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
rs3541	snp	C/T	0	0	intron-variant	FBXW8	GRCh38.p7	12:117010018	GGTTTCCAGACGGCT[C/T]TCTCTTTGTTAAGAA	26259
rs937567	snp	C/G	0.0554779	0.157039	intron-variant	FBXW8	GRCh38.p7	12:117021158	tgtcaccaatctacc[C/G]agcaaaggtaaagtt	26259
rs952934	snp	C/T	0.0260105	0.111035	intron-variant	FBXW8	GRCh38.p7	12:117005277	GGATTTGCCTGGCAT[C/T]GTGTACCAATCAGTG	26259
rs1051877	snp	C/T	0	0	utr-variant-3-prime, nc-transcript-variant	FBXW8	GRCh38.p7	12:117029239	AATTATAGAATCCCC[C/T]AACCCCAAGACACTG	26259
rs1051879	snp	A/G	0.113685	0.209567	utr-variant-3-prime, nc-transcript-variant	FBXW8	GRCh38.p7	12:117029320	CTCCAATGCAGAATA[A/G]TGAGAAATCAACAAA	26259
rs1320027	snp	A/G	0.0517044	0.152246	intron-variant	FBXW8	GRCh38.p7	12:117021496	AAACATAAACTATAA[A/G]ACATATTCAAAGGAG	26259
rs1472524	snp	A/G	0.0520825	0.152737	intron-variant	FBXW8	GRCh38.p7	12:117002828	CTTTAAAAAAACAGG[A/G]ATGAGAAAGATAGAC	26259
rs2133684	snp	A/G	0.108402	0.206034	intron-variant	FBXW8	GRCh38.p7	12:117007832	GAGAGAGAGTGCGTG[A/G]GAGGGAGGGAGAAAT	26259
rs2173652	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW8	GRCh38.p7	12:117007525	AAGTGCTTCTCTAAT[A/G]TATACCTGGTACTTA	26259
rs2242469	snp	C/G	0.45843	0.138046	utr-variant-3-prime, nc-transcript-variant	FBXW8	GRCh38.p7	12:117030562	AGGAAGGGCGAATGC[C/G]CCTGCAAAATGAACT	26259
rs2279886	snp	A/G	0.000399281	0.0141238	intron-variant	FBXW8	GRCh38.p7	12:117019434	AATGGGCACCAGAAT[A/G]TGCCAAGACAACCGA	26259
rs2279887	snp	A/G	0	0	intron-variant	FBXW8	GRCh38.p7	12:117019302	GCATTAGATGGTCTT[A/G]AAGAGGTCTGCTAGA	26259
rs2291914	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	FBXW8	GRCh38.p7	12:117028307	GGGTCAGGGAGATGC[A/G]TGCTGTCAGGCATGG	26259
rs2291915	snp	A/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	FBXW8	GRCh38.p7	12:117028239	CTGTGAAGAGGTGCC[A/T]GGCGTTTTAAGATGG	26259
rs2291916	snp	A/G	0.468875	0.120804	utr-variant-3-prime, nc-transcript-variant	FBXW8	GRCh38.p7	12:117028176	TCCCAACTGAGGCAC[A/G]TCCCTAAACATGGTT	26259
rs2393110	snp	A/G	0.386694	0.20932	intron-variant	FBXW8	GRCh38.p7	12:116932277	AAATTAGTTTGTTTA[A/G]TGGTTAGCATTTTCA	26259
rs2393111	snp	C/T	0.460702	0.134554	intron-variant	FBXW8	GRCh38.p7	12:116944485	GTACTGTAACCTACC[C/T]GCTACCACTCTTCAT	26259
rs2393112	snp	A/T	0.0517044	0.152246	intron-variant	FBXW8	GRCh38.p7	12:117012298	TGTTACATTTTTTTT[A/T]AAAACGCTCTGTCTC	26259
rs2393113	snp	A/G	0.497558	0.0348586	intron-variant	FBXW8	GRCh38.p7	12:117017560	GCTATTGATTTTGGC[A/G]TATAAGGTTATATTT	26259
rs2893701	snp	G/T	0.326741	0.23793	intron-variant	FBXW8	GRCh38.p7	12:117012192	ATGTACGCACTGCCA[G/T]GGAGGTGTTCCATGC	26259
rs2893702	snp	G/T	0.326741	0.23793	intron-variant	FBXW8	GRCh38.p7	12:117012194	GTACGCACTGCCAGG[G/T]AGGTGTTCCATGCAT	26259
rs3070246	in-del	-/TCATT			intron-variant	FBXW8	GRCh38.p7	12:117012190	TATGTACGCACTGCC[-/TCATT]AGGGAGGTGTTCCAT	26259
rs3070248	in-del	-/CACTA			intron-variant	FBXW8	GRCh38.p7	12:117012197	GCACTGCCAGGGAGG[-/CACTA]TGTTCCATGCATAGT	26259
rs3741465	snp	A/G	0.242488	0.249887	intron-variant	FBXW8	GRCh38.p7	12:117027165	TGCCAGCATGCGTAC[A/G]GGGCATGCAGACCTG	26259
rs3741466	snp	C/T	0.0150804	0.0855147	missense, nc-transcript-variant	FBXW8	GRCh38.p7	12:117027459	ACGTGCCTTACCAGA[C/T]GGTAATGCGAAACGC	26259
rs3803089	snp	A/G	0.122411	0.214991	intron-variant	FBXW8	GRCh38.p7	12:116945910	GGAGCTGAAAATGTC[A/G]TTTCTAGTAAATGTA	26259
rs3832800	in-del	-/ATTT			intron-variant	FBXW8	GRCh38.p7	12:117018745	CGCATCTTTTGGTTT[-/ATTT]GTTTATTTTGTTTGG	26259
rs3893370	snp	A/G	0.453697	0.14494	intron-variant	FBXW8	GRCh38.p7	12:116915432	CTTTACAAGGGCCTA[A/G]ATACACAGCTTGATG	26259
rs3935958	snp	G/T	0.0360663	0.129354	intron-variant	FBXW8	GRCh38.p7	12:116916099	aattcccatcaacag[G/T]agataagatgtggca	26259
rs3956801	snp	A/G	0.0279526	0.114869	intron-variant	FBXW8	GRCh38.p7	12:116932605	cagtggcgcgatctc[A/G]gctcaccgcaacctc	26259
rs3999688	snp	C/T			intron-variant	FBXW8	GRCh38.p7	12:116932612	gcgatctcagctcac[C/T]gcaacctctgcctcc	26259
rs4074147	snp	A/G	0.412416	0.190055	intron-variant	FBXW8	GRCh38.p7	12:116966133	AAAGGAAATCCATCA[A/G]TAGTGTCTACTAACA	26259
rs4076570	snp	C/T	0.0146672	0.084371	intron-variant	FBXW8	GRCh38.p7	12:116947273	GTTGATTGAGTGAAC[C/T]GGAGCGGACTGCAGG	26259
rs4076700	snp	C/T	0.333372	0.235689	missense, nc-transcript-variant	FBXW8	GRCh38.p7	12:116945515	ACCTTCCAGTTGGTT[C/T]GTAACATGTGTTCCT	26259
rs4077519	snp	C/G	0.466824	0.124448	intron-variant	FBXW8	GRCh38.p7	12:116946604	AACAGTGGTTCTCGA[C/G]TGGGAGGGGATTTTG	26259
rs4094198	snp	G/T			intron-variant	FBXW8	GRCh38.p7	12:117012008	ttttaatggaggatg[G/T]gtgtaggttatatgc	26259
rs4094199	snp	A/T	0.114738	0.210248	intron-variant	FBXW8	GRCh38.p7	12:117012236	GCTCTCTGGTCAGTT[A/T]GCAGTCCAAATCTGA	26259
rs4130068	snp	C/G	0	0	intron-variant	FBXW8	GRCh38.p7	12:116962514	TGAAAACAGTGTGCA[C/G]ACTGCTGGTGTGGTG	26259
rs4130296	snp	G/T	0.388775	0.207946	intron-variant	FBXW8	GRCh38.p7	12:116948280	TACAATAACAGAAAA[G/T]CTCTTGTGAGGGAAA	26259
rs4238049	snp	A/G	0.00676609	0.0577691	intron-variant	FBXW8	GRCh38.p7	12:116925505	CATATTTCTTAAGAT[A/G]TGGACCTTCCGTTAG	26259
rs4238050	snp	A/T	0.471196	0.1165	intron-variant	FBXW8	GRCh38.p7	12:116925652	ACAGTGACTTTTTTT[A/T]AAAAAAAGTTTGGCT	26259
rs4238051	snp	A/G	0.278399	0.248382	intron-variant	FBXW8	GRCh38.p7	12:116928494	TAAATCGAGCCTGTT[A/G]TTAGGTTGGTAGCTG	26259
rs4299000	snp	C/G	0.388587	0.208071	intron-variant	FBXW8	GRCh38.p7	12:116947346	GTCCATTTCCTGACA[C/G]TGTTAACAAGGAGAA	26259
rs4347476	snp	A/G	0.121717	0.214577	intron-variant	FBXW8	GRCh38.p7	12:116946716	TTTCCATCCACCTAC[A/G]GTAATAAACTCGTCT	26259
rs4451816	snp	A/G	0.162253	0.234095	upstream-variant-2KB	FBXW8	GRCh38.p7	12:116909381	ACCTGTAACCCCAGC[A/G]CTTTGGGAGGCTGAG	26259
rs4522274	snp	A/G	0.389152	0.207694	intron-variant	FBXW8	GRCh38.p7	12:116924407	TCCATCACCTAAAAC[A/G]TTTATTATTTGTGTT	26259
rs4529958	snp	A/G	0.198856	0.244713	synonymous-codon, nc-transcript-variant	FBXW8	GRCh38.p7	12:117028052	GTCCACCGCAAACTC[A/G]TAGGCGCGGATCAGC	26259
rs4542506	snp	C/T	0.454061	0.144427	intron-variant	FBXW8	GRCh38.p7	12:116960643	CACTCATCATTACCA[C/T]TGGAAAGTGGGCAGT	26259
rs4562925	snp	A/G	0.394538	0.203982	intron-variant	FBXW8	GRCh38.p7	12:116924648	ACATTTATGAACTGT[A/G]GGAAGTACCCAATCA	26259
rs4562926	snp	A/G	0.45889	0.13735	intron-variant	FBXW8	GRCh38.p7	12:116925245	CTGCCTTAGTGGGGT[A/G]GGAGGGGATGCAACC	26259
rs4562927	snp	G/T	0.486725	0.0803809	intron-variant	FBXW8	GRCh38.p7	12:116925361	GGAATGAGTGGGACC[G/T]GAAGCGGGATCTGAG	26259
rs4766812	snp	C/T	0.457388	0.139608	intron-variant	FBXW8	GRCh38.p7	12:116926895	TACTGTGAGTCTTGG[C/T]AGGGTCTAAATCAGT	26259
rs4766813	snp	A/C	0.00279162	0.0372561	intron-variant	FBXW8	GRCh38.p7	12:116927098	TTGGGACACAGAGTG[A/C]AGCTTTTCCTAGCTT	26259
rs4766814	snp	A/G	0.457388	0.139608	intron-variant	FBXW8	GRCh38.p7	12:116936518	agagggaggcaggac[A/G]tcagggaggagagaa	26259
rs4766815	snp	A/G	0.464523	0.128375	intron-variant	FBXW8	GRCh38.p7	12:116936703	tccggaactataagc[A/G]aataaatctgtattg	26259
rs4766816	snp	C/T	0.498346	0.0287064	intron-variant	FBXW8	GRCh38.p7	12:116943564	gtgctctctgtatat[C/T]ggggtactgcttcac	26259
rs4766817	snp	A/T	0	0	intron-variant	FBXW8	GRCh38.p7	12:116954133	aaaaaaaaaaaaaaa[A/T]agaaaaaGCAGTGGT	26259
rs4766818	snp	A/G	0.390651	0.206682	intron-variant	FBXW8	GRCh38.p7	12:116954300	TTTCATAGTGTGACT[A/G]TAGCCTTTGTTAGAT	26259
rs4766819	snp	C/T	0.0704125	0.17392	intron-variant, downstream-variant-500B, utr-variant-5-prime	FBXW8, LOC100506551	GRCh38.p7	12:116977169	AACCGACTGCAGTTT[C/T]GCCATCATTTAAATC	26259
rs4766820	snp	A/C	0.410737	0.191478	intron-variant	FBXW8, LOC100506551	GRCh38.p7	12:116982975	CCAAGTCATGACATA[A/C]CAAGTGGCTTTGGAC	26259
rs4766821	snp	A/G	0.462363	0.131916	intron-variant	FBXW8, LOC100506551	GRCh38.p7	12:116984117	CTTGGGTAAATCTTC[A/G]AAGGGAAGGAAATAG	26259
rs4766822	snp	A/G	0.482083	0.0929373	intron-variant	FBXW8	GRCh38.p7	12:116993044	acatttccaccagca[A/G]tgtataagcattccc	26259
rs4766823	snp	C/T	0.498734	0.0251279	intron-variant	FBXW8	GRCh38.p7	12:117000358	AGCAGGAAGTAAGCA[C/T]TGATAGCTGAGTAAT	26259
rs4767473	snp	A/G	0.306431	0.243548	intron-variant	FBXW8	GRCh38.p7	12:116927701	TCCACAGACCTTGAC[A/G]GTGATTCCTGTGCCG	26259
rs4767474	snp	A/C	0.4661	0.125701	intron-variant	FBXW8	GRCh38.p7	12:116928533	AGCACGAGGACAGAA[A/C]ATGTTTTAGGTGAAG	26259
rs4767476	snp	A/G	0.391583	0.206044	intron-variant	FBXW8	GRCh38.p7	12:116935813	ACATGTGAATAAGAA[A/G]GAGCCTACGGAGGGC	26259
rs4767477	snp	A/G	0.498158	0.0302955	intron-variant	FBXW8	GRCh38.p7	12:116952344	TTTAGTGACACGACT[A/G]TATAATTCATATGCC	26259
rs4767478	snp	C/T	0.454182	0.144256	intron-variant	FBXW8	GRCh38.p7	12:116952534	AGATTTCTCTAGCAC[C/T]GTAGCCTAGCGTCCA	26259
rs4767479	snp	C/T	0.0130921	0.0798413	intron-variant	FBXW8	GRCh38.p7	12:116952550	GTAGCCTAGCGTCCA[C/T]TCTTCTCGGAACTCC	26259
rs4767480	snp	A/G	0.45645	0.140991	intron-variant	FBXW8	GRCh38.p7	12:116952605	ACAGGGCAACTCATC[A/G]TGTGGCCTTGCTGTT	26259
rs4767482	snp	A/G	0.417359	0.185718	intron-variant	FBXW8	GRCh38.p7	12:116956219	ACCGTTCCTGCCTTT[A/G]CTGGAAGGAGCAGGG	26259
rs4767483	snp	A/C	0.441158	0.161117	intron-variant	FBXW8	GRCh38.p7	12:116966962	TTTGGTAAAATGCTT[A/C]GCAAGTGATTGCCAA	26259
rs4767484	snp	C/G	0.462363	0.131916	intron-variant	FBXW8	GRCh38.p7	12:116968196	ATTACTACATTTTTA[C/G]GGTTCAAAGATCAAA	26259
rs4767485	snp	A/G	0.458084	0.138567	intron-variant	FBXW8	GRCh38.p7	12:116970638	TCAGTTGTTTTGCTT[A/G]TATCTTTTGTTTGTA	26259
rs4767486	snp	A/G	0.498652	0.0259235	intron-variant	FBXW8	GRCh38.p7	12:116971053	TTTTTAACACTAGGA[A/G]TGCTCACATTTTAAA	26259
rs4767487	snp	C/T	0.462472	0.13174	intron-variant	FBXW8	GRCh38.p7	12:116971326	GATTGCTCTGCTGCA[C/T]TTCTGCCTGGGCAAC	26259
rs4767488	snp	C/T	0.465473	0.126772	intron-variant	FBXW8, LOC100506551	GRCh38.p7	12:116984310	TCTAATAAGTCGCCA[C/T]GTGGTACTGATGCTA	26259
rs4767489	snp	G/T	0.466204	0.125522	intron-variant	FBXW8, LOC100506551	GRCh38.p7	12:116984587	AAATGCTTTGAAACT[G/T]TTTAAGCACTGACAT	26259
rs4767490	snp	C/T	0.274929	0.248754	intron-variant	FBXW8	GRCh38.p7	12:116997211	CTCTGGCTTAGATGC[C/T]TTTGAGGACTGGACC	26259
rs4767491	snp	C/T	0.458545	0.137872	intron-variant	FBXW8	GRCh38.p7	12:116997566	GGTGCCTCCTTCACC[C/T]CCGGTCCCCCAGCTT	26259
rs4767492	snp	C/T	0.119978	0.213528	intron-variant	FBXW8	GRCh38.p7	12:116999056	TTAACTTATCAATTA[C/T]TGAGTTGCAGATGAA	26259
rs4767493	snp	A/G	0.459233	0.136827	intron-variant	FBXW8	GRCh38.p7	12:116999067	ATTACTGAGTTGCAG[A/G]TGAATCCTTCTAATG	26259
rs4767494	snp	C/G	0.0711525	0.174681	intron-variant	FBXW8	GRCh38.p7	12:117005965	CCTCCTAACCTTTGG[C/G]TCTCTTTGCCACTGC	26259
rs4998412	snp	A/G	0.496842	0.0396107	intron-variant	FBXW8	GRCh38.p7	12:116947750	TCAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAGA	26259
rs5801209	in-del	-/A			intron-variant	FBXW8	GRCh38.p7	12:117022355	ACTAAAGAAACTATT[-/A]AAAAAAAAAAAAAAA	26259
rs6490100	snp	C/T	0.179105	0.239737	intron-variant	FBXW8	GRCh38.p7	12:116946357	GGCAACCTCACACGG[C/T]TTCTAGCAAAGTCAA	26259
rs6490101	snp	C/T	0.102726	0.202016	intron-variant	FBXW8	GRCh38.p7	12:116964950	TGTAATCCCTCCATA[C/T]GTACACGTGGGCACA	26259
rs6490102	snp	A/T	0.376195	0.215812	intron-variant	FBXW8	GRCh38.p7	12:116996407	GTCTGGGAGAGCCTT[A/T]GGAATCAGAAATGCA	26259
rs6490103	snp	C/T	0.498346	0.0287064	intron-variant	FBXW8	GRCh38.p7	12:117004831	ACACTGGAGGGAGGG[C/T]CCAAACTAGCCCCTG	26259
rs7131746	snp	A/G	0.436408	0.16659	intron-variant	FBXW8, LOC100506551	GRCh38.p7	12:116985459	ATCTCTGGGTCTAAT[A/G]TAAGCACGTACTAAT	26259
rs7133066	snp	G/T	0.378087	0.214695	intron-variant	FBXW8	GRCh38.p7	12:116922812	AGTGTGTGTGTGTGT[G/T]TTTTTTTTCCCTTGA	26259
rs7133090	snp	C/T	0.498774	0.02473	intron-variant	FBXW8	GRCh38.p7	12:116935953	AGAGCTGACTATGTA[C/T]GTGCGAGGTACTGTT	26259
rs7133142	snp	C/T	0.159292	0.232964	intron-variant	FBXW8	GRCh38.p7	12:116913170	aaatctgATGACTGG[C/T]ATGATCAGGCAAGTT	26259
rs7133609	snp	A/T	0.114387	0.210022	intron-variant	FBXW8	GRCh38.p7	12:117001611	CAGTTTTCACTCCGT[A/T]AGATAGATATTATAA	26259
rs7136629	snp	A/G	0.122758	0.215196	intron-variant	FBXW8	GRCh38.p7	12:116949840	CAGCCCATGTGGAAG[A/G]GGGAGAGTCTCCGTG	26259
rs7136880	snp	C/T	0.159622	0.233092	intron-variant	FBXW8	GRCh38.p7	12:116913769	catgttgttcaaggg[C/T]cTGTAGTATTCTGAA	26259
rs7137006	snp	A/G	0.462472	0.13174	intron-variant, nc-transcript-variant	FBXW8, LOC100506551	GRCh38.p7	12:116987235	CAGCTCTTCTGGACC[A/G]TGTTCTGGAGGCCGG	26259
rs7137752	snp	C/T	0.459574	0.136304	intron-variant, nc-transcript-variant	FBXW8, LOC100506551	GRCh38.p7	12:116987169	TGGACCCGCAGCTTG[C/T]GGAGCTGGGCCCGAG	26259
rs7294581	snp	A/G	0.0637235	0.166737	intron-variant	FBXW8	GRCh38.p7	12:116990792	TTCCAACTCAACTAA[A/G]AGCATTAACTGTAAG	26259
rs7297155	snp	C/G	0.461813	0.132798	intron-variant	FBXW8, LOC100506551	GRCh38.p7	12:116982333	aacactaatcgaaaa[C/G]tggcgtggccatgca	26259

Full records

It may take some time, please wait.