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
rs916176	snp	C/T	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153922218	GGGAGGCTGCCACCT[C/T]CCGGAGCCTGGGTAC	393
rs1042856	snp	G/T	0	0	missense	ARHGAP4	GRCh38.p7	X:153910967	ATCTTCCGGGTATCG[G/T]GTGCCCAGCTCCGGG	393
rs2070097	snp	C/T	0.483317	0.0897951	synonymous-codon	ARHGAP4	GRCh38.p7	X:153910800	GGGCTGCACTGCCCA[C/T]GACCTGGACTCGGTG	393
rs2070098	snp	C/G	0.000191982	0.00979561	synonymous-codon	ARHGAP4	GRCh38.p7	X:153911163	GCCTGTGCCCCTGGT[C/G]GTGGAGAGCTGCATT	393
rs2070099	snp	A/C/G/T	0.0948792	0.196086	missense	ARHGAP4	GRCh38.p7	X:153909841	TTCCGGCGGGGGGAC[A/C/G/T]TACTGCGGCTGCACG	393
rs2269368	snp	C/T	0.499909	0.00675435	intron-variant	ARHGAP4	GRCh38.p7	X:153924366	TTGTGAATTGCAAGT[C/T]GATTGCATTGGTGGC	393
rs2269369	snp	A/C	0.108827	0.206325	upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153926979	GCAGCTGCACCTGCC[A/C]GTCATAGGCCTGAGG	393
rs2855585	snp	C/G			intron-variant	ARHGAP4	GRCh38.p7	X:153916387	actgagaggccccag[C/G]ctccccacggagcag	393
rs2855586	snp	C/T	0.0143533	0.0834904	missense	ARHGAP4	GRCh38.p7	X:153921747	GCTCCTGCAGCAACT[C/T]CCGCCGCAGCTCGCC	393
rs2855587	snp	A/C	0	0	upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153926574	GCTGTCCCTGGTCAC[A/C]ACTGCCAGACTGTAC	393
rs2855588	snp	A/C			upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153927685	GTCGGGAGACTCACA[A/C]GTCCCACCGCTGCCT	393
rs2857836	snp	C/T			missense	ARHGAP4	GRCh38.p7	X:153907781	CTGGGGCCCCAGCCT[C/T]ACCCTCAGCTTCCCA	393
rs2857837	snp	C/T	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153921558	AGGGCCCAAGCTCCG[C/T]TCCCAGGTCTCAGTG	393
rs2872602	snp	C/T	0	0	upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153928229	CCTCCCTTCCACCGG[C/T]GCCGGGGCGCGGCCG	393
rs3213439	snp	C/G/T	0.000794198	0.0199115	missense	ARHGAP4	GRCh38.p7	X:153909852	AGTACGTCCCCCCGC[C/G/T]GGAAGCTCAGCTCCT	393
rs3213440	snp	C/G	0.304144	0.244066	intron-variant	ARHGAP4	GRCh38.p7	X:153910132	GGGGGCTCTTCTCCA[C/G]TGGACCCCCCAGTCC	393
rs3213441	snp	A/C/G/T	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153911120	CGGGAGGGGCTGGGT[A/C/G/T]CTGCTTACCATTGAG	393
rs4898460	snp	A/G	0.410292	0.19185	intron-variant	ARHGAP4	GRCh38.p7	X:153914482	GGATGGATTATCTGA[A/G]CTCAGGAGTTGGAGA	393
rs4898461	snp	C/G	0.498666	0.0257933	intron-variant	ARHGAP4	GRCh38.p7	X:153917207	ggcgacagagaaaga[C/G]tctgtctcaaaaaat	393
rs5904376	in-del	-/C	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153913008	GCAGGGCCCCAGCCC[-/C]TCAGGGAGGACTCAC	393
rs5945374	snp	A/G	0.176813	0.239047	intron-variant	ARHGAP4	GRCh38.p7	X:153919948	cccgccatcatgccc[A/G]gctaatttttgtatt	393
rs5987181	snp	A/G	0.460948	0.134167	intron-variant	ARHGAP4	GRCh38.p7	X:153917109	tagtcccagctactc[A/G]ggaggctgaggcagg	393
rs5987182	snp	A/G	0.0220202	0.102592	missense	ARHGAP4	GRCh38.p7	X:153921489	TGCTGCAGCAGCACC[A/G]CCCAGCAGTGCAAGG	393
rs5987185	snp	A/C	0	0	upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153928211	CCGTGGGAGCCTGGG[A/C]CACCTCCCTTCCACC	393
rs6643801	snp	C/G/T	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153915214	acggacagtggaagg[C/G/T]tgggtgccagggctg	393
rs6643802	snp	C/G/T			intron-variant	ARHGAP4	GRCh38.p7	X:153924984	CCCAGAGCAAGTGAG[C/G/T]AACCCTTAGACAGTC	393
rs6643803	snp	C/G			missense	ARHGAP4	GRCh38.p7	X:153926184	CCCGCTCCCGCCGCA[C/G]CTTCCCGTGAGCGGC	393
rs6643804	snp	C/T			missense	ARHGAP4	GRCh38.p7	X:153926187	GCTCCCGCCGCAGCT[C/T]CCCGTGAGCGGCCAT	393
rs7057931	snp	C/T	0.47635	0.106139	intron-variant	ARHGAP4	GRCh38.p7	X:153908521	GAGCACGGAGCAGGG[C/T]CCCCCAGGTTGTGCG	393
rs7060505	snp	C/T	0.0131573	0.0800346	intron-variant	ARHGAP4	GRCh38.p7	X:153924021	tgacctcaggtgatc[C/T]gcccgcctcggcctc	393
rs7065799	snp	C/T	0.0147244	0.0845304	upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153926405	GCAGGGCGCCCCTTC[C/T]AGCCCCACTGTGCCC	393
rs7877284	snp	C/T	0.0709308	0.174454	intron-variant	ARHGAP4	GRCh38.p7	X:153922245	TCCCTTGCAAACACA[C/T]GGATACACAACACAC	393
rs7881265	snp	C/T	0.0840797	0.187004	intron-variant	ARHGAP4	GRCh38.p7	X:153925787	ATCAAGCTGGTTGAC[C/T]TCACTGTAGCTAAAA	393
rs7881421	snp	A/T	0.483919	0.0882151	intron-variant	ARHGAP4	GRCh38.p7	X:153911505	AGATCCACTCGTAGG[A/T]GTCTGATATTTTTGA	393
rs7890729	snp	C/T	0.0121112	0.0768695	intron-variant	ARHGAP4	GRCh38.p7	X:153908986	CAACGACTGGAACCT[C/T]GAGGAGGGAGGAGTT	393
rs10710691	in-del	-/T			intron-variant	ARHGAP4	GRCh38.p7	X:153911275	TTTTTTTTTTTTTTT[-/T]GAGACAAGGTCTCAC	393
rs11394527	in-del	-/G	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153909365	CCTCCCACTCCCACT[-/G]GGCCAAAGCCTGACC	393
rs11405331	in-del	-/A/G	0.000115548	0.00760022	intron-variant	ARHGAP4	GRCh38.p7	X:153909413	GAACAGCACACGTGT[-/A/G]TGGCCCCCTGAGCCC	393
rs11428457	in-del	-/C			intron-variant	ARHGAP4	GRCh38.p7	X:153921035	GCGGTGTTCCTCCCC[-/C]ACTGTGAGTGGCATT	393
rs11450812	in-del	-/G	0.471692	0.115554	intron-variant	ARHGAP4	GRCh38.p7	X:153911930	TAAAAAAAAAAAAAA[-/G]AAAGAAAGAAACTCA	393
rs11797283	snp	G/T	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153925953	gaagggaaaatggca[G/T]gCGGTTGAGGCCAAA	393
rs12557851	snp	C/T	0.0555816	0.157167	intron-variant	ARHGAP4	GRCh38.p7	X:153915301	AGTTCTGCGGCTGGA[C/T]GGTGGTGATGGCTGC	393
rs12832725	snp	C/T			intron-variant	ARHGAP4	GRCh38.p7	X:153908788	CTGCCACTCCCTGCT[C/T]TGAAGCTGAACATGA	393
rs12834662	snp	A/G	0	0	upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153926262	GCCGTGAGCGGGCCC[A/G]GCGCCGGGACTTGGG	393
rs34046683	in-del	-/G	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153909415	ACAGCACACGTGTGG[-/G]CCCCCTGAGCCCCGT	393
rs34153599	in-del	-/G	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153920960	GCCTAGGGAGAGAGG[-/G]CCTTTGCCCCTAGGT	393
rs34224005	in-del	-/C			intron-variant	ARHGAP4	GRCh38.p7	X:153908497	AGTGTTCACAGGGCC[-/C]ATGGTACAGAGCACG	393
rs34279017	snp	C/T	2.32159e-05	0.00340696	missense	ARHGAP4	GRCh38.p7	X:153912725	TTCTCCATGTCTCCC[C/T]CAAAGAGTCTCTGGT	393
rs34322798	in-del	-/C			upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153926988	CTGCCCGTCATAGGC[-/C]TGAGGGGGGCAGCCC	393
rs34483295	in-del	-/C			intron-variant	ARHGAP4	GRCh38.p7	X:153925021	AAACCCCAACTTTTC[-/C]AGTGTGAAATCACTG	393
rs34514067	snp	C/T	0.000933122	0.0215799	missense	ARHGAP4	GRCh38.p7	X:153907829	TTGTTCCTGCCCAGG[C/T]GGCTGCTGGGCGGGG	393
rs34635851	in-del	-/G			intron-variant	ARHGAP4	GRCh38.p7	X:153915226	GGGTGGGTGCCAGGG[-/G]CTGGGGGGTGGGGAG	393
rs34910218	in-del	-/C			intron-variant	ARHGAP4	GRCh38.p7	X:153924923	TCAAGACAGTGACCC[-/C]ACTTTGTAGAATGGT	393
rs34926983	in-del	-/G			frameshift-variant	ARHGAP4	GRCh38.p7	X:153910311	TGCAGCGCCACCGGG[-/G]TCCTGCCCAGCGGGC	393
rs34995015	in-del	-/C			intron-variant	ARHGAP4	GRCh38.p7	X:153916320	CCTGGGCCCTCCCCC[-/C]AGATCCCCTAAGGCA	393
rs35105833	in-del	-/G			intron-variant	ARHGAP4	GRCh38.p7	X:153915247	GGTGGGGAGTTGGGG[-/G]TTGAACGGGGCCAGA	393
rs35441863	in-del	-/T			intron-variant	ARHGAP4	GRCh38.p7	X:153922974	GGGAGGACCTCTTTT[-/T]AAAGGAGGGTGGTCA	393
rs35512142	snp	G/T	0.0142023	0.083063	intron-variant	ARHGAP4	GRCh38.p7	X:153924420	TCAGTTCAGACAAAC[G/T]CGTCAGCACACCCTG	393
rs35766125	snp	C/T			upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153928190	GGAAGGAGGGCGCCG[C/T]GGGCGCCGTGGGAGC	393
rs41299128	snp	C/T	0.0160072	0.0880192	intron-variant	ARHGAP4	GRCh38.p7	X:153909539	TGCTTCTCCGTCCTG[C/T]GGTGGGAAGGACCGG	393
rs41301329	snp	A/G	0.00949095	0.0682305	intron-variant	ARHGAP4	GRCh38.p7	X:153918748	AACTTGGATTCCTGA[A/G]CAAAGTGTGGGTCAT	393
rs41311386	snp	A/C/G	2.29487e-05	0.0033873	missense	ARHGAP4	GRCh38.p7	X:153919043	GCCAGGTGGAACCCT[A/C/G]TGTCACAGCACTGAG	393
rs41313418	snp	C/T	0.00422943	0.0457911	upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153926688	CCTCCTTCCCCCAGA[C/T]ATCCGATGGGGTCCT	393
rs56015121	in-del	-/C	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153909599	GTCCAGGGCCAGCAG[-/C]CTCCGCGCCAGCCAG	393
rs56069539	snp	A/T	0.0266548	0.112325	intron-variant	ARHGAP4	GRCh38.p7	X:153919798	TTTTTTTTTATTTTT[A/T]TTTTTTGAGACAGAG	393
rs56152269	snp	A/G			intron-variant	ARHGAP4	GRCh38.p7	X:153911476	CGGCACAGAGGCTTA[A/G]CACACCGTTTGTTAG	393
rs57510144	snp	G/T			intron-variant	ARHGAP4	GRCh38.p7	X:153925255	CTTGCACTGAATAAT[G/T]ATGTTAGAACCTACA	393
rs58300407	snp	C/T	0.120455	0.213818	intron-variant	ARHGAP4	GRCh38.p7	X:153915066	GAAAGTAAGGCCATT[C/T]TGAGATGGGCTCCAA	393
rs58410072	snp	A/G			missense	ARHGAP4	GRCh38.p7	X:153907772	CCCTGGGGGTGGGAA[A/G]CTGAGGGTGAGGCTG	393
rs61749033	snp	A/G	0.00397387	0.0443976	synonymous-codon	ARHGAP4	GRCh38.p7	X:153909514	AGTCTGCAGCCCTGC[A/G]CCCACCACCTGCTTC	393
rs62620964	snp	A/T	0.0282	0.115346	downstream-variant-500B, utr-variant-3-prime	AVPR2, ARHGAP4	GRCh38.p7	X:153907505	GGGCTTTCCCCAGCA[A/T]CCTTCCTCAGCTGCC	393
rs62620965	snp	A/C/T	0.140318	0.224675	synonymous-codon, missense	ARHGAP4	GRCh38.p7	X:153910830	CTCCACCAGTGGGTC[A/C/T]TCCCCTGCAGATGGG	393
rs72616464	snp	A/T	0.441523	0.160683	intron-variant	ARHGAP4	GRCh38.p7	X:153919791	ACTCTATTTTTTTTT[A/T]ATTTTTTTTTTTTGA	393
rs73627263	snp	A/G	0.0127248	0.0787432	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	AVPR2, ARHGAP4	GRCh38.p7	X:153906985	GCTGGGTGTAGGAGG[A/G]GCTGCAGCAGAGGCC	393
rs73627265	snp	C/T	0.0266548	0.112325	downstream-variant-500B, utr-variant-3-prime	AVPR2, ARHGAP4	GRCh38.p7	X:153907544	GGGCCTGGGCCAGGG[C/T]TGAGGGGCAGGCAGG	393
rs73640841	snp	A/C	0.00633741	0.0559334	intron-variant	ARHGAP4	GRCh38.p7	X:153915079	TTTTGAGATGGGCTC[A/C]AACATGGCTGACCCT	393
rs74328477	snp	A/G	0.00720314	0.0595792	intron-variant	ARHGAP4	GRCh38.p7	X:153919317	GCGTGCCAGGGTCAC[A/G]CACGTGGCCAGCCCC	393
rs74331897	snp	C/G	0.00282728	0.037492	missense	ARHGAP4	GRCh38.p7	X:153910754	AGAGTGGGGGCTCCA[C/G]GCTCCGGAAGTAGAG	393
rs74833747	snp	A/G	0.05698	0.158881	intron-variant	ARHGAP4	GRCh38.p7	X:153911930	ATAAAAAAAAAAAAA[A/G]AAAGAAAGAAACTCA	393
rs75561437	snp	G/T	0.5	0	synonymous-codon	ARHGAP4	GRCh38.p7	X:153913267	GGCCTGCAGCTTGGC[G/T]AGGATGCTCCGTCCA	393
rs77239136	in-del	-/G	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153920958	GTGCCTAGGGAGAGA[-/G]GGCCTTTGCCCCTAG	393
rs77485258	in-del	-/C	3.82431e-05	0.00437265	intron-variant	ARHGAP4	GRCh38.p7	X:153913005	GTCGCAGGGCCCCAG[-/C]CCCTCAGGGAGGACT	393
rs79022793	snp	A/C	0.0570788	0.159001	upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153926895	CCCCTTCTGCTCAGC[A/C]CCACAATTTCCCCAT	393
rs111265666	snp	A/G			intron-variant	ARHGAP4	GRCh38.p7	X:153915476	TTGGGAGGCCGAGGC[A/G]GGTGGATCACTTGAG	393
rs111513434	snp	C/G			intron-variant	ARHGAP4	GRCh38.p7	X:153914612	TGAGGCAGGGGAATC[C/G]CTTGAACCCGGGAGG	393
rs111653090	snp	C/T			missense	ARHGAP4	GRCh38.p7	X:153909471	CCGATGCCAGGAGGC[C/T]CTCGGGACTGCTCCC	393
rs111748064	snp	C/T			intron-variant	ARHGAP4	GRCh38.p7	X:153916189	AAGTGACTGTCACTT[C/T]CTTGCATCACTTCAG	393
rs112573601	snp	C/T	4.62235e-05	0.00480725	missense	ARHGAP4	GRCh38.p7	X:153920781	CATTCACGCTCTCCA[C/T]GTGATATGCCTGGTA	393
rs112645237	snp	A/G			intron-variant	ARHGAP4	GRCh38.p7	X:153911079	CATGCCAGGTGCTGG[A/G]AACTGGGTGCTGGGT	393
rs112740567	snp	A/G			intron-variant	ARHGAP4	GRCh38.p7	X:153917079	AAATCAGCCAGGCGT[A/G]GTGGCGGGCACCTGT	393
rs112925383	snp	A/G	0.00949095	0.0682305	intron-variant	ARHGAP4	GRCh38.p7	X:153913144	GAGCCAAGGACAGGC[A/G]GGAGGGGAGGACCGT	393
rs113243502	snp	C/G			upstream-variant-2KB	ARHGAP4	GRCh38.p7	X:153926400	GGGGGGCAGGGCGCC[C/G]CTTCCAGCCCCACTG	393
rs113296455	snp	A/G	0.00844089	0.0644143	intron-variant	ARHGAP4	GRCh38.p7	X:153913936	GCAGTAGGTGCCAAG[A/G]TCCCCGGGGCATAAG	393
rs113332267	snp	C/G/T	0	0	downstream-variant-500B, utr-variant-3-prime	AVPR2, ARHGAP4	GRCh38.p7	X:153907377	AGAGCTGGCTCCCAT[C/G/T]GGGGAATCAACACGA	393
rs113431005	snp	A/C	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153913652	GGGACAGGGAGGGAG[A/C]CAGGAAGTCCAAGTC	393
rs113510544	snp	A/G	0	0	intron-variant	ARHGAP4	GRCh38.p7	X:153916253	TCAAGACATCCAATC[A/G]TACAATTACCCTGCT	393
rs113818587	snp	C/T			intron-variant	ARHGAP4	GRCh38.p7	X:153915517	TGAGACCAGCCTTGG[C/T]AATATGGTAAAACCC	393
rs113896893	snp	A/G	0.0243172	0.107551	intron-variant	ARHGAP4	GRCh38.p7	X:153909398	AGTCCCCTCTGGCCT[A/G]GAACAGCACACGTGT	393
rs138254071	snp	A/G	0.000277123	0.011768	missense	ARHGAP4	GRCh38.p7	X:153910250	GGGGCGGGAAGACCC[A/G]ATCGGGCTGCACTAT	393
rs138669123	snp	C/G	0.0131573	0.0800346	intron-variant	ARHGAP4	GRCh38.p7	X:153925713	ACTGCAGTGGGGTTA[C/G]GGCCAGGTGATCTCC	393

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