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
rs3708133	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103574097	agccctagtgaccca[A/G]cctgAGTGAGCCATC	99382
rs6219381	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715194	tgggcctcaaacttg[A/G]gcaatcctcccatct	99382
rs6219974	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715314	AGTGGGGTGGGAGAG[A/G]GGGTAGNGGCCCTGC	99382
rs6219992	snp	C/T	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715321	TGGGAGAGNGGGTAG[C/T]GGCCCTGCTTTGGAA	99382
rs6220480	snp	C/G	0.359862	0.224567	intron-variant	Abtb2	Mm_Celera	2:103715389	TCCTGGGCTACAGAG[C/G]TCTCATAGGGAAAGG	99382
rs6220969	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715459	GCAGTATAGCTGTGC[A/G]GCACCACACGNGTGG	99382
rs6220987	snp	G/T	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715470	GTGCNGCACCACACG[G/T]GTGGTGTTTACNTAA	99382
rs6221001	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103715482	ACGNGTGGTGTTTAC[A/G]TAAGTCCGTTCCCAC	99382
rs6221486	snp	A/G	0.290657	0.246672	intron-variant	Abtb2	Mm_Celera	2:103715577	CATCCTGCAGGTAAG[A/G]GCAGGGCATGTAGCC	99382
rs6310195	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103693612	TAGGTAAAGTCAGCC[A/G]GACATGGTGACACAC	99382
rs6310622	snp	A/G	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103687078	TTTACAGTGTTTCAG[A/G]TCTCTCTTCTCCCTG	99382
rs27358068	snp	A/G	0.42	0.183303	intron-variant	Abtb2	Mm_Celera	2:103678537	TCTGTCTACATATTG[A/G]TAAAATCCCAGGAGA	99382
rs27358069	snp	C/G	0.21875	0.248039	intron-variant	Abtb2	Mm_Celera	2:103678391	ATCATCCAAACTGAG[C/G]AAGCATAAGTGCTAT	99382
rs27358070	snp	A/G	0.49827	0.0293608	intron-variant	Abtb2	GRCm38.p3	2:103678320	GAGAAGAAATGGACT[A/G]AGTGGGAAGGGGGAA	99382
rs27358071	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103678280	GTATCCCTTTCCAGT[A/G]ATGTCTCCTGGCCTT	99382
rs27358072	snp	A/C	0.18	0.24	intron-variant	Abtb2	Mm_Celera	2:103678269	TAGAGAGGGCAGTAT[A/C]CCTTTCCAGTAATGT	99382
rs27358073	snp	C/T	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103678245	GCTGGGACAGTCCCA[C/T]TCATGAAGTAGAGAG	99382
rs27358074	snp	A/G/T	0.277778	0.248452	intron-variant	Abtb2	GRCm38.p3	2:103678026	ATCAGAGAAGTAGCA[A/G/T]CTCCCCAGAATTTGG	99382
rs27358075	snp	C/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103677864	CATCCCTGCATGCCA[C/G]AGAGGAGACTCTTAG	99382
rs27358076	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103677793	ACATGTCAGCACAGT[A/G]TTTATAAATGCCAGA	99382
rs27358077	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103677761	CAAGTCACCCACCCA[A/G]GTTCATGTAGCTGAT	99382
rs27358078	snp	C/T	0.473373	0.11227	intron-variant	Abtb2	Mm_Celera	2:103677720	ATTTACGTTCCTCCG[C/T]CATTGTCTCCACTTA	99382
rs27358079	snp	A/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103677459	GCCCCAGGTTAGGGG[A/T]GGACTGCCCCCATGC	99382
rs27358080	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103677409	GAACTATCACTGTAC[C/T]TGCAGGGTGATCTAG	99382
rs27358081	snp	C/G	0.415225	0.187619	intron-variant	Abtb2	GRCm38.p3	2:103677262	CCAGTTCTTTCTCCT[C/G]CCATGGAAATAAACA	99382
rs27358082	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103677040	CCCAGTGTTGTTTCT[A/G]TCAATGAAAAAGGAG	99382
rs27358083	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103676947	TAGTGACATAATAGT[C/T]CTCACTGGGAATCCT	99382
rs27358084	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103676756	AAGAGAGTGAAGAGA[A/G]AGAACAATTTCTAAA	99382
rs27358085	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103676724	CTGACTGCATTATTT[C/T]CTTTGTTAGAAGAAG	99382
rs27358086	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103676062	CATTTTCAGTTTCTG[A/G]TGATCTCTGTAAGAA	99382
rs27358087	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103675984	CAAGATGGCCAAGAT[A/G]AAAATATCATTTCAT	99382
rs27358088	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103675963	CTTCCAGATACCCTA[A/G]ATGGCCAAGATGGCC	99382
rs27358089	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	GRCm38.p3	2:103675581	TGGTAAAAGCAGTAC[A/G]GCCTGGTGACTGATG	99382
rs27358090	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103675579	GGTGGTAAAAGCAGT[A/G]CGGCCTGGTGACTGA	99382
rs27358091	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103675546	AGCAGTGGCCGTGAC[C/T]AGTTTTTGAAATACT	99382
rs27358092	snp	C/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103675524	GAACAGGGAGGCCAG[C/G]GTGAGGAGCAGTGGC	99382
rs27358093	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	GRCm38.p3	2:103675465	AAAGGCAGTTGGATT[C/T]CTTCATACAGACAGC	99382
rs27358094	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103675380	TTTTGCCACTTTACC[A/G]GCAGAAAATCACTTC	99382
rs27358095	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103675180	GGGTGGAGTTTCCCT[C/T]CTAACTCAACACCAC	99382
rs27358096	snp	C/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103675138	TGGGTGGCACCTCCT[C/T]GTGAGAAGGCAGGTT	99382
rs27358097	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103675005	CAGATGAAATCATCT[C/T]CTTTTCCTTTGAACT	99382
rs27358098	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103674864	GGTTCTGTTTCTTTC[C/T]ACTGCTGACCATTTG	99382
rs27358099	snp	C/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103674801	CGCAAGCACACACAT[C/G]CTCTTATGACTGTGA	99382
rs27358100	snp	A/G	0.456747	0.140554	intron-variant	Abtb2	GRCm38.p3	2:103674616	TAGGTTGGAAGGGAA[A/G]CTATGTTGCAGCCTT	99382
rs27358101	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103674591	TAGGGAGAATGCTGT[A/G]ATGGGTTATTAGGTT	99382
rs27358102	snp	C/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103674287	ACTCCTTACCCATTC[C/T]TTCCATGGAAAAATC	99382
rs27358103	snp	A/G	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103673914	CTTCCCTTTGCTTCA[A/G]GAGGCACCCATGCCT	99382
rs27358104	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103673727	CTCCCTGTCTCAGAA[C/T]GTTGTCCTTGTTTGA	99382
rs27358105	snp	C/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103673677	CTCAGTTTGGACACC[C/G]TGCTCCATGTGTATG	99382
rs27358106	snp	A/T	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103673589	CCCTACTAAGTTTGT[A/T]TGGGCATGGAGTATA	99382
rs27358107	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103673525	CTGTGTCCCACAGGA[A/G]AATGAGACACTGCAG	99382
rs27358108	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103673452	TTGCTGCTCAGTTTG[C/T]ATTCCACTTTGCCAT	99382
rs27358109	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103672873	CAGTTGTAACTGTGC[A/G]TTTTTATTTCATTGC	99382
rs27358110	snp	A/G	0.497041	0.0383476	intron-variant	Abtb2	Mm_Celera	2:103672303	CTTAAAGTATTCAAA[A/G]TAACACAGAGCCTTT	99382
rs27358111	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103672215	AGAGGTCATTCCAAG[C/T]CTTGTGCTTCTTGGC	99382
rs27358112	snp	A/C	0.46281	0.131194	intron-variant	Abtb2	GRCm38.p3	2:103671111	AGAATTGCTTGGAGA[A/C]ATTAGAAAGGTGAAA	99382
rs27358113	snp	C/G	0.396694	0.202437	intron-variant	Abtb2	GRCm38.p3	2:103671085	GGAAGCTGAGAAAAA[C/G]TCTTCCACCCAGAAT	99382
rs27358114	snp	C/T	0.396694	0.202437	intron-variant	Abtb2	Mm_Celera	2:103671024	ACCAGATCATTTGAT[C/T]CATGTAAATTTGCCA	99382
rs27358115	snp	C/T	0.48	0.0979796	intron-variant	Abtb2	GRCm38.p3	2:103670885	TTGTCTAAAAACACC[C/T]TGAACAATGGGGGGG	99382
rs27358116	snp	A/G	0.165289	0.235211	intron-variant	Abtb2	Mm_Celera	2:103670585	TCAGGATGACTTCCT[A/G]TAAGAGGATGGAAAG	99382
rs27358117	snp	C/T	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103668857	TGAGGGAGCAAGTCA[C/T]TGTGGTCCTGCATGA	99382
rs27358118	snp	A/C	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103668852	CCTCATGAGGGAGCA[A/C]GTCACTGTGGTCCTG	99382
rs27358119	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	Mm_Celera	2:103668810	GGGGCTCCTCTCAGA[A/G]CCCAGGCCTGCTTCC	99382
rs27358120	snp	A/G	0.260355	0.249785	intron-variant	Abtb2	Mm_Celera	2:103668650	CTTGCCCTTCCAAGA[A/G]GCCTGCTCCAGGCTC	99382
rs27358121	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103668243	ACTCCACAAGACATC[A/G]GGTTGCCTCATTCAA	99382
rs27358122	snp	C/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103668168	ATCAGTCATGAGTGC[C/T]ACTTGCAGGCAGGTA	99382
rs27358123	snp	C/T	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103667933	CTGCGCTGGAAAGTC[C/T]TCACCCAGCATAGAC	99382
rs27358124	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103667922	CTCCAAGGTAGCTGC[A/G]CTGGAAAGTCCTCAC	99382
rs27358125	snp	A/T	0.5	0	intron-variant	Abtb2	Mm_Celera	2:103667348	GAAGGAAAAATAAGA[A/T]GCTGAGAGGAGTAGA	99382
rs27358126	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103667273	ATTTTCCCTCTTCCA[A/G]GGTACTCAGTGGGAA	99382
rs27358127	snp	A/C	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103667255	CTGTCTGCAGTCTAG[A/C]CCATTTTCCCTCTTC	99382
rs27358128	snp	G/T	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103667230	ATTTATTTAACCTGC[G/T]GATGGTACTCTGTCT	99382
rs27358129	snp	C/G	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103667141	TTACATACCTGGGAG[C/G]TACACAAAAAGAGAC	99382
rs27358130	snp	C/T	0.497778	0.0332592	intron-variant	Abtb2	GRCm38.p3	2:103667041	TGGAAGTTACATTCA[C/T]AGTGAGCCTCATGCT	99382
rs27358131	snp	C/T	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103667005	AGAACTGCAGGCAGC[C/T]CAGCATCCAGTGACC	99382
rs27358132	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103666861	CAGCACCCGTGCTGT[A/G]ATAAAAGTCACAGTG	99382
rs27358133	snp	A/C	0.456747	0.140554	intron-variant	Abtb2	GRCm38.p3	2:103666816	GCACCTGGAAAGAGA[A/C]GATCACGCTCAAAGT	99382
rs27358134	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103666814	ATGCACCTGGAAAGA[A/G]AAGATCACGCTCAAA	99382
rs27358135	snp	C/T	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103666773	GCCACCAGCAAGAGA[C/T]GCAGAACATTACCCA	99382
rs27358136	snp	A/G	0.35503	0.226867	intron-variant	Abtb2	GRCm38.p3	2:103666735	AGTGATTCAGGTAAT[A/G]GAGTCAACCCCGGTA	99382
rs27358137	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	Mm_Celera	2:103666692	AGAGCACTTCAGTCT[C/T]TGTGAGGCTTGAGAT	99382
rs27358138	snp	C/T	0.429688	0.173817	intron-variant	Abtb2	GRCm38.p3	2:103666527	TATTGTTTTTGCTGT[C/T]TTACAGGAGTATTAA	99382
rs27358139	snp	C/G	0.375	0.216506	intron-variant	Abtb2	Mm_Celera	2:103666466	CAGTAAGCACCCTGG[C/G]TAGGATCTGAAACCC	99382
rs27358140	snp	G/T	0.142012	0.225474	intron-variant	Abtb2	Mm_Celera	2:103666391	AAGACACACAGCAAG[G/T]CAGGCATGGAATGGT	99382
rs27358141	snp	G/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103666344	TGGGTCAAGGACTGG[G/T]CCCTTACATGGCCAT	99382
rs27358142	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103664871	GAAGCCTTCTCTTAT[C/T]CTATAATTCCACCTG	99382
rs27358143	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103664725	GTCCACCTGTGGCTT[A/G]AATTGGAGCTGGGAG	99382
rs27358144	snp	C/T	0.495868	0.0452663	intron-variant	Abtb2	GRCm38.p3	2:103664724	GGTCCACCTGTGGCT[C/T]GAATTGGAGCTGGGA	99382
rs27358145	snp	C/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103664715	CAGTGCTCTGGTCCA[C/T]CTGTGGCTTGAATTG	99382
rs27358146	snp	A/G	0.32	0.24	intron-variant	Abtb2	GRCm38.p3	2:103664635	CAAGCCTGTGTGGTC[A/G]CAGAGTTGCTGTAAA	99382
rs27358147	snp	C/T	0.345679	0.230967	intron-variant	Abtb2	Mm_Celera	2:103664634	GCAAGCCTGTGTGGT[C/T]GCAGAGTTGCTGTAA	99382
rs27358148	snp	A/G	0.277778	0.248452	intron-variant	Abtb2	Mm_Celera	2:103664524	GTGTCACACGTGTTT[A/G]TTTGTCAAGCAGGGC	99382
rs27358149	snp	A/T	0.444444	0.157135	intron-variant	Abtb2	GRCm38.p3	2:103663958	ACAGTCGACAGTATG[A/T]ACTCTCTAGGGAAGC	99382
rs27358150	snp	C/T	0.297521	0.245442	intron-variant	Abtb2	Mm_Celera	2:103663814	TGGAATGCTTACAAA[C/T]TGTGTCATCTCCTGC	99382
rs27358151	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103663685	CCTTTGAACAGTGAC[A/G]AACACATTTGAATTA	99382
rs27358152	snp	A/G	0.486111	0.0821678	intron-variant	Abtb2	GRCm38.p3	2:103663320	AGGGTAGACCGTATG[A/G]AGAAGCATAATGGGA	99382
rs27358153	snp	A/T	0.18	0.24	intron-variant	Abtb2	Mm_Celera	2:103662934	TAGGTACCATGTAGG[A/T]ATTACATACTCTGCG	99382
rs27358154	snp	A/G	0.152778	0.230321	intron-variant	Abtb2	Mm_Celera	2:103662866	TTATAGGAGCCTTCT[A/G]TGTCCACTCCCTGGC	99382
rs27358155	snp	C/T	0.152778	0.230321	intron-variant	Abtb2	GRCm38.p3	2:103662741	CTTTTCAAATGCCAA[C/T]TGTCAAGTCAACTTT	99382
rs27358156	snp	C/T	0.486111	0.0821678	intron-variant	Abtb2	Mm_Celera	2:103662401	CTACCTCTGTCTCTA[C/T]TTCAGCCAGGAGGAG	99382

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