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
rs171367	snp	A/G	0.0733688	0.176922	intron-variant	RNF150	GRCh38.p7	4:141192969	agactgaattttttg[A/G]aagaacctgaagaat	57484
rs181378	snp	A/T	0.0322114	0.122752	intron-variant	RNF150	GRCh38.p7	4:141146143	TACATTCTGTTACTT[A/T]GGGATGGATACATGT	57484
rs183055	snp	C/T	0.202035	0.245356	intron-variant	RNF150	GRCh38.p7	4:141148017	CTTAAAATATTTTCT[C/T]GTGTCTTTCCTTAAT	57484
rs187139	snp	C/T	0.371177	0.218669	intron-variant	RNF150	GRCh38.p7	4:141146323	TGAAACCTTCTTCAA[C/T]GTTTTTTATCCTATC	57484
rs189567	snp	A/G	0.0803491	0.183626	intron-variant	RNF150	GRCh38.p7	4:141148522	TGGGAGGCAGAGGTT[A/G]CAGTGAGCCAAGATG	57484
rs189568	snp	A/G	0.371785	0.218331	intron-variant	RNF150	GRCh38.p7	4:141146399	AGAAACATTCACTAC[A/G]TCATGCAAATAACTT	57484
rs193287	snp	C/G	0.400504	0.199621	intron-variant	RNF150	GRCh38.p7	4:141152956	GCTAATGCATGTGGG[C/G]CTTAATACCTAGGTA	57484
rs241866	snp	C/T	0.400504	0.199621	intron-variant	RNF150	GRCh38.p7	4:141152706	TTTATCCCCCAGAAG[C/T]GGTTAGTACACCCCA	57484
rs241867	snp	A/G	0.356169	0.226336	intron-variant	RNF150	GRCh38.p7	4:141146869	CTCTCAACTTGCTCT[A/G]ATCTTGAGAGTGGAA	57484
rs354924	snp	A/C	0.0209421	0.100162	intron-variant	RNF150	GRCh38.p7	4:141158041	CTCACACCTGTAATC[A/C]CAGCACTTTGGGAGG	57484
rs354925	snp	C/G	0.0584853	0.160693	intron-variant	RNF150	GRCh38.p7	4:141159729	tgtattttttgtaaa[C/G]gcagggtttcgtcat	57484
rs354926	snp	A/G	0.237303	0.249677	intron-variant	RNF150	GRCh38.p7	4:141193382	AGAGACTGGAATGAC[A/G]TGGACTAGGTTAAGC	57484
rs354927	snp	C/T	0.0700422	0.173537	intron-variant	RNF150	GRCh38.p7	4:141192981	ggtcttatgaagaga[C/T]tgaattttttgaaag	57484
rs354928	snp	C/T	0.143622	0.226238	intron-variant	RNF150	GRCh38.p7	4:141192368	attcactATCGAATA[C/T]TCTGTGTACTTTTAA	57484
rs354929	snp	C/T	0.140242	0.224618	intron-variant	RNF150	GRCh38.p7	4:141191835	CATCAGGAGCACACA[C/T]CTATAAGATGACCAG	57484
rs354930	snp	C/G	0.140242	0.224618	intron-variant	RNF150	GRCh38.p7	4:141191356	AAAGGATTGAGGTGG[C/G]ACACCCAAACCAGAG	57484
rs354931	snp	A/T	0.143622	0.226238	intron-variant	RNF150	GRCh38.p7	4:141191164	TAGCGGTCACCATCC[A/T]GAAAGTAACCCAGGC	57484
rs354932	snp	G/T	0.104504	0.2033	intron-variant	RNF150	GRCh38.p7	4:141190270	Tctggcaaaatggcc[G/T]aataggaacagctct	57484
rs354933	snp	A/G	0.422944	0.180528	intron-variant	RNF150	GRCh38.p7	4:141190191	atttccaactgaggt[A/G]cctggttcatctaat	57484
rs354934	snp	A/G	0.407845	0.193868	intron-variant	RNF150	GRCh38.p7	4:141154384	ACACAGGCACGCTAA[A/G]GAAGGACAGAATGAC	57484
rs354935	snp	C/G	0.400504	0.199621	intron-variant	RNF150	GRCh38.p7	4:141153962	TTGTCCCAAAGCAGA[C/G]AACTAATAAGTGGCA	57484
rs354936	snp	A/G	0.400325	0.199756	intron-variant	RNF150	GRCh38.p7	4:141148915	GAGCTGAGGAGGAAT[A/G]ATAAAGCCACCAGCT	57484
rs354937	snp	A/G	0.202343	0.245416	intron-variant	RNF150	GRCh38.p7	4:141148610	CTAGAAAATACAAAA[A/G]AAGTAGCCGGGTATG	57484
rs354938	snp	G/T	0.279726	0.248226	intron-variant	RNF150	GRCh38.p7	4:141147364	GTAGAAACTTCAGCA[G/T]CAGACTTTGAAGCTC	57484
rs354939	snp	A/T	0.37138	0.218556	intron-variant	RNF150	GRCh38.p7	4:141146785	TAGTGGAGATAACAA[A/T]GTTGCCTTGAGTGGG	57484
rs354940	snp	C/T	0.0444908	0.142359	intron-variant	RNF150	GRCh38.p7	4:141146755	CTTGCTGGACCCATC[C/T]TGTAGGTCCTACATC	57484
rs354941	snp	C/T	0.385359	0.210185	intron-variant	RNF150	GRCh38.p7	4:141146615	CTTTTTTTTAAACTC[C/T]TCAATTATGGCTTCC	57484
rs717818	snp	A/G	0.499776	0.0105807	intron-variant	RNF150	GRCh38.p7	4:140909679	TATAATGCAAGTCAT[A/G]CATGTAATTTAAATT	57484
rs729242	snp	A/G	0.444267	0.157354	utr-variant-3-prime	RNF150	GRCh38.p7	4:140864997	TCCCTGGAGGTAATT[A/G]AGCTTTTAACCTTCT	57484
rs756170	snp	A/G	0.0562307	0.157967	intron-variant	RNF150	GRCh38.p7	4:141130434	AATACTGTAGTTTGA[A/G]CGTTAAAGGAAAAAA	57484
rs767761	snp	G/T	0.469247	0.120128	intron-variant	RNF150	GRCh38.p7	4:140895503	TTATTTTCCTATCTT[G/T]ATGAACAATTACAGT	57484
rs874774	snp	C/T	0.497121	0.0378299	intron-variant	RNF150	GRCh38.p7	4:140912196	CCAGCAGAACTGAGA[C/T]AAAAGAGTAAAACTT	57484
rs874775	snp	A/G	0.498158	0.0302955	intron-variant	RNF150	GRCh38.p7	4:140911949	TGTATGATCAATACC[A/G]TATTAAGGACTTAGG	57484
rs874776	snp	C/T	0.492337	0.0614248	intron-variant	RNF150	GRCh38.p7	4:140911871	GCCTTATCCTGTGCT[C/T]TGTGTGTGTTTGAGG	57484
rs883077	snp	C/T	0.474813	0.109357	intron-variant	RNF150	GRCh38.p7	4:141074623	CTGCCTTTTTTGGTC[C/T]AGATCCCACAGACCA	57484
rs890184	snp	A/G	0.499	0.0223418	intron-variant	RNF150	GRCh38.p7	4:140968278	ACTTTGCATTCCATG[A/G]CAAAAGGGTAAAATG	57484
rs890185	snp	A/G	0.046775	0.145601	intron-variant	RNF150	GRCh38.p7	4:140930695	CTCTGTGTCACTTCA[A/G]TGGCATCGAAACTGC	57484
rs890186	snp	C/T	0.046775	0.145601	intron-variant	RNF150	GRCh38.p7	4:140930868	CAAGGCCCTGCCCTT[C/T]AAGGCAGCATCACAG	57484
rs920039	snp	G/T	0.416708	0.186302	intron-variant	RNF150	GRCh38.p7	4:141196300	AAAGACAGGAAAACT[G/T]GACCAACAGTTTCAT	57484
rs929962	snp	A/T	0.435263	0.167862	intron-variant	RNF150	GRCh38.p7	4:141050122	tatatgtacatatac[A/T]tatatatacttacat	57484
rs961402	snp	A/C	0.499872	0.0079862	intron-variant	RNF150	GRCh38.p7	4:140909098	TGTCCAATAAATGGA[A/C]AAATTCTGAGACCAC	57484
rs972778	snp	C/T	0.462909	0.131034	intron-variant	RNF150	GRCh38.p7	4:141076506	TGTCTCAGAATAATG[C/T]AAGGCTCAAGTATAA	57484
rs978670	snp	A/C	0.414905	0.187899	intron-variant	RNF150	GRCh38.p7	4:141049783	TTATAGTTAGTTTTT[A/C]TTTAAGCATCACATA	57484
rs982136	snp	C/T	0.333722	0.235565	intron-variant	RNF150	GRCh38.p7	4:140877506	ATAGATAATTTTATA[C/T]GGTTGCAGAAATGGA	57484
rs984839	snp	A/G	0.0349115	0.127424	intron-variant	RNF150	GRCh38.p7	4:140906783	CCATATCTTGATTCC[A/G]CCATTCCCACCCTCC	57484
rs984840	snp	A/T	0.486725	0.0803809	intron-variant	RNF150	GRCh38.p7	4:140907042	TTCTGTGTCTTTCTC[A/T]CACTTCTCTCTTGAG	57484
rs987302	snp	A/T	0.0973687	0.197999	intron-variant	RNF150	GRCh38.p7	4:141001010	AGAGAAAAAGAATTA[A/T]ACAAATCAGCGTAAT	57484
rs998013	snp	A/G	0.460365	0.13508	downstream-variant-500B, utr-variant-3-prime	RNF150	GRCh38.p7	4:140865391	CTAGAAGCAAATGCA[A/G]ACTGTATGTGTATTT	57484
rs1001487	snp	A/G	0.496416	0.0421803	intron-variant	RNF150	GRCh38.p7	4:140947361	GTGGCCGCCAAGTAC[A/G]AGTTTTCTTGAACAA	57484
rs1003257	snp	A/C	0.195837	0.244062	intron-variant	RNF150	GRCh38.p7	4:140984252	GATCCTTAAGAGGCC[A/C]ATTTTTTATCTGCCA	57484
rs1027815	snp	C/T	0.25045	0.25	intron-variant	RNF150	GRCh38.p7	4:141129582	aaagccattgaaatg[C/T]atactttaaatgagt	57484
rs1027816	snp	C/T	0.487621	0.0776941	intron-variant	RNF150	GRCh38.p7	4:141125674	TCTAAACAAATTAAC[C/T]TCATATCAGAGGCAC	57484
rs1030356	snp	A/G	0.216048	0.247684	intron-variant	RNF150	GRCh38.p7	4:140905626	TCCTGCTCCTCTAGT[A/G]AAAGGGGTGGAGAAA	57484
rs1039709	snp	C/T	0.0329836	0.124112	intron-variant	RNF150	GRCh38.p7	4:141124385	TCAGGGAagagtagc[C/T]tgggagtgccttcct	57484
rs1108084	snp	A/G	0.470908	0.117046	intron-variant	RNF150	GRCh38.p7	4:140931764	GGTGTTTGAAGAACT[A/G]TTTTTAAAATGTTTG	57484
rs1155225	snp	G/T	0	0	upstream-variant-2KB, intron-variant	RNF150	GRCh38.p7	4:141134035	ATGTTTGCTTCCAGG[G/T]GGGCAGTAGGAAGCC	57484
rs1318787	snp	A/G	0.48546	0.0840147	intron-variant	RNF150	GRCh38.p7	4:140980550	attatagttcccata[A/G]tccccatgtgtagtg	57484
rs1346056	snp	A/G	0.49928	0.018956	intron-variant	RNF150	GRCh38.p7	4:140938225	TTACTGAAATCACTG[A/G]AAAAAGACACTAGCC	57484
rs1346057	snp	C/T	0.0554779	0.157039	intron-variant	RNF150	GRCh38.p7	4:140901157	CATTTGGTTTTATGA[C/T]ATTAGCAGGGCATTT	57484
rs1346058	snp	A/G	0.482609	0.0916147	intron-variant	RNF150	GRCh38.p7	4:140907044	CTGTGTCTTTCTCTC[A/G]CTTCTCTCTTGAGTC	57484
rs1347403	snp	A/G	0.41275	0.189769	intron-variant	RNF150	GRCh38.p7	4:141178690	GCCAAGCTTGAAATG[A/G]TGCTGACAAGGGCCA	57484
rs1354835	snp	C/T	0.492386	0.0612297	intron-variant	RNF150	GRCh38.p7	4:141028902	GAATCTTTTCTGTAT[C/T]AATGTTATTGTATCA	57484
rs1364877	snp	A/G	0.499999	0.000599041	intron-variant	RNF150	GRCh38.p7	4:140937345	tgaacctgggtggtg[A/G]aggttgcagtcagct	57484
rs1364879	snp	C/G	0.478603	0.101197	intron-variant	RNF150	GRCh38.p7	4:140969378	TGGGAATAACTGAAA[C/G]TGGTGGCTCGATTTT	57484
rs1364880	snp	A/C	0.499104	0.0211472	intron-variant	RNF150	GRCh38.p7	4:140969529	CTAAAGAAACATGAT[A/C]TTCTTTGTATACTGG	57484
rs1364881	snp	C/T	0.194902	0.243853	intron-variant	RNF150	GRCh38.p7	4:140975816	AGGGCAGGCTCTCTG[C/T]AGTATTACTGGCTTC	57484
rs1364883	snp	C/T	0.0807149	0.183963	intron-variant	RNF150	GRCh38.p7	4:140985081	CTCTTTTTTCTTTCT[C/T]CATAGTTCTCTGATG	57484
rs1364884	snp	A/T	0.329783	0.236927	intron-variant	RNF150	GRCh38.p7	4:140897459	GGCCTATGGATCTGC[A/T]CTCCAACTACAGCCC	57484
rs1364885	snp	A/G	0.478437	0.10157	intron-variant	RNF150	GRCh38.p7	4:140897633	CTAATTCAGTTTCTT[A/G]GATATAAAAGAGTGA	57484
rs1364886	snp	C/T	0.42803	0.175514	intron-variant	RNF150	GRCh38.p7	4:140904220	GCACGTTAAGAGTCA[C/T]GGAAATGATTGTCTG	57484
rs1364887	snp	A/G	0.465892	0.126058	intron-variant	RNF150	GRCh38.p7	4:140908461	GCCATATTCATATAT[A/G]CCATCAGTCTTCTGA	57484
rs1364888	snp	C/T	0.093417	0.194889	intron-variant	RNF150	GRCh38.p7	4:141022228	TTTTTATTTTTTATT[C/T]TTTTTTCCTGCAGGC	57484
rs1364889	snp	C/T	0.093417	0.194889	intron-variant	RNF150	GRCh38.p7	4:141022325	TCCCCCCTCTAACTC[C/T]GCCTCACTTAGAAAA	57484
rs1364890	snp	A/C	0.481009	0.0955756	intron-variant	RNF150	GRCh38.p7	4:140894246	TAGGCATTAATAAAT[A/C]TTATGCTAAATCACC	57484
rs1364891	snp	C/T	0.377977	0.21476	intron-variant	RNF150	GRCh38.p7	4:141002344	CTCCTACCAGAGTTC[C/T]ATCAACAGCCTCTCA	57484
rs1364892	snp	C/T	0.200182	0.244986	intron-variant	RNF150	GRCh38.p7	4:141002525	ATGGAAATACTTCCC[C/T]TGTGAGTTGCTCAAT	57484
rs1369317	snp	A/G	0	0	intron-variant	RNF150	GRCh38.p7	4:141158471	ACTCTTTCAAAAAAA[A/G]AAAAGCCTAATCCTA	57484
rs1395664	snp	A/G	0.0685596	0.171987	intron-variant	RNF150	GRCh38.p7	4:141047195	ACTAGCTTTCTAAAT[A/G]TTTTCAGATGCAGTA	57484
rs1395666	snp	A/G	0.093417	0.194889	intron-variant	RNF150	GRCh38.p7	4:141024096	gttacctgagctgcc[A/G]atgggttggtcctaa	57484
rs1395668	snp	A/G	0.350764	0.228794	intron-variant	RNF150	GRCh38.p7	4:141104855	AGTAAGACCTGAATA[A/G]AGATTTTGGCACTTC	57484
rs1395669	snp	C/T	0.359998	0.2245	intron-variant	RNF150	GRCh38.p7	4:141104976	ATTGATTAACCCCAT[C/T]GTGATTTAACATCCA	57484
rs1425426	snp	C/G	0.499017	0.0221427	intron-variant	RNF150	GRCh38.p7	4:140938965	CATGTGTCGAGAATT[C/G]ACACAACATTCACAA	57484
rs1425427	snp	C/T	0.492966	0.0588865	intron-variant	RNF150	GRCh38.p7	4:140962686	TAATAATAAAGGATA[C/T]CATTCATTGAGTGCT	57484
rs1425428	snp	G/T	0.455144	0.142885	intron-variant	RNF150	GRCh38.p7	4:141025852	TACAGACTGAATGTT[G/T]GTGTCCTCTAAAAAT	57484
rs1425429	snp	C/T	0.0821764	0.185298	intron-variant	RNF150	GRCh38.p7	4:140970069	ATGCCCAGACTTACA[C/T]TTTTTAGTAGTCAGA	57484
rs1425430	snp	A/G	0.499879	0.0077866	intron-variant	RNF150	GRCh38.p7	4:141025940	CAATGATTAGGTCAC[A/G]AGAGTGGAGCCGTCA	57484
rs1425431	snp	C/T	0.486332	0.08153	intron-variant	RNF150	GRCh38.p7	4:140970412	AACAGGCTGTTTTAG[C/T]TGTATAGCTTTTAAC	57484
rs1425432	snp	G/T	0.478685	0.10101	intron-variant	RNF150	GRCh38.p7	4:140971253	TTGCTTCTGTGGGTG[G/T]GTGTGAGGCAGGGAA	57484
rs1425433	snp	A/G	0.484632	0.086302	intron-variant	RNF150	GRCh38.p7	4:140975396	GTGCAGGTATCTGCA[A/G]GTGGTCCTGGAACCA	57484
rs1425434	snp	A/G	0.0850919	0.187897	intron-variant	RNF150	GRCh38.p7	4:140976508	gctccctagacacac[A/G]ttcccactgttgtat	57484
rs1425435	snp	A/C	0.48546	0.0840147	intron-variant	RNF150	GRCh38.p7	4:140980124	CTTGGGTCACCGCAA[A/C]TTCTGCCTCCTGGGT	57484
rs1425436	snp	A/C	0.475965	0.106957	intron-variant	RNF150	GRCh38.p7	4:140899702	ACACTCAGAATTATC[A/C]AAACAAAGTGAAGAG	57484
rs1425437	snp	A/C	0.478603	0.101197	intron-variant	RNF150	GRCh38.p7	4:140899785	CTGGCTAAATCACTT[A/C]AGCTGCAATATATTT	57484
rs1425438	snp	C/G	0.498673	0.0257246	intron-variant	RNF150	GRCh38.p7	4:140900002	TGTGTGTGTGTGTGT[C/G]TGTCCCATTTGCTGC	57484
rs1425440	snp	A/G	0.386504	0.209444	intron-variant	RNF150	GRCh38.p7	4:140912331	TGGTGGTGGAGGAAT[A/G]TTGTCTTAAGCAGGA	57484
rs1425441	snp	G/T	0.447809	0.152878	intron-variant	RNF150	GRCh38.p7	4:140912493	TAATGATTGAATTAA[G/T]ATCACAATGACTGTT	57484
rs1425442	snp	C/G	0.0551013	0.156571	intron-variant	RNF150	GRCh38.p7	4:140912606	TGTTGTCCTAGTGTT[C/G]TGCTCTTAGCTGTAT	57484
rs1425443	snp	C/T	0.384976	0.210431	intron-variant	RNF150	GRCh38.p7	4:140960092	TTCTAAATTTAACAT[C/T]GTCAAATCCAAATTC	57484
rs1425444	snp	A/C	0.484561	0.0864924	intron-variant	RNF150	GRCh38.p7	4:140961091	TTTAGCTATTACCCT[A/C]TACCAGATTTAACTT	57484
rs1425445	snp	C/T	0.243919	0.249926	intron-variant	RNF150	GRCh38.p7	4:140992129	GTTTATTTTTATATA[C/T]CTTGTCCTTAGCCTT	57484

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