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
rs6376668	snp	C/T	0.5	0	upstream-variant-2KB	Phrf1	Mm_Celera	7:141227206	CCCCTCCATCTTAAC[C/T]ACCCCCCTGCTCCCA	101471
rs36243473	snp	C/G	0.336735	0.234472	downstream-variant-500B, utr-variant-3-prime	Phrf1, Irf7	Mm_Celera	7:141263184	ACCTGACCCAGGGCT[C/G]CACTGATTTTGAACT	101471
rs36247771	snp	G/T	0.444444	0.157135	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Phrf1	Mm_Celera	7:141228502	TGGTCCCGGGGCCGC[G/T]CCCATTCATCGCGGC	101471
rs36250893	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141233221	CATCATCTAAGGTAG[A/G]AAGGTCAGGAGCTCA	101471
rs36267339	snp	C/T	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141244055	GTCAGTATATCAAGG[C/T]CAAAGAAAAAAGGCA	101471
rs36271543	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141236181	TGGAAGTGCTCACCT[A/G]TGTAGAGGCAGAAGG	101471
rs36284984	snp	A/G	0.32	0.24	missense, nc-transcript-variant	Phrf1	Mm_Celera	7:141259309	CCCTTCTTTGGCTCT[A/G]AGGAACGGACAGTGA	101471
rs36301360	snp	C/T	0.244898	0.249948	intron-variant	Phrf1	Mm_Celera	7:141235386	AAAGTTATTCGTCAT[C/T]CCGCTATGGATGTCA	101471
rs36308395	snp	C/T	0.35503	0.226867	intron-variant	Phrf1	Mm_Celera	7:141247211	CAGCAGCCCACGGCT[C/T]TCTTCCAAGATGCAG	101471
rs36315257	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141244129	GGTTGCTTTTGGGAC[A/G]GCATCATCTTGGCTG	101471
rs36369879	snp	C/G	0.244898	0.249948	missense, nc-transcript-variant	Phrf1	Mm_Celera	7:141258296	CAGATGAGAACAGGC[C/G]CAGCCGGACACACAG	101471
rs36386174	snp	C/T	0.277778	0.248452	upstream-variant-2KB, intron-variant, utr-variant-5-prime	Phrf1	Mm_Celera	7:141228605	TCGGACAGCACACGC[C/T]CAGCAAAACACTGCT	101471
rs36390013	snp	A/T	0.459184	0.136902	intron-variant	Phrf1	Mm_Celera	7:141237418	GCTGGGTTCTGGCTG[A/T]GGCTCTGCTTAAGGG	101471
rs36394102	snp	C/T	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141235534	AACTGGGTCTCTTTA[C/T]TTTTTGTTGTTGTTT	101471
rs36414358	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141234051	CTAGAGAATGAGTCT[A/G]TCCTGGATTAATGGT	101471
rs36415797	snp	A/G	0.391111	0.206368	intron-variant, upstream-variant-2KB	Phrf1	Mm_Celera	7:141229244	GTGCTTGATGTCGCG[A/G]TTATCGTTTTCCTTA	101471
rs36422615	snp	A/C	0.244898	0.249948	intron-variant	Phrf1	Mm_Celera	7:141240990	GTAGGTGCTGTCTAT[A/C]CCTGCTTGTATTCTT	101471
rs36431194	snp	A/C	0.35503	0.226867	intron-variant	Phrf1	Mm_Celera	7:141240807	CAGTCGTGATAAGTG[A/C]TAAGTGATTGTAATA	101471
rs36433153	snp	A/G	0.124444	0.216185	intron-variant	Phrf1	Mm_Celera	7:141234870	TGAGGCTTCAGTTTA[A/G]AGGAGTCTGTGACCA	101471
rs36442934	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141244986	TATTAAAATTAACTC[A/G]TATTAGTGGTTCTTG	101471
rs36448560	snp	C/T	0.32	0.24	intron-variant	Phrf1	Mm_Celera	7:141248328	CCCAGCTCAGTGTTC[C/T]ATCCGTGGGAAGGGT	101471
rs36448583	snp	A/G	0.408163	0.193609	intron-variant	Phrf1	Mm_Celera	7:141247870	CGTATGCCCGTCTCT[A/G]TAACCTCCAGTTTTG	101471
rs36496019	snp	C/T	0.124444	0.216185	intron-variant	Phrf1	Mm_Celera	7:141244780	CCAGGAGCTGACTTT[C/T]ATCATTTCAAGGCAC	101471
rs36523382	snp	A/G	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141248259	CTCTGGTCAGTTTGC[A/G]CCATATTCAGGGATC	101471
rs36538869	snp	G/T	0.391111	0.206368	missense, nc-transcript-variant	Phrf1	Mm_Celera	7:141232471	TGATACAGGCAGTGA[G/T]CAGGATGATGACACA	101471
rs36554179	snp	A/T	0.32	0.24	missense, nc-transcript-variant	Phrf1	Mm_Celera	7:141258268	CCTCGCTCAGGTCTG[A/T]CTAGGACCCTTTCAG	101471
rs36563417	snp	A/G	0.32	0.24	missense, nc-transcript-variant	Phrf1	Mm_Celera	7:141259886	TGGACAAGCAGGAGA[A/G]TGTGACCCGGTCCCG	101471
rs36590304	snp	A/G	0.408163	0.193609	intron-variant	Phrf1	Mm_Celera	7:141243748	TCAGATGTTGAGGGT[A/G]TGTTCACTGACCAAT	101471
rs36599550	snp	C/T	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141234922	TAGGCAGGCCTGTCA[C/T]TGGAGCAGTAGCTAA	101471
rs36599608	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141234473	TGGGAGCTGGGCTGG[A/G]AGCAGAGAATTAGTG	101471
rs36609018	snp	A/C	0.32	0.24	intron-variant	Phrf1	Mm_Celera	7:141233675	AACCTTGTATTGATA[A/C]CAATTGTCCAGCTTT	101471
rs36610821	snp	A/T	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141246631	TACTGTCAGATACAG[A/T]GGGTCAAAAAGGAGA	101471
rs36636063	snp	C/T	0.132653	0.220748	intron-variant	Phrf1	Mm_Celera	7:141247884	TATAACCTCCAGTTT[C/T]GCACTTGCGTCTCAG	101471
rs36650707	snp	C/T	0.260355	0.249785	intron-variant	Phrf1	Mm_Celera	7:141236507	AGGGTAAGTTCCACT[C/T]TGTGGGTTGGTAGCA	101471
rs36650758	snp	A/G	0.124444	0.216185	missense, nc-transcript-variant	Phrf1	Mm_Celera	7:141259781	ATGAGAGTAAGAGAC[A/G]GAAGAGGCGACATTC	101471
rs36658252	snp	A/C	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141241694	ATTTTTCCTGTGCAT[A/C]AAAAGATCGGCCTTG	101471
rs36679346	snp	A/C	0.165289	0.235211	intron-variant	Phrf1	Mm_Celera	7:141236098	CCTAGCTACTGTGTT[A/C]TGCCCTCCTTTGGGA	101471
rs36687259	snp	A/G	0.124444	0.216185	intron-variant	Phrf1	Mm_Celera	7:141255540	GCCCTGCTGCCATAA[A/G]GCATATTTGGTACTT	101471
rs36705457	snp	A/G	0.336735	0.234472	missense, nc-transcript-variant	Phrf1	Mm_Celera	7:141237541	ATGGCAACGGCAGCA[A/G]TAGAGACTCAAGGGA	101471
rs36714503	snp	C/T	0.408163	0.193609	intron-variant	Phrf1	Mm_Celera	7:141242076	TGAGCCTAGGACCAG[C/T]GGCTGGGCAAGCACT	101471
rs36721569	snp	A/G	0.260355	0.249785	intron-variant	Phrf1	Mm_Celera	7:141247788	TGAAGTCATATTCCC[A/G]TGGTCAATATAGTGA	101471
rs36745753	snp	A/G	0.124444	0.216185	intron-variant	Phrf1	Mm_Celera	7:141234849	CAGTTTGTAGAAGAC[A/G]TTATTTGAGGCTTCA	101471
rs36760064	snp	C/T	0.132653	0.220748	synonymous-codon, nc-transcript-variant	Phrf1	Mm_Celera	7:141237585	CAGTGTACCCAATTC[C/T]GATGATGATGCAGAG	101471
rs36769358	snp	C/T	0.32	0.24	intron-variant	Phrf1	Mm_Celera	7:141235325	AGCAGGTCCTCTGGC[C/T]TCGCTTTGATTCTGC	101471
rs36770134	snp	C/T	0.459184	0.136902	intron-variant	Phrf1	Mm_Celera	7:141244812	AGGGTCTCCTGGGCC[C/T]TCATGCCTGTAGAAA	101471
rs36770311	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141244379	TCTGATGTACTTGAA[A/G]TCACTTTATGCTTGT	101471
rs36780236	snp	A/G	0.32	0.24	intron-variant, downstream-variant-500B	Phrf1	Mm_Celera	7:141262155	TTTGGATCTTTGGAG[A/G]AACTAAGTCTCTGAG	101471
rs36808447	snp	C/G	0.142012	0.225474	intron-variant	Phrf1	Mm_Celera	7:141233502	CAGGGCTCAGTTGGA[C/G]TGAGTTCGGGTTTCC	101471
rs36824483	snp	C/T	0.35503	0.226867	intron-variant	Phrf1	Mm_Celera	7:141244192	TTTCTATGGGTGTGG[C/T]CTATATGTGGATATG	101471
rs36856906	snp	A/G	0.231111	0.249285	intron-variant	Phrf1	Mm_Celera	7:141233967	TGCCTCAGCCTCCCA[A/G]ACTACTAGAATTAAA	101471
rs36901408	snp	A/G	0.336735	0.234472	intron-variant, downstream-variant-500B	Phrf1	Mm_Celera	7:141262335	CTTGAGATGGTCAGG[A/G]CAAGGAAGCTTGGTT	101471
rs36919403	snp	C/G	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141237078	GGGGCATTCTTAGAG[C/G]CGTAGTCATTATTTT	101471
rs36921511	snp	A/T	0.408163	0.193609	intron-variant	Phrf1	Mm_Celera	7:141238320	GGTCCTTGTGTTTGC[A/T]TAACAAATTTTCTTA	101471
rs36939857	snp	C/T	0.244898	0.249948	intron-variant, utr-variant-5-prime	Phrf1	Mm_Celera	7:141230636	GTTCTTACAGGCTTG[C/T]AAAGGAGGACTAGCA	101471
rs36960415	snp	C/T	0.277778	0.248452	intron-variant	Phrf1	Mm_Celera	7:141243938	GTTAAGTTTGTCATG[C/T]TCAGGACTGCATTGT	101471
rs37012031	snp	C/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Phrf1	Mm_Celera	7:141230278	TCTTATTTGGGGAAC[C/T]AGAGCTTGGTACAGA	101471
rs37041694	snp	A/C	0.391111	0.206368	synonymous-codon, downstream-variant-500B, nc-transcript-variant	Phrf1	Mm_Celera	7:141261889	CAAGGACATACTGCG[A/C]AAAGCCGTGCAGAAG	101471
rs37042277	snp	A/G	0.260355	0.249785	missense, nc-transcript-variant	Phrf1	Mm_Celera	7:141258488	TCCATCGGGATGGCA[A/G]TAAGAGCACGCAGGA	101471
rs37049600	snp	A/T	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141235150	TATTTGGCAAGCCAA[A/T]TGAGAGTCCAGTGAG	101471
rs37070243	snp	G/T	0.444444	0.157135	intron-variant	Phrf1	Mm_Celera	7:141245441	AGGATTTTCAGTTCC[G/T]GCCACTGACATAATA	101471
rs37072458	snp	C/G	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141236906	TAATGCCGAGATCGA[C/G]TAGCTCTTTTATAGT	101471
rs37088046	snp	G/T	0.124444	0.216185	intron-variant	Phrf1	Mm_Celera	7:141242233	ACCACGAAGTGTTCC[G/T]GCATCACAGGCTCAT	101471
rs37089020	snp	A/T	0.408163	0.193609	intron-variant	Phrf1	Mm_Celera	7:141245371	TCTGGTGTATGATGT[A/T]ACATGGACCACATTG	101471
rs37153167	snp	C/T	0.244898	0.249948	intron-variant	Phrf1	Mm_Celera	7:141256477	CATTCATTTAATTTT[C/T]TTCCTGTCACGTTGG	101471
rs37154517	snp	A/C	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141231715	TGTCTTGTTTTTAAG[A/C]TGGTGTGGTTCAGAC	101471
rs37169695	snp	C/T	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141235518	TGTGTTTTTATGGAT[C/T]AACTGGGTCTCTTTA	101471
rs37169797	snp	A/G	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141244775	TGTACCCAGGAGCTG[A/G]CTTTCATCATTTCAA	101471
rs37173361	snp	A/G	0.124444	0.216185	intron-variant	Phrf1	Mm_Celera	7:141230908	GCTCTGTTTCAGCGC[A/G]TATGTCTGTCTGGTT	101471
rs37179689	snp	A/G	0.132653	0.220748	intron-variant	Phrf1	Mm_Celera	7:141230950	TAGGACTCTTCAGGA[A/G]TGCTTGGGTGAGAGC	101471
rs37200272	snp	C/T	0.260355	0.249785	upstream-variant-2KB	Phrf1	Mm_Celera	7:141226368	ATGCAATTGAATGGT[C/T]CACAGAAAAGGGAGG	101471
rs37205716	snp	A/G	0.32	0.24	upstream-variant-2KB	Phrf1	Mm_Celera	7:141226922	TCCCAGCAAATCAGC[A/G]AATTTACTGCATAGT	101471
rs37210459	snp	G/T	0.336735	0.234472	intron-variant	Phrf1	Mm_Celera	7:141240027	CCTCAGTTTATACAT[G/T]TATCAGAATTTAGTG	101471
rs37262054	snp	C/G	0.124444	0.216185	intron-variant, downstream-variant-500B	Phrf1	Mm_Celera	7:141261719	TCTCGCCAATGGGCC[C/G]GCAGGTCAGTTTTGG	101471
rs37270883	snp	C/T	0.32	0.24	intron-variant	Phrf1	Mm_Celera	7:141233630	GGACAGTACTCATCA[C/T]ACAGGAGTAGAACTG	101471
rs37274417	snp	C/T	0.32	0.24	intron-variant	Phrf1	Mm_Celera	7:141234447	ATGAACAGGAGCTAG[C/T]CATATACTTGTGGGA	101471
rs37292929	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141262370	TGATCTTTGTGACAA[A/G]TCGAGAGAGCACTCA	101471
rs37296352	snp	A/G	0.426035	0.177515	missense, nc-transcript-variant	Phrf1	Mm_Celera	7:141258349	TCCAATGTACGGGTT[A/G]GTTCTGCCTCGACTA	101471
rs37312748	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141240396	GTTCACCCAGTTCTA[A/G]CATCTTAGCATAGGC	101471
rs37332506	snp	C/T	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141247710	TCCTCATGCCTGGCT[C/T]CTGGCACTCAGATGA	101471
rs37337134	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141231751	TTGAACCCTTGACTC[A/G]TGTGATCAGCCCAGC	101471
rs37398610	snp	A/G	0.152778	0.230321	intron-variant	Phrf1	Mm_Celera	7:141248566	TTCTGGAGTCCAGAT[A/G]TGTGGTCATTTCTGA	101471
rs37472093	snp	A/G	0.391111	0.206368	intron-variant, upstream-variant-2KB	Phrf1	Mm_Celera	7:141229887	CCAGGCAGGAGCAAC[A/G]TGTGACAATTGACAT	101471
rs37506569	snp	C/T	0.396694	0.202437	intron-variant	Phrf1	Mm_Celera	7:141256993	TCCTTCCCATGTGGC[C/T]CTTGGTGATGTGGCT	101471
rs37565933	snp	C/T	0.426035	0.177515	intron-variant	Phrf1	Mm_Celera	7:141240204	GATGCTCAGGGTCTA[C/T]TGAGCAGTTCACAGA	101471
rs37568503	snp	A/C	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141233487	GCCAGTATACAAACA[A/C]AGGGCTCAGTTGGAC	101471
rs37587813	snp	C/T	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141235406	TATGGATGTCATGAT[C/T]TTTCAAAATGTTATG	101471
rs37598454	snp	C/G	0.408163	0.193609	intron-variant	Phrf1	Mm_Celera	7:141245395	CACATTGCATGTGAC[C/G]TTCCAGTAAGGGCCA	101471
rs37601893	snp	C/T	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141232404	TGGGGCCTGTGCTTT[C/T]ACCTTGTGATCTAGA	101471
rs37641560	snp	A/G	0.48	0.0979796	intron-variant	Phrf1	Mm_Celera	7:141256317	CAGCTGAGGGTGTTG[A/G]CTCTGTTCAATCCTT	101471
rs37697191	snp	A/G	0.408163	0.193609	intron-variant	Phrf1	Mm_Celera	7:141245916	TGCTTCCCTGGCTCC[A/G]GGCTCATAATACAAG	101471
rs37713114	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141233413	CTGTCTGGTGGGAGC[A/G]TTTTCTCAGTTGAGG	101471
rs37721197	snp	A/C	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141257263	GGTGATCTCCCCACA[A/C]GCTTGATCCCCGAGA	101471
rs37741395	snp	C/T	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141234555	TGAGATAAGCCCAAT[C/T]CTGCACCTAGTGCAA	101471
rs37776217	snp	A/C	0.231111	0.249285	intron-variant	Phrf1	Mm_Celera	7:141260862	TTCTAACAGACACAT[A/C]TGCAGCTCGGCCTCG	101471
rs37817752	snp	C/T	0.32	0.24	intron-variant, downstream-variant-500B	Phrf1	Mm_Celera	7:141262023	TCTAGTTTGCATGGA[C/T]TCCTGGGTCTGTAAG	101471
rs37889329	snp	A/G	0.426035	0.177515	intron-variant	Phrf1	Mm_Celera	7:141240273	AGATGCCGTCTACCC[A/G]GTCTTTCCCTTCCCT	101471
rs37889453	snp	A/T	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141236497	TTGATCAGCGAGGGT[A/T]AGTTCCACTCTGTGG	101471
rs37916879	snp	A/T	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141236137	TAGCTGTTTGTGTCC[A/T]TCTATGCCAGCAAGA	101471
rs37995779	snp	A/G	0.391111	0.206368	intron-variant	Phrf1	Mm_Celera	7:141234069	CTGGATTAATGGTAC[A/G]GACATGGCTCTTTTG	101471
rs37999266	snp	C/G	0.32	0.24	intron-variant	Phrf1	Mm_Celera	7:141231784	AGCCTCCCAAAGTGC[C/G]GGTAGCTAAGACTAC	101471

Full records

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