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
rs11028	snp	C/T	0.445855	0.155373	utr-variant-3-prime, nc-transcript-variant	RABGEF1, GTF2IRD1P1	GRCh38.p7	7:66811230	ACATATAAAGTAGGT[C/T]ATTGAGTTGATTTTT	27342
rs974239	snp	A/G	0.486855	0.0799975	intron-variant	RABGEF1	GRCh38.p7	7:66748504	CAGGCATGGTTTATC[A/G]TGGGGGTATCACGAT	27342
rs1016265	snp	C/T	0.487995	0.0765403	intron-variant	RABGEF1	GRCh38.p7	7:66749580	AGGCAGGAGGATTGC[C/T]GGAGGTCAGGTATTA	27342
rs1027808	snp	G/T	0	0	intron-variant	RABGEF1	GRCh38.p7	7:66749527	ACAGAACTTTgcgag[G/T]tgttgttcacctgta	27342
rs1060527	snp	C/G	0.167809	0.236103	utr-variant-3-prime, nc-transcript-variant	RABGEF1, GTF2IRD1P1	GRCh38.p7	7:66811325	ATTTCTCTTAAGTCA[C/G]CATCAATACAACGGC	27342
rs1060528	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RABGEF1, GTF2IRD1P1	GRCh38.p7	7:66811417	AATACACCTTTGGAA[C/T]GGAATTCTTTATCAA	27342
rs1060796	snp	C/G			intron-variant	RABGEF1	GRCh38.p7	7:66689142	TCTCAAATCAGTCAC[C/G]TAACTATACACTTTA	27342
rs1064795	snp	A/G	0.21845	0.248001	utr-variant-3-prime, downstream-variant-500B	RABGEF1, GTF2IRD1P1	GRCh38.p7	7:66809968	TATGACACCACTAAG[A/G]TTCAGAATAAAGTTT	27342
rs1064801	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RABGEF1, GTF2IRD1P1	GRCh38.p7	7:66811189	CATATCAACTTCCCA[A/C]AAAAGCTGACTTTTT	27342
rs1110414	snp	A/G	0.495213	0.048687	utr-variant-5-prime, upstream-variant-2KB	RABGEF1	GRCh38.p7	7:66740595	CGACCCTTTGGATCC[A/G]CTCGCACTTCCTCCC	27342
rs1133267	snp	A/G	0	0	intron-variant, nc-transcript-variant	RABGEF1	GRCh38.p7	7:66685440	tgggagaatcacttg[A/G]ggctaggagttggag	27342
rs1133794	snp	C/T	0	0	utr-variant-5-prime, upstream-variant-2KB	RABGEF1	GRCh38.p7	7:66740097	cctcagcctccctgg[C/T]agttgggaccacagg	27342
rs1137890	snp	A/G			intron-variant	RABGEF1	GRCh38.p7	7:66689043	ggttgcagtgagccg[A/G]gattgcaccactgca	27342
rs1553609	snp	C/T	0.495891	0.0451408	intron-variant	RABGEF1	GRCh38.p7	7:66732152	ACCGCCCTCTCTTCC[C/T]ATGGTCCAGGCACAA	27342
rs1553610	snp	C/T	0.495213	0.048687	intron-variant	RABGEF1	GRCh38.p7	7:66732246	AGCTGCAGCTAGCCA[C/T]GGGGCTGAGCAGGCA	27342
rs1573944	snp	A/G	0.232067	0.249356	intron-variant	RABGEF1	GRCh38.p7	7:66774816	ACGAGGCTTTACAAC[A/G]GTGATGTTTGGGTGA	27342
rs1605374	snp	A/G	0.00318978	0.0398085	intron-variant	RABGEF1	GRCh38.p7	7:66784310	AAAGGGACTTTAGCA[A/G]CTATGGAGTTTCAGT	27342
rs1848168	snp	A/C			intron-variant	RABGEF1	GRCh38.p7	7:66784359	aggaagttgagagcc[A/C]aagaggataagtgac	27342
rs1882654	snp	A/C	0.125528	0.21681	upstream-variant-2KB	RABGEF1	GRCh38.p7	7:66681718	ACCCTTTAACTCGAA[A/C]ACCTGTCACATCCTA	27342
rs1882655	snp	C/T	0.230896	0.249269	upstream-variant-2KB	RABGEF1	GRCh38.p7	7:66682070	AGGCCCCGGAAGTGA[C/T]GTTTGCGCGCCGTGC	27342
rs1922722	snp	C/T	0.368938	0.219895	intron-variant	RABGEF1	GRCh38.p7	7:66709974	AACAATAAAGTTGTT[C/T]AGTGGAGAAAATATT	27342
rs1922723	snp	C/T	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66710076	AGTAGTCAGCAGCCA[C/T]GTGACTGGTACCTTC	27342
rs1962049	snp	C/G	0.0517044	0.152246	intron-variant	RABGEF1	GRCh38.p7	7:66775535	ATATACTGTCTGACC[C/G]TCAAGCCCAATTTCA	27342
rs1962050	snp	C/T	0.488545	0.074807	intron-variant	RABGEF1	GRCh38.p7	7:66775021	GTCTTCTCATACTCA[C/T]TCAGCTACTGCTCTA	27342
rs2003300	snp	C/G	0.487049	0.0794222	intron-variant	RABGEF1	GRCh38.p7	7:66682759	TCCCCTCCCAACTCC[C/G]GGACGCTTCTGTCCC	27342
rs2003301	snp	C/G	0.496034	0.0443518	intron-variant	RABGEF1	GRCh38.p7	7:66682669	GTCCGAGCGTCCCAT[C/G]CCGGCGCGTTCCGGG	27342
rs2055682	snp	A/G	0.441021	0.161279	intron-variant	RABGEF1	GRCh38.p7	7:66795302	aaggatcccgtcttt[A/G]gctgaactaaggaaa	27342
rs2055683	snp	C/T	0.0988009	0.199095	intron-variant	RABGEF1	GRCh38.p7	7:66783395	ATATATAGATCAAAG[C/T]GTGATAGATTTTGGC	27342
rs2077180	snp	C/T	0.27893	0.24832	intron-variant	RABGEF1	GRCh38.p7	7:66800458	AGAAATTACAGAAAC[C/T]AGTAATTTACTTAAC	27342
rs2141924	snp	C/T	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66721259	ttaaaaatcaaaata[C/T]ctaggaataaattta	27342
rs2178742	snp	C/T	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66732812	GCTACAGAGTGAGAG[C/T]GAGAGCAAAAGCGAG	27342
rs2244022	snp	A/G	0.502301	0.0251508	intron-variant	RABGEF1	GRCh38.p7	7:66737443	AATACGAGACTGGGT[A/G]GGGGGGGGCAGTCTA	27342
rs2279934	snp	C/G	0.0715223	0.175059	intron-variant	RABGEF1	GRCh38.p7	7:66740949	CCGCTGTCCTTCGTC[C/G]CACATTCCGTCTCCG	27342
rs2279935	snp	C/G	0.0777841	0.181223	intron-variant	RABGEF1	GRCh38.p7	7:66741130	CGGCGGCTCCCCTCG[C/G]CCCGGCTCCCACCTT	27342
rs2420827	snp	A/G	0.443195	0.158668	utr-variant-5-prime, nc-transcript-variant	RABGEF1	GRCh38.p7	7:66682114	GCTGGCGGTGCCGGG[A/G]GGGCGGGGCAAGCAG	27342
rs2659888	snp	A/C	0.495213	0.048687	intron-variant	RABGEF1	GRCh38.p7	7:66765184	AACTCCCTTTCCTAT[A/C]TCCCTCTCCAACCTC	27342
rs2659889	snp	C/T	0.495818	0.0455352	intron-variant	RABGEF1	GRCh38.p7	7:66752125	ctgtagcctcaaacg[C/T]ctggcctcaagcaat	27342
rs2659890	snp	C/T	0.471388	0.116136	intron-variant	RABGEF1	GRCh38.p7	7:66742380	AAAGTATCTTGACTG[C/T]CCCTTCTCCTCAACT	27342
rs2659891	snp	C/T	0.46974	0.119223	intron-variant	RABGEF1	GRCh38.p7	7:66736127	TGTCAGGATGCCCAC[C/T]GAGGCTTTGTTTTTT	27342
rs2659892	snp	C/T	0.470521	0.117772	intron-variant	RABGEF1	GRCh38.p7	7:66735318	GGAACAGTCATTTAA[C/T]AGCGTGATGCTGGAG	27342
rs2659893	snp	C/T	0.470618	0.117591	intron-variant	RABGEF1	GRCh38.p7	7:66735006	AATTTTCCTTAACTT[C/T]CTTAACGTTCCTGAA	27342
rs2659894	snp	C/T	0.48692	0.0798058	intron-variant	RABGEF1	GRCh38.p7	7:66733497	GTTGGCCAGTCTGGT[C/T]TTGAACTCCTGATCT	27342
rs2659895	snp	G/T	0.486984	0.079614	intron-variant	RABGEF1	GRCh38.p7	7:66731484	AGTGATCCACCTGCG[G/T]TGGCCTCCCAAACTG	27342
rs2659896	snp	A/G	0.470424	0.117954	intron-variant	RABGEF1	GRCh38.p7	7:66730706	GCCAGGTGTGGTGGC[A/G]GATGCCTGTAATCCC	27342
rs2659897	snp	C/T	0.487049	0.0794222	intron-variant	RABGEF1	GRCh38.p7	7:66722728	tggaagactcacact[C/T]cttgactttaaaact	27342
rs2659898	snp	C/T	0.470521	0.117772	intron-variant	RABGEF1	GRCh38.p7	7:66722372	GCTCACTGCAACCTC[C/T]GTCTACTAGGTTCAA	27342
rs2659899	snp	C/T	0.495963	0.0447464	intron-variant	RABGEF1	GRCh38.p7	7:66721734	gagatctgcccgcct[C/T]ggcctcccaaagtgc	27342
rs2659900	snp	C/G	0.487384	0.080253	intron-variant	RABGEF1	GRCh38.p7	7:66719456	aatcccagcacactg[C/G]ggggggccgaggtgc	27342
rs2659901	snp	A/T	0.470521	0.117772	intron-variant	RABGEF1	GRCh38.p7	7:66719392	catagcaagacccca[A/T]ctctacaaaatatat	27342
rs2659902	snp	A/T			intron-variant	RABGEF1	GRCh38.p7	7:66718196	caccacgcctaatat[A/T]tttttgtattttttg	27342
rs2659903	snp	C/T	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66715944	AAAACACTCCATCCA[C/T]AACTGTAGTCTTTTT	27342
rs2659904	snp	G/T	0.486	0.0824865	intron-variant	RABGEF1	GRCh38.p7	7:66713615	ttcaagactgaatgt[G/T]ttcacccaagttaag	27342
rs2659906	snp	A/G	0.495407	0.0477027	intron-variant	RABGEF1	GRCh38.p7	7:66700323	GACCCCTTCAAGGCG[A/G]AAGAGGAGCTCAGGC	27342
rs2659907	snp	C/T	0.470424	0.117954	intron-variant	RABGEF1	GRCh38.p7	7:66699045	CTCCTCCATGCGGCT[C/T]TGTCTCAGTGACTTC	27342
rs2659908	snp	C/T	0.470618	0.117591	intron-variant	RABGEF1	GRCh38.p7	7:66695835	GAAATTACAGGCGTT[C/T]GCTACCACACCCCTG	27342
rs2659909	snp	C/T	0.482459	0.0919928	intron-variant	RABGEF1	GRCh38.p7	7:66695292	CAGGGTCTCGCTCTG[C/T]TGCTCAGGCTGGAGT	27342
rs2659910	snp	A/C	0.0422008	0.138995	intron-variant	RABGEF1	GRCh38.p7	7:66693926	CAACTACTCTGGTGG[A/C]TGAGGCAGGAGAATC	27342
rs2659911	snp	C/T	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66693433	GACCTACCTTCTCAC[C/T]CTGAGCCAGGCCTGC	27342
rs2659912	snp	C/G	0.495252	0.0484902	intron-variant	RABGEF1	GRCh38.p7	7:66693012	CTAGGAGGGCCTGGG[C/G]CTCTAGAAAAGATCC	27342
rs2659913	snp	A/T	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66692349	TTTACATGGGAGGAG[A/T]TGCCAGGAAGCATGG	27342
rs2659914	snp	A/G	0.486332	0.08153	intron-variant	RABGEF1	GRCh38.p7	7:66691927	tgggactacagatgc[A/G]tgccagcacacttta	27342
rs2659915	snp	C/T	0.49614	0.0437598	intron-variant	RABGEF1	GRCh38.p7	7:66688114	actcctgatgtcatt[C/T]ggttacttttttttt	27342
rs2659916	snp	C/G	0.495445	0.0475058	intron-variant	RABGEF1	GRCh38.p7	7:66686365	CCCACTTTGGCCTCC[C/G]AAAGCACTGGTATTA	27342
rs2707822	snp	C/G	0.495213	0.048687	intron-variant	RABGEF1	GRCh38.p7	7:66742705	gtgggaggatcactt[C/G]agcacaggcagttga	27342
rs2707823	snp	A/G	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66718129	gggcagatcacctga[A/G]gccaggagttcgaga	27342
rs2707824	snp	A/G	0.470521	0.117772	intron-variant	RABGEF1	GRCh38.p7	7:66724256	tctacataatgtgtt[A/G]tttccttctctggct	27342
rs2707825	snp	C/T	0.000399281	0.0141238	intron-variant	RABGEF1	GRCh38.p7	7:66710328	cctatagcatcttta[C/T]tggtaaaagctaaac	27342
rs2707826	snp	A/G	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66708348	GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC	27342
rs2707827	snp	C/T	0.495999	0.0445491	intron-variant	RABGEF1	GRCh38.p7	7:66707452	GCCTGCCTTGGCCTC[C/T]CAAAGTGCTGGGATT	27342
rs2707828	snp	C/T	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66706390	TGGAAAACAGTTTGG[C/T]GGGTTTTTAAAAACT	27342
rs2707830	snp	A/G	0.230603	0.249246	intron-variant	RABGEF1	GRCh38.p7	7:66702658	catgaagatgactat[A/G]atcaaaaaatgaaag	27342
rs2707834	snp	A/G			intron-variant	RABGEF1	GRCh38.p7	7:66753420	CTTATTGGATGGTAT[A/G]TTTTTCCCCCAGGGC	27342
rs2707835	snp	A/G			intron-variant	RABGEF1	GRCh38.p7	7:66753469	GCATACTTTGGAGAT[A/G]TTACGGGTTTGGTTC	27342
rs2707836	snp	A/C	0.495291	0.0482933	intron-variant	RABGEF1	GRCh38.p7	7:66695448	TGGGCAGGGGCTTTG[A/C]CGCAAGAGGTTCCAC	27342
rs2707837	snp	C/G	0.470715	0.117409	intron-variant	RABGEF1	GRCh38.p7	7:66716086	ATATATACAGCAAAA[C/G]TGACAGAACTTGAGG	27342
rs2707838	snp	A/G	0.230896	0.249269	intron-variant	RABGEF1	GRCh38.p7	7:66694214	CCACCGCTGCCCCAC[A/G]GTGTCCCCCGCTGCA	27342
rs2707839	snp	C/T	0.487432	0.0782705	intron-variant	RABGEF1	GRCh38.p7	7:66728097	AAAGGAGCCCTGAGC[C/T]GCTGGGGGTGATGAG	27342
rs2707840	snp	A/G	0.231189	0.249291	intron-variant	RABGEF1	GRCh38.p7	7:66693028	CTGCTTTTTTCCCCC[A/G]CTAGGAGGGCCTGGG	27342
rs2707841	snp	C/T	0.495963	0.0447464	intron-variant	RABGEF1	GRCh38.p7	7:66692033	gtcttgctttgtcgc[C/T]caagctggagtgcag	27342
rs2707845	snp	A/G	0.495213	0.048687	intron-variant	RABGEF1	GRCh38.p7	7:66733811	TTCACTATGTTCACT[A/G]GGCTGGTCTCAAACT	27342
rs2707846	snp	A/T	0.00676609	0.0577691	intron-variant	RABGEF1	GRCh38.p7	7:66731427	GCACAGCCTCCAAGA[A/T]CCTTATTTACCAGCC	27342
rs2707847	snp	C/G	0.470521	0.117772	intron-variant	RABGEF1	GRCh38.p7	7:66737884	TTCCCTCTTGCTGCT[C/G]GGTGCCTAGAACATT	27342
rs2707848	snp	G/T	0.495291	0.0482933	intron-variant	RABGEF1	GRCh38.p7	7:66686252	TGCCACTGCACTCCA[G/T]CCTGGGCAACAAAGT	27342
rs2707849	snp	C/T	0.49533	0.0480965	intron-variant	RABGEF1	GRCh38.p7	7:66687725	ctataaatacagact[C/T]actttagatacaaag	27342
rs2707850	snp	G/T	0.495213	0.048687	intron-variant, upstream-variant-2KB	RABGEF1	GRCh38.p7	7:66738883	ATTACCACCATCCAA[G/T]GTACTACTGTAAATA	27342
rs2707852	snp	A/G	0.495213	0.048687	intron-variant, upstream-variant-2KB	RABGEF1	GRCh38.p7	7:66739606	ggcggaggttgcagt[A/G]agccgagatcgcacg	27342
rs2707853	snp	C/T	0.495818	0.0455352	intron-variant	RABGEF1	GRCh38.p7	7:66749023	CAGTGGAGGAAGTCA[C/T]GGTGAGCCTGAAGGC	27342
rs2707854	snp	C/T	0.495213	0.048687	intron-variant	RABGEF1	GRCh38.p7	7:66747610	AAAATAAAACTTTCA[C/T]TATGTATTTTTAACT	27342
rs2707855	snp	C/T	0.00517822	0.0506191	intron-variant	RABGEF1	GRCh38.p7	7:66747078	GGCCGGGCACGGTAG[C/T]TCACACCTGTAATCC	27342
rs2707856	snp	A/T	0.495213	0.048687	intron-variant	RABGEF1	GRCh38.p7	7:66746023	TACAGTGCTCTATGA[A/T]AGAAGTGTACATTTA	27342
rs2901267	snp	A/T	0.368938	0.219895	intron-variant, nc-transcript-variant	RABGEF1, LOC107986707	GRCh38.p7	7:66759519	acgtagttataaaga[A/T]atacctgagattgag	27342
rs3069894	in-del	-/A/AA	0	0	intron-variant	RABGEF1	GRCh38.p7	7:66742160	ATCTCAAAAAAAAAA[-/A/AA]CTAAGAGTCTGTTCC	27342
rs3194900	snp	A/G			intron-variant	RABGEF1	GRCh38.p7	7:66685271	tgattcgcctgcctc[A/G]gccttctgagtacct	27342
rs3735151	snp	C/T	0.0599851	0.162463	intron-variant	RABGEF1	GRCh38.p7	7:66772114	GCGGTTGAACAGTGA[C/T]GTGACTGGATACATA	27342
rs3735152	snp	C/T	0.0715223	0.175059	intron-variant	RABGEF1	GRCh38.p7	7:66772261	AGCTTTCAGTAGTTT[C/T]TTCATTTTGTGTTTG	27342
rs3735153	snp	A/G	0.0715223	0.175059	intron-variant	RABGEF1	GRCh38.p7	7:66808802	CTTCTGTTTTAAATG[A/G]TCTGTGATCAAAAGA	27342
rs3757420	snp	A/G	0.0777841	0.181223	utr-variant-5-prime, upstream-variant-2KB	RABGEF1	GRCh38.p7	7:66740233	CTGCCTGGGCCTCCT[A/G]AAGATTCAGCTGCTT	27342
rs3778905	snp	A/C/G	0.00953873	0.0683987	intron-variant	RABGEF1	GRCh38.p7	7:66748142	GACTTTCCAGCATGC[A/C/G]TTTCAAAGGGCTGGG	27342
rs3778906	snp	C/T	0.0715223	0.175059	intron-variant	RABGEF1	GRCh38.p7	7:66748213	GCTTTTTGTGTAAGA[C/T]GGTGACATAACATCA	27342
rs3778907	snp	A/G	0.220544	0.248259	intron-variant	RABGEF1	GRCh38.p7	7:66775851	GTGTCTTGAGGAAGT[A/G]TATTGAGAACATATA	27342

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