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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
155001	BAA02g03200	A02	1400296	C	T	upstream_gene_variant	MODIFIER	c.-541C>T\|	S216
155002	BAA02g03200	A02	1400767	C	T	upstream_gene_variant	MODIFIER	c.-70C>T\|	S121
155003	BAA02g03210	A02	1401732	G	A	missense_variant	MODERATE	c.101G>A\|p.Ser34Asn	S308
155004	BAA02g03210	A02	1401764	G	A	missense_variant	MODERATE	c.133G>A\|p.Glu45Lys	S25
155005	BAA02g03190	A02	1402108	C	T	downstream_gene_variant	MODIFIER	c.*2813C>T\|	S262
155006	BAA02g03210	A02	1402556	C	T	stop_gained	HIGH	c.331C>T\|p.Gln111*	S207
155007	BAA02g03210	A02	1402565	G	A	missense_variant	MODERATE	c.340G>A\|p.Glu114Lys	S68
155008	BAA02g03210	A02	1402775	C	T	missense_variant	MODERATE	c.550C>T\|p.Leu184Phe	S250
155009	BAA02g03210	A02	1403338	G	A	synonymous_variant	LOW	c.1113G>A\|p.Arg371Arg	S107
155010	BAA02g03190	A02	1403470	C	T	downstream_gene_variant	MODIFIER	c.*4175C>T\|	S40 S49
155011	BAA02g03190	A02	1403902	C	T	downstream_gene_variant	MODIFIER	c.*4607C>T\|	S183 S198
155012	BAA02g03190	A02	1404063	C	T	downstream_gene_variant	MODIFIER	c.*4768C>T\|	S13
155013	BAA02g03210	A02	1407882	C	T	downstream_gene_variant	MODIFIER	c.*4442C>T\|	S298
155014	BAA02g03210-BAA02g03220	A02	1410502	C	T	intergenic_region	MODIFIER	n.1410502C>T\|	S217
155015	BAA02g03210-BAA02g03220	A02	1410870	C	T	intergenic_region	MODIFIER	n.1410870C>T\|	S281
155016	BAA02g03210-BAA02g03220	A02	1412532	G	A	intergenic_region	MODIFIER	n.1412532G>A\|	S107 S120 S165 S166 S17 S184 S191 S23 S237 S279 S53 S68 S91 S96
155017	BAA02g03210-BAA02g03220	A02	1412533	T	C	intergenic_region	MODIFIER	n.1412533T>C\|	S107 S120 S165 S166 S17 S184 S191 S23 S237 S279 S53 S68 S91 S96
155018	BAA02g03210-BAA02g03220	A02	1423583	T	A	intergenic_region	MODIFIER	n.1423583T>A\|	S243 S299
155019	BAA02g03210-BAA02g03220	A02	1424969	C	T	intergenic_region	MODIFIER	n.1424969C>T\|	S138
155020	BAA02g03220	A02	1426651	C	T	downstream_gene_variant	MODIFIER	c.*4432G>A\|	S85
155021	BAA02g03220	A02	1427270	G	A	downstream_gene_variant	MODIFIER	c.*3813C>T\|	S264
155022	BAA02g03220	A02	1428469	G	A	downstream_gene_variant	MODIFIER	c.*2614C>T\|	S161
155023	BAA02g03220	A02	1429528	C	T	downstream_gene_variant	MODIFIER	c.*1555G>A\|	S108
155024	BAA02g03240	A02	1429943	C	T	upstream_gene_variant	MODIFIER	c.-4726C>T\|	S270
155025	BAA02g03240	A02	1429993	C	T	upstream_gene_variant	MODIFIER	c.-4676C>T\|	S159

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