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

USP17L8

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs11777626	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973646	cacacGGTTTCATAG[A/G]TAAAGATTTCTTCCC	392188
rs13251202	snp	A/G	0.496245	0.0431677	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974129	AGAGACTAATTGATG[A/G]CATTCCCCAAATTTA	392188
rs13257679	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974150	CCCAAATTTATGTGT[A/G]CCAGAAAAGAGAGAT	392188
rs13258372	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974401	TAATTTTGACAAAAG[A/C]AAACAAGGAAAATTA	392188
rs13259286	snp	C/T	0	0	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974066	TGAAGAGATACTCAG[C/T]GCACAAAGTAGACTG	392188
rs28696920	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973665	TGAAACCGTGTGTGT[G/T]TCTGTGTGTGTGTGT	392188
rs34844559	snp	C/G/T	0.5	0	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973391	CACCCCCACCAACCG[C/G/T]GAACACCCCACCCAC	392188
rs55684739	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973383	ATATAACTCACCCCC[A/T]CCAACCGTGAACACC	392188
rs55766577	snp	C/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973753	TACTTTTGGCAGCTA[C/T]CATCATCCTCTCAGC	392188
rs55926137	snp	C/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973343	GAGTCTTCAAATGAC[C/G]AGCTCTCTGGCCGCA	392188
rs55938735	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973557	TCCTCAGGGTGATAG[A/G]CACATATAATATGAG	392188
rs56056722	snp	A/C/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973550	AAATTACTCCTCAGG[A/C/G]TGATAGGCACATATA	392188
rs58042569	in-del	-/TTGTGTGTGT			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973700	TGTGTGTGTGTGTGT[-/TTGTGTGTGT]GTGTGTGCGCTTGTG	392188
rs59633206	snp	C/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973417	CCCACCCATCAGGTG[C/T]GCGATAAACCAATCA	392188
rs59868007	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973563	GGGTGATAGGCACAT[A/G]TAATATGAGTGTAAC	392188
rs60098696	in-del	-/AC			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973527	CATGACTTCTAGAAC[-/AC]CTGAATCAAATTACT	392188
rs62641384	snp	A/C/G/T	0.0272573	0.114054	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973179	AGCAAAAGCTGCATC[A/C/G/T]GGCCGAGGAGATGTG	392188
rs74968774	snp	A/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973597	GTTGGGACAGTGGCC[A/T]CACAGTTGCCTTATT	392188
rs75995985	snp	A/G	0.00299544	0.0385843	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973140	GAGTGGTGACTTCTC[A/G]GGGAGAGAAGTCCGC	392188
rs78915299	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974088	AGTAGACTGTGAAAG[A/C]CTTTGGGGAAATCAT	392188
rs112464135	snp	C/G	0	0	downstream-variant-500B, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971306	ATAGTAAACCATGTC[C/G]CCTGCAATAACCTCA	392188
rs112796125	snp	A/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973628	TTAGGTAAAAGAATG[A/T]CAGGGAAGAAATCTT	392188
rs113338263	snp	C/G	0	0	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973667	AAACCGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	392188
rs145140607	snp	A/G	0.264358	0.249587	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974027	ATACTAAAGCATCAA[A/G]TGGTAGAAACATGCA	392188
rs145384272	snp	A/G	0.482709	0.0913595	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972258	AGAGAAGTAATATCC[A/G]TTGTGACAACTCCAC	392188
rs148532652	snp	A/G	0.00225366	0.0334925	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972254	CATAAGAGAAGTAAT[A/G]TCCGTTGTGACAACT	392188
rs180910383	snp	A/C/G	0.000565451	0.0168049	synonymous-codon, missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972978	GCACTGCAGGGAAGC[A/C/G]TTCAAGTAGCAGGTA	392188
rs181647348	snp	C/T	0.0076432	0.0613448	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972395	CAAGTTTGTTGCCTG[C/T]GACATCGCAGAATCT	392188
rs183483361	snp	A/C	0.159292	0.232964	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973426	CAGGTGCGCGATAAA[A/C]CAATCAAATATCAGC	392188
rs183802595	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974110	GGAAATCATGCAATC[A/C]CCGAGAGACTAATTG	392188
rs184034050	snp	A/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974132	GACTAATTGATGGCA[A/T]TCCCCAAATTTATGT	392188
rs185274694	snp	A/C	0.00400113	0.0445483	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972983	GCAGGGAAGCATTCA[A/C]GTAGCAGGTATTTCC	392188
rs187300358	snp	C/G	0.0029967	0.0385923	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972403	TTGCCTGTGACATCG[C/G]AGAATCTCTTCAAGA	392188
rs188820015	snp	C/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973522	CCACATCATGACTTC[C/T]AGAACCTGAATCAAA	392188
rs189730259	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974392	AAAAAGTTCTAATTT[G/T]GACAAAAGAAAACAA	392188
rs189919259	snp	C/T			missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972260	AGAAGTAATATCCGT[C/T]GTGACAACTCCACCC	392188
rs190359008	snp	A/C	0.00113379	0.0237825	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973011	TCCCATATTCTGGAG[A/C]CCAGCCCCCACAGCA	392188
rs191814203	snp	A/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974131	AGACTAATTGATGGC[A/T]TTCCCCAAATTTATG	392188
rs192094999	snp	G/T	0.000813339	0.0201496	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972496	AGACAAAGACCGCAA[G/T]GATAGGCATTCTCTC	392188
rs199543709	snp	C/T	0.015872	0.0876588	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972777	AAATTCATGGGCATC[C/T]TCCTGCTTGCCTCTA	392188
rs199686396	snp	A/C	0.0768262	0.180308	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973275	CGCAACAAGGATCAC[A/C]AGGTTTTTCTGCTGG	392188
rs199773166	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974827	GGGCAGAATTGAGGC[A/C]CGGCGCCAAGGCCTC	392188
rs199927285	snp	C/T	0.00836139	0.0641154	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973153	TCAGGGAGAGAAGTC[C/T]GCTGGATTTCAGCAA	392188
rs199970737	snp	A/C			missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973183	AAAGCTGCATCTGGC[A/C]GAGGAGATGTGAGTT	392188
rs199984969	snp	C/G	0.0620564	0.164855	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973120	TCGACACGGGTCTCA[C/G]ATGAGAGTGGTGACT	392188
rs200095124	snp	A/T	0.118936	0.21289	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972066	CCTGTCTGTGTCTTC[A/T]GCGCCAAGGGCTCTT	392188
rs200109432	snp	A/G	0.0138271	0.08199	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973068	CTTCTCCCTGGGAGC[A/G]AGCTGTCTTGCCACA	392188
rs200201894	snp	C/T	0.00697549	0.0586437	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972250	TTGACATAAGAGAAG[C/T]AATATCCGTTGTGAC	392188
rs200356234	snp	A/C/G	0.00222514	0.0332809	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973187	CTGCATCTGGCCGAG[A/C/G]AGATGTGAGTTTTGA	392188
rs200423060	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974523	AGCATAACCTTTTTA[A/C]TGCTGGCCCTTGTTT	392188
rs200518110	snp	G/T	0.0079679	0.0626136	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973261	TCCTCCATGTCGCCC[G/T]CAACAAGGATCACAA	392188
rs200590328	snp	A/G	0.00598194	0.0543616	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973095	CACAGGAGCCAAATC[A/G]TCACAGAGGTCGACA	392188
rs200618475	snp	A/T	0.017838	0.0927405	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972810	GAAGCCAGCAGCCAA[A/T]GCCTGTGAGGGCTGG	392188
rs200693066	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974885	AGGGCCCATGAAATT[A/C]GGATGATTTTAAGGA	392188
rs200798126	in-del	-/AC			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973525	ATCATGACTTCTAGA[-/AC]ACCTGAATCAAATTA	392188
rs200849376	snp	A/C	0.00337552	0.0409434	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973169	GCTGGATTTCAGCAA[A/C]AGCTGCATCTGGCCG	392188
rs200916609	snp	A/G	0.0119281	0.0763005	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972309	ATAGAGGACATAGAC[A/G]AGAGGTCCTGTGTTC	392188
rs200919685	snp	G/T	0.293276	0.246226	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973282	AGGATCACAAGGTTT[G/T]TCTGCTGGGACCGCA	392188
rs201094494	snp	A/G/T	0.000943161	0.0216976	missense, synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973245	CAAGTAGAGTGAGTC[A/G/T]TCCTCCATGTCGCCC	392188
rs201308586	snp	C/G	0.00332267	0.0406238	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973262	CCTCCATGTCGCCCG[C/G]AACAAGGATCACAAG	392188
rs201472908	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974583	GTCTCCTGGATTCTC[G/T]CATCGATTGTTCATG	392188
rs201569670	in-del	-/GCGC			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973707	TGTGTGTGTGTGTGT[-/GCGC]TTGTGCTGGGATGAA	392188
rs201592183	snp	A/T	0.0109396	0.0731445	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973227	GAACTGCCACTCACC[A/T]CCCAAGTAGAGTGAG	392188
rs201612021	snp	C/T	0.0206163	0.0994139	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972775	AGAAATTCATGGGCA[C/T]CTTCCTGCTTGCCTC	392188
rs201670140	snp	A/G	0.13272	0.220783	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973254	TGAGTCGTCCTCCAT[A/G]TCGCCCGCAACAAGG	392188
rs201711526	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7975023	TCCTGGGGGAAGAAA[A/G]GAGCACTGCTTAGAA	392188
rs201776967	snp	A/G	0.084128	0.187047	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972925	TGAGAGTGCTCCCGG[A/G]ACAGCATGTAGTTGG	392188
rs201822520	snp	C/G	0.00399195	0.0444976	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973186	GCTGCATCTGGCCGA[C/G]GAGATGTGAGTTTTG	392188
rs201893552	snp	C/G	0.00335429	0.0408153	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973150	TTCTCAGGGAGAGAA[C/G]TCCGCTGGATTTCAG	392188
rs201918334	snp	C/T	0.0109394	0.073144	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973296	TTTCTGCTGGGACCG[C/T]AGGTTGCAGCAAGAC	392188
rs201921281	snp	A/C	0.00210637	0.0323844	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973258	TCGTCCTCCATGTCG[A/C]CCGCAACAAGGATCA	392188
rs201927052	snp	A/T	0.030956	0.120498	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973108	TCATCACAGAGGTCG[A/T]CACGGGTCTCAGATG	392188
rs202176000	snp	A/G	0.040028	0.13569	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973236	CTCACCTCCCAAGTA[A/G]AGTGAGTCGTCCTCC	392188
rs368100370	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973456	CACTCAATTAAGGAA[G/T]GAGTCACAGGGTGTG	392188
rs368343535	snp	A/G			synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972831	TGAGGGCTGGATGAC[A/G]TGGCCAGGACTGTGG	392188
rs368403724	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973505	AATTCAACAGACACA[G/T]CCCACATCATGACTT	392188
rs368649200	snp	G/T	0.260355	0.249785	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972043	TTGAGCTCTCCTTGC[G/T]TTGCTGGCCTGTCTG	392188
rs369950762	snp	A/C			missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972900	GCAGCACTTGGGACG[A/C]TGACATGTTTGAGAG	392188
rs370143318	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7975113	AGCAACGCAGATGCC[A/G]TGGCTTCACACAAGA	392188
rs370211841	snp	C/G	0.231111	0.249285	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972049	TCTCCTTGCGTTGCT[C/G]GCCTGTCTGTGTCTT	392188
rs371155804	snp	C/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973318	CAGCAAGACGCTATC[C/T]CTTCCGAGAGAGTCT	392188
rs371223086	snp	A/G	0.277778	0.248452	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972015	GGGTACCTGGAGGCA[A/G]GGGTGGTCTCTCTTG	392188
rs371617071	snp	G/T			missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972457	GTGTGTAAAGTTAAC[G/T]TGTTGGAGGCCGGCG	392188
rs371949408	snp	C/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973467	GGAATGAGTCACAGG[C/G]TGTGTCCCCTTGCAT	392188
rs372281995	snp	C/T			synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972906	CTTGGGACGCTGACA[C/T]GTTTGAGAGTGCTCC	392188
rs372606266	snp	C/T			missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972841	ATGACATGGCCAGGA[C/T]TGTGGAGGGCCCATG	392188
rs373416097	snp	C/G	0.46875	0.121031	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971966	CTAAGGTGCTTTCCT[C/G]AGTGGCTCTTTCCAC	392188
rs373838323	snp	G/T	0.293294	0.246223	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974065	TTGAAGAGATACTCA[G/T]TGCACAAAGTAGACT	392188
rs373980094	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973450	TATCAGCACTCAATT[A/C]AGGAATGAGTCACAG	392188
rs374190921	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973478	CAGGGTGTGTCCCCT[G/T]GCATCGCTGGGAATT	392188
rs374314134	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7975044	CTGCTTAGAAAGATG[A/C]TCCACAGGGAGAAAG	392188
rs374552875	snp	A/G	0.46875	0.121031	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972017	GTACCTGGAGGCAAG[A/G]GTGGTCTCTCTTGAG	392188
rs374691359	snp	A/G	0.00447508	0.0470905	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972971	ATGTCAGGCACTGCA[A/G]GGAAGCATTCAAGTA	392188
rs375197225	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974015	CTAGGCTGCCAAATA[A/C]TAAAGCATCAAATGG	392188
rs375358016	snp	A/G			missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972854	GACTGTGGAGGGCCC[A/G]TGTGATGTGAGCTTG	392188
rs376644488	snp	A/G	0.277778	0.248452	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972004	TCGTCCAACTCGGGT[A/G]CCTGGAGGCAAGGGT	392188
rs377574423	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7975060	TCCACAGGGAGAAAG[A/G]AGCCACCATTTTCAG	392188
rs377712929	snp	A/C/G	0.00993419	0.0697739	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973306	GACCGCAGGTTGCAG[A/C/G]AAGACGCTATCTCTT	392188
rs528393395	snp	A/G	0.00621756	0.0554087	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972198	ACAGGCAGTGACCTC[A/G]GCATCATCCATTTTA	392188
rs530469776	snp	C/T	0.00102018	0.0225622	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973249	TAGAGTGAGTCGTCC[C/T]CCATGTCGCCCGCAA	392188
rs532721663	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973298	TCTGCTGGGACCGCA[A/G]GTTGCAGCAAGACGC	392188
rs534063857	snp	A/G	0.00716266	0.059414	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973622	CTTATTTTAGGTAAA[A/G]GAATGTCAGGGAAGA	392188
rs536438281	snp	A/G	0.46875	0.121031	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971773	GACTCCTGATCTGTC[A/G]AGTTCATCGAAGAGA	392188
rs536773694	snp	G/T	0.00159617	0.0282053	downstream-variant-500B, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971567	GTTCGTGTTTGTGTG[G/T]GTGTGTGTGTGTTTC	392188
rs538230283	snp	A/C	0.279726	0.248226	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973023	GAGACCAGCCCCCAC[A/C]GCAGCAGGTCTCCTG	392188
rs542849604	snp	A/G	0.286243	0.247359	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972072	TGTGTCTTCAGCGCC[A/G]AGGGCTCTTGGTTCC	392188
rs545262519	snp	A/T	0.128583	0.218536	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972220	TCCATTTTATACCAC[A/T]GGCCTTCTTGAGCTT	392188
rs546887922	snp	G/T	0.00433032	0.0463294	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972417	GCAGAATCTCTTCAA[G/T]ACAAGGATGAGGACC	392188
rs548536329	in-del	-/GA	0.00597247	0.0543191	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973324	GACGCTATCTCTTCC[-/GA]GAGAGTCTTCAAATG	392188
rs550241533	snp	A/G	0.0410537	0.137264	downstream-variant-500B, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971588	TGTGTGTTTCCGTGC[A/G]CGCTTGTGGGTGTAT	392188
rs550766424	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7975041	GCACTGCTTAGAAAG[A/G]TGCTCCACAGGGAGA	392188
rs552915294	snp	C/G	0.0150556	0.0854466	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973116	GAGGTCGACACGGGT[C/G]TCAGATGAGAGTGGT	392188
rs553676134	snp	C/G	0.154661	0.231107	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971927	GCTTCATTTTGTTTT[C/G]CTCTTGGGGGAATTT	392188
rs554225299	snp	C/G	0.00716266	0.059414	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973623	TTATTTTAGGTAAAA[C/G]AATGTCAGGGAAGAA	392188
rs555144784	snp	C/G	0.0197687	0.0974348	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973033	CCCACAGCAGCAGGT[C/G]TCCTGCTACTCAGAG	392188
rs559461327	snp	A/G	0.0297994	0.118371	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972136	CATTCACTCTTCTGG[A/G]TGTAAAAGAGGACAT	392188
rs560507114	snp	C/G/T	0.00798954	0.0627091	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973260	GTCCTCCATGTCGCC[C/G/T]GCAACAAGGATCACA	392188
rs564757965	snp	C/T	0.000518538	0.0160935	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972227	TATACCACTGGCCTT[C/T]TTGAGCTTTGACATA	392188
rs566979692	snp	A/G	0.00534569	0.0514225	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973276	GCAACAAGGATCACA[A/G]GGTTTTTCTGCTGGG	392188
rs567019282	snp	A/G	0.00313381	0.0394599	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972423	TCTCTTCAAGACAAG[A/G]ATGAGGACCTTGGCA	392188
rs567020269	snp	C/T	0.00122399	0.0247082	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972391	TTGGCAAGTTTGTTG[C/T]CTGTGACATCGCAGA	392188
rs568437979	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973580	AATATGAGTGTAACC[A/G]GGTTGGGACAGTGGC	392188
rs569565186	snp	A/G	0.499154	0.0205497	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973324	GACGCTATCTCTTCC[A/G]AGAGAGTCTTCAAAT	392188
rs571190982	snp	G/T	0.00159617	0.0282053	downstream-variant-500B, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971563	CGGTGTTCGTGTTTG[G/T]GTGGGTGTGTGTGTG	392188
rs572973927	snp	A/C	0.00497509	0.0496266	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973119	GTCGACACGGGTCTC[A/C]GATGAGAGTGGTGAC	392188
rs572995946	snp	A/G	0.046775	0.145601	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974003	CTCTTGTGGAAGCTA[A/G]GCTGCCAAATACTAA	392188
rs573461318	snp	A/G	0.5	0	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971935	TTGTTTTGCTCTTGG[A/G]GGAATTTCCAGTGGT	392188
rs573919967	snp	A/G	0	0	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972050	CTCCTTGCGTTGCTG[A/G]CCTGTCTGTGTCTTC	392188
rs575183140	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974073	ATACTCAGTGCACAA[A/T]GTAGACTGTGAAAGA	392188
rs745441372	snp	A/G	0.00064255	0.0179126	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973257	GTCGTCCTCCATGTC[A/G]CCCGCAACAAGGATC	392188
rs746134425	snp	A/G	0.04875	0.148319	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972593	CCAGGGCGATGTCCA[A/G]GTAAGGGTCAAAAGT	392188
rs746578313	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974846	CGCCAAGGCCTCTAG[G/T]TTTAAAGAAACAGCC	392188
rs747168619	snp	A/G	0.000155183	0.00880724	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972243	TTGAGCTTTGACATA[A/G]GAGAAGTAATATCCG	392188
rs747399518	snp	G/T	0.00914336	0.0669931	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972554	GTTCCAAAGCTTGCT[G/T]GACACTCTGAGCTGC	392188
rs748155040	snp	C/G	0.00225433	0.0334975	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973070	TCTCCCTGGGAGCAA[C/G]CTGTCTTGCCACAGG	392188
rs748904725	in-del	-/CCG	0.000671817	0.0183155	cds-indel, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973021	GGAGACCAGCCCCCA[-/CCG]CAGCAGCAGGTCTCC	392188
rs749180205	snp	A/G	0.146436	0.22754	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972772	ATGAGAAATTCATGG[A/G]CATCTTCCTGCTTGC	392188
rs749347551	snp	C/T	0.00369912	0.0428472	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973059	CAGAGGAAGCTTCTC[C/T]CTGGGAGCAAGCTGT	392188
rs749965905	snp	A/G	0.000313234	0.0125108	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972189	AGTGATGCTACAGGC[A/G]GTGACCTCGGCATCA	392188
rs750758264	snp	A/T	0.00265604	0.0363451	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973207	GTGAGTTTTGAAAAG[A/T]GGTTGAACTGCCACT	392188
rs750764732	snp	C/G	0.000486027	0.0155813	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973141	AGTGGTGACTTCTCA[C/G]GGAGAGAAGTCCGCT	392188
rs751208436	snp	A/C/G	0.00147119	0.0270886	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972168	GGCCTGTTGACTCAG[A/C/G]ACAGAAGTGATGCTA	392188
rs752553146	snp	G/T	0.00184162	0.0302889	downstream-variant-500B, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971659	CGGTACTTCCACTCT[G/T]ATCACTGGCACACAA	392188
rs752848642	snp	A/G	0.000159502	0.00892893	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973242	TCCCAAGTAGAGTGA[A/G]TCGTCCTCCATGTCG	392188
rs753010303	snp	G/T	0.000236239	0.0108657	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973289	CAAGGTTTTTCTGCT[G/T]GGACCGCAGGTTGCA	392188
rs753244398	snp	C/T	0.001638	0.0285713	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972499	CAAAGACCGCAAGGA[C/T]AGGCATTCTCTCCAT	392188
rs753763993	snp	C/T	0.0155835	0.0868843	downstream-variant-500B, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971627	GTGTGTGTGTGTGTG[C/T]ACCCCTCAGTGTGGG	392188
rs754002906	snp	C/T	0.000386698	0.0138996	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973228	AACTGCCACTCACCT[C/T]CCAAGTAGAGTGAGT	392188
rs754976582	snp	A/C	0.0171907	0.0911034	downstream-variant-500B, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971632	TGTGTGTGTGTACCC[A/C]TCAGTGTGGGTCGGT	392188
rs754989514	snp	A/C	0.000647399	0.01798	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973172	GGATTTCAGCAAAAG[A/C]TGCATCTGGCCGAGG	392188
rs755257319	snp	C/G	0.000186029	0.00964261	stop-gained, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973233	CCACTCACCTCCCAA[C/G]TAGAGTGAGTCGTCC	392188
rs755967648	in-del	-/A	0.000152045	0.00871776	frameshift-variant, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972251	TGACATAAGAGAAGT[-/A]ATATCCGTTGTGACA	392188
rs757434420	snp	G/T	0.00431497	0.0462479	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972573	ACTCTGAGCTGCCTG[G/T]ATATCCAGGGCGATG	392188
rs757600350	snp	C/G	0.00156433	0.0279234	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973005	GGTATTTCCCATATT[C/G]TGGAGACCAGCCCCC	392188
rs757942980	snp	C/T	0.0644444	0.167538	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971738	TCCCTTGCAGAGAAG[C/T]GAGTGTGCCAGTGTT	392188
rs758373665	snp	C/T	0.00015804	0.00888792	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973243	CCCAAGTAGAGTGAG[C/T]CGTCCTCCATGTCGC	392188
rs758533516	snp	A/G	0.00030003	0.0122444	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973295	TTTTCTGCTGGGACC[A/G]CAGGTTGCAGCAAGA	392188
rs758835975	snp	A/G	0.00497922	0.0496469	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972502	AGACCGCAAGGATAG[A/G]CATTCTCTCCATTGA	392188
rs760312000	snp	C/G	0.00185701	0.0304147	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972894	GAGCATGCAGCACTT[C/G]GGACGCTGACATGTT	392188
rs760319062	snp	C/T	0.0023542	0.034228	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973094	CCACAGGAGCCAAAT[C/T]ATCACAGAGGTCGAC	392188
rs760915874	snp	A/C	0.000404122	0.0142091	stop-gained, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973223	GGTTGAACTGCCACT[A/C]ACCTCCCAAGTAGAG	392188
rs761302191	snp	C/G	0.000122392	0.00782182	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973265	CCATGTCGCCCGCAA[C/G]AAGGATCACAAGGTT	392188
rs761730438	snp	A/G	0.00630909	0.0558098	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972848	GGCCAGGACTGTGGA[A/G]GGCCCATGTGATGTG	392188
rs762246601	snp	G/T	0.0024174	0.0346822	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973194	TGGCCGAGGAGATGT[G/T]AGTTTTGAAAAGTGG	392188
rs762371076	snp	C/T	0.000509554	0.0159536	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973139	AGAGTGGTGACTTCT[C/T]AGGGAGAGAAGTCCG	392188
rs762775163	snp	A/G	0.000527398	0.0162302	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972150	GATGTAAAAGAGGAC[A/G]TAGGCCTGTTGACTC	392188
rs762824190	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973312	AGGTTGCAGCAAGAC[G/T]CTATCTCTTCCGAGA	392188
rs763496144	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7975026	TGGGGGAAGAAAGGA[A/G]CACTGCTTAGAAAGA	392188
rs763839830	snp	C/G	0.000544811	0.0164957	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972163	ACATAGGCCTGTTGA[C/G]TCAGGACAGAAGTGA	392188
rs763935507	snp	A/G			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973344	AGTCTTCAAATGACG[A/G]GCTCTCTGGCCGCAT	392188
rs763942781	snp	A/T	0.000391543	0.0139864	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972315	GACATAGACAAGAGG[A/T]CCTGTGTTCTGCTGA	392188
rs765184936	snp	A/G	0.00900882	0.0665075	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972122	CACTGTGTCTTTCCC[A/G]TTCACTCTTCTGGAT	392188
rs765850356	snp	A/G	0.000608828	0.0174368	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972949	TAGTTGGCAAGGGGC[A/G]GTGTGTATGTCAGGC	392188
rs766585630	snp	C/G	0.00036686	0.0135387	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973268	TGTCGCCCGCAACAA[C/G]GATCACAAGGTTTTT	392188
rs766815016	snp	A/G	0.00119808	0.024446	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973224	GTTGAACTGCCACTC[A/G]CCTCCCAAGTAGAGT	392188
rs767460221	snp	A/G	0.00108108	0.0232244	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972856	CTGTGGAGGGCCCAT[A/G]TGATGTGAGCTTGCA	392188
rs768032412	snp	C/G	0.000119962	0.0077438	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973206	TGTGAGTTTTGAAAA[C/G]TGGTTGAACTGCCAC	392188
rs768305517	in-del	-/T	0.000361958	0.013448	frameshift-variant, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973179	AGCAAAAGCTGCATC[-/T]GGCCGAGGAGATGTG	392188
rs768597669	snp	A/G	0.0210763	0.100469	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973066	AGCTTCTCCCTGGGA[A/G]CAAGCTGTCTTGCCA	392188
rs769289466	snp	G/T	0.150604	0.229392	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971934	TTTGTTTTGCTCTTG[G/T]GGGAATTTCCAGTGG	392188
rs769809085	snp	A/G	0.000540394	0.0164288	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972263	AGTAATATCCGTTGT[A/G]ACAACTCCACCCAGC	392188
rs769900770	snp	C/G	0.00467287	0.0481103	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972618	AAAAGTGTCTGAAAT[C/G]CCGTGGCAGTGGAGA	392188
rs770468912	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974848	CCAAGGCCTCTAGTT[G/T]TAAAGAAACAGCCCT	392188
rs771716865	snp	A/C			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974296	AGAACTGATGAAAAT[A/C]AAAACAACGTATCTC	392188
rs771990033	snp	C/T	0.00337067	0.0409142	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973074	CCTGGGAGCAAGCTG[C/T]CTTGCCACAGGAGCC	392188
rs772149916	snp	C/T	0.000272764	0.0116751	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973175	TTTCAGCAAAAGCTG[C/T]ATCTGGCCGAGGAGA	392188
rs772793057	snp	G/T			upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7974843	CGGCGCCAAGGCCTC[G/T]AGTTTTAAAGAAACA	392188
rs772986587	snp	C/T	0.00380227	0.0434359	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972891	ACAGAGCATGCAGCA[C/T]TTGGGACGCTGACAT	392188
rs773146344	snp	A/G	0.000212698	0.0103104	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973087	TGTCTTGCCACAGGA[A/G]CCAAATCATCACAGA	392188
rs773570087	snp	A/T	0.000244858	0.0110621	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973264	TCCATGTCGCCCGCA[A/T]CAAGGATCACAAGGT	392188
rs773764474	in-del	-/GA	0.000234673	0.0108297	frameshift-variant, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973194	TGGCCGAGGAGATGT[-/GA]GTTTTGAAAAGTGGT	392188
rs774238038	snp	A/C	0.230347	0.249226	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972803	CTCTATGGAAGCCAG[A/C]AGCCAATGCCTGTGA	392188
rs774982531	snp	G/T	0.00040282	0.0141862	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973189	GCATCTGGCCGAGGA[G/T]ATGTGAGTTTTGAAA	392188
rs775472309	snp	C/T	0.00030539	0.0123532	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972278	GACAACTCCACCCAG[C/T]GTGGACCAGCACAGC	392188
rs775497047	snp	C/T	0.00546444	0.0519842	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972655	ATTTGAGATCTCCAG[C/T]AGCCTCCAAATATTT	392188
rs776128977	snp	G/T	0.00149653	0.0273134	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973184	AAGCTGCATCTGGCC[G/T]AGGAGATGTGAGTTT	392188
rs776646292	snp	C/T	0.000149187	0.00863546	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972255	ATAAGAGAAGTAATA[C/T]CCGTTGTGACAACTC	392188
rs777067684	snp	C/G	0.000121959	0.00780797	upstream-variant-2KB, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973269	GTCGCCCGCAACAAG[C/G]ATCACAAGGTTTTTC	392188
rs777516237	snp	A/G	0.0644444	0.167538	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971739	CCCTTGCAGAGAAGC[A/G]AGTGTGCCAGTGTTC	392188
rs778068497	snp	C/T	0.00101704	0.0225274	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972233	ACTGGCCTTCTTGAG[C/T]TTTGACATAAGAGAA	392188
rs778144657	snp	C/T	0.000864678	0.0207748	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972507	GCAAGGATAGGCATT[C/T]TCTCCATTGAGTTCT	392188
rs779201807	snp	C/G/T	0.000273781	0.0116974	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973174	ATTTCAGCAAAAGCT[C/G/T]CATCTGGCCGAGGAG	392188
rs779505773	snp	A/C	0.000833912	0.0204025	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972216	ATCATCCATTTTATA[A/C]CACTGGCCTTCTTGA	392188
rs779831273	in-del	-/AA	0.0105076	0.0717174	frameshift-variant, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972603	GTCCAGGTAAGGGTC[-/AA]AAGTGTCTGAAATCC	392188
rs779916075	snp	A/G	0.497778	0.0332592	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971779	TGATCTGTCGAGTTC[A/G]TCGAAGAGAGGTTTA	392188
rs780122652	snp	A/G	0.000504796	0.015879	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7973045	GGTCTCCTGCTACTC[A/G]GAGGAAGCTTCTCCC	392188
rs780781763	snp	C/G	0.000358359	0.013381	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972184	ACAGAAGTGATGCTA[C/G]AGGCAGTGACCTCGG	392188
rs780783472	in-del	-/GTGC			downstream-variant-500B, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971627	TGTGTGTGTGTGTGT[-/GTGC]ACCCCTCAGTGTGGG	392188
rs780904542	snp	A/G	0.125819	0.216977	missense, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7971866	TGATGAATCACAAGT[A/G]CGTTGGGAGGCAGGG	392188
rs781365523	snp	A/G	0.00654872	0.056846	synonymous-codon, intron-variant	USP17L8, FAM66E	GRCh38.p7	8:7972585	CTGGATATCCAGGGC[A/G]ATGTCCAGGTAAGGG	392188