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
rs3602	snp	C/T	0.238171	0.24972	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986441	ACGCACTAAAAAAAA[C/T]GTGTGCTTGCTGCTG	81929
rs8566	snp	G/T	0.319376	0.240181	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985601	TGAACTAAAGTGGTA[G/T]TCCCCTCCTCCCAAC	81929
rs489221	snp	C/G/T	1.64762e-05	0.00287016	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978818	AGATCTTCCCAAATT[C/G/T]GGAGCGAATGCAATA	81929
rs498816	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12967727	gagactagcctggcc[A/C]acacagcgaaaccct	81929
rs498888	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12967760	ttctactaaaaatac[A/C]aaaattagatgggcg	81929
rs503063	snp	A/C/G	1.64795e-05	0.00287045	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978858	CTAGCCATAGCGACC[A/C/G]AAGATGTGAGAATTT	81929
rs522801	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12951317	TTAGGTAACAGAGAC[A/C]ATTAGTTACAGTCAC	81929
rs527830	snp	A/C	0	0	intron-variant	SEH1L	GRCh38.p7	18:12970793	CATTAACTATGAAAC[A/C]AAAAGTAACCCTACT	81929
rs527909	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12970760	GACTAACTTCATGAC[A/C]AAAAGATCTTAAGTG	81929
rs528699	snp	G/T	0	0	intron-variant	SEH1L	GRCh38.p7	18:12963018	GTACTTGTAGGAACT[G/T]GTGGCCCAGAGATGt	81929
rs612704	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12952784	aaaaaaaaaaaaaaa[A/G]aaaagaagagaagag	81929
rs616062	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12967884	ctctgttgcccaggc[G/T]ggagtgcagtggcat	81929
rs616083	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12967874	caggctggagtgcag[G/T]ggcatcatcttggct	81929
rs616100	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12967863	gcagtggcatcatct[G/T]ggctcactgcaacct	81929
rs621350	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12962997	CTACAAGTACATGGC[A/C]AAATACCACATATAT	81929
rs621878	snp	A/C	0	0	intron-variant	SEH1L	GRCh38.p7	18:12962871	TAATCTCTCTTAAGC[A/C]AACTGATCACAAAAA	81929
rs640682	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12970737	AGTGTTTCTTCTTTT[G/T]GTCAAAGCACTTAAG	81929
rs651176	snp	A/C	0	0	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978761	CATTAGGAAATATGC[A/C]AAAGCTGAAACTCTT	81929
rs651632	snp	A/C	0	0	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978848	TTTCCATATTCTAGC[A/C]ATAGCGACCAAAGAT	81929
rs652076	snp	C/T	0	0	intron-variant	SEH1L	GRCh38.p7	18:12978946	TGCCTTCTGATTACC[C/T]TTGTTTGTGGAGGAG	81929
rs977104	snp	C/G	0.277334	0.248501	intron-variant	SEH1L	GRCh38.p7	18:12982892	GTTGTAATTACTTTA[C/G]TTTTGAAAACTGCTC	81929
rs1300125	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12958166	aaccccggaggcgga[A/G]aatgcagtaagccga	81929
rs1474043	snp	C/T	0.354235	0.227234	intron-variant	SEH1L	GRCh38.p7	18:12951739	TAGTTAACAAAAGAA[C/T]ACAATCAGCAAGTAA	81929
rs1523064	snp	A/T	0.463881	0.12944	intron-variant	SEH1L	GRCh38.p7	18:12982265	TTTCTTTCTTCCATG[A/T]AACAGTCACTGAGTA	81929
rs1964084	snp	A/G	0.414741	0.188044	intron-variant	SEH1L	GRCh38.p7	18:12981071	ttctcagacggggcg[A/G]ttgccaggcagaggg	81929
rs1971424	snp	A/G	0.481856	0.0935034	intron-variant	SEH1L	GRCh38.p7	18:12969040	TATTTTTAGTAGAGA[A/G]GGGTTTTCTCCATGT	81929
rs2014404	snp	C/T	0.494936	0.050064	intron-variant	SEH1L	GRCh38.p7	18:12981431	TGAGCACTGAGTGAA[C/T]GCAACTCCGTCTGCC	81929
rs2902856	snp	A/C	0.349013	0.229557	intron-variant	SEH1L	GRCh38.p7	18:12984341	TTCATTTTGTTAGCT[A/C]TGTATTTGGCTTACT	81929
rs3070220	in-del	-/TTTT			intron-variant	SEH1L	GRCh38.p7	18:12962485	ttttttttttttttt[-/TTTT]gagagagggtcttac	81929
rs3809911	snp	A/G	0.067446	0.170804	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947361	CTTCGCTCTTAGGCT[A/G]CCGAGCCTGGACTGC	81929
rs3809912	snp	C/T	0.339656	0.233371	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947463	CAAACCCACGGTTCG[C/T]CTTCTCCACCTGCTC	81929
rs3809913	snp	C/G	0.0498117	0.149749	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947484	CCACCTGCTCCGCGC[C/G]CCTCGCATGTGTCTG	81929
rs3809914	snp	C/T	0.419936	0.183362	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947617	AAGCTCTTACTACTT[C/T]TCAGCACAGGTAACT	81929
rs3840889	in-del	-/T	0.467946	0.122472	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946933	CCTTCTGCAGCCTCA[-/T]TTTTTTTTTTTCTGT	81929
rs3976787	snp	C/T	0.416218	0.186739	intron-variant	SEH1L	GRCh38.p7	18:12971895	TGCATGTGGTAAGGC[C/T]GTGAGCAAGAGAGAG	81929
rs4797721	snp	C/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949616	cgccaccacgcccgg[C/G]taattttttgtattt	81929
rs4995995	snp	A/C	0.354235	0.227234	intron-variant	SEH1L	GRCh38.p7	18:12954741	GTGGCTCACGCCTGT[A/C]TTCTCAGCCCTTTAG	81929
rs6505773	snp	A/G	0.49907	0.0215454	intron-variant	SEH1L	GRCh38.p7	18:12974092	GGTGTTGGGGAAAGA[A/G]TGTCTGCAGGTGGGG	81929
rs6505774	snp	G/T	0.484421	0.0868729	intron-variant	SEH1L	GRCh38.p7	18:12976468	tctctgccacaGTAC[G/T]GGTGTTCCTCCCACT	81929
rs6505775	snp	C/T	0.349013	0.229557	intron-variant	SEH1L	GRCh38.p7	18:12978184	CTAAATGTACATTAT[C/T]AAAGGAGGAAACGTG	81929
rs6505776	snp	A/C	0.437409	0.165462	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984145	CTTCCCTAGGTTCAA[A/C]TATTCCAAGTCTTCA	81929
rs7227812	snp	A/G	0.499	0.0223418	intron-variant	SEH1L	GRCh38.p7	18:12976561	TGTGCTCTTAGCTCC[A/G]CCTGTCCTATTTCTG	81929
rs7228108	snp	C/T	0.26078	0.249767	intron-variant	SEH1L	GRCh38.p7	18:12976656	TTATAGGTACTGAAA[C/T]CATGGGTGTAGAAAC	81929
rs7228122	snp	C/T	0.498982	0.0225409	intron-variant	SEH1L	GRCh38.p7	18:12976687	CATGCATATTCTGGC[C/T]GGGCGCAGTGGCTCA	81929
rs7233600	snp	A/G	0.34989	0.229177	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986001	CTTATATACATTTGT[A/G]TATTTTTATGGTGTT	81929
rs7236729	snp	A/G	0.0566069	0.158427	intron-variant	SEH1L	GRCh38.p7	18:12953345	tctgtgtagacatat[A/G]ttttcatttcttttg	81929
rs7237381	snp	C/G	0.11228	0.208646	intron-variant	SEH1L	GRCh38.p7	18:12953664	tccaaGGTCCCCCCC[C/G]CTTttaaggtgaggt	81929
rs7359710	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12985020	ATCAAAACAATTTCA[A/G]GTTACCGTGGAAGAT	81929
rs7506801	snp	G/T	0.0283406	0.115616	intron-variant	SEH1L	GRCh38.p7	18:12954711	gggctcaagcagtct[G/T]cccacctcagccccc	81929
rs8083401	snp	C/T	0.416218	0.186739	intron-variant	SEH1L	GRCh38.p7	18:12967651	gggcacagtggctca[C/T]gcctgttatcccagc	81929
rs8083472	snp	C/T	0.0182019	0.0936463	intron-variant	SEH1L	GRCh38.p7	18:12976109	gaaacagtacagatt[C/T]ggtatttcaatgtct	81929
rs8085257	snp	C/T	0.0402882	0.136092	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946529	tcactcccactctga[C/T]aatctctggcaacca	81929
rs8086882	snp	C/G	0.467132	0.12391	intron-variant	SEH1L	GRCh38.p7	18:12982135	CCTCCCAAAGTGCTG[C/G]GATTACAGGTGTGAG	81929
rs8088313	snp	A/C	0.349452	0.229367	intron-variant	SEH1L	GRCh38.p7	18:12977207	AAAGAAGGTCAAGTG[A/C]AGAATGCTGTAGAAA	81929
rs8089123	snp	A/G	0.350109	0.229081	intron-variant	SEH1L	GRCh38.p7	18:12970263	TTAAAAAGTCATTCA[A/G]CTTATAGTTCAGGAG	81929
rs8089189	snp	C/T	0.412249	0.190198	intron-variant	SEH1L	GRCh38.p7	18:12970467	ACTCTGTTGCCCAGG[C/T]TAGAGTGCAGTGGCA	81929
rs8090667	snp	A/C	0.445987	0.155207	intron-variant	SEH1L	GRCh38.p7	18:12974074	TCAAAAACGAGGGGA[A/C]GTGGTGTTGGGGAAA	81929
rs8092888	snp	A/G	0.477684	0.103247	intron-variant	SEH1L	GRCh38.p7	18:12978067	tactgggttcaagca[A/G]ttctcccacctcagc	81929
rs8093576	snp	C/G	0.426507	0.177046	intron-variant	SEH1L	GRCh38.p7	18:12978290	actcacagttctgga[C/G]gtcggaagtctgaaa	81929
rs8096596	snp	A/T	0.498982	0.0225409	intron-variant	SEH1L	GRCh38.p7	18:12966561	TTCACCACCATGCCT[A/T]GCTAATTTTTTGTTA	81929
rs8099508	snp	C/T	0.0584853	0.160693	intron-variant	SEH1L	GRCh38.p7	18:12951290	tgctgtttaaaatgg[C/T]ctccaagcgtagtgA	81929
rs8182426	snp	C/G	0.201836	0.245317	intron-variant	SEH1L	GRCh38.p7	18:12978734	CTAAAATGTTAATGT[C/G]AATTGTTTTTCCATT	81929
rs9748518	snp	C/T	0.350327	0.228986	intron-variant	SEH1L	GRCh38.p7	18:12979221	GACCCTGCGGCCTTC[C/T]GCAGTGTTTGTGTCC	81929
rs9748528	snp	C/T	0.350982	0.228698	intron-variant	SEH1L	GRCh38.p7	18:12979435	gaatttttcttagta[C/T]agaacaaaatgaaaa	81929
rs9748873	snp	A/G	0.350982	0.228698	intron-variant	SEH1L	GRCh38.p7	18:12979436	aatttttcttagtat[A/G]gaacaaaatgaaaag	81929
rs9946408	snp	A/C	0.412416	0.190055	intron-variant	SEH1L	GRCh38.p7	18:12968759	GGAGATCCAGGTGAT[A/C]TGTCTACACTATTCA	81929
rs9947799	snp	C/T	0.42574	0.177808	intron-variant	SEH1L	GRCh38.p7	18:12956924	TACAAAAAATTAGCC[C/T]GGCATGGTGGTGGGT	81929
rs9948681	snp	A/C	0.369958	0.21934	intron-variant	SEH1L	GRCh38.p7	18:12974738	GTTTATATAGGTTAC[A/C]GGGCATTTTTATGTG	81929
rs9949126	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12969069	tacaaaattagctgg[G/T]tttggtggcacatgc	81929
rs9949380	snp	G/T	0.499673	0.0127754	intron-variant	SEH1L	GRCh38.p7	18:12953062	gctgggattacaggc[G/T]tgagccaccatgcct	81929
rs9949475	snp	C/T	0.412249	0.190198	intron-variant	SEH1L	GRCh38.p7	18:12969516	aacatggtgaaacct[C/T]atctttactaaagat	81929
rs9949532	snp	C/G	0.389152	0.207694	intron-variant	SEH1L	GRCh38.p7	18:12962367	tgacagagcaagacc[C/G]tgtccctaagaaaaa	81929
rs9949863	snp	C/T	0.176219	0.238865	intron-variant	SEH1L	GRCh38.p7	18:12953517	CTGTCTTTTTTATTA[C/T]AGCCATTTTAGTAGT	81929
rs9950241	snp	C/T	0.44768	0.153045	intron-variant	SEH1L	GRCh38.p7	18:12957024	agtgagccgagatca[C/T]gccactgcactccag	81929
rs9951081	snp	A/G	0.0755793	0.179102	intron-variant	SEH1L	GRCh38.p7	18:12957948	tcctggactgaagca[A/G]tcctctcacctcggc	81929
rs9951490	snp	G/T	0.485118	0.0849685	intron-variant	SEH1L	GRCh38.p7	18:12966059	GATTAATCTTACTTA[G/T]CACTTACCATTTGTT	81929
rs9953795	snp	C/T	0.118235	0.212457	intron-variant	SEH1L	GRCh38.p7	18:12951120	ttgcagtcatttgtg[C/T]atgtgtgaggagtgg	81929
rs9954360	snp	A/G	0.0333695	0.124785	intron-variant	SEH1L	GRCh38.p7	18:12951611	gtctaggctggtctc[A/G]aactcctgacctcag	81929
rs9958369	snp	C/G	0.349452	0.229367	intron-variant	SEH1L	GRCh38.p7	18:12977631	CAGGAGGCTGAAGCA[C/G]GAGAATCACTTGAAC	81929
rs9960379	snp	C/T	0.17654	0.238964	intron-variant	SEH1L	GRCh38.p7	18:12953270	ctgttcaccagttga[C/T]ggacatttgagttgt	81929
rs9964329	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949034	tttttttttttttgt[A/G]ttttttagtagagac	81929
rs9964794	snp	A/G	0.274124	0.248833	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949295	AGTAACTGGAAATCT[A/G]AAGGATAGTTTATCC	81929
rs9965936	snp	G/T	0.118235	0.212457	intron-variant	SEH1L	GRCh38.p7	18:12951077	GTCTACTCTGAAATT[G/T]ACTTGTACCCcaaaa	81929
rs9965977	snp	G/T	0.368938	0.219895	intron-variant	SEH1L	GRCh38.p7	18:12958329	gatctcaaatgattc[G/T]cctgccttggcctcc	81929
rs10541594	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12956455	TGTGTCTGGGGAATC[-/A]AAAAAAAAAAAAGAA	81929
rs11080616	snp	A/G	0.490063	0.0697833	intron-variant	SEH1L	GRCh38.p7	18:12962000	AGTTTCATCTTATCT[A/G]TGTGCCAGAAGATAA	81929
rs11080617	snp	A/G	0.326976	0.237854	intron-variant	SEH1L	GRCh38.p7	18:12968508	ACTCCATGATTGTCC[A/G]TGACTCATTTATATT	81929
rs11286163	in-del	-/T	0.0179954	0.0931336	intron-variant	SEH1L	GRCh38.p7	18:12955441	GTATCTGTTCTTTTC[-/T]TTTTTTTTTTTGATT	81929
rs11314030	in-del	-/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949215	TGAGATTTAGGAACC[-/T]CCCAGATGTGTTGCA	81929
rs11351617	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12964653	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC	81929
rs11480632	in-del	-/T/TT			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986813	TTGTGTTTTTTTTTT[-/T/TT]CCTGTTTTTGTTTTG	81929
rs11548616	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985372	CCAAGATACACCAGC[A/G]GCCTGCTTACTACTA	81929
rs11548617	snp	C/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985541	GTTCCTGAAACTAAT[C/T]TGGGTTTAAAGATTA	81929
rs11661908	snp	C/T	0.465996	0.12588	intron-variant	SEH1L	GRCh38.p7	18:12981827	TTCCATTCTTTCATT[C/T]TTTCCTACTTGCTGC	81929
rs11663762	snp	A/G	0.00597247	0.0543191	intron-variant	SEH1L	GRCh38.p7	18:12953790	catttttattattcc[A/G]aaaggaaaccccatC	81929
rs11876664	snp	G/T	0.444444	0.157135	intron-variant	SEH1L	GRCh38.p7	18:12962664	ttttagtagagacgg[G/T]gtcttgccatgtagc	81929
rs11876742	snp	C/T	0.0766824	0.180169	intron-variant	SEH1L	GRCh38.p7	18:12966183	CTGCAAGCTCCGCCT[C/T]CTGGGTTTAAGAGAT	81929
rs12232629	snp	G/T	0.303438	0.244222	intron-variant	SEH1L	GRCh38.p7	18:12981146	acatctcagatgatg[G/T]gcggccgggcagaga	81929
rs12326946	snp	C/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947226	TTCTACAGGCGGACT[C/G]TTCTAATTCATACTA	81929
rs12457672	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12971434	AAGAGGAGAAAGTag[A/C]ccagcctggccaata	81929

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