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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
71751	BAA01g37550	A01	25094228	C	T	upstream_gene_variant	MODIFIER	c.-2733G>A\|	S131
71752	BAA01g37550	A01	25094692	C	T	upstream_gene_variant	MODIFIER	c.-3197G>A\|	S39
71753	BAA01g37550	A01	25094951	C	T	upstream_gene_variant	MODIFIER	c.-3456G>A\|	S282
71754	BAA01g37550	A01	25095914	G	A	upstream_gene_variant	MODIFIER	c.-4419C>T\|	S71
71755	BAA01g37550	A01	25096035	G	A	upstream_gene_variant	MODIFIER	c.-4540C>T\|	S113
71756	BAA01g37550	A01	25096188	G	A	upstream_gene_variant	MODIFIER	c.-4693C>T\|	S62
71757	BAA01g37550	A01	25096298	C	T	upstream_gene_variant	MODIFIER	c.-4803G>A\|	S203
71758	BAA01g37560	A01	25097572	G	A	downstream_gene_variant	MODIFIER	c.*4121C>T\|	S58
71759	BAA01g37560	A01	25098175	C	T	downstream_gene_variant	MODIFIER	c.*3518G>A\|	S112
71760	BAA01g37570	A01	25099754	C	T	upstream_gene_variant	MODIFIER	c.-4242C>T\|	S69
71761	BAA01g37570	A01	25100573	C	T	upstream_gene_variant	MODIFIER	c.-3423C>T\|	S23
71762	BAA01g37560	A01	25101788	G	A	synonymous_variant	LOW	c.466C>T\|p.Leu156Leu	S217 S248
71763	BAA01g37560	A01	25101909	C	T	missense_variant	MODERATE	c.433G>A\|p.Val145Ile	S231
71764	BAA01g37560	A01	25102292	G	A	synonymous_variant	LOW	c.150C>T\|p.Leu50Leu	S174 S216 S241 S27
71765	BAA01g37560	A01	25103615	C	T	upstream_gene_variant	MODIFIER	c.-1174G>A\|	S167
71766	BAA01g37570	A01	25104020	C	T	missense_variant	MODERATE	c.25C>T\|p.Pro9Ser	S279
71767	BAA01g37570	A01	25104108	C	T	missense_variant	MODERATE	c.113C>T\|p.Pro38Leu	S17
71768	BAA01g37570	A01	25104389	G	A	missense_variant	MODERATE	c.394G>A\|p.Gly132Arg	S35
71769	BAA01g37570	A01	25104460	C	T	synonymous_variant	LOW	c.465C>T\|p.Tyr155Tyr	S38
71770	BAA01g37570	A01	25104794	G	A	missense_variant	MODERATE	c.799G>A\|p.Glu267Lys	S159 S188 S243 S276 S298 S299
71771	BAA01g37570	A01	25104886	C	T	synonymous_variant	LOW	c.891C>T\|p.Ala297Ala	S161
71772	BAA01g37570	A01	25104903	G	A	missense_variant	MODERATE	c.908G>A\|p.Gly303Glu	S91
71773	BAA01g37570	A01	25104931	G	A	synonymous_variant	LOW	c.936G>A\|p.Gln312Gln	S159 S243
71774	BAA01g37570	A01	25105605	G	A	missense_variant	MODERATE	c.1610G>A\|p.Gly537Asp	S221
71775	BAA01g37560	A01	25106281	C	T	upstream_gene_variant	MODIFIER	c.-3840G>A\|	S32

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