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
rs6210692	snp	C/T	0.5	0	missense	Rnf213	Mm_Celera	11:119408883	GCCAGCCTGGGCATC[C/T]CCTGGACACAGAGAA	672511
rs6211180	snp	A/G	0.444444	0.157135	missense	Rnf213	GRCm38.p3	11:119408952	GCGGCAGCCCTCTGC[A/G]GGGTCAGGCTGCAGA	672511
rs6211207	snp	A/G	0.5	0	missense	Rnf213	Mm_Celera	11:119408970	GTCAGGCTGCAGAAC[A/G]CACCGACGCTCAGAG	672511
rs6286851	snp	C/T	0.5	0	intron-variant	Rnf213	Mm_Celera	11:119464263	TCGGTCTAGCACTTT[C/T]GATCTAGCACCTTCT	672511
rs6288046	snp	A/C	0.48	0.0979796	intron-variant	Rnf213	GRCm38.p3	11:119464496	CTCTCATAAGCTACA[A/C]CCCTTAAAGGGGTGA	672511
rs6382383	snp	C/G	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475759	agacatcccagaaga[C/G]ggtatcagatctcat	672511
rs6382408	snp	A/G	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475778	atcagatctcattac[A/G]gatgtttgtgagcca	672511
rs6382901	snp	A/G	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475862	cactcataaccactg[A/G]gctatctctccagtc	672511
rs6382950	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475885	ctccagtcccCACCC[C/T]GAANCTTTTAAAATA	672511
rs6382954	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475889	agtcccCACCCNGAA[C/T]CTTTTAAAATAAGAT	672511
rs6382999	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119475927	AGAAGAAAGGGGCTT[C/T]CTGCAAACTGAACTC	672511
rs6384044	snp	G/T	0.5	0	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476047	ttttttttttttttt[G/T]ttttGGTGTGATTTC	672511
rs6384090	snp	C/T	0.5	0	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119476070	GTGATTTCACACAAA[C/T]GAGGGCATTCTAGAA	672511
rs6384210	snp	G/T	0.304688	0.243945	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476131	TTCATAGGTGTTGGT[G/T]TGTGCAGCAGCTGGA	672511
rs6384687	snp	C/T	0.304688	0.243945	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476155	AGCTGGAGTGGCTGA[C/T]GGTAGCACTGGGCAC	672511
rs6396556	snp	A/G	0.456747	0.140554	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470683	CTGAGCACATCCATC[A/G]TCCACACTACGCATA	672511
rs13459989	snp	A/G	0.486111	0.0821678	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486265	AAAGTGTGGGCACAG[A/G]CTGGATTCAAGGCCT	672511
rs13459990	snp	G/T	0.46281	0.131194	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486369	CTTAAGTCTGATGAA[G/T]GATTGTCAGTCAACT	672511
rs13459991	snp	A/T	0.375	0.216506	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119486533	GGGTAGTCAATTTTT[A/T]AAATTTTTTTACTTA	672511
rs13459992	snp	C/G/T	0.497041	0.0383476	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486721	CATGTAAACCCACCA[C/G/T]GAGCCACTGCCAACC	672511
rs27015052	snp	C/T	0.277778	0.248452	downstream-variant-500B, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119487627	TTCTGTGACAGTGTT[C/T]CTGCTGTAGTATCCA	672511
rs27015053	snp	C/G	0.473373	0.11227	utr-variant-3-prime, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119487094	AGAGTACCTGTCCTC[C/G]GATGTCTGCATCCCA	672511
rs27015054	snp	A/C	0.48	0.0979796	synonymous-codon, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486146	ACGAAAATGGGACCG[A/C]CAATCAAGGTAGAGC	672511
rs27015055	snp	C/T	0.46281	0.131194	synonymous-codon, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119486014	TCACAGCCTCAAGGA[C/T]ACTCTAGTAAGTTAC	672511
rs27015056	snp	C/T	0.48	0.0979796	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119485981	GATGTTACAAAAACT[C/T]TCTCTTGTTCCTTGA	672511
rs27015057	snp	A/C	0.49827	0.0293608	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119485677	ATCATGTCTCGGGTT[A/C]TAAAACAGCCCTCTG	672511
rs27015058	snp	G/T	0.486111	0.0821678	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119485249	ACACTCATCAGCTAT[G/T]TGTGTATGGCACAAT	672511
rs27015059	snp	A/G	0.49827	0.0293608	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119485196	TCTTTTCATTTGTAC[A/G]TCCCGACTCTGAGGC	672511
rs27015060	snp	G/T	0.497778	0.0332592	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119485134	GTAAAGGCACAGTTA[G/T]CCCTCTCTGCCAAGT	672511
rs27015061	snp	A/G	0.489796	0.070696	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119484376	AAGTCAGAGGTTAGG[A/G]ACATGGCCCAGTAGG	672511
rs27015062	snp	A/G	0.48	0.0979796	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119484140	TGCCTTGGATACTTT[A/G]TAGATTTGGTTTGCT	672511
rs27015063	snp	A/G	0.277778	0.248452	synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483735	AGAACAGCGGCTGCG[A/G]CTGAACAAAGTGAGT	672511
rs27015064	snp	C/T	0.486111	0.0821678	synonymous-codon, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119483702	TGCTCTCTGGCAGTT[C/T]CTATCTGCACATAAG	672511
rs27015065	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483588	GCTCAAGACAGAAAT[A/G]GGGGAATGTGCCTAT	672511
rs27015066	snp	C/T	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483459	ATCAGTAGACTGACA[C/T]ATGCTCTATGATGTC	672511
rs27015067	snp	A/G	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483434	TCTGCCCTGTACACC[A/G]TATACTTGGATCAGT	672511
rs27015068	snp	C/T	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119483326	TCAGCATGACCCTTG[C/T]CAAAAGCTCCTGCTT	672511
rs27015069	snp	A/G	0.49827	0.0293608	missense, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119482958	AACTTAGCAATCAGT[A/G]CCATCAGCGGACAGC	672511
rs27015070	snp	C/T	0.49827	0.0293608	missense, intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119482947	GCTCACTCCCTAACT[C/T]AGCAATCAGTACCAT	672511
rs27015071	snp	C/G	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482816	GCCTGCATCAGGCTA[C/G]TGCCTTCTGGAGAGC	672511
rs27015072	snp	C/T	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119482719	TCACAGTTATGTGTG[C/T]TGTGGCTAAACAGCC	672511
rs27015073	snp	C/T	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482542	GCTCCAGCTGCATCA[C/T]AGCTACTGTGAACAT	672511
rs27015074	snp	G/T	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482287	CTTGAATAGCTGGGT[G/T]CTGCTACTGAGTCAC	672511
rs27015075	snp	C/T	0.260355	0.249785	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119482253	CCTGGGGCAACACTG[C/T]GGGCTTTACCAGAAA	672511
rs27015076	snp	A/G	0.5	0	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119482083	TGCAGTGACTCCCTT[A/G]GTGAATGAGCTATCC	672511
rs27015077	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481612	GGTTTTTCTGCAATT[A/G]TTAATAGCACCACCA	672511
rs27015078	snp	C/G	0.32	0.24	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481542	CAAGCTCTTTGGACT[C/G]TCTGCACCTCAGTCC	672511
rs27015079	snp	C/T	0.260355	0.249785	synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119481311	ACGGCAGATCAGCAG[C/T]CGGTTCCTACAGGGC	672511
rs27015080	snp	A/G	0.277778	0.248452	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119480650	GTATTAGATGGGATG[A/G]CCATGTCTGTGAGCC	672511
rs27015081	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479673	GTCACAGTTCAGGTA[A/G]GACTCTATTCAAGCT	672511
rs27015082	snp	A/G	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479480	AAAATGTACAAGCTC[A/G]CTAGCATTCCTTAGG	672511
rs27015083	snp	A/G	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479346	CTGAAAGCCATTTGT[A/G]GGTACTTAGAGAAAG	672511
rs27015084	snp	A/C	0.35503	0.226867	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479334	AAGAGTGTAACCCTG[A/C]AAGCCATTTGTGGGT	672511
rs27015085	snp	A/G	0.432133	0.171253	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119479255	AGGATTTAGTCCTCA[A/G]GGCAGTTCTACCCAT	672511
rs27015086	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Rnf213, LOC102639982	Mm_Celera	11:119477930	TCTCACATATCCAGC[C/T]AGTCACACAAACACA	672511
rs27015087	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Rnf213, LOC102639982	Mm_Celera	11:119477829	GTGTCAGTGCTGTGA[C/T]TTCTCTCAGGGTGGT	672511
rs27015088	snp	A/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	GRCm38.p3	11:119477784	TGACCCTGAGCACCA[A/G]TGTCGGGTATTCACA	672511
rs27015089	snp	G/T	0.32	0.24	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477770	GGTGATCTTTGAGGT[G/T]ACCCTGAGCACCAGT	672511
rs27015090	snp	C/T	0.32	0.24	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477706	GAGGTGCAGCAATCC[C/T]GTCGGACCCAGGAAC	672511
rs27015091	snp	A/G	0.231111	0.249285	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477609	AGCAAACATTATTCA[A/G]CGCGTGAACATTTGT	672511
rs27015092	snp	C/G	0.336735	0.234472	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477499	AATAACACATAGGTC[C/G]GTCAGTAGTCATCAG	672511
rs27015093	snp	A/G	0.32	0.24	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119477430	AATATTAGTAGCAGG[A/G]AACTCAAGAAGGCCT	672511
rs27015094	snp	A/G	0.495	0.0497494	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	GRCm38.p3	11:119477307	CTCCAGAAGGTACGA[A/G]GGACTCCTGCTTGAC	672511
rs27015095	snp	A/T	0.444444	0.157135	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476870	AGGTGGAAGGAAAGC[A/T]GTGATTGTGGCATCT	672511
rs27015096	snp	C/G	0.495868	0.0452663	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119476642	TCTTTACCCATCATC[C/G]CTGGGGAGGGACTCC	672511
rs27015097	snp	A/G	0.32	0.24	synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476506	AACCAAAGGATGCAG[A/G]AACAACTGGGAGAAG	672511
rs27015098	snp	C/G	0.32	0.24	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119476402	TACCTGGTACTTACC[C/G]TATGCAGGATGCTAT	672511
rs27015099	snp	A/G	0.486111	0.0821678	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119476260	ACAGCAATGGAATCA[A/G]AGGAACTGTCTGAAG	672511
rs27015100	snp	C/T	0.444444	0.157135	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474843	TCTAAGCATTTAAAT[C/T]TATCAAGGAAGGACA	672511
rs27015101	snp	C/T	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474777	ACAGTTTCTCCTAGT[C/T]GGCTTTTTTTGAGCA	672511
rs27015102	snp	A/G	0.492188	0.0620098	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119474677	ATCACACAAGAATCA[A/G]TCATTAGCCTTGCTT	672511
rs27015103	snp	C/T	0.42	0.183303	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474637	AGTGCAAACCTATTG[C/T]GTGGGAGACACATGC	672511
rs27015104	snp	C/T	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119474090	GATGCTGGTGTCTTG[C/T]TCTTCTGCCCTCTCC	672511
rs27015105	snp	C/T	0.475309	0.108333	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119474072	GAAGTCATCCTCTGA[C/T]TTGATGCTGGTGTCT	672511
rs27015106	snp	A/C	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473998	GCTGATGTTTTAGAT[A/C]ATCCCACAGCCAGCT	672511
rs27015107	snp	C/T	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473813	AGTCTGGTTTTCTTC[C/T]TAACTGATACCAACT	672511
rs27015108	snp	A/G	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473681	AGCCTAATCTCCAAC[A/G]TGGCAAGGAATAGGA	672511
rs27015109	snp	A/T	0.260355	0.249785	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473344	TTCTAATGTTCACCT[A/T]GTCTTCTCTTCCTTT	672511
rs27015110	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473267	GTTCCCTCGGGGCAT[A/G]GAGCCCTACCTCCAA	672511
rs27015111	snp	A/T	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119473092	ATTTTATGCAGCCAC[A/T]TTAAGCTGAGTCTTA	672511
rs27015112	snp	C/T	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472944	TGTTCTACCAGACCT[C/T]GGATCCCAATTATTG	672511
rs27015113	snp	C/T	0.260355	0.249785	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472668	GACACAGGAGTTAGA[C/T]AGAATGCTACTCCTG	672511
rs27015114	snp	C/T	0.231111	0.249285	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472584	ATGCCTTGGTTTGTG[C/T]GAGGGGTAGGTTCTA	672511
rs27015115	snp	C/T	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472162	CAATCTCTGCACATG[C/T]CACCTAACTTGAACT	672511
rs27015116	snp	C/T	0.32	0.24	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119472140	AACACACTGAGCCAG[C/T]ATCTGCCAATCTCTG	672511
rs27015117	snp	A/G	0.132653	0.220748	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471909	CTAACTTGTGCCTCA[A/G]ACACTATTGTCCTTC	672511
rs27015118	snp	A/G	0.336735	0.234472	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471848	CTGGGAATCAGCCCT[A/G]GACATCAGCACTGCT	672511
rs27015119	snp	A/G	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471675	GCAGGGTTGTTACAC[A/G]GCAGCTCTTATGCAT	672511
rs27015120	snp	C/T	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119471597	TTAGGAGTGTCCACC[C/T]TGTCCCCATATCACT	672511
rs27015121	snp	A/G	0.5	0	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119471105	GCCTGCTAAGCAGCA[A/G]GCTACCAGGCTGCAG	672511
rs27015122	snp	A/G	0.244898	0.249948	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470752	CTTCTAGGGAGGTGC[A/G]AAGGCTGTGTCATAC	672511
rs27015123	snp	C/T	0.459184	0.136902	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119470050	ATCCTTGAGGCTGCA[C/T]AGTCAATGCCCTCCT	672511
rs27015124	snp	C/T	0.124444	0.216185	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119469709	TACAGTCTGGGTGGC[C/T]CTCCAATGGAGAGGC	672511
rs27015125	snp	C/T	0.152778	0.230321	intron-variant, downstream-variant-500B	Rnf213, LOC102639982	Mm_Celera	11:119469190	GAGTCCTAAGCACTG[C/T]GTTAGTCAGGCTTCT	672511
rs27015126	snp	A/G	0.375	0.216506	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468225	ACTACTAAAGCATAA[A/G]CTATGAGATTCTACT	672511
rs27015127	snp	A/G	0.152778	0.230321	synonymous-codon, intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119468029	GGCCTTGTACACAGA[A/G]GTGGCTGCTTTGTAC	672511
rs27015128	snp	A/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467683	TGATACTGATGTCAA[A/G]GTTTTTAGACGTCTG	672511
rs27015129	snp	C/G	0.297521	0.245442	intron-variant	Rnf213, LOC102639982	Mm_Celera	11:119467527	TAGTGGCTGGAACGG[C/G]TGCAATGACACTTGA	672511
rs27015130	snp	A/G	0.444444	0.157135	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119467476	GACACTGTACTAGAA[A/G]TCAGACTTTCATGGT	672511
rs27015131	snp	A/G	0.497041	0.0383476	intron-variant	Rnf213, LOC102639982	GRCm38.p3	11:119467428	TTACATACATCAAAT[A/G]ATGGAGTGAGCAACT	672511

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