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
rs476393	snp	A/T			intron-variant	YES1	GRCh38.p7	18:735182	aaaaaaaatcattat[A/T]tgaaaaagatacatc	7525
rs480645	snp	A/C			intron-variant	YES1	GRCh38.p7	18:771355	ctggggaataagagc[A/C]aaactttgtctcaaa	7525
rs489167	snp	A/C			intron-variant	YES1	GRCh38.p7	18:754713	agagactcccaatcc[A/C]aaaaaaaaaaaaaaa	7525
rs490678	snp	G/T	0	0	intron-variant	YES1	GRCh38.p7	18:773707	AGTTGGAACAAAGTT[G/T]GCTAAAAGAAGTGGG	7525
rs492056	snp	C/T	0.0126979	0.078662	utr-variant-3-prime	YES1	GRCh38.p7	18:722894	TCAGGAGATCGAGAC[C/T]ATCCTGGCTAACACG	7525
rs492937	snp	A/C			intron-variant	YES1	GRCh38.p7	18:748988	tttttagtagagacc[A/C]ggtttcaccatgttg	7525
rs508143	snp	A/T			intron-variant	YES1	GRCh38.p7	18:744537	ccaggcgtggtggca[A/T]gcacctgtaggctca	7525
rs523762	snp	A/G	0.0174175	0.0916809	intron-variant	YES1	GRCh38.p7	18:761893	agccATGATGTTAAC[A/G]TTTCTAAGACAACCC	7525
rs532618	snp	C/G			intron-variant	YES1	GRCh38.p7	18:791866	ttgagaacagcctga[C/G]caacatggtgaaacc	7525
rs537141	snp	A/G	0.00532576	0.0513275	synonymous-codon	YES1	GRCh38.p7	18:724612	GCTCCACTTGTTCTA[A/G]TACTTCACGGTTCAC	7525
rs541436	snp	C/T	0.375	0.216506	intron-variant	YES1	GRCh38.p7	18:779909	CAATGTATGTAGTCC[C/T]TTTTTTTTTTTTTTC	7525
rs557308	snp	A/C/G	0.00438332	0.0466095	downstream-variant-500B	YES1	GRCh38.p7	18:721554	aaaaaaaaacaaaac[A/C/G]aaacaaaaaaaaaAG	7525
rs558535	snp	G/T	0	0	intron-variant	YES1	GRCh38.p7	18:743855	gcagtggcgcaattt[G/T]ggctcactgcaacct	7525
rs564942	snp	A/G	0.426507	0.177046	utr-variant-3-prime	YES1	GRCh38.p7	18:722868	GAGGCCGAGGCGGGC[A/G]GATCACAAGGTCAGG	7525
rs572600	snp	A/T	0.0225045	0.103662	intron-variant	YES1	GRCh38.p7	18:774498	ttaacatttatcgag[A/T]tggggaagattgcag	7525
rs581987	snp	A/G			intron-variant	YES1	GRCh38.p7	18:771365	ttttttttttttgga[A/G]acaaagtttggctct	7525
rs605199	snp	A/C	0	0	intron-variant	YES1	GRCh38.p7	18:735812	aagaactAGTTTCCC[A/C]AAAACTATTGAAAAA	7525
rs631811	snp	G/T			intron-variant	YES1	GRCh38.p7	18:773719	GAAACATAGGAAAGT[G/T]GGAACAAAGTTGGCT	7525
rs642892	snp	G/T	0	0	intron-variant	YES1	GRCh38.p7	18:773549	CTTTCCTCACTGTCT[G/T]ACCAGCCTTTTAATT	7525
rs661509	snp	A/C			intron-variant, upstream-variant-2KB	YES1	GRCh38.p7	18:775634	agacctcatctctac[A/C]aaaagtaaaaaaatt	7525
rs668277	snp	A/G			intron-variant	YES1	GRCh38.p7	18:744471	ACCTGGGAGGTGGAA[A/G]TTGCAGTGAGCTGAG	7525
rs681792	snp	G/T			intron-variant	YES1	GRCh38.p7	18:743831	gcaacctctgcctcc[G/T]gggttcatgcgatcc	7525
rs694301	snp	A/C			intron-variant	YES1	GRCh38.p7	18:793752	GTTTTGTAAtatacc[A/C]aaaatagttataaag	7525
rs1060910	snp	A/G	0.495095	0.0492773	utr-variant-3-prime	YES1	GRCh38.p7	18:722830	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	7525
rs1060922	snp	A/G	0.49917	0.0203505	utr-variant-3-prime	YES1	GRCh38.p7	18:722402	ATTCTGTGCCATGGC[A/G]TATATGTTCAAATTC	7525
rs1061035	snp	C/T	0.234692	0.249531	utr-variant-3-prime	YES1	GRCh38.p7	18:722118	TTTATGTACTAAATC[C/T]AATCAGGAAAGTAAG	7525
rs1274882	snp	A/T	0	0	intron-variant	YES1	GRCh38.p7	18:771032	aaaaTCTGAAAAGTT[A/T]AAACCTAGAAAAACA	7525
rs1274883	snp	A/C	0	0	intron-variant	YES1	GRCh38.p7	18:779006	TTTAGATATACAAAC[A/C]ATTGACCTTAAAGTA	7525
rs1275321	snp	A/G	0.230896	0.249269	intron-variant	YES1	GRCh38.p7	18:800088	TCAAGTAGAATGCTT[A/G]TTTGAAATTCATCCT	7525
rs1275322	snp	C/G	0.0225045	0.103662	upstream-variant-2KB	YES1	GRCh38.p7	18:813888	GGGAGTCCAAGACAG[C/G]AGGATCACTTGAGTC	7525
rs1290012	snp	C/T			intron-variant	YES1	GRCh38.p7	18:747448	gggtcttggctctgt[C/T]gcccaggctagagtg	7525
rs1298066	snp	A/C	0	0	intron-variant	YES1	GRCh38.p7	18:773764	AATACAATCTGATCC[A/C]ATGCTGACTAATAAA	7525
rs1298343	snp	C/G			intron-variant	YES1	GRCh38.p7	18:747418	gcagtggcgtgatct[C/G]ggctcactgcaacct	7525
rs1298706	snp	A/T	0	0	intron-variant	YES1	GRCh38.p7	18:752075	TACAGAGTTTTATAA[A/T]TTGTAGAATACAGTA	7525
rs1298709	snp	A/G			intron-variant	YES1	GRCh38.p7	18:744617	agatcacttgaggtc[A/G]ggagtttgagaccag	7525
rs1299123	snp	A/C	0	0	intron-variant	YES1	GRCh38.p7	18:773754	ATTCACTTAAAATAC[A/C]ATCTGATCCCATGCT	7525
rs1299134	snp	G/T	0	0	intron-variant	YES1	GRCh38.p7	18:783111	tataGCCACTAGGTT[G/T]ggtggcacatgtctg	7525
rs1299583	snp	A/T			intron-variant	YES1	GRCh38.p7	18:747383	ctcccaggctcaagc[A/T]attctcctgcctcag	7525
rs1547856	snp	G/T	0	0	intron-variant	YES1	GRCh38.p7	18:796971	TAGAGCTAAATGACT[G/T]GTAAGACAAAACAAA	7525
rs1547857	snp	G/T	0	0	intron-variant	YES1	GRCh38.p7	18:797101	acatggaaaagtctt[G/T]gcaacataaagacaa	7525
rs1630319	snp	A/T			intron-variant	YES1	GRCh38.p7	18:732436	ttttttttttttttt[A/T]aaacacagtcttgct	7525
rs1675153	snp	A/T			intron-variant	YES1	GRCh38.p7	18:777807	gtgagactctggctt[A/T]aaaaaaaaaaaaaaa	7525
rs1675154	snp	A/C			downstream-variant-500B	YES1	GRCh38.p7	18:721559	AAAACAAAACAAAAC[A/C]AAAAAAAAAGAAAAT	7525
rs1675157	snp	A/C			intron-variant	YES1	GRCh38.p7	18:761130	CTTAAGCCTGAAGGC[A/C]AAATTGTAACAATCA	7525
rs1784804	snp	G/T			intron-variant, upstream-variant-2KB	YES1	GRCh38.p7	18:776163	gatgatgtaaagcaa[G/T]ggtaattctcatgct	7525
rs1784805	snp	A/G			intron-variant	YES1	GRCh38.p7	18:773823	gggaaaaGTGTTTAA[A/G]GGAAGAGAGAGAGAG	7525
rs1784806	snp	A/C	0	0	intron-variant	YES1	GRCh38.p7	18:734579	aacaaaacaaaaaaa[A/C]CCAGGAGCAACTACA	7525
rs1784807	snp	G/T			intron-variant	YES1	GRCh38.p7	18:734915	gtaatcccagcgctt[G/T]gggaagccaaggcgt	7525
rs1785227	snp	C/T	0.0217236	0.101931	intron-variant	YES1	GRCh38.p7	18:789839	ctgaggcaggcagat[C/T]gcctgaggtcagaag	7525
rs1785228	snp	A/G			intron-variant	YES1	GRCh38.p7	18:790489	TCCTCTTATTATAAC[A/G]AAAAATCTAGTATAG	7525
rs1785231	snp	C/T			intron-variant	YES1	GRCh38.p7	18:751816	TACCTTGGTCTTTTT[C/T]CCCTCTGATAGGTGG	7525
rs1785232	snp	G/T			intron-variant	YES1	GRCh38.p7	18:738075	AAAACAAAAATGGAT[G/T]GCCAACCTCCCCTAC	7525
rs1785233	snp	G/T	0	0	intron-variant	YES1	GRCh38.p7	18:738178	AAAGCTTTTCTGAAT[G/T]GTCAGATTCTGTGGA	7525
rs1785585	snp	G/T			intron-variant	YES1	GRCh38.p7	18:728511	atgctcaaaaagttt[G/T]ggattttggagcatt	7525
rs1785586	snp	G/T			intron-variant, upstream-variant-2KB	YES1	GRCh38.p7	18:775985	tgtttccagtttttt[G/T]gctattagaataatg	7525
rs1785590	snp	C/T			intron-variant	YES1	GRCh38.p7	18:744410	agagtgagactccat[C/T]tccaaaaaaaaaaaa	7525
rs1785591	snp	G/T			intron-variant	YES1	GRCh38.p7	18:785136	tctgtgcataacttt[G/T]gggatatccgccacc	7525
rs1940293	snp	A/G	0.387642	0.208697	intron-variant	YES1	GRCh38.p7	18:809504	AGACCAGCCTGGCCA[A/G]CGTGGTGAAACCCCA	7525
rs1940628	snp	C/T	0.48679	0.0801892	intron-variant	YES1	GRCh38.p7	18:785430	CCAGCTTTACTTGTT[C/T]CTCTTTCTCCCCCCT	7525
rs2305994	snp	C/T	0.242775	0.249896	intron-variant	YES1	GRCh38.p7	18:747825	ACACACACAGAATTA[C/T]ATACCAGTCTTAATA	7525
rs2846587	snp	C/T	0.389903	0.207189	upstream-variant-2KB	YES1	GRCh38.p7	18:813221	CAGCTGGAATCGTGT[C/T]CGTCTGAATACACGC	7525
rs2846831	snp	A/C			intron-variant	YES1	GRCh38.p7	18:810073	GACTTATGCCCAAAC[A/C]ATTTTTTAAGTGATG	7525
rs2846832	snp	A/G	0.000399281	0.0141238	intron-variant	YES1	GRCh38.p7	18:807162	acttttagtagagac[A/G]gggtttcaccatgtt	7525
rs3214047	snp	G/T	0.203987	0.24574	intron-variant	YES1	GRCh38.p7	18:745884	ATTTTGAGAAAGATA[G/T]AGTGAAAGTATTTAT	7525
rs3786347	snp	A/G	0.492902	0.0591488	intron-variant	YES1	GRCh38.p7	18:743226	TTAATCCACAGCTAA[A/G]CAATGACAGAAAACA	7525
rs3786348	snp	C/T	0.491758	0.0636642	intron-variant	YES1	GRCh38.p7	18:743436	TAAATGAATAAACTA[C/T]ACTGTAATATCAATT	7525
rs3840903	in-del	-/A	0	0	intron-variant	YES1	GRCh38.p7	18:739919	CAAAATTTAAAAAAA[-/A]TGAAAAGCTAAGAAG	7525
rs3865403	snp	A/T	0.496583	0.0411924	intron-variant	YES1	GRCh38.p7	18:756085	AAACTGTCTGAGCTT[A/T]AGGATTTTTCTTTTT	7525
rs3865404	snp	C/T	0.472522	0.113946	intron-variant	YES1	GRCh38.p7	18:755862	AAAAGCATCCTGATA[C/T]GGGACCCTTTACAAA	7525
rs3865405	snp	A/G	0.455144	0.142885	intron-variant	YES1	GRCh38.p7	18:740876	AAAAAAGATATTGGA[A/G]CATAAGAAATATAAT	7525
rs3875086	snp	C/T	0.476314	0.106217	intron-variant	YES1	GRCh38.p7	18:798446	TCTCCTTCTGACTTA[C/T]AGTGCA	7525
rs3875087	snp	C/T	0.47614	0.106587	intron-variant	YES1	GRCh38.p7	18:798268	AAGTTTCCTGAACTA[C/T]AGATTCATGACTTCT	7525
rs3897601	snp	A/G	0.441568	0.160629	intron-variant	YES1	GRCh38.p7	18:767209	ggctggagtacagtg[A/G]catgataatgggtca	7525
rs3911636	snp	A/C	0.200801	0.245111	intron-variant	YES1	GRCh38.p7	18:746846	TAGCCATTGGGGAAC[A/C]TAGTTGTAGGGTTTA	7525
rs3911637	snp	A/C	0.243061	0.249904	intron-variant	YES1	GRCh38.p7	18:746779	CAACTTTTAAAAAGT[A/C]AAAATTCACCTTCAG	7525
rs3911638	snp	C/T	0.243061	0.249904	intron-variant	YES1	GRCh38.p7	18:746578	GGTGCTTCTTACTTT[C/T]TGTTTTGTCCTTTTG	7525
rs3915597	snp	C/T	0.15665	0.231917	intron-variant	YES1	GRCh38.p7	18:805318	TTCTACATTTAGTTA[C/T]GTTTAAATACACAAA	7525
rs3915598	snp	A/G	0.437965	0.164831	intron-variant	YES1	GRCh38.p7	18:805149	gttcacataatgtca[A/G]aattgcctaatgagg	7525
rs3915753	snp	A/G	0.437824	0.164991	intron-variant	YES1	GRCh38.p7	18:797195	TTGCTCATAATCTTT[A/G]CCAGTTTTACTATTG	7525
rs3915754	snp	C/T	0.436408	0.16659	intron-variant	YES1	GRCh38.p7	18:796757	GAAGACTCTGTCTCA[C/T]AAAATAAATAAATAA	7525
rs4084145	snp	C/G	0.00835062	0.0640748	intron-variant	YES1	GRCh38.p7	18:732812	TTGCATTTTATAGCT[C/G]TTGGTTATCTCATGA	7525
rs4084146	snp	C/T	0.466515	0.124985	intron-variant	YES1	GRCh38.p7	18:758487	CACAGGGCATATGCA[C/T]TGGGGAAACAAGATT	7525
rs4085840	snp	A/G	0.480144	0.097642	intron-variant	YES1	GRCh38.p7	18:804013	AGAAACTAAAATTAC[A/G]GTGTTCTGAAAGTTT	7525
rs4085841	snp	A/C	0.499872	0.0079862	intron-variant	YES1	GRCh38.p7	18:803838	ATTTTCTGACTGATT[A/C]TCAGTTTTTGCCTGG	7525
rs4085842	snp	C/G	0.499866	0.0081858	intron-variant	YES1	GRCh38.p7	18:803577	CACCTGCTTGCTAGT[C/G]GCAGTGAAACCTGCC	7525
rs4121508	snp	A/G	0.469937	0.118861	upstream-variant-2KB	YES1	GRCh38.p7	18:813553	TTCTAGGAACTTAAG[A/G]AAATGCATATAAGGG	7525
rs4121513	snp	G/T	0.499992	0.00199679	intron-variant	YES1	GRCh38.p7	18:809772	CATGAATTTGTTGTT[G/T]TTTTTTTAAGGAATC	7525
rs4121550	snp	A/G	0.499784	0.0103811	intron-variant	YES1	GRCh38.p7	18:784547	gttcagaagtctgac[A/G]ccggtgtccctggac	7525
rs4121551	snp	C/G	0.479744	0.0985793	intron-variant	YES1	GRCh38.p7	18:784612	ctggagattcaaaga[C/G]aaaatcagttcttgc	7525
rs4121552	snp	A/G	0.479824	0.098392	intron-variant	YES1	GRCh38.p7	18:800536	TAAGCTAGTATTCCC[A/G]CTAGAAAACAATGTT	7525
rs4369751	snp	A/G	0.46855	0.121392	intron-variant	YES1	GRCh38.p7	18:730329	AGATTAGAACTGACC[A/G]AGGACCCAAGAGGAT	7525
rs4474771	snp	C/T	0.237593	0.249692	intron-variant	YES1	GRCh38.p7	18:765688	TAAATTGGCCGGGTG[C/T]GGTGGCTCACGCCTG	7525
rs4520909	snp	C/T	0.44252	0.159487	intron-variant	YES1	GRCh38.p7	18:811699	TGGGGGTCTGTGTAT[C/T]GGCCGACGCCGGTAG	7525
rs4798578	snp	A/G	0.00636936	0.0560724	intron-variant	YES1	GRCh38.p7	18:779193	aatcacttgagtcca[A/G]cagttcaggaccagc	7525
rs5009288	snp	A/G	0.0166325	0.0896639	intron-variant	YES1	GRCh38.p7	18:808138	TATATCCTGGTCTGC[A/G]TTGGGTTTACCTTTA	7525
rs5822576	in-del	-/A	0.480382	0.097079	intron-variant	YES1	GRCh38.p7	18:749859	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	7525
rs5822577	in-del	-/G/GG	0.492237	0.0618148	intron-variant	YES1	GRCh38.p7	18:756282	TACAGTGGGGGGGGG[-/G/GG]CTCAATAACTATTTG	7525
rs5822579	in-del	-/T	0.48378	0.0885831	intron-variant	YES1	GRCh38.p7	18:785154	AGTTATGCACAGACC[-/T]TTTTTTTTTTTTAAC	7525
rs5822580	in-del	-/T	0.499087	0.0213463	upstream-variant-2KB	YES1	GRCh38.p7	18:813659	CGATGCTGTATTTTC[-/T]TTAGCTACTAAAACT	7525
rs6506474	snp	A/G	0.46703	0.124089	downstream-variant-500B	YES1	GRCh38.p7	18:721198	CTGGTATAATTTTAA[A/G]AAGAAGAAAATACTT	7525

Full records

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