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
rs960608	snp	C/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18756650	CACATATTTCTGTAA[C/T]CCAGCCCAGCAAAGT	10517
rs1024657	snp	C/T	0.0104662	0.071579	missense, upstream-variant-2KB, nc-transcript-variant	FBXW10, TVP23B	GRCh38.p7	17:18779192	TTGATCCAGGAAAAG[C/T]CAGCAAAGCTGCATG	10517
rs1026259	snp	A/G	0.159882	0.233193	missense, intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18778600	CTCCTGACTGTTAGC[A/G]CCCTGCAGCACGCCC	10517
rs1318979	snp	A/G	0.029198	0.117245	missense, upstream-variant-2KB, nc-transcript-variant	FBXW10, TVP23B	GRCh38.p7	17:18779086	CCTTTTAGAGTGAAC[A/G]CTGAGTTCGTGCTGT	10517
rs2014354	snp	A/G	0.0121512	0.0769931	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXW10, TVP23B	GRCh38.p7	17:18779319	CCTTGGGAAATTACA[A/G]TGTTTTACAATAAAC	10517
rs2014360	snp	A/G	0.4488	0.151587	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779419	ATGTGGGAACTCCCA[A/G]TTATCTTCCCCTGAG	10517
rs2123375	snp	A/G	0.424659	0.17887			GRCh38.p7	17:18741366	AGCCAGCAGGGACTC[A/G]GGAAAGCACACAGGT	10517
rs2323786	snp	G/T	0.0252325	0.109451			GRCh38.p7	17:18741087	ATGTGGTATTACACT[G/T]GTTGGAAGTTGAATT	10517
rs2323787	snp	C/T	0.0252325	0.109451			GRCh38.p7	17:18741057	TTTAAAAAGCTTggc[C/T]gggcgcggtggttca	10517
rs3032059	snp	A/T	0.41275	0.189769	intron-variant	FBXW10	GRCh38.p7	17:18761962	aaaaaaaagaaaaag[A/T]aaaagaaaaaccaat	10517
rs3826384	snp	A/G	0	0	intron-variant	FBXW10	GRCh38.p7	17:18756277	TCATGTGCAAGTTTA[A/G]GGCTGGAGCTTGAGG	10517
rs4244595	snp	A/G	0.487113	0.0792303	intron-variant	FBXW10	GRCh38.p7	17:18774016	ATGTAAGACTAGATC[A/G]GCTACTATTGATTAC	10517
rs4315390	snp	A/G	0.492966	0.0588865	intron-variant	FBXW10	GRCh38.p7	17:18745734	TTCTGTATTTCTAAC[A/G]AGTTTCCAGCTAGTG	10517
rs4349204	snp	C/T	0.499551	0.0149693	intron-variant	FBXW10	GRCh38.p7	17:18745604	attttttagtagaga[C/T]ggggtttcaccatgc	10517
rs4520890	snp	A/G	0	0	intron-variant	FBXW10	GRCh38.p7	17:18759652	gagtctcactgtgtc[A/G]cccaggctggagagc	10517
rs4611519	snp	A/G	0.482534	0.0918038	intron-variant	FBXW10	GRCh38.p7	17:18766965	GAGCAACTGAGTATG[A/G]CCTTCAAGAAGGACA	10517
rs4630608	snp	C/T	0.495615	0.0466161	intron-variant, downstream-variant-500B	FBXW10	GRCh38.p7	17:18775235	AGGGAACAAGTGGCA[C/T]GGATGGTGGGCAGGA	10517
rs4924769	snp	C/T	0.499987	0.00259581	intron-variant	FBXW10	GRCh38.p7	17:18749295	TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG	10517
rs4924770	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18757189	ATCACCATACTATCT[A/G]TATTTCTTTTTTCAG	10517
rs4924914	snp	C/T	0.490453	0.0684267			GRCh38.p7	17:18740329	CTCAGATTTCAGCAC[C/T]GACTCCCTCCCTCTG	10517
rs4924915	snp	A/G	0.5	0.000399361	intron-variant	FBXW10	GRCh38.p7	17:18753346	tgcagaaagatgtat[A/G]gggacagacacacaa	10517
rs4924917	snp	C/T	0	0	intron-variant	FBXW10	GRCh38.p7	17:18757188	TATCACCATACTATC[C/T]GTATTTCTTTTTTCA	10517
rs4924918	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18757296	TCAAGCGATTCTCCT[C/G]CCTCAGTCTCCTAAG	10517
rs4924920	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18757340	AGGCACATGCCACCA[C/T]GCCTGGCTAATTTCT	10517
rs4924921	snp	C/T	0.375	0.216506	intron-variant	FBXW10	GRCh38.p7	17:18757440	GACTATACATCCCTG[C/T]TTATTGGAACAATCC	10517
rs4924923	snp	C/T	0.132653	0.220748	intron-variant	FBXW10	GRCh38.p7	17:18766028	CACTGGGCCCGGCAT[C/T]AACTTCTTCATTTTA	10517
rs4924924	snp	C/G	0.478354	0.101757	intron-variant	FBXW10	GRCh38.p7	17:18774461	AGATGGAAGGGATAA[C/G]TTCCAGCGTTTGGTT	10517
rs4924925	snp	G/T	0.475702	0.107512	intron-variant	FBXW10	GRCh38.p7	17:18777256	tttagtacagacggg[G/T]tttctccatgttggt	10517
rs5819658	in-del	-/A			intron-variant	FBXW10	GRCh38.p7	17:18767444	AGATCATGCGTCTCA[-/A]AAAAAAAAAAAAAAA	10517
rs6502669	snp	A/G	0.459687	0.136129	intron-variant	FBXW10	GRCh38.p7	17:18759758	gctgagactacaggg[A/G]cccgccaccacacca	10517
rs7209610	snp	A/G	0.00107037	0.0231093	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18751045	CCGAAGTGGAAGCTG[A/G]GAACGAAGGTGGGTT	10517
rs7212014	snp	A/C			intron-variant	FBXW10	GRCh38.p7	17:18747724	ATAAACAACTCGAGA[A/C]ATTTTACAATGGGGG	10517
rs7215492	snp	C/T	0.45762	0.139261	intron-variant	FBXW10	GRCh38.p7	17:18752174	acacaaaggaggaga[C/T]gggtcgtgtgggcag	10517
rs7216988	snp	A/G	0.0279526	0.114869	intron-variant	FBXW10	GRCh38.p7	17:18766446	AGCACTTGGGCCTCA[A/G]GGCTAAGTTCCAGGG	10517
rs7217866	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18747486	acttgaacccaggag[A/G]cggaggttgcagtga	10517
rs7217902	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18747542	ccctgggcaataaga[C/G]caaaactcagtctca	10517
rs7223011	snp	C/T	0.0091458	0.0670019	intron-variant	FBXW10	GRCh38.p7	17:18766880	AAGTGGGCAGTGGGC[C/T]ACCTTGGCGGAAAGG	10517
rs7223948	snp	A/G	0.473909	0.111197	intron-variant	FBXW10	GRCh38.p7	17:18757485	GTCCTAGTGTCATTA[A/G]TAATAGTGTCCCCAG	10517
rs7225387	snp	A/G	0.131723	0.220251	intron-variant	FBXW10	GRCh38.p7	17:18764402	agacagggtttcacc[A/G]tgttggccagtatgg	10517
rs8069260	snp	A/G	0.100588	0.200439	intron-variant	FBXW10	GRCh38.p7	17:18774049	tctaatggttgctta[A/G]cattctgctgtaaag	10517
rs8070267	snp	C/T	0.118933	0.212888	intron-variant	FBXW10	GRCh38.p7	17:18774075	taaagaggtgacaat[C/T]acaaggggAGTTGCT	10517
rs8073523	snp	C/T	0.310632	0.242536	intron-variant	FBXW10	GRCh38.p7	17:18771432	AGGGAGGCAGTGCTG[C/T]GGGGGCACAGGAAGG	10517
rs8076246	snp	A/G	0.317692	0.240661	intron-variant, synonymous-codon	FBXW10	GRCh38.p7	17:18771630	GGTCTATGAAGGAGA[A/G]GAGGCCTCCCCATTA	10517
rs8076572	snp	C/G	0	0	intron-variant	FBXW10	GRCh38.p7	17:18763281	cctgcctcagcctcc[C/G]gagtagctgggacta	10517
rs8077093	snp	A/G	0.133777	0.221342	intron-variant	FBXW10	GRCh38.p7	17:18752662	agcttgcagtgagcc[A/G]agattgcgccactgc	10517
rs9674521	snp	C/T	0.00557542	0.0525036	intron-variant	FBXW10	GRCh38.p7	17:18777381	AAGACAGGTTTTATT[C/T]TGGGCAACATTCAAG	10517
rs9674947	snp	C/T	0.482384	0.0921818	intron-variant	FBXW10	GRCh38.p7	17:18769834	AGTTATGGCCAGTGC[C/T]GCTCAATCACACACA	10517
rs9783820	snp	A/C	0.475789	0.107327	intron-variant	FBXW10	GRCh38.p7	17:18757008	AATTCTAGGTATGAC[A/C]AACGGAATAAGGGCA	10517
rs9891495	snp	C/G			intron-variant	FBXW10	GRCh38.p7	17:18752903	TTCAAGTCTGTTGCT[C/G]TTTTAAGTATAACAC	10517
rs9892842	snp	G/T	0.00199481	0.0315187	intron-variant	FBXW10	GRCh38.p7	17:18753318	aaagcagactcgggg[G/T]tatgcctgcagctgc	10517
rs9892969	snp	C/T			intron-variant	FBXW10	GRCh38.p7	17:18752880	TTGAACGTGGACCTG[C/T]TTTTGTTTTCAAGTC	10517
rs9893944	snp	C/T	0.379746	0.213696			GRCh38.p7	17:18740728	GTATATATGTGCATG[C/T]GCTGGTTTCTCATGA	10517
rs9894485	snp	A/G	0.0376037	0.131863			GRCh38.p7	17:18741026	tcggcctcccaaagt[A/G]ctgggattacaagcg	10517
rs9895749	snp	A/G	0.460046	0.135575	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18749757	CTCCGGTGTATATCC[A/G]AAATGAATAGGCTGT	10517
rs9895898	snp	C/T	0.387263	0.208947			GRCh38.p7	17:18740829	GCAGTGGTGCTATCT[C/T]GGCTCACTGCAAGCT	10517
rs9897266	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18778050	ggtcaggagatcgag[A/G]ccatcctggctaaca	10517
rs9898589	snp	C/T	0.316726	0.240931	intron-variant	FBXW10	GRCh38.p7	17:18769637	AAAAAATTAGCCAGG[C/T]GTGGTGGCGCATCAC	10517
rs9898823	snp	A/T	0.499816	0.0095829	intron-variant	FBXW10	GRCh38.p7	17:18750519	ATAAGGCTGCAAAGT[A/T]TTTTTTTAAGTTAAA	10517
rs9899562	snp	A/G	0.0263992	0.111815	intron-variant	FBXW10	GRCh38.p7	17:18757596	aggttacagggagtt[A/G]ttattgcgcccctgt	10517
rs9903004	snp	A/G	0.0023933	0.0345097	intron-variant	FBXW10	GRCh38.p7	17:18750784	CCAGAGGAACTGGCC[A/G]GAAGTGGGCCTGCCT	10517
rs9906011	snp	C/G	0.380529	0.213219	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779680	TTTCTGGTATTTTTG[C/G]ACAGAAGCCTGATAA	10517
rs9906823	snp	A/C	0.153997	0.230832	intron-variant	FBXW10	GRCh38.p7	17:18773984	ATTCAGTTTTCCATA[A/C]AAAGGCTAACATACA	10517
rs9907023	snp	A/G	0.43102	0.172429	intron-variant	FBXW10	GRCh38.p7	17:18754740	AGAGGAAGCAAAGGA[A/G]GGAGGGAAGGAGGGA	10517
rs9907681	snp	A/T	0.356811	0.226034	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779662	AGGGTCATGCATTGG[A/T]GTTTTCTGGTATTTT	10517
rs9908564	snp	C/T	0.489024	0.0732638			GRCh38.p7	17:18739168	CGAGAGCAGCCTGAC[C/T]AACATGGTGAAACTC	10517
rs9908821	snp	A/G	0.481396	0.0946345	intron-variant	FBXW10	GRCh38.p7	17:18776091	taggaggtggagatg[A/G]gcggattgcctgagg	10517
rs9909417	snp	A/G	0.467439	0.123371	intron-variant	FBXW10	GRCh38.p7	17:18776129	gtcgagaccagtctg[A/G]ccaacatggtgaaac	10517
rs9910784	snp	A/G	0.222928	0.24853	intron-variant	FBXW10	GRCh38.p7	17:18762558	caatctcctgacctc[A/G]tgatctgcccacctc	10517
rs9910881	snp	A/G	0.292008	0.246445	intron-variant	FBXW10	GRCh38.p7	17:18762350	ttgagatggagtctc[A/G]ctctgttgccaggct	10517
rs9911451	snp	A/T	0.473081	0.112848	intron-variant, upstream-variant-2KB	FBXW10, TVP23B	GRCh38.p7	17:18779697	CAGAAGCCTGATAAA[A/T]CCCATTAAGAATTTA	10517
rs9911990	snp	C/G	0	0	intron-variant	FBXW10	GRCh38.p7	17:18752187	gacgggtcgtgtggg[C/G]agtagcggacggtgt	10517
rs9912804	snp	A/G			intron-variant	FBXW10	GRCh38.p7	17:18752645	gtgaacccgggaggc[A/G]gagcttgcagtgagc	10517
rs9914084	snp	A/G	0.0267878	0.112589	intron-variant	FBXW10	GRCh38.p7	17:18758896	TACGTggccaggcgc[A/G]gtggctcacgcctgt	10517
rs9914942	snp	A/G	0.0279526	0.114869	intron-variant	FBXW10	GRCh38.p7	17:18767692	GGATCACAGTGAAAA[A/G]TGGCTGGCTTGGCCT	10517
rs10153280	snp	C/T	0.436976	0.165952	intron-variant	FBXW10	GRCh38.p7	17:18766504	GCTCCCTCAACCACC[C/T]GTATTCAGGGCGCTC	10517
rs10580273	in-del	-/AA	0.412416	0.190055	intron-variant	FBXW10	GRCh38.p7	17:18749375	AACCCCGCCTCTACT[-/AA]AAAAAAAAAAAATAC	10517
rs10659921	in-del	-/TTA/TTATT			intron-variant	FBXW10	GRCh38.p7	17:18758640	TAGAATACCTTCAGC[-/TTA/TTATT]TTTTTTTTGGCAAGG	10517
rs10775382	snp	A/C	0.314057	0.241654	intron-variant	FBXW10	GRCh38.p7	17:18768420	GTACCTACCGAGTGA[A/C]TGGCAGTCACAGATT	10517
rs11078420	snp	C/G	0.49655	0.04139	intron-variant	FBXW10	GRCh38.p7	17:18761065	AACCTGCCACTTCCT[C/G]CATTGATTTGAGGTG	10517
rs11331150	in-del	-/T			intron-variant	FBXW10	GRCh38.p7	17:18751240	TTTTTTTTTTTTTTT[-/T]AATGAGATGGAGTCT	10517
rs11336827	in-del	-/A	0.499853	0.008585	intron-variant	FBXW10	GRCh38.p7	17:18749547	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAGATTC	10517
rs11372212	in-del	-/T	0.444931	0.15653	intron-variant	FBXW10	GRCh38.p7	17:18758827	GGGAACGTGGTTTTT[-/T]ATGGGTTTGAGACAG	10517
rs11489009	snp	A/G	0.48178	0.0936921	intron-variant	FBXW10	GRCh38.p7	17:18771339	AAGAAACCTGTGCAG[A/G]GTATTTTCATTTCTT	10517
rs11510298	snp	C/G	0.469642	0.119404	upstream-variant-2KB	FBXW10	GRCh38.p7	17:18743783	TCATTGGGATAGCCA[C/G]TTTGTAACTGAACAG	10517
rs11544711	snp	A/T	0.4889	0.0736681	missense, nc-transcript-variant	FBXW10	GRCh38.p7	17:18744312	AGGGAACCGATTCCA[A/T]CCCTCTATGCCGGAA	10517
rs11651007	snp	C/T	0.484491	0.0866827	intron-variant	FBXW10	GRCh38.p7	17:18768874	ACTGTTAACCTCTTC[C/T]ACTCTCCCTTGTTTT	10517
rs11654164	snp	A/C	0.133777	0.221342			GRCh38.p7	17:18740500	ATGTGCCTAGTTTTT[A/C]ATCTCTATTTCTGGC	10517
rs11655952	snp	A/G	0.132066	0.220435	intron-variant	FBXW10	GRCh38.p7	17:18756959	ATGCTTAGTGTGGTG[A/G]TAACTGCTCTTTAGA	10517
rs11657036	snp	A/G	0.444444	0.157135	intron-variant	FBXW10	GRCh38.p7	17:18770343	TAGTTTCACTCTGTC[A/G]CACAGGCTGGAGTGC	10517
rs11657414	snp	C/G	0.416382	0.186593	intron-variant	FBXW10	GRCh38.p7	17:18765228	TGAACAACAATGGCT[C/G]CCATTTACTGAGTAC	10517
rs11657709	snp	C/T	0.131038	0.219882	intron-variant	FBXW10	GRCh38.p7	17:18755388	ggtgaaaccctgtct[C/T]tactaaaaatacaaa	10517
rs11657859	snp	G/T	0.497613	0.0344622	intron-variant	FBXW10	GRCh38.p7	17:18776035	AGAAAAAAAAAAAAA[G/T]TGGCCGGGCGCGGTG	10517
rs11867536	snp	C/T	0.109814	0.206997	intron-variant	FBXW10	GRCh38.p7	17:18759761	gagactacaggggcc[C/T]gccaccacaccaggc	10517
rs11870736	snp	C/T	0.130008	0.219321	intron-variant	FBXW10	GRCh38.p7	17:18766148	CAGTAAACCCACCCC[C/T]AGCTGTGACCATTTC	10517
rs12150401	snp	A/G	0.130351	0.219509	intron-variant	FBXW10	GRCh38.p7	17:18746651	GACTGGAGATCAACC[A/G]ACTTAATATCCTTAA	10517
rs12150592	snp	A/G	0.16618	0.23553	intron-variant	FBXW10	GRCh38.p7	17:18776520	GAGGGCTGCGCTAAC[A/G]ATGGGCATccttgta	10517
rs12452278	snp	C/T	0.38821	0.208322	intron-variant	FBXW10	GRCh38.p7	17:18769645	AGCCAGGTGTGGTGG[C/T]GCATCACTGTAATCC	10517
rs12452607	snp	A/T	0.00914312	0.0669923	intron-variant	FBXW10	GRCh38.p7	17:18765908	atttttttttttttt[A/T]agtagagacggggtt	10517
rs12602546	snp	A/G	0.464947	0.127663			GRCh38.p7	17:18741051	CAAGCGTGAACCACC[A/G]CGCCCAGCCAAGCTT	10517
rs12603304	snp	C/T	0.486	0.0824865	intron-variant	FBXW10	GRCh38.p7	17:18757963	ACTGTGTTCCTCTGA[C/T]GTTTTCCAAGAAAAA	10517

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