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
rs4048	snp	G/T	0.186105	0.241697	intron-variant	EML4	GRCh38.p7	2:42197455	ATCACCTCCTGCCAA[G/T]AGATGACTTGTGATT	27436
rs7233	snp	C/T	0.420991	0.182379	utr-variant-5-prime, intron-variant, nc-transcript-variant	EML4, LOC102723824	GRCh38.p7	2:42169582	GCCGGGCTCCGGGCT[C/T]AGAGGGGCGGGCACT	27436
rs13375	snp	A/G	0.330714	0.236612	utr-variant-3-prime, nc-transcript-variant, intron-variant	EML4, LOC107985873	GRCh38.p7	2:42332148	AGGCAGTTCTTGGAG[A/G]AGAAAGAGCATTTCT	27436
rs744916	snp	A/T	0.345482	0.231048	intron-variant	EML4	GRCh38.p7	2:42315585	TTAAAAGTAAAAAAA[A/T]AGACCTGTCTGGGCA	27436
rs997288	snp	C/G	0.239614	0.249784	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42298442	CCTTGGCAGGGATTT[C/G]AAACATTATTTGGCA	27436
rs997289	snp	A/G	0.405255	0.195948	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42298473	ACTGAAATATCAGAA[A/G]TACAGGCCCATAAGA	27436
rs1017466	snp	A/C	0.49263	0.0602539	intron-variant	EML4	GRCh38.p7	2:42219653	CTGGGTGCAGTGGCT[A/C]ACGCCTGTAATCCCA	27436
rs1017467	snp	A/G	0.468047	0.122292	intron-variant	EML4	GRCh38.p7	2:42219705	GGCAGATTACTTGAC[A/G]TCAGGACTTCAAGAC	27436
rs1044562	snp	C/G	0.243919	0.249926	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42289744	GCATTATAGCACTTT[C/G]TAGTACAAGCGACTG	27436
rs1127946	snp	A/G/T	0	0	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42289843	gagaccaaagtgggt[A/G/T]gatcattagatgtca	27436
rs1134696	snp	G/T	0	0	intron-variant	EML4	GRCh38.p7	2:42323789	GCCCCGCTAATTTTT[G/T]TTTGTTTTTTTTTTT	27436
rs1134697	snp	A/G	0	0	intron-variant	EML4	GRCh38.p7	2:42323712	TCCTGACCTGAAGTT[A/G]TCCACTTGCCCCAGC	27436
rs1269086	snp	A/G			intron-variant	EML4	GRCh38.p7	2:42263399	aaaaaaaaaaaaaaa[A/G]GATTCAAACCAGACA	27436
rs1371196	snp	C/T	0.0592355	0.161582	intron-variant	EML4	GRCh38.p7	2:42229346	aaacttgcctgggta[C/T]atagttactaaatga	27436
rs1371197	snp	A/G	0.499154	0.0205497	intron-variant	EML4	GRCh38.p7	2:42229672	GATTTTTTTTCTTGG[A/G]TAAGAAATAAAAGCA	27436
rs1439225	snp	C/G	0.39709	0.20215	intron-variant	EML4	GRCh38.p7	2:42285791	TTTTAATAGAGATGG[C/G]TTTTCACTCTTGTTA	27436
rs1439226	snp	A/G	0.404733	0.196361	intron-variant	EML4	GRCh38.p7	2:42285958	AATCTCTGTATTCCA[A/G]TTTCTTCATCTGTTA	27436
rs1439227	snp	A/G	0.441432	0.160792	intron-variant, upstream-variant-2KB	EML4, LOC107985874	GRCh38.p7	2:42311296	AAATTGGGCTGGTGC[A/G]GTGCTCACACCTGTA	27436
rs1439228	snp	A/G	0.305186	0.243833	intron-variant, upstream-variant-2KB	EML4, LOC107985874	GRCh38.p7	2:42311317	CACACCTGTAATCCC[A/G]GCACTTTGGGAGGCC	27436
rs1439229	snp	C/T	0.370568	0.219005	intron-variant	EML4	GRCh38.p7	2:42232241	TAGTAATGCACTGCA[C/T]AAGTGGGAGGTGGTG	27436
rs1439230	snp	G/T	0.463234	0.130503	intron-variant	EML4	GRCh38.p7	2:42223497	TCTCTGTTTTGTTTG[G/T]TTTCTGTTTTTTAAG	27436
rs1439231	snp	C/T	0.369754	0.219451	intron-variant	EML4	GRCh38.p7	2:42315744	ACAGGTGCATACCAC[C/T]GTGCCTGGCTAATTT	27436
rs1470051	snp	A/G	0.471578	0.115772	intron-variant	EML4	GRCh38.p7	2:42196029	TGACCAGACTTAGAT[A/G]TAGTATTTTATTCTC	27436
rs1470052	snp	C/T	0.402277	0.198272	intron-variant	EML4	GRCh38.p7	2:42215892	TGTCACTAAGATCTT[C/T]GTAAGAAAAGGAGAA	27436
rs1837357	snp	A/C	0.480697	0.0963277	intron-variant	EML4	GRCh38.p7	2:42285857	gcccgcctcggcctc[A/C]caaagtgctaggatt	27436
rs1837358	snp	A/G	0.0182019	0.0936463	intron-variant	EML4	GRCh38.p7	2:42218225	actgtgcatgcaagg[A/G]atctcggttgctcac	27436
rs1898843	snp	A/C	0.0788843	0.182262			GRCh38.p7	2:42202552	ccacactgaggagca[A/C]ggaagccagtctgag	27436
rs1992260	snp	G/T	0.392325	0.205532	intron-variant	EML4	GRCh38.p7	2:42260767	TGTGTAAAGCATACC[G/T]ACTGATGCCAAAAGA	27436
rs2033834	snp	A/G	0.0414363	0.137845	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42297641	GAAGTCCAGACCAGA[A/G]TAAGTGTCCACAGTT	27436
rs2033835	snp	C/G	0.391954	0.205789	intron-variant	EML4	GRCh38.p7	2:42239903	CCTCCCAATCTCTAA[C/G]ATGCCCCCATTCTCA	27436
rs2041355	snp	C/T	0.498832	0.0241331	intron-variant, nc-transcript-variant	EML4, LOC107985874	GRCh38.p7	2:42310137	ctcatacatctttgg[C/T]caatttgttttcaaa	27436
rs2053347	snp	A/G	0.441158	0.161117	intron-variant	EML4	GRCh38.p7	2:42320094	GTGCTGTTTCACATC[A/G]TTGGGTACCAGCCAT	27436
rs2053348	snp	C/T	0.450734	0.149016	intron-variant	EML4	GRCh38.p7	2:42319946	GACATTTATAATTTA[C/T]AGACATTTAATTAGA	27436
rs2053349	snp	A/G	0.333722	0.235565	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42289065	TCAAGCTTTTAGCTT[A/G]TTGGGCAGAAAGATG	27436
rs2058270	snp	C/G	0.474723	0.109542	intron-variant	EML4	GRCh38.p7	2:42322778	CCTTCCTCTACCCAA[C/G]TCACAGGCTAATGCA	27436
rs2058271	snp	C/T	0.0103295	0.0711199	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42289614	TAGCTAGGTGAAATG[C/T]GGAGTCAATCACTAA	27436
rs2058272	snp	C/G	0	0	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42289528	TGGTGATTTTCATTT[C/G]TGGTAGAGGACATTC	27436
rs2068421	snp	A/G	0.422473	0.180978	intron-variant	EML4	GRCh38.p7	2:42172757	ATGTATATACTGTAT[A/G]TATATTAAATCTCAG	27436
rs2109374	snp	A/G	0.485799	0.0830599	intron-variant	EML4	GRCh38.p7	2:42321109	AGTGTGAGCCACAGC[A/G]CCCGGCCTGGTACTA	27436
rs2109375	snp	C/G/T	0.622294	0.121404	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42291476	gcggaggctgcagca[C/G/T]tgagccaagatcatg	27436
rs2109376	snp	C/T	0.00914312	0.0669923	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42290036	gcaatggcgtgatct[C/T]gggtcactgcaacct	27436
rs2118888	snp	C/T	0.35809	0.225425	intron-variant	EML4	GRCh38.p7	2:42224414	AGTAATATTCTGTCA[C/T]ATGGGTATAACCGTG	27436
rs2118889	snp	A/C	0.249603	0.25	intron-variant	EML4	GRCh38.p7	2:42224543	TATGTGGTCATCTGT[A/C]TTTATTTCTCTTAGG	27436
rs2218104	snp	C/T	0.463989	0.129263	intron-variant	EML4	GRCh38.p7	2:42229069	TAGTAAAACTTTGAT[C/T]GTGTACCCTAGGTAC	27436
rs2286700	snp	A/T	0.378899	0.214208	intron-variant, nc-transcript-variant	EML4, LOC107985873	GRCh38.p7	2:42328882	CTGGCCAGACACCTT[A/T]GATATGGAAACACAG	27436
rs2286701	snp	A/G	0.220843	0.248294	intron-variant, downstream-variant-500B	EML4, LOC107985873	GRCh38.p7	2:42328496	TTCAAAAACAAAGCC[A/G]TAACACCAAGTCTTC	27436
rs2286702	snp	A/G	0.216349	0.247725	intron-variant, downstream-variant-500B	EML4, LOC107985873	GRCh38.p7	2:42328333	CCCAAGATAAGACAC[A/G]TCAAATTTAATTATT	27436
rs2286703	snp	G/T	0.343924	0.231686	intron-variant, utr-variant-3-prime, nc-transcript-variant	EML4	GRCh38.p7	2:42326070	ATTCAAACTAGCCAC[G/T]TTTACTTGTATTTAT	27436
rs2286704	snp	A/C	0.405255	0.195948	intron-variant	EML4	GRCh38.p7	2:42284487	ATCAAACAATCATCA[A/C]ATATCTGAAGATTTC	27436
rs2302345	snp	C/T	0.393987	0.204372	intron-variant	EML4	GRCh38.p7	2:42261058	AAAAAAATCAAACGA[C/T]AGAAAAGTGATTATT	27436
rs2302346	snp	C/T	0.499642	0.0133738	intron-variant	EML4	GRCh38.p7	2:42260905	TTCTAAGGCGATACA[C/T]CCCATGAAGATTGCC	27436
rs2374393	snp	C/G	0.472241	0.114494	intron-variant	EML4	GRCh38.p7	2:42187417	ttttgtgctttttac[C/G]tagcatattgcttta	27436
rs2374405	snp	A/C	0.222333	0.248464	intron-variant	EML4	GRCh38.p7	2:42252734	CTGCAATAGGATCCC[A/C]TTGTCTTATCACCGC	27436
rs2374406	snp	A/G			intron-variant	EML4	GRCh38.p7	2:42266342	AAGATAATTCTTAAT[A/G]CATTATATATCAAAA	27436
rs2374407	snp	C/T	0.460813	0.134379	intron-variant	EML4	GRCh38.p7	2:42318200	GTAGGCAGTGTAGCA[C/T]AGTGGTTAAGAGCAC	27436
rs2579961	snp	A/C	0.495818	0.0455352			GRCh38.p7	2:42181273	ataagaaacctgagt[A/C]catacagatataaac	27436
rs2579963	snp	C/T	0.499989	0.00239614			GRCh38.p7	2:42179930	CCCTCTATATGTACA[C/T]GTATCTGTGTGTATA	27436
rs2579966	snp	G/T	0.469148	0.120308			GRCh38.p7	2:42193591	TTGACCTTTTTCATT[G/T]CTGAGATTTCTTAAA	27436
rs2579967	snp	A/T	0.388021	0.208447			GRCh38.p7	2:42187736	ACCACATTTTTTATA[A/T]AGGACTTGTACCCAA	27436
rs2579968	snp	C/G	0.473359	0.112298			GRCh38.p7	2:42183965	AGAGGGCCAGAAGGT[C/G]AAAGAGGTGACCTCA	27436
rs2579969	snp	C/T	0.387453	0.208822			GRCh38.p7	2:42183579	ACATACATATACATA[C/T]ACCAAAAACCTATCA	27436
rs2579970	snp	C/T	0.476746	0.10529			GRCh38.p7	2:42189665	ACAGACATTAATATC[C/T]GTATTTTATAAAAGA	27436
rs2719127	snp	G/T	0.369754	0.219451	intron-variant	EML4	GRCh38.p7	2:42181541	tgggaggctgaggta[G/T]gtcatttgaggtcag	27436
rs2719128	snp	G/T	0.499673	0.0127754	intron-variant	EML4	GRCh38.p7	2:42183029	GGCATGGTGGTGCAC[G/T]CCTGTGATACCAGGT	27436
rs2719129	snp	A/G	0.474813	0.109357	intron-variant	EML4	GRCh38.p7	2:42185170	TTTGCTCGGGATTAG[A/G]GGTTGACAGACTACC	27436
rs2719131	snp	G/T	0.47614	0.106587	intron-variant	EML4	GRCh38.p7	2:42187653	tttctctatgaattc[G/T]cctattTGGTGCTCA	27436
rs2719132	snp	A/T	0.4582	0.138394	intron-variant	EML4	GRCh38.p7	2:42187677	GTGCTCATTTTTTTT[A/T]AAAAAAAATGGTTGC	27436
rs2719133	snp	A/G	0.373397	0.217424	intron-variant	EML4	GRCh38.p7	2:42180607	tcaaattgttATAGT[A/G]TAAAGAAGACAGGCA	27436
rs2719134	snp	C/G	0.398714	0.200958	intron-variant	EML4	GRCh38.p7	2:42193177	ATTGCCTACAGTATT[C/G]AGTGCAGTAGTATTC	27436
rs2719135	snp	C/T	0.399073	0.200692	intron-variant	EML4	GRCh38.p7	2:42193459	TGCTGTGTGATTGTT[C/T]AGACTGACAGTGGAA	27436
rs2719136	snp	C/T	0.0372196	0.131242	intron-variant	EML4	GRCh38.p7	2:42180147	AATTTTTTTTAATGC[C/T]ATACTATGAAGTATA	27436
rs2719137	snp	A/G	0.428333	0.175206	intron-variant	EML4	GRCh38.p7	2:42193750	TTGTGCAGCAGCACA[A/G]TCATGGCTCACTGCA	27436
rs2719138	snp	C/T	0.428786	0.174744	intron-variant	EML4	GRCh38.p7	2:42194194	AAATGGGATATCCTG[C/T]GGTGTTTGGTTAAGG	27436
rs2888819	snp	A/G	0.093777	0.195178	intron-variant	EML4	GRCh38.p7	2:42202355	agactagcctggTGT[A/G]TTAGTCAGTGTTCTC	27436
rs3038373	in-del	-/TT	0.031825	0.122064	intron-variant	EML4	GRCh38.p7	2:42240234	CAGAAGCAATGCATT[-/TT]ACCTTAAAGGGCATA	27436
rs3038374	in-del	-/T/TT/TTT	0	0	intron-variant	EML4	GRCh38.p7	2:42203652	CCCTTTTTTTTTTTT[-/T/TT/TTT]GTAGAAGTTCCCTCC	27436
rs3732195	snp	C/G	0.484841	0.0857308	intron-variant, downstream-variant-500B	EML4, LOC107985874	GRCh38.p7	2:42286519	AGCCATTTAGCAATA[C/G]CTAATATGTTAGCAA	27436
rs3862994	snp	G/T	0	0	intron-variant	EML4	GRCh38.p7	2:42262025	GCTTGAATAAGCATT[G/T]CTAAACAGGCAAATT	27436
rs4145345	snp	A/G	0.357451	0.225731	intron-variant	EML4	GRCh38.p7	2:42275396	AGTTTTAGAGTGGAA[A/G]TGTTTCCCGAGTTCT	27436
rs4290705	snp	C/T	0.499997	0.00119808	upstream-variant-2KB, intron-variant	EML4, LOC102723824	GRCh38.p7	2:42168854	GCTTCTGATCTGTCC[C/T]GGGCCCTGCGGCTGT	27436
rs4375914	snp	C/T	0.427727	0.175821	intron-variant	EML4	GRCh38.p7	2:42255148	TGGAGTGCAGTGGTG[C/T]GATCCCCACTAACTG	27436
rs4410332	snp	A/G	0	0	intron-variant	EML4, LOC107985874	GRCh38.p7	2:42309082	ctctgggatataaaa[A/G]agtagaattgttggg	27436
rs4428056	snp	A/T	0.37138	0.218556	intron-variant	EML4	GRCh38.p7	2:42175687	TATTTTTAATAGAGA[A/T]GAGGTTTTGCCATAT	27436
rs4494804	snp	A/T	0.24134	0.24985	upstream-variant-2KB, intron-variant	EML4, LOC102723824	GRCh38.p7	2:42168806	GGTTAGACAAGATGA[A/T]CTTTTGGGTCATGTC	27436
rs4516480	snp	G/T	0.371987	0.218218	intron-variant	EML4	GRCh38.p7	2:42174538	TCGGGTGATGGCCAC[G/T]CACCTTGGCCTCCCA	27436
rs4952720	snp	C/T	0.0794208	0.182764	intron-variant, nc-transcript-variant	EML4, LOC107985873	GRCh38.p7	2:42329047	TAGAAACTAATGTTA[C/T]AAGGCCTTCTGTCCA	27436
rs5830720	in-del	-/T			intron-variant	EML4, LOC107985874	GRCh38.p7	2:42291420	TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCATTC	27436
rs5830721	in-del	-/A			intron-variant	EML4, LOC107985874	GRCh38.p7	2:42307576	AATGGAAAAATCTTA[-/A]TGTAGCCATTCTATT	27436
rs5830723	in-del	-/T	0.363359	0.222822	intron-variant	EML4	GRCh38.p7	2:42323028	TGTCCAACATAGATG[-/T]TTTTTGCATGAATAT	27436
rs6146736	in-del	-/TTCTTATCATTCCTTAAGCATCTCAGAGTTG			intron-variant	EML4	GRCh38.p7	2:42243404	CGAGAGACTGAATTG[lengthTooLong]GACACATGTGCCTTT	27436
rs6544510	snp	A/T	0.0528381	0.153711	intron-variant	EML4	GRCh38.p7	2:42172604	TAGGTATTATTAATA[A/T]ATCTTTTAATCCACA	27436
rs6544511	snp	C/T	0.370974	0.218781	intron-variant	EML4	GRCh38.p7	2:42174977	gcccgccagcatgtc[C/T]ggctaatttttgtat	27436
rs6544512	snp	A/G	0.499982	0.00299515	intron-variant	EML4	GRCh38.p7	2:42200069	AATCCCAGCACTTTG[A/G]GAGGCCAAGGCGGGC	27436
rs6544513	snp	A/G	0.499451	0.0165644	intron-variant	EML4	GRCh38.p7	2:42200288	CGAGATTGGGCCACT[A/G]CACTCCAGCCTGGGC	27436
rs6544514	snp	A/G	0.0633504	0.166319	intron-variant	EML4	GRCh38.p7	2:42203205	cattgtgtcccataa[A/G]tacatataattatta	27436
rs6544515	snp	A/G	0.470908	0.117046	intron-variant	EML4	GRCh38.p7	2:42203260	CCTAACATTTTCCAT[A/G]AGTATATGAAGGTAA	27436
rs6544516	snp	C/T	0.475348	0.108251	intron-variant	EML4	GRCh38.p7	2:42207314	ATATTAATATAATAC[C/T]AGATATAACTAGTTT	27436
rs6544517	snp	C/G	0.330714	0.236612	intron-variant	EML4	GRCh38.p7	2:42208508	GGTGCAATCTCGGCT[C/G]ATTGCAACCTCCGCC	27436
rs6544518	snp	C/T	0.467337	0.123551	intron-variant	EML4	GRCh38.p7	2:42214400	AGCTTTTTCCTTTAC[C/T]TTGTTTTCCTCACCT	27436
rs6544519	snp	A/T	0.460702	0.134554	intron-variant	EML4	GRCh38.p7	2:42214478	CATTGAAAATGAATG[A/T]ATTGCTAAAAATGAA	27436

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