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
rs2951100	snp	C/G			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139059	TATATGTGCCTATCA[C/G]CCTGAGGAGTAATTT	377630
rs3988859	snp	C/T	1.89564e-05	0.00307861	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138555	CCAGGAAGAAGCTTC[C/T]TCTGAGTAGCAGGAG	377630
rs3988860	snp	A/T	3.88191e-05	0.00440546	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138489	GAAATACCTGCTACG[A/T]GAACGCTTCCCTGCA	377630
rs3988861	snp	C/T	1.94256e-05	0.00311647	USP17L2, FAM66D	8	allele_origin=T(somatic)/C(germline)	8:12138478	TACGAGAACGCTTCC[C/T]TGCAGTGCCTGACAT	377630
rs3988862	snp	A/G	4.89848e-05	0.00494874	synonymous-codon, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138413	GGAGCACTCTCAAAC[A/G]TGTCAGCGTCCCAAG	377630
rs3988863	snp	G/T	0.000247127	0.0111132	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138407	CTCTCAAACATGTCA[G/T]CGTCCCAAGTGCTGC	377630
rs3988864	snp	A/C			missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138402	AAACATGTCAGCGTC[A/C]CAAGTGCTGCATGCT	377630
rs3988865	snp	C/G/T	0.000162121	0.00900208	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138397	TGTCAGCGTCCCAAG[C/G/T]GCTGCATGCTCTGTA	377630
rs3988870	snp	A/G			missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138162	AAATATTTGGAGGCT[A/G]CTGGAGATCTCAAAT	377630
rs3988871	snp	C/G			synonymous-codon, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138125	TCTCCACTGCCACGG[C/G]ATTTCAGACACTTTT	377630
rs3988872	snp	A/C			missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138061	GCAGCTCAGAGTGTC[A/C]AGCAAGCTTTGGAAC	377630
rs4841752	snp	G/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139797	CTTTTGTTTATTAAA[G/T]AACTGATGAAAATAA	377630
rs4841753	snp	C/G	0.401392	0.198948	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139836	TATCTCACAGCATGG[C/G]TGATACTATTTCCAT	377630
rs4841754	snp	C/T	0.370772	0.218893	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140046	CTTTTTAATACTGGC[C/T]CTTGTTTCACTGGGA	377630
rs4841755	snp	C/G	0.352938	0.227824	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140060	CTCTTGTTTCACTGG[C/G]AAATGGCAAAAATAA	377630
rs4841756	snp	A/G	0.366679	0.221102	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140201	ATTGTAATGCTGACG[A/G]AAGTGGACATGTTCC	377630
rs9693024	snp	A/G	0.197531	0.244432	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140103	CTGGATTCTCGCATC[A/G]GTTGTTCATGCTCTG	377630
rs9693093	snp	C/T	0.473266	0.112482	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140047	TTTTTAATACTGGCT[C/T]TTGTTTCACTGGGAA	377630
rs9693300	snp	A/G	0.475789	0.107327	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140486	TCATGGGCCAGGTGT[A/G]CTTCATCAGAAGGCT	377630
rs9693352	snp	C/T	0.457154	0.139954	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140170	TGGAATTGCAGTTAG[C/T]ACCTTTGATGCAAAA	377630
rs9693390	snp	C/T	0.499776	0.0105807	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140511	AAGGCTTCCTATGCC[C/T]GATGTAAAGTGTCCT	377630
rs9694549	snp	A/G	0.457154	0.139954	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140178	CAGTTAGCACCTTTG[A/G]TGCAAAAATTGTAAT	377630
rs9774478	snp	C/G	0.000172898	0.00929619	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137966	GTGTAAAGTTAACGT[C/G]TTGGAGGCCGGCGCC	377630
rs10090565	snp	A/G	0.195837	0.244062	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140019	AGTGAGTGAAACAGA[A/G]GGTAGCATAACCTTT	377630
rs10090570	snp	A/G	0.195837	0.244062	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140021	TGAGTGAAACAGAGG[A/G]TAGCATAACCTTTTT	377630
rs11250189	snp	A/G	0	0	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139560	GTAGAAACATGCACT[A/G]AAGTTTGAAGAGTTA	377630
rs11250190	snp	A/T	0.0263992	0.111815	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139573	CTGAAGTTTGAAGAG[A/T]TACTCAGTGCACAAA	377630
rs11777425	snp	C/T	0.488363	0.0753851	downstream-variant-500B, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12136926	GTCTCTCCAGAGGTT[C/T]GGAAGACTCACGACC	377630
rs11990104	snp	G/T	0.32955	0.237006	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139386	TAATAATAAAGGAGA[G/T]ATCCGTGGCATCAAA	377630
rs11992686	snp	A/G	0.476401	0.106032	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139716	AGTGGTTTCGGACGT[A/G]CGGCGGCAGTTTAAG	377630
rs12543578	snp	C/T	0.496123	0.0438589	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137448	TGCTCTTGGGGGAAT[C/T]TCCAGTGGTCTAAGG	377630
rs12547403	snp	A/G	0.46865	0.121211	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140742	TGATGTCCTGCCTGC[A/G]TGTCATGCTCATTGC	377630
rs12677320	snp	A/G	0.449091	0.151204	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139832	AACGTATCTCACAGC[A/G]TGGGTGATACTATTT	377630
rs12677836	snp	C/T			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140048	TTTTAATACTGGCTT[C/T]TGTTTCACTGGGAAA	377630
rs13274255	snp	A/G	0.369398	0.219645	synonymous-codon, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137765	AGAGAAGTAATGTCC[A/G]TCGTGACAACTCCAC	377630
rs28396114	snp	A/C	0.0387552	0.1337	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139385	TTAATAATAAAGGAG[A/C]TATCCGTGGCATCAA	377630
rs28488512	snp	A/G	0.489665	0.0711382	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139284	CGTCATCCTCTCATC[A/G]ACGGAAGGACAAGAA	377630
rs28491134	snp	A/C/G/T	0.100281	0.204129	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138801	TTTTTCTGCTGGGAC[A/C/G/T]GCAGGTTGCAGCAAG	377630
rs28569037	snp	A/C	0.0869089	0.189476	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139811	AGAACTGATGAAAAT[A/C]AAAACAACGTATCTC	377630
rs28580271	snp	A/C	0.489434	0.0719116	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139395	AGGAGATATCCGTGG[A/C]ATCAAACAGACCTTC	377630
rs28653124	snp	C/G			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139182	TGTGTGTATCTCTCT[C/G]TGTGTGTGTGTGTGT	377630
rs34009999	in-del	-/C			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139924	CTACGGTATAATTTT[-/C]CCTTGTTTGCTTTTG	377630
rs34648338	in-del	-/C			frameshift-variant, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137330	GTGTGGGATGAAAAA[-/C]CCATCATCCTGAACA	377630
rs36114754	snp	G/T	0.457154	0.139954	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140173	AATTTTTGCATCAAA[G/T]GTGCTAACTGCAATT	377630
rs55731049	snp	G/T	0.0908922	0.192833	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140098	ATCTCCTGGATTCTC[G/T]CATCGGTTGTTCATG	377630
rs55769296	snp	A/G	0.0908922	0.192833	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140076	AAATGGCAAAAATAA[A/G]CCGTGTATCTCCTGG	377630
rs56021150	in-del	-/CT			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139175	TGTGTGTATCTCTCT[-/CT]GTGTGTGTGTGTGTG	377630
rs56335315	snp	G/T	0.378174	0.214642	downstream-variant-500B, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12136762	TCACCTTCTCGTGCC[G/T]CCCAACAACTGACGA	377630
rs62493707	snp	C/G/T	7.80792e-05	0.00624768	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137995	CCCTCTGGAGACAAA[C/G/T]ACCGCAATGATAGGC	377630
rs62493708	snp	A/G	0.00281957	0.0374411	synonymous-codon, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137999	CTGGAGACAAAGACC[A/G]CAATGATAGGCATTC	377630
rs71237667	snp	C/T	0.148284	0.228407	synonymous-codon, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138743	GGAGGACGACTCACT[C/T]TACTTGGGAGGTGAG	377630
rs73544419	snp	C/T	0.0490535	0.14873	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140295	TCCTGGCTCTAGGGA[C/T]TTTCCCAAAATGTCT	377630
rs73663091	snp	A/C	0	0	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139868	CTTACGTGATAATGG[A/C]TCAACATTTCATAGA	377630
rs74324142	snp	C/G	0.387647	0.208695	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138641	AGATGAGAGTGGTGA[C/G]TTCTCAGGGAGAGAA	377630
rs74515408	snp	A/G			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138877	CGCATCAGCCCTTAT[A/G]TAACTCACCCCCACC	377630
rs74605293	snp	C/T			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139225	GTGTGTGTGTGTGTG[C/T]TTGTGCTGGGATGAA	377630
rs74614551	snp	C/T	0.498602	0.0270118	synonymous-codon, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137975	TAACGTCTTGGAGGC[C/T]GGCGCCCTCTGGAGA	377630
rs74683378	snp	G/T			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139907	AAAAAGTTCTAATTT[G/T]GACAAAAGCAAACAA	377630
rs75173287	snp	C/T	0.375	0.216506	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139857	CTATTTCCATACTTA[C/T]GTGATAATGGATCAA	377630
rs75180221	snp	C/G/T	0.000191701	0.0097886	synonymous-codon, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137924	GGAGAATCTCTTCAA[C/G/T]ACAAGGATGAGGACC	377630
rs75476700	snp	A/G	0.382899	0.21175	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138577	TCTTCCTGGGAGCAA[A/G]CTGTCTTGCCACAGG	377630
rs75554685	snp	A/G	0.168785	0.236441	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140684	CGGGACCTAGGAATT[A/G]TTGTCCTTTAATGCT	377630
rs75807755	snp	A/G	0.379999	0.213542	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137553	AGCTCTCCTTGCGTT[A/G]CTCGCCTGTCTGTGT	377630
rs75937106	snp	A/G/T	0.010092	0.0703645	missense, synonymous-codon, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138752	CAAGTAGAGTGAGTC[A/G/T]TCCTCCATGTCGCCC	377630
rs75952964	snp	C/T	0.375	0.216506	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139851	GTGATACTATTTCCA[C/T]ACTTACGTGATAATG	377630
rs76189682	snp	C/T			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139370	AGCGTATTTTCTTCC[C/T]TAATAATAAAGGAGA	377630
rs76415856	snp	C/T			missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137377	GAATCACAAGTACGT[C/T]GGGAGGCAGGGTACC	377630
rs76662498	snp	A/C			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138875	GCCGCATCAGCCCTT[A/C]TATAACTCACCCCCA	377630
rs76753250	snp	A/T			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139647	GACTAATTGATGACA[A/T]TCCCCAAATTTATGT	377630
rs76814845	snp	C/T			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139800	TTGTTTATTAAAGAA[C/T]TGATGAAAATAAAAA	377630
rs77973456	snp	A/C			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138813	GACTGCAGGTTGCAG[A/C]AAGACGCTATCTCTT	377630
rs78280428	snp	C/T			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138881	TCAGCCCTTATATAA[C/T]TCACCCCCACCAACC	377630
rs78425152	snp	C/T			downstream-variant-500B, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12136966	GATGTTTCCCATGTG[C/T]GGGCTCATCCTGAGA	377630
rs78927706	snp	A/G			downstream-variant-500B, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12136963	CTTGATGTTTCCCAT[A/G]TGTGGGCTCATCCTG	377630
rs79412221	snp	C/T			downstream-variant-500B, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137098	GTGTTTGCGTGCGCG[C/T]TTGTGGGTGTATTTG	377630
rs79865132	snp	C/G	0.0246802	0.10831	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138578	CTTCCTGGGAGCAAG[C/G]TGTCTTGCCACAGGA	377630
rs111428074	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140316	CAAAATGTCTTAGAC[A/G]GTAAGGAACAGGGCA	377630
rs111978476	snp	A/G	0.0700422	0.173537	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139665	CCCAAATTTATGTGT[A/G]CCAGAAAAGAGAGAT	377630
rs112165118	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140020	GTGAGTGAAACAGAG[A/G]GTAGCATAACCTTTT	377630
rs112388014	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140680	TAAGCGGGACCTAGG[A/C]ATTGTTGTCCTTTAA	377630
rs112595287	snp	A/G			synonymous-codon, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138152	GAGACACTTGATTTG[A/G]GATCTCCAGCAGCCT	377630
rs112598423	snp	A/G	0.040671	0.13668	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139593	CAGTGCACAAAGTAG[A/G]CTGTGAAAGACTTTG	377630
rs112856432	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139435	CCTTTCCACGTTCAG[A/C]CTATTGACTCTCTAT	377630
rs113086230	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140304	TAGGGATTTTCCCAA[A/C]ATGTCTTAGACAGTA	377630
rs113108697	snp	C/G	3.66441e-05	0.00428027	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138424	GACATGTTTGAGAGT[C/G]CTCCCGGGACAGCAT	377630
rs113179798	snp	A/G	0.0887219	0.191022	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140024	GTGAAACAGAGGGTA[A/G]CATAACCTTTTTAAT	377630
rs113890166	snp	A/T	0.5	0	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139737	GCAGTTTAAGAAAAC[A/T]TGAAACAAAAAACTT	377630
rs114424692	snp	C/G	0.0168055	0.0901129	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140715	CATAACTGCTTTTGA[C/G]GTGAGCCGAATTGAT	377630
rs114758845	snp	G/T	0.197393	0.244402	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140006	GACGTTTAAAAGCAG[G/T]GAGTGAAACAGAGGG	377630
rs115345095	snp	C/T	0.0193772	0.0965046	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140741	TTGATGTCCTGCCTG[C/T]GTGTCATGCTCATTG	377630
rs139278194	snp	C/T			downstream-variant-500B, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137013	CAGTTGTCCCTGTTG[C/T]AGAGACAGAAACTTG	377630
rs140228481	snp	C/G			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139920	TTTGACAAAAGCAAA[C/G]AAGGAAAATTATACC	377630
rs140365730	snp	C/T	0.000607517	0.0174181	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12137493	GCTCTTTCCACCAAG[C/T]GCTCGTCCAACTCGG	377630
rs141763286	snp	C/T	0.364817	0.222075	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139120	CACACAGTTGCCTTA[C/T]TTTAGGTAAAAGAAT	377630
rs142023572	snp	C/T	0.000207506	0.0101838	missense, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12138565	TCAGAGGAAGCTTCT[C/T]CCTGGGAGCAAGCTG	377630
rs142415653	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140395	GCTTCATGGCCCATG[A/G]AATTAGGATGATTTT	377630
rs143342329	snp	C/T			downstream-variant-500B, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12136691	CTAAATGCATTCCAG[C/T]TTCCACTATTCAAGG	377630
rs143497277	in-del	-/TC			upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139174	GAAACCGTGTGTGTA[-/TC]TCTCTCTGTGTGTGT	377630
rs144549165	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12140499	GTGCTTCATCAGAAG[G/T]CTTCCTATGCCCGAT	377630
rs147997361	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP17L2, FAM66D	GRCh38.p7	8:12139994	GAAAACATCGGAGAC[A/G]TTTAAAAGCAGTGAG	377630

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