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
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

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