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
rs6204904	snp	A/G	0.5	0	intron-variant	Tle2	Mm_Celera	10:81580973	GGGGATTGTGGGTGC[A/G]GCATGTCCCCAGCCT	21886
rs6205521	snp	A/T	0.5	0	intron-variant	Tle2	Mm_Celera	10:81581108	TTATGAGACAGGGTC[A/T]CACTCACAGAGATCC	21886
rs6205546	snp	C/T	0.5	0	intron-variant	Tle2	Mm_Celera	10:81581125	ACTCACAGAGATCCT[C/T]CTGCTTCTTGGATTC	21886
rs46097994	snp	C/T			upstream-variant-2KB	Tle2	Mm_Celera	10:81572903	TAAGATGCCGTGTTT[C/T]TAGTAGCAGGTGCTG	21886
rs46302791	snp	G/T	0.124444	0.216185	intron-variant	Tle2	Mm_Celera	10:81583509	CAACTGCCAGCCACC[G/T]TGGGCTCCCACTTTA	21886
rs46331759	snp	G/T	0.244898	0.249948	intron-variant	Tle2	Mm_Celera	10:81589585	ACTTTGGGTCCCTCT[G/T]TGTACCACAGTGGAT	21886
rs46519550	snp	A/C	0.124444	0.216185	intron-variant	Tle6, Tle2	Mm_Celera	10:81592612	CTGTGACTTCTCAAA[A/C]ATTCCTTGAGCTGAC	21886
rs46634865	snp	A/G	0.124444	0.216185	intron-variant	Tle2	Mm_Celera	10:81588787	TGACCCCAGGGTCTC[A/G]GCACTCTCTCTCTTG	21886
rs46695054	snp	C/T	0.231111	0.249285	synonymous-codon, intron-variant	Tle6, Tle2	Mm_Celera	10:81592016	CAGCCAGTCTTCGGT[C/T]GGACTGTGAGCCAGG	21886
rs46921062	snp	C/G			upstream-variant-2KB	Tle2	Mm_Celera	10:81572838	AGGTGTGTTCTCGGT[C/G]TGCAAGGGGAAAATG	21886
rs47137828	snp	C/T	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Tle2	Mm_Celera	10:81586902	AGGCTCGTCTGTCTC[C/T]TTGCCTGGCATCCCT	21886
rs47213385	snp	A/C			intron-variant	Tle2	Mm_Celera	10:81585496	AGCTACGTGAAGCTC[A/C]TTATACAATTTTTAT	21886
rs47377551	snp	A/G	0.244898	0.249948	synonymous-codon, nc-transcript-variant	Tle2	Mm_Celera	10:81587185	CATCCCTCGCCACGC[A/G]AGGCAGCTACACACG	21886
rs47379030	snp	A/G	0.32	0.24	intron-variant	Tle6, Tle2	Mm_Celera	10:81591646	GTTGGAGTGTGGACA[A/G]TACCCAAGCCCTGAC	21886
rs47517866	snp	C/T	0.32	0.24	intron-variant	Tle2	Mm_Celera	10:81588666	CCTCTGCCCAGAATC[C/T]CAAGGTGCTGTGTTC	21886
rs47817107	snp	A/G	0.231111	0.249285	intron-variant	Tle2	Mm_Celera	10:81583866	TGCTCTGGGAGCTGT[A/G]ATTTTTGTTAATTGC	21886
rs48703184	snp	C/T	0.375	0.216506	intron-variant	Tle2	Mm_Celera	10:81576900	GCATGGTTGATCCCA[C/T]GGGCTTCTGAGACTC	21886
rs49014905	snp	A/T	0.124444	0.216185	intron-variant	Tle2	Mm_Celera	10:81584530	AGATTGGCTGGCCAC[A/T]GTACATGTGCCCTCG	21886
rs49528472	snp	A/G	0.231111	0.249285	intron-variant, downstream-variant-500B	Tle6, Tle2	Mm_Celera	10:81592915	GATTCCCTCAAAGCC[A/G]TGGGACTAACCCAAC	21886
rs49570830	snp	C/T	0.231111	0.249285	intron-variant	Tle2	Mm_Celera	10:81586695	AGGAATAAAGCTGGG[C/T]TAAAAAGCCTGGCCC	21886
rs49797502	snp	C/T	0.124444	0.216185	intron-variant	Tle2	Mm_Celera	10:81583806	AAGAGGTGGGTGACA[C/T]GTTTCACCTAGGGCT	21886
rs50096865	snp	C/T	0.124444	0.216185	downstream-variant-500B, missense, intron-variant	Tle2, Tle6	Mm_Celera	10:81591094	TGATGATGAGCCTGC[C/T]GTTCTCAGTCATGTC	21886
rs50103019	snp	A/G	0.124444	0.216185	intron-variant	Tle2	Mm_Celera	10:81584506	CTGTGTGCCCACCAA[A/G]TGTCTGAGAGATTGG	21886
rs50110733	snp	G/T	0.124444	0.216185	intron-variant	Tle6, Tle2	Mm_Celera	10:81592641	ACCTGGGCTGTTCCC[G/T]CTCCTGACACTGAGT	21886
rs50123562	snp	A/G	0.231111	0.249285	upstream-variant-2KB	Tle2	Mm_Celera	10:81573071	ATGCTGGAGAGTATG[A/G]CGGTCCAGATACTGA	21886
rs50131868	snp	C/T	0.124444	0.216185	downstream-variant-500B, missense, intron-variant	Tle2, Tle6	Mm_Celera	10:81591310	CCGTGATGAAGTTGC[C/T]CATACCGACGCTCGC	21886
rs50135314	snp	A/G	0.124444	0.216185	intron-variant	Tle6, Tle2	Mm_Celera	10:81592635	GAGCTGACCTGGGCT[A/G]TTCCCTCTCCTGACA	21886
rs50368959	snp	C/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Tle2	Mm_Celera	10:81588257	GGACTGCCTTACATA[C/T]GCCTTTAAAAATAAG	21886
rs50433282	snp	C/T	0.124444	0.216185	intron-variant	Tle6, Tle2	Mm_Celera	10:81592633	TTGAGCTGACCTGGG[C/T]TGTTCCCTCTCCTGA	21886
rs50470466	snp	A/G			upstream-variant-2KB	Tle2	Mm_Celera	10:81572756	ACACCACAAGCCGGG[A/G]ATCAGGAACCGCTGG	21886
rs50492547	snp	A/C			upstream-variant-2KB	Tle2	Mm_Celera	10:81572747	AGTTCTCAGACACCA[A/C]AAGCCGGGGATCAGG	21886
rs50696582	snp	A/G	0.244898	0.249948	intron-variant	Tle2	Mm_Celera	10:81586977	TGTGTTGGAGGCCTG[A/G]GTCCCTTCTTCCTGG	21886
rs50779820	snp	C/T	0.32	0.24	intron-variant	Tle2	Mm_Celera	10:81588537	CAAATAAAAAACCAC[C/T]GCTAGACTAAGAGTG	21886
rs51187420	snp	A/G			upstream-variant-2KB	Tle2	Mm_Celera	10:81572847	CTCGGTGTGCAAGGG[A/G]AAAATGAGTAAACAG	21886
rs51416360	snp	C/G	0.32	0.24	downstream-variant-500B, intron-variant, synonymous-codon	Tle2, Tle6	Mm_Celera	10:81590493	TTTCTGTGTGTGTGT[C/G]AAGCGTACAGGTGAG	21886
rs51458785	snp	A/G	0.124444	0.216185	intron-variant	Tle6, Tle2	Mm_Celera	10:81591877	GCCCAGGCTCAGTGG[A/G]CTCCTTACCATTTGG	21886
rs51544932	snp	A/G	0.231111	0.249285	intron-variant	Tle2	Mm_Celera	10:81589333	TACTGCATAGTAGGC[A/G]GCTTCAGGAAGGAGT	21886
rs51867465	snp	C/T	0.142012	0.225474	downstream-variant-500B, utr-variant-3-prime, intron-variant, synonymous-codon	Tle2, Tle6	Mm_Celera	10:81590670	CCTTATCCTGCCTGG[C/T]GTGGGCTTTACCAAC	21886
rs51905951	snp	G/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Tle2	Mm_Celera	10:81588242	TAGTCAGTGGGAGAC[G/T]GACTGCCTTACATAC	21886
rs52364399	snp	A/C	0.231111	0.249285	missense, nc-transcript-variant	Tle2	Mm_Celera	10:81587304	GGGACGTGGGCCAGC[A/C]GGGTAGCAAGACCCC	21886
rs212120108	snp	A/G			intron-variant	Tle2	Mm_Celera	10:81582896	GCCCTGGTAAGGAAG[A/G]CAGGGTGCCTGAAGC	21886
rs212162474	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81583479	AAGCCTCCCTACCCC[C/T]GCAGGTTACCATGAC	21886
rs212397023	snp	A/G			downstream-variant-500B, utr-variant-3-prime, intron-variant	Tle2, Tle6	GRCm38.p3	10:81591017	CACTGTGCAGTTAGG[A/G]GAGGGGAGTTGAAGT	21886
rs212533976	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81577957	TGTGTGCAGTACCCT[C/T]AGAGACCAGAGGAGG	21886
rs212573160	snp	A/G			intron-variant	Tle2	Mm_Celera	10:81578617	AGAGTTAGGTGAGCA[A/G]TTATGGGACTAATCT	21886
rs212747146	in-del	-/CGCCCGAA			intron-variant	Tle6, Tle2	Mm_Celera	10:81592102	AGGCTGCAAGGTCCC[-/CGCCCGAA]CGCCCGCCCACCCAA	21886
rs212768799	snp	C/G			missense, intron-variant	Tle6, Tle2	Mm_Celera	10:81591956	CACCTGGTCCCTCTT[C/G]CTGCTGTTGAACAGG	21886
rs212817201	snp	C/G			intron-variant	Tle2	Mm_Celera	10:81588619	CAGTCAAGGCTCAGC[C/G]CTGGACCTTGAGCCA	21886
rs212841014	snp	C/T			intron-variant, downstream-variant-500B	Tle2	Mm_Celera	10:81588126	GTAAAGTATTTGCCT[C/T]GATGGCAGGAGTTCA	21886
rs213127884	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81585558	TTATGTATTTTCAAA[C/T]TTGGGTTTTTAGAGT	21886
rs213171513	snp	A/C			upstream-variant-2KB	Tle2	Mm_Celera	10:81574372	GGTGGCTTCTCAGCT[A/C]TGGGGGACACCCTTA	21886
rs213289042	snp	A/G			intron-variant, missense, nc-transcript-variant	Tle2	Mm_Celera	10:81576566	AGGGTGGCACCAGCT[A/G]TCCACACTGGCCAAG	21886
rs213870650	snp	A/C			intron-variant	Tle2	Mm_Celera	10:81589727	GAAAAGCAGTCAGTG[A/C]TTTTAACCGCTGAGC	21886
rs214017298	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81581563	TGCCCCCCCACACAC[C/T]TAGGATCCCCCAATG	21886
rs214074283	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81580738	GTGGGGTTCAATGTT[C/T]GTGCTGTTTGTCCTT	21886
rs214417830	in-del	-/AGAC			intron-variant	Tle2	Mm_Celera	10:81580172	TGCAGAAATACACAT[-/AGAC]AGACAGACAGACAGA	21886
rs214449371	snp	A/T			downstream-variant-500B, utr-variant-3-prime, intron-variant	Tle2, Tle6	Mm_Celera	10:81590721	CTTTAAAACAAAAAC[A/T]GGGTGGGGCTAGTTT	21886
rs214755268	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81585608	GACTGTCCTGAAGGT[C/T]CCTGAGTTTACCATT	21886
rs214820752	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81584226	GTGGTTAGCGTCAAC[C/T]CTGGGGAGTCTGTTC	21886
rs214921402	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	Tle2	Mm_Celera	10:81574757	TCTATGCACTAAGTT[G/T]AAAGAGTCTGGTCCT	21886
rs215033474	snp	A/G			intron-variant	Tle6, Tle2	Mm_Celera	10:81592046	GCTCATGATCTGGGT[A/G]AGCCAGGCAGAGGTA	21886
rs215068895	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81588745	CCCCATTTGGGGCAC[C/T]CCTGGGCCTTCTTCC	21886
rs215487540	in-del	-/TT			intron-variant	Tle2	Mm_Celera	10:81582184	GCCTGGTCTCTCCTG[-/TT]GTTTGGGCCAGGAAT	21886
rs215499646	snp	C/T			synonymous-codon, downstream-variant-500B	Tle6, Tle2	Mm_Celera	10:81592770	CAGGTCCCAGCATCG[C/T]AGGCAGGCGTCCAGA	21886
rs215609849	in-del	-/ACCT			intron-variant	Tle2	Mm_Celera	10:81587069	GTTAGCCACCCACCC[-/ACCT]GTCTCTGCGGCCTCC	21886
rs215693845	snp	A/G			intron-variant	Tle2	Mm_Celera	10:81583587	CTAGCCAGCTGGGGA[A/G]GCCATCAAGGGCATC	21886
rs215714969	in-del	-/A			downstream-variant-500B, intron-variant, frameshift-variant	Tle2, Tle6	Mm_Celera	10:81590524	GACCCGACTGGGTAT[-/A]CAGCCTTCATTTCTC	21886
rs215721904	snp	A/T			intron-variant, downstream-variant-500B	Tle6, Tle2	Mm_Celera	10:81593209	GAGCCATCCTAGGCT[A/T]CAGAGCAAGTTCAGC	21886
rs215737565	snp	G/T			intron-variant	Tle2	Mm_Celera	10:81579868	GGTCCAGTAGGCCCT[G/T]CAAAGCATGACCTGG	21886
rs215753245	snp	A/C			intron-variant	Tle2	Mm_Celera	10:81578938	AACACAGCATCAGTA[A/C]AGACAGAGGCTGACC	21886
rs215967893	snp	A/T			downstream-variant-500B, intron-variant	Tle2, Tle6	Mm_Celera	10:81590898	CCTGGGTAAAGGACA[A/T]ATCTCTGCCATTTCA	21886
rs215977759	snp	A/G			intron-variant, downstream-variant-500B	Tle2	Mm_Celera	10:81588268	CATACGCCTTTAAAA[A/G]TAAGATTTACTTATT	21886
rs216005177	snp	C/T			intron-variant	Tle6, Tle2	Mm_Celera	10:81591815	CTGAACTCAGATCCA[C/T]CTGCCTCTGCCTCCC	21886
rs216024558	snp	A/G			intron-variant	Tle2	Mm_Celera	10:81576747	CTGAGATTTGAGATA[A/G]CCCTGAAGGTTCTGA	21886
rs216339414	snp	A/G			intron-variant, splice-acceptor-variant	Tle2	Mm_Celera	10:81586853	GACTCTCTGTTCTCC[A/G]GCAGATGGCATTTGA	21886
rs216370343	snp	C/T			synonymous-codon, utr-variant-3-prime, nc-transcript-variant	Tle2	Mm_Celera	10:81587690	AGAGCTGACTTCGTC[C/T]GCCCCGGCCTGCTAT	21886
rs216500766	snp	A/C			intron-variant	Tle2	Mm_Celera	10:81577793	CTTCATATGTCCATG[A/C]GTGTGCATATCATGA	21886
rs216704050	in-del	-/CCTC			intron-variant	Tle2	Mm_Celera	10:81583125	ATCCCAACCCTCCTG[-/CCTC]CCTCCCTTACCACAA	21886
rs216789550	snp	G/T			intron-variant	Tle2	Mm_Celera	10:81581901	CTAATCAAAAGACAC[G/T]TTGTCCTACCAGCCT	21886
rs216895314	snp	A/G			intron-variant	Tle2	Mm_Celera	10:81583666	GCCAGAAGGCATGGC[A/G]GCTCCCCATGGTGGC	21886
rs216933767	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81584470	AGTTATACCCCTGAC[C/T]CAGTCACACCCAGCT	21886
rs217064161	in-del	-/GGGGG			utr-variant-5-prime, nc-transcript-variant	Tle2	Mm_Celera	10:81575632	AGCCTCCAAGAAGCT[-/GGGGG]GGGGGGGTCCATTCT	21886
rs217267218	snp	C/G			intron-variant	Tle2	Mm_Celera	10:81579028	GACCATAGGACCTTG[C/G]TGTTGGCCATTGCCA	21886
rs217269094	snp	A/G			intron-variant	Tle2	Mm_Celera	10:81589638	GTCTTCAGACACACC[A/G]GAAGAGGGAATCAGA	21886
rs217303262	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81580374	ATGCCCTGCTCCCAG[C/T]CCAGGCACGCAGTGG	21886
rs217424408	snp	C/T			synonymous-codon, nc-transcript-variant	Tle2	Mm_Celera	10:81582763	AGAGCCCCCCAGCCC[C/T]GTGACCACCCCTTGT	21886
rs217436127	snp	A/G			intron-variant	Tle2	Mm_Celera	10:81581415	TTTTCATAGAACTCA[A/G]TTTTCCCATCTGTAC	21886
rs217526586	in-del	-/TT			intron-variant	Tle2	Mm_Celera	10:81584149	AAACCAAATAAAAAA[-/TT]TTTTTTTTTTAAAAA	21886
rs217627966	snp	C/T			synonymous-codon, intron-variant	Tle2	Mm_Celera	10:81588850	TCAGGACTGGTTGGC[C/T]GTGGGGATGGAGAGC	21886
rs217719098	snp	A/G			intron-variant	Tle2	Mm_Celera	10:81576880	CTGAGATAGCATTTG[A/G]AGTTGCATGGTTGAT	21886
rs217829842	snp	A/C			intron-variant	Tle2	Mm_Celera	10:81583192	TTTTCCCCTCCCACA[A/C]GTCTCTGTTGAGCCT	21886
rs217951333	snp	A/G			intron-variant	Tle2	Mm_Celera	10:81583743	GTAAAGTCAGTCCAG[A/G]GCTAGCCTTGGCTAC	21886
rs218093120	snp	C/T			upstream-variant-2KB	Tle2	Mm_Celera	10:81574105	ACTCCCAGAGTGGCA[C/T]ACTTCCTCCAACAAG	21886
rs218167718	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81589972	AGGATGGGGCAGAAG[C/T]ATGGTTGGTTTGAGA	21886
rs218202903	in-del	-/G			intron-variant	Tle2	Mm_Celera	10:81577563	GTCCCCTCTAGTGCT[-/G]GGGGGCTGGATGGTG	21886
rs218289498	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81581029	CCAGCGTCACCACAT[C/T]CAAAGTACAGGATGC	21886
rs218320519	snp	A/C			intron-variant	Tle2	Mm_Celera	10:81582113	GGAAATGGGAGGTGG[A/C]AAGTTTGCAGAGTTC	21886
rs218409425	in-del	-/CC			intron-variant	Tle2	Mm_Celera	10:81583292	TTTCTGCAATGGTGA[-/CC]CCCCCACAACCACAG	21886
rs218636763	snp	G/T			utr-variant-5-prime, intron-variant, nc-transcript-variant	Tle2	Mm_Celera	10:81575332	CCACAGACCTGCGGC[G/T]CTGACTGCAGCTGCC	21886
rs218673264	snp	C/T			intron-variant	Tle2	Mm_Celera	10:81576965	ATGTGGAGATTGACT[C/T]TGAGGTCTGTAATTA	21886

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