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
rs34067517	snp	A/G	0.141934	0.225437	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336343	ATACTAAAGCATCAA[A/G]TGGTAGAAACATGCA	645402
rs35820226	snp	A/G	0.375	0.216506	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336981	AACTCACCCCCACCA[A/G]CCGCGAACACCCCAC	645402
rs35836633	snp	C/G	0.5	0	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336977	CACCCCCACCAGCCG[C/G]GAACACCCCACCCAC	645402
rs36114896	snp	A/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336169	AGTGGTTTCGGACGT[A/G]CGGCGGCAGTTTAAG	645402
rs58039122	snp	A/G	0.000751258	0.0193666	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337119	TTGCGGGCGACATGG[A/G]GGACGACTCACTCTA	645402
rs58596748	snp	C/T	4.35635e-05	0.00466689	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337181	TCAAAACTCACATCT[C/T]CTCGGCCAGATGCAG	645402
rs58684851	snp	A/C			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336997	TGGTGGGGGTGAGTT[A/C]TATAAGGGATGATGC	645402
rs59466575	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337006	TGAGTTCTATAAGGG[A/C]TGATGCGGCCAGAGA	645402
rs59486279	in-del	-/CA	0.46885	0.12085	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336663	ATCCCAGCACAAGCG[-/CA]CACACACACACACAC	645402
rs59555754	in-del	-/CACACACAGA			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336689	ACACACACACACACA[-/CACACACAGA]GACACACACACGGTT	645402
rs59905325	snp	G/T	0.0103295	0.0711199	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336942	GCTGATATTTGATTG[G/T]TTTATCGCGCACCTG	645402
rs62488811	snp	A/T			missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338010	ATGTGCAATATCCTG[A/T]GTGCCTTGACATGCA	645402
rs77372001	snp	A/C	0.138546	0.223781	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336305	AGTCTACTTTGTGCG[A/C]TGAGTATCTCTTCAA	645402
rs112397662	snp	A/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336821	GTGCCTATCACCCTG[A/G]GGAGTAATTTGATTC	645402
rs112988941	snp	A/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335710	ACAATTTTTGCACCA[A/T]ATGTGCTAACTGCAA	645402
rs113847916	snp	G/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336074	GAGATACGTTGTTTT[G/T]ATTTTCATCAGTTCT	645402
rs143414176	snp	A/G			missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338108	GGGTGGAGTTGTCAC[A/G]ACGGATATTACTTCT	645402
rs149214644	snp	C/G	0.0170251	0.090679	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336969	CCTGATGGGTGGGTG[C/G]GGTGTTCCCGGCTGG	645402
rs180769379	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336995	GCTGGTGGGGGTGAG[C/T]TCTATAAGGGATGAT	645402
rs185318615	snp	A/G	0.00835141	0.0640778	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335920	TCTTCTTGAGACAGG[A/G]CCTCATTCCCGTCAC	645402
rs188291483	snp	C/G	0.00874735	0.0655527	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336990	TCCCGGCTGGTGGGG[C/G]TGAGTTCTATAAGGG	645402
rs189806469	snp	A/C/G	0.00239393	0.0345281	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335949	ACCCGGGCTTTTCTA[A/C/G]GGTATAATTTTCCTT	645402
rs199562878	snp	A/T	0.14493	0.226848	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337163	TGGCAGTTCAACCAC[A/T]TTTCAAAACTCACAT	645402
rs199714364	snp	A/T	0.00697552	0.0586438	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338019	ATCCTGAGTGCCTTG[A/T]CATGCAGCCATACAT	645402
rs199743092	snp	C/T	0.00598195	0.0543617	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337534	CCTCCACAGTCCTGG[C/T]CATGTCATCCAGCCC	645402
rs199898906	snp	C/T	0.00399198	0.0444978	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338179	TGATGCCGAGGTCAC[C/T]GTCTGTAGCATCACT	645402
rs200111135	snp	C/T	0.00399205	0.0444982	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338377	GGTACCCGAGTTGGA[C/T]GAGCACTTGGTGGAA	645402
rs200205647	snp	G/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335847	AAACAAGGGCCAGCA[G/T]TAAAAAGGTTATGCT	645402
rs200265954	snp	C/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336574	TCTCAGGTCAGAAAG[C/T]GCACTTCAGACTTCT	645402
rs200423085	snp	C/T	0.0139021	0.0822057	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337228	GCGGACTTCTCTCCC[C/T]GAGAAGTCACCACTC	645402
rs200473945	snp	A/C	0.00399197	0.0444977	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337597	CAAGCAGGAAGATGT[A/C]CATGAATTTCTCATG	645402
rs200631940	snp	A/T	0.0433415	0.140685	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338085	TCTATGCTGTGCTGG[A/T]CCACGCTGGGTGGAG	645402
rs200849774	snp	A/G	0.00399195	0.0444976	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338382	CCGAGTTGGACGAGC[A/G]CTTGGTGGAAAGAGC	645402
rs201005386	snp	C/T			downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339101	GGGGTTTGTTTCTTT[C/T]GTCAGTTGTTGGTCG	645402
rs201032502	snp	G/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335485	TCCTTAAAATCATCC[G/T]AATTTCATGGGCCCT	645402
rs201070078	snp	C/T	0.00399198	0.0444978	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338181	ATGCCGAGGTCACTG[C/T]CTGTAGCATCACTTC	645402
rs201402363	snp	C/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336816	TATATGTGCCTATCA[C/T]CCTGAGGAGTAATTT	645402
rs201404546	snp	C/T	0.00399202	0.044498	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337876	GAATGCCTATCATTG[C/T]GGTCTTTGTCTCCAG	645402
rs201436387	in-del	-/CACA	0.0103295	0.0711199	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338802	AAACACACCCACACC[-/CACA]CAAACACGAACACCG	645402
rs201515496	in-del	-/GCAC			downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338740	CCCACACTGAGGGGT[-/GCAC]ACACACACACACACA	645402
rs201672191	snp	A/C	0.0129027	0.0792772	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337473	AAACATGTCAGCGTC[A/C]CAAGTGCTGCATGCT	645402
rs201912290	snp	C/T	0.000628564	0.0177168	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338110	GTGGAGTTGTCACGA[C/T]GGATATTACTTCTCT	645402
rs201998068	snp	C/G	0.00399201	0.044498	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338184	CCGAGGTCACTGTCT[C/G]TAGCATCACTTCTGT	645402
rs202019527	snp	C/G	0.00498752	0.0496879	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338402	GTGGAAAGAGCCACT[C/G]AGGAAAGCACCTTAG	645402
rs202112245	snp	A/G	0.309648	0.24278	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336304	CAGTCTACTTTGTGC[A/G]CTGAGTATCTCTTCA	645402
rs202199312	snp	A/C			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335787	CATGAACAATCGATG[A/C]GAGAATCCAGGAGAC	645402
rs367685199	snp	C/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335912	CGATGTTTTCTTCTT[C/G]AGACAGGGCCTCATT	645402
rs368409069	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336171	TAAACTGCCGCCGCA[C/T]GTCCGAAACCACTCA	645402
rs369643631	snp	A/G			synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338542	CAAGTGTGGGATGAA[A/G]AACCACCATCCTGAA	645402
rs371209391	snp	C/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335771	AGGGAACATCTCAGA[C/T]CATGAACAATCGATG	645402
rs371655155	snp	C/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335926	TGAGACAGGGCCTCA[C/T]TCCCGTCACCCGGGC	645402
rs371919115	snp	G/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336465	TCTGAACGTGGAAAG[G/T]TCATCGCTGGAAGGT	645402
rs372211690	snp	C/T			synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338548	TGGGATGAAAAACCA[C/T]CATCCTGAACAGCAA	645402
rs375260244	snp	C/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335151	CATGACTCGCAGACA[C/G]GTTATCGATTGGGCT	645402
rs376399976	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336769	AATAAGGCAACTGTG[C/T]GGCCACTGTCCCAAC	645402
rs376799710	snp	C/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335716	TTTGCACCAAATGTG[C/T]TAACTGCAATTCCAC	645402
rs527306668	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335907	GTCTCCGATGTTTTC[C/T]TCTTGAGACAGGGCC	645402
rs527610811	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336183	GCACGTCCGAAACCA[C/T]TCACTATACAATGTC	645402
rs528645605	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336787	CCACTGTCCCAACCC[A/G]GTTACACTCATATTA	645402
rs528700270	snp	A/G	0.00358086	0.0421617	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338090	GCTGTGCTGGTCCAC[A/G]CTGGGTGGAGTTGTC	645402
rs528883615	snp	A/G	0.00110233	0.023451	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337168	GTTCAACCACTTTTC[A/G]AAACTCACATCTTCT	645402
rs530052780	snp	A/G	0.00727263	0.0598617	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338724	CAGAGTGGAAGTACC[A/G]ACCCACACTGAGGGG	645402
rs530969009	snp	C/T	0.000399281	0.0141238	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338694	GCAAGAGATCTCTGC[C/T]TGTGTGCCAGTGATC	645402
rs530975451	snp	C/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336361	GATGCTTTAGTATTT[C/G]GCAGCCTAGCTTCCA	645402
rs531284839	snp	C/G	0.000798403	0.0199641	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338141	TATGTCAAAGCTCAA[C/G]AAGGCCAGTGGTATA	645402
rs532813508	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336717	ACACACACGGTTTCA[C/T]AGATAAAGATTTCTT	645402
rs532902911	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336266	GTCTCTCGGTGATTG[A/C]ATGATTTCCCCAAAG	645402
rs535308401	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335968	ATAATTTTCCTTGTT[A/T]GCTTTTGTCAAAATT	645402
rs536201819	snp	A/G	0.000399281	0.0141238	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338171	AAAATGGATGATGCC[A/G]AGGTCACTGTCTGTA	645402
rs536534949	snp	C/T	0.0456336	0.143994	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339074	AGGGGACATGGTTTA[C/T]TATTTCCTCTTGGGG	645402
rs537064661	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336950	TTGATTGTTTTATCG[C/T]GCACCTGATGGGTGG	645402
rs537195855	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339043	TGACCTGTAGGTTTG[C/T]GTGTGAGGTTATTGC	645402
rs537381261	snp	A/C	0.000798403	0.0199641	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338368	TTGCCTCCAGGTACC[A/C]GAGTTGGACGAGCAC	645402
rs537405141	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336494	GTCTGTTGGATTCCA[C/T]GGATCTCTCCTTTAT	645402
rs538744102	snp	A/G	0.00604224	0.0546316	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338326	AGACAGGCCAGCAAC[A/G]CAAGGAGAGCTCAAG	645402
rs539167949	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338780	ATACACCCACAAGCG[C/T]GCACGGAAACACACC	645402
rs540980596	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336679	ACACACACACACACA[A/C]ACACACACACACACA	645402
rs541194778	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337044	ATTTGAAGACTCTCT[C/T]GGAAGAGATAGCGTC	645402
rs541947035	snp	A/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336333	CAAACTTCAGTGCAT[A/G]TTTCTACCATTTGAT	645402
rs542616476	snp	C/G	0.000399281	0.0141238	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338622	AGTCCATGAACACTG[C/G]CACACTCGCTTCTCT	645402
rs542690820	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336553	ATACTATACTTCATT[G/T]ACTATTCTCAGGTCA	645402
rs542753404	snp	C/T	0.000363835	0.0134828	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337184	AAACTCACATCTTCT[C/T]GGCCAGATGCAGCTT	645402
rs543592748	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336032	GCCATTATCACATAC[A/G]TGTGGAAATAGTATC	645402
rs543716343	snp	C/T	0.0196464	0.0971453	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337111	GATCCTTGTTGCGGG[C/T]GACATGGGGGACGAC	645402
rs544775790	snp	C/G	0	0	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338647	TTCTCTGCAAGGGAG[C/G]ACCAGGAGATCCAAA	645402
rs545098731	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339107	TGTTTCTTTCGTCAG[C/T]TGTTGGTCGTCAAGA	645402
rs546006554	snp	C/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335243	AAGACCCTCCGACGT[C/T]TTGTGTGAAGCCACG	645402
rs546625493	snp	C/G	0.0157968	0.0874577	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338727	AGTGGAAGTACCGAC[C/G]CACACTGAGGGGTAC	645402
rs546713468	snp	A/C	0.00372438	0.0429921	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338301	CAAGAGCCCTTGGCG[A/C]TGAAGACACAGACAG	645402
rs547112887	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335916	GTTTTCTTCTTGAGA[A/C]AGGGCCTCATTCCCG	645402
rs547668128	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336220	ATCTCTCTTTTCTGG[C/T]ACACATAAATTTGGG	645402
rs548087465	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335878	ATCTTCTGTTTCACT[C/G]CCTGCTTTTAAACGT	645402
rs549093207	snp	A/G	0.0138799	0.0821421	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336771	TAAGGCAACTGTGTG[A/G]CCACTGTCCCAACCC	645402
rs549616592	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336282	ATGATTTCCCCAAAG[C/T]CTTTCACAGTCTACT	645402
rs549840791	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335931	CAGGGCCTCATTCCC[A/G]TCACCCGGGCTTTTC	645402
rs550661644	snp	C/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336697	ACACACACACACACA[C/G]AGACACACACACGGT	645402
rs550853409	snp	G/T	0.00278043	0.0371818	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338145	TCAAAGCTCAAGAAG[G/T]CCAGTGGTATAAAAT	645402
rs550865773	snp	C/T	0.000399281	0.0141238	stop-gained, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338702	TCTCTGCTTGTGTGC[C/T]AGTGATCAGAGTGGA	645402
rs551789635	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336862	GAAGTCATGATGTGG[A/G]CTGTGTCTGTTGAAT	645402
rs551916221	snp	A/C/T	0.00118382	0.024301	missense, synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338107	TGGGTGGAGTTGTCA[A/C/T]GACGGATATTACTTC	645402

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