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
rs3786714	snp	A/G			upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697170	AAAAAAAAAAAAAAA[A/G]AAAAAAAAGTCACTT	84261
rs4468743	snp	C/T	0.00934559	0.067716	intron-variant	FBXW9	GRCh38.p7	19:12693190	ccccaagcccaagct[C/T]tcagctacCGGCCTG	84261
rs6511832	snp	C/G	0.174144	0.238214	synonymous-codon, utr-variant-5-prime	FBXW9	GRCh38.p7	19:12696252	AGACACGAGGTCGCG[C/G]AGCGCGTGGCACACC	84261
rs6511833	snp	C/T	0.122623	0.215116	missense, utr-variant-5-prime	FBXW9	GRCh38.p7	19:12696373	CTTACGGCCGAAACC[C/T]TGGACGCGGCCCGAG	84261
rs7246726	snp	C/T	0.254664	0.249956	intron-variant	FBXW9	GRCh38.p7	19:12692505	tgctgggattacagg[C/T]gtgagccactgcatc	84261
rs7246917	snp	C/T	0.266819	0.249434	intron-variant	FBXW9	GRCh38.p7	19:12692100	ggtcttgctgtgtca[C/T]ccaggcatgaatgca	84261
rs7248201	snp	C/G	0.0994999	0.200568	intron-variant	FBXW9	GRCh38.p7	19:12689676	CGAGGCTCTCCCAAG[C/G]CCCGCCCTCCCCCAC	84261
rs7254207	snp	A/C	0.253264	0.249979	intron-variant	FBXW9	GRCh38.p7	19:12690901	attatctggatttca[A/C]agatggggaaaccga	84261
rs7254682	snp	A/T			intron-variant	FBXW9	GRCh38.p7	19:12693531	aaaaaaaaaaaaaaa[A/T]atatatatatatata	84261
rs7254698	snp	C/T			intron-variant	FBXW9	GRCh38.p7	19:12693561	ATATATATATATATA[C/T]ACACACACACACACA	84261
rs7256839	snp	A/G	0.21845	0.248001	intron-variant	FBXW9	GRCh38.p7	19:12691603	GTGCCCATGGTGATA[A/G]ATGCTGCAGCAAGTA	84261
rs7257128	snp	A/G	0.258843	0.249844	intron-variant	FBXW9	GRCh38.p7	19:12691807	gtcatccaggctgga[A/G]tgcagtggcttgatc	84261
rs7258212	snp	A/C	0.254105	0.249966	intron-variant	FBXW9	GRCh38.p7	19:12691667	CATTGCATAGATGAA[A/C]CCAGAGCAAGTTCAA	84261
rs7258853	snp	C/G	0.252983	0.249982	downstream-variant-500B	LOC105372280, FBXW9	GRCh38.p7	19:12688431	CTCAATAAACATGAA[C/G]TGAATACTTCTCAGG	84261
rs10402775	snp	A/G	0.0225045	0.103662	intron-variant	FBXW9	GRCh38.p7	19:12693046	TTGCCcaccaatccc[A/G]ctgaggagggcaata	84261
rs10404612	snp	C/G	0.0174175	0.0916809	intron-variant	FBXW9	GRCh38.p7	19:12693135	tcaaggtcacacagc[C/G]aggaagcagcacagt	84261
rs10405216	snp	A/C	0.283947	0.247685	intron-variant	FBXW9	GRCh38.p7	19:12693059	ccgctgaggagggca[A/C]tattgtgtatctcat	84261
rs10409345	snp	A/T	0.253264	0.249979	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12698345	CTCTGCCTTCCTGTT[A/T]TTCTCTATAGGACTT	84261
rs10411280	snp	A/G	0.284209	0.247648	intron-variant	FBXW9	GRCh38.p7	19:12693419	atcctagcattttgg[A/G]aggctgagtcaggca	84261
rs10416965	snp	C/G	0.0916459	0.193453	synonymous-codon	FBXW9	GRCh38.p7	19:12694711	GGAGCCCGACAGACA[C/G]AGTGACCCACCCTGG	84261
rs10417846	snp	A/G	0.254105	0.249966	intron-variant	FBXW9	GRCh38.p7	19:12695134	CCCATTTCCCAGGCA[A/G]GTCTAGGACTACTCA	84261
rs10422441	snp	A/G			upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697361	ggactacaggcgcgc[A/G]ccaccacacccggct	84261
rs10424461	snp	C/T	0.0923837	0.194054	intron-variant	FBXW9	GRCh38.p7	19:12694566	cctactCAGGCCTCA[C/T]ACCTCCTATCCCCAC	84261
rs10424623	snp	C/T	0.0918135	0.19359	missense	FBXW9	GRCh38.p7	19:12694617	TACTATTTCGCTTAG[C/T]GCCTAAGGTCTTGAT	84261
rs10425615	snp	A/G	0.253824	0.249971	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697512	gaaccatcgcgcctg[A/G]TGGAAAGCTACCttt	84261
rs11552350	snp	G/T			utr-variant-5-prime	FBXW9	GRCh38.p7	19:12696588	CGGCAGCGCCCACCC[G/T]GTCGCAATGGAGCTT	84261
rs11883224	snp	A/G	0.253264	0.249979	downstream-variant-500B	LOC105372280, FBXW9	GRCh38.p7	19:12688872	CACAGCCCCAAGCAG[A/G]CACAGGCAGAACCCC	84261
rs12104166	snp	C/T	0.253824	0.249971	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697688	accactcctggctaa[C/T]ttttgtatttttcag	84261
rs12104271	snp	A/G	0.207559	0.246371	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697633	tcaagcgattctcct[A/G]cctcagcctctagag	84261
rs12977809	snp	A/G	0	0	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697208	GGAACTGGGGCCTCA[A/G]AACTACCTCTCCAGA	84261
rs12983215	snp	A/T			intron-variant	FBXW9	GRCh38.p7	19:12693529	aaaaaaaaaaaaaAa[A/T]atatatatatatata	84261
rs12985658	snp	A/G	0	0	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697917	ggttaatcacttgag[A/G]tcaggagttcaagac	84261
rs28514464	snp	C/T	0.0178098	0.0926698	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697328	AGTGATCCTCCACCT[C/T]GGCCCCCCAGGTAGC	84261
rs28677854	snp	C/T	0.0174175	0.0916809	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697327	AAGTGATCCTCCACC[C/T]CGGCCCCCCAGGTAG	84261
rs34229562	in-del	-/T			frameshift-variant	FBXW9	GRCh38.p7	19:12689988	CAGGACGCTGTTGGC[-/T]TCGGCGGTCCACCAC	84261
rs34416243	in-del	-/T	0.5	0	intron-variant	FBXW9	GRCh38.p7	19:12692077	TCTTTTTTTTTTTTT[-/T]GAGACAAGGTCTTGC	84261
rs34755979	in-del	-/A			upstream-variant-2KB	FBXW9	GRCh38.p7	19:12698062	GAGCCTGGGAGGCGG[-/A]AGGTTGCAGTGAGCC	84261
rs35117302	in-del	-/T			intron-variant	FBXW9	GRCh38.p7	19:12695727	TCTAGGGCTCAGGAG[-/T]TTTTGACATCAACAG	84261
rs35134914	in-del	-/T/TT	0.173965	0.238157	intron-variant	FBXW9	GRCh38.p7	19:12692525	CCACTGCATCCGGTC[-/T/TT]TTTTTTTTTTTTTTG	84261
rs45478502	snp	A/C	0.094384	0.195662	intron-variant	FBXW9	GRCh38.p7	19:12691339	GCCCAGGCCCCCACA[A/C]ACTTTATCTCGCCGA	84261
rs55747371	snp	C/T			upstream-variant-2KB	FBXW9	GRCh38.p7	19:12698513	TTTGGCTGGGGGCGG[C/T]GGCCCACACCTGTAA	84261
rs58000003	in-del	-/T/TT			intron-variant	FBXW9	GRCh38.p7	19:12692538	ATCCGGTCTTTTTTT[-/T/TT]TTTTTTTGAGACATA	84261
rs58312983	snp	C/G	0.0834829	0.186498	intron-variant	FBXW9	GRCh38.p7	19:12689894	GAGAGGGACAAGGGA[C/G]GGGACAGCTCAGGCC	84261
rs59299234	snp	A/G	0.254105	0.249966	intron-variant	FBXW9	GRCh38.p7	19:12695358	CAGTATCTGGAAACC[A/G]GGGAGCCTTGTCAAG	84261
rs59751558	in-del	-/C	0.253264	0.249979	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12698263	GCTCTGTTCAAACAT[-/C]CGTCTTCTCAGTGTG	84261
rs61213051	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	FBXW9	GRCh38.p7	19:12696759	GTCGGCCTTAGGCTG[A/G]AAAATGCAGGTTCCT	84261
rs62108390	snp	A/C/T	1.65641e-05	0.00287781	missense	FBXW9	GRCh38.p7	19:12689780	ATAAGCTGGAAGCAG[A/C/T]CGTTGCGGTTGGCGA	84261
rs62108391	snp	A/C			missense	FBXW9	GRCh38.p7	19:12691450	GCCAGTGACCACACC[A/C]AGCCCTGCAGGACAG	84261
rs71168624	in-del	-/A	0	0	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12697186	CCCAGTTCCTTTCTC[-/A]AAAAAAAAAAAAAAA	84261
rs73921601	snp	C/T	0.0459857	0.144493	missense	FBXW9	GRCh38.p7	19:12689783	AGCTGGAAGCAGCCG[C/T]TGCGGTTGGCGAAGA	84261
rs73923903	snp	A/C	0.0134861	0.0810011	intron-variant	FBXW9	GRCh38.p7	19:12691619	ATGCTGCAGCAAGTA[A/C]AACACCCAACTCTGG	84261
rs74180097	in-del	-/T	0.5	0	intron-variant	FBXW9	GRCh38.p7	19:12694217	TGGTGGCATGCACCT[-/T]GTAGTCCCAGCTACT	84261
rs75404765	snp	A/C			intron-variant	FBXW9	GRCh38.p7	19:12695669	TCAGGAACCAATCAA[A/C]TCAGGGCCAAGAGCC	84261
rs75929315	snp	C/T	0.0181196	0.0934424	utr-variant-3-prime	FBXW9	GRCh38.p7	19:12688950	GGTTTATTTCTCCTT[C/T]GCTCTCAACTGAGAG	84261
rs76451863	snp	G/T	0.5	0	intron-variant	FBXW9	GRCh38.p7	19:12692539	TCTTTTTTTTTTTTT[G/T]GAGACATAGTATCGC	84261
rs76679560	snp	A/G	0.0127477	0.0788122	synonymous-codon	FBXW9	GRCh38.p7	19:12690037	GCTGCCTGAGATGAT[A/G]TGCCGGTCATCCGCC	84261
rs77256012	snp	C/T	0.0236746	0.106192	intron-variant	FBXW9	GRCh38.p7	19:12690868	CCCCCATTAACCCCA[C/T]GGGGCTGCTGTGGTA	84261
rs77302244	snp	C/T	0.0383715	0.133092	intron-variant	FBXW9	GRCh38.p7	19:12695584	TGTAATACATCTTGG[C/T]TTAAGGGCCTGAGGA	84261
rs77438035	snp	A/T	0.0134861	0.0810011	intron-variant	FBXW9	GRCh38.p7	19:12695912	GATATTTGGATCCTG[A/T]GTCGTCCAGGAACCA	84261
rs78119363	snp	A/G	0.00438332	0.0466095	downstream-variant-500B	LOC105372280, FBXW9	GRCh38.p7	19:12688659	GTACCCTTTCCCACC[A/G]TGCAGACAAATGGCC	84261
rs78119753	snp	C/T	0.00557542	0.0525036	intron-variant	FBXW9	GRCh38.p7	19:12695783	CTCAGAACCTGAGGA[C/T]CCTTGGGCTCACTTT	84261
rs79473321	snp	C/T			intron-variant	FBXW9	GRCh38.p7	19:12694745	GGGAGCAAGGTGATG[C/T]TGTCAGGGCCACCCT	84261
rs111477231	snp	C/T	0.0107246	0.0724382	intron-variant	FBXW9	GRCh38.p7	19:12690756	AAACCTTGTCTCTAC[C/T]GCCTCAGCCTCTGGA	84261
rs111827159	snp	A/G	0.21845	0.248001	intron-variant	FBXW9	GRCh38.p7	19:12693666	GCTACTCAGGAGGCA[A/G]GGTTGCAGTGAGCTG	84261
rs112987154	snp	C/T	0.00269179	0.0365875	utr-variant-3-prime	FBXW9	GRCh38.p7	19:12689183	AGGAAGCCCAGCCTC[C/T]GGCAGGCAGTATCCA	84261
rs113553998	snp	C/T	0.5	0	intron-variant	FBXW9	GRCh38.p7	19:12689734	GCCCGGGGGGAGGGA[C/T]AGTCAGGGGCAGGAG	84261
rs113581497	snp	C/T	0.00874735	0.0655527	intron-variant	FBXW9	GRCh38.p7	19:12691082	TTGGTTAAGTGACTA[C/T]GACCCCAGCCAGGCT	84261
rs114172571	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-5-prime	FBXW9	GRCh38.p7	19:12696671	TGACGTTTATGCGCC[C/T]ACCGGAAGCGACGAA	84261
rs115331883	snp	A/G	0.00676609	0.0577691	intron-variant	FBXW9	GRCh38.p7	19:12692696	CCTGGCTAATTATTT[A/G]GTATTTTTTGTAGAG	84261
rs115894248	snp	C/T	0.00835141	0.0640778	downstream-variant-500B, upstream-variant-2KB	TNPO2, FBXW9	GRCh38.p7	19:12698821	AGATTGTGGTTTCCC[C/T]CCACAGCTGAAACTA	84261
rs115998909	snp	C/T	0.0236746	0.106192	intron-variant	FBXW9	GRCh38.p7	19:12696025	CGGCACCACCAGTAA[C/T]TACCTTAGCCTCCAG	84261
rs116575943	snp	C/T	0.0471551	0.14613	downstream-variant-500B, upstream-variant-2KB	TNPO2, FBXW9	GRCh38.p7	19:12698774	TGACGGAGCAAGACC[C/T]GGTCTCAAAAAAAAG	84261
rs117566511	snp	C/T	0.0342893	0.126368	missense	FBXW9	GRCh38.p7	19:12694610	TCATGGGTACTATTT[C/T]GCTTAGTGCCTAAGG	84261
rs118088305	snp	A/G	0.0228947	0.104514	intron-variant	FBXW9	GRCh38.p7	19:12693041	ACTTTTTGCCCACCA[A/G]TCCCGCTGAGGAGGG	84261
rs138069323	snp	C/T	0.000399281	0.0141238	intron-variant	FBXW9	GRCh38.p7	19:12695206	CTCTCCAGGCGCCAT[C/T]CCCCAACCCAAACTC	84261
rs138656867	snp	C/T	0.00231569	0.0339483	intron-variant	FBXW9	GRCh38.p7	19:12689878	GTAGGAGTCCAGCTA[C/T]GAGAGGGACAAGGGA	84261
rs138687993	snp	C/T	0.00676609	0.0577691	intron-variant	FBXW9	GRCh38.p7	19:12693968	GCTGAGGCGGGCAGA[C/T]CACGAGGTCTGGAGA	84261
rs138698639	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12698192	CAGCTAACCAATCCA[C/T]GTAGGTCATCTGCGC	84261
rs139535728	snp	A/C	0.00649535	0.056617	intron-variant	FBXW9	GRCh38.p7	19:12696156	GCCCCCGGTCCCCGG[A/C]CCCCGGCCCCGCGCA	84261
rs139718306	snp	A/G	8.25321e-05	0.00642334	synonymous-codon	FBXW9	GRCh38.p7	19:12689547	GAGCCTCACCCGGAT[A/G]GTCTTGTCAGTGGAT	84261
rs139736936	snp	C/G	0.0049584	0.0495441	intron-variant	FBXW9	GRCh38.p7	19:12691155	CCTGGGCCCCAGGAC[C/G]CTTGGCCCACCTCTG	84261
rs139918737	snp	C/T	0.00438332	0.0466095	intron-variant	FBXW9	GRCh38.p7	19:12695758	GTGCTGTCTCAGCTT[C/T]TAAGCTGGACTCAGA	84261
rs140209073	in-del	-/C			downstream-variant-500B	LOC105372280, FBXW9	GRCh38.p7	19:12688550	CTGCCCCCGGGGTCA[-/C]CAGCCACAGCAGCAC	84261
rs140492246	snp	A/C	0.00119737	0.0244387	intron-variant	FBXW9	GRCh38.p7	19:12691564	CAAGAGACTCACCCA[A/C]AGCCACATAGCTCTT	84261
rs140794234	snp	A/G	0.00135735	0.026016	synonymous-codon	FBXW9	GRCh38.p7	19:12689782	AAGCTGGAAGCAGCC[A/G]TTGCGGTTGGCGAAG	84261
rs141072366	snp	A/G	0.00163541	0.0285487	utr-variant-5-prime	FBXW9	GRCh38.p7	19:12696589	AGCTCCATTGCGACC[A/G]GGTGGGCGCTGCCGG	84261
rs141711253	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12698539	TGTAATCCCAGCACT[G/T]TGGGAGGCTAAAGTA	84261
rs141734078	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, utr-variant-5-prime	FBXW9	GRCh38.p7	19:12696810	AGCCGATACCGAGAG[C/T]CAGCCAACTCTAGCT	84261
rs141814234	snp	A/G	0.0244538	0.107838	upstream-variant-2KB	FBXW9	GRCh38.p7	19:12698111	TCCAGCTTGGGCAAC[A/G]AGAGCAAAACTCCGT	84261
rs142202804	snp	A/G	3.29843e-05	0.00406092	missense	FBXW9	GRCh38.p7	19:12690039	TGCCTGAGATGATGT[A/G]CCGGTCATCCGCCAG	84261
rs142463005	snp	C/T	1.66482e-05	0.0028851	missense	FBXW9	GRCh38.p7	19:12689391	TTGAGCCCATTGTCA[C/T]GCCTTCGGGTGCAAA	84261
rs142601928	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW9	GRCh38.p7	19:12690976	CCAGAACTCTAACCC[A/G]CCCCCAGGGCTGCCC	84261
rs142686174	snp	C/T	0.00159617	0.0282053	intron-variant	FBXW9	GRCh38.p7	19:12694123	GAGGTTGCAGTGAGC[C/T]GAGATTGCATCACTA	84261
rs142935382	snp	A/G	0.000447127	0.0149454	synonymous-codon	FBXW9	GRCh38.p7	19:12689980	CAGACGCTGCAGGAC[A/G]CTGTTGGCTCGGCGG	84261
rs143320263	snp	A/G	0.0505692	0.150756	intron-variant	FBXW9	GRCh38.p7	19:12692583	CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT	84261
rs143426278	snp	C/G	0.000833681	0.0203996	intron-variant	FBXW9	GRCh38.p7	19:12689342	TGGCGCTCTGGCCAG[C/G]TGGGCAGGGCACATG	84261
rs143596846	snp	C/T	0.00157224	0.0279937	missense	FBXW9	GRCh38.p7	19:12691195	ATGGTCACCTTCTTG[C/T]CATAGGTGCCAGTCA	84261
rs143742761	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW9	GRCh38.p7	19:12695760	GCTGTCTCAGCTTCT[A/G]AGCTGGACTCAGAAC	84261
rs143991227	snp	C/G	0.000399281	0.0141238	intron-variant	FBXW9	GRCh38.p7	19:12695529	ATTCCTCTCTAAGCA[C/G]AATCAAAGCTTCCAG	84261
rs144031558	snp	C/T	0.00214291	0.0326629	missense	FBXW9	GRCh38.p7	19:12689582	TGTACAAGGCTCCCA[C/T]GGAGTACTGGATCCC	84261

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