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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
87001	BAA01g46290	A01	30881389	C	T	missense_variant	MODERATE	c.70G>A\|p.Glu24Lys	S273
87002	BAA01g46300	A01	30882833	G	A	missense_variant	MODERATE	c.310G>A\|p.Ala104Thr	S217 S248
87003	BAA01g46290	A01	30884217	G	A	upstream_gene_variant	MODIFIER	c.-2759C>T\|	S83 S88
87004	BAA01g46310	A01	30885937	G	A	missense_variant	MODERATE	c.523C>T\|p.Leu175Phe	S302
87005	BAA01g46310	A01	30886081	C	T	missense_variant	MODERATE	c.379G>A\|p.Val127Ile	S239
87006	BAA01g46300	A01	30886619	G	A	downstream_gene_variant	MODIFIER	c.*2984G>A\|	S298
87007	BAA01g46310	A01	30887403	C	T	missense_variant	MODERATE	c.52G>A\|p.Val18Met	S35
87008	BAA01g46310	A01	30887439	C	T	missense_variant	MODERATE	c.16G>A\|p.Glu6Lys	S146
87009	BAA01g46310	A01	30887617	C	T	upstream_gene_variant	MODIFIER	c.-163G>A\|	S63
87010	BAA01g46310	A01	30888378	C	T	upstream_gene_variant	MODIFIER	c.-924G>A\|	S62
87011	BAA01g46310	A01	30889033	G	A	upstream_gene_variant	MODIFIER	c.-1579C>T\|	S159 S187 S188 S298
87012	BAA01g46310	A01	30889599	G	A	upstream_gene_variant	MODIFIER	c.-2145C>T\|	S9
87013	BAA01g46310	A01	30890695	C	T	upstream_gene_variant	MODIFIER	c.-3241G>A\|	S100 S82 S83 S88 S92
87014	BAA01g46310	A01	30890791	C	T	upstream_gene_variant	MODIFIER	c.-3337G>A\|	S229
87015	BAA01g46310	A01	30890907	C	T	upstream_gene_variant	MODIFIER	c.-3453G>A\|	S134
87016	BAA01g46310	A01	30891164	T	A	upstream_gene_variant	MODIFIER	c.-3710A>T\|	S138
87017	BAA01g46310	A01	30891211	C	T	upstream_gene_variant	MODIFIER	c.-3757G>A\|	S210 S225
87018	BAA01g46320	A01	30891341	C	T	splice_region_variant&stop_retained_variant	LOW	c.1733G>A\|p.Ter578Ter	S78 S83
87019	BAA01g46310	A01	30891809	C	T	upstream_gene_variant	MODIFIER	c.-4355G>A\|	S210 S225
87020	BAA01g46310	A01	30891862	G	A	upstream_gene_variant	MODIFIER	c.-4408C>T\|	S143
87021	BAA01g46310	A01	30891872	C	T	upstream_gene_variant	MODIFIER	c.-4418G>A\|	S287
87022	BAA01g46320	A01	30892206	G	A	missense_variant	MODERATE	c.1366C>T\|p.Pro456Ser	S71
87023	BAA01g46320	A01	30893176	A	T	intron_variant	MODIFIER	c.1264-32T>A\|	S129
87024	BAA01g46320	A01	30893457	C	T	missense_variant	MODERATE	c.1100G>A\|p.Gly367Glu	S177
87025	BAA01g46320	A01	30893933	C	T	intron_variant	MODIFIER	c.1092+281G>A\|	S13 S140 S168 S219 S279 S64 S72

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