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
rs510272	snp	A/C	0	0	intron-variant	USP2	GRCh38.p7	11:119370943	CCACTGGGAATCTGC[A/C]TCCTCCCCACACAGG	9099
rs511401	snp	C/G	0.207864	0.246424	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119379350	TTCAAGAGGAAAGAG[C/G]ATTGAAAAGAGCACA	9099
rs512608	snp	A/G	0.206642	0.246211	upstream-variant-2KB, intron-variant	USP2, USP2-AS1	GRCh38.p7	11:119383087	tgttATATTTCCTTA[A/G]GGCCCTCATTCCATC	9099
rs513841	snp	A/T	0.209084	0.246629	intron-variant	USP2	GRCh38.p7	11:119370539	CGTGCGGCCTGGACC[A/T]CTTCTTTCTAAAACT	9099
rs514808	snp	C/T	0.0614824	0.164198	intron-variant	USP2	GRCh38.p7	11:119370410	CCTTAGCTTCTGAAC[C/T]TGTGTCCTCCTCTGT	9099
rs565296	snp	A/G	0.22576	0.248822	intron-variant, upstream-variant-2KB	USP2, USP2-AS1	GRCh38.p7	11:119381441	GGGGATCCGGGAGGG[A/G]GGATTCGGGGATCAG	9099
rs573396	snp	C/T	0.449218	0.151037	intron-variant	USP2	GRCh38.p7	11:119368665	CACACCCTTGCCCTC[C/T]GCTCTAGGACCTGTT	9099
rs576945	snp	C/T	0.213635	0.247341	intron-variant	USP2	GRCh38.p7	11:119376186	CAGGCTGTGCTTTCA[C/T]CTGGAAGGTGCTAGG	9099
rs587726	snp	C/T	0.139903	0.224452	intron-variant	USP2	GRCh38.p7	11:119370115	GGGAGGTGGAGGTTG[C/T]AGTGAGCCGAGATCG	9099
rs587985	snp	C/T	0.46772	0.122873	intron-variant, synonymous-codon	USP2	GRCh38.p7	11:119373385	GGCCCCATAGGAGGA[C/T]GGGGTGTAGGCACCA	9099
rs602492	snp	G/T	0.210396	0.247097	intron-variant	USP2	GRCh38.p7	11:119371033	TAGTTTAGTCTGCGC[G/T]GAGGTTTTCCATCTC	9099
rs614192	snp	A/G	0.212425	0.24716	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119377999	GAGTTTCAGAAGCAC[A/G]CCTAAACAGGGTTAA	9099
rs615001	snp	C/T	0.209388	0.246679	intron-variant	USP2	GRCh38.p7	11:119371567	TTATCAAAGTTGCTC[C/T]CTCAAGACCTTTAGT	9099
rs619055	snp	A/G			intron-variant	USP2	GRCh38.p7	11:119362701	GGTCGACAGGGAGAA[A/G]GGGGCCAGAACTGCA	9099
rs656439	snp	C/T	0.205723	0.246048	intron-variant, upstream-variant-2KB	USP2, USP2-AS1	GRCh38.p7	11:119380164	TTGTGATCCGCCCGC[C/T]TTGGCCTCCCAAAGT	9099
rs658654	snp	C/T	0.24134	0.24985	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119377610	GCATCTACCCCAGCT[C/T]GGGGCCTTGGGTCCC	9099
rs658921	snp	A/G	0.0372196	0.131242	intron-variant	USP2	GRCh38.p7	11:119374475	CCCAGAGGATCATGA[A/G]TTTTAATCTATCTGT	9099
rs659705	snp	A/G	0.212728	0.247206	intron-variant	USP2	GRCh38.p7	11:119374639	TTAGGGTCAGTTGGG[A/G]ACCCCCAGAGGCCTT	9099
rs670906	snp	G/T	0.196844	0.244283	missense, utr-variant-5-prime, upstream-variant-2KB	USP2, USP2-AS1	GRCh38.p7	11:119381489	TGCCTCTTCTTGGAG[G/T]ATGGACGAGTCGAAC	9099
rs674977	snp	C/T	0.0584853	0.160693	intron-variant	USP2	GRCh38.p7	11:119375791	GGAATTGGTATTCTT[C/T]GGGCAGCGCCCCAAG	9099
rs675873	snp	C/T	0.459004	0.137176	intron-variant	USP2	GRCh38.p7	11:119375998	ATTGCCAGACCCCTC[C/T]GCCTCCTCCTAGCAG	9099
rs676465	snp	C/T	0.412249	0.190198	intron-variant	USP2	GRCh38.p7	11:119369212	GCTGAGCTGCGCCCC[C/T]CTGGCCTGGCATTTT	9099
rs677008	snp	A/G	0.257176	0.249897	intron-variant	USP2	GRCh38.p7	11:119369361	AAGTTCGTGTTGCCT[A/G]TTACTGTTAATGAGG	9099
rs679556	snp	C/G	0.148326	0.228391	intron-variant	USP2	GRCh38.p7	11:119372005	AGAGGCGTGTGCGGG[C/G]ATTAGTTGGCGAGCG	9099
rs680268	snp	A/G	0.253544	0.249975	intron-variant	USP2	GRCh38.p7	11:119368979	GGTCTATGGAAGGAC[A/G]AGCTGTTCCCATTGA	9099
rs682006	snp	C/T	0	0	upstream-variant-2KB, intron-variant	USP2, USP2-AS1	GRCh38.p7	11:119383356	cattctttccccaca[C/T]ttatgtgtagttcac	9099
rs687009	snp	C/G	0.213333	0.247296	intron-variant	USP2	GRCh38.p7	11:119375857	AGTGCTGGGGCCAAA[C/G]GAGGTCCAGAGGACA	9099
rs891290	snp	A/T	0.0379877	0.132479	intron-variant	USP2	GRCh38.p7	11:119374300	CTCTACAAACACAGA[A/T]CTCAAATTGGTCCTG	9099
rs1054953	snp	A/G			synonymous-codon	USP2	GRCh38.p7	11:119357562	GAGCTTGCTGGTTCG[A/G]ATCCTGGATTCTGAG	9099
rs1133595	snp	A/T			missense	USP2	GRCh38.p7	11:119356872	GCCAGTTCGTAGAAG[A/T]GCAGGTAGGCGTCGC	9099
rs1652024	snp	A/C	0.146623	0.228562	intron-variant	USP2	GRCh38.p7	11:119371846	TCCATCCATTCATCC[A/C]TGCAATCAGCAGGTC	9099
rs1835210	snp	G/T	0	0	intron-variant	USP2	GRCh38.p7	11:119362698	CAGGGTCGACAGGGA[G/T]AAGGGGGCCAGAACT	9099
rs1940804	snp	C/T	0.370772	0.218893	intron-variant	USP2	GRCh38.p7	11:119366507	ATATGTTTATCTTTG[C/T]TTTATAAGTGTTTCA	9099
rs2115645	snp	A/G	0.303438	0.244222	intron-variant	USP2	GRCh38.p7	11:119378778	CAAGCACCTCTGCCC[A/G]GGTACTCTCCTGGTG	9099
rs2195525	snp	C/T	0.479095	0.100076	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119364694	TCGTGAAGACCCAAA[C/T]TCATGCAGTCTGTGG	9099
rs2195526	snp	C/T	0.424193	0.179323	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119366041	CTGGGATTACAGGTG[C/T]GCACCACCACGCCTG	9099
rs2217380	snp	G/T	0.126564	0.217402	intron-variant	USP2	GRCh38.p7	11:119369169	AAGCAGAAGGTGAAG[G/T]CTCAGGGGAGGCCCT	9099
rs2241646	snp	A/G	0.408086	0.193672	synonymous-codon	USP2	GRCh38.p7	11:119359254	AACAAAGCGCGGTGC[A/G]TATCTCTGGATCTGG	9099
rs2288596	snp	A/G	0.00438332	0.0466095	intron-variant	USP2	GRCh38.p7	11:119359784	AGGCTATCCTTTCAT[A/G]GCCTCAAGTTCCTCT	9099
rs2435193	snp	G/T			intron-variant	USP2	GRCh38.p7	11:119358512	gtagagatggggttt[G/T]gccatgttggccagg	9099
rs2509401	snp	G/T	0.0360663	0.129354	utr-variant-3-prime	USP2	GRCh38.p7	11:119355222	CTGCCAACTGATTTC[G/T]CAAAGCTATTATTTA	9099
rs3195469	snp	A/C			missense	USP2	GRCh38.p7	11:119356849	GAACTGGCCAGCCCG[A/C]CCTCCCGAATGTAGC	9099
rs3195470	snp	G/T	0	0	missense	USP2	GRCh38.p7	11:119356838	CCCGCCCTCCCGAAT[G/T]TAGCGCCAGGAGCCA	9099
rs3751022	snp	C/G	0.0368353	0.130617	intron-variant	USP2	GRCh38.p7	11:119366953	AAAGCTTTAGCGTGG[C/G]AGCACTTTGAGAAGT	9099
rs3833766	in-del	-/AA	0.44638	0.154709	intron-variant	USP2	GRCh38.p7	11:119366648	GTTGATCTTGTCTCT[-/AA]AGAGGGCCAGACCAG	9099
rs4589313	snp	A/G	0.399432	0.200425	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119366084	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	9099
rs4938649	snp	C/T	0.0393691	0.134665	intron-variant, synonymous-codon	USP2	GRCh38.p7	11:119372902	GTAGTCGACCAGGTA[C/T]TCAGGGCAGCTGGCT	9099
rs5795178	in-del	-/AG	0.153997	0.230832	intron-variant	USP2	GRCh38.p7	11:119370608	CAGGAAATGACGATA[-/AG]AGGGGTGGAGAGATC	9099
rs7115997	snp	A/C	0.0162398	0.0886349	intron-variant	USP2	GRCh38.p7	11:119375572	AGACAGACAGAGGCA[A/C]AGGGTCGGGGTGGGG	9099
rs7117852	snp	C/G/T	0.100532	0.203967	utr-variant-3-prime	USP2	GRCh38.p7	11:119356534	CGAGGGTCTTCCCCC[C/G/T]CAAGACACAGTTGTT	9099
rs7126754	snp	A/G			upstream-variant-2KB, intron-variant	USP2, USP2-AS1	GRCh38.p7	11:119383103	GGCCCTCATTCCATC[A/G]CTTCATTTTACAGAT	9099
rs7127021	snp	A/G	0.0103295	0.0711199	upstream-variant-2KB, intron-variant	USP2, USP2-AS1	GRCh38.p7	11:119383276	taagagctatggggc[A/G]catcaagcaaggagg	9099
rs7927942	snp	C/T	0.0345262	0.126772	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119377906	TAACCTTCATGGCTT[C/T]TCTCTGCCCAGATCT	9099
rs7929563	snp	G/T	0.158962	0.232835	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119365898	tattttatttgtttt[G/T]ttttttttttttttg	9099
rs7936181	snp	C/T			intron-variant	USP2	GRCh38.p7	11:119371026	GGGTCTGTAGTTTAG[C/T]CTGCGCTGAGGTTTT	9099
rs7937208	snp	C/T	0.31357	0.241783	intron-variant	USP2	GRCh38.p7	11:119358664	TGCTTTGTTGAACAC[C/T]AGGCAGAAACAGGCT	9099
rs7937436	snp	A/G	0	0	intron-variant	USP2	GRCh38.p7	11:119375040	GCCCTCTGAAGGTCT[A/G]TGATAATATCAGGGC	9099
rs7943722	snp	C/T	0.299411	0.245069	upstream-variant-2KB	USP2, USP2-AS1	GRCh38.p7	11:119381738	CACTGAGTCGCGTCA[C/T]GGCTATTGGCTTGTT	9099
rs7945115	snp	A/G	0.123105	0.215401	intron-variant	USP2	GRCh38.p7	11:119369746	TACAGCCCAGCTGAT[A/G]GGTGTCCAAGGTTAG	9099
rs7949607	snp	C/G/T	0.00279162	0.0372561	intron-variant	USP2	GRCh38.p7	11:119371032	GTAGTTTAGTCTGCG[C/G/T]TGAGGTTTTCCATCT	9099
rs7949694	snp	A/G			intron-variant	USP2	GRCh38.p7	11:119370979	GATCCCCAGTAAAGG[A/G]GAATACTGCTGTCAT	9099
rs7949724	snp	C/T			intron-variant	USP2	GRCh38.p7	11:119371150	ATGAATCGTTAAGCC[C/T]TGCAGTGACTCTGAC	9099
rs7949756	snp	A/G			intron-variant	USP2	GRCh38.p7	11:119371261	CCCGCAGAGGCTTCT[A/G]GGACCCGAGCCCCTC	9099
rs7950073	snp	A/G			intron-variant	USP2	GRCh38.p7	11:119371268	AGGCTTCTAGGACCC[A/G]AGCCCCTCCGAGGAG	9099
rs10692151	in-del	-/TTT	0	0	intron-variant, upstream-variant-2KB	USP2, USP2-AS1	GRCh38.p7	11:119379934	TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTCCG	9099
rs10790291	snp	A/G	0.283947	0.247685	intron-variant	USP2	GRCh38.p7	11:119362203	AGTGCTAATGGGGGT[A/G]GGGAAATGGGAAAAC	9099
rs10892354	snp	C/T	0.36955	0.219562	intron-variant	USP2	GRCh38.p7	11:119367671	AGGCCAAAAGCTCTG[C/T]GCACCTTTGAGCCCA	9099
rs10892355	snp	C/T	0.499891	0.00738737	intron-variant	USP2	GRCh38.p7	11:119370099	AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG	9099
rs11217252	snp	A/G	0	0	utr-variant-3-prime	USP2	GRCh38.p7	11:119355322	TTGCCCTTGGGCTCA[A/G]GTTCACAGGTCTTCT	9099
rs11217253	snp	C/G	0.406468	0.194981	intron-variant	USP2	GRCh38.p7	11:119357134	GAGGGTGGAGGAGTG[C/G]GGGGAGAGTGGGTGG	9099
rs11217255	snp	A/G	0.422158	0.181278	intron-variant	USP2	GRCh38.p7	11:119360957	ACTCCTAGAAGTCCA[A/G]TATATAAAGTAACTC	9099
rs11217256	snp	C/G	0.23031	0.249223	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119365880	TGTAGTAACTATTAC[C/G]TCTATTTTATTTGTT	9099
rs11217257	snp	A/G	0.397994	0.201489	intron-variant	USP2	GRCh38.p7	11:119367745	CTCCTTCTTTTGCAT[A/G]TGTCTCCGTCTGGGG	9099
rs11217258	snp	C/T	0.233527	0.249457	intron-variant	USP2	GRCh38.p7	11:119369894	ATTTAAGAACTTCTT[C/T]TTGGCCAGGCGTGGT	9099
rs11217259	snp	G/T			intron-variant	USP2	GRCh38.p7	11:119372642	GGAGTCGAGCCCTCA[G/T]CCTGGCTGTTCTCCA	9099
rs11217260	snp	A/G	0	0	intron-variant	USP2	GRCh38.p7	11:119374103	GGGTGGGCAGGGGAG[A/G]CCGTGAGTGAGCATG	9099
rs11604901	snp	A/C			intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119364653	TGCACAAACTTTTGT[A/C]TAGAGTTCCGGGGGT	9099
rs11828770	snp	A/G	0.0134861	0.0810011	utr-variant-3-prime, downstream-variant-500B	USP2	GRCh38.p7	11:119355975	GGATATTTCAGGAGG[A/G]GCAGTTACCCCCTGG	9099
rs12161775	snp	C/G			intron-variant, missense	USP2	GRCh38.p7	11:119373185	CCTAAAGGCCGCTCA[C/G]TACCCCGGGTCTGGC	9099
rs12277700	snp	A/C	0.229723	0.249176	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119365982	TCACTGCAACCTCTG[A/C]CTCCCGGGTTCAAAC	9099
rs12285901	snp	A/G	0.232359	0.249377	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119365250	TCCCCACATGTACAC[A/G]CACACATGACCACAG	9099
rs12292387	snp	C/T	0.0482946	0.147699	intron-variant	USP2	GRCh38.p7	11:119373670	AGAAGCACACATGCA[C/T]GCAGGTGTGCACAGG	9099
rs12419866	snp	C/T	0.319616	0.240112	intron-variant	USP2	GRCh38.p7	11:119369914	CCAGGCGTGGTGGCT[C/T]ACACCTGTAATCTCA	9099
rs12419879	snp	C/T	0.349013	0.229557	intron-variant	USP2	GRCh38.p7	11:119370047	TGGTGTGGTGGTACA[C/T]GCCTGTAGTCCTAGC	9099
rs12789250	snp	C/T			intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119364394	CCCAGCCCGCTGACC[C/T]CCGGCCAGGCAGGCC	9099
rs12789449	snp	A/C			intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119364451	GAGGCCCTGGCCGGC[A/C]TCGGGGTTGAGGCTC	9099
rs33929148	snp	C/T	0.0837507	0.186711	intron-variant, missense	USP2	GRCh38.p7	11:119372960	AGCTCCTTGCGCGTC[C/T]GGGCCAGCATGGGGC	9099
rs34432859	in-del	-/A			intron-variant	USP2	GRCh38.p7	11:119360753	TTTTCAACAACCAAC[-/A]AAAATATTCTTCAGG	9099
rs34691638	snp	C/G			intron-variant	USP2	GRCh38.p7	11:119363433	GACAGTGAAGGGGAG[C/G]CGGCCCCTTTCTGCC	9099
rs35224356	snp	A/G	0.00240695	0.0346075	intron-variant, missense	USP2	GRCh38.p7	11:119372792	GTGTAGCGGCCAATG[A/G]GTCGGTAGGTTGGGC	9099
rs35310980	snp	A/T	0.0722614	0.17581	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119365700	CTCTAAGGCTGTTTG[A/T]CCACAGGCCCACCAC	9099
rs35560476	snp	G/T			intron-variant	USP2	GRCh38.p7	11:119358347	TTTGAGATGGAGTTT[G/T]GCTCTGTCCCCCAGG	9099
rs35832174	snp	A/C/G	3.3872e-05	0.00411523	intron-variant, synonymous-codon	USP2	GRCh38.p7	11:119372893	GTTCTCCAGGTAGTC[A/C/G]ACCAGGTATTCAGGG	9099
rs35957161	snp	A/G	0.00206093	0.0320346	intron-variant, missense	USP2	GRCh38.p7	11:119373021	AGCTATCTGAGGTCC[A/G]GAGGCTGGAGAAATC	9099
rs36118584	in-del	-/C			intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119376420	CCAATTGGCTGGGAT[-/C]CCCCCATACCCCTCC	9099
rs45521440	snp	A/G	0.00557542	0.0525036	intron-variant	USP2	GRCh38.p7	11:119360301	GTGCTGGGCTCTCTC[A/G]TGCAATTTCTAACCA	9099
rs45533837	snp	A/G	0.0245332	0.108003	missense	USP2	GRCh38.p7	11:119359048	TCGAGGTTCTCAGGG[A/G]TGGACTTAGGTCTCA	9099
rs45539534	snp	C/T	0.402454	0.198136	intron-variant, upstream-variant-2KB	USP2	GRCh38.p7	11:119365482	TGATCTCTACAGTCA[C/T]TGTCCTCACCCAGAC	9099
rs45570535	snp	A/T	0.0147044	0.0844746	intron-variant	USP2	GRCh38.p7	11:119358886	AGCTCAAAACTTAAG[A/T]TTAAGGGTCTGTCAA	9099
rs45575137	snp	A/G	0.00636936	0.0560724	intron-variant	USP2	GRCh38.p7	11:119368835	GAGAGGGTGGCCTGG[A/G]CAGGGTGGGGCAAGG	9099

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