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
rs768197	snp	G/T	0.460477	0.134905	intron-variant	AHCTF1	GRCh38.p7	1:246923930	GAAACATGGCCCTCT[G/T]CTCAGGTCCTGTGGC	25909
rs903462	snp	C/G	0.49621	0.0433651	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932608	TAGAAAAAACAGCAC[C/G]GTGGAAAAAGCGTTT	25909
rs903464	snp	C/T	0.097727	0.198275	intron-variant	AHCTF1	GRCh38.p7	1:246907921	TGTTAAACTAGAAAA[C/T]TGCCATCCTTATCTA	25909
rs903465	snp	A/G	0.093417	0.194889	intron-variant	AHCTF1	GRCh38.p7	1:246908051	TAACAACCATAAATA[A/G]AACTGATTTATTTCT	25909
rs923972	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246916871	CTAAGGCTTAAACGA[C/T]TTAAACTAGAAGTTA	25909
rs967953	snp	A/C/G/T	0.0934559	0.195063	intron-variant	AHCTF1	GRCh38.p7	1:246894866	TCCCAAGTTGCCTCC[A/C/G/T]TGAAGTGTTGATGTT	25909
rs1039009	snp	A/C	0.461259	0.133677	intron-variant	AHCTF1	GRCh38.p7	1:246917156	GAAGCACAGAGTAGC[A/C]GCACTGGGTGGAAGA	25909
rs1039010	snp	A/G	0.434976	0.168179	intron-variant	AHCTF1	GRCh38.p7	1:246918081	AGGTTCACTGATAAC[A/G]TGTTTAAGAGCTTAT	25909
rs1047080	snp	A/G	0.233818	0.249476	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840729	AAATATCTAGTTTGG[A/G]AGAAAATAATTTATA	25909
rs1047085	snp	A/C	0	0	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840721	AGTTTGGAAGaaaat[A/C]atttatataaattat	25909
rs1053916	snp	A/G	0.0205511	0.0992634	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839173	CTAAATGAACTTTAC[A/G]TATATTTTAAATGAA	25909
rs1472275	snp	A/G	0.483053	0.0904792	intron-variant	AHCTF1	GRCh38.p7	1:246891228	GACCAAAGTAAACTA[A/G]ATACAAAGATGAATT	25909
rs1472276	snp	C/G	0.0782148	0.181884	intron-variant	AHCTF1	GRCh38.p7	1:246867173	Gtaatttttaattat[C/G]tttaacattttatag	25909
rs1472277	snp	A/G	0.0103295	0.0711199	intron-variant	AHCTF1	GRCh38.p7	1:246866950	TGTTAGTAGACCTCT[A/G]AATGAGGGTTGTTTT	25909
rs1612610	snp	G/T	0.460252	0.135255	intron-variant	AHCTF1	GRCh38.p7	1:246905224	TATGTATCAGGCCAG[G/T]CGTGGTGACTCACAC	25909
rs1613209	snp	A/G	0.485255	0.0845871	intron-variant	AHCTF1	GRCh38.p7	1:246871877	CTGTGTCTTTAGGTT[A/G]TTATTATTTTTTAAT	25909
rs1616541	snp	C/T	0.0154538	0.0865337	intron-variant	AHCTF1	GRCh38.p7	1:246871547	GTATACCTTGTTTTT[C/T]TGGGCCCCTTTCTGT	25909
rs1619941	snp	A/T	0.454784	0.1434	intron-variant	AHCTF1	GRCh38.p7	1:246929478	GACCTGAAATTTGAG[A/T]ATTTAAAAAAGGAAA	25909
rs1630829	snp	C/T	0.435694	0.167385	intron-variant	AHCTF1	GRCh38.p7	1:246860564	AACTCTCATGCTTTC[C/T]TTCTGAGATAGGGTC	25909
rs1691238	snp	A/G	0.108755	0.206276	intron-variant	AHCTF1	GRCh38.p7	1:246928140	CCCCATCTCTACTAA[A/G]AATACAAAAAAAATT	25909
rs1691239	snp	G/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246880178	ATTTACATGCTTCAG[G/T]GTTTAAGAGCTAAGA	25909
rs1691240	snp	A/C	0.460252	0.135255	intron-variant	AHCTF1	GRCh38.p7	1:246904579	GTATGGGAAGGAGAA[A/C]GGGCAGTTGGGGGAA	25909
rs1691241	snp	A/G	0.460365	0.13508	intron-variant	AHCTF1	GRCh38.p7	1:246904829	TTTACTTGGCTTCTA[A/G]CACACCACACCTTCC	25909
rs1691242	snp	A/G	0.46014	0.13543	intron-variant	AHCTF1	GRCh38.p7	1:246905365	TAGCCAGGCATGGTG[A/G]CAGGCACCTGTAGTC	25909
rs1691243	snp	C/T	0.0908922	0.192833	intron-variant	AHCTF1	GRCh38.p7	1:246906212	TTGACCAAGAGATGA[C/T]AGTGTTAGAGAAAGC	25909
rs1691251	snp	A/G	0.431177	0.172264	intron-variant	AHCTF1	GRCh38.p7	1:246864477	TGAATTTTAGTAAAT[A/G]GATTGCCAGGGAAGC	25909
rs1691252	snp	C/T	0.433818	0.169443	intron-variant	AHCTF1	GRCh38.p7	1:246900847	acctaaaacggatgc[C/T]tttgggcattaaggc	25909
rs1691253	snp	C/T	0.108048	0.20579	intron-variant	AHCTF1	GRCh38.p7	1:246901686	AGCCAGGTGTGGTGG[C/T]GTGTGCCGGCAGTCC	25909
rs1691254	snp	A/G	0.46014	0.13543	intron-variant	AHCTF1	GRCh38.p7	1:246901773	caaccagccaagatc[A/G]tgccaccacactctg	25909
rs1691255	snp	A/G	0.485933	0.0826777	intron-variant	AHCTF1	GRCh38.p7	1:246902170	GCGATGACACTAAAG[A/G]AGACAGAGAAAACAT	25909
rs1691256	snp	G/T	0.0970103	0.197722	intron-variant	AHCTF1	GRCh38.p7	1:246902296	GCCTGTTTTGAGAAC[G/T]AGATTAAAATAAAAG	25909
rs1691257	snp	A/C	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246903806	ttgcaccactgcact[A/C]cagcctgggcgacag	25909
rs1779964	snp	A/G	0.476918	0.104919	intron-variant	AHCTF1	GRCh38.p7	1:246899907	ACATATAAATACTAA[A/G]TTTCTTGTGTGTATA	25909
rs1779965	snp	G/T	0.0973687	0.197999	intron-variant	AHCTF1	GRCh38.p7	1:246901978	TGGGTAAGTTCGCTG[G/T]GTGATTTAATCCTCA	25909
rs1779966	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246903831	cgacagagcgagact[C/T]tgtctcaaaaaaaaa	25909
rs1779967	snp	A/T	0.465052	0.127485	intron-variant	AHCTF1	GRCh38.p7	1:246904790	GATCCCTTTTAATAA[A/T]TCCTATTACTAGTTC	25909
rs1779968	snp	A/T	0.453087	0.145793	intron-variant	AHCTF1	GRCh38.p7	1:246906395	CCAGTCTGACCAACA[A/T]GGTGAAAATCCGTCT	25909
rs1779969	snp	C/T	0.485731	0.0832509	intron-variant	AHCTF1	GRCh38.p7	1:246906647	TTGAGATACACTTCC[C/T]ATAAGATAAATTACT	25909
rs1779971	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246880211	taaCAAATAACATAT[G/T]GTTTTGGATAATAAG	25909
rs1779972	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246880205	ATAACATATGGTTTT[G/T]GATAATAAGCTATTT	25909
rs1779973	snp	C/G	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246882638	AACCCACCTAACAAA[C/G]AGGAAAAATTATGCC	25909
rs1779975	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246908936	CTTAATGAATGAAAC[A/C]ATTAGCTCAAAGTAA	25909
rs1779976	snp	A/C/G	0.00404816	0.0448079	intron-variant	AHCTF1	GRCh38.p7	1:246888139	AATTTTATAATTTTA[A/C/G]TAATACATGAAACAC	25909
rs1779977	snp	A/G	0.495174	0.0488838	intron-variant	AHCTF1	GRCh38.p7	1:246869776	cctgtacatcatcag[A/G]gctcctgggtgacca	25909
rs1779978	snp	A/T	0.467132	0.12391	intron-variant	AHCTF1	GRCh38.p7	1:246869579	ttaagggccttagga[A/T]ttttggaatggtgat	25909
rs1779979	snp	A/G	0.499713	0.0119774	intron-variant	AHCTF1	GRCh38.p7	1:246869138	ACAAAACACACGGCC[A/G]GGCGTGGTGGCTCAC	25909
rs1779980	snp	C/T	0.429837	0.173662	intron-variant	AHCTF1	GRCh38.p7	1:246869133	ACACACGGCCGGGCG[C/T]GGTGGCTCACGCCTG	25909
rs1779981	snp	A/G	0.11963	0.213316	intron-variant	AHCTF1	GRCh38.p7	1:246869001	aaaagttagccaggc[A/G]tggtggcgggcgcct	25909
rs1779982	snp	A/G	0.48666	0.0805725	intron-variant	AHCTF1	GRCh38.p7	1:246868937	GAATGGCGTGAACCC[A/G]GGAGGCAGAACTTGC	25909
rs1812703	snp	A/G	0.108048	0.20579	intron-variant	AHCTF1	GRCh38.p7	1:246925347	AAAAGCATTTTTTGG[A/G]AAATGAAATATAGTA	25909
rs1892116	snp	C/T	0.375598	0.21616			GRCh38.p7	1:246917020	GTCATGTTTGGATTT[C/T]ACCCTGCCTGCAATG	25909
rs2011875	snp	A/G	0.093777	0.195178	intron-variant	AHCTF1	GRCh38.p7	1:246908130	CTGATTCCGGGTCAG[A/G]GGGAAGAAAATACAT	25909
rs2029789	snp	A/T	0.375	0.216506	intron-variant	AHCTF1	GRCh38.p7	1:246930586	CCCTTTTTTTTTTTT[A/T]AACTGTTTTTTTGTG	25909
rs2047190	snp	C/T	0.0970103	0.197722	intron-variant	AHCTF1	GRCh38.p7	1:246926469	GTTTAATAAAGTTTT[C/T]CAAATTTAACAGCCT	25909
rs2047191	snp	A/G	0.386884	0.209196	intron-variant	AHCTF1	GRCh38.p7	1:246926788	ttgaacccgggaggc[A/G]gagattgcagtcagc	25909
rs2047192	snp	A/G	0.388964	0.20782	intron-variant	AHCTF1	GRCh38.p7	1:246926904	TATggccgggccgcg[A/G]tggcacacgcctgta	25909
rs2067915	snp	C/T	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246876670	GCAGTAGGAGTTACA[C/T]AGTACAAAGATCATT	25909
rs2067916	snp	A/G	0.329084	0.237162	intron-variant	AHCTF1	GRCh38.p7	1:246876646	GATCATTGTGTGGTA[A/G]AGGAAGACGTAGAGG	25909
rs2172796	snp	A/G	0.460702	0.134554	intron-variant	AHCTF1	GRCh38.p7	1:246924316	GCATTTCATACAATA[A/G]TCTCTATGAATTCTT	25909
rs2379094	snp	A/C	0.0652144	0.168387	intron-variant	AHCTF1	GRCh38.p7	1:246866902	TAATCTTGGGTAGCT[A/C]ATTGAAGCTTTCTTC	25909
rs2379188	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246908322	TTTTTTTTTTTTTTG[G/T]ATCCCTGTGAATTTT	25909
rs2493606	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246923325	gaggctgaggcatga[A/G]aactgcttgaaccta	25909
rs2642975	snp	A/T	0.4628	0.13121	intron-variant	AHCTF1	GRCh38.p7	1:246928884	TTTCAGAAATTTCTT[A/T]CCAACTTAATTCAAA	25909
rs2642976	snp	C/T	0.448836	0.15154	intron-variant	AHCTF1	GRCh38.p7	1:246929012	CTAGAAAAGGAGATA[C/T]ATAGTCAATTATCAG	25909
rs2642977	snp	C/T	0.462144	0.132269	intron-variant	AHCTF1	GRCh38.p7	1:246929076	TAGAGGTACATATGC[C/T]GTGAGATCCCAGTAA	25909
rs2642984	snp	G/T	0.474453	0.110094	intron-variant	AHCTF1	GRCh38.p7	1:246881390	GTGTCCTGAATAATT[G/T]TTTTTCCTAGTCTGT	25909
rs2642985	snp	A/T	0.0941369	0.195465	intron-variant	AHCTF1	GRCh38.p7	1:246880645	TCATAAATTAAGTTT[A/T]TCTTACTCCTGCTAG	25909
rs2642986	snp	C/T	0.116488	0.211364	intron-variant	AHCTF1	GRCh38.p7	1:246874984	GTTTCTTCCTAAACC[C/T]CATGTAAAATATTAG	25909
rs2642990	snp	C/T	0.491245	0.0655821	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885532	TGAAGGATAACATCG[C/T]TACCACTGGACACTG	25909
rs2642991	snp	A/G	0.46014	0.13543	intron-variant	AHCTF1	GRCh38.p7	1:246886437	tacattgtattagat[A/G]ttataagtaatctac	25909
rs2800214	snp	C/T	0.461481	0.133325	intron-variant	AHCTF1	GRCh38.p7	1:246914396	CATGTGTTAAAAAGA[C/T]TAAAAGTTGTTTCAG	25909
rs2800215	snp	A/G	0.462472	0.13174	intron-variant	AHCTF1	GRCh38.p7	1:246928595	CTGGTTCAGTATTAA[A/G]CAAAACAAAATTCTT	25909
rs2800219	snp	A/C	0.460589	0.13473	intron-variant	AHCTF1	GRCh38.p7	1:246892125	AAGCCAAGAGTGAGA[A/C]TATGAACTCAAATCA	25909
rs2800220	snp	C/T	0.473909	0.111197	intron-variant	AHCTF1	GRCh38.p7	1:246894512	CGCGCCACTGCACTA[C/T]AGCCTGGCGACAGAG	25909
rs2800221	snp	C/T	0.460925	0.134204	intron-variant	AHCTF1	GRCh38.p7	1:246895403	TGAACAGACAATATG[C/T]GTTTGGGGTGTGTGT	25909
rs2800222	snp	C/G	0.434906	0.16979	intron-variant	AHCTF1	GRCh38.p7	1:246867935	TAAAATTTTTAGCTA[C/G]TATTACCACGTAATG	25909
rs2818888	snp	C/T	0.461037	0.134028	intron-variant	AHCTF1	GRCh38.p7	1:246925561	ctgatcatagcttac[C/T]gcaacctacaactcc	25909
rs2996543	snp	C/T	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246927069	tgtagtcccaggtac[C/T]cgggaggctgaggag	25909
rs2996551	snp	G/T	0.00914312	0.0669923	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246839056	TGCTACAAGGTCCGA[G/T]AATATCATTCATGCG	25909
rs2996552	snp	C/T	0.00835141	0.0640778	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839392	AGCTCTTTATTCATT[C/T]AACAAGTTCATTTAA	25909
rs3063899	in-del	-/TA			intron-variant	AHCTF1	GRCh38.p7	1:246899895	GAAACTTAGTATTTA[-/TA]TGTTTTATAAAGGAA	25909
rs3067058	in-del	-/ATTT			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933149	tttatttatttattt[-/ATTT]gagacggagtctcgc	25909
rs3104111	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246923215	aggtcaggagtttga[A/G]accagcctgactaac	25909
rs3122533	snp	A/T	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246897148	GTGTAACTCTGTCTC[A/T]ACTAAAAATAAAAAA	25909
rs4011530	snp	C/T			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850876	AAATGCAGATTTGAC[C/T]AATTTAGTGGGACAC	25909
rs4011531	in-del	-/TCTTA			intron-variant	AHCTF1	GRCh38.p7	1:246862720	AATTTAAGTAATTTA[-/TCTTA]CTAATTGGCACTTTT	25909
rs4130824	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246923824	CCCACACACATGAAG[A/G]ATGTTAGAATTCGA	25909
rs4971277	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246927191	tcaaaaaaaaaaaaa[A/G]aaagaaaTAggccag	25909
rs4971284	snp	A/T	0.296619	0.245615	intron-variant	AHCTF1	GRCh38.p7	1:246843741	TATTAAAACATTTGT[A/T]AAAAAAAAAAGTATG	25909
rs4971285	snp	A/T	0.296619	0.245615	intron-variant	AHCTF1	GRCh38.p7	1:246843742	ATTAAAACATTTGTA[A/T]AAAAAAAAAGTATGT	25909
rs4971286	snp	A/G	0.344147	0.231595	intron-variant	AHCTF1	GRCh38.p7	1:246847141	aaaatacaaaaaaat[A/G]acccaggcgtggtgg	25909
rs4971287	snp	C/T	0.361894	0.223562	intron-variant	AHCTF1	GRCh38.p7	1:246868670	TTGGACATGTGCCTT[C/T]AACTGAAATAGGAGT	25909
rs4971289	snp	A/G	0.352504	0.228019	intron-variant	AHCTF1	GRCh38.p7	1:246869824	caggcatgaaaacac[A/G]acatccattctgtaa	25909
rs5021094	snp	G/T	0.426201	0.177351	intron-variant	AHCTF1	GRCh38.p7	1:246842858	AGACAAGGAATACTA[G/T]AGCCAAACACTGATG	25909
rs6426183	snp	C/T	0.303688	0.244167	intron-variant	AHCTF1	GRCh38.p7	1:246849422	ACAGGATTTAAGTCA[C/T]GTTAACCATACTGAA	25909
rs6426188	snp	A/C	0.463989	0.129263	intron-variant	AHCTF1	GRCh38.p7	1:246930108	AGCATAAAAAGAAAA[A/C]AAAAGTCTCAAAACT	25909
rs6659764	snp	C/G	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246889109	CAAACTACCATAAAG[C/G]CCAGCGTAGTGAAAA	25909
rs6672861	snp	C/T	0.298905	0.24517	intron-variant	AHCTF1	GRCh38.p7	1:246862436	agtgagccgagattg[C/T]gccactgcactccag	25909
rs6682729	snp	A/G	0.0364509	0.129988	intron-variant	AHCTF1	GRCh38.p7	1:246918524	atattggccagatgc[A/G]gaggctcacgccttt	25909
rs6685596	snp	A/G	0.312837	0.241974	intron-variant	AHCTF1	GRCh38.p7	1:246862467	cctgggcgacagagc[A/G]agactccgtctcaaa	25909

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