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
rs3694209	snp	C/T	0.277778	0.248452	intron-variant	Kctd5	Mm_Celera	17:24055236	CCCCGGGCCTTACCA[C/T]GGTCACTGCGACCTT	69259
rs3708585	snp	C/T	0.33241	0.236027	intron-variant	Kctd5	Mm_Celera	17:24055383	GTACACTGTGGGACA[C/T]GTGCAGCTGTTGGGG	69259
rs6161355	snp	C/T	0.336735	0.234472	intron-variant	Kctd5	Mm_Celera	17:24049728	GAGAGCCCAGACTTG[C/T]TTGGCACAGAGTTCA	69259
rs6198823	snp	A/T	0.5	0	intron-variant	Kctd5	GRCm38.p3	17:24052088	cttacatataataaa[A/T]aaaaaaaaaaaaaaa	69259
rs6227999	snp	A/C	0.5	0	intron-variant	Kctd5	GRCm38.p3	17:24059437	AGCAGGTACGCCCCT[A/C]GTCCCCACACCCTGC	69259
rs6229135	snp	A/G	0.471655	0.115624	intron-variant	Kctd5	GRCm38.p3	17:24059638	TGGGAGATAACTGAC[A/G]CATTTTTTTCTGCAG	69259
rs6229227	snp	C/T	0.30839	0.243086	intron-variant	Kctd5	Mm_Celera	17:24059687	GTGCTACTGGCTCTT[C/T]CTGTTGAGAACTGGA	69259
rs6250471	snp	A/G	0.345679	0.230967	intron-variant	Kctd5	Mm_Celera	17:24054678	GGAATGTCCTTCTAT[A/G]ATTAGTTCAGAGGCT	69259
rs6250977	snp	C/T	0.444444	0.157135	intron-variant	Kctd5	Mm_Celera	17:24054766	TACTGATGCTCTGCC[C/T]CCCAAACCTGCTGCT	69259
rs6251359	snp	C/G	0.48	0.0979796	intron-variant	Kctd5	Mm_Celera	17:24054801	CTGAAACTTGCACAT[C/G]TCATGACATGCTGTG	69259
rs6251880	snp	A/G	0.336735	0.234472	intron-variant	Kctd5	Mm_Celera	17:24054931	GTACTGTATCAGCCA[A/G]TGGCAAAGATACCTG	69259
rs6252409	snp	C/G	0.5	0	intron-variant	Kctd5	GRCm38.p3	17:24055036	GAACTCTGTGCCCCC[C/G]ACCCCTGCACCCCCG	69259
rs13462160	snp	C/T			intron-variant, utr-variant-3-prime, upstream-variant-2KB	Pdpk1, Kctd5	Mm_Celera	17:24075032	GCACAGTGGCTAGGC[C/T]TTGTCATTGCCAAGG	69259
rs13464253	snp	A/G	0.408163	0.193609	utr-variant-3-prime	Kctd5, Prss27	GRCm38.p3	17:24047931	CATTGCTTCATTTAT[A/G]ACTTTGACAATAGAT	69259
rs13464254	snp	C/T	0.375	0.216506	utr-variant-3-prime	Kctd5	GRCm38.p3	17:24049206	CAGCTAGGGCTGGGT[C/T]GGCAGTCTCTGGTCT	69259
rs13464255	snp	C/G	0.375	0.216506	utr-variant-3-prime	Kctd5	Mm_Celera	17:24048994	TGGGGGTGGGTGCCT[C/G]CTCATCACTGACTGA	69259
rs13464256	snp	C/T	0.487535	0.077957	utr-variant-3-prime	Kctd5, Prss27	GRCm38.p3	17:24047791	ATTTTATCAGCTTAC[C/T]GTTTAATGCCTAAGT	69259
rs13464257	snp	A/G			utr-variant-3-prime	Kctd5	GRCm38.p3	17:24048904	ATTTCTCTCGACCTC[A/G]GCTGAGGCTCCTGAC	69259
rs29498816	snp	A/G	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24066757	CTCACTCTCCTCGTG[A/G]AACCCATGCTGCCCT	69259
rs29503029	snp	C/T	0.265928	0.249492	intron-variant	Kctd5	Mm_Celera	17:24063704	TGGAAAGTAAAGCTG[C/T]GGCACAAGGTGAGGC	69259
rs29521745	snp	A/G	0.33241	0.236027	intron-variant	Kctd5	Mm_Celera	17:24068432	CAGCTCTGCAAAGGA[A/G]CCACTGAGGCTGCAC	69259
rs29535208	snp	C/T	0.197531	0.244432	intron-variant	Kctd5	Mm_Celera	17:24063361	ATCCTGTGCTTGGAG[C/T]CCAGTGCCCTGTTTG	69259
rs29539034	snp	C/T	0.375	0.216506	intron-variant	Kctd5	GRCm38.p3	17:24064550	ATACAATTGATCAGC[C/T]GTCAACTTGACACAC	69259
rs33051054	snp	A/G	0.444444	0.157135	intron-variant	Kctd5	Mm_Celera	17:24066627	CACCAATTGCAATGG[A/G]GAAACTGAGGCTCAG	69259
rs33065722	snp	C/G	0.265928	0.249492	intron-variant	Kctd5	Mm_Celera	17:24061773	TCCAGGAAAAGGAAA[C/G]GACTCCATAAATCAG	69259
rs33065907	snp	A/G	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24058637	GGAGACAATGGGAGG[A/G]CTTTAAGTGGACCAA	69259
rs33081206	snp	A/G	0.32	0.24	intron-variant	Kctd5	Mm_Celera	17:24057027	CTCTGTATCCCCACC[A/G]GGCAGCTCTAGTTTG	69259
rs33092140	snp	A/G	0.401235	0.199068	intron-variant	Kctd5	GRCm38.p3	17:24061224	CATATGTAGAACACC[A/G]CATGCACCTGCCTGC	69259
rs33108076	snp	C/T	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24072138	AGTAGTATCTCAAAC[C/T]CTAACTTCTTGATTA	69259
rs33112328	snp	C/T	0.432133	0.171253	intron-variant	Kctd5	GRCm38.p3	17:24059783	CCTGCCCAGAGTCAC[C/T]CCTGGCTCCAGGGCT	69259
rs33116894	snp	A/G	0.32	0.24	intron-variant	Kctd5	Mm_Celera	17:24050908	CTCTTAGGAAGTCTG[A/G]GGCTCGAGAAGACGC	69259
rs33120677	snp	C/T	0.304688	0.243945	intron-variant	Kctd5	Mm_Celera	17:24069208	CCATCCCTTAGTCTA[C/T]AATATTCCTTTCATA	69259
rs33120973	snp	G/T	0.444444	0.157135	intron-variant	Kctd5	Mm_Celera	17:24069127	AACAGCTGCCATTTA[G/T]ACTCTAAGTAATCCC	69259
rs33125066	snp	C/T	0.265928	0.249492	intron-variant	Kctd5	Mm_Celera	17:24065013	CCACCATGATACACA[C/T]GGCATTGCAGGCTGT	69259
rs33128835	snp	A/G	0.345679	0.230967	intron-variant	Kctd5	Mm_Celera	17:24068936	TGCAAAGAGGGTGAG[A/G]GCACAATATCAGGAT	69259
rs33141894	snp	A/G	0.46875	0.121031	intron-variant	Kctd5	GRCm38.p3	17:24056152	AGCTCAGGGAAATGA[A/G]AGCTAGCTTTAGCCA	69259
rs33145836	snp	C/T	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24072224	GAGAAGGTGCTCTGT[C/T]AGGCCGTTTAAAGTG	69259
rs33158059	snp	A/G	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24051618	AGGAACTGGTTCCAC[A/G]CTTACATGGGTTCTG	69259
rs33164343	snp	C/T	0.255	0.24995	intron-variant	Kctd5	Mm_Celera	17:24057126	GGACCCCTGAAAGTT[C/T]GTCAACTCAGCGCTA	69259
rs33180384	snp	C/T	0.444444	0.157135	intron-variant	Kctd5	Mm_Celera	17:24069117	ATGTAGTTACAACAG[C/T]TGCCATTTAGACTCT	69259
rs33185969	snp	A/G	0.375	0.216506	utr-variant-3-prime, downstream-variant-500B	Kctd5, Prss27	Mm_Celera	17:24048541	GTGGACAGGCCTCCC[A/G]CCCCAGCCTCTATCC	69259
rs33197206	snp	C/T	0.277778	0.248452	intron-variant	Kctd5	Mm_Celera	17:24052424	TCCTCTCAGGCAATG[C/T]TCATGCTCCTCAGGA	69259
rs33233478	snp	C/T	0.46281	0.131194	intron-variant	Kctd5	Mm_Celera	17:24068471	GGGAAGAGTGCATGC[C/T]GTCCTCTCCCAAGCC	69259
rs33252024	snp	C/T	0.255	0.24995	intron-variant	Kctd5	Mm_Celera	17:24061627	AAAGGGTGAGGCTTC[C/T]ACCACCAATGCAGCC	69259
rs33306688	snp	C/G			intron-variant	Kctd5	GRCm38.p3	17:24067694	CACTGAACTAACTCT[C/G]TCTCTCTCTCTCTCT	69259
rs33327096	snp	C/T	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24052703	AGGTGTGTGCCAACA[C/T]GCCCGGCCTAAGAAG	69259
rs33345859	snp	A/G	0.401235	0.199068	intron-variant	Kctd5	GRCm38.p3	17:24056768	TCAAGGGAAACCACC[A/G]AGGCCATAGCAAGGA	69259
rs33348735	snp	G/T	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24052456	CGTCTTACCCCCACC[G/T]ACCCACTGGCCAGGG	69259
rs33353657	snp	A/G	0.33241	0.236027	intron-variant	Kctd5	Mm_Celera	17:24068561	TTATTGTTTTCTTCA[A/G]TCCTGAATGTCCAGA	69259
rs33371298	snp	G/T	0.304688	0.243945	intron-variant	Kctd5	Mm_Celera	17:24050534	GACACACGGAGGTAG[G/T]AACTCTAGGTGTCAC	69259
rs33372134	snp	C/T	0.375	0.216506	intron-variant, utr-variant-3-prime, upstream-variant-2KB	Pdpk1, Kctd5	Mm_Celera	17:24075180	CTGATTCCCAAATGG[C/T]CCAAATGCATTTCTG	69259
rs33381902	snp	A/G	0.277778	0.248452	intron-variant	Kctd5	Mm_Celera	17:24066256	GAAGATGCAGGTGGA[A/G]TGTCATGGAAGGTCT	69259
rs33417662	snp	A/G	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24053380	CTGTCAGCCCAGCCT[A/G]AGCAGTGCAGGCCTG	69259
rs33438008	snp	A/T	0.375	0.216506	intron-variant	Kctd5	GRCm38.p3	17:24062709	GTCTTCATGAATACT[A/T]AGGTAGTGAGGGGGG	69259
rs33446618	snp	C/T	0.345679	0.230967	intron-variant	Kctd5	Mm_Celera	17:24069314	ATAGTAAAACACTTT[C/T]CAAAGACCCACCTGG	69259
rs33449575	snp	A/C	0.475309	0.108333	intron-variant	Kctd5	Mm_Celera	17:24050189	CAGGCAGGACGCTTC[A/C]GAGCTGAGGGAACCC	69259
rs33456261	snp	C/T	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24063731	AGGCAGTGTGGCCTA[C/T]ACTGTGCTATGTCAG	69259
rs33456820	snp	C/T	0.32	0.24	intron-variant	Kctd5	Mm_Celera	17:24055588	GTGCAGCCGAGGCAG[C/T]TGCTGTGCTGAGGAG	69259
rs33468260	snp	G/T	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24050056	GGCCTCTTTAAACCA[G/T]GCTGGGGCTGGGGCT	69259
rs33468309	snp	C/T	0.444444	0.157135	intron-variant	Kctd5	Mm_Celera	17:24054509	CACAACCATCCATAA[C/T]GAAATCTGACTCCCT	69259
rs33469877	snp	A/G	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24064180	AGGTTAAGAGCATTC[A/G]CTGCTCTTGTGGAGG	69259
rs33470713	snp	G/T	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24058474	CCAGTTGAGGGGGAT[G/T]GGGAATCTTAGAACC	69259
rs33478130	snp	C/T	0.359862	0.224567	intron-variant	Kctd5	Mm_Celera	17:24062543	GCTCAGGAATACTCA[C/T]AGCACAATGCCCCCT	69259
rs33478839	snp	C/T	0.444444	0.157135	intron-variant	Kctd5	GRCm38.p3	17:24071414	TGCTTCATGTGGGTG[C/T]TGAATATTGAACCCT	69259
rs33527786	snp	A/C	0.33241	0.236027	intron-variant	Kctd5	Mm_Celera	17:24065626	AGACTGCTTTCTCCA[A/C]AATCATTTGCCTCTA	69259
rs33566405	snp	A/G	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24067738	TTGTTTGTTTGTTTC[A/G]AGACAGGGTTTATCT	69259
rs33568641	snp	A/G	0.32	0.24	intron-variant	Kctd5	Mm_Celera	17:24066754	CATCTCACTCTCCTC[A/G]TGGAACCCATGCTGC	69259
rs33576121	snp	C/T	0.401235	0.199068	intron-variant	Kctd5	Mm_Celera	17:24069166	TTGCCAAGCCACTGA[C/T]TCAAAGACAGTTTCC	69259
rs33581905	snp	C/T	0.265928	0.249492	intron-variant	Kctd5	Mm_Celera	17:24068305	AAGGCCTAATGAGAG[C/T]CAGCTTGCGCCTAAA	69259
rs33598827	snp	A/T	0.290657	0.246672	intron-variant	Kctd5	Mm_Celera	17:24055835	AGTTTAAAGGGAACA[A/T]CAAAAATCAGTGAAG	69259
rs33605375	snp	C/T	0.32	0.24	intron-variant	Kctd5	Mm_Celera	17:24061822	CTGGCCAGAACACTG[C/T]CAGGGCTCCTGTAGA	69259
rs33625702	snp	C/T	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24064024	AGGGGGGAACAAAAA[C/T]AAAAAAACCCAACCA	69259
rs33629709	snp	C/T	0.32	0.24	intron-variant	Kctd5	Mm_Celera	17:24058911	TGCTCTCCTCTCTGC[C/T]GTGCTGGCCATGGGC	69259
rs33651489	snp	C/T	0.265928	0.249492	intron-variant	Kctd5	Mm_Celera	17:24067527	CTCCATTCTGGCTAA[C/T]AGGTCAGCAGTTCAG	69259
rs33651670	snp	C/T	0.375	0.216506	intron-variant	Kctd5	GRCm38.p3	17:24071972	TCGTAAAGTACACAC[C/T]CTCACTATAAAAAGG	69259
rs33678408	snp	A/G	0.375	0.216506	intron-variant	Kctd5	Mm_Celera	17:24064491	CTACGCAGAGAAACC[A/G]TGTACTGAAAAAACA	69259
rs33689120	snp	C/T	0.265928	0.249492	intron-variant	Kctd5	Mm_Celera	17:24065160	CCAGGAAACGCAAAT[C/T]CAAATACAAGGCTTC	69259
rs45646683	snp	C/T			intron-variant	Kctd5	GRCm38.p3	17:24070498	GTAACACCAGTAACA[C/T]AGCTAATATGAATTA	69259
rs45704870	snp	A/G	0.231111	0.249285	intron-variant	Kctd5	GRCm38.p3	17:24070392	TATCAAGGTGGAATC[A/G]CTTGGGACACTCTTT	69259
rs45822011	snp	C/T	0.124444	0.216185	intron-variant	Kctd5	Mm_Celera	17:24060024	AGAGTCAGGCAATGA[C/T]GGATGAAAAGCTGCC	69259
rs45889775	snp	C/G	0.244898	0.249948	intron-variant	Kctd5	GRCm38.p3	17:24062673	CAGAGTCCAGTCTCC[C/G]CTGGCAACAAGAAGC	69259
rs46067843	snp	C/T	0.244898	0.249948	intron-variant	Kctd5	GRCm38.p3	17:24057406	ACAGATCTAGAAGGG[C/T]GACAGCTGCTTTCCG	69259
rs46102579	snp	C/G			intron-variant, downstream-variant-500B, upstream-variant-2KB	Pdpk1, Kctd5	Mm_Celera	17:24073659	CCGCCCCTACTCAAA[C/G]AGGCTCCATGGCAAA	69259
rs46183874	snp	C/T			intron-variant	Kctd5	GRCm38.p3	17:24069881	TGGGCTTTGAGGACA[C/T]GGGCCACAGGTACAG	69259
rs46248477	snp	C/T	0.231111	0.249285	intron-variant	Kctd5	GRCm38.p3	17:24065757	ACATTACATGAGAGC[C/T]GACTCTCCCACACAT	69259
rs46407647	snp	C/T			intron-variant, downstream-variant-500B, upstream-variant-2KB	Pdpk1, Kctd5	Mm_Celera	17:24073643	ATCCTCGGCTCAAGC[C/T]CCGCCCCTACTCAAA	69259
rs46465909	snp	C/T			intron-variant	Kctd5	Mm_Celera	17:24064454	GCCAGGCTAGTCTAT[C/T]GAGTTCCAGGGACAG	69259
rs46584509	snp	A/G			intron-variant	Kctd5	Mm_Celera	17:24051433	GTGAAGCCCTGGCTC[A/G]CCTGCAACTTACATA	69259
rs46641141	snp	C/T	0.244898	0.249948	intron-variant	Kctd5	GRCm38.p3	17:24050217	CCCCACAGGTAGCCA[C/T]GCCATAGCAGCTGTC	69259
rs46806047	snp	A/G			intron-variant	Kctd5	GRCm38.p3	17:24059157	TCCAAGGTCACACAC[A/G]GAGAAGCCACACCTG	69259
rs46947820	snp	A/G	0.124444	0.216185	intron-variant	Kctd5	Mm_Celera	17:24066476	AATCAACCTACTGAT[A/G]AATGCTTAGATTTTA	69259
rs46973542	snp	A/G	0.124444	0.216185	utr-variant-3-prime, downstream-variant-500B	Kctd5, Prss27	Mm_Celera	17:24048807	CTGGGCCAAGCTGAC[A/G]GGCCAGAACAAGAGC	69259
rs47021364	snp	A/G	0.244898	0.249948	downstream-variant-500B, utr-variant-3-prime	Kctd5, Prss27	Mm_Celera	17:24047372	GACATGCCATATTCT[A/G]GGCCATGAGGCAGGT	69259
rs47317179	snp	A/G	0.124444	0.216185	intron-variant	Kctd5	Mm_Celera	17:24066160	AGTCCTTTAGGGCAC[A/G]ATCCTAACGCAGCAT	69259
rs47480185	snp	A/C	0.124444	0.216185	utr-variant-3-prime	Kctd5, Prss27	GRCm38.p3	17:24048005	CAGAGCTACTGCCCC[A/C]GAGTGATTAAGCCAC	69259
rs47612114	snp	A/G	0.124444	0.216185	intron-variant	Kctd5	Mm_Celera	17:24067537	GCTAACAGGTCAGCA[A/G]TTCAGGCATTCTGGC	69259
rs47840882	snp	C/T	0.32	0.24	downstream-variant-500B, utr-variant-3-prime	Kctd5, Prss27	Mm_Celera	17:24047410	AGAGACCTCTCAGAG[C/T]GGGATCCAGACCCTT	69259
rs47972264	snp	C/T	0.231111	0.249285	intron-variant	Kctd5	GRCm38.p3	17:24061860	CACGGGAAAGAGTTG[C/T]ACTCACTGCCCCGTG	69259
rs47999203	snp	C/T			intron-variant	Kctd5	GRCm38.p3	17:24059187	GCTTATACAGCAAGC[C/T]CAGAAGCTACAGGCA	69259
rs48062697	snp	A/G	0.231111	0.249285	intron-variant	Kctd5	GRCm38.p3	17:24060169	CTCCTTCGGCAACGC[A/G]GGCACCTTCGAGTAA	69259

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