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
rs342	snp	A/G	0.312593	0.242037	intron-variant	ASB4	GRCh38.p7	7:95489283	CTTATTTGTAATCCA[A/G]TAGCTTTATTCTGTC	51666
rs43060	snp	C/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	LOC107986823	GRCh38.p7	7:95471806	atttgccatgtgcca[C/G]ggacaatgctaagta	51666
rs43061	snp	C/T	0.386694	0.20932	intron-variant	LOC107986823	GRCh38.p7	7:95473222	TTCAAGGAGACCTGT[C/T]GGATTGCACTGAATT	51666
rs43062	snp	C/T	0.244205	0.249933	nc-transcript-variant	LOC107986823	GRCh38.p7	7:95473786	GATGGGGAACAATGG[C/T]CAGGGACTCCAGGCC	51666
rs43063	snp	C/T	0.39214	0.205661			GRCh38.p7	7:95480475	aggatatgatagaaa[C/T]agtggtatatgactt	51666
rs43064	snp	G/T	0.245916	0.249967			GRCh38.p7	7:95481582	TTTCTTCCCTATGGT[G/T]GCATTTGATAAGTGA	51666
rs43065	snp	C/T	0.288646	0.246995			GRCh38.p7	7:95481979	GTGTAATTTGACCTC[C/T]TGAGGTGAGTTGAAG	51666
rs43066	snp	A/T	0.245631	0.249962	upstream-variant-2KB	ASB4	GRCh38.p7	7:95484880	TGTAATGGATACCAA[A/T]ATATCCCTTACTAGA	51666
rs43067	snp	C/T	0.357664	0.225629	upstream-variant-2KB	ASB4	GRCh38.p7	7:95485392	TCCCCACCTCCTCCC[C/T]TCCCAGCTTTTCATA	51666
rs43068	snp	A/T	0.317451	0.240729	upstream-variant-2KB, utr-variant-5-prime	ASB4	GRCh38.p7	7:95485618	CAGATGTTTTTATTG[A/T]GGGGAAAAAAAGAGC	51666
rs43069	snp	C/T	0.243347	0.249911	intron-variant	ASB4	GRCh38.p7	7:95486650	AATAAATGGATAAAG[C/T]GGTGCCACAGGCACC	51666
rs731910	snp	A/C	0	0	intron-variant	ASB4	GRCh38.p7	7:95514563	AGGGAGAATTTGTGT[A/C]CCCTGAAGCCAGACA	51666
rs737902	snp	C/T	0.222035	0.248431	intron-variant	ASB4	GRCh38.p7	7:95509443	GTGCTTAGTTTGGAA[C/T]AGAGGATTAATGAGC	51666
rs757035	snp	A/C	0.00597247	0.0543191	intron-variant	ASB4	GRCh38.p7	7:95535145	CTAATGTCTTGGGAT[A/C]ACAGATAAAACAGAG	51666
rs763464	snp	C/T	0.280785	0.248097	intron-variant	ASB4	GRCh38.p7	7:95532517	AGGTAACACGAGGGT[C/T]TGGGAGAGGTAAGGA	51666
rs763465	snp	C/G	0	0	intron-variant	ASB4	GRCh38.p7	7:95533035	CCCACTAATCTCTGT[C/G]CCTAACCTTCTCACT	51666
rs1015882	snp	C/T	0.40595	0.195396			GRCh38.p7	7:95467303	actccaccaacacag[C/T]ttgtgtgaccctgag	51666
rs1015883	snp	C/T	0.424659	0.17887			GRCh38.p7	7:95467335	aagttacttaatttc[C/T]GAACCCTTATTCCTT	51666
rs1015884	snp	A/G	0.407158	0.194426			GRCh38.p7	7:95467356	CTTATTCCTTTTCAC[A/G]AAAATAGATGAATTA	51666
rs1034467	snp	A/G	0.00676609	0.0577691			GRCh38.p7	7:95468016	TCCAGCAAAAGAGAT[A/G]GGTGTCAAACCTCTG	51666
rs1476515	snp	A/G	0.499424	0.0169631	intron-variant	ASB4	GRCh38.p7	7:95489949	TCATACATCTGAAGG[A/G]AGATCAAGTTGGTAA	51666
rs1476516	snp	C/G	0.35809	0.225425	intron-variant	ASB4	GRCh38.p7	7:95489898	TGGACAGTCCTTCGT[C/G]TTTCCAGTATGGAAG	51666
rs1557782	snp	A/G	0.36315	0.222928	upstream-variant-2KB	LOC107986823	GRCh38.p7	7:95469845	ATTTTCCGTTATATC[A/G]GTCTTATCAGATTGA	51666
rs2023780	snp	C/T	0.00159617	0.0282053	intron-variant	ASB4	GRCh38.p7	7:95527099	GGTATAGTAGAAATA[C/T]TCATTGAAAGAGAGA	51666
rs2074125	snp	A/G	0.494272	0.053207	intron-variant	ASB4	GRCh38.p7	7:95504704	TTACTGTTACCCTCA[A/G]TGTATGTCAAGGGAT	51666
rs2074126	snp	C/T	0.35894	0.225016	intron-variant	ASB4	GRCh38.p7	7:95501460	AGGTGGTAAGAGCAG[C/T]GTCTGTCCAGCAGGC	51666
rs2078990	snp	A/G	0.49334	0.057322	intron-variant	ASB4	GRCh38.p7	7:95506302	atcaacctgaaactc[A/G]ttggagcaggtctga	51666
rs2079081	snp	A/G	0.24449	0.249939			GRCh38.p7	7:95461293	TGCAAAGCCACAGAG[A/G]TGAAGCTGCCTAAGG	51666
rs2158047	snp	A/G	0.207253	0.246318	intron-variant	ASB4	GRCh38.p7	7:95522627	GGAGGACCAACACAG[A/G]TAAGTGCTTCCCAAC	51666
rs2158136	snp	A/T					GRCh38.p7	7:95467490	GGAGTGGGATAGGGT[A/T]TGCTAGAGGACAGAG	51666
rs2158137	snp	C/T	0.362104	0.223456			GRCh38.p7	7:95467936	CACATACATTTTTTT[C/T]TGAGGGAAGAAGAGA	51666
rs2188808	snp	C/T	0.45762	0.139261	intron-variant	ASB4	GRCh38.p7	7:95525812	AAAGATGGTCTTTCA[C/T]GAAGCCATCTGTGTT	51666
rs2240003	snp	A/G	0.356169	0.226336	intron-variant	ASB4	GRCh38.p7	7:95535962	TTCCCAGCTGCCTGG[A/G]AAACTCTTCCAGCTC	51666
rs2301681	snp	A/G	0.00119737	0.0244387	intron-variant	ASB4	GRCh38.p7	7:95495658	TTTTTTTTTGGCCAC[A/G]TTTATAAAAGTGGGG	51666
rs2375018	snp	G/T			intron-variant	ASB4	GRCh38.p7	7:95513254	tttgttttttgtttg[G/T]ttttttttttttttt	51666
rs2375019	snp	A/G	0.281313	0.248031	intron-variant	ASB4	GRCh38.p7	7:95532698	GAGAAGAGAGGCAGG[A/G]AGACTTACCTTGAAT	51666
rs3045925	in-del	-/GT	0	0			GRCh38.p7	7:95467558	tgtgtgtgtgtgtgt[-/GT]atgtatgtgtTTATA	51666
rs3046862	in-del	-/TGTGTG			intron-variant	ASB4	GRCh38.p7	7:95513322	gtgtgtgtgtgtgtg[-/TGTGTG]tgtgttcagagacag	51666
rs3046863	in-del	-/GTGTGT			intron-variant	ASB4	GRCh38.p7	7:95513332	tgtgtgtgtgtgtgt[-/GTGTGT]tcagagacagggaat	51666
rs3046864	in-del	-/ATA	0.367495	0.220669	intron-variant	ASB4	GRCh38.p7	7:95522405	gggcttaagcaaata[-/ATA]tttcattatatcatt	51666
rs3223150	microsatellite	(CA)17/18/19/20/21/22/23/24	0.724772	0.127505	intron-variant	ASB4	GRCh38.p7	7:95493363	TCCAACCTNGCTATA[(CA)17/18/19/20/21/22/23/24]TTTCATCTCTTTTNT	51666
rs3757702	snp	A/C	0.467744	0.122832	intron-variant	ASB4	GRCh38.p7	7:95535659	CAAGATGGCCAGAAT[A/C]TCCTTCAGGAGATAG	51666
rs3757703	snp	C/T	0.468047	0.122292	intron-variant	ASB4	GRCh38.p7	7:95535595	ATGGATGTTTATACA[C/T]TTAACCAACTTTTGG	51666
rs3757704	snp	A/C	0.0652144	0.168387	upstream-variant-2KB	ASB4	GRCh38.p7	7:95484108	ACTCCTAAGTTTAAG[A/C]GAACCTCCTGCCTCA	51666
rs3757705	snp	C/T	0.498632	0.0261223	upstream-variant-2KB	ASB4	GRCh38.p7	7:95483665	TGGGAATCCCTAGAT[C/T]GCCTCCATTTCCCAT	51666
rs3779488	snp	A/C	0.152667	0.230274	intron-variant	ASB4	GRCh38.p7	7:95513569	TCACATGTAAATCAG[A/C]AAACTTTGAGTTAAA	51666
rs3779489	snp	A/T	0.153332	0.230554	intron-variant	ASB4	GRCh38.p7	7:95511264	GCGTTCACTTCTTGG[A/T]GGCTCTCGGTAGGGG	51666
rs3779490	snp	A/G	0.429388	0.174127	intron-variant	ASB4	GRCh38.p7	7:95491412	TGAGGGAGAACCGGG[A/G]AACCAAGCCCATGGG	51666
rs3779491	snp	C/G	0.325563	0.238307	intron-variant	ASB4	GRCh38.p7	7:95491324	GCTACCCCATGTCTA[C/G]AGTCTGTGTGCAGTG	51666
rs3801909	snp	A/C	0.477515	0.103619	intron-variant	ASB4	GRCh38.p7	7:95532725	ATTAATACACAATCT[A/C]TTAAAAAAGAGATTC	51666
rs3801912	snp	A/G	0.316485	0.240998	intron-variant	ASB4	GRCh38.p7	7:95532341	ATTCTTTTTTCCCCC[A/G]CTTATGTAATTTACA	51666
rs3801913	snp	C/T	0.139564	0.224285	intron-variant	ASB4	GRCh38.p7	7:95526026	GCTTTAAAAAAAATC[C/T]GTTTACCATGTATTG	51666
rs3801915	snp	C/T	0	0	intron-variant	ASB4	GRCh38.p7	7:95525704	GAACGAATGAGAATG[C/T]CTTCCCAGAAGCCAT	51666
rs3801916	snp	A/G	0.367297	0.220775	intron-variant	ASB4	GRCh38.p7	7:95491707	GATGAGGCTGTGCCT[A/G]TTCACAATCTTCTGC	51666
rs3801917	snp	A/G	0.368324	0.220226	intron-variant	ASB4	GRCh38.p7	7:95490835	ATATGCAGACTAATC[A/G]TGTGTGTGTGCACGC	51666
rs3801918	snp	A/G	0.286042	0.247388	intron-variant	ASB4	GRCh38.p7	7:95490343	AAAAGTTTGAACATC[A/G]AAGAAAGGAAAAGAA	51666
rs3801919	snp	A/G	0.250168	0.25	intron-variant	ASB4	GRCh38.p7	7:95489698	TGTTTTCTTTATATC[A/G]TTTTTATTTTAAAGT	51666
rs3801920	snp	C/T	0.302686	0.244385	intron-variant	ASB4	GRCh38.p7	7:95489516	ACATGATTTCATCTG[C/T]AGATTTTATTATGAA	51666
rs3801926	snp	A/T	0.283684	0.24772	upstream-variant-2KB	LOC107986823	GRCh38.p7	7:95470659	AGCTGTGGTGTCAGA[A/T]CCTTTCTCATTTCCT	51666
rs3801927	snp	A/G	0.284733	0.247575	upstream-variant-2KB	LOC107986823	GRCh38.p7	7:95470770	ATAGGACTTTTCAAG[A/G]CACTGTCCCATCCAT	51666
rs3823954	snp	G/T	0.0142736	0.0832652	intron-variant	ASB4	GRCh38.p7	7:95488885	TTTTGTGCATTGTCT[G/T]TCTTATTAAGCCAAA	51666
rs3834352	in-del	-/TCGGAGAACATAAA			intron-variant	ASB4	GRCh38.p7	7:95535422	TTTTCCCATGAAACT[-/TCGGAGAACATAAA]TCAACCTTTCTGAGG	51666
rs3834353	in-del	-/G	0.00159617	0.0282053	intron-variant	ASB4	GRCh38.p7	7:95532046	TTCCTTTGGAGGGGG[-/G]CCAGCTCTCCTACAC	51666
rs3837137	in-del	-/GA	0.00199481	0.0315187	intron-variant	ASB4	GRCh38.p7	7:95491243	GAAAAGAAAAATAGA[-/GA]TTATTTCCCCTGTGT	51666
rs4517046	snp	C/T	0.232651	0.249397	intron-variant	ASB4	GRCh38.p7	7:95534965	TGTGCTGCCAGCTGG[C/T]TTCATCTTACCAGCT	51666
rs4727314	snp	A/G	0.23846	0.249734			GRCh38.p7	7:95466518	TTATGGAATCCAAAA[A/G]CAACAGTGAAATATG	51666
rs4729192	snp	A/G	0.359998	0.2245	intron-variant	ASB4	GRCh38.p7	7:95500522	CTGCTGTGAGCTATT[A/G]TTGGACCACTGCACA	51666
rs4729193	snp	C/G	0.00159617	0.0282053	intron-variant	ASB4	GRCh38.p7	7:95526385	CTATAAAACTTCGCT[C/G]CAGTTGCACCCTGCC	51666
rs5885914	in-del	-/TG	0.484632	0.086302			GRCh38.p7	7:95467535	GAAACATTGTAAAAT[-/TG]TGTGTGTGTGTGTGT	51666
rs5885915	in-del	-/G	0.38934	0.207568			GRCh38.p7	7:95468144	TTATTAAATTGGGTT[-/G]GGGGGGGCCCCATTC	51666
rs5885916	in-del	-/T	0.34989	0.229177			GRCh38.p7	7:95477921	TGCAATTTTTTTTTT[-/T]CCTGCAATATCCCAT	51666
rs5885917	in-del	-/C			intron-variant	ASB4	GRCh38.p7	7:95514752	AGAGGGAGCCTTACC[-/C]TGACTACACACGGGA	51666
rs6465466	snp	A/C	0.372189	0.218105	intron-variant	ASB4	GRCh38.p7	7:95502275	TAAAATGACAATTAG[A/C]TATTTTGTTGTTGTT	51666
rs6465467	snp	C/T	0.499354	0.0179596	utr-variant-3-prime, intron-variant	ASB4	GRCh38.p7	7:95537892	ACTTTACAAACACTG[C/T]CATTAATCCTAGAAT	51666
rs6465468	snp	G/T	0.266819	0.249434	utr-variant-3-prime, intron-variant	ASB4	GRCh38.p7	7:95540202	GAACTTTTATTTAGA[G/T]AACTTAAATAAAGCT	51666
rs6946568	snp	A/G	0.375996	0.215928	intron-variant	ASB4	GRCh38.p7	7:95534206	AAAAATTAGTCAGGA[A/G]TTGTGGCATGATTTG	51666
rs6950550	snp	C/G	0.499017	0.0221427			GRCh38.p7	7:95480115	AGACTTTTCTTACTT[C/G]TTGGTCCACAGGAGC	51666
rs6952627	snp	C/G	0.436692	0.166271	intron-variant	ASB4	GRCh38.p7	7:95498222	acacctataatatca[C/G]tattttgggaggcca	51666
rs6958904	snp	C/T	0.418007	0.185132	upstream-variant-2KB	ASB4	GRCh38.p7	7:95484865	AAGCTGAAAGAATAA[C/T]GTAATGGATACCAAT	51666
rs6958950	snp	C/G	0.493837	0.055168	intron-variant	ASB4	GRCh38.p7	7:95523959	tcactctgcaaccaa[C/G]aaattggctaaaatt	51666
rs6959029	snp	A/G	0.491936	0.0629843	intron-variant	ASB4	GRCh38.p7	7:95524240	gggcaatgcccatct[A/G]cagttgaatggataa	51666
rs6959064	snp	C/T	0.103082	0.202275	upstream-variant-2KB	ASB4	GRCh38.p7	7:95484961	ttacacaCACatata[C/T]atatgtgtgtatata	51666
rs6959226	snp	C/T	0.123798	0.215808	intron-variant	ASB4	GRCh38.p7	7:95515159	TTTTTCTTTCTTTCT[C/T]TCTCTTTCTCTTTCT	51666
rs6960785	snp	C/T	0.0825414	0.185628			GRCh38.p7	7:95481959	CAGTGTGAAACATGA[C/T]CACTGTGTAATTTGA	51666
rs6969315	snp	C/T	0.153	0.230415	intron-variant	ASB4	GRCh38.p7	7:95518736	ATTCCACTGCAGGAA[C/T]GACCAATGAGATTTT	51666
rs6973126	snp	C/T	0.499759	0.0109798	intron-variant	ASB4	GRCh38.p7	7:95501905	TTAAAGATCCACTTA[C/T]TCTTTCAAGCCATGT	51666
rs6973299	snp	C/G	0.439085	0.163545	intron-variant	ASB4	GRCh38.p7	7:95501998	TCAGAAGGGCAAACA[C/G]CATAAAATTAAAAGG	51666
rs6975716	snp	G/T	0.31721	0.240796	intron-variant	ASB4	GRCh38.p7	7:95520163	AATAATTTGAATTCT[G/T]AATTTTGAAAGTGTC	51666
rs6976899	snp	A/G	0.484209	0.0874434	upstream-variant-2KB	ASB4	GRCh38.p7	7:95484800	TAAGAAAAATTAAGT[A/G]TATACTTTTCTCTCC	51666
rs6979120	snp	C/T	0.493432	0.0569306	intron-variant	ASB4	GRCh38.p7	7:95524150	tagagcccagagaaa[C/T]ccctgcacgtgagca	51666
rs7455777	snp	G/T			intron-variant	ASB4	GRCh38.p7	7:95513243	TCAGGGttttttttg[G/T]tttttgtttgttttt	51666
rs7457858	snp	G/T			intron-variant	ASB4	GRCh38.p7	7:95513242	GTCAGGGtttttttt[G/T]ttttttgtttgtttt	51666
rs7779320	snp	A/C	0.206336	0.246157	intron-variant	ASB4	GRCh38.p7	7:95537254	ACTTCCATTAAATAT[A/C]TGAATATATGCATCA	51666
rs7784619	snp	A/G	0.498794	0.0245311	utr-variant-3-prime, intron-variant	ASB4	GRCh38.p7	7:95538231	ACTGTCACTAGTTTT[A/G]CAAACTCCTACTCCC	51666
rs7791764	snp	C/T	0.0562307	0.157967			GRCh38.p7	7:95463695	tgcttcctgcgcagc[C/T]tgtggaactgtgagc	51666
rs7795412	snp	A/G	0.293294	0.246223	intron-variant	ASB4	GRCh38.p7	7:95529806	ttttatttttataat[A/G]gactctgaggtgggc	51666
rs7798235	snp	C/T	0.4776	0.103433	intron-variant	ASB4	GRCh38.p7	7:95533601	TGAATGCTTTCTTCA[C/T]TTGGTATCTTTCACT	51666
rs7806277	snp	C/G	0.326506	0.238006	intron-variant	ASB4	GRCh38.p7	7:95502391	ATAGGTACCAGCCTG[C/G]GGGGGGGGGGCAAAT	51666
rs9886182	snp	A/G	0.427423	0.176128	intron-variant	ASB4	GRCh38.p7	7:95500011	cccaagtagctggga[A/G]CATCCTCATTTTTAA	51666
rs9886222	snp	G/T	0.000798403	0.0199641	intron-variant	ASB4	GRCh38.p7	7:95501444	AATCCGAAATAGATA[G/T]GCCTGCTGGACAGAC	51666

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