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
rs6558298	snp	C/T	0.192401	0.243274	intron-variant	SHARPIN	GRCh38.p7	8:144101110	aaagtgctgggatga[C/T]aggcgtgagccaccg	81858
rs6558299	snp	A/G	0.0887219	0.191022	intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144102494	GACCAGGCTGGTCTC[A/G]AACTCCTGACATCAG	81858
rs11136254	snp	A/C	0.100088	0.200066	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144103600	AGCGCGGACCCTGAG[A/C]GGCCTGGGCGCTTCC	81858
rs11136255	snp	A/G	0.311123	0.242413	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144104196	GACCTCCAATGGGCT[A/G]CCACCTTCGCCCGCA	81858
rs11136256	snp	C/T	0.0298051	0.118382	upstream-variant-2KB, synonymous-codon	WDR97, SHARPIN, MAF1	GRCh38.p7	8:144105743	GCTGACTGTGGAGAC[C/T]GGAGATGCCCACATC	81858
rs11335429	in-del	-/C	0.5	0	upstream-variant-2KB, utr-variant-5-prime	SHARPIN, MAF1	GRCh38.p7	8:144104806	ACCGACGCGGAGCGA[-/C]CCAGCCCAGCCAGAC	81858
rs11433813	in-del	-/T	0.447421	0.153379	intron-variant	SHARPIN	GRCh38.p7	8:144102275	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC	81858
rs11541802	snp	C/G			missense, nc-transcript-variant	SHARPIN	GRCh38.p7	8:144099566	TCCGCCGCGTCCTCT[C/G]CACACGTTGCCCTGC	81858
rs11541803	snp	C/T			missense, nc-transcript-variant	SHARPIN	GRCh38.p7	8:144099339	CCATCCTGCCGAACC[C/T]CGTAAGAGGCAAGGC	81858
rs11541804	snp	C/G	0.108282	0.205951	missense, nc-transcript-variant	SHARPIN	GRCh38.p7	8:144099354	CCGTAAGAGGCAAGG[C/G]TGCGCTCAGGCACAC	81858
rs11541805	snp	C/T	0.0542423	0.156054	missense, nc-transcript-variant	SHARPIN	GRCh38.p7	8:144100007	GTCTCCCTGCCCAGT[C/T]CCCCGGAAGCCTCCA	81858
rs11541806	snp	C/T			missense, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144103575	GCTTCCGGCTGGAGC[C/T]GCTGGGCGCGGGACC	81858
rs11546145	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	SHARPIN, MAF1	GRCh38.p7	8:144104713	GGATACAGTGCGGCC[C/T]GAGCGGAGGCCGCGG	81858
rs12549149	snp	C/T	0.101703	0.201266	intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144103543	CCGCGCGCCCTCCGC[C/T]CCCACTCACCGCCCC	81858
rs12550729	snp	C/T	0.204189	0.245767	intron-variant	SHARPIN	GRCh38.p7	8:144100505	AGCCACTGCCCTGGG[C/T]GTCTTCAGAGCTGAG	81858
rs13254954	snp	A/G	0.21695	0.247806	downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098235	GGTGTCCTAGCTGCA[A/G]GAGCTGAGGGGAGTG	81858
rs17852938	snp	A/G			upstream-variant-2KB, synonymous-codon	WDR97, SHARPIN, MAF1	GRCh38.p7	8:144105704	GCTATTGGAGAACTC[A/G]AGCTTTGAAGCCATC	81858
rs34173062	snp	A/G	0.146162	0.227415	missense, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144103704	AAGAGCACTGCGGCG[A/G]AGCCCAAGTCCGAGG	81858
rs34270727	in-del	-/T			intron-variant	SHARPIN	GRCh38.p7	8:144101404	TTTTTTTTTTTTTTT[-/T]GTGAGATGGAGTCTC	81858
rs34674752	snp	A/G	0.0583163	0.160491	missense, nc-transcript-variant	SHARPIN	GRCh38.p7	8:144099319	AGTAGAGGAAAGCAG[A/G]GTCCCCATCCTGCCG	81858
rs34818837	in-del	-/G			intron-variant	SHARPIN	GRCh38.p7	8:144102217	CTGGGTGAGAGAGGG[-/G]AGTCTTTGTCTGCAA	81858
rs34839093	snp	A/G	0.000234828	0.0108332	synonymous-codon, nc-transcript-variant	SHARPIN	GRCh38.p7	8:144099392	CCGTCCGATGACCCA[A/G]CGTTGCACGGCTGGC	81858
rs34857822	in-del	-/A			frameshift-variant, nc-transcript-variant	SHARPIN	GRCh38.p7	8:144099930	CCCCCACCTGTACCT[-/A]CTCTCCGTCAAGTTT	81858
rs34947229	in-del	-/A			intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144102935	CTCCACCTACTCCCT[-/A]CCTGGAAGCCTTCCC	81858
rs34948990	snp	A/G	0.00914312	0.0669923	downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098555	TGGCTGGGGAGCCCC[A/G]CCTGCTGATGAGGGC	81858
rs34960192	snp	A/G/T	0.000428471	0.0146309	intron-variant, utr-variant-3-prime	SHARPIN	GRCh38.p7	8:144098850	CCACCTCCCCTGCCT[A/G/T]TGCCACCTCTGGTAC	81858
rs35333153	in-del	-/T	0	0	intron-variant	SHARPIN	GRCh38.p7	8:144100854	CTTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCAC	81858
rs35351724	snp	A/G	0.0854556	0.188216	downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098292	GCTGAATGGGAGAAA[A/G]GTGGTACCAATAGGC	81858
rs35397593	snp	A/C/T	0.0104709	0.0715948	downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098504	CTGACCACTGAGGCT[A/C/T]AGGGTCCGGGCCCAT	81858
rs35801151	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098267	TGGCCATAGTCCAAG[C/G]AAGGCAAGAGCTGAA	81858
rs35844464	snp	A/C/G	0.00456515	0.0475596	missense, intron-variant	SHARPIN	GRCh38.p7	8:144099196	GGGTGCTGAGGGCTA[A/C/G]GTCCTGTGGCTGAGG	81858
rs57151029	in-del	-/AG	0.375	0.216506	intron-variant	SHARPIN	GRCh38.p7	8:144101602	TTTTTTTTTTTTAGT[-/AG]AGTCAGGGTTTCACC	81858
rs57242566	snp	A/G			intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144102865	CTGGCTGGGGCCTCA[A/G]ATGGTGTAGGAGACT	81858
rs58173496	in-del	-/T	0	0	intron-variant	SHARPIN	GRCh38.p7	8:144101599	TTTTTTTTTTTTTTT[-/T]AGTAGTCAGGGTTTC	81858
rs61732529	snp	C/T	0.000232994	0.0107909	missense, intron-variant	SHARPIN	GRCh38.p7	8:144099154	GATGGGGGAAACAAG[C/T]GTCCAAGTTCCCCGT	81858
rs66878813	in-del	-/CTT/TCT	0	0	upstream-variant-2KB, intron-variant	SHARPIN, MAF1	GRCh38.p7	8:144105299	GTGGCTGGAGCTCTT[-/CTT/TCT]TTGGAGTGGGCGTGG	81858
rs71516044	in-del	-/A	0.5	0	upstream-variant-2KB, frameshift-variant	WDR97, SHARPIN, MAF1	GRCh38.p7	8:144106091	ACTCAGCAAAAGCCA[-/A]GGCGGTGAGGAGGAG	81858
rs72543665	in-del	-/CTT			upstream-variant-2KB, intron-variant	SHARPIN, MAF1	GRCh38.p7	8:144105301	GGTGGCTGGAGCTCT[-/CTT]TYTGGAGTGGGCGTG	81858
rs73381305	snp	C/T	0.0785177	0.181917	intron-variant	SHARPIN	GRCh38.p7	8:144101671	TCTGCCCACATCGGC[C/T]TCCCAAAGTGCTGTG	81858
rs73717808	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098534	TTCTTCAGTAACACC[A/G]GGGTCTGGCTGGGGA	81858
rs74667328	snp	A/C	0.0726307	0.176182	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144104142	GCATCCAGCGTGCGA[A/C]TATCCCAGCGCCTAA	81858
rs75361772	snp	A/G	0.0696718	0.173152	upstream-variant-2KB, utr-variant-5-prime	SHARPIN, MAF1	GRCh38.p7	8:144104401	AGAAGGCAGAACTGA[A/G]TGGCGGGTACGGCAC	81858
rs76065466	snp	C/G	0.0197687	0.0974348	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144103986	TGGGCGAGGCTGGCG[C/G]CGTGTACGAGGCTGG	81858
rs76483965	in-del	-/TCT	0.0905309	0.192535	upstream-variant-2KB, intron-variant	SHARPIN, MAF1	GRCh38.p7	8:144105298	CATGGTGGCTGGAGC[-/TCT]TCTTTTGGAGTGGGC	81858
rs76591178	snp	A/G	0.00580766	0.0535733	intron-variant	SHARPIN	GRCh38.p7	8:144099669	ACCTGGGATGGTCAC[A/G]AGGACAAGGTGAAGA	81858
rs76889608	snp	C/T			synonymous-codon, intron-variant	SHARPIN	GRCh38.p7	8:144099135	GCCTGGGGGTAGCCC[C/T]AATGATGGGGGAAAC	81858
rs77359862	snp	A/G	0.0056191	0.0527065	missense, nc-transcript-variant	SHARPIN	GRCh38.p7	8:144099379	GCACACACAGGCACC[A/G]TCCGATGACCCAGCG	81858
rs78648437	snp	A/G	0.5	0	upstream-variant-2KB, missense	WDR97, SHARPIN, MAF1	GRCh38.p7	8:144106165	TGATTGCCACGCTCA[A/G]TGAGTCCTTCAGGCC	81858
rs111322040	snp	A/G	0	0	intron-variant	SHARPIN	GRCh38.p7	8:144100578	CCCACTGCAATGGGG[A/G]GGTCCCCATCCAGTG	81858
rs112028217	snp	A/G	0.0178098	0.0926698	downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098481	AGAGATCCCCATGCC[A/G]TGCTTTCCTGACCAC	81858
rs112063891	snp	A/G			splice-donor-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144103049	CATTACAGGGCACTG[A/G]CCATTCTGTCCTTCC	81858
rs112255220	snp	C/T	0.0162398	0.0886349	upstream-variant-2KB, intron-variant	SHARPIN, MAF1	GRCh38.p7	8:144105443	GGCTGACCTGGAGCC[C/T]GGACTTACCACCCTC	81858
rs112342688	snp	C/T	0	0	upstream-variant-2KB, intron-variant	SHARPIN, MAF1	GRCh38.p7	8:144105302	GGTGGCTGGAGCTCT[C/T]TTGGAGTGGGCGTGG	81858
rs112552278	snp	C/T	0.0161031	0.0882736	missense, nc-transcript-variant, synonymous-codon	SHARPIN	GRCh38.p7	8:144098948	ATCTCACAGCCAGGG[C/T]GGTCTGGGGCATTGA	81858
rs112813219	snp	A/G			splice-donor-variant	SHARPIN	GRCh38.p7	8:144099701	GCAGCCCCAGGCCTC[A/G]CCTGATGGGGCCAGG	81858
rs113068322	snp	C/T			upstream-variant-2KB, intron-variant	WDR97, SHARPIN, MAF1	GRCh38.p7	8:144105866	TCTCTCTGCATCCTA[C/T]AGGATTGAGAGCTAC	81858
rs113151355	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	SHARPIN, MAF1	GRCh38.p7	8:144104998	GGCCCAGGCGGGCGC[C/T]GCCTGGTGACTGCAG	81858
rs113194942	snp	C/G/T	0	0	utr-variant-3-prime, splice-donor-variant, downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098636	TGAAAGGGATGCTTG[C/G/T]TGGCTCTTAAGGGTC	81858
rs113197734	snp	G/T			intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144103048	CCATTACAGGGCACT[G/T]ACCATTCTGTCCTTC	81858
rs113472943	snp	G/T	0.00597247	0.0543191	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144104035	CTCACGTTAGAGCTG[G/T]TCTTTGGGGGCGAAG	81858
rs113734637	snp	C/T	0.0029089	0.0380262	missense, nc-transcript-variant	SHARPIN	GRCh38.p7	8:144099773	GATGCTGGGCCAGGA[C/T]GGCTGCCACTTGGGC	81858
rs113993743	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144103421	TCACCCCCATTTCAC[C/G]GACGAGAAAACAGAA	81858
rs114433070	snp	C/T	0.00597247	0.0543191	downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098225	TTTCATTGCTGGTGT[C/T]CTAGCTGCAAGAGCT	81858
rs116004300	snp	C/T	0.00636936	0.0560724	intron-variant	SHARPIN	GRCh38.p7	8:144102055	CATGTTTCTCAGTCT[C/T]AACTGCTAACTCTTC	81858
rs117299156	snp	C/T	0.0205511	0.0992634	intron-variant	SHARPIN	GRCh38.p7	8:144100763	GGTTTGTTTGCTGCT[C/T]CCTTGGTCACATGGT	81858
rs117580205	snp	A/G	0.000399281	0.0141238	intron-variant	SHARPIN	GRCh38.p7	8:144102159	CACCGTAGACCAGGA[A/G]TTCAAGGCTCCAGTG	81858
rs118008466	snp	A/G	0.000116491	0.00763098	missense, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144103111	GCTGAGCTTCCTGAG[A/G]GTTGAGGAAGTGCAG	81858
rs138032964	snp	A/C/G	0.00279258	0.0372817	upstream-variant-2KB, intron-variant, utr-variant-5-prime	SHARPIN, MAF1	GRCh38.p7	8:144104996	GTGGCCCAGGCGGGC[A/C/G]CTGCCTGGTGACTGC	81858
rs138355198	snp	C/G/T	0.0287284	0.116357	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144103902	GCGCCGAGTGGTGCA[C/G/T]TCTGGCCAAGCCTGC	81858
rs138633295	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	SHARPIN	GRCh38.p7	8:144098138	ACATGACCCAGCACC[A/G]GCCCAGTGACCTGGT	81858
rs139701481	snp	C/T	3.30896e-05	0.00406739	upstream-variant-2KB, synonymous-codon	WDR97, SHARPIN, MAF1	GRCh38.p7	8:144105722	CTTTGAAGCCATCAA[C/T]TCACAGCTGACTGTG	81858
rs139962028	snp	A/G	0.0364509	0.129988	intron-variant	SHARPIN	GRCh38.p7	8:144101534	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAT	81858
rs140040594	snp	C/T			intron-variant	SHARPIN	GRCh38.p7	8:144100871	AGACGGAGTTTCACT[C/T]GTTGCCCAGGCTGGA	81858
rs140042949	snp	C/T	1.66021e-05	0.0028811	upstream-variant-2KB, missense	WDR97, SHARPIN, MAF1	GRCh38.p7	8:144105966	CTGGAGGCACTTTCT[C/T]CACCCCAGACTTCAG	81858
rs140326885	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144102999	TCCCCAACCAGGACT[C/G]GGGGGCCAAGGCTAT	81858
rs141201044	snp	A/G	0.000399281	0.0141238	intron-variant	SHARPIN	GRCh38.p7	8:144100627	TCTCAGGCCCACTAT[A/G]TTCTACCATCTCCCT	81858
rs141573856	snp	C/T	0.000682145	0.0184555	upstream-variant-2KB, intron-variant	WDR97, SHARPIN, MAF1	GRCh38.p7	8:144105859	TCATGGTTCTCTCTG[C/T]ATCCTATAGGATTGA	81858
rs143553694	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	SHARPIN, MAF1	GRCh38.p7	8:144105525	CCTGATGTGCAGCCT[A/G]GACAGAGGCCAGACT	81858
rs143866381	snp	A/G	0.00185283	0.0303806	intron-variant	SHARPIN	GRCh38.p7	8:144100099	TGGGTGTGCTGTGCT[A/G]TGGCCTCTGTCCAGG	81858
rs144006632	snp	A/G	0.0310518	0.120672	intron-variant	SHARPIN	GRCh38.p7	8:144100993	GGCATGCACCACCAC[A/G]CCCGGCTAATTTTGT	81858
rs144249942	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144102568	GTGAGCCACCCCACC[C/T]GGCCACTAATTCCAT	81858
rs144735402	snp	C/T	0.000348597	0.0131976	upstream-variant-2KB, synonymous-codon	WDR97, SHARPIN, MAF1	GRCh38.p7	8:144105947	GGAGGGCCAGCCCCA[C/T]GTGCTGGAGGCACTT	81858
rs145431068	snp	C/G	0.0119091	0.0762411	intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144103325	GACCATTTACACGGT[C/G]CTAAGCCCTGTACGC	81858
rs145525277	snp	A/G	0.000708156	0.0188036	synonymous-codon, nc-transcript-variant, utr-variant-3-prime	SHARPIN	GRCh38.p7	8:144098911	AAGGGGGTCCCAAGT[A/G]CAGGGCCTCTGGGTG	81858
rs145703823	snp	A/C	0.000798403	0.0199641	intron-variant	SHARPIN	GRCh38.p7	8:144102076	CTAACTCTTCCATTT[A/C]AGCAGCCATGTGAGC	81858
rs146582662	snp	A/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	SHARPIN, MAF1	GRCh38.p7	8:144102848	GGAGGCTGCAACTTG[A/T]GCTGGCTGGGGCCTC	81858
rs146947779	snp	C/G	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	SHARPIN, MAF1	GRCh38.p7	8:144104955	CTGGGATTTGTAGTT[C/G]CACCGCGGCTTGGCT	81858
rs147294629	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SHARPIN, MAF1	GRCh38.p7	8:144105579	TTAGTGGGTAGGAGG[A/G]CTGAAGGCAGGGCCC	81858
rs147378643	snp	C/T	0.0023933	0.0345097	intron-variant	SHARPIN	GRCh38.p7	8:144100734	CAAGGATCACTTATA[C/T]ATGCTCACCTCAGGG	81858
rs148205171	snp	A/G	0.00119737	0.0244387	intron-variant	SHARPIN	GRCh38.p7	8:144100596	TCCCCATCCAGTGCT[A/G]ACACAGCTCCCGTGG	81858
rs148781318	snp	C/T	0.00245598	0.0349565	upstream-variant-2KB, utr-variant-5-prime	SHARPIN, MAF1	GRCh38.p7	8:144105644	TCACTCCCCAGGCAA[C/T]ACTAGCCCCTCTGGA	81858
rs149246735	snp	C/T	0.00478085	0.0486577	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144104151	GTGCGACTATCCCAG[C/T]GCCTAACGGCAGCTG	81858
rs149544330	snp	A/C	0.000119899	0.00774178	intron-variant	SHARPIN	GRCh38.p7	8:144099484	CTCCTCTGCCCCTGG[A/C]AGGGCTCCCCAGACC	81858
rs150179957	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144103788	CACCCCTCCGAGCGC[A/G]CTTCCGTGGGATCGG	81858
rs150993337	snp	A/C	0.000381534	0.0138066	missense, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144103563	CTCACCGCCCCAGGT[A/C]CCGCGCCCAGCAGCT	81858
rs180734534	snp	C/T	0.0130921	0.0798413	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SHARPIN, MAF1	GRCh38.p7	8:144104131	CGGACGTAGATGCAT[C/T]CAGCGTGCGACTATC	81858
rs180866062	snp	A/G	0.00199481	0.0315187	intron-variant	SHARPIN	GRCh38.p7	8:144100667	AGCAGGGCCTTCCAC[A/G]CACCCAGCGCTGTTC	81858
rs181377031	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	SHARPIN	GRCh38.p7	8:144098854	CTCCCCTGCCTGTGC[C/G]ACCTCTGGTACCTCT	81858
rs182009566	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	SHARPIN, MAF1	GRCh38.p7	8:144105115	TTCCTCTCCCCGGGC[A/C]AGAAAGTAGCCAAAA	81858
rs182638894	snp	C/T			intron-variant	SHARPIN	GRCh38.p7	8:144102005	CTCGTTTGTGGGCTG[C/T]CCTCTATCTGGGAGC	81858

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