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
rs3670396	snp	A/C	0.32	0.24	intron-variant	Rnf38	Mm_Celera	4:44130878	ATTCTACTAAAAAAA[A/C]CTCAAAACTGACTAT	73469
rs3671467	snp	C/G	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44130999	AGCCATCCTGACAGA[C/G]CACTGCTATTCTGAA	73469
rs3671483	snp	C/T	0.495868	0.0452663	intron-variant	Rnf38	Mm_Celera	4:44131011	AGACCACTGCTATTC[C/T]GAATCTTTGGGGGTT	73469
rs3671524	snp	C/T	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44131031	CTTTGGGGGTTTCTA[C/T]ATGCATAGGAGAAGA	73469
rs3706338	snp	C/T	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44138414	TCTAAGTTAAGTAAT[C/T]CTCTGTGCTTCTACC	73469
rs3725792	snp	A/G	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44232801	AAAAAGACACTGTAT[A/G]AACAGGCCTCCTTCC	73469
rs6152318	snp	G/T	0.304688	0.243945	intron-variant	Rnf38	Mm_Celera	4:44155525	AACTGGTCACCAAAG[G/T]TCATAAATGACAAAA	73469
rs6153428	snp	A/G	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44155758	TATAGTAAAGTGTTT[A/G]CCTTACAAGCTTAGG	73469
rs6307101	snp	A/G	0.359862	0.224567	intron-variant	Rnf38	Mm_Celera	4:44143082	ATGAAGCCCCAGTAA[A/G]GGCTAAGATCGTTAT	73469
rs6307180	snp	A/C	0.359862	0.224567	intron-variant	Rnf38	Mm_Celera	4:44143122	GCTACATTACTAAGT[A/C]TGATGCAAACCTTTA	73469
rs6307704	snp	C/T	0.48	0.0979796	intron-variant	Rnf38	Mm_Celera	4:44143211	TATATATTTTAATCA[C/T]TCTAAATAAAATGTA	73469
rs6308192	snp	A/C	0.290657	0.246672	intron-variant	Rnf38	Mm_Celera	4:44143276	AATACTTATGCTGAG[A/C]TTTTTCTTATAGTAA	73469
rs6308317	snp	C/T	0.359862	0.224567	intron-variant	Rnf38	Mm_Celera	4:44143357	GTTAGCTATCCTAAG[C/T]GAGGACTGAAGAGCC	73469
rs6312998	snp	A/G	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44224609	acagggtttctctgt[A/G]tagccctggctgtcc	73469
rs6313053	snp	C/G	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44224641	ggaactcactctgta[C/G]accaggctggcctng	73469
rs6313076	snp	C/T	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44224655	anaccaggctggcct[C/T]gaactcagaaatccg	73469
rs6313445	snp	C/T	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44224675	tcagaaatccgcctg[C/T]ctctgcctcccaagt	73469
rs6313472	snp	A/G	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44224691	ctctgcctcccaagt[A/G]ctgggattaaaggtg	73469
rs6314523	snp	G/T	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44224878	TCAATCCTGACACAG[G/T]CACTAAGCCCAGAGT	73469
rs6344903	snp	C/T	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44138913	AGGTCATTGTTGATA[C/T]ATCAAACTGAAAAAA	73469
rs6344941	snp	A/G	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44138936	TGAAAAAATATATAA[A/G]TGGACCCAAGATTTC	73469
rs6344978	snp	A/G	0.49324	0.0577452	intron-variant	Rnf38	Mm_Celera	4:44138954	GACCCAAGATTTCCT[A/G]TCTTTAATTATATTT	73469
rs6345471	snp	A/T	0.290657	0.246672	intron-variant	Rnf38	Mm_Celera	4:44139043	ACCCAAACTCTCAAA[A/T]TAGGAAATTAAAAGT	73469
rs6345577	snp	C/T	0.359862	0.224567	intron-variant	Rnf38	Mm_Celera	4:44139102	GAGATTTCCAGACAC[C/T]GAGCCTCCCTGAAGA	73469
rs6346616	snp	A/G	0.359862	0.224567	intron-variant	Rnf38	Mm_Celera	4:44139213	ACAGGCTGTAGTGTC[A/G]ATCAGTATGTGACTT	73469
rs6363634	snp	C/T	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44146678	actgaccttaggtgg[C/T]catgtgtctttacct	73469
rs6377242	snp	A/G	0.5	0	intron-variant	Rnf38	Mm_Celera	4:44146928	ccctcttctgacctc[A/G]gcaggcactaggtat	73469
rs27847714	snp	C/T	0.345679	0.230967	intron-variant	Rnf38	Mm_Celera	4:44226081	GTATGAATGAAAAAC[C/T]GAGATAGAAAAATAA	73469
rs27847715	snp	A/G	0.391111	0.206368	intron-variant	Rnf38	Mm_Celera	4:44225576	CATTCTACCCCAAAT[A/G]GCACTCCTATCCAGT	73469
rs27847716	snp	G/T	0.142012	0.225474	intron-variant	Rnf38	Mm_Celera	4:44225491	AACAGTCCTCTGCGT[G/T]CTAGCTTGCCCTAAA	73469
rs27847717	snp	C/T	0.124444	0.216185	intron-variant	Rnf38	Mm_Celera	4:44225210	AAGGCAACTCTGAAA[C/T]GAAACGTGTTTTACT	73469
rs27847718	snp	G/T	0.375	0.216506	intron-variant	Rnf38	Mm_Celera	4:44224331	TACAGTGGTCCCGCC[G/T]CTCAGAACATCCGCA	73469
rs27847719	snp	A/C	0.345679	0.230967	upstream-variant-2KB, intron-variant	Mir5106, Rnf38	Mm_Celera	4:44222760	gaaagaaagaaagaT[A/C]ATTTTCACTAAAAGT	73469
rs27847720	snp	A/G	0.46875	0.121031	upstream-variant-2KB, intron-variant	Mir5106, Rnf38	Mm_Celera	4:44221653	GTCCTTTATCCACAC[A/G]CTAAAAAGACTCCAG	73469
rs27847721	snp	A/G	0.152778	0.230321	nc-transcript-variant, intron-variant	Mir5106, Rnf38	Mm_Celera	4:44221239	CCTAGATAGGCTCTC[A/G]GGTTGTTGCTGTTGT	73469
rs27847722	snp	A/T	0.497041	0.0383476	intron-variant	Rnf38	Mm_Celera	4:44219926	CCATTGTCATACCCC[A/T]TCAATGAGGTGCTAT	73469
rs27847723	snp	A/G	0.336735	0.234472	intron-variant	Rnf38	Mm_Celera	4:44217824	GAGGTTCTATAAAAA[A/G]ATTCCAGGACTTATG	73469
rs27847724	snp	A/G	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44217571	CACACACATTCGGAA[A/G]GTCCTACAAGCACAG	73469
rs27847725	snp	C/T	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44217326	CTGCGCACCTCTATC[C/T]TGCCACAGAAGTCAC	73469
rs27847726	snp	A/G	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44216949	ACTGACAGGAACAGC[A/G]AGCCCTGAGAGCAGT	73469
rs27847727	snp	A/G	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44216942	CCTGACTACTGACAG[A/G]AACAGCGAGCCCTGA	73469
rs27847728	snp	G/T	0.124444	0.216185	intron-variant	Rnf38	Mm_Celera	4:44216746	ATTCAGAACTCAAAA[G/T]CAGGCCATTTTTCTA	73469
rs27847729	snp	G/T	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44216583	TCTTCTCAACTGCCC[G/T]CGTTAACCGGTCCTC	73469
rs27847730	snp	C/T	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44216523	ATTCTGAAGCTAGAT[C/T]TGTTAAGAAACTCAA	73469
rs27847731	snp	A/G	0.456747	0.140554	intron-variant	Rnf38	Mm_Celera	4:44216250	AACACAGTTAACAGC[A/G]TCTTCACTAAGAACC	73469
rs27847732	snp	G/T	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44216173	TAACTGCTCCCAACA[G/T]TACATGCAGTTTTAG	73469
rs27847733	snp	C/T	0.429688	0.173817	intron-variant	Rnf38	Mm_Celera	4:44215750	TGTTAACAGCAGCTT[C/T]TAGCTAAGTCTTTTT	73469
rs27847734	snp	A/C	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44215648	TTTTTATCTCAACCG[A/C]AACTTAACAGAGTTA	73469
rs27847735	snp	C/T	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44215639	TCACCTCTGTTTTTA[C/T]CTCAACCGCAACTTA	73469
rs27847736	snp	C/T	0.244898	0.249948	intron-variant	Rnf38	Mm_Celera	4:44215563	TGACTTCAGAGGTTG[C/T]TGCTGTTTGGGGTAA	73469
rs27847737	snp	C/T	0.35503	0.226867	intron-variant	Rnf38	Mm_Celera	4:44215205	CACACAGATGAGTGT[C/T]TGGAGTGTGTGTACG	73469
rs27847738	snp	C/G	0.124444	0.216185	intron-variant	Rnf38	Mm_Celera	4:44214185	TTTTAAATGATTTTG[C/G]TATGAGGCTGGTGAG	73469
rs27847739	snp	C/T	0.21875	0.248039	intron-variant	Rnf38	Mm_Celera	4:44214057	AAGGGAGTTTAATAG[C/T]CTTAAAATCAATTTG	73469
rs27847740	snp	A/G	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44213035	CTCATTTTGTACTGG[A/G]AATCCATCATCTTAA	73469
rs27847741	snp	C/G	0.493827	0.0552116	intron-variant	Rnf38	Mm_Celera	4:44212802	TCTCTAACTGTGAGC[C/G]GATCTCTGAGCAGTC	73469
rs27847742	snp	C/T	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44212666	GGTAAAGCTGAGAGG[C/T]GCTGCCTAACTCAGA	73469
rs27847743	snp	C/T	0.244898	0.249948	intron-variant	Rnf38	Mm_Celera	4:44210852	CCAGTCTTGAGCTCC[C/T]GACTTTAGGTGTCTG	73469
rs27847744	snp	A/G	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44210840	AGAGCGCTTAAGCCA[A/G]TCTTGAGCTCCCGAC	73469
rs27847745	snp	C/G	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44210331	CCTGGCACACTGGCT[C/G]TGGACTGACTGAAAG	73469
rs27847746	snp	A/G	0.32	0.24	intron-variant	Rnf38	Mm_Celera	4:44210310	CATGGTGGAGTGGAC[A/G]GCTTGCCTGGCACAC	73469
rs27847747	snp	A/G	0.32	0.24	intron-variant	Rnf38	Mm_Celera	4:44210244	ACATGGACACACCAC[A/G]AAGACCAGTAAATAC	73469
rs27847748	snp	C/G	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44210104	GAAGCAGAGGACAAG[C/G]TGTGGGTAAAGGTTT	73469
rs27847749	snp	A/T	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44209571	CAAATAAAAAGTATT[A/T]TACGATCAGCAGCTA	73469
rs27847750	snp	G/T	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44209372	AAACATCCCAAGAAA[G/T]TCAGGTTATCAAGTC	73469
rs27847751	snp	A/G	0.142012	0.225474	intron-variant	Rnf38	Mm_Celera	4:44209267	AAACAGAGGAAAATA[A/G]TAAAAGGAGTCTAAA	73469
rs27847752	snp	C/T	0.142012	0.225474	intron-variant	Rnf38	Mm_Celera	4:44209218	CTCAAAAGCCTAAAG[C/T]TATAGTTTAACTGCA	73469
rs27847753	snp	C/T	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44209062	AATTAGCGGCAATAC[C/T]ATACTGAGAATAAAA	73469
rs27847754	snp	A/G	0.142012	0.225474	intron-variant	Rnf38	Mm_Celera	4:44209025	CAATAAGTAAATCCA[A/G]AATGGTAAGACTTAT	73469
rs27847755	snp	A/G	0.495868	0.0452663	intron-variant	Rnf38	Mm_Celera	4:44208954	TATCCTAATTAGCAT[A/G]GGAAAAAATATAAAA	73469
rs27847756	snp	A/G	0.142012	0.225474	intron-variant	Rnf38	Mm_Celera	4:44208902	AACAAAATAGAGATG[A/G]GTATTACCTCTTACC	73469
rs27847757	snp	C/T	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44206994	ATCCATGCAACCAAA[C/T]GCAACATTTAAGAAC	73469
rs27847758	snp	A/G	0.124444	0.216185	intron-variant	Rnf38	Mm_Celera	4:44206753	ATGTGGGGATCTAGA[A/G]CGCAATCTTGAGTGT	73469
rs27847759	snp	A/C	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44206733	CTATGTAAGTGAACC[A/C]TGTCATGTGGGGATC	73469
rs27847760	snp	A/G	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44206659	TCAGGGCTGTCTTTG[A/G]GCAGTGAAAATGTGT	73469
rs27847761	snp	A/C	0.165289	0.235211	intron-variant	Rnf38	Mm_Celera	4:44206373	AGAAGGATAGGCTAT[A/C]TATTTTGTTAATGGA	73469
rs27847762	snp	A/G	0.391111	0.206368	intron-variant	Rnf38	Mm_Celera	4:44206027	ACTCTGTTCCTGACA[A/G]TGAGAAAGCCTTCAT	73469
rs27847763	snp	C/T	0.124444	0.216185	intron-variant	Rnf38	Mm_Celera	4:44205278	CATGAGAAAAGAATG[C/T]GTTCGATTATGTCAC	73469
rs27847764	snp	A/T	0.487535	0.077957	intron-variant	Rnf38	Mm_Celera	4:44205205	AGGCCCGTCTCTGTC[A/T]GTTCTTCCAAAGGTA	73469
rs27847765	snp	C/T	0.124444	0.216185	intron-variant	Rnf38	Mm_Celera	4:44205193	ATTCTCTACAAAAGG[C/T]CCGTCTCTGTCAGTT	73469
rs27847766	snp	C/G	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44205107	ATCACATCGGAACAA[C/G]GGTAAATGTGCTGAT	73469
rs27847767	snp	A/G	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44204907	TGGGGAGAAAGGATC[A/G]AGCTGAAGGGGCTGA	73469
rs27847768	snp	C/T	0.124444	0.216185	intron-variant	Rnf38	Mm_Celera	4:44204906	ATGGGGAGAAAGGAT[C/T]GAGCTGAAGGGGCTG	73469
rs27847769	snp	C/G	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44204877	ACTGATGACAGCAAA[C/G]AGCAGCTTCCGAGAT	73469
rs27847770	snp	C/T	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44204823	CTGTTAAAGACCCAG[C/T]GAGAAGTGGCCTGGG	73469
rs27847771	snp	A/G	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44204805	CCTGGGAAGGTAAAA[A/G]CTCTGTTAAAGACCC	73469
rs27847772	snp	C/T	0.444444	0.157135	intron-variant	Rnf38	Mm_Celera	4:44204123	CATGTAAAGTATGAA[C/T]TTCTTGTAAAATACA	73469
rs27847773	snp	C/T	0.188366	0.242283	intron-variant	Rnf38	Mm_Celera	4:44203976	TGGAGAATGATGTGG[C/T]GGAGAGAGATATACA	73469
rs27847774	snp	A/G	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44203460	CCTGGCTCCCTCTGC[A/G]TTCTCAGAGCTGCAC	73469
rs27847775	snp	C/T	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44203355	AAACTGAAAAGACAT[C/T]GGGTAAGTTCAAATG	73469
rs27847776	snp	C/G	0.124444	0.216185	intron-variant	Rnf38	Mm_Celera	4:44203320	AGCAGGAGCTATAGT[C/G]TCAAGTCAGAGAAAG	73469
rs27847777	snp	A/G	0.33241	0.236027	intron-variant	Rnf38	Mm_Celera	4:44203262	GAAGGGAAGAGGGCA[A/G]TAAGAAAGGAGGCTT	73469
rs27847778	snp	C/T	0.32	0.24	intron-variant	Rnf38	Mm_Celera	4:44203079	CAGGGACTGGAGAAA[C/T]GGCTCTGTACTTAAG	73469
rs27847779	snp	C/T	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44203045	ATTGTCATCCAACAG[C/T]TACAAATATGAACAA	73469
rs27847780	snp	A/G	0.124444	0.216185	intron-variant	Rnf38	Mm_Celera	4:44202747	TCTCCCAATTGCAAA[A/G]ATTATAGGCACAGGT	73469
rs27847781	snp	A/C	0.132653	0.220748	intron-variant	Rnf38	Mm_Celera	4:44201184	TGAACAGTGTGTTCG[A/C]TTAGCAAACACTCAT	73469
rs27847782	snp	C/T	0.387812	0.208586	intron-variant	Rnf38	Mm_Celera	4:44201098	ATTAAAAGTTTTAAT[C/T]CGATACCAAATAATT	73469
rs27847783	snp	C/T	0.277778	0.248452	intron-variant	Rnf38	Mm_Celera	4:44201031	GAAAAGGACTCTAAG[C/T]TAGTGACTGTGTCAC	73469
rs27847784	snp	A/G	0.475309	0.108333	intron-variant	Rnf38	Mm_Celera	4:44200639	GGGAAAATGTTTAAC[A/G]TGAGGCTGGAGAGGT	73469
rs27847785	snp	A/C	0.493827	0.0552116	intron-variant	Rnf38	Mm_Celera	4:44200555	AGTATGTGGTTCAGT[A/C]CCAACAAGTACCATA	73469
rs27847786	snp	A/G	0.231111	0.249285	intron-variant	Rnf38	Mm_Celera	4:44200521	GCTAAAGTATGGATT[A/G]GTGGTAGAGTTACTA	73469

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