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
rs710183	snp	A/C	0.0577344	0.159793	intron-variant	KCTD17	GRCh38.p7	22:37054720	CATCCTCCGgccagg[A/C]actgagctccatgct	79734
rs710184	snp	A/G	0.0919752	0.193722	intron-variant	KCTD17	GRCh38.p7	22:37057219	GAGATGGTGCCTGGT[A/G]AATGCCTGGTGAGGA	79734
rs710185	snp	C/T	0.231937	0.249347	synonymous-codon, nc-transcript-variant	KCTD17	GRCh38.p7	22:37057412	GGTCCCACCCAAGCA[C/T]GTGTACCGCGTGCTG	79734
rs855792	snp	A/G			intron-variant	KCTD17	GRCh38.p7	22:37059645	CGGCTGCACCCTGGG[A/G]ATGCTCTCATTTCAC	79734
rs855793	snp	A/G	0.273856	0.248859	intron-variant	KCTD17	GRCh38.p7	22:37053568	GCCTGTCAACACTGC[A/G]TTCCTGTCACCCCAG	79734
rs855794	snp	A/G	0.00159617	0.0282053	intron-variant	KCTD17	GRCh38.p7	22:37052820	GGTGAGAGGATGTCT[A/G]AGTGGCAACTGGCCC	79734
rs855795	snp	A/C	0	0	intron-variant	KCTD17	GRCh38.p7	22:37052333	TAGCTCCCTGCACCC[A/C]TCCGCCACCCACATC	79734
rs855796	snp	C/T	0.00517822	0.0506191	intron-variant	KCTD17	GRCh38.p7	22:37052154	GGCCGCGGCCTGCGT[C/T]GTCCCGTTGCCACGG	79734
rs855797	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37050937	TCAGTTTTTCCACGT[C/T]CTCCCTAAGAAGGAG	79734
rs2142825	snp	A/G	0.0298908	0.118541	intron-variant	KCTD17	GRCh38.p7	22:37058209	CACGCCCACCCACAC[A/G]TTCCCTGGCACATGG	79734
rs2235320	snp	G/T	0.147656	0.228091	intron-variant	KCTD17	GRCh38.p7	22:37057216	AGTGAGATGGTGCCT[G/T]GTAAATGCCTGGTGA	79734
rs5756501	snp	A/G			intron-variant	KCTD17	GRCh38.p7	22:37053739	GCAGGAGAGGGGGGA[A/G]TCTGCTTCCCAGTGG	79734
rs6000544	snp	C/T	0.0287284	0.116357	intron-variant	KCTD17	GRCh38.p7	22:37057967	CAGCATTGCAACATG[C/T]AGGGGAGCCCAAAGC	79734
rs6000545	snp	A/G	0.0295035	0.117819	intron-variant	KCTD17	GRCh38.p7	22:37059200	TGGGCCCGACAAGCC[A/G]CAAGATTAGGACCTG	79734
rs6000546	snp	A/G	0	0	missense, nc-transcript-variant	KCTD17	GRCh38.p7	22:37059361	AGCGAGGACCAGGCA[A/G]AGTTCCTGTGTGTGG	79734
rs6000547	snp	C/T	0.117537	0.212022	downstream-variant-500B	KCTD17	GRCh38.p7	22:37063788	CTCCCTTCTCTGACC[C/T]TGCTGGACCCAGCCC	79734
rs7287067	snp	A/G	0.0205511	0.0992634	intron-variant	KCTD17	GRCh38.p7	22:37054440	TATCTGGGGGCTAGG[A/G]GATCACACAGGGCTA	79734
rs7287458	snp	A/G	0.0178098	0.0926698	intron-variant	KCTD17	GRCh38.p7	22:37054411	TATCTGGGGGCTAGG[A/G]GATCACACAGGGCTA	79734
rs7287464	snp	A/G	0.02016	0.0983543	intron-variant	KCTD17	GRCh38.p7	22:37054432	CACAGGGCTATCTGG[A/G]GGCTAGGAGATCACA	79734
rs7292681	snp	C/T	0.104504	0.2033	intron-variant, utr-variant-3-prime	KCTD17	GRCh38.p7	22:37062157	ctgctccctgtggct[C/T]ctttcGCCTGGGGCA	79734
rs8138791	snp	A/G	0.0655868	0.168795	downstream-variant-500B	KCTD17	GRCh38.p7	22:37063499	CAAAAGCCCAGGGAC[A/G]CTGCCCTGTTGTCAT	79734
rs9610639	snp	A/T	0.0376037	0.131863	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37049953	TCGttttattttttt[A/T]aaatagagatggggg	79734
rs9610640	snp	A/C			intron-variant	KCTD17	GRCh38.p7	22:37058689	TTAGCCAGAAGGGCT[A/C]TGTGGGCGTGGTTAT	79734
rs11542756	snp	C/G			missense, nc-transcript-variant	KCTD17	GRCh38.p7	22:37056394	CGGATGGAAGAGAAG[C/G]ACTACACGGTCACCC	79734
rs11542757	snp	C/T			utr-variant-3-prime, nc-transcript-variant	KCTD17	GRCh38.p7	22:37063272	CCATACCCACTCTCC[C/T]CGGGCAGTTCCTGAG	79734
rs11913600	snp	C/T	0.0655868	0.168795	intron-variant	KCTD17	GRCh38.p7	22:37056095	CTGGGTCACCGCACT[C/T]AGCACAGCAGAGCTG	79734
rs11913810	snp	C/G	0.278664	0.248351	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37051006	ACTCGGATCCAGGGC[C/G]TGCTCTACTCTTCCT	79734
rs12159304	snp	A/C	0.109814	0.206997	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37050359	tcaagcgagccttgg[A/C]ctcccaaagtgctgg	79734
rs12159325	snp	A/G	0.134119	0.221521	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37050261	ctcaaaaaagaaaaa[A/G]agagagagagagaga	79734
rs12160419	snp	A/G	0.0479149	0.147179	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37051501	TTTGGGGAAGCCCTC[A/G]TTCTTTTCCCAGAGG	79734
rs12160438	snp	C/T	0.0524604	0.153226	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37051428	TTATCAGCTGTTGGA[C/T]GACGGAGACGGCACA	79734
rs13054696	snp	C/T	0.5	0	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37051453	GGCACAAAGGAAAAA[C/T]AAGAATGCTCGGACC	79734
rs17852877	snp	C/G	0	0	missense, nc-transcript-variant	KCTD17	GRCh38.p7	22:37051890	CGGCAGACGCTGTGC[C/G]GCGAGCAGAAGTCCT	79734
rs17852879	snp	A/C			synonymous-codon, nc-transcript-variant	KCTD17	GRCh38.p7	22:37057463	CACGCAAATGGTCTC[A/C]ACCATGTCTGATGGC	79734
rs17852880	snp	C/G			synonymous-codon, nc-transcript-variant	KCTD17	GRCh38.p7	22:37059330	GGTGAACATCGGCTC[C/G]TCCTACAACTACGGC	79734
rs28412036	snp	C/G			intron-variant	KCTD17	GRCh38.p7	22:37052329	TTGGGATGTGGGTGG[C/G]GGATGGGTGCAGGGA	79734
rs34289157	in-del	-/G			intron-variant	KCTD17	GRCh38.p7	22:37056004	TCATGGTGACATTCT[-/G]GGGGATCAGTCCCAA	79734
rs34306072	in-del	-/C			intron-variant	KCTD17	GRCh38.p7	22:37059561	ACCGCCCATGCACAA[-/C]CCCCATGCTCACAGC	79734
rs34395802	snp	C/T	0.000530724	0.0162813	synonymous-codon, nc-transcript-variant	KCTD17	GRCh38.p7	22:37059324	CTAGCTGGTGAACAT[C/T]GGCTCCTCCTACAAC	79734
rs34493724	in-del	-/G			intron-variant	KCTD17	GRCh38.p7	22:37059030	TAGGCTGGAGGTGGT[-/G]GGTGGGGACAGCGGT	79734
rs34745899	in-del	-/T			intron-variant	KCTD17	GRCh38.p7	22:37054794	GGGCACTGGGGATAA[-/T]TTCTCGTAATCAGGC	79734
rs34948303	in-del	-/A			upstream-variant-2KB	KCTD17	GRCh38.p7	22:37050260	TCTCAAAAAAGAAAA[-/A]GAGAGAGAGAGAGAG	79734
rs35182982	in-del	-/T			intron-variant	KCTD17	GRCh38.p7	22:37059113	GGTCCTGGGGCACAG[-/T]ACCACAGGCACAGGT	79734
rs35505327	in-del	-/G			intron-variant, utr-variant-3-prime	KCTD17	GRCh38.p7	22:37062298	CTGGATGGGTTAGTT[-/G]GGGGAGCCCTTGCTG	79734
rs35901190	snp	A/G	0.00170555	0.0291524	synonymous-codon, nc-transcript-variant	KCTD17	GRCh38.p7	22:37056357	CTACAACATCGGCCC[A/G]CTGATCCGCATCATC	79734
rs35975182	in-del	-/T			intron-variant	KCTD17	GRCh38.p7	22:37052056	ACCCGGCCGGGTTCA[-/T]TTTCCGAGGAACTGG	79734
rs55897262	snp	A/G			intron-variant	KCTD17	GRCh38.p7	22:37059217	AAGATTAGGACCTGA[A/G]CTGGTATCTTGATTT	79734
rs56126639	snp	A/G			intron-variant	KCTD17	GRCh38.p7	22:37059209	CAAGCCGCAAGATTA[A/G]GACCTGAGCTGGTAT	79734
rs56340423	in-del	-/GAGA			upstream-variant-2KB	KCTD17	GRCh38.p7	22:37050295	AGAGAGAGAGAGAGA[-/GAGA]TAGGGGTCTCACTAT	79734
rs56381800	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	KCTD17	GRCh38.p7	22:37063432	GCCACTTTTGGGGAC[A/G]GGGCTAAACTAAAGG	79734
rs56852782	snp	G/T	0.0652144	0.168387	intron-variant	KCTD17	GRCh38.p7	22:37054275	AGGCCCCATCGGGAG[G/T]GAAGTAAACACCCCA	79734
rs56979751	snp	A/C			intron-variant, missense, nc-transcript-variant	KCTD17	GRCh38.p7	22:37061423	GGAGGAGGGGCGCAG[A/C]TGCACCTCCTCTGTG	79734
rs57980010	snp	A/G			intron-variant	KCTD17	GRCh38.p7	22:37055938	TGCACCTGGCACTTA[A/G]AATGTGCTTAATAAA	79734
rs58201239	in-del	-/C	0.0298908	0.118541	intron-variant, utr-variant-3-prime	KCTD17	GRCh38.p7	22:37061830	CCATCAGCACCAGAG[-/C]CCAGGCTGGTGGGGA	79734
rs58843694	snp	C/T	0.0410537	0.137264	intron-variant	KCTD17	GRCh38.p7	22:37059705	CCGCTTAGTGGCCAC[C/T]GGGCACTGTGGCATG	79734
rs59355258	in-del	-/AAGA/GA			upstream-variant-2KB	KCTD17	GRCh38.p7	22:37050298	AGAGAGAGAGAGAGA[-/AAGA/GA]TAGGGGTCTCACTAT	79734
rs59772675	snp	C/T			intron-variant	KCTD17	GRCh38.p7	22:37058706	GTGGGCGTGGTTATT[C/T]TAGGGACCCTGGAAC	79734
rs61214014	snp	C/G	0.0349115	0.127424	downstream-variant-500B	KCTD17	GRCh38.p7	22:37063419	CCTCTTTCTCTGGGC[C/G]ACTTTTGGGGACGGG	79734
rs71317024	snp	A/G	0.5	0	intron-variant	KCTD17	GRCh38.p7	22:37054249	CATGGGCGTGGCCTA[A/G]GCTCAGGAGCAGGCC	79734
rs71707926	in-del	-/AA	0.0524604	0.153226	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37051400	GGATTCCTGGAGGGG[-/AA]AGTTTCTTCCCTTAT	79734
rs73415522	snp	A/C	0.109814	0.206997	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37050742	AGGCCAGGACCAGGA[A/C]TGAAACCAGTAAGGA	79734
rs73884697	snp	C/G/T	0.010564	0.0719074	intron-variant	KCTD17	GRCh38.p7	22:37059263	TCGTATCCTGCCCCA[C/G/T]GGCCCCCAACACCAA	79734
rs73884698	snp	C/T	0.0410537	0.137264	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	KCTD17	GRCh38.p7	22:37062827	TGTCTCTCCGGCACC[C/T]GCGTCCCCTCTCCCG	79734
rs73886910	snp	A/G	0.0298908	0.118541	utr-variant-3-prime, nc-transcript-variant	KCTD17	GRCh38.p7	22:37063051	GGAAGGACCCAGCCC[A/G]ACCCCTGGGCATAAC	79734
rs73886911	snp	C/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	KCTD17	GRCh38.p7	22:37063310	GCCAGGGGCCCTCCT[C/G]TGTTTGACTTCCCGG	79734
rs74844925	snp	C/G	0.0524604	0.153226	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37051378	CACATGCGGGTCAAT[C/G]CTATGGGGATTCCTG	79734
rs75327537	snp	C/T	0.0543475	0.155628	intron-variant	KCTD17	GRCh38.p7	22:37054777	CCTGCAGGGCTCCGC[C/T]CAGGGCACTGGGGAT	79734
rs75883417	snp	C/T	0.0517044	0.152246	intron-variant	KCTD17	GRCh38.p7	22:37052192	GCTCTCCAGCCGCCC[C/T]GGATCGGGGCCTCTC	79734
rs76442271	snp	A/G	0.000339006	0.0130149	missense, nc-transcript-variant	KCTD17	GRCh38.p7	22:37056352	GAGTTCTACAACATC[A/G]GCCCGCTGATCCGCA	79734
rs76498710	snp	G/T	0.0471551	0.14613	intron-variant	KCTD17	GRCh38.p7	22:37052370	TGGAGGAGCCCTGGG[G/T]CGCCTTCTGAGCGGG	79734
rs76664375	snp	A/G	0.00159617	0.0282053	intron-variant	KCTD17	GRCh38.p7	22:37054060	ATCCTGCACCTGTGC[A/G]TGCCTTCCTGCTCTG	79734
rs76833367	in-del	-/T	0.448452	0.152042	intron-variant	KCTD17	GRCh38.p7	22:37058506	GTGTCATGCAAATCA[-/T]TAGAAATCCATATTG	79734
rs77519495	snp	A/G	0.0185938	0.0946107	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37051520	TTTTCCCAGAGGCCG[A/G]GAGTTCGACCTTCCC	79734
rs77644444	snp	C/T	0.00119737	0.0244387	intron-variant	KCTD17	GRCh38.p7	22:37055110	TCGCCCGCCCCTTCT[C/T]GAGAGCTTGTTTGGA	79734
rs77673159	snp	A/G	0	0	intron-variant	KCTD17	GRCh38.p7	22:37059605	CCCATGCCACCTGCC[A/G]TTACCCAGGCCCAGG	79734
rs78029853	snp	C/T	0.0130921	0.0798413	intron-variant	KCTD17	GRCh38.p7	22:37059834	AGGATCACATACTCT[C/T]TGTAGTGCCTTGGAG	79734
rs78329095	snp	C/T	0.00546817	0.0520018	intron-variant	KCTD17	GRCh38.p7	22:37052612	CAAGTCGCCTCACCT[C/T]TCAATGTCTCCGATC	79734
rs78379299	snp	G/T			splice-donor-variant	KCTD17	GRCh38.p7	22:37053210	CATGGCTGAGGAGGG[G/T]GAGTTGGTCCAGGGG	79734
rs78578257	snp	A/G	0.0185938	0.0946107	intron-variant	KCTD17	GRCh38.p7	22:37053355	CGGGGCTGATTCCCA[A/G]GCATCTGCCTGTGCC	79734
rs79517127	snp	C/T	0.0279526	0.114869	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37051414	GAAAGTTTCTTCCCT[C/T]ATCAGCTGTTGGACG	79734
rs79570630	snp	A/G	0.000798403	0.0199641	intron-variant	KCTD17	GRCh38.p7	22:37055872	TTTCCCAGTTGTTCA[A/G]TGCAGATGATGAAAG	79734
rs79695422	snp	A/G	0.00716266	0.059414	intron-variant	KCTD17	GRCh38.p7	22:37057316	GGGTATGTTGCGGGG[A/G]TGGTGGCAGCAGGTG	79734
rs79883813	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	KCTD17	GRCh38.p7	22:37062759	CAAGGTGGGCCCCAG[A/G]ACCTCTGGGCAGAGT	79734
rs80086725	snp	A/G	0.0283406	0.115616	intron-variant	KCTD17	GRCh38.p7	22:37054800	CTGGGGATAATTCTC[A/G]TAATCAGGCAGCTGC	79734
rs80165807	snp	C/G	0.0298908	0.118541	upstream-variant-2KB	KCTD17	GRCh38.p7	22:37049764	CTTCCTGAGTAGCTG[C/G]AACTACAGGCGTGAG	79734
rs80271594	snp	C/G	0.00517822	0.0506191	intron-variant	KCTD17	GRCh38.p7	22:37059590	GCCACCGCCATCCAT[C/G]CCATGCCACCTGCCG	79734
rs111412516	snp	C/T	0.00527187	0.05107	intron-variant	KCTD17	GRCh38.p7	22:37059466	GCCTCAGCCTGTGTC[C/T]GGAGAAGTCTCCTGT	79734
rs111459900	snp	A/G	0.0256215	0.110247	intron-variant	KCTD17	GRCh38.p7	22:37057799	GAGTCTGTGGCCCCC[A/G]AAGGACAGCTCAGGT	79734
rs111518907	snp	A/G	0.0115144	0.0749975	intron-variant, missense, nc-transcript-variant	KCTD17	GRCh38.p7	22:37061467	CCGGGCACCTCTGAG[A/G]CTGGGCCCTGGCTGC	79734
rs111538548	snp	A/C	0.5	0	intron-variant	KCTD17	GRCh38.p7	22:37053092	CCGAGCATCCCTCAC[A/C]TCCATAGGATGAGAC	79734
rs111672049	snp	C/G	0.0150606	0.0854603	intron-variant	KCTD17	GRCh38.p7	22:37054650	ATCTGTGAAATGGGG[C/G]ACCATAGCACCCACC	79734
rs111832378	snp	A/G	0.0150606	0.0854603	intron-variant, utr-variant-3-prime	KCTD17	GRCh38.p7	22:37061895	GTCCCTGCACATCCA[A/G]GAGCTCCTGTGTCAC	79734
rs112009022	snp	C/T	0.0150606	0.0854603	intron-variant	KCTD17	GRCh38.p7	22:37053295	TTTGGACAACCAGGA[C/T]GGCCATCTGCCTGCT	79734
rs112030530	snp	A/G	0.00398564	0.0444627	intron-variant	KCTD17	GRCh38.p7	22:37057880	CCTCTTAGAACTCAG[A/G]GTCAGCATCATGCGA	79734
rs112058074	snp	C/T	0.0249893	0.10895	intron-variant	KCTD17	GRCh38.p7	22:37052654	TCGCATGGAAGCCCA[C/T]CCTGCCTCCCTGCCC	79734
rs112358168	snp	A/G	0.5	0	intron-variant	KCTD17	GRCh38.p7	22:37055563	GAGCCTAGGGGAGTC[A/G]AAACAGCTGCAAGCT	79734
rs112587587	snp	C/G			missense, nc-transcript-variant	KCTD17	GRCh38.p7	22:37051752	AGGATGCAGACGCCG[C/G]GGCCGGCGATGAGGA	79734
rs113014472	snp	A/C	0.5	0	intron-variant	KCTD17	GRCh38.p7	22:37057003	ATTAAAGAGGGGAGG[A/C]TCCGTGTCTCCTTGA	79734
rs113075613	snp	A/G	0	0	intron-variant	KCTD17	GRCh38.p7	22:37060561	TCATCCCCTCCCTCC[A/G]GCCTCGCTCTATGTA	79734
rs113412072	in-del	-/G	0	0	intron-variant	KCTD17	GRCh38.p7	22:37061009	GCTGCAGAACCGGGG[-/G]CCCCGGGGCTGCTGG	79734

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