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
rs4220205	snp	C/T	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93888158	AAGGTGAGCTGTATA[C/T]GTATCTCATTAACAT	110749
rs4220206	snp	A/G	0.5	0	intron-variant	Chaf1b	Mm_Celera	16:93889466	AGGAAGTAGAATGGA[A/G]CCCAAAGCCCATCCC	110749
rs4220207	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93895595	CTATGTCTTCATCTG[A/G]AGGCTACTAGCAGAA	110749
rs4220208	snp	C/T	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93899856	CCTGCCATCGGGTGC[C/T]TCTCCCTGCAGATCC	110749
rs4220209	snp	C/T	0.46281	0.131194	intron-variant	Chaf1b	Mm_Celera	16:93905590	CCTAGCTGTAGTCAG[C/T]GTCTCACTGGGCCAC	110749
rs6323022	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93890944	tgaggagacaccatg[C/T]ccaaggcacctctta	110749
rs6323161	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891023	ctgttatcatcatgg[C/T]gggaagcntggcagc	110749
rs6323571	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891031	atcatggngggaagc[A/C]tggcagcgtacaggc	110749
rs6323607	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891050	cagcgtacaggcaga[C/T]atggtgctggagagg	110749
rs6323655	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891078	agggagctgagagtt[C/T]tacctctggatcctc	110749
rs6323717	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891112	cagcagggagtgaac[C/T]tagacacacttcctc	110749
rs6324161	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891139	cctccaacgagacca[C/T]gcctactttaacatg	110749
rs13463333	snp	G/T	0.5	0	synonymous-codon	Chaf1b	Mm_Celera	16:93887198	GGATGAGGAGGAGGC[G/T]CAGCTGAATAAGGAG	110749
rs13463334	snp	A/G			synonymous-codon, utr-variant-5-prime	Chaf1b	Mm_Celera	16:93892785	GTCGTTCTTCCGAAG[A/G]CTCAGCTTTACTCCA	110749
rs32577585	snp	A/G	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93890416	TGCACGTGCACACAT[A/G]CATACATAGTTAAGG	110749
rs32623814	snp	C/T	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93889043	CTTTGATAGGCCTGA[C/T]CTTGCTTTTGTTTGG	110749
rs32626099	snp	C/T	0.375	0.216506	upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883622	GTAGGTAGGACGTCT[C/T]GCATCTCGGGTTAGC	110749
rs32650214	snp	A/G	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93899763	TTGAGCTCATTGCAT[A/G]TGTGCTGGTCAGAGG	110749
rs32692974	snp	C/T	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93890387	GGCTAGCCTGGGCTA[C/T]GAGATGAGATGTGTG	110749
rs32815045	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93888591	TACTTTTCTATTGCT[A/G]TGATAAGTCACCATC	110749
rs32927394	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	GRCm38.p3	16:93897273	TTCTCACCAGAGACT[A/G]TGAAAGCTAGAAGAT	110749
rs32944815	snp	A/G	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93899008	AGCCTTTCAGCGGGG[A/G]GGCTTCTAGGCCACG	110749
rs32965016	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93888706	TGTTGGAGGAAGTGT[A/G]TCACTGTGGGGGTGG	110749
rs45755726	snp	C/T	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93893299	AAGGTGTGTAAGGCT[C/T]TGGGGTCAACCCTTA	110749
rs45854472	snp	A/T			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906596	CCAGGCACAGCACAC[A/T]CTTCAGGGCAACCAG	110749
rs45860696	snp	C/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93902835	TGGTCGCAACTGTTC[C/T]GAGGCTTCCCGTTGG	110749
rs46007323	snp	A/T	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93890529	CTCAGGCCTCGCCCA[A/T]CCATCCTTCAGTTTC	110749
rs46030149	snp	C/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93902894	ACTTACTCCAGAGCT[C/T]ACTCCTCGTCTGGCC	110749
rs46150905	snp	G/T	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93893188	AATGTATCCTATACC[G/T]CGGCCCTCTCACTTG	110749
rs46158181	snp	A/T	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93895371	AGGCTTTTTGTTGTT[A/T]TGTGGCTTTTGGGGA	110749
rs46222996	snp	A/G	0.142012	0.225474	intron-variant	Chaf1b	Mm_Celera	16:93894072	AGTAGGGTCCTCTCT[A/G]GCAGTTCCAGAATCG	110749
rs46531190	snp	C/T	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93886518	AGACCATTGCTCCGT[C/T]AGGCTGACATGGCTG	110749
rs46682108	snp	A/G	0.231111	0.249285	synonymous-codon	Chaf1b	Mm_Celera	16:93905960	GAGACCCAGGCTTGA[A/G]GAACGTGAAGGAGAT	110749
rs46756019	snp	A/G	0.260355	0.249785	intron-variant	Chaf1b	Mm_Celera	16:93900805	ACAGTCTGTCGTGCC[A/G]GTCCCCTGTCTAACA	110749
rs46830996	snp	A/C	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93894098	AATCGTCACATGTTA[A/C]GATGGCGTGTGTAGG	110749
rs46966661	snp	A/T	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93893267	ACTTAGATGAAGCTC[A/T]TTAGTCAGGTGTGTC	110749
rs47090767	snp	A/G	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93893892	CGTAGCACTGCAGAG[A/G]CTGACTTTTATGGAC	110749
rs47150383	snp	A/C	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93899484	TGGCGCGCAGAAGTC[A/C]TTGATTACTGGTCTG	110749
rs47238196	snp	C/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93892948	AACCGACTACTGCAT[C/G]CCATTTGTTCTGAGT	110749
rs47259276	snp	A/C	0.277778	0.248452	synonymous-codon	Chaf1b	Mm_Celera	16:93905024	AATAAATTTAACACC[A/C]TTGAAAACAGACACT	110749
rs47274567	snp	C/T	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93893951	TGCAGTTCTCTAGTC[C/T]TACAACAAATGCATT	110749
rs47275317	snp	A/G	0.493827	0.0552116	intron-variant	Chaf1b	Mm_Celera	16:93899145	AGTGTATCGGGGACC[A/G]GAAATCTGGTCCCCG	110749
rs47423866	snp	C/T	0.124444	0.216185	synonymous-codon, utr-variant-5-prime	Chaf1b	Mm_Celera	16:93892758	CCGGATGTTTCACGA[C/T]GACAGCATGAAGTCG	110749
rs47445888	snp	A/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93893543	TGATAACGCCATCCA[A/G]TCCTATGCCTCACAG	110749
rs47573211	snp	G/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93893165	GCGCCACCTGGTGCC[G/T]TTGATACAATGTATC	110749
rs47599950	snp	A/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93895296	CTCATTGTCCAGAAT[A/G]CAACTTTCTCATCTA	110749
rs47743664	snp	G/T			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906468	TTGTCTAGAGTTGTG[G/T]ATCTGGTGGCAGCAC	110749
rs47751454	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891259	TGAGGGCTCTGATAT[C/T]GCTCCTAATTTCTCG	110749
rs47764205	snp	C/T	0.277778	0.248452	intron-variant	Chaf1b	Mm_Celera	16:93898750	AAATAACTATTCTGT[C/T]TGTTGAATATCAACA	110749
rs47854157	snp	C/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93894534	AAGCTCCTGGCTTGG[C/T]GTCGTCACTCAGGTG	110749
rs47856349	snp	A/G	0.260355	0.249785	intron-variant	Chaf1b	GRCm38.p3	16:93904945	TTGAACCTTGGCTTC[A/G]TACCTAAACGGCTCC	110749
rs48003120	snp	C/T	0.375	0.216506	downstream-variant-500B	Chaf1b	Mm_Celera	16:93906349	AAATTCAAGTGAGAG[C/T]ATGCAGTGCTTCCAA	110749
rs48139339	snp	A/T	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93895912	ATCCCTCCATCTTCC[A/T]TTTGTGTGTCTGTTT	110749
rs48271425	snp	A/T	0.260355	0.249785	intron-variant	Chaf1b	Mm_Celera	16:93894049	GGATAGCTGTACGAT[A/T]AAGTAAGAGTAGGGT	110749
rs48335103	snp	C/T	0.142012	0.225474	intron-variant	Chaf1b	Mm_Celera	16:93894086	TAGCAGTTCCAGAAT[C/T]GTCACATGTTAAGAT	110749
rs48367003	snp	C/T	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93899229	ATGACATCAGTAAGT[C/T]GACAGAGCTCTAAAA	110749
rs48539904	snp	C/T	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93899912	CTTCATGGTTTACCG[C/T]AAACTGGCTTTTAGT	110749
rs48634014	snp	A/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93894854	CTTTTTGCCTCTGAC[A/G]AGCATCTGTGCCTGT	110749
rs48976386	snp	A/G			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906296	TTGGTAGAGAGGAGG[A/G]CTAGGAGAAGACAGG	110749
rs49006166	snp	C/T	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93893107	TGTAAAACTTCCATA[C/T]GGTAAAGGTGTAGCA	110749
rs49061553	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93899806	CCTCAGTGCTTCCAC[A/G]TGTGGGTCCTGTGAA	110749
rs49078370	snp	A/G	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93894389	CTTAAAGGCTGGCTC[A/G]GAGAGAGGACAGCCA	110749
rs49088394	snp	A/C	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93893844	GACTGGTTTTCTGCT[A/C]GTAAATATTACAGAG	110749
rs49115530	snp	A/G	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93904717	CAAATTTAAAACGGG[A/G]TTGAGTGTGGTTTGG	110749
rs49236241	snp	A/C	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93894622	GTGCTTGTCTCTGTC[A/C]CAGATGCCCTGTCAG	110749
rs49283852	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891611	GGTTCGTAAGTAACA[C/T]GAACGTGTTTTGCAA	110749
rs49364355	snp	C/G	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93902980	ATGTGAGACCAAGCC[C/G]GGTGGAACCATGCTA	110749
rs49473439	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93896215	CACGCCCAGGATCAC[A/T]GGATCACAGGATCAC	110749
rs49738361	snp	G/T	0.132653	0.220748	intron-variant	Chaf1b	Mm_Celera	16:93901494	TCCCGTGATTCCGTG[G/T]GCTAGGTGGGCTGCT	110749
rs49890927	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93896283	TCCCAGAGGCAACTT[G/T]ACTTCCAGGAGCTCT	110749
rs49904238	snp	C/G	0.132653	0.220748	intron-variant	Chaf1b	Mm_Celera	16:93904883	ACACTGAAGGCCATG[C/G]GTGATATGCTCTGCA	110749
rs49973450	snp	G/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892618	ACTTGCCCGACCTGC[G/T]GGCCAACTGATGAGG	110749
rs50011492	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891607	GACAGGTTCGTAAGT[A/G]ACATGAACGTGTTTT	110749
rs50057015	snp	C/T	0.5	0	intron-variant	Chaf1b	Mm_Celera	16:93886331	AGAGTGTTGATCTGT[C/T]CAGCCATCTCATCTC	110749
rs50059813	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93890110	GAGCAGGCCTCTGGA[A/G]GAACAATAGAGAAAT	110749
rs50201505	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93899701	GAATTCTGTATTTTT[A/T]TTTTATTTTATTATT	110749
rs50215802	snp	A/G	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93893132	GTAGCAGACTAAGTC[A/G]GTAGACACATGGTGG	110749
rs50384652	snp	A/C	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93893430	AACTTAGATGTTGCT[A/C]TTCTGTTCAGGTTGA	110749
rs50448695	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93899765	GAGCTCATTGCATAT[A/G]TGCTGGTCAGAGGAA	110749
rs50464734	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93904811	GTGTGGTGAACATTG[A/T]CTGTGGCTGTGATGC	110749
rs50618759	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891682	TTTGGCTTTTTTGTT[C/T]GGATCTGCTATTCTG	110749
rs50733452	snp	C/T	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93899431	GATAGTGTTCCTAAA[C/T]GAAACCATTTTCCTG	110749
rs50744051	snp	A/G	0.336735	0.234472	intron-variant	Chaf1b	Mm_Celera	16:93901851	AGCCCTGCATCGGGA[A/G]GTTTTCTGACACGGT	110749
rs50946690	snp	A/G	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93899208	ACCTTTAAATCCTGA[A/G]TATAAATGACATCAG	110749
rs50958601	snp	A/G	0.391111	0.206368	intron-variant, utr-variant-5-prime	Chaf1b	Mm_Celera	16:93892845	GCCTGACGGCATGTG[A/G]CATAGGGGTGTGATG	110749
rs51030621	snp	A/C/G			intron-variant	Chaf1b	GRCm38.p3	16:93904751	CGCATTCAGCAAGGT[A/C/G]TGTACTGGACTCCTC	110749
rs51043672	snp	A/G	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93900713	TGAAGTTGAGAGGAA[A/G]GTACATAGATCAAGA	110749
rs51122935	snp	C/G	0.408163	0.193609	intron-variant	Chaf1b	Mm_Celera	16:93900207	AACAGACACGGGTGT[C/G]GAGGATAGACCTCTG	110749
rs51196038	snp	A/C/T			intron-variant	Chaf1b	Mm_Celera	16:93899387	AACACACACACACAC[A/C/T]TACTCCTACAAAAAA	110749
rs51234037	snp	C/G	0.142012	0.225474	intron-variant	Chaf1b	Mm_Celera	16:93902043	CCGGAGGGTAGCACT[C/G]AGAAGGAACCTGTGT	110749
rs51243797	snp	A/G	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93899491	CAGAAGTCCTTGATT[A/G]CTGGTCTGGCCTCAT	110749
rs51400260	snp	A/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93895263	GTAGTGTCCCATGAT[A/G]CATAGTGTGTCTTTT	110749
rs51414044	snp	C/T	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93899530	GTGTAAATGTAAGAA[C/T]TGATTTTTTTACCCC	110749
rs51430194	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93899780	GTGCTGGTCAGAGGA[A/C]AACTTACAGCCCTCA	110749
rs51883938	snp	C/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93903202	GGGCCAAGTAGCGGC[C/T]GCCTTTGTCCTTCTG	110749
rs51988881	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93887706	AATACTCCACCCTAT[C/T]CCCTCAGTTTCCTAG	110749
rs52029908	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93896238	TGTGACCAAGCTCCT[A/G]GGATCCTGGGATCCT	110749
rs52410750	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93904706	AAGCCAAACTCCAAA[A/T]ATAAAACGGGATTGA	110749
rs108462872	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93897254	TATCAGAATTACACC[A/T]GACTTCTCACCAGAG	110749
rs108553745	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93897281	AGAGACTGTGAAAGC[C/T]AGAAGATCCTGGGCC	110749

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