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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
151401	BAA02g00160	A02	117365	C	T	upstream_gene_variant	MODIFIER	c.-552C>T\|	S124
151402	BAA02g00160	A02	117368	G	A	upstream_gene_variant	MODIFIER	c.-549G>A\|	S134
151403	BAA02g00170	A02	118240	C	T	upstream_gene_variant	MODIFIER	c.-2868C>T\|	S37
151404	BAA02g00170	A02	120155	C	T	upstream_gene_variant	MODIFIER	c.-953C>T\|	S207
151405	BAA02g00170	A02	120762	G	A	upstream_gene_variant	MODIFIER	c.-346G>A\|	S256
151406	BAA02g00170	A02	120949	G	A	upstream_gene_variant	MODIFIER	c.-159G>A\|	S184
151407	BAA02g00170	A02	121383	G	A	synonymous_variant	LOW	c.276G>A\|p.Gly92Gly	S265
151408	BAA02g00170	A02	121697	C	T	missense_variant	MODERATE	c.590C>T\|p.Ser197Phe	S267
151409	BAA02g00170	A02	121753	G	A	missense_variant	MODERATE	c.646G>A\|p.Asp216Asn	S44
151410	BAA02g00170	A02	122169	C	T	synonymous_variant	LOW	c.1062C>T\|p.Ile354Ile	S116
151411	BAA02g00170	A02	122262	C	T	synonymous_variant	LOW	c.1155C>T\|p.Thr385Thr	S281
151412	BAA02g00170	A02	122969	G	A	missense_variant	MODERATE	c.1862G>A\|p.Gly621Glu	S136
151413	BAA02g00160	A02	124219	G	A	downstream_gene_variant	MODIFIER	c.*4794G>A\|	S5
151414	BAA02g00170	A02	124499	C	T	downstream_gene_variant	MODIFIER	c.*1292C>T\|	S228
151415	BAA02g00170	A02	125165	G	A	downstream_gene_variant	MODIFIER	c.*1958G>A\|	S95
151416	BAA02g00170	A02	125255	C	T	downstream_gene_variant	MODIFIER	c.*2048C>T\|	S234
151417	BAA02g00180	A02	125738	A	T	synonymous_variant	LOW	c.783T>A\|p.Thr261Thr	S201 S213 S267
151418	BAA02g00180	A02	125741	A	T	synonymous_variant	LOW	c.780T>A\|p.Ala260Ala	S201 S213 S267
151419	BAA02g00180	A02	125747	G	C	synonymous_variant	LOW	c.774C>G\|p.Ala258Ala	S201 S213 S267
151420	BAA02g00180	A02	125756	A	C	synonymous_variant	LOW	c.765T>G\|p.Ala255Ala	S201 S213 S267
151421	BAA02g00180	A02	125780	G	C	synonymous_variant	LOW	c.741C>G\|p.Ala247Ala	S201 S213 S267
151422	BAA02g00180	A02	125789	A	T	synonymous_variant	LOW	c.732T>A\|p.Ala244Ala	S201 S213 S267
151423	BAA02g00180	A02	125792	G	A	synonymous_variant	LOW	c.729C>T\|p.His243His	S201 S213 S267
151424	BAA02g00180	A02	125816	C	T	synonymous_variant	LOW	c.705G>A\|p.Gln235Gln	S201 S213 S267
151425	BAA02g00180	A02	125822	C	A	missense_variant	MODERATE	c.699G>T\|p.Met233Ile	S201 S213 S267

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