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
rs4366224	snp	A/G	0.490622	0.0678316	intron-variant	ASB11	GRCh38.p7	X:15306079	CCTCCAGCTCCATCC[A/G]TGTCTCTGCAAAGGA	140456
rs4370686	snp	C/T	0.491815	0.0634477	intron-variant	ASB11	GRCh38.p7	X:15306032	ATGTGGCATTTGGTT[C/T]TCTGTTCCTGTTAGT	140456
rs4830529	snp	A/T	0.00633741	0.0559334	upstream-variant-2KB	ASB11	GRCh38.p7	X:15315720	CTCCTGTTACCGAGA[A/T]CTCTGTAGGTTCTAA	140456
rs4830935	snp	A/C	0.327237	0.23777			GRCh38.p7	X:15278266	ATAATGTCATAAAAA[A/C]CAGATGATTAGTCTG	140456
rs5008833	snp	C/T	0.481456	0.0944889	intron-variant	ASB11	GRCh38.p7	X:15294611	CCTGGGTTCAAATGA[C/T]CCTCCTGCCTCAGCC	140456
rs5901555	in-del	-/TC	0.488319	0.0755258	intron-variant	ASB11	GRCh38.p7	X:15294882	GATTTCCTATAAATT[-/TC]TCTCTTAGTTCACGT	140456
rs5901557	in-del	-/TCTTA			intron-variant	ASB11	GRCh38.p7	X:15305777	GTTTTTTGACTTTTA[-/TCTTA]AGTTCAGGGGTACAT	140456
rs5934230	snp	G/T	0.499997	0.00128534	intron-variant	ASB11	GRCh38.p7	X:15289981	GTGAGCCGAGATAGC[G/T]CCACTGCACTCCAGC	140456
rs5934231	snp	C/T	0.474111	0.11079	intron-variant	ASB11	GRCh38.p7	X:15291764	TTATATGGCTGAGCA[C/T]GGTGGCTCATGCCTG	140456
rs5934232	snp	A/T	0.454162	0.144284	intron-variant	ASB11	GRCh38.p7	X:15295243	AGACGGGGTTTCACC[A/T]TGTTGGCCAGGATGG	140456
rs5934233	snp	C/G	0.415877	0.188383	intron-variant	ASB11	GRCh38.p7	X:15299108	ACCATTTCCCTCCCT[C/G]TGATGATCACGTTCT	140456
rs5935921	snp	C/T	0.488319	0.0755258			GRCh38.p7	X:15275854	TCCTGGTACAGGCTC[C/T]GCTAAGGGAAGGAGA	140456
rs5935922	snp	A/G	0.493114	0.0582701			GRCh38.p7	X:15278997	TTCAATATTTGGGGC[A/G]CATTGAATTGTACCT	140456
rs5935923	snp	G/T	0.476119	0.10663			GRCh38.p7	X:15279538	TGCCTTTGATATATT[G/T]CAAAAATGCTTTCCC	140456
rs5935924	snp	C/G	0.492736	0.0598256	downstream-variant-500B	ASB11	GRCh38.p7	X:15281434	ACAAAAGTGAAACTC[C/G]GTCTAAAAAAGAAAA	140456
rs5935925	snp	A/G	0.491541	0.0644807	utr-variant-3-prime	ASB11	GRCh38.p7	X:15283411	CATTTAAAGATACTA[A/G]GAGTCTAAGCTGTTG	140456
rs5935926	snp	A/G	0.491679	0.0639643	intron-variant	ASB11	GRCh38.p7	X:15287159	TCACCATTTAGTCGG[A/G]TTTCTGAAATACTCT	140456
rs5935927	snp	C/T	0.481456	0.0944889	intron-variant	ASB11	GRCh38.p7	X:15287403	GTGATCTCTGCTCAT[C/T]GCAACCTCCGCCTCC	140456
rs5935928	snp	G/T	0.482063	0.0929878	intron-variant	ASB11	GRCh38.p7	X:15289062	TAGATTTCCCAAAGG[G/T]AAACCACCCTCTTGT	140456
rs5935929	snp	A/G	0.474111	0.11079	intron-variant	ASB11	GRCh38.p7	X:15289369	ACTCATTTCTCTAGA[A/G]AAGTTTTGTTTTTAG	140456
rs5935930	snp	C/T	0.453679	0.144965	intron-variant	ASB11	GRCh38.p7	X:15289441	ACAAGAACTTCATCT[C/T]TGAAGCTGTAGAAAA	140456
rs5935931	snp	A/T	0.474231	0.110546	intron-variant	ASB11	GRCh38.p7	X:15292627	CAGCCTTTTCTTTTC[A/T]ATAACTATGACCTTG	140456
rs5935932	snp	A/G	0.454001	0.144511	intron-variant	ASB11	GRCh38.p7	X:15292966	AAGCATTCCGAAGTT[A/G]TAAGTAGGGCTCTTT	140456
rs5935933	snp	A/G	0.45384	0.144738	intron-variant	ASB11	GRCh38.p7	X:15294387	GTTGCAATATAACCC[A/G]TGAAACAGGGTCTTG	140456
rs5935934	snp	C/T	0.415597	0.187291	intron-variant	ASB11	GRCh38.p7	X:15295283	CTTGATCTCATGATC[C/T]ACCTGCCTCAGCCTC	140456
rs5935935	snp	C/T	0.398695	0.200972	intron-variant	ASB11	GRCh38.p7	X:15296257	GACTCTGTCTAAAAA[C/T]AAAAAGATGGAAAAA	140456
rs5935936	snp	C/T	0.474948	0.109081	intron-variant	ASB11	GRCh38.p7	X:15296656	TTTATTAAAAGCTCG[C/T]TCATTTTGATAATTT	140456
rs5935937	snp	A/G	0.489502	0.0716857	intron-variant	ASB11	GRCh38.p7	X:15300243	AAGATCATCTAGAGT[A/G]GATCACCTCAATTGT	140456
rs5935938	snp	C/T	0.477263	0.10417	intron-variant	ASB11	GRCh38.p7	X:15301214	GTGATCCACCCACCT[C/T]GGCCTCCTAAAGTGC	140456
rs5935939	snp	A/G	0.48872	0.0742474	intron-variant	ASB11	GRCh38.p7	X:15301540	AGACAGAGAGAGAGA[A/G]AGAAAGAAAAAGAGA	140456
rs5935940	snp	C/T	0.49091	0.0668016	intron-variant	ASB11	GRCh38.p7	X:15304823	gaggttgcagtgagc[C/T]aagattatgccactg	140456
rs5935941	snp	A/G	0.497499	0.0352757	intron-variant	ASB11	GRCh38.p7	X:15307068	CCATTTAAAAATAAA[A/G]ACAGGATTTAAGTGG	140456
rs5935942	snp	C/G	0.491882	0.0631893	intron-variant	ASB11	GRCh38.p7	X:15307221	TCCCATTAGACTCAA[C/G]TCATATACACAACAT	140456
rs5935943	snp	C/T	0.460503	0.134865	intron-variant	ASB11	GRCh38.p7	X:15310982	ATAAGAGCGAAACTC[C/T]AACTCAAAAAATAAA	140456
rs5935944	snp	A/G	0.472357	0.11427	synonymous-codon, intron-variant	ASB11	GRCh38.p7	X:15314436	TCCGGACCTTCTGAT[A/G]CGTTCTGAAACTTCA	140456
rs5935945	snp	G/T	0.460055	0.135562	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316062	TTTTCTCTTAATTCT[G/T]AAGTTTATAGAGGAT	140456
rs5935946	snp	A/T	0.460354	0.135097	upstream-variant-2KB	ASB11	GRCh38.p7	X:15317047	ATATTTCATGAATCA[A/T]CCTTCTCTAGTTGGG	140456
rs5980146	snp	C/G	0.0183711	0.0940641	intron-variant	ASB11	GRCh38.p7	X:15284208	agtgagccgagatcg[C/G]gccactgcactccag	140456
rs6527420	snp	C/T	0.352982	0.227804	intron-variant	ASB11	GRCh38.p7	X:15285521	CCAGGATATCCAGGT[C/T]TACAAATCCTAGTCC	140456
rs6628932	snp	A/G	0.455909	0.141779	intron-variant	ASB11	GRCh38.p7	X:15284267	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	140456
rs6628937	snp	A/T			intron-variant	ASB11	GRCh38.p7	X:15287407	tctctgctcatcgca[A/T]cctccgcctcccagg	140456
rs6628942	snp	A/T	0.48	0.0979796	intron-variant	ASB11	GRCh38.p7	X:15290041	AATAAATAAATAAAT[A/T]AATTAATTAAATAAC	140456
rs6628943	snp	G/T	0.491264	0.0655128	intron-variant	ASB11	GRCh38.p7	X:15290425	ATATGGCCTGCAACA[G/T]TACTTTGGTTAGTCT	140456
rs6628945	snp	C/T	0.480942	0.0957375	intron-variant	ASB11	GRCh38.p7	X:15291559	AAAAAATACAAAAAT[C/T]AGCTGGGCACTGTGA	140456
rs6628949	snp	A/G	0.45384	0.144738	intron-variant	ASB11	GRCh38.p7	X:15294018	ACTCTAAAACTTAAA[A/G]TATAATAAAAAATAA	140456
rs6628964	snp	A/G	0.489655	0.0711726	intron-variant	ASB11	GRCh38.p7	X:15303736	TTTCCTTACTGGTAA[A/G]ATGGAAATATAATAA	140456
rs6628967	snp	C/T	0.491264	0.0655128	intron-variant	ASB11	GRCh38.p7	X:15306238	TAATGAACATATGCA[C/T]GTATGTGTCCTTATA	140456
rs6628971	snp	A/C	0	0	intron-variant	ASB11	GRCh38.p7	X:15312282	CAAAGAAGCTTAAAA[A/C]CCAAAACTAATAACA	140456
rs6632183	snp	C/T	0.472271	0.114437	intron-variant	ASB11	GRCh38.p7	X:15283844	TTTAAGTTAATCTTC[C/T]AATGGTACTTGGATT	140456
rs6632267	snp	C/T	0.4608	0.1344	intron-variant	ASB11	GRCh38.p7	X:15307448	CAGGCATTAGATTCT[C/T]ATAAAGAGAATGTAA	140456
rs6632268	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15309147	gtcttgaactcctga[C/T]ctcaagtgatccact	140456
rs6653931	snp	A/G	0.359796	0.224599	intron-variant	ASB11	GRCh38.p7	X:15292949	GGAAATTGGAGTCAG[A/G]AAAGCATTCCGAAGT	140456
rs7049370	snp	A/G	0.481149	0.0952383	intron-variant	ASB11	GRCh38.p7	X:15285643	AAGCTCGGATCTGCT[A/G]AGGAAGATCATAATT	140456
rs7062793	snp	G/T	0.0126344	0.0784702	intron-variant	ASB11	GRCh38.p7	X:15284952	CCAAGGAGCATCCAT[G/T]AGATAGAAAGCTACC	140456
rs7066009	snp	C/T	0.263	0.249662	intron-variant	ASB11	GRCh38.p7	X:15311173	AGATATCTAAAATAT[C/T]GTAATAAAACTGAGT	140456
rs7881570	snp	A/G	0.00158814	0.0281345			GRCh38.p7	X:15279917	caaaaaagtttttTC[A/G]tttaattttatttgg	140456
rs11094674	snp	A/C	0	0	intron-variant	ASB11	GRCh38.p7	X:15307311	CGTGTGATTTGGTTT[A/C]TATAAAGCAGCAGTC	140456
rs12006793	snp	C/T	0.425108	0.17843	intron-variant	ASB11	GRCh38.p7	X:15284068	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTGT	140456
rs12006826	snp	C/G	0.0389457	0.134	intron-variant	ASB11	GRCh38.p7	X:15284168	gaggcaggagaatgg[C/G]gtgaacccgggaggc	140456
rs12010915	snp	G/T	0.0317957	0.122012	intron-variant	ASB11	GRCh38.p7	X:15304936	aaataaacaataaga[G/T]attatatcttatcaa	140456
rs12013880	snp	A/T	0.0317957	0.122012	intron-variant	ASB11	GRCh38.p7	X:15309074	gacacacatcaccac[A/T]cccagctaattttag	140456
rs12401027	snp	C/G			intron-variant	ASB11	GRCh38.p7	X:15300902	GAGAAGAGGTGGGTG[C/G]GAGACTGAGAGAGAA	140456
rs12557809	snp	G/T	0.352406	0.228063	intron-variant	ASB11	GRCh38.p7	X:15309585	gtccatggagaaatt[G/T]tcttccatgaaacca	140456
rs12687741	snp	G/T			utr-variant-3-prime	ASB11	GRCh38.p7	X:15281712	ttttttttttttttg[G/T]tttgagacggagtct	140456
rs12688765	snp	G/T	0	0	intron-variant	ASB11	GRCh38.p7	X:15292886	GCCACCAAAACACCA[G/T]CAAAGAGGATCTGGA	140456
rs12690160	snp	A/G	0.47326	0.112495	intron-variant	ASB11	GRCh38.p7	X:15300905	AAGAGGTGGGTGGGA[A/G]ACTGAGAGAGAAGAG	140456
rs12834070	snp	C/T	0.291966	0.246453	intron-variant	ASB11	GRCh38.p7	X:15284027	ggaggccaaggtggg[C/T]ggatcacgaggtcag	140456
rs12834451	snp	C/G	0	0	intron-variant	ASB11	GRCh38.p7	X:15284048	ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT	140456
rs12841882	snp	A/G	0.261904	0.249716	intron-variant	ASB11	GRCh38.p7	X:15307716	agtcaaaagcacccc[A/G]aggaggggtgaggac	140456
rs12843347	snp	A/G	0	0	intron-variant	ASB11	GRCh38.p7	X:15302663	CTCTGCTACAGCCAA[A/G]GCTAATAAAGAATGA	140456
rs12843560	snp	A/C	0	0	intron-variant	ASB11	GRCh38.p7	X:15302698	TAATTATAGCATAAG[A/C]ATGAAGGATCAAGTC	140456
rs12843739	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15285137	AGTTGGTATTTAATC[C/T]ttctttttttttttt	140456
rs12843742	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15285141	GGTATTTAATCtttc[C/T]ttttttttttttttt	140456
rs12845370	snp	A/T	0	0	intron-variant	ASB11	GRCh38.p7	X:15296296	aaaaaaaGAAAATGC[A/T]CGACCACAATGGCAT	140456
rs12846060	snp	A/C			intron-variant	ASB11	GRCh38.p7	X:15312246	AAGAAAAAAAAATAT[A/C]CATATAATAGACAAA	140456
rs12846066	snp	A/C			intron-variant	ASB11	GRCh38.p7	X:15312257	ATATACATATAATAG[A/C]CAAAATAAACAAAGA	140456
rs12846074	snp	A/C	0	0	intron-variant	ASB11	GRCh38.p7	X:15312266	TAATAGACAAAATAA[A/C]CAAAGAAGCTTAAAA	140456
rs12851814	snp	A/C	0	0	intron-variant	ASB11	GRCh38.p7	X:15312356	GTAATAGTTTAAGCC[A/C]CAAAGACATATAAAA	140456
rs12859158	snp	C/T	0.374005	0.217078	intron-variant	ASB11	GRCh38.p7	X:15301249	ATTACAGGCGTGAGC[C/T]ACCACATCCGGCCAG	140456
rs16979812	snp	A/G	0.0660089	0.169255	intron-variant	ASB11	GRCh38.p7	X:15298525	GGAAATGGAGCACCT[A/G]TGAAGTCTGCTAGGC	140456
rs16979814	snp	A/G	0.0328205	0.123827	intron-variant	ASB11	GRCh38.p7	X:15303771	ATATTTGTCAAGTGC[A/G]TTGGTCTCTAAGTAG	140456
rs34025595	snp	C/T	0.0104621	0.0715654	missense	ASB11	GRCh38.p7	X:15287983	GGTTAGCTCCATAGT[C/T]GGTTAGCAGGTGGAT	140456
rs34057288	in-del	-/C			intron-variant	ASB11	GRCh38.p7	X:15297018	TGGTACAAGGCCGGG[-/C]CGCGGTGGCTCACGC	140456
rs34332247	in-del	-/T			intron-variant	ASB11	GRCh38.p7	X:15311660	AGCTTAAAATAGCCC[-/T]TTTTTTTTTTTGAAA	140456
rs34551144	snp	A/G	0.421791	0.181625	intron-variant	ASB11	GRCh38.p7	X:15284080	ACACGGTGAAACCCC[A/G]TGTCCACTAAAAATA	140456
rs34660573	in-del	-/T			upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315342	AAGTATAAATATAAT[-/T]CTGCCTTCCAGAAAT	140456
rs34670756	in-del	-/C			intron-variant	ASB11	GRCh38.p7	X:15288203	TTTGAAAATATGCAA[-/C]CTCAAGCCTAGAACC	140456
rs34708436	in-del	-/CT/TC			intron-variant	ASB11	GRCh38.p7	X:15294883	ATTTCCTATAAATTT[-/CT/TC]CTCTTAGTTCACGTC	140456
rs34773033	snp	C/T	0.417974	0.185161	intron-variant	ASB11	GRCh38.p7	X:15284085	GTGAAACCCCGTGTC[C/T]ACTAAAAATACAAAA	140456
rs34826963	in-del	-/A			intron-variant	ASB11	GRCh38.p7	X:15284270	AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAGAA	140456
rs35110928	in-del	-/G			intron-variant	ASB11	GRCh38.p7	X:15294686	AACCCCCATTAAATT[-/G]GGAAAGTTAAAGATA	140456
rs35413500	in-del	-/A			intron-variant	ASB11	GRCh38.p7	X:15296574	CTCAGTCACCCTTTG[-/A]AAAAAGTTTGGAGAT	140456
rs35650807	snp	A/T	0.0714214	0.174956	intron-variant	ASB11	GRCh38.p7	X:15290037	TCAAAATAAATAAAT[A/T]AATTAATTAATTAAA	140456
rs35762920	in-del	-/AGTC	0.382114	0.21224			GRCh38.p7	X:15276721	TGTCTACATAGACAT[-/AGTC]AGATGGTTTATGGAT	140456
rs35775215	snp	C/T	0.423873	0.179634			GRCh38.p7	X:15276461	AGCTGGGACTACAGG[C/T]GCCCGCCAACACGCC	140456
rs35859007	snp	C/T	0.0333887	0.124818	missense	ASB11	GRCh38.p7	X:15287941	CCAGATCAAGCGCAC[C/T]TTTGCCCTGAGCATT	140456
rs36040626	snp	C/G	0.417974	0.185161	intron-variant	ASB11	GRCh38.p7	X:15284082	ACGGTGAAACCCCGT[C/G]TCCACTAAAAATACA	140456
rs41309559	snp	C/G	0.0989831	0.199233	utr-variant-3-prime	ASB11	GRCh38.p7	X:15283502	TCCCAGGAACACTTA[C/G]GACTATTGGTATAGG	140456
rs55651049	snp	A/G	0.127804	0.218101	intron-variant	ASB11	GRCh38.p7	X:15300495	TTTAACAGTGTATAA[A/G]AGTAAAGAAGTAGGG	140456
rs56075342	snp	A/G	0.0312828	0.12109	intron-variant	ASB11	GRCh38.p7	X:15304179	TAAACTTGGTGAAAC[A/G]AAAATCCCAGCAAAA	140456

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