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
rs6218200	snp	A/T	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80278544	ATCCTCAAACTCCTC[A/T]CAGTTTAAGGGTTCC	106794
rs6223553	snp	A/G	0.260355	0.249785	intron-variant	Dhx57	Mm_Celera	17:80272908	CCAGACCTGAGGGAG[A/G]TGGCGCTGGCCCTTA	106794
rs6224199	snp	C/T	0.290657	0.246672	synonymous-codon, nc-transcript-variant	Dhx57	Mm_Celera	17:80273055	ATTCTCCACGATAAT[C/T]GATGCAGGTCCTTCA	106794
rs6224791	snp	A/C	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80273158	TGCCCTTTCTTTAGG[A/C]AAGGGNTAACACCAC	106794
rs6224795	snp	A/G	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80273164	TTCTTTAGGNAAGGG[A/G]TAACACCACTAACAA	106794
rs6225223	snp	A/G	0.401235	0.199068	intron-variant	Dhx57	Mm_Celera	17:80273189	TAACAAAGTAACAGC[A/G]CCTTGAGACAGGAAA	106794
rs6225333	snp	A/G	0.471655	0.115624	intron-variant	Dhx57	Mm_Celera	17:80273259	CTGCTCTGAAACAGG[A/G]ATTTAGGATGCTAAC	106794
rs6225714	snp	C/T	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80273283	TGCTAACTTGAGCtt[C/T]ctccaagaaagggtc	106794
rs6225747	snp	A/G	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80273305	gaaagggtctctttg[A/G]gtagttttggaactt	106794
rs6225856	snp	C/T	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80273363	tcatagatccccctg[C/T]ctctgtcttccaagt	106794
rs6242262	snp	G/T	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80240753	TCTTGCTCACACAGG[G/T]AGAGTGGGCCTTTAT	106794
rs6242922	snp	A/G	0.408163	0.193609	intron-variant	Dhx57	Mm_Celera	17:80240911	GAAGAGTGTAAGCAC[A/G]CCTGACTTTAGAGAC	106794
rs6242928	snp	A/G	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80240916	gtgtaagcacncctg[A/G]ctttagagacttaat	106794
rs6243405	snp	G/T	0.408163	0.193609	intron-variant	Dhx57	Mm_Celera	17:80241008	GCTGGGTATATTAGG[G/T]TAAATAAAATATATT	106794
rs6243927	snp	A/G	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80241089	CTAATGCTTTATGCT[A/G]CATGCTCTACCTCTG	106794
rs6243953	snp	A/G	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80241106	ATGCTCTACCTCTGA[A/G]GTATGTtttctttct	106794
rs6244026	snp	C/T	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80241135	cttctttctttcttt[C/T]tttctttccttcttt	106794
rs6297377	snp	C/T	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80244051	ttccttgagacaggg[C/T]ctcactctncagctc	106794
rs6297389	snp	A/T	0.5	0	intron-variant	Dhx57	Mm_Celera	17:80244060	acagggnctcactct[A/T]cagctctggctgtcc	106794
rs6298585	snp	G/T	0.290657	0.246672	intron-variant	Dhx57	Mm_Celera	17:80244265	CCTGTCCTCATGGAT[G/T]TTATAATTCCAGGAC	106794
rs6298698	snp	A/G	0.290657	0.246672	intron-variant	Dhx57	Mm_Celera	17:80244320	ACAAATGCATACCCA[A/G]TGGCAGCAGAACAGA	106794
rs6362368	snp	C/T	0.290657	0.246672	intron-variant	Dhx57	Mm_Celera	17:80259948	GGTCCTCCGTTACTA[C/T]TTTGCCTTTGTCCTT	106794
rs29497781	snp	C/T	0.375	0.216506	intron-variant	Dhx57	Mm_Celera	17:80257716	AACAAGAAAGCCCTG[C/T]TCTTTTTGTTTTGGT	106794
rs29500527	snp	A/G	0.487535	0.077957	intron-variant	Dhx57	Mm_Celera	17:80250360	TTTTCAGGCTCTGTC[A/G]TTTGGCTCTTTCTAC	106794
rs29501418	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Dhx57	Mm_Celera	17:80282071	TGGCTCCTCAGGGTG[C/T]GGTGATCCCCCATCA	106794
rs29501915	snp	C/T	0.32	0.24	intron-variant	Dhx57	Mm_Celera	17:80259461	TGTAGAATCTCAGTG[C/T]AGGTGTTCAGCGCAT	106794
rs29515512	snp	C/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Dhx57, Morn2	Mm_Celera	17:80290651	AATACAGTGAAGTAA[C/G]CCTGTACAAATGGAA	106794
rs29517329	snp	A/G	0.304688	0.243945	intron-variant	Dhx57	Mm_Celera	17:80254901	AATGGAAATCCCAAG[A/G]CAGCATCTGTCAGCT	106794
rs29522740	snp	A/T	0.375	0.216506	intron-variant	Dhx57	Mm_Celera	17:80247832	GCTGACTTCAGACAC[A/T]CCAGAAGAGGGTGTC	106794
rs29541956	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Dhx57	Mm_Celera	17:80282317	GAACAAACACAAGAC[A/G]TTTTGTTGACAACAA	106794
rs29709564	snp	C/G	0.165289	0.235211	intron-variant	Dhx57	Mm_Celera	17:80272705	AGAAAAGTCTAAGCG[C/G]TCAGGAAGGGAGTGG	106794
rs29709565	snp	C/T	0.152778	0.230321	intron-variant	Dhx57	Mm_Celera	17:80272630	CACATGCGTTTGATA[C/T]TGGCTAGCTGAGTGT	106794
rs29709566	snp	C/T	0.152778	0.230321	intron-variant	Dhx57	Mm_Celera	17:80272234	ATACATTTTTGCTGA[C/T]CTATGGGCACACAGT	106794
rs29709567	snp	A/G	0.152778	0.230321	intron-variant	Dhx57	Mm_Celera	17:80271392	GAAGTTCAATAGGAC[A/G]GAAAGCCTGTAATGC	106794
rs29709568	snp	C/G	0.152778	0.230321	intron-variant	Dhx57	Mm_Celera	17:80270973	TGAGCACTGATCTGA[C/G]CCTTGCCAATAGCAA	106794
rs29709569	snp	C/T	0.277778	0.248452	intron-variant	Dhx57	Mm_Celera	17:80270337	TAGCCACTGCTCCTG[C/T]CTTGCACGTACACGT	106794
rs29709570	snp	A/T	0.345679	0.230967	intron-variant	Dhx57	Mm_Celera	17:80270302	GCTACATATCTTTTT[A/T]AAAGCAGATCTGGTT	106794
rs29709571	snp	C/T	0.345679	0.230967	intron-variant	Dhx57	Mm_Celera	17:80270152	GCCTCATGGCAGAGG[C/T]ATACATCCACAGGGT	106794
rs29709572	snp	A/G	0.345679	0.230967	intron-variant	Dhx57	Mm_Celera	17:80270065	AGCTTTCCAGCTGTC[A/G]GAACAGAATTCTCCT	106794
rs29709573	snp	C/T	0.297521	0.245442	intron-variant	Dhx57	Mm_Celera	17:80269985	GGAAAAAATGTTACT[C/T]AAGGTGTTGGTAAGA	106794
rs29709814	snp	A/G	0.124444	0.216185	intron-variant	Dhx57	Mm_Celera	17:80249803	CCCCTCTGGGCAACT[A/G]CCAGCTACGCCAGCG	106794
rs29709815	snp	A/G	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80249635	TGAAACAAAAGCTTT[A/G]TAGAGACCTTCTCCA	106794
rs29709816	snp	C/G	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80249606	CTCCCTTTCTCCAGT[C/G]TCCAGATTGTTAGTG	106794
rs29709817	snp	G/T	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80249182	TCCTACCTTATGGAG[G/T]CCCTGGATCACAGCT	106794
rs29709818	snp	A/T	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80249122	TGAGCCGAGAGTAGC[A/T]AGCATTTCTCTCAGT	106794
rs29709819	snp	A/C	0.265928	0.249492	intron-variant	Dhx57	Mm_Celera	17:80248641	TTTAAAGAAGGAGCT[A/C]GCAACACATCCAAGG	106794
rs29709820	snp	A/G	0.231111	0.249285	synonymous-codon	Dhx57	Mm_Celera	17:80248337	AATTTCTTTTGCTCG[A/G]AGTCCTTCTTTCACA	106794
rs29709821	snp	C/T	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80248173	TCTGTGGACCGGAGA[C/T]GGAGTGTGCCACTGC	106794
rs29709822	snp	C/T	0.484429	0.0868505	intron-variant	Dhx57	Mm_Celera	17:80248057	AAACATTACTACAGC[C/T]TACTGTGAACTACAG	106794
rs29709823	snp	A/G	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80247713	ATGCATCATGGAAAG[A/G]AAGAGCCTGGTTTGT	106794
rs29710494	snp	A/T	0.32	0.24	intron-variant	Dhx57	Mm_Celera	17:80269886	AAAACTAACAATGCT[A/T]AGTGTGATCCTGAGT	106794
rs29710495	snp	A/C	0.165289	0.235211	intron-variant	Dhx57	Mm_Celera	17:80269870	AGTTGAGTCTCAGTG[A/C]AAAACTAACAATGCT	106794
rs29710496	snp	A/G	0.375	0.216506	intron-variant	Dhx57	Mm_Celera	17:80269700	TCCTCTCTACACAAG[A/G]CCTTACACACCTGTA	106794
rs29710497	snp	C/G	0.165289	0.235211	intron-variant	Dhx57	Mm_Celera	17:80268961	ATCTGTATGTCAAAA[C/G]AAAGGAGTCCTAAAA	106794
rs29710498	snp	C/T	0.152778	0.230321	intron-variant	Dhx57	Mm_Celera	17:80268617	TCCTTCTCGAGGGAT[C/T]TGAACCGCACGGAAA	106794
rs29710499	snp	C/G	0.32	0.24	intron-variant	Dhx57	Mm_Celera	17:80267817	TCACATTAAAACTAT[C/G]AAAGAGGCCGGGTGG	106794
rs29710500	snp	A/G	0.375	0.216506	intron-variant	Dhx57	Mm_Celera	17:80267729	GACAACATTAATTCC[A/G]CTTAACAGCAATTCC	106794
rs29710501	snp	A/G	0.142012	0.225474	intron-variant	Dhx57	Mm_Celera	17:80267675	GTCACACATTAACGA[A/G]ATTTTGGAAAAGTAA	106794
rs29710502	snp	G/T	0.197531	0.244432	intron-variant	Dhx57	Mm_Celera	17:80267439	AGTCTGAAACTCCAC[G/T]GGAAGCAAGCAACCA	106794
rs29710503	snp	C/G	0.444444	0.157135	intron-variant	Dhx57	Mm_Celera	17:80267310	TGGCATGATGCCCAG[C/G]AGACACTCCTGGTGA	106794
rs29710694	snp	C/T	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80247631	GCAAGTCCTGATGCC[C/T]AGCATGATCAAAGTG	106794
rs29710695	snp	C/T	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80247568	AGCCAGTGCTCTCGA[C/T]TGGGATGTGGTTAAG	106794
rs29710696	snp	G/T	0.124444	0.216185	intron-variant	Dhx57	Mm_Celera	17:80247252	TGCCAGCATTTGTCT[G/T]TCTTTTTTCTTTTGA	106794
rs29710697	snp	C/T	0.244898	0.249948	intron-variant	Dhx57	Mm_Celera	17:80247089	CAAAAACCAGGAGGA[C/T]TCAGGAAGTGTCCTG	106794
rs29710698	snp	A/C	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80246893	AAGATGACTAATGAG[A/C]AATTTTTTTTCTTTT	106794
rs29710699	snp	C/T	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80246864	GAATCCTTTCGCGCT[C/T]TGTGCAGCTACTGAA	106794
rs29710700	snp	A/G	0.244898	0.249948	intron-variant	Dhx57	Mm_Celera	17:80246662	TTAAGGACTCACACC[A/G]AATCAGTATTAAGTA	106794
rs29710701	snp	C/T	0.244898	0.249948	intron-variant	Dhx57	Mm_Celera	17:80246658	TTATTTAAGGACTCA[C/T]ACCGAATCAGTATTA	106794
rs29710702	snp	A/G	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80246550	AGAATCCTCCTGGCT[A/G]CAACTTTGTGCACAT	106794
rs29710703	snp	A/T	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80246510	AAATTTAGACTTGTC[A/T]GGTGAAAATTCGATC	106794
rs29711384	snp	C/G	0.165289	0.235211	intron-variant	Dhx57	Mm_Celera	17:80267252	TGCTTACAGAATGAT[C/G]AAAACAACAAAAGCA	106794
rs29711385	snp	C/T	0.297521	0.245442	intron-variant	Dhx57	Mm_Celera	17:80267229	AACGCTTTAAGTTCC[C/T]GAGTGAATGCTTACA	106794
rs29711386	snp	A/T	0.18	0.24	intron-variant	Dhx57	Mm_Celera	17:80267220	CTGGATGTCAACGCT[A/T]TAAGTTCCCGAGTGA	106794
rs29711387	snp	C/T	0.396694	0.202437	intron-variant, upstream-variant-2KB	Dhx57	Mm_Celera	17:80265902	CTTAGGGTCTCTGCA[C/T]GTCAGTAACATGGCA	106794
rs29711388	snp	A/G	0.18	0.24	intron-variant, upstream-variant-2KB	Dhx57	Mm_Celera	17:80265867	CAGGACTCCACTCTC[A/G]TTGTCCTTGAGGAAT	106794
rs29711389	snp	A/G	0.165289	0.235211	intron-variant, upstream-variant-2KB	Dhx57	Mm_Celera	17:80265802	AGTGCTTACTGACAT[A/G]GCTCACTGCGCCCTC	106794
rs29711390	snp	C/G	0.18	0.24	intron-variant, upstream-variant-2KB	Dhx57	Mm_Celera	17:80265746	ACTCAAATGTCATCC[C/G]AGTATGCCACTCCTC	106794
rs29711391	snp	C/T	0.336735	0.234472	intron-variant, upstream-variant-2KB	Dhx57	Mm_Celera	17:80265245	GTTAAGGGTCAGACA[C/T]GTGCCACATAGGAAA	106794
rs29711392	snp	A/G	0.165289	0.235211	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	Dhx57	Mm_Celera	17:80265203	CAAAACTAGCAGTAA[A/G]AAGTCACTGGAGACA	106794
rs29711393	snp	A/C	0.165289	0.235211	missense, upstream-variant-2KB, nc-transcript-variant	Dhx57	Mm_Celera	17:80265127	TGGAGAACAGCCCAG[A/C]GTCCAGAGTTGCACT	106794
rs29711584	snp	A/G	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80246487	CCACAGCTGCCACAC[A/G]TTACTGCAAATTTAG	106794
rs29711585	snp	C/T	0.132653	0.220748	intron-variant	Dhx57	Mm_Celera	17:80245620	GCTTTAGGGACAGAC[C/T]GTGCTTCTCATTTGA	106794
rs29711586	snp	C/T	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80245536	CTGTCAGTCTCTTTA[C/T]ACAGAGTCAACCTTC	106794
rs29711587	snp	C/G	0.391111	0.206368	intron-variant	Dhx57	Mm_Celera	17:80245421	TCATGACTTCCTAAA[C/G]CAACGCACAGGCGCG	106794
rs29711588	snp	A/C	0.244898	0.249948	intron-variant	Dhx57	Mm_Celera	17:80245359	CAGGCTGAAGGAAGG[A/C]CAGAATAAAGGATTG	106794
rs29711589	snp	A/G	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80245287	CCTTTAGAATTGACA[A/G]CTACTGTGACCACAG	106794
rs29711590	snp	C/T	0.444444	0.157135	intron-variant	Dhx57	Mm_Celera	17:80244881	AAGTCTTCATGACAT[C/T]AGGCTGATTCGGATG	106794
rs29711591	snp	C/G	0.345679	0.230967	intron-variant	Dhx57	Mm_Celera	17:80244842	GAACTTGGTGACCAA[C/G]TGAATCAATATGGAG	106794
rs29711592	snp	A/G	0.231111	0.249285	intron-variant	Dhx57	Mm_Celera	17:80244761	TAGTACTTTGGGCAC[A/G]AAACAATGGAATTTG	106794
rs29711593	snp	C/T	0.244898	0.249948	intron-variant	Dhx57	Mm_Celera	17:80244546	GCATGTCTGGTGTCA[C/T]GGTAATGGAAAACCC	106794
rs29712274	snp	C/T	0.396694	0.202437	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	Dhx57	Mm_Celera	17:80263995	CTGATCAACAGGAAA[C/T]GCACGGCCTAGGAAA	106794
rs29712275	snp	A/G	0.18	0.24	intron-variant	Dhx57	Mm_Celera	17:80263727	TACTAGCGATAGACA[A/G]ATAGTCACACTCCAT	106794
rs29712276	snp	C/G	0.32	0.24	intron-variant	Dhx57	Mm_Celera	17:80263702	CTGGTCCCTGTGACC[C/G]GGGAAATGCTACTAG	106794
rs29712277	snp	C/T	0.396694	0.202437	intron-variant	Dhx57	Mm_Celera	17:80263659	TTCTTGTTACTTGAG[C/T]TAGACTATTACTCTA	106794
rs29712278	snp	C/T	0.18	0.24	intron-variant	Dhx57	Mm_Celera	17:80262697	AGAGAAACCTGTTTG[C/T]ATACAATAGAAATGA	106794
rs29712279	snp	A/G	0.375	0.216506	intron-variant	Dhx57	Mm_Celera	17:80262581	AAAGAGCCTGATCTA[A/G]AAGTGACAGCTAAAA	106794
rs29712280	snp	G/T	0.32	0.24	intron-variant	Dhx57	Mm_Celera	17:80261694	GCTGAGGCTTCTACA[G/T]CGAGCTGCTCCACTG	106794
rs29712281	snp	A/G	0.244898	0.249948	intron-variant	Dhx57	Mm_Celera	17:80261664	AATGCTGCCCGAGGA[A/G]CAGCGGCTGATACTG	106794
rs29712282	snp	C/T	0.35503	0.226867	intron-variant	Dhx57	Mm_Celera	17:80261577	CATCAAGGCAGCTGG[C/T]GTGCAAGCTGAGGGT	106794
rs29712283	snp	C/T	0.32	0.24	intron-variant	Dhx57	Mm_Celera	17:80261424	GATGCGTGGTAAGTA[C/T]AGAGAGCCTTTTAAG	106794

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