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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
21451	BAA01g15600	A01	7572231	C	T	downstream_gene_variant	MODIFIER	c.*3733G>A\|	S128
21452	BAA01g15600	A01	7572690	C	T	downstream_gene_variant	MODIFIER	c.*3274G>A\|	S136
21453	BAA01g15600	A01	7572769	C	T	downstream_gene_variant	MODIFIER	c.*3195G>A\|	S132 S137 S89
21454	BAA01g15600	A01	7572806	G	A	downstream_gene_variant	MODIFIER	c.*3158C>T\|	S257
21455	BAA01g15600	A01	7573018	C	T	downstream_gene_variant	MODIFIER	c.*2946G>A\|	S153
21456	BAA01g15600	A01	7580820	G	A	upstream_gene_variant	MODIFIER	c.-2808C>T\|	S263
21457	BAA01g15600	A01	7581576	G	A	upstream_gene_variant	MODIFIER	c.-3564C>T\|	S32
21458	BAA01g15620	A01	7583418	C	T	upstream_gene_variant	MODIFIER	c.-3246C>T\|	S247
21459	BAA01g15620	A01	7586001	C	T	upstream_gene_variant	MODIFIER	c.-663C>T\|	S213
21460	BAA01g15620	A01	7586832	G	A	missense_variant	MODERATE	c.169G>A\|p.Val57Ile	S73 S91
21461	BAA01g15620	A01	7587346	C	T	missense_variant	MODERATE	c.683C>T\|p.Ala228Val	S286
21462	BAA01g15620	A01	7587404	G	A	synonymous_variant	LOW	c.741G>A\|p.Lys247Lys	S17 S74
21463	BAA01g15610	A01	7588200	T	G	downstream_gene_variant	MODIFIER	c.*3208T>G\|	S107 S15 S159 S286 S291 S44 S84
21464	BAA01g15620	A01	7588432	C	T	synonymous_variant	LOW	c.1422C>T\|p.Leu474Leu	S82 S92
21465	BAA01g15610	A01	7589047	C	T	downstream_gene_variant	MODIFIER	c.*4055C>T\|	S128
21466	BAA01g15620	A01	7590326	C	T	downstream_gene_variant	MODIFIER	c.*1358C>T\|	S134
21467	BAA01g15620	A01	7590538	G	A	downstream_gene_variant	MODIFIER	c.*1570G>A\|	S162
21468	BAA01g15620	A01	7591605	C	T	downstream_gene_variant	MODIFIER	c.*2637C>T\|	S242
21469	BAA01g15620	A01	7592617	G	A	downstream_gene_variant	MODIFIER	c.*3649G>A\|	S292
21470	BAA01g15620	A01	7593524	C	T	downstream_gene_variant	MODIFIER	c.*4556C>T\|	S179
21471	BAA01g15620	A01	7593895	C	T	downstream_gene_variant	MODIFIER	c.*4927C>T\|	S93
21472	BAA01g15620-BAA01g15630	A01	7594543	G	A	intergenic_region	MODIFIER	n.7594543G>A\|	S96
21473	BAA01g15620-BAA01g15630	A01	7594642	C	T	intergenic_region	MODIFIER	n.7594642C>T\|	S302
21474	BAA01g15620-BAA01g15630	A01	7595486	C	T	intergenic_region	MODIFIER	n.7595486C>T\|	S167
21475	BAA01g15620-BAA01g15630	A01	7597341	C	T	intergenic_region	MODIFIER	n.7597341C>T\|	S169

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