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
rs2572	snp	A/G	0.164219	0.234823	utr-variant-3-prime, intron-variant	DCAF4	GRCh38.p7	14:72959582	GAATAAACATCTCAC[A/G]AACTGTCGCTCCTAG	26094
rs741227	snp	C/T	0.0422008	0.138995	intron-variant	DCAF4	GRCh38.p7	14:72942063	GAGAGAGGATGGGGA[C/T]GTAGGCAGAGATGTC	26094
rs887936	snp	A/G	0.361894	0.223562	intron-variant	DCAF4	GRCh38.p7	14:72939960	TTCCAAGCCAGGAAC[A/G]GGTCTCAGCCTTCCC	26094
rs1076458	snp	A/G	0.469049	0.120489	intron-variant	DCAF4	GRCh38.p7	14:72927170	GTGGGCTCCCCGGGG[A/G]CTTCAGAAACCATGA	26094
rs1079560	snp	G/T	0.107341	0.205301	intron-variant, utr-variant-5-prime	DCAF4	GRCh38.p7	14:72926849	GCCTTCAGCAGCAGG[G/T]CTCAGAGAAGCGCTT	26094
rs1110058	snp	C/G	0.0185938	0.0946107	intron-variant	DCAF4	GRCh38.p7	14:72957584	AACAGGTGAAAAATC[C/G]ACTTAAAAAGGAGGC	26094
rs2098321	snp	A/G	0.37778	0.214877	intron-variant	DCAF4	GRCh38.p7	14:72927414	CAGTGAGTCGAGATC[A/G]TGCCACTGCACTCCA	26094
rs2098322	snp	C/T	0.494143	0.0537956	intron-variant, upstream-variant-2KB	DCAF4	GRCh38.p7	14:72926576	CAGCCCTCGAATCGA[C/T]GCCAGTAGGCACCCC	26094
rs2240980	snp	C/G	0.449718	0.150375	intron-variant	DCAF4	GRCh38.p7	14:72942975	TCAGCATCCATGCCC[C/G]CACCCTCTGTTTCTG	26094
rs2240981	snp	C/T	0.375	0.216506	intron-variant	DCAF4	GRCh38.p7	14:72943490	TGGCTAAACCTGCAG[C/T]CCAGTGTGCCTTTGG	26094
rs2243443	snp	C/G	0.330249	0.23677	intron-variant	DCAF4	GRCh38.p7	14:72947257	TGGACCTGGGTATCT[C/G]TGGGCTTCATGACAT	26094
rs2243596	snp	A/G	0.498774	0.02473	utr-variant-3-prime	DCAF4	GRCh38.p7	14:72961952	CCCCAGCTCTCCGTC[A/G]GAGCACGTCTGTCTT	26094
rs2246976	snp	C/T	0.392186	0.20897	intron-variant	DCAF4	GRCh38.p7	14:72946031	ACCAACCGGAAGGTA[C/T]GTTGCCCATCCCTGT	26094
rs2247080	snp	A/C	0.375399	0.216275	intron-variant	DCAF4	GRCh38.p7	14:72945756	TCTCCACTCTCGCTC[A/C]TGGAGAGGAACTCTC	26094
rs2286833	snp	A/G	0.0454566	0.143743	intron-variant	DCAF4	GRCh38.p7	14:72947122	ATAACTTTCCATCTC[A/G]CTGTGTGCTTCCTCA	26094
rs2286834	snp	A/G	0.0633504	0.166319	intron-variant	DCAF4	GRCh38.p7	14:72952136	GCTCAGAACAGATTC[A/G]GACGCCCGTGCACAT	26094
rs2302586	snp	C/G	0.371791	0.218327	intron-variant	DCAF4	GRCh38.p7	14:72938117	CCCAGTGTGCTTCTG[C/G]CATTGTACACATGGC	26094
rs2302587	snp	C/T	0.393594	0.204648	intron-variant	DCAF4	GRCh38.p7	14:72938087	GCAAAAGTGGCTCCC[C/T]AGAGCGGCACACTTG	26094
rs2302588	snp	C/G	0.167495	0.236042	missense, intron-variant, utr-variant-5-prime	DCAF4	GRCh38.p7	14:72938044	ATCACGGAGTCTGAA[C/G]CAAGGGTTCTGCTGG	26094
rs2333012	snp	A/G	0.336702	0.234484	intron-variant	DCAF4	GRCh38.p7	14:72942905	CGAGGAGAGATGGGC[A/G]TCAGCGGGGCAGGGA	26094
rs2535908	snp	C/G/T	0.00157319	0.0280047	synonymous-codon, intron-variant	DCAF4	GRCh38.p7	14:72958724	GCCCCCCAGCCGCGA[C/G/T]GAGAAGGCCACACTG	26094
rs2535909	snp	C/G	0.0637235	0.166737	intron-variant	DCAF4	GRCh38.p7	14:72955258	CCCCTGCACTGTCCC[C/G]TTTGGCCTTTCTCTC	26094
rs2535910	snp	C/T	0.32955	0.237006	intron-variant	DCAF4	GRCh38.p7	14:72953934	GTCGTGTTTACAGTA[C/T]GAATAGTACTGATAT	26094
rs2535912	snp	A/G	0.330249	0.23677	intron-variant	DCAF4	GRCh38.p7	14:72951492	TCCTGAGTAGCTGGG[A/G]TTACAGGCATGTGCC	26094
rs2535913	snp	C/T	0.330249	0.23677	intron-variant	DCAF4	GRCh38.p7	14:72948525	CTTGGCCTCTTTAGC[C/T]CTCTGGTTAGATCAT	26094
rs2535914	snp	A/G	0.330249	0.23677	intron-variant	DCAF4	GRCh38.p7	14:72943913	GGGCCCTGCTGTGGC[A/G]GTCTCCTGGGGCAGG	26094
rs2806031	snp	C/T	0.227074	0.248947	utr-variant-3-prime	DCAF4	GRCh38.p7	14:72961868	GCATTGTAGTGGCCA[C/T]CTGCTGGAGAGGATG	26094
rs2806032	snp	A/G	0.00636936	0.0560724	intron-variant	DCAF4	GRCh38.p7	14:72958247	CTTGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG	26094
rs2806033	snp	A/G	0.49607	0.0441545	intron-variant	DCAF4	GRCh38.p7	14:72958106	TTTTTTTTTGAGATA[A/G]GGTCTTGCTGTGTTG	26094
rs2806034	snp	A/C	0.388709	0.208002	synonymous-codon	DCAF4	GRCh38.p7	14:72955642	TTGGAGGATCCGCAC[A/C]GAGGTCACTGCTGAA	26094
rs2806035	snp	C/T			intron-variant	DCAF4	GRCh38.p7	14:72953764	AAATAAATAAATAAA[C/T]tatatatatatatat	26094
rs2806036	snp	A/T			intron-variant	DCAF4	GRCh38.p7	14:72953734	TATATATATATATAT[A/T]TTTTTTTTTTTTTTT	26094
rs2806037	snp	A/T			intron-variant	DCAF4	GRCh38.p7	14:72952719	caataagagcaaaac[A/T]ccgtctcaaaaaaaa	26094
rs2806038	snp	C/T	0.331874	0.236213	intron-variant	DCAF4	GRCh38.p7	14:72951155	TGTCTCTACAAAAAA[C/T]ACAAAAACTAGCTGG	26094
rs2806039	snp	A/G	0.377187	0.215229	intron-variant	DCAF4	GRCh38.p7	14:72949109	CATACCGCTCTGGGT[A/G]GTAAGCTCCAAATTA	26094
rs2806040	snp	A/G	0.330016	0.236849	intron-variant	DCAF4	GRCh38.p7	14:72948357	CTATGACCCTTTGAA[A/G]TGTAAGCTGGGTGTG	26094
rs2806041	snp	A/C	0.371987	0.218218	intron-variant	DCAF4	GRCh38.p7	14:72948187	AAAAAAATTAAAATC[A/C]AAAAAAACTCCTTTG	26094
rs2806042	snp	C/T	0.499982	0.00299515	intron-variant	DCAF4	GRCh38.p7	14:72947939	ATTAACATGTGGTTT[C/T]GGGTGAGTCAAGTCT	26094
rs2806043	snp	C/T	0.376791	0.215463	intron-variant	DCAF4	GRCh38.p7	14:72947613	TGTGCTGCTCCTTTC[C/T]GCCTTGTTCCTCTGC	26094
rs2806044	snp	C/T	0.463881	0.12944	intron-variant	DCAF4	GRCh38.p7	14:72947608	TGCTCCTTTCTGCCT[C/T]GTTCCTCTGCTACCA	26094
rs2806045	snp	A/G	0.46865	0.121211	intron-variant	DCAF4	GRCh38.p7	14:72944816	caggtgtgagccacc[A/G]cacctggccCTAttt	26094
rs2907953	snp	C/T	0.432797	0.170544	downstream-variant-500B	DCAF4	GRCh38.p7	14:72962412	CTCAAGCAATCCTCC[C/T]GTCTCGGCATCACTT	26094
rs2998006	snp	A/G	0.493386	0.0571263	downstream-variant-500B	DCAF4	GRCh38.p7	14:72962406	CAATCCTCCTGTCTC[A/G]GCATCACTTCGGCCT	26094
rs3061066	in-del	-/AC/ACACGCAC/ACGCAC	0	0	downstream-variant-500B	DCAF4	GRCh38.p7	14:72962511	CACACACACACACAC[-/AC/ACACGCAC/ACGCAC]GCATGCACACTCTCT	26094
rs3213729	snp	C/G	0.320814	0.239761	utr-variant-5-prime, upstream-variant-2KB	DCAF4	GRCh38.p7	14:72926538	ACAGTCTTACCTGTT[C/G]AGCGTGTCCCTTCCG	26094
rs3214336	in-del	-/T	0.376989	0.215346	intron-variant	DCAF4	GRCh38.p7	14:72952025	TACCAGAAGCATGTG[-/T]TTTTTTTACAGCATC	26094
rs3742832	snp	C/T	0.444267	0.157354	intron-variant	DCAF4	GRCh38.p7	14:72941647	ATGTAATGAAGGAAA[C/T]AGGCACTAAATTGGC	26094
rs3815460	snp	C/G	0.164445	0.234905	missense	DCAF4	GRCh38.p7	14:72955551	TTAATGGCTGCCGCT[C/G]TGGGGAAATCTTTGC	26094
rs3815500	snp	G/T	0.376876	0.215412	utr-variant-5-prime, intron-variant	DCAF4	GRCh38.p7	14:72937972	TTTATTCATTTCTGT[G/T]CCTAAAAGAGAAAAA	26094
rs3832967	in-del	-/A	0.330249	0.23677	intron-variant	DCAF4	GRCh38.p7	14:72941661	TTTAGTTCCATAGGA[-/A]TGTAATGAAGGAAAC	26094
rs3832968	in-del	-/A	0.364609	0.222182	intron-variant	DCAF4	GRCh38.p7	14:72941611	TTATATGCATAAAAA[-/A]TCTGACGGTGTCCTT	26094
rs3965998	snp	C/T	0.0115144	0.0749975	intron-variant	DCAF4	GRCh38.p7	14:72927640	acaggcgtgagccac[C/T]gcgcccggccTGAGG	26094
rs4395014	snp	C/T	0.367708	0.220556	intron-variant	DCAF4	GRCh38.p7	14:72945531	TTTTTCCTATTGCGC[C/T]ACAGCCTTCGTGATG	26094
rs4903078	snp	A/G	0.363359	0.222822	intron-variant, upstream-variant-2KB	DCAF4	GRCh38.p7	14:72937730	GGCCGACCTGGCAAC[A/G]TTTCTGTGGGGTAGG	26094
rs4903079	snp	A/G	0.372391	0.217992	intron-variant	DCAF4	GRCh38.p7	14:72941186	GGCCAGGCTGGTCTC[A/G]AACTCCTGGCCTCAA	26094
rs4903080	snp	A/G	0.410061	0.192043	intron-variant	DCAF4	GRCh38.p7	14:72949416	AGCTGTGATCACACT[A/G]CTGCACTCCAGCCTG	26094
rs4903081	snp	C/T	0.409721	0.192325	downstream-variant-500B, intron-variant	DCAF4	GRCh38.p7	14:72959718	TGGGACCAGCTTTCA[C/T]AGCCTTCCTGGAGAG	26094
rs6574112	snp	A/G	0.0640965	0.167152	intron-variant	DCAF4	GRCh38.p7	14:72929739	GCCCATTTCTCCTTG[A/G]AGACCTTCAGTGACT	26094
rs7141910	snp	C/T	0.478354	0.101757	intron-variant	DCAF4	GRCh38.p7	14:72952972	tgctgggattacagg[C/T]gtgagccacaatgcc	26094
rs7141933	snp	A/T			intron-variant	DCAF4	GRCh38.p7	14:72953022	tttttttttttgaga[A/T]ggagtttcactcttg	26094
rs7142086	snp	C/T	0.281049	0.248064	upstream-variant-2KB	DCAF4	GRCh38.p7	14:72924885	CCTGTCACTTCCCAA[C/T]TCTAGAACCCTCAGA	26094
rs7142161	snp	A/G	0.121369	0.214369	intron-variant	DCAF4	GRCh38.p7	14:72940686	ACCTCCACCTCCCAG[A/G]TTCAAGCAATTCTCC	26094
rs7142775	snp	G/T	0.160938	0.233598	intron-variant	DCAF4	GRCh38.p7	14:72955191	CCCTTAAAAGTGAAT[G/T]AACCCACTAACCTGC	26094
rs7143528	snp	C/T	0.44755	0.153212	intron-variant, upstream-variant-2KB	DCAF4	GRCh38.p7	14:72934132	CTGCAGGCCCCCCGC[C/T]CCCACTGCCTTACGT	26094
rs7143683	snp	C/T	0.409721	0.192325	intron-variant	DCAF4	GRCh38.p7	14:72958345	TTGAACGTTCCGTGA[C/T]ATCAAGAGCAGCAGA	26094
rs7144128	snp	A/G			intron-variant	DCAF4	GRCh38.p7	14:72928329	ctcccgagtagctga[A/G]actacgggcgcacgc	26094
rs7144193	snp	C/T	0.390745	0.206618	intron-variant	DCAF4	GRCh38.p7	14:72958607	GTGTCTCTCCTCTTT[C/T]CTAGTGGGCCAGGAC	26094
rs7144310	snp	G/T	0.0275645	0.114116	intron-variant	DCAF4	GRCh38.p7	14:72928438	ccgacctcgtgatcc[G/T]cccgcctcggcctcc	26094
rs7144738	snp	A/C	0.372391	0.217992	utr-variant-3-prime, intron-variant	DCAF4	GRCh38.p7	14:72958973	TGGAGATGCTCAGGA[A/C]AGTTATTTGAGTTAA	26094
rs7145222	snp	A/C	0.323434	0.238972	intron-variant	DCAF4	GRCh38.p7	14:72929079	TGCGGGCGGCACGGA[A/C]GCCCGGGGCTGCTCC	26094
rs7149675	snp	A/G	0.00159617	0.0282053	intron-variant	DCAF4	GRCh38.p7	14:72929295	GTGTGGAAAACTGCT[A/G]GACTGTGAGAGAGAG	26094
rs7150054	snp	C/T	0.0103295	0.0711199	intron-variant	DCAF4	GRCh38.p7	14:72929423	TCTCAGATTTGCTgc[C/T]gcgcgtggtggctca	26094
rs7154677	snp	A/G			intron-variant	DCAF4	GRCh38.p7	14:72942626	CCTGGGGCTCTTCCC[A/G]GCAGCCGTATCCTGG	26094
rs7155130	snp	A/G	0.446902	0.154045	intron-variant	DCAF4	GRCh38.p7	14:72935643	GCCTGTATGAGTTAG[A/G]GGTGAACACATGCTC	26094
rs7155812	snp	A/G	0.00194459	0.031121	missense	DCAF4	GRCh38.p7	14:72951866	CATCACTGTTCGTCA[A/G]TAGTCACCCAGGTAC	26094
rs7156296	snp	C/T	0.0111196	0.0737302	intron-variant	DCAF4	GRCh38.p7	14:72952065	TTACCCATCTTGGGC[C/T]ATTTCAGTCATTTCA	26094
rs7160796	snp	C/G	0.370568	0.219005	intron-variant	DCAF4	GRCh38.p7	14:72927906	ATGTTGTTTTACAGT[C/G]AACAACTCCTAACTg	26094
rs7160837	snp	C/G	0.267091	0.249415	intron-variant	DCAF4	GRCh38.p7	14:72928060	cccacctcagcctcc[C/G]aaagtgctgggatta	26094
rs7493034	snp	A/G			downstream-variant-500B	DCAF4	GRCh38.p7	14:72962504	AACACACACACACAC[A/G]CACACACGCATGCAC	26094
rs7493035	snp	A/G	0.444444	0.157135	downstream-variant-500B	DCAF4	GRCh38.p7	14:72962508	CACACACACACACAC[A/G]CACGCATGCACACTC	26094
rs7493937	snp	C/T	0.0418186	0.138422	intron-variant	DCAF4	GRCh38.p7	14:72956952	GCGCGGTGGCTCACG[C/T]CCGTAATCCCAACAC	26094
rs8003923	snp	C/T	0.121369	0.214369	intron-variant, upstream-variant-2KB	DCAF4	GRCh38.p7	14:72936879	AATGAGCAAAGGATT[C/T]ATTTAGCAAGAAGAA	26094
rs8004641	snp	A/G	0.16911	0.236552	intron-variant, upstream-variant-2KB	DCAF4	GRCh38.p7	14:72933330	ctttgggaggccgag[A/G]tgggcagatcacaag	26094
rs8005272	snp	A/G	0.101658	0.201233	intron-variant	DCAF4	GRCh38.p7	14:72940881	CAGGCGTGAGCCACC[A/G]CACCCAGCCTTCTTC	26094
rs8010674	snp	C/T	0.493386	0.0571263	downstream-variant-500B	DCAF4	GRCh38.p7	14:72962458	CACTTGAAACCAGCC[C/T]GGGCAACATGCCAAA	26094
rs8022709	snp	A/C	0.0260105	0.111035	intron-variant, upstream-variant-2KB	DCAF4	GRCh38.p7	14:72936823	AAAAGGATCTAGGAC[A/C]GAACAATGGAAAGCA	26094
rs9788482	snp	C/T	0.443195	0.158668	intron-variant	DCAF4	GRCh38.p7	14:72935197	GAAAGGTACTGTCTT[C/T]GTCCTAGCCTTTAAA	26094
rs10130567	snp	C/G	0	0	intron-variant	DCAF4	GRCh38.p7	14:72955220	GCTTTTGGTGGAGAT[C/G]GAATGCTATCTCTGG	26094
rs10134292	snp	C/T	0.169435	0.236663	intron-variant, upstream-variant-2KB	DCAF4	GRCh38.p7	14:72934488	AGAGTTGGGGTTTCG[C/T]CATGTTGGTCAGGCT	26094
rs10148121	snp	A/T	0.443195	0.158668	intron-variant	DCAF4	GRCh38.p7	14:72935344	ACTGCAACCTCCGCC[A/T]CCTGGGTTCAAACGA	26094
rs10149638	snp	A/T			intron-variant	DCAF4	GRCh38.p7	14:72953732	aaaaaaaaaaaaaaa[A/T]atatatatatatata	26094
rs10483851	snp	C/T	0.17332	0.23795	upstream-variant-2KB	DCAF4	GRCh38.p7	14:72924632	TGTCCCCTGGCTCTT[C/T]AGTGGAAAATCCAGC	26094
rs10873253	snp	C/T	0.112631	0.208878	intron-variant	DCAF4	GRCh38.p7	14:72928361	accgcgcccggctaa[C/T]tttttgtattttagt	26094
rs11158993	snp	C/T	0.199254	0.244796	intron-variant	DCAF4	GRCh38.p7	14:72928562	TCACTTTAACTATTA[C/T]AGCATGGTGTAGTAA	26094
rs11158994	snp	A/T			intron-variant	DCAF4	GRCh38.p7	14:72928598	CTTtatatatatata[A/T]atatatatatatata	26094
rs11158995	snp	C/T	0.040671	0.13668	intron-variant	DCAF4	GRCh38.p7	14:72930155	AAATAAATAAAGTGG[C/T]ATCTCACTGTGGTTT	26094
rs11158996	snp	C/T	0.3742	0.216966	intron-variant	DCAF4	GRCh38.p7	14:72930254	GCTTTTTCTTTTTTT[C/T]TTTTGAGACGGAGTT	26094
rs11158997	snp	C/G	0.375399	0.216275	intron-variant	DCAF4	GRCh38.p7	14:72944690	CCAGCTACTCGGGAG[C/G]CTATGGTGGGAGTAT	26094
rs11158998	snp	A/G	0.410061	0.192043	intron-variant	DCAF4	GRCh38.p7	14:72951036	CCCAGGCTGGAGTGC[A/G]GTCACATGATCACAG	26094
rs11158999	snp	A/G	0.409891	0.192184	intron-variant	DCAF4	GRCh38.p7	14:72957119	CGGAAGTCAGAAGCA[A/G]GAGAATTGCTTGGAC	26094

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