Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
179801	BAA02g20030-BAA02g20040	A02	10546759	G	A	intergenic_region	MODIFIER	n.10546759G>A\|	S272
179802	BAA02g20030-BAA02g20040	A02	10547309	C	T	intergenic_region	MODIFIER	n.10547309C>T\|	S249
179803	BAA02g20030-BAA02g20040	A02	10548178	G	A	intergenic_region	MODIFIER	n.10548178G>A\|	S122
179804	BAA02g20030-BAA02g20040	A02	10548210	C	T	intergenic_region	MODIFIER	n.10548210C>T\|	S32
179805	BAA02g20030-BAA02g20040	A02	10548438	C	T	intergenic_region	MODIFIER	n.10548438C>T\|	S75
179806	BAA02g20030-BAA02g20040	A02	10549538	G	A	intergenic_region	MODIFIER	n.10549538G>A\|	S223
179807	BAA02g20030-BAA02g20040	A02	10551354	C	T	intergenic_region	MODIFIER	n.10551354C>T\|	S203
179808	BAA02g20030-BAA02g20040	A02	10551903	G	A	intergenic_region	MODIFIER	n.10551903G>A\|	S256
179809	BAA02g20040	A02	10552850	G	A	downstream_gene_variant	MODIFIER	c.*4707C>T\|	S200
179810	BAA02g20040	A02	10554290	C	T	downstream_gene_variant	MODIFIER	c.*3267G>A\|	S77 S82
179811	BAA02g20040	A02	10554669	C	T	downstream_gene_variant	MODIFIER	c.*2888G>A\|	S194
179812	BAA02g20040	A02	10554881	C	T	downstream_gene_variant	MODIFIER	c.*2676G>A\|	S138
179813	BAA02g20040	A02	10555256	C	T	downstream_gene_variant	MODIFIER	c.*2301G>A\|	S51
179814	BAA02g20040	A02	10555413	C	T	downstream_gene_variant	MODIFIER	c.*2144G>A\|	S51 S85
179815	BAA02g20040	A02	10555824	C	T	downstream_gene_variant	MODIFIER	c.*1733G>A\|	S94
179816	BAA02g20050	A02	10556592	C	T	upstream_gene_variant	MODIFIER	c.-4974C>T\|	S32
179817	BAA02g20050	A02	10556610	C	T	upstream_gene_variant	MODIFIER	c.-4956C>T\|	S32
179818	BAA02g20050	A02	10557542	G	A	upstream_gene_variant	MODIFIER	c.-4024G>A\|	S230
179819	BAA02g20040	A02	10557822	C	T	missense_variant	MODERATE	c.838G>A\|p.Asp280Asn	S25
179820	BAA02g20040	A02	10558208	G	A	missense_variant	MODERATE	c.452C>T\|p.Ser151Phe	S218 S267 S268 S269
179821	BAA02g20040	A02	10558228	C	T	synonymous_variant	LOW	c.432G>A\|p.Lys144Lys	S212
179822	BAA02g20040	A02	10558429	C	T	synonymous_variant	LOW	c.231G>A\|p.Glu77Glu	S80
179823	BAA02g20040	A02	10558559	G	A	missense_variant	MODERATE	c.101C>T\|p.Pro34Leu	S257
179824	BAA02g20040	A02	10559394	C	T	upstream_gene_variant	MODIFIER	c.-735G>A\|	S138
179825	BAA02g20040	A02	10559442	C	A	upstream_gene_variant	MODIFIER	c.-783G>T\|	S124 S256 S261 S27 S284 S290 S37 S51 S66

Users can query the SNP information according to the gene ID.