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
rs8460	snp	A/C	0.456406	0.141076	synonymous-codon	TBL3	GRCh38.p7	16:1978401	TGTGCTCTTGAGGCG[A/C]GAGGCCCCCGAGGAG	10607
rs17602	snp	A/C	0.233067	0.249426	synonymous-codon	TBL3	GRCh38.p7	16:1975677	CCACAACCTGTTGCT[A/C]TACGAGGCTCGCTCC	10607
rs17603	snp	C/G/T	0.00692867	0.0584975	missense	TBL3	GRCh38.p7	16:1976870	CTGTGAAGCTGTGGC[C/G/T]TCTTCCCAAAGCCTT	10607
rs17604	snp	C/T	0.141914	0.225427	synonymous-codon	TBL3	GRCh38.p7	16:1976291	CGGTCACACACACAG[C/T]GTGGGCACCGTCTGC	10607
rs17605	snp	C/T	0.135717	0.22235	missense	TBL3	GRCh38.p7	16:1976890	CCCAAAGCCTTGCTG[C/T]CCAAGAACACAGCCC	10607
rs20548	snp	C/T	0.00104706	0.0228568	synonymous-codon	TBL3	GRCh38.p7	16:1975650	CGGCGTGGTCCTCAC[C/T]GCCACCGCCGACCAC	10607
rs1860236	snp	A/C	0.369142	0.219784	intron-variant	TBL3	GRCh38.p7	16:1973371	GGAGGTGGAGCTTGC[A/C]GTGAGCTGAGATCGT	10607
rs2159247	snp	C/T			upstream-variant-2KB	TBL3	GRCh38.p7	16:1970875	CGGCCACCCAAAGTG[C/T]TAGGATTACAGGCGT	10607
rs2230086	snp	A/G	0.166599	0.235678	missense	TBL3	GRCh38.p7	16:1975601	CGCCGGGCCCTGGGC[A/G]GGAGCTGACCCACTG	10607
rs2240690	snp	C/G	0.310632	0.242536	intron-variant	TBL3	GRCh38.p7	16:1976441	AGGCTCCAGCCCAAA[C/G]ATGTGGAACAGAACA	10607
rs2302178	snp	A/G	0.326741	0.23793	upstream-variant-2KB	TBL3	GRCh38.p7	16:1971892	GGTCTACCCCCACCG[A/G]CCCGCGAAGCACCCT	10607
rs3178284	snp	A/G			downstream-variant-500B, synonymous-codon	NOXO1, TBL3	GRCh38.p7	16:1978670	CTGGGAAACCCATAA[A/G]GGCGCACTGCCCTAG	10607
rs3743849	snp	A/C/T	1.69309e-05	0.0029095	intron-variant	TBL3	GRCh38.p7	16:1974701	TCTGTGCCCACGACC[A/C/T]ACCTGCACGGCAGGG	10607
rs3743850	snp	A/C	0.245372	0.249982	intron-variant	TBL3	GRCh38.p7	16:1974354	GAAAGAGTGGTGTGC[A/C]GAGCACGGTGTGAGT	10607
rs3743851	snp	A/G	0.477881	0.102812	intron-variant	TBL3	GRCh38.p7	16:1974130	CTGGCTGCCCGCCCC[A/G]CTGCCCTTCCCCAGG	10607
rs4325553	snp	C/T	0.33303	0.235809	intron-variant	TBL3	GRCh38.p7	16:1972358	AGGCTGCGGTGATAC[C/T]AGGCGGGAGAGCCGG	10607
rs8052713	snp	C/G	0.250819	0.249999	missense	TBL3	GRCh38.p7	16:1975603	CCGGGCCCTGGGCAG[C/G]AGCTGACCCACTGCA	10607
rs8053843	snp	A/C	0.365654	0.22164	synonymous-codon	TBL3	GRCh38.p7	16:1975205	CGGCCGTGACAAGAT[A/C]TGTATCATCTGGGAC	10607
rs8055439	snp	C/T	0.493613	0.0561475	upstream-variant-2KB	TBL3	GRCh38.p7	16:1971104	GGCCTGTGCCCTGGC[C/T]GTTCTCAACACCATT	10607
rs9933908	snp	A/C	0.0109809	0.0732794	intron-variant	TBL3	GRCh38.p7	16:1974897	CCACCCAGGCTGCAC[A/C]GCTCACCCATCCTGT	10607
rs9937671	snp	C/G	0.274929	0.248754	intron-variant	TBL3	GRCh38.p7	16:1972410	ACGGCGATCGGAGCC[C/G]GGCCGCCGGGAGCAG	10607
rs11555443	snp	G/T			missense	TBL3	GRCh38.p7	16:1974585	GGCTCAGTGGGCCTG[G/T]CAAGAGGGCAGCGTT	10607
rs11647257	snp	A/G	0.273484	0.248895	synonymous-codon, downstream-variant-500B	NOXO1, TBL3	GRCh38.p7	16:1979082	GGGGTGCGGCACAGA[A/G]TCCACGCACCCTCGA	10607
rs11859495	snp	A/G	0.143724	0.226286	intron-variant	TBL3	GRCh38.p7	16:1977954	TCTCCTCCCCTCCCC[A/G]CAGGCAGCAAGAGCT	10607
rs11863523	snp	C/T	0.0122943	0.0774339	intron-variant	TBL3	GRCh38.p7	16:1977942	CCCTCAGTGGCCTCT[C/T]CTCCCCTCCCCACAG	10607
rs11864416	snp	C/T	0.0133875	0.0807125	intron-variant	TBL3	GRCh38.p7	16:1978099	GAGGGGCTGGGTCTT[C/T]GGACCACTGGGCTCT	10607
rs12921076	snp	A/G	0.00368168	0.0427468	synonymous-codon	TBL3	GRCh38.p7	16:1974946	AGTGGCCTTCCACCC[A/G]GACCCTACACGCCTG	10607
rs12925447	snp	C/G	0.136965	0.222987	synonymous-codon	TBL3	GRCh38.p7	16:1975410	TGTGAAGTCCCCAGG[C/G]CTGTACTTTCTGACA	10607
rs12927376	snp	A/G	0.121223	0.214281	synonymous-codon, downstream-variant-500B	NOXO1, TBL3	GRCh38.p7	16:1979151	GCGTGTGACGGTGCA[A/G]CAGCGGCTCTGGATG	10607
rs12927588	snp	A/G	0.136265	0.222631	intron-variant	TBL3	GRCh38.p7	16:1975764	ACCAGCCCTCCTCTT[A/G]CACAGGTCCTGGCTC	10607
rs13334590	snp	A/T			intron-variant	TBL3	GRCh38.p7	16:1973718	TACCCAGGCCTGGCC[A/T]CCCACCGCCGGCAGG	10607
rs13334591	snp	A/T			intron-variant	TBL3	GRCh38.p7	16:1973722	CAGGCCTGGCCACCC[A/T]CCGCCGGCAGGGGTG	10607
rs17853425	snp	C/G			missense	TBL3	GRCh38.p7	16:1974611	GCGTTACCCGCCTGT[C/G]GAAGGCGATACACAC	10607
rs28396225	snp	C/T	0.105569	0.204058	utr-variant-5-prime	TBL3	GRCh38.p7	16:1972073	GCGCCGGGAGTGTGG[C/T]GTTCTGTGAAGAGTT	10607
rs34051952	in-del	-/C			intron-variant	TBL3	GRCh38.p7	16:1972676	GCCCCGTCACTCCCC[-/C]AAGCCTTTGCCGAAC	10607
rs34143457	snp	A/C	0.109108	0.206518	downstream-variant-500B	NOXO1, TBL3	GRCh38.p7	16:1978880	CCTGGCCTGGCAGAG[A/C]TCCAGCCCGCGGCTC	10607
rs34396682	snp	C/T	0.004633	0.0479065	synonymous-codon	TBL3	GRCh38.p7	16:1975392	TGGGGACTTCACACC[C/T]AGCTGGGACACTGGC	10607
rs34396773	snp	A/G	0.114036	0.209795	downstream-variant-500B	NOXO1, TBL3	GRCh38.p7	16:1978913	CACGCTTAGACGGTG[A/G]GGGTCATGCAGAACA	10607
rs34593003	snp	A/G	0.0916144	0.193427	intron-variant	TBL3	GRCh38.p7	16:1976442	GGCTCCAGCCCAAAG[A/G]TGTGGAACAGAACAG	10607
rs34660191	in-del	-/G			downstream-variant-500B	NOXO1, TBL3	GRCh38.p7	16:1978916	CTTAGACGGTGGGGG[-/G]TCATGCAGAACAAGC	10607
rs34731323	in-del	-/C			intron-variant	TBL3	GRCh38.p7	16:1976201	CTCTCCTCAACTCCC[-/C]TGTCCCCAGGATCAG	10607
rs34775709	snp	C/T	0.108402	0.206034	intron-variant	TBL3	GRCh38.p7	16:1976506	CCTCAGAAGTAGCCC[C/T]GGTGAAGTGGTTAAA	10607
rs34968293	snp	A/G	0.142202	0.225565	downstream-variant-500B, synonymous-codon	NOXO1, TBL3	GRCh38.p7	16:1978676	AACCCATAAAGGCGC[A/G]CTGCCCTAGCCGGTC	10607
rs35189805	snp	C/T	0.013199	0.0801579	synonymous-codon	TBL3	GRCh38.p7	16:1974558	AGCCAGCAGCAATGC[C/T]CGACTGGCTGTCACC	10607
rs35265313	snp	C/T	0.00436438	0.0465096	missense	TBL3	GRCh38.p7	16:1975254	TCCCCACCTCAAACA[C/T]AGGCACGGTCCTCGT	10607
rs35438477	snp	C/G	0.0551013	0.156571	intron-variant	TBL3	GRCh38.p7	16:1972803	GGAAAGTCCCAGGCT[C/G]GCAGCACCGTCGTGG	10607
rs35544607	snp	C/T	0.00569636	0.0530635	synonymous-codon	TBL3	GRCh38.p7	16:1975353	CAACAGCACAGCAGC[C/T]TCCACGCTCTGGAGA	10607
rs35637038	snp	G/T	0.112631	0.208878	downstream-variant-500B	NOXO1, TBL3	GRCh38.p7	16:1978831	GAAGGGCACTGGAGC[G/T]GATGGTCTCGGCCCT	10607
rs35795901	snp	A/G	0.130989	0.219855	intron-variant	TBL3	GRCh38.p7	16:1975957	CCACACGGGTGAGTG[A/G]GGCCAGCCCACCTGA	10607
rs35938501	snp	A/G	0.0919752	0.193722	intron-variant	TBL3	GRCh38.p7	16:1976634	GCCACCCGGTGCTGC[A/G]GGTGGACAATGTAGA	10607
rs35955001	snp	C/T	0.0704125	0.17392	intron-variant	TBL3	GRCh38.p7	16:1973853	ATCACCAGCCAGCTG[C/T]GGGTCTCTACTTCTC	10607
rs35958398	snp	A/G	0.0916144	0.193427	intron-variant	TBL3	GRCh38.p7	16:1976377	AGGCCTGCCAGCAGG[A/G]CTGCCGCTCAGGGAG	10607
rs36118556	snp	C/T	0.136347	0.222676	intron-variant	TBL3	GRCh38.p7	16:1976176	CACGCAGTAGGCCCA[C/T]GGACCAGCCTCTCTC	10607
rs56675820	snp	C/G	0.14933	0.228835	intron-variant	TBL3	GRCh38.p7	16:1973226	GCGGGCGGATCACGA[C/G]GTCAGGAGATTGAGA	10607
rs57349007	in-del	-/T			upstream-variant-2KB	TBL3	GRCh38.p7	16:1971226	CTTCTGTTTTTTTTT[-/T]CTTTCTTTCTTTCTT	10607
rs57455320	in-del	-/T			upstream-variant-2KB	TBL3	GRCh38.p7	16:1970624	TTACTTTTTTTTTTT[-/T]CTCTGAGACAGTCTT	10607
rs59669934	in-del	-/A	0.144296	0.226554	intron-variant	TBL3	GRCh38.p7	16:1973324	GTCCCAGCTACTCGG[-/A]GAGGCTGAGGCAGGA	10607
rs60529427	snp	C/G	0.178144	0.239451	intron-variant	TBL3	GRCh38.p7	16:1973752	GTTCCCAAGGAGCCC[C/G]CTGGCTCTCACTGGG	10607
rs60652688	in-del	-/GT/TG	0.0398539	0.13542	upstream-variant-2KB	TBL3	GRCh38.p7	16:1970551	CTACTAAATTTTCTG[-/GT/TG]TGTGTGTGTGTGTGT	10607
rs61516948	snp	C/T	0.144969	0.226867	intron-variant	TBL3	GRCh38.p7	16:1973321	GTAGTCCCAGCTACT[C/T]GGAGAGGCTGAGGCA	10607
rs62038785	snp	A/C	0.5	0	intron-variant	TBL3	GRCh38.p7	16:1973190	CTCACGCCTGTAATC[A/C]CAGCGCTTTTGGAGG	10607
rs62038786	snp	A/G	0.5	0	intron-variant	TBL3	GRCh38.p7	16:1973192	CACGCCTGTAATCCC[A/G]GCGCTTTTGGAGGCC	10607
rs66471978	snp	C/T	0.141883	0.225412	intron-variant	TBL3	GRCh38.p7	16:1977290	CTGTCTCAAGGTAAG[C/T]GGCGCTCCAGACCCT	10607
rs66748999	snp	C/T	0.140459	0.224724	intron-variant	TBL3	GRCh38.p7	16:1977312	CCAGACCCTCCCCAC[C/T]TCCCGCCCTGGTGAC	10607
rs67220861	snp	A/G	0.135574	0.222276	intron-variant	TBL3	GRCh38.p7	16:1976985	ATAGCCACTGGGGTG[A/G]GGGTGTGGCCAAGCC	10607
rs71385727	snp	C/T	0.0126979	0.078662	intron-variant	TBL3	GRCh38.p7	16:1973216	GGAGGCCGAAGCGGG[C/T]GGATCACGAGGTCAG	10607
rs72764901	snp	A/G	0.0209421	0.100162	intron-variant	TBL3	GRCh38.p7	16:1973728	TGGCCACCCACCGCC[A/G]GCAGGGGTGTTCCCA	10607
rs74002751	snp	C/T	0.000399281	0.0141238	intron-variant	TBL3	GRCh38.p7	16:1977879	GGCTGAGTGCCAGGC[C/T]CCCTGCCTGCTGACT	10607
rs74907106	snp	C/T	0.00967442	0.0688739	synonymous-codon	TBL3	GRCh38.p7	16:1975656	GGTCCTCACCGCCAC[C/T]GCCGACCACAACCTG	10607
rs76059545	snp	A/G	0.0240643	0.107019	intron-variant	TBL3	GRCh38.p7	16:1973083	TGGGCAGAAGGGAGG[A/G]GCTAACGCAGGGCAG	10607
rs76890223	snp	C/G	0.5	0	missense	TBL3	GRCh38.p7	16:1974777	GGTGGCTGTGATGGG[C/G]CCGTGCGCGTCTGGG	10607
rs77311024	snp	C/T	0.000217161	0.0104179	missense	TBL3	GRCh38.p7	16:1974783	TGTGATGGGGCCGTG[C/T]GCGTCTGGGACATCG	10607
rs77402400	snp	C/G	0.00641623	0.0562756	intron-variant	TBL3	GRCh38.p7	16:1974306	AGGTGAGGGCAGCCT[C/G]GGTGGGTGAGGGGCA	10607
rs77771180	snp	C/T	0.0162398	0.0886349	upstream-variant-2KB	TBL3	GRCh38.p7	16:1971810	AAAAGCAGGAGTAAA[C/T]GCTGGCTACAAATGC	10607
rs77882016	snp	C/G	0.185472	0.241529	intron-variant	TBL3	GRCh38.p7	16:1973748	GGGTGTTCCCAAGGA[C/G]CCCCCTGGCTCTCAC	10607
rs78086648	snp	C/G	0.0530448	0.153976	upstream-variant-2KB	TBL3	GRCh38.p7	16:1970549	CCCCTACTAAATTTT[C/G]TGTGTGTGTGTGTGT	10607
rs78289321	snp	C/T	0.000599269	0.0172996	missense	TBL3	GRCh38.p7	16:1974655	ACCATGGCCTTCGAC[C/T]CCACCTCCACTCTGC	10607
rs79259772	snp	A/G	0.0236746	0.106192	intron-variant	TBL3	GRCh38.p7	16:1973660	GAAGAGGTATGCCAG[A/G]CCTCAGGGATGAAGA	10607
rs79378611	snp	C/T	0.0941369	0.195465	upstream-variant-2KB	TBL3	GRCh38.p7	16:1970950	AGCCAGTAGCACAAA[C/T]GGCTCAAAACCTTGA	10607
rs79412280	snp	A/G	0.00761655	0.0612394	missense	TBL3	GRCh38.p7	16:1978155	CTCCCACAGCCATCC[A/G]GAGGGACCCTGAGGC	10607
rs79976559	snp	C/G	0.0103295	0.0711199	utr-variant-3-prime, downstream-variant-500B	NOXO1, TBL3	GRCh38.p7	16:1978996	GAGATCCGCCCTCCC[C/G]GCTCCTCCCCAGCCC	10607
rs111267541	snp	A/G	0.5	0	intron-variant	TBL3	GRCh38.p7	16:1974321	GGGTGGGTGAGGGGC[A/G]AGTGGAGAGGGCAGC	10607
rs111440237	in-del	-/G	0	0	intron-variant	TBL3	GRCh38.p7	16:1973748	GGGTGTTCCCAAGGA[-/G]CCCCCTGGCTCTCAC	10607
rs111549353	snp	C/G	0.00597247	0.0543191	intron-variant	TBL3	GRCh38.p7	16:1973734	CCCACCGCCGGCAGG[C/G]GTGTTCCCAAGGAGC	10607
rs111968775	snp	A/G	1.66938e-05	0.00288905	missense	TBL3	GRCh38.p7	16:1977234	CTGGCCACGGCCTCA[A/G]CTGATGGCACCATCA	10607
rs111994180	snp	A/G	0.000156556	0.00884609	missense	TBL3	GRCh38.p7	16:1977515	CACCCCAAACCCAGC[A/G]GTTCGGATGGCCTCG	10607
rs112060107	snp	C/G	0.0182019	0.0936463	intron-variant	TBL3	GRCh38.p7	16:1973558	GAAGGAAGGAGAAGG[C/G]GCACGAGTGAGGTCA	10607
rs112167806	snp	C/T	0.0729998	0.176553	intron-variant	TBL3	GRCh38.p7	16:1973908	CTGCAGTACTGCTGG[C/T]TCCACCCCATGCCCT	10607
rs112196938	snp	A/G	0.5	0	synonymous-codon	TBL3	GRCh38.p7	16:1978186	CTGCGAGAAGCTGGA[A/G]GCCACCATGCTCCGA	10607
rs112544386	snp	C/T	0.0134861	0.0810011	intron-variant	TBL3	GRCh38.p7	16:1973703	GTGCTCTGGGCTGGC[C/T]ACCCAGGCCTGGCCA	10607
rs112842863	snp	A/G	0.00863075	0.0651221	intron-variant	TBL3	GRCh38.p7	16:1977703	CAGGGAAGAGTCGGG[A/G]TGGAGTGGAGGCCCC	10607
rs112862967	snp	A/G	0.000399281	0.0141238	intron-variant	TBL3	GRCh38.p7	16:1972394	GCTGCTCTCGGGGAG[A/G]ACGGCGATCGGAGCC	10607
rs113040184	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	TBL3	GRCh38.p7	16:1971420	TTTCTGTTTTTAGTA[A/G]AGACGGGGTTTCTCC	10607
rs113851238	in-del	-/G	0	0	intron-variant	TBL3	GRCh38.p7	16:1973752	TTCCCAAGGAGCCCC[-/G]CTGGCTCTCACTGGG	10607
rs113941997	snp	C/T	0.5	0	missense	TBL3	GRCh38.p7	16:1974816	CGGCACTACGGGACA[C/T]ACCACTTCCGAGGCT	10607
rs114412717	snp	C/T	0.00047826	0.0154564	intron-variant	TBL3	GRCh38.p7	16:1976023	CCTTCCCCCGTCTTG[C/T]TGTGTGACCTATACC	10607
rs114835742	snp	A/G	0.0788843	0.182262	intron-variant	TBL3	GRCh38.p7	16:1973875	CTACTTCTCAGTGAC[A/G]ACGGTAGCTACAGCC	10607
rs115260840	snp	A/G	0.0711525	0.174681	intron-variant	TBL3	GRCh38.p7	16:1972315	TGGAGGCGAGAGGCT[A/G]TGTGTGCGCCGGCCC	10607
rs115403611	snp	A/G	0.00295351	0.0383149	intron-variant	TBL3	GRCh38.p7	16:1974924	CTGTCCCGTCCGCCC[A/G]CAGCCTAGTGGCCTT	10607
rs115975390	snp	C/T	0.0766824	0.180169	intron-variant	TBL3	GRCh38.p7	16:1972813	AGGCTGGCAGCACCG[C/T]CGTGGGAGGGTCAAC	10607

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