A/G]GGCAGGAGCGTCACC	9759
rs631292	snp	C/T	0.197703	0.244469	intron-variant, nc-transcript-variant	HDAC4, MGC16025	GRCh38.p7	2:239195145	CAGGAGGTGCCGTAG[C/T]GAGAACAGCGACAGC	9759
rs637265	snp	C/T	0.499995	0.00159744	intron-variant	HDAC4	GRCh38.p7	2:239218124	AAACAGAATATAAAA[C/T]TGGATGAAAATTTTA	9759
rs640780	snp	G/T			intron-variant	HDAC4	GRCh38.p7	2:239172425	catttacatttaatg[G/T]aattattgatatatt	9759
rs645357	snp	C/G	0.245346	0.249957	intron-variant	HDAC4	GRCh38.p7	2:239187170	GTTGGCCTGCAGGAA[C/G]GCAGGGAAGCCGGAG	9759
rs646326	snp	C/T	0.490007	0.0699769	intron-variant	HDAC4	GRCh38.p7	2:239187391	AATGTGAGCCTATGG[C/T]GCAAAAACTAAATAA	9759
rs653976	snp	A/G	0.444666	0.15686	intron-variant	HDAC4	GRCh38.p7	2:239192777	TGTGTTTATCCCTGG[A/G]AAGCACGGGCCCGCT	9759
rs669106	snp	A/G	0.48955	0.071525	intron-variant	HDAC4	GRCh38.p7	2:239184460	GCTGTGCCCTATGAG[A/G]GGGGGTCCCTCAGTG	9759
rs672183	snp	C/T	0.197082	0.244335	intron-variant	HDAC4	GRCh38.p7	2:239178567	TTTCTTCTTTTTTGA[C/T]GAAACAAGATCTTGC	9759
rs673912	snp	A/G	0.356169	0.226336	intron-variant	HDAC4	GRCh38.p7	2:239172340	AAAACATACACTAAA[A/G]GCAAGACAAGTGCAT	9759
rs674540	snp	A/G	0.197393	0.244402	intron-variant	HDAC4	GRCh38.p7	2:239189081	GATATAGATAACTTA[A/G]TCTGGTTTTGTGGGA	9759
rs675093	snp	A/C	0.499977	0.00339449	intron-variant	HDAC4	GRCh38.p7	2:239209937	CAGACCCCTGGAGAC[A/C]CCACTTTACGCCCAC	9759
rs675525	snp	C/T	0.198324	0.244601	intron-variant	HDAC4	GRCh38.p7	2:239198031	ctaatttctctccct[C/T]cctcccttccttcca	9759
rs678228	snp	A/G	0.499859	0.0083854	intron-variant	HDAC4	GRCh38.p7	2:239205328	GCGAAACAGCAGACC[A/G]CTGAGACAGAGTTCA	9759
rs680392	snp	C/T	0.0501905	0.150254	intron-variant	HDAC4	GRCh38.p7	2:239217984	gtggttccagctact[C/T]ggaaggctgaggcag	9759
rs680564	snp	A/G	0.432944	0.170387	intron-variant	HDAC4	GRCh38.p7	2:239192672	GCGGAAGAGGGAACC[A/G]CAACCTGACAGTCAT	9759
rs681715	snp	A/T	0.388021	0.208447	intron-variant	HDAC4	GRCh38.p7	2:239182693	GCCATCAGGACAAAC[A/T]GGATTTCAACACTCC	9759
rs686606	snp	C/T	0.0486741	0.148216	intron-variant	HDAC4	GRCh38.p7	2:239179399	AGCTCAAGCTCCTGC[C/T]GGATCAGTGGTGGCA	9759
rs687778	snp	C/T	0.418491	0.184691	intron-variant	HDAC4	GRCh38.p7	2:239205021	ACCTTCCCCCGTCCC[C/T]GAGCCGCCTCTGTCC	9759
rs688680	snp	A/G	0.141258	0.225111	intron-variant, upstream-variant-2KB	HDAC4	GRCh38.p7	2:239232067	CGTCCTCCCCGAAGC[A/G]CCCCTCTCCTCAATC	9759
rs709271	snp	C/T	0.499866	0.0081858	intron-variant	HDAC4	GRCh38.p7	2:239219062	agatccctgaggaat[C/T]gccacactgatttcc	9759
rs709272	snp	A/G	0.499977	0.00339449	intron-variant	HDAC4	GRCh38.p7	2:239219169	ccgcaataaacatac[A/G]tgtgcatgtgtcttt	9759
rs747787	snp	A/G	0.498982	0.0225409	intron-variant	HDAC4	GRCh38.p7	2:239110623	GAGAGTGAGAACCTC[A/G]CAGACTGCAGAACAC	9759
rs753302	snp	C/T	0.310632	0.242536	intron-variant	HDAC4	GRCh38.p7	2:239192441	AAAGTCTGAAGCAAA[C/T]GTAGGTGAACGCTGA	9759
rs843461	snp	A/G	0.362941	0.223034	intron-variant	HDAC4	GRCh38.p7	2:239397395	ACGAGCAGCTGTCAC[A/G]TGCTCCCGTAGCTGA	9759
rs843462	snp	A/G	0.148326	0.228391	intron-variant	HDAC4	GRCh38.p7	2:239397060	TGTTGACTGTTCTTG[A/G]CGCTGTTACAGGCGC	9759
rs843463	snp	C/T	0.0107246	0.0724382	intron-variant	HDAC4	GRCh38.p7	2:239396636	CCTGTGTAAGCTTAA[C/T]AGTCAATATATAAAG	9759
rs843469	snp	A/G	0.247905	0.249991	intron-variant	HDAC4	GRCh38.p7	2:239183921	ACTAGGTTCCTTTCC[A/G]TGTTAGTTCCTCCCT	9759
rs843470	snp	C/T	0.170084	0.236883	intron-variant	HDAC4	GRCh38.p7	2:239208060	gggcgcggtggctca[C/T]gcctgtaatcccagc	9759
rs860022	snp	C/T	0	0	intron-variant	HDAC4	GRCh38.p7	2:239218456	tccttacatcttata[C/T]aaaaattaattcaag	9759
rs860023	snp	C/G	0	0	intron-variant	HDAC4	GRCh38.p7	2:239219018	acttttacactgttg[C/G]tgggactgtaaacta	9759
rs860936	snp	A/G	0.472147	0.114677	intron-variant	HDAC4	GRCh38.p7	2:239396183	TTCAAGACCAGCCTG[A/G]GCAACATAGTGAGAC	9759
rs863617	snp	C/T	0.4444	0.15719	intron-variant	HDAC4	GRCh38.p7	2:239208283	agtgagccgagatcg[C/T]gccactgcactccag	9759
rs864012	snp	A/G	0	0	intron-variant	HDAC4	GRCh38.p7	2:239218946	cccagttagaatggc[A/G]atcattaaaaagtca	9759
rs870790	snp	A/G	0.417034	0.18601	intron-variant	HDAC4	GRCh38.p7	2:239394311	AATATGTTTGTGTAC[A/G]TAAACATTTTGGAGT	9759
rs895802	snp	A/T	0.49928	0.018956	intron-variant	HDAC4	GRCh38.p7	2:239169095	GTCTGGTAAACTCTG[A/T]GGAAGTAATTTAGAC	9759
rs895803	snp	C/T	0.494358	0.0528145	intron-variant	HDAC4	GRCh38.p7	2:239191350	CGTCTCTGGACTGGC[C/T]TAAGACCAGGCCTTG	9759
rs895804	snp	C/T	0.310386	0.242597	intron-variant	HDAC4	GRCh38.p7	2:239191506	CAGGTCCCACACTGG[C/T]TTTGTCTCCAAACCA	9759
rs895805	snp	C/T	0.494315	0.0530107	intron-variant	HDAC4	GRCh38.p7	2:239191669	CACCTGAGCTCCTGG[C/T]GCCCAGGGTGAGGGG	9759
rs895806	snp	C/T	0.489665	0.0711382	intron-variant	HDAC4	GRCh38.p7	2:239191678	TCCTGGTGCCCAGGG[C/T]GAGGGGTGCTCTCAG	9759
rs895807	snp	C/T	0.48955	0.071525	intron-variant	HDAC4	GRCh38.p7	2:239191698	GGTGCTCTCAGCTTC[C/T]CTGGCTGACTTCACT	9759

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