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
rs7498	snp	C/T	0.379464	0.213867	synonymous-codon, downstream-variant-500B	FLII, LLGL1	GRCh38.p7	17:18245171	TACCCGCTGCTTCCA[C/T]GCCTGGAGCGCCTTC	3996
rs8821	snp	A/G	0.0344789	0.126691	missense, downstream-variant-500B	FLII, LLGL1	GRCh38.p7	17:18245220	GGCCGCGCCGGCTGC[A/G]CCTGGTCCGCAAGGG	3996
rs11382	snp	G/T	0	0	utr-variant-3-prime, downstream-variant-500B	FLII, LLGL1	GRCh38.p7	17:18244960	TGCCCTCAGGGGTCT[G/T]GGAAATCCAACTCTC	3996
rs1063682	snp	A/G/T	3.34448e-05	0.00408917	missense	LLGL1	GRCh38.p7	17:18236710	ACAGACTGTGAGCAC[A/G/T]CTGACAGCCTGGCCC	3996
rs1063683	snp	C/G	0	0	missense	LLGL1	GRCh38.p7	17:18237519	TGTGCCGGTGGAGCA[C/G]GCGGTCAGCGTGGCC	3996
rs1063684	snp	C/T	0	0	synonymous-codon	LLGL1	GRCh38.p7	17:18237534	GGCGGTCAGCGTGGC[C/T]ATCATAGACCTCCTC	3996
rs1063685	snp	C/T	5.11252e-05	0.00505569	missense	LLGL1	GRCh38.p7	17:18237608	GCCCACGCACGGGGC[C/T]GCTGCCCTGGCCTGC	3996
rs1063686	snp	C/T	0	0	missense	LLGL1	GRCh38.p7	17:18237637	GCTGGCTTCCAGCCC[C/T]GTGTCCTGGTGCAGT	3996
rs1063687	snp	A/G	3.35632e-05	0.0040964	synonymous-codon	LLGL1	GRCh38.p7	17:18238515	CGACGTGGAGATGAC[A/G]CCCGTGCAGCGCCGC	3996
rs1063688	snp	C/G	0	0	missense	LLGL1	GRCh38.p7	17:18240823	CTGGCGCAGGCACCT[C/G]ACATGCAGGGTGGTC	3996
rs1063689	snp	G/T	0	0	synonymous-codon	LLGL1	GRCh38.p7	17:18240837	TGACATGCAGGGTGG[G/T]CACGCTGTGCTCATC	3996
rs1063690	snp	C/G/T	8.09881e-05	0.00636298	synonymous-codon	LLGL1	GRCh38.p7	17:18240849	TGGTCACGCTGTGCT[C/G/T]ATCGCATCTGAGGAG	3996
rs1063691	snp	C/G			missense	LLGL1	GRCh38.p7	17:18241640	GTGCCTCTGCGGCCC[C/G]AGGTGCACTATTCCT	3996
rs2245430	snp	C/T	0.410905	0.191336	intron-variant	LLGL1	GRCh38.p7	17:18238391	TAACAGAACGTAGGG[C/T]GCAAAGCAGGATGCA	3996
rs2245737	snp	C/T	0.494149	0.0537694	intron-variant	LLGL1	GRCh38.p7	17:18241406	GAGGGGCCCTGGGGA[C/T]GAGGACAGGGCCAGG	3996
rs2290502	snp	A/G	0.349671	0.229272	intron-variant	LLGL1	GRCh38.p7	17:18230181	AGTGGGGGCTTCTGC[A/G]GAGGTTGGCGTGGCT	3996
rs2290503	snp	C/T	0.346368	0.23068	intron-variant	LLGL1	GRCh38.p7	17:18232439	GAGCCTTGGGTGTCT[C/T]CCTCACTGTGGTTTG	3996
rs2290504	snp	C/T	0.346147	0.230772	intron-variant	LLGL1	GRCh38.p7	17:18233674	GGCCCTGGTGAGTGC[C/T]GTGGGGCCAGTGATG	3996
rs2290505	snp	A/G	0.365994	0.221462	missense	LLGL1	GRCh38.p7	17:18233827	CTGCTGGTGGCTGCC[A/G]GCGACATAGCAGCCC	3996
rs2290506	snp	A/G	0.000116033	0.00761598	intron-variant	LLGL1	GRCh38.p7	17:18234835	CACCTCCCTCTGCAC[A/G]TAGGGGCCACTTTAT	3996
rs2290507	snp	A/G	0.27893	0.24832	intron-variant	LLGL1	GRCh38.p7	17:18235775	CCCAGGGCTCCACCC[A/G]CCCAGCCTGCCTGCC	3996
rs2290508	snp	A/G	0.021333	0.101051	intron-variant	LLGL1	GRCh38.p7	17:18235834	CGCTGAGCTGCCCAG[A/G]GAAGGTGCCAGAGAG	3996
rs2290509	snp	A/G	0.0550147	0.156463	intron-variant	LLGL1	GRCh38.p7	17:18242136	TCAAGTCATCCACCT[A/G]TGGTCCCCATCATGG	3996
rs2290510	snp	C/G/T	0.0002482	0.0111374	missense, synonymous-codon	LLGL1	GRCh38.p7	17:18242551	CTCACCCATGTCCAT[C/G/T]GACTCAGCCACCAGT	3996
rs2305563	snp	C/T	0.00437657	0.0465739	synonymous-codon	LLGL1	GRCh38.p7	17:18237729	TGGCACCAGTCATGG[C/T]TTTGGCCTCTTCGAC	3996
rs2473656	snp	A/G	0.396727	0.202413	intron-variant	LLGL1	GRCh38.p7	17:18237259	CTTTGCCCTCAGAGG[A/G]CAGGGACTAGTGTGT	3996
rs2605131	snp	C/T	0.472803	0.113397			GRCh38.p7	17:18225127	TGGAGTTCTGTGAAA[C/T]TGGTAAAATATAAAC	3996
rs2605132	snp	A/G	0.358728	0.225118			GRCh38.p7	17:18225160	GGCAATCACTTGACC[A/G]ATGGTGTAGATGGGG	3996
rs2605133	snp	C/T	0.41325	0.18934			GRCh38.p7	17:18226468	ATCCCTTCAAGGAGC[C/T]TCTCCTTCCTTCCCC	3996
rs2605134	snp	C/T	0.49703	0.0384237			GRCh38.p7	17:18226830	ACTGCTCTGGGGACG[C/T]TGGTTTTGTCCTCAT	3996
rs2605135	snp	C/T	0.493568	0.0563433			GRCh38.p7	17:18227773	CTCAGCCCACTCTGG[C/T]TAGCCTTGGGGTGGC	3996
rs2605136	snp	C/T	0.36315	0.222928			GRCh38.p7	17:18233436	CAGGAGATGTCTGAG[C/T]GCTGGCAGCGGGATT	3996
rs2605137	snp	A/G	0.318174	0.240525			GRCh38.p7	17:18236086	CTGGGGCCCTGCTTG[A/G]ACTCTGCAGCTGTGT	3996
rs2605138	snp	C/T	0.318174	0.240525			GRCh38.p7	17:18241369	TTGTGGTGGGGGCTG[C/T]TGGGTCAGCAGCCAC	3996
rs2746026	snp	C/T	0.491577	0.0643472	intron-variant	LLGL1	GRCh38.p7	17:18231040	GTGCTGCGCTGCGTG[C/T]GCACATGTGTCCCTG	3996
rs2746027	snp	A/G	0.317933	0.240593	intron-variant	LLGL1	GRCh38.p7	17:18232087	TGCCTGATCCCATCC[A/G]GCAAGGCGCAGCTCC	3996
rs2746028	snp	G/T	0.490697	0.0675648	intron-variant	LLGL1	GRCh38.p7	17:18236582	CCAGGAACTCGGGTA[G/T]CCCTGACATCTGCCC	3996
rs2746029	snp	C/G	0.497502	0.035255	intron-variant	LLGL1	GRCh38.p7	17:18239426	AAAAATAGAGAGGTG[C/G]AAAGTTGTCCCACAT	3996
rs2746030	snp	A/G	0.318174	0.240525	intron-variant	LLGL1	GRCh38.p7	17:18242065	TCTCATCCCACCCCC[A/G]AGATCTGCCTTCCCT	3996
rs2746031	snp	A/C			intron-variant	LLGL1	GRCh38.p7	17:18243423	ACAAGACCAGATTAA[A/C]CCACTTAGAGGTGGC	3996
rs3794782	snp	C/G	0.497881	0.0324789	upstream-variant-2KB	LLGL1	GRCh38.p7	17:18224600	GGAGCTGACCTCTGA[C/G]CCCGAGGCGGCTGCC	3996
rs3829589	snp	A/G	0.348134	0.229934	intron-variant	LLGL1	GRCh38.p7	17:18230952	CACACTCACCAACAG[A/G]GGCCGCTGGGGCCAT	3996
rs3829590	snp	G/T	0.348134	0.229934	intron-variant	LLGL1	GRCh38.p7	17:18230951	ACACTCACCAACAGA[G/T]GCCGCTGGGGCCATG	3996
rs3829591	snp	A/G	0.0182019	0.0936463	intron-variant	LLGL1	GRCh38.p7	17:18230926	GCCATGGGAGAGAAG[A/G]GGACATCTCAGCCCA	3996
rs3862147	snp	A/C	0.349013	0.229557	intron-variant	LLGL1	GRCh38.p7	17:18230399	CACCAGGGCCCCCAG[A/C]CCACCTGCCACCCTC	3996
rs3889544	snp	C/T	0.349013	0.229557	intron-variant	LLGL1	GRCh38.p7	17:18230474	AAAGGGGCCTGGGGG[C/T]AGTGCCAGGCTCGGC	3996
rs4386179	snp	A/G	0.333261	0.235728	intron-variant	LLGL1	GRCh38.p7	17:18231460	CCTGCACCCTCTGTC[A/G]TGGGGCCCCCTCAGG	3996
rs4450455	snp	A/G	0.334642	0.235236	intron-variant	LLGL1	GRCh38.p7	17:18237133	AACCACAGTGTTGAG[A/G]GGAGGGAACTCATGT	3996
rs4556848	snp	C/G	0.348574	0.229746	intron-variant	LLGL1	GRCh38.p7	17:18231553	AGCAGGTCATCCACC[C/G]CCTCCAAGTCTGTGT	3996
rs4925151	snp	C/G	0.339882	0.233284	intron-variant	LLGL1	GRCh38.p7	17:18226818	CACTCCTGGCTCACT[C/G]CTCTGGGGACGTTGG	3996
rs4925152	snp	C/T	0.0126979	0.078662	intron-variant	LLGL1	GRCh38.p7	17:18240052	GGTCGTCCTAGGTGT[C/T]CCCAGGCTTGGCGGC	3996
rs6502641	snp	A/G	0.396364	0.202676	intron-variant	LLGL1	GRCh38.p7	17:18229665	AGCCTGTGTGCATTG[A/G]GGGGCACAGGGGCTT	3996
rs7211573	snp	C/T	0.34101	0.232846	intron-variant	LLGL1	GRCh38.p7	17:18228299	TGAGGAGATTACTCC[C/T]GAGCGACAGGAAGTG	3996
rs7215678	snp	A/C	0.33303	0.235809	intron-variant	LLGL1	GRCh38.p7	17:18236479	TATTGTTTTTTGTAA[A/C]AGTAGGATTCCGGTC	3996
rs7405677	snp	C/T	0.333261	0.235728	intron-variant	LLGL1	GRCh38.p7	17:18227922	CCCCTGATTCCTGAG[C/T]TTAGGGGGTGGGAGA	3996
rs8066959	snp	C/T	0.000188597	0.0097089	synonymous-codon	LLGL1	GRCh38.p7	17:18235243	CGTGGCCAGTGTCCC[C/T]GCCAAGCTGTGGGCC	3996
rs8071028	snp	C/G	0.0748431	0.178382	intron-variant	LLGL1	GRCh38.p7	17:18226793	CTGATGTTAGAGCAG[C/G]GCCTCAGCCCACTCC	3996
rs8073330	snp	C/G	0.00330285	0.0405033	intron-variant	LLGL1	GRCh38.p7	17:18238063	GGACCCTGTCTTCCC[C/G]CAGGTGCACTCTTCA	3996
rs9896725	snp	A/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	LLGL1	GRCh38.p7	17:18242979	CCATGGAGTGCCTCA[A/T]TTGGGGACTTCTGGT	3996
rs9897554	snp	C/G	0.067446	0.170804	intron-variant	LLGL1	GRCh38.p7	17:18243190	ttggctcactgcaac[C/G]tctgcctcctgggtt	3996
rs9907277	snp	C/T	0.0644693	0.167566	intron-variant	LLGL1	GRCh38.p7	17:18237146	AGAGGAGGGAACTCA[C/T]GTCAGTGCTGTGCTC	3996
rs11540885	snp	G/T			utr-variant-3-prime, downstream-variant-500B	FLII, LLGL1	GRCh38.p7	17:18245004	CCCCAGTAGCCTCAA[G/T]CAGCACCAATGGGGA	3996
rs11653817	snp	A/G	0	0	synonymous-codon, downstream-variant-500B	FLII, LLGL1	GRCh38.p7	17:18245156	GGCCAGGGCCTTGCA[A/G]AAGGCGCTCCAGGCG	3996
rs11867895	snp	A/C	0.340784	0.232934	intron-variant	LLGL1	GRCh38.p7	17:18243407	CCACCGCACCCGGCC[A/C]ACAAGACCAGATTAA	3996
rs11869582	snp	A/G	0.177182	0.23916	intron-variant	LLGL1	GRCh38.p7	17:18233267	TGTGCTTGGTAAGGC[A/G]CTGGCAGCATGCCCC	3996
rs12939851	snp	A/T	0.345037	0.231231	intron-variant	LLGL1	GRCh38.p7	17:18228271	CAGCCAGGGTGGCCT[A/T]GGGAGGCTTCTCTGA	3996
rs12944747	snp	C/T			missense, intron-variant, downstream-variant-500B	LLGL1	GRCh38.p7	17:18242745	CCCCATCTCGCAGCT[C/T]CTCTGAGGAGTCAGA	3996
rs12944748	snp	C/T			missense, intron-variant, downstream-variant-500B	LLGL1	GRCh38.p7	17:18242748	CATCTCGCAGCTCCT[C/T]TGAGGAGTCAGAGAA	3996
rs12952091	snp	A/C			intron-variant	LLGL1	GRCh38.p7	17:18225953	GGACTCTGGGTGGGT[A/C]TGGGTCTCCGGCCGA	3996
rs28523978	snp	C/T	0.0726307	0.176182	utr-variant-3-prime, missense	LLGL1	GRCh38.p7	17:18243925	AGGCCAGAACTATCC[C/T]GACCTCCACCTGCCC	3996
rs34181252	in-del	-/G			intron-variant	LLGL1	GRCh38.p7	17:18231475	GTGGGGCCCCCTCAG[-/G]CCCTGCTGTCCACCA	3996
rs34217595	snp	A/G	0.00262712	0.0361477	intron-variant	LLGL1	GRCh38.p7	17:18238632	AGGGGCAGGGGCAGG[A/G]ACAGGGCAAGGGTTG	3996
rs34411623	in-del	-/C			upstream-variant-2KB	LLGL1	GRCh38.p7	17:18224622	TCAGCTCCTGCTCCC[-/C]TGGACACAGCTGGTG	3996
rs34513508	in-del	-/C			intron-variant	LLGL1	GRCh38.p7	17:18225924	GCACCCCTCGGCGGG[-/C]CCCGCTCTGGCTCGG	3996
rs34604631	snp	C/G			utr-variant-3-prime	LLGL1	GRCh38.p7	17:18244181	GGTGGGGCCCAGCAC[C/G]TGTGCCACCTCCCCC	3996
rs34709206	in-del	-/A			frameshift-variant	LLGL1	GRCh38.p7	17:18237695	CACACTCCACACCGA[-/A]GTGGAGCCTCGTGGC	3996
rs34800060	in-del	-/T	0	0	intron-variant	LLGL1	GRCh38.p7	17:18227396	CACTTTTTTTTTTTT[-/T]GAAATGGGGTCTCAC	3996
rs34971811	in-del	-/A			intron-variant	LLGL1	GRCh38.p7	17:18233605	TGACATCCTGATGAA[-/A]TAATTGAGCGGGCTG	3996
rs35062334	snp	A/G	0.00636936	0.0560724	intron-variant	LLGL1	GRCh38.p7	17:18240126	GTGAAGCAGGGCTAA[A/G]ACAAGGCACACCTGT	3996
rs35135234	in-del	-/T			intron-variant	LLGL1	GRCh38.p7	17:18232986	TATACTCTGAACTTT[-/T]CAGGTTAAATGGGAG	3996
rs35187870	in-del	-/C			intron-variant	LLGL1	GRCh38.p7	17:18235003	GGATGGTGCGTGCCC[-/C]TGCCGTACCCTACCC	3996
rs35212748	in-del	-/G			intron-variant	LLGL1	GRCh38.p7	17:18230261	ACGGGTGGTGGGGGG[-/G]TCAGTTTGCAGTAGC	3996
rs35666460	in-del	-/G			frameshift-variant	LLGL1	GRCh38.p7	17:18235106	TTTGATGACCCCCAG[-/G]CCCTGGCTGTGCTGC	3996
rs35754280	in-del	-/C			intron-variant	LLGL1	GRCh38.p7	17:18238286	TCTGGCCTGGGACCC[-/C]TGGGGCCTGCTTAGC	3996
rs55775920	snp	C/T	0.0123036	0.0774623	intron-variant	LLGL1	GRCh38.p7	17:18237247	TAAGGGTGGACACTT[C/T]GCCCTCAGAGGGCAG	3996
rs55854919	snp	C/T	0.0737376	0.17729	utr-variant-3-prime	LLGL1	GRCh38.p7	17:18244196	CTGTGCCACCTCCCC[C/T]CCTCCACACACCATC	3996
rs56309886	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	LLGL1	GRCh38.p7	17:18223754	TTTTTTGTATTTTTA[A/G]TAGAGACTGGGTTTT	3996
rs56367302	snp	A/G			missense	LLGL1	GRCh38.p7	17:18241548	TGGCCACGTTTGCCA[A/G]TGTGGCCTGCGAGGA	3996
rs56406965	snp	A/G			synonymous-codon	LLGL1	GRCh38.p7	17:18241507	GCTGACGGCCCATGA[A/G]GGCTGTCGTGTGCGC	3996
rs57808902	snp	C/T	0.270621	0.249148	intron-variant	LLGL1	GRCh38.p7	17:18243586	CACCTAGATGTGGGG[C/T]CCATAGATCTGCCCA	3996
rs57956221	snp	C/G	0.00227225	0.0336298	synonymous-codon	LLGL1	GRCh38.p7	17:18240783	TGGCCGCCCACTGCC[C/G]GAGCCCTACGAGGCC	3996
rs60814048	snp	C/T	0.0752113	0.178743	intron-variant	LLGL1	GRCh38.p7	17:18227806	AAAGTAAGGGCCCTC[C/T]GCTGAGGATGAAGCG	3996
rs61576260	snp	A/G/T	0.111928	0.208413	intron-variant	LLGL1	GRCh38.p7	17:18231834	CCGGCTAATTTTTGC[A/G/T]TTTTTAGTAGAGACG	3996
rs62072500	snp	A/C	0.304937	0.243889	upstream-variant-2KB	LLGL1	GRCh38.p7	17:18223604	TTGTTTTTTTCATTT[A/C]TCACGCTTGTTGCCC	3996
rs62072501	snp	C/T	0.0138799	0.0821421	upstream-variant-2KB	LLGL1	GRCh38.p7	17:18224374	CCCTCGTAGAGCTAC[C/T]GACAGCACTAAGTCA	3996
rs66493242	multinucleotide-polymorphism	AC/CT	0	0	intron-variant	LLGL1	GRCh38.p7	17:18230952	CATGGCCCCAGCGGC[AC/CT]CTGTTGGTGAGTGTG	3996
rs71355559	in-del	-/C	0.5	0	upstream-variant-2KB	LLGL1	GRCh38.p7	17:18223852	AGCCACTGCTCCTGG[-/C]CTTTTTTTCGAGATG	3996
rs71367435	snp	A/G	0.5	0	intron-variant	LLGL1	GRCh38.p7	17:18230462	CATGTGTTCAGCAAA[A/G]GGGCCTGGGGGTAGT	3996
rs71367436	snp	C/T	0.5	0	missense	LLGL1	GRCh38.p7	17:18232678	ACACACCAGGGCCGC[C/T]TCCTGTCCCTGCTTG	3996
rs71367437	snp	C/T	0.5	0	intron-variant	LLGL1	GRCh38.p7	17:18235790	GCCCAGCCTGCCTGC[C/T]CTGGGACTGGAAAAT	3996

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