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
rs936058	snp	C/T	0.47802	0.102502	intron-variant	LLGL2	GRCh38.p7	17:75571272	AGCTGACTCAGAGGC[C/T]GAGGCAGGGGAGGGG	3993
rs936059	snp	A/C	0.489492	0.0717183	intron-variant	LLGL2	GRCh38.p7	17:75569429	TCCACCGGAAAAGCA[A/C]AGGACACAGAATGTG	3993
rs936060	snp	C/T	0.385168	0.210309	intron-variant	LLGL2	GRCh38.p7	17:75563261	CCCATCGCCTGCACC[C/T]CATGCCTCTGCACAG	3993
rs936061	snp	A/G	0.0186639	0.0947819	intron-variant	LLGL2	GRCh38.p7	17:75558282	GGAAGCAGTGAAGGC[A/G]AGGAGGGCATGGAAG	3993
rs960511	snp	A/G	0.433236	0.170072	intron-variant	LLGL2	GRCh38.p7	17:75565337	CCCTTTCAGGCCAGC[A/G]TCATTAGGAGAGGGC	3993
rs960512	snp	C/G	0.433236	0.170072	intron-variant	LLGL2	GRCh38.p7	17:75565238	TGTCACACAATTTAC[C/G]AGGCTGACTCAGGGC	3993
rs1042861	snp	C/T	0.467919	0.122521	utr-variant-3-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574949	CACCGGCCTCTCCGG[C/T]TGGGGCAGGGACCCC	3993
rs1126939	snp	C/G	0.408695	0.193201	synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574637	GCGTTCACATCGAGC[C/G]GCCGTGGGGTGCAGC	3993
rs1128126	snp	C/G/T	0.00013221	0.00812941	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524445	GGATGGAGCTTGCTC[C/G/T]GGGGGACCGGGACTG	3993
rs1470941	snp	A/G	0.384976	0.210431	intron-variant	LLGL2	GRCh38.p7	17:75562236	TAGCCCCATAAAACA[A/G]AACTCTGTGTGAGTT	3993
rs1620378	snp	A/G	0.497558	0.0348586	intron-variant	LLGL2	GRCh38.p7	17:75561462	tttttattttttgtg[A/G]ggagagacagggtct	3993
rs1626316	snp	C/T			intron-variant	LLGL2	GRCh38.p7	17:75560747	tgtaatcccagcact[C/T]tgggaggctgaggcg	3993
rs1661712	snp	A/C	0.405033	0.196124	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574675	CACTCAAGCCCAGAG[A/C]CCCCACCTCCGCCAT	3993
rs1661713	snp	A/G	0.48818	0.0759629	intron-variant	LLGL2	GRCh38.p7	17:75572929	GGCCCTCCCCTCCCC[A/G]CATGCCTCCCGGTGT	3993
rs1661714	snp	A/G	0.357353	0.225777	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571974	CACTTCGAGGGGCTC[A/G]GGAAGGGGTACGCTG	3993
rs1661715	snp	A/G	0.400456	0.199657	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75571765	GCTCTGCCCGCACAG[A/G]CTCATCCATTCTCCG	3993
rs1661716	snp	A/C	0.47802	0.102502	intron-variant	LLGL2	GRCh38.p7	17:75571454	AGGGAGAGACACGTC[A/C]TCTGGAGACCAGCAG	3993
rs1661718	snp	A/C	0.0910124	0.192936	intron-variant	LLGL2	GRCh38.p7	17:75571127	GCCCACTACCCCCTG[A/C]CCCCCAACCCCAGGC	3993
rs1661721	snp	A/C	0.34101	0.232846	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566796	CTCAGACTTGATCCC[A/C]GCCCAGCTGAGCTTG	3993
rs1661722	snp	A/G	0.426966	0.176587	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566340	tctttgctccactcc[A/G]tgtcccccacatggc	3993
rs1661723	snp	A/G	0.426047	0.177503	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566210	tctatacgatctggc[A/G]cTGGCCACATCTGGA	3993
rs1661725	snp	A/G	0.499801	0.00998203	intron-variant	LLGL2	GRCh38.p7	17:75564053	CAACTAAAGGAGTTT[A/G]AGACCTGCTGCTCAG	3993
rs1661727	snp	C/T	0.384976	0.210431	intron-variant	LLGL2	GRCh38.p7	17:75561647	AGGCGTGAGCCACCG[C/T]GCCCGGCCTAATTTT	3993
rs1661728	snp	C/T	0.387453	0.208822	intron-variant	LLGL2	GRCh38.p7	17:75560696	GAGTTCGAGACTAGT[C/T]TGACCACCATGGAGA	3993
rs1661729	snp	C/T	0.029116	0.117091	intron-variant	LLGL2	GRCh38.p7	17:75556944	cctcccaggttcaaa[C/T]gattctcccatctca	3993
rs1671016	snp	C/T	0.360548	0.22423	intron-variant, downstream-variant-500B	LLGL2	GRCh38.p7	17:75574693	CAGCACGGTTGGCAG[C/T]TGCACTCAAGCCCAG	3993
rs1671018	snp	A/G	0.00183678	0.0302493	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LLGL2	GRCh38.p7	17:75574623	CCGCTCGATGTGAAC[A/G]CCAGTTGCCGCTCCT	3993
rs1671019	snp	A/C	0.479258	0.0997024	intron-variant	LLGL2	GRCh38.p7	17:75573846	CAGCCTGTCCTGAGC[A/C]GGAGAGCCTGGGAGG	3993
rs1671020	snp	C/T	0.427423	0.176128	intron-variant	LLGL2	GRCh38.p7	17:75572903	GGTGTCCTGACAAAC[C/T]CTTGGCTCTCAGATG	3993
rs1671021	snp	A/G	0.469911	0.118908	missense, nc-transcript-variant	LLGL2	GRCh38.p7	17:75569090	CGCCCTGGGCACTGA[A/G]GTTCTCGTTGGGGTC	3993
rs1671022	snp	C/T	0.338523	0.233803	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566357	Ctctcactgggctcc[C/T]gtctttgctccactc	3993
rs1671023	snp	C/T	0.424659	0.17887	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75566135	GGAGCAAGCCAAGAG[C/T]CCTCCCAGCTCAGTC	3993
rs1671025	snp	C/T	0.432504	0.170857	intron-variant	LLGL2	GRCh38.p7	17:75564137	GCCACTCCTGCCTCA[C/T]GCTGGGTGCCCCCAC	3993
rs1671026	snp	C/T	0.384976	0.210431	intron-variant	LLGL2	GRCh38.p7	17:75564122	TGCTGGGTGCCCCCA[C/T]CAATTCTGTTTGAAC	3993
rs1671027	snp	C/T	0.388021	0.208447	intron-variant	LLGL2	GRCh38.p7	17:75563548	TACCCTCTCTGGCCC[C/T]GGAGTTTGCTTCAGA	3993
rs1671028	snp	C/T	0.382572	0.211954	intron-variant	LLGL2	GRCh38.p7	17:75563482	GGGGTGGGCCCTGCC[C/T]GGCGGGTGAAACACT	3993
rs1671029	snp	A/G	0.335101	0.23507	intron-variant	LLGL2	GRCh38.p7	17:75562680	TTGGGAGGCGGAGGC[A/G]GGAGAATTGCTTGAA	3993
rs1671031	snp	C/G	0.497586	0.0346604	intron-variant	LLGL2	GRCh38.p7	17:75560526	GCACTCTAGCCTGGG[C/G]AACAAGAGTGAAACT	3993
rs1671032	snp	C/T	0.497776	0.0332724	intron-variant	LLGL2	GRCh38.p7	17:75559824	TTTTAGCCACGGAGC[C/T]TGCGAGCAAATGGAA	3993
rs1671033	snp	C/G	0.49703	0.0384237	intron-variant	LLGL2	GRCh38.p7	17:75558442	ACACACTGGGGCCAC[C/G]CAGCCCCAGTTGTTT	3993
rs1671035	snp	A/G	0.439918	0.162576	intron-variant	LLGL2	GRCh38.p7	17:75557847	GATCCTGAGCTGCAA[A/G]AGACATGTTGGCTGT	3993
rs1671036	snp	C/T	0.499986	0.00264766	missense, utr-variant-5-prime, nc-transcript-variant	LLGL2	GRCh38.p7	17:75556104	CCGATGGCCAGGATG[C/T]GCAGGGACGGGCTGT	3993
rs1671037	snp	A/G	0.0444908	0.142359	intron-variant	LLGL2	GRCh38.p7	17:75555955	CCAGACGACCCAGCA[A/G]GAAGCAGGGCTTCGG	3993
rs2017625	snp	A/G	0.493477	0.0567349	intron-variant	LLGL2	GRCh38.p7	17:75556985	CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTCACT	3993
rs2305525	snp	C/T	0.388355	0.208294	synonymous-codon, nc-transcript-variant	LLGL2	GRCh38.p7	17:75570480	TCCTGGGGGGCCAGC[C/T]GGGTGCCGCTTCCGG	3993
rs2305526	snp	A/T	0.20849	0.24653	intron-variant	LLGL2	GRCh38.p7	17:75569181	AGCAGCCACGGGGAC[A/T]GGACCCAGCTGGCCT	3993
rs2305527	snp	A/T	0.095934	0.196885	intron-variant	LLGL2	GRCh38.p7	17:75559504	GAATTCCCAGCAGAG[A/T]AATGACAGCTCCTGA	3993
rs2305528	snp	C/G	0.495135	0.0490805	intron-variant	LLGL2	GRCh38.p7	17:75555981	CCACCATGGCTGCTG[C/G]AGCTGCAGCACCAGA	3993
rs3785430	snp	C/T	0.335559	0.234904	intron-variant	LLGL2	GRCh38.p7	17:75565636	CTCAGCAAGTTTCTT[C/T]CCTCCCTTCCTGACC	3993
rs3862478	snp	C/T	0.497668	0.0340657	intron-variant	LLGL2	GRCh38.p7	17:75572844	AAAAAAAAATCCAGA[C/T]AGGGAAGTCGGTGAC	3993
rs3896707	snp	C/T	0.493523	0.0565391	intron-variant	LLGL2	GRCh38.p7	17:75556827	CATTGACCAGGCTGG[C/T]CTTGAACTCCTGACC	3993
rs3910704	snp	C/T	0.487746	0.0773096	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75567943	TTTTTTTTCTTTTCT[C/T]GAGACAGGGTTTCAC	3993
rs4073421	snp	C/T	0.450609	0.149185	intron-variant	LLGL2	GRCh38.p7	17:75546115	CCTCCCCATCCCCTC[C/T]CTCTTTACTGCCCCA	3993
rs4073422	snp	C/T	0.450609	0.149185	intron-variant	LLGL2	GRCh38.p7	17:75545929	CTAAATAATCTACAA[C/T]GCACAGGACAGCCTC	3993
rs4076354	snp	C/T	0	0	upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524870	CTATCCCGCGGGCTT[C/T]TCTCACTCTTAGATC	3993
rs4076967	snp	C/G	0.460813	0.134379	intron-variant	LLGL2	GRCh38.p7	17:75550243	CTGCAAAGGTACACA[C/G]AGCAACCCTGAATCG	3993
rs4077852	snp	C/T	0.392881	0.205147	intron-variant	LLGL2	GRCh38.p7	17:75549460	CCGTGCCCACCCTCC[C/T]CTGTCCCCTTAGGCC	3993
rs4788896	snp	C/T	0.295599	0.245806	intron-variant	LLGL2	GRCh38.p7	17:75532127	actctgtggcccagg[C/T]tggagtgcaatggca	3993
rs4788897	snp	G/T			intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541756	ttttttgagatactg[G/T]ttttgctctgttgcc	3993
rs4788898	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75541777	CTCTGTTGCCCAGGC[C/T]GGAGTGCAATGGCCT	3993
rs4788900	snp	C/T	0.384785	0.210554	intron-variant	LLGL2	GRCh38.p7	17:75560956	cctgcctcagccttc[C/T]gagtagctgggatta	3993
rs4789208	snp	C/T	0.450483	0.149354	intron-variant	LLGL2	GRCh38.p7	17:75548079	GAATGCTCACTGGAG[C/T]GTTTCAGATTTTGAA	3993
rs4789209	snp	A/C/G	0.331874	0.236213	intron-variant	LLGL2	GRCh38.p7	17:75548267	TTTTACAGAAGGACA[A/C/G]TTTTTTTTTTCCTTT	3993
rs4789210	snp	C/T	0.444444	0.157135	intron-variant	LLGL2	GRCh38.p7	17:75548273	AGAAGGACAATTTTT[C/T]TTTTCCTTTTTTTTT	3993
rs4789211	snp	C/G	0.467744	0.122832	intron-variant	LLGL2	GRCh38.p7	17:75551088	ATCCCCTGGGAGACA[C/G]GTCATTTACACATGA	3993
rs4789212	snp	A/G	0.473909	0.111197	intron-variant, utr-variant-5-prime	LLGL2	GRCh38.p7	17:75551286	GCAGGGTGGCCTCAG[A/G]TCCATCATCTCCAAT	3993
rs4789213	snp	C/G	0.493568	0.0563433	intron-variant	LLGL2	GRCh38.p7	17:75556445	TGTCCTTTCAGGACC[C/G]TTCATGTGGTCTGCT	3993
rs5015927	snp	C/T	0.0295035	0.117819	intron-variant	LLGL2	GRCh38.p7	17:75559005	CCTCCATCTGCACCC[C/T]GCCTCCTCCATCCGC	3993
rs5822090	in-del	-/G	0.0287284	0.116357	intron-variant	LLGL2	GRCh38.p7	17:75557438	TGGTTCTGGCCGACT[-/G]GGGGCTCCCAGTGTT	3993
rs5822091	in-del	-/A	0.477768	0.103061	intron-variant	LLGL2	GRCh38.p7	17:75572360	GACTACTAAAAATAC[-/A]AAAAAAAAATAGCCC	3993
rs6416848	snp	C/T	0.365439	0.221752	intron-variant	LLGL2	GRCh38.p7	17:75544752	GGTCAGCGCTCCCAA[C/T]GTGCCCTGCCATTTC	3993
rs6501821	snp	C/G	0.123798	0.215808	intron-variant	LLGL2	GRCh38.p7	17:75526740	AGTTCTCTTGAAGGG[C/G]CTACAGAGAGGATTC	3993
rs6501822	snp	A/G	0.265113	0.249543	intron-variant	LLGL2	GRCh38.p7	17:75543550	GGTTTTCGGCCAAGC[A/G]GCTCAGGCTGGGGCT	3993
rs6501823	snp	C/G	0.251859	0.249993	intron-variant	LLGL2	GRCh38.p7	17:75543714	TGGGACTTCTCATCT[C/G]AAGGCTTTCACTGGC	3993
rs6501824	snp	C/T	0.393619	0.204631	intron-variant	LLGL2	GRCh38.p7	17:75544532	CCCAACTTTGCCACA[C/T]AGAAGCTGGATGGCC	3993
rs6501825	snp	G/T	0.396364	0.202676	intron-variant	LLGL2	GRCh38.p7	17:75544774	TGCCATTTCTCTCTG[G/T]GTTTCTTAGCCTGTG	3993
rs6501826	snp	C/T	0.245346	0.249957	intron-variant	LLGL2	GRCh38.p7	17:75551661	CTGCCCGCCCTTGAC[C/T]TGTGGCCTGAGAGCC	3993
rs7208126	snp	A/C	0.393065	0.205018	intron-variant	LLGL2	GRCh38.p7	17:75545131	CCCCTGCCCCCTTGC[A/C]CCAAGTTCTGTCTGT	3993
rs7208430	snp	A/G	0.484138	0.0876334	intron-variant	LLGL2	GRCh38.p7	17:75548818	tggtctcctacagtg[A/G]tattttggggtggta	3993
rs7208892	snp	A/G	0.328148	0.237472	intron-variant	LLGL2	GRCh38.p7	17:75553966	ATAAACCTCTGGTGA[A/G]TTAGGATATCTACAG	3993
rs7209370	snp	C/T	0.484279	0.0872533	intron-variant	LLGL2	GRCh38.p7	17:75548130	gaccggtaagtataa[C/T]gcaaatattccgaaa	3993
rs7210253	snp	A/G	0.484066	0.0878235	intron-variant	LLGL2	GRCh38.p7	17:75548820	gtctcctacagtggt[A/G]ttttggggtggtatg	3993
rs7211129	snp	C/G	0.32153	0.239548	intron-variant	LLGL2	GRCh38.p7	17:75536492	CCGGGCCTAACTATT[C/G]CGTGTCTCTAGGGGG	3993
rs7211130	snp	C/G	0.32153	0.239548	intron-variant	LLGL2	GRCh38.p7	17:75536493	CGGGCCTAACTATTC[C/G]GTGTCTCTAGGGGGT	3993
rs7211793	snp	C/T	0.295343	0.245854	intron-variant	LLGL2	GRCh38.p7	17:75530398	tctcacgcctgtaat[C/T]ccagcactttgggag	3993
rs7214191	snp	C/T	0.483995	0.0880135	intron-variant	LLGL2	GRCh38.p7	17:75548742	gcctgggtgacagag[C/T]gagattctgtctcaa	3993
rs7214407	snp	A/C	0.0966517	0.197444	upstream-variant-2KB, downstream-variant-500B	LLGL2, TSEN54, LOC107985023	GRCh38.p7	17:75524944	GTCGGAGGGGATGGG[A/C]CGTCGCAGGCTTCCC	3993
rs7219049	snp	A/G	0.0287284	0.116357	intron-variant	LLGL2	GRCh38.p7	17:75555501	TCCCTTTCTGGGAAG[A/G]TGGTTGGAATTTGGT	3993
rs7219929	snp	A/G	0	0	intron-variant	LLGL2	GRCh38.p7	17:75551144	TAGAGTCGCTGTGAA[A/G]GTCACTGCCCTTATT	3993
rs7222559	snp	C/G	0.0414363	0.137845	intron-variant	LLGL2	GRCh38.p7	17:75547908	AGGTGAATGAAGgtt[C/G]TCTTGTTATGCAGAG	3993
rs7222924	snp	G/T	0.484279	0.0872533	intron-variant	LLGL2	GRCh38.p7	17:75548096	tttcagattttgaaa[G/T]tttggatttgggatg	3993
rs7223552	snp	A/G	0.00664444	0.0572545	intron-variant	LLGL2	GRCh38.p7	17:75526859	TGGCCCAGCCCGGGG[A/G]AAGCCAAGGTCAGAA	3993
rs7224904	snp	C/T	0.272241	0.249009	intron-variant, upstream-variant-2KB	LLGL2	GRCh38.p7	17:75542143	CCACGCTGCCCAGAT[C/T]ACATGGGATCCTATC	3993
rs7225150	snp	G/T	0.135825	0.222405	intron-variant	LLGL2	GRCh38.p7	17:75530287	gagggaggattgctt[G/T]aacccaggagttcaa	3993
rs7225291	snp	A/G	0.0236746	0.106192	intron-variant	LLGL2	GRCh38.p7	17:75530389	ggcgcggtgtctcac[A/G]cctgtaattccagca	3993
rs7225594	snp	A/G	0.393065	0.205018	intron-variant	LLGL2	GRCh38.p7	17:75545001	GGGTCTCAAAGCTTC[A/G]GTGTCCACGGGAGAT	3993
rs7502310	snp	A/G	0.252421	0.249988	intron-variant	LLGL2	GRCh38.p7	17:75531507	ACTCATTTGTCCTCA[A/G]TCCTCAACTCTGAGA	3993
rs7502311	snp	A/G	0.25214	0.249991	intron-variant	LLGL2	GRCh38.p7	17:75531514	TGTCCTCAATCCTCA[A/G]CTCTGAGAGGCCCTC	3993
rs7502339	snp	A/C	0.250567	0.250298	intron-variant	LLGL2	GRCh38.p7	17:75531631	AGGAGCAGTTTGCAG[A/C]GAGAAAACTGGGGAC	3993
rs7502353	snp	G/T	0.456095	0.141508	intron-variant	LLGL2	GRCh38.p7	17:75549602	GAGGGCCAGGCTGCC[G/T]CCACTGCCAGGAATC	3993

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