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
rs162725	snp	A/G	0.0387552	0.1337	intron-variant	VAV1	GRCh38.p7	19:6819717	TTGGCCTCTCCCACA[A/G]CCCCCAACACTCTCC	7409
rs162726	snp	A/C	0.450105	0.149859	intron-variant	VAV1	GRCh38.p7	19:6845459	TGCCAGTAACAATTA[A/C]AAGGTTAATTTTATG	7409
rs162727	snp	A/C	0.417196	0.185864	intron-variant	VAV1	GRCh38.p7	19:6844995	atgaacaaacatcaa[A/C]attttgaataaagac	7409
rs164014	snp	A/C	0.130008	0.219321	intron-variant	VAV1	GRCh38.p7	19:6848561	gcgcctgtgaccatg[A/C]ccagctaatttttgt	7409
rs164015	snp	A/G	0.000399281	0.0141238	intron-variant	VAV1	GRCh38.p7	19:6821177	GAGGCTGAGGTGGGC[A/G]GATCACGAGGTCAGG	7409
rs164016	snp	C/T	0.454302	0.144085	intron-variant	VAV1	GRCh38.p7	19:6820940	AGGCCATATACAAGA[C/T]GCAAATAGCACTGGC	7409
rs164017	snp	C/T	0.206642	0.246211	intron-variant	VAV1	GRCh38.p7	19:6820401	ATCCACATTGTAGTA[C/T]GAATCAGTGCTTCAT	7409
rs164018	snp	A/T	0.305186	0.243833	intron-variant	VAV1	GRCh38.p7	19:6820197	TGCGACACATGACTG[A/T]AGTCCTAGCTACCTG	7409
rs164019	snp	C/T	0.40386	0.197046	intron-variant	VAV1	GRCh38.p7	19:6819522	aaggttcatccatgt[C/T]gtagtgtggaacagt	7409
rs164020	snp	A/T	0.496905	0.0392151	intron-variant	VAV1	GRCh38.p7	19:6818617	acctcagaatgtggc[A/T]gtatttggatatgga	7409
rs164021	snp	C/G	0	0	intron-variant	VAV1	GRCh38.p7	19:6829377	GCTCCACCCACCTGT[C/G]CATCTAGGAGCCTGG	7409
rs164022	snp	C/G	0.484403	0.0869204	intron-variant	VAV1	GRCh38.p7	19:6828029	GGCAGGTCCCAGAAA[C/G]AGCCAGTTGCAGGGT	7409
rs164023	snp	C/G	0.0659589	0.169201	intron-variant	VAV1	GRCh38.p7	19:6827554	gctaggattacaggc[C/G]tgagcaatcgtgccc	7409
rs164024	snp	C/T	0.0659589	0.169201	intron-variant	VAV1	GRCh38.p7	19:6827457	tttttgtgttttttg[C/T]agagatggggtttca	7409
rs170711	snp	A/C			intron-variant	VAV1	GRCh38.p7	19:6844105	TCTCAGCCTCATTTG[A/C]aaaaaaaaaaaaaaa	7409
rs180864	snp	A/G	0.221141	0.248329	intron-variant	VAV1	GRCh38.p7	19:6823073	tataaaggtatatat[A/G]tctacatatggacat	7409
rs186295	snp	C/T	0.249484	0.249999	intron-variant	VAV1	GRCh38.p7	19:6833766	GTTGCCCATTATTTG[C/T]GGTACACAGGAAGGA	7409
rs308194	snp	C/T	0.460813	0.134379	intron-variant	VAV1	GRCh38.p7	19:6836825	TGTGTGTCCATCTCT[C/T]TGCTCAATGGTCACT	7409
rs308195	snp	A/G	0.246485	0.249975	intron-variant	VAV1	GRCh38.p7	19:6836749	TGATAATGAGTATTA[A/G]CTTCCTGGGAAGATG	7409
rs308196	snp	G/T	0.291235	0.246576	intron-variant	VAV1	GRCh38.p7	19:6836260	tggggatactctttg[G/T]aaaactatttggcaa	7409
rs308197	snp	A/T	0.464841	0.127841	intron-variant	VAV1	GRCh38.p7	19:6835429	ACGTGAGCAAAAAAA[A/T]TTTTAAGGTGATTTC	7409
rs308198	snp	A/G	0.296619	0.245615	intron-variant	VAV1	GRCh38.p7	19:6834384	tggtgacatgtgcct[A/G]taatcccagctactt	7409
rs308199	snp	A/C	0.337753	0.234093	intron-variant	VAV1	GRCh38.p7	19:6833978	TTTTCCTCCTGCCCC[A/C]ACACAGCAACCCCTG	7409
rs308200	snp	A/G	0.460365	0.13508	intron-variant	VAV1	GRCh38.p7	19:6833061	CTCATTCATTGATTG[A/G]CTTTTGGGTCGTTTT	7409
rs331677	snp	A/T	0.485049	0.0851591	intron-variant	VAV1	GRCh38.p7	19:6849895	gacacacacccttgt[A/T]tgttcatcacagcag	7409
rs331678	snp	A/T	0.48498	0.0853497	intron-variant	VAV1	GRCh38.p7	19:6848787	taataataataaaat[A/T]aaaTTAAAAAAATTA	7409
rs331679	snp	C/T	0.5	0	intron-variant	VAV1	GRCh38.p7	19:6848209	GGTGGATGCTATTAC[C/T]GTACACTTCTATAAA	7409
rs331680	snp	C/T	0.374341	0.216885	intron-variant	VAV1	GRCh38.p7	19:6847963	ACAGAGGTGGCACGG[C/T]CCCCGTGCCTGGGTC	7409
rs331681	snp	A/G	0.41408	0.188621	intron-variant	VAV1	GRCh38.p7	19:6844934	cctcctcttactccc[A/G]gctctattggatcct	7409
rs331682	snp	A/G	0.471673	0.115589	intron-variant	VAV1	GRCh38.p7	19:6844024	GTATGGGGGCAGAGA[A/G]TAAGAATCAAATCTA	7409
rs331683	snp	C/T	0.46845	0.121572	intron-variant	VAV1	GRCh38.p7	19:6842785	gtgcagcagtatgat[C/T]atagctcactgcagc	7409
rs332423	snp	A/G	0.0955749	0.196603	intron-variant	VAV1	GRCh38.p7	19:6790154	gtgcactccagcctg[A/G]gtgagagagtgagac	7409
rs332424	snp	A/G	0.00318978	0.0398085	intron-variant	VAV1	GRCh38.p7	19:6799229	ctggagtgcagtggc[A/G]caatctcggctcact	7409
rs332425	snp	A/C	0.219648	0.248151	intron-variant	VAV1	GRCh38.p7	19:6801942	ATTTGCATATGGGCA[A/C]GATGCCAGCACAGTG	7409
rs332426	snp	A/G	0.21303	0.247251	intron-variant	VAV1	GRCh38.p7	19:6801955	CACGATGCCAGCACA[A/G]TGGGTGCCCGCCTCT	7409
rs347031	snp	C/T	0.0287284	0.116357	intron-variant	VAV1	GRCh38.p7	19:6818270	gaggaaagacaaaga[C/T]gttggcaaggaactt	7409
rs347032	snp	A/G	0.0850919	0.187897	intron-variant	VAV1	GRCh38.p7	19:6824330	agtaagctcgtggtt[A/G]ccatggaccggggga	7409
rs347033	snp	A/G	0.385704	0.209963	intron-variant	VAV1	GRCh38.p7	19:6822208	TCGCTGTGGGTTGTG[A/G]GGTCAGGGATCCCTT	7409
rs347034	snp	C/T	0.129149	0.21885	intron-variant	VAV1	GRCh38.p7	19:6822188	AGGGATCCCTTGGAC[C/T]TCTCCCAGATCACAG	7409
rs369632	snp	A/C/T	0.031499	0.121847	intron-variant	VAV1	GRCh38.p7	19:6817718	GCCTGGGCAACAGAG[A/C/T]GAGACCCCATCTCAG	7409
rs370209	snp	A/G	0.241053	0.24984	intron-variant	VAV1	GRCh38.p7	19:6835553	AGACAGTGGTTCCCT[A/G]TGGGAGATAGGTGAG	7409
rs374119	snp	C/T	0.228547	0.249078	intron-variant	VAV1	GRCh38.p7	19:6812091	ATCTCTCCTTGCATG[C/T]GGATGCAGTCATGTG	7409
rs385677	snp	A/G	0	0	upstream-variant-2KB	VAV1	GRCh38.p7	19:6771800	AAGAAAGAAAGGAAG[A/G]AAGGAAGGAAGGAAG	7409
rs392497	snp	A/G	0.00478085	0.0486577	intron-variant	VAV1	GRCh38.p7	19:6777475	aacaaagtggaacag[A/G]gtatgaggggggcac	7409
rs394436	snp	C/G	0.468148	0.122112	intron-variant	VAV1	GRCh38.p7	19:6840543	tgaccttgtgttcct[C/G]ccgcttcggcttccc	7409
rs397337	snp	G/T	0.5	0	downstream-variant-500B	VAV1	GRCh38.p7	19:6857516	TTTGTCTGTGGATTG[G/T]TGAGGGGGCTTTGTC	7409
rs398118	snp	A/C/T	0.000399281	0.0141238	intron-variant	VAV1	GRCh38.p7	19:6773847	TTCCCACCCAGCAGC[A/C/T]CTGGGGAACCAGACA	7409
rs398650	snp	A/G	0.185155	0.241444	intron-variant	VAV1	GRCh38.p7	19:6809361	cttggggttacaggc[A/G]tgagccaccataccc	7409
rs415218	snp	A/T	0.0329836	0.124112	intron-variant	VAV1	GRCh38.p7	19:6815526	ACAAAAGAGTTAAAG[A/T]TCATGTTCCATATGC	7409
rs415306	snp	C/T	0.135484	0.22223	intron-variant	VAV1	GRCh38.p7	19:6812671	TGTATTTTGGGTTGT[C/T]TTTGTTTCTGTTTTT	7409
rs419098	snp	A/G	0	0	intron-variant	VAV1	GRCh38.p7	19:6855425	gatttgtggatagat[A/G]gatggatagatggat	7409
rs426815	snp	G/T	0.229723	0.249176	intron-variant	VAV1	GRCh38.p7	19:6812353	TTTGAAACTGGAAAA[G/T]ACCTCAGATATTAAT	7409
rs428020	snp	A/G	0.078151	0.181571	intron-variant	VAV1	GRCh38.p7	19:6812404	gcctcccaaagtgct[A/G]ggatcacaggtgtga	7409
rs432249	snp	A/G	0.458545	0.137872	intron-variant	VAV1	GRCh38.p7	19:6838964	ctggagtgcagtggg[A/G]tgatctcggctcatt	7409
rs432280	snp	C/T	0.0325976	0.123435	intron-variant	VAV1	GRCh38.p7	19:6817763	accgtcgtggctcac[C/T]gcagcctccacctcc	7409
rs446841	snp	C/T	0	0	intron-variant	VAV1	GRCh38.p7	19:6850498	TTGCTACTCTAAAGC[C/T]TTAATGTCTTCCTCT	7409
rs461970	snp	C/T	0.499053	0.0217445	downstream-variant-500B	VAV1	GRCh38.p7	19:6857629	GCTGTTCTCTGTCAT[C/T]TATTAATACAATACA	7409
rs462793	snp	A/C			intron-variant	VAV1	GRCh38.p7	19:6843385	cgtcatcatcattgt[A/C]accatTTTCCTTCCA	7409
rs472835	snp	A/G	0.348574	0.229746	intron-variant	VAV1	GRCh38.p7	19:6788968	GCAGCTCCCAGGACA[A/G]AAAATGATCCGGCCC	7409
rs473021	snp	A/C	0.323434	0.238972	intron-variant	VAV1	GRCh38.p7	19:6788896	TTTAGAAGTCACTGC[A/C]CATATAAACACTGAT	7409
rs479660	snp	A/G	0.338976	0.23363	intron-variant	VAV1	GRCh38.p7	19:6782487	AAAATAATGACTCTC[A/G]TTCATTTAGCACTCA	7409
rs481623	snp	C/T	0.338069	0.233974	intron-variant	VAV1	GRCh38.p7	19:6782262	GCTCACTACAACCTC[C/T]GCCTCCTGGGTTCAA	7409
rs500562	snp	C/T			upstream-variant-2KB	VAV1	GRCh38.p7	19:6771812	cttccttccttcctt[C/T]cttccttccttcctt	7409
rs544138	snp	A/G	0.437118	0.165792	intron-variant	VAV1	GRCh38.p7	19:6780023	ggctgaagcaggaga[A/G]tggcatgaacctggg	7409
rs544901	snp	G/T	0.43655	0.16643	intron-variant	VAV1	GRCh38.p7	19:6779977	ttagccgggcgtggt[G/T]gcgggcgcctgtagt	7409
rs568259	snp	A/G	0.33693	0.2344	intron-variant	VAV1	GRCh38.p7	19:6782563	CAGCAGTTAACATAC[A/G]TACCCTGACTTATAT	7409
rs579371	snp	C/T	0.383632	0.211288	intron-variant	VAV1	GRCh38.p7	19:6786492	cccagccataatttt[C/T]atttttaatttttta	7409
rs580314	snp	C/T	0.321292	0.23962	intron-variant	VAV1	GRCh38.p7	19:6786369	gctcaagcgatcctc[C/T]catctcagcctcccg	7409
rs625828	snp	A/T	0.47919	0.0998605	intron-variant	VAV1	GRCh38.p7	19:6832049	TGTGCTCCCACCCTC[A/T]GCGGGGGCAGTGCCT	7409
rs642553	snp	G/T	0.314057	0.241654	intron-variant	VAV1	GRCh38.p7	19:6786846	ataaaaataGTAAAC[G/T]TCAAATCAATACCAA	7409
rs645030	snp	C/T			intron-variant	VAV1	GRCh38.p7	19:6836871	acacacacacacaca[C/T]gcacacGAGTGATGG	7409
rs645031	snp	A/G	0	0	intron-variant	VAV1	GRCh38.p7	19:6836872	CACACACACACACAC[A/G]CACACACGAGTGATG	7409
rs657410	snp	G/T	0.33875	0.233717	intron-variant	VAV1	GRCh38.p7	19:6782435	GATTAAACATGATAA[G/T]GTAAATGAAATTCCC	7409
rs657469	snp	C/T	0.339203	0.233544	intron-variant	VAV1	GRCh38.p7	19:6782472	GCAATTAACATATAG[C/T]GAGTGCTAAATGAAC	7409
rs659657	snp	C/T	0.376989	0.215346	intron-variant	VAV1	GRCh38.p7	19:6788928	TTAAGCCAGAATTTC[C/T]GATTCTCAGTCCTGT	7409
rs660134	snp	C/T	0.36955	0.219562	intron-variant	VAV1	GRCh38.p7	19:6789069	agtatctccagacat[C/T]gccaaatgtcccctg	7409
rs675614	snp	C/T	0.369958	0.21934	intron-variant	VAV1	GRCh38.p7	19:6780607	gacggagtctcactc[C/T]attcctcaggctgga	7409
rs676528	snp	A/G	0.316243	0.241064	intron-variant	VAV1	GRCh38.p7	19:6780821	tcagatgatctgccc[A/G]cctcagcctcccaaa	7409
rs682626	snp	C/T	0.249603	0.25	intron-variant	VAV1	GRCh38.p7	19:6774058	CCCCTGAAAACCACC[C/T]GCCAGGAACCCCCAT	7409
rs691469	snp	A/G	0.147321	0.227941	intron-variant	VAV1	GRCh38.p7	19:6812937	TAAAAAGGGCTGGAC[A/G]TTTCAAGTTCTGGAA	7409
rs691486	snp	A/C	0.314057	0.241654	intron-variant	VAV1	GRCh38.p7	19:6786834	AACGTCAAATCAATA[A/C]CAAGAAAAGTAAATA	7409
rs691502	snp	A/C	0.321292	0.23962	intron-variant	VAV1	GRCh38.p7	19:6786664	tcttgagtagctggg[A/C]ctataggcgcacacc	7409
rs691503	snp	A/G	0.383632	0.211288	intron-variant	VAV1	GRCh38.p7	19:6786619	atttttatatttttt[A/G]tagagatggggtttt	7409
rs691528	snp	C/T	0.383439	0.21141	intron-variant	VAV1	GRCh38.p7	19:6786260	AGCCCCTGTGTTAAG[C/T]GAATGAATGAAGCAA	7409
rs691713	snp	A/G	0.373598	0.21731	intron-variant	VAV1	GRCh38.p7	19:6780008	cccagctactcggga[A/G]gctgaagcaggagaa	7409
rs691715	snp	A/G	0.434398	0.168811	intron-variant	VAV1	GRCh38.p7	19:6780060	AGCTTGCAGTGAGCC[A/G]AGATCAGGCCACTGC	7409
rs692221	snp	A/G	0.384017	0.211044	intron-variant	VAV1	GRCh38.p7	19:6781742	cctcacaagtagctg[A/G]gattacaggtgtgcg	7409
rs692222	snp	C/T	0.384017	0.211044	intron-variant	VAV1	GRCh38.p7	19:6781752	agctgagattacagg[C/T]gtgcgccaagatgcc	7409
rs692397	snp	C/T	0.384017	0.211044	intron-variant	VAV1	GRCh38.p7	19:6789052	AAGTAGCACCTCTCC[C/T]Cagtatctccagaca	7409
rs694271	snp	A/G	0.350982	0.228698	intron-variant	VAV1	GRCh38.p7	19:6787466	TGGAGggctgggtgc[A/G]gtgactcacgcctgc	7409
rs797622	snp	C/T	0.361474	0.223771	intron-variant	VAV1	GRCh38.p7	19:6780161	aataataataataaC[C/T]TCATCCATGAATCAT	7409
rs797629	snp	A/G	0.320096	0.239972	intron-variant	VAV1	GRCh38.p7	19:6785868	agttcaagaccagct[A/G]gccaacatggtgaaa	7409
rs808843	snp	C/T	0.314301	0.241589	intron-variant	VAV1	GRCh38.p7	19:6785950	aatctgggctgggcg[C/T]ggtggctcattacct	7409
rs811292	snp	A/G	0.337386	0.23423	intron-variant	VAV1	GRCh38.p7	19:6782041	ggaaATCTATAAAAT[A/G]AGAATGTTggccgtg	7409
rs813430	snp	A/G	0.464523	0.128375	intron-variant	VAV1	GRCh38.p7	19:6847024	caggaggctgaggca[A/G]gagaatcgcttgaac	7409
rs906331	snp	C/G	0.370365	0.219117	intron-variant	VAV1	GRCh38.p7	19:6821920	GGCCATGTCCCCCCA[C/G]ACCCTCCACCCCCAG	7409
rs1619409	snp	A/T	0	0	intron-variant	VAV1	GRCh38.p7	19:6847604	TCAGGTGCAAAATGT[A/T]AGTGAGAGCCAAAAA	7409
rs1651876	snp	C/T	0.132066	0.220435	intron-variant	VAV1	GRCh38.p7	19:6817027	GAATGCCTAACCATG[C/T]GTAGTAGGCATCCAA	7409
rs1651879	snp	A/G	0.227664	0.249	intron-variant	VAV1	GRCh38.p7	19:6836900	CCCATAACCCTACAC[A/G]TGGATCCTGCCCCAT	7409
rs1702378	snp	C/T	0.461037	0.134028	intron-variant	VAV1	GRCh38.p7	19:6812554	aagtgcctcagcctc[C/T]cgaacagctgggatt	7409

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