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
rs6187395	snp	A/C/G	0.290657	0.246672	intron-variant	Katnb1	Mm_Celera	8:95085057	ATGCCCCTGGAGCCT[A/C/G]AGGGCAGGAAGCTCT	74187
rs6187503	snp	C/T	0.498615	0.0262793	intron-variant	Katnb1	GRCm38.p3	8:95085109	GGCCTAGAGCAGATG[C/T]CTAGAAGCCTCTTCT	74187
rs6187533	snp	C/T	0.21875	0.248039	intron-variant	Katnb1	Mm_Celera	8:95085132	CCTCTTCTGTTAGAC[C/T]GCCACAGCTGTCTCT	74187
rs6187950	snp	A/G	0.5	0	intron-variant	Katnb1	Mm_Celera	8:95085177	GGCCTGTTGAGATGG[A/G]GACTCAACCAGATCT	74187
rs6188512	snp	A/G	0.5	0	intron-variant	Katnb1	Mm_Celera	8:95085313	TTCCCCTCCTGCTGG[A/G]CTGGCCACATATAGA	74187
rs6188570	snp	C/T	0.5	0	intron-variant	Katnb1	Mm_Celera	8:95085340	TAGAAGGGTCTGTGG[C/T]CCAAGCTTGTGGGCA	74187
rs6188937	snp	C/T	0.489796	0.070696	intron-variant	Katnb1	GRCm38.p3	8:95085368	GCAGCTGTCCCCAAG[C/T]GTGCAGAGGACAAGA	74187
rs6188993	snp	A/G	0.290657	0.246672	intron-variant	Katnb1	Mm_Celera	8:95085405	TTGAGCTGAGAATTA[A/G]AGCAAGACCCTCCTC	74187
rs6189446	snp	C/T	0.290657	0.246672	intron-variant	Katnb1	Mm_Celera	8:95085464	TACCTAGATTGAAAG[C/T]GTCTGGGCTTACAAT	74187
rs6228880	snp	A/G	0.5	0	intron-variant	Katnb1	Mm_Celera	8:95081643	GGCAAGAGAAGTAAA[A/G]AGGGTCTGGCGAAGC	74187
rs6259910	snp	C/G	0.5	0	intron-variant	Katnb1	Mm_Celera	8:95094711	CTTACTCTTTCCACC[C/G]TTGCCTAGCTTTGGG	74187
rs6263377	snp	C/T	0.5	0	intron-variant	Katnb1	Mm_Celera	8:95083376	gcttgggacatgttc[C/T]tctgcctcctgtgtg	74187
rs6263938	snp	A/C	0.48	0.0979796	intron-variant	Katnb1	GRCm38.p3	8:95083511	GTTTCTCTGTGTAGC[A/C]CTGGCTGTCCTGGAA	74187
rs6278493	snp	G/T	0.290657	0.246672	intron-variant	Katnb1	Mm_Celera	8:95083908	AGGCCTGGAGGACCT[G/T]CATCTCACCTCTGTG	74187
rs13474081	snp	A/G			utr-variant-3-prime, downstream-variant-500B	Kifc3, Katnb1	GRCm38.p3	8:95100161	TGGCCCTTGGGCTGG[A/G]CTGTTCTCTACTAGT	74187
rs32562832	snp	C/T	0.290657	0.246672	intron-variant	Katnb1	GRCm38.p3	8:95097391	GGCTCAGCCTCTGCT[C/T]CCTGCAGCTCGAGGT	74187
rs32589020	snp	A/G	0.375	0.216506	intron-variant	Katnb1	GRCm38.p3	8:95081829	TTCCGACTCACACCT[A/G]GACTGGAGACTCAAT	74187
rs32634153	snp	C/T	0.401235	0.199068	intron-variant	Katnb1	GRCm38.p3	8:95094707	GGCTCTTACTCTTTC[C/T]ACCCTTGCCTAGCTT	74187
rs32637354	snp	A/G	0.444444	0.157135	intron-variant	Katnb1	Mm_Celera	8:95091835	AAGGGAAGGGCGCAG[A/G]CTTGCTGGATCCCAC	74187
rs32795872	snp	A/C	0.5	0	intron-variant	Katnb1	Mm_Celera	8:95093903	CCCACCTCTGCTTCT[A/C]TCCTCTATAGCTCTG	74187
rs32858979	snp	A/C	0.359862	0.224567	intron-variant	Katnb1	GRCm38.p3	8:95083696	AAAGTCACACTTACC[A/C]ATATATTCTGTTAGA	74187
rs32885221	snp	C/T	0.444444	0.157135	intron-variant	Katnb1	GRCm38.p3	8:95090764	GAGTTAAAGCCCAGC[C/T]TAGCCTGTGGTGTAA	74187
rs32968168	snp	C/T	0.375	0.216506	synonymous-codon, nc-transcript-variant	Katnb1	Mm_Celera	8:95096396	GCCCTTCCCAGCACC[C/T]CCAGAAGATGGTGAG	74187
rs32987598	snp	A/G	0.359862	0.224567	intron-variant	Katnb1	GRCm38.p3	8:95092022	CACTCGGTGTGGGGT[A/G]TAGCTGAGTTCGACA	74187
rs33171187	snp	A/C	0.444444	0.157135	intron-variant	Katnb1	GRCm38.p3	8:95090710	GGTGCCTGCCTAGAG[A/C]CCCAGCACTCAGGAA	74187
rs33182448	snp	C/T	0.375	0.216506	intron-variant, utr-variant-3-prime, downstream-variant-500B	Kifc3, Katnb1	Mm_Celera	8:95099650	GAGGTGATACTGCAA[C/T]GGGATGGAATGGTTA	74187
rs33201857	snp	C/T	0.375	0.216506	upstream-variant-2KB	Katnb1	GRCm38.p3	8:95079203	TCATGTGGTAGCCCA[C/T]GCCTTTAATGCCAGC	74187
rs33221131	snp	A/G	0.492188	0.0620098	intron-variant	Katnb1	GRCm38.p3	8:95084815	AGTTTCGGCTGAGGT[A/G]TGCCAGTTCGGCTGA	74187
rs33262225	snp	A/G	0.387812	0.208586	upstream-variant-2KB	Katnb1	Mm_Celera	8:95080091	CAAATGTTATTCTCC[A/G]AATCCAGGTCTCTTA	74187
rs33286029	snp	C/T	0.375	0.216506	intron-variant	Katnb1	Mm_Celera	8:95086263	GACAGAACTTGAATT[C/T]TTCTCAGTGTTTGTC	74187
rs33360459	snp	A/T	0.277778	0.248452	intron-variant	Katnb1	Mm_Celera	8:95093703	TACCATCCTCGGGAC[A/T]GAGGACATGTGGACG	74187
rs33443628	snp	A/T	0.375	0.216506	intron-variant	Katnb1	GRCm38.p3	8:95081828	ATTCCGACTCACACC[A/T]AGACTGGAGACTCAA	74187
rs33452083	snp	C/T	0.32	0.24	utr-variant-3-prime, downstream-variant-500B	Katnb1	Mm_Celera	8:95099101	GCTCTCCCAGACACA[C/T]TGTGGCCTGCCTAGA	74187
rs33494836	snp	A/G	0.18	0.24	utr-variant-3-prime, downstream-variant-500B	Katnb1	Mm_Celera	8:95099124	TGCCTAGAGGTCGCT[A/G]GAAGCAGAGACTGTC	74187
rs33551874	snp	A/G	0.456747	0.140554	intron-variant	Katnb1	GRCm38.p3	8:95092492	AAGAATGAAGGTCGA[A/G]AGGACAGACTGGAGG	74187
rs36270839	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95086276	TTCTTCTCAGTGTTT[A/G]TCCCAGATGGGCTTT	74187
rs36278768	snp	A/G	0.244898	0.249948	intron-variant	Katnb1	Mm_Celera	8:95082055	TCAGTCTCTCTGTTC[A/G]TCTCCGTGTATCTCT	74187
rs36345015	snp	A/G	0.124444	0.216185	intron-variant	Katnb1	Mm_Celera	8:95089773	GGGTCACAGGTGTCT[A/G]AAGGGCCGCTTCATC	74187
rs36370959	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95091546	GAGAGCTAAGGTCTC[A/G]GGGCCACTGCCATTC	74187
rs36386317	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95083173	GTCCAAGAACCCCAG[A/G]CATGTCCCAGGTCCC	74187
rs36398395	snp	C/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95087200	GTGGGGGTTACCTGG[C/G]TGTCCTGCTCAGAGC	74187
rs36404974	snp	C/T	0.444444	0.157135	intron-variant	Katnb1	GRCm38.p3	8:95090339	AAGGACATCAAATCC[C/T]AGGAGGTAGCCTGCA	74187
rs36435702	snp	G/T	0.124444	0.216185	intron-variant	Katnb1	Mm_Celera	8:95087216	TGTCCTGCTCAGAGC[G/T]GGTGGCTAAGCATCC	74187
rs36467805	snp	C/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95092042	TGAGTTCGACATCCA[C/T]GCCGCAGATGAGTCA	74187
rs36488928	snp	C/T	0.231111	0.249285	intron-variant, downstream-variant-500B	Katnb1	Mm_Celera	8:95098547	TGTCAGAGCACGGGC[C/T]TTTTGTGTCCCTGCA	74187
rs36499996	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95091044	ATCCTTTAGTCCTCT[A/G]GAGTGACTGCATGTT	74187
rs36554046	snp	C/T	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Katnb1	Mm_Celera	8:95095946	CGAAGATGACAGGGA[C/T]GAGCGAGAGTCCCGG	74187
rs36584112	snp	A/G	0.244898	0.249948	intron-variant	Katnb1	Mm_Celera	8:95086444	AGATAAAAATGGGAA[A/G]CCAGTTATTTATTTA	74187
rs36599770	snp	C/T	0.244898	0.249948	synonymous-codon, nc-transcript-variant	Katnb1	Mm_Celera	8:95089998	TGTGGAGAGTGTCCG[C/T]CTCAACACTCCTGAG	74187
rs36600555	snp	C/T	0.244898	0.249948	intron-variant	Katnb1	Mm_Celera	8:95096132	CTAAAACCAGAAACC[C/T]AGCTGGACACCTGTA	74187
rs36662727	snp	A/G	0.142012	0.225474	intron-variant	Katnb1	Mm_Celera	8:95093368	AATGGCTGTAAGACT[A/G]TCAGGGTGACAGGGC	74187
rs36724907	snp	C/T	0.124444	0.216185	intron-variant	Katnb1	Mm_Celera	8:95086944	TGCCTTCGCCGCCCA[C/T]GTGCTGAGTTTACAA	74187
rs36780417	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95087871	GCAGGCCTGGAGTAT[A/G]CAGTTCTGAGAAGCT	74187
rs36822625	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95087939	CCGCAGCATGGGAGC[A/G]TGGCTGTGTCCCGTG	74187
rs36824067	snp	G/T	0.165289	0.235211	intron-variant	Katnb1	GRCm38.p3	8:95087106	CAGGAGGAAGTGTCC[G/T]AGCAGGGCAGGCTAA	74187
rs36832697	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95086880	AGGTGCTTGTTTCCC[A/G]ACAGGGTCTTGCATG	74187
rs36878252	snp	C/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95086158	TCTCCACACAAGGAC[C/T]CTCTCTCACTCATGA	74187
rs36889488	snp	A/G	0.231111	0.249285	upstream-variant-2KB	Katnb1	Mm_Celera	8:95080172	ACTTTTGTTCCCGTA[A/G]AGGTTTTGCATTTAA	74187
rs36917789	snp	C/G	0.231111	0.249285	upstream-variant-2KB	Katnb1	Mm_Celera	8:95080328	CCGGACTGTGTAGAG[C/G]AGAACGCCAGATGCA	74187
rs36932406	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95093405	TGGTCTCCTGTTTTC[A/G]CATCGGCATCTCAGT	74187
rs36940908	snp	C/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95092754	TAGCTACTCAGTTCT[C/T]TGTTCTTGGATCTCT	74187
rs36960623	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95082929	ACCCTGTTGTTTTGT[A/G]AGCTGAGTAGTCTTA	74187
rs36970791	snp	A/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95084074	TTAAGTTGTCCCCCA[A/T]AGCTGTAAGGTTCTG	74187
rs37022025	snp	A/G	0.489796	0.070696	intron-variant	Katnb1	Mm_Celera	8:95084025	AAAGCTGTTTTGGTG[A/G]CTCAGTCTCCTCATT	74187
rs37038727	snp	G/T	0.124444	0.216185	intron-variant	Katnb1	Mm_Celera	8:95091096	CCCAGGACGCCCTTA[G/T]GACAAACAGCTGTGC	74187
rs37043960	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95087556	CAGTAATTTCAGGCC[A/G]TTCTGAATGACCAGG	74187
rs37100137	snp	C/G	0.132653	0.220748	intron-variant	Katnb1	Mm_Celera	8:95082033	tctctGAACgtctgc[C/G]tatctctcagtctct	74187
rs37166936	snp	A/C	0.124444	0.216185	intron-variant	Katnb1	Mm_Celera	8:95089938	CCTGCAGTTCATTGG[A/C]GCTGCCACCTTCTCT	74187
rs37174526	snp	A/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95091610	TTCTGAGAGAGCCAC[A/T]GTTAACCGTGGAGGA	74187
rs37202128	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95090953	TACTGCATAACAGTA[A/G]CCCCTGGCATGTGTG	74187
rs37208793	snp	C/G/T	0.231111	0.249285	intron-variant	Katnb1	GRCm38.p3	8:95086195	AAGCCCATGCAGCTG[C/G/T]CAGATTAGCACCATT	74187
rs37224459	snp	C/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95092180	GATGGCTGGCTAGGA[C/T]GGCTGTTGCCTATGT	74187
rs37246156	snp	C/T	0.231111	0.249285	upstream-variant-2KB	Katnb1	Mm_Celera	8:95080825	CTCAGAGCTGGTTCT[C/T]CAATAACACTAACGT	74187
rs37257580	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95084408	CGAGTGCAAAGGCCC[A/G]AAACAGGAAGCTTTA	74187
rs37274839	snp	C/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95092919	AGAGATAGACTTGAA[C/T]GCTGCCAGGAATACT	74187
rs37314685	snp	A/C	0.444444	0.157135	intron-variant	Katnb1	Mm_Celera	8:95085362	TTGTGGGCAGCTGTC[A/C]CCAAGTGTGCAGAGG	74187
rs37448221	snp	A/T	0.497041	0.0383476	intron-variant	Katnb1	GRCm38.p3	8:95086030	CCTGCCATTATCTCT[A/T]TGGAACCTACTCCCT	74187
rs37545027	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95096661	TACCGCAGACGTGAC[A/G]TGATGGGGACTCTGA	74187
rs37546720	snp	C/T	0.231111	0.249285	intron-variant, utr-variant-3-prime, downstream-variant-500B	Kifc3, Katnb1	Mm_Celera	8:95099622	TTGAAGCCTAGTTTT[C/T]CTTCTGTAACATGAG	74187
rs37555950	snp	G/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95086818	TTCTTGCATTGTATC[G/T]TTCATGGACTAGCAA	74187
rs37586025	snp	C/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95088877	TGAAGAATTGTGGCG[C/T]TGTTGTTTTTATGAG	74187
rs37689937	snp	C/T	0.124444	0.216185	intron-variant	Katnb1	Mm_Celera	8:95083194	CCCAGGTCCCTTTTC[C/T]TCCATCAGATGCAAG	74187
rs37723470	snp	A/T	0.444444	0.157135	upstream-variant-2KB	Katnb1	Mm_Celera	8:95079969	GATCTGTAATGTACA[A/T]ATAATTGTATAAACA	74187
rs37802496	snp	A/G	0.497778	0.0332592	intron-variant	Katnb1	GRCm38.p3	8:95084109	GACCCTGTTCATGGC[A/G]ACTTTTGGCAGAGTA	74187
rs37838885	snp	C/T	0.231111	0.249285	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Katnb1	Mm_Celera	8:95098861	GCCCACGAGCCTCAG[C/T]CTGGCCTCCATTCCT	74187
rs37874965	snp	A/T	0.277778	0.248452	intron-variant	Katnb1	Mm_Celera	8:95081821	AGGAGTCATTCCGAC[A/T]CACACCTAGACTGGA	74187
rs38075652	snp	A/C	0.244898	0.249948	intron-variant	Katnb1	Mm_Celera	8:95085736	CCAGCTCCTTTAGGG[A/C]ACCTGCATGTTGGGG	74187
rs38094954	snp	A/G	0.124444	0.216185	intron-variant	Katnb1	Mm_Celera	8:95095827	CCCGGCAGGGTGTAT[A/G]TCCCAAGAAGGCACC	74187
rs38147229	snp	A/G	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95093740	AGACACTTCAACTTG[A/G]AATTCCCAACTTGGG	74187
rs38223682	snp	G/T	0.124444	0.216185	intron-variant	Katnb1	Mm_Celera	8:95088114	ACCACTCAGATCAGA[G/T]CCGGTACGTCCAGGT	74187
rs38597806	snp	A/G	0.132653	0.220748	intron-variant	Katnb1	Mm_Celera	8:95086021	CTGCTGTCTCCTGCC[A/G]TTATCTCTTTGGAAC	74187
rs38619325	snp	G/T	0.132653	0.220748	intron-variant	Katnb1	Mm_Celera	8:95084281	TGTTTCCAGTCCTGC[G/T]CTAATTCTGAgtgtg	74187
rs38698688	snp	A/G	0.336735	0.234472	intron-variant	Katnb1	GRCm38.p3	8:95097598	CCTGTGCCAGCATCT[A/G]GGTACCATCCCCACA	74187
rs38747904	snp	C/T	0.231111	0.249285	intron-variant	Katnb1	Mm_Celera	8:95088704	ACAAGAAAATACATC[C/T]GGTTTCCCTCCAGAG	74187
rs38958409	snp	A/G/T	0.231111	0.249285	intron-variant	Katnb1	GRCm38.p3	8:95083125	GTCTGGTCAAGCTGA[A/G/T]GAGCGGAGTGTTGCG	74187
rs39212685	snp	G/T	0.260355	0.249785	intron-variant	Katnb1	Mm_Celera	8:95087467	CGCCTCTGCACACCA[G/T]CAGTGCTACCCCAGT	74187
rs39307207	snp	A/T	0.231111	0.249285	upstream-variant-2KB	Katnb1	Mm_Celera	8:95080241	TAAGTCCTGGGTCCG[A/T]TCTTCCAAATGTCTG	74187
rs48961559	snp	C/T			intron-variant	Katnb1	Mm_Celera	8:95089671	TTTTCTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT	74187
rs49404360	snp	A/G			intron-variant	Katnb1	Mm_Celera	8:95093852	TGACCTAGCCTCCAG[A/G]GACATAACAACTTCC	74187
rs50336565	snp	A/C			intron-variant	Katnb1	GRCm38.p3	8:95094113	GGACCGCCACCCCCC[A/C]AGGCTTCCCACCAAC	74187

Full records

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