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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
99151	BAA10g06440	A10	3304329	C	T	upstream_gene_variant	MODIFIER	c.-3111G>A\|	S28
99152	BAA10g06440	A10	3304688	G	A	upstream_gene_variant	MODIFIER	c.-3470C>T\|	S182
99153	BAA10g06440	A10	3305138	C	T	upstream_gene_variant	MODIFIER	c.-3920G>A\|	S73 S91
99154	BAA10g06440	A10	3305190	C	T	upstream_gene_variant	MODIFIER	c.-3972G>A\|	S15 S4 S6
99155	BAA10g06440	A10	3305404	C	T	upstream_gene_variant	MODIFIER	c.-4186G>A\|	S98
99156	BAA10g06450	A10	3306000	C	T	synonymous_variant	LOW	c.54C>T\|p.Phe18Phe	S206 S26
99157	BAA10g06450	A10	3308559	G	A	downstream_gene_variant	MODIFIER	c.*383G>A\|	S65
99158	BAA10g06450	A10	3309841	C	T	downstream_gene_variant	MODIFIER	c.*1665C>T\|	S273
99159	BAA10g06450	A10	3310419	G	A	downstream_gene_variant	MODIFIER	c.*2243G>A\|	S211 S227
99160	BAA10g06450	A10	3310874	C	T	downstream_gene_variant	MODIFIER	c.*2698C>T\|	S297
99161	BAA10g06450	A10	3310963	C	T	downstream_gene_variant	MODIFIER	c.*2787C>T\|	S195 S196
99162	BAA10g06450	A10	3311312	C	T	downstream_gene_variant	MODIFIER	c.*3136C>T\|	S42
99163	BAA10g06450	A10	3311862	G	A	downstream_gene_variant	MODIFIER	c.*3686G>A\|	S250
99164	BAA10g06450	A10	3312872	C	T	downstream_gene_variant	MODIFIER	c.*4696C>T\|	S186
99165	BAA10g06450-BAA10g06460	A10	3313671	G	A	intergenic_region	MODIFIER	n.3313671G>A\|	S20
99166	BAA10g06450-BAA10g06460	A10	3314364	C	T	intergenic_region	MODIFIER	n.3314364C>T\|	S152 S232
99167	BAA10g06450-BAA10g06460	A10	3314372	C	T	intergenic_region	MODIFIER	n.3314372C>T\|	S11
99168	BAA10g06450-BAA10g06460	A10	3314553	C	T	intergenic_region	MODIFIER	n.3314553C>T\|	S8
99169	BAA10g06450-BAA10g06460	A10	3315153	G	A	intergenic_region	MODIFIER	n.3315153G>A\|	S129
99170	BAA10g06460	A10	3320829	G	A	upstream_gene_variant	MODIFIER	c.-2093G>A\|	S45
99171	BAA10g06460	A10	3323098	G	A	synonymous_variant	LOW	c.177G>A\|p.Glu59Glu	S33
99172	BAA10g06470	A10	3323460	G	A	missense_variant	MODERATE	c.13G>A\|p.Val5Ile	S295
99173	BAA10g06470	A10	3323789	G	A	synonymous_variant	LOW	c.342G>A\|p.Leu114Leu	S207
99174	BAA10g06470	A10	3323894	G	A	synonymous_variant	LOW	c.447G>A\|p.Lys149Lys	S286
99175	BAA10g06470	A10	3324087	G	A	missense_variant	MODERATE	c.640G>A\|p.Val214Ile	S290

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