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
rs23282	snp	C/T	0.468349	0.121752	intron-variant	ARHGAP26	GRCh38.p7	5:142890736	AACTGGAAAGTGTCC[C/T]GTGCATGTCGGTGGT	23092
rs26690	snp	A/G	0.483852	0.0883933	intron-variant	ARHGAP26	GRCh38.p7	5:142904475	CTGGAGTACAGTGGT[A/G]GCAATCTCAGCTCAC	23092
rs26691	snp	C/T	0.446249	0.154875	intron-variant	ARHGAP26	GRCh38.p7	5:142904177	AAGTGAGCCTTTGTT[C/T]CTACTTTTCATAAAA	23092
rs26692	snp	G/T	0.0103295	0.0711199	intron-variant	ARHGAP26	GRCh38.p7	5:142903003	GTATTCAGGGCGACT[G/T]TGAAGGATCATCCCA	23092
rs26693	snp	C/T	0.468949	0.12067	intron-variant	ARHGAP26	GRCh38.p7	5:142900701	CTTACTAAACATAAT[C/T]CCATCCCACTTATTT	23092
rs26696	snp	A/T	0.455383	0.142541	intron-variant	ARHGAP26	GRCh38.p7	5:142885037	CCAAGATTCCCCCTC[A/T]AAGAACTTTGTGAAA	23092
rs26697	snp	A/C	0.438526	0.164189	intron-variant	ARHGAP26	GRCh38.p7	5:142944847	AGAACACAAGCGAAA[A/C]TTAGGTTTGTACCTT	23092
rs26698	snp	A/G	0.440884	0.161442	intron-variant	ARHGAP26	GRCh38.p7	5:142945989	ATCTGGACATCAGCT[A/G]GTGGTGATGTTCCTT	23092
rs26699	snp	C/T	0.437401	0.165472	intron-variant	ARHGAP26	GRCh38.p7	5:142946278	CCAACAACTACAATA[C/T]AGATAACAAACTGTA	23092
rs26706	snp	C/G	0.4582	0.138394	intron-variant	ARHGAP26	GRCh38.p7	5:142877295	CAGGAAGTCAGGAAA[C/G]GCTTCCCAGAGAAGG	23092
rs26707	snp	C/G	0.489893	0.0703642	intron-variant	ARHGAP26	GRCh38.p7	5:142874108	GGCGGGGACCTCCCT[C/G]TCCACAGCACAGGAG	23092
rs27131	snp	A/G	0.21725	0.247846	intron-variant	ARHGAP26	GRCh38.p7	5:142945927	AAATGAGACTGAGGA[A/G]ATGTGACAACTAATT	23092
rs27546	snp	A/T	0.477345	0.103991	intron-variant	ARHGAP26	GRCh38.p7	5:142886180	AACATATGACAGAGG[A/T]CAAGCAAACTGTTGA	23092
rs27779	snp	G/T	0.475259	0.108435	intron-variant	ARHGAP26	GRCh38.p7	5:142879518	ATTTCTGAAGACTTT[G/T]TTTTAAAGAAAGGTG	23092
rs27899	snp	C/G	0.483923	0.0882034	intron-variant	ARHGAP26	GRCh38.p7	5:142904030	CCAAAGGATACACTG[C/G]TGATAGATAACAGGG	23092
rs27958	snp	C/T	0.487241	0.0788465	intron-variant	ARHGAP26	GRCh38.p7	5:142874121	AGGAAACAGGAGTGG[C/T]GGGGACCTCCCTGTC	23092
rs28052	snp	C/G	0.472052	0.11486	intron-variant	ARHGAP26	GRCh38.p7	5:142900305	AGTGGTAAGCCCCAT[C/G]GAGTCACTAGAGACT	23092
rs28053	snp	A/C	0.214541	0.247473	intron-variant	ARHGAP26	GRCh38.p7	5:142946674	AAACAACCTAATTTG[A/C]AGACTTTCTAATACT	23092
rs28304	snp	A/G	0.442655	0.159323	intron-variant	ARHGAP26	GRCh38.p7	5:142902294	GCTACAGACGCTACA[A/G]ATTTGAAACATAACC	23092
rs35290	snp	C/T	0.496968	0.0388195	intron-variant, nc-transcript-variant	ARHGAP26, LOC107986457	GRCh38.p7	5:142970658	GATGGCTCCCCTGTC[C/T]GTTACACCCTGGCCA	23092
rs35291	snp	A/G	0.497558	0.0348586	intron-variant, nc-transcript-variant	ARHGAP26, LOC107986457	GRCh38.p7	5:142969500	ATAAAATCAAGCTTT[A/G]TTTGTTTAAATCTGG	23092
rs35292	snp	C/T	0.0383493	0.133136	intron-variant	ARHGAP26	GRCh38.p7	5:142903490	ACAAAGTATCTGTTT[C/T]AACAATCCAGATCAA	23092
rs35293	snp	C/T	0.325799	0.238232	intron-variant	ARHGAP26	GRCh38.p7	5:142849036	TCACCATGGAACCAA[C/T]AAACAACATGGAAGA	23092
rs35294	snp	G/T	0.457037	0.140127	intron-variant	ARHGAP26	GRCh38.p7	5:142979472	TTGAGTCAAAAGGAA[G/T]ATGTCCCATAGTCTC	23092
rs35295	snp	A/C	0.497359	0.0362457	intron-variant	ARHGAP26	GRCh38.p7	5:142977551	CAAAGATCCGTATCC[A/C]GCAGGGGGAAAAAAA	23092
rs35296	snp	A/T	0.486984	0.079614	intron-variant	ARHGAP26	GRCh38.p7	5:142835841	TCTAATTGAGATCAC[A/T]GTAAGAGCTAAATTA	23092
rs35297	snp	A/G	0.356597	0.226135	intron-variant	ARHGAP26	GRCh38.p7	5:142837505	TGAGCTTCACTTGGC[A/G]ATGATAAGAAGGCCT	23092
rs35298	snp	C/T	0.361263	0.223876	intron-variant	ARHGAP26	GRCh38.p7	5:142841643	GCTCCCTTGCACTCA[C/T]GGGACAAGCTTTCAG	23092
rs35299	snp	C/T	0.425894	0.177655	intron-variant	ARHGAP26	GRCh38.p7	5:142823211	CTCATGTGTTTAGCA[C/T]GAGCTTCCATGCCAG	23092
rs35300	snp	A/G	0.29789	0.24537	intron-variant	ARHGAP26	GRCh38.p7	5:142823490	GTCACACAGTCCCAA[A/G]AGCCAGGCTTTAGGG	23092
rs35301	snp	C/T	0.29789	0.24537	intron-variant	ARHGAP26	GRCh38.p7	5:142823642	ACCCTTGGTCCTACA[C/T]CTTGAGGAAGGAAAC	23092
rs35302	snp	A/G	0.474272	0.110462	intron-variant	ARHGAP26	GRCh38.p7	5:142824508	TCTGGCTCTCTTGCC[A/G]GGACACCCACTCTGG	23092
rs35303	snp	C/T	0.474363	0.110278	intron-variant	ARHGAP26	GRCh38.p7	5:142824985	ACCAATGAAAATGGA[C/T]CAGCAACTCTTTTCA	23092
rs35314	snp	A/G/T	0.00636936	0.0560724	intron-variant	ARHGAP26	GRCh38.p7	5:142877620	TATGGCTGGGCGAAG[A/G/T]ACTTGGGGGTCCTGA	23092
rs37184	snp	A/G	0.41441	0.188333	intron-variant	ARHGAP26	GRCh38.p7	5:142932405	GAGGTAAGTTACTAC[A/G]GGAGGCTGAACCAGA	23092
rs37185	snp	A/G	0.499831	0.00918375	intron-variant	ARHGAP26	GRCh38.p7	5:142931334	CACAAATGGTACTCC[A/G]CAAGAAAAAGAGACT	23092
rs37186	snp	A/G	0.581317	0.151092	intron-variant	ARHGAP26	GRCh38.p7	5:142930327	TGCCAGACTCAGTGG[A/G]TATCTGCAGACTGCT	23092
rs37187	snp	C/G	0.472989	0.113031	intron-variant	ARHGAP26	GRCh38.p7	5:142928625	GCTGGCAAGATAATA[C/G]AGCCAGGATGTGAAC	23092
rs37188	snp	A/C	0.427727	0.175821	intron-variant	ARHGAP26	GRCh38.p7	5:142928233	TAAAAAAAAAAAAAA[A/C]ACACACACacacaaa	23092
rs37189	snp	A/G	0.234109	0.249494	intron-variant	ARHGAP26	GRCh38.p7	5:142924620	TGAGAGACAGAGGAA[A/G]TAAGAAACCAGAAGA	23092
rs37190	snp	A/C	0.209997	0.246779	intron-variant	ARHGAP26	GRCh38.p7	5:142923927	ttgcagtgagcggag[A/C]ttgcgccactgcact	23092
rs37191	snp	A/G	0.22263	0.248497	intron-variant	ARHGAP26	GRCh38.p7	5:142920928	GGGAATGAATTCAGC[A/G]TATTCCAGTCATGCC	23092
rs37192	snp	C/T	0.419135	0.184101	intron-variant	ARHGAP26	GRCh38.p7	5:142918578	AAATCATGTAGAAGC[C/T]AATACAAAAGGGTGT	23092
rs37193	snp	A/G	0.204803	0.245881	intron-variant	ARHGAP26	GRCh38.p7	5:142979182	TCCTATCTTCTTTAA[A/G]CTAATAACGTTTTTT	23092
rs37194	snp	A/C	0.244776	0.249945	intron-variant	ARHGAP26	GRCh38.p7	5:142978337	GCCAAGGATTTCTCA[A/C]ACATTATCTCATACC	23092
rs37195	snp	C/T	0.204803	0.245881	intron-variant	ARHGAP26	GRCh38.p7	5:142978193	AGGCCTTGGGCAAAC[C/T]CTAAGCCCCTCTGAA	23092
rs37196	snp	A/G	0.20511	0.245937	intron-variant	ARHGAP26	GRCh38.p7	5:142977412	TTTTTTTTTAATAAG[A/G]TTAATTGATGGCCCT	23092
rs37197	snp	C/G	0.20511	0.245937	intron-variant	ARHGAP26	GRCh38.p7	5:142975503	AAGAAACAATAACCA[C/G]ATTCAGGTCATTTAA	23092
rs37198	snp	A/C	0.21695	0.247806	intron-variant	ARHGAP26	GRCh38.p7	5:142973843	TCCCACCCACCTCCC[A/C]CTAAACCAACGGAGA	23092
rs37199	snp	G/T	0.301681	0.2446	intron-variant	ARHGAP26	GRCh38.p7	5:142973532	ACTATACAGAAAAGT[G/T]TAAAAATGGAAGGTT	23092
rs37200	snp	A/G	0.221737	0.248397	intron-variant, nc-transcript-variant	ARHGAP26, LOC107986457	GRCh38.p7	5:142971111	ATCATTATAATGGAC[A/G]TCTCTGAAAAAAAAT	23092
rs37201	snp	A/C	0.216649	0.247765	intron-variant, nc-transcript-variant	ARHGAP26, LOC107986457	GRCh38.p7	5:142969171	GGCAGATTGCTTGAG[A/C]ACAGGAGTTCAAGAC	23092
rs37202	snp	A/C	0.222928	0.24853	intron-variant	ARHGAP26, LOC107986457	GRCh38.p7	5:142965939	AAGATTAAACTAAAA[A/C]TTTTTACAGGCCCTT	23092
rs37203	snp	A/G	0.218151	0.247963	intron-variant	ARHGAP26, LOC107986457	GRCh38.p7	5:142964735	ATTTCGGGTGATCCA[A/G]AAATGCATGTCAGGT	23092
rs37204	snp	C/T	0.216649	0.247765	intron-variant, nc-transcript-variant	ARHGAP26, LOC107986457	GRCh38.p7	5:142963509	aaaaaataagagatg[C/T]tggtaaggttgtgga	23092
rs37205	snp	C/T	0.431621	0.171796	intron-variant, upstream-variant-2KB	ARHGAP26, LOC107986457	GRCh38.p7	5:142962560	AACAAGGAAAATTCT[C/T]GTGGATTTCTGGTTG	23092
rs37206	snp	A/C	0.440609	0.161766	intron-variant, upstream-variant-2KB	ARHGAP26, LOC107986457	GRCh38.p7	5:142961210	AGCCACCGTGCCCAG[A/C]GTGGATCCATTTTTT	23092
rs37207	snp	A/G	0.223225	0.248562	intron-variant, upstream-variant-2KB	ARHGAP26, LOC107986457	GRCh38.p7	5:142960629	TTTCTTTCACATTAc[A/G]gtagtctcccctcat	23092
rs37208	snp	C/G	0.182933	0.240836	intron-variant	ARHGAP26	GRCh38.p7	5:142958768	GTTGAATTTGCTAAT[C/G]ACACTCATTTTTCCC	23092
rs37209	snp	A/C	0.27008	0.249192	intron-variant	ARHGAP26	GRCh38.p7	5:142958748	TCATTTTTCCCAGCT[A/C]ATTAGCATACCTGTA	23092
rs37210	snp	C/T	0.417521	0.185571	intron-variant	ARHGAP26	GRCh38.p7	5:142956623	CACAGATGTCTTGAA[C/T]GATTTACAATTTCTG	23092
rs37211	snp	A/C	0.416218	0.186739	intron-variant	ARHGAP26	GRCh38.p7	5:142955601	CTACAATGATTGAGG[A/C]GGGAGGTTTGTGATA	23092
rs37212	snp	A/G	0.430285	0.173197	intron-variant	ARHGAP26	GRCh38.p7	5:142953438	AAGACTTTTTGCATG[A/G]AAGTTTTAAAAATGA	23092
rs37213	snp	G/T	0.415563	0.18732	intron-variant	ARHGAP26	GRCh38.p7	5:142953310	GGTGACCAATCTGTT[G/T]GCTTGTTGACTCTCT	23092
rs37214	snp	A/G	0.361263	0.223876	intron-variant	ARHGAP26	GRCh38.p7	5:142899071	TGAGGATGAAGGACT[A/G]GAGGGAGGCATCTAT	23092
rs37215	snp	A/T	0.230017	0.2492	intron-variant	ARHGAP26	GRCh38.p7	5:142894893	CATCATGGTCCACTC[A/T]GCAGAGTCTCTATGC	23092
rs37216	snp	C/T	0.110029	0.207142	intron-variant	ARHGAP26	GRCh38.p7	5:142894382	TGAGGGATGAATATA[C/T]GGGTACATCATTAAA	23092
rs37221	snp	C/G	0.428333	0.175206	intron-variant	ARHGAP26	GRCh38.p7	5:142939212	AAAAATAGCACAGAA[C/G]TGGAAGCTAAGAGAC	23092
rs37222	snp	A/T	0.473266	0.112482	intron-variant	ARHGAP26	GRCh38.p7	5:142938090	ttaactagactatac[A/T]cgttgttcaaactcc	23092
rs37223	snp	C/T	0.447809	0.152878	intron-variant	ARHGAP26	GRCh38.p7	5:142937659	tgtttaaccattcac[C/T]cattaaaggacatct	23092
rs37224	snp	C/T	0.430732	0.172731	intron-variant	ARHGAP26	GRCh38.p7	5:142935706	GATGACCTTCTGCCA[C/T]CATTTATACagctcc	23092
rs40127	snp	A/G	0.32768	0.237625	intron-variant	ARHGAP26	GRCh38.p7	5:142850686	AATAGAGGACCTACT[A/G]TGTGTCTGACATTGA	23092
rs40128	snp	A/G	0.417521	0.185571	intron-variant	ARHGAP26	GRCh38.p7	5:142826017	GTTAACCAGCAAATC[A/G]ATAAGAAAATCTAGG	23092
rs40193	snp	A/C	0.223225	0.248562	intron-variant, nc-transcript-variant	ARHGAP26, LOC107986457	GRCh38.p7	5:142967138	CACTAAAAGAACATT[A/C]AGAATAACACCTTAA	23092
rs40360	snp	C/T	0.215747	0.247642	intron-variant	ARHGAP26	GRCh38.p7	5:142956044	CATTACACAATATGG[C/T]TTTGAATATTCTCAG	23092
rs42464	snp	C/T	0.419296	0.183954	intron-variant	ARHGAP26	GRCh38.p7	5:142952069	GAGACAGAAGAGCAG[C/T]GAAAGAGAAGTGGTC	23092
rs42465	snp	C/G	0.213333	0.247296	intron-variant	ARHGAP26	GRCh38.p7	5:142937052	taccagggtctttca[C/G]acacaaagcaaaagc	23092
rs42466	snp	C/T	0.418653	0.184544	intron-variant	ARHGAP26	GRCh38.p7	5:142934665	AATAAGGCAACGACA[C/T]TAACACCGACTAGAG	23092
rs42866	snp	A/T	0.438386	0.164349	intron-variant	ARHGAP26	GRCh38.p7	5:142852691	CTTCCCATTGTCTCC[A/T]TCCAAGACACTCGAC	23092
rs43158	snp	A/G	0.219349	0.248114	intron-variant, nc-transcript-variant	ARHGAP26, LOC107986457	GRCh38.p7	5:142971509	TTGCTCAAACTTCCT[A/G]CAGCGCTGCTAATTA	23092
rs114534	snp	A/G	0.476487	0.105846	intron-variant	ARHGAP26	GRCh38.p7	5:143154092	attcattccacaaat[A/G]tcaattgaactccta	23092
rs114539	snp	C/T	0.40733	0.194287	intron-variant	ARHGAP26	GRCh38.p7	5:143119238	CAATATAAAAATACA[C/T]GGTTTGGATGATGAT	23092
rs121882	snp	A/G	0.471292	0.116318	intron-variant	ARHGAP26	GRCh38.p7	5:143153779	CGTGTGTGTTAAGAC[A/G]GAAGGACGAGAAAAA	23092
rs121883	snp	A/G	0.476918	0.104919	intron-variant	ARHGAP26	GRCh38.p7	5:143153164	TAGAATCTCAGTTAC[A/G]AGTTGTTTTCTTTCC	23092
rs151972	snp	A/C	0.421051	0.182323	intron-variant	ARHGAP26	GRCh38.p7	5:142996417	caacctccacctccc[A/C]ggttcaagcaattct	23092
rs151973	snp	A/T	0.448066	0.152544	intron-variant	ARHGAP26	GRCh38.p7	5:142993975	ATCTTAGATTCAGTT[A/T]ACATTAACTTCAAAA	23092
rs151974	snp	A/G	0.419135	0.184101	intron-variant	ARHGAP26	GRCh38.p7	5:142991245	ctcagagggtcccac[A/G]cccacggagccttgc	23092
rs151975	snp	C/T	0.38286	0.211774	intron-variant	ARHGAP26	GRCh38.p7	5:142990247	acaagcttcagtagc[C/T]gatttgatcaagtgg	23092
rs153163	snp	A/G	0	0	intron-variant	ARHGAP26	GRCh38.p7	5:142953174	GTCAAGAATGAGAGC[A/G]GTAGTGGGAATCCAG	23092
rs153164	snp	A/G	0.433673	0.1696	intron-variant	ARHGAP26	GRCh38.p7	5:142937363	aattttagtcattct[A/G]gaaggtgatagttca	23092
rs153165	snp	C/T	0.434831	0.168337	intron-variant	ARHGAP26	GRCh38.p7	5:142922100	TGAAGCATGTATCAA[C/T]AACAGGTTATCACAT	23092
rs153166	snp	C/T	0.423726	0.179776	intron-variant	ARHGAP26	GRCh38.p7	5:142923052	ACATGAATTCTAAGA[C/T]TCCAAGAACTTCTCC	23092
rs153167	snp	C/G	0.43555	0.167544	intron-variant	ARHGAP26	GRCh38.p7	5:142913637	CAATCATGCTAAATA[C/G]TTTTCTTTAAAAGTC	23092
rs153168	snp	A/C	0.447809	0.152878	intron-variant	ARHGAP26	GRCh38.p7	5:142896181	ATGTGACAGCATTTG[A/C]ATTCCTGCCCTGACC	23092
rs153169	snp	A/C	0.454664	0.143571	intron-variant	ARHGAP26	GRCh38.p7	5:142897567	TTACTAAACTACAGG[A/C]TACTGGGCCCCTCCC	23092
rs153170	snp	C/T	0.44768	0.153045	intron-variant	ARHGAP26	GRCh38.p7	5:142897686	GCTTAGCACGGTACA[C/T]GACAGTTTCAGATAA	23092
rs153171	snp	C/T	0.478768	0.100824	intron-variant	ARHGAP26	GRCh38.p7	5:142898154	GTGTGTATATATATA[C/T]ACACACATATATATC	23092
rs153172	snp	G/T	0.473359	0.112298	intron-variant	ARHGAP26	GRCh38.p7	5:142898453	GAAATATTCAGGATG[G/T]AAAACTCGGAGGATG	23092
rs154786	snp	C/T	0.406814	0.194704	utr-variant-3-prime, nc-transcript-variant	ARHGAP26	GRCh38.p7	5:143227406	AGTCAGCAGGATGTC[C/T]TCTCACCCACCCTGT	23092
rs154787	snp	A/C	0.456332	0.141164	utr-variant-3-prime, nc-transcript-variant	ARHGAP26	GRCh38.p7	5:143226736	TCTTATGTCAGACCA[A/C]ACTGTCTTTTTGAAT	23092

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