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
rs41544	snp	A/C	0.00496275	0.0495656	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778188	GGGCCAAACCCAGGA[A/C]TCCTGTGCGCGAGTC	84182
rs41545	snp	A/T	0.0298908	0.118541	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796700	AGGTGTAGCAAAGTT[A/T]TTTTCATAAACTCTG	84182
rs41546	snp	C/G	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797599	aagaaaggaagcaag[C/G]gcttggtcatgtggg	84182
rs41547	snp	C/T	0.031825	0.122064	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800047	cctcctagatgagtt[C/T]ggcaaaggacgattc	84182
rs718930	snp	A/C	0.295343	0.245854	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776561	acagatgaaagtccc[A/C]gtcctcagggagctt	84182
rs739978	snp	C/T	0.078151	0.181571	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873143	GGGCCTGTGGTTTGT[C/T]CAGGGCACCCACAGA	84182
rs739979	snp	C/T	0.420892	0.182472	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873744	CTGCTCCCTGATCTG[C/T]GTCTAAAATCTTCCT	84182
rs739980	snp	C/T	0.421051	0.182323	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873799	TTTTTCAGGCAAGTT[C/T]GAGTTTTCCCATCTG	84182
rs739981	snp	A/G	0.486725	0.0803809	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796263	CTCTTTTTTATCTGG[A/G]CCTTGTGTGGAAAAG	84182
rs740819	snp	A/C	0.0482946	0.147699	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770939	CTCATTACGGGAAAG[A/C]AGGCACCAAGGGGGC	84182
rs757486	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777003	tttcttCTTTCtttc[C/T]ttttctttttctttt	84182
rs763287	snp	A/G	0.293551	0.246177	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870488	CTTCTGGGAAGGGTG[A/G]TTGAGGCTCACCCAC	84182
rs765508	snp	C/T	0.243919	0.249926	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795653	TCCAGAACCATCAAT[C/T]TGTGTTTGTCCTCAA	84182
rs882533	snp	C/T	0.242201	0.249878	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830912	CATCTCACACTGACC[C/T]CCACATCCTCCCCAA	84182
rs882534	snp	A/G	0.497329	0.0364438	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830898	CCCCACATCCTCCCC[A/G]ACAGGGCCATTACCT	84182
rs1017012	snp	A/G	0.492727	0.0598633	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797387	gggagccctggggac[A/G]gagctgctattttat	84182
rs1034750	snp	C/G	0.482831	0.0910472	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798531	agacagagtctcgct[C/G]tgtcgcccaggctgg	84182
rs1203181	snp	C/T	0.489024	0.0732638	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891692	CCCAGCAGTGCCAGG[C/T]GCAAAGTAGGTTGTG	84182
rs1468311	snp	G/T	0.124144	0.21601	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847793	CACCTAGGCTAGAAT[G/T]CAGTGGCACGATCAT	84182
rs1468312	snp	C/T	0.239902	0.249796	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848165	ATGGAGTTTTTCCAG[C/T]TTAGGTGTTCTAGGC	84182
rs1468313	snp	G/T	0.239902	0.249796	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848166	TGGAGTTTTTCCAGC[G/T]TAGGTGTTCTAGGCA	84182
rs1557909	snp	A/G	0.0352966	0.128072	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797188	acaccacctgcgatg[A/G]cctactgtgtgccag	84182
rs1557910	snp	C/T	0.492727	0.0598633	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797558	tgattgaggctggac[C/T]acatgagggagagag	84182
rs1990010	snp	A/C	0.496034	0.0443518	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805134	TGCAGCAGGTCTGAG[A/C]AAGGTGACTGGCAGC	84182
rs1990011	snp	C/G	0.305934	0.243663	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805368	GTTTCTGGATATGTC[C/G]AGTGGAGCTTTTGTT	84182
rs2040834	snp	A/C	0.485324	0.0843964	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811661	gtagttaaagatcga[A/C]ccctgacctaatcag	84182
rs2040835	snp	A/G	0.499035	0.0219437	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825667	tgtgtaagccaccta[A/G]cttctgtgAGAATCA	84182
rs2040836	snp	G/T	0.389903	0.207189	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825832	gctgccataacaaat[G/T]accacaaagtggctt	84182
rs2040837	snp	A/G	0.389715	0.207315	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826360	TAGCCTCACATGTGT[A/G]CTGGGTGAGTGAGTG	84182
rs2040838	snp	A/G	0.497641	0.0342639	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856824	GAGCTGGTACAAGGG[A/G]CTGGTGACCCAAGTC	84182
rs2040839	snp	A/T	0.242775	0.249896	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858656	GATGTTTTAAAAATA[A/T]ATATATATATATATA	84182
rs2107549	snp	C/T	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873531	GTTGAAGAGCaggct[C/T]agattcagtgggtct	84182
rs2107550	snp	A/G	0.496314	0.0427728	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878748	GGAAAACAGCTTGAC[A/G]GGCAAGAGTTCTGAA	84182
rs2107551	snp	G/T	0.469346	0.119947	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784142	ATTCAGAGGTGGAGG[G/T]TCATAAGGGGCTATG	84182
rs2107552	snp	A/G	0.498652	0.0259235	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821089	AAATGTGAGATTTTA[A/G]GAAGCTTTAACTCTG	84182
rs2107553	snp	A/G	0.498813	0.0243321	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824971	GCAGTAATCCAGCTC[A/G]TGCCTCTCTCTGGGG	84182
rs2158463	snp	A/G	0.437683	0.165152	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824757	TTATTTATTTTTTGT[A/G]GAGAGAGGGTCTTGA	84182
rs2158464	snp	A/G	0.495291	0.0482933	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871173	AAGTGGGGGGGACAG[A/G]CCTGGGACCCAGGCT	84182
rs2269921	snp	C/G	0.493293	0.0575177	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785613	TGTCTTTCATGATAA[C/G]GCACTGGCTGGTTAG	84182
rs2391916	snp	A/G	0.469544	0.119585	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784174	AGAAGCTCTTCCTCC[A/G]AGGCACTTACTACCT	84182
rs2391917	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789397	AGAATTTCGCCAGAT[C/T]CTCTAGAAGGGACAT	84182
rs2391918	snp	C/G	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795348	TTTTATCCTCCCTTA[C/G]GAATTCAACCCACAG	84182
rs2391919	snp	C/T	0.487621	0.0776941	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795951	CCAGAACACTCAGCA[C/T]ATCTCAAGGTCAGCT	84182
rs2391920	snp	C/T	0.497586	0.0346604	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822018	CCAATATATATTAAT[C/T]GTATTTATATATACA	84182
rs2391921	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856587	GTTACAGGCATTGGC[A/G]GAAGGGGAAACAGAC	84182
rs2893395	snp	C/T	0.305934	0.243663	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809173	gtaccactttgttgt[C/T]agtgtaaacaagggt	84182
rs3076403	in-del	-/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776985	cttttcttttctttc[-/TT]cttttcttCTTTCtt	84182
rs3076404	in-del	-/CT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776998	tccttttcttCTTTC[-/CT]tttctttttcttttt	84182
rs3076405	in-del	-/AGC	0.469642	0.119404	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784162	AAGGGGCTATGAAGA[-/AGC]TCTTCCTCCGAGGCA	84182
rs3138796	microsatellite	(TG)10/11/12/14/15/16/17	0.634826	0.140861	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785271	AGGTGTGCCAATGGG[(TG)10/11/12/14/15/16/17]TCAGAGAGAGAGAGA	84182
rs3223240	microsatellite	(CA)21/22/23/24/25	0.600806	0.138185	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782331	ATATGCNTATAGATA[(CA)21/22/23/24/25]AGAGACTATATTGAT	84182
rs3801323	snp	G/T	0.475081	0.108804	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872369	CCTCAGAGAGGGAGA[G/T]GTCCTCCTCCCTCCT	84182
rs3801324	snp	A/C	0.46703	0.124089	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872392	TCCCTCCTCTTGCCC[A/C]AGAAAAAGACAAGTC	84182
rs3801325	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872408	AGAAAAAGACAAGTC[C/T]TTCTTGCCTCTGCCA	84182
rs3801326	snp	C/G	0.419776	0.18351	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872542	TTTATGTGCACTGAT[C/G]TATGTGCTCAGAGCT	84182
rs3801327	snp	G/T	0.395453	0.203331	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883402	CCTGGCCCAGCCTGG[G/T]GGTGGCAGGAGGTGC	84182
rs3823766	snp	A/C	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872757	TTACAGAGGGGCCCT[A/C]AATGGACCTCACAGG	84182
rs3823767	snp	A/G	0.496382	0.0423778	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883429	GTGCTGCCTGGAGCG[A/G]CACCCTCTGCTTGCG	84182
rs3888593	snp	C/G/T	0.0569829	0.158885	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776935	AGGACTGGCTGACTC[C/G/T]CAAGGGCACCCTTGT	84182
rs4134403	snp	A/G	0.47726	0.104176	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865005	CTCTTGGAGGTTTAA[A/G]TGTGCTGTTCTGAAC	84182
rs4141290	snp	C/G	0.499631	0.0135733	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869069	CAGCTTCCATTTTGT[C/G]TGGTTCTGGGCCCTC	84182
rs4336510	snp	A/G	0.316243	0.241064	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857217	TTCTCCTTTTGGAGC[A/G]ACGTTCACTTTTCTG	84182
rs4509209	snp	C/T	0.492533	0.0606443	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798621	cctgcctcagcctcc[C/T]gagtagctgggactg	84182
rs4628165	snp	C/G	0.361263	0.223876	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856428	TGCAGAGAGGCATGT[C/G]CAGGGCTCAAGGGGT	84182
rs4723016	snp	A/C	0.390426	0.2107	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780998	GTTTGGTTGTAGTCC[A/C]TGGGCTGTGGGTCTT	84182
rs4723017	snp	C/T	0.484066	0.0878235	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802793	ATATATCTAGCCAAC[C/T]AAACAACTAACCAGC	84182
rs4723018	snp	C/T	0.480382	0.097079	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803046	AACTAACCAACCCAC[C/T]CAATCAAACCAGCCA	84182
rs4723019	snp	A/G	0.0498117	0.149749	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842133	CAATGGTTTTGCACA[A/G]TAATAATTGAGGTGT	84182
rs5026597	snp	A/T	0.495782	0.0457324	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858654	TTGATGTTTTAAAAA[A/T]ATATATATATATATA	84182
rs5883256	in-del	-/A/AA	0.49949	0.0159663	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796897	TGGAGTCATACCCTC[-/A/AA]AAAAAAAAAAAAAAG	84182
rs5883257	in-del	-/A	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796898	CAAAAAAAAAAAAAA[-/A]GACCCTGTCAATTCA	84182
rs5883258	in-del	-/C	0.317583	0.242826	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812279	GTGTTGAGGGGGGGG[-/C]GGTGTATGTATGTAT	84182
rs5883259	snp	G/T	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812281	TGTTGAGGGGGGGGG[G/T]GTATGTATGTATGCA	84182
rs5883262	in-del	-/C	0.425586	0.17796	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871137	CCAGGGCTGTGTGTT[-/C]CCCCCCAGGGTCATG	84182
rs6462224	snp	A/G	0.46014	0.13543	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783443	catagttaaccaaaa[A/G]tgggttaacccactt	84182
rs6462228	snp	A/G	0.369346	0.219673	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855792	TCTGGACTCAAAGCA[A/G]TCGCCTCCTCGCCTG	84182
rs6462229	snp	C/T	0.498158	0.0302955	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889737	CCACATCCAATGGAG[C/T]AAGTGATGATGCTGG	84182
rs6462230	snp	C/G	0.454423	0.143914	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890208	AACCTTTTATGCCGA[C/G]TGTTTTAACAAGAAG	84182
rs6942480	snp	A/G	0.24134	0.24985	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885935	TCCACCTTGGCAGTT[A/G]TTCCTAGAAAAGCTG	84182
rs6944321	snp	C/T	0.274124	0.248833	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769821	TTGTGTTTGTTTTAA[C/T]GTGTATTAGAGATTT	84182
rs6945015	snp	A/T	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867311	GGGTTCTTGGCCGTG[A/T]TATGAGTGGTTGAGA	84182
rs6945458	snp	A/G	0.0244538	0.107838	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779753	gtgttttgattccca[A/G]ttcTATTGTAGGAGT	84182
rs6946714	snp	C/T	0.216649	0.247765	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797277	ccacttccagtgaga[C/T]gaggcagcccacaat	84182
rs6947469	snp	C/T	0.151334	0.229706	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791799	TCTAGAcaggggtgt[C/T]caaccttttggcttc	84182
rs6947493	snp	A/C	0.167809	0.236103	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791904	aaaattgcaaaaaaa[A/C]ctcaatgttttaaga	84182
rs6947717	snp	A/T	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812958	AAGCTCCAGATACCT[A/T]TGGTCAGCGCTCTTC	84182
rs6948085	snp	C/T	0.497722	0.0336691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792202	tacattgattgattt[C/T]tgaatgttaaaccaa	84182
rs6948436	snp	C/T	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792454	agattgatgtgattt[C/T]tttcttaaatatttg	84182
rs6949578	snp	C/T	0.482609	0.0916147	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779898	ACCACTTGAAAACTA[C/T]GCAAGTACATGTCAT	84182
rs6950663	snp	C/T	0.464309	0.12873	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889318	ACCCAGCAGATGTAA[C/T]AGATGAACTCAGTAC	84182
rs6951406	snp	C/T	0.377582	0.214995	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856158	CTGTGGAGTGCAGAG[C/T]AGCACTGGAAGAATA	84182
rs6951701	snp	A/T	0.499451	0.0165644	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796122	GTTGGAGCACTGTAC[A/T]TTTTTTTTTTTTGTC	84182
rs6956006	snp	A/C	0.00358891	0.0422285	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811555	atattgtcttatgcc[A/C]gatttctgcttccaa	84182
rs6956143	snp	C/G	0.352504	0.228019	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781490	TCTCTGTGCTCTTCA[C/G]ATTGACCTGCTTCAG	84182
rs6956261	snp	A/G	0.296364	0.245663	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781426	TGAAGACTTTCATTT[A/G]CCTTTTGTTTTTAAG	84182
rs6956593	snp	A/G	0.0399052	0.1355	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811736	gaaaatccctgtcct[A/G]ttctgttccgttcta	84182
rs6956870	snp	A/G	0.00755907	0.0610114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805961	CTTGGGTGGGGCCCG[A/G]AAGGGGACAGTGCTG	84182
rs6957048	snp	G/T	0.424659	0.17887	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850001	GGCCCTGGCAGTGAA[G/T]AGCACCTGCCTGTAC	84182
rs6958083	snp	C/T	0.295343	0.245854	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769481	ATTCTTTCATTATTA[C/T]ACATCATCCATCAGT	84182
rs6958406	snp	C/T	0.258565	0.249853	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769702	GCCACATTAAAGCTA[C/T]GTCCTATGGAGACTG	84182

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