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
rs923530	snp	G/T	0.496314	0.0427728	intron-variant	PHF21A	GRCh38.p7	11:46087968	CGCCATGTTGCCTAG[G/T]CTGGTCTTGAGCTCC	51317
rs939106	snp	A/C	0.217851	0.247924	intron-variant	PHF21A	GRCh38.p7	11:45954709	ACTGAAATAATTTTA[A/C]AACAGAAAATATCAA	51317
rs939107	snp	A/G	0.491157	0.065903	intron-variant	PHF21A	GRCh38.p7	11:45960800	CATGATGCAGACTCG[A/G]AATTGTCTTGCAGAT	51317
rs950105	snp	A/T	0.472241	0.114494	intron-variant	PHF21A	GRCh38.p7	11:46115871	CTTAACTTCAGTATG[A/T]CTTCACAGAAAGCTT	51317
rs953230	snp	A/G	0.484771	0.0859212	intron-variant	PHF21A	GRCh38.p7	11:46043423	AATTAATCCTTTCTG[A/G]TTAACATACTACCTT	51317
rs953577	snp	G/T	0.0755793	0.179102	intron-variant	PHF21A	GRCh38.p7	11:46054967	TACCTAAGCATTTTA[G/T]TTTAGTTTAAATGAA	51317
rs959241	snp	A/C	0.0898077	0.191933	intron-variant	PHF21A	GRCh38.p7	11:46097373	ccagtgttgctggaa[A/C]ggattgagcgatagg	51317
rs1006909	snp	C/T	0.0329836	0.124112	intron-variant	PHF21A	GRCh38.p7	11:46113121	TTGATTTAAACAGTA[C/T]GGAAAACCCTTCCTT	51317
rs1038733	snp	A/G	0.167158	0.235875	intron-variant	PHF21A	GRCh38.p7	11:46075867	ACTAAATAACATTAA[A/G]TAACAACATAAAAAT	51317
rs1063809	snp	A/G	0	0	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934030	GCCACCTCCACGCCG[A/G]CCCCTTCCCCCTCCT	51317
rs1063810	snp	C/G/T	1.69232e-05	0.00290883	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934029	CCACCTCCACGCCGG[C/G/T]CCCTTCCCCCTCCTC	51317
rs1125290	snp	C/G	0.489318	0.0722982	intron-variant	PHF21A	GRCh38.p7	11:45985503	TCCAGTGCAGATTCT[C/G]TTATTGAATTTTACT	51317
rs1125291	snp	C/T	0.491368	0.0651254	intron-variant	PHF21A	GRCh38.p7	11:45985186	TGAGTTTTAGTTAGA[C/T]GGTAGAAAGTCTTTT	51317
rs1132657	snp	A/C			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119371	GTATGGATTTCTAGA[A/C]TTTCAAATCTGAGTG	51317
rs1135457	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46019316	GATTCATTTGACATG[A/G]TACTTAATTTTGATG	51317
rs1135458	snp	A/C	0	0	intron-variant	PHF21A	GRCh38.p7	11:46019233	CGACATTCTTTTCCC[A/C]TATCTTCTAGAAAGA	51317
rs1352643	snp	A/C	0	0	intron-variant	PHF21A	GRCh38.p7	11:46044290	TTAAACCAAATGTAC[A/C]TTAAATGAGCAGGAA	51317
rs1401420	snp	C/G	0.204803	0.245881	intron-variant	PHF21A	GRCh38.p7	11:45961081	AAAAGCGGGATATCT[C/G]TTATACTCATGTTCC	51317
rs1401421	snp	A/G	0.205723	0.246048	intron-variant	PHF21A	GRCh38.p7	11:45984278	AAACAATAAGCCAAC[A/G]TGCCAGGCCTCCAGA	51317
rs1490082	snp	C/T	0.167809	0.236103	intron-variant	PHF21A	GRCh38.p7	11:46117734	GTGGGATGTTGAGCA[C/T]GTATTTTAAAAAATT	51317
rs1490087	snp	A/G	0.16846	0.236329	intron-variant	PHF21A	GRCh38.p7	11:46086859	ACATAACAAAGGGCT[A/G]ATACAGTTTATATAT	51317
rs1490088	snp	C/T	0.133777	0.221342	intron-variant	PHF21A	GRCh38.p7	11:46086891	TAGGGCCCTCAAAAA[C/T]TGATAACAAAAATCT	51317
rs1490089	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46086899	TCAAAAATTGATAAC[A/C]AAAATCTATGAAAAA	51317
rs1542724	snp	G/T	0.272511	0.248984	intron-variant	PHF21A	GRCh38.p7	11:46095632	ATATTATAACCATAT[G/T]AGAAATCTGGATGAT	51317
rs1554339	snp	C/T	0.206029	0.246103	intron-variant	PHF21A	GRCh38.p7	11:45984949	GAATCAACATGCAAT[C/T]TAAAAATACAACCTT	51317
rs1565412	snp	C/G	0.463881	0.12944	intron-variant	PHF21A	GRCh38.p7	11:46064596	AAGATACTAGTTAAA[C/G]AGTAAACTTCTTTTT	51317
rs1907003	snp	C/T	0.168135	0.236216	intron-variant	PHF21A	GRCh38.p7	11:46066944	AATACTGAATTATAC[C/T]GTATGTCTGTTTTAC	51317
rs1973721	snp	A/G	0.206029	0.246103	intron-variant	PHF21A	GRCh38.p7	11:45972868	tgagtgcagtggcac[A/G]atttctgctcactgc	51317
rs1976182	snp	A/C	0.471958	0.115042	intron-variant	PHF21A	GRCh38.p7	11:46070393	TGGAGTGCAGTGGCA[A/C]CATCTTGGCTCCCTG	51317
rs1994599	snp	A/C	0.167809	0.236103	intron-variant	PHF21A	GRCh38.p7	11:46068872	GCATCTGGTACAAGT[A/C]ACCAACTGACTTGAT	51317
rs1996573	snp	C/G	0.470715	0.117409	intron-variant	PHF21A	GRCh38.p7	11:45953092	ATACAATGGTTGTAA[C/G]AAAAACGCACACTTA	51317
rs2013010	snp	C/G	0.463126	0.13068	intron-variant	PHF21A	GRCh38.p7	11:46059707	gatgacaggcataag[C/G]cattgtacctggccT	51317
rs2056261	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45981468	ACCTGATGTGTAAAG[G/T]GGTGGGACCAAAGAC	51317
rs2056262	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45981471	TGATGTGTAAAGTGG[G/T]GGGACCAAAGACCAA	51317
rs2130469	snp	A/G	0.16846	0.236329	intron-variant	PHF21A	GRCh38.p7	11:46087381	TTTACTTTCTCCATC[A/G]GATTGTTGTCTGCTT	51317
rs2130470	snp	C/T	0.167809	0.236103	intron-variant	PHF21A	GRCh38.p7	11:46087624	GAAAGAAACAAATTA[C/T]AGACATGTATTTATA	51317
rs2130471	snp	C/T	0.167484	0.23599	intron-variant	PHF21A	GRCh38.p7	11:46091423	GAGCCATTAAAAAAA[C/T]CTCTCAAAGTAGATA	51317
rs2130473	snp	C/T	0.167484	0.23599	intron-variant	PHF21A	GRCh38.p7	11:46094668	GTCTCGATCTCCTGA[C/T]CTCGTGATCCACCCA	51317
rs2130475	snp	C/T	0.384017	0.211044	intron-variant	PHF21A	GRCh38.p7	11:46107488	GGCTGGTAAAAAACG[C/T]TGACTACTCTATAGT	51317
rs2130476	snp	A/G	0.384017	0.211044	intron-variant	PHF21A	GRCh38.p7	11:46107551	TTCTTAGAATTTTAC[A/G]GCAAGGCTTTAGCAC	51317
rs2171895	snp	C/T	0.168135	0.236216	intron-variant	PHF21A	GRCh38.p7	11:46091564	AGACATGAAGCTAAC[C/T]AATCCAATATTAATT	51317
rs2220546	snp	A/G	0.395453	0.203331	intron-variant	PHF21A	GRCh38.p7	11:46072994	TCAAAAAATCAGGGT[A/G]TGGGGAGTGAGAATG	51317
rs2860376	snp	G/T	0.216649	0.247765	intron-variant	PHF21A	GRCh38.p7	11:45951910	CTCCTGGGTTCAAGC[G/T]ATTCTCCAGCCTCAG	51317
rs2860403	snp	C/T	0.167809	0.236103	intron-variant	PHF21A	GRCh38.p7	11:46074462	ATATGCCTTCCCCCC[C/T]CCCGCCAAAAGAGCC	51317
rs2860404	snp	A/G	0.485528	0.0838238	intron-variant	PHF21A	GRCh38.p7	11:46074016	CTCAGTTTCTCCCTT[A/G]AAACTATGTAATCGT	51317
rs2860433	snp	C/T	0.205417	0.245993	intron-variant	PHF21A	GRCh38.p7	11:45977045	ACACTGTTTTGGAGG[C/T]AGCCCTGGGCCTCTT	51317
rs2863714	snp	A/G	0.185472	0.241529	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930760	CTCTCTGAAGTGACT[A/G]CAAAGCCAGCTGGTC	51317
rs2902550	snp	C/T	0.168135	0.236216	intron-variant	PHF21A	GRCh38.p7	11:46058348	GTTGGTAAAACGAAA[C/T]CTGATTAAGACTTTG	51317
rs2932510	snp	C/G	0.167158	0.235875	intron-variant	PHF21A	GRCh38.p7	11:46080167	TTTATCTAACTACTA[C/G]TTTTTTTTTGAGACA	51317
rs2932512	snp	A/G	0.168135	0.236216	intron-variant	PHF21A	GRCh38.p7	11:46059348	tcctgaagaataatt[A/G]agaatgtaaagaaat	51317
rs2932513	snp	A/G	0.464096	0.129085	intron-variant	PHF21A	GRCh38.p7	11:46048627	ATACAAAAATTAGCC[A/G]GGCATGGTGGCATAC	51317
rs2932514	snp	A/G	0.463881	0.12944	intron-variant	PHF21A	GRCh38.p7	11:46048749	CACTCCAGCTTGGGC[A/G]ACAGAGCAAGACTCC	51317
rs2932515	snp	A/G	0.146066	0.227371	intron-variant	PHF21A	GRCh38.p7	11:46084137	CATTACTTAACAACA[A/G]TGTGGGAGAAGCCAA	51317
rs2932516	snp	G/T	0.167809	0.236103	intron-variant	PHF21A	GRCh38.p7	11:46056833	GGAGGACAGCATGAG[G/T]ATTGTTGACTAAAAG	51317
rs2932517	snp	C/T	0	0	intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46075067	TTAAAATTCCAGTTT[C/T]TGAAATGCAAACTTA	51317
rs2945996	snp	A/G	0.204496	0.245824	intron-variant	PHF21A	GRCh38.p7	11:45951828	TTTTTTTTTTTTGAG[A/G]CGGAGTCTCACTCTG	51317
rs2945997	snp	A/G	0.475789	0.107327	intron-variant	PHF21A	GRCh38.p7	11:45955788	GAAGCCAGCTGCCAC[A/G]TTGTGAGCAGCACTA	51317
rs2945998	snp	C/G	0.217551	0.247885	intron-variant	PHF21A	GRCh38.p7	11:45956066	ccaagaattctatat[C/G]ctgcaaaactattct	51317
rs2945999	snp	G/T	0.479014	0.100263	intron-variant	PHF21A	GRCh38.p7	11:45961406	GGTCACTTGGAACTA[G/T]TTTCTCTACTATTGC	51317
rs2946000	snp	A/G	0.217551	0.247885	intron-variant	PHF21A	GRCh38.p7	11:45961497	AAATTTGAAGATAAT[A/G]CATTGGATAATATTA	51317
rs2946001	snp	A/G	0.475525	0.107882	intron-variant	PHF21A	GRCh38.p7	11:45966083	CCTCATCCTAAATGT[A/G]AGTATTTCTTAGGAT	51317
rs2946002	snp	A/G	0.206029	0.246103	intron-variant	PHF21A	GRCh38.p7	11:45966344	ATTGCCTCAGTAAGT[A/G]CCCTTTTCTTGACAA	51317
rs2946003	snp	C/T	0.493432	0.0569306	intron-variant	PHF21A	GRCh38.p7	11:45975963	TCGTCCTTGCCCTCA[C/T]ACATTAAATATATGT	51317
rs2946004	snp	C/G	0.475702	0.107512	intron-variant	PHF21A	GRCh38.p7	11:45976254	CCATTCATCTGACAG[C/G]GCCCTGCTCAGATGC	51317
rs2946005	snp	C/G	0.206029	0.246103	intron-variant	PHF21A	GRCh38.p7	11:45979678	TGAGCTTAGTATAGT[C/G]TGAGACAGGACCCAG	51317
rs2946006	snp	A/T	0.277867	0.248442	intron-variant	PHF21A	GRCh38.p7	11:45983506	TGTGAAAAAAAAAAA[A/T]TTTTAAATCAAGATT	51317
rs2946008	snp	C/G	0.21695	0.247806	intron-variant	PHF21A	GRCh38.p7	11:45987420	TAATCCTGGCACTTT[C/G]GGAGGCCGAGGTGGG	51317
rs2946009	snp	A/G	0.205723	0.246048	intron-variant	PHF21A	GRCh38.p7	11:45993555	TAACAAAAAGCTGGA[A/G]CTCATTTTTCTGAGC	51317
rs2959082	snp	C/G	0.168135	0.236216	intron-variant	PHF21A	GRCh38.p7	11:46051411	AAACCAGAGCATTTA[C/G]CATTACCTCCCACCT	51317
rs2959083	snp	A/T	0.166832	0.235761	intron-variant	PHF21A	GRCh38.p7	11:46055224	TTACCCAAATATAAC[A/T]AAGCAGCAAATTTTT	51317
rs2959084	snp	A/G	0.484841	0.0857308	intron-variant	PHF21A	GRCh38.p7	11:46057105	AAACTACAATTGAGA[A/G]GTTTTTTTCCCCAAG	51317
rs2959085	snp	C/T	0.168785	0.236441	intron-variant	PHF21A	GRCh38.p7	11:46072810	TCAGGCTGGGGAAAC[C/T]GAAGCTGCAACCACG	51317
rs2959086	snp	A/T	0.462909	0.131034	intron-variant	PHF21A	GRCh38.p7	11:46080768	CAACTCCTGGGCTTC[A/T]GCAATCTTCCCACCT	51317
rs2959087	snp	A/C	0.475613	0.107697	intron-variant	PHF21A	GRCh38.p7	11:45962418	AATGTGATACTGGAA[A/C]TGAAATATAAATAGA	51317
rs2959088	snp	C/T	0.206029	0.246103	intron-variant	PHF21A	GRCh38.p7	11:45963147	TCTGGGGGCCGGGTG[C/T]GGTGGCTCACACCTG	51317
rs2959089	snp	C/T	0.206029	0.246103	intron-variant	PHF21A	GRCh38.p7	11:45963393	CCATTGCACTCCAGC[C/T]TGGGTGACAAGAGTA	51317
rs2959090	snp	A/G	0.475437	0.108066	intron-variant	PHF21A	GRCh38.p7	11:45968388	acttctccaacctca[A/G]ctctaactaactcta	51317
rs2959091	snp	A/G	0.475525	0.107882	intron-variant	PHF21A	GRCh38.p7	11:45969306	CATGCAGAGCTGCTC[A/G]GGCCTAGGGAGAAAG	51317
rs2959092	snp	A/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45975469	CTAACTTCCACATCT[A/G]TTTTATATTATTTTG	51317
rs2959093	snp	A/G	0.227664	0.249	intron-variant	PHF21A	GRCh38.p7	11:45976634	ATCACTTGAGCTCCG[A/G]AGTTTGAGACCAGCC	51317
rs2959094	snp	A/C	0.21725	0.247846	intron-variant	PHF21A	GRCh38.p7	11:45976635	TCACTTGAGCTCCGG[A/C]GTTTGAGACCAGCCT	51317
rs2959095	snp	A/G	0.206029	0.246103	intron-variant	PHF21A	GRCh38.p7	11:45983212	TGCTCCTCCCCCAGG[A/G]CCTGAAACAAAGCCG	51317
rs2959096	snp	C/G	0.206029	0.246103	intron-variant	PHF21A	GRCh38.p7	11:45951317	TATCCTCGATATTAT[C/G]CTACTTTGGCCTGAA	51317
rs2959097	snp	A/T	0.217551	0.247885	intron-variant	PHF21A	GRCh38.p7	11:45985826	CAATGTCTACAAAAG[A/T]AGGTCTCTTTCCTGG	51317
rs2959098	snp	C/G	0.487995	0.0765403	intron-variant	PHF21A	GRCh38.p7	11:45988866	ATTGTACTTCAGCCT[C/G]GGTGACAGAGCGAGA	51317
rs2959099	snp	A/G	0.493154	0.0581045	intron-variant	PHF21A	GRCh38.p7	11:45992251	CTTAGAAAATTTTTC[A/G]GCCCGGCATGGTGGC	51317
rs2959100	snp	C/G	0.430583	0.172886	intron-variant	PHF21A	GRCh38.p7	11:45993587	AACTTTTCTGGGGCT[C/G]ACAGGAGGTTGGGTG	51317
rs2959101	snp	C/T	0.427879	0.175668	intron-variant	PHF21A	GRCh38.p7	11:45996588	GCCAGGAATGCTACT[C/T]TCCATATGCACAAAG	51317
rs2959102	snp	C/G	0.475789	0.107327	intron-variant	PHF21A	GRCh38.p7	11:45954046	TCGTTGCCCAGGCTG[C/G]AGTGCAATGGCATGA	51317
rs2959103	snp	C/T	0.203575	0.245652	intron-variant	PHF21A	GRCh38.p7	11:45948533	GGAACACCTTGGCAA[C/T]GGCAGTGCTCTGTTC	51317
rs2959104	snp	A/G	0.165527	0.235296	intron-variant	PHF21A	GRCh38.p7	11:46043485	TAAAGCCCATATCAC[A/G]GTCTATTAGTTATTA	51317
rs3021404	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45966649	tgtttgagatggagt[C/T]tcgctctgttgccag	51317
rs3021405	snp	C/T	0.277778	0.248452	intron-variant	PHF21A	GRCh38.p7	11:45971886	GGACAGTGTCTTTTT[C/T]TTTCTTTTTTTTTTT	51317
rs3061870	in-del	-/T/TT			intron-variant	PHF21A	GRCh38.p7	11:45943139	TCATCTTTCTTTCCT[-/T/TT]TTTTTTTTTTTTTTT	51317
rs3061874	in-del	-/CA			intron-variant	PHF21A	GRCh38.p7	11:45955307	acacacacacacaca[-/CA]CTTTTTAATCAAAAA	51317
rs3061876	in-del	-/CT	0.205417	0.245993	intron-variant	PHF21A	GRCh38.p7	11:45962308	ATACGGGTTTGGTAA[-/CT]CTGTGAACAGGTGTG	51317
rs3061877	in-del	-/AAT			intron-variant	PHF21A	GRCh38.p7	11:45978354	AGAGATGGTAATAAT[-/AAT]AACTTCCTCTTAGGA	51317
rs3061959	in-del	-/GTT/GTTGTT/GTTGTTGTT	0.350103	0.234577	intron-variant	PHF21A	GRCh38.p7	11:46088408	gttgttgttgttgtt[-/GTT/GTTGTT/GTTGTTGTT]ATTGGAAAGTTAGAG	51317
rs3061961	in-del	-/AAAAG			intron-variant	PHF21A	GRCh38.p7	11:46087553	GAGATCTTTCTGAAG[-/AAAAG]AAAAAGAATTTCAAA	51317
rs3107239	snp	C/T	0.206029	0.246103	intron-variant	PHF21A	GRCh38.p7	11:45966685	agtgcagtggcgcga[C/T]ctcggctcacagcag	51317

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