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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
81151	BAA01g42920-BAA01g42930	A01	28410645	T	A	intergenic_region	MODIFIER	n.28410645T>A\|	S94
81152	BAA01g42920-BAA01g42930	A01	28412827	G	A	intergenic_region	MODIFIER	n.28412827G>A\|	S208
81153	BAA01g42920-BAA01g42930	A01	28412953	G	A	intergenic_region	MODIFIER	n.28412953G>A\|	S212
81154	BAA01g42920-BAA01g42930	A01	28414340	C	T	intergenic_region	MODIFIER	n.28414340C>T\|	S41
81155	BAA01g42930	A01	28415474	C	T	upstream_gene_variant	MODIFIER	c.-4983C>T\|	S183
81156	BAA01g42930	A01	28416427	C	T	upstream_gene_variant	MODIFIER	c.-4030C>T\|	S111
81157	BAA01g42930	A01	28416966	C	T	upstream_gene_variant	MODIFIER	c.-3491C>T\|	S292
81158	BAA01g42930	A01	28418184	G	A	upstream_gene_variant	MODIFIER	c.-2273G>A\|	S138
81159	BAA01g42930	A01	28418444	G	A	upstream_gene_variant	MODIFIER	c.-2013G>A\|	S252
81160	BAA01g42930	A01	28418778	C	T	upstream_gene_variant	MODIFIER	c.-1679C>T\|	S170
81161	BAA01g42930	A01	28418858	G	A	upstream_gene_variant	MODIFIER	c.-1599G>A\|	S262
81162	BAA01g42930	A01	28419958	T	A	upstream_gene_variant	MODIFIER	c.-499T>A\|	S134
81163	BAA01g42930	A01	28420489	C	T	synonymous_variant	LOW	c.33C>T\|p.Pro11Pro	S61
81164	BAA01g42930	A01	28420655	G	A	missense_variant	MODERATE	c.199G>A\|p.Ala67Thr	S117
81165	BAA01g42930	A01	28420718	C	T	missense_variant	MODERATE	c.262C>T\|p.Leu88Phe	S44
81166	BAA01g42930	A01	28421202	C	T	missense_variant	MODERATE	c.746C>T\|p.Pro249Leu	S72 S78
81167	BAA01g42940	A01	28423120	G	A	upstream_gene_variant	MODIFIER	c.-2887G>A\|	S157 S163
81168	BAA01g42940	A01	28424376	G	A	upstream_gene_variant	MODIFIER	c.-1631G>A\|	S237
81169	BAA01g42940	A01	28426478	C	T	missense_variant	MODERATE	c.472C>T\|p.Pro158Ser	S205
81170	BAA01g42940	A01	28427178	C	T	downstream_gene_variant	MODIFIER	c.*167C>T\|	S205 S240
81171	BAA01g42940	A01	28428769	G	A	downstream_gene_variant	MODIFIER	c.*1758G>A\|	S237
81172	BAA01g42940	A01	28428990	G	A	downstream_gene_variant	MODIFIER	c.*1979G>A\|	S238
81173	BAA01g42950	A01	28430109	C	T	missense_variant	MODERATE	c.832G>A\|p.Val278Met	S282
81174	BAA01g42950	A01	28430555	C	T	synonymous_variant	LOW	c.561G>A\|p.Glu187Glu	S174 S27
81175	BAA01g42940	A01	28430849	G	A	downstream_gene_variant	MODIFIER	c.*3838G>A\|	S306 S308

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