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
rs346438805	snp	A/T			intron-variant	?	TAIR10	1:7114632	TTAATTTGCACGCTT[A/T]TAATTTGTGTCAATT	838642
rs346470962	snp	A/G			intron-variant	?	TAIR10	1:7114764	ATTTCAAATCTCCTA[A/G]ACATCCTTGCACCGA	838642
rs346473712	snp	C/T			synonymous-codon	?	TAIR10	1:7113677	AGCTGGGATGTTGCA[C/T]TCTTTATCTGGTGGA	838642
rs346483840	snp	C/T			intron-variant	?	TAIR10	1:7114411	TTTTTTGTCAAATTT[C/T]ACAGGACTTGGGCTG	838642
rs346525966	snp	A/T			missense	?	TAIR10	1:7113681	GGGATGTTGCATTCT[A/T]TATCTGGTGGAGCAT	838642
rs346558512	snp	A/G			synonymous-codon	?	TAIR10	1:7113656	ATAGGTTCTATCTAA[A/G]GATTCAGCTGGGATG	838642
rs346588760	snp	A/G			missense	?	TAIR10	1:7113666	TCTAAGGATTCAGCT[A/G]GGATGTTGCATTCTT	838642
rs346590366	snp	A/T			synonymous-codon	?	TAIR10	1:7113217	GTTTGGAGCAGCGAT[A/T]TGGCAAATTCCTGAG	838642
rs346647475	snp	A/G			synonymous-codon	?	TAIR10	1:7114740	TGATGACAAAACCTC[A/G]GAAAGGTTATTTCAA	838642
rs346748460	snp	A/C			synonymous-codon	?	TAIR10	1:7115030	TTGGGTTTTTGCATC[A/C]TTATCATATGACGGA	838642
rs346888810	snp	A/G			splice-acceptor-variant	?	TAIR10	1:7113437	CTCTCTGGTGGAAAC[A/G]GTGTTCTTTGGTGGC	838642
rs346910180	snp	C/G			intron-variant	?	TAIR10	1:7114550	TCGCAGTTGTTTTAG[C/G]TGAAATGTGCAGTTT	838642
rs346928052	snp	C/G			intron-variant	?	TAIR10	1:7114150	GAGCTGAACTGAATT[C/G]TTATGGAGCTCAACC	838642
rs346937960	snp	A/G			missense	?	TAIR10	1:7113699	TCTGGTGGAGCATGG[A/G]ATCCACATGATGTAA	838642
rs346938860	snp	A/T			intron-variant	?	TAIR10	1:7113418	AAGCTGACTCTCAAT[A/T]TTTCTCTCTGGTGGA	838642
rs346945947	snp	C/T			synonymous-codon	?	TAIR10	1:7114239	GGTAACTGCAGAGGA[C/T]GAATCTGGCATACAT	838642
rs346949066	snp	A/C			intron-variant	?	TAIR10	1:7113412	CTTATGAAGCTGACT[A/C]TCAATTTTTCTCTCT	838642
rs346957001	snp	A/G			missense	?	TAIR10	1:7114852	CTGTGGAATCCACAC[A/G]ACAGCGTGTGAACCC	838642
rs346962535	snp	C/G			missense	?	TAIR10	1:7113687	TTGCATTCTTTATCT[C/G]GTGGAGCATGGGATC	838642
rs346971767	snp	C/G			missense	?	TAIR10	1:7113220	TGGAGCAGCGATATG[C/G]CAAATTCCTGAGTTA	838642
rs346980654	snp	A/T			intron-variant	?	TAIR10	1:7113824	GCAGTTAGGAGGTTT[A/T]ACGCATTGATTTTAT	838642
rs346998206	snp	A/T			intron-variant	?	TAIR10	1:7113152	TTTGTATTGATTTAT[A/T]GCGTGAGTGTGTCAA	838642
rs347030085	snp	C/G			intron-variant	?	TAIR10	1:7113782	TATGAAGTATGGTAT[C/G]ACTGTTGCTATCCTC	838642
rs347047317	snp	C/T			missense	?	TAIR10	1:7114718	GGTATGCTTCAGCAA[C/T]ATCCAGTGATGACAA	838642
rs347063661	snp	C/T			missense	?	TAIR10	1:7113718	CACATGATGTAAATG[C/T]TGTTGCAGCAACGGG	838642
rs347179223	snp	A/C			intron-variant	?	TAIR10	1:7114142	TCAGCATTGAGCTGA[A/C]CTGAATTGTTATGGA	838642
rs347251697	snp	C/T			missense	?	TAIR10	1:7113455	GTTCTTTGGTGGCCT[C/T]CTGGAAGATGTGACA	838642
rs347257925	snp	C/G			intron-variant	?	TAIR10	1:7114538	TATGTATGTCAGTCG[C/G]AGTTGTTTTAGCTGA	838642
rs347284446	snp	C/G			missense	?	TAIR10	1:7113726	GTAAATGCTGTTGCA[C/G]CAACGGGTGAATCAT	838642
rs347293502	snp	A/C			missense	?	TAIR10	1:7113648	GGATTTATATAGGTT[A/C]TATCTAAGGATTCAG	838642
rs347317978	snp	C/T			intron-variant	?	TAIR10	1:7113112	CTTGTCTTGAGTTGA[C/T]TAGCAAGAATTTGGA	838642
rs347330020	snp	G/T			missense	?	TAIR10	1:7113219	TTGGAGCAGCGATAT[G/T]GCAAATTCCTGAGTT	838642
rs347415758	snp	C/T			missense	?	TAIR10	1:7113727	TAAATGCTGTTGCAG[C/T]AACGGGTGAATCATC	838642
rs347476064	snp	C/T			synonymous-codon	?	TAIR10	1:7114459	TATGATGGACTGATT[C/T]TGGTACTCTACTCTC	838642

Full records

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