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
rs2806	snp	A/T	0	0	utr-variant-3-prime	HLTF	GRCh38.p7	3:149031252	TGTAAACAATTGTTA[A/T]GTGTTTAGAATCAGA	6596
rs746671	snp	A/G	0.294064	0.246086	intron-variant	HLTF	GRCh38.p7	3:149071106	AACACAGTTTTTCCT[A/G]TAGTTTTTAGTTAAA	6596
rs751845	snp	C/T	0.407845	0.193868	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087266	CTCAGAGCGCCCCTC[C/T]GCAGTTCCTTGAGGA	6596
rs772813	snp	A/G	0.382279	0.212137	intron-variant	HLTF	GRCh38.p7	3:149077204	ctggagtgcaggggc[A/G]ctatcttggctcact	6596
rs772814	snp	C/T	0.294064	0.246086	intron-variant	HLTF	GRCh38.p7	3:149072136	AGTGAGTAGTGTAAT[C/T]CTAGAGTTGATTTAT	6596
rs772815	snp	C/T	0.294064	0.246086	intron-variant	HLTF	GRCh38.p7	3:149068981	aaacagttttgactt[C/T]gcattttcgtgaagg	6596
rs772816	snp	C/T	0.364193	0.222396	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085892	GCGCTAGTAGAGATA[C/T]GCGCCACTTGCAAGG	6596
rs772817	snp	C/T	0.382279	0.212137	intron-variant	HLTF	GRCh38.p7	3:149083285	TTATTTTATAATTAA[C/T]GCATGTTCTTTTATT	6596
rs810082	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149079331	gctggtctcaaactt[C/T]ttttgacagtttgat	6596
rs812248	snp	A/G	0	0	intron-variant	HLTF	GRCh38.p7	3:149079245	cttcttatatgtgta[A/G]agtagtggtttccat	6596
rs812249	snp	A/G	0.406591	0.194883	synonymous-codon	HLTF	GRCh38.p7	3:149068321	GGGTAAAACTCTTAC[A/G]GCCATTGCAGTAATC	6596
rs812820	snp	C/G	0.293551	0.246177	intron-variant	HLTF	GRCh38.p7	3:149082414	tggagcgcagtggcg[C/G]gatctcggctcattg	6596
rs813853	snp	A/C	0	0	intron-variant	HLTF	GRCh38.p7	3:149079338	tgcccaggctggtct[A/C]aaacttcttttgaca	6596
rs975922	snp	A/C/G	0.0134861	0.0810011	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030894	TTCAATGTGTGCCCT[A/C/G]TAACACAACATTGTC	6596
rs1017489	snp	C/T	0.475096	0.108775	intron-variant	HLTF	GRCh38.p7	3:149046303	AACTTTTAATTTCTA[C/T]ATAAATTGATCCAAG	6596
rs1042835	snp	A/G	0	0	missense	HLTF	GRCh38.p7	3:149074284	ACTTTTTGGGGAAAA[A/G]AAGAAAATAGAAAAG	6596
rs1081819	snp	A/T	0.409721	0.192325	intron-variant	HLTF	GRCh38.p7	3:149078323	cctggcctcaagaga[A/T]cctcacacttcagcc	6596
rs1272861	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149043608	TGTTGTCATTGTACC[A/C]CTGTATTTTGTATAA	6596
rs1350359	snp	A/T	0.409552	0.192466	intron-variant	HLTF	GRCh38.p7	3:149051236	AATATAAGGAAGTTT[A/T]AAAAAAAAAAAAAAG	6596
rs1457604	snp	C/T	0.29432	0.24604	intron-variant	HLTF	GRCh38.p7	3:149040348	ATGTGGTAAGTAGAA[C/T]GGATAAAGGAGGGAG	6596
rs1457605	snp	C/T	0.00874735	0.0655527	intron-variant	HLTF	GRCh38.p7	3:149043891	TTATTTAATTTAATA[C/T]ATGTAAAGTATTTAA	6596
rs1457606	snp	A/T	0.0894459	0.191631	intron-variant	HLTF	GRCh38.p7	3:149075097	TCTTAAATACAAAAA[A/T]CTTATTTTTCTCTTG	6596
rs1879170	snp	A/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149072065	CCCAAAAAATTAAGA[A/T]ATTGAAATTAAATTA	6596
rs1965258	snp	C/T	0.431769	0.17164	intron-variant	HLTF	GRCh38.p7	3:149051609	CTCATGCCTGTAATC[C/T]CGGCACTTTGGGAGG	6596
rs1965259	snp	C/T	0.00358779	0.0422022	intron-variant	HLTF	GRCh38.p7	3:149051740	GTGGTGATGGTGATG[C/T]GCACCTATAATTCCA	6596
rs2034905	snp	C/T	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149064459	GTTGTATTTAAAATG[C/T]AATATGCATGGATAA	6596
rs2034906	snp	A/G	0.382279	0.212137	intron-variant	HLTF	GRCh38.p7	3:149054135	TAAATTTGACAATTA[A/G]ACTATCACAAGTAGT	6596
rs2054197	snp	A/G	0.432357	0.171014	intron-variant	HLTF	GRCh38.p7	3:149045719	ATCTTGCTTGGACCA[A/G]AATTTCATACCTTCT	6596
rs2119341	snp	A/C			utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031773	AAAATTAATTCTTGT[A/C]TAGTCTGTATATATT	6596
rs2119342	snp	C/T	0.40733	0.194287	utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031834	AATCGGAGGCTTTGG[C/T]AAATAACTAAGTGTC	6596
rs2228257	snp	C/G	0.0133149	0.0804996	missense	HLTF	GRCh38.p7	3:149063507	GCATCTAGATGTAGT[C/G]AACAACCCAGTATTT	6596
rs2229361	snp	A/G	0.0594826	0.161874	missense	HLTF	GRCh38.p7	3:149040077	CAGAAGAATTAGCAC[A/G]TGACAGTGAGAAAAA	6596
rs2290725	snp	C/T	0.43424	0.168984	synonymous-codon	HLTF	GRCh38.p7	3:149041538	TTTACAAAATACATG[C/T]GCACAATGTGTTATC	6596
rs2290726	snp	A/C	0.432063	0.171327	intron-variant	HLTF	GRCh38.p7	3:149041773	TAGGGAAAGTCTCTC[A/C]TCATTTTCTGCCATA	6596
rs2305867	snp	C/G/T	0.000979748	0.0221119	intron-variant	HLTF	GRCh38.p7	3:149040172	CTATATAAGAAAGAA[C/G/T]GAAGTATGAGCAACA	6596
rs2305868	snp	A/G	0.0535406	0.154608	missense	HLTF	GRCh38.p7	3:149068298	CAGTAATCCTTACCA[A/G]CTTCCATGATGGCAG	6596
rs2607999	snp	A/C	0.410568	0.191619			GRCh38.p7	3:149087754	ACTAAAAATACAAAA[A/C]TTAGCTGGGCGTGGT	6596
rs2608003	snp	A/T	0.404384	0.196635			GRCh38.p7	3:149077284	ttatttttatttatt[A/T]atttatttatttatt	6596
rs2608004	snp	A/T	0.325799	0.238232			GRCh38.p7	3:149077268	atttatttatttatt[A/T]atttatttatttatt	6596
rs2877411	snp	C/T	0.134119	0.221521	intron-variant	HLTF	GRCh38.p7	3:149051695	GCGAAACCCTGCCTC[C/T]ACTAAAAATACAAAA	6596
rs3070552	in-del	-/GTCTA	0	0	intron-variant	HLTF	GRCh38.p7	3:149047213	AGTTGAACCACATTA[-/GTCTA]CATCTTGCAAAATGG	6596
rs3070582	in-del	-/AA	0	0	intron-variant	HLTF	GRCh38.p7	3:149083761	tacaaaaaaaaaaaa[-/AA]tacaaaaattagctg	6596
rs3182285	snp	A/G	0.424659	0.17887	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030593	GTATGGGTTCTCCAT[A/G]TAGCAATACTTCAGT	6596
rs3213908	snp	A/G	0.0103356	0.0711407	utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031566	AATGAGTGTAGTACT[A/G]CTTAACTAAAATGGA	6596
rs3765075	snp	C/T			synonymous-codon	HLTF	GRCh38.p7	3:149059719	GGATATTTACTGACC[C/T]TTTTTCAACATTTTC	6596
rs3772565	snp	A/G	0.3744	0.216852	intron-variant	HLTF	GRCh38.p7	3:149053525	TTTACAGGAAGTATC[A/G]TGCTGGCATCTGCTT	6596
rs3816570	snp	C/G	0.487746	0.0773096	intron-variant	HLTF	GRCh38.p7	3:149042498	GCTGCCAATTGCAGT[C/G]TAAGTCAGATAGGAA	6596
rs3836276	in-del	-/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149040436	ATTGTTATTCATAGA[-/T]TTTTTTTTTTAAACT	6596
rs4681479	snp	A/C	0.496034	0.0443518	intron-variant	HLTF	GRCh38.p7	3:149052289	TCTTTTTAAAAAATT[A/C]TATGTTGTATGGAAA	6596
rs4681480	snp	G/T	0.405082	0.196086	intron-variant	HLTF	GRCh38.p7	3:149069858	tggaaaagttgtgtg[G/T]gacactatgaacata	6596
rs4974388	snp	C/G	0.431916	0.171483	intron-variant	HLTF	GRCh38.p7	3:149071154	TCTAGTCCCAAACTG[C/G]TACCAACATATTCCT	6596
rs6440581	snp	C/G	0.301429	0.244653	intron-variant	HLTF	GRCh38.p7	3:149044564	accatccacacatag[C/G]tgactttgaactcga	6596
rs6440583	snp	C/T	0.431473	0.171952	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087412	TGAGGAGGCTGCTGT[C/T]CCCGAAGCTGGCCTT	6596
rs6764352	snp	A/G	0.0480316	0.147428	intron-variant	HLTF	GRCh38.p7	3:149039038	CTGAAAAAATTTACA[A/G]AACTACTTACTGGAT	6596
rs6767681	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149032976	AAAAAAAAAAAAAAA[A/C]ACAAAAAACTATTCC	6596
rs6771107	snp	C/T	0.424193	0.179323	intron-variant	HLTF	GRCh38.p7	3:149062102	ATATTCTTCAATGCC[C/T]GTTTCCTCATAAGAA	6596
rs6772943	snp	A/C	0.0566069	0.158427	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087435	CTGGCCTTTTAATCG[A/C]ACAGGGCAGGAAGCT	6596
rs6783991	snp	A/G	0.0256215	0.110247	intron-variant	HLTF	GRCh38.p7	3:149049993	gcaaaactccatcGA[A/G]AGGGAGGGGGAGGGG	6596
rs6792312	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149032978	AAAAAAAAAAAAAAA[A/C]AAAAAACTATTCCCA	6596
rs6792730	snp	A/C	0.29432	0.24604	intron-variant	HLTF	GRCh38.p7	3:149033468	ATTTTCAAAAAGGGT[A/C]ATCAGAACATTTTAC	6596
rs6796555	snp	C/T	0.495891	0.0451408	intron-variant	HLTF	GRCh38.p7	3:149079836	aacctcgtgatccac[C/T]caccttggcctccca	6596
rs6800063	snp	A/C	0	0	downstream-variant-500B	HLTF	GRCh38.p7	3:149029942	AAGCACTCTTGATTT[A/C]TGAACAAGAATTTCA	6596
rs6800629	snp	A/G	0.0275645	0.114116	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149088292	tcccagcactttggg[A/G]ggccgagttgggtgg	6596
rs6809084	snp	G/T	0.279991	0.248195	intron-variant	HLTF	GRCh38.p7	3:149037784	ACAGAAACAGCAGAG[G/T]GTTGCCTTTAGCCCA	6596
rs7611003	snp	C/G	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149044215	AGCACTAAGATCAAT[C/G]TATAACACCTAGTGA	6596
rs7611297	snp	C/G	0.0577344	0.159793	intron-variant	HLTF	GRCh38.p7	3:149038739	gctgctctcaaactc[C/G]tgagctcaggcaatc	6596
rs7624263	snp	A/G	0.382473	0.212016	intron-variant	HLTF	GRCh38.p7	3:149066204	GGTATGCGCCACCAC[A/G]CCCAGCTAATTTTGT	6596
rs7625832	snp	C/T	0.431473	0.171952	intron-variant	HLTF	GRCh38.p7	3:149078741	gggtgcctgtagtcc[C/T]agttactcgggaagc	6596
rs7625894	snp	A/G	0.431916	0.171483	intron-variant	HLTF	GRCh38.p7	3:149054481	CCTCTGACATAAGAA[A/G]AATGGCGATGAGAGA	6596
rs7635712	snp	C/T	0.424503	0.179021	intron-variant	HLTF	GRCh38.p7	3:149052077	caggatcacttgaac[C/T]tgggaggtggaggtt	6596
rs7637603	snp	C/T	0.452103	0.147154	intron-variant	HLTF	GRCh38.p7	3:149054668	ATTCCAATGTCAATG[C/T]TTCAGAACAGAAAAG	6596
rs9289779	snp	G/T	0.372592	0.217879	intron-variant	HLTF	GRCh38.p7	3:149066822	ATAAAACATTAGGTT[G/T]CTCAGGGTGAGGAAT	6596
rs9683270	snp	A/G	0.432063	0.171327	intron-variant	HLTF	GRCh38.p7	3:149046756	CCCCAAAATAAAAAG[A/G]TAATATGGTAATTCA	6596
rs9822226	snp	A/G	0.406986	0.194565	intron-variant	HLTF	GRCh38.p7	3:149060303	AATGTAAACAATAAT[A/G]GTATTGCCAGGAAGA	6596
rs9834138	snp	A/C	0.489796	0.070696	intron-variant	HLTF	GRCh38.p7	3:149032971	TCAAAAAAAAAAAAA[A/C]AAAAAACAAAAAACT	6596
rs9835785	snp	C/T	0.382473	0.212016	intron-variant	HLTF	GRCh38.p7	3:149080928	ATGACAGACCACATG[C/T]ATTATGCAACAGTTG	6596
rs9850529	snp	A/G	0.406986	0.194565	intron-variant	HLTF	GRCh38.p7	3:149058824	TGTGACTTTGAAAAT[A/G]TTCTCTCTTGTATCA	6596
rs9864549	snp	A/C	0.3746	0.216737	intron-variant	HLTF	GRCh38.p7	3:149044028	TAGGCAAAATAATAC[A/C]AAGATTAAACTTACA	6596
rs10513347	snp	C/T	0.111224	0.207945	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030729	CCTGCAGAAAGGTCT[C/T]GGTTTTGATGAAAAT	6596
rs10513348	snp	A/G	0.43221	0.171171	intron-variant	HLTF	GRCh38.p7	3:149038074	GATCCTAGACCACCT[A/G]TACCTCAATCACCTA	6596
rs10513349	snp	A/G	0.409382	0.192607	intron-variant	HLTF	GRCh38.p7	3:149065156	AAATGACACATTATT[A/G]TGAGAAAAATTCAAG	6596
rs10550068	in-del	-/G	0.5	0	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087584	TTTTTTCTTTTTTTT[-/G]TTTTTTCTTTTTTAT	6596
rs10651075	in-del	-/GTC			utr-variant-3-prime	HLTF	GRCh38.p7	3:149030478	AAGAAGCAAGCTGTC[-/GTC]CTCCCTTTACCTTCA	6596
rs10935740	snp	C/G	0.0255019	0.110003	intron-variant	HLTF	GRCh38.p7	3:149073333	TAAAGCTATAATTTA[C/G]AAAATAAAAAGAATA	6596
rs11306648	in-del	-/A	0.424659	0.17887	intron-variant	HLTF	GRCh38.p7	3:149033371	AATAATAAATTCAAT[-/A]AATCTCAAGATATCT	6596
rs11559143	snp	C/G	0	0	missense, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084818	CACGCCTCTCATATC[C/G]AACTTTCTTTCCACG	6596
rs11710438	snp	A/G	0.495999	0.0445491	intron-variant	HLTF	GRCh38.p7	3:149067547	tcacagtgtcactga[A/G]ggtggagtgcaatag	6596
rs11715474	snp	G/T	0.495891	0.0451408	intron-variant	HLTF	GRCh38.p7	3:149084128	CATAAAATGCCACAA[G/T]TATGAAAATATAAAA	6596
rs11917715	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149078961	Caccaaacagcaatt[C/T]tagagtcaaaaggta	6596
rs11918527	snp	C/G/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149079080	ttgagattatacaat[C/G/T]taaggaacaaaaaaa	6596
rs11918628	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149079372	gggtaacgacagttt[C/T]taaaaaaaaaaaaaa	6596
rs11926206	snp	A/C	0.00952359	0.0683454	intron-variant	HLTF	GRCh38.p7	3:149079159	cacatacataagagt[A/C]ccataaggagaaaag	6596
rs12106722	snp	C/T	0.371177	0.218669	intron-variant	HLTF	GRCh38.p7	3:149065698	AGCCAGGCATGGTGG[C/T]GGGCACCTGTAATCC	6596
rs12152447	snp	A/G	0.0364509	0.129988	intron-variant	HLTF	GRCh38.p7	3:149078102	attatttaaaatgtc[A/G]atttttcaagaaaaa	6596
rs12488819	snp	C/T	0.45198	0.147323	intron-variant	HLTF	GRCh38.p7	3:149049329	CACTGAACTGTTCTA[C/T]CTCGGATTAAAACAT	6596
rs12488889	snp	G/T	0.431916	0.171483	intron-variant	HLTF	GRCh38.p7	3:149049370	TAGAAAATGGCAGTT[G/T]TAAGAATTACTTGAA	6596
rs12490157	snp	C/T	0.406986	0.194565	intron-variant	HLTF	GRCh38.p7	3:149036692	GAGGCTGAGGGAGGA[C/T]TGCTTGAGCTCAGGA	6596
rs12634247	snp	C/T	0.406986	0.194565	intron-variant	HLTF	GRCh38.p7	3:149043813	aggttgcttaaccta[C/T]gtcttgagcttcctc	6596
rs13062076	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149065646	actagcctggccaac[A/C]cagcaaaaccctgtc	6596
rs13062476	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149065639	gctcgagactagcct[A/G]gccaacacagcaaaa	6596

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