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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
168151	BAA02g13560	A02	6270746	G	A	splice_region_variant&intron_variant	LOW	c.1268+5G>A\|	S61
168152	BAA02g13560	A02	6270978	G	A	missense_variant	MODERATE	c.1381G>A\|p.Glu461Lys	S37
168153	BAA02g13560	A02	6271160	C	T	downstream_gene_variant	MODIFIER	c.*6C>T\|	S181
168154	BAA02g13560	A02	6272097	A	T	downstream_gene_variant	MODIFIER	c.*943A>T\|	S130
168155	BAA02g13560	A02	6272864	G	A	downstream_gene_variant	MODIFIER	c.*1710G>A\|	S53 S75 S82 S92
168156	BAA02g13560	A02	6274766	G	A	downstream_gene_variant	MODIFIER	c.*3612G>A\|	S184
168157	BAA02g13560	A02	6275439	C	T	downstream_gene_variant	MODIFIER	c.*4285C>T\|	S182
168158	BAA02g13560	A02	6275489	G	A	downstream_gene_variant	MODIFIER	c.*4335G>A\|	S231
168159	BAA02g13560	A02	6275820	G	A	downstream_gene_variant	MODIFIER	c.*4666G>A\|	S288
168160	BAA02g13560	A02	6275860	G	A	downstream_gene_variant	MODIFIER	c.*4706G>A\|	S247
168161	BAA02g13560	A02	6276130	G	A	downstream_gene_variant	MODIFIER	c.*4976G>A\|	S79 S91
168162	BAA02g13560-BAA02g13570	A02	6278983	C	T	intergenic_region	MODIFIER	n.6278983C>T\|	S211 S227
168163	BAA02g13560-BAA02g13570	A02	6278991	G	A	intergenic_region	MODIFIER	n.6278991G>A\|	S170
168164	BAA02g13560-BAA02g13570	A02	6279494	G	A	intergenic_region	MODIFIER	n.6279494G>A\|	S160
168165	BAA02g13560-BAA02g13570	A02	6279846	C	T	intergenic_region	MODIFIER	n.6279846C>T\|	S8
168166	BAA02g13560-BAA02g13570	A02	6280394	G	A	intergenic_region	MODIFIER	n.6280394G>A\|	S156
168167	BAA02g13560-BAA02g13570	A02	6281884	C	T	intergenic_region	MODIFIER	n.6281884C>T\|	S162 S34
168168	BAA02g13560-BAA02g13570	A02	6282596	C	T	intergenic_region	MODIFIER	n.6282596C>T\|	S181
168169	BAA02g13570	A02	6284912	G	A	upstream_gene_variant	MODIFIER	c.-3112G>A\|	S62
168170	BAA02g13570	A02	6285009	C	T	upstream_gene_variant	MODIFIER	c.-3015C>T\|	S289 S290
168171	BAA02g13570	A02	6286326	C	T	upstream_gene_variant	MODIFIER	c.-1698C>T\|	S183 S198
168172	BAA02g13570	A02	6286944	G	A	upstream_gene_variant	MODIFIER	c.-1080G>A\|	S82 S92
168173	BAA02g13570	A02	6288581	G	A	missense_variant	MODERATE	c.304G>A\|p.Asp102Asn	S105 S106
168174	BAA02g13570	A02	6289847	G	A	intron_variant	MODIFIER	c.1146+102G>A\|	S297
168175	BAA02g13570	A02	6291847	G	A	downstream_gene_variant	MODIFIER	c.*772G>A\|	S288

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