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
rs3675358	snp	A/T	0.375	0.216506	intron-variant	Neb	Mm_Celera	2:52241179	GACAACAGAAATTTG[A/T]TTCATTGCCCTCAGG	17996
rs3675868	snp	A/T	0.48	0.0979796	intron-variant	Neb	Mm_Celera	2:52241218	AAAAGGATGATTAAA[A/T]ATCTCTCATTTGGAT	17996
rs3676547	snp	C/T	0.359862	0.224567	intron-variant	Neb	GRCm38.p3	2:52241373	CGATTTTACCTCATT[C/T]TGTCACCACAGAAAA	17996
rs3715363	snp	A/G	0.5	0	intron-variant	Neb	GRCm38.p3	2:52145548	ATACTGTAATCTGAT[A/G]CAGCCACTCTGGAAA	17996
rs3715946	snp	C/T	0.5	0	intron-variant	Neb	GRCm38.p3	2:52145615	AGCTACCATGCGATC[C/T]AACTGTACCACTCCT	17996
rs3715963	snp	C/T	0.5	0	intron-variant	Neb	GRCm38.p3	2:52145626	GATCTAACTGTACCA[C/T]TCCTTGGCATATGCC	17996
rs3716558	snp	G/T	0.5	0	intron-variant	Neb	GRCm38.p3	2:52145709	CTGCTCTACTCAACA[G/T]TAGCTAAGACCTGCA	17996
rs3716644	snp	C/T	0.5	0	intron-variant	Neb	GRCm38.p3	2:52145753	ATTCAACTGAGTGGA[C/T]AGGGAAAACATACAT	17996
rs3716685	snp	A/G	0.5	0	intron-variant	Neb	GRCm38.p3	2:52145775	AACATACATACACAC[A/G]ATAGAATACTATTCA	17996
rs3716726	snp	A/G	0.5	0	intron-variant	Neb	GRCm38.p3	2:52145796	ATACTATTCAGCTCA[A/G]AACAAGAAAACTTGC	17996
rs3717256	snp	A/G	0.5	0	intron-variant	Neb	Mm_Celera	2:52145825	GCTGGTAAATGGTTG[A/G]ACTACATATTATCCT	17996
rs3717276	snp	A/T	0.5	0	intron-variant	Neb	Mm_Celera	2:52145834	TGGTTGGACTACATA[A/T]TATCCTAGATCCTAG	17996
rs6225087	snp	C/T	0.444444	0.157135	intron-variant	Neb	GRCm38.p3	2:52185258	TGCTTCTTCACACCC[C/T]CTTGAACATTACCTG	17996
rs6290422	snp	A/T	0.5	0	intron-variant	Neb	GRCm38.p3	2:52234707	TATTTCAAATTAATT[A/T]TTTGAAAATGAAAGT	17996
rs6386254	snp	C/T	0.5	0	intron-variant	Neb	Mm_Celera	2:52331028	TTCACTTAGGAAGTT[C/T]GAGNAAAGCTAAAAA	17996
rs6386267	snp	G/T	0.5	0	intron-variant	Neb	Mm_Celera	2:52331032	CTTAGGAAGTTNGAG[G/T]AAAGCTAAAAATGCA	17996
rs6401006	snp	A/G	0.5	0	intron-variant	Neb	Mm_Celera	2:52331467	gccccacaggcttgc[A/G]tactgaccaatctga	17996
rs6402064	snp	C/T	0.5	0	intron-variant	Neb	Mm_Celera	2:52331646	AAAACAAAACACAAA[C/T]CTACTGTGAGCAAAT	17996
rs6403101	snp	A/G	0.336735	0.234472	intron-variant	Neb	Mm_Celera	2:52331783	TCAGCACTTGCCTCC[A/G]CTGAAGCAGCAGGTG	17996
rs13476497	snp	C/T	0.448558	0.151903	missense	Neb	GRCm38.p3	2:52137402	ATCCGCATCTGCAGC[C/T]ATATAGTCATATATA	17996
rs13476498	snp	A/G	0.406327	0.195095	synonymous-codon, intron-variant	Neb	GRCm38.p3	2:52245290	ACTCACGTCACTGGC[A/G]ATATCTCTGGAGGCC	17996
rs27893868	snp	A/G	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52151317	AGGCCAAACTGCAAG[A/G]GTTACTTTGTAAAAT	17996
rs27893869	snp	A/C	0.244898	0.249948	intron-variant	Neb	GRCm38.p3	2:52150949	GAATTGTAATGGTTG[A/C]TTTTTACTCTCAAAT	17996
rs27893870	snp	A/G	0.391111	0.206368	intron-variant	Neb	GRCm38.p3	2:52150641	ATACCTAGGGGAGCC[A/G]AGAGTATCCCAACAT	17996
rs27893871	snp	A/G	0.33241	0.236027	intron-variant	Neb	GRCm38.p3	2:52150239	GGGTCAATTTGTTAT[A/G]TAGCTGGTTATGAGA	17996
rs27893872	snp	A/G	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52150201	TTAGAAATAACAGCA[A/G]AAGGTTGAAGATGTT	17996
rs27893873	snp	A/G	0.33241	0.236027	intron-variant	Neb	GRCm38.p3	2:52149843	TATTTGGACCTAGTG[A/G]ACCAGATCAGCACAA	17996
rs27893874	snp	G/T	0.375	0.216506	intron-variant	Neb	GRCm38.p3	2:52149775	TCAAAGACTAACAGA[G/T]TGAAATGGAAGTAAC	17996
rs27893875	snp	A/G	0.124444	0.216185	synonymous-codon	Neb	Mm_Celera	2:52149686	TTTCCGGAAGCTATC[A/G]GAGTAAAGAACCTAT	17996
rs27893876	snp	C/T	0.336735	0.234472	intron-variant	Neb	GRCm38.p3	2:52149000	AAAGGTGGCAGAAGG[C/T]ACTTCTCAGGTCTCA	17996
rs27893877	snp	C/T	0.33241	0.236027	intron-variant	Neb	GRCm38.p3	2:52148979	AGGTTCTGGTCTTCT[C/T]AGAGCAAAGGTGGCA	17996
rs27893878	snp	C/T	0.33241	0.236027	intron-variant	Neb	GRCm38.p3	2:52148866	GACCTGAAAAGAAAG[C/T]GAGTATTCAGAACAA	17996
rs27893879	snp	C/T	0.432133	0.171253	intron-variant	Neb	GRCm38.p3	2:52148729	GAACATTCATTGATT[C/T]TAGTCCACTAGACAG	17996
rs27893880	snp	A/C	0.265928	0.249492	intron-variant	Neb	GRCm38.p3	2:52148605	GGATCTGAAGGAGAC[A/C]GGAAGTGAAACAGTT	17996
rs27893881	snp	C/T	0.33241	0.236027	intron-variant	Neb	GRCm38.p3	2:52148501	AATGGTCCTGATGAG[C/T]GTGTATATTCTCTTC	17996
rs27893882	snp	A/G	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52148145	GGAGGTTCCTTTCCT[A/G]TGTTTCATGGTCTTG	17996
rs27893883	snp	C/T	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52147918	CTATAATTCCTCTAG[C/T]GTGTAGCTGTTCTTC	17996
rs27893884	snp	A/G	0.33241	0.236027	intron-variant	Neb	GRCm38.p3	2:52147794	TTGAGCTTGGACTGG[A/G]AGACATGTGGAAAAG	17996
rs27893885	snp	A/G	0.124444	0.216185	synonymous-codon	Neb	Mm_Celera	2:52147725	CTCAGATTTCTCCTC[A/G]CCCCCACTGATACTC	17996
rs27893886	snp	A/G	0.124444	0.216185	synonymous-codon	Neb	Mm_Celera	2:52147668	GAAGAAGGCACCTCC[A/G]TCACTGTATGTGGAA	17996
rs27893887	snp	C/T	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52147630	ATCTGGAAAAGTCTC[C/T]TTATACCTGTTGAAG	17996
rs27893888	snp	C/T	0.32	0.24	intron-variant	Neb	GRCm38.p3	2:52147487	CTTGACTGTTAGTAC[C/T]ATTCACTTAATGGTT	17996
rs27893889	snp	A/C	0.124444	0.216185	synonymous-codon	Neb	Mm_Celera	2:52147173	TGATGGGATAGAGGA[A/C]AGTGTTGTCTGCTGG	17996
rs27893890	snp	C/G	0.391111	0.206368	intron-variant	Neb	GRCm38.p3	2:52139960	ATTGGCACCTTCTTT[C/G]TGGATGTTTGCAACA	17996
rs27893891	snp	C/T	0.231111	0.249285	intron-variant	Neb	GRCm38.p3	2:52139044	TATTACTCTGGTTTC[C/T]GCTCCATCATGCCAC	17996
rs27893892	snp	A/G	0.391111	0.206368	intron-variant	Neb	GRCm38.p3	2:52138959	CCAGTGTTGTGCACA[A/G]TCCCACATTCACCAT	17996
rs27893893	snp	A/G	0.32	0.24	intron-variant	Neb	GRCm38.p3	2:52138885	GGAAAGTCCAATATC[A/G]GCTTCAGATGTCCTT	17996
rs27893894	snp	A/G	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52138804	GAGCACACCATGGCC[A/G]CATTGACACCAGACT	17996
rs27893895	snp	C/T	0.42	0.183303	intron-variant	Neb	GRCm38.p3	2:52138778	AGTCCCACCAAACCA[C/T]AGGTGGCTGTGAGCA	17996
rs27893896	snp	G/T	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52138120	ACTGGCAAAGCTCGT[G/T]CGTGCGCTCTCTCTC	17996
rs27893897	snp	A/G	0.444444	0.157135	intron-variant	Neb	GRCm38.p3	2:52138094	TCTACAATGCTTTAG[A/G]CCTGGCTGAGACTGG	17996
rs27893898	snp	A/G	0.32	0.24	intron-variant	Neb	GRCm38.p3	2:52138069	ACCAAGGACTCCAGG[A/G]CAAAGCCTGTCTACA	17996
rs27893899	snp	G/T	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52137710	AAAAGATATTTTACT[G/T]TTAGCCAAGCTCTCA	17996
rs27893900	snp	C/T	0.33241	0.236027	utr-variant-3-prime	Neb	GRCm38.p3	2:52137161	TGCTACAGGTGAAAA[C/T]ATGAGAGAGCTTGAA	17996
rs27893901	snp	A/T	0.132653	0.220748	utr-variant-3-prime	Neb	Mm_Celera	2:52137115	GTAACCATGGTTTCT[A/T]TAGAAGAGATTGTAA	17996
rs27893902	snp	A/C	0.345679	0.230967	utr-variant-3-prime	Neb	GRCm38.p3	2:52136767	AACACATAGTAAACA[A/C]GGGAAAGGGCTTCTC	17996
rs27893903	snp	A/T	0.345679	0.230967	downstream-variant-500B	Neb	GRCm38.p3	2:52136584	CTGGGAATCACACAA[A/T]GAGCACCAACTCACA	17996
rs27897768	snp	C/G	0.32	0.24	intron-variant	Neb	Mm_Celera	2:52323012	CGTTCTCTAACATCC[C/G]AGACTCATGTGGCCC	17996
rs27897769	snp	A/G	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52322980	AAGAACCCTACAAAT[A/G]AGGCACCCACTTTTA	17996
rs27897770	snp	C/T	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52322932	GACTTGTACACCAGT[C/T]TGATTCCTAAGGTCC	17996
rs27897771	snp	A/G	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52322922	TTATTGCCCAGACTT[A/G]TACACCAGTTTGATT	17996
rs27897772	snp	C/T	0.142012	0.225474	intron-variant	Neb	Mm_Celera	2:52322847	TCTTTTGGTCTATCA[C/T]GAGTTTCTTCAGACT	17996
rs27897773	snp	A/G	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52322787	CCCTTTGCTACATCT[A/G]CACTGCCAAATTAGA	17996
rs27897774	snp	C/T	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52322770	TTATGGTTCCTTTCT[C/T]TCCCTTTGCTACATC	17996
rs27897775	snp	C/T	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52322725	TTTGTCTCCAATATC[C/T]ACTGTCATTAACACT	17996
rs27897776	snp	A/G	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52322701	CTTTCCCATGGCTTC[A/G]TTCTCTCCTTTGTCT	17996
rs27897777	snp	A/G	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52322623	AACACTTTCCCTGTC[A/G]TTTTATGTCTGTTTC	17996
rs27897778	snp	C/T	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52322605	ATAGAATGCCTCGAT[C/T]CAAACACTTTCCCTG	17996
rs27897779	snp	A/T	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52322595	TACTTTATCCATAGA[A/T]TGCCTCGATCCAAAC	17996
rs27897780	snp	C/T	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52322394	GCCTCTCTGTCCCCT[C/T]GTCTTGTGCTGGCTC	17996
rs27897781	snp	A/C	0.32	0.24	intron-variant	Neb	Mm_Celera	2:52322317	GAGAGGTGTGCAGAC[A/C]GGGTCTTCTTGGACA	17996
rs27897782	snp	A/G	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52322246	TGCGATATCTCAAAG[A/G]CACAGCCAACTTTAA	17996
rs27897783	snp	C/T	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52322056	TTCTGTAGACAACAG[C/T]TCTGAGCTAGAGACT	17996
rs27897784	snp	A/G	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52321919	CCAGATCAGTTTAAA[A/G]ACATTCTTAATCCAA	17996
rs27897785	snp	C/T	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52321616	GATGCTTATCAAGTG[C/T]GACAACTCGTCAAAA	17996
rs27897786	snp	A/G	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52320928	ATACCTGGTCTAAAT[A/G]TCTCTTAATAGTATC	17996
rs27897787	snp	C/T	0.124444	0.216185	intron-variant	Neb	Mm_Celera	2:52320624	CTCACTCCTTACTAC[C/T]TCCTTCCTTTCAGCC	17996
rs27897788	snp	C/T	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52320592	ACTGTCCCTGCTATG[C/T]CTCACAGCTTCTGCC	17996
rs27897789	snp	A/G	0.231111	0.249285	intron-variant	Neb	Mm_Celera	2:52320308	CTGGAACTTGCCTGG[A/G]GCTCTATGTCTACCA	17996
rs27897790	snp	A/G	0.260355	0.249785	intron-variant	Neb	Mm_Celera	2:52320197	AACATTGTAAGTGGG[A/G]TTAAGAAGGGCATAG	17996
rs27897791	snp	C/T	0.132653	0.220748	intron-variant	Neb	Mm_Celera	2:52319880	TGCACTACTGAGCCT[C/T]GACTGTCCCCTGGTT	17996
rs27897792	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52319237	TGAGAGCTCACTCAT[A/G]CAGTCTGTCCACATC	17996
rs27897793	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52319079	GCCTATGTACCAGCC[A/G]AACACTTGTCTCCCT	17996
rs27897794	snp	C/T	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52318534	AATATGCAAAGTCCT[C/T]CATTTAACCTCTTTC	17996
rs27897795	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52318307	ATGGAGAGTGGCTAT[A/G]GGAAAGTTTGAAAGC	17996
rs27897796	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317696	AGCCACTCAGCTCAG[A/G]TTATTCTACAAGGTC	17996
rs27897797	snp	A/T	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317614	TGATGCACAACAGAC[A/T]CTAGGAATCTGGATA	17996
rs27897798	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317527	CCCTTGGCAGCCTGG[A/G]CCTCTGCTTGGATGC	17996
rs27897799	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317347	TAAAAAGGACAGTAG[A/G]CACGGAAGGCATAGC	17996
rs27897800	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317312	CAGAGTATGATCATT[A/G]CCAGCTGAACAGGAA	17996
rs27897801	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317263	AGAGTAAGAAGAGCC[A/G]ATGGAGAGGATGTAA	17996
rs27897802	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317211	AAAGCTCCTGGTTTT[A/G]GCAAAGATAAAAGGA	17996
rs27897803	snp	C/T	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317159	CACCTAAGTCACACC[C/T]ACACAGCATACCCAA	17996
rs27897804	snp	A/C	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317137	CAAGTCAGGATCCTG[A/C]GTTATTCACCTAAGT	17996
rs27897805	snp	A/G	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52317068	GTATGCAGAATCCAC[A/G]TTCAGCAGGTCCTGG	17996
rs27897806	snp	A/G	0.336735	0.234472	intron-variant	Neb	Mm_Celera	2:52316948	ACTTAACAATGTGCC[A/G]CTGCAAGACATACTT	17996
rs27897807	snp	C/T	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52316927	AGAAGATCAGGGCTC[C/T]GTGTTACTTAACAAT	17996
rs27897808	snp	C/T	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52316775	TAGCAGAGAAGTTAT[C/T]GTTCAGAGCATGTAG	17996
rs27897809	snp	C/T	0.244898	0.249948	intron-variant	Neb	Mm_Celera	2:52316753	CTGAGCTACCAGTCA[C/T]CTCCATTAGCAGAGA	17996
rs27897810	snp	G/T	0.277778	0.248452	intron-variant	Neb	Mm_Celera	2:52316624	TCCTGGTGTTTTGCT[G/T]AAACTCATGGCTTCA	17996

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