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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
68301	BAA01g35770	A01	23946980	C	T	synonymous_variant	LOW	c.1092G>A\|p.Glu364Glu	S288
68302	BAA01g35770	A01	23946989	C	T	splice_region_variant&intron_variant	LOW	c.1087-4G>A\|	S81 S85
68303	BAA01g35770	A01	23948036	C	T	synonymous_variant	LOW	c.201G>A\|p.Lys67Lys	S204
68304	BAA01g35770	A01	23948861	G	A	upstream_gene_variant	MODIFIER	c.-625C>T\|	S106
68305	BAA01g35770	A01	23950432	G	A	upstream_gene_variant	MODIFIER	c.-2196C>T\|	S281
68306	BAA01g35770	A01	23950728	G	A	upstream_gene_variant	MODIFIER	c.-2492C>T\|	S257
68307	BAA01g35770-BAA01g35780	A01	23953247	G	A	intergenic_region	MODIFIER	n.23953247G>A\|	S199
68308	BAA01g35770-BAA01g35780	A01	23955361	C	T	intergenic_region	MODIFIER	n.23955361C>T\|	S240
68309	BAA01g35770-BAA01g35780	A01	23955578	C	T	intergenic_region	MODIFIER	n.23955578C>T\|	S55
68310	BAA01g35770-BAA01g35780	A01	23956070	C	T	intergenic_region	MODIFIER	n.23956070C>T\|	S289 S290
68311	BAA01g35770-BAA01g35780	A01	23956710	C	T	intergenic_region	MODIFIER	n.23956710C>T\|	S210
68312	BAA01g35780	A01	23963488	C	T	upstream_gene_variant	MODIFIER	c.-2307C>T\|	S4
68313	BAA01g35780	A01	23966810	C	T	missense_variant	MODERATE	c.625C>T\|p.Leu209Phe	S187 S188 S276
68314	BAA01g35780	A01	23967134	C	T	missense_variant&splice_region_variant	MODERATE	c.869C>T\|p.Ser290Phe	S184
68315	BAA01g35800	A01	23967991	G	A	upstream_gene_variant	MODIFIER	c.-4755G>A\|	S283
68316	BAA01g35790	A01	23968170	C	T	missense_variant	MODERATE	c.902G>A\|p.Gly301Glu	S104 S52
68317	BAA01g35790	A01	23968376	C	T	stop_gained	HIGH	c.696G>A\|p.Trp232*	S148 S210 S30 S31
68318	BAA01g35790	A01	23968446	C	T	missense_variant	MODERATE	c.626G>A\|p.Arg209Lys	S146
68319	BAA01g35790	A01	23968495	G	A	missense_variant	MODERATE	c.577C>T\|p.Pro193Ser	S298
68320	BAA01g35790	A01	23968773	G	A	missense_variant	MODERATE	c.299C>T\|p.Thr100Ile	S287
68321	BAA01g35790	A01	23969590	C	T	upstream_gene_variant	MODIFIER	c.-519G>A\|	S201
68322	BAA01g35790	A01	23969823	C	T	upstream_gene_variant	MODIFIER	c.-752G>A\|	S178
68323	BAA01g35790	A01	23973358	C	T	upstream_gene_variant	MODIFIER	c.-4287G>A\|	S16
68324	BAA01g35800	A01	23974478	C	T	intron_variant	MODIFIER	c.851-49C>T\|	S46
68325	BAA01g35800	A01	23974569	C	T	missense_variant	MODERATE	c.893C>T\|p.Ser298Leu	S270

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