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
rs16763	snp	A/C	0.479663	0.0987666	intron-variant	VAV2	GRCh38.p7	9:133927643	TGGCCCCACTCCAAG[A/C]GGCCCCCAGATCCTC	7410
rs16767	snp	C/T	0.422158	0.181278	intron-variant	VAV2	GRCh38.p7	9:133953784	GAAACCCAGCTCCCA[C/T]GACCCCGGCTCCCAG	7410
rs16803	snp	C/T	0.400147	0.19989	intron-variant	VAV2	GRCh38.p7	9:133950235	TGCTGGGTTTCCTCT[C/T]GAGTGCTGCTGAGGA	7410
rs16819	snp	C/T	0.446249	0.154875	intron-variant	VAV2	GRCh38.p7	9:133954235	GGGACACCAGGCACA[C/T]GCCGCTTCTCAGAAA	7410
rs23149	snp	C/T	0.492287	0.0616198	intron-variant	VAV2	GRCh38.p7	9:133924407	TTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCC	7410
rs370641	snp	C/T	0.471673	0.115589	intron-variant	VAV2	GRCh38.p7	9:133986277	AGCAGCGTCAGGTCA[C/T]GCAACTGTAGGGGTC	7410
rs370869	snp	C/G	0.47802	0.102502	intron-variant	VAV2	GRCh38.p7	9:133984075	ctgaggcaggagaat[C/G]gcttgaacccagaag	7410
rs375871	snp	C/T	0.28052	0.24813	intron-variant	VAV2	GRCh38.p7	9:133982650	TTGCAGGGCCCACCA[C/T]CTGGTTTTGCAGGGC	7410
rs378285	snp	C/G			intron-variant	VAV2	GRCh38.p7	9:133898903	accctggaggcggag[C/G]ttgcagtgagccgag	7410
rs378732	snp	A/G	0.447032	0.153878	intron-variant	VAV2	GRCh38.p7	9:133924781	CAGGACTAAATGACC[A/G]TGAAtattcacagga	7410
rs379485	snp	C/G	0.422473	0.180978	intron-variant	VAV2	GRCh38.p7	9:133979441	CCCCTGCCTGGGGAC[C/G]CATCTCCTCTGGGCC	7410
rs379996	snp	A/G	0.28052	0.24813	intron-variant	VAV2	GRCh38.p7	9:133983756	TGACAGGGACTGACC[A/G]GGAGTGGGACTTGAG	7410
rs381017	snp	G/T	0.441432	0.160792	intron-variant	VAV2	GRCh38.p7	9:133966896	aaaaatcagttgggc[G/T]tggtggcgggcgcct	7410
rs383749	snp	A/C	0.000399281	0.0141238	intron-variant	VAV2	GRCh38.p7	9:133947194	GAAGCATCTCTTCCG[A/C]AAACAAGCAAGCAGG	7410
rs386372	snp	A/C			intron-variant	VAV2	GRCh38.p7	9:133955758	ggaacgtgggggggg[A/C]gttggggggagtggg	7410
rs400924	snp	A/G	0.342134	0.232404	intron-variant	VAV2	GRCh38.p7	9:133881082	CAGCCTCTCTGGGAC[A/G]TGGGTGGGCCATGGC	7410
rs405004	snp	A/T	0.337158	0.234315	intron-variant	VAV2	GRCh38.p7	9:133924997	TGTTCTGGACATTTC[A/T]TATAAGTGGAATCCT	7410
rs410383	snp	A/C			intron-variant	VAV2	GRCh38.p7	9:133955692	ccccaaagctcctcc[A/C]cactcccccacactc	7410
rs412472	snp	G/T	0.441568	0.160629	intron-variant	VAV2	GRCh38.p7	9:133966894	caaaaaatcagttgg[G/T]cttggtggcgggcgc	7410
rs414848	snp	C/T	0.417845	0.185278	intron-variant	VAV2	GRCh38.p7	9:133978446	AGACGGGCTCCCCAA[C/T]CCTGGGAAGGCCACA	7410
rs416060	snp	C/T	0.280785	0.248097	intron-variant	VAV2	GRCh38.p7	9:133982134	TGCCTGGCTCACTGC[C/T]GCCATCTGCTTAGAG	7410
rs419240	snp	C/G	0.375797	0.216044	intron-variant	VAV2	GRCh38.p7	9:133979511	GTCCGAGTTCCGGAC[C/G]GCTGCGGCGTCCGCT	7410
rs420897	snp	A/G	0.404907	0.196224	intron-variant	VAV2	GRCh38.p7	9:133986641	AAAGTTATGAGTACA[A/G]CACAGGTAACttttt	7410
rs421510	snp	A/G	0.499104	0.0211472	intron-variant	VAV2	GRCh38.p7	9:133985122	TATGTGTGTGTATGT[A/G]TTTATTTATGTATGT	7410
rs421771	snp	A/C	0.472147	0.114677	intron-variant	VAV2	GRCh38.p7	9:133986273	gcgtcaggtcacgca[A/C]ctgtaggggtctagc	7410
rs422999	snp	C/T	0.409382	0.192607	intron-variant	VAV2	GRCh38.p7	9:133979632	GCAGCCAGGCACTAA[C/T]CCGGGCCCGGCCCCG	7410
rs425078	snp	C/T	0.0422008	0.138995	intron-variant	VAV2	GRCh38.p7	9:133890382	TGGGAAGCTGCAGTC[C/T]GTGCTCACTCCTGGA	7410
rs425790	snp	A/C	0.484701	0.0861117	intron-variant	VAV2	GRCh38.p7	9:133978919	ACCGGGCACCTGAGC[A/C]GGGGGCTGGCCCCGG	7410
rs425850	snp	C/T	0.316	0.241131	intron-variant	VAV2	GRCh38.p7	9:133978852	AAGCCAAACAGCGTC[C/T]CCAGCTCCAGGCAAA	7410
rs429461	snp	C/G	0.349452	0.229367	intron-variant	VAV2	GRCh38.p7	9:133986970	GGAGGCACAAAGCCT[C/G]CGTGGCACACAGCAG	7410
rs431743	snp	C/T	0.481627	0.0940692	intron-variant	VAV2	GRCh38.p7	9:133922850	agtctgatgtagtct[C/T]atttgtctgttttcg	7410
rs431791	snp	C/T	0.303438	0.244222	intron-variant	VAV2	GRCh38.p7	9:133986152	TGGTGAAGGTGGAGT[C/T]TGCTTGATTTCACTG	7410
rs433035	snp	G/T	0.312104	0.242163	intron-variant	VAV2	GRCh38.p7	9:133978920	CCGGGCACCTGAGCC[G/T]GGGGCTGGCCCCGGT	7410
rs435586	snp	C/T	0.406641	0.194842	intron-variant	VAV2	GRCh38.p7	9:133979851	CGGCAGGCTCCCTGA[C/T]GAGGTGACAGGGCGG	7410
rs435943	snp	C/T	0.409041	0.192888	intron-variant	VAV2	GRCh38.p7	9:133979664	TCAGTGGTGGGGCTC[C/T]GGGACATGGCCGGAG	7410
rs436817	snp	C/G	0.428937	0.17459	intron-variant	VAV2	GRCh38.p7	9:133966811	ttgacctcaagtgat[C/G]tgcccgccacggcct	7410
rs437062	snp	A/G			intron-variant	VAV2	GRCh38.p7	9:133952997	GGTGTCAGTGGGGCC[A/G]TGCTCCCTCCAGGTT	7410
rs438210	snp	A/G	0.495095	0.0492773	intron-variant	VAV2	GRCh38.p7	9:133970364	ACCGAACGTGGTGCC[A/G]TCCCCCAGCCTCCGC	7410
rs441533	snp	C/T	0.306927	0.243432	intron-variant	VAV2	GRCh38.p7	9:133978444	TGGCCTTCCCAGGAT[C/T]GGGGAGCCCGTCTCC	7410
rs452943	snp	A/G	0.477853	0.102875	intron-variant	VAV2	GRCh38.p7	9:133967455	agtgctacggtaaag[A/G]tgggagtgcagatat	7410
rs452999	snp	A/G	0.422473	0.180978	intron-variant	VAV2	GRCh38.p7	9:133967406	ctttcttttgtttac[A/G]tgcctggtggtagga	7410
rs453703	snp	C/T	0.28052	0.24813	intron-variant	VAV2	GRCh38.p7	9:133982904	GCAGCACGACAGCAG[C/T]CCTGGGTGGTCTGTA	7410
rs471858	snp	C/G	0.41441	0.188333	intron-variant	VAV2	GRCh38.p7	9:133937621	CCAGGGTGCTGCAGG[C/G]AAATTCATCTCTGCT	7410
rs471882	snp	C/G	0.432063	0.171327	intron-variant	VAV2	GRCh38.p7	9:133960277	ACAGATAAGAACTTT[C/G]TGGCCCAGCTTGGTC	7410
rs478393	snp	C/T	0.448708	0.151707	intron-variant	VAV2	GRCh38.p7	9:133954467	TGCGATGTGCTGCTG[C/T]GGCACTGAGTACTTT	7410
rs478403	snp	C/T	0.39214	0.205661	intron-variant	VAV2	GRCh38.p7	9:133774131	cagatgttaaaccaa[C/T]cttgcattcctggaa	7410
rs478645	snp	C/T	0.462144	0.132269	intron-variant	VAV2	GRCh38.p7	9:133925567	GATCACCCAGGGCTC[C/T]AGCCCCAAAGTCCCC	7410
rs481964	snp	A/G	0.432504	0.170857	intron-variant	VAV2	GRCh38.p7	9:133948219	AGACAAAATCAACTC[A/G]TGACACTCCTCAATC	7410
rs484440	snp	C/G	0.428635	0.174898	intron-variant	VAV2	GRCh38.p7	9:133957912	TGTTTCAGAGAGCAC[C/G]GGGTTGGGGGTAAGG	7410
rs485458	snp	A/G	0.433673	0.1696	intron-variant	VAV2	GRCh38.p7	9:133948531	CAGGGCAGGCGGCCC[A/G]CGTGCCCTCAGGAGT	7410
rs490177	snp	C/G	0.383439	0.21141	intron-variant	VAV2	GRCh38.p7	9:133958543	acacatccccctctc[C/G]gagaaacacccacga	7410
rs493433	snp	A/G	0.454423	0.143914	intron-variant	VAV2	GRCh38.p7	9:133950868	GGTCAACATGAGGGC[A/G]TTCGCACGCTCTCTG	7410
rs503376	snp	C/G	0.438666	0.164028	intron-variant	VAV2	GRCh38.p7	9:133954840	TTAGCTTTATTTATC[C/G]TAATGCAGACACACA	7410
rs503596	snp	A/G	0.415891	0.18703	intron-variant	VAV2	GRCh38.p7	9:133945402	GGGGCTGACCTGATT[A/G]ATCGGCACATAATAA	7410
rs504375	snp	A/C	0.5	0	intron-variant	VAV2	GRCh38.p7	9:133926001	CTGTGGACATGGACC[A/C]AAAAAAAAAAAAAAA	7410
rs506278	snp	C/T	0.405603	0.195673	intron-variant	VAV2	GRCh38.p7	9:133773400	ctaggccttcacatt[C/T]actcaccactctcca	7410
rs508878	snp	C/T	0.444444	0.157135	intron-variant	VAV2	GRCh38.p7	9:133773134	TGCAGTAGGCTCTGC[C/T]GTCCAGCCTAGGTGT	7410
rs509590	snp	A/G	0.499663	0.0129749	utr-variant-3-prime	VAV2	GRCh38.p7	9:133763648	AGGGGACCTGCCCCC[A/G]CACCCTCTGCTCAGC	7410
rs520308	snp	A/G	0.429238	0.174281	intron-variant	VAV2	GRCh38.p7	9:133942116	CTCAGTGTCTTCTCC[A/G]GTTTTCCTCTAGAGC	7410
rs521418	snp	A/C	0.488241	0.0757703	intron-variant	VAV2	GRCh38.p7	9:133782891	GGGTCGGGGGCATAC[A/C]TTTGGGGTTGTGCCC	7410
rs524538	snp	G/T	0.459574	0.136304	intron-variant	VAV2	GRCh38.p7	9:133951976	atctctgctgtgtaa[G/T]ggtacaaggagaagc	7410
rs525060	snp	A/G	0.468148	0.122112	intron-variant	VAV2	GRCh38.p7	9:133782502	CCCTAACCTGGGGAG[A/G]GGGCCAGAAGGTCAG	7410
rs526581	snp	A/G	0.460252	0.135255	intron-variant	VAV2	GRCh38.p7	9:133952229	ATGGGTGGGCCCCAA[A/G]GAGACAGGTCTGCAT	7410
rs527316	snp	C/G	0.46014	0.13543	intron-variant	VAV2	GRCh38.p7	9:133952260	CCAGACCCTGAGAAG[C/G]CTATTTGTGACCTTA	7410
rs532646	snp	A/C	0.463774	0.129618	intron-variant	VAV2	GRCh38.p7	9:133946231	CTCAAGGCAGCTGCC[A/C]GGGACTGGGGGAGGG	7410
rs533771	snp	C/T	0.5	0.00019968	intron-variant	VAV2	GRCh38.p7	9:133766134	ACCTTTCCCAGGGCT[C/T]CCCATTTCCTCCTGC	7410
rs538287	snp	C/T	0.476574	0.105661	intron-variant	VAV2	GRCh38.p7	9:133927411	ATGGGAGGCCACCCA[C/T]GGTCAGAGAACACAG	7410
rs540626	snp	C/G	0.417472	0.185615	intron-variant	VAV2	GRCh38.p7	9:133779957	CCTCATCTCTGTGTT[C/G]TGTCCTTGTCCTCAC	7410
rs545246	snp	A/G	0.243919	0.249926	intron-variant	VAV2	GRCh38.p7	9:133779410	CCCAGCCCAGCTCCC[A/G]CCTGGCCCAGCAGCA	7410
rs556664	snp	A/C	0.45645	0.140991	intron-variant	VAV2	GRCh38.p7	9:133765902	aaatttcaacttaaa[A/C]gtgtcagtaacctgc	7410
rs557327	snp	A/G	0.464309	0.12873	intron-variant	VAV2	GRCh38.p7	9:133946650	GTGCTGACTCCCTGG[A/G]GCCACAATGCTGCGT	7410
rs557430	snp	A/G	0.499999	0.000599041	intron-variant	VAV2	GRCh38.p7	9:133765843	cccatttgctttatc[A/G]tttgcactgtgtgtg	7410
rs557500	snp	C/T	0.452965	0.145963	intron-variant	VAV2	GRCh38.p7	9:133953297	GCTTGGGGGGCACAG[C/T]GCCAAGGGCACAGGA	7410
rs561257	snp	A/C	0.483995	0.0880135	intron-variant	VAV2	GRCh38.p7	9:133947129	GCCTTCCAAGACGTC[A/C]GGGGCCCCCAAGGAC	7410
rs562000	snp	C/G	0.483995	0.0880135	intron-variant	VAV2	GRCh38.p7	9:133947161	GCCACTGCTGCTTAG[C/G]TGGCAACCTCGCTTC	7410
rs562143	snp	C/G	0.421209	0.182174	intron-variant	VAV2	GRCh38.p7	9:133929870	AGGCAGGTTTCCTCA[C/G]CTGTGACGGATCAAT	7410
rs567208	snp	C/T	0.42574	0.177808	intron-variant	VAV2	GRCh38.p7	9:133957167	CCGTAACTGCCAGGC[C/T]GAGCCTCAGTTTCCC	7410
rs578151	snp	C/G	0.496245	0.0431677	intron-variant	VAV2	GRCh38.p7	9:133950406	GCCGCCCAGCCGTGC[C/G]TGTTCAGAGCCAGCA	7410
rs581622	snp	C/T	0.484771	0.0859212	intron-variant	VAV2	GRCh38.p7	9:133773336	gacagctgtatgggg[C/T]gcttatcatgactgg	7410
rs582682	snp	A/G	0.41023	0.191902	intron-variant	VAV2	GRCh38.p7	9:133773602	acacagctgtacaaa[A/G]atattttattctttg	7410
rs583505	snp	C/T	0.498852	0.0239341	intron-variant	VAV2	GRCh38.p7	9:133915383	CACGATCTGGCGTTC[C/T]ACAGACTCCACCTGC	7410
rs583538	snp	A/C	0.499809	0.00978247	intron-variant	VAV2	GRCh38.p7	9:133773755	AGTATTTTTTTGCTG[A/C]GTAGAAGGAGTATGC	7410
rs584396	snp	A/G	0.46014	0.13543	intron-variant	VAV2	GRCh38.p7	9:133960545	AAATAATTGGCGGCC[A/G]CTATTAAGCGGAGAC	7410
rs584738	snp	A/G	0.478768	0.100824	intron-variant	VAV2	GRCh38.p7	9:133928105	CTGGAAAGGAAAGCA[A/G]AGAAAAACCTCTCCC	7410
rs590614	snp	C/T	0.499121	0.020948	intron-variant	VAV2	GRCh38.p7	9:133770287	CCTGCCCTCACAGAC[C/T]CAGACCAGGAGTCCC	7410
rs591797	snp	C/T	0.419296	0.183954	intron-variant	VAV2	GRCh38.p7	9:133765682	catattcaaatctta[C/T]cagtcatcccaatca	7410
rs591866	snp	A/G	0.419296	0.183954	intron-variant	VAV2	GRCh38.p7	9:133765629	CTGGTCCTGGATCCA[A/G]TCCAGGATCATGAAT	7410
rs592252	snp	C/T	0.419296	0.183954	intron-variant	VAV2	GRCh38.p7	9:133765586	ctgtgatccttaact[C/T]tctttaatctggaat	7410
rs592820	snp	C/T	0.41325	0.18934	intron-variant	VAV2	GRCh38.p7	9:133765414	tggggacgttggcac[C/T]ttctcagtgccgtag	7410
rs593590	snp	A/G	0.499187	0.0201513	intron-variant	VAV2	GRCh38.p7	9:133765276	TGACTGTAATTAGCA[A/G]GTAATTTGCAGGGTA	7410
rs594130	snp	A/G	0.416545	0.186448	intron-variant	VAV2	GRCh38.p7	9:133765106	agttggcattctact[A/G]taaggaaaactttct	7410
rs595291	snp	A/G	0.0588605	0.161139	intron-variant	VAV2	GRCh38.p7	9:133913431	TGTCAGGGGTGGTGC[A/G]CGCTTCCTGGTGCCC	7410
rs598184	snp	C/T	0.480223	0.0974544	intron-variant	VAV2	GRCh38.p7	9:133914054	ACAAGCAACCAAAGA[C/T]GATGCTCACCGCAAA	7410
rs601764	snp	C/T	0.451856	0.147493	intron-variant	VAV2	GRCh38.p7	9:133967793	caaaaattagccgga[C/T]gtggtggtgtgcacc	7410
rs602990	snp	C/T	0.499995	0.00158753	missense	VAV2	GRCh38.p7	9:133778872	CATGGTAATTCTGCA[C/T]GGCCACCATCTTGGG	7410
rs603601	snp	C/T	0.481932	0.0933148	intron-variant	VAV2	GRCh38.p7	9:133932785	CACTGCACCTGCCTT[C/T]TGGTGCCTCCTCTCA	7410
rs604481	snp	A/G	0	0	intron-variant	VAV2	GRCh38.p7	9:133827427	CCGCTGCGCCCACTG[A/G]GGCTGACCACTGAGC	7410
rs604525	snp	A/G	0	0	intron-variant	VAV2	GRCh38.p7	9:133827452	CTGAGCGGGGGCATC[A/G]CCAGCTACTGCTGTG	7410
rs605476	snp	C/G	0.5	0.235702	intron-variant	VAV2	GRCh38.p7	9:133828416	GTGGGGGCATCACCA[C/G]CTACCGCTGCGCCCA	7410
rs605855	snp	A/G	0.21875	0.248039	intron-variant	VAV2	GRCh38.p7	9:133828460	CTGAGTGGGGGCATC[A/G]CCACCTACCGCTGCG	7410

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