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
rs888428	snp	A/G	0.00277597	0.0371521	utr-variant-3-prime, nc-transcript-variant, intron-variant	DCAF17	GRCh38.p7	2:171483454	TGATGCTCTGAGAAT[A/G]CAGAAACTTAGATCC	80067
rs997666	snp	C/T	0.470327	0.118136	intron-variant	DCAF17	GRCh38.p7	2:171452567	GAAGTGCTCCTCTCA[C/T]GTCACCCTCCTGAGT	80067
rs1185477	snp	C/T	0	0	intron-variant	DCAF17	GRCh38.p7	2:171462586	AACAATAAATGAAAG[C/T]GCCTAAACTTTTACC	80067
rs1476111	snp	C/G	0.393619	0.204631	intron-variant	DCAF17	GRCh38.p7	2:171452100	AAAGATTCTCCCTTC[C/G]AAAGGGATAAATTTT	80067
rs1558936	snp	C/T	0.32768	0.237625	intron-variant	DCAF17	GRCh38.p7	2:171471940	ggagccttgacctct[C/T]ggcctcaatcaattc	80067
rs1558937	snp	A/G	0.32768	0.237625	intron-variant	DCAF17	GRCh38.p7	2:171471939	gagccttgacctctt[A/G]gcctcaatcaattct	80067
rs1861899	snp	C/T	0.355096	0.226837	intron-variant	DCAF17	GRCh38.p7	2:171480473	ATTTTTCCAAATTTA[C/T]AATTGAAAGAAAATC	80067
rs1882378	snp	A/G	0.0755793	0.179102	intron-variant	DCAF17	GRCh38.p7	2:171480753	GAACTCTGGACCCAG[A/G]AGTCTAAATACCCAG	80067
rs1921776	snp	C/T	0.461592	0.133149	intron-variant, downstream-variant-500B	DCAF17	GRCh38.p7	2:171470393	ACCTTTCACCACGCA[C/T]GTTACAGATCACCTT	80067
rs1981788	snp	C/T	0.327445	0.237702	intron-variant	DCAF17	GRCh38.p7	2:171470829	acggatatagaaggc[C/T]ggctgTATCTGTACG	80067
rs2193621	snp	C/T	0.0444908	0.142359	intron-variant, upstream-variant-2KB	DCAF17, METTL8	GRCh38.p7	2:171436215	ctaacaactgataaa[C/T]ggatacgtaaaatgt	80067
rs2356709	snp	A/G	0.461481	0.133325	intron-variant	DCAF17	GRCh38.p7	2:171438282	atggctcagaatgtg[A/G]tctaccttggtgaac	80067
rs2356781	snp	A/G	0.327445	0.237702	intron-variant	DCAF17	GRCh38.p7	2:171480499	AAAATTTTTTAAAAT[A/G]AGAGAATACGGTAAT	80067
rs3054497	in-del	-/ATA			intron-variant	DCAF17	GRCh38.p7	2:171466593	TTTTCATTGAGAATA[-/ATA]TTAGAGATCAAAATT	80067
rs3731979	snp	C/T	0.00205205	0.0319658	utr-variant-3-prime, nc-transcript-variant, intron-variant	DCAF17	GRCh38.p7	2:171482148	CCTTTACTTGGGTTG[C/T]CTTTATTTAACATTC	80067
rs3731980	snp	A/G	0.00531452	0.0512739	DCAF17	2	allele_origin=G(germline)/A(germline)	2:171480091	ATCTATTTGAGTAAC[A/G]GCTACCACAGAAAGC	80067
rs3731981	snp	A/G	0.347954	0.230011	DCAF17	2	allele_origin=G(germline)/A(germline)	2:171480031	TTTGAAAGTCTTTGG[A/G]ATAGATAGATAAAAT	80067
rs3731982	snp	C/T	0.354881	0.226936	intron-variant	DCAF17	GRCh38.p7	2:171479769	ATAATTGAAATTCTC[C/T]ACAGTGACAGCAAAT	80067
rs3731983	snp	C/T	0.350574	0.228877	DCAF17	2	allele_origin=T(germline)/C(germline)	2:171473883	ACAACAATCCATTTC[C/T]TGGATCCCATTTTTT	80067
rs3731984	snp	A/T	0.0518822	0.152477	DCAF17	2	allele_origin=T(germline)/A(germline)	2:171453141	AAGGTACAGCAAAAC[A/T]TGTTGTTGAATGCCT	80067
rs3731985	snp	A/T	0.328148	0.237472	intron-variant	DCAF17	GRCh38.p7	2:171452996	CATATTATGAAAACA[A/T]CCATCTATCTAGATT	80067
rs3795996	snp	A/G	0.0332515	0.12458	utr-variant-3-prime, nc-transcript-variant, intron-variant	DCAF17	GRCh38.p7	2:171481464	GATGAGTTCTTAAAG[A/G]ATGGTATGGAATTTT	80067
rs3795997	snp	C/T	0.00184672	0.0303307	utr-variant-3-prime, nc-transcript-variant, intron-variant	DCAF17	GRCh38.p7	2:171481492	TTTGTTTGTTAAGGC[C/T]AGGAAAGACAGGGAG	80067
rs3795998	snp	A/G	0.387914	0.208518	utr-variant-3-prime, nc-transcript-variant, intron-variant	DCAF17	GRCh38.p7	2:171481684	TTGTATATAGTATCA[A/G]GAATTGGTTCTAGTT	80067
rs3821084	snp	A/C	0.387784	0.208604	utr-variant-3-prime, nc-transcript-variant, intron-variant	DCAF17	GRCh38.p7	2:171481790	TTAAGGTTTGCTTGG[A/C]ATCTTTTACATTAGC	80067
rs4404240	snp	A/T	0.337841	0.23406	intron-variant	DCAF17	GRCh38.p7	2:171463223	CGATGGAGCGAGATT[A/T]TAAAAAAAAAAAAAA	80067
rs4404241	snp	A/T	0.351418	0.228505	intron-variant	DCAF17	GRCh38.p7	2:171463224	GATGGAGCGAGATTT[A/T]AAAAAAAAAAAAAAA	80067
rs4417688	snp	A/G	0.327914	0.237549	intron-variant	DCAF17	GRCh38.p7	2:171463187	GGTGAGTGAGACTGC[A/G]CCACTGCACTCCAGC	80067
rs4458186	snp	C/T	0.32768	0.237625	intron-variant	DCAF17	GRCh38.p7	2:171458701	CTGAGCCTTGCTTGG[C/T]CACAGACCTTTAGCA	80067
rs4496302	snp	C/T	0.350982	0.228698	intron-variant	DCAF17	GRCh38.p7	2:171463183	TTGCGGTGAGTGAGA[C/T]TGCGCCACTGCACTC	80067
rs4522571	snp	A/G	0.328148	0.237472	intron-variant	DCAF17	GRCh38.p7	2:171440924	gctatgaggacagac[A/G]ggtggcacttccagg	80067
rs4668385	snp	A/G	0.354019	0.227333	intron-variant	DCAF17	GRCh38.p7	2:171450641	GTTTCTTTATACACC[A/G]GGACACCTAGAAAAA	80067
rs4668386	snp	C/T	0.32768	0.237625	intron-variant	DCAF17	GRCh38.p7	2:171461202	GTAATCCCAGCACTT[C/T]AGGAGGCTGACGCGG	80067
rs4668387	snp	C/T	0.327445	0.237702	intron-variant	DCAF17	GRCh38.p7	2:171476785	ATTTGTTGAGTTTTA[C/T]TTCAGTACTTAAACT	80067
rs5836336	in-del	-/A	0.5	0	intron-variant, upstream-variant-2KB	METTL8, DCAF17	GRCh38.p7	2:171432227	GTCAAAAAAAAAAAA[-/A]TCCTGTGTCACAAGT	80067
rs5836337	in-del	-/T	0.462253	0.132093	intron-variant	DCAF17	GRCh38.p7	2:171461850	CAACCAGTGATCTGC[-/T]TTTTTTTCACAGTAG	80067
rs5836338	in-del	-/AAT	0.480223	0.0974544	intron-variant	DCAF17	GRCh38.p7	2:171466589	GCCTTTTTCATTGAG[-/AAT]AATATTAGAGATCAA	80067
rs6433291	snp	A/G	0.391954	0.205789	intron-variant	DCAF17	GRCh38.p7	2:171439031	accAGaacactttag[A/G]tatttatgtctctct	80067
rs6433292	snp	C/G	0.351635	0.228408	intron-variant	DCAF17	GRCh38.p7	2:171439369	ttttcctcttttatt[C/G]ccccagcttgggaag	80067
rs6433293	snp	A/G	0.00478085	0.0486577	intron-variant, utr-variant-3-prime	DCAF17	GRCh38.p7	2:171474828	tttttaaatctgcct[A/G]tttctgcccttggcc	80067
rs6713612	snp	A/G	0.354881	0.226936	intron-variant	DCAF17	GRCh38.p7	2:171444798	AAAGGATAAGAGGCT[A/G]TACGCTAAATTTATT	80067
rs6718740	snp	C/G	0.392325	0.205532	intron-variant	DCAF17	GRCh38.p7	2:171440567	caacagagcgagaca[C/G]tgtctcaaaaaaTTT	80067
rs6720250	snp	A/T	0.32768	0.237625	intron-variant	DCAF17	GRCh38.p7	2:171458958	AGAAAATTATATACA[A/T]GTCTATAAATATAGT	80067
rs6729749	snp	G/T	0.0479149	0.147179	intron-variant, utr-variant-3-prime, downstream-variant-500B	DCAF17	GRCh38.p7	2:171469753	GATAAGTGCAAAAAG[G/T]GAGTTAAGGGGGGAG	80067
rs6730160	snp	C/T	0.0479149	0.147179	intron-variant, utr-variant-3-prime	DCAF17	GRCh38.p7	2:171470066	tctcactctggtgcc[C/T]agcctagagtgcagt	80067
rs6737818	snp	C/T			intron-variant	DCAF17	GRCh38.p7	2:171450868	ttacaggtgaggatt[C/T]tgagccccagagaag	80067
rs6740733	snp	G/T	0.32768	0.237625	intron-variant	DCAF17	GRCh38.p7	2:171456788	tcttggcttgactgt[G/T]gttgttgtataggaa	80067
rs6741663	snp	C/T	0.0437281	0.141251	intron-variant	DCAF17	GRCh38.p7	2:171472692	GTTTCTGCCTCCCCC[C/T]AGACTATAAGCTTCT	80067
rs6741806	snp	A/G	0.328148	0.237472	intron-variant	DCAF17	GRCh38.p7	2:171444727	AGGTCTTTGAATCTG[A/G]TTGGCTGTCCTTTAG	80067
rs6743290	snp	A/G	0.355096	0.226837	intron-variant, utr-variant-3-prime	DCAF17	GRCh38.p7	2:171470072	TCTGGTGCCTAGCCT[A/G]GAGTGCAGTGGCACA	80067
rs6751956	snp	C/T	0.396327	0.202703	DCAF17, METTL8	2	allele_origin=T(germline)/C(germline)	2:171435106	TAAATTTAAGAATGT[C/T]TGGACAACTCATTCC	80067
rs7563499	snp	A/G	0.0748431	0.178382	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	DCAF17, METTL8	GRCh38.p7	2:171433987	GGCCGAGAAGCTTGT[A/G]AGTACCGGGGCAGTG	80067
rs7564602	snp	C/T	0.0718919	0.175435	intron-variant, utr-variant-3-prime	DCAF17	GRCh38.p7	2:171474890	cactagccaaggcta[C/T]agtaatagcccactc	80067
rs7568037	snp	C/T	0.334138	0.239331	intron-variant	DCAF17	GRCh38.p7	2:171445495	TCTCTTAAGAAAAAC[C/T]AGGAGCATTTTGAAT	80067
rs7572334	snp	A/C	0.35445	0.227135	intron-variant, downstream-variant-500B	DCAF17	GRCh38.p7	2:171477142	AAGAAAGTTGACTAT[A/C]TTGAGTTTGTCTTTT	80067
rs7572973	snp	C/T	0.000399281	0.0141238	intron-variant	DCAF17	GRCh38.p7	2:171441645	gaaaacagggagcct[C/T]gtactcttggctgca	80067
rs7576894	snp	C/T	0.325091	0.238456	intron-variant	DCAF17	GRCh38.p7	2:171442740	taacaattagctaag[C/T]gtagtagcatgagct	80067
rs7591821	snp	A/C			intron-variant, utr-variant-3-prime, downstream-variant-500B	DCAF17	GRCh38.p7	2:171469633	atttattgagggcct[A/C]ccatgtgccagacaT	80067
rs7594714	snp	A/G	0.426507	0.177046	intron-variant	DCAF17	GRCh38.p7	2:171445808	CCACCTTGGCCTCCT[A/G]AGTAGCTGGGACTAC	80067
rs7599416	snp	A/C	0.040671	0.13668	intron-variant	DCAF17	GRCh38.p7	2:171441632	gagtggaagcttgga[A/C]aacagggagcctcgt	80067
rs7600478	snp	C/T	0.422158	0.181278	downstream-variant-500B	DCAF17	GRCh38.p7	2:171491110	AGGGTGGGAGGATCA[C/T]GAGGTCAGGAGTTCG	80067
rs7606658	snp	A/C	0.35445	0.227135	intron-variant	DCAF17	GRCh38.p7	2:171473496	CAAATGATTTATTCT[A/C]TTTGTGTATCAGTTT	80067
rs9646734	snp	C/T	0.133777	0.221342	intron-variant	DCAF17	GRCh38.p7	2:171465937	TTTGCATACTTTAAA[C/T]ATTTAATCTTCTTTC	80067
rs9678149	snp	A/G	0.32768	0.237625	intron-variant	DCAF17	GRCh38.p7	2:171460121	CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCTA	80067
rs9678164	snp	A/G	0.32768	0.237625	intron-variant	DCAF17	GRCh38.p7	2:171460310	CCTGGGCGATTGAGC[A/G]AGATTCCATCTCAAA	80067
rs9679537	snp	A/T	0.327914	0.237549	intron-variant	DCAF17	GRCh38.p7	2:171460275	TTGCAGTGAGCCGAG[A/T]TCGTGCCACTGCACT	80067
rs9679547	snp	A/T	0.277778	0.248452	intron-variant	DCAF17	GRCh38.p7	2:171460543	attattattattatt[A/T]Attttgagacagggt	80067
rs9789380	snp	A/G	0.42263	0.180829	downstream-variant-500B, intron-variant	DCAF17	GRCh38.p7	2:171485236	TCCACACATTCTCCA[A/G]CATGTGTGGTTGTTA	80067
rs9789572	snp	A/G	0.388025	0.208445	utr-variant-3-prime, nc-transcript-variant, intron-variant	DCAF17	GRCh38.p7	2:171484817	AAATTTACCTGTTCT[A/G]AACTTCATATGAGTG	80067
rs9789596	snp	C/T	0.326506	0.238006	intron-variant	DCAF17	GRCh38.p7	2:171488772	TACCAGCTGGACTCA[C/T]GATCCAGTAGTTTCC	80067
rs10177689	snp	G/T	0.114387	0.210022	intron-variant	DCAF17	GRCh38.p7	2:171479162	TAAATCCATATAAAT[G/T]TTTATGTCTTAGGGT	80067
rs10445722	snp	C/G	0.328148	0.237472	intron-variant	DCAF17	GRCh38.p7	2:171446973	ACTGAAATGTATTGT[C/G]TTTACTATCAAGAAC	80067
rs10445762	snp	A/G	0.198944	0.244731	intron-variant	DCAF17	GRCh38.p7	2:171447045	TAGAGATTTCTGACC[A/G]AATTAAGGAACACTG	80067
rs10460358	snp	A/G	0.463234	0.130503	intron-variant	DCAF17	GRCh38.p7	2:171439284	ccttctggtattccc[A/G]ttatgtggatgttat	80067
rs10490604	snp	C/G	0.425432	0.178112	intron-variant	DCAF17	GRCh38.p7	2:171457403	TTTTTATACAATTCA[C/G]CAGCTTAATCAAAAA	80067
rs10515933	snp	A/G	0.327914	0.237549	intron-variant	DCAF17	GRCh38.p7	2:171468652	ATCTGTTTTCAGGAG[A/G]TATATGTGGCCCGCA	80067
rs11311213	in-del	-/T	0.0482946	0.147699	intron-variant	DCAF17	GRCh38.p7	2:171479535	AAAAGGATTTTTTTT[-/T]AAAGGTGGTAAAAAG	80067
rs11366327	in-del	-/A	0.32768	0.237625	intron-variant	DCAF17	GRCh38.p7	2:171473624	ATCTCTTGGGTTATT[-/A]ACTCCTGTTTGTGAG	80067
rs11449615	in-del	-/T	0.5	0	intron-variant	DCAF17	GRCh38.p7	2:171477454	AATAATTTTTTTTTT[-/T]GCCCATTCTGGCATT	80067
rs11677265	snp	A/G	0.0146672	0.084371	intron-variant, utr-variant-3-prime	DCAF17	GRCh38.p7	2:171474256	GTCTTAGTTAATTCT[A/G]TAGGGTTAATAAGAA	80067
rs11677562	snp	A/G	0.463343	0.130326	intron-variant	DCAF17	GRCh38.p7	2:171444745	GGCTGTCCTTTAGGA[A/G]AAACGGAACTCATAA	80067
rs11696032	snp	C/T	0.379354	0.213933	intron-variant	DCAF17	GRCh38.p7	2:171454245	GATCTAGAATTAAAA[C/T]AGATTGGCTACTTTA	80067
rs11887983	snp	A/T	0.00917871	0.0671201	intron-variant	DCAF17	GRCh38.p7	2:171478121	TGTGTCCTTGCATTG[A/T]GAATTTCATATTAAT	80067
rs11901352	snp	G/T	0.040671	0.13668	intron-variant	DCAF17	GRCh38.p7	2:171471608	tcttttatgtaaaat[G/T]taataataCCACTAT	80067
rs12052810	snp	G/T	0.462472	0.13174	intron-variant	DCAF17	GRCh38.p7	2:171451085	TTTAATTTTACCTTG[G/T]TTAGATAACTACATC	80067
rs12151641	snp	A/T	0.388903	0.207861	utr-variant-3-prime, nc-transcript-variant, intron-variant	DCAF17	GRCh38.p7	2:171483539	AGAAAACAAAACAAA[A/T]CCTATCCTATTTACT	80067
rs12471094	snp	A/G	0.462472	0.13174	intron-variant	DCAF17	GRCh38.p7	2:171466414	CCTTTTTTTCACAAT[A/G]TAGGAAGTGGAAGCC	80067
rs12612865	snp	A/G	0.0123036	0.0774623	intron-variant	DCAF17	GRCh38.p7	2:171468306	GTGGTAGTAGTGACT[A/G]TCCTGTAATAAAGCT	80067
rs12620294	snp	A/C			intron-variant	DCAF17	GRCh38.p7	2:171439815	cacccataatcccag[A/C]tactccagaggccaa	80067
rs12620336	snp	C/G			intron-variant	DCAF17	GRCh38.p7	2:171439867	tgggaggtggaggtt[C/G]cagtgagttgtgatt	80067
rs12620343	snp	C/T	0	0	intron-variant	DCAF17	GRCh38.p7	2:171440053	tgtagccccaaactc[C/T]tgcactccagtgatc	80067
rs13005833	snp	A/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	DCAF17	GRCh38.p7	2:171469593	TTTAAAAATGGCTTA[A/G]GCGTTGATTTGTCAT	80067
rs13024497	snp	A/G	0.247277	0.249985	intron-variant, utr-variant-5-prime	DCAF17	GRCh38.p7	2:171447401	atggagtcttctgtc[A/G]ccaggctggagtgca	80067
rs13031705	snp	C/T			intron-variant	DCAF17	GRCh38.p7	2:171439512	atttcttttttttcc[C/T]ttttttttttttttt	80067
rs13396824	snp	A/T	0.114036	0.209795	intron-variant	DCAF17	GRCh38.p7	2:171449506	TTTTAACTATTAGTT[A/T]TATAAATTAGATGTA	80067
rs13402901	snp	A/G	0.114036	0.209795	intron-variant	DCAF17	GRCh38.p7	2:171465386	TTTCATTTTGTTTTC[A/G]ATTTTGGGGTTTGCT	80067
rs13404032	snp	C/T	0.0150606	0.0854603	intron-variant	DCAF17	GRCh38.p7	2:171451533	GTGTCTTGTCTGATG[C/T]ACCTTTTTAATAATT	80067
rs13404120	snp	G/T	0	0	intron-variant	DCAF17	GRCh38.p7	2:171451628	gttgccaggctagag[G/T]gtcgtggtgagctct	80067
rs13417427	snp	G/T			intron-variant	DCAF17	GRCh38.p7	2:171439419	aaactcactgattct[G/T]tccttggctgcatcc	80067
rs16859388	snp	A/G	0.0170251	0.090679	upstream-variant-2KB, intron-variant	DCAF17, METTL8	GRCh38.p7	2:171433706	AGCAATTATCGCAAA[A/G]CCAGTCAGTGTCCCC	80067

Full records

It may take some time, please wait.