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
rs26837	snp	A/G	0.49889	0.0235361	intron-variant	E4F1	GRCh38.p7	16:2230317	AGGTCTGGATGGGCA[A/G]GCTCTCATCGGGGAC	1877
rs26838	snp	C/G	0.499598	0.0141716	intron-variant	E4F1	GRCh38.p7	16:2231150	CTAGTGGAGATGGCA[C/G]AGGGTCCTGCCTGCT	1877
rs26839	snp	A/G	0.0133536	0.0806142	missense, nc-transcript-variant	E4F1	GRCh38.p7	16:2232255	CCCCGGGCAGCCCCC[A/G]CCAGCAGGGGCTGGG	1877
rs26840	snp	C/T	0.477489	0.103676	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	E4F1, DNASE1L2	GRCh38.p7	16:2235356	CGACACCATCACCAT[C/T]GCCACCCCCGAGAGC	1877
rs27382	snp	A/G	0.49889	0.0235361	intron-variant	E4F1	GRCh38.p7	16:2230276	GATGTCTCTCTCCCT[A/G]ATGTGCTGTGGGAGG	1877
rs27709	snp	A/G	0.435263	0.167862	intron-variant	E4F1	GRCh38.p7	16:2231828	GCAGGACAGGCGGCT[A/G]TCTCTTCACCCAAGG	1877
rs30985	snp	A/G	0.00597247	0.0543191	intron-variant	E4F1	GRCh38.p7	16:2226663	AGTGTCAGGGACAGT[A/G]CCTGTTTACACAAAG	1877
rs30986	snp	A/G	0.432797	0.170544	intron-variant	E4F1	GRCh38.p7	16:2225866	cctcgggatccgccc[A/G]tctcagcctcccaaa	1877
rs30987	snp	A/G	0.499908	0.00678851	intron-variant	E4F1	GRCh38.p7	16:2225685	cgggagttcaagacc[A/G]gcctggccaacatgg	1877
rs30988	snp	A/G	0.499759	0.0109798	intron-variant	E4F1	GRCh38.p7	16:2224299	ACCCAGGATCAAAGA[A/G]CTAGAAAGCGGCAAG	1877
rs30989	snp	C/G	0.251014	0.249998	upstream-variant-2KB	E4F1	GRCh38.p7	16:2221605	ggagttcaagaccaa[C/G]caggccaacatggca	1877
rs313910	snp	G/T	0.175576	0.238665	intron-variant	E4F1	GRCh38.p7	16:2229370	ACCCTGGCCCGGGGG[G/T]GAAGGGATTGGACTG	1877
rs1056834	snp	C/G	0	0	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	E4F1, DNASE1L2	GRCh38.p7	16:2235260	GCAGATCGTGCACCA[C/G]GCTAGCGCCGGCCAC	1877
rs1056869	snp	C/T	0	0	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	E4F1, DNASE1L2	GRCh38.p7	16:2235620	ACAGGGCAGAGGACT[C/T]TGAGCGCCCCACCCA	1877
rs1612140	snp	A/G	0.164546	0.234942	intron-variant	E4F1	GRCh38.p7	16:2225767	AGACTGGGAGGAGCC[A/G]GGCACGGTGGCGCAC	1877
rs1640780	snp	C/T	0.164219	0.234823	intron-variant	E4F1	GRCh38.p7	16:2225699	CTGGTCTTGAACTCC[C/T]GACCTCAGGTGATCT	1877
rs1804823	snp	A/C/T	1.84862e-05	0.00304019	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	E4F1, DNASE1L2	GRCh38.p7	16:2235483	GTGACCATGGTGTCA[A/C/T]CAGAGGACATCGAGA	1877
rs2241070	snp	A/G	0.0966694	0.197458	synonymous-codon, nc-transcript-variant	E4F1	GRCh38.p7	16:2228508	CCCTGCCACCACAGC[A/G]TTGCTGGGCCAGGAG	1877
rs2241071	snp	A/G	0.373397	0.217424	intron-variant	E4F1	GRCh38.p7	16:2229369	GACCCTGGCCCGGGG[A/G]TGAAGGGATTGGACT	1877
rs2302584	snp	A/C/T	0.00207496	0.032143	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	E4F1, DNASE1L2	GRCh38.p7	16:2234763	CACGGCACGCTGAAC[A/C/T]GGCACCTGCGCACCA	1877
rs3096278	snp	C/T	0.165527	0.235296	intron-variant	E4F1	GRCh38.p7	16:2226088	TTTTTTCTTTCAAGG[C/T]GGAGTCTCGCTTTGT	1877
rs3114131	snp	C/G	0.202343	0.245416	intron-variant, upstream-variant-2KB	E4F1, DNASE1L2	GRCh38.p7	16:2234514	TCTCCCCTCCCGCCT[C/G]TGGCCCAAGGGAGGG	1877
rs8056361	snp	A/G	0.175897	0.238765	upstream-variant-2KB	E4F1	GRCh38.p7	16:2222891	gcctggcgtggtggc[A/G]gacacctgtagtccc	1877
rs8057731	snp	A/G	0.0479149	0.147179	upstream-variant-2KB	E4F1	GRCh38.p7	16:2222654	tggtttgaggctagg[A/G]gtttgagaccagcct	1877
rs9928419	snp	C/T			intron-variant	E4F1	GRCh38.p7	16:2225526	ttgcccaggctggag[C/T]gcaatggtgcgatct	1877
rs11640867	snp	C/T	0.000177984	0.00943188	intron-variant	E4F1	GRCh38.p7	16:2233668	TGCCAGCACCACCTG[C/T]GGGCTCCTCCCAGGG	1877
rs11641096	snp	A/G	0.495927	0.0449436	upstream-variant-2KB	E4F1	GRCh38.p7	16:2221670	aagtgctgggattac[A/G]ggagtgagccactgt	1877
rs11648028	snp	C/T	0.5	0	intron-variant	E4F1	GRCh38.p7	16:2231341	CCCCATCAGAGGCCT[C/T]TGTCCTTTGGAAGAT	1877
rs11648224	snp	C/G	0	0	intron-variant	E4F1	GRCh38.p7	16:2226492	TGCAGGCGAGTCATA[C/G]CTGTGGTTTGGCCCT	1877
rs12935005	snp	C/T	0	0	intron-variant, missense, nc-transcript-variant	E4F1	GRCh38.p7	16:2223849	CCCGGATGGCCCGAG[C/T]TGCGGGCTCGACCGA	1877
rs34008168	in-del	-/T			intron-variant	E4F1	GRCh38.p7	16:2227844	TTTTTTTTTTTTTTT[-/T]GGTAGAGATGGGTCT	1877
rs34062468	in-del	-/C			intron-variant	E4F1	GRCh38.p7	16:2228672	GGTGTGGGAGGGTCC[-/C]GGGTGTGTGAGCCTG	1877
rs34166917	in-del	-/T			intron-variant	E4F1	GRCh38.p7	16:2231555	AACCTGAACTGTGTT[-/T]ACAACCTAGCTTTGC	1877
rs34243234	in-del	-/T			intron-variant	E4F1	GRCh38.p7	16:2225490	CTTTTTTTTTTTTTT[-/T]GAGACGGCGTTTCTC	1877
rs34274744	in-del	-/T			upstream-variant-2KB	E4F1	GRCh38.p7	16:2222930	GGAGGCTGAGGCAGG[-/T]AGAATGGCGTGAACC	1877
rs34615954	snp	C/T			intron-variant	E4F1	GRCh38.p7	16:2230274	AAGATGTCTCTCTCC[C/T]TAATGTGCTGTGGGA	1877
rs35080768	in-del	-/T	0	0	intron-variant	E4F1	GRCh38.p7	16:2227844	TTTTTTTTTTTTTTT[-/T]GGTAGAGATGGGTCT	1877
rs35320604	in-del	-/G			downstream-variant-500B, upstream-variant-2KB	E4F1, DNASE1L2	GRCh38.p7	16:2235867	CCGCCCCACCCAGGG[-/G]CTTCTGCCAGCCCTG	1877
rs35337547	snp	C/T	0.0168055	0.0901129	synonymous-codon, nc-transcript-variant	E4F1	GRCh38.p7	16:2228385	GCGGCCGCATCTGTG[C/T]ACATCGTCCTCATCT	1877
rs35339015	in-del	-/G			intron-variant	E4F1	GRCh38.p7	16:2233814	GGGTGGGGCCCATGG[-/G]TTGTGTTCTTGGTAC	1877
rs35368180	in-del	-/GA	0.473451	0.112115	upstream-variant-2KB	E4F1	GRCh38.p7	16:2221663	CTCCCAAAGTGCTGG[-/GA]GATTACGGGAGTGAG	1877
rs35436732	snp	C/T	0.0729998	0.176553	intron-variant	E4F1	GRCh38.p7	16:2231323	CATGTTCCCCCAGGT[C/T]CTCCCCATCAGAGGC	1877
rs35483132	snp	C/T	0.0836354	0.186609	intron-variant	E4F1	GRCh38.p7	16:2231011	GCCCCTCTTGGCACC[C/T]CTGCCACTCTGGCAC	1877
rs35508264	snp	C/G	0.00528437	0.0511299	missense, nc-transcript-variant	E4F1	GRCh38.p7	16:2233474	GGTTCTCACGGCTGC[C/G]CTCGCTGGAGCAGGG	1877
rs35589455	in-del	-/G			intron-variant	E4F1	GRCh38.p7	16:2231669	CGTTCACTCTCCCAG[-/G]CCAAGCCTGCCTTGG	1877
rs35739041	in-del	-/C			frameshift-variant, intron-variant, nc-transcript-variant	E4F1	GRCh38.p7	16:2233509	CACCAGGCCATGCAG[-/C]AACTCCGGCATCGTC	1877
rs56828353	snp	A/G	0.0248432	0.108648	intron-variant	E4F1	GRCh38.p7	16:2229845	GCAGGAGGAGGAAGC[A/G]TTGGGCACTGGGCCT	1877
rs57106550	snp	C/T			intron-variant	E4F1	GRCh38.p7	16:2225691	TGGCCAGGCTGGTCT[C/T]GAACTCCCGACCTCA	1877
rs57862391	snp	A/G/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	E4F1	GRCh38.p7	16:2223517	CTCCGGTTCTGCCCC[A/G/T]CCCTCCTCTTGCCGT	1877
rs58584758	snp	C/T	0.0252325	0.109451	intron-variant	E4F1	GRCh38.p7	16:2234058	CGGGGTGCTTCTGGG[C/T]GTCCAGGGTGGGTCC	1877
rs58700030	snp	C/T			intron-variant	E4F1	GRCh38.p7	16:2225720	CAGGTGATCTGCCCG[C/T]CTCAGCCTCCCAAAG	1877
rs59007121	snp	C/T			intron-variant	E4F1	GRCh38.p7	16:2225714	CGACCTCAGGTGATC[C/T]GCCCGCCTCAGCCTC	1877
rs59101267	snp	A/G			intron-variant	E4F1	GRCh38.p7	16:2225865	CTTTGGGAGGCTGAG[A/G]CGGGCGGATCCCGAG	1877
rs59563983	snp	G/T	0.0287284	0.116357	intron-variant	E4F1	GRCh38.p7	16:2229747	GATGGGGCCCCTGCT[G/T]CCTGTATGCTCGTCT	1877
rs59620278	snp	A/T			intron-variant	E4F1	GRCh38.p7	16:2225661	ATTTTTAGTAGAGAC[A/T]GGATTTCTCCATGTT	1877
rs59759998	snp	C/T	0.0185399	0.0944786	intron-variant	E4F1	GRCh38.p7	16:2233843	ACTGCCAGGGCACAG[C/T]CTGCCCCGGGTGCTG	1877
rs59784157	snp	A/G/T	0.0112773	0.0742411	missense, nc-transcript-variant	E4F1	GRCh38.p7	16:2233444	CCCCTGCAGCCCCCC[A/G/T]TCTCCCAGGAGCTCC	1877
rs59845216	snp	G/T	0.0244538	0.107838	intron-variant	E4F1	GRCh38.p7	16:2233327	AGGGCCAGTGGGAGC[G/T]CCATGGGGGTCTGAG	1877
rs60013960	in-del	-/G			intron-variant	E4F1	GRCh38.p7	16:2229369	ACCCTGGCCCGGGGG[-/G]TGAAGGGATTGGACT	1877
rs60612119	snp	G/T	0.029116	0.117091	intron-variant	E4F1	GRCh38.p7	16:2231788	CCTATGTTGGTGGGA[G/T]CAGTGGCAGGAGCAG	1877
rs62040662	snp	G/T			intron-variant	E4F1	GRCh38.p7	16:2228798	TTCTTGGAGCTGGAG[G/T]GTCTCCTTTGGCTCT	1877
rs71394733	in-del	-/A	0.5	0	intron-variant	E4F1	GRCh38.p7	16:2227024	GCTCAAACTCCCGCA[-/A]GTTTTTGTTTGTTTG	1877
rs72766666	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	E4F1	GRCh38.p7	16:2222687	TCTAAACAGCAAGAC[C/T]CTGTCTCTATTTAAA	1877
rs73500107	snp	G/T	0.029116	0.117091	intron-variant	E4F1	GRCh38.p7	16:2226796	GGTGCTTGGCACACA[G/T]TGAGGGGGTGGTCTC	1877
rs74367875	snp	C/T	0.0182019	0.0936463	intron-variant	E4F1	GRCh38.p7	16:2224662	AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAGTGG	1877
rs74695663	snp	A/G	0.0209421	0.100162	downstream-variant-500B, upstream-variant-2KB	E4F1, DNASE1L2	GRCh38.p7	16:2235846	CTCCTAGACTCACGT[A/G]CCTGGCCGCCCCACC	1877
rs75636456	snp	A/G	0.0524604	0.153226	intron-variant	E4F1	GRCh38.p7	16:2231923	GGTCTCCCTGTGGAC[A/G]CATTTAGGGGCCCTG	1877
rs75956074	snp	G/T	0.5	0	intron-variant	E4F1	GRCh38.p7	16:2225489	TCTTTTTTTTTTTTT[G/T]TGAGACGGCGTTTCT	1877
rs76885746	snp	A/G	0.00716266	0.059414	intron-variant	E4F1	GRCh38.p7	16:2224387	GCCAGTAATGTAACA[A/G]GCCCTTATCCTGCTT	1877
rs77536843	snp	C/T	0.00993419	0.0697739	intron-variant	E4F1	GRCh38.p7	16:2230326	TGGGCAGGCTCTCAT[C/T]GGGGACAGATGCTTG	1877
rs78398423	snp	C/T	0.0325976	0.123435	downstream-variant-500B, upstream-variant-2KB	E4F1, DNASE1L2	GRCh38.p7	16:2235852	GACTCACGTGCCTGG[C/T]CGCCCCACCCAGGGG	1877
rs78729709	snp	G/T	0	0	intron-variant	E4F1	GRCh38.p7	16:2225491	TTTTTTTTTTTTTTT[G/T]AGACGGCGTTTCTCT	1877
rs79253733	snp	C/G	0.5	0	intron-variant	E4F1	GRCh38.p7	16:2224994	AAGGTGGGTGGATCA[C/G]CTGAGGTCAGGAGTT	1877
rs79982505	snp	A/C	0.00159617	0.0282053	intron-variant	E4F1	GRCh38.p7	16:2230456	AGACGCGAGGGAAGG[A/C]GCTGTCTAGGGACCT	1877
rs80084951	snp	A/C	0.5	0	missense, intron-variant, nc-transcript-variant	E4F1	GRCh38.p7	16:2233553	CTGGGGAGGAGGGTG[A/C]CCTGGAGCCAGCTCC	1877
rs111361324	snp	C/T			intron-variant	E4F1	GRCh38.p7	16:2224956	AGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG	1877
rs111514458	snp	A/G	0.5	0	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	E4F1	GRCh38.p7	16:2223501	CCTGTCCGTCAATCC[A/G]CTCCGGTTCTGCCCC	1877
rs111767084	in-del	-/G	0.17461	0.238362	intron-variant	E4F1	GRCh38.p7	16:2229364	CGCTGACCCTGGCCC[-/G]GGGGGTGAAGGGATT	1877
rs111797145	snp	A/C	0.5	0	intron-variant	E4F1	GRCh38.p7	16:2231330	CCCCAGGTCCTCCCC[A/C]TCAGAGGCCTCTGTC	1877
rs112325888	in-del	-/T	0	0	intron-variant	E4F1	GRCh38.p7	16:2225806	AAAAAAAAAAAAAAA[-/T]AAAAAAAGGCTGGGC	1877
rs112564078	snp	C/T	0.5	0	intron-variant	E4F1	GRCh38.p7	16:2229002	CCGCACACGCCGCAG[C/T]GGGCGCTTGTCATCC	1877
rs112862402	snp	C/T	0.000798403	0.0199641	intron-variant	E4F1	GRCh38.p7	16:2231823	AGCGAGCAGGACAGG[C/T]GGCTGTCTCTTCACC	1877
rs112919582	snp	A/T	0.128632	0.218563	intron-variant	E4F1	GRCh38.p7	16:2225810	AAAAAAAAAAAAAAA[A/T]AAAGGCTGGGCGCAA	1877
rs112938340	snp	A/C/G/T	0.000302858	0.0123026	intron-variant, upstream-variant-2KB	E4F1, DNASE1L2	GRCh38.p7	16:2234790	ACCAAAGGTCTGGGC[A/C/G/T]GGTGGAGGTGGGAGG	1877
rs112969870	snp	A/G	0.5	0	upstream-variant-2KB	E4F1	GRCh38.p7	16:2222816	TCACGAGGTCAGGAG[A/G]TCGAGACCATCCTGG	1877
rs113062677	snp	C/T	0.0244538	0.107838	intron-variant	E4F1	GRCh38.p7	16:2225144	CTTGAGCCCAGGAGA[C/T]GGAGGTCGCAGTAAG	1877
rs113244233	snp	A/G	0.5	0	intron-variant	E4F1	GRCh38.p7	16:2225497	TTTTTTTTTGAGACG[A/G]CGTTTCTCTCTTGTT	1877
rs113268992	snp	A/G	0.00636936	0.0560724	upstream-variant-2KB	E4F1	GRCh38.p7	16:2221577	TTTTGTATTTTTAGT[A/G]AAGACGTAATTTTGC	1877
rs113270919	snp	C/G/T	6.98731e-05	0.00591036	missense, synonymous-codon, intron-variant, nc-transcript-variant	E4F1	GRCh38.p7	16:2234184	AGGGCCGAGGCCGTT[C/G/T]GCCTGCGCGCAGTGT	1877
rs113465416	snp	A/G	0.0146672	0.084371	intron-variant	E4F1	GRCh38.p7	16:2226397	GAGTAGGGTGGGAAG[A/G]GGAAGAGGGTGGTGG	1877
rs113710566	snp	C/T	0.5	0	intron-variant	E4F1	GRCh38.p7	16:2232698	TGCCTGCCTTCGCCT[C/T]GTCACCTTGTCGCCA	1877
rs113976652	snp	A/C/T	0.000399281	0.0141238	intron-variant	E4F1	GRCh38.p7	16:2229560	CCCTGTTTTCTTCCC[A/C/T]CTTTGGCAGGTGGTG	1877
rs114147924	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	E4F1, DNASE1L2	GRCh38.p7	16:2235854	CTCACGTGCCTGGCC[A/G]CCCCACCCAGGGGCT	1877
rs114578394	snp	A/G	0.0524604	0.153226	downstream-variant-500B, upstream-variant-2KB	E4F1, DNASE1L2	GRCh38.p7	16:2235918	GGGTGTCATTGGCAT[A/G]TTGACCAACAGCCTC	1877
rs115208946	snp	A/G	0.000399281	0.0141238	intron-variant	E4F1	GRCh38.p7	16:2230188	GTGGGAGTGGTGATT[A/G]CTACACTGGTCCTCA	1877
rs115624510	snp	A/G	0.000720898	0.0189718	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	E4F1, DNASE1L2	GRCh38.p7	16:2235460	CAAGTGGCACTGAAC[A/G]GGCCACTGTGACCAT	1877
rs116064450	snp	G/T	0.00874735	0.0655527	upstream-variant-2KB	E4F1	GRCh38.p7	16:2223198	CCCTGGTTGGAGCTG[G/T]GGCGGCTTCCCAGCA	1877
rs117057799	snp	C/T	0.000374366	0.0136764	intron-variant	E4F1	GRCh38.p7	16:2232371	TTCAAGACGGTGAGC[C/T]GGCGTGCGGGGAGCC	1877
rs117454577	snp	C/T	0.0146672	0.084371	intron-variant	E4F1	GRCh38.p7	16:2231966	GCAGCCTGACAGAGT[C/T]GGGAGGTGTCTCTCC	1877
rs137969975	snp	A/G	0.000466656	0.0152679	missense, intron-variant, nc-transcript-variant	E4F1	GRCh38.p7	16:2234191	AGGCCGTTCGCCTGC[A/G]CGCAGTGTGGCAAGG	1877

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