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
rs800977	snp	C/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74781492	ataataataataata[C/T]ctaacattaatggag	653361
rs800978	snp	A/G	0.23031	0.249223	intron-variant	NCF1	GRCh38.p7	7:74781743	tcactacattgccca[A/G]gctggtcttaaactc	653361
rs800979	snp	A/G	0.466412	0.125164	intron-variant	NCF1	GRCh38.p7	7:74781755	ccaagctggtcttaa[A/G]ctcttggcctcaagc	653361
rs800980	snp	C/T	0.161267	0.233723	intron-variant	NCF1	GRCh38.p7	7:74781899	ctgacctcattttaa[C/T]ttaattacctcttga	653361
rs800981	snp	C/T	0.214239	0.247429	intron-variant	NCF1	GRCh38.p7	7:74782019	gatgtcagccaataC[C/T]Aaacagcatcagcac	653361
rs997440	snp	A/G	0.5	0	intron-variant	NCF1	GRCh38.p7	7:74786460	ttgctctgactccca[A/G]gctggagcacaatca	653361
rs1637415	snp	C/T	0.0654984	0.168698	intron-variant	NCF1	GRCh38.p7	7:74775890	aggtgcgcgccacca[C/T]gcccagctcgcattt	653361
rs2465932	snp	G/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74785746	acatgagccgggtgt[G/T]gtggtgggagcctgt	653361
rs2472047	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74785652	ctttgggagcccagg[A/G]caggacgatcacgtg	653361
rs2472048	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74785664	agggcaggacgatca[C/T]gtgaggtcaggagtt	653361
rs2523327	snp	C/T	0.142012	0.225474	intron-variant	NCF1	GRCh38.p7	7:74781945	acctttctcttaata[C/T]acccacactgtaagg	653361
rs2523332	snp	A/T	0.276443	0.248598	intron-variant	NCF1	GRCh38.p7	7:74783255	TGTGGGCATCTGTGC[A/T]TGGCAGGCCGGGGCG	653361
rs2523333	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74784449	tgagacaaagtctgg[C/T]tctgtcacccaggct	653361
rs2523335	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74787450	tgtctTGGGGTTGGG[C/T]GGGGGAAAAGCATTT	653361
rs2528941	snp	A/G	0.435837	0.167226	intron-variant	NCF1	GRCh38.p7	7:74783387	GTGACCTCATTGTCC[A/G]GTGTGGTGAAGGTGA	653361
rs2529296	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74777234	GCCTCTTTGGAGGCT[A/G]AATGGGGTCCCCCGA	653361
rs2529297	snp	A/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74782015	ggcggatgtcagccA[A/T]TACTAaacagcatca	653361
rs2539044	snp	C/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74788173	TGAGAGCCCCCGCCC[C/T]GGCACTGCCAAGCTA	653361
rs2718280	snp	C/T	0.395087	0.203592	downstream-variant-500B	NCF1	GRCh38.p7	7:74789738	GAGGATCCGTTGAGC[C/T]CAGGAGTTCGAGACC	653361
rs2737400	snp	A/C			intron-variant	NCF1	GRCh38.p7	7:74782581	agaccttgtctttac[A/C]agaaattagccgggt	653361
rs2737401	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74782583	accttgtctttacca[A/G]aaattagccgggtgt	653361
rs2906281	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74776039	GCATCCTCCGCCTCC[C/T]AGGTTCAAGCAATTC	653361
rs2953669	snp	G/T			intron-variant	NCF1	GRCh38.p7	7:74775973	tttttatgagatgga[G/T]tcttactctgtcacc	653361
rs2953670	snp	G/T			intron-variant	NCF1	GRCh38.p7	7:74775998	gtcacccaggctgga[G/T]tgcaatggcacaatc	653361
rs17356100	snp	A/G	0.00137622	0.0261957	synonymous-codon	NCF1	GRCh38.p7	7:74779372	CACCTTGAAGAAGTC[A/G]AGGAGGTGGGGACAG	653361
rs28668454	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74782204	AGCACTTTGGGAGGC[C/T]GAGGCGGTTGAATCA	653361
rs35067650	snp	C/T	0.1638	0.234669	intron-variant	NCF1	GRCh38.p7	7:74785057	GAAGAGGGGGAACTG[C/T]GGGCCCTGGGTGGGT	653361
rs60312903	in-del	-/A			intron-variant	NCF1	GRCh38.p7	7:74786255	AAAAAAAAAAAAAAA[-/A]GCTTCCATTGCAATT	653361
rs62475422	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74778615	TGCTGGTGACTTGCA[C/T]ATGGGAGGGAGAGAG	653361
rs62475427	snp	C/G			utr-variant-3-prime	NCF1	GRCh38.p7	7:74789202	TCTCGGCCCTTGCCG[C/G]CCCGTGCCTGTACAT	653361
rs75207809	snp	A/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74775961	AGTCTTTTTTTTTTT[A/T]TATGAGATGGAGTCT	653361
rs77875067	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	NCF1	GRCh38.p7	7:74789533	AGAAACCACCTGCTT[A/G]GACTCTGGCGGAAGA	653361
rs78031146	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74779032	GTGATTTTCCAAGTG[C/T]TGTAAACTACAAATA	653361
rs111979289	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772242	CAGGAGATCAGGTCC[A/G]GACCATGAGCTGACC	653361
rs112000369	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74783077	GTCAGACCTCCCACC[C/T]TACGGGGCTCCTTCC	653361
rs112894340	snp	G/T			intron-variant	NCF1	GRCh38.p7	7:74777495	TTTATTTATATAAAT[G/T]TTTGTGACAGGGTCT	653361
rs113297930	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74775965	TTTTTTTTTTTTTAT[A/G]AGATGGAGTCTTACT	653361
rs113623758	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74787032	AGATGGATTTCCATA[C/T]TGGAAAAAAAAAAAA	653361
rs119103270	snp	A/G			missense	NCF1	GRCh38.p7	7:74777319	AGAAGGTGGTCTACC[A/G]GCGCTTCACCGAGAT	653361
rs119103271	snp	C/T			stop-gained	NCF1	GRCh38.p7	7:74779298	GCCGCCGAGAACCGC[C/T]AGGGCACACTTACCG	653361
rs119103272	snp	A/T	3.56831e-05	0.00422377	NCF1	7	allele_origin=T(germline)/A(germline)	7:74779360	CAAGATCTCCCGCTG[A/T]CCCCACCTCCTCGAC	653361
rs119103273	snp	A/G	6.84521e-05	0.0058499	NCF1	7	allele_origin=G(germline)/A(germline)	7:74783061	GAGAAGAGCGAGAGC[A/G]GTCAGACCTCCCACC	653361
rs138054188	snp	C/T	0.0532157	0.154195	intron-variant	NCF1	GRCh38.p7	7:74775882	GGGAATACAGGTGCG[C/T]GCCACCATGCCCAGC	653361
rs138406096	snp	A/G	0.0185938	0.0946107	intron-variant	NCF1	GRCh38.p7	7:74785612	TCCTAGCTAGGCGCA[A/G]TGGCTCAGGCCTGTA	653361
rs139225348	snp	A/G	0.0179533	0.0930287	missense	NCF1	GRCh38.p7	7:74779274	CCCAAGTGGTTTGAC[A/G]GGCAGCGGGCCGCCG	653361
rs140034807	snp	A/G	0.0379877	0.132479	intron-variant	NCF1	GRCh38.p7	7:74775881	TGGGAATACAGGTGC[A/G]CGCCACCATGCCCAG	653361
rs140463577	snp	C/T	0.000408956	0.0142937	synonymous-codon	NCF1	GRCh38.p7	7:74783060	AGAGAAGAGCGAGAG[C/T]GGTCAGACCTCCCAC	653361
rs140969778	snp	A/G	0.00358779	0.0422022	intron-variant	NCF1	GRCh38.p7	7:74781714	ATTTTTAATTTTCTG[A/G]TAGAGATGGGGTCTC	653361
rs141286916	snp	A/C			intron-variant	NCF1	GRCh38.p7	7:74787053	AAAAAAAAAAAAGAG[A/C]AAAAAACAAACCTAG	653361
rs141305543	snp	A/G			upstream-variant-2KB	NCF1	GRCh38.p7	7:74773052	AAAAAAAAAAAATTA[A/G]CCAGGTGTGGTGGCA	653361
rs142050799	snp	C/T	0.00398564	0.0444627	intron-variant	NCF1	GRCh38.p7	7:74777567	AGGCATGAGCCCCCA[C/T]GCTCGGCCTTTTAGG	653361
rs142480486	snp	A/G	0.000340248	0.0130387	missense	NCF1	GRCh38.p7	7:74782989	GCCATTGCCAACTAC[A/G]AGAAGACCTCGGGCT	653361
rs144018361	snp	G/T	0.00145853	0.0269655	missense	NCF1	GRCh38.p7	7:74779319	ACACTTACCGAGTAC[G/T]GCGGCACGCTCATGA	653361
rs144372615	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74775883	GGAATACAGGTGCGC[A/G]CCACCATGCCCAGCT	653361
rs145360423	snp	A/G	0.00129198	0.0253835	stop-gained	NCF1	GRCh38.p7	7:74783529	CTCTGGCACAGGTTG[A/G]TGGTTCTGTCAGATG	653361
rs146125534	snp	C/T	0.00887071	0.0660051	missense	NCF1	GRCh38.p7	7:74779326	CCGAGTACTGCGGCA[C/T]GCTCATGAGCCTGCC	653361
rs146173318	snp	A/G	0.000524761	0.0161897	synonymous-codon	NCF1	GRCh38.p7	7:74777302	ATGGCAGGACCTGTC[A/G]GAGAAGGTGGTCTAC	653361
rs147659773	snp	C/T	8.5139e-05	0.00652397	missense	NCF1	GRCh38.p7	7:74783606	ACAGTCCTGACGAGA[C/T]GGAAGACCCTGAGCC	653361
rs148767467	snp	C/T	9.10258e-05	0.00674571	missense	NCF1	GRCh38.p7	7:74779355	CCCACCAAGATCTCC[C/T]GCTGTCCCCACCTCC	653361
rs149204001	snp	A/G			missense	NCF1	GRCh38.p7	7:74783602	CTGGACAGTCCTGAC[A/G]AGACGGAAGACCCTG	653361
rs151319713	snp	A/G	6.69299e-05	0.0057845	synonymous-codon	NCF1	GRCh38.p7	7:74783051	GGAGGTCGTAGAGAA[A/G]AGCGAGAGCGGTCAG	653361
rs181692881	snp	A/G	0.00159617	0.0282053	intron-variant	NCF1	GRCh38.p7	7:74782011	AGAAGGCGGATGTCA[A/G]CCAATACCAAACAGC	653361
rs181788842	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74781963	CCACACTGTAAGGTA[C/T]TGGGTGGTTAGGACT	653361
rs182413790	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74785865	TCCAGCCTGGGCAAC[A/G]AGAGCGAAACTCCGT	653361
rs183580334	snp	C/G			intron-variant	NCF1	GRCh38.p7	7:74777569	GCATGAGCCCCCACG[C/G]TCGGCCTTTTAGGTG	653361
rs185170050	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74787238	ATGTCAGGAGTTTGA[A/G]ACCAGCCATGACCAA	653361
rs185872833	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74782002	TGAATTTTGAGAAGG[C/T]GGATGTCAGCCAATA	653361
rs190079672	snp	A/G	0.00279162	0.0372561	intron-variant	NCF1	GRCh38.p7	7:74782003	GAATTTTGAGAAGGC[A/G]GATGTCAGCCAATAC	653361
rs199789198	snp	A/C	0.0154538	0.0865337	intron-variant	NCF1	GRCh38.p7	7:74781840	GCCCGGCTTTTTCTT[A/C]TTCTTATAAGGACAC	653361
rs199886863	snp	G/T	0.00106549	0.0230566	intron-variant	NCF1	GRCh38.p7	7:74777359	CCATGTGAGTGTGGG[G/T]ACGGAGGAGGGACAG	653361
rs199908473	snp	G/T			intron-variant	NCF1	GRCh38.p7	7:74784586	CACGCCAGGCTAATT[G/T]TTTGTATTTTTAGTA	653361
rs199938434	snp	C/T	6.90286e-05	0.00587448	synonymous-codon	NCF1	GRCh38.p7	7:74779285	TGACGGGCAGCGGGC[C/T]GCCGAGAACCGCCAG	653361
rs200050981	snp	C/G			intron-variant	NCF1	GRCh38.p7	7:74778391	CCTCCCAAATTGCTA[C/G]GATTACAGGTTTGAG	653361
rs200205449	snp	A/G	0.499977	0.00339449	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773424	TGATCCCACCACTGC[A/G]CTTAAGCCTGGATAA	653361
rs200459715	snp	G/T	0.00123077	0.0247764	intron-variant	NCF1	GRCh38.p7	7:74782896	CTGGAGGCCCAGATG[G/T]GCCCTGCAATGCCCA	653361
rs200623471	snp	A/G	0.22263	0.248497	intron-variant	NCF1	GRCh38.p7	7:74778736	atggagtgcagtggc[A/G]ccatctcggctcact	653361
rs200655630	in-del	-/A	0.49263	0.0602539	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773035	ACCCAGTCTCTAATT[-/A]AAAAAAAAAAAAATT	653361
rs200663210	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74777247	CTGAATGGGGTCCCC[C/T]GACTCTGGCTTTCCC	653361
rs201522178	snp	A/G	0.000497934	0.0157708	missense	NCF1	GRCh38.p7	7:74782972	TCCTGCAGACGTACC[A/G]CGCCATTGCCAACTA	653361
rs201586849	snp	A/T			intron-variant	NCF1	GRCh38.p7	7:74775963	TCTTTTTTTTTTTTT[A/T]TGAGATGGAGTCTTA	653361
rs201802880	snp	A/G	0.00208105	0.03219	missense	NCF1	GRCh38.p7	7:74779296	GGGCCGCCGAGAACC[A/G]CCAGGGCACACTTAC	653361
rs201978343	snp	C/T			downstream-variant-500B	NCF1	GRCh38.p7	7:74789697	GGCTCACGCCTGTAA[C/T]CCAGCACTTTGGGAG	653361
rs202195500	snp	C/T	0.000187606	0.00968337	missense	NCF1	GRCh38.p7	7:74782981	CGTACCGCGCCATTG[C/T]CAACTACGAGAAGAC	653361
rs273585651	in-del	-/GT			frameshift-variant	NCF1	GRCh38.p7	7:74777269	GGCTTTCCCCCAGGT[-/GT]ACATGTTCCTGGTGA	653361
rs367985113	snp	A/G	0.000627254	0.0176984	missense	NCF1	GRCh38.p7	7:74782974	CTGCAGACGTACCGC[A/G]CCATTGCCAACTACG	653361
rs368254704	snp	A/G	0.000137872	0.00830161	intron-variant	NCF1	GRCh38.p7	7:74777248	TGAATGGGGTCCCCC[A/G]ACTCTGGCTTTCCCC	653361
rs368358726	snp	C/T			upstream-variant-2KB	NCF1	GRCh38.p7	7:74772150	CTTGGGCAACAAGAG[C/T]GAAACTTCGCTTCAA	653361
rs368662637	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74781827	CATGAGCCACTGTGC[C/T]CGGCTTTTTCTTCTT	653361
rs368945669	snp	C/G	3.35272e-05	0.0040942	synonymous-codon	NCF1	GRCh38.p7	7:74783018	CTCCGAGATGGCTCT[C/G]TCCACGGGGGACGTG	653361
rs368948045	snp	A/T	0.000153988	0.00877328	missense	NCF1	GRCh38.p7	7:74777337	GCTTCACCGAGATCT[A/T]CGAGTTCCATGTGAG	653361
rs369249526	snp	C/T	0.000153988	0.00877328	synonymous-codon	NCF1	GRCh38.p7	7:74783042	GGACGTGGTGGAGGT[C/T]GTAGAGAAGAGCGAG	653361
rs369461764	snp	A/G	0.00660348	0.0570801	intron-variant	NCF1	GRCh38.p7	7:74779228	CTCCCAGCCCCTCTC[A/G]GGCTTGACCTCATGT	653361
rs369485834	snp	A/G	0.208474	0.246527	intron-variant	NCF1	GRCh38.p7	7:74784878	ACCTTCATCGTTATG[A/G]GATCTCTGGTCCCCA	653361
rs370513174	snp	A/C/T	0.000397452	0.0140914	intron-variant	NCF1	GRCh38.p7	7:74779428	CGGACAACCAGTGAG[A/C/T]GAACTTTTCACCCTG	653361
rs371061025	snp	C/G			intron-variant	NCF1	GRCh38.p7	7:74781786	AACCCTCCTGCCTCA[C/G]CCTCCCAAAGTGCTG	653361
rs371075194	snp	A/G	6.55645e-05	0.0057252	synonymous-codon	NCF1	GRCh38.p7	7:74779327	CGAGTACTGCGGCAC[A/G]CTCATGAGCCTGCCC	653361
rs371241620	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74785449	TCAGTAGCAGGGAGG[A/G]ATGAGCCCACCCTTG	653361
rs372176579	snp	A/G	1.6588e-05	0.00287988	missense	NCF1	GRCh38.p7	7:74783037	ACGGGGGACGTGGTG[A/G]AGGTCGTAGAGAAGA	653361
rs372181124	snp	C/T	0.00358779	0.0422022	intron-variant	NCF1	GRCh38.p7	7:74784210	CTGGGATTACAAGCA[C/T]GCACCACCATGCCTG	653361
rs372741570	snp	A/G	0.000153988	0.00877328	missense	NCF1	GRCh38.p7	7:74783569	CGAGGCTGGATCCCA[A/G]CGTCCTTCCTCGAGC	653361

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