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
rs4230425	snp	G/T	0.59256	0.192248	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67742051	GGTCCTCTGCAGACA[G/T]ATCTGAGGCTGCAGA	105440
rs4230426	snp	A/G	0.226843	0.248925	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Kctd9	Mm_Celera	14:67742190	TCTTGCTTTTCTAAG[A/G]CAGCACTTTCTGCAT	105440
rs6155147	snp	C/T	0.359862	0.224567	intron-variant	Kctd9	Mm_Celera	14:67737443	GTAGCTCTTCCAAAA[C/T]TTCTTAGCTCTTTCT	105440
rs6157245	snp	C/G	0.21875	0.248039	intron-variant	Kctd9	Mm_Celera	14:67737785	GGTGAAACAGGAAGG[C/G]TCTGGGCAGAGCATA	105440
rs6212285	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Cdca2, Kctd9	Mm_Celera	14:67714235	AATGAGTGTCACTCT[A/G]GCTTCGCCTAGCTCA	105440
rs30123573	snp	C/T	0.444444	0.157135	intron-variant	Kctd9	Mm_Celera	14:67719467	ACAATTAAATAAATA[C/T]ACAATTGATTGACCT	105440
rs30217442	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67724168	AGGAAGAGTCCCAAG[A/G]GTATGCACAAGAGTC	105440
rs30244786	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67724221	TTAGGAGGCCCACAA[A/G]CCCACCAAGCTACAG	105440
rs30291794	snp	C/T	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67725184	CAGGTAGAGACCACA[C/T]CAGCAGTGTGTGCTC	105440
rs30332365	snp	G/T	0.444444	0.157135	intron-variant	Kctd9	Mm_Celera	14:67735917	TAAAGTGTGTGTGTG[G/T]GGGGGGGTATTTTTT	105440
rs30361920	snp	C/T	0.444444	0.157135	intron-variant	Kctd9	Mm_Celera	14:67724044	CTCCTCCCAGCTGTC[C/T]CCACCTTTCCCTTCC	105440
rs30386925	snp	A/C	0.375	0.216506	intron-variant	Kctd9	Mm_Celera	14:67726851	GAAAAGACCTAATAC[A/C]TAAGTAGGCAACTAT	105440
rs30441424	snp	C/G	0.375	0.216506	intron-variant	Kctd9	Mm_Celera	14:67721156	ATCAGTTTTGAGTCT[C/G]ACCATTGTCTGGTAC	105440
rs30578499	snp	C/T	0.345679	0.230967	intron-variant	Kctd9	Mm_Celera	14:67738620	TCCACCTAACATGGC[C/T]GGGCAGCTGGAAGGC	105440
rs30619076	snp	C/G	0.375	0.216506	intron-variant	Kctd9	Mm_Celera	14:67719860	GACACAGTAGGCAAG[C/G]AAATACCTGTGTTCT	105440
rs30891204	snp	A/C	0.375	0.216506	intron-variant	Kctd9	Mm_Celera	14:67730192	GTCTCTCAAACAGTA[A/C]CACCAGATATGGGAC	105440
rs30898073	snp	A/G	0.33241	0.236027	intron-variant	Kctd9	Mm_Celera	14:67725380	TAGTCGTTTTCAACA[A/G]GTAGACCAAGATCTG	105440
rs30949979	snp	A/T	0.375	0.216506	intron-variant	Kctd9	Mm_Celera	14:67728115	GTACATCAGTCATGT[A/T]CTGACTGTCCCTCCT	105440
rs30980712	snp	C/T	0.375	0.216506	intron-variant	Kctd9	Mm_Celera	14:67723437	GGCAGTAACCCTCAC[C/T]TTGTTAGTTACTACA	105440
rs31153361	snp	A/G	0.375	0.216506	intron-variant	Kctd9	Mm_Celera	14:67725496	ATTAACTAGCAAACT[A/G]AGCAGGTAGAAAATA	105440
rs31162848	snp	A/T	0.142012	0.225474	downstream-variant-500B	Kctd9	Mm_Celera	14:67742669	AAGTCATTATTATGA[A/T]GGATTCCATTATTAA	105440
rs31162850	snp	G/T	0.244898	0.249948	downstream-variant-500B	Kctd9	Mm_Celera	14:67742490	GAGGAAGGTTCCAAA[G/T]AGAAAGGCTTGGCGT	105440
rs31162852	snp	A/G	0.124444	0.216185	downstream-variant-500B	Kctd9	Mm_Celera	14:67742379	TTTCTGCACTAGGGA[A/G]GACACCCAGTGATTT	105440
rs31162854	snp	C/T	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67733908	AAGCAGTTCACCTGT[C/T]AGTGTAGTGTAGCCA	105440
rs31162856	snp	A/G	0.42	0.183303	intron-variant	Kctd9	Mm_Celera	14:67733654	AATTGTGCTTTATGT[A/G]GCGGTTCTTGAGTAA	105440
rs31162858	snp	G/T	0.124444	0.216185	intron-variant	Kctd9	GRCm38.p3	14:67733547	TTATTTCTCTTTGTT[G/T]AATGTAAGATACAAT	105440
rs31162859	snp	A/G	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67733151	AAAGTCATGCTTTGT[A/G]TTTTGATAGGTGTGC	105440
rs31162860	snp	C/T	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67733092	ATTGTGAGGGTTTAA[C/T]GGAAAAAAAATTATA	105440
rs31162862	snp	A/T	0.244898	0.249948	intron-variant	Kctd9	Mm_Celera	14:67732747	TGCTTGTTGCCACTG[A/T]CCAAGCCTAGGGAGA	105440
rs31163765	snp	A/G	0.124444	0.216185	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Kctd9	Mm_Celera	14:67742162	GTGTGGAACGCTGAC[A/G]GCCTGTTTCTGCTCT	105440
rs31163767	snp	A/G	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67742107	GTGTGTGGGAACTGC[A/G]GGGTTCAGAGCTGAT	105440
rs31163770	snp	G/T	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67741645	TCCCAGTGTCCTTAT[G/T]TGTTGCCCAAAAGCA	105440
rs31163772	snp	A/G	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67741467	ACAAAGGAAGCATTT[A/G]GCTAGGACACGATGC	105440
rs31163884	snp	A/G	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67732335	CTGTTCACTCCATTA[A/G]TAAAGTAGATGAATT	105440
rs31163886	snp	A/G	0.142012	0.225474	intron-variant	Kctd9	Mm_Celera	14:67732259	TTGTGAATTTACTTC[A/G]ATATTACTCATTTTC	105440
rs31163888	snp	A/G	0.244898	0.249948	intron-variant	Kctd9	Mm_Celera	14:67732062	TTTTGTAATTCCTAA[A/G]TCAGTTTAGCAACCA	105440
rs31163890	snp	C/G	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67731917	TGCACCACTCTGAGC[C/G]TTGCTTCTCAGTTGG	105440
rs31163892	snp	C/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67731791	GTTGATACTTACACT[C/G]CCTCTTGGGAGGGAT	105440
rs31164714	snp	A/T	0.336735	0.234472	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67741393	GCTGAAACCCTGCAG[A/T]GGGGACTAAGAAATT	105440
rs31164716	snp	A/C	0.231111	0.249285	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67741171	CTACTCTTTCCCTTC[A/C]CTCGTCCAGTTCTCA	105440
rs31164718	snp	A/G	0.231111	0.249285	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67741079	GCAGGAGAAGGAAGG[A/G]CTCACCAGTACTGCA	105440
rs31164720	snp	C/G	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67741058	AAAGCTCTTGTGTAT[C/G]CTTGTGCAGGAGAAG	105440
rs31164722	snp	A/G	0.132653	0.220748	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67740993	TTAAAGAAGAAAACA[A/G]CTAAATTTGAGTCAT	105440
rs31164754	snp	C/T	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67731761	AAAGTCTCTTTATTC[C/T]GGGTTTCTTTTGGGG	105440
rs31164756	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67731682	TAGAAAAGCAGCCAT[A/G]CCACATTCCCCAAGA	105440
rs31164758	snp	A/G	0.142012	0.225474	intron-variant	Kctd9	Mm_Celera	14:67729969	CTTATTATTATTTGA[A/G]TAGTGAGGTCACAAG	105440
rs31164760	snp	A/G	0.132653	0.220748	intron-variant	Kctd9	Mm_Celera	14:67729967	GACTTATTATTATTT[A/G]AATAGTGAGGTCACA	105440
rs31164761	snp	A/G	0.231111	0.249285	intron-variant, utr-variant-5-prime	Kctd9	Mm_Celera	14:67729307	TAAATATGTTTGTTT[A/G]TAAAGACACATGAAG	105440
rs31164763	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67728395	TTTTTGGGTATTGTA[A/G]GTAAGTTATTTCACT	105440
rs31165374	snp	C/T	0.32	0.24	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67740950	CTCCCTGTGGCTCTT[C/T]TGAGATTCATTTCTA	105440
rs31165376	snp	A/G	0.32	0.24	utr-variant-3-prime, nc-transcript-variant	Kctd9	Mm_Celera	14:67740726	GCATTGTGTGGAAGT[A/G]CCATCTTGGTTCAAG	105440
rs31165378	snp	A/G	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67739521	GTTATGTTAAACAAT[A/G]TGACATGGCACAGAT	105440
rs31165380	snp	A/C	0.260355	0.249785	intron-variant	Kctd9	Mm_Celera	14:67739144	CTATTATTTTTTATA[A/C]GACCTGTATTCTATG	105440
rs31165382	snp	C/T	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67738947	TTTTCTTGGGTCTTT[C/T]TCAAGCATATTGCAA	105440
rs31165735	snp	C/T	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67728245	TCTGGCATCTTGCAA[C/T]CTAGACAGTTTGTCT	105440
rs31165737	snp	C/T	0.35503	0.226867	intron-variant	Kctd9	Mm_Celera	14:67727995	CTTCAGAGGAACAAT[C/T]AATATTTCAATACTA	105440
rs31165739	snp	A/G	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67727704	ACTAGAGTTGGAGAT[A/G]TATAAGTAGCTAGAG	105440
rs31165741	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67727523	GGTCAGTGGAAACCT[A/G]CTCGTTTTTAACTCA	105440
rs31165743	snp	A/G	0.132653	0.220748	intron-variant	Kctd9	Mm_Celera	14:67726661	GAAATAATTTTCTTT[A/G]AAAGCAATGGCTAGC	105440
rs31166234	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67738843	ATTACACCTAGATAG[A/G]CCACTGTTACCTAAG	105440
rs31166236	snp	A/G	0.244898	0.249948	intron-variant	Kctd9	Mm_Celera	14:67738795	TAAGGGGAGTCCCTC[A/G]CTGTTGAATGATTTT	105440
rs31166239	snp	C/T	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67738365	ACTCCTTCAAAAACA[C/T]GCTTCTTGCAGGTGC	105440
rs31166241	snp	A/C	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67738343	AACTATAAAGTTTTC[A/C]GGTTAAACTCCTTCA	105440
rs31166243	snp	A/G	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67737999	TTAATCCTGTTAACC[A/G]TGTTTTGTCAGGTTT	105440
rs31166635	snp	A/G	0.244898	0.249948	intron-variant	Kctd9	Mm_Celera	14:67726634	GGACATGATAAGATA[A/G]TTTTGATTTTAGAAA	105440
rs31166637	snp	A/G	0.336735	0.234472	intron-variant	Kctd9	Mm_Celera	14:67726592	ACGTGCTTTTAAGAT[A/G]TCCTAGATATGTACG	105440
rs31166639	snp	A/G	0.244898	0.249948	intron-variant	Kctd9	Mm_Celera	14:67726471	TGAAAACATCATGAT[A/G]ACTAAACTCAGGTCT	105440
rs31166641	snp	A/G	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67726408	TCTTGCCACAGTAAC[A/G]AACATGAAACAGTAA	105440
rs31166643	snp	A/G	0.244898	0.249948	intron-variant	Kctd9	Mm_Celera	14:67726267	CAGCTCAGACGAGCC[A/G]TCAGTTAACAAGCGT	105440
rs31167115	snp	A/G	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67737858	TCATAGGCAGAGGCT[A/G]GGCTAGGCAACACCC	105440
rs31167118	snp	C/T	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67737553	TTCTTTCTTATTGCT[C/T]GCACAGATGTTATCA	105440
rs31167120	snp	C/T	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67737528	GTTGAATTGGACCTT[C/T]CCTATTAATTTCTTT	105440
rs31167123	snp	C/T	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67737402	ATGGACATACTGTTG[C/T]TATTTTGCTGTTTAT	105440
rs31167534	snp	G/T	0.244898	0.249948	intron-variant	Kctd9	Mm_Celera	14:67726177	TTAGACCTGGTCAGG[G/T]TTAAACAGAGCCCTG	105440
rs31167536	snp	A/C/G	0.32	0.24	intron-variant	Kctd9	GRCm38.p3	14:67726168	GTTTGATTTTTAGAC[A/C/G]TGGTCAGGTTTAAAC	105440
rs31167538	snp	A/T	0.244898	0.249948	intron-variant	Kctd9	Mm_Celera	14:67726088	TATGCCAAATTCATA[A/T]ATTTTGATAGTGAGT	105440
rs31167540	snp	A/G	0.244898	0.249948	intron-variant	Kctd9	Mm_Celera	14:67726056	TGAACATAAATTAGT[A/G]CATTCTTCAATTAAT	105440
rs31167542	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67725954	CTAAAGTGCCCAGCA[A/G]CTAATTATTTGAGAA	105440
rs31167799	snp	A/G	0.375	0.216506	intron-variant	Kctd9	Mm_Celera	14:67717906	GGATATGTAGTGTAT[A/G]CATAGTCCCTATATC	105440
rs31167935	snp	A/G	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67737182	ACTGGTGACATTAGT[A/G]TCCTGGCCTTTGAAG	105440
rs31167937	snp	C/G	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67737071	TGCTTTCTTCATTAT[C/G]CATTGTGCACAGGGT	105440
rs31167939	snp	A/G	0.124444	0.216185	intron-variant	Kctd9	Mm_Celera	14:67737002	GGCCTGGATGCACTG[A/G]GTCCCTTAAGAAGAC	105440
rs31167941	snp	A/G	0.132653	0.220748	intron-variant	Kctd9	Mm_Celera	14:67736641	CTTGGCAGACCTTCT[A/G]TGCCTCCTCATTAGG	105440
rs31167943	snp	G/T	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67735830	TAGTCTGACCTTATT[G/T]TATAGGCTGATAATC	105440
rs31168304	snp	A/G	0.142012	0.225474	intron-variant	Kctd9	Mm_Celera	14:67725855	AAGTGTGCTCATGGT[A/G]GATGGGTGGTGAGTA	105440
rs31168306	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67725775	TGAGTTACACTAATG[A/G]AGCAAGGGTGGTCAG	105440
rs31168308	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67725721	GATTGTATGAGGCTT[A/G]CACTGTGCTTTCTGG	105440
rs31168310	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67725400	ACCAAGATCTGAGAA[A/G]TGAGGGGTCTTACCC	105440
rs31168312	snp	A/T	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67725253	TACGTTTTTAATCTG[A/T]TGGTCTAAAGACTGT	105440
rs31168765	snp	A/C	0.124444	0.216185	intron-variant, downstream-variant-500B	Kctd9	Mm_Celera	14:67735544	TCCTATGGCTCCCAT[A/C]TTTTGCTGAGCTACT	105440
rs31168767	snp	A/G	0.124444	0.216185	intron-variant, downstream-variant-500B	Kctd9	Mm_Celera	14:67735477	TGATTAACAGCCATG[A/G]GTACTGCAGTGTCTA	105440
rs31168769	snp	A/G	0.152778	0.230321	intron-variant, downstream-variant-500B	Kctd9	Mm_Celera	14:67735437	AACTAATTTCTCATT[A/G]CCTTTGGTACAAGAA	105440
rs31168771	snp	C/T	0.231111	0.249285	intron-variant, downstream-variant-500B	Kctd9	Mm_Celera	14:67735385	AAAATTGGCTTATAT[C/T]GAGGACTATTGCTGA	105440
rs31168773	snp	A/C	0.132653	0.220748	intron-variant, downstream-variant-500B	Kctd9	Mm_Celera	14:67735342	ATGAAGTAAAATGGT[A/C]TAGGACTGTAAGTTA	105440
rs31169394	snp	A/G	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67725126	ATGAGACAGTTGTAG[A/G]ACAGGGAAGTAGCTG	105440
rs31169396	snp	A/G	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67725054	CTTTTTGGTTTTTCA[A/G]TGTCCCAGGTAGACT	105440
rs31169398	snp	A/G	0.142012	0.225474	intron-variant	Kctd9	Mm_Celera	14:67724970	TTACAAGGAACTGAT[A/G]CTAAATACTACAAAA	105440
rs31169399	snp	G/T	0.32	0.24	intron-variant	Kctd9	Mm_Celera	14:67724687	TTGATCAGGTAACCT[G/T]CCCTTTCTAAGGCTG	105440
rs31169401	snp	A/G	0.231111	0.249285	intron-variant	Kctd9	Mm_Celera	14:67723858	GTTGACTGATAGAAA[A/G]TGCTAATCTAAATTT	105440
rs31169403	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Cdca2, Kctd9	Mm_Celera	14:67714205	TCTTTTATGTGATAA[C/T]TCTGAGCGGTAGAGA	105440

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