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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
63901	BAA01g33540	A01	22392266	G	A	synonymous_variant	LOW	c.633G>A\|p.Lys211Lys	S155 S211
63902	BAA01g33550	A01	22392545	G	A	upstream_gene_variant	MODIFIER	c.-862G>A\|	S158
63903	BAA01g33550	A01	22392723	C	T	upstream_gene_variant	MODIFIER	c.-684C>T\|	S213
63904	BAA01g33550	A01	22393185	C	T	upstream_gene_variant	MODIFIER	c.-222C>T\|	S256
63905	BAA01g33550	A01	22393361	G	A	upstream_gene_variant	MODIFIER	c.-46G>A\|	S294
63906	BAA01g33560	A01	22393802	G	A	upstream_gene_variant	MODIFIER	c.-2880G>A\|	S225 S73
63907	BAA01g33550	A01	22394225	G	A	missense_variant	MODERATE	c.581G>A\|p.Ser194Asn	S80 S86 S90
63908	BAA01g33560	A01	22395374	G	A	upstream_gene_variant	MODIFIER	c.-1308G>A\|	S33
63909	BAA01g33560	A01	22396246	C	T	upstream_gene_variant	MODIFIER	c.-436C>T\|	S206 S26
63910	BAA01g33560	A01	22396850	G	A	missense_variant	MODERATE	c.169G>A\|p.Gly57Arg	S99
63911	BAA01g33560	A01	22397020	G	A	missense_variant	MODERATE	c.339G>A\|p.Met113Ile	S294
63912	BAA01g33560	A01	22397320	G	A	stop_gained	HIGH	c.639G>A\|p.Trp213*	S299
63913	BAA01g33550	A01	22398516	C	T	downstream_gene_variant	MODIFIER	c.*4284C>T\|	S298
63914	BAA01g33550	A01	22398531	G	A	downstream_gene_variant	MODIFIER	c.*4299G>A\|	S181
63915	BAA01g33560	A01	22399600	C	T	downstream_gene_variant	MODIFIER	c.*1416C>T\|	S290
63916	BAA01g33570	A01	22401522	C	T	upstream_gene_variant	MODIFIER	c.-3316C>T\|	S56
63917	BAA01g33570	A01	22404060	C	T	upstream_gene_variant	MODIFIER	c.-778C>T\|	S183 S198
63918	BAA01g33570	A01	22405721	C	T	intron_variant	MODIFIER	c.519+39C>T\|	S120
63919	BAA01g33570	A01	22405930	G	A	intron_variant	MODIFIER	c.636-44G>A\|	S208 S219
63920	BAA01g33570	A01	22406535	C	T	splice_region_variant&intron_variant	LOW	c.1012+8C>T\|	S164
63921	BAA01g33570	A01	22406902	G	A	missense_variant	MODERATE	c.1202G>A\|p.Gly401Glu	S294
63922	BAA01g33570	A01	22407944	C	T	downstream_gene_variant	MODIFIER	c.*888C>T\|	S142
63923	BAA01g33570	A01	22409876	G	A	downstream_gene_variant	MODIFIER	c.*2820G>A\|	S61
63924	BAA01g33580	A01	22411687	G	A	missense_variant	MODERATE	c.2038C>T\|p.Leu680Phe	S260
63925	BAA01g33580	A01	22411697	G	A	synonymous_variant	LOW	c.2028C>T\|p.Phe676Phe	S252

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