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
rs8359	snp	C/T	0.227074	0.248947	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80394251	ATCTAGTTTCTCTCA[C/T]AATTTCAAAATGTCA	57674
rs1128358	snp	C/G	0.0349115	0.127424	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80395224	TTGTACAGAAATATA[C/G]TGGCCTAGCAGAGGC	57674
rs3185057	snp	A/G	0.145533	0.227127	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80390047	TTCAAGGTACAAAGC[A/G]GATCTGAGCCCGGAA	57674
rs3193455	snp	A/C	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80382063	GTTCCGAAGTCAGCC[A/C]CGTAGGTCATTCCCC	57674
rs3923128	snp	A/G	0.0115895	0.0752359	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389123	GGCTGGGTTTCTGGC[A/G]TCTCACCACCTGGTA	57674
rs4073111	snp	C/G	0.490398	0.0686206	intron-variant	RNF213	GRCh38.p7	17:80283792	GGCGGTCCAGAGCCT[C/G]AGGATTCTCCGTCTA	57674
rs4075499	snp	A/G	0.495252	0.0484902	intron-variant	RNF213	GRCh38.p7	17:80327059	CATAGCATATGCAAA[A/G]AGAGAAACAGCCATG	57674
rs4078429	snp	A/G	0.218151	0.247963	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361572	TAGGGAATTGAAGGA[A/G]TAGTCACTGTCTAGA	57674
rs4523980	snp	C/T	0.382279	0.212137	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80373864	AAGCACCCACCATCA[C/T]GTCCAGCTAATTTTT	57674
rs4609905	snp	A/G	0.40853	0.193309	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80387972	ACTCCGTCTCAAAAA[A/G]AAAAAAAAAAAAAAA	57674
rs4889843	snp	C/T	0.448066	0.152544	intron-variant	RNF213	GRCh38.p7	17:80325519	AGATCAGGAAACAAA[C/T]GGAGAAGGCAATGCG	57674
rs4889844	snp	A/G	0.465892	0.126058	intron-variant	RNF213	GRCh38.p7	17:80325697	GCCCCCCGCGCCCCA[A/G]GTGTTTTGTGGTCAA	57674
rs4889845	snp	A/G	0.452473	0.146644	intron-variant	RNF213	GRCh38.p7	17:80329760	cacttgagcctggga[A/G]gtcgaggctgcagtg	57674
rs4889846	snp	A/G	0.493718	0.0556925	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355824	ATGGGGGCTTACAGG[A/G]GAAGAAGCGGGGTGA	57674
rs4889847	snp	A/G	0.0550842	0.15655	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80372748	AGGCAAGTCTTCTCT[A/G]CCTTGCTTTCCTTTG	57674
rs4889848	snp	C/T	0.347418	0.230239	synonymous-codon, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80380861	AACGCAGACCGGCCA[C/T]GTGCTGGGCAACCCG	57674
rs4889968	snp	A/G	0.275197	0.248727	intron-variant	RNF213	GRCh38.p7	17:80263005	AGGTCCTCCACTGTT[A/G]GGTGGCCAAGCGCCC	57674
rs4890007	snp	G/T	0.179425	0.239831	intron-variant	RNF213	GRCh38.p7	17:80330752	AACCATCTCTTGGCT[G/T]CTGGGGTGAAGAAGG	57674
rs4890008	snp	G/T	0.162581	0.234218	intron-variant	RNF213	GRCh38.p7	17:80331819	TGCTTTCTTTATCAT[G/T]AATATTGGTTAACAA	57674
rs4890009	snp	A/G	0.457173	0.139926	synonymous-codon	RNF213	GRCh38.p7	17:80337708	CTATGTGATCCAGGC[A/G]CCCAAAGGTGGCCAA	57674
rs4890010	snp	A/G	0.498693	0.0255257	intron-variant	RNF213	GRCh38.p7	17:80342379	GAGGTGACCAGGAGA[A/G]TGAGTAGGTAACGGC	57674
rs4890011	snp	A/G			intron-variant	RNF213	GRCh38.p7	17:80342754	ATATATTGTATGTAT[A/G]TATATATTATATATA	57674
rs4890012	snp	A/C/G/T	0.49098	0.0668198	synonymous-codon	RNF213	GRCh38.p7	17:80345580	CCGGTGTGGGATCCC[A/C/G/T]GTTATCATCATGGGA	57674
rs4890013	snp	A/G	0.273856	0.248859	intron-variant	RNF213	GRCh38.p7	17:80351225	CAGGGGCTGTTTcct[A/G]taatcctagctactt	57674
rs4890014	snp	C/T	0.494936	0.050064	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361256	ATATCCTAGGCCAGG[C/T]GCAGTGGTTCACAAC	57674
rs4890015	snp	A/G	0.496583	0.0411924	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80361400	TGGTGCATGCCTGTA[A/G]TCCCAGCTACTTGGT	57674
rs4890016	snp	A/G	0.00636936	0.0560724	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80364057	GGCTATTGTGATGCC[A/G]TGTGAGAAATGCTGT	57674
rs4890017	snp	A/G	0.0733688	0.176922	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80378606	GGATTATGAGCCACT[A/G]TGCCCAGCCTGATAC	57674
rs4890018	snp	C/T	0.0961445	0.197049	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80386201	CACGCCTAGATTCTG[C/T]GAGGAGTTGGAACTC	57674
rs4890019	snp	A/G	0.382085	0.212258	utr-variant-3-prime, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80398190	tttggttttgacctg[A/G]cttggatatcctgat	57674
rs4890020	snp	A/T	0.382473	0.212016	downstream-variant-500B, intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80399034	cattcaatctgtagc[A/T]gcaactgctttgcta	57674
rs5822349	in-del	-/T/TT	0.45866	0.137698	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80368433	ATGTAGACGCCAGTG[-/T/TT]TTTTTTTTTTTTTTT	57674
rs5822350	in-del	-/A			intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80377438	ACAAAAAAAAAAAAA[-/A]TCAAGGAAAATAGAA	57674
rs5822351	in-del	-/CC	0.0337553	0.125452	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80389070	TAGAGAGTTGGCCCC[-/CC]GCATGTGGCTTGGGC	57674
rs6420491	snp	A/G	0.0456336	0.143994	intron-variant	RNF213	GRCh38.p7	17:80331236	ctgtgacataaaact[A/G]ctcagctctcagtgt	57674
rs6565662	snp	G/T	0.448452	0.152042	intron-variant	RNF213	GRCh38.p7	17:80276370	ctcccaaagtgctgg[G/T]attacgggcgtgagc	57674
rs6565663	snp	A/G	0.492137	0.0622048	intron-variant	RNF213	GRCh38.p7	17:80285865	TTAGTAGAGATGGGG[A/G]GGATCTCACCATGTT	57674
rs6565664	snp	G/T	0.0923359	0.194016	intron-variant	RNF213	GRCh38.p7	17:80285919	GACCTCCAGTGATCC[G/T]CCTGCCTCGGCCTCC	57674
rs6565666	snp	A/G	0.291266	0.246571	intron-variant	RNF213	GRCh38.p7	17:80319145	ATAGAGCACTGGAGC[A/G]CTGCATCCGAAAGCT	57674
rs6565667	snp	A/C	0.470034	0.11868	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320375	tgttgtttttgagac[A/C]gagtttcactctttt	57674
rs6565668	snp	A/G	0.495135	0.0490805	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320436	tggctcaccgcaacc[A/G]ctgcctcccgggttc	57674
rs6565669	snp	C/T	0.494442	0.0524218	intron-variant, downstream-variant-500B	RNF213	GRCh38.p7	17:80321945	gggtcatgatggtct[C/T]gatctcttgacctca	57674
rs6565670	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80322152	gcccctcatcccccc[A/C]acccccccttttttt	57674
rs6565671	snp	A/C			intron-variant	RNF213	GRCh38.p7	17:80322153	cccctcatccccccc[A/C]ccccccctttttttt	57674
rs6565672	snp	C/T	0.491421	0.0649309	intron-variant	RNF213	GRCh38.p7	17:80322448	gggcatggtggcatg[C/T]gcctgtagtcccagc	57674
rs6565673	snp	A/T	0.0228947	0.104514	intron-variant	RNF213	GRCh38.p7	17:80322587	tctcaaaaaaaaaaa[A/T]tttttttcgtagaga	57674
rs6565674	snp	A/G	0.000113993	0.00754873	missense	RNF213	GRCh38.p7	17:80325138	ACCGCGGACAACTTC[A/G]ATGACATTTTAAAGC	57674
rs6565675	snp	A/G	0.497445	0.0356514	intron-variant	RNF213	GRCh38.p7	17:80326282	ggcgtgcaccaccat[A/G]cccagccTGTTTATA	57674
rs6565676	snp	G/T	0.49614	0.0437598	intron-variant	RNF213	GRCh38.p7	17:80326326	tttttagagcacttt[G/T]atgtgtacagaaaaa	57674
rs6565677	snp	C/T	0.427119	0.176434	intron-variant	RNF213	GRCh38.p7	17:80343642	CCAATTGTAAAACGG[C/T]GTATTTATGTGTCTA	57674
rs6565678	snp	A/G	0.442791	0.15916	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80357847	AAAAATTAGCTGGGC[A/G]TGGTGGCACTGGGTG	57674
rs6565679	snp	C/T	0.211819	0.247067	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80360717	GCTGAGCTCTGCTGC[C/T]AGATGCCAGAAGATT	57674
rs6565680	snp	A/G	0.485528	0.0838238	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80366804	tcaaacttggaacag[A/G]aaggaactctcctTG	57674
rs6565681	snp	A/G	0.321449	0.239573	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80374694	ATGGACCACTGATGC[A/G]GCCCATCACGTGACA	57674
rs6565682	snp	A/G	0.251578	0.249995	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388469	TGGTGGGTTAATGAC[A/G]GAGAGGGGCGCTCTT	57674
rs6565683	snp	A/T	0.381503	0.21262	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388500	AGCCAAGGGATACAC[A/T]GGGCAGCGCGGCACT	57674
rs7206993	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287635	CCCCGACCCTGCCCA[C/T]CCCCCACTTTTGTTT	57674
rs7207660	snp	C/T	0.457154	0.139954	intron-variant	RNF213	GRCh38.p7	17:80341643	ctaggaaggctgact[C/T]gggaggatcgctcca	57674
rs7208006	snp	C/G/T	0.00127898	0.0252576	intron-variant, downstream-variant-500B	RNF213, LOC100294362	GRCh38.p7	17:80361684	CTGGAGGCAGGGGAG[C/G/T]GCCATGACTTAGACG	57674
rs7208136	snp	C/T	0.427271	0.176281	intron-variant	RNF213	GRCh38.p7	17:80341931	cctgcctcagcctcc[C/T]gagtagctgggacta	57674
rs7209174	snp	A/T	0.452227	0.146984	intron-variant	RNF213	GRCh38.p7	17:80323949	cctgcaacattgctg[A/T]gctcatttggtagct	57674
rs7209233	snp	A/G	0.438526	0.164189	intron-variant	RNF213	GRCh38.p7	17:80335932	CAGTGAGCCGAGATC[A/G]TGTCACTTCACTCCA	57674
rs7209557	snp	C/T	0.441432	0.160792	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80359636	TAAAGAAAGAAAGAG[C/T]GAGAGAAAGAAAGAA	57674
rs7209771	snp	C/G	0.375	0.216506	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355442	GGGGTGGATGGGAAT[C/G]GGGGCTCACGGAGGA	57674
rs7211876	snp	C/T	0.32593	0.23819	intron-variant	RNF213	GRCh38.p7	17:80337560	GCTCCAACCGTGGCC[C/T]GTGTTCTCTCCTTTT	57674
rs7212829	snp	G/T	0.494568	0.0518327	intron-variant	RNF213	GRCh38.p7	17:80324800	TTGGTGTGTGTTTGT[G/T]TGTGTGTCTTCACAT	57674
rs7213539	snp	A/G	0.0209421	0.100162	intron-variant	RNF213	GRCh38.p7	17:80340841	acagagtctcactct[A/G]ttgcccagattggag	57674
rs7213699	snp	A/G	0	0	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355408	GTGAATGGGAATGGG[A/G]GCTCACGGAGGAAGA	57674
rs7213818	snp	A/G	0.375	0.216506	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355433	GGAAGAAGCGGGGTG[A/G]ATGGGAATCGGGGCT	57674
rs7214019	snp	A/G	0.485664	0.0834419	intron-variant	RNF213	GRCh38.p7	17:80261796	GGCCAAGGCGGGTGG[A/G]TCACCTGAGGTCGGG	57674
rs7214614	snp	A/G	0.43978	0.162738	intron-variant	RNF213	GRCh38.p7	17:80284995	TAGAGTAAGGCTGAT[A/G]TTACTCAAACCATGC	57674
rs7215078	snp	A/T	0.498009	0.0314867	intron-variant, upstream-variant-2KB	RNF213	GRCh38.p7	17:80287290	TGCCTGAGCCTGAGA[A/T]TTCAAAACCAGCTTG	57674
rs7215243	snp	A/G	0.438666	0.164028	synonymous-codon, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288006	GCCGAGCCAGCCCCC[A/G]GGCACAGCCACCACG	57674
rs7216493	snp	A/G	0.445108	0.15631	synonymous-codon, nc-transcript-variant	RNF213, LOC100294362	GRCh38.p7	17:80353558	TGAGGAGGCGATGGA[A/G]ACGGAGGCCAGCACA	57674
rs7217256	snp	A/G	0.49703	0.0384237	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355371	GTGAACGGGAATGGG[A/G]GCTTACAGGGGAAGA	57674
rs7217421	snp	A/G	0.476918	0.104919	intron-variant	RNF213	GRCh38.p7	17:80261661	AGCGGATTGAATGCA[A/G]CAGTGTTGGGTGCCT	57674
rs7219131	snp	C/T	0.489608	0.0713316	intron-variant	RNF213	GRCh38.p7	17:80278971	CATGCTGGCACAGCC[C/T]GGCACGGCCACCTCG	57674
rs7219660	snp	C/T	0.457388	0.139608	intron-variant	RNF213	GRCh38.p7	17:80279301	GGAGCCCAAGGGGGC[C/T]TAGAGGGCCAGGCCC	57674
rs7220243	snp	C/T	0.00203195	0.0318096	missense, upstream-variant-2KB	RNF213	GRCh38.p7	17:80288043	GAGGGTGACGGCCTC[C/T]CCGCGCCCACCGAGG	57674
rs7220465	snp	A/G	0.495708	0.0461266	intron-variant	RNF213	GRCh38.p7	17:80286212	TGTCGGACGCAGGCC[A/G]GTGTTGGACGCAGGC	57674
rs7221291	snp	C/T	0.485187	0.0847778	intron-variant, utr-variant-3-prime	RNF213, LOC100294362	GRCh38.p7	17:80370543	cagtagctggaggta[C/T]tgttttcttcaccgc	57674
rs7222014	snp	A/G	0.444267	0.157354	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80319669	TTGCTCAGTAGGTGT[A/G]CGGGAAGAGACTCCA	57674
rs7222128	snp	C/T	0.42	0.183303	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80355398	AAGAAGCGGGGTGAA[C/T]GGGAATGGGGGCTCA	57674
rs7223115	snp	C/T	0.444829	0.156658	intron-variant	RNF213	GRCh38.p7	17:80349957	CCCCAGCCGCAGCCG[C/T]GTGGCTTCTGCGTGG	57674
rs7223701	snp	G/T	0.212425	0.24716	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80388851	CAGCAAATCAGCAAG[G/T]TTTCTTGTAGAGTAA	57674
rs7224239	snp	A/G	0.472522	0.113946	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80381376	AACAGAAAAGCCAGC[A/G]GCCGTTCCGCTTGCT	57674
rs7224493	snp	C/G	0.458315	0.13822	intron-variant	RNF213	GRCh38.p7	17:80349020	GGAGGCCGCTGGAAC[C/G]GTACAAAGGAGAGGA	57674
rs7224585	snp	C/G	0.184838	0.241358	intron-variant	RNF213	GRCh38.p7	17:80335689	TGCTATTAACAGACA[C/G]TACAggctgggcgtg	57674
rs7225029	snp	A/G	0.180383	0.240111	intron-variant	RNF213	GRCh38.p7	17:80323979	tcaaattgtgtgtgc[A/G]tgtgtgtgtgtgtgt	57674
rs7501563	snp	A/G	0.495407	0.0477027	intron-variant	RNF213	GRCh38.p7	17:80326746	agctaacttcgtttt[A/G]ccactgaataatatt	57674
rs7501761	snp	A/T	0.499683	0.0125759	intron-variant	RNF213	GRCh38.p7	17:80316385	cagtttacaaaacag[A/T]tggcctgaacttttc	57674
rs7501767	snp	C/T	0.000477598	0.0154457	synonymous-codon	RNF213	GRCh38.p7	17:80291715	TCCTTACAAGTACGT[C/T]ATTTATAATGGGGAA	57674
rs7501942	snp	C/T	0.00318978	0.0398085	intron-variant	RNF213	GRCh38.p7	17:80292343	gaagtgttgggatta[C/T]aggtgtaagccacta	57674
rs7501987	snp	A/G	0.41141	0.19091	intron-variant	RNF213	GRCh38.p7	17:80317664	gcaggagcaagctcc[A/G]tgcaggccctgcagc	57674
rs7502336	snp	C/T	0.496968	0.0388195	intron-variant	RNF213	GRCh38.p7	17:80307970	ACTTGTAAATAGTCA[C/T]GATACTGCATATGCC	57674
rs7502410	snp	C/T	0.276534	0.248588	intron-variant	RNF213	GRCh38.p7	17:80316696	TGCCCAGGTATGTAG[C/T]GGCAAGGTGCCATGA	57674
rs7502437	snp	C/T	0.40263	0.198	intron-variant	RNF213	GRCh38.p7	17:80308348	ACACCGCCTTCCCAG[C/T]CCCCTCCATCAACTC	57674
rs7502832	snp	A/C	0.312837	0.241974	intron-variant	RNF213	GRCh38.p7	17:80302238	aacgactgtaattta[A/C]aatttattacgtttt	57674
rs7503136	snp	C/T	0.482905	0.0908579	intron-variant, utr-variant-3-prime	RNF213	GRCh38.p7	17:80320426	ggtgcgatcctggct[C/T]accgcaaccgctgcc	57674
rs7503198	snp	A/G	0.0573587	0.15934	intron-variant	RNF213, LOC100294362	GRCh38.p7	17:80365210	TCCAGAGCCCTCACC[A/G]CCAGGGGGTCTGGAA	57674

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