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
rs76277875	snp	A/G			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7979005	TCAGAAGGTATCCCA[A/G]CTATAACCTTTTGTT	645836
rs78947321	snp	C/T	0.081446	0.184634	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7975938	GGTGAGAATGATCCA[C/T]GGATGTGCCACATGA	645836
rs79407094	snp	C/T	0.0998734	0.199905	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978340	GTGGCCACACAGTTG[C/T]CTTATTTTAGGTAAA	645836
rs79753474	snp	C/T	0.385359	0.210185	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978378	CAGGGAAGAAATCTT[C/T]ACCTATGAAACCCTG	645836
rs111485122	snp	A/G			missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976598	TGATGAATCACAAGT[A/G]CGTTGGGAGGCAGGG	645836
rs112255439	snp	C/T			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976375	ACCCCTACGTGTGGG[C/T]CGACACTTCCACTGA	645836
rs112257485	snp	C/T			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978050	CAGCAAGACGCTATC[C/T]CTTCCGAGAGAGTCT	645836
rs142906685	snp	G/T	0.4628	0.13121	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978441	TGTGTGTGTGTGTGT[G/T]TATGTGTGTGTGTGC	645836
rs150980083	snp	C/G			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7979012	GTATCCCAACTATAA[C/G]CTTTTGTTTATTAAA	645836
rs180915307	snp	A/T			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7979056	TAAAAACAACTTATC[A/T]CACAGCATTGGTGAT	645836
rs182610233	snp	A/G			synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977563	TGAGGGCTGGATGAC[A/G]TGGCCAGGACTGTGG	645836
rs183176031	snp	C/T			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976199	GCTCATCCTGAGATG[C/T]AGCCATCACTATCCA	645836
rs183612317	snp	C/G			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976018	CCCCAAGAGAAAATA[C/G]GAAACCGAGTCCCCT	645836
rs185001671	snp	A/C			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978980	AACATGAAACAAAAA[A/C]CTTGAGAAATCAGAA	645836
rs186055634	snp	A/C	0.329317	0.237084	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7979099	CGTATGTGATAATGG[A/C]TCAACATTTCATAGA	645836
rs186967106	snp	A/G			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976126	ACAAACACACAGACA[A/G]TCCCTCCAGAGGTTC	645836
rs187598865	snp	C/T			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976351	GTGTGTGTGTGTGTG[C/T]GTGCGTGCACCCCTA	645836
rs188014243	snp	A/G	0.127599	0.217986	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977977	CAAGTAGAGTGAGTC[A/G]TCCCCCATGTCGCCC	645836
rs189010362	snp	A/G			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978331	GTTTGGGCAGTGGCC[A/G]CACAGTTGCCTTATT	645836
rs189286845	snp	A/C/G	0.00875628	0.0656872	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978992	AAACCTTGAGAAATC[A/C/G]GAAGGTATCCCAACT	645836
rs189790985	snp	A/G			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7979105	TGATAATGGATCAAC[A/G]TTTCATAGATATGAA	645836
rs190989637	snp	C/T			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976157	GGAAGACTCACGACC[C/T]CAAAACTTGATGTTT	645836
rs191361756	snp	A/C			missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977535	CTCTATGGAAGCCAG[A/C]AGCCAATGCCTGTGA	645836
rs199527832	snp	A/C			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978989	CAAAAACCTTGAGAA[A/C]TCAGAAGGTATCCCA	645836
rs199904548	snp	A/G	0.00697544	0.0586435	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976990	AGAGAAGTAATGTCC[A/G]TCGTGACAACTCCAC	645836
rs199988858	snp	A/T	0.149716	0.229004	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977714	TGCAGGGAAGCGTTC[A/T]CGTAGCAGGTATTTC	645836
rs199999223	snp	A/G			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978538	GACAAGAAATCGGAA[A/G]TGTGCTTTCTGACCT	645836
rs200143156	snp	A/G	0.0129155	0.0793154	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977665	CTCCCGGGACAGCAT[A/G]TAGTTGGCAAGGGGC	645836
rs200263085	snp	A/G	0.0922954	0.193983	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977800	CTTCTCCCTGGGAGC[A/G]AGCTGTCTTGCCACA	645836
rs200415368	snp	A/C/G	0.015189	0.0858125	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977919	CTGCATCTGGCCGAG[A/C/G]AGATGTGAGTTTTGA	645836
rs200689566	snp	C/T	0.0584021	0.160593	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976992	AGAAGTAATGTCCGT[C/T]GTGACAACTCCACCC	645836
rs200743959	snp	A/G	0.198912	0.244724	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977681	TAGTTGGCAAGGGGC[A/G]GTGTGTATGTCAGGC	645836
rs200975552	snp	C/G	0.017838	0.0927406	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977852	TCGACACGGGTCTCA[C/G]ATGAGAGTGGTGACT	645836
rs201264829	snp	A/C	0.00498757	0.0496881	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977743	TCCCATATTCTGGAG[A/C]CCAGCCCCCACCGCA	645836
rs201374304	snp	A/G	0.267438	0.249391	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977703	ATGTCAGGCACTGCA[A/G]GGAAGCGTTCTCGTA	645836
rs201523459	snp	A/T	0.00697555	0.058644	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977047	GACATAGACAAGAGG[A/T]CCTGTGTTCTGCTGA	645836
rs201549590	snp	A/T	0.113679	0.209563	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977959	GAACTGCCACTCACC[A/T]CCCAAGTAGAGTGAG	645836
rs201888439	snp	G/T			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7979014	ATCCCAACTATAACC[G/T]TTTGTTTATTAAAGA	645836
rs202084160	snp	A/G	0.00299544	0.0385843	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977872	GAGTGGTGACTTCTC[A/G]GGGAGAGAAGTCCGC	645836
rs202157266	snp	C/T	0.00498749	0.0496877	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977750	TTCTGGAGCCCAGCC[C/T]CCACCGCAGCAGGTC	645836
rs368397272	snp	G/T			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978244	CAGACACAGCCCACA[G/T]CATGACTTCTAGAAC	645836
rs368911443	snp	A/G			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976178	CTTGATGTTTCCCAT[A/G]TGTGGGCTCATCCTG	645836
rs369546680	snp	C/T			missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976488	GTGTGCCAGTGTTCA[C/T]GGACTCCTGATCTGT	645836
rs370184970	snp	G/T	0.0110605	0.0735385	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977911	AGCAAAAGCTGCATC[G/T]GGCCGAGAAGATGTG	645836
rs371345748	snp	C/T			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976181	GATGTTTCCCATGTG[C/T]GGGCTCATCCTGAGA	645836
rs371418825	snp	C/T			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978254	CCACATCATGACTTC[C/T]AGAACACCTGAATCA	645836
rs371860002	snp	A/G			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976245	GAGACAGAAACTTGG[A/G]CTCCTCATTACTTTA	645836
rs374225581	snp	A/G	0.00234344	0.0341501	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976919	GAAGTGATGCTACAG[A/G]CAGTGACCTCGGCAT	645836
rs374515369	in-del	-/TG	0.0663309	0.169604	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976334	GCTTGTGGGTGTATT[-/TG]TGTGTGTGTGTGTGT	645836
rs375323113	snp	G/T			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978188	CACTCAATTAAGGAA[G/T]GAGTCACAGGGTGTG	645836
rs375748325	snp	C/T			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976197	GGGCTCATCCTGAGA[C/T]GCAGCCATCACTATC	645836
rs376093255	snp	A/C			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978038	GACCGCAGGTTGCAG[A/C]AAGACGCTATCTCTT	645836
rs376440294	in-del	-/GT			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976294	CGGGTTTGTTTGGGG[-/GT]GTGTGTGTGTGTGTT	645836
rs376860796	snp	C/G			downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976256	TTGGACTCCTCATTA[C/G]TTTATGTAGGATTGA	645836
rs527932174	snp	C/T	0.0023933	0.0345097	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977981	TAGAGTGAGTCATCC[C/T]CCATGTCGCCCGCAA	645836
rs532069270	snp	C/G	0.0626037	0.165477	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976009	TGAAACATACCCCAA[C/G]AGAAAATAGGAAACC	645836
rs534190166	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976235	CCCTGTTGTAGAGAC[A/G]GAAACTTGGACTCCT	645836
rs537638030	snp	C/T	0.00835141	0.0640778	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978507	GCAGCTATCATCATC[C/T]TCTCAGCGACAGAAG	645836
rs537775759	snp	A/G	0.00335723	0.0408331	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976368	TGCGTGCACCCCTAC[A/G]TGTGGGTCGACACTT	645836
rs539509123	snp	C/T	0.00199481	0.0315187	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976313	GTGTGTGTGTGTTTG[C/T]GTGCGTGCTTGTGGG	645836
rs540218636	snp	C/T	0.00150263	0.0273689	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976540	TAGCAGGGAGCTTTG[C/T]TGTTCAGGATGATGG	645836
rs545889094	snp	A/G	0.00316956	0.0396829	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976717	GGCTCTTTCCACCAA[A/G]TGCTCGTCCAACTCG	645836
rs547623541	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976293	TCGGGTTTGTTTGGG[G/T]GTGTGTGTGTGTGTG	645836
rs547779268	snp	A/C	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978115	ATAGAACTCACCCCC[A/C]CCAGCCGCTAACACC	645836
rs548880696	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976110	GTCATCTACCATGAA[C/T]ACAAACACACAGACA	645836
rs548941570	snp	A/C	0.00262123	0.0361074	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977554	CAATGCCTGTGAGGG[A/C]TGGATGACATGGCCA	645836
rs553753972	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978993	AACCTTGAGAAATCA[A/G]AAGGTATCCCAACTA	645836
rs554488473	snp	A/C	0.0584853	0.160693	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978967	GGCAGTTTAAGAAAA[A/C]ATGAAACAAAAACCT	645836
rs558344810	snp	C/G	0.0337553	0.125452	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976317	GTGTGTGTTTGCGTG[C/G]GTGCTTGTGGGTGTA	645836
rs559844578	snp	A/G	0.000798403	0.0199641	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976667	TTGTTTTGCTCTTGG[A/G]GGAATTTCCAGTGGT	645836
rs563040214	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7975970	CAAAATTTCACCTTC[C/T]CGTGCCGCCCAACAA	645836
rs563105091	snp	A/G	0.000399281	0.0141238	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976741	CAACTCGGGTGCCTG[A/G]AGGCAGGGGTGGTCT	645836
rs568503412	snp	C/T	0.0524604	0.153226	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976228	CAGTTGTCCCTGTTG[C/T]AGAGACAGAAACTTG	645836
rs570721241	snp	A/C	0.0252325	0.109451	upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978158	CAGGTGCGCGATAAA[A/C]CAATCAAATATCAGC	645836
rs570928011	snp	G/T	0.0410537	0.137264	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976295	GGGTTTGTTTGGGGG[G/T]GTGTGTGTGTGTGTT	645836
rs574388455	snp	C/G	0.000402739	0.0141847	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976432	CTTGCTGTGTTTGTT[C/G]TTCCCTTTGGCTCTC	645836
rs575067265	snp	G/T	0.00209289	0.032281	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976358	TGTGTGTGTGTGCGT[G/T]CACCCCTACGTGTGG	645836
rs576878678	snp	C/G	0.00472067	0.0483534	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976698	CTAAGGTGCTTTCCT[C/G]AGTGGCTCTTTCCAC	645836
rs745683217	snp	C/G	0.000155364	0.00881237	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976363	GTGTGTGCGTGCACC[C/G]CTACGTGTGGGTCGA	645836
rs746307146	snp	C/T	0.00485827	0.0490462	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977387	ATTTGAGATCTCCAG[C/T]AGCCTCCAAATATTT	645836
rs746432120	snp	C/T	0.00135135	0.0259586	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976726	CACCAAGTGCTCGTC[C/T]AACTCGGGTGCCTGG	645836
rs747416643	snp	A/T	0.00157924	0.0280558	stop-gained, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976434	TGCTGTGTTTGTTCT[A/T]CCCTTTGGCTCTCCT	645836
rs747710994	in-del	-/GG	0.000129946	0.00805954	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976349	TGTGTGTGTGTGTGT[-/GG]GTGTGCGTGCACCCC	645836
rs747723797	snp	C/T	0.00117924	0.0242535	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976704	TGCTTTCCTGAGTGG[C/T]TCTTTCCACCAAGTG	645836
rs748988053	snp	G/T	0.000200931	0.0100212	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976372	TGCACCCCTACGTGT[G/T]GGTCGACACTTCCAC	645836
rs749697358	snp	C/T	0.000440626	0.0148364	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977505	TGAGAAATTCATGGA[C/T]ATCTTCCTGCTTGCC	645836
rs750049362	in-del	-/TGTGTGTGTG			upstream-variant-2KB, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7978402	AACCCTGTGTGTGTC[-/TGTGTGTGTG]TGTGTGTGTGTGTGT	645836
rs750348015	snp	C/T	0.0127383	0.0787839	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976826	CTTGGTTCCCTGCCT[C/T]TTGACACACTCTCAC	645836
rs750402917	snp	A/G	0.000753154	0.019391	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976649	TTGAACTCAGGCTTC[A/G]TTTTGTTTTGCTCTT	645836
rs751141756	snp	C/G			missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977976	CCAAGTAGAGTGAGT[C/G]ATCCCCCATGTCGCC	645836
rs751677062	snp	A/G	0.00122474	0.0247158	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976594	TGATTGATGAATCAC[A/G]AGTGCGTTGGGAGGC	645836
rs752387672	snp	A/T	0.00153257	0.0276394	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977937	ATGTGAGTTTTGAAA[A/T]GTGGTTGAACTGCCA	645836
rs753655411	snp	A/G	0.00117855	0.0242464	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976975	TTGAGCTTTGACATA[A/G]GAGAAGTAATGTCCG	645836
rs754546529	snp	G/T	0.00117509	0.0242108	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976978	AGCTTTGACATAAGA[G/T]AAGTAATGTCCGTCG	645836
rs754672401	snp	A/C	0.00353564	0.0418965	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976671	TTTGCTCTTGGAGGA[A/C]TTTCCAGTGGTCTAA	645836
rs754969934	snp	C/T	0.000931098	0.0215565	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7977915	AAAGCTGCATCTGGC[C/T]GAGAAGATGTGAGTT	645836
rs755882162	snp	C/T	0.000187529	0.0096814	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976660	CTTCGTTTTGTTTTG[C/T]TCTTGGAGGAATTTC	645836
rs757097028	snp	C/T	0.000255297	0.0112953	missense, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976625	AGGGTACCTTCGACT[C/T]TTCCGACGTTGAACT	645836
rs757219258	snp	A/C	0.00013224	0.00813035	downstream-variant-500B, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976360	TGTGTGTGTGCGTGC[A/C]CCCCTACGTGTGGGT	645836
rs757910406	snp	A/G	0.000633112	0.0177807	synonymous-codon, intron-variant	USP17L3, FAM66E	GRCh38.p7	8:7976993	GAAGTAATGTCCGTC[A/G]TGACAACTCCACCCA	645836

Full records

It may take some time, please wait.