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

USP17L7

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs2466115	snp	A/G	0.459687	0.136129	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134830	ATGCACTGAAGTTTG[A/G]AGAGTTACTCAGTGC	392197
rs2698949	snp	C/G	0.405776	0.195535	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132039	TGAAACAAACCCCAA[C/G]AGGAAATAGTAAACC	392197
rs2698950	snp	C/T	0.24019	0.249807	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132227	GGGCTCATCCTGAGA[C/T]GCAGCCATCACTATC	392197
rs2698968	snp	C/T	0.104489	0.20329	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133936	TCACATCTTCTCGGC[C/T]AGATGCAGCTTTTGC	392197
rs2719627	snp	C/T	0.417196	0.185864	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134488	gtgtgtgtgtgtgtg[C/T]gCTTGTGCTGGGATG	392197
rs2954096	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134423	TGAAACCgtgtgtgt[A/G]tctgtgtgtgtgtgt	392197
rs2954097	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134535	CTTTTGGCAGCTACC[A/G]TCATCCTCTCAGCGA	392197
rs2954098	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134557	TCTCAGCGATGGAAG[C/G]ACAAGAAGTCTGAAG	392197
rs2954099	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134576	AGAAGTCTGAAGTGC[A/G]CTTTCTGACCTGAGA	392197
rs3958835	snp	C/T	0.375399	0.216275	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135849	ACAGGGAGAAAGAAG[C/T]CACCATTTTCAGGAG	392197
rs3958836	snp	A/G	0.487621	0.0776941	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135924	ACAAGACGTCGGAGG[A/G]TCTTATTCCTGCAGC	392197
rs3989687	snp	A/G	0	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135941	CTTATTCCTGCAGCC[A/G]GGACCTGGGCATCGG	392197
rs3989704	snp	C/T	0.00222215	0.0332586	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132959	CAGTGACCTCGGCAT[C/T]ATCCATTTTATACCA	392197
rs3989705	snp	A/G	0.0117151	0.0756327	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133014	AGAGAAGTAATGTCC[A/G]TTGTGACAACTCCAC	392197
rs3989706	snp	C/G/T	0.00441842	0.0467949	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133016	AGAAGTAATGTCCGT[C/G/T]GTGACAACTCCACCC	392197
rs5889395	in-del	-/TG/TGTG	0.625	0.125	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132364	GTGTGTGTGTGTGTG[-/TG/TGTG]CACCCATCAGTGTGG	392197
rs9329263	snp	A/C	0.366083	0.221415	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132388	TGTGTGTGTGCACCC[A/C]TCAGTGTGGGTCGGT	392197
rs9694757	snp	C/G	0.10021	0.200157	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132477	TTTGGATCTCCTGGT[C/G]CTCCCTTGCAGAGAA	392197
rs9694759	snp	A/G	0.0952597	0.196355	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132529	GACTCCTGATCTGTC[A/G]GTTTCGTCGAAGAGA	392197
rs9694780	snp	A/G/T	0.103409	0.202512	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132799	TTGAGCTCTCCTTGC[A/G/T]TTGCTGGCCTGTCTG	392197
rs9720197	snp	A/G	0.356615	0.226126	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133601	CATGGCCAGGACTGT[A/G]GAGGGCCCATGTGAT	392197
rs9720235	snp	C/T	0.494653	0.051427	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133373	CAAAGGTGTCTGAAA[C/T]GCCGTGGCAGTGGAG	392197
rs9720236	snp	C/T	0.00915577	0.0670377	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133413	TTGAGATCTCCAATA[C/T]GCTCCAAATATTTGG	392197
rs9721012	snp	G/T	0.356697	0.226154	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133598	TGACATGGCCAGGAC[G/T]GTGGAGGGCCCATGT	392197
rs9772134	snp	A/G	0	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134927	CCCAAATTTATGTGT[A/G]CCAGAAAAGAGAGAT	392197
rs9772207	snp	C/G	0.473543	0.111932	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134679	AAACAGACCTTCCAG[C/G]GATAACCTTTCCACG	392197
rs9772248	snp	A/C	0	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135011	AACATGAAACAAAAA[A/C]CTTGAGAAATCCAAA	392197
rs9772263	snp	A/C	0.132409	0.220618	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135073	AGAACTGATGAAAAT[A/C]AAAACAACATATCTC	392197
rs9773954	snp	A/G	0.0948562	0.196037	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135082	GAAAATCAAAACAAC[A/G]TATCTCACAGCATGG	392197
rs9801894	snp	C/T	0.112983	0.209108	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135891	GAAGCATGAGCAATG[C/T]AGATGTCGTGGCTTC	392197
rs11779232	snp	G/T			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12131973	GAATGATCCACGGAT[G/T]TACCACATGAGCAAA	392197
rs11989796	snp	A/G	0.368324	0.220226	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134841	TTTGAAGAGTTACTC[A/G]GTGCACAAAGTAGAC	392197
rs11989822	snp	A/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134999	GCAGTTTAAGAAAAC[A/T]TGAAACAAAAAACTT	392197
rs11991871	snp	A/G	0.000793426	0.0199018	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133329	ACTCTGAGCTGCCTG[A/G]ATATCCAGGGCGATG	392197
rs11991960	snp	C/G	0.00489112	0.0492101	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133621	GCCCATGTGATGTGA[C/G]CTTGCATAGTACAGA	392197
rs13278959	snp	C/T	0.389702	0.207324	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132686	TCGTTTTGTTTTGCT[C/T]TTGGGGGAATTTCCA	392197
rs17815120	snp	C/G	0.18865	0.242872	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133528	ATGAGAAATTCATGG[C/G]CATCCTCCTGCTCAC	392197
rs28546619	snp	A/G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134464	GTGTGTGTGTGTGTG[A/G/T]GTGTGTTTGTGTGTG	392197
rs28594743	snp	C/G	0.102634	0.20196	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133546	TCCTCCTGCTCACCT[C/G]TATGGAAGCCAGCAG	392197
rs28734770	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134439	TCTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	392197
rs35096499	in-del	-/GCAAAAAT			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135343	CAAAAATGCAAAAAT[-/GCAAAAAT]AAGCCGTGTGTCTCC	392197
rs35367402	in-del	-/T			frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133435	CCAAGGACACCACCC[-/T]TCATCCACCAAATAT	392197
rs55751927	snp	A/G	0.399968	0.200024	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134146	TCACCCCCTCCAACC[A/G]CGAACACCCCACCCA	392197
rs56195358	snp	A/G	0.110285	0.207319	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133910	CAGAGAGAGAAGTCC[A/G]CTGGATTTCAGCAAA	392197
rs56236622	in-del	-/GCAAAAAT	0.357238	0.225832	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135328	TTTCACAGGGAAAAG[-/GCAAAAAT]GCAAAAATAAGCCGT	392197
rs71205056	in-del	-/GTGTGTGTGT	0	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134461	TGTGTGTGTGTGTGT[-/GTGTGTGTGT]TTGTGTGTGTGTGTG	392197
rs72496213	snp	G/T			missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132532	TCCTGATCTGTCGGT[G/T]TCGTCGAAGAGAGGT	392197
rs73663089	snp	A/G	0.100927	0.200699	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133382	CTGAAACGCCGTGGC[A/G]GTGGAGATACTTGAT	392197
rs73663090	snp	C/G	0.00226387	0.033568	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133625	ATGTGATGTGAGCTT[C/G]CATAGTACAGAACAT	392197
rs74450497	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134865	AGTAGACTGTGAAAG[A/C]CTTTGGGGAAATCAT	392197
rs75237423	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134801	TGCCAAATAAAGCAT[C/G]AAATGGTAGAAACAT	392197
rs75673018	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134471	TGTGTGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT	392197
rs75826165	snp	A/G	0.370564	0.219008	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133940	AAGCTGCATCTAGCC[A/G]AGAAGATGTGAGTTT	392197
rs76116057	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134490	GTGTGTGTGTGTGTG[C/T]TTGTGCTGGGATGAA	392197
rs76248036	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134368	CCACACAGTTGCCTT[A/C]TTTTAGGTAAAAGAA	392197
rs77046746	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134887	GGAAATCATGCAATC[A/C]CCGAGAGACTAATTG	392197
rs77358782	snp	G/T	0.5	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134455	TGTGTGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT	392197
rs77948924	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134473	TGTGTGTGTGTGTTT[G/T]TGTGTGTGTGTGTGT	392197
rs78158094	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134532	GTACTTTTGGCAGCT[A/G]CCATCATCCTCTCAG	392197
rs78624849	snp	C/G/T	3.97109e-05	0.00445577	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132524	TCATGGACTCCTGAT[C/G/T]TGTCGGTTTCGTCGA	392197
rs79380368	snp	A/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134835	CTGAAGTTTGAAGAG[A/T]TACTCAGTGCACAAA	392197
rs80158797	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134441	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	392197
rs111280009	snp	C/G	0.5	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134744	CCTGCCAGTGGAGAA[C/G]AAGACAAGTCTTTGC	392197
rs111711022	snp	C/T	0.0562307	0.157967	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134878	AGACTTTGGGGAAAT[C/T]ATGCAATCACCGAGA	392197
rs112027963	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134551	TCATCCTCTCAGCGA[C/T]GGAAGCACAAGAAGT	392197
rs112191142	snp	C/G	0.220843	0.248294	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135631	CGCCAAGGCCTCTGG[C/G]TGTAAAGAAACAGCC	392197
rs112608396	snp	A/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134370	ACACAGTTGCCTTAT[A/T]TTAGGTAAAAGAATG	392197
rs115365463	snp	A/C/T	0.000278735	0.0118021	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133662	CTTGTGAAGATGACA[A/C/T]GTTTGAGAGTCCTCC	392197
rs115444041	snp	A/C/G/T	0.0188297	0.0955158	missense, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134001	CAAATAGAGTGAGTC[A/C/G/T]TCTTCCATGTCGCCC	392197
rs117041743	snp	C/T	0.11157	0.208194	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133701	CATGTAGTTGGAAAG[C/T]GGCAGTGTGTATGTC	392197
rs117044628	snp	C/T	0.338261	0.233902	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133115	GCATGTCACGGCACT[C/T]AGGATATTGCACATT	392197
rs138063292	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135492	GACATGTTCCCTGAA[C/G]TAAGAGGGACAGCAT	392197
rs138217195	snp	A/C/G	0.249415	0.250021	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132805	TCTCCTTGCGTTGCT[A/C/G]GCCTGTCTGTGTCTT	392197
rs138886240	snp	A/G	0.0681886	0.171594	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135779	CAGAAGGCTTCGTGC[A/G]CCTGATGTAAAGTGT	392197
rs139243416	snp	C/T	1.8369e-05	0.00303054	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133791	CACCGCAGCAGGTCT[C/T]CTGCTACTCAGAGGA	392197
rs139723955	snp	A/C	0.021333	0.101051	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132094	GCAAACCTACAGGTC[A/C]ATAGGTCACATTAAG	392197
rs140155563	snp	A/C/G	0.00332191	0.0406209	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133906	TTTTCAGAGAGAGAA[A/C/G]TCCGCTGGATTTCAG	392197
rs141172525	in-del	-/TG			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134472	GTGTGTGTGTGTGTT[-/TG]TGTGTGTGTGTGTGT	392197
rs141263690	snp	A/G	0.00115827	0.0240374	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132645	AGGCAGGGTACCTTC[A/G]ACTTTTCTGACGTTG	392197
rs141419210	snp	A/G	0.000872754	0.0208714	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133630	ATGTGAGCTTGCATA[A/G]TACAGAACATGCAGC	392197
rs143104523	snp	C/T	0.117188	0.211804	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132626	GAATCACAAGTACGT[C/T]GGGAGGCAGGGTACC	392197
rs143142287	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135216	GAAAAGCCCGGGTGA[A/C]GGGAGTGAGGCCCTG	392197
rs143752696	snp	A/G	7.42942e-05	0.00609439	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133965	GAGTTTTGAAAAGTG[A/G]TTGAACTGCCAGTCA	392197
rs144333235	snp	A/C/G	0.0121149	0.076882	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133819	GGAAGCTTCTCCCTG[A/C/G]GAGCAAGCTGTCTTG	392197
rs145870845	snp	C/T	0.0119116	0.076249	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134027	CGCCCGCAACAAGGA[C/T]CACAAGGTTTTTCTG	392197
rs145911199	snp	A/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134682	CAGACCTTCCAGCGA[A/T]AACCTTTCCACGTTC	392197
rs146637764	snp	A/T			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132414	TCGGTACTTCCACTG[A/T]GATCACTGGCACACA	392197
rs146951254	snp	A/C/T	0.000205892	0.0101443	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133597	ATGACATGGCCAGGA[A/C/T]TGTGGAGGGCCCATG	392197
rs147245467	in-del	-/GAT	0.122411	0.214991	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135688	GATGATTTTAAGGAG[-/GAT]GATGGAATGAGAGGA	392197
rs148208217	snp	A/C	0.012319	0.0775097	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132630	CACAAGTACGTTGGG[A/C]GGCAGGGTACCTTCA	392197
rs148843344	snp	A/G	1.8738e-05	0.00306082	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133587	TGAGGGCTGGATGAC[A/G]TGGCCAGGACTGTGG	392197
rs149455714	snp	C/G/T	0.000523132	0.0161661	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132559	AGGTTTAGCAGGGAG[C/G/T]TTTGCTGTTCAGGAT	392197
rs150389377	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135468	AAAATTGTAATGCTG[A/C]CGAAAGTGGACATGT	392197
rs150814956	snp	G/T	0.00772242	0.0616979	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133663	TTGTGAAGATGACAC[G/T]TTTGAGAGTCCTCCC	392197
rs151150377	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134278	CCACATCATGACTTC[C/T]AGAACACCTGAATCA	392197
rs151205280	snp	A/T	0.00557542	0.0525036	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135289	AAACAGAAGATAGCA[A/T]AACCTTTTTAATGCT	392197
rs180723571	snp	A/C	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132033	GACGAATGAAACAAA[A/C]CCCAAGAGGAAATAG	392197
rs180755326	snp	A/G	0.0792508	0.182605	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135799	ATGTAAAGTGTCCTG[A/G]GGGAAGAAAGGAGCA	392197
rs180969344	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134884	TGGGGAAATCATGCA[A/G]TCACCGAGAGACTAA	392197
rs181210111	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135549	TTACCAGGAATGAAG[A/C]TCCTGGCTCTAGGGA	392197
rs181389292	snp	A/G	1.91316e-05	0.0030928	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132831	GTCTTCAGCACCAAG[A/G]GCTCTTGGTTCCCTG	392197
rs181526248	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134768	TCTTTGCATGAAATA[C/T]TCTTGTGGAAGCTAG	392197
rs181719434	snp	A/G	0.000297597	0.0121947	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132673	TTGAACTCAGGCTTC[A/G]TTTTGTTTTGCTCTT	392197
rs182112681	snp	C/T			synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133140	CACATTCTTGGCAAG[C/T]TTGTTGCCTGTGACA	392197
rs182492012	snp	A/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135205	ATTATACCGTAGAAA[A/T]GCCCGGGTGACGGGA	392197
rs183048633	snp	A/T	0.0356406	0.128647	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133357	ATGTCCAGGTAAGGG[A/T]CAAAGGTGTCTGAAA	392197
rs183320421	snp	A/C/G/T	7.40513e-05	0.00608448	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133702	ATGTAGTTGGAAAGC[A/C/G/T]GCAGTGTGTATGTCA	392197
rs183330396	snp	A/T	0.0103295	0.0711199	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135083	AAAATCAAAACAACA[A/T]ATCTCACAGCATGGG	392197
rs183715994	snp	C/G	0.00755907	0.0610114	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134138	TATATAACTCACCCC[C/G]TCCAACCGCGAACAC	392197
rs184084068	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134973	TAGTGAGTGGTTTCG[A/G]ACGTGCGGCGGCAGT	392197
rs184094604	snp	A/C/G	0.108493	0.2061	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133257	AAGACCACAATGATA[A/C/G]GCATTCTCTCCATTG	392197
rs184989495	snp	A/G			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132262	TGTCCCTGTTGTAGA[A/G]ACAGAAACTGGGGCT	392197
rs185065491	snp	A/C/T	0.00518157	0.0506848	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134889	AAATCATGCAATCAC[A/C/T]GAGAGACTAATTGAT	392197
rs185108255	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135361	GCCGTGTGTCTCCTG[A/G]ATTCTCTCATCGATT	392197
rs185302713	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135629	GGCGCCAAGGCCTCT[A/G]GGTGTAAAGAAACAG	392197
rs185388681	snp	C/T	0.0209421	0.100162	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134404	GGGAAGAAATCTTTA[C/T]CTATGAAACCGTGTG	392197
rs185754382	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135286	GTGAAACAGAAGATA[A/G]CATAACCTTTTTAAT	392197
rs186384198	snp	A/C	1.85737e-05	0.00304738	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133187	ATACAAGAATGAGGA[A/C]CTTGGCAGAAGTGGG	392197
rs186655681	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134779	AATACTCTTGTGGAA[G/T]CTAGGCTGCCAAATA	392197
rs186811742	snp	C/G	0.0174175	0.0916809	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135235	AGTGAGGCCCTGTCT[C/G]AAGAAGAAAACATCG	392197
rs187291009	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135098	TATCTCACAGCATGG[C/G]TGATACTGTTTCCAT	392197
rs187577668	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135809	TCCTGGGGGAAGAAA[A/G]GAGCACTGCTTAGAA	392197
rs187862332	snp	A/G	0.0331392	0.124384	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134010	TGAGTCGTCTTCCAT[A/G]TCGCCCGCAACAAGG	392197
rs188210824	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135782	AAGGCTTCGTGCGCC[G/T]GATGTAAAGTGTCCT	392197
rs188462716	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134855	CAGTGCACAAAGTAG[A/G]CTGTGAAAGACTTTG	392197
rs188668641	snp	A/C/G	0.000612791	0.0174939	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133374	AAAGGTGTCTGAAAC[A/C/G]CCGTGGCAGTGGAGA	392197
rs188728937	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135416	CATTTCCAGTTATGC[A/G]TTGTATGGTGGAATT	392197
rs188779607	snp	G/T	0.00994996	0.0698282	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133310	GTTCCAAAGCTTGCT[G/T]GACACTCTGAGCTGC	392197
rs189370611	snp	A/C/G	0.000911984	0.0213348	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132668	TGACGTTGAACTCAG[A/C/G]CTTCGTTTTGTTTTG	392197
rs189531010	snp	A/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134908	AGACTAATTGATGAC[A/T]TTCCCCAAATTTATG	392197
rs189625608	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134140	TATAACTCACCCCCT[C/T]CAACCGCGAACACCC	392197
rs189777952	snp	A/C/G/T	0.000232418	0.0107781	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133109	ATGGCTGCATGTCAC[A/C/G/T]GCACTTAGGATATTG	392197
rs190277747	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135303	ATAACCTTTTTAATG[C/G]TGGCCCTTGTTTCAC	392197
rs190855865	snp	C/G/T	0.00112131	0.0236531	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133265	AATGATAGGCATTCT[C/G/T]TCCATTGAGTTCTTT	392197
rs191271043	snp	A/G	0.0263992	0.111815	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135238	GAGGCCCTGTCTGAA[A/G]AAGAAAACATCGGAG	392197
rs191378034	snp	A/G	0.113278	0.209301	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132747	TTCCACCAAGTGCTC[A/G]TCCAACTCGGGTACC	392197
rs191477508	snp	G/T			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132364	TGGGTGTATTTGTGT[G/T]TGTGTGTGTGTGTGT	392197
rs191528258	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134136	CTTATATAACTCACC[A/C/G]CCTCCAACCGCGAAC	392197
rs191737058	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135111	GGGTGATACTGTTTC[C/T]ATACGTATGTGATAA	392197
rs191905989	snp	C/T	0.0894459	0.191631	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135918	CTTCACACAAGACGT[C/T]GGAGGGTCTTATTCC	392197
rs191958986	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135053	TATAAGCTTTTGTTT[A/G]TTAAAGAACTGATGA	392197
rs192516006	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134144	ACTCACCCCCTCCAA[A/C]CGCGAACACCCCACC	392197
rs192820076	snp	G/T	1.88004e-05	0.00306591	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133570	CCAGCAGCCAATACC[G/T]GTGAGGGCTGGATGA	392197
rs193183127	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135349	ATGCAAAAATAAGCC[A/G]TGTGTCTCCTGGATT	392197
rs199636962	snp	C/T	0.00189254	0.0307032	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133013	AAGAGAAGTAATGTC[C/T]GTTGTGACAACTCCA	392197
rs199704775	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134155	CCAACCGCGAACACC[A/C]CACCCACCCATCAGG	392197
rs199944267	snp	A/G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134516	ATGAACTTCCAAGTA[A/G/T]GTACTTTTGGCAGCT	392197
rs200053052	snp	A/G	0.00100361	0.0223785	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133341	CTGGATATCCAGGGC[A/G]ATGTCCAGGTAAGGG	392197
rs200106662	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135335	GGGAAAAGGCAAAAA[G/T]GCAAAAATAAGCCGT	392197
rs200322250	snp	A/C/G/T	0.0176358	0.0922354	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132773	GTACCTGGAGGCAAG[A/C/G/T]GTGGTCTCTCTTGAG	392197
rs200388551	snp	G/T	0.010127	0.0704341	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133201	ACCTTGGCAGAAGTG[G/T]GTAAAGTTAACGTCT	392197
rs200461881	in-del	-/CAAAAATA			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135337	GAAAAGGCAAAAATG[-/CAAAAATA]AGCCGTGTGTCTCCT	392197
rs200504108	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134697	TAACCTTTCCACGTT[C/G]AGACTATTGATTCTC	392197
rs200535890	in-del	-/GC			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134489	TGTGTGTGTGTGTGT[-/GC]TTGTGCTGGGATGAA	392197
rs200727456	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135169	AAAAAGTTCTAATTT[G/T]GACAAAAGCAAACAA	392197
rs200816630	snp	A/G	0.000627037	0.0176953	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132825	GTCTGTGTCTTCAGC[A/G]CCAAGGGCTCTTGGT	392197
rs200847529	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135384	CATCGATTGTTCATG[C/G]TCTGAGATGTTCCCT	392197
rs200862172	snp	C/T	0.000394244	0.0140345	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133034	GACAACTCCACCCAG[C/T]GTGGACCAGCACAGC	392197
rs201019658	snp	A/C			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132185	TCGGAAGACTCACGA[A/C]CCCAAAACTTGATGT	392197
rs201299300	snp	C/T	0.0239126	0.106698	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132989	ACTGGCCTTCTTGAG[C/T]TTTGACATAAGAGAA	392197
rs201407597	snp	A/T			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132002	AAATTTCACCTTCTC[A/T]TGCCGACCAACAACT	392197
rs201409115	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134700	CCTTTCCACGTTCAG[A/C]CTATTGATTCTCTAT	392197
rs201559161	snp	C/T	0.00210784	0.0323956	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133280	CTCCATTGAGTTCTT[C/T]GGGCTTCACCAACTG	392197
rs201590848	snp	A/G	1.85389e-05	0.00304452	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132691	TTGTTTTGCTCTTGG[A/G]GGAATTTCCAGTGGT	392197
rs201847687	snp	C/G/T	1.86998e-05	0.0030577	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133244	CCTTCTGGAGACAAA[C/G/T]ACCACAATGATAGGC	392197
rs201911351	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135200	GGAAAATTATACCGT[A/G]GAAAAGCCCGGGTGA	392197
rs202073430	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134425	AAACCGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	392197
rs202147612	in-del	-/GC			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135336	GGAAAAGGCAAAAAT[-/GC]AAAAATAAGCCGTGT	392197
rs367882189	snp	C/T	0.00462055	0.0478427	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133147	TTGGCAAGTTTGTTG[C/T]CTGTGACATCGGAGA	392197
rs368104450	snp	A/G			synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132906	GATGTAAAAGAGGAC[A/G]TAGGCCTGTTGACTC	392197
rs368507136	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134170	CCACCCACCCATCAG[G/T]TGTGCGATAAACCAA	392197
rs368540113	snp	A/G	0.0252325	0.109451	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134080	GACGCTATCTCTTCC[A/G]AGAGAGTCTTCAAAT	392197
rs368663151	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135159	GAGATGAAATAAAAA[A/G]TTCTAATTTTGACAA	392197
rs368676698	snp	A/G	3.6916e-05	0.00429612	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133721	GTGTGTATGTCAGGC[A/G]CTGCAGGGAAACGTT	392197
rs368788418	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134760	AAGACAAGTCTTTGC[A/G]TGAAATACTCTTGTG	392197
rs369359218	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134234	CAGGGTGTGTCCCCT[G/T]GCATCGCTGGGAATT	392197
rs369544672	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135000	CAGTTTAAGAAAACA[C/T]GAAACAAAAACCTTG	392197
rs369667197	snp	A/G			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132344	TGTGTTTCCGTGCGC[A/G]CTTGTGGGTGTATTT	392197
rs369691004	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134642	ATTTTTCCTTAATAA[G/T]AAAGGAGAGATCCGT	392197
rs369926544	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135775	CCATCAGAAGGCTTC[A/G]TGCGCCTGATGTAAA	392197
rs370291799	snp	C/T	0.160938	0.233598	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134708	CGTTCAGACTATTGA[C/T]TCTCTATCCGAGTGA	392197
rs370371800	snp	A/C/T	0.326203	0.238165	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133108	TATGGCTGCATGTCA[A/C/T]GGCACTTAGGATATT	392197
rs370584913	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134692	AGCGATAACCTTTCC[A/G]CGTTCAGACTATTGA	392197
rs371172384	snp	A/G	9.19227e-05	0.00677886	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133826	TCTCCCTGGGAGCAA[A/G]CTGTCTTGCCACAGG	392197
rs371377323	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135113	GTGATACTGTTTCCA[C/T]ACGTATGTGATAATG	392197
rs371380053	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135599	ACAGTAAGGAACAGG[A/G]CAGAATTGAGGCCCG	392197
rs371723489	snp	G/T	0.0213662	0.101127	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133173	GGAGAATCTCTTCAA[G/T]ACAAGAATGAGGACC	392197
rs371854419	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135268	GACGTTTAAAAGCAG[G/T]GAGTGAAACAGAAGA	392197
rs372373230	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134206	TATCAGCACTCAATT[A/C]AGGAATGAGTCACAG	392197
rs373078712	snp	A/G/T	0.0222155	0.10303	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132535	TGATCTGTCGGTTTC[A/G/T]TCGAAGAGAGGTTTA	392197
rs373524943	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134663	AGAGATCCGTGGAAT[C/T]AAACAGACCTTCCAG	392197
rs373572965	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134587	GTGCACTTTCTGACC[G/T]GAGAATAGTCAATGA	392197
rs374095675	snp	A/C/G	0.000185774	0.00963612	synonymous-codon, missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132456	CTTGCTGTGTTTGTT[A/C/G]TTCCCTTTGGATCTC	392197
rs374305787	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135130	CGTATGTGATAATGG[A/C]TCAACATTTCATAGA	392197
rs374740639	snp	A/C/G	0.000632386	0.0177712	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134017	TCTTCCATGTCGCCC[A/C/G]CAACAAGGATCACAA	392197
rs374933685	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134881	CTTTGGGGAAATCAT[G/T]CAATCACCGAGAGAC	392197
rs375363545	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134212	CACTCAATTAAGGAA[G/T]GAGTCACAGGGTGTG	392197
rs376125387	snp	A/G	0.000115741	0.00760638	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133449	GAGGGTGGTGTCCTT[A/G]GAGTGATGATCTAGC	392197
rs376133460	snp	C/G			missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133823	GCTTCTCCCTGGGAG[C/G]AAGCTGTCTTGCCAC	392197
rs376386893	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134640	ATATTTTTCCTTAAT[A/G]ATAAAGGAGAGATCC	392197
rs376713833	snp	C/G	0.0130921	0.0798413	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132316	ACGGTGTTCGTGTTT[C/G]TGTGGGTGTGTGTGT	392197
rs376967632	snp	A/G/T	7.5886e-05	0.00615939	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133353	GGCGATGTCCAGGTA[A/G/T]GGGTCAAAGGTGTCT	392197
rs377016217	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135106	AGCATGGGTGATACT[A/G]TTTCCATACGTATGT	392197
rs377222340	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134147	CACCCCCTCCAACCG[C/T]GAACACCCCACCCAC	392197
rs377271473	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134981	GGTTTCGGACGTGCG[A/G]CGGCAGTTTAAGAAA	392197
rs377289436	snp	A/G	0.0216535	0.101774	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133179	TCTCTTCAATACAAG[A/G]ATGAGGACCTTGGCA	392197
rs377424512	in-del	-/GAG			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134642	TTTTTCCTTAATAAT[-/GAG]AAAGGAGAGATCCGT	392197
rs377522933	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135062	TTGTTTATTAAAGAA[C/T]TGATGAAAATCAAAA	392197
rs397703652	in-del	-/GC/TA/TG/TGTG/TT	0.00283887	0.037569	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132382	GTGTGTGTGTGTGTG[-/GC/TA/TG/TGTG/TT]CACCCATCAGTGTGG	392197
rs398007085	in-del	-/GCAAAAAT	0	0	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135336	GGAAAAGGCAAAAAT[-/GCAAAAAT]AAGCCGTGTGTCTCC	392197
rs527428362	snp	A/T	1.84035e-05	0.00303338	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133858	GCCAAATCATCACAG[A/T]GGTCGAAACGGGTCT	392197
rs528107039	snp	A/G	0.0107246	0.0724382	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135225	GGGTGACGGGAGTGA[A/G]GCCCTGTCTGAAGAA	392197
rs528370889	snp	A/C/T	0.00161994	0.0284142	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133494	AAGGCATGCCTTTTT[A/C/T]ATGGCATCCACAGTA	392197
rs528404548	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135518	AGCATTTGGGTGTGT[C/T]TTCAGGCTCTCTGGC	392197
rs528506213	snp	C/G/T	7.54423e-05	0.00614136	synonymous-codon, missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132750	CACCAAGTGCTCGTC[C/G/T]AACTCGGGTACCTGG	392197
rs528575230	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134964	GACATTGTATAGTGA[A/G]TGGTTTCGGACGTGC	392197
rs528594703	snp	C/G	0.00895317	0.0663055	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132554	AAGAGAGGTTTAGCA[C/G]GGAGCTTTGCTGTTC	392197
rs528620689	snp	G/T	0.00755907	0.0610114	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134731	CCGAGTGAAATTACC[G/T]GCCAGTGGAGAACAA	392197
rs528849923	snp	A/G	0.000353196	0.0132843	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133637	CTTGCATAGTACAGA[A/G]CATGCAGCACTTGTG	392197
rs528884685	snp	A/G	0.00130458	0.0255066	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133530	GAGAAATTCATGGGC[A/G]TCCTCCTGCTCACCT	392197
rs528904489	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135898	GAGCAATGCAGATGT[C/T]GTGGCTTCACACAAG	392197
rs528994004	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135614	GCAGAATTGAGGCCC[A/G]GCGCCAAGGCCTCTG	392197
rs529866508	snp	C/T	0.000436147	0.0147609	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132803	GCTCTCCTTGCGTTG[C/T]TGGCCTGTCTGTGTC	392197
rs530047259	snp	A/G	0.00795532	0.062565	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134185	GTGTGCGATAAACCA[A/G]TCAAATATCAGCACT	392197
rs530239874	snp	G/T	0.000160449	0.00895538	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132506	AAGCGAGTGTGCCAG[G/T]GTTCATGGACTCCTG	392197
rs530415582	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132171	GTCCCTCCAGAGGTT[C/T]GGAAGACTCACGAAC	392197
rs530455785	snp	G/T	0.0134861	0.0810011	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134445	TGTGTGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT	392197
rs530582665	snp	A/G	1.91933e-05	0.00309779	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133470	ATGATCTAGCTGCTT[A/G]TGCCCGGGAAGGCAT	392197
rs530629997	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135482	GACGAAAGTGGACAT[C/G]TTCCCTGAACTAAGA	392197
rs530811802	snp	C/T	0.00279162	0.0372561	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132182	GGTTCGGAAGACTCA[C/T]GAACCCAAAACTTGA	392197
rs530899859	snp	A/C/T	0.000844926	0.0205368	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132534	CTGATCTGTCGGTTT[A/C/T]GTCGAAGAGAGGTTT	392197
rs530929945	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134717	TATTGATTCTCTATC[C/T]GAGTGAAATTACCTG	392197
rs531015741	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134533	TACTTTTGGCAGCTA[C/T]CATCATCCTCTCAGC	392197
rs531790636	snp	C/G/T	0.000148815	0.00862492	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134016	GTCTTCCATGTCGCC[C/G/T]GCAACAAGGATCACA	392197
rs531998950	snp	A/G	3.71443e-05	0.00430938	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133627	GTGATGTGAGCTTGC[A/G]TAGTACAGAACATGC	392197
rs532543164	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132159	AACACACAGACAGTC[C/T]CTCCAGAGGTTCGGA	392197
rs532579418	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134381	TTATTTTAGGTAAAA[C/G]AATGTCAGGGAAGAA	392197
rs532666103	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134173	CCCACCCATCAGGTG[C/T]GCGATAAACCAATCA	392197
rs532910719	snp	A/G	0.00953873	0.0683987	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135950	GCAGCCGGGACCTGG[A/G]CATCGGTGTGCTTTC	392197
rs532970163	snp	A/G	0.000533083	0.0163174	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133824	CTTCTCCCTGGGAGC[A/G]AGCTGTCTTGCCACA	392197
rs534219585	snp	C/G	0.00138964	0.0263228	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133571	CAGCAGCCAATACCT[C/G]TGAGGGCTGGATGAC	392197
rs534256114	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135672	GGGCTCATGAAATTC[A/G]GATGATTTTAAGGAG	392197
rs534336835	snp	A/G	4.95013e-05	0.00497475	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132901	TTCTGGATGTAAAAG[A/G]GGACATAGGCCTGTT	392197
rs534375376	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135023	AAACCTTGAGAAATC[A/C]AAAGGTATCCCAACT	392197
rs534423786	snp	A/G	0.000130069	0.00806335	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133679	TTTGAGAGTCCTCCC[A/G]GGACAGCATGTAGTT	392197
rs535156418	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132310	GGATTGACGGTGTTC[A/G]TGTTTGTGTGGGTGT	392197
rs535190169	snp	A/T	0.000283364	0.0118996	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133330	CTCTGAGCTGCCTGG[A/T]TATCCAGGGCGATGT	392197
rs535563714	snp	C/T	2.1017e-05	0.00324161	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132966	CTCGGCATCATCCAT[C/T]TTATACCACTGGCCT	392197
rs536061475	snp	A/G	7.56058e-05	0.00614794	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132620	ATTGATGAATCACAA[A/G]TACGTTGGGAGGCAG	392197
rs536219475	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12131956	ACTATTCAAGGTGGC[A/G]AGAATGATCCACGGA	392197
rs536375858	snp	A/G	0.000277667	0.0117795	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133927	TGGATTTCAGCAAAA[A/G]CTGCATCTAGCCGAG	392197
rs536538963	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132325	GTGTTTGTGTGGGTG[C/T]GTGTGTGTTTCCGTG	392197
rs536577892	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134623	AGTATTTAGCACAGC[A/G]TATATTTTTCCTTAA	392197
rs536672912	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134840	GTTTGAAGAGTTACT[C/T]AGTGCACAAAGTAGA	392197
rs536710686	snp	A/C	0.00795532	0.062565	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134660	AGGAGAGATCCGTGG[A/C]ATCAAACAGACCTTC	392197
rs536743588	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134097	GAGAGTCTTCAAATG[A/G]CCAGCTCTCTGGCCG	392197
rs536751070	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135430	CATTGTATGGTGGAA[C/T]TGCAGTTAGTACATT	392197
rs536984464	snp	A/G/T	0.00088094	0.0209697	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132637	ACGTTGGGAGGCAGG[A/G/T]TACCTTCAACTTTTC	392197
rs537541378	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12131988	GTACCACATGAGCAA[A/G]ATTTCACCTTCTCTT	392197
rs537568298	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134199	AATCAAATATCAGCA[C/G]TCAATTAAGGAATGA	392197
rs538138262	snp	A/G	0.000399281	0.0141238	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133903	GACTTTTCAGAGAGA[A/G]AAGTCCGCTGGATTT	392197
rs538670571	snp	A/G/T	0.000222027	0.0105341	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133914	GAGAGAAGTCCGCTG[A/G/T]ATTTCAGCAAAAGCT	392197
rs538706813	snp	A/C/G	0.00101341	0.0224887	missense, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133734	GCACTGCAGGGAAAC[A/C/G]TTCACATAGAAGGTA	392197
rs538858249	snp	C/G	0.00199481	0.0315187	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132029	AACTGACGAATGAAA[C/G]AAACCCCAAGAGGAA	392197
rs538884548	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134228	GAGTCACAGGGTGTG[C/T]CCCCTTGCATCGCTG	392197
rs538982704	snp	C/T	0.00323347	0.0400784	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134039	GGATCACAAGGTTTT[C/T]CTGCTGGGACCGCAG	392197
rs539577868	snp	A/G	1.88656e-05	0.00307123	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133554	CTCACCTCTATGGAA[A/G]CCAGCAGCCAATACC	392197
rs540206220	in-del	-/A	0.00114284	0.0238771	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133017	AAGTAATGTCCGTTG[-/A]TGACAACTCCACCCA	392197
rs540207737	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135879	GAATGATCCCCAGAA[C/G]CATGAGCAATGCAGA	392197
rs540286411	snp	A/G	0.000798403	0.0199641	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133135	TATTGCACATTCTTG[A/G]CAAGTTTGTTGCCTG	392197
rs540439944	snp	A/G	0.000972986	0.0220351	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133780	AGCCCAGCCCCCACC[A/G]CAGCAGGTCTCCTGC	392197
rs540642030	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135443	AATTGCAGTTAGTAC[A/T]TTTGGTGCAAAAATT	392197
rs540682599	snp	C/T	0.000149276	0.00863804	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132656	CTTCAACTTTTCTGA[C/T]GTTGAACTCAGGCTT	392197
rs540951599	snp	C/T	0.000211402	0.0102789	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133390	CCGTGGCAGTGGAGA[C/T]ACTTGATTTGAGATC	392197
rs541213317	snp	A/G/T	0.000441241	0.0148467	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133843	TGTCTTGCCACAGGA[A/G/T]CCAAATCATCACAGA	392197
rs541243966	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132166	AGACAGTCCCTCCAG[A/G]GGTTCGGAAGACTCA	392197
rs541666502	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134394	AAGAATGTCAGGGAA[G/T]AAATCTTTACCTATG	392197
rs542274020	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134255	GCTGGGAATTCAACA[G/T]ACACAGCCCACATCA	392197
rs542459665	snp	C/T	0.000535083	0.0163479	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132528	GGACTCCTGATCTGT[C/T]GGTTTCGTCGAAGAG	392197
rs542547810	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134694	CGATAACCTTTCCAC[A/G]TTCAGACTATTGATT	392197
rs542585191	snp	C/T	0.0107246	0.0724382	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132078	TGCAATAACCTCACA[C/T]GCAAACCTACAGGTC	392197
rs542660392	snp	A/C/T	0.00398691	0.0444912	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134145	CTCACCCCCTCCAAC[A/C/T]GCGAACACCCCACCC	392197
rs543038276	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132343	GTGTGTTTCCGTGCG[C/T]GCTTGTGGGTGTATT	392197
rs543162081	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134326	ATAGACACATGTAAT[A/G]TGAGTGTAACCGGGT	392197
rs543595482	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134164	AACACCCCACCCACC[A/C]ATCAGGTGTGCGATA	392197
rs544330872	snp	A/G	3.86056e-05	0.00439332	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133438	ATTTGGTGGATGAGG[A/G]TGGTGTCCTTGGAGT	392197
rs544348557	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135469	AAATTGTAATGCTGA[C/G]GAAAGTGGACATGTT	392197
rs544607536	snp	A/G	0.000112444	0.00749728	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133590	GGGCTGGATGACATG[A/G]CCAGGACTGTGGAGG	392197
rs545142644	snp	A/G	1.85493e-05	0.00304537	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133602	ATGGCCAGGACTGTG[A/G]AGGGCCCATGTGATG	392197
rs545366408	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134139	ATATAACTCACCCCC[A/T]CCAACCGCGAACACC	392197
rs545576177	snp	C/G/T	9.60613e-05	0.00692983	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133473	ATCTAGCTGCTTGTG[C/G/T]CCGGGAAGGCATGCC	392197
rs545747311	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135485	GAAAGTGGACATGTT[A/C]CCTGAACTAAGAGGG	392197
rs545957171	snp	C/T	0.0193772	0.0965046	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135815	GGGAAGAAAGGAGCA[C/T]TGCTTAGAAAGATGC	392197
rs546202967	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134909	GACTAATTGATGACT[A/T]TCCCCAAATTTATGT	392197
rs546256179	snp	A/C/T	0.00118843	0.0243479	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133325	TGACACTCTGAGCTG[A/C/T]CTGGATATCCAGGGC	392197
rs546560301	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135068	ATTAAAGAACTGATG[A/G]AAATCAAAACAACAT	392197
rs546561236	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135577	GGATTTTCCCAAAAT[G/T]TCTTAGACAGTAAGG	392197
rs546566395	snp	G/T	1.87549e-05	0.0030622	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132743	CTCTTTCCACCAAGT[G/T]CTCGTCCAACTCGGG	392197
rs546913965	snp	A/G	0.000266236	0.0115346	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133509	CATGGCATCCACAGT[A/G]AACATGAGAAATTCA	392197
rs547069010	snp	G/T	5.68015e-05	0.00532893	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132776	CCTGGAGGCAAGGGT[G/T]GTCTCTCTTGAGCTC	392197
rs547113292	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134971	TATAGTGAGTGGTTT[C/T]GGACGTGCGGCGGCA	392197
rs547254256	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134767	GTCTTTGCATGAAAT[A/G]CTCTTGTGGAAGCTA	392197
rs547749183	snp	A/C/G/T	7.44693e-05	0.00610167	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134050	TTTTTCTGCTGGGAC[A/C/G/T]GCAGGTTGCAGCAAG	392197
rs547817241	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134175	CACCCATCAGGTGTG[C/T]GATAAACCAATCAAA	392197
rs547966532	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134127	GCATCAGCCCTTATA[G/T]AACTCACCCCCTCCA	392197
rs548054319	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134975	GTGAGTGGTTTCGGA[C/T]GTGCGGCGGCAGTTT	392197
rs548549377	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12131968	GGCGAGAATGATCCA[C/T]GGATGTACCACATGA	392197
rs548637790	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134186	TGTGCGATAAACCAA[G/T]CAAATATCAGCACTC	392197
rs548641023	snp	A/G/T	0.00239393	0.0345281	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132172	TCCCTCCAGAGGTTC[A/G/T]GAAGACTCACGAACC	392197
rs549389102	in-del	-/AC	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134256	CTGGGAATTCAACAG[-/AC]ACAGCCCACATCATG	392197
rs549530089	snp	C/G/T	3.68224e-05	0.0042907	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133860	CAAATCATCACAGAG[C/G/T]TCGAAACGGGTCTCA	392197
rs550377621	snp	A/G/T	0.000397133	0.014086	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133542	GGCATCCTCCTGCTC[A/G/T]CCTCTATGGAAGCCA	392197
rs550580622	snp	A/G	5.57823e-05	0.00528091	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133644	AGTACAGAACATGCA[A/G]CACTTGTGAAGATGA	392197
rs550697685	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135617	GAATTGAGGCCCGGC[A/G]CCAAGGCCTCTGGGT	392197
rs551103705	snp	A/G	0.000427712	0.0146176	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133194	AATGAGGACCTTGGC[A/G]GAAGTGGGTAAAGTT	392197
rs551471066	snp	C/T	0.00176441	0.0296495	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133835	GAGCAAGCTGTCTTG[C/T]CACAGGAGCCAAATC	392197
rs551560082	in-del	-/C	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134654	TAATAAAGGAGAGAT[-/C]CGTGGAATCAAACAG	392197
rs551735499	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135250	GAAGAAGAAAACATC[A/G]GAGACGTTTAAAAGC	392197
rs551749569	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134983	TTTCGGACGTGCGGC[A/G]GCAGTTTAAGAAAAC	392197
rs551756980	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135656	ACAGCCCTGGCTTCA[A/G]GGGCTCATGAAATTC	392197
rs551932769	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135980	CATGTTCCTAACTGA[C/T]TTTGAGGGGAGCCCA	392197
rs552054122	snp	A/G	0.00842648	0.0643602	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134008	AGTGAGTCGTCTTCC[A/G]TGTCGCCCGCAACAA	392197
rs552058028	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135198	AAGGAAAATTATACC[A/G]TAGAAAAGCCCGGGT	392197
rs552060040	snp	C/G/T	0.000312369	0.0124936	synonymous-codon, missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132843	AAGGGCTCTTGGTTC[C/G/T]CTGCCTCTTGACACA	392197
rs552674625	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134720	TGATTCTCTATCCGA[A/G]TGAAATTACCTGCCA	392197
rs552711585	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134539	TGGCAGCTACCATCA[C/T]CCTCTCAGCGATGGA	392197
rs552996051	snp	G/T	0.000286448	0.0119642	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132936	CAGGACAGAGGTGAT[G/T]CCAGAGGCAGTGACC	392197
rs553043205	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135024	AACCTTGAGAAATCC[A/G]AAGGTATCCCAACTA	392197
rs553545552	snp	A/G	0.00151991	0.0275254	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133575	AGCCAATACCTGTGA[A/G]GGCTGGATGACATGG	392197
rs553783683	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134229	AGTCACAGGGTGTGT[C/T]CCCTTGCATCGCTGG	392197
rs553814815	snp	A/G	3.7022e-05	0.00430228	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133921	GTCCGCTGGATTTCA[A/G]CAAAAGCTGCATCTA	392197
rs553851468	snp	A/G	0.000147205	0.00857793	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133743	GGAAACGTTCACATA[A/G]AAGGTATTTCCTATC	392197
rs554141240	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134627	TTTAGCACAGCGTAT[A/T]TTTTTCCTTAATAAT	392197
rs554487879	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135302	CATAACCTTTTTAAT[A/G]CTGGCCCTTGTTTCA	392197
rs554577803	snp	C/T	0.00199481	0.0315187	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132341	GTGTGTGTTTCCGTG[C/T]GCGCTTGTGGGTGTA	392197
rs554584958	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134308	AAATTACTCCTCAGG[C/G]TGATAGACACATGTA	392197
rs554777805	snp	C/G	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134099	GAGTCTTCAAATGAC[C/G]AGCTCTCTGGCCGCA	392197
rs554822461	snp	C/G/T	0.000547583	0.0165378	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132623	GATGAATCACAAGTA[C/G/T]GTTGGGAGGCAGGGT	392197
rs555476569	snp	A/G	3.85862e-05	0.00439222	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133410	GATTTGAGATCTCCA[A/G]TACGCTCCAAATATT	392197
rs555503028	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135447	GCAGTTAGTACATTT[G/T]GTGCAAAAATTGTAA	392197
rs555732756	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135758	CATGGGCCAGGTGTG[C/G]TCCATCAGAAGGCTT	392197
rs555747527	snp	A/G	3.70858e-05	0.00430599	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133689	CTCCCGGGACAGCAT[A/G]TAGTTGGAAAGCGGC	392197
rs556110099	snp	A/C/G	1.85824e-05	0.00304809	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133633	TGAGCTTGCATAGTA[A/C/G]AGAACATGCAGCACT	392197
rs556134232	snp	A/G	0.000738907	0.019207	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133712	AAAGCGGCAGTGTGT[A/G]TGTCAGGCACTGCAG	392197
rs556387659	snp	G/T	0.0475351	0.146656	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134223	GGAATGAGTCACAGG[G/T]TGTGTCCCCTTGCAT	392197
rs556424497	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134137	TTATATAACTCACCC[C/T]CTCCAACCGCGAACA	392197
rs557579262	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135298	ATAGCATAACCTTTT[C/T]AATGCTGGCCCTTGT	392197
rs557616126	snp	G/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135059	CTTTTGTTTATTAAA[G/T]AACTGATGAAAATCA	392197
rs558199378	snp	C/G	0.000385027	0.0138696	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132413	GTCGGTACTTCCACT[C/G]TGATCACTGGCACAC	392197
rs558236188	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134670	CGTGGAATCAAACAG[A/G]CCTTCCAGCGATAAC	392197
rs558363901	snp	A/C	0.00016956	0.00920605	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133559	CTCTATGGAAGCCAG[A/C]AGCCAATACCTGTGA	392197
rs558436075	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135383	TCATCGATTGTTCAT[A/G]GTCTGAGATGTTCCC	392197
rs558456148	snp	C/T	0.000516286	0.016059	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133376	AGGTGTCTGAAACGC[C/T]GTGGCAGTGGAGATA	392197
rs559032544	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135396	ATGGTCTGAGATGTT[C/G]CCTCCATTTCCAGTT	392197
rs559101155	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132001	AAAATTTCACCTTCT[C/T]TTGCCGACCAACAAC	392197
rs559244329	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134972	ATAGTGAGTGGTTTC[A/G]GACGTGCGGCGGCAG	392197
rs559508834	snp	A/G/T	0.000362997	0.013468	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132498	TTGCAGAGAAGCGAG[A/G/T]GTGCCAGTGTTCATG	392197
rs559557771	snp	A/G	0.0185938	0.0946107	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132167	GACAGTCCCTCCAGA[A/G]GTTCGGAAGACTCAC	392197
rs559919344	snp	C/T	0.0017465	0.0294991	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134004	ATAGAGTGAGTCGTC[C/T]TCCATGTCGCCCGCA	392197
rs559922453	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134683	AGACCTTCCAGCGAT[A/G]ACCTTTCCACGTTCA	392197
rs560430139	snp	G/T	0.000350939	0.0132418	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133897	AGTGGTGACTTTTCA[G/T]AGAGAGAAGTCCGCT	392197
rs560546561	snp	C/G	0.000283616	0.0119049	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132812	GCGTTGCTGGCCTGT[C/G]TGTGTCTTCAGCACC	392197
rs560937111	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132079	GCAATAACCTCACAC[A/G]CAAACCTACAGGTCA	392197
rs561490947	snp	A/G/T	7.44025e-05	0.00609889	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134013	GTCGTCTTCCATGTC[A/G/T]CCCGCAACAAGGATC	392197
rs562149368	snp	A/G	0.000242282	0.0110037	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133158	GTTGCCTGTGACATC[A/G]GAGAATCTCTTCAAT	392197
rs562649093	in-del	-/TGTG	0.117537	0.212022	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134426	AACCGTGTGTGTGTC[-/TGTG]TGTGTGTGTGTGTGT	392197
rs562661936	snp	G/T	9.60716e-05	0.00693012	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133466	AGTGATGATCTAGCT[G/T]CTTGTGCCCGGGAAG	392197
rs562776638	snp	A/G	1.85813e-05	0.003048	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133976	AGTGATTGAACTGCC[A/G]GTCACCTCCCAAATA	392197
rs563099266	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135470	AATTGTAATGCTGAC[A/G]AAAGTGGACATGTTC	392197
rs563186874	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135115	GATACTGTTTCCATA[C/T]GTATGTGATAATGGC	392197
rs563295803	snp	A/G/T	0.000130821	0.00808673	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133228	GTCTTGGAGGCAGGC[A/G/T]CCTTCTGGAGACAAA	392197
rs563941093	snp	A/C/G/T	0.000500973	0.0158199	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132697	TGCTCTTGGGGGAAT[A/C/G/T]TCCAGTGGTCTAAGG	392197
rs563967441	snp	A/G	0.00089716	0.0211607	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133486	TGCCCGGGAAGGCAT[A/G]CCTTTTTCATGGCAT	392197
rs563993136	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134900	TCACCGAGAGACTAA[C/T]TGATGACTTTCCCCA	392197
rs564428642	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135513	GGGACAGCATTTGGG[C/T]GTGTCTTCAGGCTCT	392197
rs564501069	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134961	CCTGACATTGTATAG[C/T]GAGTGGTTTCGGACG	392197
rs564586486	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134730	TCCGAGTGAAATTAC[C/T]TGCCAGTGGAGAACA	392197
rs564643394	snp	C/T	0.0178098	0.0926698	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132158	AAACACACAGACAGT[C/T]CCTCCAGAGGTTCGG	392197
rs564774899	snp	A/G	4.1474e-05	0.0045536	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133032	GTGACAACTCCACCC[A/G]GCGTGGACCAGCACA	392197
rs565130127	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134337	TAATATGAGTGTAAC[C/T]GGGTTGGGACAGTGG	392197
rs565166725	snp	A/G	0.0107246	0.0724382	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134169	CCCACCCACCCATCA[A/G]GTGTGCGATAAACCA	392197
rs565783916	snp	G/T	0.00199481	0.0315187	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132322	TTCGTGTTTGTGTGG[G/T]TGTGTGTGTGTTTCC	392197
rs565820621	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134612	CAATGAAGTATAGTA[A/T]TTAGCACAGCGTATA	392197
rs565827300	snp	C/G/T	0.000380495	0.0137881	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132603	ACCACACTTGTATTT[C/G/T]GATTGATGAATCACA	392197
rs565870350	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135277	AAGCAGGGAGTGAAA[C/G]AGAAGATAGCATAAC	392197
rs566025666	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134184	GGTGTGCGATAAACC[A/T]ATCAAATATCAGCAC	392197
rs566057511	snp	A/G	0.00358779	0.0422022	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12131949	AGTATCCACTATTCA[A/G]GGTGGCGAGAATGAT	392197
rs567032274	snp	A/C/G/T	0.00116945	0.0241534	missense, stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133676	ACGTTTGAGAGTCCT[A/C/G/T]CCGGGACAGCATGTA	392197
rs567129233	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135657	CAGCCCTGGCTTCAA[C/G]GGCTCATGAAATTCG	392197
rs567424715	snp	A/G	0.00716266	0.059414	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134112	ACCAGCTCTCTGGCC[A/G]CATCAGCCCTTATAT	392197
rs567808536	snp	C/T	0.000239351	0.010937	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133862	AATCATCACAGAGGT[C/T]GAAACGGGTCTCAGA	392197
rs568528232	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135043	GTATCCCAACTATAA[A/G]CTTTTGTTTATTAAA	392197
rs568901860	snp	G/T	0.000204459	0.0101088	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133651	AACATGCAGCACTTG[G/T]GAAGATGACACGTTT	392197
rs569433131	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135623	AGGCCCGGCGCCAAG[A/G]CCTCTGGGTGTAAAG	392197
rs569631835	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134980	TGGTTTCGGACGTGC[A/G]GCGGCAGTTTAAGAA	392197
rs569861778	snp	A/G	3.80996e-05	0.00436444	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132828	TGTGTCTTCAGCACC[A/G]AGGGCTCTTGGTTCC	392197
rs569995585	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12131976	TGATCCACGGATGTA[C/T]CACATGAGCAAAATT	392197
rs570065479	snp	C/T	9.86748e-05	0.00702337	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132848	CTCTTGGTTCCCTGC[C/T]TCTTGACACACTCTC	392197
rs570110213	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134527	AGTATGTACTTTTGG[C/T]AGCTACCATCATCCT	392197
rs570146943	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134190	CGATAAACCAATCAA[A/C]TATCAGCACTCAATT	392197
rs570314293	snp	C/T	0.00597247	0.0543191	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135222	CCCGGGTGACGGGAG[C/T]GAGGCCCTGTCTGAA	392197
rs570427202	snp	C/T	3.74483e-05	0.00432698	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133278	CTCTCCATTGAGTTC[C/T]TTGGGCTTCACCAAC	392197
rs570476851	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135020	CAAAAACCTTGAGAA[A/G]TCCAAAGGTATCCCA	392197
rs570885648	snp	A/C/T	0.00170468	0.0291455	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132537	ATCTGTCGGTTTCGT[A/C/T]GAAGAGAGGTTTAGC	392197
rs570973429	snp	A/T	0.00478085	0.0486577	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132299	TACTTTATGTAGGAT[A/T]GACGGTGTTCGTGTT	392197
rs571398824	snp	C/G			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132119	ATTAAGAAATACACA[C/G]TGAATGTCATCTACC	392197
rs571419920	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134542	CAGCTACCATCATCC[A/T]CTCAGCGATGGAAGC	392197
rs571506388	snp	C/G	0.0178098	0.0926698	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134227	TGAGTCACAGGGTGT[C/G]TCCCCTTGCATCGCT	392197
rs571871421	snp	A/C/T	0.000551222	0.0165926	missense, stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133814	TCAGAGGAAGCTTCT[A/C/T]CCTGGGAGCAAGCTG	392197
rs571978682	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134240	GTGTCCCCTTGCATC[A/G]CTGGGAATTCAACAG	392197
rs572366882	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135401	CTGAGATGTTCCCTC[C/T]ATTTCCAGTTATGCA	392197
rs572404585	snp	A/G	4.23146e-05	0.00459951	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132423	CCACTGTGATCACTG[A/G]CACACAAGCAGAGAT	392197
rs572487704	snp	A/T	0.00177551	0.0297423	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133925	GCTGGATTTCAGCAA[A/T]AGCTGCATCTAGCCG	392197
rs572673992	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135753	CTTTTCATGGGCCAG[G/T]TGTGCTCCATCAGAA	392197
rs572923022	snp	C/T	9.1894e-05	0.0067778	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133753	ACATAGAAGGTATTT[C/T]CTATCTTCTGGAGCC	392197
rs573083335	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135852	GGGAGAAAGAAGCCA[C/T]CATTTTCAGGAGAAT	392197
rs573118805	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135410	TCCCTCCATTTCCAG[C/T]TATGCATTGTATGGT	392197
rs573193008	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135081	TGAAAATCAAAACAA[C/T]ATATCTCACAGCATG	392197
rs573247048	snp	A/C/G/T	7.56435e-05	0.00614954	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133127	ACTTAGGATATTGCA[A/C/G/T]ATTCTTGGCAAGTTT	392197
rs573704047	snp	C/T	0.00716266	0.059414	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135761	GGGCCAGGTGTGCTC[C/T]ATCAGAAGGCTTCGT	392197
rs573713380	in-del	-/T	0.00501886	0.0498422	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133952	CCGAGAAGATGTGAG[-/T]TTTTGAAAAGTGATT	392197
rs573777495	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135448	CAGTTAGTACATTTG[C/G]TGCAAAAATTGTAAT	392197
rs573797037	snp	C/G/T	0.000166768	0.00913008	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133939	AAAGCTGCATCTAGC[C/G/T]GAGAAGATGTGAGTT	392197
rs573860450	snp	C/G/T	7.35071e-05	0.00606211	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133795	GCAGCAGGTCTCCTG[C/G/T]TACTCAGAGGAAGCT	392197
rs573920491	snp	A/G	0.000399281	0.0141238	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133580	ATACCTGTGAGGGCT[A/G]GATGACATGGCCAGG	392197
rs574021705	snp	C/T	0.00119737	0.0244387	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133411	ATTTGAGATCTCCAA[C/T]ACGCTCCAAATATTT	392197
rs574064126	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134894	ATGCAATCACCGAGA[G/T]ACTAATTGATGACTT	392197
rs574433245	snp	C/T	2.14931e-05	0.00327812	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132951	GCCAGAGGCAGTGAC[C/T]TCGGCATCATCCATT	392197
rs574526302	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135420	TCCAGTTATGCATTG[C/T]ATGGTGGAATTGCAG	392197
rs575026724	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134690	CCAGCGATAACCTTT[C/T]CACGTTCAGACTATT	392197
rs575673848	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134906	AGAGACTAATTGATG[A/G]CTTTCCCCAAATTTA	392197
rs575674557	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134630	AGCACAGCGTATATT[C/T]TTCCTTAATAATAAA	392197
rs575710148	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134318	TCAGGCTGATAGACA[C/T]ATGTAATATGAGTGT	392197
rs575946653	snp	A/G	0.0532157	0.154195	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132342	TGTGTGTTTCCGTGC[A/G]CGCTTGTGGGTGTAT	392197
rs575948213	snp	C/G/T	5.57567e-05	0.00527975	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133660	CACTTGTGAAGATGA[C/G/T]ACGTTTGAGAGTCCT	392197
rs575984940	snp	C/T	0.000543381	0.0164741	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132742	GCTCTTTCCACCAAG[C/T]GCTCGTCCAACTCGG	392197
rs575995191	snp	C/G	0.00119737	0.0244387	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132090	ACACGCAAACCTACA[C/G]GTCAATAGGTCACAT	392197
rs576469109	snp	A/C/G/T	0.000298866	0.0122214	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132647	GCAGGGTACCTTCAA[A/C/G/T]TTTTCTGACGTTGAA	392197
rs576516813	snp	C/G	0.00130375	0.0254986	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132428	GTGATCACTGGCACA[C/G]AAGCAGAGATCTCTT	392197
rs576608041	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135613	GGCAGAATTGAGGCC[C/T]GGCGCCAAGGCCTCT	392197
rs576839570	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134854	TCAGTGCACAAAGTA[G/T]ACTGTGAAAGACTTT	392197
rs577342244	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134674	GAATCAAACAGACCT[C/T]CCAGCGATAACCTTT	392197
rs577655176	snp	A/G/T	7.38776e-05	0.00607734	stop-gained, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133719	CAGTGTGTATGTCAG[A/G/T]CACTGCAGGGAAACG	392197
rs577863670	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132024	CCAACAACTGACGAA[A/T]GAAACAAACCCCAAG	392197
rs745370993	in-del	-/GG/GTGC/GTGG	5.00388e-05	0.00500169	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132369	TATTTGTGTTTGTGT[-/GG/GTGC/GTGG]GTGTGTGTGTGTGCA	392197
rs745374238	snp	C/T	2.00254e-05	0.00316422	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132509	CGAGTGTGCCAGTGT[C/T]CATGGACTCCTGATC	392197
rs745486493	snp	A/C/T	9.36731e-05	0.00684316	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133588	GAGGGCTGGATGACA[A/C/T]GGCCAGGACTGTGGA	392197
rs745510677	snp	C/G	3.72592e-05	0.00431604	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133159	TTGCCTGTGACATCG[C/G]AGAATCTCTTCAATA	392197
rs745569689	snp	A/C	5.57885e-05	0.00528121	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133193	GAATGAGGACCTTGG[A/C]AGAAGTGGGTAAAGT	392197
rs745673298	snp	C/G	7.48769e-05	0.00611824	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132738	AGTGGCTCTTTCCAC[C/G]AAGTGCTCGTCCAAC	392197
rs745677004	snp	C/T	1.84756e-05	0.00303932	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133715	GCGGCAGTGTGTATG[C/T]CAGGCACTGCAGGGA	392197
rs745679655	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135227	GTGACGGGAGTGAGG[C/T]CCTGTCTGAAGAAGA	392197
rs745766893	snp	A/G	0.00022941	0.0107076	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133377	GGTGTCTGAAACGCC[A/G]TGGCAGTGGAGATAC	392197
rs745784575	snp	A/C/T	9.19454e-05	0.00677977	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133748	CGTTCACATAGAAGG[A/C/T]ATTTCCTATCTTCTG	392197
rs745858553	snp	A/G	1.92951e-05	0.00310599	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133412	TTTGAGATCTCCAAT[A/G]CGCTCCAAATATTTG	392197
rs746036683	snp	A/G	8.29067e-05	0.00643789	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133035	ACAACTCCACCCAGC[A/G]TGGACCAGCACAGCA	392197
rs746062640	snp	C/G	0.000167492	0.00914974	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133952	GCCGAGAAGATGTGA[C/G]TTTTGAAAAGTGATT	392197
rs746144415	snp	A/T	5.68015e-05	0.00532893	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132616	TTTGATTGATGAATC[A/T]CAAGTACGTTGGGAG	392197
rs746162646	snp	A/C	1.85758e-05	0.00304755	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133622	CCCATGTGATGTGAG[A/C]TTGCATAGTACAGAA	392197
rs746169547	snp	A/G	3.71775e-05	0.00431131	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133989	CCAGTCACCTCCCAA[A/G]TAGAGTGAGTCGTCT	392197
rs746247556	snp	C/T	1.85858e-05	0.00304837	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133648	CAGAACATGCAGCAC[C/T]TGTGAAGATGACACG	392197
rs746337329	snp	A/C	5.61729e-05	0.00529937	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133277	TCTCTCCATTGAGTT[A/C]TTTGGGCTTCACCAA	392197
rs746442485	snp	G/T	3.4718e-05	0.00416627	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132814	GTTGCTGGCCTGTCT[G/T]TGTCTTCAGCACCAA	392197
rs746450006	snp	C/G	5.50989e-05	0.00524847	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133786	GCCCCCACCGCAGCA[C/G]GTCTCCTGCTACTCA	392197
rs746530084	snp	G/T	2.11822e-05	0.00325433	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132868	GACACACTCTCACTG[G/T]GTCTTTCCCATTCAC	392197
rs746622009	snp	A/C	0.000122662	0.00783044	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132467	TGTTATTCCCTTTGG[A/C]TCTCCTGGTGCTCCC	392197
rs746643596	snp	A/G	1.89906e-05	0.00308139	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133517	CCACAGTAAACATGA[A/G]AAATTCATGGGCATC	392197
rs746731461	snp	C/G/T	5.79384e-05	0.00538204	synonymous-codon, missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133113	CTGCATGTCACGGCA[C/G/T]TTAGGATATTGCACA	392197
rs746733417	snp	A/C/G	7.55687e-05	0.00614643	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133544	CATCCTCCTGCTCAC[A/C/G]TCTATGGAAGCCAGC	392197
rs746793142	snp	A/G	3.73065e-05	0.00431878	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132657	TTCAACTTTTCTGAC[A/G]TTGAACTCAGGCTTC	392197
rs746811018	snp	A/G	0.00346432	0.0414748	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133155	TTTGTTGCCTGTGAC[A/G]TCGGAGAATCTCTTC	392197
rs746824423	snp	A/G	1.86083e-05	0.00305021	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134032	GCAACAAGGATCACA[A/G]GGTTTTTCTGCTGGG	392197
rs746916783	snp	A/T	1.85424e-05	0.00304481	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132694	TTTTGCTCTTGGGGG[A/T]ATTTCCAGTGGTCTA	392197
rs746987891	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134134	CCCTTATATAACTCA[A/C]CCCCTCCAACCGCGA	392197
rs747005763	in-del	-/GT	0.000266165	0.0115331	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132799	TTGAGCTCTCCTTGC[-/GT]TGCTGGCCTGTCTGT	392197
rs747207727	snp	C/G	3.84882e-05	0.00438664	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133402	AGATACTTGATTTGA[C/G]ATCTCCAATACGCTC	392197
rs747270552	snp	C/G	5.96285e-05	0.00545992	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132521	TGTTCATGGACTCCT[C/G]ATCTGTCGGTTTCGT	392197
rs747297497	snp	A/G	6.27464e-05	0.00560083	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132971	CATCATCCATTTTAT[A/G]CCACTGGCCTTCTTG	392197
rs747360618	snp	A/G/T	3.89077e-05	0.00441051	missense, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132551	TCGAAGAGAGGTTTA[A/G/T]CAGGGAGCTTTGCTG	392197
rs747367780	snp	A/C/T	0.000148483	0.00861525	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133947	ATCTAGCCGAGAAGA[A/C/T]GTGAGTTTTGAAAAG	392197
rs747454586	snp	A/T	9.28152e-05	0.00681168	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133611	ACTGTGGAGGGCCCA[A/T]GTGATGTGAGCTTGC	392197
rs747586885	snp	A/G	3.73972e-05	0.00432402	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133239	AGGCGCCTTCTGGAG[A/G]CAAAGACCACAATGA	392197
rs747645601	snp	A/G	5.58186e-05	0.00528263	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134024	TGTCGCCCGCAACAA[A/G]GATCACAAGGTTTTT	392197
rs747764168	snp	G/T	0.000321656	0.0126777	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132809	CTTGCGTTGCTGGCC[G/T]GTCTGTGTCTTCAGC	392197
rs747804572	snp	A/T	4.28229e-05	0.00462705	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132406	AGTGTGGGTCGGTAC[A/T]TCCACTGTGATCACT	392197
rs747859174	snp	A/G	9.58396e-05	0.00692175	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133476	TAGCTGCTTGTGCCC[A/G]GGAAGGCATGCCTTT	392197
rs747902733	snp	A/C	0.000488878	0.0156269	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133064	CATAGAGGACATAGA[A/C]AAGAGGTCCTGTGTT	392197
rs747945569	snp	A/G	5.70706e-05	0.00534154	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133507	TTCATGGCATCCACA[A/G]TAAACATGAGAAATT	392197
rs748119800	snp	C/T	1.86079e-05	0.00305018	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134028	GCCCGCAACAAGGAT[C/T]ACAAGGTTTTTCTGC	392197
rs748198755	snp	A/G	1.85761e-05	0.00304758	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133661	ACTTGTGAAGATGAC[A/G]CGTTTGAGAGTCCTC	392197
rs748209827	snp	A/G	1.85493e-05	0.00304537	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133685	AGTCCTCCCGGGACA[A/G]CATGTAGTTGGAAAG	392197
rs748350543	snp	A/G	5.68629e-05	0.00533181	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133344	GATATCCAGGGCGAT[A/G]TCCAGGTAAGGGTCA	392197
rs748380480	snp	A/G	9.2465e-05	0.00679882	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133705	TAGTTGGAAAGCGGC[A/G]GTGTGTATGTCAGGC	392197
rs748440093	snp	C/G	0.00627439	0.0556581	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132885	TCTTTCCCATTCACT[C/G]TTCTGGATGTAAAAG	392197
rs748440277	snp	A/G	1.90022e-05	0.00308233	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133369	GGGTCAAAGGTGTCT[A/G]AAACGCCGTGGCAGT	392197
rs748528383	snp	A/G/T	0.000316154	0.0125696	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132931	TGACTCAGGACAGAG[A/G/T]TGATGCCAGAGGCAG	392197
rs748545592	snp	A/C	0.00215352	0.0327433	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133865	CATCACAGAGGTCGA[A/C]ACGGGTCTCAGATGA	392197
rs748554467	snp	C/T	2.03184e-05	0.00318728	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132481	GATCTCCTGGTGCTC[C/T]CTTGCAGAGAAGCGA	392197
rs748561283	snp	C/T	1.99507e-05	0.00315832	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132516	GCCAGTGTTCATGGA[C/T]TCCTGATCTGTCGGT	392197
rs748631445	snp	G/T	1.88699e-05	0.00307158	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133551	CTGCTCACCTCTATG[G/T]AAGCCAGCAGCCAAT	392197
rs748701722	snp	A/G/T	5.856e-05	0.00541078	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132545	GTTTCGTCGAAGAGA[A/G/T]GTTTAGCAGGGAGCT	392197
rs748845669	snp	C/T	3.7372e-05	0.00432257	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133229	TCTTGGAGGCAGGCG[C/T]CTTCTGGAGACAAAG	392197
rs748937319	snp	A/G	9.44742e-05	0.00687228	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132771	GGGTACCTGGAGGCA[A/G]GGGTGGTCTCTCTTG	392197
rs749137668	snp	C/T	0.000330585	0.0128524	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133773	CTTCTGGAGCCCAGC[C/T]CCCACCGCAGCAGGT	392197
rs749223308	snp	A/C/G/T	0.000383606	0.0138449	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133475	CTAGCTGCTTGTGCC[A/C/G/T]GGGAAGGCATGCCTT	392197
rs749300446	snp	A/G	4.11921e-05	0.0045381	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133045	CCAGCGTGGACCAGC[A/G]CAGCATAGAGGACAT	392197
rs749321161	snp	A/G	3.71547e-05	0.00430998	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133970	TTGAAAAGTGATTGA[A/G]CTGCCAGTCACCTCC	392197
rs749347120	snp	C/G	5.57699e-05	0.00528032	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133994	CACCTCCCAAATAGA[C/G]TGAGTCGTCTTCCAT	392197
rs749481096	snp	A/C	0.000204394	0.0101072	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133656	GCAGCACTTGTGAAG[A/C]TGACACGTTTGAGAG	392197
rs749566888	snp	C/T	1.87542e-05	0.00306214	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133284	ATTGAGTTCTTTGGG[C/T]TTCACCAACTGTTCC	392197
rs749653115	snp	A/G	5.67951e-05	0.00532863	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133339	GCCTGGATATCCAGG[A/G]CGATGTCCAGGTAAG	392197
rs749664876	snp	A/C	1.90823e-05	0.00308882	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132829	GTGTCTTCAGCACCA[A/C]GGGCTCTTGGTTCCC	392197
rs749706852	snp	A/C	2.28324e-05	0.00337871	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132881	TGTGTCTTTCCCATT[A/C]ACTCTTCTGGATGTA	392197
rs749803310	snp	A/G	6.12101e-05	0.00553185	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132475	CCTTTGGATCTCCTG[A/G]TGCTCCCTTGCAGAG	392197
rs749859514	in-del	-/GC			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132379	TGTGTGTGTGTGTGT[-/GC]GTGCACCCATCAGTG	392197
rs750109653	snp	A/C	0.000267135	0.011554	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132588	ATGATGGTTTTTCAT[A/C]CCACACTTGTATTTT	392197
rs750156517	snp	A/G	0.000111359	0.00746102	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133606	CCAGGACTGTGGAGG[A/G]CCCATGTGATGTGAG	392197
rs750244444	snp	C/T	0.00022432	0.0105882	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133227	CGTCTTGGAGGCAGG[C/T]GCCTTCTGGAGACAA	392197
rs750317099	snp	A/T	9.44938e-05	0.00687299	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132763	TCCAACTCGGGTACC[A/T]GGAGGCAAGGGTGGT	392197
rs750382127	snp	C/T	1.83643e-05	0.00303015	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133769	CTATCTTCTGGAGCC[C/T]AGCCCCCACCGCAGC	392197
rs750494432	snp	A/C	2.17924e-05	0.00330087	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132390	TGTGTGTGCACCCAT[A/C]AGTGTGGGTCGGTAC	392197
rs750519742	snp	A/G	0.00038582	0.0138838	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133801	GGTCTCCTGCTACTC[A/G]GAGGAAGCTTCTCCC	392197
rs750582338	snp	C/G	1.78787e-05	0.00298982	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132449	GAGATCTCTTGCTGT[C/G]TTTGTTATTCCCTTT	392197
rs750712082	snp	G/T	0.000217725	0.0104314	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133103	ACATGTATGGCTGCA[G/T]GTCACGGCACTTAGG	392197
rs750744170	snp	C/T	1.87468e-05	0.00306154	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132638	CGTTGGGAGGCAGGG[C/T]ACCTTCAACTTTTCT	392197
rs750800108	snp	A/G	7.55972e-05	0.00614759	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133128	CTTAGGATATTGCAC[A/G]TTCTTGGCAAGTTTG	392197
rs750879013	snp	A/G	0.000260117	0.0114013	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132678	CTCAGGCTTCGTTTT[A/G]TTTTGCTCTTGGGGG	392197
rs750895295	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135616	AGAATTGAGGCCCGG[C/T]GCCAAGGCCTCTGGG	392197
rs750904815	snp	C/T	3.72287e-05	0.00431427	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134043	CACAAGGTTTTTCTG[C/T]TGGGACCGCAGGTTG	392197
rs750994451	snp	A/G/T	1.8517e-05	0.00304272	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133699	AGCATGTAGTTGGAA[A/G/T]GCGGCAGTGTGTATG	392197
rs751129365	snp	A/T	2.37668e-05	0.00344715	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132922	TAGGCCTGTTGACTC[A/T]GGACAGAGGTGATGC	392197
rs751279766	snp	A/G	9.22433e-05	0.00679066	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133883	GGGTCTCAGATGAGA[A/G]TGGTGACTTTTCAGA	392197
rs751309469	snp	A/G	2.00773e-05	0.00316832	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132504	AGAAGCGAGTGTGCC[A/G]GTGTTCATGGACTCC	392197
rs751357084	snp	A/G	1.87756e-05	0.0030639	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133577	CCAATACCTGTGAGG[A/G]CTGGATGACATGGCC	392197
rs751490883	snp	C/G	1.86485e-05	0.00305351	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132730	CTTTCCTGAGTGGCT[C/G]TTTCCACCAAGTGCT	392197
rs751537116	snp	A/C/T	0.00050496	0.015882	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133224	TAACGTCTTGGAGGC[A/C/T]GGCGCCTTCTGGAGA	392197
rs751644125	snp	A/G	3.77922e-05	0.0043468	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132756	GTGCTCGTCCAACTC[A/G]GGTACCTGGAGGCAA	392197
rs751696339	snp	A/G	1.84045e-05	0.00303347	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133742	GGGAAACGTTCACAT[A/G]GAAGGTATTTCCTAT	392197
rs751711218	snp	A/C	3.80467e-05	0.00436141	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132789	GTGGTCTCTCTTGAG[A/C]TCTCCTTGCGTTGCT	392197
rs751730006	in-del	-/A	1.86187e-05	0.00305106	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134053	TTCTGCTGGGACCGC[-/A]GGTTGCAGCAAGACG	392197
rs751755026	snp	C/T	0.00121125	0.0245796	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132383	GTGTGTGTGTGTGTG[C/T]ACCCATCAGTGTGGG	392197
rs751806728	snp	G/T	3.67222e-05	0.00428483	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133766	TTCCTATCTTCTGGA[G/T]CCCAGCCCCCACCGC	392197
rs751882415	snp	C/T	2.07574e-05	0.00322154	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133025	GTCCGTTGTGACAAC[C/T]CCACCCAGCGTGGAC	392197
rs751966997	snp	C/T	7.62689e-05	0.00617484	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133492	GGAAGGCATGCCTTT[C/T]TCATGGCATCCACAG	392197
rs752022254	snp	A/T	1.89622e-05	0.00307908	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132612	GTATTTTGATTGATG[A/T]ATCACAAGTACGTTG	392197
rs752063001	snp	A/G	3.97622e-05	0.00445865	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133100	GAGACATGTATGGCT[A/G]CATGTCACGGCACTT	392197
rs752110423	snp	C/G	1.877e-05	0.00306344	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132635	GTACGTTGGGAGGCA[C/G]GGTACCTTCAACTTT	392197
rs752164555	snp	C/G	7.43273e-05	0.00609575	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133673	GACACGTTTGAGAGT[C/G]CTCCCGGGACAGCAT	392197
rs752179388	snp	C/T	0.000111537	0.00746698	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133645	GTACAGAACATGCAG[C/T]ACTTGTGAAGATGAC	392197
rs752447823	snp	C/T	3.97567e-05	0.00445834	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132850	CTTGGTTCCCTGCCT[C/T]TTGACACACTCTCAC	392197
rs752496797	snp	A/G	1.83984e-05	0.00303296	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133854	AGGAGCCAAATCATC[A/G]CAGAGGTCGAAACGG	392197
rs752525914	snp	C/T	0.000123033	0.00784228	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132911	AAAAGAGGACATAGG[C/T]CTGTTGACTCAGGAC	392197
rs752532647	snp	C/T	2.05231e-05	0.0032033	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132460	CTGTGTTTGTTATTC[C/T]CTTTGGATCTCCTGG	392197
rs752586513	snp	C/T	0.000128984	0.00802964	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133871	AGAGGTCGAAACGGG[C/T]CTCAGATGAGAGTGG	392197
rs752730437	snp	G/T	3.6846e-05	0.00429204	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133869	ACAGAGGTCGAAACG[G/T]GTCTCAGATGAGAGT	392197
rs752810835	snp	A/G	5.57243e-05	0.00527817	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133185	CAATACAAGAATGAG[A/G]ACCTTGGCAGAAGTG	392197
rs752814774	snp	A/G			missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132854	GTTCCCTGCCTCTTG[A/G]CACACTCTCACTGTG	392197
rs752856962	snp	A/G	0.000316506	0.0125759	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134051	TTTTCTGCTGGGACC[A/G]CAGGTTGCAGCAAGA	392197
rs752890914	in-del	-/T	1.90463e-05	0.00308591	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132600	CATACCACACTTGTA[-/T]TTTGATTGATGAATC	392197
rs752896850	snp	A/G	3.72703e-05	0.00431669	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132726	GGTGCTTTCCTGAGT[A/G]GCTCTTTCCACCAAG	392197
rs752910672	snp	C/T	1.88731e-05	0.00307184	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132753	CAAGTGCTCGTCCAA[C/T]TCGGGTACCTGGAGG	392197
rs752930744	snp	A/T	0.00424595	0.0458797	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133738	TGCAGGGAAACGTTC[A/T]CATAGAAGGTATTTC	392197
rs753015733	in-del	-/AA	1.848e-05	0.00303968	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133904	ACTTTTCAGAGAGAG[-/AA]GTCCGCTGGATTTCA	392197
rs753020927	snp	G/T	1.92269e-05	0.0031005	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133395	GCAGTGGAGATACTT[G/T]ATTTGAGATCTCCAA	392197
rs753123547	snp	C/G/T	5.50922e-05	0.0052482	synonymous-codon, missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133761	GGTATTTCCTATCTT[C/G/T]TGGAGCCCAGCCCCC	392197
rs753254697	snp	A/G	4.1561e-05	0.00455838	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133019	AGTAATGTCCGTTGT[A/G]ACAACTCCACCCAGC	392197
rs753268694	snp	C/T			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132302	TTTATGTAGGATTGA[C/T]GGTGTTCGTGTTTGT	392197
rs753294807	snp	C/T	1.8582e-05	0.00304806	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133979	GATTGAACTGCCAGT[C/T]ACCTCCCAAATAGAG	392197
rs753341106	snp	A/G	0.000133378	0.00816524	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132597	TTTCATACCACACTT[A/G]TATTTTGATTGATGA	392197
rs753377543	in-del	-/TGTGTGTGTG			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134430	GTGTGTGTGTCTGTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT	392197
rs753404257	snp	A/C/T	3.71368e-05	0.00430894	stop-gained, missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133609	GGACTGTGGAGGGCC[A/C/T]ATGTGATGTGAGCTT	392197
rs753431189	snp	G/T	1.87972e-05	0.00306565	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132632	CAAGTACGTTGGGAG[G/T]CAGGGTACCTTCAAC	392197
rs753493917	snp	A/C/T	5.57847e-05	0.00528108	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133642	ATAGTACAGAACATG[A/C/T]AGCACTTGTGAAGAT	392197
rs753572049	snp	A/G	1.86935e-05	0.00305719	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133260	ACCACAATGATAGGC[A/G]TTCTCTCCATTGAGT	392197
rs753653976	snp	A/G	1.96581e-05	0.00313507	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132846	GGCTCTTGGTTCCCT[A/G]CCTCTTGACACACTC	392197
rs753673038	snp	C/G	3.76449e-05	0.00433832	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133311	TTCCAAAGCTTGCTT[C/G]ACACTCTGAGCTGCC	392197
rs753698762	snp	A/G	3.67512e-05	0.00428652	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133807	CTGCTACTCAGAGGA[A/G]GCTTCTCCCTGGGAG	392197
rs753706431	snp	C/T	0.000107932	0.00734536	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132400	CCCATCAGTGTGGGT[C/T]GGTACTTCCACTGTG	392197
rs753787382	snp	A/C	5.71543e-05	0.00534545	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133499	ATGCCTTTTTCATGG[A/C]ATCCACAGTAAACAT	392197
rs753882811	snp	A/C	3.67823e-05	0.00428833	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133850	CCACAGGAGCCAAAT[A/C]ATCACAGAGGTCGAA	392197
rs754009423	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134135	CCTTATATAACTCAC[A/C]CCCTCCAACCGCGAA	392197
rs754057837	snp	C/T	1.86048e-05	0.00304993	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134018	CTTCCATGTCGCCCG[C/T]AACAAGGATCACAAG	392197
rs754068779	snp	A/C/G/T	0.000528037	0.0162407	missense, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132624	ATGAATCACAAGTAC[A/C/G/T]TTGGGAGGCAGGGTA	392197
rs754158929	snp	G/T	1.85451e-05	0.00304503	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132690	TTTGTTTTGCTCTTG[G/T]GGGAATTTCCAGTGG	392197
rs754248696	snp	C/T	0.00024193	0.0109958	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132715	CAGTGGTCTAAGGTG[C/T]TTTCCTGAGTGGCTC	392197
rs754283040	in-del	-/C	1.83653e-05	0.00303023	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133778	GGAGCCCAGCCCCCA[-/C]CGCAGCAGGTCTCCT	392197
rs754290457	snp	A/G/T	3.79544e-05	0.00435615	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133363	AGGTAAGGGTCAAAG[A/G/T]TGTCTGAAACGCCGT	392197
rs754296160	snp	A/G	0.00436113	0.0464924	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133732	AGGCACTGCAGGGAA[A/G]CGTTCACATAGAAGG	392197
rs754405115	snp	C/T	2.32485e-05	0.00340936	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132926	CCTGTTGACTCAGGA[C/T]AGAGGTGATGCCAGA	392197
rs754472719	snp	C/G	1.85844e-05	0.00304826	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133981	TTGAACTGCCAGTCA[C/G]CTCCCAAATAGAGTG	392197
rs754588256	snp	C/T	0.000468371	0.0152959	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133231	TTGGAGGCAGGCGCC[C/T]TCTGGAGACAAAGAC	392197
rs754673564	snp	A/G	0.000378881	0.0137585	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132806	CTCCTTGCGTTGCTG[A/G]CCTGTCTGTGTCTTC	392197
rs754677814	snp	A/T	3.73895e-05	0.00432358	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133262	CACAATGATAGGCAT[A/T]CTCTCCATTGAGTTC	392197
rs754717792	snp	C/G/T	0.000257104	0.0113356	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133778	GGAGCCCAGCCCCCA[C/G/T]CGCAGCAGGTCTCCT	392197
rs754759266	snp	A/G	6.46921e-05	0.00568699	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132401	CCATCAGTGTGGGTC[A/G]GTACTTCCACTGTGA	392197
rs754809811	snp	A/G	1.83768e-05	0.00303118	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133808	TGCTACTCAGAGGAA[A/G]CTTCTCCCTGGGAGC	392197
rs754897553	snp	A/G	0.00148923	0.027247	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133851	CACAGGAGCCAAATC[A/G]TCACAGAGGTCGAAA	392197
rs754919341	snp	G/T	0.000267086	0.011553	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132458	TGCTGTGTTTGTTAT[G/T]CCCTTTGGATCTCCT	392197
rs754932953	snp	C/T	3.80786e-05	0.00436324	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133503	CTTTTTCATGGCATC[C/T]ACAGTAAACATGAGA	392197
rs754950385	snp	C/G	1.89034e-05	0.0030743	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133539	ATGGGCATCCTCCTG[C/G]TCACCTCTATGGAAG	392197
rs755038308	snp	G/T	1.87661e-05	0.00306312	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133143	ATTCTTGGCAAGTTT[G/T]TTGCCTGTGACATCG	392197
rs755205358	snp	A/G	1.85565e-05	0.00304596	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133681	TGAGAGTCCTCCCGG[A/G]ACAGCATGTAGTTGG	392197
rs755306820	snp	C/T	1.86093e-05	0.0030503	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132716	AGTGGTCTAAGGTGC[C/T]TTCCTGAGTGGCTCT	392197
rs755475025	snp	A/G	3.84135e-05	0.00438238	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133391	CGTGGCAGTGGAGAT[A/G]CTTGATTTGAGATCT	392197
rs755475377	snp	G/T	4.58989e-05	0.00479034	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132928	TGTTGACTCAGGACA[G/T]AGGTGATGCCAGAGG	392197
rs755517325	snp	C/G	2.00298e-05	0.00316457	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132510	GAGTGTGCCAGTGTT[C/G]ATGGACTCCTGATCT	392197
rs755635471	snp	A/G	0.000221697	0.0105261	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133898	GTGGTGACTTTTCAG[A/G]GAGAGAAGTCCGCTG	392197
rs755706782	snp	A/C/T	0.000111419	0.00746315	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133607	CAGGACTGTGGAGGG[A/C/T]CCATGTGATGTGAGC	392197
rs755920949	snp	G/T	3.77936e-05	0.00434688	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132765	CAACTCGGGTACCTG[G/T]AGGCAAGGGTGGTCT	392197
rs756018706	snp	G/T	3.79032e-05	0.00435318	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132804	CTCTCCTTGCGTTGC[G/T]GGCCTGTCTGTGTCT	392197
rs756090163	snp	A/G	1.8368e-05	0.00303046	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133771	ATCTTCTGGAGCCCA[A/G]CCCCCACCGCAGCAG	392197
rs756098533	snp	C/G	4.42057e-05	0.00470116	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132392	TGTGTGCACCCATCA[C/G]TGTGGGTCGGTACTT	392197
rs756106055	snp	A/T	3.67492e-05	0.0042864	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133803	TCTCCTGCTACTCAG[A/T]GGAAGCTTCTCCCTG	392197
rs756307794	snp	C/G	2.06682e-05	0.0032146	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133041	CCACCCAGCGTGGAC[C/G]AGCACAGCATAGAGG	392197
rs756307801	snp	G/T	1.90612e-05	0.00308711	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133496	GGCATGCCTTTTTCA[G/T]GGCATCCACAGTAAA	392197
rs756329627	snp	A/G	5.57667e-05	0.00528018	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133991	AGTCACCTCCCAAAT[A/G]GAGTGAGTCGTCTTC	392197
rs756395704	snp	A/G	9.89658e-05	0.00703371	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133104	CATGTATGGCTGCAT[A/G]TCACGGCACTTAGGA	392197
rs756447152	snp	A/G	3.74693e-05	0.00432819	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132639	GTTGGGAGGCAGGGT[A/G]CCTTCAACTTTTCTG	392197
rs756462032	snp	C/G	1.85782e-05	0.00304775	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132683	GCTTCGTTTTGTTTT[C/G]CTCTTGGGGGAATTT	392197
rs756463377	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134810	AAGCATCAAATGGTA[A/G]AAACATGCACTGAAG	392197
rs756559953	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135625	GCCCGGCGCCAAGGC[C/T]TCTGGGTGTAAAGAA	392197
rs756564399	snp	A/G	1.89206e-05	0.0030757	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133337	CTGCCTGGATATCCA[A/G]GGCGATGTCCAGGTA	392197
rs756653576	snp	C/T	2.22269e-05	0.00333361	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132876	CTCACTGTGTCTTTC[C/T]CATTCACTCTTCTGG	392197
rs756666137	in-del	-/GCACCCATCA	7.43909e-05	0.00609835	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132382	TGTGTGTGTGTGTGT[-/GCACCCATCA]GTGTGGGTCGGTACT	392197
rs756715482	snp	A/C/G	0.000609437	0.0174458	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133362	CAGGTAAGGGTCAAA[A/C/G]GTGTCTGAAACGCCG	392197
rs756811802	snp	A/G	9.45403e-05	0.00687468	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132923	AGGCCTGTTGACTCA[A/G]GACAGAGGTGATGCC	392197
rs756870479	snp	C/T	1.78912e-05	0.00299086	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133887	CTCAGATGAGAGTGG[C/T]GACTTTTCAGAGAGA	392197
rs756958287	snp	A/C	3.75368e-05	0.00433209	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133578	CAATACCTGTGAGGG[A/C]TGGATGACATGGCCA	392197
rs757093323	snp	A/G	1.85976e-05	0.00304933	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133191	AAGAATGAGGACCTT[A/G]GCAGAAGTGGGTAAA	392197
rs757181275	snp	C/G	1.86921e-05	0.00305707	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132735	CTGAGTGGCTCTTTC[C/G]ACCAAGTGCTCGTCC	392197
rs757267356	snp	G/T	1.88956e-05	0.00307367	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132758	GCTCGTCCAACTCGG[G/T]TACCTGGAGGCAAGG	392197
rs757451118	snp	A/C	3.67262e-05	0.00428506	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133767	TCCTATCTTCTGGAG[A/C]CCAGCCCCCACCGCA	392197
rs757451217	snp	C/G	1.92989e-05	0.00310629	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133407	CTTGATTTGAGATCT[C/G]CAATACGCTCCAAAT	392197
rs757537775	snp	C/G	0.000288525	0.0120075	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133463	TGGAGTGATGATCTA[C/G]CTGCTTGTGCCCGGG	392197
rs757583209	snp	C/G	0.000563732	0.0167794	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133101	AGACATGTATGGCTG[C/G]ATGTCACGGCACTTA	392197
rs757607477	snp	C/T	1.85872e-05	0.00304848	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133985	ACTGCCAGTCACCTC[C/T]CAAATAGAGTGAGTC	392197
rs757663451	snp	A/T	3.79046e-05	0.00435326	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132614	ATTTTGATTGATGAA[A/T]CACAAGTACGTTGGG	392197
rs757695378	snp	A/C	1.85882e-05	0.00304857	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133646	TACAGAACATGCAGC[A/C]CTTGTGAAGATGACA	392197
rs757739251	snp	C/G/T	0.00039024	0.0139633	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133984	AACTGCCAGTCACCT[C/G/T]CCAAATAGAGTGAGT	392197
rs757882252	snp	G/T	5.57108e-05	0.00527753	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133675	CACGTTTGAGAGTCC[G/T]CCCGGGACAGCATGT	392197
rs757915876	snp	C/T	1.87033e-05	0.00305799	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133267	TGATAGGCATTCTCT[C/T]CATTGAGTTCTTTGG	392197
rs758071712	snp	A/G/T	4.09385e-05	0.00452415	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132463	TGTTTGTTATTCCCT[A/G/T]TGGATCTCCTGGTGC	392197
rs758095877	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134842	TTGAAGAGTTACTCA[G/T]TGCACAAAGTAGACT	392197
rs758119917	snp	C/T	3.97583e-05	0.00445843	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132851	TTGGTTCCCTGCCTC[C/T]TGACACACTCTCACT	392197
rs758154240	snp	C/G	1.83994e-05	0.00303305	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133855	GGAGCCAAATCATCA[C/G]AGAGGTCGAAACGGG	392197
rs758330149	snp	A/C	1.87799e-05	0.00306424	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133574	CAGCCAATACCTGTG[A/C]GGGCTGGATGACATG	392197
rs758352095	snp	G/T	3.73525e-05	0.00432144	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133152	AAGTTTGTTGCCTGT[G/T]ACATCGGAGAATCTC	392197
rs758438219	snp	G/T	3.72974e-05	0.00431825	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132727	GTGCTTTCCTGAGTG[G/T]CTCTTTCCACCAAGT	392197
rs758444853	snp	A/G/T	3.70839e-05	0.00430591	missense, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132693	GTTTTGCTCTTGGGG[A/G/T]AATTTCCAGTGGTCT	392197
rs758448410	snp	A/G	1.8492e-05	0.00304067	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133706	AGTTGGAAAGCGGCA[A/G]TGTGTATGTCAGGCA	392197
rs758505145	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134052	TTTCTGCTGGGACCG[C/T]AGGTTGCAGCAAGAC	392197
rs758583219	in-del	-/C	1.86956e-05	0.00305736	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132737	GAGTGGCTCTTTCCA[-/C]CAAGTGCTCGTCCAA	392197
rs758637147	snp	A/G/T	0.00424459	0.045873	stop-gained, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133740	CAGGGAAACGTTCAC[A/G/T]TAGAAGGTATTTCCT	392197
rs758723084	snp	A/G	1.92162e-05	0.00309963	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133396	CAGTGGAGATACTTG[A/G]TTTGAGATCTCCAAT	392197
rs758787426	snp	A/T	8.38153e-05	0.00647307	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132969	GGCATCATCCATTTT[A/T]TACCACTGGCCTTCT	392197
rs758844341	snp	A/C	5.56633e-05	0.00527528	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133944	TGCATCTAGCCGAGA[A/C]GATGTGAGTTTTGAA	392197
rs758871430	snp	A/G	6.22827e-05	0.00558009	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133023	ATGTCCGTTGTGACA[A/G]CTCCACCCAGCGTGG	392197
rs758883307	snp	A/C/G	0.000214139	0.0103454	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132954	AGAGGCAGTGACCTC[A/C/G]GCATCATCCATTTTA	392197
rs758910864	snp	A/T	5.6933e-05	0.0053351	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133522	GTAAACATGAGAAAT[A/T]CATGGGCATCCTCCT	392197
rs758987891	snp	C/G	1.9894e-05	0.00315382	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133098	CTGAGACATGTATGG[C/G]TGCATGTCACGGCAC	392197
rs759077837	snp	C/T	5.68672e-05	0.00533201	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133120	TCACGGCACTTAGGA[C/T]ATTGCACATTCTTGG	392197
rs759077967	snp	A/C/G	0.000544759	0.0164954	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132633	AAGTACGTTGGGAGG[A/C/G]AGGGTACCTTCAACT	392197
rs759226158	snp	C/T	3.72218e-05	0.00431387	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134037	AAGGATCACAAGGTT[C/T]TTCTGCTGGGACCGC	392197
rs759260449	snp	A/G	1.85696e-05	0.00304704	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133670	GATGACACGTTTGAG[A/G]GTCCTCCCGGGACAG	392197
rs759347877	snp	C/G	3.76683e-05	0.00433967	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133315	AAAGCTTGCTTGACA[C/G]TCTGAGCTGCCTGGA	392197
rs759350105	snp	A/G	1.85338e-05	0.0030441	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133691	CCCGGGACAGCATGT[A/G]GTTGGAAAGCGGCAG	392197
rs759369571	snp	A/C	2.47216e-05	0.0035157	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132905	GGATGTAAAAGAGGA[A/C]ATAGGCCTGTTGACT	392197
rs759457495	snp	C/T	6.07306e-05	0.00551014	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132494	TCCCTTGCAGAGAAG[C/T]GAGTGTGCCAGTGTT	392197
rs759575372	snp	C/T	6.57873e-05	0.00573492	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132938	GGACAGAGGTGATGC[C/T]AGAGGCAGTGACCTC	392197
rs759649600	snp	A/G	0.000130994	0.00809197	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133595	GGATGACATGGCCAG[A/G]ACTGTGGAGGGCCCA	392197
rs759687973	snp	A/G	0.000112905	0.00751264	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133567	AAGCCAGCAGCCAAT[A/G]CCTGTGAGGGCTGGA	392197
rs759775079	snp	A/C	1.85606e-05	0.0030463	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133180	CTCTTCAATACAAGA[A/C]TGAGGACCTTGGCAG	392197
rs759940117	in-del	-/CTC	1.83683e-05	0.00303048	cds-indel, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133789	CCCACCGCAGCAGGT[-/CTC]CTGCTACTCAGAGGA	392197
rs760033958	in-del	-/A	1.84463e-05	0.00303691	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133730	TCAGGCACTGCAGGG[-/A]AACGTTCACATAGAA	392197
rs760084110	snp	A/G/T	7.34772e-05	0.00606086	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133759	AAGGTATTTCCTATC[A/G/T]TCTGGAGCCCAGCCC	392197
rs760124425	snp	A/C	1.92847e-05	0.00310516	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133445	GGATGAGGGTGGTGT[A/C]CTTGGAGTGATGATC	392197
rs760219926	snp	C/T	1.90583e-05	0.00308688	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132595	TTTTTCATACCACAC[C/T]TGTATTTTGATTGAT	392197
rs760391238	snp	C/G/T	0.000872964	0.0208745	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133977	GTGATTGAACTGCCA[C/G/T]TCACCTCCCAAATAG	392197
rs760441634	snp	G/T	1.884e-05	0.00306915	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132627	AATCACAAGTACGTT[G/T]GGAGGCAGGGTACCT	392197
rs760481152	snp	C/T	1.85889e-05	0.00304862	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133638	TTGCATAGTACAGAA[C/T]ATGCAGCACTTGTGA	392197
rs760502152	snp	A/C/T	3.75885e-05	0.0043351	stop-gained, missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133300	TTCACCAACTGTTCC[A/C/T]AAGCTTGCTTGACAC	392197
rs760745770	snp	G/T	2.06217e-05	0.00321099	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132453	TCTCTTGCTGTGTTT[G/T]TTATTCCCTTTGGAT	392197
rs760803537	snp	A/C/G/T	7.36847e-05	0.00606945	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133868	CACAGAGGTCGAAAC[A/C/G/T]GGTCTCAGATGAGAG	392197
rs760814893	snp	A/G	0.000495565	0.0157333	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132894	TTCACTCTTCTGGAT[A/G]TAAAAGAGGACATAG	392197
rs760835837	snp	G/T	2.02867e-05	0.00318479	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132484	CTCCTGGTGCTCCCT[G/T]GCAGAGAAGCGAGTG	392197
rs760893381	snp	C/T	1.88631e-05	0.00307103	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133555	TCACCTCTATGGAAG[C/T]CAGCAGCCAATACCT	392197
rs760971742	snp	C/T	9.46298e-05	0.00687793	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133533	AAATTCATGGGCATC[C/T]TCCTGCTCACCTCTA	392197
rs761059931	snp	C/T	1.88863e-05	0.00307291	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133132	GGATATTGCACATTC[C/T]TGGCAAGTTTGTTGC	392197
rs761066639	snp	C/G	1.86166e-05	0.00305089	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134045	CAAGGTTTTTCTGCT[C/G]GGACCGCAGGTTGCA	392197
rs761157802	snp	C/G/T	0.00011137	0.00746156	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133178	ATCTCTTCAATACAA[C/G/T]AATGAGGACCTTGGC	392197
rs761218472	snp	C/G	1.86038e-05	0.00304984	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132712	TTCCAGTGGTCTAAG[C/G]TGCTTTCCTGAGTGG	392197
rs761244415	snp	A/G	3.69181e-05	0.00429624	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133724	TGTATGTCAGGCACT[A/G]CAGGGAAACGTTCAC	392197
rs761336436	snp	A/G	9.18687e-05	0.00677687	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133756	TAGAAGGTATTTCCT[A/G]TCTTCTGGAGCCCAG	392197
rs761458905	in-del	-/GTGTGC	2.43294e-05	0.00348771	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132378	TTTGTGTGTGTGTGT[-/GTGTGC]ACCCATCAGTGTGGG	392197
rs761498415	snp	C/G	3.86675e-05	0.00439685	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133427	ACGCTCCAAATATTT[C/G]GTGGATGAGGGTGGT	392197
rs761560267	snp	A/G	1.85799e-05	0.00304789	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133973	AAAAGTGATTGAACT[A/G]CCAGTCACCTCCCAA	392197
rs761588346	snp	C/G	2.07998e-05	0.00322482	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133012	TAAGAGAAGTAATGT[C/G]CGTTGTGACAACTCC	392197
rs761589285	in-del	-/ATAC	0.000212144	0.0102969	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133410	GATTTGAGATCTCCA[-/ATAC]GCTCCAAATATTTGG	392197
rs761701570	snp	C/T	1.91573e-05	0.00309488	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132580	TGTTCAGGATGATGG[C/T]TTTTCATACCACACT	392197
rs761908916	snp	A/C	3.75488e-05	0.00433278	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133293	TTTGGGCTTCACCAA[A/C]TGTTCCAAAGCTTGC	392197
rs761908940	snp	C/T	3.80156e-05	0.00435963	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132792	GTCTCTCTTGAGCTC[C/T]CCTTGCGTTGCTGGC	392197
rs761996642	snp	C/G/T	7.73835e-05	0.00621985	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132838	GCACCAAGGGCTCTT[C/G/T]GTTCCCTGCCTCTTG	392197
rs762011920	snp	G/T	8.29996e-05	0.0064415	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132443	CAAGCAGAGATCTCT[G/T]GCTGTGTTTGTTATT	392197
rs762076942	snp	A/C	2.54482e-05	0.003567	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132385	GTGTGTGTGTGTGCA[A/C]CCATCAGTGTGGGTC	392197
rs762200588	snp	A/G	1.83859e-05	0.00303193	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133829	CCCTGGGAGCAAGCT[A/G]TCTTGCCACAGGAGC	392197
rs762202282	snp	C/T	3.81366e-05	0.00436656	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133493	GAAGGCATGCCTTTT[C/T]CATGGCATCCACAGT	392197
rs762279931	snp	A/G	3.71941e-05	0.00431227	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133171	TCGGAGAATCTCTTC[A/G]ATACAAGAATGAGGA	392197
rs762286455	snp	C/G	0.000170343	0.00922727	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133529	TGAGAAATTCATGGG[C/G]ATCCTCCTGCTCACC	392197
rs762377861	snp	C/G	3.71747e-05	0.00431115	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132702	TTGGGGGAATTTCCA[C/G]TGGTCTAAGGTGCTT	392197
rs762405907	snp	C/G/T	5.58418e-05	0.00528378	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134042	TCACAAGGTTTTTCT[C/G/T]CTGGGACCGCAGGTT	392197
rs762416610	snp	G/T	3.70659e-05	0.00430483	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133695	GGACAGCATGTAGTT[G/T]GAAAGCGGCAGTGTG	392197
rs762444079	snp	C/T	9.30207e-05	0.00681921	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132672	GTTGAACTCAGGCTT[C/T]GTTTTGTTTTGCTCT	392197
rs762590043	in-del	-/TGTT	1.80234e-05	0.00300189	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132370	ATTTGTGTTTGTGTG[-/TGTT]TGTGTGTGTGTGCAC	392197
rs762776638	snp	A/T	2.42228e-05	0.00348006	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132918	GACATAGGCCTGTTG[A/T]CTCAGGACAGAGGTG	392197
rs762789177	snp	A/G	1.7886e-05	0.00299044	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133879	AAACGGGTCTCAGAT[A/G]AGAGTGGTGACTTTT	392197
rs762870864	snp	C/G/T	0.00107252	0.0231368	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132953	CAGAGGCAGTGACCT[C/G/T]GGCATCATCCATTTT	392197
rs762959003	snp	A/G	4.17772e-05	0.00457021	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133000	TGAGCTTTGACATAA[A/G]AGAAGTAATGTCCGT	392197
rs762962543	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134685	ACCTTCCAGCGATAA[C/G]CTTTCCACGTTCAGA	392197
rs762964876	snp	G/T	7.8782e-05	0.00627573	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132531	CTCCTGATCTGTCGG[G/T]TTCGTCGAAGAGAGG	392197
rs763041128	snp	A/C	7.46561e-05	0.00610921	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133220	AAGTTAACGTCTTGG[A/C]GGCAGGCGCCTTCTG	392197
rs763054272	snp	C/T	1.91926e-05	0.00309773	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132577	TGCTGTTCAGGATGA[C/T]GGTTTTTCATACCAC	392197
rs763074219	in-del	-/AAG			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134793	GCTAGGCTGCCAAAT[-/AAG]AAAGCATCAAATGGT	392197
rs763140876	snp	A/C	1.9013e-05	0.00308321	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132781	AGGCAAGGGTGGTCT[A/C]TCTTGAGCTCTCCTT	392197
rs763202606	snp	G/T	1.88624e-05	0.00307097	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132754	AAGTGCTCGTCCAAC[G/T]CGGGTACCTGGAGGC	392197
rs763250677	snp	A/G	1.92766e-05	0.0031045	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133450	AGGGTGGTGTCCTTG[A/G]AGTGATGATCTAGCT	392197
rs763274856	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135300	AGCATAACCTTTTTA[A/C]TGCTGGCCCTTGTTT	392197
rs763464728	snp	A/G	0.000263507	0.0114754	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132487	CTGGTGCTCCCTTGC[A/G]GAGAAGCGAGTGTGC	392197
rs763471800	snp	G/T	3.57699e-05	0.00422891	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132434	ACTGGCACACAAGCA[G/T]AGATCTCTTGCTGTG	392197
rs763510579	snp	C/G/T	3.81936e-05	0.00436985	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133487	GCCCGGGAAGGCATG[C/G/T]CTTTTTCATGGCATC	392197
rs763584233	snp	C/T			missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133264	CAATGATAGGCATTC[C/T]CTCCATTGAGTTCTT	392197
rs763624920	snp	C/G	1.85906e-05	0.00304877	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132707	GGAATTTCCAGTGGT[C/G]TAAGGTGCTTTCCTG	392197
rs763625204	snp	A/C	9.26209e-05	0.00680455	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133697	ACAGCATGTAGTTGG[A/C]AAGCGGCAGTGTGTA	392197
rs763717112	snp	C/G/T	0.000170794	0.00923959	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133358	TGTCCAGGTAAGGGT[C/G/T]AAAGGTGTCTGAAAC	392197
rs763788372	snp	A/G	1.84476e-05	0.00303702	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133882	CGGGTCTCAGATGAG[A/G]GTGGTGACTTTTCAG	392197
rs763841273	snp	C/T	2.40174e-05	0.00346527	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132920	CATAGGCCTGTTGAC[C/T]CAGGACAGAGGTGAT	392197
rs763906940	in-del	-/GTGC	2.43911e-05	0.00349213	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132375	TGTTTGTGTGTGTGT[-/GTGC]GTGTGTGCACCCATC	392197
rs763933510	snp	C/G	4.0286e-05	0.00448792	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132502	AGAGAAGCGAGTGTG[C/G]CAGTGTTCATGGACT	392197
rs764030772	snp	C/T	1.85146e-05	0.00304252	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133929	GATTTCAGCAAAAGC[C/T]GCATCTAGCCGAGAA	392197
rs764137077	snp	G/T	5.60135e-05	0.00529184	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133222	GTTAACGTCTTGGAG[G/T]CAGGCGCCTTCTGGA	392197
rs764145048	snp	C/T	3.77729e-05	0.00434569	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132755	AGTGCTCGTCCAACT[C/T]GGGTACCTGGAGGCA	392197
rs764387803	snp	A/G	1.90054e-05	0.00308259	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132787	GGGTGGTCTCTCTTG[A/G]GCTCTCCTTGCGTTG	392197
rs764446129	snp	A/G	3.67289e-05	0.00428522	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133763	TATTTCCTATCTTCT[A/G]GAGCCCAGCCCCCAC	392197
rs764481838	snp	G/T	9.90136e-05	0.00703541	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132382	TGTGTGTGTGTGTGT[G/T]CACCCATCAGTGTGG	392197
rs764499783	snp	A/C/T	3.84773e-05	0.00438605	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133461	CTTGGAGTGATGATC[A/C/T]AGCTGCTTGTGCCCG	392197
rs764512838	snp	C/T	1.98702e-05	0.00315194	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133099	TGAGACATGTATGGC[C/T]GCATGTCACGGCACT	392197
rs764519837	snp	C/T	1.83694e-05	0.00303057	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133792	ACCGCAGCAGGTCTC[C/T]TGCTACTCAGAGGAA	392197
rs764587683	snp	C/T	2.07781e-05	0.00322314	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133024	TGTCCGTTGTGACAA[C/T]TCCACCCAGCGTGGA	392197
rs764777093	snp	C/T	9.29982e-05	0.00681839	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134012	AGTCGTCTTCCATGT[C/T]GCCCGCAACAAGGAT	392197
rs764804541	snp	C/G/T	7.41268e-05	0.00608758	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133694	GGGACAGCATGTAGT[C/G/T]GGAAAGCGGCAGTGT	392197
rs764862476	snp	C/T	3.71478e-05	0.00430958	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133672	TGACACGTTTGAGAG[C/T]CCTCCCGGGACAGCA	392197
rs764988083	snp	A/G	7.54219e-05	0.00614046	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133321	TGCTTGACACTCTGA[A/G]CTGCCTGGATATCCA	392197
rs765076098	snp	A/T	9.8866e-05	0.00703017	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132849	TCTTGGTTCCCTGCC[A/T]CTTGACACACTCTCA	392197
rs765100507	snp	A/G/T	7.5899e-05	0.00615991	missense, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133356	GATGTCCAGGTAAGG[A/G/T]TCAAAGGTGTCTGAA	392197
rs765102816	snp	C/T	1.83971e-05	0.00303285	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133852	ACAGGAGCCAAATCA[C/T]CACAGAGGTCGAAAC	392197
rs765190409	snp	A/G	3.51914e-05	0.00419458	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132909	GTAAAAGAGGACATA[A/G]GCCTGTTGACTCAGG	392197
rs765191501	snp	A/G/T	5.91341e-05	0.00543729	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132530	ACTCCTGATCTGTCG[A/G/T]TTTCGTCGAAGAGAG	392197
rs765192902	snp	A/G	3.68473e-05	0.00429212	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133870	CAGAGGTCGAAACGG[A/G]TCTCAGATGAGAGTG	392197
rs765234783	snp	A/G	6.06459e-05	0.00550629	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132495	CCCTTGCAGAGAAGC[A/G]AGTGTGCCAGTGTTC	392197
rs765255328	snp	C/T	0.000396994	0.0140833	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133541	GGGCATCCTCCTGCT[C/T]ACCTCTATGGAAGCC	392197
rs765303548	snp	A/G	3.71271e-05	0.00430838	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133184	TCAATACAAGAATGA[A/G]GACCTTGGCAGAAGT	392197
rs765510960	snp	C/T	1.86621e-05	0.00305462	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133216	GGTAAAGTTAACGTC[C/T]TGGAGGCAGGCGCCT	392197
rs765568954	snp	C/T	1.86111e-05	0.00305044	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132718	TGGTCTAAGGTGCTT[C/T]CCTGAGTGGCTCTTT	392197
rs765624845	in-del	-/AG	3.69406e-05	0.00429755	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133896	GAGTGGTGACTTTTC[-/AG]AGAGAGAAGTCCGCT	392197
rs765651353	snp	C/G	1.92143e-05	0.00309948	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133392	GTGGCAGTGGAGATA[C/G]TTGATTTGAGATCTC	392197
rs765738953	snp	C/G	1.92929e-05	0.00310581	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133446	GATGAGGGTGGTGTC[C/G]TTGGAGTGATGATCT	392197
rs765915221	snp	A/C	2.01485e-05	0.00317393	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133080	AAGAGGTCCTGTGTT[A/C]TGCTGAGACATGTAT	392197
rs765951433	snp	G/T	1.90605e-05	0.00308705	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132596	TTTTCATACCACACT[G/T]GTATTTTGATTGATG	392197
rs766067824	snp	A/G	9.34553e-05	0.00683512	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133258	AGACCACAATGATAG[A/G]CATTCTCTCCATTGA	392197
rs766161477	snp	A/G	7.43218e-05	0.00609552	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133639	TGCATAGTACAGAAC[A/G]TGCAGCACTTGTGAA	392197
rs766176572	in-del	-/TGTG			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134436	GTGTCTGTGTGTGTG[-/TGTG]TGTGTGTGTGTGTGT	392197
rs766254382	snp	A/G	3.71402e-05	0.00430914	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133668	AAGATGACACGTTTG[A/G]GAGTCCTCCCGGGAC	392197
rs766331193	snp	C/G	2.48007e-05	0.00352132	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132900	CTTCTGGATGTAAAA[C/G]AGGACATAGGCCTGT	392197
rs766339676	snp	C/G	1.839e-05	0.00303227	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133845	TCTTGCCACAGGAGC[C/G]AAATCATCACAGAGG	392197
rs766360987	snp	A/G	1.83744e-05	0.00303098	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133804	CTCCTGCTACTCAGA[A/G]GAAGCTTCTCCCTGG	392197
rs766429651	snp	A/G/T	3.78252e-05	0.00434873	missense, stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133538	CATGGGCATCCTCCT[A/G/T]CTCACCTCTATGGAA	392197
rs766492898	snp	G/T	0.000142064	0.00842686	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132485	TCCTGGTGCTCCCTT[G/T]CAGAGAAGCGAGTGT	392197
rs766632713	snp	A/G	5.66374e-05	0.00532123	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133558	CCTCTATGGAAGCCA[A/G]CAGCCAATACCTGTG	392197
rs766759743	snp	A/G	0.000148918	0.00862767	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134048	GGTTTTTCTGCTGGG[A/G]CCGCAGGTTGCAGCA	392197
rs766887803	snp	G/T	9.3057e-05	0.00682055	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132714	CCAGTGGTCTAAGGT[G/T]CTTTCCTGAGTGGCT	392197
rs766901626	snp	C/G	5.535e-05	0.00526041	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133727	ATGTCAGGCACTGCA[C/G]GGAAACGTTCACATA	392197
rs766974250	in-del	-/G	1.84369e-05	0.00303614	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133734	GCACTGCAGGGAAAC[-/G]TTCACATAGAAGGTA	392197
rs766989492	snp	A/G	1.91834e-05	0.00309698	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133387	ACGCCGTGGCAGTGG[A/G]GATACTTGATTTGAG	392197
rs767097322	snp	A/C/T	5.55863e-05	0.00527168	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133938	AAAAGCTGCATCTAG[A/C/T]CGAGAAGATGTGAGT	392197
rs767104643	in-del	-/GTGC	9.70791e-05	0.00696636	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132380	TGTGTGTGTGTGTGT[-/GTGC]ACCCATCAGTGTGGG	392197
rs767117530	snp	A/C/T	0.000106076	0.00728203	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132958	GCAGTGACCTCGGCA[A/C/T]CATCCATTTTATACC	392197
rs767173107	snp	A/T	1.90842e-05	0.00308897	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132586	GGATGATGGTTTTTC[A/T]TACCACACTTGTATT	392197
rs767185230	snp	A/G	1.85537e-05	0.00304574	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133604	GGCCAGGACTGTGGA[A/G]GGCCCATGTGATGTG	392197
rs767353584	snp	G/T	0.000317629	0.0125982	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133226	ACGTCTTGGAGGCAG[G/T]CGCCTTCTGGAGACA	392197
rs767388919	snp	C/T	3.71602e-05	0.0043103	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133974	AAAGTGATTGAACTG[C/T]CAGTCACCTCCCAAA	392197
rs767401621	snp	A/G	0.00011147	0.00746477	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133634	GAGCTTGCATAGTAC[A/G]GAACATGCAGCACTT	392197
rs767491523	snp	C/T	0.000130894	0.00808886	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133255	CAAAGACCACAATGA[C/T]AGGCATTCTCTCCAT	392197
rs767709286	snp	A/C	2.0729e-05	0.00321933	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132445	AGCAGAGATCTCTTG[A/C]TGTGTTTGTTATTCC	392197
rs767787164	snp	C/G	3.67492e-05	0.0042864	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133798	GCAGGTCTCCTGCTA[C/G]TCAGAGGAAGCTTCT	392197
rs767898553	snp	A/G	0.00021804	0.010439	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133102	GACATGTATGGCTGC[A/G]TGTCACGGCACTTAG	392197
rs768044896	snp	C/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135611	AGGGCAGAATTGAGG[C/T]CCGGCGCCAAGGCCT	392197
rs768103685	snp	A/C	1.88209e-05	0.00306759	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132744	TCTTTCCACCAAGTG[A/C]TCGTCCAACTCGGGT	392197
rs768243732	snp	C/G	1.86405e-05	0.00305286	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133207	GCAGAAGTGGGTAAA[C/G]TTAACGTCTTGGAGG	392197
rs768350502	snp	A/C/G/T	0.00150611	0.027404	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133414	TGAGATCTCCAATAC[A/C/G/T]CTCCAAATATTTGGT	392197
rs768352653	snp	A/G	1.89077e-05	0.00307465	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132772	GGTACCTGGAGGCAA[A/G]GGTGGTCTCTCTTGA	392197
rs768358330	snp	C/T	0.000110276	0.00742467	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133754	CATAGAAGGTATTTC[C/T]TATCTTCTGGAGCCC	392197
rs768461258	snp	C/T	0.000288036	0.0119973	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133049	CGTGGACCAGCACAG[C/T]ATAGAGGACATAGAC	392197
rs768505651	snp	C/T	3.71568e-05	0.0043101	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133971	TGAAAAGTGATTGAA[C/T]TGCCAGTCACCTCCC	392197
rs768549809	in-del	-/AA	1.87005e-05	0.00305776	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133241	GCGCCTTCTGGAGAC[-/AA]AGACCACAATGATAG	392197
rs768608694	snp	A/G	2.09115e-05	0.00323347	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133005	TTTGACATAAGAGAA[A/G]TAATGTCCGTTGTGA	392197
rs768695428	snp	G/T	3.7143e-05	0.0043093	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133628	TGATGTGAGCTTGCA[G/T]AGTACAGAACATGCA	392197
rs768705010	snp	C/G/T	0.00032591	0.0127615	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132579	CTGTTCAGGATGATG[C/G/T]TTTTTCATACCACAC	392197
rs768757290	snp	C/T	1.85924e-05	0.00304891	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133995	ACCTCCCAAATAGAG[C/T]GAGTCGTCTTCCATG	392197
rs768875169	snp	A/C	3.75453e-05	0.00433258	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133289	GTTCTTTGGGCTTCA[A/C]CAACTGTTCCAAAGC	392197
rs768953808	snp	A/T	4.16701e-05	0.00456435	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132438	GCACACAAGCAGAGA[A/T]CTCTTGCTGTGTTTG	392197
rs768967041	snp	C/T	0.00125	0.0249687	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133340	CCTGGATATCCAGGG[C/T]GATGTCCAGGTAAGG	392197
rs769110625	snp	C/T	2.3142e-05	0.00340154	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132883	TGTCTTTCCCATTCA[C/T]TCTTCTGGATGTAAA	392197
rs769133503	snp	A/T	5.66064e-05	0.00531978	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133547	CCTCCTGCTCACCTC[A/T]ATGGAAGCCAGCAGC	392197
rs769194061	snp	A/G	1.84103e-05	0.00303394	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133859	CCAAATCATCACAGA[A/G]GTCGAAACGGGTCTC	392197
rs769225504	snp	C/G	3.7219e-05	0.00431371	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133165	GTGACATCGGAGAAT[C/G]TCTTCAATACAAGAA	392197
rs769272975	snp	C/T	0.000569806	0.0168694	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133750	TTCACATAGAAGGTA[C/T]TTCCTATCTTCTGGA	392197
rs769296837	snp	A/G	1.89489e-05	0.003078	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133121	CACGGCACTTAGGAT[A/G]TTGCACATTCTTGGC	392197
rs769341853	snp	G/T			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12131917	AGAGCACCGTTCCTA[G/T]CTTCCAATTGAATTC	392197
rs769447440	snp	A/G			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132228	GGCTCATCCTGAGAC[A/G]CAGCCATCACTATCC	392197
rs769508744	snp	C/G	0.000131151	0.00809682	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132741	GGCTCTTTCCACCAA[C/G]TGCTCGTCCAACTCG	392197
rs769607265	snp	C/T	0.000110848	0.00744392	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133716	CGGCAGTGTGTATGT[C/T]AGGCACTGCAGGGAA	392197
rs769776265	in-del	-/TC	2.17488e-05	0.00329757	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132874	CTCTCACTGTGTCTT[-/TC]CCATTCACTCTTCTG	392197
rs769777535	snp	G/T	3.82409e-05	0.00437253	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133378	GTGTCTGAAACGCCG[G/T]GGCAGTGGAGATACT	392197
rs769846564	snp	C/G	3.7022e-05	0.00430228	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133922	TCCGCTGGATTTCAG[C/G]AAAAGCTGCATCTAG	392197
rs769866476	snp	C/G	2.15227e-05	0.00328038	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132950	TGCCAGAGGCAGTGA[C/G]CTCGGCATCATCCAT	392197
rs769907288	snp	C/G	1.89245e-05	0.00307602	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132617	TTGATTGATGAATCA[C/G]AAGTACGTTGGGAGG	392197
rs769916138	snp	A/T	1.85658e-05	0.00304673	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133954	CGAGAAGATGTGAGT[A/T]TTGAAAAGTGATTGA	392197
rs769953341	snp	C/T	4.15818e-05	0.00455951	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132995	CTTCTTGAGCTTTGA[C/T]ATAAGAGAAGTAATG	392197
rs770003787	snp	C/G/T	3.73952e-05	0.00432394	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133246	TTCTGGAGACAAAGA[C/G/T]CACAATGATAGGCAT	392197
rs770094674	snp	C/T	1.89406e-05	0.00307733	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132775	ACCTGGAGGCAAGGG[C/T]GGTCTCTCTTGAGCT	392197
rs770342396	snp	C/G/T	7.34786e-05	0.00606091	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133789	CCCACCGCAGCAGGT[C/G/T]TCCTGCTACTCAGAG	392197
rs770380078	snp	C/T	5.73433e-05	0.00535428	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133483	TTGTGCCCGGGAAGG[C/T]ATGCCTTTTTCATGG	392197
rs770389000	snp	A/C/T	3.79617e-05	0.00435656	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133519	ACAGTAAACATGAGA[A/C/T]ATTCATGGGCATCCT	392197
rs770590166	snp	C/G	0.000102317	0.0071518	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132469	TTATTCCCTTTGGAT[C/G]TCCTGGTGCTCCCTT	392197
rs770672355	snp	C/T	7.46032e-05	0.00610705	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133157	TGTTGCCTGTGACAT[C/T]GGAGAATCTCTTCAA	392197
rs770692024	snp	C/T	1.86346e-05	0.00305237	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132664	TTTCTGACGTTGAAC[C/T]CAGGCTTCGTTTTGT	392197
rs770739509	snp	C/T	3.71927e-05	0.00431219	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134005	TAGAGTGAGTCGTCT[C/T]CCATGTCGCCCGCAA	392197
rs770762436	snp	A/G	3.7103e-05	0.00430699	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132695	TTTGCTCTTGGGGGA[A/G]TTTCCAGTGGTCTAA	392197
rs770831075	snp	A/T	1.86097e-05	0.00305033	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134035	ACAAGGATCACAAGG[A/T]TTTTCTGCTGGGACC	392197
rs770921013	snp	C/T	1.86211e-05	0.00305126	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134057	GCTGGGACCGCAGGT[C/T]GCAGCAAGACGCTAT	392197
rs770921179	snp	A/T	1.85424e-05	0.00304481	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133688	CCTCCCGGGACAGCA[A/T]GTAGTTGGAAAGCGG	392197
rs771044883	snp	A/T	8.31964e-05	0.00644913	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132976	TCCATTTTATACCAC[A/T]GGCCTTCTTGAGCTT	392197
rs771151346	snp	A/T	3.74518e-05	0.00432718	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133593	CTGGATGACATGGCC[A/T]GGACTGTGGAGGGCC	392197
rs771244554	snp	A/C/T	5.60987e-05	0.00529592	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133247	TCTGGAGACAAAGAC[A/C/T]ACAATGATAGGCATT	392197
rs771370598	snp	A/G	5.57046e-05	0.00527723	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133619	GGGCCCATGTGATGT[A/G]AGCTTGCATAGTACA	392197
rs771463070	snp	A/G	5.59675e-05	0.00528967	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133213	GTGGGTAAAGTTAAC[A/G]TCTTGGAGGCAGGCG	392197
rs771551001	snp	A/G	3.73993e-05	0.00432414	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133241	GCGCCTTCTGGAGAC[A/G]AAGACCACAATGATA	392197
rs771551085	snp	A/C/T	0.00432783	0.0463168	synonymous-codon, missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133758	GAAGGTATTTCCTAT[A/C/T]TTCTGGAGCCCAGCC	392197
rs771553045	snp	C/T	1.88283e-05	0.00306819	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132748	TCCACCAAGTGCTCG[C/T]CCAACTCGGGTACCT	392197
rs771574145	in-del	-/CAGC	0.000212657	0.0103094	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133414	GAGATCTCCAATACG[-/CAGC]CTCCAAATATTTGGT	392197
rs771724007	snp	A/C	2.14149e-05	0.00327215	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132408	TGTGGGTCGGTACTT[A/C]CACTGTGATCACTGG	392197
rs771729162	snp	G/T	7.65477e-05	0.00618611	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133478	GCTGCTTGTGCCCGG[G/T]AAGGCATGCCTTTTT	392197
rs771813328	snp	A/C/G	3.87246e-05	0.00440012	missense, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133110	TGGCTGCATGTCACG[A/C/G]CACTTAGGATATTGC	392197
rs771863135	snp	A/G	0.000101701	0.00713024	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133066	TAGAGGACATAGACA[A/G]GAGGTCCTGTGTTCT	392197
rs771897307	snp	A/T	1.8659e-05	0.00305436	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132655	CCTTCAACTTTTCTG[A/T]CGTTGAACTCAGGCT	392197
rs771909706	snp	C/G/T	3.77829e-05	0.00434627	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133543	GCATCCTCCTGCTCA[C/G/T]CTCTATGGAAGCCAG	392197
rs771999413	snp	A/T	3.75587e-05	0.00433335	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133294	TTGGGCTTCACCAAC[A/T]GTTCCAAAGCTTGCT	392197
rs772141293	snp	A/C	7.44311e-05	0.0061	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134029	CCCGCAACAAGGATC[A/C]CAAGGTTTTTCTGCT	392197
rs772143053	snp	A/C/G/T	7.41656e-05	0.00608922	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133687	TCCTCCCGGGACAGC[A/C/G/T]TGTAGTTGGAAAGCG	392197
rs772236941	snp	A/C	1.89582e-05	0.00307876	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133346	TATCCAGGGCGATGT[A/C]CAGGTAAGGGTCAAA	392197
rs772270937	snp	C/G	4.87234e-05	0.00493552	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132888	TTCCCATTCACTCTT[C/G]TGGATGTAAAAGAGG	392197
rs772300057	snp	A/G	1.84177e-05	0.00303456	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133866	ATCACAGAGGTCGAA[A/G]CGGGTCTCAGATGAG	392197
rs772344836	in-del	-/GC/GTGC			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132381	TGTGTGTGTGTGTGT[-/GC/GTGC]GCACCCATCAGTGTG	392197
rs772354326	snp	C/T	2.03159e-05	0.00318709	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132482	ATCTCCTGGTGCTCC[C/T]TTGCAGAGAAGCGAG	392197
rs772445941	snp	C/G	5.97247e-05	0.00546432	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132519	AGTGTTCATGGACTC[C/G]TGATCTGTCGGTTTC	392197
rs772555466	snp	C/T	3.69781e-05	0.00429973	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133909	TCAGAGAGAGAAGTC[C/T]GCTGGATTTCAGCAA	392197
rs772628660	snp	A/C	1.88653e-05	0.0030712	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133553	GCTCACCTCTATGGA[A/C]GCCAGCAGCCAATAC	392197
rs772699196	snp	A/T	9.65167e-05	0.00694615	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133439	TTTGGTGGATGAGGG[A/T]GGTGTCCTTGGAGTG	392197
rs772763020	snp	C/G/T	6.07371e-05	0.00551049	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133074	ATAGACAAGAGGTCC[C/G/T]GTGTTCTGCTGAGAC	392197
rs772766100	snp	C/T	3.67289e-05	0.00428522	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133781	GCCCAGCCCCCACCG[C/T]AGCAGGTCTCCTGCT	392197
rs772788974	snp	A/G/T	7.64853e-05	0.00618366	stop-gained, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133482	CTTGTGCCCGGGAAG[A/G/T]CATGCCTTTTTCATG	392197
rs772790579	in-del	-/G	1.92996e-05	0.00310635	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133434	AAATATTTGGTGGAT[-/G]AGGGTGGTGTCCTTG	392197
rs772830588	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134121	CTGGCCGCATCAGCC[C/G]TTATATAACTCACCC	392197
rs773165144	snp	C/G	1.89665e-05	0.00307943	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133350	CAGGGCGATGTCCAG[C/G]TAAGGGTCAAAGGTG	392197
rs773253316	snp	A/C	3.75947e-05	0.00433543	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133299	CTTCACCAACTGTTC[A/C]AAAGCTTGCTTGACA	392197
rs773257019	snp	C/G	1.83839e-05	0.00303176	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133841	GCTGTCTTGCCACAG[C/G]AGCCAAATCATCACA	392197
rs773280303	snp	A/G	7.74728e-05	0.00622338	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132839	CACCAAGGGCTCTTG[A/G]TTCCCTGCCTCTTGA	392197
rs773367053	snp	A/G	2.46831e-05	0.00351297	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132892	CATTCACTCTTCTGG[A/G]TGTAAAAGAGGACAT	392197
rs773450756	snp	C/T	2.0292e-05	0.00318521	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132483	TCTCCTGGTGCTCCC[C/T]TGCAGAGAAGCGAGT	392197
rs773512861	snp	G/T			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132168	ACAGTCCCTCCAGAG[G/T]TTCGGAAGACTCACG	392197
rs773523994	snp	C/T	5.52613e-05	0.0052562	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133867	TCACAGAGGTCGAAA[C/T]GGGTCTCAGATGAGA	392197
rs773542601	snp	C/T	0.00041759	0.0144437	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132520	GTGTTCATGGACTCC[C/T]GATCTGTCGGTTTCG	392197
rs773606291	snp	C/T	1.89181e-05	0.0030755	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133532	GAAATTCATGGGCAT[C/T]CTCCTGCTCACCTCT	392197
rs773610939	snp	G/T	1.86055e-05	0.00304999	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132711	TTTCCAGTGGTCTAA[G/T]GTGCTTTCCTGAGTG	392197
rs773790291	snp	A/C/T	0.000262302	0.0114493	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133591	GGCTGGATGACATGG[A/C/T]CAGGACTGTGGAGGG	392197
rs773792448	snp	A/G	1.85623e-05	0.00304645	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133174	GAGAATCTCTTCAAT[A/G]CAAGAATGAGGACCT	392197
rs773792880	snp	C/G			missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133417	GATCTCCAATACGCT[C/G]CAAATATTTGGTGGA	392197
rs773880411	snp	A/C/T	0.000205181	0.010127	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133212	AGTGGGTAAAGTTAA[A/C/T]GTCTTGGAGGCAGGC	392197
rs773883622	snp	C/T	5.64956e-05	0.00531456	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132746	TTTCCACCAAGTGCT[C/T]GTCCAACTCGGGTAC	392197
rs773921902	snp	A/G	1.93086e-05	0.00310707	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133423	CAATACGCTCCAAAT[A/G]TTTGGTGGATGAGGG	392197
rs773951485	snp	C/T	0.0043289	0.0463218	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133755	ATAGAAGGTATTTCC[C/T]ATCTTCTGGAGCCCA	392197
rs774009585	snp	A/G	0.0163664	0.0889682	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133010	CATAAGAGAAGTAAT[A/G]TCCGTTGTGACAACT	392197
rs774018125	snp	A/T	1.85207e-05	0.00304303	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133935	AGCAAAAGCTGCATC[A/T]AGCCGAGAAGATGTG	392197
rs774135250	in-del	-/TGTA	4.87436e-05	0.00493654	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132376	GTTTGTGTGTGTGTG[-/TGTA]TGTGTGCACCCATCA	392197
rs774186549	in-del	-/G	1.88067e-05	0.00306643	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133307	ACTGTTCCAAAGCTT[-/G]CTTGACACTCTGAGC	392197
rs774193678	snp	C/G	5.57719e-05	0.00528042	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133998	TCCCAAATAGAGTGA[C/G]TCGTCTTCCATGTCG	392197
rs774290731	snp	A/T	4.1099e-05	0.00453297	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133050	GTGGACCAGCACAGC[A/T]TAGAGGACATAGACA	392197
rs774294816	snp	A/T	1.85792e-05	0.00304783	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133972	GAAAAGTGATTGAAC[A/T]GCCAGTCACCTCCCA	392197
rs774396771	snp	A/G/T	0.00142859	0.0266896	stop-gained, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133248	CTGGAGACAAAGACC[A/G/T]CAATGATAGGCATTC	392197
rs774429022	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135307	CCTTTTTAATGCTGG[A/C]CCTTGTTTCACAGGG	392197
rs774487818	snp	A/C	1.87749e-05	0.00306384	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133291	TCTTTGGGCTTCACC[A/C]ACTGTTCCAAAGCTT	392197
rs774574096	snp	A/G	0.000172369	0.00928197	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132832	TCTTCAGCACCAAGG[A/G]CTCTTGGTTCCCTGC	392197
rs774632310	snp	C/T	2.03469e-05	0.00318952	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132478	TTGGATCTCCTGGTG[C/T]TCCCTTGCAGAGAAG	392197
rs774671797	snp	C/T	2.33108e-05	0.00341392	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132884	GTCTTTCCCATTCAC[C/T]CTTCTGGATGTAAAA	392197
rs774751951	snp	C/T	6.23215e-05	0.00558183	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132442	ACAAGCAGAGATCTC[C/T]TGCTGTGTTTGTTAT	392197
rs774768858	snp	A/G	1.89145e-05	0.00307521	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133126	CACTTAGGATATTGC[A/G]CATTCTTGGCAAGTT	392197
rs774821025	snp	A/G			synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133896	GAGTGGTGACTTTTC[A/G]GAGAGAGAAGTCCGC	392197
rs774865648	snp	C/G	1.83849e-05	0.00303185	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133827	CTCCCTGGGAGCAAG[C/G]TGTCTTGCCACAGGA	392197
rs774978624	snp	G/T	3.72204e-05	0.00431379	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132670	ACGTTGAACTCAGGC[G/T]TCGTTTTGTTTTGCT	392197
rs775005104	snp	A/C/T	0.000293826	0.0121172	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133779	GAGCCCAGCCCCCAC[A/C/T]GCAGCAGGTCTCCTG	392197
rs775040993	snp	A/G	1.848e-05	0.00303968	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133717	GGCAGTGTGTATGTC[A/G]GGCACTGCAGGGAAA	392197
rs775043478	snp	C/G	3.77451e-05	0.00434409	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133550	CCTGCTCACCTCTAT[C/G]GAAGCCAGCAGCCAA	392197
rs775054340	snp	A/G			downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132274	AGAGACAGAAACTGG[A/G]GCTCCTCATTACTTT	392197
rs775058697	snp	C/T	1.85986e-05	0.00304942	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133170	ATCGGAGAATCTCTT[C/T]AATACAAGAATGAGG	392197
rs775066931	snp	G/T	0.000186119	0.00964495	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134041	ATCACAAGGTTTTTC[G/T]GCTGGGACCGCAGGT	392197
rs775124660	snp	A/C			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135287	TGAAACAGAAGATAG[A/C]ATAACCTTTTTAATG	392197
rs775403371	snp	A/C	3.84549e-05	0.00438474	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132573	GCTTTGCTGTTCAGG[A/C]TGATGGTTTTTCATA	392197
rs775411714	snp	C/G/T	7.65732e-05	0.00618721	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133381	TCTGAAACGCCGTGG[C/G/T]AGTGGAGATACTTGA	392197
rs775533975	snp	A/G	1.86659e-05	0.00305493	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133219	AAAGTTAACGTCTTG[A/G]AGGCAGGCGCCTTCT	392197
rs775587739	snp	A/G	2.07898e-05	0.00322405	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132996	TTCTTGAGCTTTGAC[A/G]TAAGAGAAGTAATGT	392197
rs775647378	snp	C/T	1.85758e-05	0.00304755	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133626	TGTGATGTGAGCTTG[C/T]ATAGTACAGAACATG	392197
rs775739823	snp	G/T			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134651	TAATAATAAAGGAGA[G/T]ATCCGTGGAATCAAA	392197
rs776101730	snp	G/T	1.83883e-05	0.00303213	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133822	AGCTTCTCCCTGGGA[G/T]CAAGCTGTCTTGCCA	392197
rs776115530	snp	C/T	2.01408e-05	0.00317332	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133081	AGAGGTCCTGTGTTC[C/T]GCTGAGACATGTATG	392197
rs776188819	snp	G/T	1.86104e-05	0.00305038	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134036	CAAGGATCACAAGGT[G/T]TTTCTGCTGGGACCG	392197
rs776288222	snp	G/T	1.86242e-05	0.00305152	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132667	CTGACGTTGAACTCA[G/T]GCTTCGTTTTGTTTT	392197
rs776380717	snp	A/T	1.85558e-05	0.00304591	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132696	TTGCTCTTGGGGGAA[A/T]TTCCAGTGGTCTAAG	392197
rs776467872	snp	G/T	1.85723e-05	0.00304727	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133669	AGATGACACGTTTGA[G/T]AGTCCTCCCGGGACA	392197
rs776542728	snp	C/T	8.79237e-05	0.00662979	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132937	AGGACAGAGGTGATG[C/T]CAGAGGCAGTGACCT	392197
rs776641624	snp	C/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12135096	CATATCTCACAGCAT[C/G]GGTGATACTGTTTCC	392197
rs776645815	snp	A/G/T	3.79552e-05	0.00435619	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133355	CGATGTCCAGGTAAG[A/G/T]GTCAAAGGTGTCTGA	392197
rs776947783	snp	A/G	1.86977e-05	0.00305753	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133243	GCCTTCTGGAGACAA[A/G]GACCACAATGATAGG	392197
rs776965213	snp	C/G	1.87184e-05	0.00305922	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133594	TGGATGACATGGCCA[C/G]GACTGTGGAGGGCCC	392197
rs777049366	snp	A/C/G	0.000655161	0.0180876	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133215	GGGTAAAGTTAACGT[A/C/G]TTGGAGGCAGGCGCC	392197
rs777222260	snp	C/T	1.88418e-05	0.00306929	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132749	CCACCAAGTGCTCGT[C/T]CAACTCGGGTACCTG	392197
rs777228060	snp	A/G	1.83835e-05	0.00303174	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133818	AGGAAGCTTCTCCCT[A/G]GGAGCAAGCTGTCTT	392197
rs777310148	snp	A/G/T	7.56392e-05	0.00614937	missense, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132774	TACCTGGAGGCAAGG[A/G/T]TGGTCTCTCTTGAGC	392197
rs777386482	snp	C/T	3.77986e-05	0.00434717	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132813	CGTTGCTGGCCTGTC[C/T]GTGTCTTCAGCACCA	392197
rs777426256	snp	A/T	1.89968e-05	0.00308189	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133513	GCATCCACAGTAAAC[A/T]TGAGAAATTCATGGG	392197
rs777482158	snp	C/G	2.00078e-05	0.00316283	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132853	GGTTCCCTGCCTCTT[C/G]ACACACTCTCACTGT	392197
rs777484152	snp	G/T	2.13295e-05	0.00326562	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132412	GGTCGGTACTTCCAC[G/T]GTGATCACTGGCACA	392197
rs777506130	snp	A/T	3.68006e-05	0.0042894	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133856	GAGCCAAATCATCAC[A/T]GAGGTCGAAACGGGT	392197
rs777603114	snp	A/G	3.73399e-05	0.00432071	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133153	AGTTTGTTGCCTGTG[A/G]CATCGGAGAATCTCT	392197
rs777717606	snp	A/C/T	3.7159e-05	0.00431026	synonymous-codon, missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133188	TACAAGAATGAGGAC[A/C/T]TTGGCAGAAGTGGGT	392197
rs777793852	in-del	-/ACAAGGATC	1.86048e-05	0.00304993	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134020	TCCATGTCGCCCGCA[-/ACAAGGATC]ACAAGGTTTTTCTGC	392197
rs777815193	snp	A/C	1.86083e-05	0.00305021	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134030	CCGCAACAAGGATCA[A/C]AAGGTTTTTCTGCTG	392197
rs777887550	snp	C/G	1.86482e-05	0.00305348	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132728	TGCTTTCCTGAGTGG[C/G]TCTTTCCACCAAGTG	392197
rs777888833	snp	A/C	1.92387e-05	0.00310145	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133401	GAGATACTTGATTTG[A/C]GATCTCCAATACGCT	392197
rs777907765	snp	A/C/G	7.39664e-05	0.00608099	stop-gained, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133710	GGAAAGCGGCAGTGT[A/C/G]TATGTCAGGCACTGC	392197
rs777909218	snp	A/G/T	3.72434e-05	0.00431516	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134055	CTGCTGGGACCGCAG[A/G/T]TTGCAGCAAGACGCT	392197
rs777934376	in-del	-/CTC	1.90148e-05	0.00308335	cds-indel, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132791	GGTCTCTCTTGAGCT[-/CTC]CTTGCGTTGCTGGCC	392197
rs777978178	snp	C/T	2.09352e-05	0.0032353	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132970	GCATCATCCATTTTA[C/T]ACCACTGGCCTTCTT	392197
rs778004223	snp	A/C/G	0.000536357	0.0163683	missense, synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132933	ACTCAGGACAGAGGT[A/C/G]ATGCCAGAGGCAGTG	392197
rs778176441	snp	C/T	1.94903e-05	0.00312166	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132547	TTCGTCGAAGAGAGG[C/T]TTAGCAGGGAGCTTT	392197
rs778277631	snp	G/T	1.85558e-05	0.00304591	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133945	GCATCTAGCCGAGAA[G/T]ATGTGAGTTTTGAAA	392197
rs778281912	snp	A/C	0.00013194	0.00812111	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133136	ATTGCACATTCTTGG[A/C]AAGTTTGTTGCCTGT	392197
rs778447630	snp	A/G	7.42666e-05	0.00609326	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133610	GACTGTGGAGGGCCC[A/G]TGTGATGTGAGCTTG	392197
rs778454909	snp	A/G			upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134815	TCAAATGGTAGAAAC[A/G]TGCACTGAAGTTTGA	392197
rs778539519	snp	C/T	1.86893e-05	0.00305685	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133234	GAGGCAGGCGCCTTC[C/T]GGAGACAAAGACCAC	392197
rs778612463	snp	C/T	4.10855e-05	0.00453222	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132459	GCTGTGTTTGTTATT[C/T]CCTTTGGATCTCCTG	392197
rs778633367	snp	C/T	3.48292e-05	0.00417294	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132807	TCCTTGCGTTGCTGG[C/T]CTGTCTGTGTCTTCA	392197
rs778661346	snp	A/G	0.000513694	0.0160182	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133504	TTTTTCATGGCATCC[A/G]CAGTAAACATGAGAA	392197
rs778675191	snp	C/G	1.83761e-05	0.00303112	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133809	GCTACTCAGAGGAAG[C/G]TTCTCCCTGGGAGCA	392197
rs778719078	snp	C/T	8.59051e-05	0.00655326			GRCh38.p7	8:12132403	ATCAGTGTGGGTCGG[C/T]ACTTCCACTGTGATC	392197
rs778741377	in-del	GTGTGTGTGTTTG/T					GRCh38.p7	8:12134461	TGTGTGTGTGTGTGT[GTGTGTGTGTTTG/T]TGTGTGTGTGTGTGT	392197
rs779029740	snp	A/G	1.87306e-05	0.00306022	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133146	CTTGGCAAGTTTGTT[A/G]CCTGTGACATCGGAG	392197
rs779123555	snp	C/G	1.85541e-05	0.00304577	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133683	AGAGTCCTCCCGGGA[C/G]AGCATGTAGTTGGAA	392197
rs779199706	snp	A/G/T	5.56199e-05	0.00527322	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132692	TGTTTTGCTCTTGGG[A/G/T]GAATTTCCAGTGGTC	392197
rs779221154	snp	C/T	5.69503e-05	0.00533591	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133366	TAAGGGTCAAAGGTG[C/T]CTGAAACGCCGTGGC	392197
rs779311443	snp	A/G	4.55208e-05	0.00477057	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132930	TTGACTCAGGACAGA[A/G]GTGATGCCAGAGGCA	392197
rs779379530	snp	A/G	1.95624e-05	0.00312743	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132539	CTGTCGGTTTCGTCG[A/G]AGAGAGGTTTAGCAG	392197
rs779401180	snp	A/T	0.000168269	0.00917093	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132965	CCTCGGCATCATCCA[A/T]TTTATACCACTGGCC	392197
rs779475319	snp	C/T	3.99832e-05	0.00447102	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132512	GTGTGCCAGTGTTCA[C/T]GGACTCCTGATCTGT	392197
rs779512535	snp	A/G	1.86197e-05	0.00305115	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133197	GAGGACCTTGGCAGA[A/G]GTGGGTAAAGTTAAC	392197
rs779521859	snp	A/G	0.000570613	0.0168814	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133863	ATCATCACAGAGGTC[A/G]AAACGGGTCTCAGAT	392197
rs779704508	snp	A/G/T	7.49546e-05	0.00612148	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133589	AGGGCTGGATGACAT[A/G/T]GCCAGGACTGTGGAG	392197
rs779788939	snp	C/T	0.000257074	0.0113345	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133772	TCTTCTGGAGCCCAG[C/T]CCCCACCGCAGCAGG	392197
rs779854328	in-del	-/AA	2.23656e-05	0.003344	frameshift-variant, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132877	CACTGTGTCTTTCCC[-/AA]ATTCACTCTTCTGGA	392197
rs779880641	snp	G/T	9.45474e-05	0.00687494	stop-gained, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132768	CTCGGGTACCTGGAG[G/T]CAAGGGTGGTCTCTC	392197
rs779977750	snp	A/G	0.00017251	0.00928577	downstream-variant-500B, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132396	TGCACCCATCAGTGT[A/G]GGTCGGTACTTCCAC	392197
rs780149163	snp	A/G	0.000133444	0.00816726	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133498	CATGCCTTTTTCATG[A/G]CATCCACAGTAAACA	392197
rs780248394	snp	A/G	2.06562e-05	0.00321367	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133043	ACCCAGCGTGGACCA[A/G]CACAGCATAGAGGAC	392197
rs780299201	snp	A/C	0.000204493	0.0101096	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133654	ATGCAGCACTTGTGA[A/C]GATGACACGTTTGAG	392197
rs780342645	snp	A/C	3.7815e-05	0.00434811	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132619	GATTGATGAATCACA[A/C]GTACGTTGGGAGGCA	392197
rs780392957	snp	C/T	0.00016717	0.00914095	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133678	GTTTGAGAGTCCTCC[C/T]GGGACAGCATGTAGT	392197
rs780432469	snp	A/C	1.87285e-05	0.00306005	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132640	TTGGGAGGCAGGGTA[A/C]CTTCAACTTTTCTGA	392197
rs780541479	snp	A/G	9.39783e-05	0.00685422	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132924	GGCCTGTTGACTCAG[A/G]ACAGAGGTGATGCCA	392197
rs780549802	snp	A/G	0.00024594	0.0110864	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133338	TGCCTGGATATCCAG[A/G]GCGATGTCCAGGTAA	392197
rs780637517	snp	C/G	2.00535e-05	0.00316644	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132507	AGCGAGTGTGCCAGT[C/G]TTCATGGACTCCTGA	392197
rs780639913	snp	A/G	0.000514593	0.0160322	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132878	CACTGTGTCTTTCCC[A/G]TTCACTCTTCTGGAT	392197
rs780827880	snp	C/T	0.000240094	0.010954	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133893	TGAGAGTGGTGACTT[C/T]TCAGAGAGAGAAGTC	392197
rs780829149	snp	C/G	4.0823e-05	0.00451772	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132474	CCCTTTGGATCTCCT[C/G]GTGCTCCCTTGCAGA	392197
rs780932864	snp	G/T	7.43978e-05	0.00609864	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133192	AGAATGAGGACCTTG[G/T]CAGAAGTGGGTAAAG	392197
rs781020687	snp	C/T	3.74104e-05	0.00432479	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132737	GAGTGGCTCTTTCCA[C/T]CAAGTGCTCGTCCAA	392197
rs781032279	snp	A/G	3.72523e-05	0.00431564	upstream-variant-2KB, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12134058	CTGGGACCGCAGGTT[A/G]CAGCAAGACGCTATC	392197
rs781108720	snp	A/G	1.76574e-05	0.00297126	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132760	TCGTCCAACTCGGGT[A/G]CCTGGAGGCAAGGGT	392197
rs781211877	snp	G/T	3.69665e-05	0.00429906	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133714	AGCGGCAGTGTGTAT[G/T]TCAGGCACTGCAGGG	392197
rs781325442	snp	A/C	0.00427815	0.0460519	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133744	GAAACGTTCACATAG[A/C]AGGTATTTCCTATCT	392197
rs781390464	snp	C/T	1.78411e-05	0.00298667	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132615	TTTTGATTGATGAAT[C/T]ACAAGTACGTTGGGA	392197
rs781413515	snp	C/T	3.6733e-05	0.00428546	missense, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12133768	CCTATCTTCTGGAGC[C/T]CAGCCCCCACCGCAG	392197
rs781418031	snp	G/T	6.2284e-05	0.00558015	synonymous-codon, intron-variant	USP17L7, FAM66D	GRCh38.p7	8:12132978	CATTTTATACCACTG[G/T]CCTTCTTGAGCTTTG	392197

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