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
rs3691523	snp	C/T	0.408163	0.193609	intron-variant	Atg16l1	Mm_Celera	1:87788072	ATCAAAGGCGTGTGC[C/T]ATCATGCCCAGCTAA	77040
rs3691529	snp	C/T	0.408163	0.193609	intron-variant	Atg16l1	Mm_Celera	1:87788077	AGGCGTGTGCTATCA[C/T]GCCCAGCTAAGGCTG	77040
rs3692232	snp	A/G	0.48	0.0979796	intron-variant	Atg16l1	Mm_Celera	1:87788218	TTAGAATTTAATGAA[A/G]ATGAAGACACATCAT	77040
rs4222498	snp	G/T	0.21875	0.248039	synonymous-codon	Atg16l1	Mm_Celera	1:87791270	ACATGTTGTCAGTGT[G/T]GACAAAGGAAGCAGA	77040
rs4222499	snp	C/T	0.21875	0.248039	utr-variant-3-prime	Atg16l1	Mm_Celera	1:87791440	AAGGTCTCTAATGGC[C/T]GAGAAGAACCAACAC	77040
rs4222500	snp	A/G	0.497041	0.0383476	utr-variant-3-prime	Atg16l1	Mm_Celera	1:87791454	CTGAGAAGAACCAAC[A/G]CTGAACCAAACTGAC	77040
rs4222501	snp	C/T	0.21875	0.248039	utr-variant-3-prime	Atg16l1	Mm_Celera	1:87791499	GCAGAGGTTCAGATT[C/T]TTGTCTGCATTTGGG	77040
rs6257942	snp	C/T	0.5	0	intron-variant	Atg16l1	Mm_Celera	1:87768921	TGTTCTGCTTTTATT[C/T]GAGGTTGATAAGATG	77040
rs6258833	snp	G/T	0.5	0	intron-variant	Atg16l1	Mm_Celera	1:87769056	ACACTCTCAGCCCCT[G/T]AAACTTCTAAGAAAA	77040
rs13461819	snp	A/T			missense, nc-transcript-variant	Atg16l1	Mm_Celera	1:87765377	TGATAGTCAACTACA[A/T]GAAATGGCCCAGTTG	77040
rs13461820	snp	C/T			intron-variant	Atg16l1	Mm_Celera	1:87786141	GGTCTCATTTCATTT[C/T]GTGATTTTGGGGGCT	77040
rs13461821	snp	C/T	0.387812	0.208586	utr-variant-3-prime	Atg16l1	Mm_Celera	1:87792171	CGTTTGTCTGTCACA[C/T]TTACTTTGCACTTTA	77040
rs13461822	snp	C/T	0.426035	0.177515	utr-variant-3-prime	Atg16l1	Mm_Celera	1:87791722	GGCTCACTGTAGGCA[C/T]TGGGTCAGTGGAAAC	77040
rs13475968	snp	A/G	0.495	0.0497494	intron-variant	Atg16l1	Mm_Celera	1:87790830	CTTCCTATTTCCAGG[A/G]CTGATTGACTAAAAT	77040
rs30554641	snp	A/C	0.493827	0.0552116	intron-variant	Atg16l1	Mm_Celera	1:87787303	CAGATGGCCACATAC[A/C]AAAGATTTGGAGTAG	77040
rs30706723	snp	C/T	0.375	0.216506	intron-variant	Atg16l1	Mm_Celera	1:87790100	TGCTCCACCACTCCC[C/T]CTAGTCCCTTGAGGC	77040
rs30947374	snp	C/T	0.444444	0.157135	intron-variant	Atg16l1	Mm_Celera	1:87786774	GATGGGGTGAGTGGA[C/T]ATCAGATGTCCACCT	77040
rs30952829	snp	A/G	0.260355	0.249785	intron-variant	Atg16l1	Mm_Celera	1:87774370	GAGAGTGGAAGGGAG[A/G]CAGGGTACCAGTGGC	77040
rs31088358	snp	A/G	0.375	0.216506	intron-variant	Atg16l1	Mm_Celera	1:87790171	GCCTGTCTTTTCCCC[A/G]GCAGGCCTGGATTTC	77040
rs31228664	snp	C/T	0.375	0.216506	intron-variant	Atg16l1	Mm_Celera	1:87761300	GCCGATACCTAGTAA[C/T]TATTAAAAACTAAGT	77040
rs31330442	snp	A/T	0.375	0.216506	intron-variant	Atg16l1	Mm_Celera	1:87780889	ATTTTGTTGCCCTCC[A/T]TGGGAGAGGTGCCAT	77040
rs31340798	snp	A/T	0.444444	0.157135	downstream-variant-500B	Atg16l1	Mm_Celera	1:87792898	ATTATATTTTATTTT[A/T]AAAATGGGAAGTTGT	77040
rs31421766	snp	A/G	0.304688	0.243945	intron-variant	Atg16l1	Mm_Celera	1:87770692	AGAAGACTTAGACTT[A/G]AGCGTCTGCAGACTG	77040
rs31460975	snp	A/G	0.493827	0.0552116	intron-variant	Atg16l1	Mm_Celera	1:87790543	GAAGTGGTCGTGCGA[A/G]GCTAAAAGTTTATAG	77040
rs31677386	snp	A/G	0.375	0.216506	intron-variant	Atg16l1	Mm_Celera	1:87770255	TGACGACCTGTGTTC[A/G]ATCCCCGGTGGGATC	77040
rs31751685	snp	A/G	0.21875	0.248039	intron-variant	Atg16l1	Mm_Celera	1:87779598	TAGCTCAGCAGTAGA[A/G]CACTTGCCTAGCTAT	77040
rs31918573	snp	C/T	0.375	0.216506	intron-variant	Atg16l1	Mm_Celera	1:87763025	CCCTGTTACTCTTTT[C/T]AACCCCTCCTAACCA	77040
rs32165594	snp	C/G	0.415225	0.187619	intron-variant	Atg16l1	Mm_Celera	1:87785362	TTCTATCACTTGTGA[C/G]AGACCTAAGTAAGAC	77040
rs32206159	snp	A/G	0.493827	0.0552116	intron-variant	Atg16l1	Mm_Celera	1:87777518	TGTGGGTGTTCATTC[A/G]TGCTAATCTTAGAAA	77040
rs32208897	snp	C/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87763674	TGCCAAGAACCTTTT[C/T]TTCAGTTGTAGTCAG	77040
rs32243229	snp	C/T	0.375	0.216506	intron-variant	Atg16l1	Mm_Celera	1:87774326	CATATGTACCCAGAG[C/T]CCCCACGCCCTGTCC	77040
rs32284376	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Atg16l1, Scarna6	Mm_Celera	1:87783342	TGCAGACTCCTTTAT[A/C]CTGGAGGAAAAGAGA	77040
rs32315583	snp	C/T	0.444444	0.157135	intron-variant	Atg16l1	Mm_Celera	1:87770647	ATATCTTTGCATTTC[C/T]TTAGGAAGCCAAAGT	77040
rs32335693	snp	C/T	0.489796	0.070696	intron-variant, downstream-variant-500B	Atg16l1, Scarna6	Mm_Celera	1:87785124	GTTTCTAAGGTTGGG[C/T]TTGTATTTCTCTTTA	77040
rs32353729	snp	A/T	0.401235	0.199068	intron-variant	Atg16l1	Mm_Celera	1:87773512	AAACCAGGCACAGCC[A/T]TGTTCTTTATTCTCT	77040
rs32354679	snp	C/T	0.444444	0.157135	intron-variant	Atg16l1	Mm_Celera	1:87770666	GGAAGCCAAAGTCAC[C/T]TAAAGATAACAGAAG	77040
rs32492989	snp	A/G	0.429688	0.173817	intron-variant	Atg16l1	Mm_Celera	1:87790537	AGCATAGAAGTGGTC[A/G]TGCGAAGCTAAAAGT	77040
rs32516394	snp	C/G	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87780800	AGCTGGCGCAGGGTG[C/G]GTCCAGAAGCTGCTC	77040
rs32618465	snp	C/G	0.401235	0.199068	downstream-variant-500B	Atg16l1	Mm_Celera	1:87792870	GTTTTAGTTCTCAAA[C/G]TAGGCTGTCTGAATT	77040
rs32661665	snp	A/G	0.375	0.216506	intron-variant	Atg16l1	Mm_Celera	1:87770356	GTGTGCACACACAAA[A/G]TGTAAAAACAAAGCC	77040
rs32792017	snp	G/T	0.5	0	intron-variant	Atg16l1	Mm_Celera	1:87778119	AAAACAAGCGTGCGC[G/T]TGTGCACACGAGCAC	77040
rs45661328	snp	A/G	0.132653	0.220748	intron-variant	Atg16l1	Mm_Celera	1:87778063	TTCAAGTTCAGTGCG[A/G]AGTCTTGTCTCAGGG	77040
rs45694089	snp	A/G	0.124444	0.216185	intron-variant	Atg16l1	Mm_Celera	1:87765916	ACCTCAAAGCCACCC[A/G]AGGTTCTCAGGAAGA	77040
rs45715138	snp	C/T	0.260355	0.249785	intron-variant, downstream-variant-500B	Atg16l1, Scarna6	Mm_Celera	1:87785299	CTGGGACTGTGTATG[C/T]AATACCTGCCTTTAT	77040
rs45785204	snp	C/T	0.124444	0.216185	intron-variant	Atg16l1	Mm_Celera	1:87773936	CACACACGTTTAGGT[C/T]TTGCTTTGGGAAATT	77040
rs45869029	snp	C/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87771734	GTCTTTGACAGTATT[C/T]AAAATCAGTTACTTG	77040
rs45974506	snp	A/C	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87765614	GGACACAACAGAGGA[A/C]CCATCAAGCAACATG	77040
rs46036711	snp	C/T	0.165289	0.235211	intron-variant	Atg16l1	GRCm38.p3	1:87787886	ATATTCCTGTAGGCT[C/T]TTTTTTTTTGGGAAT	77040
rs46085498	snp	A/G	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87786614	AAGACAGTATAAGCA[A/G]TGAGCACCGTGGGAT	77040
rs46099354	snp	C/T	0.244898	0.249948	intron-variant	Atg16l1	Mm_Celera	1:87764895	GGATGGGATGCAATA[C/T]TTGCAATGAGTGGGT	77040
rs46112948	snp	A/G	0.336735	0.234472	intron-variant	Atg16l1	Mm_Celera	1:87781449	TGAGTTTGGGGTGTT[A/G]ACTGCACTCTTGTCA	77040
rs46166889	snp	C/T	0.375	0.216506	intron-variant	Atg16l1	Mm_Celera	1:87788893	GCATATAAGGGCCTT[C/T]GAATATATTTCTTAA	77040
rs46281129	snp	A/G	0.231111	0.249285	intron-variant	Atg16l1	Mm_Celera	1:87765629	ACCATCAAGCAACAT[A/G]AGGCCTGTTAGCAGG	77040
rs46314471	snp	C/T	0.231111	0.249285	intron-variant	Atg16l1	Mm_Celera	1:87762819	TTGTTTGCTTGGAAA[C/T]GTGTTAAGAGTACTC	77040
rs46380766	snp	C/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87765870	CTGAGTCAGCCACAG[C/T]GTGGAAGCATAGACG	77040
rs46394897	snp	A/G	0.132653	0.220748	intron-variant	Atg16l1	Mm_Celera	1:87779561	GCAGATGTTCTTTGT[A/G]AAAGTTAATCAGTTG	77040
rs46438850	snp	C/T	0.132653	0.220748	intron-variant	Atg16l1	Mm_Celera	1:87782414	TTAGAGGGATCCTTA[C/T]GGTTAGCTTGCTGGT	77040
rs46445145	snp	A/G	0.231111	0.249285	intron-variant	Atg16l1	Mm_Celera	1:87767189	CTAGCCAAAGTAGCA[A/G]TGTGGGAATCGGAGA	77040
rs46471361	snp	A/T	0.124444	0.216185	intron-variant	Atg16l1	Mm_Celera	1:87764042	TGATTAACTTTTATC[A/T]CTACCCATCCACCCT	77040
rs46534822	snp	A/G	0.124444	0.216185	intron-variant	Atg16l1	Mm_Celera	1:87767488	AAAAGGAATTTTAAA[A/G]CCATCCAGTTAATAC	77040
rs46567952	snp	C/G	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87786626	GCAATGAGCACCGTG[C/G]GATGTTCCTGTAGTG	77040
rs46653169	snp	G/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87762627	TTACCTCAAACTCCT[G/T]ATTCTGTCCAGTGGT	77040
rs46738945	snp	C/T	0.260355	0.249785	intron-variant	Atg16l1	Mm_Celera	1:87788844	CACAGATATATAACG[C/T]ACCTTAAATACTCTC	77040
rs46754416	snp	A/G			intron-variant	Atg16l1	Mm_Celera	1:87778264	CGAGGCTAGAGAGAT[A/G]TCTCAGTAGTTAAGT	77040
rs46824531	snp	A/G	0.132653	0.220748	intron-variant	Atg16l1	Mm_Celera	1:87782474	AGGCTTCAGGAGCAC[A/G]TTAACTCACCACTTT	77040
rs46983413	snp	A/C			intron-variant	Atg16l1	Mm_Celera	1:87781545	ACACTTGACAAGATG[A/C]TACAATGTTATGTCA	77040
rs47022799	snp	C/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87766704	ATGGACCAGGTGTGG[C/T]GGCCAGTGTTCCCAT	77040
rs47059770	snp	A/C	0.152778	0.230321	intron-variant	Atg16l1	Mm_Celera	1:87787231	AACATAAAACATGGA[A/C]GTTTAGAAATTCACT	77040
rs47083288	snp	A/G	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87762992	TCTTGTCTGCAGTCC[A/G]CCATCTTAGGAAGTC	77040
rs47086192	snp	A/G	0.32	0.24	synonymous-codon, nc-transcript-variant	Atg16l1	Mm_Celera	1:87765371	GTGGAATGATAGTCA[A/G]CTACAAGAAATGGCC	77040
rs47137552	snp	A/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87772581	TGGTGTATTTTTTCA[A/T]ACCCACAAAGTAAAT	77040
rs47147895	snp	A/G/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87763948	GATATTTCTCTGATC[A/G/T]GGGTTAGTGGCCCTG	77040
rs47160455	snp	A/G	0.231111	0.249285	intron-variant, downstream-variant-500B	Atg16l1	Mm_Celera	1:87776811	GAACGGCTCCTGGGC[A/G]CTAGAACTTTTGGTT	77040
rs47301551	snp	C/T			intron-variant	Atg16l1	Mm_Celera	1:87772688	GTCTTTTCGCCTCTA[C/T]AATCAAGCTCTCCCA	77040
rs47376805	snp	A/C	0.124444	0.216185	intron-variant	Atg16l1	Mm_Celera	1:87787269	ACAAGTCTCCTAGCC[A/C]ATCCCTTAACTTGAT	77040
rs47459532	snp	C/T	0.124444	0.216185	intron-variant	Atg16l1	Mm_Celera	1:87779044	TAAGAGCCTTGGTGG[C/T]CTTAGAAGACAGCTC	77040
rs47605785	snp	A/G			intron-variant	Atg16l1	Mm_Celera	1:87763910	GAAATGATTACTTCT[A/G]GATCTGTTTGGGTTT	77040
rs47638532	snp	C/T	0.231111	0.249285	missense, nc-transcript-variant	Atg16l1	Mm_Celera	1:87775849	TCCCAACTACTGCCT[C/T]GTATGTCTTCGTAAG	77040
rs47679253	snp	C/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87790780	CAGTCTTTGGTTGGG[C/T]GCGAACCTCAGTGGG	77040
rs47927021	snp	C/T	0.231111	0.249285	synonymous-codon	Atg16l1	Mm_Celera	1:87790601	CCCTGATGGCAGTTA[C/T]GTGGCAGCAGGCTCA	77040
rs47953546	snp	G/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87772210	CAGACCTACTGTTAC[G/T]TAAACGTGTATTGGC	77040
rs48039776	snp	A/G	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87789965	ACCATACTTTCCTCA[A/G]GTGTATTCTGGGATT	77040
rs48072360	snp	A/G	0.231111	0.249285	intron-variant	Atg16l1	Mm_Celera	1:87762556	CCACAAGTTGTCTGG[A/G]GTTCCTCTTCCCTGG	77040
rs48121141	snp	C/T	0.260355	0.249785	intron-variant, upstream-variant-2KB	Atg16l1, Scarna6	Mm_Celera	1:87782728	TAAACGTGGAGAAGG[C/T]GCCTGGCCATTGCTA	77040
rs48160879	snp	G/T	0.124444	0.216185	intron-variant	Atg16l1	Mm_Celera	1:87770462	TGGCTAGAAAGTAGG[G/T]AGACATGATTCTGAG	77040
rs48177100	snp	A/C	0.142012	0.225474	intron-variant, upstream-variant-2KB	Atg16l1, Scarna6	Mm_Celera	1:87782616	ATACAAGCTGTGAAG[A/C]GTGAAAAGTCAGCCT	77040
rs48197054	snp	C/T			intron-variant	Atg16l1	Mm_Celera	1:87778382	AGGGATCTGATACCT[C/T]CTTCTGGCCCACACA	77040
rs48257529	snp	C/T	0.18	0.24	intron-variant	Atg16l1	Mm_Celera	1:87774457	AAACTTTATTATACA[C/T]AGTGATGAGAGCCTA	77040
rs48292593	snp	A/G	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87762662	ATTTATTTTGCCGCC[A/G]CCTTTCTTTTCATTC	77040
rs48293184	snp	G/T	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87786368	TGCCTTAAGAGCTTG[G/T]TGGGAGGCTGGTGAG	77040
rs48335157	snp	C/T			intron-variant	Atg16l1	Mm_Celera	1:87778501	CTTTCAGCAGTGTGT[C/T]TGCTTTCTGGGGGCT	77040
rs48375434	snp	C/T	0.231111	0.249285	intron-variant	Atg16l1	Mm_Celera	1:87766582	CAAGGCCCTTTGCCA[C/T]TTGGAAATGCCTGGA	77040
rs48402585	snp	A/G/T	0.132653	0.220748	intron-variant	Atg16l1	Mm_Celera	1:87773864	AGGTGCCTGGCATCC[A/G/T]CTGGGATAAAGGAGC	77040
rs48422660	snp	A/G	0.152778	0.230321	intron-variant	Atg16l1	Mm_Celera	1:87782506	GCTTTTCATTTTCCC[A/G]GAGGAGCTGTGCGGT	77040
rs48473274	snp	C/T	0.124444	0.216185	intron-variant	Atg16l1	Mm_Celera	1:87777390	GTACTTGGAGCAAAA[C/T]GTAGACATCAGCTTT	77040
rs48592924	snp	C/G	0.32	0.24	intron-variant	Atg16l1	Mm_Celera	1:87764596	TAAGTCTTGGTTCTC[C/G]GTCCCTTTCACTGAC	77040
rs48683291	snp	C/T	0.132653	0.220748	intron-variant	Atg16l1	Mm_Celera	1:87775004	CTTAATTCAGCTTGT[C/T]GTTTAGCTTCTTCCT	77040
rs48718637	snp	G/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Atg16l1	Mm_Celera	1:87789894	GGAACGGCACAGTCT[G/T]TTTGGAGGTGACACT	77040
rs48842557	snp	A/G	0.244898	0.249948	intron-variant	Atg16l1	Mm_Celera	1:87786386	GGAGGCTGGTGAGAG[A/G]ACATATAAAGAGCTG	77040
rs48886711	snp	C/T	0.244898	0.249948	intron-variant	Atg16l1	Mm_Celera	1:87787550	GTCCCATGTCTGAAG[C/T]AGCCTCAGTCAAGCT	77040

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