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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
113901	BAA10g09050	A10	11114365	C	T	intron_variant	MODIFIER	c.804+34C>T\|	S79 S91
113902	BAA10g09050	A10	11115966	G	A	downstream_gene_variant	MODIFIER	c.*1170G>A\|	S125
113903	BAA10g09050	A10	11116136	G	A	downstream_gene_variant	MODIFIER	c.*1340G>A\|	S181
113904	BAA10g09050	A10	11117358	G	A	downstream_gene_variant	MODIFIER	c.*2562G>A\|	S280
113905	BAA10g09050	A10	11117404	G	A	downstream_gene_variant	MODIFIER	c.*2608G>A\|	S57
113906	BAA10g09050	A10	11117578	G	A	downstream_gene_variant	MODIFIER	c.*2782G>A\|	S13 S140 S219 S279 S64 S72
113907	BAA10g09050	A10	11117975	G	A	downstream_gene_variant	MODIFIER	c.*3179G>A\|	S48
113908	BAA10g09050	A10	11118544	C	T	downstream_gene_variant	MODIFIER	c.*3748C>T\|	S20
113909	BAA10g09050	A10	11118603	G	A	downstream_gene_variant	MODIFIER	c.*3807G>A\|	S262
113910	BAA10g09050	A10	11119262	G	A	downstream_gene_variant	MODIFIER	c.*4466G>A\|	S151 S263
113911	BAA10g09050	A10	11119543	C	T	downstream_gene_variant	MODIFIER	c.*4747C>T\|	S156
113912	BAA10g09060	A10	11119819	C	T	downstream_gene_variant	MODIFIER	c.*3921G>A\|	S287
113913	BAA10g09060	A10	11120186	C	T	downstream_gene_variant	MODIFIER	c.*3554G>A\|	S270
113914	BAA10g09060	A10	11120386	C	T	downstream_gene_variant	MODIFIER	c.*3354G>A\|	S282
113915	BAA10g09060	A10	11120465	G	A	downstream_gene_variant	MODIFIER	c.*3275C>T\|	S161
113916	BAA10g09060	A10	11120924	G	A	downstream_gene_variant	MODIFIER	c.*2816C>T\|	S157 S163
113917	BAA10g09060	A10	11121557	C	T	downstream_gene_variant	MODIFIER	c.*2183G>A\|	S284
113918	BAA10g09060	A10	11123457	G	A	downstream_gene_variant	MODIFIER	c.*283C>T\|	S151 S263
113919	BAA10g09060	A10	11124004	C	T	synonymous_variant	LOW	c.1482G>A\|p.Gln494Gln	S17
113920	BAA10g09060	A10	11124374	G	A	intron_variant	MODIFIER	c.1289+39C>T\|	S125
113921	BAA10g09060	A10	11125123	C	T	missense_variant	MODERATE	c.878G>A\|p.Gly293Glu	S155 S211
113922	BAA10g09060	A10	11125757	C	T	splice_acceptor_variant&intron_variant	HIGH	c.358-1G>A\|	S56
113923	BAA10g09060	A10	11126194	C	T	missense_variant	MODERATE	c.35G>A\|p.Gly12Glu	S10
113924	BAA10g09060	A10	11128110	G	A	upstream_gene_variant	MODIFIER	c.-1882C>T\|	S112
113925	BAA10g09060	A10	11128399	C	T	upstream_gene_variant	MODIFIER	c.-2171G>A\|	S133

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