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
rs6291718	snp	A/C	0.5	0	intron-variant	Psen2	Mm_Celera	1:180250511	ACAGTGGAGAGAGGC[A/C]CAGGATTGCCCTGAT	19165
rs30473421	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263759	TTTTGCTTGCATTTA[C/T]ATCTGTGCACGGTGT	19165
rs30505573	snp	C/T	0.444444	0.157135	intron-variant	Psen2	Mm_Celera	1:180231650	TCTGTGACTTTGCCT[C/T]CTCTTGCTGCCTCCT	19165
rs30507380	snp	A/G	0.444444	0.157135	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180260443	CATGCATATATTCAC[A/G]TATACCATCTATCTA	19165
rs30616461	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Psen2, Gm31728	GRCm38.p3	1:180255303	AGTCATTTCACAACC[A/G]TTCATATCTTTAAAG	19165
rs30667956	snp	C/T	0.260355	0.249785	intron-variant	Psen2, Gm31728	Mm_Celera	1:180262285	TAAGAGTTGTATAAC[C/T]GATGCACTTATCTTT	19165
rs30670767	snp	A/G	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180250302	TGGACCGTGTGCAGA[A/G]GACAGGCTGTTCTGG	19165
rs30984606	snp	C/T	0.345679	0.230967	downstream-variant-500B	Psen2	Mm_Celera	1:180226715	GGACATCTGTCAAAG[C/T]AACCACTCAGCTTTT	19165
rs31052399	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180245470	AGGGGAGAGGACATT[C/T]CCTTATGATCTCCAT	19165
rs31126107	snp	A/T	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180251357	CTGCATAGACTAGTG[A/T]GACATGAACCATACT	19165
rs31153288	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254591	GAGCAACCACAGAAG[A/G]GCCACTGGACAGGGT	19165
rs31302683	snp	C/T	0.495868	0.0452663	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180261326	AATTGTCATGGTCTA[C/T]ACTTGAAACTTTAAT	19165
rs31344197	snp	C/T	0.444444	0.157135	intron-variant	Psen2	Mm_Celera	1:180231003	ACATGAAGGGACCTA[C/T]GGGCTCCAGCTGCAT	19165
rs31417850	snp	C/G	0.375	0.216506	intron-variant	Psen2	Mm_Celera	1:180250139	AGCATAGAAAAACAA[C/G]CCCCGCTGGATCCGC	19165
rs31431681	snp	A/G	0.345679	0.230967	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180260167	TCCCAGTCATGAACA[A/G]GTATGGTTGTTTTGC	19165
rs31450547	snp	C/T	0.489796	0.070696	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255132	AAGGCCTGAGAGGCT[C/T]AGGTGTCCACAGAGG	19165
rs31462499	snp	A/G	0.48	0.0979796	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180259781	CTCTTCACAGCAATG[A/G]AACTAAGTCAGGGGG	19165
rs31548221	snp	A/G	0.5	0	intron-variant	Psen2	Mm_Celera	1:180231084	GCTCTGTGGAAGCTC[A/G]ATGCCCCAGCATAGG	19165
rs31562572	snp	C/T	0.375	0.216506	intron-variant	Psen2	GRCm38.p3	1:180233557	ACTTCCACGCCTCCA[C/T]GAAAGGCCACCTGCT	19165
rs31651455	snp	C/T	0.375	0.216506	intron-variant	Psen2	Mm_Celera	1:180228192	CAAATCACCAAAGTG[C/T]CTGCCCTGCCCTTGG	19165
rs31670154	snp	A/G	0.5	0	intron-variant, downstream-variant-500B	Psen2, Gm31728	GRCm38.p3	1:180258797	GTAGATGAACAGATG[A/G]GCAAATGGGTTCTAG	19165
rs31709105	snp	A/G	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180250776	CCCCTGGAAAGTCCC[A/G]GTCTTCCTCCACACT	19165
rs31763341	snp	A/C	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180230020	GAAAGCCTGCAGAGC[A/C]CCTCTGTCCCGAGGC	19165
rs31771102	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180248549	AGTACCTCCCACTCC[C/T]ATGACTTGTAGGGAT	19165
rs31774241	snp	C/G	0.32	0.24	intron-variant	Psen2, Gm31728	Mm_Celera	1:180259758	AAGAGTTGCCATGGT[C/G]ATGGTGTCTCTTCAC	19165
rs31819863	snp	C/T	0.444444	0.157135	intron-variant	Psen2, Gm31728	Mm_Celera	1:180260404	TGCTGATAATAATTA[C/T]GTATGTATATGTGTG	19165
rs31819908	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255953	CCAGAGCTGCACCCT[A/G]CGCTCCTTCCAAGCC	19165
rs31837949	snp	C/T	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180236576	AGAATGAAAGGGAAG[C/T]CCAGGCAAGGGTGGG	19165
rs31849057	snp	C/T	0.260355	0.249785	intron-variant	Psen2, Gm31728	Mm_Celera	1:180262450	CTTTCACTCTCTTTT[C/T]CCATTTTTCCAAAGC	19165
rs31852556	snp	C/T	0.486111	0.0821678	intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258833	GTGGACAGAGTATTG[C/T]CTAAAGGAGCTGCTC	19165
rs31870962	snp	G/T	0.375	0.216506	intron-variant	Psen2	Mm_Celera	1:180250171	CAGGAGGTCCTGGGG[G/T]AGCCTGACTCAGCAC	19165
rs31893827	snp	A/G	0.277778	0.248452	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254719	TTCATTTCCACATAC[A/G]AATGGATGTACAGCC	19165
rs31947168	snp	C/T	0.32	0.24	intron-variant	Psen2	GRCm38.p3	1:180254049	TTTTGGGGATAGTGT[C/T]TCACTACATAGCTCA	19165
rs31950085	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180251492	TGGCTAGTCAGTGAA[C/T]GGGAGCCTCGATGGG	19165
rs31960160	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Psen2	GRCm38.p3	1:180247870	GATCTCTTCCGTATC[C/T]CTTCTGGCAACAGTG	19165
rs31961746	snp	C/T	0.375	0.216506	intron-variant	Psen2	GRCm38.p3	1:180238316	ACGGGGTGAGGGTAC[C/T]GCTCAGTGGTACATT	19165
rs31966860	snp	A/G	0.290657	0.246672	intron-variant	Psen2	Mm_Celera	1:180232264	CTGGGTTGTTTCTCC[A/G]TGTCCAAACCGGCTC	19165
rs32001496	snp	A/C	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180237415	CTTAAGGACTGTCCG[A/C]GGTCACCAGCTCAGC	19165
rs32026433	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Psen2	GRCm38.p3	1:180247285	AGGACCAGGCGCTCC[A/G]TCTCTTGGGTCTTGA	19165
rs32085490	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254608	CCACTGGACAGGGTA[C/T]GGCTAGACACTGCTC	19165
rs32129149	snp	A/G	0.5	0	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180261260	GTGTGTACTGGGGGC[A/G]GGGAAGAGTTCCACA	19165
rs32193659	snp	C/T	0.375	0.216506	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180262014	GTCACTAGTCTTCAG[C/T]GTGTTCGCTCGGAAC	19165
rs32216262	snp	A/G	0.375	0.216506	intron-variant	Psen2, Gm31728	Mm_Celera	1:180259576	AGCATTAGAATAGAA[A/G]CAGGTACAATATTAT	19165
rs32220633	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180234240	TTGTTATCATGTGAA[C/T]GTGAAATGTCCCCTA	19165
rs32230437	snp	C/T	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180249586	TGCTTGGATCACAGG[C/T]ATGAACCTCTACATC	19165
rs32315325	snp	C/T	0.48	0.0979796	intron-variant	Psen2	GRCm38.p3	1:180251851	AAACTGCCCACAGAA[C/T]GATGTCATCTCCCAG	19165
rs32378604	snp	C/T	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180229493	GAGTCTTCTTCTAAG[C/T]GTCCAGGAACAAAGG	19165
rs32435302	snp	A/G	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180228285	CTGACACACATGTGG[A/G]CAGAGACAAGCTCTT	19165
rs32456894	snp	A/G	0.32	0.24	intron-variant	Psen2	Mm_Celera	1:180254332	TACAGATGGTTGTGG[A/G]CCTCCATGTTGAACA	19165
rs32520209	snp	A/G	0.46875	0.121031	intron-variant	Psen2	GRCm38.p3	1:180240419	TATGCAGAGCTCAAA[A/G]CTACAGTACCAGAGC	19165
rs32539316	snp	A/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180248579	TGAAGGGGTAAACTG[A/T]ACAGCCCTTAATCCT	19165
rs32552715	snp	A/G	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180229490	TAGGAGTCTTCTTCT[A/G]AGTGTCCAGGAACAA	19165
rs32553311	snp	C/T	0.444444	0.157135	downstream-variant-500B	Psen2	GRCm38.p3	1:180226965	CGCCCCTAGCCCCTC[C/T]CACTACACAGCGGAG	19165
rs32570462	snp	A/G	0.375	0.216506	intron-variant	Psen2	Mm_Celera	1:180231257	CCAATTTTTTAAAAA[A/G]AGGAAATGATTTTCA	19165
rs32591046	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246468	CCAAGCTAGGCCAGG[C/T]TAGACAAGGTTAGCC	19165
rs32610029	snp	A/G	0.336735	0.234472	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254799	CTCCAAACCGGACCC[A/G]GCTTCCAGCTCAGTC	19165
rs32610934	snp	C/T	0.375	0.216506	intron-variant, downstream-variant-500B	Psen2, Gm31728	GRCm38.p3	1:180258889	GTGTCAGAATAGTCT[C/T]AGTCGGAGGTGTGGT	19165
rs32685017	snp	C/T	0.46875	0.121031	downstream-variant-500B	Psen2	GRCm38.p3	1:180226839	CCTCCCAATGCCCTG[C/T]TATGGAACTTTTTAG	19165
rs32685020	snp	G/T	0.375	0.216506	utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227552	GCCCCCATAGCTCTC[G/T]GAGCCTCCGCCTGGC	19165
rs32685775	snp	C/T	0.375	0.216506	intron-variant	Psen2	GRCm38.p3	1:180230395	GGTGTCTCCGTGTTC[C/T]AGGAGACAAACCTGT	19165
rs32685778	snp	A/G	0.426035	0.177515	intron-variant	Psen2	Mm_Celera	1:180231534	TGTATTCAGATCTGC[A/G]AAAAAAAACCCAGCT	19165
rs32685781	snp	A/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180232925	GGGATTACCCGGCTC[A/T]GCAGCGGGCTTCCAG	19165
rs32685783	snp	A/G	0.493827	0.0552116	intron-variant	Psen2	GRCm38.p3	1:180233041	TGAACTCACATAACC[A/G]TGCCTCCTGTGAGAC	19165
rs32685945	snp	A/C	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180236630	CACTTAGTTACAACT[A/C]TCTCTTACCTTCTAC	19165
rs32685948	snp	G/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180236919	CTGAAGCCCTGGACA[G/T]CCTTCTCAGCTACAC	19165
rs32685951	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180237067	TGTGTGCACAGGCTG[A/G]CAATCTAAACATGCA	19165
rs32686754	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180237168	TAGCAGGTAGGATGA[A/G]GGTCACGCTGGTCCA	19165
rs32686757	snp	A/G	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180237300	GACAGGTCCGTCCTC[A/G]GGAGAGCTGTCTTTT	19165
rs32686759	snp	A/T	0.165289	0.235211	intron-variant	Psen2	Mm_Celera	1:180237452	GGTCTCCAGCAGTCT[A/T]CCTGGAGGAAGGGCC	19165
rs32686761	snp	A/G	0.132653	0.220748	intron-variant	Psen2	Mm_Celera	1:180237553	TCCCAACTATGACTT[A/G]CTTGTCTGGGCAATG	19165
rs32686925	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180233073	TCTATGCCACACACA[A/G]GAGCTACGGGTAAGT	19165
rs32686927	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180233288	CCTCTGAAGGTGGCA[C/T]GTTCATGCGATGTGG	19165
rs32686929	snp	A/G	0.142012	0.225474	intron-variant	Psen2	Mm_Celera	1:180233490	TATGATAAGACCCTC[A/G]TCTTTGGTTAAGATA	19165
rs32686930	snp	C/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180233527	ATAACCTGTCAGATA[C/T]CAAAACCACGGCCCA	19165
rs32686932	snp	A/G	0.132653	0.220748	intron-variant	Psen2	Mm_Celera	1:180233537	AGATATCAAAACCAC[A/G]GCCCACTTCCACGCC	19165
rs32687464	snp	A/C	0.132653	0.220748	intron-variant	Psen2	Mm_Celera	1:180237651	ATGACATGTACTGAC[A/C]ACAGCACGGTCATTC	19165
rs32687467	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180237688	TGTTCCTAGTTTGTT[A/G]CCATGTTCTCTATAT	19165
rs32687470	snp	C/T	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180237961	ACACAAGGGCCCACG[C/T]TTTGCCCGTGGCAGC	19165
rs32687473	snp	G/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180238031	CTTTCATGTTTCAAA[G/T]CCTGCTGCCTAAAAC	19165
rs32688036	snp	C/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180238082	CACAGTTAGGTCTAG[C/T]AATACAGGTCTGTTT	19165
rs32688039	snp	A/C	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180238456	GAGGCTCAAGATCCA[A/C]AGGAGAACCCAACTC	19165
rs32688042	snp	C/T	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180238469	CAAAGGAGAACCCAA[C/T]TCACAGGCTTCCCGG	19165
rs32688324	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180233699	TTTGGGGCACAGCAC[A/G]GCCACGAGATCTGGG	19165
rs32688326	snp	C/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180233801	CACCAGGAACCTAAG[C/T]GAACTCTGGGCCACC	19165
rs32688329	snp	A/G	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180233827	CCACCATGCTGCTGG[A/G]CTTGGGTCCCAAGGC	19165
rs32688331	snp	C/T	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180233860	CTTATCCAGTTTGCA[C/T]TGATGGAGCCGAAGC	19165
rs32688333	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180234144	GTGGTCACTTGGGGT[A/G]TGTGCTTCAAGTATC	19165
rs32688755	snp	C/T	0.32	0.24	intron-variant	Psen2	Mm_Celera	1:180238787	GAGAAAGTTGCCGTG[C/T]GGTAGTAGCTCCAGC	19165
rs32688758	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Psen2	GRCm38.p3	1:180238906	GTAGAGTACCACGAG[A/G]AAGATGGTCATGACT	19165
rs32688760	snp	A/C	0.391111	0.206368	synonymous-codon, nc-transcript-variant	Psen2	GRCm38.p3	1:180238951	CATGATGAGGGTGTT[A/C]AGCACGGAGTTGAGG	19165
rs32688763	snp	A/G	0.32	0.24	intron-variant	Psen2	GRCm38.p3	1:180239113	CCCTAGAAACCCCAC[A/G]CTGCTCTGTTAGAAC	19165
rs32689166	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180235032	CCAGGCAGACCACTC[C/T]GGCAGGTACTTGATG	19165
rs32689169	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180235143	CATGCCCACTGCCCC[A/G]AAGTTCCAGACAGCC	19165
rs32689172	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180235353	CACACGTCCCAGTCT[A/G]GGTTTAATTCACAAC	19165
rs32689324	snp	C/T	0.197531	0.244432	intron-variant	Psen2	Mm_Celera	1:180253175	TTTTGTTAGAAAGAT[C/T]CATGTGACCTACACA	19165
rs32689327	snp	C/T	0.46875	0.121031	intron-variant	Psen2	Mm_Celera	1:180253361	TTTATTTTTTATTTT[C/T]CTATAGCCAGGATGA	19165
rs32689330	snp	A/G	0.48	0.0979796	intron-variant	Psen2	GRCm38.p3	1:180253434	ACAGCCAGTAGTAGT[A/G]ACATTAAACTCCAGA	19165
rs32689333	snp	C/T	0.46875	0.121031	intron-variant	Psen2	GRCm38.p3	1:180253484	CCAAGCACTGGCATA[C/T]AGGCATTTTGGGTTG	19165
rs32689336	snp	A/G	0.197531	0.244432	intron-variant	Psen2, Gm31728	Mm_Celera	1:180260764	CATCCTTTTCTCCAC[A/G]CCGTTGGATGATTTT	19165
rs32689339	snp	A/G	0.444444	0.157135	intron-variant	Psen2, Gm31728	Mm_Celera	1:180260797	TTCTCTGAGGAGGAC[A/G]TTTGTTTCCTTTTGA	19165

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