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
rs183969	snp	A/G	0.471578	0.115772	intron-variant	RNF182	GRCh38.p7	6:13973018	tgaaagcagccagga[A/G]ggaggctgtacccta	221687
rs184898	snp	C/T	0.106278	0.204558	intron-variant	RNF182	GRCh38.p7	6:13939800	cacccgcctcagcct[C/T]ccaaagtgctgggat	221687
rs280143	snp	A/G	0.377582	0.214995	intron-variant	RNF182	GRCh38.p7	6:13929271	TGGCCAACATATTGT[A/G]TTTGAGTGAGAAGTT	221687
rs280144	snp	C/T	0.00478085	0.0486577	intron-variant	RNF182	GRCh38.p7	6:13930044	CATATATTAAAAGAA[C/T]ATagtcagccttgca	221687
rs280145	snp	C/G	0.375797	0.216044	intron-variant	RNF182	GRCh38.p7	6:13934257	GATTCAGAGTCACTC[C/G]TCACCCTGTCTCTTA	221687
rs280146	snp	C/T	0.406468	0.194981	intron-variant	RNF182	GRCh38.p7	6:13935559	CAGTGGAATGACTTA[C/T]AAGCTACATATTAAT	221687
rs280147	snp	C/T	0.107694	0.205546	intron-variant	RNF182	GRCh38.p7	6:13937103	TCACAATCACATTAC[C/T]TGTTTTGTGTTGTAT	221687
rs280148	snp	A/G	0.377187	0.215229	intron-variant	RNF182	GRCh38.p7	6:13937184	ttattgaaggttaac[A/G]tacatatagaaaagt	221687
rs280149	snp	A/G	0.37246	0.264737	intron-variant	RNF182	GRCh38.p7	6:13938375	agaagtcctttgtgc[A/G]atgtatgtgttacag	221687
rs280150	snp	A/T	0.391954	0.205789	intron-variant	RNF182	GRCh38.p7	6:13938552	gaagatattctccta[A/T]gctaccaagaagttt	221687
rs280151	snp	C/G	0.496874	0.0394129	intron-variant	RNF182	GRCh38.p7	6:13942600	acttgcctcagccta[C/G]cagagtgctgggatt	221687
rs280152	snp	C/T	0.353587	0.22753	intron-variant	RNF182	GRCh38.p7	6:13943550	TGGTACTTATCTTAC[C/T]GCCTTGGAACTGCTA	221687
rs280153	snp	G/T	0.349671	0.229272	intron-variant	RNF182	GRCh38.p7	6:13944836	GATTCCAACCCAGAT[G/T]TTTTTGACTTCAAAT	221687
rs280154	snp	C/T	0.362523	0.223246	intron-variant	RNF182	GRCh38.p7	6:13945881	gtgcaataaagaatt[C/T]gaggtgagtccacag	221687
rs280157	snp	A/G	0.373598	0.21731	intron-variant	RNF182	GRCh38.p7	6:13970610	tagataccaagtaga[A/G]gaattgctgggttgt	221687
rs280158	snp	A/G	0.471578	0.115772	intron-variant	RNF182	GRCh38.p7	6:13971505	agtaccaggagtggg[A/G]tactgctataaggat	221687
rs280159	snp	A/G	0.455977	0.141681	intron-variant	RNF182	GRCh38.p7	6:13975439	CTGTATTTCAAAACT[A/G]CTACCACGAACCAAG	221687
rs280160	snp	A/T	0.456568	0.140818	intron-variant	RNF182	GRCh38.p7	6:13976738	CAGCTAAGCATGGAA[A/T]TAACACTTTTCCGTT	221687
rs280161	snp	C/T	0.386504	0.209444	intron-variant	RNF182	GRCh38.p7	6:13976755	AACACTTTTCCGTTC[C/T]AGGGACAGAAGTGTG	221687
rs280162	snp	A/C	0.456095	0.141508	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978044	AAAATGTTCATTTCT[A/C]CTTAGGGGTTAGCAA	221687
rs280163	snp	C/G	0.464735	0.128019	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978387	ACTTGTTTCCTCTGC[C/G]CATTCTCCCTTGCCA	221687
rs280164	snp	G/T	0.460027	0.135605	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978606	AAGAATGGAGGAGAA[G/T]GAACTTCTCATACAG	221687
rs280166	snp	C/T	0.490563	0.0680388	intron-variant	RNF182	GRCh38.p7	6:13951279	ttcaaggaacagggt[C/T]aggaaagcatgcagt	221687
rs280167	snp	A/G	0.492188	0.0620098	intron-variant	RNF182	GRCh38.p7	6:13952555	gaaatgtatcctacg[A/G]tttatccaaagtcgg	221687
rs280168	snp	C/G	0.492237	0.0618148	intron-variant	RNF182	GRCh38.p7	6:13952561	tatcctacggtttat[C/G]caaagtcggccaatt	221687
rs280169	snp	C/T	0.420096	0.183214	intron-variant	RNF182	GRCh38.p7	6:13952996	caaaactTATTCTTT[C/T]TTCCTTTTGAGATGG	221687
rs280170	snp	C/T	0.101301	0.200969	intron-variant	RNF182	GRCh38.p7	6:13953807	TGGCTGAGTTCCTTA[C/T]GGGCTCCCCCTCTAG	221687
rs280171	snp	A/G	0.444799	0.156695	intron-variant	RNF182	GRCh38.p7	6:13954401	acaaggactactcat[A/G]tatttagctaataaa	221687
rs280172	snp	C/G	0.372592	0.217879	intron-variant	RNF182	GRCh38.p7	6:13955333	Atcattggttgaaat[C/G]cttctataaaaagaa	221687
rs280173	snp	A/G	0.373799	0.217195	intron-variant	RNF182	GRCh38.p7	6:13956077	cttctttcacttcac[A/G]taatgtcgttcagac	221687
rs280174	snp	A/G	0.456685	0.140646	intron-variant	RNF182	GRCh38.p7	6:13956152	gctgaatagtatttc[A/G]ttgtgtatacctacc	221687
rs280175	snp	C/G	0.456095	0.141508	intron-variant	RNF182	GRCh38.p7	6:13956413	cactgcaacctccac[C/G]tcccagattcaattg	221687
rs280176	snp	G/T	0.320575	0.239832	intron-variant	RNF182	GRCh38.p7	6:13957413	CAAGCTTGGATTAAG[G/T]CATGTATTAAATGTG	221687
rs280177	snp	A/G	0.456803	0.140473	intron-variant	RNF182	GRCh38.p7	6:13957461	TTTAAATTTCCTTTT[A/G]AAACCTTTTTGCCCA	221687
rs280178	snp	G/T	0.3752	0.216391	intron-variant	RNF182	GRCh38.p7	6:13959074	ctgagatcctcttca[G/T]atgcagatgtccagt	221687
rs280179	snp	A/G	0.45574	0.142025	intron-variant	RNF182	GRCh38.p7	6:13960588	AAATGTATTGATGAA[A/G]GACAGTTGGTGATTT	221687
rs280180	snp	A/G	0.383053	0.211653	intron-variant	RNF182	GRCh38.p7	6:13960646	ACTTTTTTGATGGAG[A/G]GAGAGAGAGAgtgtg	221687
rs280181	snp	A/T	0.374	0.217081	intron-variant	RNF182	GRCh38.p7	6:13961763	ATCAAATTAAATTGC[A/T]TGTTCTTGGAGGAGG	221687
rs280182	snp	A/C	0.327914	0.237549	intron-variant	RNF182	GRCh38.p7	6:13962226	ACTGGACTTTCTTGG[A/C]GGTAGATGCCACATG	221687
rs280183	snp	C/T	0.455383	0.142541	intron-variant	RNF182	GRCh38.p7	6:13962867	AATATTTTGAAGAAA[C/T]TCAACTTACCCTAAG	221687
rs280184	snp	C/T	0.455383	0.142541	intron-variant	RNF182	GRCh38.p7	6:13963052	GGAAAGATACTTCAA[C/T]GGATGTTCATATGCC	221687
rs280185	snp	C/T	0.454784	0.1434	intron-variant	RNF182	GRCh38.p7	6:13964400	ATTGCCAATGTTCTG[C/T]CCAAATTAAACTTTT	221687
rs280186	snp	G/T	0.322007	0.239405	intron-variant	RNF182	GRCh38.p7	6:13964695	GGGCTGGCATCCATT[G/T]GATGAGTCCCACCAG	221687
rs280187	snp	G/T	0.481703	0.0938806	intron-variant	RNF182	GRCh38.p7	6:13964848	AAATCCATAGTTGGG[G/T]GCGTCCTTTGGAGCA	221687
rs280188	snp	A/G	0.375797	0.216044	intron-variant	RNF182	GRCh38.p7	6:13965926	aagcaatcatgatca[A/G]tgaggggcccctcaa	221687
rs280189	snp	C/T	0.454423	0.143914	intron-variant	RNF182	GRCh38.p7	6:13966151	CAGCAGCCAGAAAAT[C/T]CCATACATTTCCCTG	221687
rs280190	snp	A/G	0.455502	0.142369	intron-variant	RNF182	GRCh38.p7	6:13966292	AACACAGACCTTGAG[A/G]TACAGGAAGATGACA	221687
rs280191	snp	A/G	0.455383	0.142541	intron-variant	RNF182	GRCh38.p7	6:13966543	CAAGGTAGGTGGATC[A/G]CTTGAGTACAGGAGT	221687
rs364998	snp	A/G	0.4444	0.15719	intron-variant	RNF182	GRCh38.p7	6:13960697	TGTGTGTGTGTGCGC[A/G]CGTGCACATGCATGT	221687
rs380669	snp	A/G	0.378174	0.214642	intron-variant	RNF182	GRCh38.p7	6:13927498	TAATTTTTGGTATAA[A/G]CTGTAAAATATGGCC	221687
rs402711	snp	A/G	0.455621	0.142197	intron-variant	RNF182	GRCh38.p7	6:13968058	TGAATTGGGAAAAAA[A/G]TCATAACAAACAAAA	221687
rs408909	snp	C/G	0.209084	0.246629	intron-variant	RNF182	GRCh38.p7	6:13940762	tggctttaatagtat[C/G]ctcttaaattctgtc	221687
rs409463	snp	A/G	0.460813	0.134379	intron-variant	RNF182	GRCh38.p7	6:13969497	AGGAAACACTACCCC[A/G]AAGAAGTGGGGGCAG	221687
rs411501	snp	G/T	0.106278	0.204558	upstream-variant-2KB	RNF182	GRCh38.p7	6:13923745	TCATTAGTTAATATA[G/T]GTGTACCTTCAAATG	221687
rs418858	snp	A/T	0	0	intron-variant	RNF182	GRCh38.p7	6:13929164	AGGCCCAATAATAAA[A/T]TTTTTCCACATGAGA	221687
rs432578	snp	C/G	0.455263	0.142713	intron-variant	RNF182	GRCh38.p7	6:13967849	acaggcgtgagccac[C/G]atgcctggccCTGTA	221687
rs433765	snp	A/G	0	0	intron-variant	RNF182	GRCh38.p7	6:13959784	tgagaggtgagggtt[A/G]aaatttgtcttagac	221687
rs439034	snp	A/C	0.455024	0.143057	intron-variant	RNF182	GRCh38.p7	6:13969192	GGCTTTATTCTTCTT[A/C]TTCTCCCTCTTGCTG	221687
rs439797	snp	C/T	0.164546	0.234942	upstream-variant-2KB	RNF182	GRCh38.p7	6:13924337	TCAACAAGACAGATA[C/T]ACGGGTTGGGTGGAG	221687
rs445781	snp	G/T	0.413582	0.189052	intron-variant	RNF182	GRCh38.p7	6:13926793	TGTGTGTGTGTGTGT[G/T]TTTTTTTTTTTCCTG	221687
rs579538	snp	C/T	0.339882	0.233284	intron-variant	RNF182	GRCh38.p7	6:13969219	GCTGCCATGGCAGTT[C/T]CTTGATACATCTTTT	221687
rs1001575	snp	G/T	0.0162558	0.0886773	intron-variant	RNF182	GRCh38.p7	6:13960434	atcacttgaggccag[G/T]aatttgagaccagtc	221687
rs1041035	snp	A/T	0.453939	0.144598	intron-variant	RNF182	GRCh38.p7	6:13975025	CATTTGGGTGGGCTG[A/T]AGTCTGTGTGTGGCT	221687
rs1192057	snp	A/G	0.364817	0.222075	intron-variant	RNF182	GRCh38.p7	6:13948158	aatatttatgaatac[A/G]ttagttttccaagag	221687
rs1330116	snp	A/G	0.450231	0.149691	intron-variant	RNF182	GRCh38.p7	6:13970032	CCCTCTTTTGTTAAT[A/G]TATAATAATTTACAT	221687
rs1330119	snp	G/T	0.00676609	0.0577691	intron-variant	RNF182	GRCh38.p7	6:13926795	tgtgtgtgtgtgtgt[G/T]tTTTTTTTTCCTGAG	221687
rs1330120	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943305	TTTTTTCTTTTTGTA[A/G]AAATAGGGTCTCACC	221687
rs1330121	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13943396	AAAGTGATAGGATTA[A/G]AGGCCTGAGCCACTG	221687
rs1536949	snp	A/C			intron-variant	RNF182	GRCh38.p7	6:13960494	aaaaaacaaacaaaC[A/C]CAAACAAAAAACCAA	221687
rs2057536	snp	A/G	0.45235	0.146814	intron-variant	RNF182	GRCh38.p7	6:13933179	TTTCAGGTAGTATTG[A/G]TTTTTTAATCCTTAG	221687
rs2147197	snp	C/T			intron-variant	RNF182	GRCh38.p7	6:13960700	gtgtgtgtgcgcgcg[C/T]gCACATGCATGTGAT	221687
rs2147200	snp	G/T	0.454904	0.143228	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978623	AACTTCTCATACAGC[G/T]GTTATTATTGATGAA	221687
rs2147201	snp	A/G	0.454784	0.1434	utr-variant-3-prime	RNF182	GRCh38.p7	6:13979295	TAGGCAAAAATTTAA[A/G]AAAACATTCTAGTCT	221687
rs2210081	snp	A/G	0.456803	0.140473	intron-variant	RNF182	GRCh38.p7	6:13971658	tccaaacttccccac[A/G]tctttctgtctctga	221687
rs2308199	in-del	-/CTC	0.455263	0.142713	cds-indel	RNF182	GRCh38.p7	6:13978572	TGTCTGTTTTCCTCT[-/CTC]CTCAGTCTTATCTGA	221687
rs3040808	snp	C/T	0.444444	0.157135	intron-variant	RNF182	GRCh38.p7	6:13960692	gtgtgtgtgtgtgtg[C/T]gcgcgcgtgCACATG	221687
rs3885772	snp	A/T	0	0	intron-variant	RNF182	GRCh38.p7	6:13960658	GAGAGAGAGAGAGAg[A/T]gtgtgtgtgtgtgtg	221687
rs4464798	snp	A/T	0	0	intron-variant	RNF182	GRCh38.p7	6:13951681	tacctttttgccagc[A/T]tgccaggtttctggg	221687
rs4715723	snp	A/G	0.375996	0.215928	intron-variant	RNF182	GRCh38.p7	6:13958423	ATCTATAATCTGAAA[A/G]TCTACATTATAAAAT	221687
rs4715849	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF182	GRCh38.p7	6:13978775	CAATACTTTTTTTCC[C/T]TATTATATTTTTGGT	221687
rs6459295	snp	A/G	0.455024	0.143057	downstream-variant-500B	RNF182	GRCh38.p7	6:13980296	TGAAATAAAAATATC[A/G]TCTTTATAAATAAAT	221687
rs6907416	snp	C/T	0.453818	0.144769	intron-variant	RNF182	GRCh38.p7	6:13961314	AATTTCTAGTCGCAT[C/T]CATATAGTGCTTATG	221687
rs6917710	snp	A/G	0.405082	0.196086	intron-variant	RNF182	GRCh38.p7	6:13952251	ttgtcagttgtgaag[A/G]gatcttctccagcag	221687
rs6938461	snp	C/T	0.384976	0.210431	intron-variant	RNF182	GRCh38.p7	6:13952132	gaggaaagggaaggg[C/T]gaaaagcattgtctg	221687
rs7739694	snp	A/T			intron-variant	RNF182	GRCh38.p7	6:13968080	CAAACAAAAATAAAT[A/T]AGAGGGAATAATAAA	221687
rs7745956	snp	A/G	0.284995	0.247539	intron-variant	RNF182	GRCh38.p7	6:13934835	AAAGGGTAAGGTAAC[A/G]TTTAAATAGGGATTT	221687
rs7758489	snp	A/G			intron-variant	RNF182	GRCh38.p7	6:13969080	cagaaactcagttca[A/G]gtctcatcaggcttg	221687
rs7758493	snp	A/G	0.000399281	0.0141238	intron-variant	RNF182	GRCh38.p7	6:13969090	gttcaggtctcatca[A/G]gcttgtctctgtttt	221687
rs7764529	snp	A/C/G	0.181191	0.243488	intron-variant	RNF182	GRCh38.p7	6:13934949	gagtcagatgaaatg[A/C/G]ggttagaaagaaaag	221687
rs7765960	snp	A/G	0.456568	0.140818	intron-variant	RNF182	GRCh38.p7	6:13958154	ATCTGTTGGGAGGCC[A/G]AGGCAGGCAGATCAC	221687
rs7771397	snp	C/T	0.366266	0.221319	intron-variant	RNF182	GRCh38.p7	6:13949442	ATCTATAGGTTTCTT[C/T]GACTTCATTCTGGCC	221687
rs9349847	snp	C/T	0.497907	0.0322805	intron-variant	RNF182	GRCh38.p7	6:13927480	ATGACGTAAAATTGG[C/T]CCTAATTTTTGGTAT	221687
rs9357947	snp	C/T	0.0693013	0.172766	intron-variant	RNF182	GRCh38.p7	6:13942364	aaattttttttgaga[C/T]aaaatcttgctctgt	221687
rs9370570	snp	A/T	0.00716266	0.059414	intron-variant	RNF182	GRCh38.p7	6:13933212	CAGTGCTGTCCAata[A/T]gtacttttaagttat	221687
rs9370575	snp	C/T	0.467132	0.12391	intron-variant	RNF182	GRCh38.p7	6:13938955	aggtgtggtggttca[C/T]gcctgtaatcccagc	221687
rs9370576	snp	A/C	0.465683	0.126415	intron-variant	RNF182	GRCh38.p7	6:13939005	tgtgaattgcttgaa[A/C]ccaggaggcagaggt	221687
rs9370637	snp	A/G	0.375	0.216506	intron-variant	RNF182	GRCh38.p7	6:13966834	tgtgtgcgcgtgcgt[A/G]tgtgtgtgtgtgtgt	221687
rs9382687	snp	C/T	0.282105	0.24793	intron-variant	RNF182	GRCh38.p7	6:13925495	AGCCCATTTTTATGC[C/T]TGTGGCTGAAGCATT	221687
rs9382688	snp	A/T	0.465996	0.12588	intron-variant	RNF182	GRCh38.p7	6:13926515	AACAGTTTGCAGGTT[A/T]TTTCACAATTGGGCT	221687
rs9382713	snp	C/T	0.384785	0.210554	intron-variant	RNF182	GRCh38.p7	6:13943724	AAGTTTTGCAGCCGA[C/T]ACTTTTAAAAATGAT	221687

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