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
rs346474673	snp	A/C			synonymous-codon	?	TAIR10	1:9563618	GGCTGGATAGGTAAT[A/C]GGGATATCGAACTGG	839644
rs346677043	snp	A/G			synonymous-codon	?	TAIR10	1:9563446	TGAAATGCACAGTCA[A/G]ACATATCTTCCCACC	839644
rs346738312	snp	A/G			utr-variant-3-prime	?	TAIR10	1:9562744	ATTTCTGAGATTGAT[A/G]GAAAGGTTACATAGA	839644
rs346749633	snp	C/T			intron-variant	?	TAIR10	1:9563086	TTAGCACTAGAGTTT[C/T]CCGGCCTAATTGAAT	839644
rs346774118	snp	A/T			intron-variant	?	TAIR10	1:9562950	GCTGTGCTCATATTC[A/T]TGATAGAAATGGATT	839644
rs346774552	snp	C/T			synonymous-codon	?	TAIR10	1:9562803	ATCTTTGTGCTTAAT[C/T]GCGCCGGAGTCCACA	839644
rs346792621	snp	C/G			intron-variant	?	TAIR10	1:9563388	ACAATGTCTATGCAA[C/G]CAGAAAGCATATAAA	839644
rs346799668	snp	G/T			intron-variant	?	TAIR10	1:9563283	GTACACAAGAAGATC[G/T]ACAACAAACCAATCT	839644
rs346813881	snp	A/G			synonymous-codon	?	TAIR10	1:9562841	GAATCTCTGCAGCTA[A/G]CCACGGAGCGAGCCC	839644
rs346837929	snp	A/C			missense	?	TAIR10	1:9563808	TGCGTCCATGCCGCG[A/C]CGTCTCTTGGACCCG	839644
rs346880899	snp	C/G			intron-variant	?	TAIR10	1:9563361	TGATCTAAAACACTG[C/G]ATGCTTCTCTAACAA	839644
rs346954975	snp	A/C			synonymous-codon	?	TAIR10	1:9563426	GTTTTTGGCCCATAG[A/C]GGCTTGAAATGCACA	839644
rs346969916	snp	C/T			synonymous-codon	?	TAIR10	1:9563864	CGTTAACGTCGACTT[C/T]GTGTTCGGATCCCAT	839644
rs346992331	snp	C/T			intron-variant	?	TAIR10	1:9563323	CTTTCTTTCAGAATT[C/T]CTCTAAAAATCTGAG	839644
rs347097482	snp	A/G			intron-variant	?	TAIR10	1:9563212	TGCTCCTCTTACAAT[A/G]TCTATGCAACCAGAG	839644
rs347183435	snp	A/T			intron-variant	?	TAIR10	1:9563216	CCTCTTACAATATCT[A/T]TGCAACCAGAGAAAG	839644

Full records

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