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
rs3656611	snp	A/G	0.493827	0.0552116	intron-variant	D7Ertd443e	GRCm38.p3	7:134296232	CAGGAGAGGCAAGGA[A/G]CCTGTGAGGAGTTTC	71007
rs3668877	snp	A/G	0.375	0.216506	intron-variant	D7Ertd443e	GRCm38.p3	7:134515592	TCTGCTGGGATCAGT[A/G]GATAAAGACAGATGG	71007
rs3669956	snp	A/C	0.48	0.0979796	intron-variant	D7Ertd443e	GRCm38.p3	7:134515744	TGAGCTACATTTCTT[A/C]GTCTAGCTTTGGAAG	71007
rs3695686	snp	A/G	0.5	0	upstream-variant-2KB	D7Ertd443e	GRCm38.p3	7:134520450	AACCAAACGAGGTCA[A/G]GGGGGATTTATGATC	71007
rs6166875	snp	C/T	0.359862	0.224567	intron-variant	D7Ertd443e	Mm_Celera	7:134375021	GTTACTCTATGACAA[C/T]CTTTGTGTTACTTAC	71007
rs6167434	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134375127	ctggcctgtaggcaa[A/G]catgtaatgcatttt	71007
rs6167483	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134375154	ttttcttgattgaca[A/G]ttgncatggagnggc	71007
rs6167487	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134375158	cttgattgacanttg[C/T]catggagnggcntga	71007
rs6167502	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134375166	acanttgncatggag[A/G]ggcntgatccactgt	71007
rs6167517	snp	A/C	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134375170	ttgncatggagnggc[A/C]tgatccactgtnagt	71007
rs6167536	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134375182	ggcntgatccactgt[A/G]agtagtgcnagctct	71007
rs6167552	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134375191	cactgtnagtagtgc[C/T]agctctgggcaggtg	71007
rs6167974	snp	A/C	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134375227	gactatataagaaag[A/C]aaactgagcaaacca	71007
rs6168015	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134375248	gagcaaaccacaggg[A/G]aaaagtcattaagca	71007
rs6171478	snp	C/T	0.21875	0.248039	intron-variant	D7Ertd443e	Mm_Celera	7:134302334	TCTGACAGGAGAAGC[C/T]CAGTATAAATGGGAT	71007
rs6171514	snp	G/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134302351	AGTATAAATGGGATA[G/T]CGAGGATCTTGGCAA	71007
rs6171547	snp	A/G	0.21875	0.248039	intron-variant	D7Ertd443e	Mm_Celera	7:134302371	GATCTTGGCAATATA[A/G]GGTCAGCCAAGAAGG	71007
rs6173829	snp	C/T	0.21875	0.248039	intron-variant	D7Ertd443e	Mm_Celera	7:134302783	CACATGTAGAACTCA[C/T]GTTTCCATCACTGAT	71007
rs6181754	snp	C/G	0.359862	0.224567	intron-variant	D7Ertd443e	Mm_Celera	7:134375432	gaagcctgactgaaa[C/G]aGCCTTGCAGGGACT	71007
rs6181921	snp	G/T	0.475309	0.108333	intron-variant	D7Ertd443e	GRCm38.p3	7:134421377	AGCAGTCCATGCTAC[G/T]CAGTTCTCTGGTCCC	71007
rs6184253	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134421840	aggggaaaggagGAA[C/T]GGTGGNTCAGGATCA	71007
rs6184267	snp	A/G	0.231111	0.249285	intron-variant	D7Ertd443e	Mm_Celera	7:134421846	aaggagGAANGGTGG[A/G]TCAGGATCANGAAGA	71007
rs6184698	snp	C/T	0.444444	0.157135	intron-variant	D7Ertd443e	GRCm38.p3	7:134421856	GGTGGGTCAGGATCA[C/T]GAAGAAGTCAAGTGG	71007
rs6190392	snp	A/G	0.5	0	downstream-variant-500B	D7Ertd443e	Mm_Celera	7:134265947	GGTGGTGAAGATGCT[A/G]NCAGCTTTACTCAGT	71007
rs6190393	snp	C/T	0.415225	0.187619	downstream-variant-500B	D7Ertd443e	Mm_Celera	7:134265948	GTGGTGAAGATGCTN[C/T]CAGCTTTACTCAGTC	71007
rs6191361	snp	C/T	0.290657	0.246672	downstream-variant-500B	D7Ertd443e	Mm_Celera	7:134266108	CAGCCTCTGACACTC[C/T]AGGATGTGTACAGAA	71007
rs6191930	snp	G/T	0.5	0	downstream-variant-500B	D7Ertd443e	Mm_Celera	7:134266199	AGACTTTTGCAAAAA[G/T]TTTGGAAAAAAAAAA	71007
rs6192011	snp	A/G	0.5	0	downstream-variant-500B	D7Ertd443e	Mm_Celera	7:134266250	CCCAAAAAAAAAAAA[A/G]AAAAACAAGCATCCA	71007
rs6193081	snp	C/T	0.5	0	utr-variant-3-prime	D7Ertd443e	Mm_Celera	7:134266431	TGATCCATTGCCTGC[C/T]GGACTGTTGCTTCTG	71007
rs6198561	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134422156	GTTTAAGACACTTCC[A/G]CCCCAACCAGCAGAG	71007
rs6252254	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134425183	tatttatttattttg[C/T]ggggaggagggggat	71007
rs6265707	snp	C/G	0.429688	0.173817	intron-variant	D7Ertd443e	Mm_Celera	7:134465355	AATCGTTACAGGTCC[C/G]AGACACATTCAGGAA	71007
rs6266794	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134438548	tctccatcaagacca[C/T]gcctcctaatccttc	71007
rs6335161	snp	A/G	0.359862	0.224567	intron-variant	D7Ertd443e	Mm_Celera	7:134369436	ACAAATGAGGCTGGC[A/G]CAGTGTCTGAAAGCC	71007
rs6335697	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134369539	GGGAGAGGCACCATC[A/G]CTGGGCTGGATCTGA	71007
rs6335754	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134369562	GGATCTGAGAGTACA[A/G]CACCAGAGGAAAAGC	71007
rs6339111	snp	A/G	0.304688	0.243945	intron-variant	D7Ertd443e	Mm_Celera	7:134436089	AAAGAGTTTGATGTT[A/G]AAGATTACAGTAAGT	71007
rs6339563	snp	G/T	0.304688	0.243945	intron-variant	D7Ertd443e	Mm_Celera	7:134436161	AGAAATCCATCATCA[G/T]CTGTAGAAGAAACAG	71007
rs6340143	snp	G/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370354	acctggtattgttag[G/T]caaacaaaccctttc	71007
rs6340172	snp	C/T	0.304688	0.243945	intron-variant	D7Ertd443e	Mm_Celera	7:134436312	CCATCTTGTGATTAC[C/T]TAAGCCTGTCCTGCT	71007
rs6340757	snp	A/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134436422	AGAGCTGTTCACTCC[A/T]CGGAAGCCAAAAACG	71007
rs6341159	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134436489	TGTGTTATTTGGATC[A/G]NTTCCTTTCTTGTTT	71007
rs6341161	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134436490	GTGTTATTTGGATCN[C/T]TTCCTTTCTTGTTTC	71007
rs6353727	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370601	GAAAGGCCTGGTTCA[A/G]tgacttcagaaaacc	71007
rs6354162	snp	A/C	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370620	cttcagaaaacctct[A/C]actcctcccaaagaa	71007
rs6354760	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370758	tgaaatgacaggagg[C/T]ntggcctcgtngggc	71007
rs6354762	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370759	gaaatgacaggaggn[A/G]tggcctcgtngggct	71007
rs6354780	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370769	gaggnntggcctcgt[C/T]gggcttctttcattt	71007
rs6354825	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370798	ttaacaGCTCCCTTG[C/T]GTTNTACATACACTG	71007
rs6354838	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370802	caGCTCCCTTGNGTT[A/G]TACATACACTGTTCA	71007
rs6355304	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370853	AAAGGGAAAGACTGC[A/G]TGGGAGCTGCTAGCC	71007
rs6355352	snp	A/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370881	GCCATTCAGCTGATG[A/G]GCATGTAGGCTGACC	71007
rs6355745	snp	A/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134370914	GTctaccataaacat[A/T]tgtgtacaggtattc	71007
rs6386154	snp	A/G	0.5	0	upstream-variant-2KB	D7Ertd443e	Mm_Celera	7:134520649	gctaagactgggcaa[A/G]tcanagacaagagaa	71007
rs6386175	snp	A/T	0.5	0	upstream-variant-2KB	D7Ertd443e	Mm_Celera	7:134520653	agactgggcaantca[A/T]agacaagagaacagt	71007
rs6386786	snp	G/T	0.5	0	upstream-variant-2KB	D7Ertd443e	Mm_Celera	7:134520811	TATGAGAGCTATTTA[G/T]CCATAGTTTAGTAAA	71007
rs31010149	snp	A/G	0.5	0	intron-variant	D7Ertd443e	GRCm38.p3	7:134416717	AGAGACAGAGACAGA[A/G]AAACTGAGACAGACA	71007
rs31031889	snp	A/G	0.444444	0.157135	intron-variant	D7Ertd443e	Mm_Celera	7:134405321	CATGTGCACTGTAAT[A/G]TACCAGAACAGCTGG	71007
rs31043666	snp	A/G	0.444444	0.157135	intron-variant	D7Ertd443e	GRCm38.p3	7:134423780	AAGAAGAAGCCTAGA[A/G]GGCTTTCAGGGGAGC	71007
rs31044124	snp	A/G	0.401235	0.199068	intron-variant	D7Ertd443e	GRCm38.p3	7:134417756	TCACAAGTTAATTTG[A/G]GTTGGTTTAATCTGA	71007
rs31080497	snp	A/C	0.48	0.0979796	intron-variant	D7Ertd443e	GRCm38.p3	7:134513594	GTTTATGTCTTGTAT[A/C]TCAGTCCGTTGAGTC	71007
rs31087817	snp	A/G	0.188366	0.242283	intron-variant	D7Ertd443e	Mm_Celera	7:134268676	CAGGAGGCTTTTAAG[A/G]GGAAGAGAAAGGAGA	71007
rs31101047	snp	A/G	0.48	0.0979796	intron-variant	D7Ertd443e	GRCm38.p3	7:134506403	TCATCTGAGATACTG[A/G]CTTCTGGTCATGTCT	71007
rs31111879	snp	C/G	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134462713	GTTAAATTTAATGGA[C/G]GAAAGATGCTCACGG	71007
rs31128063	snp	A/G	0.456747	0.140554	intron-variant	D7Ertd443e	GRCm38.p3	7:134425919	CTATGTGTGCACTTC[A/G]ATAGTTTGAATGGAA	71007
rs31128254	snp	A/G	0.444444	0.157135	intron-variant	D7Ertd443e	Mm_Celera	7:134407555	CTATACTATACCGGT[A/G]GTATTGTTGGTACCT	71007
rs31140360	snp	A/G	0.49827	0.0293608	intron-variant	D7Ertd443e	GRCm38.p3	7:134425603	TCATGAGGTGTGTGA[A/G]AGTCTTACAGGAAGA	71007
rs31147629	snp	G/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134425960	ACGGGCTGTCTTAGT[G/T]TGGGCTTTATTGCTT	71007
rs31154498	snp	A/C	0.5	0	intron-variant	D7Ertd443e	GRCm38.p3	7:134381524	TATATATCTGGAAGT[A/C]CATACTGGGAGCCTT	71007
rs31207027	snp	C/T	0.48	0.0979796	intron-variant	D7Ertd443e	GRCm38.p3	7:134506161	TCTGTCATCACACCG[C/T]GGTGACTAAACATGT	71007
rs31228206	snp	A/G	0.48	0.0979796	intron-variant	D7Ertd443e	GRCm38.p3	7:134513640	AGACTGTGATCTTCA[A/G]TCTGATGAATAGGCT	71007
rs31273666	snp	C/T	0.32	0.24	intron-variant	D7Ertd443e	GRCm38.p3	7:134513543	CACCTTTGTATTCTA[C/T]CCTACCTGTCTCCCT	71007
rs31311316	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134422326	GTCCCGGTTCTGCAG[C/T]TTTAAGGATCTCTGC	71007
rs31371519	snp	C/T	0.408163	0.193609	intron-variant	D7Ertd443e	GRCm38.p3	7:134423531	CAACCATCACGGTAA[C/T]GTAACAGGGTACTTT	71007
rs31443773	snp	C/T	0.5	0	intron-variant	D7Ertd443e	GRCm38.p3	7:134406184	TCTAAAGCCTCATGC[C/T]GTGCAGCTGAAGAGC	71007
rs31455803	snp	A/T	0.5	0	intron-variant	D7Ertd443e, Gm35970	Mm_Celera	7:134412436	AACCACAGGCAACTG[A/T]GTGCATCTAAAAAAA	71007
rs31488445	snp	C/T	0.375	0.216506	intron-variant	D7Ertd443e	Mm_Celera	7:134462054	TATGGACATGCCCCC[C/T]GACATACACACACAC	71007
rs31509277	snp	C/T	0.492188	0.0620098	intron-variant	D7Ertd443e	GRCm38.p3	7:134398332	GTCAGGATTCTCAGT[C/T]GCTATTCCTTTGAGG	71007
rs31544678	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	D7Ertd443e, Gm35970	GRCm38.p3	7:134408963	ATGCTGCTGGGCAAC[C/T]TGTGAGCTGCACACA	71007
rs31575300	snp	C/T	0.375	0.216506	intron-variant	D7Ertd443e	GRCm38.p3	7:134417918	GTGCATGCATGAATG[C/T]GCATGTATACAAGTA	71007
rs31595542	snp	C/G	0.375	0.216506	intron-variant	D7Ertd443e	GRCm38.p3	7:134461236	AATCATTACTTTGTA[C/G]GTTCTTTATTTGTGA	71007
rs31601321	snp	C/T	0.444444	0.157135	intron-variant	D7Ertd443e, Gm35970	GRCm38.p3	7:134412719	AGGGAACCTTGGGAA[C/T]AGTCTTGCTTGCCTT	71007
rs31617645	snp	A/T	0.359862	0.224567	intron-variant	D7Ertd443e	GRCm38.p3	7:134508003	TGAAATACAATACGT[A/T]TCAGCAAAACCCCTA	71007
rs31622093	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	D7Ertd443e, Gm35970	GRCm38.p3	7:134409658	TTGGGAACCTTCAAG[G/T]AGCTGATAGCCTAAC	71007
rs31646253	snp	C/T	0.444444	0.157135	intron-variant	D7Ertd443e	Mm_Celera	7:134398444	AATCATAACTCTGAG[C/T]CCAAGGGCAGAGTTA	71007
rs31650437	snp	A/G	0.401235	0.199068	intron-variant	D7Ertd443e	GRCm38.p3	7:134416830	AAGATTCACGAAACT[A/G]TATGCATAGGATAGG	71007
rs31654399	snp	C/T	0.444444	0.157135	intron-variant	D7Ertd443e	GRCm38.p3	7:134406441	TCTGGCCAGCCCCAT[C/T]CTCACTGGTAGCCAG	71007
rs31662356	snp	C/T	0.49827	0.0293608	intron-variant	D7Ertd443e	GRCm38.p3	7:134513106	GAGGTCAACCATGTG[C/T]GTTACTCCCAGTAGA	71007
rs31668143	snp	A/G	0.375	0.216506	intron-variant	D7Ertd443e	GRCm38.p3	7:134417523	TTGCTAGAGGCTGAC[A/G]TCTGGTTCTTTTGAA	71007
rs31670913	snp	A/G	0.444444	0.157135	intron-variant	D7Ertd443e	GRCm38.p3	7:134508898	TGACAACAGCAAGGG[A/G]ATGGAAACGATGCAT	71007
rs31675917	snp	A/C	0.493827	0.0552116	intron-variant	D7Ertd443e	GRCm38.p3	7:134425679	AGAGATGAAGATGGA[A/C]GACGAGAGGTAGGAA	71007
rs31705683	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	D7Ertd443e, Gm35970	GRCm38.p3	7:134408645	ACTCCCCAGAAGTTC[C/T]GAGATCCGTACGCTC	71007
rs31709883	snp	G/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134461965	CCAATGAGAGAGACT[G/T]TCTCAAAAGAATAAG	71007
rs31737641	snp	C/T	0.359862	0.224567	intron-variant	D7Ertd443e	GRCm38.p3	7:134442950	AGCTATACCACCCAT[C/T]CCAGGGCCATTGGAT	71007
rs31771633	snp	A/T	0.444444	0.157135	intron-variant	D7Ertd443e	Mm_Celera	7:134511535	AGCACCTGAAAAAAA[A/T]GTTCAACATCCTTAA	71007
rs31783536	snp	C/T	0.444444	0.157135	intron-variant	D7Ertd443e	GRCm38.p3	7:134403985	GCTGAATGTTCAAAG[C/T]GCAGTGACAAATAGC	71007
rs31883120	snp	C/T	0.5	0	intron-variant	D7Ertd443e	Mm_Celera	7:134408398	TGGTGTCTGTCTTTC[C/T]TTCTTTCTTTTCTTT	71007
rs31894912	snp	C/T	0.375	0.216506	intron-variant	D7Ertd443e	GRCm38.p3	7:134515404	GAAATTGTAAGACAG[C/T]CACAATTAAATGTTT	71007
rs31897519	snp	C/T	0.465374	0.126941	intron-variant	D7Ertd443e	GRCm38.p3	7:134418042	TGCCCTCCAACTAGC[C/T]GTTAGTGACATTACC	71007
rs31906567	snp	C/G/T	0.444444	0.157135	intron-variant	D7Ertd443e, Gm35970	GRCm38.p3	7:134412681	CAGCAGAGAGATACC[C/G/T]GATTCTCTACAGCAC	71007

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