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

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
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

Full records

It may take some time, please wait.