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
rs3024181	snp	A/G			intron-variant	Prex2	GRCm38.p3	1:11297067	CCCCTTAGTACCACA[A/G]GGACATAGATAATGT	109294
rs3024182	snp	A/G			intron-variant	Prex2	Mm_Celera	1:11297149	CTGCAAGATAGCTAT[A/G]CTAGACAAGGTATTA	109294
rs3024196	snp	G/T			intron-variant	Prex2	GRCm38.p3	1:11036917	TAAATTTATAATTAC[G/T]GTGGCTAGTTCTTAG	109294
rs3024197	snp	C/T			intron-variant	Prex2	GRCm38.p3	1:11036899	GGCTAGTTCTTAGAG[C/T]TGTTGAGAAAACTAA	109294
rs3671759	snp	A/T	0.455	0.143091	intron-variant	Prex2	GRCm38.p3	1:11182359	TTTCCCTTTTCTTTT[A/T]ACATATTGCACTTTA	109294
rs3672887	snp	C/G	0.486111	0.0821678	intron-variant	Prex2	GRCm38.p3	1:11182511	GCTCCAGGCTTGCAT[C/G]CTTACCATGTAAATT	109294
rs3672901	snp	C/T	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11182519	CTTGCATCCTTACCA[C/T]GTAAATTGTCATCTT	109294
rs3672956	snp	C/T	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11182545	ATCTTCCCTCTGTGG[C/T]TCCTTGTGTGACCTC	109294
rs3674105	snp	C/G	0.456747	0.140554	intron-variant	Prex2	GRCm38.p3	1:11182714	GTTAACATTCAGTAC[C/G]TCTTCCTGCTCAATG	109294
rs3674168	snp	A/G	0.456747	0.140554	intron-variant	Prex2	Mm_Celera	1:11182754	AAGAGTTCCATCTCT[A/G]AAAGTGCTTTTTGCT	109294
rs3674698	snp	C/G	0.359862	0.224567	intron-variant	Prex2	Mm_Celera	1:11182825	AACTAGTCACATGAA[C/G]TATGTGTGCAGCATC	109294
rs3679024	snp	A/C	0.489796	0.070696	intron-variant	Prex2	Mm_Celera	1:11055168	TAATTAAAAAATTGC[A/C]AGCATCTCAGGCTGT	109294
rs3680189	snp	C/T	0.304688	0.243945	intron-variant	Prex2	GRCm38.p3	1:11186585	CTCTAAAGCCAGTGG[C/T]CTTGACTGAGAACCA	109294
rs3681510	snp	C/G	0.456747	0.140554	intron-variant	Prex2	GRCm38.p3	1:11186791	AAGGCAGGGAACATT[C/G]TGATAACGTGGATAC	109294
rs3682122	snp	C/G	0.415225	0.187619	intron-variant	Prex2	GRCm38.p3	1:11186867	TGTAGTGCTTCGTTG[C/G]TATCTGCAGTGATTT	109294
rs3709040	snp	A/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11224039	AGATGACCTTGGCCA[A/G]GGGGGCTAAGCAGTT	109294
rs3710150	snp	C/T	0.495868	0.0452663	intron-variant	Prex2	Mm_Celera	1:11118344	TGGATATAAATAGAT[C/T]GGATAAAAAGCACTG	109294
rs3710796	snp	A/G	0.32	0.24	intron-variant	Prex2	GRCm38.p3	1:11272555	AGAAAATGTCAGATA[A/G]ATTTCTGGCTATTGT	109294
rs3711521	snp	A/G	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11069038	AGACTTATTTATAGG[A/G]TTTGCCATGAGTTAT	109294
rs3711594	snp	C/T	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11069076	ATGCACTAGCCGGTC[C/T]GGGGCATAAATTCTC	109294
rs3722284	snp	A/C	0.48	0.0979796	intron-variant	Prex2	GRCm38.p3	1:11269182	TAGAAGGCCCTCAAC[A/C]CTGGAATTCTTCCTC	109294
rs3722295	snp	A/C	0.401235	0.199068	intron-variant	Prex2	GRCm38.p3	1:11269188	GCCCTCAACCCTGGA[A/C]TTCTTCCTCAGCCTC	109294
rs3722996	snp	A/C	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11269353	TTAATGATTATTGTC[A/C]CCCCCTACAGTTGCA	109294
rs3724763	snp	A/G	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11269584	TATTGCTCTTAATTG[A/G]GGGACAATTATATTC	109294
rs6153126	snp	A/G	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11093394	ggcagacagatttct[A/G]agtttgaggccagcc	109294
rs6153707	snp	A/C	0.207612	0.24638	intron-variant	Prex2	Mm_Celera	1:11093519	AAGTTAGCTAATGAT[A/C]GACTCTCTCACCTTA	109294
rs6167362	snp	A/C	0.5	0	intron-variant	Prex2	Mm_Celera	1:11093694	tgttcttcttttttc[A/C]cctttcatgtagttc	109294
rs6167480	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11093762	ggtgtgttcttcata[C/T]tcagtttaacctcca	109294
rs6182992	snp	A/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11173284	ttatatccctgtttt[A/G]ttgctaattttgtta	109294
rs6184117	snp	A/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11173456	gaccagagtttattt[A/G]tttcttgtcatgtac	109294
rs6185168	snp	A/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11173625	cttgttagaactgcc[A/G]ccactgtctccctta	109294
rs6185251	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11173677	cattttcattcaatt[C/T]tggagggtanttagt	109294
rs6185268	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11173687	caattntggagggta[C/T]ttagttcttcnctta	109294
rs6185684	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11173698	ggtanttagttcttc[C/T]cttaatttntgtttg	109294
rs6185698	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11173707	ttcttcncttaattt[C/T]tgtttgaacccattt	109294
rs6185788	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11173767	ttaatttgtaagcct[C/T]ctcctgcttatgtag	109294
rs6228078	snp	A/G	0.5	0	utr-variant-5-prime	Prex2	Mm_Celera	1:10993518	GCCTCCCCTCGGGCT[A/G]GAGCCGCGTGAGGCC	109294
rs6228152	snp	C/T	0.5	0	utr-variant-5-prime	Prex2	Mm_Celera	1:10993555	GCGGGCCGGGCTGGG[C/T]TCCCGCTCTCCGGGG	109294
rs6228328	snp	A/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11187905	CCCAATTAATGAATA[A/T]TTTTTAAATGAATGG	109294
rs6242335	snp	C/G	0.5	0	missense	Prex2	Mm_Celera	1:10993801	GGCCACCATGAGCGA[C/G]GAAAGCGCCAGGGAA	109294
rs6259073	snp	A/G	0.509512	0.086336	intron-variant	Prex2	GRCm38.p3	1:11027020	ACTAGATCTCTGAAC[A/G]TTTATAAGACAGTCT	109294
rs6260132	snp	A/G	0.290657	0.246672	intron-variant	Prex2	Mm_Celera	1:11027225	TAGAGATTGGATTGA[A/G]TGTTTGTCCTTGCCT	109294
rs6260654	snp	A/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11027324	AGGAAGGGTGGGTTC[A/G]CTGTAATCCCTGTCC	109294
rs6288198	snp	C/T	0.497778	0.0332592	intron-variant	Prex2	GRCm38.p3	1:11113153	GCAGGGTGAATAGAA[C/T]GTAAAACAACAGATG	109294
rs6288746	snp	A/C	0.456747	0.140554	intron-variant	Prex2	GRCm38.p3	1:11113269	GATTCTCATGTGGCT[A/C]TTCTATACTATGAGC	109294
rs6289257	snp	A/C	0.21875	0.248039	intron-variant	Prex2	Mm_Celera	1:11113363	AGGACAACACATTGG[A/C]TGTGTATTGAAGGGC	109294
rs6289696	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11113388	AAGGGCAGGAGAAGA[C/T]GCNTATTTTTACATG	109294
rs6289697	snp	A/C	0.5	0	intron-variant	Prex2	Mm_Celera	1:11113391	GGCAGGAGAAGANGC[A/C]TATTTTTACATGAAG	109294
rs6293530	snp	C/T	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11009626	ctgttctattctatt[C/T]tattctattctattc	109294
rs6297340	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11198111	CTCTAATTATTCTGT[C/T]GGTGTGGATTTTGGC	109294
rs6297841	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11198157	AGGACATAGAGAATG[C/T]ACCAGTGACCACATG	109294
rs6297961	snp	A/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11198220	agccatcagctaggg[A/G]tatggcatatagagc	109294
rs6298478	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11198282	agcttaatttttgta[C/T]aggccttgtntatgt	109294
rs6298497	snp	A/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11198292	ttgtanaggccttgt[A/G]tatgtattcatagct	109294
rs6298967	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11198337	ttgcaacaaccgtgt[C/T]atgtccagagaccag	109294
rs6304316	snp	G/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11113710	TTGAAGAGTAGGCAT[G/T]GAGCAGTGCTTGTGG	109294
rs6304347	snp	A/G	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11113726	GAGCAGTGCTTGTGG[A/G]NAAAGGTTGGANTTA	109294
rs6304349	snp	A/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11113727	AGCAGTGCTTGTGGN[A/G]AAAGGTTGGANTTAC	109294
rs6304364	snp	C/T	0.495868	0.0452663	intron-variant	Prex2	GRCm38.p3	1:11113738	TGGNNAAAGGTTGGA[C/T]TTACAACATCGAAAA	109294
rs6304396	snp	A/G	0.456747	0.140554	intron-variant	Prex2	GRCm38.p3	1:11113758	AACATCGAAAACAAG[A/G]AGAAAGTGGTGCTGA	109294
rs6304796	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11113799	AAAGCTAGAAGATGC[C/T]CAAGTGAAAAGGCAG	109294
rs6307423	snp	A/C	0.5	0	intron-variant	Prex2	Mm_Celera	1:11009791	CATCTGTTTGTAAGT[A/C]CAGTTCTAGGGAGTC	109294
rs6315127	snp	C/T	0.21875	0.248039	intron-variant	Prex2	Mm_Celera	1:11271434	CCCATGGAATAAAAG[C/T]TTTACAACTATTGTC	109294
rs6315659	snp	C/T	0.207612	0.24638	intron-variant	Prex2	Mm_Celera	1:11271526	GCTTCCTTTTCATAA[C/T]TCAGATGTCAATTTG	109294
rs6315683	snp	A/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11271543	CAGATGTCAATTTGT[A/G]TTATGAGTNCTCTTC	109294
rs6315698	snp	C/T	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11271552	ATTTGTNTTATGAGT[C/T]CTCTTCCTTAGAAGT	109294
rs6316095	snp	A/C	0.231111	0.249285	intron-variant	Prex2	Mm_Celera	1:11271585	CTTAAATATTGCAGA[A/C]TTTTCCAATAAGCAA	109294
rs6316157	snp	C/T	0.304688	0.243945	intron-variant	Prex2	Mm_Celera	1:11271625	AAAATTTCTGCTGAT[C/T]TGATAAACAGATAAA	109294
rs6316191	snp	C/T	0.257117	0.249899	intron-variant	Prex2	Mm_Celera	1:11271646	AACAGATAAATAACA[C/T]AGGTGTATGTAATTT	109294
rs6325251	snp	A/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11187745	GAAAGGTTCCCCAGA[A/T]AAGTAACATGTTTTA	109294
rs6325308	snp	C/T	0.359862	0.224567	intron-variant	Prex2	Mm_Celera	1:11187776	TTCAATGATGAAATA[C/T]TTTCTTATTTGTAAC	109294
rs6325739	snp	C/T	0.21875	0.248039	intron-variant	Prex2	Mm_Celera	1:11187796	TTATTTGTAACTAAA[C/T]TTCTTGGCTATATTT	109294
rs6345992	snp	C/T	0.207612	0.24638	intron-variant	Prex2	Mm_Celera	1:11083441	CTAGCAGATAGATGG[C/T]TCAGTTCAGACTTTG	109294
rs6346583	snp	A/G	0.207612	0.24638	intron-variant	Prex2	Mm_Celera	1:11083520	TTTAAGGAACCTATT[A/G]TGAATTAGATTTAca	109294
rs6347189	snp	A/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11083629	cacagatatttatgt[A/T]ataatttacaacaat	109294
rs6347231	snp	A/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11083653	caacaatagtaaaaa[A/T]tagttataaagtaac	109294
rs6357764	snp	A/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11123496	TACTGAAATATAACT[A/T]AGCACATTCTAGATT	109294
rs6358124	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11123514	CACATTCTAGATTTA[C/T]TGCTATTTNAACTTT	109294
rs6358132	snp	A/G	0.48	0.0979796	intron-variant	Prex2	Mm_Celera	1:11123523	GATTTANTGCTATTT[A/G]AACTTTCTGTTTGAA	109294
rs6358714	snp	A/G	0.336735	0.234472	intron-variant	Prex2	Mm_Celera	1:11123646	TTCTTCAGTGACTTA[A/G]CTCCTACATTTATCC	109294
rs6359243	snp	C/G	0.5	0	intron-variant	Prex2	Mm_Celera	1:11123780	TTCTCTTGAGTGATC[C/G]TANCCGTTTCTGATT	109294
rs6359244	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11123783	TCTTGAGTGATCNTA[C/T]CCGTTTCTGATTTGC	109294
rs6360236	snp	A/C	0.345679	0.230967	intron-variant	Prex2	Mm_Celera	1:11083825	AACTGTGAGGGGGCA[A/C]CCAACGGTAGTCTTT	109294
rs6360841	snp	A/C	0.30839	0.243086	intron-variant	Prex2	Mm_Celera	1:11090509	ATAAAATCGGCACTT[A/C]TGCTATAAAAATAAG	109294
rs6372231	snp	A/G	0.484429	0.0868505	synonymous-codon	Prex2	Mm_Celera	1:11123822	CACACAGGGTGTAAG[A/G]CTCTACTGTCGTCTT	109294
rs6372808	snp	A/C	0.5	0	intron-variant	Prex2	Mm_Celera	1:11123938	AGTCATTTCATTTTA[A/C]GTAATTGTTTATGTC	109294
rs6383525	snp	A/C	0.304688	0.243945	intron-variant	Prex2	Mm_Celera	1:11045870	TCCCAGACTGGTCTG[A/C]AACAAACCTTTCTGT	109294
rs6383562	snp	C/T	0.5	0	intron-variant	Prex2	Mm_Celera	1:11045888	CAAACCTTTCTGTCT[C/T]CACCTCTCAGTGCTG	109294
rs6384765	snp	A/G	0.444444	0.157135	intron-variant	Prex2	Mm_Celera	1:11046081	TCTGTAGCCAGGGAT[A/G]AGCTTGAACTCCTGA	109294
rs6385334	snp	C/G	0.336735	0.234472	intron-variant	Prex2	Mm_Celera	1:11046163	CGTCTTCTTGAAGGT[C/G]TTCCTCAAGACACTG	109294
rs13475723	snp	G/T	0.5	0	synonymous-codon	Prex2	GRCm38.p3	1:11149879	TGGACCTTCAGTTGT[G/T]CATGCGGTGGGAAGA	109294
rs30465546	snp	A/G	0.375	0.216506	intron-variant	Prex2	GRCm38.p3	1:11285945	AGATATGCTTTTGTA[A/G]TCATGACCACTTTAT	109294
rs30468596	snp	G/T	0.345679	0.230967	intron-variant	Prex2	GRCm38.p3	1:11242221	CACCCTTGTCTCTGT[G/T]TAGATCCATTTTACT	109294
rs30471054	snp	A/G	0.444444	0.157135	intron-variant	Prex2	GRCm38.p3	1:11295499	CTGCTGTATGCTGGG[A/G]ACAGCCTGGGCCAAA	109294
rs30473216	snp	A/G	0.5	0	intron-variant	Prex2	GRCm38.p3	1:11076005	GTTCAAGGCCAGCCT[A/G]GTCTACAAAGTGAGT	109294
rs30474984	snp	A/G	0.375	0.216506	intron-variant	Prex2	GRCm38.p3	1:11277829	GAGCTGGAGATTGAT[A/G]CAATAAGCAAGAGGT	109294
rs30493056	snp	A/T	0.375	0.216506	intron-variant	Prex2	GRCm38.p3	1:11244690	CCCAAATATATTTTT[A/T]ATAATACATAGAAAA	109294
rs30505799	snp	A/G	0.304688	0.243945	intron-variant	Prex2	Mm_Celera	1:11099895	AACTAGAAATTCTCA[A/G]CTCCTGAAAAGTGAG	109294
rs30534831	snp	C/T	0.415225	0.187619	intron-variant	Prex2	GRCm38.p3	1:11265955	AGCTAAAATGAAAAG[C/T]GAGGGACACAAAGCT	109294
rs30552273	snp	A/G	0.444444	0.157135	intron-variant	Prex2	Mm_Celera	1:11134904	TAACCAGTATTTGGT[A/G]CCAGCTGTGCTAAAA	109294

Full records

It may take some time, please wait.