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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
21801	BAA01g15840	A01	7700860	C	T	synonymous_variant	LOW	c.222C>T\|p.Leu74Leu	S50
21802	BAA01g15850	A01	7701733	C	T	upstream_gene_variant	MODIFIER	c.-2876C>T\|	S278
21803	BAA01g15840	A01	7703450	C	T	synonymous_variant	LOW	c.1894C>T\|p.Leu632Leu	S148 S210 S30 S31
21804	BAA01g15850	A01	7704313	C	T	upstream_gene_variant	MODIFIER	c.-296C>T\|	S210
21805	BAA01g15850	A01	7705042	C	T	missense_variant	MODERATE	c.434C>T\|p.Ser145Leu	S138
21806	BAA01g15840	A01	7705976	G	A	downstream_gene_variant	MODIFIER	c.*2308G>A\|	S174
21807	BAA01g15840	A01	7706172	G	A	downstream_gene_variant	MODIFIER	c.*2504G>A\|	S273
21808	BAA01g15850	A01	7706753	G	A	missense_variant	MODERATE	c.1273G>A\|p.Gly425Arg	S289 S290
21809	BAA01g15850	A01	7706978	C	T	synonymous_variant	LOW	c.1498C>T\|p.Leu500Leu	S144
21810	BAA01g15850	A01	7707155	G	A	missense_variant	MODERATE	c.1675G>A\|p.Asp559Asn	S105 S106
21811	BAA01g15850	A01	7707422	C	T	missense_variant	MODERATE	c.1942C>T\|p.Leu648Phe	S153
21812	BAA01g15840	A01	7707656	T	A	downstream_gene_variant	MODIFIER	c.*3988T>A\|	S146
21813	BAA01g15840	A01	7707681	G	A	downstream_gene_variant	MODIFIER	c.*4013G>A\|	S183
21814	BAA01g15840	A01	7708244	C	T	downstream_gene_variant	MODIFIER	c.*4576C>T\|	S132 S137
21815	BAA01g15840	A01	7708338	C	T	downstream_gene_variant	MODIFIER	c.*4670C>T\|	S25
21816	BAA01g15860	A01	7708918	G	A	synonymous_variant	LOW	c.93C>T\|p.Ile31Ile	S224
21817	BAA01g15860	A01	7709496	C	T	upstream_gene_variant	MODIFIER	c.-486G>A\|	S185
21818	BAA01g15860	A01	7711920	G	A	upstream_gene_variant	MODIFIER	c.-2910C>T\|	S188
21819	BAA01g15860-BAA01g15870	A01	7714136	G	A	intergenic_region	MODIFIER	n.7714136G>A\|	S240
21820	BAA01g15870	A01	7716776	G	A	upstream_gene_variant	MODIFIER	c.-4108G>A\|	S131
21821	BAA01g15870	A01	7717376	C	T	upstream_gene_variant	MODIFIER	c.-3508C>T\|	S148 S30 S31
21822	BAA01g15870	A01	7717418	C	T	upstream_gene_variant	MODIFIER	c.-3466C>T\|	S132 S137
21823	BAA01g15870	A01	7720318	C	T	upstream_gene_variant	MODIFIER	c.-566C>T\|	S42
21824	BAA01g15870	A01	7721152	C	T	missense_variant	MODERATE	c.269C>T\|p.Ser90Phe	S299
21825	BAA01g15870	A01	7721485	G	A	missense_variant	MODERATE	c.406G>A\|p.Glu136Lys	S281

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