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
rs868934	snp	C/T	0.45866	0.137698	upstream-variant-2KB	RNF7	GRCh38.p7	3:141736939	GAATGCATTAATATA[C/T]AGAAACATAAATATG	9616
rs1065369	snp	C/T	0.00119737	0.0244387	intron-variant	RNF7	GRCh38.p7	3:141738934	CTGAATCACGGCCTT[C/T]ACCCTGACCACCTTG	9616
rs1829258	snp	A/G	0.459004	0.137176	upstream-variant-2KB	RNF7	GRCh38.p7	3:141736683	CCACTGGCCCTGAAG[A/G]CCTCCCATGTTCCCC	9616
rs1879284	snp	A/G	0.159622	0.233092	intron-variant	RNF7	GRCh38.p7	3:141739888	CCACCATGCCTGGTC[A/G]GCTTTTTATTTTAAT	9616
rs1879285	snp	C/T	0.159622	0.233092	intron-variant	RNF7	GRCh38.p7	3:141739881	GCCTGGTCAGCTTTT[C/T]ATTTTAATTTTTAAT	9616
rs1879286	snp	C/T	0.0528381	0.153711	intron-variant	RNF7	GRCh38.p7	3:141739808	ACTCCTGGGCTCAAG[C/T]GATCCATGTAAAATA	9616
rs1980190	snp	A/G	0.472335	0.114312	intron-variant	RNF7	GRCh38.p7	3:141739156	GCGTGGCTTGAAGGG[A/G]ACAGTGTGGTTCAAG	9616
rs1980191	snp	A/T	0.332106	0.236133	upstream-variant-2KB	RNF7	GRCh38.p7	3:141737833	ATCTTTAAGATCATT[A/T]ATTCACTCAACAAAT	9616
rs1980192	snp	A/G	0.169435	0.236663	upstream-variant-2KB	RNF7	GRCh38.p7	3:141737984	CAAGATAATTTCTGA[A/G]AGCAGTAGGTTTAAT	9616
rs2681694	snp	C/T	0.117537	0.212022	upstream-variant-2KB	RNF7	GRCh38.p7	3:141737528	CCTGTAATGAGGTTA[C/T]TACTGTGATTTTTAA	9616
rs3052146	in-del	-/AATA	0.154661	0.231107	upstream-variant-2KB	RNF7	GRCh38.p7	3:141737628	TACAGGAAATGTATG[-/AATA]TATATATGAATATAC	9616
rs3052148	in-del	-/AT			upstream-variant-2KB	RNF7	GRCh38.p7	3:141737709	tatatatatatatat[-/AT]tTACACATTTcctac	9616
rs3184648	snp	A/G	0.210875	0.246919	utr-variant-3-prime, nc-transcript-variant	RNF7	GRCh38.p7	3:141745304	AGGCTTCTTAGCGCA[A/G]TTGTTCAGAGCCCTG	9616
rs3773840	snp	A/G	0.159622	0.233092	downstream-variant-500B	RNF7	GRCh38.p7	3:141746949	AAAGGTCAAACAGAA[A/G]GTTACTAAAACAGTT	9616
rs3836425	in-del	-/G/GC			upstream-variant-2KB	RNF7	GRCh38.p7	3:141738152	GCCAGCGCCAGGGGG[-/G/GC]GGGCAGGCCCCGCCC	9616
rs4538350	snp	A/G	0.157642	0.232314	intron-variant	RNF7	GRCh38.p7	3:141739226	TTTTTTCAGAAACGT[A/G]AAACTTCACCTCCAT	9616
rs6769676	snp	G/T	0.472616	0.113763	intron-variant	RNF7	GRCh38.p7	3:141743005	CAGAAATTGAGGAAG[G/T]TATGTATATTACCTG	9616
rs6785010	snp	A/C	0.147321	0.227941	intron-variant	RNF7	GRCh38.p7	3:141744347	CTTTTTTTCTGCCTT[A/C]TTTCTTTCATTTAAT	9616
rs6785106	snp	A/G	0.147321	0.227941	intron-variant	RNF7	GRCh38.p7	3:141744425	ATAGCTCAGTTGATC[A/G]AGCAAGGGACAGATG	9616
rs9789959	snp	C/T	0.170084	0.236883	upstream-variant-2KB	RNF7	GRCh38.p7	3:141737961	GAAGAGACAAACGAA[C/T]AAATTAACAAGATAA	9616
rs9789973	snp	G/T	0.159622	0.233092	intron-variant	RNF7	GRCh38.p7	3:141741927	AGTAATTTATTAAAA[G/T]ACTTTACCATTGTTG	9616
rs9789997	snp	A/G	0.45946	0.136478	intron-variant	RNF7	GRCh38.p7	3:141742099	CATCACCCAGGTATT[A/G]AGCCTAGTACCCATT	9616
rs9790069	snp	G/T	0.0528381	0.153711	intron-variant	RNF7	GRCh38.p7	3:141741690	ATTAAGCTGATAGTA[G/T]TCCAGATTGAATTTT	9616
rs9790073	snp	C/T	0.0528381	0.153711	intron-variant	RNF7	GRCh38.p7	3:141741845	AATAACCCATACATA[C/T]AATGTTAGTATTTGT	9616
rs9790075	snp	A/T	0.257732	0.24988	intron-variant	RNF7	GRCh38.p7	3:141741997	CTTTCTTTTTTTTTT[A/T]AAAAAAACTTTTAGG	9616
rs10660073	in-del	-/GAG			intron-variant	RNF7	GRCh38.p7	3:141743026	GTATATTACCTGGAA[-/GAG]GAGTGAAAACTCTCC	9616
rs11452917	in-del	-/A	0.158962	0.232835	intron-variant	RNF7	GRCh38.p7	3:141741785	AGTTACTATAAGCTC[-/A]ACTGGGCATGCTCAT	9616
rs11542226	snp	C/T	0.0930568	0.194599	utr-variant-3-prime, nc-transcript-variant	RNF7	GRCh38.p7	3:141745389	TCTTCAAATAGGAGC[C/T]GATGGATCTGTGGTC	9616
rs11918543	snp	C/T	0.147321	0.227941	utr-variant-3-prime, nc-transcript-variant	RNF7	GRCh38.p7	3:141746286	ctggccCAGATGATA[C/T]AATTTAACTGTGTTT	9616
rs16851717	snp	A/G	0.159622	0.233092	intron-variant	RNF7	GRCh38.p7	3:141743906	TCACTTTTGGTTCTA[A/G]TAAGGCATTTCACTT	9616
rs16851720	snp	A/C	0.302435	0.244439	intron-variant	RNF7	GRCh38.p7	3:141744456	AATCCCAAATTCGAG[A/C]TTGCATTCTAGATTG	9616
rs17195449	snp	G/T	0.127944	0.218179	intron-variant	RNF7	GRCh38.p7	3:141744961	AACAGTGATGGAAAG[G/T]CTCTCAAACAGTGAC	9616
rs17850027	snp	C/G/T	7.30034e-05	0.00604122	synonymous-codon, nc-transcript-variant	RNF7	GRCh38.p7	3:141738455	GAAGTGGAACGCGGT[C/G/T]GCCATGTGGAGCTGG	9616
rs34131180	in-del	-/C			upstream-variant-2KB	RNF7	GRCh38.p7	3:141738112	ATAAGGGCCCGAGCC[-/C]TCTCAGTTGGCCTAG	9616
rs34247627	in-del	-/C			frameshift-variant, nc-transcript-variant	RNF7	GRCh38.p7	3:141745203	ACAACTGCTGCATGT[-/C]CCCTGTGGGTGAAAC	9616
rs34462617	in-del	-/G			upstream-variant-2KB	RNF7	GRCh38.p7	3:141738103	CGTCGCCCCATAAGG[-/G]CCCGAGCCCTCTCAG	9616
rs34529210	in-del	-/TA			upstream-variant-2KB	RNF7	GRCh38.p7	3:141737708	GTATATATATATATA[-/TA]TTTACACATTTCCTA	9616
rs34684789	in-del	-/T			intron-variant	RNF7	GRCh38.p7	3:141739669	AGAATCAAGAGATTT[-/T]CGCAGTTTATGCTCT	9616
rs35165405	in-del	-/AT			upstream-variant-2KB	RNF7	GRCh38.p7	3:141737635	AATGTATGTATATAT[-/AT]GAATATACATATATT	9616
rs35208508	in-del	-/G			intron-variant	RNF7	GRCh38.p7	3:141741788	TACTATAAGCTCACT[-/G]GGGCATGCTCATGGG	9616
rs35306264	snp	C/T			upstream-variant-2KB	RNF7	GRCh38.p7	3:141738157	GGCCTGCCCGCCCCC[C/T]TGGCGCTGGCGTCAG	9616
rs35404891	in-del	-/G			intron-variant	RNF7	GRCh38.p7	3:141740924	CTTTCTGCTCCCAAG[-/G]ACTTGCCTGTCAGCC	9616
rs35463789	in-del	-/T			intron-variant	RNF7	GRCh38.p7	3:141740495	TATAGCAAGTATTCT[-/T]GCTACTACAGGATCA	9616
rs35717595	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	RNF7	GRCh38.p7	3:141745528	GTGTGTGTCGCGCAC[-/A]CAGCTTAGAAGTGCT	9616
rs35765606	snp	C/T			upstream-variant-2KB	RNF7	GRCh38.p7	3:141738154	CGGGGCCTGCCCGCC[C/T]CCCTGGCGCTGGCGT	9616
rs35786989	in-del	-/AATA			upstream-variant-2KB	RNF7	GRCh38.p7	3:141737629	ACAGGAAATGTATGT[-/AATA]ATATATGAATATACA	9616
rs35815506	in-del	-/C			intron-variant	RNF7	GRCh38.p7	3:141738706	CCTGAGGGCTGCGGC[-/C]GCCGCCTGGGGCTGC	9616
rs35928742	in-del	-/GCCC			intron-variant	RNF7	GRCh38.p7	3:141738544	CGCGAGTCCAGGGCC[-/GCCC]TGCGGCCTCCGGGAG	9616
rs57365200	in-del	-/T	0.243919	0.249926	intron-variant	RNF7	GRCh38.p7	3:141739211	AAGAATTGTAAGCCC[-/T]TTTTTCAGAAACGTA	9616
rs59998648	snp	C/T	0.145978	0.227331	upstream-variant-2KB	RNF7	GRCh38.p7	3:141736248	GCAGTGTGTCAAAAC[C/T]GTACTCATCTCCTCC	9616
rs72998395	snp	A/C/G	0.152799	0.230723	intron-variant	RNF7	GRCh38.p7	3:141741763	TACACCTACTCCACT[A/C/G]TATTAGAAGTTACTA	9616
rs72998398	snp	A/G	0.0466346	0.145407	intron-variant	RNF7	GRCh38.p7	3:141743490	ATCAGAATGAGAATC[A/G]CTATTTGTTTACTTT	9616
rs73226658	snp	A/G	0.00398564	0.0444627	downstream-variant-500B	RNF7	GRCh38.p7	3:141747262	CTGAAAGTTTAATAC[A/G]TACTCATCAGAGGGA	9616
rs73870348	snp	A/G	0.0379877	0.132479	upstream-variant-2KB	RNF7	GRCh38.p7	3:141737323	GGAGCGGGGCCTGAA[A/G]AATAAGTGTGGGTTG	9616
rs73870349	snp	A/G	0.00795532	0.062565	intron-variant	RNF7	GRCh38.p7	3:141740370	AGTAAGTGGAAATGT[A/G]TAACCTGAAATAATG	9616
rs73870351	snp	A/G	0.00874735	0.0655527	intron-variant	RNF7	GRCh38.p7	3:141743444	GCTTTTGACTTTGAA[A/G]TGTCTGGTTTTTAAA	9616
rs74776152	snp	C/T	0.0103295	0.0711199	intron-variant	RNF7	GRCh38.p7	3:141744871	GAAGGTTCAAGAACA[C/T]TCATCTAACTTCAAG	9616
rs75171144	snp	A/G	0.226779	0.248919	intron-variant	RNF7	GRCh38.p7	3:141740126	CCACTTAGGAATCAT[A/G]ATTTCTAGTTTGGGA	9616
rs75854649	snp	A/C	0.0980852	0.198549	upstream-variant-2KB	RNF7	GRCh38.p7	3:141736426	CATCCTTTTGACTTT[A/C]AAACTTCTCACCAAC	9616
rs76037255	snp	C/T	0	0	intron-variant	RNF7	GRCh38.p7	3:141740169	TGATCCAGGAGACTC[C/T]TTTTTTTTTTTTTTA	9616
rs76285412	snp	C/G	0.158962	0.232835	utr-variant-3-prime, nc-transcript-variant	RNF7	GRCh38.p7	3:141745873	GTTACTATTCTGTAT[C/G]ATTGATTCATCAAGA	9616
rs76642309	snp	A/T	0.0603597	0.1629	upstream-variant-2KB	RNF7	GRCh38.p7	3:141738013	ATGAAGCCGTAAAGC[A/T]GGACACATATCCCTG	9616
rs76776164	snp	A/G			downstream-variant-500B	RNF7	GRCh38.p7	3:141746920	GCCATTTAAATGTTT[A/G]TCATTGTGCAGTGAA	9616
rs77870385	snp	G/T	0.169908	0.237249	intron-variant	RNF7	GRCh38.p7	3:141739636	CTCACCTTAAGGGGG[G/T]TGAGACTGTAAACAT	9616
rs77971862	snp	A/G	0.0130921	0.0798413	intron-variant	RNF7	GRCh38.p7	3:141744618	AAATTTCATCGTCAC[A/G]TGAGGAATTGCACTG	9616
rs78477651	snp	C/T	0.0879971	0.190408	intron-variant	RNF7	GRCh38.p7	3:141743988	TCTAAGTCTCAAGTA[C/T]ATTTTTGGAATGTGG	9616
rs79073808	snp	C/T	0.0248432	0.108648	utr-variant-3-prime, nc-transcript-variant	RNF7	GRCh38.p7	3:141745467	TTCAGAAATTCTCTG[C/T]GATTAAGAAGATAAT	9616
rs80061564	snp	A/G	0.0825414	0.185628	intron-variant	RNF7	GRCh38.p7	3:141738799	AAACGGAGTTAAACA[A/G]GGTAATTTCAGGTAG	9616
rs80238227	snp	A/G	0.159622	0.233092	intron-variant	RNF7	GRCh38.p7	3:141744191	GTTTGCATGGTGTAC[A/G]TAGAACACAAATACA	9616
rs111262302	snp	A/G	0	0	intron-variant	RNF7	GRCh38.p7	3:141742156	TTCCACCCTCCAAAA[A/G]GCCCCAGTGTGTGTT	9616
rs111369760	snp	A/G	0.147321	0.227941	intron-variant	RNF7	GRCh38.p7	3:141742105	CCAGGTATTGAGCCT[A/G]GTACCCATTAGTTAT	9616
rs111558867	snp	A/G	0.0023933	0.0345097	intron-variant	RNF7	GRCh38.p7	3:141738572	CGGGAGCCGACCTCG[A/G]GGTTGGGAAGGGACG	9616
rs111796549	snp	A/G	0.5	0	intron-variant	RNF7	GRCh38.p7	3:141743660	CAATACACAAAAATA[A/G]ACTGTAAAGCAGTGA	9616
rs111805180	snp	A/C			intron-variant	RNF7	GRCh38.p7	3:141738692	CTCCTGCTGCGGCTC[A/C]TGAGGGCTGCGGCCG	9616
rs111814392	snp	A/G	0.5	0	intron-variant	RNF7	GRCh38.p7	3:141743304	AATAGAGGATTTGTT[A/G]ACCCTTGTGAAATTG	9616
rs112162512	snp	A/G	0.00676609	0.0577691	intron-variant	RNF7	GRCh38.p7	3:141744785	AATAAAAATTGGAAG[A/G]ACATTTTCCCATAAA	9616
rs112619890	snp	A/C	0.0271762	0.113356	intron-variant	RNF7	GRCh38.p7	3:141742311	GGCTCACTGCAAGCT[A/C]TGCCTCCTGGGTTCA	9616
rs113738510	snp	G/T	0.000798403	0.0199641	intron-variant	RNF7	GRCh38.p7	3:141740204	AAGTTTCGCTAAACA[G/T]TTTATCTCCTAAATA	9616
rs114584193	snp	C/T	0.0197687	0.0974348	upstream-variant-2KB	RNF7	GRCh38.p7	3:141737974	AATAAATTAACAAGA[C/T]AATTTCTGAGAGCAG	9616
rs115219219	snp	A/T	0.0248432	0.108648	intron-variant	RNF7	GRCh38.p7	3:141742004	TTTTTTTTTAAAAAA[A/T]CTTTTAGGTTCAGGG	9616
rs115267388	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	RNF7	GRCh38.p7	3:141737160	GGAAACACATGTGAT[G/T]GTGGGCTAGCCGTAG	9616
rs116335480	snp	C/T	0.158962	0.232835	intron-variant	RNF7	GRCh38.p7	3:141741792	TATAAGCTCACTGGG[C/T]ATGCTCATGGGCAGT	9616
rs116389135	snp	A/G	0.0626037	0.165477	utr-variant-3-prime, nc-transcript-variant	RNF7	GRCh38.p7	3:141746665	GATATGAATTTAAGA[A/G]AAAACCTTAGAATCT	9616
rs116444897	snp	C/T	0.0663309	0.169604	intron-variant	RNF7	GRCh38.p7	3:141744297	TTCACCCTTGCTTCC[C/T]ACCCCCTGTAGCCAA	9616
rs117481781	snp	A/G	0.0528381	0.153711	intron-variant	RNF7	GRCh38.p7	3:141743944	CTCTTATAATACAGT[A/G]TTTAACTTTAAAACC	9616
rs137871830	in-del	-/TG	0.225005	0.248747	intron-variant	RNF7	GRCh38.p7	3:141738683	GAGCCACGCTCCTGC[-/TG]TGCGGCTCCTGAGGG	9616
rs138166487	snp	C/T	0.00676609	0.0577691	intron-variant	RNF7	GRCh38.p7	3:141738604	GCGTCCGTCAGAAGC[C/T]TCGGAAAGTGCCCTG	9616
rs138261482	snp	A/C	0.0678174	0.1712	intron-variant	RNF7	GRCh38.p7	3:141741410	TTGTTTTTAATCCAC[A/C]CTGAAGAGACTAGGG	9616
rs138840258	snp	C/G	0.00636936	0.0560724	intron-variant	RNF7	GRCh38.p7	3:141739752	TTCAGATATTTTTAT[C/G]TTTCTCTTTTGAAAG	9616
rs139318917	snp	A/G	0.00159617	0.0282053	downstream-variant-500B	RNF7	GRCh38.p7	3:141747219	TGCTGCTCAGCCTGC[A/G]ATGATTACAGCTCAT	9616
rs140291324	snp	A/C			intron-variant	RNF7	GRCh38.p7	3:141744343	TTTTCTTTTTTTCTG[A/C]CTTATTTCTTTCATT	9616
rs141023810	in-del	-/C	0.159622	0.233092	utr-variant-3-prime, nc-transcript-variant	RNF7	GRCh38.p7	3:141746554	CAAGAAAATACTAAA[-/C]AACTTTATCAAACTG	9616
rs141114694	snp	A/G	0.00119737	0.0244387	intron-variant	RNF7	GRCh38.p7	3:141744622	TTCATCGTCACATGA[A/G]GAATTGCACTGCTTA	9616
rs141479027	snp	A/G	0.0528381	0.153711	intron-variant	RNF7	GRCh38.p7	3:141740143	TTTCTAGTTTGGGAA[A/G]CATTTTTAACTGATC	9616
rs142106107	snp	A/G	0.00318978	0.0398085	intron-variant	RNF7	GRCh38.p7	3:141744054	CAAAAGTTGTCGTAG[A/G]CTAAATATTTTAGGC	9616
rs142463798	in-del	-/TTTC	0.00364892	0.0425575	intron-variant	RNF7	GRCh38.p7	3:141745153	TCTTCTTTTTCTTTC[-/TTTC]AGTGGTCTGGGGAGA	9616
rs142492597	in-del	-/ACA	0.159622	0.233092	cds-indel, nc-transcript-variant	RNF7	GRCh38.p7	3:141745599	TTTACCCATTTCTAT[-/ACA]ACAGGCAGTGGAAGC	9616
rs142752523	snp	C/T	0.02016	0.0983543	intron-variant	RNF7	GRCh38.p7	3:141738880	GGAAACACTTCGGTT[C/T]GTGTGTCCAGCCCCA	9616
rs143654555	in-del	-/TTTCA	0.0103295	0.0711199	utr-variant-3-prime, nc-transcript-variant	RNF7	GRCh38.p7	3:141746454	TTGTCAAGTAAATAC[-/TTTCA]TTTAATTTGAAAGAA	9616
rs143709172	snp	A/C	0.0681886	0.171594	RNF7	3	allele_origin=A(somatic)/C(germline)	3:141746225	CAGGTGATTCGCCCA[A/C]CTCAGCCTCCCAAAG	9616

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