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
rs3697398	snp	C/T	0.444444	0.157135	intron-variant	Ppp2r2c	GRCm38.p3	5:36934639	CATATCTCACAACAC[C/T]ACCACTTGAGGTACT	269643
rs3698586	snp	A/G	0.465374	0.126941	intron-variant	Ppp2r2c	GRCm38.p3	5:36934826	AGTGTGACAGCAAGC[A/G]TTGGTCTACAGCCCA	269643
rs6203571	snp	C/T	0.484429	0.0868505	intron-variant, nc-transcript-variant	Ppp2r2c, LOC105244727	GRCm38.p3	5:36926140	acacacacaTCCCTG[C/T]ACACACATGTACACG	269643
rs6204137	snp	A/G	0.492188	0.0620098	intron-variant, nc-transcript-variant	Ppp2r2c, LOC105244727	GRCm38.p3	5:36926241	CTGCCTCCCTCTTCC[A/G]TGGGCACTCCTTCGG	269643
rs6319962	snp	A/G	0.5	0	intron-variant	Ppp2r2c	Mm_Celera	5:36879303	GTGAAGTCAGGGAGG[A/G]GAACGGCCTTGCAGG	269643
rs6321131	snp	C/T	0.5	0	intron-variant	Ppp2r2c	Mm_Celera	5:36879515	TGTAATATCACAGAA[C/T]AAATGCTCAAGTATA	269643
rs29500348	snp	G/T	0.48	0.0979796	intron-variant	Ppp2r2c	Mm_Celera	5:36914637	GCAGCTATCTGCTCC[G/T]GGGTCATCTGCAAAT	269643
rs29507963	snp	A/C	0.495	0.0497494	intron-variant	Ppp2r2c	GRCm38.p3	5:36891576	ATGTGAGCCTCACTT[A/C]TTCCAGTTGGCGCCT	269643
rs29508458	snp	C/T	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36915989	TTGGGGAGGAAAGGG[C/T]TTATTTAGCTTAAAT	269643
rs29513288	snp	A/C	0.444444	0.157135	intron-variant	Ppp2r2c	GRCm38.p3	5:36921178	CATGGTGTTAGCCGT[A/C]GTGTTGCTGGACTCT	269643
rs29523010	snp	A/G	0.48	0.0979796	intron-variant	Ppp2r2c	GRCm38.p3	5:36936974	ACCACTCTTCTCTGT[A/G]TGTCCAATAAAGACA	269643
rs29527356	snp	A/G	0.49827	0.0293608	intron-variant	Ppp2r2c	GRCm38.p3	5:36905938	TTTTCATCTGCACTT[A/G]GCCACTGGTAGGTGA	269643
rs29531170	snp	A/G	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36911695	CCACAGGGCAGGAAC[A/G]CAGTATCAGAACCCT	269643
rs29546785	snp	C/T	0.32	0.24	intron-variant	Ppp2r2c	GRCm38.p3	5:36941911	AAGCAAATTCCTATC[C/T]GCTACACCTGGGAGG	269643
rs29549263	snp	A/G	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36912035	AGAGAAGAGTAGAGC[A/G]GTGCCCTGGGGGCTG	269643
rs29549811	snp	C/T	0.444444	0.157135	intron-variant	Ppp2r2c	GRCm38.p3	5:36928361	ATACAGTTCCTCAAA[C/T]GTATGGTGACCCCAG	269643
rs29549972	snp	A/C	0.46875	0.121031	intron-variant, upstream-variant-2KB	Ppp2r2c, LOC105244727	GRCm38.p3	5:36927338	AGTGAGTAGAAGATG[A/C]AGCAGAAACAGATTG	269643
rs29555502	snp	C/G	0.5	0	intron-variant	Ppp2r2c	GRCm38.p3	5:36931212	TCCCCTGCCCTTGTG[C/G]TGCTGACCGCCTCTT	269643
rs29560172	snp	C/G	0.49827	0.0293608	intron-variant	Ppp2r2c	GRCm38.p3	5:36921028	TTTACCATCCAAGTC[C/G]GGGGCGTGTGAGTTC	269643
rs29560999	snp	C/T	0.492188	0.0620098	utr-variant-3-prime	Ppp2r2c	GRCm38.p3	5:36952691	AGAGGACAGGATGAG[C/T]GTGGTGGCCATTTGT	269643
rs29580510	snp	A/G	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36911866	AGGACAGGGGCTTGT[A/G]CAAGCCGACACAGGC	269643
rs29583535	snp	C/T	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36932785	TCCTCCCTGTGTCAC[C/T]GGCTCCTCCTCCCAT	269643
rs29583875	snp	C/T	0.408163	0.193609	intron-variant	Ppp2r2c	GRCm38.p3	5:36915810	GAACACCGCATCTTA[C/T]ATCATCGCTCTCTGT	269643
rs29588725	snp	G/T	0.42	0.183303	intron-variant	Ppp2r2c	GRCm38.p3	5:36912565	TCCCTCTGAGTGCTC[G/T]GGAGACTGAGTGTGC	269643
rs29628076	snp	A/G	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36939278	ATAGTTCCTATTCTA[A/G]TCTATTGTATAGTCC	269643
rs29629430	snp	C/T	0.498615	0.0262793	intron-variant	Ppp2r2c	GRCm38.p3	5:36904386	GGGAAGTCTTGCCCA[C/T]CTGTCATTTGGAGAG	269643
rs29634508	snp	C/T	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36911573	CCTTTAACTCCTGGC[C/T]TGATTTTCTCATCTA	269643
rs29634955	snp	A/G	0.375	0.216506	intron-variant	Ppp2r2c	Mm_Celera	5:36912219	CCCTGCGCATGGCGG[A/G]GGCTCCGGGGGAGTC	269643
rs29670724	snp	A/G	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36893247	CAGGTGGAAGGAAGG[A/G]TCTCTTCCCACACAC	269643
rs29678157	snp	G/T	0.32	0.24	utr-variant-3-prime	Ppp2r2c	Mm_Celera	5:36954333	AGAATGTGGCCAGTC[G/T]TATTTAATCCCATTG	269643
rs29679282	snp	A/G	0.484429	0.0868505	intron-variant	Ppp2r2c	GRCm38.p3	5:36903639	GGGCTGCATTTAGTG[A/G]GAGCCTCCCTGCTTT	269643
rs29679965	snp	C/T	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36904574	CCAAACTCCTGTCCC[C/T]AGGGCCTGAGAATGG	269643
rs29681002	snp	C/T	0.493827	0.0552116	intron-variant	Ppp2r2c	GRCm38.p3	5:36904130	TGTGTCCCTTTGGAG[C/T]CAGAAGTTACACACA	269643
rs29683399	snp	C/G	0.32	0.24	intron-variant	Ppp2r2c	Mm_Celera	5:36913048	CTTAGTTAGGAAGCT[C/G]CTCTCGGCTGGCCTG	269643
rs29728599	snp	A/C	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36932893	ATGACATGCTTGACG[A/C]TGGCACTAGGCATGC	269643
rs29731515	snp	C/T	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36911031	GCCCTGTCTATAAGT[C/T]AGTGGCTGGGTCGCC	269643
rs29733194	snp	A/C	0.429688	0.173817	intron-variant	Ppp2r2c	GRCm38.p3	5:36935548	TTCTGGAGCTGTTAC[A/C]TTAAATCTAAGCCAC	269643
rs29776700	snp	C/G	0.375	0.216506	intron-variant	Ppp2r2c	Mm_Celera	5:36872104	TACCATTAGTAAGTG[C/G]CTTAGAGACCATTCT	269643
rs29777691	snp	A/C	0.456747	0.140554	intron-variant	Ppp2r2c	GRCm38.p3	5:36941799	GTTCAGGTTTTATAC[A/C]GTCACAAGGACAAGT	269643
rs29817923	snp	A/G	0.415225	0.187619	intron-variant	Ppp2r2c	GRCm38.p3	5:36945145	CTTGGCTGTCATGAG[A/G]TTCCCAGGGCCAGAG	269643
rs29823848	snp	C/T	0.444444	0.157135	intron-variant	Ppp2r2c	GRCm38.p3	5:36945923	CAGCTGCTAAAGCTA[C/T]CACACCTTGGCTACC	269643
rs32662625	snp	C/T	0.35503	0.226867	intron-variant	Ppp2r2c	Mm_Celera	5:36946001	TTCATACCAGTGTGG[C/T]GGGAAGAGGCCTCTC	269643
rs32662627	snp	C/G	0.32	0.24	intron-variant	Ppp2r2c	Mm_Celera	5:36945755	CCTCAGCCTCCTCAC[C/G]ATGTTGCCCTGGAGC	269643
rs32662629	snp	C/T	0.336735	0.234472	intron-variant	Ppp2r2c	Mm_Celera	5:36943496	GAGCCAACACACTCT[C/T]TGGTATGCAAATAAA	269643
rs32662631	snp	A/G	0.142012	0.225474	intron-variant	Ppp2r2c	Mm_Celera	5:36943445	AAGAGAAGGTGAGAG[A/G]TGCAGGTGAGAGGAG	269643
rs32662633	snp	G/T	0.132653	0.220748	intron-variant	Ppp2r2c	Mm_Celera	5:36942551	CTTTCTTTTTTCTTT[G/T]AACACAAGAATTTAT	269643
rs32663225	snp	A/G	0.132653	0.220748	downstream-variant-500B	Ppp2r2c	Mm_Celera	5:36955531	GGAAGGCAGCCACTG[A/G]ATTGTGAGCAAGTCA	269643
rs32663227	snp	C/T	0.231111	0.249285	downstream-variant-500B	Ppp2r2c	Mm_Celera	5:36955522	AGAATGGGTGGAAGG[C/T]AGCCACTGAATTGTG	269643
rs32663229	snp	A/G	0.244898	0.249948	downstream-variant-500B	Ppp2r2c	Mm_Celera	5:36955500	CCTGCAGAGGCTGCA[A/G]GTTCTTAGAATGGGT	269643
rs32663231	snp	C/T	0.432133	0.171253	utr-variant-3-prime	Ppp2r2c	GRCm38.p3	5:36954385	GGCCTTACACACTGG[C/T]CTGGATCTCTGGCAC	269643
rs32663233	snp	G/T	0.345679	0.230967	utr-variant-3-prime	Ppp2r2c	Mm_Celera	5:36954382	GAGGGCCTTACACAC[G/T]GGCCTGGATCTCTGG	269643
rs32663505	snp	A/G	0.244898	0.249948	intron-variant	Ppp2r2c	Mm_Celera	5:36942468	TTGGCATAGTAACCC[A/G]TCCCTTGAGGCCTTG	269643
rs32663507	snp	C/T	0.492188	0.0620098	intron-variant	Ppp2r2c	GRCm38.p3	5:36942419	CCTTCTGCCTTCCTC[C/T]GAAGAACTGCAGGTC	269643
rs32663509	snp	C/T	0.336735	0.234472	intron-variant	Ppp2r2c	Mm_Celera	5:36942397	CTCTCTGCACTGTTG[C/T]TAGCATCCTTCTGCC	269643
rs32663511	snp	G/T	0.336735	0.234472	intron-variant	Ppp2r2c	Mm_Celera	5:36942236	AACTCACTTAGAAGC[G/T]TTGACTGCATCAGCC	269643
rs32663513	snp	G/T	0.132653	0.220748	intron-variant	Ppp2r2c	Mm_Celera	5:36942024	AGAGGTGGATCTCAC[G/T]TTGCAGTGCCTCTCT	269643
rs32664034	snp	C/T	0.473373	0.11227	utr-variant-3-prime	Ppp2r2c	Mm_Celera	5:36954052	GTGATGGAGTTTTTT[C/T]TCTCTCTCTCTCTCT	269643
rs32664035	snp	G/T	0.231111	0.249285	utr-variant-3-prime	Ppp2r2c	Mm_Celera	5:36953995	GCAGAGAGCAGAGGG[G/T]CTTTGGTTTTTACAA	269643
rs32664036	snp	A/C	0.231111	0.249285	utr-variant-3-prime	Ppp2r2c	Mm_Celera	5:36953672	GGTTTTAGAAGGGAA[A/C]CATTTCCACGCCAGG	269643
rs32664038	snp	A/G	0.244898	0.249948	utr-variant-3-prime	Ppp2r2c	Mm_Celera	5:36953570	AAGTGGGGTGCCTAG[A/G]GAGTCATACCCCGAG	269643
rs32664040	snp	C/T	0.244898	0.249948	utr-variant-3-prime	Ppp2r2c	Mm_Celera	5:36953453	CACGAGACAGGTGTC[C/T]GCTCATTTCCATAAC	269643
rs32664042	snp	A/G	0.336735	0.234472	utr-variant-3-prime	Ppp2r2c	Mm_Celera	5:36953188	GGCCGGGTCCCTCGG[A/G]TGGGTTTTTCCAGGC	269643
rs32664127	snp	G/T	0.244898	0.249948	intron-variant	Ppp2r2c	Mm_Celera	5:36941755	AGGCACTTTATACTC[G/T]GAGGGTTATGACAGG	269643
rs32664129	snp	A/C	0.244898	0.249948	intron-variant	Ppp2r2c	Mm_Celera	5:36941689	GAGAACTGAGCTGAT[A/C]AACGAGGCAGACTAA	269643
rs32664131	snp	C/T	0.244898	0.249948	intron-variant	Ppp2r2c	Mm_Celera	5:36941649	CGTGGGATGATGTCA[C/T]TGCTTTAGAGAGGGT	269643
rs32664133	snp	A/C	0.244898	0.249948	intron-variant	Ppp2r2c	Mm_Celera	5:36941603	GGTGGTCAGGGTCTT[A/C]AGTGAGGTTGACACT	269643
rs32664995	snp	C/T	0.459184	0.136902	intron-variant	Ppp2r2c	GRCm38.p3	5:36941573	GGGGTGTGGAACAGT[C/T]GGTGCACAGATGCTG	269643
rs32664997	snp	A/C	0.32	0.24	intron-variant	Ppp2r2c	Mm_Celera	5:36941340	GAAGAGCAAACATTA[A/C]AGAGGGAAGAGACAG	269643
rs32664999	snp	A/C	0.426035	0.177515	intron-variant	Ppp2r2c	GRCm38.p3	5:36941137	ATCAAATCATAGGGG[A/C]AAATGCTTCAAGTTG	269643
rs32665001	snp	C/T	0.124444	0.216185	intron-variant	Ppp2r2c	Mm_Celera	5:36940794	AGAGAAGTGGAGGTG[C/T]AGATAGTCCAGGCTT	269643
rs32665003	snp	A/C	0.32	0.24	intron-variant	Ppp2r2c	Mm_Celera	5:36940523	TCTCGCATGATGGTC[A/C]CATCCCTCCAAGGTA	269643
rs32665024	snp	C/G	0.49827	0.0293608	utr-variant-3-prime	Ppp2r2c	GRCm38.p3	5:36953003	CAGCCAGCCATGTGC[C/G]CTGGCTCAGAGCTGC	269643
rs32665027	snp	C/T	0.489796	0.070696	synonymous-codon	Ppp2r2c	GRCm38.p3	5:36952567	GGCCTGGCACCCAGC[C/T]GAGAATATCATTGCC	269643
rs32665029	snp	A/T	0.124444	0.216185	intron-variant	Ppp2r2c	Mm_Celera	5:36951297	CCTGAACTTGGTCTG[A/T]CTATGGTTAGGGACC	269643
rs32665031	snp	A/G	0.489796	0.070696	intron-variant	Ppp2r2c	GRCm38.p3	5:36951236	GTTGTCCATGTTTCT[A/G]GCCAGTGAAGAGCAA	269643
rs32665033	snp	A/G	0.5	0	intron-variant	Ppp2r2c	GRCm38.p3	5:36951206	GAGGGACCTCAGGAG[A/G]GTGTCCAAGCAATGG	269643
rs32665075	snp	C/T	0.244898	0.249948	intron-variant	Ppp2r2c	GRCm38.p3	5:36933299	CAAGTAATGTGTAGC[C/T]CCAGTTGTGTCAAAG	269643
rs32665077	snp	G/T	0.486111	0.0821678	intron-variant	Ppp2r2c	GRCm38.p3	5:36933108	GGGATTGTTGATCTC[G/T]GGGAATCTGTGCTGG	269643
rs32665079	snp	C/T	0.32	0.24	intron-variant	Ppp2r2c	Mm_Celera	5:36932995	ACGTTTTTCATCCAC[C/T]TCTGCTGTAGGCCAT	269643
rs32665081	snp	C/T	0.473373	0.11227	intron-variant	Ppp2r2c	GRCm38.p3	5:36932923	CAAAGGCCAGACGTG[C/T]GGGAGTGCTTAGTGA	269643
rs32665083	snp	A/G	0.497778	0.0332592	intron-variant	Ppp2r2c	GRCm38.p3	5:36932811	CCCATCTGGAATATG[A/G]GAATTACGCTCACCC	269643
rs32665105	snp	C/T	0.297521	0.245442	intron-variant	Ppp2r2c	GRCm38.p3	5:36907950	GCGTGCCTGCCTGGG[C/T]CCTGAGCGCCCGTGA	269643
rs32665107	snp	A/G	0.426035	0.177515	intron-variant	Ppp2r2c	GRCm38.p3	5:36907935	TGAGGGAACAAGCAC[A/G]CGTGCCTGCCTGGGC	269643
rs32665109	snp	A/C	0.497041	0.0383476	intron-variant	Ppp2r2c	GRCm38.p3	5:36907760	CCCTGCCATCCCAGC[A/C]GGCCATCTAGAGCAT	269643
rs32665111	snp	G/T	0.32	0.24	intron-variant	Ppp2r2c	Mm_Celera	5:36907570	CTTTACAGCCCAGCT[G/T]CACACCCAATGCCCA	269643
rs32665113	snp	C/T	0.415225	0.187619	intron-variant	Ppp2r2c	GRCm38.p3	5:36907543	GCTCAAGTGTGCATA[C/T]TCCAGAGTGGCCTTT	269643
rs32665125	snp	C/G	0.244898	0.249948	intron-variant	Ppp2r2c	Mm_Celera	5:36916596	ATGGGAGCCCTTCTG[C/G]AGCCTGAAGTTCAGA	269643
rs32665126	snp	G/T	0.32	0.24	intron-variant	Ppp2r2c	Mm_Celera	5:36916563	CTAGAACCTTCATTA[G/T]TAGAGAAGCTGGGTT	269643
rs32665127	snp	C/T	0.375	0.216506	intron-variant	Ppp2r2c	Mm_Celera	5:36916392	CTCGTTTAATCCTTG[C/T]GTGTATTATAACCAT	269643
rs32665128	snp	C/T	0.493827	0.0552116	intron-variant	Ppp2r2c	GRCm38.p3	5:36916374	CTATCCTGCCTCTGC[C/T]GTCTCGTTTAATCCT	269643
rs32665129	snp	A/G	0.5	0	intron-variant	Ppp2r2c	Mm_Celera	5:36916320	CAGTGCAGTGATGAC[A/G]ATGACAACGATGTAC	269643
rs32665130	snp	C/T	0.375	0.216506	intron-variant	Ppp2r2c	GRCm38.p3	5:36915830	TCGCTCTCTGTATGC[C/T]TGTTATTCATGTGTC	269643
rs32665131	snp	A/G	0.375	0.216506	intron-variant	Ppp2r2c	Mm_Celera	5:36915817	GCATCTTACATCATC[A/G]CTCTCTGTATGCCTG	269643
rs32665165	snp	C/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Ppp2r2c, LOC105244727	Mm_Celera	5:36923925	GGTACAGATGCACAC[C/G]CACTTACAGACAGAT	269643
rs32665167	snp	G/T	0.244898	0.249948	intron-variant, nc-transcript-variant	Ppp2r2c, LOC105244727	Mm_Celera	5:36923858	CAGACCCTGTGCTGA[G/T]CATTCTCCTTCCACA	269643
rs32665169	snp	C/G	0.244898	0.249948	intron-variant, nc-transcript-variant	Ppp2r2c, LOC105244727	Mm_Celera	5:36923774	AGAGACCATCCACCC[C/G]AGAGGTCATTTCTGA	269643
rs32665171	snp	A/G	0.260355	0.249785	intron-variant, downstream-variant-500B	Ppp2r2c, LOC105244727	Mm_Celera	5:36923504	AACTCTGCCCGACTG[A/G]CAGGTTTTGCTCAGG	269643
rs32665173	snp	A/G	0.260355	0.249785	intron-variant, downstream-variant-500B	Ppp2r2c, LOC105244727	Mm_Celera	5:36923176	GAGATGTGGCCCCCA[A/G]CAGGATGCAGGCCAT	269643
rs32665765	snp	A/G	0.231111	0.249285	intron-variant	Ppp2r2c	Mm_Celera	5:36940316	GTGCACTACTGTGGC[A/G]CATGCACAAGGGTGA	269643
rs32665767	snp	C/G	0.152778	0.230321	intron-variant	Ppp2r2c	Mm_Celera	5:36938880	CCAAAATAGCAGGAA[C/G]TAGAGGGCAAGCATC	269643

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