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
rs1963	snp	A/G	0.0759472	0.179459	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93670315	GGCCAGGTTTGAGCC[A/G]CAGGGAAGTGGGCAG	5253
rs8690	snp	C/T	0.139225	0.224118	utr-variant-3-prime	PHF2	GRCh38.p7	9:93679468	TCTAACAAAGTTTAT[C/T]GTGGCTATTAAAGTG	5253
rs914417	snp	G/T	0.301932	0.244547	intron-variant	PHF2	GRCh38.p7	9:93597513	GGGCCCTGGAATCAG[G/T]CAGGCTGTGGGGCAG	5253
rs928368	snp	A/G	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93610202	aggagaagaaaaaga[A/G]aaaggaatagaggat	5253
rs928369	snp	C/T	0.29046	0.246704	intron-variant	PHF2	GRCh38.p7	9:93586007	ACTGATTTAGGGGTT[C/T]AGGCCCATTTCCCTG	5253
rs951447	snp	C/G	0	0	upstream-variant-2KB	PHF2	GRCh38.p7	9:93575816	TGGGGCTGAGCATCA[C/G]GGAAGTCCGCGGGAT	5253
rs1000850	snp	A/G	0.493247	0.0577133	intron-variant	PHF2	GRCh38.p7	9:93585436	AGGGACAGCAAGCAC[A/G]GTTATGGAGCAGTGC	5253
rs1000851	snp	C/G	0.493201	0.0579089	intron-variant	PHF2	GRCh38.p7	9:93585467	CAGCCGCTCTGTGTG[C/G]GCAGCACGTGGCCTC	5253
rs1000852	snp	A/G	0.497613	0.0344622	intron-variant	PHF2	GRCh38.p7	9:93585608	TTGGACAAACATGAG[A/G]ATCTGATTGGCCTTG	5253
rs1041500	snp	A/G	0.498459	0.0277128	intron-variant	PHF2	GRCh38.p7	9:93590029	GCTATCCTGGTCTGT[A/G]TGTTTTTGTGCATGT	5253
rs1123475	snp	A/G	0.0520825	0.152737	intron-variant	PHF2	GRCh38.p7	9:93622669	gtctcaccgggctaa[A/G]atcaaggtgtgggca	5253
rs1132003	snp	C/T	0.168785	0.236441	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678446	TCTTGCCCTGCTGGC[C/T]ACACTCTGGAGAAGC	5253
rs1132004	snp	A/C	0.384401	0.210799	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678526	GGGCAGGGACAGTGG[A/C]CAGGCGGCCCGAGGA	5253
rs1132027	snp	C/T	0.0771285	0.180597	utr-variant-3-prime	PHF2	GRCh38.p7	9:93679273	GCAGTCCCTAGGGCC[C/T]GAGACTGGGTGGGAG	5253
rs1140722	snp	A/G	0.384785	0.210554	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678046	AGACAGAGTGAGCCA[A/G]TGCTCACCAGCCCCA	5253
rs1317260	snp	C/T	0.290977	0.246619	intron-variant	PHF2	GRCh38.p7	9:93592338	CACTCAGGGCGGGCC[C/T]ATTCTTTACTCATTT	5253
rs1412048	snp	C/T	0.421368	0.182025	intron-variant	PHF2	GRCh38.p7	9:93600685	GCCACAGCATGGAGC[C/T]TGTGTTACCATTTAC	5253
rs1412049	snp	A/T	0.349671	0.229272	intron-variant	PHF2	GRCh38.p7	9:93600641	ATGCCAGGGCCACCA[A/T]CCCACAACCTGCGAG	5253
rs1806458	snp	A/G	0.49645	0.0419827	intron-variant	PHF2	GRCh38.p7	9:93634049	CACTCGGTGTTCCTC[A/G]CAGGTGGTGACCTAA	5253
rs1806524	snp	A/C	0.34437	0.231505	intron-variant	PHF2	GRCh38.p7	9:93622242	GGCCTTGACCAGACC[A/C]CAAGCCCAAACTGAA	5253
rs1806673	snp	G/T	0.067446	0.170804	intron-variant	PHF2	GRCh38.p7	9:93631908	GCCCCTGGCCCAGGG[G/T]TTTCTGACACTTTCT	5253
rs1810886	snp	C/G	0.308123	0.244277	intron-variant	PHF2	GRCh38.p7	9:93596912	TACAGGCACGCGCCA[C/G]CACGCCCAGCTAATT	5253
rs1901280	snp	A/G					GRCh38.p7	9:93624941	gatgTCACTCTCAAA[A/G]GGGCAAGTTCTTTTT	5253
rs2001315	snp	C/T	0.45235	0.146814	intron-variant	PHF2	GRCh38.p7	9:93632120	AGGGTCTGGGTGAGG[C/T]AGGCACACAGGGCTC	5253
rs2001316	snp	G/T	0.20111	0.245173	intron-variant	PHF2	GRCh38.p7	9:93632064	GATGTCTGGGGACAT[G/T]AGAGAAATCAAAACA	5253
rs2001368	snp	C/T	0.237593	0.249692	intron-variant	PHF2	GRCh38.p7	9:93621740	AAAGTAGGCTTGTGC[C/T]GTCTGCCCCCAGGAT	5253
rs2001587	snp	C/T	0.0341408	0.126114	intron-variant	PHF2	GRCh38.p7	9:93633734	CACTGAGGCCAGGGG[C/T]CCCCGGCTACACCTG	5253
rs2001588	snp	A/C	0.0341408	0.126114	intron-variant	PHF2	GRCh38.p7	9:93633555	CCTATCCCAGAGCCA[A/C]ATGCGGAGCATGAGG	5253
rs2001589	snp	C/T	0.451856	0.147493	intron-variant	PHF2	GRCh38.p7	9:93633519	GCCCCTGTGACAACA[C/T]ACCCACTGAGACAAC	5253
rs2001609	snp	C/T	0.108402	0.206034	intron-variant	PHF2	GRCh38.p7	9:93633081	GCCTTGAACCTGCCT[C/T]CACCTGTCCTGCTCC	5253
rs2001610	snp	C/T	0.426507	0.177046	intron-variant	PHF2	GRCh38.p7	9:93633147	TCAGGGTTCCCAGAG[C/T]GAGCTGTGCCTGAGG	5253
rs2001994	snp	A/T	0.495782	0.0457324	intron-variant	PHF2	GRCh38.p7	9:93631567	TAAAGGGTAGGAAGG[A/T]TCAGCCCAGCGGGGC	5253
rs2001995	snp	C/T	0.190205	0.242744	intron-variant	PHF2	GRCh38.p7	9:93631645	GCCAAGCTGTCTTTA[C/T]GACAGGAATGACACA	5253
rs2026942	snp	A/C	0.498369	0.0285077	intron-variant	PHF2	GRCh38.p7	9:93588593	GCACTCCCTGCCCCC[A/C]AGAAAAACACTTTAT	5253
rs2150751	snp	A/G	0.290977	0.246619	intron-variant	PHF2	GRCh38.p7	9:93590784	TGAAGGGACCACCCC[A/G]GAGGCCATGGGCTGG	5253
rs2150752	snp	G/T	0.290718	0.246662	intron-variant	PHF2	GRCh38.p7	9:93590837	CTGGTTGTGGTGGTG[G/T]TTTCTGACTCCCCTT	5253
rs2250236	snp	C/T	0.299158	0.245119	intron-variant	PHF2	GRCh38.p7	9:93615515	CCAGTATTTCTGTCA[C/T]TGACCTTCTACTAGA	5253
rs2250344	snp	C/T	0.434398	0.168811	intron-variant	PHF2	GRCh38.p7	9:93614116	ACTTGCCCTCTACCT[C/T]AGACCATGGCCACCT	5253
rs2254389	snp	A/G	0.434543	0.168653	intron-variant	PHF2	GRCh38.p7	9:93604133	TTCTGAGATGGGGAC[A/G]CCCCTCTGAGATGGG	5253
rs2254712	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93601577	TGTGGTTGGCAGGAT[A/G]GTTGGCACCCCCAGG	5253
rs2254715	snp	C/T	0.299664	0.245017	intron-variant	PHF2	GRCh38.p7	9:93601418	TGCTAAGTTTGCAAA[C/T]AGGCTGTGGCAGGTG	5253
rs2265300	snp	A/G	0.470908	0.117046	intron-variant	PHF2	GRCh38.p7	9:93607553	ctctcaaaatgttgg[A/G]attacaggtgtgagc	5253
rs2265573	snp	A/G	0.299158	0.245119	intron-variant	PHF2	GRCh38.p7	9:93607207	TTTACTTCTCCATGT[A/G]AACTTCAGAATCAAT	5253
rs2265574	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93608493	CCCTCTGCTTCTATC[A/G]TCTGAAAGAGACTGT	5253
rs2265575	snp	A/G	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93609482	ATTTTCTGAACTGTT[A/G]TTTGTCTGATAGACT	5253
rs2265576	snp	C/T	0.470908	0.117046	intron-variant	PHF2	GRCh38.p7	9:93609519	ctccttcacttttga[C/T]ggataattttgctgg	5253
rs2274851	snp	C/T	0.291235	0.246576	intron-variant	PHF2	GRCh38.p7	9:93592807	GGGGCCAAGCACCAG[C/T]ACGTGGCCTTGCACC	5253
rs2398845	snp	G/T	0.421842	0.181577	intron-variant	PHF2	GRCh38.p7	9:93603330	CCGACTTAGCTGTGG[G/T]TGTCTACGGCAGGGA	5253
rs2398846	snp	A/T	0.404035	0.196909	intron-variant	PHF2	GRCh38.p7	9:93603461	TAATGCTGGCTCTGG[A/T]CTCCTGTAGGACACA	5253
rs2398847	snp	A/G	0.404209	0.196773	intron-variant	PHF2	GRCh38.p7	9:93603476	ACTCCTGTAGGACAC[A/G]CTGCTGGGGTCACTG	5253
rs2398848	snp	G/T	0.426047	0.177503	intron-variant	PHF2	GRCh38.p7	9:93633903	TTTTCTTTGATCTCC[G/T]CAGCCAGCCCTGAGG	5253
rs2398849	snp	C/G	0.487809	0.0771174	intron-variant	PHF2	GRCh38.p7	9:93636088	CCTTTTCAGGAGGTG[C/G]CTCTCTGGTGGTCTC	5253
rs2398850	snp	C/T	0.0349115	0.127424	intron-variant	PHF2	GRCh38.p7	9:93636172	TCAGGGAATGGAGGA[C/T]ACTGGTGCCATCCAT	5253
rs2398851	snp	A/G	0.495891	0.0451408	intron-variant	PHF2	GRCh38.p7	9:93636226	ACACGAGGTCGAGGT[A/G]GGGGGTTGACTCCTC	5253
rs2398852	snp	A/G	0.0731253	0.176679	intron-variant	PHF2	GRCh38.p7	9:93636374	CCCTGCTGGGGCTGC[A/G]CTGTGTGACCGACCT	5253
rs2398853	snp	C/T	0.490119	0.0695896	intron-variant	PHF2	GRCh38.p7	9:93637160	AGAATCCTAAGTTGG[C/T]GGGTTTTTTTTCTTT	5253
rs2398854	snp	A/C	0.0260105	0.111035	intron-variant	PHF2	GRCh38.p7	9:93645888	GCCCTGGCTGTGTCC[A/C]TGTGTGCCGTGAGCA	5253
rs2398855	snp	A/C	0.498206	0.0298983	intron-variant	PHF2	GRCh38.p7	9:93646898	TTGGGTGTCCATGCA[A/C]AGGGGCTGATTCTGT	5253
rs2398856	snp	C/T	0.421842	0.181577	intron-variant	PHF2	GRCh38.p7	9:93647088	CTGTTTCTGTCTTGC[C/T]GCACAATGCTGGTCA	5253
rs2398861	snp	A/G	0.469049	0.120489	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668465	GCCCCTAAACACCCT[A/G]GGCCCCTCCCGAGGT	5253
rs2398862	snp	A/G	0.0360663	0.129354	intron-variant	PHF2	GRCh38.p7	9:93677416	TTTGCCAGTGATCCC[A/G]GACTCCTGAAGGGTG	5253
rs2895249	snp	A/G	0.349233	0.229462	intron-variant	PHF2	GRCh38.p7	9:93603471	TCTGGACTCCTGTAG[A/G]ACACACTGCTGGGGT	5253
rs2989751	snp	A/G	0.434543	0.168653	intron-variant	PHF2	GRCh38.p7	9:93604365	TTTGAGACGGAGAGC[A/G]AGACTTCTTTATATT	5253
rs2989752	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93605461	caccattgcaatgta[A/G]tacagaagagtttca	5253
rs2989753	snp	A/G	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93613446	CACTTAGGGTTGGCC[A/G]AGGGCCCTAAAACAG	5253
rs2989754	snp	A/G	0.434398	0.168811	intron-variant	PHF2	GRCh38.p7	9:93613875	CACCACACCTGGCCC[A/G]CATTGTCAGACCAGA	5253
rs2989755	snp	A/G	0.470908	0.117046	intron-variant	PHF2	GRCh38.p7	9:93613971	CTGCTGCCTCTACAC[A/G]TCCCTTTCTTGCTGT	5253
rs2989756	snp	C/T	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93616328	CTGGCCTGAAGGGTG[C/T]AAATCTTTTTAAAGC	5253
rs2994365	snp	C/T	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93612092	CTGCAACTTGTGCTC[C/T]TTGCTGAACAATATA	5253
rs2994366	snp	C/G	0.299411	0.245069	intron-variant	PHF2	GRCh38.p7	9:93602180	AAAAGTATGTAAATT[C/G]TTCGTTGAGTATGTA	5253
rs2994367	snp	A/G	0.298905	0.24517	intron-variant	PHF2	GRCh38.p7	9:93613532	AGTAGGTCCCGGTGG[A/G]GATTGGGGTTCTTCT	5253
rs2994368	snp	A/G	0.298905	0.24517	intron-variant	PHF2	GRCh38.p7	9:93614618	CGCAGTCCTGGAGGA[A/G]TGGACATAGCACACT	5253
rs2994369	snp	C/T	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93604231	GCAGGTGCCGGGGAC[C/T]GAGTGAGTGAGTTGG	5253
rs2994370	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93605538	aaacctctgataacc[A/G]ctgatgtttttactg	5253
rs3080731	in-del	-/GGG	0.495963	0.0447464	intron-variant	PHF2	GRCh38.p7	9:93631803	GGTCCTACCTGAGTT[-/GGG]GGGCTTGGGAGGATG	5253
rs3080732	in-del	-/GTCT			intron-variant	PHF2	GRCh38.p7	9:93632941	CTGTGCCCAGAGGCT[-/GTCT]ATGATGCCCCAGTTG	5253
rs3080758	in-del	-/AT	0.418653	0.184544	intron-variant	PHF2	GRCh38.p7	9:93649687	CTCGTGGACACACTC[-/AT]GACACTCACACTGAC	5253
rs3750353	snp	A/G	0.0560246	0.157714	intron-variant	PHF2	GRCh38.p7	9:93653130	CACTGCAGGGGAAAT[A/G]AAAAAGGGAGTCCCA	5253
rs3750354	snp	C/T	0.456707	0.140614	intron-variant	PHF2	GRCh38.p7	9:93653371	CGTGCTCAAGGTGAG[C/T]CACGCCCCTCGGGGC	5253
rs3750355	snp	C/T	0.0410144	0.137204	intron-variant	PHF2	GRCh38.p7	9:93654617	TGTACTAGGGCTTGC[C/T]GGCCCTCATCAAGCT	5253
rs3750356	snp	A/G	0.0689305	0.172377	intron-variant	PHF2	GRCh38.p7	9:93654821	GGCTTGTGTTGTCTC[A/G]TCAGCATGGGCACTC	5253
rs3750357	snp	C/T	0.394171	0.204242	intron-variant	PHF2	GRCh38.p7	9:93659837	ACTGAGAAATGGCAC[C/T]AGCCTCTCTGAAACT	5253
rs3750358	snp	C/T	0.490839	0.0670581	intron-variant	PHF2	GRCh38.p7	9:93662856	GTGGCTCAAGAGAGT[C/T]CCACCAGCCCTCTAT	5253
rs3750359	snp	A/G	0.317933	0.240593	intron-variant	PHF2	GRCh38.p7	9:93663081	GCTTGGTGAGTGTGA[A/G]CAGAGGTGAATCTGT	5253
rs3750360	snp	A/G	0.075454	0.179954	intron-variant	PHF2	GRCh38.p7	9:93663206	TGTGACCACCCATGG[A/G]CTACATCTTCCTCTG	5253
rs3750361	snp	C/T	0.484066	0.0878235	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669538	CACACCTCAATCCTG[C/T]TCAGTCCCTGTGAAA	5253
rs3750362	snp	A/G	0.49998	0.00319482	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669577	GCAACGCAGTCCAGT[A/G]TGTCTCAGACAGGGC	5253
rs3750363	snp	C/T	0.00279162	0.0372561	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669647	TGCCCCGGCACTGGG[C/T]ATCTTCCTGAGTCTG	5253
rs3750364	snp	C/G	0.167809	0.236103	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669851	GAACCAGGACTGGTC[C/G]TGGTGGGGCCACTGC	5253
rs3763605	snp	A/G	0.484672	0.0861922	intron-variant	PHF2	GRCh38.p7	9:93658108	GCACCTGTGGGCAGC[A/G]GGCACCCACCCACCT	5253
rs3813386	snp	C/T	0.0759472	0.179459	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678263	CATTCAGGCTGAACA[C/T]CCACCATCCTGCTGC	5253
rs3829059	snp	C/T	0.0759472	0.179459	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668874	CTCTCCCAAAGTCTC[C/T]CATTTGGAGCGTAGG	5253
rs3829758	snp	A/G	0.390838	0.206555	intron-variant, utr-variant-3-prime	PHF2, LOC107987098	GRCh38.p7	9:93673427	GGCAGTGAGCTGATG[A/G]CTTCTCCCTTGGAAG	5253
rs3922729	snp	C/T	0.462363	0.131916	intron-variant	PHF2	GRCh38.p7	9:93587303	CAACCAGGGCTCCTC[C/T]GTCATCCCTCACCCA	5253
rs3957504	snp	C/T	0.029116	0.117091	intron-variant	PHF2	GRCh38.p7	9:93636061	ACCTGC[C/T]	5253
rs4073155	snp	A/G	0.459118	0.137002	intron-variant	PHF2	GRCh38.p7	9:93592272	AGTTGCCTCTGCAGG[A/G]GCTGCTGGTCCCCAC	5253
rs4146138	snp	C/T	0.290977	0.246619	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593157	ACTGTTCCAGCAGGA[C/T]GGGACATGGCAGCAC	5253
rs4403473	snp	C/G	0.461703	0.132974	intron-variant	PHF2	GRCh38.p7	9:93636892	GCATGCTCCCATGGC[C/G]CAGGCAGGCGTTGTC	5253
rs4568663	snp	A/G	0.404384	0.196635	intron-variant	PHF2	GRCh38.p7	9:93610043	ttgatttttttttgc[A/G]gtttgaatgtgatat	5253
rs4743929	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93606355	aatgaatgagagttc[A/G]tgttgctctacatcc	5253

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