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
rs9724	snp	C/G	0.0700422	0.173537	utr-variant-3-prime, nc-transcript-variant	ARHGAP10	GRCh38.p7	4:148072706	TCGGTGCTCCTCACC[C/G]GTGTGCTGTTTTCCA	79658
rs168367	snp	A/G	0.0941369	0.195465	intron-variant	ARHGAP10	GRCh38.p7	4:147935156	TTAATCACAACAGAC[A/G]GCTCGACCATCACCC	79658
rs168368	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147945091	GCTGGGCTTACACGC[C/T]TCTAACAACCTGGCC	79658
rs180952	snp	C/T	0.180702	0.240204	intron-variant	ARHGAP10	GRCh38.p7	4:147932728	ggtttgctgcacaga[C/T]catcccattactcag	79658
rs182989	snp	C/T	0.104149	0.203046	intron-variant	ARHGAP10	GRCh38.p7	4:147930597	ATTTCACAGGAATTG[C/T]TGAGTACTTATATTT	79658
rs187005	snp	C/T	0.161924	0.233971	intron-variant	ARHGAP10	GRCh38.p7	4:147934906	CCCACAGTGATACTC[C/T]CTTCTTCTAAACATA	79658
rs187006	snp	A/T	0.438666	0.164028	intron-variant	ARHGAP10	GRCh38.p7	4:147945437	AGTTTTCTTTATCCA[A/T]ATAGCGTGTAATTAT	79658
rs187007	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147943090	CATGAACTATTGTAA[G/T]TGATATTTTACATTC	79658
rs238866	snp	C/T	0.0810805	0.184299	intron-variant	ARHGAP10	GRCh38.p7	4:147926433	tcgttttcactttcc[C/T]ctctccctgacttcc	79658
rs349023	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147917134	ATCCTTTGATTCAGG[A/T]GTAGGATAGCTCTCA	79658
rs349024	snp	C/T	0.0402882	0.136092	intron-variant	ARHGAP10	GRCh38.p7	4:147933716	ATCCATCTGGGCCAC[C/T]AGAACAGTCTTCTGG	79658
rs349025	snp	C/T	0.104504	0.2033	intron-variant	ARHGAP10	GRCh38.p7	4:147930394	TTAGCCTATGGTATA[C/T]ATTTAACAAATGAAT	79658
rs731989	snp	A/G	0.0839998	0.186933	intron-variant	ARHGAP10	GRCh38.p7	4:147863500	CCAATGCCCATGGAT[A/G]GATGGATGAGTAAAT	79658
rs744031	snp	C/T	0.287606	0.247155	intron-variant	ARHGAP10	GRCh38.p7	4:147810833	TTCCTAAAGCCATCA[C/T]GACAGGGTCTGTCAC	79658
rs747097	snp	C/T	0.465892	0.126058	intron-variant	ARHGAP10	GRCh38.p7	4:147809674	GGTCCCCAACCTTTT[C/T]GGCACCAGGGACTGG	79658
rs869762	snp	C/G	0.26326	0.249648	intron-variant	ARHGAP10	GRCh38.p7	4:148005323	GTGTGCTGGCTCATG[C/G]CTGAAATCTGATCAC	79658
rs869763	snp	A/C	0.266	0.249487	intron-variant	ARHGAP10	GRCh38.p7	4:148005327	GCTGGCTCATGGCTG[A/C]AATCTGATCACTTTG	79658
rs869764	snp	C/G	0.26271	0.249677	intron-variant	ARHGAP10	GRCh38.p7	4:148005929	GAGATACATGTATTT[C/G]TTTCACCTAATATTG	79658
rs893022	snp	A/G	0.447162	0.153712	intron-variant	ARHGAP10	GRCh38.p7	4:147832084	GTGTGTGTATGTCGG[A/G]CGGGGCAGTCAGGGG	79658
rs893023	snp	C/T	0.238171	0.24972	intron-variant	ARHGAP10	GRCh38.p7	4:147831208	CGAAACAATTTAGAG[C/T]GTATCCAACGTCCAG	79658
rs893024	snp	A/G	0.391954	0.205789	intron-variant	ARHGAP10	GRCh38.p7	4:147843101	GAAGCCCACAAACCC[A/G]TTTGTACTGGGCACC	79658
rs893025	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147943159	TGTTTTAAACTAAAG[A/T]AGGGAAGAAGGAAGA	79658
rs893026	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147811057	CCACAGGAAAAAGAG[A/G]ATTAAGGCGAGGAGC	79658
rs893030	snp	A/G	0.136166	0.22258	intron-variant	ARHGAP10	GRCh38.p7	4:147863400	tactacaacatggat[A/G]aaccttgaggacatc	79658
rs893031	snp	A/T			intron-variant	ARHGAP10	GRCh38.p7	4:147862671	CAGTCAACCTCTATC[A/T]CCACCCCCTTAATGT	79658
rs893032	snp	C/T	0.0505692	0.150756	intron-variant	ARHGAP10	GRCh38.p7	4:147899332	gtgtgtgcatgcgtg[C/T]gtgtgtgtgtgtctg	79658
rs893033	snp	A/G	0.41408	0.188621	intron-variant	ARHGAP10	GRCh38.p7	4:147899481	TTTCATAGGTTCTCC[A/G]TCTTGTTCTTATTGG	79658
rs893034	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147899561	caACAGTTCTCTAAT[A/G]ATTAATTGCTTGAAT	79658
rs906124	snp	C/T	0.487621	0.0776941	intron-variant	ARHGAP10	GRCh38.p7	4:148069209	CAGCCTTATCTGCAA[C/T]TGCGGAGCCACTTTT	79658
rs906125	snp	A/T	0.487809	0.0771174	intron-variant	ARHGAP10	GRCh38.p7	4:147924039	CCTCCCACAGAAGAC[A/T]GTCCTCTATTTCCAC	79658
rs924780	snp	A/C	0.487495	0.0780784	intron-variant	ARHGAP10	GRCh38.p7	4:147764846	TAAAACACACTTAAT[A/C]AATGTTTACTGGGCT	79658
rs924781	snp	C/T	0.00159617	0.0282053	intron-variant	ARHGAP10	GRCh38.p7	4:147757774	CCGAAACAAGGACAA[C/T]GGTAATTAGCTGGGC	79658
rs924782	snp	A/G	0.00159617	0.0282053	intron-variant	ARHGAP10	GRCh38.p7	4:147757643	AGTAAGCCAATGTTC[A/G]GAGGAAGCAGAGGCT	79658
rs924784	snp	G/T	0.00279162	0.0372561	intron-variant	ARHGAP10	GRCh38.p7	4:147740511	CAGTCATCATACTAA[G/T]GTAAAAAGAATATCC	79658
rs937020	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147931297	TCTCTTAATAAATTA[A/G]ATTGAGATTCGTTCT	79658
rs964170	snp	A/C	0.434976	0.168179	intron-variant	ARHGAP10	GRCh38.p7	4:147774805	AGACTCTGTCAATGA[A/C]AAAATGTTCTTCTCA	79658
rs969032	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147955286	CAGCTCAGAATTATC[A/G]AATAAATCCAAACAA	79658
rs975371	snp	C/T	0.34303	0.232046	intron-variant	ARHGAP10	GRCh38.p7	4:147923075	AATTGTTGAGACACA[C/T]AATATTACCAATATG	79658
rs975372	snp	C/T	0.342806	0.232136	intron-variant	ARHGAP10	GRCh38.p7	4:147922932	ATAAGACATTTTCTC[C/T]GAGTAAACAGTAAAG	79658
rs988112	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147866362	TGACACAATCTTTAA[A/G]AAAGTAAAATCACAG	79658
rs990245	snp	A/C	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147956457	ATGTGAAAACAAAAA[A/C]GAATAGAACCAGTTT	79658
rs992572	snp	C/T	0.0275645	0.114116	intron-variant	ARHGAP10	GRCh38.p7	4:148039488	TATTTTTAGTAAAGA[C/T]GAGGTTTCACTGTGT	79658
rs1013842	snp	A/G	0.418169	0.184985	intron-variant	ARHGAP10	GRCh38.p7	4:147862251	ggcaacagtacctgg[A/G]cttggctacaacttt	79658
rs1021956	snp	G/T	0.240478	0.249819	intron-variant	ARHGAP10	GRCh38.p7	4:148058023	CTCGGTGTGCTCGTG[G/T]GGAGCCAAACAATGT	79658
rs1036441	snp	C/T	0.145642	0.227177	intron-variant	ARHGAP10	GRCh38.p7	4:147909102	taaattgggggttcc[C/T]gtgaacccctcatca	79658
rs1036444	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147940014	CAAAAAACTCCTGTA[G/T]AAAGTATAGGAATGG	79658
rs1039660	snp	C/T	0.29432	0.24604	intron-variant	ARHGAP10	GRCh38.p7	4:147973402	CCAACTATGTACCCA[C/T]GAAAATTAAAAATAA	79658
rs1113688	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147732709	ACCAGGCGGGGCCCA[G/T]GCGGGGCCCGCTGGC	79658
rs1119887	snp	C/T	0.272241	0.249009	intron-variant	ARHGAP10	GRCh38.p7	4:147803955	ccagcattcccacta[C/T]cgaatatttatccaa	79658
rs1161575	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147778549	CCCTGCTCTAGGGCT[G/T]TAACAAAACTGAAAT	79658
rs1161576	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147778525	CTGAAATATGAAAAA[G/T]GGCTGTGAAAGACCC	79658
rs1161577	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147807162	ACCTCAAGGGAAGCA[A/T]AATATGTCACACAGT	79658
rs1177326	snp	A/G	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147803332	tttctttttttattg[A/G]tacataactgtacat	79658
rs1182742	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147790271	aataattccataagg[G/T]gggcttcacctttgt	79658
rs1183548	snp	C/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147774425	CCCAGGTCATGTTTT[C/T]CACCTGCACACTCTT	79658
rs1185058	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147774492	TTGACTTCAAAATTG[G/T]CCTTATATAACCCTT	79658
rs1185059	snp	G/T			intron-variant	ARHGAP10	GRCh38.p7	4:147790130	agtccaaaatcaagg[G/T]gctggtatattcggt	79658
rs1185487	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147790122	ggctgggaagtccaa[A/G]atcaaggggctggta	79658
rs1317354	snp	A/G	0.266	0.249487	intron-variant	ARHGAP10	GRCh38.p7	4:148005306	ATACATATATAAGCT[A/G]GGTGTGCTGGCTCAT	79658
rs1347596	snp	A/G	0.427119	0.176434	intron-variant	ARHGAP10	GRCh38.p7	4:147838927	TATCTGAAACTAAAT[A/G]TGATTAGGGCTATTT	79658
rs1369958	snp	A/C	0.278399	0.248382	intron-variant	ARHGAP10	GRCh38.p7	4:147903580	tcatacagaagattt[A/C]actgccctaaaaatc	79658
rs1369959	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147927500	TGAGAGAGTGTGAGA[G/T]ACTCCAAAAACATAA	79658
rs1395296	snp	C/G	0.0696718	0.173152	intron-variant	ARHGAP10	GRCh38.p7	4:147993423	TATCAGGTCATTTAA[C/G]TATTGTTATGAATAA	79658
rs1436489	snp	A/G	0.265453	0.249522	intron-variant	ARHGAP10	GRCh38.p7	4:147840563	TGCTTACCTTGTTTG[A/G]ATTCAGGCGGTATGT	79658
rs1436490	snp	C/G	0.239037	0.24976	intron-variant	ARHGAP10	GRCh38.p7	4:147844325	GTTCAAGCATTTATC[C/G]TTTGTGTTACAATCT	79658
rs1436491	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147951830	caaacttaccgaaac[G/T]tacactataaatata	79658
rs1436492	snp	A/G	0.0513262	0.151752	intron-variant	ARHGAP10	GRCh38.p7	4:147951792	tattgtatgtcaact[A/G]tgtttcaataaagct	79658
rs1436493	snp	A/G/T	0.000399281	0.0141238	intron-variant	ARHGAP10	GRCh38.p7	4:147940007	CTCCTGTATAAAGTA[A/G/T]AGGAATGGAATGACA	79658
rs1469865	snp	C/T	0.415727	0.187175	intron-variant	ARHGAP10	GRCh38.p7	4:147860045	GAGCATCTCAATTCA[C/T]TGAAAATTAGCATTA	79658
rs1469866	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147860018	ATTACATTAACCACT[C/G]CCAAAAGTAATGAAT	79658
rs1469867	snp	G/T	0.455024	0.143057	intron-variant	ARHGAP10	GRCh38.p7	4:147859979	CTAACATTTTCCCCT[G/T]TAAAAAGCATCCCCC	79658
rs1469868	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147859640	caagaagcttacatt[C/G]tagtggaagaagcca	79658
rs1529935	snp	C/T	0.47802	0.102502	intron-variant	ARHGAP10	GRCh38.p7	4:147909321	tcatgttcaccaaca[C/T]ggaagctTATCAGAG	79658
rs1529939	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147909577	gatgctctgtgtcag[A/G]aAGTGGGGATGCAGA	79658
rs1567062	snp	C/T	0.499382	0.017561	intron-variant	ARHGAP10	GRCh38.p7	4:147993952	gatacatcaatacta[C/T]ctaccctttcagggt	79658
rs1583541	snp	G/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147927502	TGTGAGAGAGTGTGA[G/T]AGACTCCAAAAACAT	79658
rs1604785	snp	A/G	0.440057	0.162414	intron-variant	ARHGAP10	GRCh38.p7	4:147803487	ttgttattttgaaat[A/G]tttttaattatagtc	79658
rs1811406	snp	C/T	0.394721	0.203852	intron-variant	ARHGAP10	GRCh38.p7	4:147893064	TTGAATGGAAGTAAA[C/T]ttttttttttttgag	79658
rs1811407	snp	C/G			intron-variant	ARHGAP10	GRCh38.p7	4:147893150	tgcaacctctgcctc[C/G]tgggttctagcgatt	79658
rs1873175	snp	A/C	0.3744	0.216852	intron-variant	ARHGAP10	GRCh38.p7	4:148004638	ctgactatgggctgg[A/C]ggctgcctcagctcc	79658
rs1876196	snp	C/T	0.000798403	0.0199641	intron-variant	ARHGAP10	GRCh38.p7	4:148071353	gggagtggtggctca[C/T]gcctgtaatcccagc	79658
rs1966686	snp	A/T	0	0	intron-variant	ARHGAP10	GRCh38.p7	4:147853099	TCTGAGCTGCTGAAA[A/T]GGGCTCTAGCCACCT	79658
rs1969102	snp	A/G	0.43978	0.162738	intron-variant	ARHGAP10	GRCh38.p7	4:147738482	GGCGTGGACCCAGGA[A/G]GTGGAGCTTTCAGCG	79658
rs1969103	snp	A/C	0.451732	0.147663	intron-variant	ARHGAP10	GRCh38.p7	4:147738560	TCTGTCTCCCCCCCC[A/C]AAAAAAAATTATAAT	79658
rs1969104	snp	A/G	0.0275645	0.114116	intron-variant	ARHGAP10	GRCh38.p7	4:147757258	GCAGTGAGCCCAGAT[A/G]GCACCACTGCACTCC	79658
rs1971125	snp	C/T			intron-variant	ARHGAP10	GRCh38.p7	4:147835403	ttttcccttaagtct[C/T]gctctgtcgcccagg	79658
rs2015429	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147940030	AATTGTCTCTGCTCA[A/G]CAAAAAACTCCTGTA	79658
rs2015431	snp	A/G			intron-variant	ARHGAP10	GRCh38.p7	4:147940027	TGTCTCTGCTCAACA[A/G]AAAACTCCTGTATAA	79658
rs2017857	snp	C/G	0.416218	0.186739	intron-variant	ARHGAP10	GRCh38.p7	4:148067248	CTTACTGTACCCTTT[C/G]AAGAAGTGTTCCTAT	79658
rs2043643	snp	C/G	0.413748	0.188909	intron-variant	ARHGAP10	GRCh38.p7	4:147898772	cctgtcttcttctga[C/G]ccctccaaactgttt	79658
rs2043644	snp	C/T	0.451856	0.147493	intron-variant	ARHGAP10	GRCh38.p7	4:147819068	TGGGGCTCATTTGCA[C/T]AACTAATCTGATGTA	79658
rs2043645	snp	A/G	0.379942	0.213577	intron-variant	ARHGAP10	GRCh38.p7	4:147881071	ggccaggccagtctc[A/G]aactcctgacctcaa	79658
rs2055551	snp	A/G	0.439502	0.163061	intron-variant	ARHGAP10	GRCh38.p7	4:147771018	gtgggccctaatcca[A/G]tattactggtctcct	79658
rs2076947	snp	C/T	0.370365	0.219117	intron-variant	ARHGAP10	GRCh38.p7	4:148067008	CAGGACTTTGCTGGC[C/T]GGGGCACCCCGGGTG	79658
rs2118032	snp	A/G	0.0799831	0.183287	intron-variant	ARHGAP10	GRCh38.p7	4:147937138	taTTCAGCAGCCCCC[A/G]tccccaacctttttg	79658
rs2118033	snp	A/C	0.465052	0.127485	intron-variant	ARHGAP10	GRCh38.p7	4:147936949	tcctataacaatcta[A/C]tgtcgccactgatct	79658
rs2118034	snp	C/T	0.141258	0.225111	intron-variant	ARHGAP10	GRCh38.p7	4:147869497	TATTAAGGATTCCAA[C/T]CAGGTCATTTTGTGA	79658
rs2118035	snp	G/T	0.3746	0.216737	intron-variant	ARHGAP10	GRCh38.p7	4:147929976	ACATTTCATCATTAA[G/T]GAGGCACATGTGCAT	79658
rs2118036	snp	A/G	0.429688	0.173817	intron-variant	ARHGAP10	GRCh38.p7	4:147795339	TACCTTTTATCCTAC[A/G]TTTGTCTTTTTATAC	79658
rs2134706	snp	A/G	0.428484	0.175052	intron-variant	ARHGAP10	GRCh38.p7	4:147787353	GGGAGGAGTATTTTC[A/G]GTTTAGGAAACACAT	79658

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