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
rs6297342	snp	A/G	0.5	0	intron-variant	Phf2	Mm_Celera	13:48812204	CTCCCTACGCCTCAG[A/G]TTCCCCAATTATCNA	18676
rs6297360	snp	A/C	0.5	0	intron-variant	Phf2	Mm_Celera	13:48812218	GNTTCCCCAATTATC[A/C]AGTTAAAGTCTGAAG	18676
rs6297936	snp	A/G	0.5	0	intron-variant	Phf2	Mm_Celera	13:48812299	CGTGGAGGGTCTTGC[A/G]GTGGGGGGAGAGGGG	18676
rs6297966	snp	A/C	0.5	0	intron-variant	Phf2	Mm_Celera	13:48812318	GGGGGAGAGGGGGGT[A/C]CAGGCTGTGCCCCAT	18676
rs6298006	snp	G/T	0.5	0	intron-variant	Phf2	Mm_Celera	13:48812336	GGCTGTGCCCCATCA[G/T]TCACCTATCAGTGCC	18676
rs6298561	snp	C/T	0.5	0	intron-variant	Phf2	Mm_Celera	13:48812424	AACCCAAGTCAGCAA[C/T]GCATGAATCTAACTG	18676
rs6351705	snp	A/G	0.5	0	intron-variant	Phf2	Mm_Celera	13:48853730	GACTCTAAACACAGG[A/G]GGTGAGCTTAATCTC	18676
rs6352216	snp	G/T	0.5	0	intron-variant	Phf2	Mm_Celera	13:48853821	AAGACTTCTTACAAC[G/T]CCAGGAGATCCCCCA	18676
rs6353747	snp	C/T	0.5	0	intron-variant	Phf2	Mm_Celera	13:48854100	GTGATTGGCTGGAGC[C/T]GGGGACAGGCNGGAA	18676
rs6353763	snp	A/C	0.5	0	intron-variant	Phf2	Mm_Celera	13:48854111	GAGCNGGGGACAGGC[A/C]GGAAGAGGGGTGGAC	18676
rs13470923	snp	A/G			missense	Phf2	GRCm38.p3	13:48807715	AGATTGGTGGTGGCA[A/G]CAAAGGCACAGGCAA	18676
rs45635301	snp	A/C	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48841076	TCCCTGATGACAGTG[A/C]TCTAAGTCCTCTCTA	18676
rs45641088	snp	C/T	0.391111	0.206368	intron-variant	Phf2	Mm_Celera	13:48837699	CCGTCCCTGCAGAGT[C/T]CCATCTCACTACAAG	18676
rs45690174	snp	G/T	0.375	0.216506	intron-variant	Phf2	Mm_Celera	13:48831449	CTTTCACAATAAACA[G/T]CAGAAACCCACCAAC	18676
rs45698062	snp	C/T	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48819254	CAGATGTGTGGTCAC[C/T]GCGCCAGCTGCCTCC	18676
rs45707365	snp	A/G	0.21875	0.248039	intron-variant	Phf2	Mm_Celera	13:48857123	TTGGCCTGTCACTGG[A/G]TGCTGCTGTGCGTGC	18676
rs45715033	snp	A/G	0.297521	0.245442	intron-variant	Phf2	Mm_Celera	13:48856197	GCTGTCTCACCTTCC[A/G]GAGTCATAGGACATT	18676
rs45715536	snp	A/C	0.48	0.0979796	intron-variant	Phf2	Mm_Celera	13:48849254	CAGAGCCTCACTGGC[A/C]CTCCAGCTTCCACAA	18676
rs45722831	snp	A/G	0.152778	0.230321	intron-variant	Phf2	Mm_Celera	13:48856023	AGCACCATGATACCC[A/G]CCAAGTGCCACTGGA	18676
rs45729497	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Phf2	Mm_Celera	13:48803118	CACTGGTCAAGTGAT[A/G]TAAGCCTCGCTCAGG	18676
rs45796003	snp	C/T	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48815339	TCCCTGCTGCCTCGC[C/T]GGCCCACACTGAGGC	18676
rs45797377	snp	A/G	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48855615	CTAACCTCCTGTAGC[A/G]TGACAGTTTCCCACT	18676
rs45797984	snp	A/G	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48819051	AAGCTGGCATCCTGC[A/G]GTCTTTGAGAAGCAG	18676
rs45835497	snp	A/G	0.21875	0.248039	intron-variant	Phf2	Mm_Celera	13:48859623	CACACTTGCCTGAAC[A/G]TTGGCCTCTGCCTGG	18676
rs45841781	snp	C/T	0.244898	0.249948	intron-variant	Phf2	Mm_Celera	13:48814539	GGTCTTCAGGACATA[C/T]TTTTCTCAACAGGAG	18676
rs45849081	snp	G/T	0.244898	0.249948	intron-variant	Phf2	Mm_Celera	13:48817049	GCCTTCTCCTAGTGC[G/T]CTCAAACAGATGCAC	18676
rs45883370	snp	C/T	0.165289	0.235211	intron-variant	Phf2	Mm_Celera	13:48855926	ACTGGTAGGACCAGG[C/T]GCTTACAGGGGAGAG	18676
rs45888197	snp	C/T	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48818818	TTGGTGAAGACAGGC[C/T]ATGGACATGATTCCC	18676
rs45890107	snp	A/G	0.260355	0.249785	intron-variant	Phf2	Mm_Celera	13:48828567	GCTCAGATGCCCAGC[A/G]CTCATTTAAAATGGA	18676
rs45892834	snp	C/T	0.277778	0.248452	intron-variant	Phf2	Mm_Celera	13:48821327	TTGCACCAGTTGAAG[C/T]GTTCCTTAGGAAGAC	18676
rs45894532	snp	A/G	0.165289	0.235211	intron-variant	Phf2	Mm_Celera	13:48857789	GCCTGGCTTTGTGTC[A/G]AACGTTGAGAAGGGC	18676
rs45913769	snp	A/G	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48821806	GGATGCTGGTGTGGC[A/G]GGTAGAGCCTACTGG	18676
rs45913877	snp	A/G	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48837426	TTTAGGGCCTTAACC[A/G]AGCTAGACAAGGATT	18676
rs45928821	snp	C/T	0.336735	0.234472	intron-variant	Phf2	Mm_Celera	13:48815766	ATGTCACATATACAC[C/T]GCATGCAGACTCAAG	18676
rs45960341	snp	A/C	0.260355	0.249785	intron-variant	Phf2	Mm_Celera	13:48831432	TCAGCTGCCCATGTG[A/C]GCTTTCACAATAAAC	18676
rs46057250	snp	C/T	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48803949	ACCTGTGGGTAGCCA[C/T]GCCGCTGAAACTTGA	18676
rs46111349	snp	A/C	0.277778	0.248452	intron-variant	Phf2	Mm_Celera	13:48850645	CCAACACTGGCACAA[A/C]CCTATAACTGAGCCT	18676
rs46138327	snp	C/T	0.5	0	intron-variant	Phf2	Mm_Celera	13:48852142	GTACAGAGCTGGTGA[C/T]AGGATAGCCCACCGC	18676
rs46169462	snp	A/T	0.42	0.183303	intron-variant	Phf2	Mm_Celera	13:48856886	ACGTTGAATGAATGG[A/T]AGTACTCAGCAACCG	18676
rs46184047	snp	C/G	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48814898	ACTTGGGACCTGTCT[C/G]TCCATCACCCACAGT	18676
rs46197815	snp	C/T	0.444444	0.157135	intron-variant	Phf2	Mm_Celera	13:48843509	TGAGTCTTAGTTTGC[C/T]TAGGAAACTTTGACT	18676
rs46212599	snp	C/T	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48835515	ACAGTTGCAGCTCAC[C/T]ACATGGACCCAGTGA	18676
rs46276329	snp	A/G	0.336735	0.234472	intron-variant	Phf2	Mm_Celera	13:48827411	CACACAGAAGGAGAT[A/G]TAAGGGACACACAAG	18676
rs46277420	snp	C/T	0.32	0.24	intron-variant	Phf2	Mm_Celera	13:48844151	GAAGATCAGGGAACA[C/T]ACGGAATCCTGAGCC	18676
rs46278656	snp	A/T	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48824936	GGCAGTTCAGTCCTG[A/T]GTAGGTGAGTACGCA	18676
rs46302217	snp	C/T	0.375	0.216506	intron-variant	Phf2	Mm_Celera	13:48852128	CCCCAGATACACAAG[C/T]ACAGAGCTGGTGATA	18676
rs46313743	snp	C/T	0.142012	0.225474	intron-variant	Phf2	Mm_Celera	13:48806308	CCTGCATGGCCACTA[C/T]GGAGCTTCCCGGGCT	18676
rs46402429	snp	G/T	0.18	0.24	intron-variant	Phf2	Mm_Celera	13:48857730	AAAGCCTTCAGTCTA[G/T]CTGGCTGGCTCTGCT	18676
rs46477319	snp	G/T	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48821308	AGCTGCTCAGGACTT[G/T]ACATTGCACCAGTTG	18676
rs46496067	snp	A/G	0.142012	0.225474	intron-variant	Phf2	Mm_Celera	13:48858079	TCTCTCTGGTCTCCA[A/G]GCAGTCATTTCTCAC	18676
rs46498306	snp	A/G	0.408163	0.193609	intron-variant	Phf2	Mm_Celera	13:48836165	TGTCCAGAAGCCACC[A/G]GTGAACACTATGCAG	18676
rs46582411	snp	C/T	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48852067	TCCACACCTGACTGA[C/T]TCGTTCACTACCCTT	18676
rs46591866	snp	C/T	0.277778	0.248452	intron-variant	Phf2	Mm_Celera	13:48834753	AGCTCAAAGCCCACT[C/T]AGATGAAACTGCATG	18676
rs46610071	snp	A/G	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48820199	CTTCAAACAGACCAC[A/G]CAAGGGAGAGCCCAG	18676
rs46621185	snp	A/G	0.152778	0.230321	intron-variant	Phf2	Mm_Celera	13:48810493	AGAGACATTTCCTGA[A/G]CCCGAGGAGAGGGAA	18676
rs46662289	snp	C/T	0.444444	0.157135	intron-variant	Phf2	Mm_Celera	13:48840091	GGATTGGCATTCTGT[C/T]GATGCCCAGTCAGAG	18676
rs46667173	snp	A/G	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48821406	TCCCATGCCAAAGTC[A/G]GCTGGCCACACAGCC	18676
rs46678364	snp	A/T	0.5	0	intron-variant	Phf2	Mm_Celera	13:48843504	CCAAGTGAGTCTTAG[A/T]TTGCCTAGGAAACTT	18676
rs46711693	snp	C/T	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48827025	CAGAAGGTTCACAAC[C/T]AAGAGAGGAGGAAAT	18676
rs46716926	snp	A/G	0.375	0.216506	intron-variant	Phf2	Mm_Celera	13:48848750	ACACCTGGGCACCCC[A/G]AGAGCTTGCAGCAGG	18676
rs46740973	snp	C/T	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48857170	ATGGCTGAAGGTGTT[C/T]AGTTTATCGCAGCTC	18676
rs46745747	snp	C/T	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48840527	TATTCACACCGGCCA[C/T]TGAGAATTCACACCA	18676
rs46750917	snp	C/G	0.165289	0.235211	intron-variant	Phf2	Mm_Celera	13:48862189	AGGATTTCATCACAG[C/G]AGTGAGCACAGCACA	18676
rs46793130	snp	A/T	0.32	0.24	intron-variant	Phf2	Mm_Celera	13:48851376	ACATAATCCATATGG[A/T]CAGGAAATCGTTCCT	18676
rs46803959	snp	A/G	0.260355	0.249785	intron-variant	Phf2	GRCm38.p3	13:48823451	GAGATGCTTCTCAAC[A/G]GTGCCTTGTGTGCCA	18676
rs46839645	snp	A/G	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48803749	AGCGACAGGAGGAGA[A/G]GATCCCACATGACTC	18676
rs46916694	snp	C/G	0.142012	0.225474	intron-variant	Phf2	Mm_Celera	13:48818266	ACATCTCCCTAGCAG[C/G]TTCCCTTGGTCCTAG	18676
rs46986001	snp	A/G	0.391111	0.206368	intron-variant	Phf2	Mm_Celera	13:48824877	TGCTGGGACCTCTAC[A/G]TGTGGCCTCATAGGT	18676
rs47000636	snp	A/G	0.336735	0.234472	intron-variant	Phf2	Mm_Celera	13:48841057	CACTGAGCACATCTC[A/G]GTGTCCCTGATGACA	18676
rs47001222	snp	A/G	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48816366	TGTGACTCCAGGCTC[A/G]CACAGACTTTCCTCG	18676
rs47030390	snp	A/G	0.32	0.24	intron-variant	Phf2	Mm_Celera	13:48841923	ATAAAGACAATTCAG[A/G]ACAATGGAACAGCTT	18676
rs47052726	snp	C/T	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48824766	AACCACAGCCTAGTC[C/T]TGTTGGCCCAGTCTG	18676
rs47181062	snp	A/C	0.244898	0.249948	intron-variant	Phf2	Mm_Celera	13:48829203	TGCATGCTGGCCACC[A/C]TTTGTACTGCAGCAG	18676
rs47183726	snp	A/G	0.244898	0.249948	intron-variant	Phf2	Mm_Celera	13:48834954	AATAGGGCCACACAC[A/G]TATGGGGCTTGCCTG	18676
rs47199339	snp	C/T	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48803824	CCGGGTTTAGAAATC[C/T]CCCATGGACCCAACG	18676
rs47214381	snp	C/T	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48815371	GTACTCTCTATGGTC[C/T]CTGCAGCTCGGACTG	18676
rs47238855	snp	C/T	0.32	0.24	intron-variant	Phf2	Mm_Celera	13:48842084	TGTACAAAGATCACT[C/T]GAAGAAATGGTATCT	18676
rs47262772	snp	C/T	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48838575	AATGTACCTCAAATT[C/T]AGGCAAGATTTGTCC	18676
rs47275911	snp	C/T	0.48	0.0979796	intron-variant	Phf2	Mm_Celera	13:48844161	GAACATACGGAATCC[C/T]GAGCCCAGCATTTTT	18676
rs47396553	snp	C/T	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48820445	CAGCATAGCAACCCA[C/T]AGGCTGAGCCCAGAA	18676
rs47429283	snp	A/G	0.297521	0.245442	intron-variant	Phf2	Mm_Celera	13:48830273	TAAAAGAGCCTGCCA[A/G]CAGGTCTGTTCATAT	18676
rs47469773	snp	C/T	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48833668	CCAGGGCAGTGTGAC[C/T]CTAGCATCTTCCAGA	18676
rs47492983	snp	A/G	0.142012	0.225474	intron-variant	Phf2	Mm_Celera	13:48819257	ATGTGTGGTCACCGC[A/G]CCAGCTGCCTCCTGG	18676
rs47500816	snp	A/G	0.336735	0.234472	intron-variant	Phf2	Mm_Celera	13:48841032	GTGTTACTCAGCTCC[A/G]CAGCTGTTTCACTGA	18676
rs47669495	snp	C/T	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48825151	TTCCTGAGTGTGAAA[C/T]GTCCCTAAGTGTGTC	18676
rs47682560	snp	A/G	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48835762	AAGCTTCGCTCGCTC[A/G]GGAGACAGCGACTGG	18676
rs47690685	snp	A/C	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48818054	CAAGAAATGTTCACA[A/C]ATCCCTACAGCCCAC	18676
rs47719201	snp	A/G	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48823785	CCTGCTGGTACATGG[A/G]GAAGCACCTATTGGA	18676
rs47757285	snp	A/C/G	0.132653	0.220748	intron-variant	Phf2	GRCm38.p3	13:48840834	CTCACAGGAGCCACG[A/C/G]AGCATTCGTACGGGC	18676
rs47771202	snp	C/T	0.35503	0.226867	intron-variant	Phf2	Mm_Celera	13:48837770	CAGGGATCATGTGAC[C/T]GTCACCCACTTCTGA	18676
rs47781588	snp	A/G	0.32	0.24	intron-variant	Phf2	Mm_Celera	13:48823438	TTGGCGCTCAGAAGA[A/G]ATGCTTCTCAACGGT	18676
rs47829093	snp	G/T	0.345679	0.230967	intron-variant	Phf2	Mm_Celera	13:48834104	CCAGGCCCCAGAAGA[G/T]CCAAGACACAGCAGA	18676
rs47841213	snp	G/T	0.231111	0.249285	intron-variant	Phf2	Mm_Celera	13:48803985	CTGGAGTATAGGTCG[G/T]CGGGATAAGGGAGGC	18676
rs47904723	snp	C/G	0.124444	0.216185	intron-variant	Phf2	Mm_Celera	13:48828163	TCACCAGGGATGGAT[C/G]AAACCATGTTCAGCT	18676
rs47916275	snp	A/C	0.244898	0.249948	intron-variant	Phf2	Mm_Celera	13:48819667	TAGTTAGTGTGGTGT[A/C]TGCTTAGCCTGCCCC	18676
rs47916277	snp	A/G	0.132653	0.220748	intron-variant	Phf2	Mm_Celera	13:48833376	TATGCCTTCCCCAGC[A/G]GATAGGTTGTTGACA	18676
rs47968898	snp	C/G	0.46281	0.131194	intron-variant	Phf2	Mm_Celera	13:48852323	AAAGTACTCTCGGGG[C/G]TGAGGCCACGGTGGA	18676
rs47992656	snp	C/G	0.32	0.24	intron-variant	Phf2	Mm_Celera	13:48862104	AGCCTAAAAAATGTG[C/G]CCAAGTCACCACATC	18676
rs47995360	snp	C/T	0.32	0.24	synonymous-codon	Phf2	Mm_Celera	13:48817521	CTTCCCTTTCTTCGG[C/T]GGCTCCATCTTGGTC	18676
rs48002150	snp	C/G	0.391111	0.206368	intron-variant	Phf2	Mm_Celera	13:48835499	GCAGTGGGAGTCACA[C/G]ACAGTTGCAGCTCAC	18676

Full records

It may take some time, please wait.