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
rs3679297	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770566	ACCTACCAGGCATGC[C/G]TAAGACTCCCACGAG	19013
rs3679322	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770578	TGCGTAAGACTCCCA[C/T]GAGCTACAGCTCATT	19013
rs3679344	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770588	TCCCACGAGCTACAG[C/G]TCATTGACAGAGTCT	19013
rs3679946	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770664	GTTGAAAGCAAAGTA[A/G]TGGTGCTTTTAAAGT	19013
rs3680606	snp	A/G	0.46875	0.121031	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770745	GCCTGGCTGTCCATC[A/G]TTGCTTATTTTTCCC	19013
rs3680770	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770821	ATGAGATGCCCTTTT[C/T]CCTTTTCTATTGAGT	19013
rs3681229	snp	A/G	0.489796	0.070696	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770830	CCTTTTCCCTTTTCT[A/G]TTGAGTTTCTGGTCA	19013
rs3681406	snp	A/G	0.46875	0.121031	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85770922	CAACTGTTTGCTTAC[A/G]TGTACCTCTTATGGT	19013
rs6253977	snp	C/T	0.32	0.24	utr-variant-3-prime	Ppara	Mm_Celera	15:85802674	CCAAGGAGTCGAGGA[C/T]GTAGCCCAGTGGATG	19013
rs6254040	snp	C/T	0.290657	0.246672	utr-variant-3-prime	Ppara	Mm_Celera	15:85802711	CTTGGTTCCTGGTGC[C/T]GATTTATggacatgg	19013
rs6255204	snp	A/G	0.5	0	utr-variant-3-prime	Ppara	Mm_Celera	15:85802940	TTTGCACCCTTACTG[A/G]ccttccccnctccct	19013
rs6255595	snp	A/C	0.444444	0.157135	utr-variant-3-prime	Ppara	Mm_Celera	15:85802949	TTACTGACCTTCCCC[A/C]CTCCCTCCTGCTCTT	19013
rs6311008	snp	A/G	0.495	0.0497494	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85774379	CCTCATTACCCTACC[A/G]TTCTGGAATATCTAG	19013
rs6312031	snp	C/T	0.265928	0.249492	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85774569	TGTGTTGGGGTGTGC[C/T]CATGTGACCTCTGTT	19013
rs6313052	snp	A/G	0.487293	0.0786907	intron-variant, upstream-variant-2KB	Ppara	GRCm38.p3	15:85774741	GTGTTATCTCATCTC[A/G]TTTGTGCATGGCAAG	19013
rs8238200	snp	C/T	0.345679	0.230967	upstream-variant-2KB, utr-variant-5-prime, intron-variant	Ppara	Mm_Celera	15:85735014	TCTNAAGATCAGATT[C/T]CGCCTGTCCGTCCAC	19013
rs8238201	snp	C/T	0.18	0.24	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85735199	GCGCACCCTTCCCAC[C/T]GACTGTTCTCCCCCG	19013
rs8238202	snp	C/T	0.128419	0.218444	synonymous-codon	Ppara	Mm_Celera	15:85798088	CTTGATGAACAAAGA[C/T]GGGATGCTGATCGCG	19013
rs8238203	snp	A/T	0.113866	0.209684	synonymous-codon	Ppara	Mm_Celera	15:85798136	CACACGCGAGTTCCT[A/T]AAGAACCTGAGGAAG	19013
rs13466761	snp	A/C	0.375	0.216506	utr-variant-3-prime	Ppara	Mm_Celera	15:85806285	CCTTGGCGTGTCTTC[A/C]TAACTCCAAGATCCA	19013
rs13475195	snp	C/T	0.375	0.216506	intron-variant, utr-variant-3-prime, downstream-variant-500B	Ppara, Cdpf1	GRCm38.p3	15:85807102	CAAACAACACAATGT[C/T]ATCTGTCTAGGGAAT	19013
rs13475196	snp	C/T	0.444444	0.157135	intron-variant, utr-variant-3-prime, downstream-variant-500B	Ppara, Cdpf1	GRCm38.p3	15:85806997	TGACTCTGTATCATA[C/T]TTATCATTAAAAACC	19013
rs16783499	snp	A/G	0.0980975	0.198559	synonymous-codon	Ppara	GRCm38.p3	15:85791012	CTTTCCCGCGAGTAT[A/G]ACCCGGGCCTTGACC	19013
rs16783500	snp	C/T	0.188366	0.242283	intron-variant	Ppara	GRCm38.p3	15:85791087	CTGGCGCTGACATAT[C/T]GCCAAGGGACATTTC	19013
rs16783501	snp	A/T	0.0980975	0.198559	intron-variant	Ppara	Mm_Celera	15:85791128	TATTTCNTGCACTGG[A/T]CAGTGTTCTCAGCCA	19013
rs16783502	snp	A/C	0.090703	0.192677	intron-variant	Ppara	Mm_Celera	15:85791137	GATAAATTCTATTTC[A/C]TGCACTGGNCAGTGT	19013
rs16783503	snp	C/T	0.290657	0.246672	intron-variant	Ppara	Mm_Celera	15:85798282	AGTGGATCTGTCACT[C/T]GCAGGNNTTCACNGG	19013
rs16783504	snp	C/T	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85798288	TCTGTCACTNGCAGG[C/T]NTTCACNGGCTTCCC	19013
rs16783505	snp	A/G	0.235537	0.249581	intron-variant	Ppara	Mm_Celera	15:85798289	CTGTCACTNGCAGGN[A/G]TTCACNGGCTTCCCC	19013
rs16783506	snp	C/T	0.463593	0.129916	intron-variant	Ppara	GRCm38.p3	15:85798295	CTNGCAGGNNTTCAC[C/T]GGCTTCCCCTTCTNT	19013
rs16783507	snp	A/G	0.165289	0.235211	intron-variant	Ppara	Mm_Celera	15:85798309	CNGGCTTCCCCTTCT[A/G]TAGGAACTCAGTGGT	19013
rs16783508	snp	G/T	0.4352	0.167931	intron-variant	Ppara	GRCm38.p3	15:85798356	ATATGTATGCCGATA[G/T]NGTGANNTGAGCTCT	19013
rs16783509	snp	A/T	0.4352	0.167931	intron-variant	Ppara	GRCm38.p3	15:85798357	TATGTATGCCGATAN[A/T]GTGANNTGAGCTCTG	19013
rs16783510	snp	C/T	0.0849383	0.187762	intron-variant	Ppara	Mm_Celera	15:85798362	ATGCCGATANNGTGA[C/T]NTGAGCTCTGGCAGG	19013
rs16783511	snp	A/G	0.0849383	0.187762	intron-variant	Ppara	Mm_Celera	15:85798363	TGCCGATANNGTGAN[A/G]TGAGCTCTGGCAGGG	19013
rs16783512	snp	G/T	0.235537	0.249581	intron-variant	Ppara	Mm_Celera	15:85798380	GAGCTCTGGCAGGGT[G/T]GGGTGATGTCTTGAG	19013
rs16783513	snp	C/T	0.231111	0.249285	intron-variant	Ppara	Mm_Celera	15:85798401	ATGTCTTGAGTAACT[C/T]CAAATTTCTGTGGAG	19013
rs16783514	snp	A/G	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85798430	AGTGGAACTGAGTGA[A/G]AACAGTATAGCTATG	19013
rs16783515	snp	A/T	0.0849383	0.187762	intron-variant	Ppara	Mm_Celera	15:85798498	TGTATAGTAGCATAT[A/T]ATATGTATACATTAA	19013
rs16783516	snp	A/C	0.0849383	0.187762	intron-variant	Ppara	Mm_Celera	15:85798525	TTAAACATATACTCC[A/C]CTGGTAATATACAAT	19013
rs16820243	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733375	CTAGAACCCCTCAAC[A/C]CCTTAGGAAGCAAAG	19013
rs16820244	in-del	-/A/C/T	0.119908	0.219859	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733474	ATAGGACAAGTCCTT[-/A/C/T]NNNNNNTCCTCTCAA	19013
rs16820251	snp	A/G	0.18	0.24	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733492	CTCTCAATACAGTCT[A/G]TCAAACAAAATTCAC	19013
rs16820252	in-del	-/G	0.095	0.19615	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733543	GAGCCATTTGAGGAG[-/G]ANATGTTCAGGATCT	19013
rs16820254	snp	A/G	0.197531	0.244432	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733597	AGTCTATGTTCCAAA[A/G]NNATTCTTCTGGACA	19013
rs16820255	snp	A/T	0.30839	0.243086	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733598	GTCTATGTTCCAAAN[A/T]NATTCTTCTGGACAG	19013
rs16820257	snp	C/T	0.362812	0.2231	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733644	AAAACCAAACAAAAC[C/T]CCCATATTTTCTCAT	19013
rs16820258	snp	C/T	0.095	0.19615	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733670	CTCATCTTGAAACCT[C/T]GGGCGCTCCAANAAT	19013
rs16820259	snp	A/G	0.117188	0.211804	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733682	CCTNGGGCGCTCCAA[A/G]AATCCCAACTGTCAT	19013
rs16820260	snp	G/T	0.099723	0.199792	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733719	TTTCTGTGTTCTCTG[G/T]GCTCAGCAGTTACTC	19013
rs16820261	snp	A/G	0.18	0.24	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733754	GGCCCCTCTCATTCC[A/G]AACCATTCTTTCCAN	19013
rs16820262	snp	A/G	0.473373	0.11227	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733769	NAACCATTCTTTCCA[A/G]ATTATTCCAAATGTC	19013
rs16820263	snp	A/G	0.152778	0.230321	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85733790	TCCAAATGTCTGGTA[A/G]AACTGGGTTAACAGC	19013
rs16820264	snp	C/G	0.095	0.19615	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734266	TCGAAGCTTGCAAAA[C/G]TGAGACCCTGgagat	19013
rs16820265	snp	A/G	0.110727	0.207612	upstream-variant-2KB, intron-variant	Ppara	GRCm38.p3	15:85734201	gatgacctggattcc[A/G]acctggggactcaca	19013
rs16820266	snp	G/T	0.172336	0.23763	upstream-variant-2KB, intron-variant	Ppara	GRCm38.p3	15:85734040	GTATGATTTCCTGAA[G/T]GGCCCAGGGGATATT	19013
rs16820267	snp	A/G	0.244898	0.249948	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734627	AGGAGCGGCGTCCTG[A/G]GGNGTTGGCACCCCG	19013
rs16820268	snp	C/T	0.408163	0.193609	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734630	AGCGGCGTCCTGNGG[C/T]GTTGGCACCCCGGGG	19013
rs16820269	snp	A/G	0.188366	0.242283	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734675	GTGACTGAAGATCCA[A/G]GGNCGACACAAGCAA	19013
rs16820270	snp	A/G	0.244898	0.249948	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734678	ACTGAAGATCCANGG[A/G]CGACACAAGCAAAGN	19013
rs16820271	snp	A/C	0.090703	0.192677	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734693	NCGACACAAGCAAAG[A/C]GGCTGCTCTGGGTCG	19013
rs16820272	snp	A/G	0.444444	0.157135	upstream-variant-2KB, intron-variant	Ppara	GRCm38.p3	15:85734711	CTGCTCTGGGTCGCA[A/G]CCTGCTCCCAGTTGC	19013
rs16820273	snp	A/G	0.35124	0.228584	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734755	CGCTGTCAGTTGGCA[A/G]AGCCCCAGTGCCTNA	19013
rs16820274	snp	A/G	0.362812	0.2231	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734769	ANAGCCCCAGTGCCT[A/G]AGCTGGACACAGTCA	19013
rs16820275	snp	A/G	0.35124	0.228584	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734816	AGCGTATGCAGAGGG[A/G]CCACAGCCCGGGGCG	19013
rs16820276	snp	A/G	0.362812	0.2231	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734854	GGCGGAGGGTGGGTC[A/G]GAGCGGCCGCGCCTC	19013
rs16820277	snp	A/C	0.090703	0.192677	upstream-variant-2KB, intron-variant	Ppara	Mm_Celera	15:85734874	GGCCGCGCCTCCCTG[A/C]GACCGTCCTCGATGC	19013
rs16820278	snp	A/G	0.287335	0.247197	upstream-variant-2KB, utr-variant-5-prime, intron-variant	Ppara	Mm_Celera	15:85735002	TCATCCTGGGACTCT[A/G]AAGATCAGATTNCGC	19013
rs16820279	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Ppara	Mm_Celera	15:85735771	CGGACTAGGGGCGCG[A/G]GTCTGGAGACCCACA	19013
rs16820280	snp	C/G	0.090703	0.192677	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85735830	GGCACACGCGTGCGA[C/G]TTTTCAGGGCCCNCG	19013
rs16820281	snp	A/G	0.090703	0.192677	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85735843	GANTTTTCAGGGCCC[A/G]CGGAACTGTCCGCCA	19013
rs16820282	snp	A/G	0.099723	0.199792	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85735955	TCCTGGAACTGGAGC[A/G]ACGCTGGGTCCTCTG	19013
rs16820283	snp	C/T	0.244898	0.249948	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736000	GGGAGGGCACACGGG[C/T]GGGGACATCGGGGCG	19013
rs16820284	snp	A/T	0.0831758	0.186198	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736049	GTGCATTTGGGCGTA[A/T]CTCACCGGGAGGCGT	19013
rs16820285	snp	C/T	0.15879	0.232768	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736078	GTTTCCTGAGACCCT[C/T]GGGGAACTTAGAGGA	19013
rs16820286	snp	C/T	0.0831758	0.186198	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736108	AGAGGTAACTGGAGG[C/T]TCCCTGACAGACTGA	19013
rs16820287	snp	C/T	0.0867769	0.189363	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Ppara	Mm_Celera	15:85736171	CCTGAGAAACGCTGC[C/T]GGTGGGTTTGAGTCA	19013
rs16820288	snp	A/G	0.099723	0.199792	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85736231	TTCCTCATTGCTCCT[A/G]ATCGTAGTGGGGCGA	19013
rs16820289	snp	G/T	0.095	0.19615	intron-variant, utr-variant-5-prime	Ppara	Mm_Celera	15:85736250	GTAGTGGGGCGATGT[G/T]GGCCCCAACAGTAGG	19013
rs16820290	snp	C/T	0.48	0.0979796	intron-variant	Ppara	Mm_Celera	15:85736755	CGGTTACAATATGTT[C/T]TNTGGATCTCCCCCA	19013
rs16820291	snp	C/T	0.444444	0.157135	intron-variant	Ppara	Mm_Celera	15:85736753	GTTACAATATGTTNT[C/T]TGGATCTCCCCCAAC	19013
rs16820292	snp	C/T	0.277778	0.248452	intron-variant	Ppara	Mm_Celera	15:85736736	GGATCTCCCCCAACT[C/T]TCCACCNCCTTGGGA	19013
rs16820293	snp	A/C	0.408163	0.193609	intron-variant	Ppara	Mm_Celera	15:85736729	CCCCAACTNTCCACC[A/C]CCTTGGGAAAGTCAC	19013
rs16820294	snp	C/T	0.117188	0.211804	intron-variant	Ppara	GRCm38.p3	15:85736658	CGCCCAAGAAAGTTC[C/T]GTGCTCCTCCCCCAA	19013
rs16820295	snp	A/G	0.260355	0.249785	intron-variant	Ppara	GRCm38.p3	15:85736409	TCCGGACTAGCACAC[A/G]GGCACTCCCGGCTCC	19013
rs16820296	snp	A/G	0.165289	0.235211	intron-variant	Ppara	GRCm38.p3	15:85737243	TGCTTCTTGGGGGCC[A/G]TCCCTGCCTGGCTAA	19013
rs16820297	snp	C/T	0.095	0.19615	intron-variant	Ppara	GRCm38.p3	15:85737214	AATGATGAAACTAAC[C/T]NACTACTTCATTGAA	19013
rs16820298	snp	A/G	0.104938	0.20361	intron-variant	Ppara	GRCm38.p3	15:85737213	ATGATGAAACTAACN[A/G]ACTACTTCATTGAAT	19013
rs16820299	in-del	-/C/CT/T	0.466759	0.178654	intron-variant	Ppara	Mm_Celera	15:85737114	AACGCAATACCACCT[-/C/CT/T]NTTTNAAACTACGCC	19013
rs16820301	in-del	-/T	0.391111	0.206368	intron-variant	Ppara	Mm_Celera	15:85737111	AATACCACCTNNTTT[-/T]AAACTACGCCGACGC	19013
rs16820302	snp	A/C	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85737083	CGCAGCCTGCCATAA[A/C]GAAATGNGGTTCCCA	19013
rs16820303	snp	C/T	0.35503	0.226867	intron-variant	Ppara	GRCm38.p3	15:85737076	TGCCATAANGAAATG[C/T]GGTTCCCATGAAGCA	19013
rs16820304	snp	C/T	0.0831758	0.186198	intron-variant	Ppara	GRCm38.p3	15:85736964	ACAAAATAACCACTA[C/T]CCAAGCCCTGTTGCT	19013
rs16820305	snp	G/T	0.0867769	0.189363	intron-variant	Ppara	GRCm38.p3	15:85736947	CAAGCCCTGTTGCTA[G/T]TCTGAAGTGCAACCA	19013
rs16820306	snp	A/G	0.4992	0.019984	intron-variant	Ppara	Mm_Celera	15:85777129	GGTTGCCAACTGCAC[A/G]GCAGCTTGGCACCTT	19013
rs16820307	snp	G/T	0.5	0	intron-variant	Ppara	Mm_Celera	15:85777264	tgcccacagaggtca[G/T]aagatcccctggaac	19013
rs16820308	snp	G/T	0.197531	0.244432	intron-variant	Ppara	Mm_Celera	15:85777304	agatgtttgtgagct[G/T]ccacgtaggtgttgg	19013
rs16820309	snp	A/G	0.0831758	0.186198	intron-variant	Ppara	Mm_Celera	15:85777367	agtactcccaactgc[A/G]gagtcatccctcnag	19013
rs16820310	snp	C/T	0.0831758	0.186198	intron-variant	Ppara	Mm_Celera	15:85777380	gcngagtcatccctc[C/T]agacccTGTTTGGAG	19013
rs16820311	snp	A/C	0.0867769	0.189363	intron-variant	Ppara	Mm_Celera	15:85777455	GCTGCCACTGCTGAG[A/C]TTTGAGCTTAGACAG	19013

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