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
rs9401	snp	A/T	0	0	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620154	TATTTTTACTACCAG[A/T]AGGTAAAGAAAAAGT	54476
rs710939	snp	C/T	0.040671	0.13668	intron-variant	RNF216	GRCh38.p7	7:5651059	CGGAAGTGAGATATA[C/T]GTATATAATTCCTGT	54476
rs710940	snp	C/T	0.0337553	0.125452	intron-variant	RNF216	GRCh38.p7	7:5634204	AGCCTCCTGTGACCA[C/T]GGGGGAAGAACGGGT	54476
rs710941	snp	C/T	0.32885	0.23724	intron-variant	RNF216	GRCh38.p7	7:5633798	GCAAGCACCCGGCCT[C/T]TCCAGAAACGTGCTG	54476
rs752909	snp	C/T	0.217145	0.247832	intron-variant	RNF216	GRCh38.p7	7:5726328	ACAGGTAAAATCACA[C/T]GACAATGGGCTGGTG	54476
rs752910	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5726355	GGTGAGTCCCATTCT[A/G]TAGGCAAATCTTCCA	54476
rs852257	snp	A/G	0.333722	0.235565	intron-variant	RNF216	GRCh38.p7	7:5700001	GCCTAAGCTGAAGCT[A/G]CTGTTGGGTGGAATT	54476
rs852258	snp	A/C	0.32955	0.237006	intron-variant	RNF216	GRCh38.p7	7:5699759	CATCACTGCAAGTGG[A/C]ATCAACCACCCAGCC	54476
rs852259	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5698416	CATGCGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT	54476
rs852260	snp	C/T	0.00755907	0.0610114	intron-variant	RNF216	GRCh38.p7	7:5693917	TAGAACAGTTATTAA[C/T]TTTCGTTGTGTCATT	54476
rs852261	snp	A/G	0.253544	0.249975	intron-variant	RNF216	GRCh38.p7	7:5690865	ATTTTACACATGTGC[A/G]TATGTGTTATTAAGT	54476
rs852262	snp	C/T	0.0387552	0.1337	intron-variant	RNF216	GRCh38.p7	7:5690585	GTACAGGGAAAGCAC[C/T]GCTGATGGGAGCTGC	54476
rs852263	snp	G/T	0.48	0.0979796	intron-variant	RNF216	GRCh38.p7	7:5689934	TCTTTTTTTTTTTTT[G/T]TTTGAGACAGAGTCA	54476
rs852264	snp	C/G	0.0310518	0.120672	intron-variant	RNF216	GRCh38.p7	7:5689384	TTCACTTTTCTTCTT[C/G]TTTCTTTTTTTTTTT	54476
rs852265	snp	C/T	0.326741	0.23793	intron-variant	RNF216	GRCh38.p7	7:5688906	GAGTTCAGACTTAAA[C/T]TTTATATTGAAGAAC	54476
rs852266	snp	C/T	0.334871	0.235153	intron-variant	RNF216	GRCh38.p7	7:5688368	GCTGGGCAATTTCCT[C/T]TGACATGCGGTTTGT	54476
rs852267	snp	C/G	0.335788	0.23482	intron-variant	RNF216	GRCh38.p7	7:5686934	gtgagtgagcattac[C/G]acctgagctctgcct	54476
rs852374	snp	A/G	0.340108	0.233197	intron-variant	RNF216	GRCh38.p7	7:5636488	CGAGGGAGTTGTCCC[A/G]TCATGGTTTTGGAGG	54476
rs852375	snp	C/T	0.303688	0.244167	intron-variant	RNF216	GRCh38.p7	7:5636069	CTGGCAGTCTGGATT[C/T]GAGAGTATGGCAAAA	54476
rs852376	snp	A/G	0.32955	0.237006	intron-variant	RNF216	GRCh38.p7	7:5635674	ATTTGTCCTCGGAGT[A/G]TTCCCAGGCCTGCCT	54476
rs852377	snp	C/T	0.00636936	0.0560724	intron-variant	RNF216	GRCh38.p7	7:5635470	AGGTATTTTAGACTT[C/T]TAGGTTGGAAACTGA	54476
rs852378	snp	A/G	0.0912534	0.193131	intron-variant	RNF216	GRCh38.p7	7:5635078	tccctagcttggtga[A/G]accaggatgtgagcc	54476
rs852393	snp	C/T	0.0341408	0.126114	intron-variant	RNF216	GRCh38.p7	7:5682471	GCAGTAAGACAAGAC[C/T]GCGCCACTGCACTGC	54476
rs852394	snp	C/T	0.499997	0.00119808	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5681817	TTTCTGGGTGTTTCC[C/T]GTTTATGTAGTCAGG	54476
rs852395	snp	C/T	0.138546	0.223781	intron-variant, upstream-variant-2KB	RNF216, RNF216-IT1	GRCh38.p7	7:5680624	ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCC	54476
rs852396	snp	C/T	0.296619	0.245615	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5680108	CCCTTGTGTGAAGAA[C/T]GTGGACTTCTTCCTG	54476
rs852397	snp	C/T	0.333491	0.235646	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679926	AGGGTCCCTATTGTG[C/T]TTCTTAAAGCCGACT	54476
rs852398	snp	C/G	0.030665	0.119967	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679186	CACCACCACCCCTAC[C/G]CGAGGGTGACAGGAT	54476
rs852399	snp	C/G	0.030278	0.119257	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5679129	TAAATGACTTGATAA[C/G]TAAGATGTTTCATCC	54476
rs852400	snp	G/T	0.34101	0.232846	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678846	ACCTTTGCCTCTTAA[G/T]TTATCCAGTCCAGCT	54476
rs852401	snp	G/T	0.0360663	0.129354	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5678159	CAATACTCAGGCATG[G/T]GCCCAAATCTAGGTT	54476
rs852402	snp	C/G	0.334871	0.235153	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677630	TCAGATTGGAAAGAA[C/G]TGACTAAGAACAGGT	54476
rs852403	snp	C/T	0.17461	0.238362	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677218	TGATTTAGAGACTGC[C/T]CAGCACGTGCTTCTG	54476
rs852404	snp	C/T	0.030278	0.119257	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5677174	TTAATTCTAATTTGT[C/T]CAGGTGTTAATTTTA	54476
rs852405	snp	A/G	0.17654	0.238964	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5676414	ATCATACTTTTTGCA[A/G]CTGCCGTCAGCACTT	54476
rs852406	snp	A/C	0.327445	0.237702	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5675759	tcgcaccattgcgtt[A/C]cagcctgggcaacaa	54476
rs852407	snp	C/T	0.0314385	0.121371	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674976	agagtctctctctgt[C/T]gcccaggctggagtg	54476
rs852408	snp	G/T	0.030665	0.119967	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5674392	aggcaggcggatcat[G/T]aggtcaggagtttga	54476
rs852409	snp	C/T	0.329783	0.236927	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673884	gatagagcaagactc[C/T]gtctcaaaaaaaaaa	54476
rs852410	snp	A/G	0.331179	0.236453	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5673365	ATGCTTTCTCCCACA[A/G]AGCTATCTCCAGCCC	54476
rs852411	snp	C/G	0.186105	0.241697	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672775	CGCAAGGTAGAGGAT[C/G]GATATGAGGGAGGAC	54476
rs852412	snp	A/G	0.030665	0.119967	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5672666	TGCTTATGTGATCAC[A/G]TAAGTATTTATGCGA	54476
rs852413	snp	C/T	0.0356815	0.128715	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668895	TATCTAGTTAGCATA[C/T]TATCCACCTGATGCC	54476
rs852414	snp	G/T	0.242201	0.249878	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5668267	cactgcactccagcc[G/T]gggccaacggagcga	54476
rs852415	snp	C/T	0.331642	0.236293	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5667192	CCTAGTATTTTTGTT[C/T]TAACTTTAAATCCAC	54476
rs852416	snp	G/T	0.0310518	0.120672	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5665999	TTTTTGTATTTTTAG[G/T]AGAAACGGGGTTTCA	54476
rs852417	snp	C/T	0.353154	0.227726	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5664038	CAAAGATACCTGAGA[C/T]GTACGGTGGTTGATT	54476
rs852418	snp	C/T	0.0513262	0.151752	intron-variant	RNF216, RNF216-IT1	GRCh38.p7	7:5663281	GTGAACTTTTTTTTA[C/T]TGGATGAATTGAGCC	54476
rs852419	snp	A/G	0.0364509	0.129988	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5662033	TGGTCTTCTCACACA[A/G]GATGCCATTGTAACC	54476
rs852420	snp	C/T	0.342806	0.232136	intron-variant, downstream-variant-500B	RNF216, RNF216-IT1	GRCh38.p7	7:5661960	ACAGTGACCTGCTTT[C/T]GCTAGCAAACGCCAT	54476
rs852421	snp	A/C	0.241627	0.24986	intron-variant	RNF216	GRCh38.p7	7:5661265	AATAGAGTGAGACCC[A/C]ATCCCTTCGAAAAAC	54476
rs852437	snp	A/G	0.0475351	0.146656	utr-variant-3-prime	RNF216	GRCh38.p7	7:5622005	CCCCTGGCTTTCTGG[A/G]GGAGGAGTGGGCCTC	54476
rs852438	snp	C/G	0.25214	0.249991	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621780	CCCTGGGTTTCTAGC[C/G]GTGCCTGAGGCATCA	54476
rs852439	snp	A/G	0.0479149	0.147179	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621397	TTGGGAGGCCGAGGC[A/G]GGCGGATGAGTTGAG	54476
rs852440	snp	A/G	0.0482946	0.147699	utr-variant-3-prime	RNF216	GRCh38.p7	7:5621303	CCTATAATCCCAGGT[A/G]CTCAGGAGGCTGAGG	54476
rs852441	snp	C/T	0.274124	0.248833	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5621055	GGCAGCCTGCTGCTA[C/T]GTCCTTGCTGGCGCC	54476
rs852442	snp	A/T	0.251859	0.249993	utr-variant-3-prime, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5620426	GCACTGGGGGTCTTC[A/T]GACCAGCCAGCAAGG	54476
rs852443	snp	C/T	0.0322114	0.122752	downstream-variant-500B, upstream-variant-2KB	RNF216, LOC107986762	GRCh38.p7	7:5619754	TGCAGTCGGTTTCTT[C/T]TGCAGGCCCCTTCCC	54476
rs852448	snp	A/G	0.32885	0.23724	intron-variant	RNF216	GRCh38.p7	7:5632838	TTGGATCCCACTGTG[A/G]TCCATAGGTACACCT	54476
rs852449	snp	A/T	0.0460142	0.144533	intron-variant	RNF216	GRCh38.p7	7:5632573	gccaggctggtctcg[A/T]acccctgacatcagg	54476
rs852450	snp	A/G	0.328616	0.237317	intron-variant	RNF216	GRCh38.p7	7:5630930	CGATTCAGAAACCTG[A/G]GGGGTTATGTGGTTA	54476
rs852451	snp	C/G	0.0345262	0.126772	intron-variant	RNF216	GRCh38.p7	7:5630841	ctcatctgcagcgtg[C/G]caatcagttcatagt	54476
rs852452	snp	A/G	0.388964	0.20782	intron-variant	RNF216	GRCh38.p7	7:5630710	GTCACTGTGCTTGGC[A/G]CTTTATAAGAGTGAT	54476
rs852453	snp	C/T	0.304188	0.244057	intron-variant	RNF216	GRCh38.p7	7:5630041	TGTGTCCTAGATTTG[C/T]AGCGTGGCCTTTTTC	54476
rs852454	snp	C/T	0.47709	0.104548	intron-variant	RNF216	GRCh38.p7	7:5628435	GTTGTATTAAAGTTA[C/T]TAAGCACAGTGTCCT	54476
rs852455	snp	C/T	0.189261	0.242509	intron-variant	RNF216	GRCh38.p7	7:5628002	TCTGTATCAGAAACC[C/T]GGGCTCGCGCTCCTA	54476
rs852456	snp	A/G	0.466515	0.124985	intron-variant	RNF216	GRCh38.p7	7:5627783	GGGGAGAGTCTGAGG[A/G]AAAAAAGGGGGTTAG	54476
rs852457	snp	A/G	0.328148	0.237472	intron-variant	RNF216	GRCh38.p7	7:5626985	TGTTGGTTGTGATTA[A/G]TAACGGACCAGAGTG	54476
rs852458	snp	C/T	0.0345262	0.126772	intron-variant	RNF216	GRCh38.p7	7:5626226	GAAGGTAGTAAGTTC[C/T]CCCTTGTGGAGTGTT	54476
rs852459	snp	C/T	0.221141	0.248329	intron-variant	RNF216	GRCh38.p7	7:5626149	CTTATGTGTTAACCC[C/T]GGAGAGAGACAGCTC	54476
rs852460	snp	C/T	0.0482946	0.147699	intron-variant	RNF216	GRCh38.p7	7:5625708	CTGAAGTTTAATCAG[C/T]AAACTTAGAACAGTG	54476
rs852461	snp	A/C	0.334182	0.235401	intron-variant	RNF216	GRCh38.p7	7:5624972	GAGGGGGGTTAAGGT[A/C]AGCGCCACTCATGAA	54476
rs852462	snp	A/C	0.0429648	0.14013	intron-variant	RNF216	GRCh38.p7	7:5624426	CATATCCACCACTTG[A/C]ACGCAGCTCAGTGCA	54476
rs852463	snp	A/G			intron-variant	RNF216	GRCh38.p7	7:5647332	aaaaaaaaaaaaaaa[A/G]aaagaaagaaagaaa	54476
rs852464	snp	G/T	0	0	intron-variant	RNF216	GRCh38.p7	7:5647073	gcctcccagtggatt[G/T]tgttgaaagcatttg	54476
rs852465	snp	C/G	0.0325976	0.123435	intron-variant	RNF216	GRCh38.p7	7:5645623	agcgtggggacagag[C/G]aagactctgttgcaa	54476
rs852466	snp	C/T	0.0678174	0.1712	intron-variant	RNF216	GRCh38.p7	7:5644570	tgcagtgagctgata[C/T]tacactactgcactc	54476
rs852467	snp	A/G	0.0505692	0.150756	intron-variant	RNF216	GRCh38.p7	7:5644388	ctataataagatacc[A/G]cttcacacctattag	54476
rs852468	snp	A/G	0.325327	0.238382	intron-variant	RNF216	GRCh38.p7	7:5642892	CCACACCTTAAAGCC[A/G]CACCTCAGCCTCAGG	54476
rs852469	snp	C/T	0.202343	0.245416	intron-variant	RNF216	GRCh38.p7	7:5642562	gctgagacatgtgaa[C/T]cgtttgaacccagga	54476
rs852470	snp	A/G	0.0437281	0.141251	intron-variant	RNF216	GRCh38.p7	7:5640661	AACAATTCTATTAAC[A/G]TAAATCATTATATGG	54476
rs852471	snp	G/T	0.0926964	0.194308	intron-variant	RNF216	GRCh38.p7	7:5640222	ATAAACAAAGATTAG[G/T]GATACATGAAAAACT	54476
rs852472	snp	A/G	0.326035	0.238157	intron-variant	RNF216	GRCh38.p7	7:5639852	gaatggcgtgaaccc[A/G]ggaggcagagcttgc	54476
rs852473	snp	A/G	0.0879971	0.190408	intron-variant	RNF216	GRCh38.p7	7:5639461	aaaaaaTGTGGAGCC[A/G]TGTGTGGTGGCTCAT	54476
rs852474	snp	A/C	0.209997	0.246779	intron-variant	RNF216	GRCh38.p7	7:5639183	ctaaagagcctgctt[A/C]cctatctcttaagga	54476
rs852475	snp	A/C	0.0352966	0.128072	intron-variant	RNF216	GRCh38.p7	7:5638813	acccccatctttaca[A/C]aatatcaaaaattag	54476
rs852476	snp	A/G	0.0322114	0.122752	intron-variant	RNF216	GRCh38.p7	7:5637720	AAACTCCATCTCTAC[A/G]AAAAATCCCAAAGTT	54476
rs852477	snp	A/C	0.21695	0.247806	intron-variant	RNF216	GRCh38.p7	7:5637711	CTCTACAAAAAATCC[A/C]AAAGTTATCCAGGGG	54476
rs852514	snp	G/T	0.0463947	0.145069	intron-variant	RNF216	GRCh38.p7	7:5659924	TTAAAATATTAAGAA[G/T]AATAGTAATAAAGTC	54476
rs852515	snp	A/G	0.0611083	0.163768	intron-variant	RNF216	GRCh38.p7	7:5658425	ACGTGATCTGCCCAC[A/G]TCGGCTTCCCAGAGT	54476
rs852516	snp	A/G	0.252702	0.249985	intron-variant	RNF216	GRCh38.p7	7:5658297	TATGTTTCATTGTTG[A/G]AATGTTTGGTTTGAG	54476
rs852517	snp	G/T	0.371177	0.218669	intron-variant	RNF216	GRCh38.p7	7:5657948	CACATAACAGCCGAA[G/T]AAGGCTTGGTCCTTG	54476
rs852518	snp	A/G	0.0372196	0.131242	intron-variant	RNF216	GRCh38.p7	7:5657698	ACAACTAGAAGACAC[A/G]GATGGCCTGGAAGCC	54476
rs852519	snp	A/G	0.354418	0.227615	intron-variant	RNF216	GRCh38.p7	7:5656494	CCGTGGTTTCCCCCA[A/G]TCGGAAAGGCACAAG	54476
rs852520	snp	G/T	0.273587	0.248885	intron-variant	RNF216	GRCh38.p7	7:5655636	CTAGCTACATGGTCT[G/T]GTCTTGTCTTTTTTT	54476
rs852521	snp	C/T	0.121369	0.214369	intron-variant	RNF216	GRCh38.p7	7:5655392	CAGGCTGGTCTCTAA[C/T]GTCTGACCTCAGGTG	54476
rs852522	snp	C/T	0.263809	0.249618	intron-variant	RNF216	GRCh38.p7	7:5653912	CTCCAGGGCCATGCT[C/T]ACTGTCTGCAGTCCA	54476
rs852523	snp	C/T	0.0333695	0.124785	intron-variant	RNF216	GRCh38.p7	7:5652855	GAGAGAAATTTTTCC[C/T]TGTGCGTCCTTCTAA	54476
rs852524	snp	A/G	0.0356815	0.128715	intron-variant	RNF216	GRCh38.p7	7:5649991	tgttcaccaggttct[A/G]tctgcatgtcgttca	54476
rs852525	snp	A/C	0.040671	0.13668	intron-variant	RNF216	GRCh38.p7	7:5649487	gtgtcttattctgtc[A/C]tccaggctggaatac	54476

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