iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

USP17L4

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
rs552377731	snp	A/C	0.000798403	0.0199641	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338784	ACCCACAAGCGCGCA[A/C]GGAAACACACCCACA	645402
rs552419935	snp	A/G			downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338813	CACCCACACAAACAC[A/G]AACACCGTGAATCCT	645402
rs552981467	snp	C/G	0.000798403	0.0199641	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339087	TACTATTTCCTCTTG[C/G]GGTTTGTTTCTTTCG	645402
rs555190136	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336555	ACTATACTTCATTGA[A/C]TATTCTCAGGTCAGA	645402
rs556118850	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335951	CCGGGCTTTTCTACG[A/G]TATAATTTTCCTTGT	645402
rs556966288	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336962	TCGCGCACCTGATGG[A/G]TGGGTGGGGTGTTCC	645402
rs557054694	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336541	ACGCTGTGCTAAATA[C/T]TATACTTCATTGACT	645402
rs557249227	snp	C/G	0.0419388	0.138602	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338586	TGCTAAACCTCTCTT[C/G]GATGAACTCGACAGA	645402
rs557314462	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339044	GACCTGTAGGTTTGC[A/G]TGTGAGGTTATTGCA	645402
rs557784922	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337064	GAGATAGCGTCTTGC[G/T]GCAACCTGCGGTCCC	645402
rs557893188	snp	A/G/T	0.0154817	0.0868488	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336017	TCTATGAAATGTTGA[A/G/T]CCATTATCACATACG	645402
rs557958676	snp	C/T	0.0146672	0.084371	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338351	CTCAAGAGAGACCAC[C/T]CTTGCCTCCAGGTAC	645402
rs558417799	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336432	GCCGGTAATTTCACT[C/T]GGATAGAGAATCAAT	645402
rs559197894	snp	A/T	0.000399281	0.0141238	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338626	CATGAACACTGGCAC[A/T]CTCGCTTCTCTGCAA	645402
rs559486076	snp	A/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335267	AGCCACGGCATCTGC[A/G]TTGCTCATGCTTCTG	645402
rs561221381	snp	C/G	0.0788843	0.182262	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338711	GTGTGCCAGTGATCA[C/G]AGTGGAAGTACCGAC	645402
rs561530892	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336180	GCCGCACGTCCGAAA[C/T]CACTCACTATACAAT	645402
rs561601140	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335903	AAACGTCTCCGATGT[A/T]TTCTTCTTGAGACAG	645402
rs563602412	snp	C/G/T	0.00358923	0.042236	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336750	CTGACATTCTTTTAC[C/G/T]TAAAATAAGGCAACT	645402
rs563761275	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336123	TAGTTGGGATACCTT[C/T]GGATTTCTCAAGGTT	645402
rs563968848	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336263	TTAGTCTCTCGGTGA[C/T]TGCATGATTTCCCCA	645402
rs564361287	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336709	ACAGAGACACACACA[C/G]GGTTTCATAGATAAA	645402
rs564782612	snp	A/G	0.00119737	0.0244387	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339113	TTTCGTCAGTTGTTG[A/G]TCGTCAAGAGAAGGT	645402
rs565316593	snp	A/C/T	7.78489e-05	0.00623854	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338125	CGGATATTACTTCTC[A/C/T]TATGTCAAAGCTCAA	645402
rs565516782	snp	C/G	0.000798403	0.0199641	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338658	GGAGGACCAGGAGAT[C/G]CAAAGGGAAGAACAA	645402
rs566315459	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336786	GCCACTGTCCCAACC[C/T]GGTTACACTCATATT	645402
rs566728751	snp	A/G	0.0130921	0.0798413	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338779	AATACACCCACAAGC[A/G]CGCACGGAAACACAC	645402
rs566924712	snp	A/G	0.00755907	0.0610114	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338316	CTGAAGACACAGACA[A/G]GCCAGCAACGCAAGG	645402
rs567320264	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336966	GCACCTGATGGGTGG[A/G]TGGGGTGTTCCCGGC	645402
rs567332948	snp	A/G	0.000126398	0.00794878	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338161	CCAGTGGTATAAAAT[A/G]GATGATGCCGAGGTC	645402
rs570405946	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335918	TTTCTTCTTGAGACA[C/G]GGCCTCATTCCCGTC	645402
rs571427085	snp	A/C	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338811	CACACCCACACAAAC[A/C]CGAACACCGTGAATC	645402
rs571560416	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336456	AATCAATAGTCTGAA[C/G]GTGGAAAGGTCATCG	645402
rs572196711	snp	A/G	0.00755907	0.0610114	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336573	TTCTCAGGTCAGAAA[A/G]TGCACTTCAGACTTC	645402
rs572446772	in-del	-/CA			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336665	CCCAGCACAAGCGCA[-/CA]CACACACACACACAC	645402
rs572740715	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335962	TACGGTATAATTTTC[C/G]TTGTTTGCTTTTGTC	645402
rs572742934	snp	A/G	0.00716266	0.059414	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339102	GGGTTTGTTTCTTTC[A/G]TCAGTTGTTGGTCGT	645402
rs572927038	snp	C/T	0.0377219	0.132053	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338629	GAACACTGGCACACT[C/T]GCTTCTCTGCAAGGG	645402
rs573682568	snp	C/T	0.00119737	0.0244387	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338594	CTCTCTTCGATGAAC[C/T]CGACAGATCAGGAGT	645402
rs573832387	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336543	GCTGTGCTAAATACT[A/T]TACTTCATTGACTAT	645402
rs573946894	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339069	ATTGCAGGGGACATG[G/T]TTTACTATTTCCTCT	645402
rs575457513	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7339118	TCAGTTGTTGGTCGT[C/T]AAGAGAAGGTGAAAT	645402
rs575833794	snp	G/T	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336124	AGTTGGGATACCTTT[G/T]GATTTCTCAAGGTTT	645402
rs577756705	snp	C/T	0.000399281	0.0141238	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338364	ACCCTTGCCTCCAGG[C/T]ACCCGAGTTGGACGA	645402
rs577901479	snp	C/T	0.00189215	0.0307	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337066	GATAGCGTCTTGCTG[C/T]AACCTGCGGTCCCAG	645402
rs745474279	snp	C/T			synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338296	GGAACCAAGAGCCCT[C/T]GGCGCTGAAGACACA	645402
rs745551738	snp	C/G	2.59892e-05	0.00360471	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338124	ACGGATATTACTTCT[C/G]TTATGTCAAAGCTCA	645402
rs746231963	snp	A/G	4.23191e-05	0.00459976	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338745	CACTGAGGGGTACAC[A/G]CACACACACACAAAC	645402
rs746618057	snp	A/C	4.62203e-05	0.00480708	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337238	CTCCCTGAGAAGTCA[A/C]CACTCTCATCTGAGA	645402
rs746750613	snp	A/T	2.60794e-05	0.00361096	stop-gained, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338116	TTGTCACGACGGATA[A/T]TACTTCTCTTATGTC	645402
rs747433178	snp	G/T	5.77918e-05	0.00537518	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338734	GTACCGACCCACACT[G/T]AGGGGTACACACACA	645402
rs747762105	snp	A/C			synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337951	GGTCCTCATCCTTGT[A/C]TTGAAGAGATTCTCC	645402
rs747919799	snp	G/T	0.000717617	0.0189286	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337094	CAGCAGAAAAACCTT[G/T]TGATCCTTGTTGCGG	645402
rs748763060	snp	A/G	6.93842e-05	0.00588959	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338317	TGAAGACACAGACAG[A/G]CCAGCAACGCAAGGA	645402
rs749060735	snp	A/G			missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337491	AGTGCTGCATGCTCT[A/G]TACTATGCAAGCTCA	645402
rs749206974	snp	C/T	1.97147e-05	0.00313958	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337079	TGCAACCTGCGGTCC[C/T]AGCAGAAAAACCTTG	645402
rs750578429	snp	A/G	0.000131149	0.00809674	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337124	GGCGACATGGGGGAC[A/G]ACTCACTCTACTTGG	645402
rs750806733	snp	C/T	1.83145e-05	0.00302604	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338089	TGCTGTGCTGGTCCA[C/T]GCTGGGTGGAGTTGT	645402
rs751283010	snp	A/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336060	ATCACCCATGCTGTG[A/T]GATACGTTGTTTTGA	645402
rs751390643	snp	C/T	3.8684e-05	0.00439778	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338636	GGCACACTCGCTTCT[C/T]TGCAAGGGAGGACCA	645402
rs751572842	snp	C/G	0.000100175	0.00707655	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338203	CATCACTTCTGTCCT[C/G]AGTCAACAGGCCTAT	645402
rs751806040	in-del	-/TTAA			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336917	CCTGTGACTCATTCC[-/TTAA]TTGAGTGCTGATATT	645402
rs752130882	snp	A/G/T	0.00087776	0.020933	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337121	GCGGGCGACATGGGG[A/G/T]ACGACTCACTCTACT	645402
rs752222866	in-del	-/GCGC			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336660	TTCATCCCAGCACAA[-/GCGC]ACACACACACACACA	645402
rs753307947	in-del	-/G	0.000180382	0.00949518	frameshift-variant, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338135	TTCTCTTATGTCAAA[-/G]CTCAAGAAGGCCAGT	645402
rs753949129	snp	A/C	2.55699e-05	0.00357551	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338142	ATGTCAAAGCTCAAG[A/C]AGGCCAGTGGTATAA	645402
rs754151918	snp	A/G	6.29228e-05	0.00560869	stop-gained, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338097	TGGTCCACGCTGGGT[A/G]GAGTTGTCACGACGG	645402
rs754453870	in-del	-/CT	0.000108867	0.00737711	frameshift-variant, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338221	CAACAGGCCTATGTC[-/CT]CTCTTTTACATCCAG	645402
rs754999461	snp	G/T	4.27487e-05	0.00462304	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338103	ACGCTGGGTGGAGTT[G/T]TCACGACGGATATTA	645402
rs755125135	snp	C/T	6.27372e-05	0.00560042	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337174	CCACTTTTCAAAACT[C/T]ACATCTTCTCGGCCA	645402
rs755941182	snp	G/T	7.59071e-05	0.00616018	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338696	AAGAGATCTCTGCTT[G/T]TGTGCCAGTGATCAG	645402
rs756162854	snp	C/T	0.000313234	0.0125108	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337070	GCGTCTTGCTGCAAC[C/T]TGCGGTCCCAGCAGA	645402
rs756323226	snp	C/G	0.000283006	0.0118921	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337139	GACTCACTCTACTTG[C/G]GAGGTGAGTGGCAGT	645402
rs756944068	snp	C/T	0.00237248	0.03436	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338224	ACAGGCCTATGTCCT[C/T]TTTTACATCCAGAAG	645402
rs757253895	snp	C/T	7.6118e-05	0.00616873	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338637	GCACACTCGCTTCTC[C/T]GCAAGGGAGGACCAG	645402
rs757686909	snp	A/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336720	cacacGGTTTCATAG[A/G]TAAAGATTTCTTCCC	645402
rs758008744	in-del	-/AC	0.00938946	0.0678717	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338741	CCCACACTGAGGGGT[-/AC]ACACACACACACACA	645402
rs758593663	snp	A/G	3.29234e-05	0.00405717	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338172	AAATGGATGATGCCG[A/G]GGTCACTGTCTGTAG	645402
rs758830756	in-del	-/ACAC	0.00240384	0.0345853	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338741	CCCACACTGAGGGGT[-/ACAC]ACACACACACACAAA	645402
rs758964561	snp	A/G	0.00432898	0.0463223	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337894	TCTTTGTCTCCAGAG[A/G]GCGCCGGCCTCCAAC	645402
rs759137651	snp	C/G	0.000160424	0.00895466	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337114	CCTTGTTGCGGGCGA[C/G]ATGGGGGACGACTCA	645402
rs760086103	in-del	-/GC			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336662	CATCCCAGCACAAGC[-/GC]ACACACACACACACA	645402
rs760413713	snp	A/G	0.000737871	0.0191935	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337108	TGTGATCCTTGTTGC[A/G]GGCGACATGGGGGAC	645402
rs762260966	snp	C/T	2.59004e-05	0.00359854	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338128	ATATTACTTCTCTTA[C/T]GTCAAAGCTCAAGAA	645402
rs762315917	snp	A/C	0.00011441	0.00756253	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338081	GTCCTCTATGCTGTG[A/C]TGGTCCACGCTGGGT	645402
rs763272292	snp	C/T	1.95984e-05	0.00313031	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338754	GTACACACACACACA[C/T]ACAAACACAAATACA	645402
rs764265825	snp	C/T			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7335410	GGACCACACCTGGCC[C/T]ATGAAAAGACAAGGG	645402
rs764860262	snp	C/T	0.000222247	0.0105392	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338067	GACCTCTTGTCTATG[C/T]CCTCTATGCTGTGCT	645402
rs765366258	snp	C/T	0.000382795	0.0138293	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338146	CAAAGCTCAAGAAGG[C/T]CAGTGGTATAAAATG	645402
rs765526325	snp	A/G	0.000259034	0.0113776	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338417	GAGGAAAGCACCTTA[A/G]ACCACTGGAAATTCC	645402
rs766475210	snp	C/G	3.63709e-05	0.00426429	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338093	GTGCTGGTCCACGCT[C/G]GGTGGAGTTGTCACG	645402
rs766820840	snp	C/G	5.14973e-05	0.00507405	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338136	TCTCTTATGTCAAAG[C/G]TCAAGAAGGCCAGTG	645402
rs767171073	snp	A/G	3.58224e-05	0.00423201	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338642	CTCGCTTCTCTGCAA[A/G]GGAGGACCAGGAGAT	645402
rs767883200	snp	C/T	0.00232355	0.0340055	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337123	GGGCGACATGGGGGA[C/T]GACTCACTCTACTTG	645402
rs768218594	snp	C/T	0.000304206	0.0123292	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338325	CAGACAGGCCAGCAA[C/T]GCAAGGAGAGCTCAA	645402
rs768472455	snp	G/T			synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337912	GCCGGCCTCCAACAC[G/T]TTAACTTTACACACT	645402
rs768498141	snp	C/G	3.90274e-05	0.00441726	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337082	AACCTGCGGTCCCAG[C/G]AGAAAAACCTTGTGA	645402
rs770342558	snp	A/G	8.16827e-05	0.0063902	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338747	CTGAGGGGTACACAC[A/G]CACACACACAAACAC	645402
rs770470319	snp	A/G	0.000895723	0.0211438	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337262	TCTGAGACCCGTGTC[A/G]ACCTCTGTGATGATT	645402
rs770826811	snp	C/G/T	5.19659e-05	0.00509713	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338123	GACGGATATTACTTC[C/G/T]CTTATGTCAAAGCTC	645402
rs771931171	snp	A/G	0.000365698	0.0135172	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337185	AACTCACATCTTCTC[A/G]GCCAGATGCAGCTTT	645402
rs772055532	snp	C/G	0.000383362	0.0138396	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337106	CTTGTGATCCTTGTT[C/G]CGGGCGACATGGGGG	645402
rs772537769	snp	A/G	0.0037383	0.0430718	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338737	CCGACCCACACTGAG[A/G]GGTACACACACACAC	645402
rs772543539	snp	C/T	2.58715e-05	0.00359654	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338130	ATTACTTCTCTTATG[C/T]CAAAGCTCAAGAAGG	645402
rs772982550	snp	C/T	0.000377287	0.0137296	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337107	TTGTGATCCTTGTTG[C/T]GGGCGACATGGGGGA	645402
rs773142214	snp	A/C	8.9811e-05	0.00670055	stop-gained, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337236	CTCTCCCTGAGAAGT[A/C]ACCACTCTCATCTGA	645402
rs773745124	snp	A/C/G	7.73452e-05	0.00621833	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338135	TTCTCTTATGTCAAA[A/C/G]CTCAAGAAGGCCAGT	645402
rs774168261	snp	C/T			synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337945	TGCCAAGGTCCTCAT[C/T]CTTGTCTTGAAGAGA	645402
rs774394946	snp	G/T	1.90736e-05	0.00308811	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337093	CCAGCAGAAAAACCT[G/T]GTGATCCTTGTTGCG	645402
rs774786353	snp	G/T	3.76556e-05	0.00433894	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338075	GTCTATGTCCTCTAT[G/T]CTGTGCTGGTCCACG	645402
rs775798171	snp	C/G	2.00282e-05	0.00316445	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338750	AGGGGTACACACACA[C/G]ACACACAAACACAAA	645402
rs775922829	snp	C/T	0.000891398	0.0210928	synonymous-codon, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338434	CCACTGGAAATTCCC[C/T]CAAGAGCAAAACAAA	645402
rs776030482	snp	A/G	0.000167043	0.00913747	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337112	ATCCTTGTTGCGGGC[A/G]ACATGGGGGACGACT	645402
rs776387377	snp	C/G	0.000841397	0.0204937	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337363	GGGGGCTGGGCTCCA[C/G]AATATGGGAAATACC	645402
rs777052084	snp	A/G	5.00939e-05	0.00500444	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338741	CCCACACTGAGGGGT[A/G]CACACACACACACAC	645402
rs777096214	snp	A/G			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336662	CATCCCAGCACAAGC[A/G]CACACACACACACAC	645402
rs777849931	snp	C/T	0.000774293	0.0196608	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338193	CTGTCTGTAGCATCA[C/T]TTCTGTCCTGAGTCA	645402
rs777909045	snp	A/G	8.54762e-05	0.00653688	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338111	TGGAGTTGTCACGAC[A/G]GATATTACTTCTCTT	645402
rs778490142	snp	G/T	5.95362e-05	0.00545569	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338733	AGTACCGACCCACAC[G/T]GAGGGGTACACACAC	645402
rs779449584	in-del	-/G	0.00361662	0.0423702	frameshift-variant, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338297	GAACCAAGAGCCCTT[-/G]GCGCTGAAGACACAG	645402
rs779673363	snp	G/T	0.00340715	0.0411335	downstream-variant-500B, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338708	CTTGTGTGCCAGTGA[G/T]CAGAGTGGAAGTACC	645402
rs780003940	snp	A/G	4.0097e-05	0.00447738	upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7337074	CTTGCTGCAACCTGC[A/G]GTCCCAGCAGAAAAA	645402
rs781050527	snp	A/T	0.0149916	0.0852706	missense, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7338240	TTTTACATCCAGAAG[A/T]GTGAATGGGAAAGAC	645402
rs796421144	in-del	-/CA			upstream-variant-2KB, intron-variant	USP17L4, FAM66B	GRCh38.p7	8:7336695	ACACACACACACACA[-/CA]GAGACACACACACGG	645402