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
rs1954	snp	A/G	0.000378928	0.0137594	missense	DCAF13	GRCh38.p7	8:103441608	CATACTTTCGTCGAC[A/G]AGCTTCTTTCATGAT	25879
rs750509	snp	A/G	0.0486741	0.148216	intron-variant, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103416628	AGAATCACAGAAGAC[A/G]GGTGCTGAAGGGGGC	25879
rs750605	snp	A/G			intron-variant, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103416181	TGAACCTAAGGCATA[A/G]AAAGAAGGGCTGTGT	25879
rs750606	snp	C/T	0.316726	0.240931	intron-variant, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103416302	TGTGAGCATTGCTAA[C/T]AAGTCTCTGCTCAAA	25879
rs751725	snp	A/G	0.0486741	0.148216	intron-variant	DCAF13	GRCh38.p7	8:103436854	TTTTCTCAAAAAATT[A/G]TGATAATTGGATGAT	25879
rs893044	snp	C/T	0.489665	0.0711382	intron-variant	DCAF13	GRCh38.p7	8:103436870	TGATAATTGGATGAT[C/T]ATGGTCATAGTCAAT	25879
rs975440	snp	A/G	0.376989	0.215346	intron-variant	DCAF13	GRCh38.p7	8:103435425	GGAAAATGTGTTGGT[A/G]TATATATAAGTGGAG	25879
rs1370005	snp	A/C	0.362014	0.223501	intron-variant	DCAF13	GRCh38.p7	8:103432781	ACAATTAAGCCATTC[A/C]TGATAGAAATACACA	25879
rs1370006	snp	C/T	0.378174	0.214642	intron-variant	DCAF13	GRCh38.p7	8:103426335	CAAAAAAAAAAAAAA[C/T]TGTTAAAATTCTTTA	25879
rs1436595	snp	C/T	0.489665	0.0711382	intron-variant	DCAF13	GRCh38.p7	8:103433132	CTGTAAAGGGCCAAA[C/T]GTTAAACATTTTCAG	25879
rs2304501	snp	C/T	0.376989	0.215346	intron-variant	DCAF13	GRCh38.p7	8:103431055	AGTGTACATGTCATA[C/T]GATAATCATGGGGCT	25879
rs2304502	snp	C/T	0.0232847	0.105357	intron-variant	DCAF13	GRCh38.p7	8:103442718	TCAGAAAAATCAAAG[C/T]ATTTTCTTTCACTAG	25879
rs2892544	snp	A/G	0.0240643	0.107019	intron-variant, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103417051	ACATTATCATTTTGG[A/G]TATGCTTTCTTTGTG	25879
rs3098214	snp	G/T	0.489722	0.0709447	intron-variant	DCAF13	GRCh38.p7	8:103442566	TAAGTTTAAAAACCT[G/T]CCACAGTTAATAAAA	25879
rs3098215	snp	C/T	0.376791	0.215463	intron-variant	DCAF13	GRCh38.p7	8:103441375	AGAAAGCACCCTTTT[C/T]CCCCTAACCTAATCT	25879
rs3098216	snp	C/T	0.00129525	0.0254155	intron-variant	DCAF13	GRCh38.p7	8:103440125	CCTCCCTATAGAAAA[C/T]GAATTAAGTTAAAAC	25879
rs3098217	snp	C/T	0.376592	0.215579	intron-variant	DCAF13	GRCh38.p7	8:103440053	TAAGTATCAGGATAC[C/T]ATTTCTGAGTCCTAT	25879
rs3098218	snp	C/T	0.493293	0.0575177	intron-variant	DCAF13	GRCh38.p7	8:103439971	CAACTAATAAGGTTC[C/T]GTGTTAAGTGCTGGG	25879
rs3098219	snp	A/G	0.48978	0.0707512	intron-variant	DCAF13	GRCh38.p7	8:103439813	ATATGATGTTCAACC[A/G]AGGTAACTTTGTAAC	25879
rs3098220	snp	A/T	0.371582	0.218444	intron-variant	DCAF13	GRCh38.p7	8:103439306	CTGATAAGTTGAGGT[A/T]AGAATAATTTAATAG	25879
rs3098221	snp	C/G	0.489893	0.0703642	intron-variant	DCAF13	GRCh38.p7	8:103438254	GCTTTTTCTTCTCCC[C/G]CTCAGTGCTCTGCTT	25879
rs3098222	snp	C/T	0.499187	0.0201513	intron-variant	DCAF13	GRCh38.p7	8:103435961	AAGCAACAGGCCATA[C/T]CATATGACCACACAG	25879
rs3098223	snp	C/T	0.498832	0.0241331	intron-variant	DCAF13	GRCh38.p7	8:103434877	atgtaagagtgAACA[C/T]GGCCTTTCAAAGGGT	25879
rs3098224	snp	A/G	0.376592	0.215579	intron-variant	DCAF13	GRCh38.p7	8:103434468	TCCTGCCTAAGAACA[A/G]TGGTTTTCAGCTAGG	25879
rs3098225	snp	C/T	0.376592	0.215579	intron-variant	DCAF13	GRCh38.p7	8:103434448	TTTCAGCTAGGTTTG[C/T]TTGGTTCCAGCAAAC	25879
rs3098226	snp	A/G	0.0486741	0.148216	intron-variant	DCAF13	GRCh38.p7	8:103428834	ATCCCTAATAATTAC[A/G]ATTTTAGAATTGGTG	25879
rs3098227	snp	A/G	0.370974	0.218781	intron-variant	DCAF13	GRCh38.p7	8:103428523	GAGAAAGATATAATA[A/G]AGACAGACACTCCAG	25879
rs3098234	snp	G/T	0.0486741	0.148216	intron-variant	DCAF13	GRCh38.p7	8:103423677	ACTTATTATTTTGTG[G/T]TGAGAACATTTAATT	25879
rs3098235	snp	C/G	0.0460142	0.144533	intron-variant	DCAF13	GRCh38.p7	8:103422974	CCGAATCTTTTAACA[C/G]TAACACCTATTTCCA	25879
rs3098236	snp	G/T	0.378765	0.214288	intron-variant	DCAF13	GRCh38.p7	8:103422794	CCTACATTTTATAAC[G/T]CAGCTCAACCTGTTT	25879
rs3098237	snp	A/G	0.499187	0.0201513	intron-variant	DCAF13	GRCh38.p7	8:103422120	TCAATCCTCCAAAGT[A/G]TCAACCACTGATTTC	25879
rs3098238	snp	A/G	0.0941315	0.195461	synonymous-codon	DCAF13	GRCh38.p7	8:103420403	ATGCTTTGCCAAGCA[A/G]TTGACTCCATCACGG	25879
rs3098239	snp	A/G	0.0460142	0.144533	intron-variant	DCAF13	GRCh38.p7	8:103419175	CGCTTAGggccgggc[A/G]tggtggctcacgcct	25879
rs3098240	snp	A/G	0.489722	0.0709447	intron-variant	DCAF13	GRCh38.p7	8:103417596	GGAGTGCAGTGACGC[A/G]ATCTCGGCTCACTGC	25879
rs3098241	snp	C/T	0.331411	0.236373	upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103413076	TGACAGATAAAAGGA[C/T]TGAGTTTGGATTGGA	25879
rs3133817	snp	A/G	0.372995	0.217652	upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103414017	CCCATACAGCAGTCT[A/G]CAAATATTAAGAGAA	25879
rs3133818	snp	A/C/G			intron-variant	DCAF13	GRCh38.p7	8:103419127	ctgacctcgtgatcc[A/C/G]tccgtcccggccccc	25879
rs3133819	snp	C/T	0.345037	0.231231	intron-variant	DCAF13	GRCh38.p7	8:103419177	GCGTGAGCCACCACG[C/T]CCGGCCCTAAGCGTG	25879
rs3134249	snp	A/C			intron-variant, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103416634	TTCAGCACCTGTCTT[A/C]TGTGATTCTATCACT	25879
rs3134250	snp	A/G	0.373196	0.217538	intron-variant	DCAF13	GRCh38.p7	8:103417997	gccgggcatggtggc[A/G]ggtgcctgtagtccc	25879
rs3134251	snp	A/G	0.378174	0.214642	intron-variant	DCAF13	GRCh38.p7	8:103418970	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	25879
rs3134252	snp	A/G	0.0460142	0.144533	intron-variant	DCAF13	GRCh38.p7	8:103419517	CATAATCACAACTTC[A/G]TGTGTCTATCAGCAC	25879
rs3134253	snp	A/G	0.359518	0.224735	missense	DCAF13	GRCh38.p7	8:103420317	GTCCCACGAGAATAT[A/G]TAAGAGCTTTAAATG	25879
rs3134257	snp	A/C	0.0486741	0.148216	intron-variant	DCAF13	GRCh38.p7	8:103423309	ACCTAAAGTGTCCAG[A/C]AATGGATGAATGAAT	25879
rs3134258	snp	G/T	0.373397	0.217424	intron-variant	DCAF13	GRCh38.p7	8:103423506	ccaaactcttagaaa[G/T]ggagtaaaatggtca	25879
rs3134260	snp	C/T	0.0463947	0.145069	intron-variant	DCAF13	GRCh38.p7	8:103424650	GCAGAACAGCTTGGT[C/T]ATTTACAAGCAAATT	25879
rs3134261	snp	C/T	0.378174	0.214642	intron-variant	DCAF13	GRCh38.p7	8:103426425	CCCATGGGAAGACCA[C/T]GGAGAAAAAGATAGA	25879
rs3134263	snp	A/G	0.000399281	0.0141238	intron-variant	DCAF13	GRCh38.p7	8:103428048	TTAGGTAGTATGAGA[A/G]AAAAATCCTAATATG	25879
rs3134264	snp	C/T	0.489608	0.0713316	intron-variant	DCAF13	GRCh38.p7	8:103428815	CTGTGTCAGAAGAGC[C/T]GATCACCAATTCTAA	25879
rs3134265	snp	A/G	0.376592	0.215579	intron-variant	DCAF13	GRCh38.p7	8:103429695	GAGAGTTAACAACAC[A/G]AAGAAACATTTACTA	25879
rs3134267	snp	C/T	0.376592	0.215579	intron-variant	DCAF13	GRCh38.p7	8:103434641	GAAACTATGTAGATA[C/T]CCTCTTCTCAGACTT	25879
rs3134268	snp	G/T	0.000798403	0.0199641	intron-variant	DCAF13	GRCh38.p7	8:103437533	ATATTTCATTTCTAA[G/T]AAATTGTCTCCTGAT	25879
rs3134270	snp	C/G	0.379158	0.214052	intron-variant	DCAF13	GRCh38.p7	8:103439213	GTTTCACCTGGTCTC[C/G]ATCTCCTGACCTCGT	25879
rs3134271	snp	C/T	0.371177	0.218669	intron-variant	DCAF13	GRCh38.p7	8:103439309	TTAAATTATTCTTAC[C/T]TCAACTTATCAGACA	25879
rs3134272	snp	C/G	0.49917	0.0203505	intron-variant	DCAF13	GRCh38.p7	8:103441913	TAGGACTACAGGCAC[C/G]CGCCACCATGCGCGG	25879
rs3134273	snp	C/T	0.498832	0.0241331	intron-variant	DCAF13	GRCh38.p7	8:103442084	GGCCATTTCTTTTTC[C/T]TTTTCCCAAAAAAGG	25879
rs3134274	snp	C/T	0.0198	0.0975088	utr-variant-3-prime	DCAF13	GRCh38.p7	8:103443164	TACTTTCTCTTTGAT[C/T]TATTATTGTAGACAC	25879
rs3134291	snp	C/T	0.489722	0.0709447	upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103413381	CTTATAGAGGTAATA[C/T]GGTGAGGGGTTAAGT	25879
rs3134292	snp	A/C	0.372995	0.217652	upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103413817	CAATCTTCCACTGAA[A/C]CTTAAAGATACACAT	25879
rs3134293	snp	C/T	0.316968	0.240864	upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103413856	GTAATGTAGAATTTT[C/T]TTAACGGTTTACCTG	25879
rs3134294	snp	A/C	0.0460142	0.144533	upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103414570	CTCAGACTTCTCTAC[A/C]TACATGCCCCCTCTC	25879
rs3134295	snp	A/C	0.49294	0.0589944	missense, utr-variant-5-prime, nc-transcript-variant	DCAF13, SLC25A32	GRCh38.p7	8:103415131	AAGAACGGGGCACAG[A/C]CACTACGTCACGCCG	25879
rs3134296	snp	C/T	0.301032	0.244736	missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103415313	AGGATCCAGTTGAGC[C/T]AGCAGGCCGCCGCTC	25879
rs3134297	snp	C/T	0.360292	0.224356	synonymous-codon, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103415350	TCACGTGACTGGAAG[C/T]AGTCTGGGAAAAGCG	25879
rs3814106	snp	A/C/G	0.000102697	0.00716517	missense, utr-variant-5-prime, nc-transcript-variant	DCAF13, SLC25A32	GRCh38.p7	8:103415006	GCGACCGTCGCCACG[A/C/G]TGGCGGCCACTGCAT	25879
rs3837183	in-del	-/ACAAA			intron-variant	DCAF13	GRCh38.p7	8:103426042	CATCATCATAATAAA[-/ACAAA]TATTTCTAGGTTGGT	25879
rs4634606	snp	A/T	0	0	intron-variant	DCAF13	GRCh38.p7	8:103418868	tatatatatatatat[A/T]tTTtttttttttttt	25879
rs5025988	snp	A/C			upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103414678	CCAACGCGGACAGCA[A/C]CSCTCCCTTCAACGC	25879
rs5893653	snp	C/G			upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103414680	CAACGCGGACAGCAC[C/G]CCCCTTCAACGCTCC	25879
rs5893654	in-del	-/T			upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103414682	ACGCGGACAGCACCC[-/T]CCCTTCAACGCTCCT	25879
rs5893655	in-del	-/A	0.372391	0.217992	intron-variant	DCAF13	GRCh38.p7	8:103417343	TTTCTTAAAAAAAAA[-/A]GATCTTTGGCTGGGC	25879
rs7813024	snp	A/T			intron-variant	DCAF13	GRCh38.p7	8:103418866	tatatatatatatat[A/T]tTTTTtttttttttt	25879
rs7815341	snp	A/G	0.0898077	0.191933	intron-variant	DCAF13	GRCh38.p7	8:103430052	gtaggtaagtaaaat[A/G]tgTTTTATTACAAAT	25879
rs7816297	snp	A/G	0.376592	0.215579	intron-variant	DCAF13	GRCh38.p7	8:103430438	CATGAGGATTTTACA[A/G]TGAAAATACTTGGTT	25879
rs7820295	snp	C/T	0.0287284	0.116357	intron-variant	DCAF13	GRCh38.p7	8:103438277	GAAAAAGCAGTCTAT[C/T]TCATCTAGTTTTCAT	25879
rs7833434	snp	C/G	0.0240643	0.107019	intron-variant, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103415938	GTGGATGTTGGAAGA[C/G]ACAAAGATGAATTTA	25879
rs7835639	snp	C/T	0.0178098	0.0926698	intron-variant	DCAF13	GRCh38.p7	8:103434416	CATGTAGAAATAAAG[C/T]ATCTTACTAAAAAGC	25879
rs10093237	snp	A/G	0.0887219	0.191022	intron-variant	DCAF13	GRCh38.p7	8:103423006	TTTGGTGTAAAAAAA[A/G]AAAACTTATTTGCTG	25879
rs10094939	snp	G/T	0.290718	0.246662	intron-variant	DCAF13	GRCh38.p7	8:103432039	GCTACTTTCTGTTGC[G/T]TCTTTGCTCCATCTA	25879
rs10108112	snp	A/T	0.274393	0.248807	intron-variant	DCAF13	GRCh38.p7	8:103422909	TACAATTTGAAAGAT[A/T]GTCATGTGAAAAAGA	25879
rs10112317	snp	A/G	0.290718	0.246662	intron-variant	DCAF13	GRCh38.p7	8:103433487	TGATAGATTCTTAAT[A/G]CATGTTTTTTTTAAG	25879
rs10541932	in-del	-/TAAA	0.489722	0.0709447	intron-variant	DCAF13	GRCh38.p7	8:103430392	GCAAGACTCTGTCTC[-/TAAA]TAAATAAATAAATAA	25879
rs10709873	in-del	-/A	0	0	upstream-variant-2KB, intron-variant	DCAF13, SLC25A32	GRCh38.p7	8:103414677	GCCAACGCGGACAGC[-/A]ACGCTCCCTTCAACG	25879
rs11290677	in-del	-/T	0.396546	0.202545	intron-variant	DCAF13	GRCh38.p7	8:103428907	GTATTTGTTCAGCTG[-/T]TTTTTTTTTTAATTG	25879
rs11985510	snp	A/G	0.0901694	0.192235	intron-variant, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103416811	tcagttTCTCCATCT[A/G]TAAAGATTCATTTTT	25879
rs11985609	snp	A/G	0.0901694	0.192235	intron-variant, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103417101	TTTGCACAGTACCAT[A/G]TTAACTGAACCAGTC	25879
rs12547432	snp	G/T	0	0	intron-variant	DCAF13	GRCh38.p7	8:103438927	CACTTACTAATATAG[G/T]ATCACCTGTGAATTC	25879
rs12675902	snp	A/G			intron-variant	DCAF13	GRCh38.p7	8:103435805	GGTATGTGCCTACCA[A/G]TAAGCCATTTATATt	25879
rs12677876	snp	C/G	0.346368	0.23068	intron-variant	DCAF13	GRCh38.p7	8:103419877	AGCTGGGCGTGGTGG[C/G]ATGCGCCTGTAATCC	25879
rs13261525	snp	A/G			intron-variant	DCAF13	GRCh38.p7	8:103417536	agtcacagctactca[A/G]gaggctgaggcggga	25879
rs13272825	snp	A/G	0.00273758	0.0368957	missense	DCAF13	GRCh38.p7	8:103420402	ACCGTGATGGAGTCA[A/G]TTGCTTGGCAAAGCA	25879
rs13276522	snp	G/T			missense, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103415424	CGGACACCTCGTGGA[G/T]TCCGGCCGGAAGAGC	25879
rs13278059	snp	A/T			missense, upstream-variant-2KB	DCAF13, SLC25A32	GRCh38.p7	8:103415425	GGACACCTCGTGGAG[A/T]CCGGCCGGAAGAGCA	25879
rs13280790	snp	G/T			intron-variant	DCAF13	GRCh38.p7	8:103418869	atatatatatatatT[G/T]TTttttttttttttt	25879
rs13280792	snp	G/T			intron-variant	DCAF13	GRCh38.p7	8:103418875	atatatatTTTTttt[G/T]ttttttttttttttt	25879
rs13280803	snp	G/T			intron-variant	DCAF13	GRCh38.p7	8:103418884	TTTtttttttttttt[G/T]ttttttttttttttt	25879
rs13439598	snp	C/G	0.0217236	0.101931	intron-variant	DCAF13	GRCh38.p7	8:103419142	gtccgtcccggcccc[C/G]caaagtgctgggatt	25879
rs16870396	snp	A/G	0.322483	0.239262	intron-variant	DCAF13	GRCh38.p7	8:103426940	GTCTTGTCTCATTAT[A/G]GTATTGTTTCCCCCT	25879
rs17229709	snp	A/G	0.040671	0.13668	intron-variant	DCAF13	GRCh38.p7	8:103427761	TGCTCAGAAGTCTGA[A/G]TTGTGATTCCCAGTT	25879
rs17230038	snp	A/G	0.00716266	0.059414	intron-variant	DCAF13	GRCh38.p7	8:103442253	AAAAAATAATTTCTG[A/G]TGTAGCTGGAATTAA	25879

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