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
rs15036	snp	A/C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	USP10, LOC105371378	GRCh38.p7	16:84779661	GTACACATTGCAGAT[A/C/G]AAATATTTGGAGTTA	9100
rs173419	snp	A/C	0.24019	0.249807	intron-variant	USP10	GRCh38.p7	16:84773925	CTGTATTTTTATATC[A/C]GCTGCCACCTCCAAT	9100
rs244562	snp	C/T	0.340333	0.233109	intron-variant	USP10	GRCh38.p7	16:84773655	CACACTTCTAGCTGC[C/T]TTATCACTCATCAGC	9100
rs244563	snp	A/G	0.264084	0.249603	intron-variant	USP10	GRCh38.p7	16:84773352	TGGGAAGCAGAAAAG[A/G]GGACACTGGGCCTCA	9100
rs244564	snp	A/G	0.250168	0.25	intron-variant	USP10	GRCh38.p7	16:84772178	tgcctctgccaccca[A/G]gtagctggggttaca	9100
rs744838	snp	A/G	0.499984	0.00279548	intron-variant	USP10	GRCh38.p7	16:84741080	AGGAAACTGATGCCA[A/G]ACTTTTTCTTTGAGA	9100
rs744839	snp	C/T	0.499502	0.0157669	intron-variant	USP10	GRCh38.p7	16:84740830	TGACTCTTGGGAACT[C/T]AGGTCAACTCTTCAC	9100
rs774294	snp	A/G	0.485664	0.0834419	intron-variant	USP10	GRCh38.p7	16:84769017	GATGTGCCAGCTTAT[A/G]GCTATTTTGTACTCT	9100
rs774295	snp	A/C	0.484701	0.0861117	intron-variant	USP10	GRCh38.p7	16:84769085	TGTGGCAGTGAATTC[A/C]TAAAAATGCACTGGG	9100
rs774296	snp	A/G	0.376592	0.215579	intron-variant	USP10	GRCh38.p7	16:84769282	GTGTGCTCTGAGTCA[A/G]AAAGAGCAAAGTAGG	9100
rs774297	snp	C/G	0.380919	0.21298	intron-variant	USP10	GRCh38.p7	16:84770803	AAATCTCCAGTGGCT[C/G]ATGCCTGTAATCCCA	9100
rs774298	snp	C/G	0.502104	0.0366843	synonymous-codon, nc-transcript-variant	USP10	GRCh38.p7	16:84775218	CCGAACCTATCGGCT[C/G]TTTGCAGGTGAGTAA	9100
rs774299	snp	A/G	0.46885	0.12085	intron-variant	USP10	GRCh38.p7	16:84775294	TACAGCTGGGCACAG[A/G]TTTGCTGCAACTTAG	9100
rs774300	snp	C/T	0.361053	0.22398	intron-variant	USP10	GRCh38.p7	16:84775378	GTCACGTGAGAGTTT[C/T]ACCTGAAACTCTGCG	9100
rs774301	snp	C/G	0.000399281	0.0141238	intron-variant	USP10	GRCh38.p7	16:84776465	ACTTGCTGGGCCTCA[C/G]ATGGGACGGCCATGG	9100
rs774302	snp	C/T	0.326741	0.23793	intron-variant	USP10	GRCh38.p7	16:84776618	GGCCAGCAGTTTCTC[C/T]GCCTTCTCCCTGCAC	9100
rs774303	snp	A/G	0.102014	0.201495	intron-variant	USP10	GRCh38.p7	16:84777083	TTAGAATTACCTGTA[A/G]AGTGAGCAAAGGAAC	9100
rs774304	snp	A/G	0.428937	0.17459	intron-variant	USP10	GRCh38.p7	16:84777343	CCCCCAGGCCCTGCA[A/G]ATTCTACTGATGGTC	9100
rs774305	snp	C/G	0.187685	0.242109	intron-variant	USP10	GRCh38.p7	16:84777997	ATGTGTTCTGTGGCT[C/G]TCTTAATGTTTTCAT	9100
rs774306	snp	A/G	0.349233	0.229462	intron-variant	USP10	GRCh38.p7	16:84778355	TAATATACCATAAGC[A/G]TATTCCCGCATCACC	9100
rs774307	snp	A/G	0.476746	0.10529	downstream-variant-500B, upstream-variant-2KB	USP10, LOC105371378	GRCh38.p7	16:84780193	AGCCCACCGTTTTCA[A/G]TATCACCAAAATAGT	9100
rs774308	snp	C/T	0.0648419	0.167978	downstream-variant-500B, upstream-variant-2KB	USP10, LOC105371378	GRCh38.p7	16:84780359	AGGGTGCCCGTGCCC[C/T]GGCTTCTGGCCCTGT	9100
rs811330	snp	A/C	0.462363	0.131916	downstream-variant-500B, upstream-variant-2KB	USP10, LOC105371378	GRCh38.p7	16:84780102	TTAGTGATTTGGGTA[A/C]ACGAAGTTTTTGACT	9100
rs958309	snp	A/G	0.287606	0.247155	intron-variant	USP10	GRCh38.p7	16:84733364	CAGAAAAAATGCTAC[A/G]TATTTTAACAATCCT	9100
rs958310	snp	A/G	0	0	intron-variant	USP10	GRCh38.p7	16:84733285	AGGATCTGCAACTCA[A/G]AGTTCTAGGTTGTTT	9100
rs958311	snp	A/G			intron-variant	USP10	GRCh38.p7	16:84733147	GTCCTGCTTGCAGGA[A/G]ATTTTTATTGGTTCA	9100
rs963246	snp	G/T	0.0275645	0.114116	intron-variant	USP10	GRCh38.p7	16:84754999	AAACACAGCTCCTTT[G/T]TTTTTTTTTCTGGGA	9100
rs964453	snp	A/G	0.379942	0.213577	intron-variant	USP10	GRCh38.p7	16:84734629	ttgacattaaagttg[A/G]aagtgtactcctctt	9100
rs1050423	snp	G/T	0	0	utr-variant-5-prime, nc-transcript-variant	USP10	GRCh38.p7	16:84700063	TGAGCAGCCGGAGGA[G/T]CGCGGAGTCCCAATG	9100
rs1050424	snp	C/G			utr-variant-5-prime, nc-transcript-variant	USP10	GRCh38.p7	16:84700067	CAGCCGGAGGATCGC[C/G]GAGTCCCAATGAAAC	9100
rs1050435	snp	A/G			missense, intron-variant, nc-transcript-variant	USP10	GRCh38.p7	16:84745500	CTGTCAGCCAGCCCA[A/G]GTCCTGGGCCAGCCT	9100
rs1477392	snp	C/T	0.496517	0.0415876	intron-variant	USP10	GRCh38.p7	16:84755342	CCCACCCAGAAACTT[C/T]GCTGCATCTTCCTGG	9100
rs1541696	snp	C/T	0.482534	0.0918038	intron-variant	USP10	GRCh38.p7	16:84761238	TCCACCTGTGCTAGG[C/T]GGGCCCCTCTGGGTT	9100
rs1541697	snp	C/T	0.288386	0.247035	intron-variant	USP10	GRCh38.p7	16:84761030	CTTAAGACCCTATGC[C/T]ACCCCTGGTGGTATC	9100
rs1541698	snp	C/T	0.481242	0.0950111	intron-variant	USP10	GRCh38.p7	16:84761026	AGACCCTATGCTACC[C/T]CTGGTGGTATCCTGC	9100
rs1541699	snp	A/G	0.308166	0.243139	intron-variant	USP10	GRCh38.p7	16:84714290	TTTTACTAAACAAGT[A/G]TCATTCCACATTTTA	9100
rs1812061	snp	C/G	0.326436	0.238028	missense, intron-variant, nc-transcript-variant	USP10	GRCh38.p7	16:84745091	AAGTCCTGGGCGTAA[C/G]TGACGGGGGCATGTC	9100
rs1812062	snp	A/G	0.326247	0.238089	synonymous-codon, intron-variant, nc-transcript-variant	USP10	GRCh38.p7	16:84745084	GGGCGTAACTGACGG[A/G]GGCATGTCACCCATA	9100
rs1820246	snp	C/T	0.28052	0.24813	intron-variant	USP10	GRCh38.p7	16:84725628	agtctgttctctgac[C/T]cctgacctcaggtga	9100
rs1862792	snp	A/G	0.354634	0.22705	missense, intron-variant, nc-transcript-variant	USP10	GRCh38.p7	16:84745079	GAATTTATGGGTGAC[A/G]TGCCCCCGTCAGTTA	9100
rs1862794	snp	C/T	0.370162	0.219229	intron-variant	USP10	GRCh38.p7	16:84716989	TTCATAGTAGAGCTT[C/T]GGGATTACATGAGAT	9100
rs1968266	snp	C/T	0.278399	0.248382	intron-variant	USP10	GRCh38.p7	16:84705606	CCTCTTTCTTTCTTC[C/T]TGATCTGATGGTGCT	9100
rs2012708	snp	C/T	0.495213	0.048687	intron-variant	USP10	GRCh38.p7	16:84756953	GAGCCCTTTCCTCAA[C/T]ATATAAGGGGCTTCA	9100
rs2012733	snp	A/C	0.284995	0.247539	intron-variant	USP10	GRCh38.p7	16:84757222	CTTAATATGGAATAC[A/C]GAACTGGGCCTTGAA	9100
rs2113253	snp	C/T	0.278399	0.248382	intron-variant	USP10	GRCh38.p7	16:84707994	gaggtgggaggatcg[C/T]ttgaacctgggaggt	9100
rs2161692	snp	C/T	0.301681	0.2446	intron-variant	USP10	GRCh38.p7	16:84736881	GCAAGCTCCGCCTCC[C/T]GGGTTCACACCATTC	9100
rs2216762	snp	C/T	0.422315	0.181128	intron-variant	USP10	GRCh38.p7	16:84725840	TTAAGGCTTTAATCA[C/T]GCCAAACAGTCTATT	9100
rs2288017	snp	C/G	0.131898	0.220361	intron-variant	USP10	GRCh38.p7	16:84760143	AGTTCATTGTAGTTA[C/G]GAAAACCTGTGTCCT	9100
rs2291648	snp	C/T	0.49263	0.0602539	intron-variant	USP10	GRCh38.p7	16:84766879	CTTTATTCACACCAA[C/T]TGAAAGATTTACTTC	9100
rs2291649	snp	A/G	0.373397	0.217424	intron-variant	USP10	GRCh38.p7	16:84767301	AATGAGAGATGGGCC[A/G]AACACACAATTTTTA	9100
rs2303231	snp	G/T	0.227959	0.249026	intron-variant	USP10	GRCh38.p7	16:84775016	ATGAGTCAATTTTTG[G/T]GCAACTGAAGGGATA	9100
rs2303232	snp	C/G	0.307176	0.243374	intron-variant	USP10	GRCh38.p7	16:84775363	CTTGTGAGTCGGGGA[C/G]TCACGTGAGAGTTTT	9100
rs2326391	snp	C/T	0.326376	0.238048	missense, intron-variant, nc-transcript-variant	USP10	GRCh38.p7	16:84745088	GGTGACATGCCCCCG[C/T]CAGTTACGCCCAGGA	9100
rs2326392	snp	C/G	0.416708	0.186302	intron-variant	USP10	GRCh38.p7	16:84747182	TGGATTCCACCAAGC[C/G]TGGTGACCAGATCTT	9100
rs2550409	snp	C/T	0.379158	0.214052			GRCh38.p7	16:84767876	GGGAAGGTCAGCAGA[C/T]AAACAAGTGAACAAA	9100
rs2641688	snp	A/G	0.361667	0.223675	intron-variant	USP10	GRCh38.p7	16:84768145	ATCTTAAGGGAAAGT[A/G]GCAAGGAGTGGTCTC	9100
rs2641694	snp	A/T			intron-variant	USP10	GRCh38.p7	16:84770168	GGACTCCGGAAGATA[A/T]AAAGGATGCTGCCAG	9100
rs2641695	snp	A/G	0.00199481	0.0315187	intron-variant	USP10	GRCh38.p7	16:84766518	GTTTAGGATTGTGAG[A/G]ACACCCCCTCGGGAT	9100
rs3180185	snp	A/G	0.277067	0.24853	intron-variant	USP10	GRCh38.p7	16:84755657	AATAATTATGATTGG[A/G]TATGGTGGCACACAT	9100
rs3213810	snp	A/T	0.419616	0.183658	intron-variant	USP10	GRCh38.p7	16:84764031	GATCTGTGCCTTTTT[A/T]TTTTTTGCTGTTCTT	9100
rs3751759	snp	C/T	0.411282	0.191019	intron-variant	USP10	GRCh38.p7	16:84744616	TGTTTAGAAAGAAAA[C/T]TATTAGTTAAGAACC	9100
rs3751760	snp	C/G	0.322245	0.239334	intron-variant	USP10	GRCh38.p7	16:84744443	ATTATTTAATTTGGG[C/G]ATATGAAAAGCAGAA	9100
rs3751761	snp	C/G	0.252702	0.249985	upstream-variant-2KB	USP10	GRCh38.p7	16:84699945	GGGCGCGGGGAGGCC[C/G]GCCCGCTGCTGCGCC	9100
rs3751866	snp	A/G	0.412082	0.190341	intron-variant	USP10	GRCh38.p7	16:84737698	GGTGACAGTGCCAGC[A/G]GGTGACACTGCCAGT	9100
rs3764281	snp	C/T	0.322858	0.239148	intron-variant	USP10	GRCh38.p7	16:84733546	AAACATAACTATTAA[C/T]TGTATCTACCCACGG	9100
rs3764283	snp	C/T	0.00795532	0.062565	intron-variant	USP10	GRCh38.p7	16:84733234	AACCTTTCCTACAAA[C/T]TGTCAAAGAACACTA	9100
rs3764284	snp	A/G	0.0456336	0.143994	intron-variant	USP10	GRCh38.p7	16:84708075	CTTTTCTTTTTTGAC[A/G]TAAGAGTCTCGCTCT	9100
rs3764286	snp	A/G	0.412416	0.190055	intron-variant	USP10	GRCh38.p7	16:84707737	ATGTTATAAGTTGTG[A/G]CAGCACTTCCACAAT	9100
rs3764331	snp	C/T	0.40853	0.193309	intron-variant	USP10	GRCh38.p7	16:84759742	AGTGAACTCAAGTCT[C/T]TTCTATATGCATTTT	9100
rs3764332	snp	A/T	0.231775	0.249335	intron-variant	USP10	GRCh38.p7	16:84759679	GCTAAAATATTTTCT[A/T]CTGAATCTAAAGAAC	9100
rs3764333	snp	C/T	0.361053	0.22398	intron-variant	USP10	GRCh38.p7	16:84759655	AAAGAACACAGATCA[C/T]CAATGCTCCAATTCC	9100
rs3829516	snp	A/G	0.412082	0.190341	intron-variant	USP10	GRCh38.p7	16:84744320	TAAAAATACCCCCCA[A/G]TGGAATCTGACTTTC	9100
rs3829554	snp	A/G	0.499999	0.000798721	intron-variant	USP10	GRCh38.p7	16:84737437	GTCTGTGGTAACTGG[A/G]TATCTAAATACACAA	9100
rs3893782	snp	A/C	0.479824	0.098392	intron-variant	USP10	GRCh38.p7	16:84773231	AGCACAGCTTCAAGA[A/C]GACTTTTCTTGAAAG	9100
rs4510001	snp	A/G	0.287346	0.247195	intron-variant	USP10	GRCh38.p7	16:84740514	TCAAAGTGATTCAGC[A/G]ATTAAATACATTACA	9100
rs4553618	snp	A/G	0.370457	0.219066	synonymous-codon, intron-variant, nc-transcript-variant	USP10	GRCh38.p7	16:84745156	TCCGGGGAAAGGACT[A/G]TCAGGCACAATGTCA	9100
rs4782652	snp	C/G	0.292008	0.246445	intron-variant	USP10	GRCh38.p7	16:84738159	TCCCAGCCTGCTGCA[C/G]TCTCTCGGGTCTGGA	9100
rs4782653	snp	C/T	0.300169	0.244914	intron-variant	USP10	GRCh38.p7	16:84746794	gaaattaaccttaac[C/T]tactgtaactttttt	9100
rs4782654	snp	A/G	0.245916	0.249967	intron-variant	USP10	GRCh38.p7	16:84755444	GCTGTCTTCACTCCT[A/G]CACGCTGCCCCCACT	9100
rs4782655	snp	C/G	0.287606	0.247155	intron-variant	USP10	GRCh38.p7	16:84763593	TGACACGGTAATACC[C/G]ACTTTGCAGAGCATC	9100
rs4782656	snp	G/T	0.420574	0.182769	intron-variant	USP10	GRCh38.p7	16:84765028	tgcagtgagccaaga[G/T]tacaccactgcactc	9100
rs4783053	snp	C/T	0.283158	0.247791	upstream-variant-2KB	USP10	GRCh38.p7	16:84699591	ATAAACCAGACCCTC[C/T]TCGGGGATCTAATGC	9100
rs4783054	snp	A/G	0.456214	0.141336	intron-variant	USP10	GRCh38.p7	16:84701475	TGTTTAGACCTTTCT[A/G]TTAAAAAAAAAGATT	9100
rs4783055	snp	A/C	0.389715	0.207315	intron-variant	USP10	GRCh38.p7	16:84708597	AAACTGGGTAATTCA[A/C]CTGAATTTTTCTCCA	9100
rs4783056	snp	A/G	0.303938	0.244112	intron-variant	USP10	GRCh38.p7	16:84748526	ccaggctggtcttga[A/G]ctcctgacctcaagt	9100
rs4783057	snp	A/G	0.420255	0.183066	intron-variant	USP10	GRCh38.p7	16:84752066	CAACTCCATTTTTCT[A/G]TATGTCAGCAGATTT	9100
rs4783058	snp	G/T	0.00597534	0.0543715	intron-variant	USP10	GRCh38.p7	16:84756994	GTCAGGTGGACCCAG[G/T]TTCAcaggtcatttc	9100
rs5818506	in-del	-/T	0.360842	0.224085	intron-variant	USP10	GRCh38.p7	16:84731776	AGCTCTTTTTTTTTT[-/T]GTGATAGTCTGTGCT	9100
rs6564067	snp	A/G	0.273587	0.248885	intron-variant	USP10	GRCh38.p7	16:84700806	CAGTAGCTAAAGCTT[A/G]GGGGCCCTTTACAAT	9100
rs6564068	snp	C/T	0.456568	0.140818	intron-variant	USP10	GRCh38.p7	16:84711144	GAGATTTCAGTTTGG[C/T]TTGGCATTCATTAAG	9100
rs6564069	snp	A/T	0.494013	0.0543839	intron-variant, utr-variant-5-prime	USP10	GRCh38.p7	16:84719921	CTTAGCTAGTATACC[A/T]CTTTTTGCATTCTTT	9100
rs6564070	snp	A/T	0.29432	0.24604	intron-variant	USP10	GRCh38.p7	16:84724011	AATGAATATGAAAGT[A/T]GGTGGAATCTTGAAC	9100
rs6564071	snp	C/G	0.0150606	0.0854603	intron-variant	USP10	GRCh38.p7	16:84724826	TTGGCGAACTTCCTG[C/G]TGTGCATTCACTAGT	9100
rs6564072	snp	C/G	0.316726	0.240931	intron-variant	USP10	GRCh38.p7	16:84727881	ATGCAGTACTTTTTT[C/G]TAACCTGTCCATATT	9100
rs6564073	snp	C/T	0.0142736	0.0832652	intron-variant	USP10	GRCh38.p7	16:84732413	CTCCGTTGTGGAAAT[C/T]GCTAATTCTTCTCAA	9100
rs6564074	snp	A/C	0.41325	0.18934	intron-variant	USP10	GRCh38.p7	16:84752644	AAGACCTGACTTTTG[A/C]ATGATAACAATAGGA	9100
rs6564075	snp	A/G	0.493881	0.054972	intron-variant	USP10	GRCh38.p7	16:84752741	TTTTTCACTGCGAGG[A/G]AGAAGAGGAGCTCAC	9100
rs6564076	snp	A/G	0.388587	0.208071	intron-variant	USP10	GRCh38.p7	16:84766813	GGTAAAGCAAAGATA[A/G]GGAATTCTTACAACG	9100
rs7184644	snp	A/C	0.352721	0.227922	intron-variant	USP10	GRCh38.p7	16:84752854	TGTTACAAAAGTGGA[A/C]CTTAAATGTTTCTTG	9100
rs7185379	snp	C/G	0.245631	0.249962	intron-variant	USP10	GRCh38.p7	16:84753109	GTAGTTGGGACTATA[C/G]GCAGGCACCACCATG	9100

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