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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
11151	BAA01g09070	A01	3977671	C	T	missense_variant	MODERATE	c.944G>A\|p.Arg315His	S62
11152	BAA01g09070	A01	3977844	C	T	stop_gained	HIGH	c.771G>A\|p.Trp257*	S25 S264
11153	BAA01g09050	A01	3978467	G	A	upstream_gene_variant	MODIFIER	c.-4930C>T\|	S183 S198
11154	BAA01g09060	A01	3979003	G	A	upstream_gene_variant	MODIFIER	c.-1841C>T\|	S63
11155	BAA01g09060	A01	3981336	C	T	upstream_gene_variant	MODIFIER	c.-4174G>A\|	S54
11156	BAA01g09080	A01	3981620	G	A	synonymous_variant	LOW	c.816C>T\|p.Ser272Ser	S207
11157	BAA01g09070	A01	3982489	G	A	upstream_gene_variant	MODIFIER	c.-3720C>T\|	S75 S81
11158	BAA01g09080	A01	3983945	G	A	upstream_gene_variant	MODIFIER	c.-1510C>T\|	S103
11159	BAA01g09080	A01	3984755	G	A	upstream_gene_variant	MODIFIER	c.-2320C>T\|	S247
11160	BAA01g09080	A01	3985571	C	T	upstream_gene_variant	MODIFIER	c.-3136G>A\|	S302
11161	BAA01g09080	A01	3985806	G	A	upstream_gene_variant	MODIFIER	c.-3371C>T\|	S6
11162	BAA01g09090	A01	3987662	G	A	upstream_gene_variant	MODIFIER	c.-451C>T\|	S308
11163	BAA01g09090	A01	3987908	C	T	upstream_gene_variant	MODIFIER	c.-697G>A\|	S120
11164	BAA01g09100	A01	3988767	G	A	missense_variant	MODERATE	c.98G>A\|p.Gly33Glu	S298
11165	BAA01g09100	A01	3989543	A	C	missense_variant	MODERATE	c.874A>C\|p.Ile292Leu	S109 S12 S149 S159 S44 S61 S69
11166	BAA01g09100	A01	3989649	C	T	missense_variant	MODERATE	c.980C>T\|p.Ser327Phe	S1 S90
11167	BAA01g09090	A01	3990525	G	A	upstream_gene_variant	MODIFIER	c.-3314C>T\|	S107
11168	BAA01g09090	A01	3990746	C	T	upstream_gene_variant	MODIFIER	c.-3535G>A\|	S42
11169	BAA01g09090	A01	3991448	C	T	upstream_gene_variant	MODIFIER	c.-4237G>A\|	S176
11170	BAA01g09110	A01	3991535	G	A	missense_variant	MODERATE	c.76C>T\|p.Leu26Phe	S220 S257 S267 S91
11171	BAA01g09110	A01	3991546	G	T	missense_variant	MODERATE	c.65C>A\|p.Ser22Tyr	S220 S257 S267 S91
11172	BAA01g09110	A01	3991547	A	G	missense_variant	MODERATE	c.64T>C\|p.Ser22Pro	S220 S257 S267 S91
11173	BAA01g09110	A01	3991566	C	G	synonymous_variant	LOW	c.45G>C\|p.Val15Val	S220 S257 S267 S91
11174	BAA01g09110	A01	3991569	A	C	missense_variant	MODERATE	c.42T>G\|p.Asp14Glu	S220 S257 S267 S91
11175	BAA01g09090	A01	3992037	G	A	upstream_gene_variant	MODIFIER	c.-4826C>T\|	S124

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