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
rs14542	snp	C/T	0.0596104	0.162024	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650772	AAAGCAGGAAGGGAA[C/T]GGAGAAGAAAAGTGT	51147
rs2365101	snp	C/T	0.243919	0.249926	intron-variant	ING4	GRCh38.p7	12:6651645	ctcccgagttcaagc[C/T]attctcctgcctcag	51147
rs2365102	snp	C/T	0.251014	0.249998	intron-variant	ING4	GRCh38.p7	12:6651784	tgatctcaagtgatc[C/T]gctcaccttggcctc	51147
rs3809244	snp	A/C	0.258843	0.249844	upstream-variant-2KB	ING4	GRCh38.p7	12:6663709	TGAGAAAGATGATCA[A/C]CTTTCTACTTATAAA	51147
rs3809245	snp	C/T	0.228253	0.249052	upstream-variant-2KB	ING4	GRCh38.p7	12:6664435	TTAGTAAGATAGTAT[C/T]TTAGAGATAGCTGCC	51147
rs4764503	snp	A/G	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6659293	gctagaattacaggc[A/G]tgagccaccgtgcct	51147
rs4764504	snp	A/G	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6659179	CACCTGCCTTCCAGA[A/G]TGCTGGATTACAGGC	51147
rs4764505	snp	A/G	0.0107246	0.0724382	intron-variant	ING4	GRCh38.p7	12:6658962	ATGGGATGAGGAAAA[A/G]CGAGCGGTGCATTCC	51147
rs4764506	snp	A/G	0.0667028	0.170006	intron-variant	ING4	GRCh38.p7	12:6652860	TCTTCATCTGGTGGG[A/G]AGTTTGGCACCAGGT	51147
rs4764615	snp	A/G	0.396	0.202938	intron-variant	ING4	GRCh38.p7	12:6657031	aagtagctgggatta[A/G]agatgcccaccgtca	51147
rs4764616	snp	C/T	0.284733	0.247575	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655665	CAAAAACCCTGGACA[C/T]AGTTCCCTGAGAACT	51147
rs4764617	snp	C/T	0.251859	0.249993	intron-variant	ING4	GRCh38.p7	12:6655326	ccgggtgcggtggct[C/T]acgcctgtaatccca	51147
rs4764618	snp	A/G	0.411074	0.191194	intron-variant	ING4	GRCh38.p7	12:6655192	GTCGGGTGTGGTGGC[A/G]CATGCCAGTAATCCC	51147
rs4764619	snp	C/G	0.251859	0.249993	intron-variant	ING4	GRCh38.p7	12:6654816	AATCCCTTGAACCCA[C/G]GAGGCAGAGGTTGAG	51147
rs5796244	in-del	-/G			intron-variant	ING4	GRCh38.p7	12:6661079	AAGGCTGGGAGCGGT[-/G]GCTCACGCCTATAAT	51147
rs6416323	snp	C/T	0.284995	0.247539	intron-variant	ING4	GRCh38.p7	12:6657480	aaacaaaaaataaaG[C/T]GCAGCTCAGTTTTCC	51147
rs7316048	snp	C/T	0.039522	0.134904	intron-variant	ING4	GRCh38.p7	12:6652106	ctcacgtgatctgcc[C/T]gcctcagcctcccaa	51147
rs7397940	snp	G/T	0.251859	0.249993	intron-variant	ING4	GRCh38.p7	12:6662711	GAGGTCTTTACCGCT[G/T]CTCCAAATGGCAGTG	51147
rs7958346	snp	G/T	0.0471551	0.14613	intron-variant	ING4	GRCh38.p7	12:6659437	gcttaaatccgggag[G/T]tggaggttgcagtga	51147
rs7961940	snp	C/T	0.0577344	0.159793	downstream-variant-500B	ING4	GRCh38.p7	12:6650402	CCCTGGTCTGAGGCC[C/T]ACCCTCCAGCACCTC	51147
rs7962047	snp	C/T	0.0209421	0.100162	downstream-variant-500B	ING4	GRCh38.p7	12:6650513	GCCATCCTCTCACAT[C/T]GCATCCAACCCAGAG	51147
rs7964213	snp	C/T	0.13446	0.221699	intron-variant	ING4	GRCh38.p7	12:6655333	acaggcgtaagccac[C/T]gcacccggccCCAAA	51147
rs7979340	snp	C/G	0.0475351	0.146656	intron-variant	ING4	GRCh38.p7	12:6657329	tggcgggcgcctgta[C/G]tcccagctactcagg	51147
rs7979794	snp	C/T	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6659608	acgaggtcaggagat[C/T]gagaccatcctggct	51147
rs10849494	snp	G/T	0.197531	0.244432	intron-variant	ING4	GRCh38.p7	12:6661414	AGCCTTTGTTTTTTT[G/T]TTTTTTTTTTTTTTT	51147
rs11064301	snp	C/T	0.00517822	0.0506191	downstream-variant-500B	ING4	GRCh38.p7	12:6650479	ACTCTGGTTTCATGT[C/T]GTGTCCTAATTCTGG	51147
rs11064302	snp	G/T	0.00795532	0.062565	intron-variant	ING4	GRCh38.p7	12:6651504	TTTGGAGAATTCTTG[G/T]AAGTCCCAAGGCCAA	51147
rs11064303	snp	A/G	0.0422008	0.138995	intron-variant	ING4	GRCh38.p7	12:6653704	TCCATGTTTGAAGAT[A/G]CTTCTTTGAAGGGCT	51147
rs11064304	snp	A/G	0.0138799	0.0821421	intron-variant	ING4	GRCh38.p7	12:6653992	CTCAGGCACCACCAC[A/G]CCTGGCTAATTTTTT	51147
rs11064305	snp	C/T	0.0130921	0.0798413	intron-variant	ING4	GRCh38.p7	12:6654013	CTAATTTTTTCTATT[C/T]TTTTGTAGAGACAGG	51147
rs11064306	snp	A/C	0.281577	0.247998	intron-variant	ING4	GRCh38.p7	12:6654864	CAAGTAGCTGGGACT[A/C]CAGGTGTGCGCCACC	51147
rs11551179	snp	C/T	0	0	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652971	GAGCTGTCATAGTCA[C/T]TTGACTCAATCTGTT	51147
rs12300751	snp	C/T	0.00557542	0.0525036	intron-variant	ING4	GRCh38.p7	12:6660015	TCTCCCcaggccgaa[C/T]atggctatcatattc	51147
rs12306554	snp	A/T	0.136506	0.222754	intron-variant	ING4	GRCh38.p7	12:6654507	cctgataattttttt[A/T]aaaaaattatttcta	51147
rs12311071	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6661271	cctggctattttttt[A/T]atttttagtagagac	51147
rs12314060	snp	A/G	0.00557542	0.0525036	intron-variant	ING4	GRCh38.p7	12:6660537	cacttgaacccggga[A/G]gcagaggttgcagtg	51147
rs12581338	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6659740	gtggcgtgcatccag[C/G]aggtggagctttcag	51147
rs12825615	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6659734	aggagagtggcgtgc[A/C]tccaggaggtggagc	51147
rs28455167	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6659773	AGCCGAGATCGCTCC[A/T]CTGCACTCCAGCCTG	51147
rs34283927	snp	A/G	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6660146	AAATCTCTTGCCAAG[A/G]CTCCACCTAAAACTT	51147
rs34568819	in-del	-/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6663843	TTTTTTTTTTTTTTT[-/T]GAGACAGAATTTTCA	51147
rs34961465	in-del	-/CT			intron-variant	ING4	GRCh38.p7	12:6662179	ATTCCTTTTTTCTCT[-/CT]CCTCACTGGCAAATA	51147
rs35667235	snp	A/G	0.0711525	0.174681	upstream-variant-2KB	ING4	GRCh38.p7	12:6663748	ATGACTCATAATAAA[A/G]CTATAATTCTGCACA	51147
rs35710003	in-del	-/AA			intron-variant	ING4	GRCh38.p7	12:6659830	AAAAAAAAAAAAAAA[-/AA]TAGATGGGCATGGTG	51147
rs35762960	snp	C/T	0.0785177	0.181917	intron-variant	ING4	GRCh38.p7	12:6660562	GCAGTGGGCCAAGAT[C/T]GCACCATTGCGCTCC	51147
rs35787939	snp	C/T	0.0333695	0.124785	intron-variant	ING4	GRCh38.p7	12:6659685	GGCCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	51147
rs55641348	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6662337	TGTCACAGTGTTTTA[A/T]AATTATTTGCAGAAT	51147
rs55986948	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6662241	GCTGTAAAGCTTTTC[C/T]TACATCCCCAGGTAA	51147
rs58105040	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6658467	CAGGTGGGCGCATCA[C/G]CTGAGCTGAGGAGTT	51147
rs61495500	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6658462	AGGCCCAGGTGGGCG[C/G]ATCAGCTGAGCTGAG	51147
rs74057051	snp	A/G	0.0471551	0.14613	downstream-variant-500B	ING4	GRCh38.p7	12:6650480	CTCTGGTTTCATGTC[A/G]TGTCCTAATTCTGGC	51147
rs74057052	snp	C/T	0.0471551	0.14613	intron-variant	ING4	GRCh38.p7	12:6652167	GTCCAGCCCATCTTT[C/T]TTCTATTCTGAAGTC	51147
rs74057056	snp	C/T	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6662332	TCACTTGTCACAGTG[C/T]TTTATAATTATTTGC	51147
rs74239562	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655340	TRAGCCACCGCACCC[A/G]GCCCCAAATGTTTTA	51147
rs74651259	snp	C/T	0.00835141	0.0640778	intron-variant	ING4	GRCh38.p7	12:6659791	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC	51147
rs74743984	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6655026	CACGGCACCCGGTCT[C/T]CCAGATGTTTTATTT	51147
rs75082820	snp	C/T	0.0126979	0.078662	intron-variant	ING4	GRCh38.p7	12:6660805	GCATGATCTTTTCTC[C/T]GCTGAGTAACTTTCT	51147
rs75155588	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	ING4	GRCh38.p7	12:6664185	TCTCGTGTTTTTGTT[C/T]TCCTTTTGTTTATAT	51147
rs75418571	snp	G/T	0	0	intron-variant	ING4	GRCh38.p7	12:6654345	TCTTTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA	51147
rs76126701	snp	C/T	0.0174175	0.0916809	intron-variant	ING4	GRCh38.p7	12:6662249	GCTTTTCCTACATCC[C/T]CAGGTAATTACCCCC	51147
rs76290581	snp	C/T	0.00874735	0.0655527	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650927	GCACCGACCTCAGCA[C/T]GGAGGCAAAAGGACA	51147
rs76327967	snp	C/T	0.100216	0.200162	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651201	GGCCCTTATCTATTT[C/T]TTCTTCCGTTCTTGG	51147
rs76463160	snp	G/T	0.5	0	intron-variant	ING4	GRCh38.p7	12:6656185	TCTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTTG	51147
rs76592027	snp	A/C	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6658726	CAAAAATAAAAAATG[A/C]AAACCTAATCAAGTC	51147
rs76783851	snp	A/T	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6660129	TCACCCCAGTACAAG[A/T]GAAATCTCTTGCCAA	51147
rs76846620	snp	A/C	0.5	0	intron-variant	ING4	GRCh38.p7	12:6656264	CACTACAACCTCCAC[A/C]TCCCAGGTTCAAACG	51147
rs77114558	snp	A/C	0.5	0	intron-variant	ING4	GRCh38.p7	12:6659814	CGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA	51147
rs77283008	snp	A/G	0.00106447	0.0230456	synonymous-codon, intron-variant, nc-transcript-variant	ING4	GRCh38.p7	12:6652271	CAAAATGTTTCTCAC[A/G]TCAGGGTTGTCACAG	51147
rs77426127	snp	C/T	0.00199481	0.0315187	intron-variant	ING4	GRCh38.p7	12:6662765	ATGGGGAAAAAAATC[C/T]ACCGAGGCTGGAGAC	51147
rs77516085	snp	A/G	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6658957	TAGTTGGAATGCACC[A/G]CTCGCTTTTCCTCAT	51147
rs77742335	in-del	-/T			intron-variant	ING4	GRCh38.p7	12:6661589	ACCATGCCCAGCTAA[-/T]TTTTTTTTTTTTTTA	51147
rs78086878	snp	A/G	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6662484	TGAATAAATGACTCC[A/G]GGCCCTAAAACAAAT	51147
rs78166458	snp	A/T	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6662526	GAGCAATAGGCTTTC[A/T]GCAGGGGTGGTTTAC	51147
rs78194930	snp	A/C	0.0376037	0.131863	upstream-variant-2KB	ING4	GRCh38.p7	12:6663321	TTTTGCATGGTAGCC[A/C]CGACCGCCCACAGTG	51147
rs78635226	snp	G/T	0.5	0	intron-variant	ING4	GRCh38.p7	12:6656186	CTTTTTTTTTTTTTT[G/T]GAGACAGAGTCTTGC	51147
rs79526248	snp	A/T	0.5	0	intron-variant	ING4	GRCh38.p7	12:6659830	AAAAAAAAAAAAAAA[A/T]TAGATGGGCATGGTG	51147
rs79655322	snp	A/G	0.0437281	0.141251	intron-variant	ING4	GRCh38.p7	12:6660233	GGGAGGCCAAGGCAG[A/G]TAGATCGCTTGATCT	51147
rs79682518	snp	A/G	0.0498117	0.149749	intron-variant	ING4	GRCh38.p7	12:6654475	GTAGCTGGGACCACA[A/G]GCACATGCCACTACA	51147
rs79906574	snp	G/T	0.5	0	intron-variant	ING4	GRCh38.p7	12:6656187	TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT	51147
rs79942815	snp	A/C/T	0.0741367	0.177809	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655642	CTGGTTCTCACCATT[A/C/T]GGCAGGCAGTTCTCA	51147
rs80101392	snp	A/C	0.5	0	intron-variant	ING4	GRCh38.p7	12:6659812	AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	51147
rs80223260	snp	A/G	0.5	0	downstream-variant-500B	ING4	GRCh38.p7	12:6650264	AAAGGAAAAAAAAAA[A/G]GAAGTCAAGCTAATG	51147
rs111594180	snp	A/C	0.5	0	downstream-variant-500B	ING4	GRCh38.p7	12:6650429	CCTCTGTCTTTCCCA[A/C]GTTGAGAACTTACAA	51147
rs111933102	snp	C/G	0.00517822	0.0506191	intron-variant	ING4	GRCh38.p7	12:6659010	GCCTATTAAATTCCT[C/G]TTCGTTCTTCCAAAG	51147
rs112500523	in-del	-/A	0.5	0	downstream-variant-500B	ING4	GRCh38.p7	12:6650254	ACTTCGCCTCAAAGG[-/A]AAAAAAAAAAGAAGT	51147
rs112505199	snp	A/G	0.5	0	intron-variant	ING4	GRCh38.p7	12:6653548	CTGTGCCATGCACTC[A/G]AGTAATGGAACATAC	51147
rs112962175	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6656345	CACACCTGGCTAGTT[C/T]TTGTATTTTTAGTAG	51147
rs113711890	snp	C/G	0	0	splice-acceptor-variant, intron-variant	ING4	GRCh38.p7	12:6652419	CCATACTCAGGACTT[C/G]TGCATGCCAAGAGGA	51147
rs113932069	snp	A/C	0.5	0	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652668	ATCACTCACGTGCGC[A/C]CGAGCTTTAACTTCT	51147
rs114082659	snp	C/G	0.0182019	0.0936463	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650828	GAGGGGGAATGAAGA[C/G]GTCTGGGGGACTGCC	51147
rs114423275	snp	A/G	0.00398564	0.0444627	intron-variant	ING4	GRCh38.p7	12:6654143	TGCCTGGCCTAATCT[A/G]TTTATTTTTAGAGGC	51147
rs114905789	snp	A/T	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655782	CATGGCTACATAGAA[A/T]GAAGACAAGACTACA	51147
rs114937023	snp	G/T	0.0209421	0.100162	upstream-variant-2KB	ING4	GRCh38.p7	12:6665008	AAAAGCAGTAAATAT[G/T]CAGGGAGCTAAGAAA	51147
rs115021376	snp	C/G	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6651985	TCGCCTCAGCCTCCC[C/G]AGTAGCTGGGATGAC	51147
rs115151324	snp	A/T	0.00676609	0.0577691	intron-variant	ING4	GRCh38.p7	12:6662321	TTTCCATTATCTCAC[A/T]TGTCACAGTGTTTTA	51147
rs115808834	snp	A/G	0.0368353	0.130617	intron-variant	ING4	GRCh38.p7	12:6653800	TCTGCCGCAAATCAG[A/G]CTGAGTCATCTGCTG	51147
rs115876538	snp	A/T	0.0387552	0.1337	intron-variant	ING4	GRCh38.p7	12:6655056	TTATTTTATTTATTT[A/T]TTTTTGAGACCAAGT	51147
rs116142617	snp	C/G	0.0368353	0.130617	intron-variant	ING4	GRCh38.p7	12:6651897	TGCTCTTGTCGCCCA[C/G]GTTAGAGTGTGGTGG	51147
rs116416840	snp	A/G	0.00199481	0.0315187	intron-variant	ING4	GRCh38.p7	12:6655389	TGTCCCAGGACATTG[A/G]GACTATAGATGTTTA	51147
rs116693623	snp	C/T	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6652139	TGCTGGGATTTCAGG[C/T]AAGAGCTACTACGTC	51147

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