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
rs1467379	snp	C/T	0	0				:	GCACAGGCTTCACCG[C/T]CAACGTGGCATGGAA	10013
rs4411026	snp	A/C	0	0				:	TCCCTTACTCCCTTT[A/C]TGGCTCCCCACTGTC	10013
rs34826345	snp	A/C	0.375	0.216506				:	TGGTACATTTGTATC[A/C]CCAACTCTTGGCACA	10013
rs35189789	snp	A/G	0	0				:	ATCTTAGGCTTTGCA[A/G]GCCACATACGGTCTC	10013
rs1127346	snp	C/T	0	0	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823380	CACTGGCCCAGACCA[C/T]CTCGGAGGCAGCCAT	10013
rs1985411	snp	A/C	0.447863	0.152807	intron-variant	HDAC6	GRCh38.p7	X:48819689	agacgtggtggcggg[A/C]gcctgtagtcccagc	10013
rs2008290	snp	C/G	0.119068	0.212972	intron-variant	HDAC6	GRCh38.p7	X:48810110	agacagggtatcact[C/G]tgtcacccaggctgg	10013
rs2075837	snp	A/G	0.35347	0.227583	intron-variant	HDAC6	GRCh38.p7	X:48818432	AGCTCAGGATAGATC[A/G]CAGGACGTATGTGAC	10013
rs2075840	snp	A/G	0.369713	0.219474	intron-variant	HDAC6	GRCh38.p7	X:48814381	GCAACTGTTGGGTTG[A/G]GGGTGTCTATGGGGA	10013
rs5905711	snp	A/C/G	0.001583	0.0280909	intron-variant	HDAC6	GRCh38.p7	X:48816100	TGGGGGTCCCTCCCC[A/C/G]TCAGGCACTAAGCCT	10013
rs5906711	snp	C/T	0.446659	0.154354	intron-variant	HDAC6	GRCh38.p7	X:48809768	GATCGCACCACTGCA[C/T]TCCAGCCTGGGTGAT	10013
rs5906712	snp	C/G	0.420951	0.182417	intron-variant	HDAC6	GRCh38.p7	X:48817519	ACCTGGATGCTCCCC[C/G]CAGCCCATTGTTTAC	10013
rs5906713	snp	C/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48817852	GAAGAGCCCAGGGCC[C/T]AGCCCCGAGCACTTG	10013
rs6609797	snp	C/T	0.00211696	0.0324653	intron-variant	HDAC6	GRCh38.p7	X:48821498	acctgCCTCtttttt[C/T]ttttttttttttttt	10013
rs12397055	snp	G/T			intron-variant	HDAC6	GRCh38.p7	X:48810727	aatcctcatgcctca[G/T]cctcctgagtagctg	10013
rs12557774	snp	C/G			intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806867	TTGTCACCCAGACAC[C/G]TGCCTCCTCTCATGG	10013
rs12847613	snp	G/T	0	0	intron-variant	HDAC6	GRCh38.p7	X:48813237	TTTTATGTCCTACTG[G/T]GTTTCTCTTCCTCTA	10013
rs17281209	snp	A/G	0.0389457	0.134	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800821	AGCTGACATTTAGAC[A/G]TGGAGTGGGAGTTGC	10013
rs17281216	snp	C/T	0.0256233	0.11025	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802028	GCTGAAGAGGGTTAG[C/T]GAAACGTTAGCGGTC	10013
rs28711341	snp	G/T	0	0	intron-variant	HDAC6	GRCh38.p7	X:48808193	TGGGGTGTCCTGGTC[G/T]GGGCTCTTCCCCCAG	10013
rs34423449	in-del	-/A			intron-variant	HDAC6	GRCh38.p7	X:48810666	AGTCGTATTTGTGCC[-/A]CTGTACTCCAGTCTG	10013
rs34717743	in-del	-/T			intron-variant	HDAC6	GRCh38.p7	X:48810227	TTAGCTGGGTGTGGT[-/T]GGCACATGCCTGCAG	10013
rs34955786	snp	A/G	0	0	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800180	TGGTATTCTTTTGCA[A/G]GATTGAGGGTAGGGG	10013
rs34985248	in-del	-/C			frameshift-variant, nc-transcript-variant, intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48820248	AAAGTTACCTCTAGG[-/C]ATAAGGATAATGCGG	10013
rs34988126	in-del	-/C			intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801497	CCAGTCACTTAGGAG[-/C]CCTTCGGGTCGGCGG	10013
rs35112134	in-del	-/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800243	TTGGCTTGAATGCCA[-/T]TAGTTTGCCGATCTG	10013
rs35306795	snp	A/T			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800328	CACATACGGTCTCAG[A/T]GGCATTTTTCTTTTT	10013
rs35738141	in-del	-/A			upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801029	AGTTGCTGAACAGTT[-/A]CTGTGCTCCGTTTCC	10013
rs41298472	snp	A/T			intron-variant	HDAC6	GRCh38.p7	X:48817682	GGGCACTTACAAAAC[A/T]GGATCCAGGGTCCCA	10013
rs41310599	snp	A/C	0.0214859	0.101397	downstream-variant-500B, upstream-variant-2KB	HDAC6, ERAS	GRCh38.p7	X:48825106	CCATCCATTGCCCCC[A/C]AAAAACTAACTGAAA	10013
rs41312114	snp	A/G	0.00427135	0.0460155	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823730	GAGAGGCAGCTGGAG[A/G]TCAGGACATGGCTGA	10013
rs45441102	snp	C/T	0.0147244	0.0845304	intron-variant	HDAC6	GRCh38.p7	X:48803061	CCAAAGGTTCCCCAC[C/T]CTGGACAGTTCCCTC	10013
rs55842933	snp	A/G	0.0173306	0.0914601	intron-variant	HDAC6	GRCh38.p7	X:48805336	GACACCACAGTTTTG[A/G]GGTAAGCAGCTGTGG	10013
rs56747159	snp	A/G	0.0110639	0.0735497	intron-variant	HDAC6	GRCh38.p7	X:48817613	ACCCAGAGAAGGACC[A/G]AGGATGGAGCCTCTC	10013
rs57333741	snp	A/C/G	3.86294e-05	0.00439468	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815428	AGGCGTCAGTGCTTC[A/C/G]CTCCACACCCTTCTG	10013
rs57466824	in-del	-/C			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815333	ATTATTATTATTCCC[-/C]TGGTCATGTCTGGTC	10013
rs57913011	snp	C/T			synonymous-codon, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48817403	CGGTTTTTGCTTTTT[C/T]AACTCTGTGGCTGTG	10013
rs61735967	snp	A/G/T	0.0499518	0.149936	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822777	ATCGCAGATACTGGC[A/G/T]CAGCTTACGGGTCAT	10013
rs61737931	snp	C/T	0.0363512	0.129824	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814457	TCCTCTATTTCTCCA[C/T]CCACCGCTACGAGCA	10013
rs73209760	snp	C/T	0.00357207	0.0421103	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806443	CCTAGCAGACACCTA[C/T]GACTCAGTTTATCTG	10013
rs77316228	snp	C/T	0.5	0	intron-variant	HDAC6	GRCh38.p7	X:48810070	GGTTATCTTGGTGTT[C/T]TTTTTTTTTTTTTTT	10013
rs77409607	snp	G/T	0.5	0	intron-variant	HDAC6	GRCh38.p7	X:48810626	TTTATTTATTTTTTT[G/T]GAGACAAGGTCTTGC	10013
rs111255849	snp	A/G/T	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48819995	ATCTCTCTGACTTGC[A/G/T]TCTCCATGTCTTCAT	10013
rs111860068	snp	A/T			synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823156	CACAGGGGGAGCCAC[A/T]CTGGCCCAGACCATT	10013
rs112140048	snp	A/T			intron-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48807386	TTATAAAAATAAAAT[A/T]TTATTTTACACTAAC	10013
rs112427413	snp	C/T	0.5	0	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48808114	GGCAGCCCGCTATGC[C/T]CAACAGAAACACCGC	10013
rs113247595	snp	A/G	0.017851	0.0927731	intron-variant, utr-variant-3-prime, downstream-variant-500B	HDAC6	GRCh38.p7	X:48806108	GAAGAGGGTGACTGA[A/G]GGAAGGGAAGAACAG	10013
rs113573430	snp	A/C			intron-variant, upstream-variant-2KB	HDAC6	GRCh38.p7	X:48801698	GCGGTGTGGCTCAGC[A/C]CAGCTGGCGTAGCAC	10013
rs113585645	snp	A/G			intron-variant	HDAC6	GRCh38.p7	X:48816981	AGGTCCGGGCGTGAT[A/G]GCTCACACCTGTAAT	10013
rs113753590	snp	A/G	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48812203	CACACACAGATGTGA[A/G]ACACTGTGAATATAT	10013
rs116427806	snp	A/G	0.00896606	0.0663524	intron-variant	HDAC6	GRCh38.p7	X:48811516	AGTGTTTGTAGGTCT[A/G]TTTTCCTGAAAGGCA	10013
rs137925626	snp	C/T	0.00422943	0.0457911	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800113	CCCTGCCCATGAATC[C/T]CTGTCCTCACACACC	10013
rs138084502	snp	C/T	0.00448983	0.0471673	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823473	AAACTCCTCTAGCCT[C/T]GAGCACAGACCACCA	10013
rs138154887	snp	C/G	0.00942664	0.0680034	intron-variant	HDAC6	GRCh38.p7	X:48819923	TATTTCTTTTCTTCC[C/G]TTCTTCATTTTCAGT	10013
rs138420803	snp	A/G	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48809576	TTGGGAGGCCGAGGC[A/G]GATCACCTGAGGTCA	10013
rs138466917	snp	C/T	4.95577e-05	0.00497759	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816239	TGACACCGCGCCCTG[C/T]CACAGAGGCTGAGCT	10013
rs139032847	snp	C/T	0.0168099	0.0901243	intron-variant	HDAC6	GRCh38.p7	X:48819025	AAAGGGTGTGAGCAC[C/T]GCTCTGTCACCCTGG	10013
rs139240691	snp	C/T			missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822942	AAGGACCCTCCAGTT[C/T]TAAGTTGGTCACCAA	10013
rs139330641	snp	C/T	4.84966e-05	0.00492402	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822776	CATCGCAGATACTGG[C/T]GCAGCTTACGGGTCA	10013
rs139655181	snp	C/T	0.00317376	0.039709	intron-variant	HDAC6	GRCh38.p7	X:48821957	GACTCCATCAGAGAG[C/T]CCAAGTTCAAACCCC	10013
rs139669611	snp	A/G	0.0772873	0.180749	intron-variant	HDAC6	GRCh38.p7	X:48814155	GTCTCTCACCAGAAC[A/G]TCTCCCTCAGCAAAC	10013
rs139742976	snp	C/T	0.0115877	0.0752302	intron-variant	HDAC6	GRCh38.p7	X:48803809	CATGAACAGATAATA[C/T]AGGTGAGGTTGGAAG	10013
rs139773351	snp	A/G	5.99251e-05	0.00547348	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802921	TATCCCCAATCTAGC[A/G]GAGGTAAAGAAGAAA	10013
rs140347117	in-del	-/T			intron-variant	HDAC6	GRCh38.p7	X:48808226	TCACCTTGATCTCCT[-/T]GCACAGAGTCCCCTC	10013
rs141268593	snp	C/G/T	0.000265197	0.0115125	missense, nc-transcript-variant, intron-variant	HDAC6	GRCh38.p7	X:48802784	ACTCCAGTGTCACTT[C/G/T]GGTGAGGCCCTAGAC	10013
rs141405349	snp	C/T	0.00528398	0.051128	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806842	ATAATTAAAAATCTG[C/T]CTCCCATCCTTGTCA	10013
rs141406512	snp	C/T	2.38447e-05	0.00345279	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823022	CGAGAAAAGAAGGTT[C/T]TGGAAGCAGGCATGG	10013
rs141467577	snp	A/G	0.000118887	0.00770903	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48814982	GATGGCCGCCACTCC[A/G]GCAGGGTTCGCCCAG	10013
rs141641633	snp	G/T	4.57509e-05	0.00478261	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48815634	TCTGGGAGGTTCTTG[G/T]GAGATCAAGTAGGAA	10013
rs141938903	snp	C/T	0.000623247	0.0176419	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48816207	GGAGCTGGGCCTTGC[C/T]GGGCGCTGCCTCACC	10013
rs142007727	snp	A/G	0.00707718	0.0590636	intron-variant	HDAC6	GRCh38.p7	X:48808177	TGGGGGTGGCATGGG[A/G]TGGGGTGTCCTGGTC	10013
rs142276149	snp	A/G	0.000140103	0.00836852	missense, nc-transcript-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48822669	TGGCTGCCTGCACTC[A/G]CTCCCTCCTTGGAGA	10013
rs142774634	snp	A/G	3.71581e-05	0.00431018	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823226	ACCTCAGAGGAGGCT[A/G]TCGGGGGAGCCACTC	10013
rs143030911	snp	C/T	0.00229762	0.0338162	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823185	TTTCTGAGGCAGCCA[C/T]TGGGGGAGCCATGCT	10013
rs143074853	snp	C/T	0.01368	0.0815649	intron-variant	HDAC6	GRCh38.p7	X:48808380	CACCTCCCACCCTTA[C/T]AGGCCCAGCCAGAAG	10013
rs143480781	snp	A/G	0.00317376	0.039709	upstream-variant-2KB	HDAC6	GRCh38.p7	X:48800703	CTGTCAGTCTGATGC[A/G]GAACCCCCGGACTGC	10013
rs143498608	snp	C/T	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48817987	AGGGGTCTAGCCCAG[C/T]CCTCTTCCAGGGCGT	10013
rs143642817	snp	A/G	5.37844e-05	0.00518549	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823474	AACTCCTCTAGCCTC[A/G]AGCACAGACCACCAG	10013
rs143689285	snp	C/T	0.00728761	0.0599224	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48805666	AGAGCTGATGTTGGT[C/T]CACAGGTGAAGGCTT	10013
rs143759049	snp	A/G	5.77901e-05	0.0053751	synonymous-codon, intron-variant, nc-transcript-variant	HDAC6	GRCh38.p7	X:48818280	CCCCATGGGGGATGA[A/G]GGTGCCAGCAGCCAG	10013
rs144079643	in-del	-/A			intron-variant	HDAC6	GRCh38.p7	X:48812794	TTCTGTTTTCTTTTT[-/A]AACTTAGCTTGAGTG	10013
rs144699758	snp	A/G/T	0.00182387	0.0301473	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48824244	CTGGTCCTCAGCTAC[A/G/T]TCGACCTGTCAGCCT	10013
rs145147896	snp	A/G	0.00192692	0.0309798	synonymous-codon, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823066	GGCATCATTTGGGGA[A/G]GAGTCCACTCCAGGC	10013
rs145152846	snp	C/T	0.00158814	0.0281345	intron-variant	HDAC6	GRCh38.p7	X:48818716	TGGATCTGTGTTGTA[C/T]GTGCGTGCCATCACA	10013
rs145223784	snp	C/G	8.20681e-05	0.00640526	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48815023	TGCTCATGGGTCTGG[C/G]AGGAGGCAAGCTGAT	10013
rs145263943	snp	A/G	0.016289	0.0887646	intron-variant	HDAC6	GRCh38.p7	X:48822287	CTGTATAGATTGAGC[A/G]CCTGTGGTTGTGAGG	10013
rs145349858	snp	C/G	0.000709384	0.0188199	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48802995	TCGTGGGACTGCAAG[C/G]GATGGTGAGCAGGGC	10013
rs145577593	snp	C/T	0.000529661	0.016265	intron-variant, utr-variant-3-prime	HDAC6	GRCh38.p7	X:48806814	TATATTCTCTTTTTT[C/T]CCTTTGGATTCTTGA	10013
rs145768118	snp	A/G	0.000452408	0.0150333	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	HDAC6	GRCh38.p7	X:48806665	CAGGCTGGTGGATGC[A/G]GTCCTGGGGGCTGAG	10013
rs145799176	snp	A/C	0.000189982	0.00974449	missense, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814563	CAATGTGCCTTGGAA[A/C]CAGGTCAGCATCTAC	10013
rs145874648	snp	A/G	0.000189982	0.00974449	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48823095	GCCAGACTAACTCAG[A/G]GACAGCTGTGGTGGC	10013
rs146047260	snp	C/T	0.00738971	0.0603345	intron-variant	HDAC6	GRCh38.p7	X:48805097	TGGGCATGGGTAATA[C/T]TTTGGCTTTTACTCA	10013
rs146616822	snp	A/T	2.4039e-05	0.00346683	missense, nc-transcript-variant, downstream-variant-500B	HDAC6	GRCh38.p7	X:48822998	AGGTTAGCTGAGCGG[A/T]TGACCACACGAGAAA	10013
rs146634571	snp	C/T	0.000189982	0.00974449	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48814698	GCGGGATGCTGACTA[C/T]ATTGCTGCTTTCCTG	10013
rs146979948	snp	A/G	0.00190101	0.0307716	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823438	GTCAGAGGAGGCTCC[A/G]GGGGGCACCGAGCTG	10013
rs147012956	snp	C/T	0.00581083	0.0535878	intron-variant	HDAC6	GRCh38.p7	X:48807536	TTATTTATTTTGAGA[C/T]GGAGTCTCGCTCTGT	10013
rs147198199	snp	A/G	0.0256233	0.11025	intron-variant	HDAC6	GRCh38.p7	X:48822299	AGCGCCTGTGGTTGT[A/G]AGGATTGAGTTAATA	10013
rs147206457	snp	C/G			intron-variant	HDAC6	GRCh38.p7	X:48821718	TCACCATGTTGGCCA[C/G]GCTGGCCTCAAACTC	10013
rs147207522	snp	C/T	0.00110224	0.02345	synonymous-codon, nc-transcript-variant	HDAC6	GRCh38.p7	X:48823571	CTCAGGACCTTGGAG[C/T]TAGGCAGCGAATCTC	10013
rs147285278	snp	A/G	0.000529661	0.016265	intron-variant	HDAC6	GRCh38.p7	X:48821881	GGCTTGCAAAAAGTC[A/G]CACTTACTATGTGCC	10013

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