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
rs717954	snp	A/G	0.404907	0.196224	intron-variant	ARHGEF37	GRCh38.p7	5:149601466	GAGGAACATGCTTAC[A/G]GTCACGGAATTGTTA	389337
rs755858	snp	G/T	0.0970103	0.197722	intron-variant	ARHGEF37	GRCh38.p7	5:149579314	AATCAGGAAGTCTGA[G/T]CTAGGAATCAGTCTC	389337
rs921977	snp	A/T	0.345482	0.231048	intron-variant	ARHGEF37	GRCh38.p7	5:149576333	ctttgaagtcatact[A/T]ctgaggtttcagtcc	389337
rs921978	snp	A/G	0.335788	0.23482	intron-variant	ARHGEF37	GRCh38.p7	5:149576469	ATCATCTAGCAGAAT[A/G]CCTGGCTTATAGGCT	389337
rs965876	snp	A/G	0.427119	0.176434	intron-variant	ARHGEF37	GRCh38.p7	5:149614039	cagtggctcatgctt[A/G]taatcctagcccttt	389337
rs1037714	snp	C/T	0.493013	0.058691	intron-variant	ARHGEF37	GRCh38.p7	5:149573831	atgtaaggatatcca[C/T]gttatagatatgata	389337
rs1056189	snp	A/G	0.265453	0.249522	utr-variant-3-prime	ARHGEF37	GRCh38.p7	5:149634855	GTTGTGGAGATGAGG[A/G]CAAGATTACAATATC	389337
rs1056993	snp	C/T	0.428126	0.175417	synonymous-codon	ARHGEF37	GRCh38.p7	5:149628840	CACATGGTACAGCTG[C/T]AGTTTCCCAGCCGGC	389337
rs1135093	snp	C/T	0.423768	0.179735	missense	ARHGEF37	GRCh38.p7	5:149628958	TACTCACCTGGTTCA[C/T]GGTGGGAATAGAGGG	389337
rs1379544	snp	C/T	0.466412	0.125164	intron-variant	ARHGEF37	GRCh38.p7	5:149601483	TCACGGAATTGTTAG[C/T]GATGCAGCTAAATCT	389337
rs1379545	snp	A/G	0.493881	0.054972	intron-variant	ARHGEF37	GRCh38.p7	5:149613041	TGTCAGGGTGGAAAA[A/G]GCGGCCTTGCAGAGG	389337
rs1457699	snp	C/T	0.453453	0.145282	intron-variant	ARHGEF37	GRCh38.p7	5:149591362	tttgaggattacagg[C/T]gtgagccaccgtgct	389337
rs1457700	snp	A/G	0.473359	0.112298	intron-variant	ARHGEF37	GRCh38.p7	5:149591420	atgaggtctctctct[A/G]ttgcccaggctggag	389337
rs1531233	snp	C/T	0.432797	0.170544	intron-variant	ARHGEF37	GRCh38.p7	5:149588704	GATTGTTTTCCTTTT[C/T]CCCCCCTTCCTTAAA	389337
rs1531234	snp	G/T	0.479824	0.098392	intron-variant	ARHGEF37	GRCh38.p7	5:149588729	CTTAAATGTTTAAAT[G/T]GGCTCCTCCTGGGAG	389337
rs1531235	snp	A/G	0.406296	0.19512	intron-variant	ARHGEF37	GRCh38.p7	5:149588812	TTAAAGCCTTGGGCA[A/G]CTAGCTGATGGATCC	389337
rs1531236	snp	A/G	0.349671	0.229272	intron-variant	ARHGEF37	GRCh38.p7	5:149615102	CCAGATACACCACTG[A/G]TGCATGGATGACTAG	389337
rs1563625	snp	A/G	0.496681	0.0405994	intron-variant	ARHGEF37	GRCh38.p7	5:149598822	tatgtgtgtgtgtgt[A/G]tatatatatatgtat	389337
rs1563626	snp	A/T	0.372995	0.217652	intron-variant	ARHGEF37	GRCh38.p7	5:149608376	AAATATGCAAACAAA[A/T]ttttttttttttgag	389337
rs1870229	snp	C/T	0.471958	0.115042	intron-variant	ARHGEF37	GRCh38.p7	5:149599314	GAGCCCAGCCCCTCT[C/T]CTGTGGCTGAGCAGG	389337
rs1902794	snp	C/G	0.452473	0.146644			GRCh38.p7	5:149593577	gtagttaagtttttg[C/G]tgagtcagaagttat	389337
rs1960010	snp	A/G	0.472429	0.114129	intron-variant	ARHGEF37	GRCh38.p7	5:149602257	AGACAGGGTTTCACC[A/G]TATTGGTCAGACTTG	389337
rs1960011	snp	A/G	0.437542	0.165312	intron-variant	ARHGEF37	GRCh38.p7	5:149602182	CTGCCTCAGCCTCCC[A/G]AGTAGCTGAGACTAC	389337
rs1968762	snp	A/G			intron-variant	ARHGEF37	GRCh38.p7	5:149588083	tttgtattgttagta[A/G]agacagggtttcacc	389337
rs1968763	snp	A/G	0.406296	0.19512	intron-variant	ARHGEF37	GRCh38.p7	5:149588186	ACAGGCGTGAGCCAC[A/G]GTGCCCGGCCTTTTT	389337
rs2125131	snp	C/T	0.406296	0.19512	intron-variant	ARHGEF37	GRCh38.p7	5:149587953	GCTGAGATCATGCCA[C/T]TGCACTCCAGCCTGG	389337
rs2125132	snp	A/G	0.0558544	0.157504	intron-variant	ARHGEF37	GRCh38.p7	5:149587927	cctgggcgacagagt[A/G]agactttgtctccaa	389337
rs2168773	snp	G/T	0.0558544	0.157504	intron-variant	ARHGEF37	GRCh38.p7	5:149588301	taaatattttacttg[G/T]attatcttaagaaat	389337
rs2168774	snp	A/G	0.361894	0.223562	intron-variant	ARHGEF37	GRCh38.p7	5:149572671	ctttactcaaagtct[A/G]ctgatgtaaaggtta	389337
rs2279019	snp	C/T	0.172028	0.23753	utr-variant-5-prime, upstream-variant-2KB	CSNK1A1, ARHGEF37	GRCh38.p7	5:149551313	CTGGGCCGGAGCCGG[C/T]GGCAGTGGTGGCAGC	389337
rs2279132	snp	C/T	0.2768	0.248559	utr-variant-3-prime	ARHGEF37	GRCh38.p7	5:149634024	CACACAGTAGGCCTT[C/T]GGTAGGTATCTGTGG	389337
rs2279133	snp	A/G	0.14665	0.227637	utr-variant-3-prime	ARHGEF37	GRCh38.p7	5:149632490	GACTGGCCATAACCT[A/G]TGGAGAGTCCTGGCC	389337
rs2279134	snp	C/G	0.439224	0.163383	utr-variant-3-prime	ARHGEF37	GRCh38.p7	5:149632488	CTGGCCATAACCTAT[C/G]GAGAGTCCTGGCCAA	389337
rs2400884	snp	C/T	0.406296	0.19512	intron-variant	ARHGEF37	GRCh38.p7	5:149587982	GCTCAGTGCAACCTC[C/T]GCCTCCTGGGTTCAA	389337
rs2400885	snp	C/T	0.445987	0.155207	intron-variant, upstream-variant-2KB	ARHGEF37	GRCh38.p7	5:149596102	cttccttacccaccc[C/T]tctactttgggccac	389337
rs2400886	snp	A/T	0.38286	0.211774	intron-variant	ARHGEF37	GRCh38.p7	5:149597267	TTATCTATTAAAAAA[A/T]AATTTTTTTTGTAAG	389337
rs2400887	snp	A/T	0.483563	0.0891524	intron-variant	ARHGEF37	GRCh38.p7	5:149597268	TATCTATTAAAAAAA[A/T]ATTTTTTTTGTAAGA	389337
rs2400888	snp	A/T	0.483126	0.0902898	intron-variant	ARHGEF37	GRCh38.p7	5:149597269	ATCTATTAAAAAAAA[A/T]TTTTTTTTGTAAGAA	389337
rs2400889	snp	C/T	0.44546	0.155869	intron-variant	ARHGEF37	GRCh38.p7	5:149598542	GGTCTCTTTATTCGA[C/T]CACAAAGTCACTGTC	389337
rs2400890	snp	A/G	0.497907	0.0322805	intron-variant	ARHGEF37	GRCh38.p7	5:149609260	GCACTGTCCAAATGT[A/G]AGCATTATTAATATT	389337
rs2400891	snp	C/T	0.49762	0.0344131	synonymous-codon, utr-variant-5-prime	ARHGEF37	GRCh38.p7	5:149609559	TCAGGTAACATATTT[C/T]TGGAATTCCAAGAGG	389337
rs2400892	snp	C/T	0.484066	0.0878235	intron-variant	ARHGEF37	GRCh38.p7	5:149616316	ctgctgtggagaggc[C/T]gagcaagctgagggc	389337
rs2895862	snp	C/T	0.431325	0.172108	intron-variant	ARHGEF37	GRCh38.p7	5:149587895	TCCCTCCCTTTAGTC[C/T]TTTTTTTTTTTTTTT	389337
rs2895863	snp	C/T	0.123105	0.215401	intron-variant	ARHGEF37	GRCh38.p7	5:149591962	ATCAGGACATAACCT[C/T]ATTGTAAGTCGAAGA	389337
rs2895864	snp	C/T	0.330249	0.23677	intron-variant	ARHGEF37	GRCh38.p7	5:149592062	aatagcaaagggagg[C/T]cctctgtactgttca	389337
rs2895865	snp	C/T	0.453331	0.145452	intron-variant	ARHGEF37	GRCh38.p7	5:149593403	attctggtcatttca[C/T]ataaatgcaataata	389337
rs2895866	snp	A/T	0.0532157	0.154195	intron-variant, upstream-variant-2KB	ARHGEF37	GRCh38.p7	5:149595354	CTAATTACAAAAAAA[A/T]TTTTTCTGTAGAGAC	389337
rs2895867	snp	A/G	0.471673	0.115589	intron-variant	ARHGEF37	GRCh38.p7	5:149598544	TCTCTTTATTCGATC[A/G]CAAAGTCACTGTCAG	389337
rs3073426	in-del	-/AAAGA	0.480382	0.097079	intron-variant	ARHGEF37	GRCh38.p7	5:149582668	GTTCTAGCATAAAGA[-/AAAGA]CAAATATTTAAAGTG	389337
rs3073427	in-del	-/CTTG/TTTG	0	0	intron-variant	ARHGEF37	GRCh38.p7	5:149588230	TTGTTTGTTTGTTTG[-/CTTG/TTTG]CTTTGAGACAGAATC	389337
rs3073428	in-del	-/GCTT			intron-variant	ARHGEF37	GRCh38.p7	5:149588233	TTTGTTTGTTTGCTT[-/GCTT]TGAGACAGAATCTTG	389337
rs3073459	in-del	-/CT	0.375	0.216506	intron-variant	ARHGEF37	GRCh38.p7	5:149598750	CTCatatatatatat[-/CT]atatatagatataga	389337
rs3073460	in-del	-/TA			intron-variant	ARHGEF37	GRCh38.p7	5:149598763	atctatatatagata[-/TA]gatatagatatagat	389337
rs3073461	in-del	-/TTT			intron-variant	ARHGEF37	GRCh38.p7	5:149602072	ttctttttttttttt[-/TTT]gagacggagtctcac	389337
rs3205250	snp	A/G	0	0	utr-variant-3-prime	ARHGEF37	GRCh38.p7	5:149632660	GCTGACTCATTGGTT[A/G]TGATGTCTCCTGATA	389337
rs3205251	snp	G/T	0	0	utr-variant-3-prime	ARHGEF37	GRCh38.p7	5:149632571	TCCTGCAACCACACA[G/T]CACGCAGGTAACATT	389337
rs3733658	snp	C/T	0.388964	0.20782	utr-variant-3-prime	ARHGEF37	GRCh38.p7	5:149633219	GCATGCTTAGCCCCA[C/T]GTCATTCTCAGCACA	389337
rs3733659	snp	A/G	0.0601824	0.162694	intron-variant	ARHGEF37	GRCh38.p7	5:149628998	CCGGATGGCCGATGG[A/G]AGGCAAGCCCCCAGC	389337
rs3733661	snp	C/T	0.0549504	0.156383	synonymous-codon	ARHGEF37	GRCh38.p7	5:149628921	AGCTGGGCTGGGCTC[C/T]GGTGTTAGACATCGG	389337
rs3733662	snp	G/T	0.273334	0.248909	missense	ARHGEF37	GRCh38.p7	5:149628904	GTGTTAGACATCGGG[G/T]GTCTTTGTTCAGCCC	389337
rs3994917	in-del	-/T			intron-variant	ARHGEF37	GRCh38.p7	5:149587913	TTTTTTTTTTTTTTT[-/T]GGAGACAAAGTCTCA	389337
rs4075280	snp	A/C	0.344815	0.231323	intron-variant	ARHGEF37	GRCh38.p7	5:149624688	TCTGCCTTCCAGGCT[A/C]AAGCAATTCTTCTGC	389337
rs4075281	snp	A/G	0.410737	0.191478	intron-variant	ARHGEF37	GRCh38.p7	5:149624553	CTCTTGGCCTCAAGT[A/G]ATCCACCCACCTCGG	389337
rs4235744	snp	C/G	0.470908	0.117046	intron-variant	ARHGEF37	GRCh38.p7	5:149622504	CCTGTTTGGAGCACT[C/G]TCCATGCATGATCTC	389337
rs4291000	snp	A/G	0.0524604	0.153226	intron-variant	ARHGEF37	GRCh38.p7	5:149624480	TTCAAATTGTCATCA[A/G]AAGGTATCCTTGGCC	389337
rs4320246	snp	A/G/T	0.226248	0.267174	intron-variant	ARHGEF37	GRCh38.p7	5:149624302	TATTTGAGCTGGGGT[A/G/T]GGGGGACACACCCAG	389337
rs4382154	snp	A/G	0.135484	0.22223	intron-variant	ARHGEF37	GRCh38.p7	5:149620780	AGGTTGCAGTGAGCC[A/G]AGATCATGCCACCGC	389337
rs4409073	snp	A/G	0.410737	0.191478	intron-variant	ARHGEF37	GRCh38.p7	5:149622387	CTAGAAGTTGATGAC[A/G]GAGACAGAAGGTCGT	389337
rs4443410	snp	C/G	0.450859	0.148847	intron-variant	ARHGEF37	GRCh38.p7	5:149571221	ggctgggattacagg[C/G]atgagccaccgcgtc	389337
rs4489048	snp	C/T	0.290201	0.246747	intron-variant	ARHGEF37	GRCh38.p7	5:149631240	GCAGTGCCATGATCT[C/T]GGCTTACTGCAGCCT	389337
rs4499821	snp	A/C	0.466412	0.125164	intron-variant	ARHGEF37	GRCh38.p7	5:149619822	cgcctgtaatcccag[A/C]attttggaaggccga	389337
rs4629585	snp	A/C	0.486704	0.080444	missense	ARHGEF37	GRCh38.p7	5:149621988	TGGCTGGGCCAGATC[A/C]TGTGCACATTCGTGA	389337
rs4705074	snp	A/G	0.472147	0.114677	intron-variant	ARHGEF37	GRCh38.p7	5:149610444	TTTCGAATGGGTAAC[A/G]TGATTATAAGATTAA	389337
rs4705075	snp	G/T	0.325091	0.238456	intron-variant	ARHGEF37	GRCh38.p7	5:149610650	CATTTTCCCTTTTTA[G/T]TCATCCTTCATGGGT	389337
rs4705076	snp	C/G	0.248716	0.249997	intron-variant	ARHGEF37	GRCh38.p7	5:149615946	AGGCAGCAGACCATT[C/G]TATTAAATAAGATAT	389337
rs4705077	snp	A/G	0.292211	0.246411	utr-variant-3-prime	ARHGEF37	GRCh38.p7	5:149633851	TGAAGACTGCATGAC[A/G]CAAGAGAAATGCAAG	389337
rs4705349	snp	A/G	0.33875	0.233717	intron-variant	ARHGEF37	GRCh38.p7	5:149557478	TTTGTTTGTTTGTTT[A/G]TTTATTTATTTATTT	389337
rs4705350	snp	A/G	0.474723	0.109542	intron-variant	ARHGEF37	GRCh38.p7	5:149559672	CAACAATTTCCAATT[A/G]TGTTTTGATATAGTT	389337
rs4705351	snp	C/T	0.431473	0.171952	intron-variant	ARHGEF37	GRCh38.p7	5:149559739	CTTTTCATTTATCTT[C/T]ACAGACTTAAAAGAG	389337
rs4705352	snp	C/T	0.407502	0.194147	intron-variant	ARHGEF37	GRCh38.p7	5:149569912	aggtgtgagccactg[C/T]acctgaccAtatgtt	389337
rs4705353	snp	A/G	0.400325	0.199756	intron-variant	ARHGEF37	GRCh38.p7	5:149585334	ttgtaatagtgaaac[A/G]ggaaacaaacagttg	389337
rs4705354	snp	A/T	0.480302	0.0972668	intron-variant	ARHGEF37	GRCh38.p7	5:149585662	agctgggattacagg[A/T]gtctgccaccacgcc	389337
rs4705355	snp	A/C	0.480302	0.0972668	intron-variant	ARHGEF37	GRCh38.p7	5:149585665	tgggattacaggtgt[A/C]tgccaccacgcccag	389337
rs4705356	snp	C/T	0.480302	0.0972668	intron-variant	ARHGEF37	GRCh38.p7	5:149585674	aggtgtctgccacca[C/T]gcccagctaattttt	389337
rs4705357	snp	A/C	0.472429	0.114129	intron-variant	ARHGEF37	GRCh38.p7	5:149604438	CTCTCTCCCCTGCAA[A/C]TTTGGCAGTCCTGTT	389337
rs4705358	snp	C/T	0.434398	0.168811	intron-variant	ARHGEF37	GRCh38.p7	5:149604785	CCTCCTGGGTTCAAG[C/T]GATTCTCATGTCTCA	389337
rs5872137	in-del	-/TTGC	0.40386	0.197046	intron-variant	ARHGEF37	GRCh38.p7	5:149588227	TGTTTGTTTGTTTGT[-/TTGC]TTGCTTTGAGACAGA	389337
rs5872138	in-del	-/T			intron-variant	ARHGEF37	GRCh38.p7	5:149613765	TTCTACAGTGTTTTC[-/T]TTTTTTTTTTTTTTT	389337
rs5872139	in-del	-/TATAA/TGTAA	0.436643	0.173512	intron-variant	ARHGEF37	GRCh38.p7	5:149624649	GTGGTGGTGTGCACC[-/TATAA/TGTAA]TCCCAGCTACTTGGG	389337
rs5872140	in-del	-/GTAAT			intron-variant	ARHGEF37	GRCh38.p7	5:149624650	TGGTGGTGTGCACCT[-/GTAAT]CCCAGCTACTTGGGA	389337
rs6149294	in-del	-/ATAATAAATATATTACATATGTAATATGACATAT	0	0	intron-variant	ARHGEF37	GRCh38.p7	5:149608305	TGTAATATGACATAT[lengthTooLong]GAGGATGGCGATTAA	389337
rs6579743	snp	G/T	0.32955	0.237006	intron-variant	ARHGEF37	GRCh38.p7	5:149591063	gaggacctctttTAG[G/T]tctttttttcttttt	389337
rs6579744	snp	A/G	0.0345262	0.126772	intron-variant	ARHGEF37	GRCh38.p7	5:149600097	TATTGCTCCTAGGCT[A/G]TAAGTGTGTTCAGCA	389337
rs6579745	snp	C/T	0.324619	0.238604	intron-variant	ARHGEF37	GRCh38.p7	5:149600585	CCCCGGTTCAGCTTT[C/T]CTTCCCCACTGAGTA	389337
rs6579746	snp	C/G	0.324619	0.238604	intron-variant	ARHGEF37	GRCh38.p7	5:149606813	agttgcttcctgcaa[C/G]catcagaataaaacc	389337
rs6579747	snp	A/G	0.407674	0.194008	intron-variant	ARHGEF37	GRCh38.p7	5:149606980	gagtgcagtggtgca[A/G]tctcagctcactgct	389337
rs6579748	snp	G/T	0.471388	0.116136	intron-variant	ARHGEF37	GRCh38.p7	5:149611927	taatggcttcactaa[G/T]aaaggagaaataaaa	389337
rs6579749	snp	A/G	0.150333	0.229274	intron-variant	ARHGEF37	GRCh38.p7	5:149617628	CATCACTTGCTTCCT[A/G]TCGCAGAACTGGTAA	389337
rs6579750	snp	A/G	0.150333	0.229274	intron-variant	ARHGEF37	GRCh38.p7	5:149618123	ATGTCCGTGACATCC[A/G]CTTTCCTGAGTTGGC	389337
rs6859243	snp	C/G	0.49827	0.0293608	intron-variant	ARHGEF37	GRCh38.p7	5:149590934	ACACTTAATAAAATA[C/G]AATAGAACAATCAAA	389337

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