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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
17401	BAA01g13070	A01	6204030	C	T	missense_variant	MODERATE	c.53C>T\|p.Ser18Phe	S230
17402	BAA01g13070	A01	6204328	C	T	synonymous_variant	LOW	c.351C>T\|p.Val117Val	S161
17403	BAA01g13070	A01	6204950	C	T	missense_variant	MODERATE	c.635C>T\|p.Ser212Phe	S239 S33
17404	BAA01g13070	A01	6205180	C	T	missense_variant	MODERATE	c.865C>T\|p.Pro289Ser	S171
17405	BAA01g13070	A01	6205416	G	A	splice_region_variant&intron_variant	LOW	c.1096+5G>A\|	S271
17406	BAA01g13070	A01	6205442	C	T	intron_variant	MODIFIER	c.1096+31C>T\|	S81 S85
17407	BAA01g13070	A01	6206288	C	T	downstream_gene_variant	MODIFIER	c.*696C>T\|	S196
17408	BAA01g13070	A01	6206311	G	A	downstream_gene_variant	MODIFIER	c.*719G>A\|	S60
17409	BAA01g13070	A01	6206673	G	A	downstream_gene_variant	MODIFIER	c.*1081G>A\|	S110 S114 S125 S20 S202 S221 S23 S286 S289 S299 S46 S84 S99
17410	BAA01g13070	A01	6208869	G	A	downstream_gene_variant	MODIFIER	c.*3277G>A\|	S12
17411	BAA01g13070	A01	6208945	G	A	downstream_gene_variant	MODIFIER	c.*3353G>A\|	S129
17412	BAA01g13070	A01	6208984	G	A	downstream_gene_variant	MODIFIER	c.*3392G>A\|	S197
17413	BAA01g13070	A01	6209379	C	T	downstream_gene_variant	MODIFIER	c.*3787C>T\|	S44
17414	BAA01g13070	A01	6210119	C	T	downstream_gene_variant	MODIFIER	c.*4527C>T\|	S58
17415	BAA01g13080	A01	6217297	C	T	upstream_gene_variant	MODIFIER	c.-3387G>A\|	S82 S92
17416	BAA01g13080	A01	6218460	G	A	upstream_gene_variant	MODIFIER	c.-4550C>T\|	S95
17417	BAA01g13090	A01	6222348	C	T	upstream_gene_variant	MODIFIER	c.-1247G>A\|	S259
17418	BAA01g13090	A01	6222506	G	A	upstream_gene_variant	MODIFIER	c.-1405C>T\|	S241
17419	BAA01g13100	A01	6222762	C	T	missense_variant	MODERATE	c.151C>T\|p.Leu51Phe	S155
17420	BAA01g13090	A01	6223854	G	A	upstream_gene_variant	MODIFIER	c.-2753C>T\|	S308
17421	BAA01g13100	A01	6224101	C	T	synonymous_variant	LOW	c.1249C>T\|p.Leu417Leu	S221
17422	BAA01g13090	A01	6225003	G	A	upstream_gene_variant	MODIFIER	c.-3902C>T\|	S271
17423	BAA01g13090	A01	6225900	C	T	upstream_gene_variant	MODIFIER	c.-4799G>A\|	S303
17424	BAA01g13110	A01	6226600	C	T	upstream_gene_variant	MODIFIER	c.-605C>T\|	S247
17425	BAA01g13110	A01	6227676	G	A	missense_variant	MODERATE	c.388G>A\|p.Ala130Thr	S6

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