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
rs699240	snp	C/T	0.477004	0.104734	intron-variant	NCF2	GRCh38.p7	1:183585314	CACACCATGCACAGA[C/T]CATTTTCACTGTCAG	4688
rs699241	snp	A/G	0.0919752	0.193722	intron-variant	NCF2	GRCh38.p7	1:183577367	TGCATGGTCCTTTGC[A/G]CTTCACATTAATAAA	4688
rs699242	snp	C/T	0.352287	0.228117	intron-variant	NCF2	GRCh38.p7	1:183577338	CAAAAATGAGCCCCC[C/T]GGGCTCTCTGAAGGG	4688
rs699243	snp	A/G	0.0998734	0.199905	intron-variant	NCF2	GRCh38.p7	1:183568799	AGCTATGTTCCACAG[A/G]ACACCACTGCCCCTC	4688
rs699244	snp	G/T	0.135967	0.227142	intron-variant	NCF2	GRCh38.p7	1:183556317	ACAGAATTTGTTATC[G/T]GTCACCCTTCCCCAC	4688
rs789180	snp	A/T	0.295343	0.245854	intron-variant	NCF2	GRCh38.p7	1:183556485	GTTACCAGATAGAGA[A/T]GAAGGGTCAAAGAAA	4688
rs789181	snp	A/G	0.114387	0.210022	intron-variant	NCF2	GRCh38.p7	1:183557203	AGACAACTTAGGTAT[A/G]ATCTCCAAAGCCCAC	4688
rs789182	snp	C/T	0.302435	0.244439	intron-variant	NCF2	GRCh38.p7	1:183557968	caagctccatgtccc[C/T]agttcaagtgattct	4688
rs789183	snp	C/T	0.301932	0.244547	intron-variant	NCF2	GRCh38.p7	1:183558123	aagtgatccactcac[C/T]ttggcctcccaaagt	4688
rs789184	snp	C/G	0.301932	0.244547	intron-variant	NCF2	GRCh38.p7	1:183558855	aggtgtgagccacca[C/G]gcccagccTACCCTC	4688
rs789185	snp	A/G	0.463989	0.129263	intron-variant	NCF2	GRCh38.p7	1:183585146	GCAACAGCTGCATAC[A/G]TGGGTTTTACAGGCT	4688
rs789186	snp	A/G	0.189576	0.242588	intron-variant	NCF2	GRCh38.p7	1:183585398	tgggaggccgaggcg[A/G]gtggatcacaaggtc	4688
rs789187	snp	C/G/T	0.0698336	0.173994	intron-variant	NCF2	GRCh38.p7	1:183586035	CTGTTTTGAAATCTG[C/G/T]TTTTAAATTTAACAT	4688
rs789188	snp	G/T	0.187369	0.242028	intron-variant	NCF2	GRCh38.p7	1:183586094	AATCCCAGCACTTTG[G/T]GGGGCTGAGGTGGGC	4688
rs789189	snp	C/T	0.0372196	0.131242	intron-variant	NCF2	GRCh38.p7	1:183586271	CCTGGGAGGCGGAGG[C/T]TGCGGTGAGCTGAGA	4688
rs789190	snp	C/T	0.0376037	0.131863	intron-variant	NCF2	GRCh38.p7	1:183586622	GACACTGGTGGGGTG[C/T]CACACCAGCTGAGTA	4688
rs789191	snp	A/G	0.183886	0.241099	intron-variant	NCF2	GRCh38.p7	1:183586744	GCTTCTGCCTCACCT[A/G]CTGATTTATTGCATA	4688
rs789192	snp	A/G	0.493201	0.0579089	intron-variant	NCF2	GRCh38.p7	1:183587156	CGCTCTCACATTTAG[A/G]AGCTGAAGTCTGGGA	4688
rs796860	snp	A/C	0.114036	0.209795	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555720	TGTTTTTGTAAGATG[A/C]TAGGTTTTTTTTTAT	4688
rs1126596	snp	C/T			synonymous-codon	NCF2	GRCh38.p7	1:183566949	CTTGAACCAGTTGAG[C/T]TGCGGATCCACCCTC	4688
rs2236384	snp	C/G	0.499502	0.0157669	intron-variant	NCF2	GRCh38.p7	1:183568724	TGCCCCCGTCAGAGG[C/G]GACTGCAGCCAGTGC	4688
rs2236385	snp	A/G	0.495818	0.0455352	intron-variant	NCF2	GRCh38.p7	1:183568890	ACGTAGCTGCAGCCA[A/G]GCCCTGATGGCCAGC	4688
rs2274064	snp	C/T	0.499779	0.0105108	missense, intron-variant	NCF2	GRCh38.p7	1:183573252	TTTGGTCGAAACAGC[C/T]TGCCCACAGGGATCA	4688
rs2274065	snp	A/C	0.325091	0.238456	utr-variant-5-prime, intron-variant, upstream-variant-2KB	NCF2	GRCh38.p7	1:183590569	gagagaaaaggaaag[A/C]agcagagagagagag	4688
rs2296164	snp	C/T	0.499437	0.0167719	intron-variant	NCF2	GRCh38.p7	1:183565800	GGCAACAGGGAGCGA[C/T]GGTCAGAACCTTCAT	4688
rs2296165	snp	C/T	0.0182019	0.0936463	intron-variant	NCF2	GRCh38.p7	1:183586828	CTCAAACACCAAGCC[C/T]GCAACACTGAGACCC	4688
rs2308167	in-del	-/TGTT	0.462187	0.132199	downstream-variant-500B	NCF2	GRCh38.p7	1:183555507	CTCTGTGGAATTGAG[-/TGTT]TGTTGTAGTCCATGA	4688
rs2333681	snp	C/T	0.327211	0.237778	upstream-variant-2KB, intron-variant	NCF2	GRCh38.p7	1:183590726	AGCTTCTGGCCAAAG[C/T]TCTGCTTCTAGAGCC	4688
rs2333682	snp	A/G	0.32768	0.237625	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591626	TAGCTGGGATTACAG[A/G]AGCCTGCCACCACGC	4688
rs2333683	snp	A/G	0.177503	0.239258	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591722	aactcctgacctcag[A/G]tgattcggcctcctc	4688
rs3768582	snp	A/G	0.351418	0.228505	intron-variant	NCF2	GRCh38.p7	1:183584735	ACTCCCCCTTACCCC[A/G]TCTCCAGACTATAGA	4688
rs3768583	snp	A/T	0.49949	0.0159663	intron-variant	NCF2	GRCh38.p7	1:183569590	AAAAAAATTTTTTTT[A/T]AATTAATTTAAAAAT	4688
rs3768584	snp	C/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183567905	TCAGACTTAAGGGAA[C/T]CGACACTGCACCACG	4688
rs3818364	snp	G/T	0.49975	0.0111793	intron-variant	NCF2	GRCh38.p7	1:183573612	CACCACCACGACAAG[G/T]CTGGCCCGGGATCAA	4688
rs3820690	snp	A/G	0.299158	0.245119	intron-variant	NCF2	GRCh38.p7	1:183582027	GGCCTGCAGCAGGGA[A/G]CGAGGGGGCTGGGAA	4688
rs3820691	snp	C/T	0.499741	0.0113788	intron-variant	NCF2	GRCh38.p7	1:183569990	AGGCCATGAGGGGAA[C/T]GCAGCCCAGGTAACT	4688
rs3843292	snp	A/G	0.0314385	0.121371	intron-variant	NCF2	GRCh38.p7	1:183561366	AGAGTCCACAGAGAA[A/G]ggtttgtatcccacc	4688
rs3843293	snp	G/T	0.49934	0.0181589	intron-variant	NCF2	GRCh38.p7	1:183570314	GTTCACTCTCAGTGC[G/T]CTGCCTGTGTTCCCG	4688
rs3845461	snp	A/G	0.126909	0.217598	intron-variant	NCF2	GRCh38.p7	1:183563065	GGGAGGCAGAGCTGT[A/G]ACTTATTACACACCA	4688
rs3845462	snp	G/T	0.49621	0.0433651	intron-variant	NCF2	GRCh38.p7	1:183568339	ACTCAGCTAATTTTT[G/T]CATGTTTAGTAGACA	4688
rs3845463	snp	G/T	0.499477	0.0161657	intron-variant	NCF2	GRCh38.p7	1:183568343	AGCTAATTTTTTCAT[G/T]TTTAGTAGACATGGG	4688
rs3845464	snp	A/C	0.499801	0.00998203	intron-variant	NCF2	GRCh38.p7	1:183572707	TACAGTGGTGCAATC[A/C]TAGCTCACTGTAGCC	4688
rs3845465	snp	C/T	0.499784	0.0103811	intron-variant	NCF2	GRCh38.p7	1:183572731	TGTAGCCTTGAACTC[C/T]TGGGCTCAAGTGATC	4688
rs3845466	snp	A/G	0.325327	0.238382	intron-variant	NCF2	GRCh38.p7	1:183582625	AAGTCAAAACTTCAG[A/G]CATCTTTGGGATGCT	4688
rs3903837	snp	C/T	0.416545	0.186448	intron-variant	NCF2	GRCh38.p7	1:183587485	TGTGGTCCCAGCTAC[C/T]TGGGGGACTGAGGTA	4688
rs3905122	snp	C/T	0.067446	0.170804	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592900	TGCATCTGTGBGACT[C/T]GTGCTAGTTCCTCTT	4688
rs3929721	snp	C/T	0.175897	0.238765	intron-variant	NCF2	GRCh38.p7	1:183579508	gaggcgggtggatca[C/T]gaggtcaggagatcg	4688
rs4652813	snp	C/G	0.178465	0.239547	intron-variant	NCF2	GRCh38.p7	1:183565409	TTCTTCCTGAGACAT[C/G]GTTTCCCTACCTAAT	4688
rs4987079	snp	A/G	0.191775	0.243125	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591061	aggaaagtcccccca[A/G]tgcgggtgagtctgg	4688
rs4987080	snp	A/G	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591057	aagtccccccagtgc[A/G]ggtgagtctggggct	4688
rs6667363	snp	C/T	0.499793	0.0101816	intron-variant	NCF2	GRCh38.p7	1:183571963	cgtagtattctgttg[C/T]atggatatatcacat	4688
rs6668645	snp	A/G	0.0341408	0.126114	intron-variant	NCF2	GRCh38.p7	1:183567126	TCTGCAAAGAAGGCA[A/G]CAGATACTGCTCCAC	4688
rs7520027	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183557025	TTTGTTAAATATAAA[C/T]ATTTTAATAGCTCCT	4688
rs7521394	snp	A/C	0.0391387	0.134304	intron-variant	NCF2	GRCh38.p7	1:183584502	GGTCTTACTTTTAGA[A/C]GTTTCCAAGATCTTT	4688
rs7531724	snp	A/G/T	0.00716266	0.059414	intron-variant	NCF2	GRCh38.p7	1:183580775	tgaggtcaggggttc[A/G/T]agaccagcctggcca	4688
rs9425306	snp	A/G	0.304937	0.243889	intron-variant	NCF2	GRCh38.p7	1:183560519	AGATGAATGGTGGTG[A/G]GTGGTGGGTTGGGGG	4688
rs10689990	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183578356	CCTCCTTTTTTTTTT[-/T]CTTTTTTTTTGAGAC	4688
rs10797887	snp	A/G	0.231482	0.249313	intron-variant	NCF2	GRCh38.p7	1:183575559	CAGAATCAAATAATC[A/G]TTTGGATGCATTACC	4688
rs10797888	snp	C/T	0.14933	0.228835	intron-variant	NCF2	GRCh38.p7	1:183577897	CCTTGGGAATGGTGT[C/T]CCCCCCAGGGCTGTG	4688
rs10911357	snp	G/T	0.499325	0.0183582	intron-variant	NCF2	GRCh38.p7	1:183571641	TTTTAAAAATCAGAT[G/T]TAAAGCTAGCTTTAT	4688
rs10911358	snp	C/T	0.499784	0.0103811	intron-variant	NCF2	GRCh38.p7	1:183571991	cattttgattactca[C/T]tcatcagttgataga	4688
rs10911359	snp	C/T	0.499784	0.0103811	intron-variant	NCF2	GRCh38.p7	1:183573918	AACATGGCAAAACCC[C/T]GTCTCTATTAAAAAT	4688
rs10911360	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576990	TCTCCCTTTTGATAA[C/T]AGAGAAAAGAAGTTG	4688
rs10911361	snp	C/T	0.29046	0.246704	intron-variant	NCF2	GRCh38.p7	1:183579361	TTTGAGTCTTGGCTC[C/T]GTCACTTACTATCTG	4688
rs10911362	snp	A/G	0.295854	0.245759	intron-variant	NCF2	GRCh38.p7	1:183579857	TGCCTGGCACACACC[A/G]TAATTTTTTTACTAT	4688
rs10911363	snp	G/T	0.46845	0.121572	intron-variant	NCF2	GRCh38.p7	1:183580622	GAAGTGACACCACCT[G/T]GGTCTATCTGGCATT	4688
rs10911364	snp	A/G	0.169435	0.236663	intron-variant	NCF2	GRCh38.p7	1:183583391	ACACATTAAGAAGTA[A/G]TTTCTCTAGCCCCCA	4688
rs10911365	snp	A/G	0.323434	0.238972	intron-variant	NCF2	GRCh38.p7	1:183589970	TGCTCTCCACCTGGA[A/G]AGCTTTTAAAACTGG	4688
rs10911366	snp	C/T	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592150	TAGCAACTGAAAGAA[C/T]TCACTCATTATCACC	4688
rs10911367	snp	C/T	0.484632	0.086302	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592382	TGCTAAATCTAGCCC[C/T]GAACTCTGGGTAGTA	4688
rs11287969	in-del	-/A			intron-variant	NCF2	GRCh38.p7	1:183587625	AAAAAAAAAAAAAAA[-/A]TCCAATGATACAAAT	4688
rs11414367	in-del	-/A	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183580979	CAAAAAAAAAAAAAA[-/A]GGTGTCTACAGATTT	4688
rs11540867	snp	C/T			utr-variant-5-prime	NCF2	GRCh38.p7	1:183590341	TCTTGGCCTCCTAGT[C/T]TCTACCTAATCATGT	4688
rs11577618	snp	C/T	0.0622301	0.165053	intron-variant	NCF2	GRCh38.p7	1:183568691	ATTCTAGATTCCTGA[C/T]TCCAGAGAGCTCTGG	4688
rs11578964	snp	C/T	0.416218	0.186739	intron-variant	NCF2	GRCh38.p7	1:183586644	AGCTGAGTATCAGGC[C/T]CATGGTGGTTACCTA	4688
rs11588654	snp	C/T	0.301429	0.244653	intron-variant	NCF2	GRCh38.p7	1:183587260	ATACCATCTGATTTC[C/T]GCTTTTGTTAGTCAT	4688
rs11590384	snp	A/C	0	0	intron-variant	NCF2	GRCh38.p7	1:183587296	GCCTAGAAAAGCTAC[A/C]CAAGAATCCAATAAT	4688
rs11806305	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183561842	tctctctgtcaccca[A/G]actggagtgcagtgg	4688
rs11811630	snp	C/T	0.499203	0.0199521	intron-variant	NCF2	GRCh38.p7	1:183564775	ATTGAGCAGGAGCAA[C/T]GGGAGAAATTTGAAT	4688
rs12022723	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183561905	tgggttcaagcaatt[C/T]tgcctcagcctccca	4688
rs12027051	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587292	TATGGCCTAGAAAAG[C/T]TACACAAGAATCCAA	4688
rs12027057	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587327	TCccaggtgcggttg[C/T]tcacacctgtaatcc	4688
rs12027823	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587481	tgcctgtggtcccag[C/T]tacttgggggactga	4688
rs12036973	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183561913	agcaattctgcctca[A/G]cctcccaagtagctg	4688
rs12045169	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183580833	aatatttaaaaatta[C/G]ccgggcgtggtggtg	4688
rs12046252	snp	A/G	0.302184	0.244493	intron-variant	NCF2	GRCh38.p7	1:183581910	CTTACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC	4688
rs12057355	snp	G/T	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592306	AGGCCTTCCCAGCTC[G/T]CTTCTTTGCCTGGCA	4688
rs12066019	snp	A/C	0.192088	0.2432	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592425	TCTCCTTTGTACCAC[A/C]TTTACCCAAAAACTT	4688
rs12066221	snp	A/C	0.0182019	0.0936463	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592769	TATCCCACCCTGACA[A/C]TCAGAACTCTCCTTA	4688
rs12086606	snp	C/G	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592383	GCTAAATCTAGCCCT[C/G]AACTCTGGGTAGTAG	4688
rs12086699	snp	G/T	0.192088	0.2432	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592590	AATTAGAAATCATTG[G/T]TAAATGACCTGCAGG	4688
rs12091406	snp	A/G	0.192401	0.243274	upstream-variant-2KB, intron-variant	NCF2	GRCh38.p7	1:183590706	TCCCACCCCTGTTCT[A/G]TGGCAGCTTCTGGCC	4688
rs12091848	snp	C/T	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592389	TCTAGCCCTGAACTC[C/T]GGGTAGTAGGAGAAT	4688
rs12094036	snp	C/T	0.324145	0.238752	intron-variant	NCF2	GRCh38.p7	1:183589039	GTGGGGCCATGTCCT[C/T]CCTCCAGCCAGAGGT	4688
rs12094228	snp	G/T	0.287346	0.247195	intron-variant	NCF2	GRCh38.p7	1:183578737	AGCTGACTGGCTCGA[G/T]GTATACCAGGGCTGC	4688
rs12095261	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183571081	AAAAGAAATGttttt[A/T]attgaggtgcaattt	4688
rs12095618	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183579568	catctctactaaaaa[A/T]aaaaaaataaaaaaa	4688
rs12096702	snp	A/G	0.192088	0.2432	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592562	ACATGATGAAGGGAT[A/G]CATTCTAAAAGAAAT	4688
rs12119260	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183581315	aagaaagaaaGAAAG[A/G]AAAGAAAGTCCAACA	4688
rs12122217	snp	C/T	0.482309	0.0923707	intron-variant	NCF2	GRCh38.p7	1:183576530	CCACGATGCGCAGGA[C/T]GCACCACAACCCCTC	4688

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