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
rs1858	snp	C/T	0.027999	0.114959	synonymous-codon, utr-variant-3-prime	NCF4	GRCh38.p7	22:36877763	CCAGAAGCGCCTCTT[C/T]CCCTGGAAGCTGCAC	4689
rs729749	snp	C/T	0.437118	0.165792	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36867804	AGGTACCCACTGTCC[C/T]ATGGGAATGCCAACA	4689
rs738148	snp	A/G	0.497776	0.0332724	intron-variant	NCF4	GRCh38.p7	22:36874460	TGGTTTAGCCAGTTT[A/G]GCAGTTTCCATTTTA	4689
rs741997	snp	A/G	0.202651	0.245475	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36862771	CAGCGGGGACTTTCT[A/G]GAACCCCAAGGTGAG	4689
rs741998	snp	A/G	0.271972	0.249033	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36862802	ACATCCAAAGATGGG[A/G]AGGGCTGCCTTAGGG	4689
rs741999	snp	A/G	0.480931	0.0957637	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36863231	GAGGGCAAGGACTCT[A/G]CTCACCCTACATCCC	4689
rs746713	snp	A/G	0.441158	0.161117	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36863317	CTGTAAAATGGGGAC[A/G]GGAGAAGTACTTATG	4689
rs746934	snp	C/T			intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36862621	GAGGGGGAGGGACTG[C/T]TTTTCATGAGGCCTT	4689
rs760517	snp	C/T	0.461923	0.132621	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36862944	GGCAGGCTCCAAAAC[C/T]TCCCCCAGGCCAGGC	4689
rs760518	snp	C/T	0.317114	0.240823	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36863563	TCACGTTCCACCTCC[C/T]GCTCTGTGCTCCAGC	4689
rs760519	snp	C/T	0.299158	0.245119	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36867664	TAGGAGCAGGAGCAA[C/T]GGAGAAGGTAAAAGA	4689
rs909483	snp	A/G	0.211212	0.246973	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36864432	CAGCATAATACTAAG[A/G]TTGAGAAATCCTGAT	4689
rs909484	snp	A/G	0.245916	0.249967	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36864559	GAGGGGGCATCCTGC[A/G]CCCACAGCACAGCCA	4689
rs909485	snp	A/G	0.211212	0.246973	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36864635	ATTTCTTGGGCCTGA[A/G]TGTGTGTTTGGCCTA	4689
rs1003500	snp	C/T	0.0448719	0.142907	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36866727	GTTCCACCAGTGCGC[C/T]CACATGAAGGCACCT	4689
rs1003501	snp	C/T	0.0663309	0.169604	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36866900	ttggtggtatgtgga[C/T]gtgccttgagagatg	4689
rs1883112	snp	A/G	0.485187	0.0847778	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36860804	CAAGACACCCTGATG[A/G]CTGGGACCCCATCTC	4689
rs2056912	snp	C/G	0.279991	0.248195	downstream-variant-500B	NCF4	GRCh38.p7	22:36878352	TGCTGCTCTGTGGAG[C/G]AGGAAGGCAGGTCTC	4689
rs2072706	snp	A/G	0.469544	0.119585	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36870937	GTGTGTTGGAGCTCC[A/G]TGGGGCCAGCTATGG	4689
rs2072708	snp	A/G	0.41732	0.185753	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36871725	GTAACCCCCGCCCCC[A/G]CGCTGGCCAGGCTCT	4689
rs2072709	snp	A/C	0.417034	0.18601	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36871901	CAGCTAAGGGGAGGG[A/C]ATGTGACCAGCGTGC	4689
rs2072710	snp	A/G	0.403876	0.197034	intron-variant	NCF4	GRCh38.p7	22:36872459	ATGGAGGTGAGATTG[A/G]AGGTGAGGTTGGAGG	4689
rs2072711	snp	A/G	0.284209	0.247648	intron-variant	NCF4	GRCh38.p7	22:36872513	TGAGGGTGGAAGTGC[A/G]ATTGGAGGTGAGGAT	4689
rs2072712	snp	C/T	0.169196	0.236586	synonymous-codon	NCF4	GRCh38.p7	22:36875760	GCGTTGCTACTACTA[C/T]GAAGACACCATCAGC	4689
rs2075938	snp	A/G	0.470715	0.117409	intron-variant, nc-transcript-variant	NCF4, LOC107985578	GRCh38.p7	22:36870280	TCTTTTAAACAACGC[A/G]TTTCTGTTATCAGGC	4689
rs2075939	snp	C/T	0.277246	0.248511	intron-variant, missense	NCF4	GRCh38.p7	22:36875840	CATCCCTACGACCAC[C/T]GCCCCTCACATCACC	4689
rs2092031	snp	A/G	0.211212	0.246973	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36864771	GGCGCCAGCCTTTTG[A/G]CTTGACAGGGGTCTC	4689
rs2284027	snp	C/G	0.462582	0.131564	intron-variant, downstream-variant-500B	NCF4, LOC107985578	GRCh38.p7	22:36869037	GGAACTGCGTGAAGA[C/G]CTTTGACTGGCAACC	4689
rs2284028	snp	A/C	0.20111	0.245173	intron-variant, downstream-variant-500B	NCF4, LOC107985578	GRCh38.p7	22:36869130	TGTGAGTTAAGTGTG[A/C]CAGAGCAGTTAGGTA	4689
rs2284029	snp	C/T	0.225005	0.248747	intron-variant, downstream-variant-500B	NCF4, LOC107985578	GRCh38.p7	22:36869344	CCACGAGGGAGAGGC[C/T]ATTATTGTCCCCATT	4689
rs2413426	snp	A/G	0.352287	0.228117	intron-variant, utr-variant-5-prime	NCF4, LOC107985578	GRCh38.p7	22:36861813	CTGCTGTATCACTAG[A/G]AGGTAGCTCATCCCT	4689
rs3221695	microsatellite	(CA)16/17/18/19/20/21	0.754826	0.141247	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36867112	CTGTTCATCCAAGCG[(CA)16/17/18/19/20/21]CGACTCTTAGTTCTA	4689
rs3788523	snp	C/T	0.498034	0.0312882	intron-variant	NCF4	GRCh38.p7	22:36873465	GTATGCTTCAGAGAC[C/T]GAGGATGGTCTCAGA	4689
rs3788524	snp	C/T	0.285519	0.247464	intron-variant	NCF4	GRCh38.p7	22:36873514	GCTATCTGAGGATAG[C/T]CCTGGAGATCCAGGC	4689
rs3827352	snp	A/G	0.466927	0.124269	intron-variant	NCF4	GRCh38.p7	22:36873136	GGTGAGATTGGAGGT[A/G]AGATTAGAGGTGAAG	4689
rs4820258	snp	C/T	0.343477	0.231866	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36859811	ATGCTTTCTTGTTTT[C/T]TTTAGCTGGGACTTG	4689
rs4820259	snp	C/T	0.451732	0.147663	intron-variant	NCF4	GRCh38.p7	22:36874083	GGAGGTGGTAGATGG[C/T]CAGGGCTCGCCCCAG	4689
rs4821544	snp	C/T	0.456685	0.140646	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36862461	GCACGCAAACTCGAA[C/T]CTTCCGGAAGCAGCA	4689
rs4821546	snp	A/G	0.467439	0.123371	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36872037	GACAAGGCCCAGCCC[A/G]CGATGAAGCCTGGGG	4689
rs4821547	snp	C/G	0.134119	0.221521	intron-variant	NCF4	GRCh38.p7	22:36873716	GCACTATTGACATTG[C/G]GGCCAGATGGTCCCT	4689
rs4821548	snp	A/G	0.285519	0.247464	intron-variant	NCF4	GRCh38.p7	22:36873903	GTACATACCTTGCCC[A/G]CAGCAGTAAAAGCTG	4689
rs4821549	snp	A/G	0.13446	0.221699	intron-variant	NCF4	GRCh38.p7	22:36874048	AAATGTTTCTTCATC[A/G]GCTTCCTGGAAAGGG	4689
rs4821550	snp	A/G	0.451483	0.148002	intron-variant	NCF4	GRCh38.p7	22:36874106	CGCCCCAGAGCCTGG[A/G]TGTGCGGCGCCTGGC	4689
rs4821551	snp	G/T	0.230896	0.249269	intron-variant	NCF4	GRCh38.p7	22:36874401	TTAAGAGTTGGGTTG[G/T]GTCCCTAGCGTCCAG	4689
rs4821552	snp	A/C	0.430136	0.173352	intron-variant	NCF4	GRCh38.p7	22:36875389	CTGGTTCTCAAGAAG[A/C]CTTTGTTGAATGAAT	4689
rs4821553	snp	A/G	0.0543475	0.155628	intron-variant	NCF4	GRCh38.p7	22:36875456	AATCCAGATTCTGGC[A/G]TATTGTAAAACCCAA	4689
rs5756374	snp	C/T	0.431405	0.172023	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36872215	AGTCGCTTATTCTCC[C/T]CAAGCCTCAGTTTCT	4689
rs5756375	snp	A/T	0.00398564	0.0444627	intron-variant	NCF4	GRCh38.p7	22:36873591	CGGTGGCAGCAGAAC[A/T]TTCTTGGAGCTCATG	4689
rs5756376	snp	C/G	0.362523	0.223246	intron-variant	NCF4	GRCh38.p7	22:36874971	CACAGCGCGCACAGC[C/G]TGTCATTCCCCATCA	4689
rs5995360	snp	G/T	0.265727	0.249505	intron-variant	NCF4	GRCh38.p7	22:36877138	GAAAGTCTCTTCTCC[G/T]TCTCCtttttttttt	4689
rs5995361	snp	A/C/T	0.000313893	0.0125243	missense, utr-variant-3-prime	NCF4	GRCh38.p7	22:36877714	CGGATGAGGACGTAG[A/C/T]GCTCATGGTGCGGCA	4689
rs6000454	snp	C/G	0.0168391	0.0901998	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36870562	GTGACCAGCCCCTGG[C/G]CTTCCACATGGCCAG	4689
rs6000455	snp	A/C/G	0.0552829	0.156821	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36871727	AACCCCCGCCCCCAC[A/C/G]CTGGCCAGGCTCTCA	4689
rs6000456	snp	A/G	0.143284	0.226079	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36871881	CACTGGGGGTCCCCC[A/G]AGCCCAGCTAAGGGG	4689
rs6000460	snp	A/G	0.493703	0.0557558	intron-variant	NCF4	GRCh38.p7	22:36875265	GAACTACTGATCTCA[A/G]GTGATTCACCAGCTT	4689
rs6000461	snp	A/G	0.0143261	0.0834135	intron-variant	NCF4	GRCh38.p7	22:36876144	ACTCTGGAGAAGAGA[A/G]CGCAGGGAGAAATGT	4689
rs6000462	snp	A/G	0.305186	0.243833	downstream-variant-500B	NCF4	GRCh38.p7	22:36878305	TCGGCTGTGTGATGA[A/G]GGTCAGAAGCTCTCC	4689
rs7288939	snp	A/G	0.00676609	0.0577691	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36866489	GGGATCCTCTGAGCA[A/G]ACATCCTCTCTCCCC	4689
rs7289110	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36859505	CTGGTACACACGTCC[C/T]TTGTTCCACCCATGG	4689
rs8137456	snp	C/G	0.235564	0.249583	downstream-variant-500B	NCF4	GRCh38.p7	22:36878401	TGTAAGTAGACACAG[C/G]GGGAGGACTCTAGTC	4689
rs9607387	snp	C/T	0.494143	0.0537956	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36859500	CTGATCTGGTACACA[C/T]GTCCCTTGTTCCACC	4689
rs9607388	snp	G/T	0.110519	0.207473	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36860309	AGCATAGGCCTTGGG[G/T]CGGACGTCTTAGAAC	4689
rs9610594	snp	A/T	0.0119091	0.0762411	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36860350	cggaaaggaggccag[A/T]gAGAAAAAGGGAGCT	4689
rs9610595	snp	A/G			missense, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36870425	CACAGAGCCTGCTCA[A/G]CCTGCCGGTCTGGGT	4689
rs9610596	snp	A/G	0.00159617	0.0282053	intron-variant	NCF4	GRCh38.p7	22:36873906	CATACCTTGCCCACA[A/G]CAGTAAAAGCTGCtg	4689
rs9619637	snp	C/G	0.241914	0.249869	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36862609	CCTTAGCCCTCAGAG[C/G]GGGAGGGACTGCTTT	4689
rs9619638	snp	C/T			intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36868216	CTGGCAAGCGAAGCC[C/T]TCCTCCCAGCCCAGC	4689
rs9941970	snp	A/G	0.303938	0.244112	intron-variant	NCF4	GRCh38.p7	22:36877414	AATGCTGGAATTATA[A/G]GCGTGAGCCACCGCA	4689
rs10622881	in-del	-/TCTT	0.204803	0.245881	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36859193	CACTAATAACCCTGC[-/TCTT]CTCTGTGTTTCATTT	4689
rs10656921	in-del	-/TTCT	0.193762	0.243592	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36859196	TAATAACCCTGCTCT[-/TTCT]GTGTTTCATTTCATC	4689
rs10671614	in-del	-/TG/TGTG/TGTGTG/TGTGTGCG	0.625	0.125	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36867143	GTGTGTGTGTGTGTG[-/TG/TGTG/TGTGTG/TGTGTGCG]CGCTTGGATGAACAG	4689
rs10854694	snp	A/G	0.481856	0.0935034	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36860434	AGGGCAAGGACTCTG[A/G]ACTTTATCCTGAGCA	4689
rs10854695	snp	A/G	0.0763428	0.179842	synonymous-codon, utr-variant-5-prime, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36864081	TGATGTTGCCATCTC[A/G]GCCAACATTGCTGAC	4689
rs11089806	snp	A/G	0.485255	0.0845871	upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36860220	GTCAGGGAAGGCCTC[A/G]CTAAAGATGTAGCTT	4689
rs11552115	snp	A/G	0.170482	0.237016	synonymous-codon, utr-variant-3-prime	NCF4	GRCh38.p7	22:36877700	GGTTCGGCTGCTGTC[A/G]GATGAGGACGTAGCG	4689
rs11703711	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36861025	TGGAGAGAAGCAGGC[C/T]TGAGCCTCCCCAAAG	4689
rs11912791	snp	C/T	0.32885	0.23724	intron-variant, utr-variant-5-prime	NCF4, LOC107985578	GRCh38.p7	22:36861780	GCAAGCTCCACGAGG[C/T]TGTGTCCGTTTTGAT	4689
rs12158689	snp	A/G	0.0970103	0.197722	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36870076	AGATGGAGCAAGGGC[A/G]CGCATGTGATACCCA	4689
rs12158690	snp	A/G	0.0437281	0.141251	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36870078	ATGGAGCAAGGGCGC[A/G]CATGTGATACCCACC	4689
rs12159790	snp	C/T	0.0437281	0.141251	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36871385	gcaagtgaaaggcac[C/T]gaatgagcgTGTATC	4689
rs12160812	snp	A/G	0.0437281	0.141251	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36871917	ATGTGACCAGCGTGC[A/G]GAGCCAGAGGAGAAT	4689
rs12483961	snp	A/G			downstream-variant-500B	NCF4	GRCh38.p7	22:36878162	TCCCTGTGTTGGGGG[A/G]AAACCCGAGGGTCCC	4689
rs12485228	snp	C/T			intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36865782	CAAGCCTCAGGGACC[C/T]TTCCCCAAGCTCCAA	4689
rs13054824	snp	A/G	0.0944967	0.195752	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36868404	GTTGGGATCTGTCGA[A/G]AACAGGATGAGAAAG	4689
rs13057803	snp	A/C/T	1.64762e-05	0.00287016	missense, utr-variant-5-prime, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36864098	CCAACATTGCTGACA[A/C/T]CGAGGAGAAGAGAGG	4689
rs16997451	snp	G/T	0.0562307	0.157967	intron-variant	NCF4	GRCh38.p7	22:36877070	CTTCACAACTCTTAA[G/T]CCTTTAGCACATTTA	4689
rs17811059	snp	A/G	0.115438	0.210697	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36868788	GCCTCTTTGTGTCCA[A/G]TTGGGTTCCTGGAAG	4689
rs28363915	snp	A/T			upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36859731	TTTTCCCATGGGCTG[A/T]TGGCCACGTTCCTCT	4689
rs28445840	snp	A/G	0.000297039	0.0121832	splice-acceptor-variant, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36864918	CCTCTGTCCTCCTTA[A/G]GTTTTCGTCATCGAG	4689
rs28485904	snp	C/T	0.0433465	0.140692	intron-variant, nc-transcript-variant	NCF4, LOC107985578	GRCh38.p7	22:36870342	GTCAGGGCTCGGGGA[C/T]GGGACATCTAGGCTG	4689
rs28669668	snp	A/G	0.0166499	0.0897091	synonymous-codon, utr-variant-3-prime	NCF4	GRCh38.p7	22:36877814	CAGGGTCTACAACAC[A/G]ATGCCATGAGCTGAC	4689
rs28759151	snp	C/T			intron-variant, nc-transcript-variant	NCF4, LOC107985578	GRCh38.p7	22:36869420	TGGTGACAGGCAGAG[C/T]TGGGATTCGATCCCA	4689
rs33918925	in-del	-/TCTT			upstream-variant-2KB, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36859194	ACTAATAACCCTGCT[-/TCTT]CTGTGTTTCATTTCA	4689
rs34018301	snp	G/T	0.00318978	0.0398085	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36864262	AGTGGTTCTCAACAG[G/T]ACCGATTTTGCCCAT	4689
rs34023794	snp	A/C	0.0829062	0.185956	intron-variant, upstream-variant-2KB	NCF4, LOC107985578	GRCh38.p7	22:36871120	GAGCTCCTGAGCTCC[A/C]CACCAGCTCCTCCCT	4689
rs34028655	snp	C/T	0.000798403	0.0199641	intron-variant	NCF4	GRCh38.p7	22:36873769	CAGGCTGTTCAGCAA[C/T]ATCCCTGGCCTCTCC	4689
rs34029541	snp	A/G	0.00428649	0.0460963	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36867491	TTGCCACCTTGGCAC[A/G]TGGAAGGGCATGCAG	4689
rs34072404	snp	C/T	8.25157e-05	0.0064227	synonymous-codon, utr-variant-5-prime, intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36867426	GAAACAGGAGATCGC[C/T]GAGATGCGGATACCT	4689
rs34121963	snp	C/T	0.0103295	0.0711199	intron-variant	NCF4, LOC107985578	GRCh38.p7	22:36864847	CTCCTCCTCCTCCCC[C/T]TTTCCCTTCCACCTC	4689
rs34123598	in-del	-/ATCT	0.442055	0.160046	intron-variant	NCF4	GRCh38.p7	22:36873502	CAGGGAAGAGATGCT[-/ATCT]GAGGATAGTCCTGGA	4689

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