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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
43901	BAA01g26780	A01	15058958	C	T	missense_variant	MODERATE	c.721G>A\|p.Val241Ile	S275
43902	BAA01g26780	A01	15059027	C	T	missense_variant	MODERATE	c.652G>A\|p.Asp218Asn	S104 S52
43903	BAA01g26780	A01	15059096	C	T	missense_variant	MODERATE	c.583G>A\|p.Gly195Arg	S10
43904	BAA01g26780	A01	15059164	C	T	missense_variant	MODERATE	c.515G>A\|p.Cys172Tyr	S153
43905	BAA01g26780	A01	15059591	G	A	synonymous_variant	LOW	c.360C>T\|p.Pro120Pro	S126
43906	BAA01g26780	A01	15059731	G	A	missense_variant	MODERATE	c.220C>T\|p.Pro74Ser	S274
43907	BAA01g26780	A01	15061425	G	A	upstream_gene_variant	MODIFIER	c.-1388C>T\|	S74
43908	BAA01g26780	A01	15061911	C	T	upstream_gene_variant	MODIFIER	c.-1874G>A\|	S166
43909	BAA01g26780	A01	15062282	C	T	upstream_gene_variant	MODIFIER	c.-2245G>A\|	S114
43910	BAA01g26780	A01	15062403	C	T	upstream_gene_variant	MODIFIER	c.-2366G>A\|	S205
43911	BAA01g26780	A01	15063201	C	T	upstream_gene_variant	MODIFIER	c.-3164G>A\|	S4
43912	BAA01g26780	A01	15063801	T	A	upstream_gene_variant	MODIFIER	c.-3764A>T\|	S226
43913	BAA01g26780	A01	15063862	G	A	upstream_gene_variant	MODIFIER	c.-3825C>T\|	S240
43914	BAA01g26780	A01	15064908	G	A	upstream_gene_variant	MODIFIER	c.-4871C>T\|	S103
43915	BAA01g26780-BAA01g26790	A01	15065572	C	T	intergenic_region	MODIFIER	n.15065572C>T\|	S186
43916	BAA01g26780-BAA01g26790	A01	15068337	C	T	intergenic_region	MODIFIER	n.15068337C>T\|	S117 S23 S266 S297 S55
43917	BAA01g26780-BAA01g26790	A01	15069046	C	T	intergenic_region	MODIFIER	n.15069046C>T\|	S242
43918	BAA01g26780-BAA01g26790	A01	15069519	G	A	intergenic_region	MODIFIER	n.15069519G>A\|	S159 S243
43919	BAA01g26790	A01	15070956	C	T	upstream_gene_variant	MODIFIER	c.-4874C>T\|	S192
43920	BAA01g26790	A01	15072208	G	A	upstream_gene_variant	MODIFIER	c.-3622G>A\|	S123
43921	BAA01g26790	A01	15072225	C	T	upstream_gene_variant	MODIFIER	c.-3605C>T\|	S132 S137 S215
43922	BAA01g26790	A01	15076829	C	T	synonymous_variant	LOW	c.612C>T\|p.Phe204Phe	S203
43923	BAA01g26790	A01	15076852	G	A	missense_variant	MODERATE	c.635G>A\|p.Gly212Glu	S149
43924	BAA01g26790	A01	15076981	C	T	missense_variant	MODERATE	c.764C>T\|p.Ser255Phe	S54
43925	BAA01g26790	A01	15077261	G	A	downstream_gene_variant	MODIFIER	c.*246G>A\|	S159 S243 S276 S298 S299

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