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
rs110675	snp	A/G	0.26818	0.249338	intron-variant	TRIM16	GRCh38.p7	17:15675538	TACAAAACATATAAA[A/G]GTCTACACTGGAGAG	10626
rs149261	snp	C/T	0.261056	0.249755	upstream-variant-2KB	TRIM16	GRCh38.p7	17:15683986	TATCCGAGACACCTC[C/T]GGGTCGTTTGCTTGG	10626
rs151315	snp	A/G	0.441841	0.160303	intron-variant	TRIM16	GRCh38.p7	17:15680201	AAAGTCCTTTTAAGC[A/G]GCTCCTAGGCTAATG	10626
rs163368	snp	C/T	0.244205	0.249933	intron-variant	TRIM16	GRCh38.p7	17:15666661	atagtgcctactata[C/T]atttccatttatatg	10626
rs163369	snp	A/G	0.290201	0.246747	intron-variant	TRIM16	GRCh38.p7	17:15665794	tgagctgagacatca[A/G]tttgtgagccataaa	10626
rs163370	snp	C/T	0.42	0.183303	intron-variant	TRIM16	GRCh38.p7	17:15665366	acccaccaccatgcc[C/T]ggctaattttttgtg	10626
rs163378	snp	C/T	0.46875	0.121031	intron-variant	TRIM16	GRCh38.p7	17:15679806	GGGACTACAGGCACC[C/T]GCCACCGCGCCCGGC	10626
rs163379	snp	G/T	0.475348	0.108251	intron-variant	TRIM16	GRCh38.p7	17:15679853	GCCTCCCAGGTTCAC[G/T]CCATTCTCCTGCCTC	10626
rs163380	snp	A/G	0.46014	0.13543	intron-variant	TRIM16	GRCh38.p7	17:15680042	GTACATTGAAATCAC[A/G]GAGGTGTTGTTCCAC	10626
rs163381	snp	C/T	0.322483	0.239262	intron-variant	TRIM16	GRCh38.p7	17:15680449	AGATATGCAAAGGCA[C/T]GTGAGGCATTTCTTG	10626
rs163382	snp	A/C	0.473266	0.112482	intron-variant	TRIM16	GRCh38.p7	17:15680663	ATGAGATGGTGTTTG[A/C]GTGTTCCTCAGTTGT	10626
rs163383	snp	C/G	0.46014	0.13543	intron-variant	TRIM16	GRCh38.p7	17:15682501	TGTATCTCCTTAAGA[C/G]AAAGCGCTTTTTAAG	10626
rs163384	snp	A/G	0.441568	0.160629	intron-variant	TRIM16	GRCh38.p7	17:15682836	GAGTGTGCGAAGAAT[A/G]GTGGTGATTTTACTA	10626
rs163385	snp	A/G	0.250168	0.25	upstream-variant-2KB	TRIM16	GRCh38.p7	17:15684031	ACCCCACTCCCACAC[A/G]CACAAAACCCAAAGA	10626
rs163386	snp	C/T	0.366473	0.221211	upstream-variant-2KB	TRIM16	GRCh38.p7	17:15684560	gtaatcccagctact[C/T]gggagtctgaggagg	10626
rs163388	snp	G/T	0	0	intron-variant	TRIM16	GRCh38.p7	17:15674315	TGGCATGATCTCAGC[G/T]CACTGTGACCTCCGC	10626
rs163389	snp	A/G	0.24449	0.249939	intron-variant	TRIM16	GRCh38.p7	17:15676160	catcctacaatgcac[A/G]ggacggggccccaca	10626
rs163390	snp	A/G	0.29432	0.24604	intron-variant	TRIM16	GRCh38.p7	17:15676580	ggcgtggtggcgggc[A/G]cctgtagtcccagct	10626
rs163391	snp	A/G	0.360421	0.224293	intron-variant	TRIM16	GRCh38.p7	17:15676815	GGAAAgaatttgaat[A/G]attttaaggatataa	10626
rs170912	snp	A/C	0.264358	0.249587	upstream-variant-2KB	TRIM16	GRCh38.p7	17:15684089	CAAGGTGGCCGAACC[A/C]TAGCTCCAGCAGAAG	10626
rs186840	snp	G/T	0.330482	0.236691	intron-variant	TRIM16	GRCh38.p7	17:15667828	attagttcattaatt[G/T]tgacaaactatcata	10626
rs189280	snp	A/G	0.372794	0.217765	intron-variant	TRIM16	GRCh38.p7	17:15677060	CATCTTCACTTGACC[A/G]CATCAGAATCCTAAT	10626
rs234607	snp	A/G	0.327914	0.237549	intron-variant	TRIM16	GRCh38.p7	17:15670803	ACCGTGATACTGAAT[A/G]AGCAAAGAATCCTAA	10626
rs234608	snp	A/G	0.372391	0.217992	intron-variant	TRIM16	GRCh38.p7	17:15680241	GAGAGATTTAGGAAG[A/G]TTTTATTCATTCAAC	10626
rs489698	snp	C/G	0.317783	0.244462	intron-variant	TRIM16	GRCh38.p7	17:15669802	TTGTCCCACCCAAAA[C/G]GGCAGTAGCACTGAG	10626
rs494460	snp	C/T	0.282632	0.247861	intron-variant	TRIM16	GRCh38.p7	17:15669243	ATTCAGTGGTCATGC[C/T]GCTATTTCTGTAGGA	10626
rs498213	snp	C/T	0.283684	0.24772	intron-variant	TRIM16	GRCh38.p7	17:15668833	AGCCAATTGAACTAA[C/T]TGTCCTTATTGAATA	10626
rs510387	snp	A/G			intron-variant	TRIM16	GRCh38.p7	17:15652508	tcactctgtcgccca[A/G]gctggagtgcagtgt	10626
rs535972	snp	A/G	0.1638	0.234669	intron-variant	TRIM16	GRCh38.p7	17:15670815	TGAAGTCATGGCTTA[A/G]GATTCTTTGCTTATT	10626
rs642537	snp	C/G	0	0	intron-variant	TRIM16	GRCh38.p7	17:15656797	aaactttgtcgccca[C/G]gctgtaacgtagtgg	10626
rs656485	snp	G/T	0	0	intron-variant	TRIM16	GRCh38.p7	17:15651017	GCGTCAGTGGACCTA[G/T]CAGCTGCAGCCAGCT	10626
rs657363	snp	A/G/T	1.64738e-05	0.00286995	missense, synonymous-codon	TRIM16	GRCh38.p7	17:15651202	GAAGGCAGACAGTGG[A/G/T]CTGTGGTGGGCAGGA	10626
rs657380	snp	A/G	0	0	synonymous-codon	TRIM16	GRCh38.p7	17:15651217	TCTGTGGTGGGCAGG[A/G]CAGTATCGCCAGTTG	10626
rs671150	snp	C/T	0.267091	0.249415	intron-variant	TRIM16	GRCh38.p7	17:15668555	gcgtcattccccctc[C/T]tcctcaggccctcgt	10626
rs673343	snp	A/G			intron-variant	TRIM16	GRCh38.p7	17:15652490	tttttttgagacaca[A/G]tctcactctgtcgcc	10626
rs685251	snp	A/G	0.287606	0.247155	intron-variant	TRIM16	GRCh38.p7	17:15669339	ATAGGACATCCATAC[A/G]TCAGAACACAATGCA	10626
rs886915	snp	A/G	0.1302	0.219426	intron-variant	TRIM16	GRCh38.p7	17:15636992	GAGGAAACCTTCAGA[A/G]CTTGGAAAGATGTTG	10626
rs886916	snp	C/G	0	0	intron-variant	TRIM16	GRCh38.p7	17:15636909	AGTCCACATGCATGT[C/G]CCCCATCATTCAAAC	10626
rs886917	snp	A/C/T	0.0582	0.160352	intron-variant	TRIM16	GRCh38.p7	17:15636894	GCCCCATCATTCAAA[A/C/T]CCTTAATGTTTCTCA	10626
rs886918	snp	A/G	0.00318978	0.0398085	intron-variant	TRIM16	GRCh38.p7	17:15636791	TTGGGTGCCATGGTC[A/G]TCTGCACCCTAAACA	10626
rs1060899	snp	G/T	0	0	missense	TRIM16	GRCh38.p7	17:15628747	GACTCTGGTTCACAA[G/T]TTTGCCTGCAAATTT	10626
rs1060903	snp	G/T	0.399196	0.200601	missense	TRIM16	GRCh38.p7	17:15628628	CACCGTCCTTGGTGG[G/T]GACTGCTCCCTAGAC	10626
rs1060904	snp	G/T	0.0176531	0.0922763	utr-variant-3-prime	TRIM16	GRCh38.p7	17:15628547	TTTTAGGGTGATTTG[G/T]GGGCAGAAATAACTG	10626
rs1060926	snp	G/T	0	0	utr-variant-3-prime	TRIM16	GRCh38.p7	17:15628150	AGTGCTGGGATTACA[G/T]GCGTGAGCCACTGCG	10626
rs1138102	snp	C/T			utr-variant-3-prime	TRIM16	GRCh38.p7	17:15628358	gcagtggcgcgatct[C/T]ggctcactgcaagct	10626
rs1138113	snp	C/T	0.277778	0.248452	utr-variant-3-prime	TRIM16	GRCh38.p7	17:15628200	GGCAGATCTCAAACT[C/T]CTGACCTCGTGATGC	10626
rs1138116	snp	C/T	0.277778	0.248452	utr-variant-3-prime	TRIM16	GRCh38.p7	17:15628182	GACCTCGTGATGCAC[C/T]CACCTCGGCCTCCCA	10626
rs1377218	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15634988	ACACCAACAAAGCGT[C/T]TGTCAGTTTCTTTGC	10626
rs1377219	snp	A/G	0.4872	0.0789694	intron-variant	TRIM16	GRCh38.p7	17:15634966	TTTCTTTGCTTTTCA[A/G]TATCAAAACACGAAG	10626
rs1377220	snp	A/G	0.474813	0.109357	intron-variant	TRIM16	GRCh38.p7	17:15634954	TCAGTATCAAAACAC[A/G]AAGAAAATATGAATA	10626
rs1476728	snp	C/T	0.498277	0.0293024	intron-variant	TRIM16	GRCh38.p7	17:15661232	CATTTTCTCACAAAC[C/T]GTAAGGTTTTTGTAA	10626
rs1503130	snp	A/C	0.326976	0.237854	intron-variant	TRIM16	GRCh38.p7	17:15663265	AGCGATCCTGAGTGG[A/C]GAGGAGAGTGGCACG	10626
rs1563010	snp	C/T	0.101658	0.201233	intron-variant	TRIM16	GRCh38.p7	17:15664464	TCCGCCCACCTCGGC[C/T]TCCTAGAATGCTGGG	10626
rs1563011	snp	C/T	0.151668	0.229849	intron-variant	TRIM16	GRCh38.p7	17:15662638	AGAGCAGATCAGCCT[C/T]TGAAAGCTGCCACTG	10626
rs1566722	snp	A/C	0.0696804	0.173161	intron-variant	TRIM16	GRCh38.p7	17:15675120	TCATTTCAGGTACAG[A/C]CAAAAATACACACAT	10626
rs1875692	snp	C/T	0.400682	0.199487	intron-variant	TRIM16	GRCh38.p7	17:15654889	AAGTATCCTCCTCAA[C/T]CCCTTGGTCTCTTTG	10626
rs1901691	snp	A/C	0.0905871	0.19279			GRCh38.p7	17:15659505	GCGTGACATTTTATG[A/C]GGCACATAGCACATT	10626
rs1910344	snp	C/G	0.3942	0.204221	intron-variant	TRIM16	GRCh38.p7	17:15636483	ATCCATTTGATGAGA[C/G]AGTGAATTCCTCTAT	10626
rs1910345	snp	C/T	0.42	0.183303	intron-variant	TRIM16	GRCh38.p7	17:15636557	GTCAAGTTTCCGAAA[C/T]TGATTTTCCTACCAG	10626
rs2012604	snp	C/T	0.067446	0.170804	intron-variant	TRIM16	GRCh38.p7	17:15664757	gtgagccaccgcgcc[C/T]ggccTGTTTCCTGGT	10626
rs2074890	snp	G/T	0.14418	0.226504	missense	TRIM16	GRCh38.p7	17:15651247	CCACCTGCTGACCGA[G/T]CCAGTGAAGGACCAC	10626
rs2159084	snp	C/T	0.107694	0.205546	intron-variant	TRIM16	GRCh38.p7	17:15662915	ATACCTAGTAGTAGC[C/T]CTGCCCTATCCTGGA	10626
rs2252683	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15680155	AAGAATTTACTCAGC[C/T]TTCAGGGCCCACATC	10626
rs2323790	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15634684	aggtgtggtggcggg[C/T]gcctgtaatcccagc	10626
rs2323791	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15634704	gtaatcccagctact[C/T]gggaggctgaggcag	10626
rs2323792	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15634735	agaattgcttgaatc[C/T]gggaggcggaggttg	10626
rs2323793	snp	A/G	4.99276e-05	0.00499613	intron-variant	TRIM16	GRCh38.p7	17:15636275	ACACCGACACCTGGC[A/G]GGGGGTGGGGGTGGA	10626
rs2323794	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15636531	ACAACTCTGACACTC[C/T]GGGATTGTTAGTCAA	10626
rs2323795	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15636580	CCTACCAGAGCAATG[C/T]GTGTATTCAGTCTAC	10626
rs2323796	snp	A/G	0.139903	0.224452	intron-variant	TRIM16	GRCh38.p7	17:15639619	AGCCCTGTTGTCCAG[A/G]GCTGGCCCTCACCCT	10626
rs2323797	snp	A/T			intron-variant	TRIM16	GRCh38.p7	17:15641285	TACATTCAAGGAGCC[A/T]GCAGGTAATGGTTTA	10626
rs2323798	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15680151	TTTCAAGAATTTACT[C/T]AGCTTTCAGGGCCCA	10626
rs2455770	snp	G/T			intron-variant	TRIM16	GRCh38.p7	17:15676121	tgtctgtctaaaacg[G/T]caacagtgctgcagt	10626
rs2530092	snp	A/G			intron-variant	TRIM16	GRCh38.p7	17:15682222	GTATAGAAAGAAAGC[A/G]CCATAAAGTCTTGGT	10626
rs2530096	snp	A/G	0.5	0	intron-variant	TRIM16	GRCh38.p7	17:15681585	AGACCAAGGGAATTT[A/G]GGGCTCATTCATTAA	10626
rs2530099	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15680838	ATTTTCCTCTCTTCT[C/T]GGAAATTTTATTTTA	10626
rs2530103	snp	G/T	0.0569829	0.158885	intron-variant	TRIM16	GRCh38.p7	17:15678940	tgcggtaagccgaga[G/T]catcgtggccactgc	10626
rs2530104	snp	A/C			intron-variant	TRIM16	GRCh38.p7	17:15678924	catcgtggccactgc[A/C]ctccagcaacagagt	10626
rs2530107	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15678574	ctagcctctttacca[C/T]atggcttccaaactc	10626
rs2530108	snp	C/T			intron-variant	TRIM16	GRCh38.p7	17:15675651	TTCCCACACTCCTGA[C/T]AATCAAATGGTTTCT	10626
rs2530111	snp	A/G			intron-variant	TRIM16	GRCh38.p7	17:15673964	CAGAAAGTAAGAACC[A/G]TTTACCTTGGAAACT	10626
rs2530113	snp	C/T	0.00478085	0.0486577	intron-variant	TRIM16	GRCh38.p7	17:15671611	ATACGGTTAAAAAAA[C/T]CACGTGAAATAGAGT	10626
rs2601964	snp	A/G	0.497984	0.0316851			GRCh38.p7	17:15646680	AGAGATGAAAAATAG[A/G]AAGAACAGGGAGAGT	10626
rs2601968	snp	C/G					GRCh38.p7	17:15669929	gtgacaaccaaaact[C/G]tctccagacactggc	10626
rs2601972	snp	G/T	0.5	0			GRCh38.p7	17:15671425	TTGGTGCATATGGGT[G/T]AATTCTTGTTAAGTA	10626
rs2601978	snp	A/G					GRCh38.p7	17:15675246	CAAGAGAAAATAACC[A/G]GGGTAGGAGAGGAGG	10626
rs2601979	snp	C/T					GRCh38.p7	17:15675330	AGTATAATTCTTTGG[C/T]ATTTAACCAAATGAA	10626
rs2601980	snp	C/T					GRCh38.p7	17:15680097	ATCAGTATCTTGCTT[C/T]GATTCTAAGTCATTT	10626
rs2601984	snp	C/T					GRCh38.p7	17:15680575	TTCCCATCCTGCCCC[C/T]ACCATCCTTTCTCTA	10626
rs2601985	snp	C/T					GRCh38.p7	17:15680589	CTACCATCCTTTCTC[C/T]ACACTGCCAACTGAT	10626
rs2601988	snp	C/T	0	0			GRCh38.p7	17:15682472	GAAGTCCCTTCTAAT[C/T]TGGGGGATCCCTTTG	10626
rs2601989	snp	G/T					GRCh38.p7	17:15684799	gattgtatttttcat[G/T]taattcattggattc	10626
rs2649445	snp	A/C/G	0.000399281	0.0141238	intron-variant	TRIM16	GRCh38.p7	17:15665921	cctccctagatccca[A/C/G]cacaacaaatttaac	10626
rs2649446	snp	A/C	0.00914312	0.0669923	intron-variant	TRIM16	GRCh38.p7	17:15666047	acaacccatgtccat[A/C]ccatcaccattttac	10626
rs2649448	snp	C/G			intron-variant	TRIM16	GRCh38.p7	17:15666685	gcactattgtgtctg[C/G]cttatttcactcaat	10626
rs2649454	snp	A/G	0.498652	0.0259235	intron-variant	TRIM16	GRCh38.p7	17:15646254	ACCTCAAAAGGTGGA[A/G]CCACTTTGAAAGACT	10626
rs2649456	snp	A/G	0.5	0	intron-variant	TRIM16	GRCh38.p7	17:15670900	TATCAATAATATACA[A/G]ATGAATATTGTCTAA	10626
rs2649462	snp	A/T			intron-variant	TRIM16	GRCh38.p7	17:15672587	aaatacaaacaaatt[A/T]gccgggtgtggtgac	10626
rs2649463	snp	A/T	0.046775	0.145601	intron-variant	TRIM16	GRCh38.p7	17:15672753	aacaaacaaacaaac[A/T]aaTCTGAGAGGAGAG	10626
rs2654347	snp	A/G	0	0	intron-variant	TRIM16	GRCh38.p7	17:15681664	AGTTCTCTCCCTACA[A/G]GCAAAAAAATCAAAA	10626

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