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
rs10847	snp	A/G	0.290201	0.246747	upstream-variant-2KB, utr-variant-3-prime	CTSK, ARNT	GRCh38.p7	1:150810321	TTTTAAATGTGATCA[A/G]GACTATAATATTGTA	405
rs955156	snp	C/T	0.0119091	0.0762411	intron-variant	ARNT	GRCh38.p7	1:150865632	AAAAGACAGATTTAC[C/T]CTCTGGAGAGTATAA	405
rs1027699	snp	C/T	0.477853	0.102875	intron-variant	ARNT	GRCh38.p7	1:150839236	GTTCTCAAATATTAA[C/T]ACTTATTAGCTTATT	405
rs1268831	snp	A/G	0.0193405	0.0964168	intron-variant	ARNT	GRCh38.p7	1:150841287	TCTGTTACCACTTAA[A/G]AATTCTACTTGAACA	405
rs1272965	snp	C/T			upstream-variant-2KB	ARNT	GRCh38.p7	1:150877235	ccactgcacgccagt[C/T]tgggcaacaagagcg	405
rs1805133	snp	A/G	0.0111726	0.0739019	missense	ARNT	GRCh38.p7	1:150817408	CAGCAAACAGAATTG[A/G]ACATGGTACCAGGAA	405
rs1889740	snp	A/G	0.498346	0.0287064			GRCh38.p7	1:150827279	CAGTGAATGTGTTCT[A/G]AAACTGGATTGTGGT	405
rs2039590	snp	C/T	0.447291	0.153545	intron-variant	ARNT	GRCh38.p7	1:150840839	GAGAAACTTAATGGG[C/T]TTTTAAAAATTCCTG	405
rs2089081	snp	A/G	0.445987	0.155207	intron-variant	ARNT	GRCh38.p7	1:150827641	cacccatagatttgt[A/G]cacagttcatatctg	405
rs2089082	snp	A/C	0.477004	0.104734	intron-variant	ARNT	GRCh38.p7	1:150827614	TCTGTATTATTCATA[A/C]TAGCCAAAAAAATGA	405
rs2134688	snp	A/G	0.312348	0.242101	intron-variant	ARNT	GRCh38.p7	1:150844410	TACAATGCATTTTAT[A/G]TAATACCCTCTAATT	405
rs2228099	snp	C/G	0.483541	0.0892109	synonymous-codon	ARNT	GRCh38.p7	1:150836413	CAGGGTGGTGTATGT[C/G]TCTGACTCCGTGACT	405
rs2229175	snp	A/C/G/T	1.64754e-05	0.00287009	missense	ARNT	GRCh38.p7	1:150823299	TCTTGGTTCTTAGAC[A/C/G/T]GGAACCGGAACATGA	405
rs2256355	snp	C/T	0.498437	0.0279115	intron-variant	ARNT	GRCh38.p7	1:150839318	TGTTATAGCCAAGGA[C/T]TGAAATTCGTTTTCC	405
rs2275237	snp	C/T	0.00267563	0.0364781	missense	ARNT	GRCh38.p7	1:150813335	CTGTATTTCTAGCTC[C/T]TGAGACTGGACAGAC	405
rs2864873	snp	A/G	0.480302	0.0972668	intron-variant	ARNT	GRCh38.p7	1:150841698	AACAACAGTCTCCCA[A/G]GAGAATTCTAGAGTC	405
rs3062353	in-del	-/T/TT	0	0	intron-variant, upstream-variant-2KB	ARNT	GRCh38.p7	1:150858633	TTTTTTTTTTTTTTT[-/T/TT]GAGACCAGGTCTCAC	405
rs3062354	in-del	-/CAGT			intron-variant	ARNT	GRCh38.p7	1:150866278	gtgagccaccaaggt[-/CAGT]cagcctgttccaagg	405
rs3215133	in-del	-/T	0.100231	0.200173	intron-variant	ARNT	GRCh38.p7	1:150829797	ATTTTGAGAGTTTTA[-/T]GGAATTCTTCATTTG	405
rs3738482	snp	A/C/G/T	0.00915317	0.0671402	intron-variant	ARNT	GRCh38.p7	1:150842525	CCTTCCTCCCTCCCC[A/C/G/T]CTTCCTTCCTTCTTT	405
rs3738483	snp	A/G	0.300421	0.244863	intron-variant	ARNT	GRCh38.p7	1:150828990	ATATCAACCTCAGTT[A/G]AGAAAAAGAGATCAT	405
rs3768012	snp	A/G	0.0513262	0.151752	intron-variant	ARNT	GRCh38.p7	1:150875822	GCCTACGTCGAGGCA[A/G]TTTCCAAACTCTTTC	405
rs3768013	snp	C/T	0.498481	0.027514	intron-variant	ARNT	GRCh38.p7	1:150842935	CTCTGTCTTTAATTT[C/T]TTCATTATAGAATAG	405
rs3768015	snp	C/T	0.477004	0.104734	intron-variant	ARNT	GRCh38.p7	1:150840478	TAAGAGAGAGGCTTA[C/T]CATATTTTATAGACC	405
rs3768016	snp	A/G	0.47743	0.103805	intron-variant	ARNT	GRCh38.p7	1:150837443	GGAAAAGGGACTTGA[A/G]TTGGTAATTAGGAGG	405
rs3768017	snp	G/T	0.173289	0.23794	intron-variant	ARNT	GRCh38.p7	1:150826636	AAGTATATATCTTAC[G/T]CTTCTTTCTGTATTC	405
rs3820541	snp	C/G	0.143959	0.226396	intron-variant	ARNT	GRCh38.p7	1:150876205	TTTTAACCCTCTGCC[C/G]GCTGGAGCCGCTTGA	405
rs3820543	snp	A/T	0.144969	0.226867	intron-variant	ARNT	GRCh38.p7	1:150840382	GGTCCTTTTATTTTC[A/T]GGCCTTTAAATAGTT	405
rs3894771	snp	A/T	0.499526	0.0153875	intron-variant	ARNT	GRCh38.p7	1:150817485	AAAAAAATTTTTTTT[A/T]AAAAAGAATCTGGAG	405
rs4987112	snp	C/T	0	0	missense	ARNT	GRCh38.p7	1:150817409	TCCTGGTACCATGTC[C/T]AATTCTGTTTGCTGT	405
rs6587523	snp	A/G	0.0349115	0.127424	intron-variant	ARNT	GRCh38.p7	1:150813675	TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG	405
rs6656967	snp	A/T	0	0	intron-variant	ARNT	GRCh38.p7	1:150864769	aagtataataaaaaa[A/T]aaataaataaataaa	405
rs6660845	snp	A/G	0.476487	0.105846	intron-variant	ARNT	GRCh38.p7	1:150868590	gcaggaggatcactc[A/G]aggacagtagttcaa	405
rs6671703	snp	C/T	0.143959	0.226396	intron-variant	ARNT	GRCh38.p7	1:150824494	ggagtctcgctctgt[C/T]gccaggctggagtgc	405
rs6679794	snp	C/T	0.00874735	0.0655527	intron-variant	ARNT	GRCh38.p7	1:150822188	aagaattttctaata[C/T]atttactgaaaaaaa	405
rs6689204	snp	C/T	0.00874735	0.0655527	intron-variant	ARNT	GRCh38.p7	1:150860497	ctaggattacaggca[C/T]gagccaccgtgccca	405
rs7513824	snp	A/G	0.132409	0.220618	intron-variant	ARNT	GRCh38.p7	1:150868499	TATCAAGAACTTGTA[A/G]AGGATTCTAATAACA	405
rs7514004	snp	C/T	0.498459	0.0277128	intron-variant	ARNT	GRCh38.p7	1:150845758	aatacaaaaattagc[C/T]gggcgtggtggcagg	405
rs7515228	snp	A/T	0.0325976	0.123435	upstream-variant-2KB	ARNT	GRCh38.p7	1:150877383	AAAGAGCACCTAAAC[A/T]TCACATGGTGATTTG	405
rs7517566	snp	A/G	0.222035	0.248431	upstream-variant-2KB	ARNT	GRCh38.p7	1:150877559	AAAATTGGAGGCAAT[A/G]GATGAAGAAAGTAAT	405
rs7517945	snp	A/G	0.0341408	0.126114	upstream-variant-2KB	ARNT	GRCh38.p7	1:150878022	gagtcttgctccatc[A/G]cccaggctggagtgc	405
rs7518440	snp	A/G	0.0345262	0.126772	intron-variant	ARNT	GRCh38.p7	1:150818286	ATTCAAAACCTGGTT[A/G]TTGTGAATGTGTGTA	405
rs7518546	snp	A/G	0.0345262	0.126772	intron-variant	ARNT	GRCh38.p7	1:150818353	AAAAAATGAAAGTAC[A/G]TACACTGTACATCAA	405
rs7521592	snp	A/C	0.472241	0.114494	intron-variant	ARNT	GRCh38.p7	1:150849215	tctcaaaaaaaaaga[A/C]agaaagaaaataaat	405
rs7529204	snp	C/G	0.146532	0.228245	intron-variant	ARNT	GRCh38.p7	1:150872904	aaggtcaaggctgca[C/G]tgagccatgattgtg	405
rs7532045	snp	A/G	0.498415	0.0281103	intron-variant	ARNT	GRCh38.p7	1:150849371	AAAAAAGCAGATTGC[A/G]GTCAAAGTTCTCTTC	405
rs7533914	snp	A/G	0.0322494	0.12282	intron-variant	ARNT	GRCh38.p7	1:150822580	gtctgaaagctctgc[A/G]ctccttcctccttac	405
rs9325978	snp	C/G	0.0263992	0.111815	intron-variant	ARNT	GRCh38.p7	1:150832008	TGATTATCCTGTTTT[C/G]TAAACTCCTAAGAGC	405
rs9325979	snp	C/T	0.0382008	0.13282	intron-variant	ARNT	GRCh38.p7	1:150832427	ATAAAGAGATTAAAA[C/T]CAATCAGACTGCCCT	405
rs10305645	in-del	-/T	0.499551	0.0149693	upstream-variant-2KB	ARNT	GRCh38.p7	1:150878429	AGCGATACATGAAAA[-/T]GGAAGTACTTTGTAG	405
rs10305646	snp	A/G	0.0894459	0.191631	upstream-variant-2KB	ARNT	GRCh38.p7	1:150877889	gcctgtaatcccaac[A/G]gtttgtgagaccgag	405
rs10305647	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	ARNT	GRCh38.p7	1:150877225	gcccagactggcgtg[C/T]agtggcgctatctcg	405
rs10305648	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB	ARNT	GRCh38.p7	1:150876858	TCACTGGACTGGCTG[C/G]CGCAGTGAGTAGCCC	405
rs10305649	snp	G/T	0.0325976	0.123435	utr-variant-5-prime, upstream-variant-2KB	ARNT	GRCh38.p7	1:150876627	GAGGAGCCGCCGCCA[G/T]CGAACCGGGAGGGAG	405
rs10305650	snp	A/C/G/T	0.0570107	0.158919	intron-variant	ARNT	GRCh38.p7	1:150876501	TTGTCAGCCCCTTCG[A/C/G/T]CCCCTCCCCTTTAGA	405
rs10305651	snp	A/T	0.00199481	0.0315187	intron-variant	ARNT	GRCh38.p7	1:150876482	AGGGGCTGACAACTA[A/T]GGAGACCCAGGGCTG	405
rs10305652	snp	G/T	0.00119737	0.0244387	intron-variant	ARNT	GRCh38.p7	1:150876330	GGGAGCGAGGGGGCA[G/T]GTGGGAGTTGAGGGG	405
rs10305653	in-del	-/AC	0.0733688	0.176922	intron-variant	ARNT	GRCh38.p7	1:150875501	GATATGTGTGTGTGT[-/AC]TGCGTGGGGCGGAGA	405
rs10305654	snp	C/T	0.00517822	0.0506191	intron-variant	ARNT	GRCh38.p7	1:150868402	TTGTTCCTTCTTTGT[C/T]CTTTTTGCTTATCTT	405
rs10305655	snp	C/T	0.00318978	0.0398085	intron-variant	ARNT	GRCh38.p7	1:150868203	tgtacacttgtaatc[C/T]cagctactcaggaag	405
rs10305656	snp	C/G	0.00993419	0.0697739	intron-variant	ARNT	GRCh38.p7	1:150868044	ACCTACCATAGTCCT[C/G]TTCCCTTtgtattag	405
rs10305657	snp	G/T	0.0138799	0.0821421	intron-variant	ARNT	GRCh38.p7	1:150867941	gccctgcctcccata[G/T]agcctgcggaactat	405
rs10305658	snp	C/T	0.132409	0.220618	intron-variant	ARNT	GRCh38.p7	1:150867870	cagccatgtgaagac[C/T]tgcttgcttcccctt	405
rs10305659	snp	A/G	0.0209421	0.100162	intron-variant	ARNT	GRCh38.p7	1:150867787	tctcttgagaactct[A/G]tcatgagagagcatt	405
rs10305660	snp	C/T	0.0170251	0.090679	intron-variant	ARNT	GRCh38.p7	1:150867608	GGAATGAAATTTTTG[C/T]AGTCTTTTATACATA	405
rs10305661	snp	C/T	0.0129027	0.0792771	intron-variant	ARNT	GRCh38.p7	1:150867585	TTCATTCCTGGCTTC[C/T]CACATAAACTACTTT	405
rs10305662	snp	A/G	0.124491	0.216211	intron-variant	ARNT	GRCh38.p7	1:150867574	AAAAATATAGGAAAG[A/G]AGTTTATGTGAGAAG	405
rs10305663	snp	G/T	0.0599851	0.162463	intron-variant	ARNT	GRCh38.p7	1:150867222	AATCTGTTTTTTTTT[G/T]TTGTTGTTGTTTTTT	405
rs10305664	snp	G/T	0.478685	0.10101	intron-variant	ARNT	GRCh38.p7	1:150867210	TTTGTTGTTGTTGTT[G/T]TTTTTAAAGACAGAG	405
rs10305665	snp	A/G	0.0130921	0.0798413	intron-variant	ARNT	GRCh38.p7	1:150866995	tggtcttgaactccc[A/G]tcctcaagtgatcca	405
rs10305666	snp	C/T	0.0136048	0.0813469	intron-variant	ARNT	GRCh38.p7	1:150866962	tgccttggcctccca[C/T]agtgctgggattaca	405
rs10305667	snp	A/G	0.438246	0.16451	intron-variant	ARNT	GRCh38.p7	1:150859632	CAGTGGCTCAAACCT[A/G]TAATTCCAGTGCTCT	405
rs10305668	snp	C/T	0.0755793	0.179102	intron-variant	ARNT	GRCh38.p7	1:150859618	TGTAATTCCAGTGCT[C/T]TGGGAAGCTGAGGTG	405
rs10305669	snp	A/T	0.0227243	0.104143	intron-variant, upstream-variant-2KB	ARNT	GRCh38.p7	1:150858613	aaaaaaaaaaaaTCA[A/T]GAAGAGCAATCTGGA	405
rs10305670	snp	C/G	0.00696856	0.058615	intron-variant, upstream-variant-2KB	ARNT	GRCh38.p7	1:150858612	aaaaaaaaaaaTCAA[C/G]AAGAGCAATCTGGAT	405
rs10305671	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	ARNT	GRCh38.p7	1:150857880	aatcagcacaatgcc[A/G]taacactaattagga	405
rs10305672	snp	C/T	0.472335	0.114312	intron-variant	ARNT	GRCh38.p7	1:150853154	AGCTGAGATTACAGG[C/T]ACCCGCCACCATGCC	405
rs10305673	snp	A/G	0.477004	0.104734	intron-variant	ARNT	GRCh38.p7	1:150853035	CCTCAGCCTTCCAAA[A/G]TGCTGGGATTACAGG	405
rs10305674	snp	G/T	0.00356505	0.0420692	intron-variant	ARNT	GRCh38.p7	1:150852195	gtgagtgtgtgaggg[G/T]gttacacaaggaagt	405
rs10305675	snp	A/G	0.131723	0.220251	intron-variant	ARNT	GRCh38.p7	1:150847362	ctcactgcaacctcc[A/G]cctcccaggttcaag	405
rs10305676	snp	C/T	0.00874735	0.0655527	intron-variant	ARNT	GRCh38.p7	1:150846748	aaaactgaaactcta[C/T]actcatcaaacacca	405
rs10305677	snp	A/T	0.0138799	0.0821421	intron-variant	ARNT	GRCh38.p7	1:150846616	ttttttaccagaatt[A/T]aaaaaaAACCCAAAA	405
rs10305678	snp	A/G	0.00181167	0.0300425	intron-variant, synonymous-codon	ARNT	GRCh38.p7	1:150842447	TCTCTCTTTATCCGC[A/G]GAGCTCTGCTCATCA	405
rs10305679	snp	C/T	0.123105	0.215401	intron-variant	ARNT	GRCh38.p7	1:150842326	GCCACAGATAAGGAA[C/T]AATACAAAGAGAAAG	405
rs10305680	snp	C/T	0.124491	0.216211	intron-variant	ARNT	GRCh38.p7	1:150842199	AAAAAACTTAAAACT[C/T]ATAGCAATTTCTTAA	405
rs10305681	snp	A/G	0.0129027	0.0792771	intron-variant	ARNT	GRCh38.p7	1:150842054	AATAAATATATCTGT[A/G]TTTGTGATTAGTTCC	405
rs10305682	snp	C/T	0.123452	0.215605	intron-variant	ARNT	GRCh38.p7	1:150838962	GCAGAAAATGTTTAC[C/T]CCTTCTTTTTTTCAT	405
rs10305683	snp	C/T	0.00676609	0.0577691	intron-variant	ARNT	GRCh38.p7	1:150838864	GCATAAAGAGAGGAA[C/T]TGTATTTTTTAATTA	405
rs10305684	snp	A/G	0.00199481	0.0315187	intron-variant	ARNT	GRCh38.p7	1:150838779	AATGGCTAGACTTGA[A/G]TGAGGATGGTTAGGG	405
rs10305685	snp	A/G	0.108048	0.20579	intron-variant	ARNT	GRCh38.p7	1:150838529	TATAGCTACAAAGTA[A/G]GTAGTTTTAAGTAGA	405
rs10305686	snp	A/C/G/T	0.0142736	0.0832652	intron-variant	ARNT	GRCh38.p7	1:150838426	TCTCACAGCACAACA[A/C/G/T]ACCTGGTTTGCCCAC	405
rs10305687	snp	A/G	0.00676609	0.0577691	intron-variant	ARNT	GRCh38.p7	1:150838330	CATAGAACTAGTTCT[A/G]TAATAGAAGTGCTGT	405
rs10305688	snp	G/T	0.00874735	0.0655527	intron-variant	ARNT	GRCh38.p7	1:150837731	CCAAGTCTATAGCCC[G/T]AGACATGACTAACGT	405
rs10305689	snp	A/C/G/T	0.00318978	0.0398085	intron-variant	ARNT	GRCh38.p7	1:150837647	AAAGTTCATCTTAAG[A/C/G/T]CCTCTTTATTAATAC	405
rs10305690	snp	C/T	0.0023933	0.0345097	intron-variant	ARNT	GRCh38.p7	1:150837507	AAAGGATAAGATGGA[C/T]GACATTGTCACATTC	405
rs10305691	snp	A/G	0.000399281	0.0141238	intron-variant	ARNT	GRCh38.p7	1:150837381	GCTGTTCCTGGCAGA[A/G]CAAAAACCAAACCAA	405
rs10305692	in-del	-/ATT	0.0138799	0.0821421	intron-variant	ARNT	GRCh38.p7	1:150837276	AGTGAATATAACATT[-/ATT]CTTAGTATAAGCTTG	405
rs10305693	snp	A/G	0.0138799	0.0821421	intron-variant	ARNT	GRCh38.p7	1:150836912	aaacaaaaacaaaaa[A/G]aaaactagccaggtg	405
rs10305694	snp	C/T	0.0217236	0.101931	intron-variant	ARNT	GRCh38.p7	1:150836773	ATTACCGGCGGGAGC[C/T]GCTGTGCCTAGCCCA	405
rs10305695	snp	A/G	0.0232847	0.105357	intron-variant	ARNT	GRCh38.p7	1:150836640	ACAGCCACAGGTTTC[A/G]ACCCTAAATGTAGTT	405

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