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
rs717739	snp	G/T	0	0	intron-variant	FBXO10	GRCh38.p7	9:37543793	CAAGTAGATGACCTA[G/T]AGCAACTTCCAAGTC	26267
rs927930	snp	A/G	0.097727	0.198275	intron-variant	FBXO10	GRCh38.p7	9:37537001	TTTAAACTTATTCAC[A/G]CACGCTTGACGTCAT	26267
rs1055396	snp	A/C			intron-variant	FBXO10	GRCh38.p7	9:37521376	GGGTTGCACAGCGGC[A/C]AGGCAGAGGCGCTCC	26267
rs1128206	snp	C/T	0	0	utr-variant-3-prime, nc-transcript-variant	FBXO10	GRCh38.p7	9:37510971	TGCCGTTACTATTTT[C/T]TAAGAAATGACTTTT	26267
rs1475414	snp	G/T	0.474091	0.11083	intron-variant	FBXO10	GRCh38.p7	9:37526451	TGAGGAATATCATAA[G/T]TAGATCAGTGTTGGG	26267
rs1536551	snp	C/T	0.0599851	0.162463	intron-variant	FBXO10	GRCh38.p7	9:37557358	ACCTCTTTACCCCTT[C/T]GGAGGCCTTGGATGG	26267
rs1571233	snp	C/G	0.132066	0.220435	intron-variant	FBXO10	GRCh38.p7	9:37561212	agaagtgaggtctct[C/G]tgtgttgcccaggct	26267
rs1854159	snp	C/T	0.257454	0.249889	intron-variant	FBXO10	GRCh38.p7	9:37564530	AGGAGGTGGGTTGTA[C/T]CCTGCAAAGCCACAG	26267
rs1854160	snp	C/T	0.499396	0.0173617	intron-variant	FBXO10	GRCh38.p7	9:37564702	GCCCCTTTGGCCAAT[C/T]TCTCCCATTTGGAGT	26267
rs1927153	snp	C/T	0.0948562	0.196037	intron-variant	FBXO10	GRCh38.p7	9:37564228	agtcaagaactgagg[C/T]atagaaacctctact	26267
rs1969936	snp	C/T	0.205723	0.246048	intron-variant	FBXO10	GRCh38.p7	9:37561169	caaaacaaaacaaaa[C/T]CAACttttttttttt	26267
rs1977448	snp	G/T	0.0107246	0.0724382	intron-variant	FBXO10	GRCh38.p7	9:37523386	tttttgtattttttt[G/T]tagagacaggatttc	26267
rs2182745	snp	C/T	0.200492	0.245049	intron-variant	FBXO10	GRCh38.p7	9:37538450	aacgtgctggaacta[C/T]gggcgtgagccacca	26267
rs2182746	snp	A/G	0.093417	0.194889	intron-variant	FBXO10	GRCh38.p7	9:37531196	ATAGCCACCATTAAT[A/G]CATAATGCTTATTAT	26267
rs3739572	snp	A/G	0.295088	0.245901	intron-variant, downstream-variant-500B	FBXO10	GRCh38.p7	9:37515714	TCCCCAGGAGGGAAC[A/G]AGCTTTTTAAGAGTC	26267
rs4077401	snp	C/T	0.208779	0.246578	intron-variant, upstream-variant-2KB	FBXO10	GRCh38.p7	9:37576103	CCGCTCAGTCCTGGC[C/T]GAGGCTGAGCGTCTG	26267
rs4242642	snp	A/G	0.313814	0.241719	intron-variant	FBXO10	GRCh38.p7	9:37539322	GCTAAGGTTCTCCTT[A/G]GAAGTCACTGAAAAC	26267
rs4354400	snp	C/T	0.0930568	0.194599	intron-variant	FBXO10	GRCh38.p7	9:37530813	CCCAGCTAATTTTTA[C/T]AATTTTTTGTAGAGA	26267
rs4457420	snp	A/G	0.450357	0.149522	intron-variant	FBXO10	GRCh38.p7	9:37513689	cttcctcccaggttc[A/G]agtgatcctcctggc	26267
rs4581142	snp	C/T	0.493568	0.0563433	intron-variant	FBXO10	GRCh38.p7	9:37513746	agttgcgtgccatga[C/T]gcccagctaattttt	26267
rs4878154	snp	C/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	FBXO10	GRCh38.p7	9:37515477	ACGTGAAAGGACAGA[C/G]AGGTTTGAGGAAGAT	26267
rs4878155	snp	A/G	0.165853	0.235413	intron-variant, downstream-variant-500B	FBXO10	GRCh38.p7	9:37515535	GCAGAGTGACTAAAG[A/G]ACAGCAGCAGCATCA	26267
rs4878156	snp	A/G	0.16618	0.23553	intron-variant	FBXO10	GRCh38.p7	9:37516854	taatcccagctactt[A/G]ggaggctgaggcagg	26267
rs4878157	snp	A/G	0.499859	0.0083854	intron-variant	FBXO10	GRCh38.p7	9:37517039	acagaatgaaataac[A/G]gcctttgcagcaatt	26267
rs4878158	snp	A/G	0.168135	0.236216	intron-variant	FBXO10	GRCh38.p7	9:37519711	CTCTGACCTGGGAGG[A/G]GACAGAACTCATTTT	26267
rs4878696	snp	C/T	0.124144	0.21601	intron-variant	FBXO10	GRCh38.p7	9:37525384	AAGTCCACAGGGGCA[C/T]AAAAGCATTTCCTAA	26267
rs4878697	snp	C/T	0.496416	0.0421803	intron-variant	FBXO10	GRCh38.p7	9:37549283	TCCCCTGGGCTCCCA[C/T]AGCACCCAGAGAACA	26267
rs4878698	snp	A/T	0.365439	0.221752	intron-variant	FBXO10	GRCh38.p7	9:37551528	tgcttgtgccctggg[A/T]tctgtagcccagcca	26267
rs4878699	snp	C/T	0.234401	0.249513	intron-variant	FBXO10	GRCh38.p7	9:37563808	tgcaggagatcattt[C/T]ggaattttaaggttt	26267
rs4878700	snp	G/T	0.133435	0.221162	intron-variant	FBXO10	GRCh38.p7	9:37564549	gcaaagccacagggg[G/T]ggagctgcccaaggc	26267
rs5897689	in-del	-/AC	0.00517822	0.0506191	intron-variant	FBXO10	GRCh38.p7	9:37523222	CCCGGCACCTACTAT[-/AC]ACCCAATGGCCTTGA	26267
rs6476636	snp	A/G	0.496616	0.0409947	intron-variant	FBXO10	GRCh38.p7	9:37514783	AGGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC	26267
rs6476637	snp	C/T	0.197703	0.244469	intron-variant	FBXO10	GRCh38.p7	9:37534478	AAAAAGAAAGACAGG[C/T]GCCTCCAAGGAGACG	26267
rs6476638	snp	A/G	0.242201	0.249878	intron-variant	FBXO10	GRCh38.p7	9:37554888	gctattatggataat[A/G]ctgctgtgaatattc	26267
rs6476639	snp	A/T	0.24449	0.249939	intron-variant	FBXO10	GRCh38.p7	9:37558310	GCTAATGGTTGGTAT[A/T]CCAAGTCTCAGGAGG	26267
rs6476640	snp	C/G	0.498632	0.0261223	intron-variant	FBXO10	GRCh38.p7	9:37558488	GCACTGACAATTTCT[C/G]TCCCAGATGGGTTTC	26267
rs6476643	snp	G/T	0.279991	0.248195	upstream-variant-2KB, utr-variant-5-prime	FBXO10	GRCh38.p7	9:37576451	CCCGACCACCGCGCA[G/T]AAAAGCTGTATCTGC	26267
rs7018980	snp	G/T	0.499017	0.0221427	intron-variant	FBXO10	GRCh38.p7	9:37570224	GCTGAGGAGGCAGGA[G/T]AATCCCTTGAACCCG	26267
rs7020950	snp	A/G	0.128288	0.218372	intron-variant	FBXO10	GRCh38.p7	9:37514578	cggtggctcacacct[A/G]taatctcaatacttt	26267
rs7023107	snp	C/T	0.499846	0.00878459	intron-variant	FBXO10	GRCh38.p7	9:37550161	gttttcTTTTTTTGT[C/T]GTCTCAGGTtttttt	26267
rs7024249	snp	A/G	0.00472811	0.0483911	intron-variant	FBXO10	GRCh38.p7	9:37520727	tttctgcctctctaa[A/G]aaggaaaactcactg	26267
rs7027678	snp	C/T	0.356811	0.226034	intron-variant	FBXO10	GRCh38.p7	9:37528459	TTTGCTCATGCTGTT[C/T]CATTACTAGGAACAT	26267
rs7027892	snp	A/G	0.356811	0.226034	intron-variant	FBXO10	GRCh38.p7	9:37528407	CAAGCCACCGTCAAC[A/G]GTTTGCTAACCCCTG	26267
rs7028288	snp	C/G	0	0	missense, downstream-variant-500B, nc-transcript-variant	FBXO10	GRCh38.p7	9:37521654	CTTCTCCAGCTCTGT[C/G]TCCCAGAGGATGGCG	26267
rs7031794	snp	C/T	0.499053	0.0217445	intron-variant	FBXO10	GRCh38.p7	9:37552095	acctcatcagactag[C/T]cttcactgttgcaac	26267
rs7035751	snp	C/T	0.0154538	0.0865337	intron-variant	FBXO10	GRCh38.p7	9:37535832	CTGGGCCTTCACACA[C/T]ACCTCCTTTGCCTCG	26267
rs7037295	snp	C/T	0.0799831	0.183287	intron-variant	FBXO10	GRCh38.p7	9:37523848	cttgaacctgggagg[C/T]ggaggttgcagtgag	26267
rs7037435	snp	C/T	0.0599851	0.162463	intron-variant	FBXO10	GRCh38.p7	9:37524001	AAGCCTGTGAGAAGG[C/T]GCTAGCCTCACCTGC	26267
rs7039920	snp	C/T	0.499203	0.0199521	intron-variant	FBXO10	GRCh38.p7	9:37557723	TACTATGTCCCCACA[C/T]GGTTTACATTTATCT	26267
rs7041752	snp	A/G	0.497855	0.0326773	intron-variant	FBXO10	GRCh38.p7	9:37524778	GGGCGGAGGTTTCCA[A/G]AGCAGGCAGAGGTCC	26267
rs7043428	snp	A/C	0.0345262	0.126772	intron-variant	FBXO10	GRCh38.p7	9:37567218	tgtgatcttggctca[A/C]tacagcctcaatctc	26267
rs7044153	snp	A/G	0.472309	0.114363	synonymous-codon, nc-transcript-variant	FBXO10	GRCh38.p7	9:37537560	CTTTGGGGAGCTAGA[A/G]GCTGGGCTGGTAGGG	26267
rs7044233	snp	C/T	0.498611	0.0263212	intron-variant	FBXO10	GRCh38.p7	9:37560610	ATGAAACAACAGGGA[C/T]TTCTTAGAACAAGGT	26267
rs7044561	snp	G/T	0.00843964	0.0644096	missense, nc-transcript-variant	FBXO10	GRCh38.p7	9:37537895	CATGGACCTGGATGT[G/T]CCCGTTCTCAAAGTT	26267
rs7048273	snp	A/G	0.494976	0.0498674	intron-variant	FBXO10	GRCh38.p7	9:37538388	AGGTATACTGCCATT[A/G]CCAGGAAGCATTGAA	26267
rs7048462	snp	A/G	0.161267	0.233723	intron-variant	FBXO10	GRCh38.p7	9:37538751	cgggggttgactgca[A/G]gtgttatcttggaca	26267
rs7341712	snp	C/T	0.0314385	0.121371	intron-variant	FBXO10	GRCh38.p7	9:37553973	agatcctttgcttgg[C/T]ttaccccaatggtaa	26267
rs7341863	snp	A/G	0.0539704	0.155153	intron-variant	FBXO10	GRCh38.p7	9:37554091	tgtactcacttgtgt[A/G]tgtgtattaagttct	26267
rs7850177	snp	C/T	0.498611	0.0263212	intron-variant	FBXO10	GRCh38.p7	9:37562519	GGAATTAAATGTTTT[C/T]CTTCATTTATTGTCT	26267
rs7851820	snp	A/G	0	0	intron-variant	FBXO10	GRCh38.p7	9:37550762	gcgattataggcacc[A/G]cacccagccTATTTC	26267
rs7851984	snp	A/G	0	0	intron-variant	FBXO10	GRCh38.p7	9:37520548	ttttttttttttgta[A/G]aaaccaagtcttgtt	26267
rs7852508	snp	C/T	0.046775	0.145601	intron-variant	FBXO10	GRCh38.p7	9:37515117	GACAGGTGACATTGG[C/T]GGTGCAGGAGTGATA	26267
rs7855367	snp	C/T	0.167158	0.235875	intron-variant	FBXO10	GRCh38.p7	9:37519155	ACCTCGTGATCCACC[C/T]GCCTCGGCCTCCCAA	26267
rs7855746	snp	C/T	0.0437281	0.141251	intron-variant	FBXO10	GRCh38.p7	9:37551452	gaggcacacaagcct[C/T]cacagctcttgtact	26267
rs7865784	snp	A/G	0.161267	0.233723	intron-variant	FBXO10	GRCh38.p7	9:37518987	CCATCTCGGCTCACT[A/G]CAAGCTCCGCCTCCC	26267
rs7865834	snp	A/G	0.340559	0.233022	intron-variant	FBXO10	GRCh38.p7	9:37518764	CGCCATCCTACTGCC[A/G]CTTACACCTCCCTGA	26267
rs7865842	snp	A/G	0.0733688	0.176922	intron-variant	FBXO10	GRCh38.p7	9:37518778	CGCTTACACCTCCCT[A/G]ACGGGGTGCTCACTG	26267
rs7866748	snp	A/G	0.47743	0.103805	intron-variant	FBXO10	GRCh38.p7	9:37566459	TGAGACTCTGTCTCG[A/G]AAAAAAAAAAAAAAA	26267
rs7868084	snp	C/T			intron-variant	FBXO10	GRCh38.p7	9:37545314	cctgagtagctggga[C/T]tacaggcgcacaccg	26267
rs7868924	snp	A/G	0.167484	0.23599	intron-variant	FBXO10	GRCh38.p7	9:37519185	AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCAT	26267
rs7873615	snp	C/T	0.0314385	0.121371	intron-variant	FBXO10	GRCh38.p7	9:37543275	AGGTAAGGTTCCCAG[C/T]AGATGTATATGTAGA	26267
rs9775795	snp	C/G			intron-variant, upstream-variant-2KB	FBXO10	GRCh38.p7	9:37533456	gaggctaaggcagga[C/G]aatctcttgaatcag	26267
rs9969717	snp	C/T	0.215747	0.247642	intron-variant, upstream-variant-2KB	FBXO10	GRCh38.p7	9:37532401	CGCCTCCCAGGCTCA[C/T]GTGATCCTCCCACCT	26267
rs10114827	snp	C/T	0.12932	0.218944	intron-variant, downstream-variant-500B	FBXO10	GRCh38.p7	9:37515442	acactgagtggatgg[C/T]gatgtcgctgaaatg	26267
rs10116329	snp	C/T	0.0912534	0.193131	intron-variant	FBXO10	GRCh38.p7	9:37561993	agtctaacatctcaa[C/T]ggcatgacatggaaa	26267
rs10116373	snp	C/T	0.180064	0.240019	intron-variant	FBXO10	GRCh38.p7	9:37526056	CCTCCAGAAAGGATC[C/T]GTGGCCACCTGGAGA	26267
rs10117312	snp	A/G	0.498774	0.02473	intron-variant	FBXO10	GRCh38.p7	9:37557384	GATGGCTCTGCCTCT[A/G]ATTATTCTTTTCTTA	26267
rs10117614	snp	A/G	0.12932	0.218944	intron-variant, downstream-variant-500B	FBXO10	GRCh38.p7	9:37515459	atgtcgctgaaatgg[A/G]gaacgtgaaaggaca	26267
rs10118103	snp	A/G	0.499424	0.0169631	intron-variant	FBXO10	GRCh38.p7	9:37563939	TCACCAAGATAATGT[A/G]GAAAATGTCTGCAGG	26267
rs10118277	snp	A/C	0.437683	0.165152	intron-variant	FBXO10	GRCh38.p7	9:37558783	AATTAAGCACTACTG[A/C]AGCTTATAGAGATCA	26267
rs10119802	snp	C/G	0.0926964	0.194308	intron-variant	FBXO10	GRCh38.p7	9:37565941	CTTAGGACATGTTGG[C/G]AGGTTCAGTCTGGCT	26267
rs10121333	snp	C/T	0.499477	0.0161657	intron-variant	FBXO10	GRCh38.p7	9:37563938	ATCACCAAGATAATG[C/T]GGAAAATGTCTGCAG	26267
rs10121547	snp	A/G	0.0916144	0.193427	intron-variant	FBXO10	GRCh38.p7	9:37567777	tcaggtgatctgtcc[A/G]cctcggcctcccaaa	26267
rs10122666	snp	A/G	0.499017	0.0221427	intron-variant	FBXO10	GRCh38.p7	9:37556841	TGAGCCACCGCATCC[A/G]GCCTGTTCTGTATTC	26267
rs10122829	snp	C/T	0.0711525	0.174681	intron-variant	FBXO10	GRCh38.p7	9:37540922	CTCCAGTTGGTCCAG[C/T]TGGAAAGGGAAGAGG	26267
rs10123823	snp	G/T	0.12932	0.218944	intron-variant, downstream-variant-500B	FBXO10	GRCh38.p7	9:37515495	gtttgaggaagaTGG[G/T]TGGCGGCAATTGTGA	26267
rs10124667	snp	C/T	0.125182	0.216612	intron-variant	FBXO10	GRCh38.p7	9:37516503	AAAGTCACTAACCCA[C/T]GAAGCTGCAGAACTG	26267
rs10124731	snp	C/T	0.125182	0.216612	intron-variant	FBXO10	GRCh38.p7	9:37516745	ctgaggcaggtggat[C/T]gatcacctgaggtca	26267
rs10124736	snp	C/T	0.125182	0.216612	intron-variant	FBXO10	GRCh38.p7	9:37516773	tcaggagtttgagac[C/T]agcctgaccaacatg	26267
rs10125441	snp	C/T	0.228842	0.249103	intron-variant	FBXO10	GRCh38.p7	9:37547259	ATACAAAGGGATAAA[C/T]CATTGATGTAGACAA	26267
rs10217806	snp	C/T	0.178465	0.239547	intron-variant	FBXO10	GRCh38.p7	9:37544182	gctgagacaggagaa[C/T]tgcttgaacctggga	26267
rs10570076	in-del	-/GA	0.19646	0.2442	intron-variant	FBXO10	GRCh38.p7	9:37534688	AAACTGGGGGCAGAT[-/GA]GAGACTGGAGACAGC	26267
rs10696134	in-del	-/T			intron-variant	FBXO10	GRCh38.p7	9:37561194	TTTTTTTTTTTTTTT[-/T]AAAGAAGTGAGGTCT	26267
rs10701235	in-del	-/AT/ATTTT			intron-variant	FBXO10	GRCh38.p7	9:37560645	TTTTTATTTTATTTT[-/AT/ATTTT]TTTTAATGCATTCAA	26267
rs10733488	snp	C/G	0.00159617	0.0282053	intron-variant	FBXO10	GRCh38.p7	9:37517684	GACTGCAGTGCAAGG[C/G]GGGCAGGAGGTATGC	26267
rs10758436	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO10	GRCh38.p7	9:37517494	GGGAGACAAATAGGT[A/G]AAGGAAGAGATACCA	26267
rs10758437	snp	C/T	0.496681	0.0405994	intron-variant	FBXO10	GRCh38.p7	9:37520443	gggctcaagcgatcc[C/T]cccgcctcctgagta	26267
rs10758438	snp	C/T	0.498832	0.0241331	intron-variant	FBXO10	GRCh38.p7	9:37550639	cctgcaccacacacc[C/T]ggctaatttttgtag	26267
rs10758439	snp	A/G	0.498632	0.0261223	intron-variant	FBXO10	GRCh38.p7	9:37559728	TTCATTGCCTATGCA[A/G]GATCATCCACAGCTT	26267
rs10758440	snp	A/C	0.272511	0.248984	intron-variant	FBXO10	GRCh38.p7	9:37573333	AACCCAGCCTGGTGA[A/C]AAGCTCAACAAAAGC	26267

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