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
rs11986	snp	A/G	0	0	utr-variant-3-prime	KCTD5	GRCh38.p7	16:2708739	TAAGTCTGCCTTCTA[A/G]AAAGGCTTTTATAAA	54442
rs732055	snp	A/G	0.470521	0.117772	intron-variant	KCTD5	GRCh38.p7	16:2700191	ACACAGAGGTGCCAG[A/G]TGATGCGAAGAAAGC	54442
rs732057	snp	C/G	0.309154	0.242901	intron-variant	KCTD5	GRCh38.p7	16:2700617	GGGAGGGCTGGGTGA[C/G]GTCACTGTCCCCACC	54442
rs732058	snp	C/T	0.332568	0.235971	intron-variant	KCTD5	GRCh38.p7	16:2700870	AGTCACCCCGGCCCC[C/T]GGCCTAGGGGTCCAG	54442
rs739717	snp	A/G	0.478603	0.101197	intron-variant	KCTD5	GRCh38.p7	16:2702153	GGAAGAGCTCGCCCC[A/G]TGCCATGCCACGGCG	54442
rs757168	snp	C/G	0.234109	0.249494	intron-variant	KCTD5	GRCh38.p7	16:2700209	ACGCCAGTCCCCTCC[C/G]TCACACAGAGGTGCC	54442
rs1859137	snp	C/T	0.454544	0.143743	intron-variant	KCTD5	GRCh38.p7	16:2700454	AGCACTCAGGTGGCT[C/T]CCGTGGAAGCTGCTG	54442
rs2074368	snp	C/G	0	0	intron-variant	KCTD5	GRCh38.p7	16:2695469	CCTACATGCAGGAAC[C/G]GGGGGTCAGGGTGAC	54442
rs2335152	snp	C/G	0.117886	0.21224	intron-variant	KCTD5	GRCh38.p7	16:2696842	GCTGTGAGCCATGAT[C/G]CCCACTCCTGTCTCT	54442
rs2335153	snp	C/T			intron-variant	KCTD5	GRCh38.p7	16:2696882	AATGTCTTTCACATG[C/T]ACTCTCTCTGGTCGC	54442
rs2335154	snp	C/T	0	0	intron-variant	KCTD5	GRCh38.p7	16:2696936	TGGAGCCGCTCGAGT[C/T]GAGGCTTCGCTTTAT	54442
rs2335155	snp	A/G	0.0444908	0.142359	intron-variant	KCTD5	GRCh38.p7	16:2696986	GATTGGCTCAGAAAC[A/G]GGCGCTAGACACAGA	54442
rs2335156	snp	A/G			intron-variant	KCTD5	GRCh38.p7	16:2696990	GGCTCAGAAACGGGC[A/G]CTAGACACAGACCAA	54442
rs2907052	snp	A/G	0.000798403	0.0199641	intron-variant	KCTD5	GRCh38.p7	16:2696543	CCAACGCGTGTGGGC[A/G]CCGTCCCTGCACCAC	54442
rs2965989	snp	C/G/T	0.000798403	0.0199641	intron-variant	KCTD5	GRCh38.p7	16:2696747	TGGGCCTCTGGGCCT[C/G/T]GGCATCTGCCTGCCT	54442
rs3030700	in-del	-/GA			intron-variant	KCTD5	GRCh38.p7	16:2700642	CCCTCCCTGTCCTGA[-/GA]GTTTCCTCTGTCACT	54442
rs3030702	in-del	-/C/CC			intron-variant	KCTD5	GRCh38.p7	16:2700814	TGGAGCCCCCCCCCC[-/C/CC]TTAAAATGTCACTAA	54442
rs3032675	in-del	-/CT			intron-variant	KCTD5	GRCh38.p7	16:2696916	GCAGCCGCTTGTGTT[-/CT]GTCGTGGAGCCGCTC	54442
rs3094470	snp	C/T	0.320335	0.239902	intron-variant	KCTD5	GRCh38.p7	16:2704259	TCCAGCTCTGGCCCC[C/T]GCAATCCCCCACGGC	54442
rs3094471	snp	A/G	0.333722	0.235565	intron-variant	KCTD5	GRCh38.p7	16:2703179	AGGAAATGCCACCAG[A/G]ATGGGTCACCTGTGG	54442
rs3094473	snp	C/T	0.470853	0.11715	intron-variant	KCTD5	GRCh38.p7	16:2699194	GGTGGCCCCACATCC[C/T]GGACAGTCACTACGG	54442
rs3094474	snp	A/G	0.308661	0.24302	intron-variant	KCTD5	GRCh38.p7	16:2698062	GGCAGCCGGTCGGGG[A/G]AGTAAAGGGGAGCCC	54442
rs3094475	snp	A/G	0.487232	0.078872	intron-variant	KCTD5	GRCh38.p7	16:2697856	CCAAACTAAACCAAA[A/G]AATCCACGCTTTACA	54442
rs3094476	snp	C/T	0.428484	0.175052	intron-variant	KCTD5	GRCh38.p7	16:2697615	CAGTGACCCGCCAGG[C/T]ATGGAGCCGCTGCTT	54442
rs3094477	snp	C/T	0.471388	0.116136	intron-variant	KCTD5	GRCh38.p7	16:2697076	CACAGCCCCCTTCTC[C/T]AGCACCCAGGGCGTG	54442
rs3094478	snp	C/T	0.308908	0.242961	intron-variant	KCTD5	GRCh38.p7	16:2697049	CGTGAGTGGCTGCAT[C/T]GGGGCGGGATAGAGG	54442
rs3094479	snp	C/T	0.45946	0.136478	intron-variant	KCTD5	GRCh38.p7	16:2696660	GGGGGAGCAGGGCCA[C/T]GCCCGCACGCAGGTG	54442
rs3112710	snp	A/G			upstream-variant-2KB	KCTD5	GRCh38.p7	16:2680955	CCACATAGCCTAACC[A/G]TCTGGCAGAATGACT	54442
rs3112711	snp	C/T			upstream-variant-2KB	KCTD5	GRCh38.p7	16:2680956	CACATAGCCTAACCG[C/T]CTGGCAGAATGACTA	54442
rs3112712	snp	C/T	0	0	intron-variant	KCTD5	GRCh38.p7	16:2683297	TTCCCTGGTGACTTG[C/T]ATTTAGAGAGTTGGC	54442
rs3112713	snp	A/G			intron-variant	KCTD5	GRCh38.p7	16:2683374	TTAGAAGATGCGTCC[A/G]TAGTATATAGTATGA	54442
rs3112714	snp	C/G			intron-variant	KCTD5	GRCh38.p7	16:2683384	CGTCCGTAGTATATA[C/G]TATGATTTTTCGAAG	54442
rs3112715	snp	A/G			intron-variant	KCTD5	GRCh38.p7	16:2683386	TCCGTAGTATATAGT[A/G]TGATTTTTCGAAGGG	54442
rs3112716	snp	C/T	0.000399281	0.0141238	intron-variant	KCTD5	GRCh38.p7	16:2683447	GATGTCCAGGAAGGG[C/T]CAGGTAAGGAATCTT	54442
rs3112724	snp	A/C	0.0298908	0.118541	intron-variant	KCTD5	GRCh38.p7	16:2696590	CTGTGTGCTGCGGTG[A/C]TGGCTTGGCTCAGAA	54442
rs3112725	snp	C/G	0.470811	0.117228	intron-variant	KCTD5	GRCh38.p7	16:2697098	GGGGCTGTGCGGGAC[C/G]CATGCGGGGCCGGGA	54442
rs3112726	snp	C/T	0.444267	0.157354	intron-variant	KCTD5	GRCh38.p7	16:2698698	GTCCACGTAGAGCCC[C/T]GGGCCCTGTGCAGAC	54442
rs3112727	snp	C/T	0.304688	0.243945	intron-variant	KCTD5	GRCh38.p7	16:2699529	AGACGTGGACGCTCT[C/T]GTGTCGTCATGTCGA	54442
rs3112728	snp	C/T	0.311859	0.242226	intron-variant	KCTD5	GRCh38.p7	16:2701172	TGGGCACCTGCCTCC[C/T]GGGGCAGCTTCAGGT	54442
rs3743929	snp	C/T	0.00159617	0.0282053	downstream-variant-500B	KCTD5	GRCh38.p7	16:2709200	GCCAAGCCGGCACCC[C/T]GTGGATGGCCCAGCT	54442
rs3785340	snp	C/T	0.00119737	0.0244387	intron-variant	KCTD5	GRCh38.p7	16:2706546	GAGGACAGGCTCAGG[C/T]GCTGGCCAATGCTGC	54442
rs3785341	snp	A/G	0	0	intron-variant	KCTD5	GRCh38.p7	16:2705045	CAAACCCCCACGCCC[A/G]GTGACCTTCCAGTGA	54442
rs3785342	snp	A/C	0.00159617	0.0282053	intron-variant	KCTD5	GRCh38.p7	16:2703616	GAGAGACATGCTTGG[A/C]GGCCCCACCCCTCTG	54442
rs3826244	snp	C/T	0.00119737	0.0244387	intron-variant	KCTD5	GRCh38.p7	16:2704727	AGGAGGGATCAGCCA[C/T]GGGGGCAGGCGGTGG	54442
rs3837778	in-del	-/GGCCCCCAGCC			intron-variant	KCTD5	GRCh38.p7	16:2703512	CAGAGGCCCCCAGCC[-/GGCCCCCAGCC]AAGAGTCTGCGGTTG	54442
rs3842363	in-del	-/AAG	0.00478275	0.0486673	cds-indel	KCTD5	GRCh38.p7	16:2707897	AGCCCGTGTCAGAAG[-/AAG]GCCCGGCCTCGGAAT	54442
rs4045847	in-del	-/TCGCTTGG			intron-variant	KCTD5	GRCh38.p7	16:2696894	ATGTACTCTCTCTGG[-/TCGCTTGG]GCAGCCGCTTGTGTT	54442
rs4296261	snp	A/G	0.0905309	0.192535	intron-variant	KCTD5	GRCh38.p7	16:2700695	TCCATGGCCCAGTGC[A/G]CCTGCCAGGTTGTGG	54442
rs4785900	snp	C/G	0.284209	0.247648	intron-variant	KCTD5	GRCh38.p7	16:2684324	TAAGGTGGTTGATCC[C/G]TTTGCTTTACTGTTC	54442
rs4786320	snp	G/T	0.167809	0.236103	intron-variant	KCTD5	GRCh38.p7	16:2705879	TGCAGGTCTCCAGGG[G/T]GTCTCCTGCCCTCAT	54442
rs5815130	in-del	-/AG			intron-variant	KCTD5	GRCh38.p7	16:2700639	CCTCCCTGTCCTGAG[-/AG]TTTCCTCTGTCACTT	54442
rs5815131	in-del	-/C	0.402201	0.19833	intron-variant	KCTD5	GRCh38.p7	16:2700804	TGGAGCCCCCCCCCC[-/C]TTAAAATGTCACTAA	54442
rs7188619	snp	C/T	0.00874735	0.0655527	utr-variant-3-prime	KCTD5	GRCh38.p7	16:2709016	AAATAGCAAATAAAA[C/T]TGTGTATTTATGAAT	54442
rs7188658	snp	C/T	0.00557542	0.0525036	intron-variant	KCTD5	GRCh38.p7	16:2698595	GAGAGCTGAGCCCGC[C/T]CCCCCCACCCAAGCT	54442
rs7194693	snp	C/G	0.481473	0.0944461	intron-variant	KCTD5	GRCh38.p7	16:2689766	cactgcaacggggct[C/G]tcaggttcaagtgat	54442
rs7201996	snp	A/G	0.00874735	0.0655527	intron-variant	KCTD5	GRCh38.p7	16:2705567	CAGGACCAGTGCGGC[A/G]GACAGCAGACCCCTA	54442
rs7206555	snp	A/G	0.0174175	0.0916809	downstream-variant-500B	KCTD5	GRCh38.p7	16:2709409	tgctgggctcaagtg[A/G]tcctcctgcctcagc	54442
rs8044323	snp	A/G	0	0	intron-variant	KCTD5	GRCh38.p7	16:2698949	ATGACGCAGGTGGGC[A/G]GGAAATGGTGCAGGT	54442
rs8048298	snp	C/T	0.000399281	0.0141238	intron-variant	KCTD5	GRCh38.p7	16:2698851	CTGCGTCCCGCGCCC[C/T]GGGTCACCTTGTCCA	54442
rs8048336	snp	C/G	0	0	intron-variant	KCTD5	GRCh38.p7	16:2698912	CTGTGTGGGCACTCC[C/G]TGCCTCAGTCTACCT	54442
rs8049286	snp	C/T	0.102726	0.202016	intron-variant	KCTD5	GRCh38.p7	16:2705187	CAGATTAAGTGTGAA[C/T]GTCATGGTGAGCTCC	54442
rs8057370	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB	KCTD5	GRCh38.p7	16:2681358	cactctgtcgcccag[A/G]ctagagtgcagtggc	54442
rs8059207	snp	A/G	0	0	intron-variant	KCTD5	GRCh38.p7	16:2699237	GAGCAGCTCCATGCA[A/G]GCGGGCGGCCCTGGT	54442
rs8059210	snp	A/G	0	0	intron-variant	KCTD5	GRCh38.p7	16:2699240	CAGCTCCATGCAGGC[A/G]GGCGGCCCTGGTGGC	54442
rs8063137	snp	C/T	0	0	intron-variant	KCTD5	GRCh38.p7	16:2699134	ACCTCTGAACCCCTT[C/T]TCACTGCTGCGTTTC	54442
rs8063286	snp	C/G			intron-variant	KCTD5	GRCh38.p7	16:2699188	AGTCCTCCGTAGTGA[C/G]TGTCCAGGATGTGGG	54442
rs9926188	snp	C/T	0.427727	0.175821	intron-variant	KCTD5	GRCh38.p7	16:2692732	gggacctaccccctt[C/T]ttcccaggaatctat	54442
rs9935912	snp	A/T	0.5	0	intron-variant	KCTD5	GRCh38.p7	16:2688247	TATATATATATATAT[A/T]TATTTATTTATTTAT	54442
rs9941296	snp	A/G	0.0558544	0.157504	downstream-variant-500B	KCTD5	GRCh38.p7	16:2709498	TTTGAAAGTCCTGAT[A/G]CCTCAAGTTAGCATC	54442
rs10500324	snp	A/G	0.308414	0.24308	intron-variant	KCTD5	GRCh38.p7	16:2691811	GGCTGCTCCTTTCAA[A/G]TCTCTTCCTAACTGG	54442
rs11077332	snp	A/G	0.465996	0.12588	intron-variant	KCTD5	GRCh38.p7	16:2684980	GGAATCAATTCTTTG[A/G]GCGAGGGGTAATTAA	54442
rs11077336	snp	A/G	0.459004	0.137176	intron-variant	KCTD5	GRCh38.p7	16:2692019	CCTGGTCCCTCTGTC[A/G]GGAGCCTGAGCTCCA	54442
rs11552505	snp	A/C			utr-variant-3-prime	KCTD5	GRCh38.p7	16:2708633	TGGTTAATCAGGTGA[A/C]TGGCAAAGAGGAGGA	54442
rs11642384	snp	G/T	0.122411	0.214991	intron-variant	KCTD5	GRCh38.p7	16:2693417	AAGCTGCCTCCTAAA[G/T]GGGGTGTTTAATGGA	54442
rs11644881	snp	A/G	0.490563	0.0680388	intron-variant	KCTD5	GRCh38.p7	16:2690840	GCTGCCTTTGTCTCC[A/G]TGAGCCTCGGAGTAT	54442
rs11645410	snp	C/T	0.494526	0.0520291	intron-variant	KCTD5	GRCh38.p7	16:2687070	CTCTGCGATGGTCCC[C/T]GCGGTGCTGGGGGCT	54442
rs11646634	snp	C/T	0.208474	0.246527	intron-variant	KCTD5	GRCh38.p7	16:2693451	GCCAGCCCCGCCCAG[C/T]GGTAGGAGTGGCCAA	54442
rs11860950	snp	C/T	0.5	0	intron-variant	KCTD5	GRCh38.p7	16:2702879	CTGAGTGCAGGGACA[C/T]GGGGGTCCAGTTGTC	54442
rs12149376	snp	C/T	0.178785	0.239642	intron-variant	KCTD5	GRCh38.p7	16:2688349	TCTGCCTCCTGGGTT[C/T]AAGCATTTCTCCTGC	54442
rs12149789	snp	A/G	0.43088	0.172575	intron-variant	KCTD5	GRCh38.p7	16:2690266	GGCTGTGTGTGCCCT[A/G]GCTCGGCGCTGTCTG	54442
rs12448477	snp	C/T	0.286303	0.24735	intron-variant	KCTD5	GRCh38.p7	16:2684531	agcactttgggaggc[C/T]gaggcaggcggatca	54442
rs12926029	snp	G/T	0.335788	0.23482	intron-variant	KCTD5	GRCh38.p7	16:2689714	GACAGAGGCTCACTG[G/T]ATCGCCCAGGCTGGA	54442
rs13331521	snp	A/G	0.0429648	0.14013	intron-variant	KCTD5	GRCh38.p7	16:2687396	GGAGGAAATGCTGTC[A/G]CTGCAGGGCAGTTCC	54442
rs13331631	snp	A/C/G	0.0360663	0.129354	intron-variant	KCTD5	GRCh38.p7	16:2687634	GCCAGGGCTGTGGCC[A/C/G]TGATGGGGGCGCCTG	54442
rs13331679	snp	G/T	0.110167	0.207236	intron-variant	KCTD5	GRCh38.p7	16:2687662	CTGCTGCCTGGTCTC[G/T]CCCCGGCCCTGTCGT	54442
rs13333623	snp	A/G	0.0391387	0.134304	intron-variant	KCTD5	GRCh38.p7	16:2706895	GGTCCGGGCGTCGGG[A/G]TGGGGGTGGGGGCTG	54442
rs13337854	snp	A/G	0.227664	0.249	intron-variant	KCTD5	GRCh38.p7	16:2702687	CCTCCCAGCCTGCAT[A/G]CAGAGCTGCTCCTGG	54442
rs17136030	snp	C/G	0.014814	0.0847794	utr-variant-3-prime	KCTD5	GRCh38.p7	16:2708214	GGAGCTGAAGGTCTG[C/G]GTCACGGTGAAAATT	54442
rs17598822	snp	A/G	0.482757	0.0912364	intron-variant	KCTD5	GRCh38.p7	16:2696544	TGGTGCAGGGACGGC[A/G]CCCACACGCGTTGGG	54442
rs28379781	snp	A/G	0.0364509	0.129988	intron-variant	KCTD5	GRCh38.p7	16:2697685	GTGTTCAGTCCACAC[A/G]TCGGCCCTCTCACCA	54442
rs28536680	snp	C/G			intron-variant	KCTD5	GRCh38.p7	16:2693182	CAGCTCTGCATCGGG[C/G]CCCCTCTCCACCCAA	54442
rs28567711	snp	A/T			intron-variant	KCTD5	GRCh38.p7	16:2688228	ATAAATAAATAAATA[A/T]ATATATATATATATA	54442
rs28572556	snp	C/G/T	0.0744748	0.178019	upstream-variant-2KB	KCTD5	GRCh38.p7	16:2680637	TGGGGTCCCTTCTTA[C/G/T]GCAGCACACGTGGCA	54442
rs28576266	snp	A/T			intron-variant	KCTD5	GRCh38.p7	16:2688224	TTAAATAAATAAATA[A/T]ATAAATATATATATA	54442
rs28580368	snp	A/T			intron-variant	KCTD5	GRCh38.p7	16:2688239	AATAAATATATATAT[A/T]TATATATTTATTTAT	54442
rs28593320	snp	A/T			intron-variant	KCTD5	GRCh38.p7	16:2688243	AATATATATATATAT[A/T]TATTTATTTATTTAT	54442
rs28711015	snp	G/T	0.499946	0.00519141	intron-variant	KCTD5	GRCh38.p7	16:2689536	GTCTCCGAGCACCGG[G/T]AATGACTGAGAGCCG	54442
rs34064394	in-del	-/C			intron-variant	KCTD5	GRCh38.p7	16:2700808	GTACTTGGAGCCCCC[-/C]CCCCCCTTAAAATGT	54442
rs34835609	in-del	-/T			upstream-variant-2KB	KCTD5	GRCh38.p7	16:2681723	ATTTTACAACTTTTT[-/T]CTGGCTTTATTACAA	54442
rs35317991	snp	A/G	0.428786	0.174744	intron-variant	KCTD5	GRCh38.p7	16:2694030	AGGTAGCAGTGAGCC[A/G]TGAATAATTCCTGAG	54442

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