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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
167651	BAA02g13300	A02	6050474	G	A	missense_variant	MODERATE	c.3020C>T\|p.Ser1007Phe	S308
167652	BAA02g13300	A02	6051365	G	A	intron_variant	MODIFIER	c.2926+148C>T\|	S56
167653	BAA02g13300	A02	6051391	C	T	intron_variant	MODIFIER	c.2926+122G>A\|	S208 S219
167654	BAA02g13300	A02	6051692	G	A	intron_variant	MODIFIER	c.2839-10C>T\|	S298
167655	BAA02g13300	A02	6051799	G	A	missense_variant	MODERATE	c.2803C>T\|p.Pro935Ser	S140
167656	BAA02g13300	A02	6052060	G	A	missense_variant	MODERATE	c.2542C>T\|p.Leu848Phe	S169
167657	BAA02g13300	A02	6052634	A	C	missense_variant	MODERATE	c.2143T>G\|p.Phe715Val	S165
167658	BAA02g13300	A02	6052647	G	A	synonymous_variant	LOW	c.2130C>T\|p.Phe710Phe	S105 S106
167659	BAA02g13310	A02	6053529	C	T	upstream_gene_variant	MODIFIER	c.-3805C>T\|	S171
167660	BAA02g13300	A02	6054513	G	A	missense_variant	MODERATE	c.1049C>T\|p.Pro350Leu	S136
167661	BAA02g13300	A02	6054531	G	A	missense_variant	MODERATE	c.1031C>T\|p.Thr344Ile	S153 S213
167662	BAA02g13300	A02	6056128	C	T	missense_variant	MODERATE	c.19G>A\|p.Asp7Asn	S63
167663	BAA02g13300	A02	6056292	G	A	upstream_gene_variant	MODIFIER	c.-146C>T\|	S136
167664	BAA02g13300	A02	6057236	C	T	upstream_gene_variant	MODIFIER	c.-1090G>A\|	S175
167665	BAA02g13300	A02	6057299	G	A	upstream_gene_variant	MODIFIER	c.-1153C>T\|	S11
167666	BAA02g13310	A02	6057887	G	A	missense_variant	MODERATE	c.238G>A\|p.Ala80Thr	S289 S290
167667	BAA02g13300	A02	6058018	G	A	upstream_gene_variant	MODIFIER	c.-1872C>T\|	S34
167668	BAA02g13300	A02	6058402	C	T	upstream_gene_variant	MODIFIER	c.-2256G>A\|	S255
167669	BAA02g13320	A02	6059597	T	A	synonymous_variant	LOW	c.51T>A\|p.Ala17Ala	S226 S238 S91
167670	BAA02g13320	A02	6059609	G	A	synonymous_variant	LOW	c.63G>A\|p.Glu21Glu	S226 S238 S257 S91
167671	BAA02g13320	A02	6059615	C	T	synonymous_variant	LOW	c.69C>T\|p.Asp23Asp	S226 S238 S246 S257 S91
167672	BAA02g13320	A02	6059618	C	T	synonymous_variant	LOW	c.72C>T\|p.Leu24Leu	S226 S238 S257 S91
167673	BAA02g13320	A02	6059623	G	C	missense_variant	MODERATE	c.77G>C\|p.Gly26Ala	S226 S238 S257 S91
167674	BAA02g13320	A02	6059624	C	T	synonymous_variant	LOW	c.78C>T\|p.Gly26Gly	S226 S238 S257 S91
167675	BAA02g13320	A02	6059627	C	A	synonymous_variant	LOW	c.81C>A\|p.Ser27Ser	S226 S238 S257 S91

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