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
rs12221	snp	C/T	0.312083	0.242169	synonymous-codon, downstream-variant-500B	STAM	GRCh38.p7	10:17714597	CCAGGCGCCAGTATA[C/T]AGTCCTCCTCCTGCC	8027
rs723790	snp	C/T	0.186421	0.24178	intron-variant	STAM	GRCh38.p7	10:17683432	GCTCACACCTATAAT[C/T]CCAGCATTTTGGGAG	8027
rs723791	snp	A/C	0.175254	0.238565	intron-variant	STAM	GRCh38.p7	10:17683367	TGGGACCAGCCTGGG[A/C]AACACTGTGAAACCC	8027
rs723792	snp	A/G	0.176861	0.239062	intron-variant	STAM	GRCh38.p7	10:17683307	GCCAGAAATGGTCCC[A/G]GCTCCTATGGGCGCA	8027
rs942775	snp	C/T	0.145978	0.227331	intron-variant	STAM	GRCh38.p7	10:17709047	TCTGGCTAATAAATA[C/T]CTGTGGTCAGCGTCA	8027
rs1007264	snp	A/G	0.29432	0.24604	intron-variant	STAM	GRCh38.p7	10:17668275	AGTTTTAGGAAAGAG[A/G]GAGAGTGGTTTGGAA	8027
rs1061162	snp	A/G	0.136166	0.22258	utr-variant-3-prime	STAM	GRCh38.p7	10:17715297	CTTCAAGAAAACAAA[A/G]TTGTTAGCGTATTTA	8027
rs1359506	snp	C/G	0.0244538	0.107838	intron-variant	STAM	GRCh38.p7	10:17699188	TGGAAAGATTAAAAA[C/G]TTTTGTAAAAGAGAA	8027
rs1359507	snp	A/G	0.0244538	0.107838	intron-variant	STAM	GRCh38.p7	10:17698794	CTAACAGCTCTTGAC[A/G]CGCAAGTTTGCAACC	8027
rs1801675	snp	A/T			utr-variant-3-prime	STAM	GRCh38.p7	10:17715113	TGTTATGTACATATA[A/T]TGATATGTAACTGCA	8027
rs1937348	snp	A/G	0.44858	0.151875	intron-variant	STAM	GRCh38.p7	10:17648683	CTTGCCACTGACTAT[A/G]AGAGATAACAATGAC	8027
rs1937349	snp	A/T	0.130008	0.219321	intron-variant	STAM	GRCh38.p7	10:17653395	TTTTGATAAAACAGG[A/T]TAAAAACTCTGAACA	8027
rs1977342	snp	A/G	0.296364	0.245663	intron-variant	STAM	GRCh38.p7	10:17707175	tgatccacccgcctc[A/G]gcctcccaacgtgct	8027
rs2001832	snp	G/T	0.00517822	0.0506191	intron-variant	STAM	GRCh38.p7	10:17675700	ttcttgttcactact[G/T]tattcctaaagcctt	8027
rs2031514	snp	A/G	0.496968	0.0388195	intron-variant	STAM	GRCh38.p7	10:17676700	TTTCGCGAGTGAAAG[A/G]TGGTGTTAACTGGAC	8027
rs2031515	snp	C/T	0.12932	0.218944	intron-variant	STAM	GRCh38.p7	10:17676495	TTCCAATGTCTTTTT[C/T]TCAAATCACAGACCA	8027
rs2182158	snp	C/T	0.136506	0.222754	intron-variant, upstream-variant-2KB	STAM	GRCh38.p7	10:17689273	ACAGACTGTAATGAG[C/T]GATGTGAAACCATGA	8027
rs2243617	snp	A/G	0.346147	0.230772	upstream-variant-2KB, nc-transcript-variant	STAM, STAM-AS1	GRCh38.p7	10:17643728	GACTTCATCCGAGCA[A/G]GTTTGTCACCTCACG	8027
rs2244877	snp	A/G	0.127599	0.217986	intron-variant	STAM	GRCh38.p7	10:17654793	ATATTTTTCAAAAAA[A/G]TCTAGGTCTTGTTGT	8027
rs2244878	snp	C/G	0.127599	0.217986	intron-variant	STAM	GRCh38.p7	10:17654795	ATTTTTCAAAAAAGT[C/G]TAGGTCTTGTTGTTT	8027
rs2246058	snp	C/T	0.128632	0.218563	intron-variant	STAM	GRCh38.p7	10:17677951	AGTAAAAACTTTTAT[C/T]GGGCAATTTGAACTC	8027
rs2251596	snp	C/T	0.473174	0.112665	upstream-variant-2KB, nc-transcript-variant	STAM, STAM-AS1	GRCh38.p7	10:17642399	TGTACTATGATTTAA[C/T]TGACCAGTGTAAATT	8027
rs2251710	snp	A/T	0.3748	0.216622	upstream-variant-2KB, nc-transcript-variant	STAM, STAM-AS1	GRCh38.p7	10:17643342	ATTATTCTCTGTGTG[A/T]TGGAGAAGTTTTAAG	8027
rs2253965	snp	C/T	0.258843	0.249844	intron-variant, upstream-variant-2KB	STAM, LOC105376438	GRCh38.p7	10:17697804	GCATATCAACCTATA[C/T]ATATAAGCTCTTTAA	8027
rs2255065	snp	A/G	0.137187	0.223099	intron-variant	STAM	GRCh38.p7	10:17647389	ggatttcaggacacc[A/G]aactttttctcattt	8027
rs2255153	snp	A/C	0.137527	0.223271	intron-variant	STAM	GRCh38.p7	10:17647578	cctgggactgaatcc[A/C]agcagtgtggcccca	8027
rs2255426	snp	G/T	0.467337	0.123551	intron-variant	STAM	GRCh38.p7	10:17650311	TGTATAATGGATATT[G/T]CTATCCCTATTTACC	8027
rs2255657	snp	C/G	0.47517	0.10862	intron-variant	STAM	GRCh38.p7	10:17651913	TTTCTCAAAATTTAT[C/G]ACTGTCAAAGATCTG	8027
rs2255760	snp	C/T	0.475081	0.108804	intron-variant	STAM	GRCh38.p7	10:17652606	ACCTGCCACCTTATT[C/T]AAAAACATAATAGCT	8027
rs2264643	snp	C/T	0.00914312	0.0669923	intron-variant	STAM	GRCh38.p7	10:17656111	agagacgggtttcac[C/T]gtgttagccaggatg	8027
rs2272143	snp	A/T	0.142358	0.22564	intron-variant	STAM	GRCh38.p7	10:17709003	TGTTACAGCTGTTTA[A/T]GTGCCCCCAGTTATC	8027
rs2272146	snp	C/T	0.185788	0.241613	intron-variant	STAM, LOC105376438	GRCh38.p7	10:17696485	ATTGTCAGCTTCAGA[C/T]GGTTCACAGGCTCCA	8027
rs2280583	snp	C/T	0.0693013	0.172766	upstream-variant-2KB, nc-transcript-variant	STAM, STAM-AS1	GRCh38.p7	10:17643818	GGGAATACAAGGTTA[C/T]GATAACCGAGAGAGC	8027
rs2357291	snp	A/G	0.173643	0.238054	intron-variant	STAM	GRCh38.p7	10:17662373	ATCCTTTCAGACCCA[A/G]TGTAGATACCACTTC	8027
rs2357292	snp	A/T	0.472989	0.113031	intron-variant	STAM	GRCh38.p7	10:17662634	TACTCTAGAGGGAGA[A/T]TGCCTGGGTTCAAAT	8027
rs2357293	snp	C/T	0.0287284	0.116357	intron-variant	STAM	GRCh38.p7	10:17662889	CTGTTGAAGACTGGG[C/T]ACCAAGCTAGACCAC	8027
rs2357294	snp	G/T			intron-variant	STAM	GRCh38.p7	10:17669905	ttttttttttttttg[G/T]atttttagtagacac	8027
rs2461890	snp	C/T	0.46754	0.123192	intron-variant	STAM	GRCh38.p7	10:17649636	AATGTTCTAGAAAAA[C/T]ACCAATAATTCATTA	8027
rs2570276	snp	A/C	0.090703	0.192677			GRCh38.p7	10:17702220	ATCATTACCTTATAC[A/C]TATGAATGAATCTAA	8027
rs2570277	snp	A/G	0.34101	0.232846			GRCh38.p7	10:17709798	TCCTCAAAGAGTTAC[A/G]TGTTAGAGATGCTTG	8027
rs2570278	snp	C/T	0.48679	0.0801892			GRCh38.p7	10:17712538	CCAAGTACAAGAGCA[C/T]TGAATTTCCCAACAA	8027
rs2570284	snp	C/T	0.488424	0.0751925			GRCh38.p7	10:17674872	TTAGAATTATTTTTT[C/T]CTAATGGTATTTTTC	8027
rs2570285	snp	C/G	0.138886	0.22395			GRCh38.p7	10:17678337	aacctgggaggtgca[C/G]gttacagtgaactga	8027
rs2570286	snp	A/C	0.130008	0.219321			GRCh38.p7	10:17683712	ttccagcatgcttat[A/C]atagcttatataaag	8027
rs2570287	snp	A/G	0.492287	0.0616198			GRCh38.p7	10:17684071	GGCCTCATCTCTGAC[A/G]ACTGTGTGAGCGTTG	8027
rs2570288	snp	A/C	0.130351	0.219509			GRCh38.p7	10:17686518	AGTAGCTGGGAATAC[A/C]GGCATGCGCCACCAC	8027
rs2570289	snp	A/G	0.130694	0.219696			GRCh38.p7	10:17695869	tccatttgggctgcc[A/G]taacaaactaccgta	8027
rs2688786	snp	C/T	0.360632	0.224189	intron-variant	STAM	GRCh38.p7	10:17706173	CAAGTAAAAAAATTC[C/T]GTTAAACTTTATTTT	8027
rs2688787	snp	C/T	0.240478	0.249819	intron-variant	STAM	GRCh38.p7	10:17703997	CCTCTTATGTCATGC[C/T]AGAGGATTTTGCTTT	8027
rs2688788	snp	C/T	0.492188	0.0620098	intron-variant	STAM	GRCh38.p7	10:17692247	TTAAACAAGGTACTG[C/T]GATATGAGTGGTTAA	8027
rs2688789	snp	C/T	0.485255	0.0845871	intron-variant	STAM	GRCh38.p7	10:17691015	AACTTCACAATTAGA[C/T]AGATTTGAACTTTTA	8027
rs2688790	snp	A/G	0.489434	0.0719116	intron-variant	STAM	GRCh38.p7	10:17683856	AATATAAAATTCAAA[A/G]TACTAAGCATTCAAT	8027
rs2688791	snp	C/T	0.425123	0.178415	intron-variant	STAM	GRCh38.p7	10:17708636	GTTTTTCAAAATGCC[C/T]GTTGACAGAAATAAC	8027
rs2688797	snp	G/T	0.128976	0.218754	intron-variant	STAM	GRCh38.p7	10:17670809	AATTATTCCCTTAAT[G/T]TTAAGCTTATTAAGT	8027
rs2764800	snp	A/T	0	0	intron-variant	STAM	GRCh38.p7	10:17686514	CCTGAGTAGCTGGGA[A/T]TACAGGCATGCGCCA	8027
rs2764801	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	STAM	GRCh38.p7	10:17689470	GAAGCAAAGGACATT[C/T]TTCTTCTTAAAAAAA	8027
rs2764804	snp	A/G	0.401747	0.198678	intron-variant	STAM	GRCh38.p7	10:17712813	TTCTTTCTTTTTTTA[A/G]TGGGAGCAGTGCACA	8027
rs2764805	snp	A/C	0.459574	0.136304	utr-variant-3-prime, downstream-variant-500B	STAM	GRCh38.p7	10:17715961	TATTGTTTTCTTTCA[A/C]ACTGGATTTTTGGGT	8027
rs3780960	snp	A/G	0.333722	0.235565	intron-variant, upstream-variant-2KB	STAM, STAM-AS1	GRCh38.p7	10:17645554	ATATTATTTAACTGC[A/G]GAATGGAATGATGTG	8027
rs3813860	snp	C/G	0.0912534	0.193131	intron-variant	STAM	GRCh38.p7	10:17694586	TAGGTTGAGTCTTTA[C/G]ACTGGTAAGAATTAC	8027
rs3813861	snp	C/G	0.0023933	0.0345097	intron-variant	STAM	GRCh38.p7	10:17694841	AGTTTTCATGCTGTT[C/G]CAATTTTGTTAATTT	8027
rs3824629	snp	G/T	0.0930568	0.194599	intron-variant	STAM	GRCh38.p7	10:17704612	TGAGAAATGTTCCAT[G/T]TTTAATATTATCCTC	8027
rs3830598	in-del	-/A			intron-variant	STAM	GRCh38.p7	10:17684423	GTAGGAAAAAAAAAA[-/A]GGTTTGAAAATAAAA	8027
rs3832661	in-del	-/G/GG			utr-variant-3-prime, downstream-variant-500B	STAM	GRCh38.p7	10:17714959	CAGGGGCGGGGGGGG[-/G/GG]AAGAACCTCTAAAAA	8027
rs4281393	snp	C/G	0	0	intron-variant	STAM	GRCh38.p7	10:17678850	aatttgtctattcta[C/G]atacctcatggaagt	8027
rs4400696	snp	A/G	0.466721	0.124627	intron-variant	STAM	GRCh38.p7	10:17669438	TTTCAAATTGAGTTG[A/G]CTGGGTTAAAAACAA	8027
rs4551659	snp	C/T	0.304438	0.244001	intron-variant	STAM	GRCh38.p7	10:17704769	GCACTTTAAGATTTT[C/T]AGATTAATATTTTAG	8027
rs4556434	snp	A/G	0.474272	0.110462	intron-variant	STAM	GRCh38.p7	10:17703125	AATTTTAAATATTGT[A/G]TAGTATTCTGTAAGC	8027
rs4589180	snp	A/G	0	0	intron-variant	STAM	GRCh38.p7	10:17648426	aagctgggcacccta[A/G]ccagcagcAgcaacc	8027
rs4747317	snp	A/G	0.158962	0.232835	intron-variant	STAM	GRCh38.p7	10:17655052	CTCTTCTTATTTTCT[A/G]AATACATCGGGAAGC	8027
rs4747318	snp	C/T	0.123452	0.215605	intron-variant	STAM	GRCh38.p7	10:17655342	TTGTATTAATTCTTA[C/T]GCAAGGAATTAATCT	8027
rs4747319	snp	A/G	0.17461	0.238362	intron-variant	STAM	GRCh38.p7	10:17658859	acaacatacagttgt[A/G]tgttgttttttgatt	8027
rs4747320	snp	C/G	0.164546	0.234942	intron-variant	STAM	GRCh38.p7	10:17666479	ggctcactgcaagct[C/G]cgcctgccgggttca	8027
rs4747321	snp	C/T	0.0905309	0.192535	intron-variant	STAM	GRCh38.p7	10:17674879	ACCATTAGGAAAAAA[C/T]AATTCTAATAAACAA	8027
rs4748393	snp	A/T	0.163236	0.234461	intron-variant	STAM	GRCh38.p7	10:17646511	ATACTCCTTAATGAG[A/T]GGTTGCTACATAGGA	8027
rs4748394	snp	A/G	0.16976	0.236773	intron-variant	STAM	GRCh38.p7	10:17653718	ttaggcatgataagt[A/G]atctagagaaattaa	8027
rs4748395	snp	G/T	0.137187	0.223099	intron-variant	STAM	GRCh38.p7	10:17655348	TAATTCTTATGCAAG[G/T]AATTAATCTGTGTGA	8027
rs4748396	snp	A/G	0.161596	0.233848	intron-variant	STAM	GRCh38.p7	10:17659265	cttcccatcccttgc[A/G]tcattgctgtcattc	8027
rs4748397	snp	A/G	0.157311	0.232183	intron-variant	STAM	GRCh38.p7	10:17670298	GACTTATAGAATTCT[A/G]ATGACTGTTGTGctt	8027
rs4748398	snp	C/T	0.151668	0.229849	intron-variant, upstream-variant-2KB	STAM	GRCh38.p7	10:17688417	CTACTTCTTTATAAA[C/T]GAATTGGTTTAACAT	8027
rs4748399	snp	C/T	0.136506	0.222754	intron-variant, upstream-variant-2KB	STAM	GRCh38.p7	10:17689391	GCTTTCTTCCCAAGG[C/T]ATTTCCAGTTTATCT	8027
rs4748400	snp	C/G	0.140919	0.224948	intron-variant	STAM	GRCh38.p7	10:17692361	ACTGACTGATGTGTT[C/G]AAACTCAAAAGGGAA	8027
rs4748401	snp	A/G	0.184521	0.241273	intron-variant	STAM	GRCh38.p7	10:17694875	TTTAAACTTTCAGTT[A/G]TGAATGAATGAATAA	8027
rs4748402	snp	C/T	0.139225	0.224118	intron-variant, nc-transcript-variant	STAM, LOC105376438	GRCh38.p7	10:17696627	GGCTTCTTCTTCTTT[C/T]GTAATAAAGGAAGAT	8027
rs4748403	snp	A/T	0.114738	0.210248	intron-variant	STAM	GRCh38.p7	10:17703589	TTTTTTAAAAAACAT[A/T]AATACATATATACTT	8027
rs4748404	snp	A/C	0.114738	0.210248	intron-variant	STAM	GRCh38.p7	10:17703594	TAAAAAACATAAATA[A/C]ATATATACTTATATA	8027
rs4748405	snp	C/G	0.139723	0.224364	intron-variant	STAM	GRCh38.p7	10:17705054	GTGCATTTATGTTGT[C/G]TACCTTCTTTCCTGA	8027
rs4748406	snp	A/G	0.115088	0.210473	intron-variant	STAM	GRCh38.p7	10:17705276	AAACAAGGGCTAGCT[A/G]TGTAATTCTCTTTGC	8027
rs4748407	snp	C/G	0.183886	0.241099	intron-variant	STAM	GRCh38.p7	10:17711159	TCAGTTTATATATAT[C/G]TGAGAGGCTATCTCT	8027
rs4748408	snp	C/T	0.114738	0.210248	intron-variant	STAM	GRCh38.p7	10:17711294	TAAAGCTACCTGTAG[C/T]GATGGTAGTATTATA	8027
rs5783557	in-del	-/T	0.146314	0.227484	intron-variant	STAM	GRCh38.p7	10:17675799	TTGGTACCTATTGAA[-/T]TTTTTTTTTAACAGT	8027
rs6602207	snp	C/T	0.462144	0.132269	intron-variant	STAM	GRCh38.p7	10:17656879	agaaatccaagtggg[C/T]gacttgaagagtaag	8027
rs7070105	snp	A/T	0.32885	0.23724	intron-variant	STAM	GRCh38.p7	10:17650917	AAAAATACAAAAAAT[A/T]AGCCGGGCGTAGTGG	8027
rs7070402	snp	A/G	0.16976	0.236773	intron-variant	STAM	GRCh38.p7	10:17654105	aagtctttgctgact[A/G]ggtagttagcatcag	8027
rs7072026	snp	C/G	0.00478085	0.0486577	intron-variant	STAM	GRCh38.p7	10:17648010	tccttgcccttctca[C/G]tagacgacaacatga	8027
rs7073509	snp	A/G			intron-variant	STAM	GRCh38.p7	10:17660214	ATATAATTTTTTTAT[A/G]AAGAAAAATCAATGC	8027
rs7073595	snp	C/T	0.172674	0.237741	intron-variant	STAM	GRCh38.p7	10:17657056	cccatcggaggcttt[C/T]ttcccttttctggtg	8027
rs7075270	snp	A/C	0.126219	0.217206	intron-variant, missense	STAM	GRCh38.p7	10:17713291	ccaggggacctcatg[A/C]agcccggtgattctg	8027
rs7076184	snp	A/T	0.00835141	0.0640778	intron-variant	STAM	GRCh38.p7	10:17704697	TGAATTCTTATAATT[A/T]TCTATCCAAACGAAG	8027
rs7076634	snp	C/T	0.145305	0.227022	intron-variant	STAM	GRCh38.p7	10:17673293	ATGTTTTCCACTTAG[C/T]GAACTCAGTGGAAGA	8027

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