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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
155301	BAA02g03430	A02	1527511	C	T	synonymous_variant	LOW	c.39C>T\|p.His13His	S250
155302	BAA02g03430	A02	1527898	C	T	synonymous_variant	LOW	c.426C>T\|p.Tyr142Tyr	S185
155303	BAA02g03430	A02	1527921	C	T	missense_variant	MODERATE	c.449C>T\|p.Pro150Leu	S159 S187 S188 S243 S276 S299
155304	BAA02g03440	A02	1528476	G	A	missense_variant	MODERATE	c.16G>A\|p.Glu6Lys	S96
155305	BAA02g03440	A02	1529439	C	T	missense_variant	MODERATE	c.280C>T\|p.Leu94Phe	S239
155306	BAA02g03420	A02	1529564	G	A	upstream_gene_variant	MODIFIER	c.-4675C>T\|	S78
155307	BAA02g03450	A02	1529903	G	A	upstream_gene_variant	MODIFIER	c.-657G>A\|	S223
155308	BAA02g03450	A02	1530252	C	T	upstream_gene_variant	MODIFIER	c.-308C>T\|	S15
155309	BAA02g03450	A02	1530868	G	A	synonymous_variant	LOW	c.309G>A\|p.Gln103Gln	S271
155310	BAA02g03460	A02	1531301	G	A	upstream_gene_variant	MODIFIER	c.-660G>A\|	S122
155311	BAA02g03460	A02	1531913	C	T	upstream_gene_variant	MODIFIER	c.-48C>T\|	S39
155312	BAA02g03470	A02	1532225	T	G	upstream_gene_variant	MODIFIER	c.-2309T>G\|	S172 S217
155313	BAA02g03470	A02	1532286	A	G	upstream_gene_variant	MODIFIER	c.-2248A>G\|	S116 S118 S148 S210 S30 S31 S54
155314	BAA02g03460	A02	1532770	C	T	synonymous_variant	LOW	c.225C>T\|p.Leu75Leu	S37
155315	BAA02g03470	A02	1533304	G	A	upstream_gene_variant	MODIFIER	c.-1230G>A\|	S226
155316	BAA02g03470	A02	1533450	C	T	upstream_gene_variant	MODIFIER	c.-1084C>T\|	S20
155317	BAA02g03470	A02	1533582	G	A	upstream_gene_variant	MODIFIER	c.-952G>A\|	S43
155318	BAA02g03470	A02	1533996	C	T	upstream_gene_variant	MODIFIER	c.-538C>T\|	S138
155319	BAA02g03470	A02	1534025	G	A	upstream_gene_variant	MODIFIER	c.-509G>A\|	S191
155320	BAA02g03470	A02	1534553	G	A	missense_variant	MODERATE	c.20G>A\|p.Ser7Asn	S105 S106
155321	BAA02g03480	A02	1535590	G	A	upstream_gene_variant	MODIFIER	c.-819G>A\|	S165
155322	BAA02g03480	A02	1536236	G	A	upstream_gene_variant	MODIFIER	c.-173G>A\|	S288
155323	BAA02g03490	A02	1538324	C	T	synonymous_variant	LOW	c.144C>T\|p.Asp48Asp	S82 S92
155324	BAA02g03490	A02	1538374	C	T	missense_variant	MODERATE	c.194C>T\|p.Ser65Phe	S117
155325	BAA02g03490	A02	1538502	C	T	missense_variant	MODERATE	c.322C>T\|p.Pro108Ser	S289 S290

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