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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
7901	BAA01g06350	A01	2824722	C	T	missense_variant	MODERATE	c.1538G>A\|p.Arg513Lys	S221
7902	BAA01g06330	A01	2825942	G	A	upstream_gene_variant	MODIFIER	c.-3617C>T\|	S180
7903	BAA01g06350	A01	2827369	C	T	synonymous_variant	LOW	c.528G>A\|p.Lys176Lys	S99
7904	BAA01g06340	A01	2827760	C	T	upstream_gene_variant	MODIFIER	c.-4198G>A\|	S266
7905	BAA01g06360	A01	2829510	C	T	stop_gained	HIGH	c.1071G>A\|p.Trp357*	S176
7906	BAA01g06360	A01	2829593	C	T	missense_variant	MODERATE	c.988G>A\|p.Asp330Asn	S46
7907	BAA01g06350	A01	2830710	C	T	upstream_gene_variant	MODIFIER	c.-2360G>A\|	S291
7908	BAA01g06350	A01	2831366	C	T	upstream_gene_variant	MODIFIER	c.-3016G>A\|	S134
7909	BAA01g06350	A01	2831648	C	T	upstream_gene_variant	MODIFIER	c.-3298G>A\|	S158
7910	BAA01g06350	A01	2831753	C	A	upstream_gene_variant	MODIFIER	c.-3403G>T\|	S233
7911	BAA01g06370	A01	2832912	G	A	splice_region_variant&intron_variant	LOW	c.682-7C>T\|	S17
7912	BAA01g06360	A01	2835586	C	T	upstream_gene_variant	MODIFIER	c.-4227G>A\|	S48
7913	BAA01g06360	A01	2835661	C	T	upstream_gene_variant	MODIFIER	c.-4302G>A\|	S74
7914	BAA01g06360	A01	2835980	G	A	upstream_gene_variant	MODIFIER	c.-4621C>T\|	S286
7915	BAA01g06360	A01	2836225	C	T	upstream_gene_variant	MODIFIER	c.-4866G>A\|	S252
7916	BAA01g06370	A01	2836975	C	T	upstream_gene_variant	MODIFIER	c.-2174G>A\|	S59
7917	BAA01g06370	A01	2838050	G	A	upstream_gene_variant	MODIFIER	c.-3249C>T\|	S57
7918	BAA01g06380	A01	2838625	C	T	splice_region_variant&stop_retained_variant	LOW	c.611G>A\|p.Ter204Ter	S100
7919	BAA01g06380	A01	2839999	G	A	upstream_gene_variant	MODIFIER	c.-764C>T\|	S139
7920	BAA01g06380	A01	2840939	C	T	upstream_gene_variant	MODIFIER	c.-1704G>A\|	S134
7921	BAA01g06380	A01	2840956	G	A	upstream_gene_variant	MODIFIER	c.-1721C>T\|	S224
7922	BAA01g06390	A01	2841530	C	T	synonymous_variant	LOW	c.204G>A\|p.Glu68Glu	S25 S264
7923	BAA01g06390	A01	2841568	C	T	missense_variant	MODERATE	c.166G>A\|p.Ala56Thr	S19
7924	BAA01g06390	A01	2841720	C	T	missense_variant	MODERATE	c.14G>A\|p.Gly5Glu	S100
7925	BAA01g06380	A01	2842511	C	T	upstream_gene_variant	MODIFIER	c.-3276G>A\|	S148 S210 S30 S31

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