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
rs6291191	snp	A/G	0.207612	0.24638	intron-variant	Nbr1	Mm_Celera	11:101566162	TTTCCTGGTGCTGGA[A/G]CTGAGTTTTCCTACC	17966
rs6305642	snp	C/T	0.5	0	intron-variant	Nbr1	Mm_Celera	11:101566436	CCTGGGCAGGGGCAG[C/T]NACCAACTAGCATTC	17966
rs6305643	snp	C/G	0.5	0	intron-variant	Nbr1	Mm_Celera	11:101566437	CTGGGCAGGGGCAGN[C/G]ACCAACTAGCATTCT	17966
rs6412022	snp	A/G	0.5	0	upstream-variant-2KB	Nbr1, Brca1	Mm_Celera	11:101551988	CAGCGGAAGGGAAGG[A/G]AGGAGCGAGTTGGGG	17966
rs13473437	snp	C/G/T	0.444444	0.157135	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	Nbr1, Tmem106a	GRCm38.p3	11:101581487	ACTGTCACAGTGGAT[C/G/T]GGAAGGACAAGCATG	17966
rs13473438	snp	A/G	0.32	0.24	missense, synonymous-codon, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101580609	TCTGAAGATCAGACC[A/G]CAGCCCTGATGGCCC	17966
rs28273194	snp	C/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Nbr1, Tmem106a	Mm_Celera	11:101582401	TGGGCTTACTCAGCG[C/T]CCAACACGTTGTTGC	17966
rs28273195	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB, downstream-variant-500B	Nbr1, Tmem106a	Mm_Celera	11:101582194	GCAGAGCCGGAAGTG[C/T]CTTCCAGTGGCCTCT	17966
rs28273196	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB, downstream-variant-500B	Nbr1, Tmem106a	Mm_Celera	11:101582152	TAGTTTGGTCCTGGC[A/G]ATAGCAACATTTGTC	17966
rs28273197	snp	A/T	0.124444	0.216185	intron-variant, upstream-variant-2KB, downstream-variant-500B	Nbr1, Tmem106a	Mm_Celera	11:101582099	GTAGCAACTTAAAAG[A/T]ATTGTGAATACGTGT	17966
rs28273198	snp	A/G	0.231111	0.249285	intron-variant, upstream-variant-2KB, downstream-variant-500B	Nbr1, Tmem106a	Mm_Celera	11:101582084	CCGTTGTACTTGCAC[A/G]TAGCAACTTAAAAGA	17966
rs28273199	snp	C/T	0.231111	0.249285	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101581937	AAATAAACCACAATT[C/T]AAACTGCAAGCCAAC	17966
rs28273200	snp	A/G	0.32	0.24	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101581752	CAGATGGTGAAAGAA[A/G]AGGCAACACAACACT	17966
rs28273201	snp	A/G	0.231111	0.249285	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101581626	CGAGAACAGGAAGTA[A/G]TGCTTTGGGGCTAAC	17966
rs28273202	snp	C/T	0.260355	0.249785	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101581537	AAGGTCGGGTGTGGG[C/T]GAAAGGACACAGAAC	17966
rs28273203	snp	A/G	0.231111	0.249285	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101581507	GGACAAGCATGTGCA[A/G]ATACTCATCTCAGTA	17966
rs28273204	snp	G/T	0.32	0.24	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101581315	AAGGACAGGAGGCAT[G/T]CGGGTTAACCCACAG	17966
rs28273205	snp	A/G	0.32	0.24	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101581287	GCTTTCAGAAGGCCT[A/G]GCAGGAACCTGGAAG	17966
rs28273206	snp	A/G	0.32	0.24	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101581067	TCTGCTTGTATTGAA[A/G]TTGAGTATTTTCCTT	17966
rs28273207	snp	A/G	0.495	0.0497494	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101580955	TGTAGAAATGGGATG[A/G]ATGGTAGGAAGACAG	17966
rs28273208	snp	A/G	0.124444	0.216185	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant	Nbr1, Tmem106a	Mm_Celera	11:101580832	TGAGTGTGGGTGGAA[A/G]CCCTTGCTTGCTTTT	17966
rs28273209	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Nbr1, Tmem106a	Mm_Celera	11:101580405	CCTCTCCTTCAGTTA[C/T]GCACACACATAGTCA	17966
rs28273210	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Nbr1, Tmem106a	Mm_Celera	11:101580350	CCACTGTGCCTGAGC[A/G]CGCTGCTTTCAGAAA	17966
rs28273211	snp	A/G	0.244898	0.249948	intron-variant	Nbr1	Mm_Celera	11:101580225	TCTTGCTCTTCAATT[A/G]TTACTTGGCTGAAGA	17966
rs28273212	snp	C/T	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101580205	GTCTTCGAGGCTTCT[C/T]GTCATCTTGCTCTTC	17966
rs28273213	snp	A/C	0.132653	0.220748	intron-variant	Nbr1	Mm_Celera	11:101579859	AAACATGTTATCAGT[A/C]CAAATGAGAGGAAAG	17966
rs28273214	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101579822	TTATAAAAGAGACTT[A/G]AGGTTGGCAAGCCTA	17966
rs28273215	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101579634	CTTAGAAGAAACAGG[A/G]CCACTGCTGCAACTT	17966
rs28273216	snp	A/C	0.142012	0.225474	intron-variant	Nbr1	Mm_Celera	11:101579003	AGGAGTGCAAGGATA[A/C]AGCTCAGGCTTTAGC	17966
rs28273217	snp	C/T	0.231111	0.249285	intron-variant	Nbr1	Mm_Celera	11:101578947	TTAACAGGAAAGAGA[C/T]AGGCGCGTGAGGACC	17966
rs28273218	snp	A/T	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101578290	CAACGTAGTGGACAT[A/T]CTACGGGATAATAAG	17966
rs28273219	snp	A/G	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101578258	AAGACTGCATGTACA[A/G]AGTTGCTGTTCTACA	17966
rs28273220	snp	A/G	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101577699	CAGCTGGGATGGAAA[A/G]CTGGCGTAGTAACTA	17966
rs28273221	snp	A/T	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101577346	CAGGTGGCGAGCACC[A/T]TAAATGAGCACCTTC	17966
rs28273222	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101576963	CCTAAAACTCTGCGA[A/G]CTAACACATCAGGGT	17966
rs28273223	snp	A/G	0.231111	0.249285	intron-variant	Nbr1	Mm_Celera	11:101576168	GCTAGAGAGGACATC[A/G]GAGAGTGGAACTCAG	17966
rs28273224	snp	C/T	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101576039	CACGTCTACTGGAGC[C/T]GGGTCATTGTCTCTA	17966
rs28273225	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	GRCm38.p3	11:101575919	ATTTGTCAGCTCCAA[A/G]GTTTGCCTGGTGAGT	17966
rs28273226	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Nbr1	Mm_Celera	11:101575384	GGTGCCTCTAGTCCC[C/T]GAGGTGGCAGGACTT	17966
rs28273227	snp	C/T	0.124444	0.216185	missense, nc-transcript-variant	Nbr1	Mm_Celera	11:101575004	TATTCCTTAGTGAAA[C/T]TTGCCTTGCCTGAAG	17966
rs28273228	snp	A/G	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101574977	GGCCTCTTCCCTCAC[A/G]GTGGTTACTTTTATT	17966
rs28273229	snp	C/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101574939	TCTTTCCACTGTGCC[C/T]GTTGTGCTAGCTCGT	17966
rs28273230	snp	C/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101574358	TAAACCAGTTATTCA[C/T]AGTTACTGCTCTGAT	17966
rs28273231	snp	A/G	0.336735	0.234472	intron-variant	Nbr1	Mm_Celera	11:101573570	AAAGATGTGGGAATG[A/G]CTTCTAGGGAACTAC	17966
rs28273232	snp	A/G	0.231111	0.249285	missense, nc-transcript-variant	Nbr1	Mm_Celera	11:101573165	CCTGGATTCTGCAGA[A/G]AGGATTCTTCCTGTA	17966
rs28273233	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101573045	TGACGATGCTGGCAC[A/G]CTTACTAGAGCACCG	17966
rs28273234	snp	C/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101572632	CCACCTCTCCTCACA[C/T]GTCCATTCCTCATTA	17966
rs28273235	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101572321	AAAAGTTCTGATGAC[A/G]TGACAGCTGGTGGAG	17966
rs28273236	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101571832	CCAGGAGACCTGATG[A/G]TCCATTCAGGAAAGA	17966
rs28273237	snp	C/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101571439	GACTGCCCAGGTAAG[C/T]AGTCCGCGCTCGGAG	17966
rs28273238	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Nbr1	Mm_Celera	11:101571391	ACGCGCTGCCAGTGA[A/G]AGGGAGCTGTACATT	17966
rs28273239	snp	A/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101570884	CTCAAAAAGAAAGGC[A/T]ACCTGGCCTGCTGCT	17966
rs28273240	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101570626	CATTATTATGCTGGT[A/G]TTTGGCCTAGTCCTC	17966
rs28273241	snp	C/T	0.244898	0.249948	synonymous-codon, nc-transcript-variant	Nbr1	Mm_Celera	11:101569578	CTTGAAGGCTGGCCA[C/T]GTTGGGGTCGTGTCT	17966
rs28273242	snp	A/G	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101569460	GGATGTGCAATAGCA[A/G]AGGGCGCACCTGACA	17966
rs28273243	snp	C/T	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101569214	ATGTTTGGAGGCCAT[C/T]ACACCAGTAGCAAGT	17966
rs28273244	snp	C/T	0.132653	0.220748	intron-variant	Nbr1	Mm_Celera	11:101568926	ATGGACACTTATAAT[C/T]ACCCTTTAGGCAGCG	17966
rs28273245	snp	C/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101568068	TGTGTAATGAAACAA[C/T]TGTCTGAGACTCATC	17966
rs28273246	snp	A/G	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101567966	GCTAAGCTATGTAGT[A/G]AGTCAGTCTCATAGC	17966
rs28273247	snp	A/G	0.32	0.24	missense, nc-transcript-variant	Nbr1	Mm_Celera	11:101567144	GAAGCTGGACCATAC[A/G]CCCATGACACTAACC	17966
rs28273248	snp	A/G	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Nbr1	Mm_Celera	11:101567104	ACACAGCCTATGCCC[A/G]TCCTACAACATTTGT	17966
rs28273249	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101567032	AGCTTAAACTGGTTC[A/G]TTGCTCTCTACTTCA	17966
rs28273250	snp	A/C	0.132653	0.220748	intron-variant	Nbr1	GRCm38.p3	11:101566563	TGCTATTCAGATACG[A/C]ATTTGGGTTAACTGA	17966
rs28273251	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101566543	ATAGCGGGAACTGTT[A/G]AGAGTGCTATTCAGA	17966
rs28273252	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101566092	CTCCAGCAGCCATTA[A/G]CCATGTTCTTGAGTT	17966
rs28273253	snp	C/G	0.231111	0.249285	intron-variant	Nbr1	Mm_Celera	11:101565816	TGGGTGTTAGCAGCA[C/G]TGTTGGCACAGGTAG	17966
rs28273254	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Nbr1	Mm_Celera	11:101565769	AGATTGGTTTACAAG[C/T]TACCTGGAGATGGTG	17966
rs28273255	snp	A/C	0.231111	0.249285	missense, nc-transcript-variant	Nbr1	Mm_Celera	11:101565705	GTATTTTCTCCCAGC[A/C]ATGTTCTTCTGCTCC	17966
rs28273256	snp	C/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101564864	TGACCAACTCTGACC[C/T]TACATCTCATTGTCT	17966
rs28273257	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101562998	GACTCTCAGGCTGAG[A/G]TAAAGGAAAACAGCT	17966
rs28273258	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101562469	CAGCAGGCAGTTCCT[A/G]CTACAGTTCAGGTGA	17966
rs28273259	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101562431	AGTTAGAGAGTCTGT[A/G]GTAAGTAGGGCAAAT	17966
rs28273260	snp	A/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101562404	AGTACTAAGAATAGA[A/T]TGACTCCCGTTAGTT	17966
rs28273261	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101561661	TCAAGACCTCTTGCA[A/G]CTAGAGAAAGGAGTG	17966
rs28273262	snp	C/T	0.231111	0.249285	intron-variant	Nbr1	Mm_Celera	11:101561308	GGTTGATATTTTGTG[C/T]TTAGAAGGCTAGAGC	17966
rs28273263	snp	C/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101561193	GTAGTCCATATTGTA[C/G]TCCCCACATCCTTAT	17966
rs28273264	snp	A/G	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101561086	TGTCACATGCAACTC[A/G]TTCTGCTGGTATTGC	17966
rs28273265	snp	C/T	0.132653	0.220748	intron-variant	Nbr1	Mm_Celera	11:101561014	GGTCATAAGGACAGG[C/T]CTTATCCAACATGGT	17966
rs28273266	snp	A/G	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101560626	CGATGAGATGTTTCC[A/G]TTTAAACCATGCTTT	17966
rs28273267	snp	C/T	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101560470	AGTTCCTGAGAAAAA[C/T]CTTGTTAGCTTTACT	17966
rs28273268	snp	G/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101560385	TAGTCAACAAAATGC[G/T]CAGGTGATGAGACTT	17966
rs28273269	snp	C/T	0.231111	0.249285	intron-variant	Nbr1	Mm_Celera	11:101560374	GAGACCGATCCTAGT[C/T]AACAAAATGCTCAGG	17966
rs28273270	snp	A/C	0.244898	0.249948	intron-variant	Nbr1	Mm_Celera	11:101560305	AAGATAAAACAGAGC[A/C]CATTATTTAAGCAGT	17966
rs28273271	snp	A/T	0.165289	0.235211	intron-variant	Nbr1	Mm_Celera	11:101560135	GCGCTAGACTAGCAG[A/T]ACTGTATATCTGGTA	17966
rs28273272	snp	C/T	0.244898	0.249948	intron-variant	Nbr1	Mm_Celera	11:101560110	GAACCCTTTATGAAG[C/T]GGTTAAAGTGCGCTA	17966
rs28273273	snp	A/C	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101560043	CAGAGAAAGAACCTA[A/C]AATTATAGCAAGACT	17966
rs28273274	snp	G/T	0.48	0.0979796	intron-variant	Nbr1	Mm_Celera	11:101559990	ACTATTGGCATCTGA[G/T]CTGGAGTTGAGAAAT	17966
rs28273275	snp	C/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101559596	GGTAAAGTGTCTGAA[C/T]GCCATTGTTAGAGAT	17966
rs28273276	snp	A/G	0.132653	0.220748	intron-variant	Nbr1	Mm_Celera	11:101559402	GGCAGAATACTCTCC[A/G]GCTCCACCATTACTG	17966
rs28273277	snp	A/G	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101558217	CCAAGTGGTCCACAG[A/G]ATAATTATAACAATG	17966
rs28273278	snp	A/T	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101557540	TCTCCAGCCCGGAAA[A/T]TTTTAAATTATATCC	17966
rs28273279	snp	A/G	0.231111	0.249285	intron-variant	Nbr1	Mm_Celera	11:101557146	TCTAGCAGCTGTTGG[A/G]TGAGTTGGCAGCTTG	17966
rs28273280	snp	C/T	0.231111	0.249285	intron-variant	Nbr1	Mm_Celera	11:101556816	GCAGCAGCTCCTCTG[C/T]TCCGTGCTTTGGTTT	17966
rs28273281	snp	C/T	0.456747	0.140554	intron-variant	Nbr1	Mm_Celera	11:101556810	GCCCATGCAGCAGCT[C/T]CTCTGCTCCGTGCTT	17966
rs28273282	snp	A/C	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101556754	TGGGTCAAAGGTTGG[A/C]TGTCTCAGAGCTGGC	17966
rs28273283	snp	A/G	0.231111	0.249285	intron-variant	Nbr1	Mm_Celera	11:101556596	TTAGGGTTTAGAGAC[A/G]TTCTGGGGATAAGTT	17966
rs28273284	snp	A/G	0.32	0.24	intron-variant	Nbr1	Mm_Celera	11:101555933	ATATAAGTGGTAGCT[A/G]TAACATAAGTGCAGA	17966
rs28273285	snp	C/T	0.124444	0.216185	intron-variant	Nbr1	Mm_Celera	11:101555633	CACCTTGCTGGATTA[C/T]GCTACAGATGCTCAA	17966
rs28273286	snp	A/G	0.231111	0.249285	intron-variant	Nbr1	Mm_Celera	11:101555629	AATCCACCTTGCTGG[A/G]TTACGCTACAGATGC	17966
rs28273287	snp	C/G	0.391111	0.206368	intron-variant	Nbr1	Mm_Celera	11:101554911	TGCCTCTTGTGTGTG[C/G]AGCAGAATCTGGCCC	17966

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