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
rs11801	snp	A/G	0.450483	0.149354	intron-variant	USP7	GRCh38.p7	16:8896382	GTGAGACCCTAATCT[A/G]TTACCTAATAAGAGT	7874
rs30761	snp	A/T	0.0256215	0.110247	intron-variant	USP7	GRCh38.p7	16:8921395	AAATTCCCATTTATG[A/T]TTTCATTGCTCTCTC	7874
rs30762	snp	A/T	0.0980852	0.198549	intron-variant	USP7	GRCh38.p7	16:8922359	TGGGTGTGGTGGCAC[A/T]CGCCTATAGTCCCAG	7874
rs30763	snp	C/T	0.421051	0.182323	intron-variant	USP7	GRCh38.p7	16:8922767	ACATTTCATAATATA[C/T]ATGAATGTTTAAATG	7874
rs30764	snp	A/G	0.409212	0.192748	intron-variant	USP7	GRCh38.p7	16:8954495	TAACAGGGTAATCCT[A/G]AAATCTCACAAGCTG	7874
rs39863	snp	A/T	0.0926964	0.194308	intron-variant	USP7	GRCh38.p7	16:8921902	TTAAGGTTTGCGATT[A/T]AAGTGGGGCCTTATC	7874
rs39864	snp	G/T	0.137867	0.223442	intron-variant	USP7	GRCh38.p7	16:8952115	AAAAAAATGGCCAGG[G/T]GTGGTGTGCCTGTAG	7874
rs42554	snp	C/G	0.0295553	0.11824	intron-variant	USP7	GRCh38.p7	16:8921071	ATCTGACTCTAAAAT[C/G]AATAAAGGACTTGAA	7874
rs166231	snp	C/T	0.449599	0.150533	intron-variant	USP7	GRCh38.p7	16:8939733	GAAGGAAAACACATA[C/T]ACTATTCACATTACG	7874
rs166232	snp	C/T	0.445987	0.155207	intron-variant	USP7	GRCh38.p7	16:8941527	GACATGTCCAGTAAC[C/T]TGTCCTAAGCCAAAA	7874
rs173863	snp	A/G	0.0998734	0.199905	intron-variant	USP7	GRCh38.p7	16:8948652	ggaatattattctgc[A/G]agaaaagggaacgac	7874
rs173864	snp	G/T	0.0232847	0.105357	downstream-variant-500B, intron-variant	USP7, LOC101929989	GRCh38.p7	16:8891662	TGCAACGTGGGTGCC[G/T]TGACAGGGCGAGAAG	7874
rs183725	snp	A/G	0.341685	0.232581	intron-variant	USP7	GRCh38.p7	16:8954178	TCTGCCTCCAGTGGC[A/G]CCGCAGGGGGCACGT	7874
rs187614	snp	C/T	0.432357	0.171014	intron-variant	USP7	GRCh38.p7	16:8939020	atacccttttcctag[C/T]ttccccttacagcac	7874
rs254943	snp	A/G	0.0322114	0.122752	intron-variant	USP7	GRCh38.p7	16:8940566	TGGCCCCTGCATCAG[A/G]AAGGGAGAGGTGGGA	7874
rs254944	snp	C/T	0.030278	0.119257	intron-variant, upstream-variant-2KB	USP7	GRCh38.p7	16:8950009	CTGTCCCACCAACCA[C/T]AGAAGCCAGGAGCTG	7874
rs876884	snp	C/T	0.357451	0.225731	intron-variant	USP7	GRCh38.p7	16:8902931	ATTCTAATTCTTCCC[C/T]GGTTGATTTGGACAA	7874
rs899253	snp	A/C	0.436265	0.166749	intron-variant, utr-variant-3-prime	USP7	GRCh38.p7	16:8894278	CCCACACCCTGACTG[A/C]GCCTCAGAGCCACTG	7874
rs899254	snp	A/G	0.459687	0.136129	intron-variant, utr-variant-3-prime	USP7	GRCh38.p7	16:8894331	TCACCCTGCACACAT[A/G]TCCAAGCTTCTCTCC	7874
rs960733	snp	A/G			intron-variant	USP7	GRCh38.p7	16:8952471	cccctagaacctcca[A/G]aaggagtgtggccct	7874
rs960734	snp	A/G	0.0463947	0.145069	intron-variant	USP7	GRCh38.p7	16:8952465	GAACCTCCAGAAGGA[A/G]TGTGGCCCTGCTGGC	7874
rs1050394	snp	A/G	0	0	utr-variant-3-prime, nc-transcript-variant	USP7	GRCh38.p7	16:8893721	CGCAATGGGGGAGAA[A/G]AGGTTAGTGGATCGG	7874
rs1058329	snp	C/G	0.194902	0.243853	intron-variant, nc-transcript-variant	USP7, LOC105371074	GRCh38.p7	16:8962683	CTGCGTTCCTTGCAG[C/G]TATTTTCGAACGTAA	7874
rs1347580	snp	C/T	0.4231	0.180378	intron-variant	USP7	GRCh38.p7	16:8905691	GCCATACTGAGCACA[C/T]CAAACGAGAGTTCAA	7874
rs1382390	snp	C/G	0.0127356	0.0788577	synonymous-codon, utr-variant-5-prime, intron-variant	USP7	GRCh38.p7	16:8936587	CCACAGGCTTGGGCT[C/G]GAAGGTGAGTCAGGT	7874
rs1471435	snp	C/T	0.44755	0.153212	intron-variant	USP7	GRCh38.p7	16:8941267	TGGAAAAATTAACTA[C/T]GCTCAAACATAACCC	7874
rs1529916	snp	C/T	0.396364	0.202676	intron-variant	USP7	GRCh38.p7	16:8897333	ACAGGCTTCTTGCAT[C/T]AAGGCCACTTTTGTT	7874
rs1542540	snp	C/T	0.0256215	0.110247	intron-variant	USP7	GRCh38.p7	16:8932322	tataatcctagcact[C/T]tgggaggcaaagatg	7874
rs1542541	snp	A/G	0.386884	0.209196	intron-variant	USP7	GRCh38.p7	16:8932543	TCAAGACACAGGATG[A/G]AGAGAAGGAAAAATG	7874
rs1600194	snp	A/C	0.0603597	0.1629	upstream-variant-2KB, intron-variant	USP7, LOC105371074	GRCh38.p7	16:8964602	AAACAAAACCCAAAA[A/C]CTTTGTAGAGAGGGT	7874
rs1622768	snp	C/G	0.404559	0.196498	intron-variant	USP7	GRCh38.p7	16:8936339	TTGAACTCCCTCTGG[C/G]TTCTGCATGGTCCTC	7874
rs1657066	snp	A/C	0.408871	0.193029	intron-variant	USP7	GRCh38.p7	16:8906228	TTACTCACAAAGAGA[A/C]GCACAAATGCTAATT	7874
rs1657076	snp	C/T	0.0260105	0.111035	intron-variant	USP7	GRCh38.p7	16:8896648	AACAGAGGAAGGATA[C/T]GATTCCATTTGAACG	7874
rs1657077	snp	C/T	0.0379877	0.132479	intron-variant	USP7	GRCh38.p7	16:8896363	CCTAATAAGAGTAAG[C/T]GAGGAAAACGCCACT	7874
rs1657084	snp	A/G	0.00835141	0.0640778	intron-variant	USP7	GRCh38.p7	16:8925295	TAACACACACAAAAC[A/G]CAGGCCTCAACAAAA	7874
rs1657086	snp	C/G	0.403334	0.197456	upstream-variant-2KB, intron-variant	USP7	GRCh38.p7	16:8937059	TAAAAAGGCAAAGTA[C/G]AATGCCCTCTCAGCC	7874
rs1657087	snp	A/C/G	0.375	0.216506	intron-variant	USP7	GRCh38.p7	16:8953704	GAAGACACGTGCCCC[A/C/G]TGCGGCGCCACCGGA	7874
rs1657088	snp	C/T	0.367091	0.220884	intron-variant	USP7	GRCh38.p7	16:8953716	CCCGTGCGGCGCCAC[C/T]GGAGGCAGAGGGAAG	7874
rs1657091	snp	C/T	0.415563	0.18732	intron-variant	USP7	GRCh38.p7	16:8901557	GGAAGAGCGTTGCCA[C/T]GGGAAGATTGCGCAT	7874
rs1677468	snp	A/G	0.00914312	0.0669923	intron-variant	USP7	GRCh38.p7	16:8935752	CCTACTTGGTGTTTC[A/G]AAAACATATTTTCTG	7874
rs1677470	snp	C/T	0.00760928	0.0612106	intron-variant	USP7	GRCh38.p7	16:8920493	GAATAAGAACACACA[C/T]TTTATTCCCAAGAGA	7874
rs1677472	snp	C/T	0.0260105	0.111035	intron-variant, utr-variant-3-prime	USP7	GRCh38.p7	16:8894381	CAAAGGATGTAAGGA[C/T]CTGTTAAGAACTCGT	7874
rs1677473	snp	A/G	0.0260105	0.111035	intron-variant	USP7	GRCh38.p7	16:8895546	TGGTATAAAAACACA[A/G]ATCAAGCTACTTGTA	7874
rs1677480	snp	G/T	0.435263	0.167862	intron-variant	USP7	GRCh38.p7	16:8933584	GTAGTTTCTTCACTG[G/T]ATATGCACACACTCA	7874
rs1677490	snp	C/G	0.426354	0.177198	intron-variant	USP7	GRCh38.p7	16:8934684	GATTGGCCACACCAA[C/G]TCAGATGTGTTAATT	7874
rs1677491	snp	G/T	0.441705	0.160466	intron-variant	USP7	GRCh38.p7	16:8909393	TGTACATCAGCTCAT[G/T]TAAGAGGACAGAGCT	7874
rs1816548	snp	G/T	0.00479614	0.0487346	utr-variant-3-prime, nc-transcript-variant	USP7	GRCh38.p7	16:8893915	TGCACGTGCCCTCTA[G/T]CCGAAGTCTTCAGCA	7874
rs1865807	snp	G/T	0.0558544	0.157504	intron-variant	USP7	GRCh38.p7	16:8948554	AAATCCCTTTAAAAA[G/T]ACTGACTAAAGCCTA	7874
rs1871210	snp	A/G	0.0995161	0.199636	intron-variant	USP7	GRCh38.p7	16:8948744	aGCATGGACAACACA[A/G]CGATAAAAGCAGCCA	7874
rs1972295	snp	G/T	0.0562307	0.157967	intron-variant	USP7	GRCh38.p7	16:8927707	caggcgtggtggcat[G/T]tgcctgtaatcccag	7874
rs2086154	snp	A/C	0.392696	0.205275	intron-variant	USP7	GRCh38.p7	16:8948774	AAAAACAAGCATGGA[A/C]AACACAGCGAAACCC	7874
rs2126999	snp	C/T	0.0477023	0.146886	intron-variant	USP7	GRCh38.p7	16:8919607	ACTCCCAGAGCTTTT[C/T]TTATTTTGTGATTTT	7874
rs2164506	snp	A/G	0.0928121	0.194402	intron-variant	USP7	GRCh38.p7	16:8919178	GGGGATCTTGCAGAT[A/G]CCCCATTGCTCCTGC	7874
rs2164507	snp	A/G	0.0463947	0.145069	intron-variant	USP7	GRCh38.p7	16:8919839	GGAGACACCTACTGC[A/G]CAGTACCATTCACCA	7874
rs2217910	snp	A/G	0.0275645	0.114116	intron-variant	USP7	GRCh38.p7	16:8909348	ACTGGGGACCATGAC[A/G]AGGCACACCCATATG	7874
rs2248797	snp	C/T	0.445724	0.155538	intron-variant	USP7	GRCh38.p7	16:8946462	CTCCAGAAAGACTTA[C/T]GCTCCAGAAAGAAGC	7874
rs2248802	snp	A/G	0.101301	0.200969	intron-variant	USP7	GRCh38.p7	16:8946690	TCTGGTCACTGGCCT[A/G]TACCCCAGCCCCACA	7874
rs2257181	snp	G/T	0.407845	0.193868	intron-variant	USP7	GRCh38.p7	16:8896823	CTCAACACAGACCCA[G/T]TGTTGCTCCAGTTTT	7874
rs2289109	snp	A/C	0.489893	0.0703642	intron-variant	USP7	GRCh38.p7	16:8898971	TGTCACCACTCACAT[A/C]TTGACCACATTACTC	7874
rs2289110	snp	A/G	0.0577344	0.159793	intron-variant, missense	USP7	GRCh38.p7	16:8894418	GACCTGTGGAACCAG[A/G]AGCAATAGCATTCCA	7874
rs2289111	snp	A/G	0.000115448	0.00759675	synonymous-codon, nc-transcript-variant	USP7	GRCh38.p7	16:8915520	ATTTTCCACATTATC[A/G]AGCAACTGAAAAAGA	7874
rs2304464	snp	A/G	0.0566069	0.158427	intron-variant	USP7	GRCh38.p7	16:8898695	TGCTCACTCACAGAT[A/G]TTTGTTTTTAGGCAA	7874
rs2304465	snp	C/T	0.479029	0.100229	intron-variant	USP7	GRCh38.p7	16:8898485	CATAAAGAGAAGGCT[C/T]GGGGTTTTGGTGACG	7874
rs2304466	snp	A/G	0.5	0.00040385	intron-variant	USP7	GRCh38.p7	16:8902070	GCAGGCAGGCGTCTC[A/G]TGGGCACTTACGATC	7874
rs2304467	snp	C/G	0.438666	0.164028	intron-variant	USP7	GRCh38.p7	16:8894920	TTGGTTTTGGCGGCT[C/G]CCACGTGACGTGGCC	7874
rs2304473	snp	A/G	0.0554779	0.157039	intron-variant	USP7	GRCh38.p7	16:8919251	ACCGAGGCCAGGAAC[A/G]CTTATCACACAGCAT	7874
rs2437711	snp	C/T	0.442655	0.159323	intron-variant	USP7	GRCh38.p7	16:8912328	gtggtggtgggcacc[C/T]gtaatcccagctact	7874
rs2437713	snp	G/T	0.132066	0.220435	intron-variant	USP7	GRCh38.p7	16:8926952	ACGAAGTTCCCACTG[G/T]GCACTTTGTTACAGC	7874
rs2437714	snp	C/T	0.0346268	0.126943	intron-variant	USP7	GRCh38.p7	16:8934124	CTTGGTTCAAACTTA[C/T]CCTACGACAATAGCT	7874
rs2437715	snp	A/G	0.0252325	0.109451	intron-variant	USP7	GRCh38.p7	16:8934955	ACATGGTAAATCCCT[A/G]GTCCAGAAGTAAATG	7874
rs2437716	snp	C/T	0.143959	0.226396	upstream-variant-2KB, intron-variant	USP7	GRCh38.p7	16:8937247	acgaaacaacgtgta[C/T]aagacaagcaatctg	7874
rs2437717	snp	C/T	0.0352966	0.128072	intron-variant	USP7	GRCh38.p7	16:8942676	CCTCAAGCTCTTGAG[C/T]AGCTGGGACTACAGG	7874
rs2437718	snp	A/G	0.0228947	0.104514	intron-variant	USP7	GRCh38.p7	16:8942840	GACATGAGCCACCAC[A/G]TCCAGCCACTTTGTG	7874
rs2437719	snp	C/G	0.0352966	0.128072	intron-variant	USP7	GRCh38.p7	16:8944407	CACCTTGGCAACTAA[C/G]TAGCAGCTTCCTCTC	7874
rs2437724	snp	A/C	0.0236746	0.106192	intron-variant	USP7	GRCh38.p7	16:8899011	CTAAGCAAGAAATGG[A/C]CTGTCAGGTGAAATG	7874
rs2437725	snp	A/C	0.0260105	0.111035	intron-variant	USP7	GRCh38.p7	16:8899012	TAAGCAAGAAATGGA[A/C]TGTCAGGTGAAATGG	7874
rs2437726	snp	A/T	0.455621	0.142197	intron-variant	USP7	GRCh38.p7	16:8900035	GCACCTGCTCTCCTC[A/T]ACAGGAGCAGACCCA	7874
rs2437727	snp	C/G	0.432082	0.197628	intron-variant	USP7	GRCh38.p7	16:8904714	TTGGGAGGCTGAGGC[C/G]GGCCGATCACGAGGT	7874
rs2447911	snp	A/C	0.442249	0.159814	intron-variant	USP7	GRCh38.p7	16:8924808	CTCAAAGAAGGTAGA[A/C]GTGCTTACCGTCACA	7874
rs2447912	snp	A/C	0.0256215	0.110247	intron-variant	USP7	GRCh38.p7	16:8920577	GTCTAAAATTAGCAA[A/C]AAAGTTGGGATGTAT	7874
rs2447913	snp	G/T	0.119281	0.213102	intron-variant	USP7	GRCh38.p7	16:8916234	ATTGGTATATATACA[G/T]GAGTTATTAATCCAG	7874
rs2447914	snp	C/T	0.443464	0.15834	intron-variant	USP7	GRCh38.p7	16:8911783	ttctcactgaCAGCT[C/T]CGGAAGAAACTGCAC	7874
rs2447915	snp	A/G	0.45645	0.140991	intron-variant	USP7	GRCh38.p7	16:8911210	GAGGTTTTCCTTGTC[A/G]TTCTGCCACATCAGC	7874
rs2447916	snp	G/T	0.00745915	0.060613	intron-variant	USP7	GRCh38.p7	16:8910707	GTGTCCTGTTGTAGC[G/T]TTCTTCTTTATTTTC	7874
rs2447917	snp	C/T	0.0368353	0.130617	intron-variant	USP7	GRCh38.p7	16:8906799	TATATTTGGAATTCC[C/T]CCACCCTAAATTATT	7874
rs2447918	snp	A/G	0.470724	0.117425	intron-variant	USP7	GRCh38.p7	16:8902520	GACTAAAATATGAGC[A/G]TGTTTTTATTTTAAT	7874
rs2447919	snp	A/G	0.386694	0.20932	intron-variant	USP7	GRCh38.p7	16:8900706	AGAGAAAATACTTAA[A/G]TACATGGAAGACTAT	7874
rs2447931	snp	C/G	0.372995	0.217652	intron-variant	USP7	GRCh38.p7	16:8942424	TCAGACCCTCACAGT[C/G]CTGCAGAACAGCAAA	7874
rs2447933	snp	A/G	0.442655	0.159323	intron-variant	USP7	GRCh38.p7	16:8934773	TGTACTCGGTGGCCA[A/G]CCAGTGGCCCTTTGC	7874
rs3214650	in-del	-/C	0.0407518	0.136803	intron-variant, frameshift-variant	USP7	GRCh38.p7	16:8894530	GGGTTCTCCCCCCCC[-/C]GGGGGCTGGTGTGGG	7874
rs3826203	snp	A/G	0.0166325	0.0896639	intron-variant	USP7	GRCh38.p7	16:8911174	GTCTCAAAAGCAGAG[A/G]TGCACAAATGTGAAT	7874
rs3841558	in-del	-/TTTCTGAATTAGGTCT			intron-variant	USP7	GRCh38.p7	16:8916405	AACAAAGATGGGCAT[-/TTTCTGAATTAGGTCT]GAGGTTTTACTTGGT	7874
rs4076904	snp	A/C	0.347032	0.230401	intron-variant	USP7	GRCh38.p7	16:8958616	GATGTGGGATAGAGA[A/C]AGCAGAGTTCAAAGC	7874
rs4539593	snp	C/T	0.0460142	0.144533	intron-variant	USP7	GRCh38.p7	16:8931395	GTTTCACCATGTCGG[C/T]CAACTGGTCTCGAAC	7874
rs4985011	snp	A/T	0.45889	0.13735	intron-variant	USP7	GRCh38.p7	16:8902981	ATCGAATGCCCATTT[A/T]CAAAAATAAAGAGGG	7874
rs4985012	snp	A/G	0.494692	0.0512434	intron-variant	USP7	GRCh38.p7	16:8906146	GGGTAATTATCCCAC[A/G]AGCATTCAGAAGAAA	7874
rs4985013	snp	A/G	0.45574	0.142025	intron-variant	USP7	GRCh38.p7	16:8914618	ctcatgaatgtgctg[A/G]gcaaaaggaatcaga	7874
rs4985014	snp	C/G	0.0376037	0.131863	intron-variant	USP7	GRCh38.p7	16:8941448	ACAGGAAGGACCTGA[C/G]GGGTAAAGGCACGTA	7874
rs4985061	snp	C/G	0.487809	0.0771174	intron-variant	USP7	GRCh38.p7	16:8900335	AATTTTTAAGAAATT[C/G]AGAAGAGCTTTATGA	7874
rs4985062	snp	C/T	0.463018	0.130857	intron-variant	USP7	GRCh38.p7	16:8902779	TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	7874

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