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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
30301	BAA01g21210	A01	10490726	G	A	upstream_gene_variant	MODIFIER	c.-3048C>T\|	S134 S179 S193
30302	BAA01g21210	A01	10490751	G	A	upstream_gene_variant	MODIFIER	c.-3073C>T\|	S240
30303	BAA01g21210	A01	10492177	G	A	upstream_gene_variant	MODIFIER	c.-4499C>T\|	S95
30304	BAA01g21210-BAA01g21220	A01	10495397	G	A	intergenic_region	MODIFIER	n.10495397G>A\|	S156 S213 S4 S6
30305	BAA01g21210-BAA01g21220	A01	10496171	G	A	intergenic_region	MODIFIER	n.10496171G>A\|	S142
30306	BAA01g21210-BAA01g21220	A01	10496390	G	A	intergenic_region	MODIFIER	n.10496390G>A\|	S265
30307	BAA01g21210-BAA01g21220	A01	10496698	C	T	intergenic_region	MODIFIER	n.10496698C>T\|	S249
30308	BAA01g21210-BAA01g21220	A01	10496822	G	A	intergenic_region	MODIFIER	n.10496822G>A\|	S306 S308
30309	BAA01g21210-BAA01g21220	A01	10497119	G	A	intergenic_region	MODIFIER	n.10497119G>A\|	S284
30310	BAA01g21210-BAA01g21220	A01	10497176	G	A	intergenic_region	MODIFIER	n.10497176G>A\|	S172 S217
30311	BAA01g21210-BAA01g21220	A01	10497201	C	T	intergenic_region	MODIFIER	n.10497201C>T\|	S166
30312	BAA01g21220	A01	10502944	C	T	synonymous_variant	LOW	c.1500G>A\|p.Lys500Lys	S305
30313	BAA01g21220	A01	10503043	C	T	synonymous_variant	LOW	c.1401G>A\|p.Ala467Ala	S48
30314	BAA01g21220	A01	10503047	G	A	missense_variant	MODERATE	c.1397C>T\|p.Ser466Phe	S125
30315	BAA01g21220	A01	10504415	G	A	intron_variant	MODIFIER	c.447+32C>T\|	S240
30316	BAA01g21220	A01	10505961	C	T	upstream_gene_variant	MODIFIER	c.-1068G>A\|	S266
30317	BAA01g21220	A01	10506003	G	A	upstream_gene_variant	MODIFIER	c.-1110C>T\|	S190
30318	BAA01g21220	A01	10506443	C	T	upstream_gene_variant	MODIFIER	c.-1550G>A\|	S231
30319	BAA01g21220	A01	10508610	G	A	upstream_gene_variant	MODIFIER	c.-3717C>T\|	S181
30320	BAA01g21220	A01	10508748	G	A	upstream_gene_variant	MODIFIER	c.-3855C>T\|	S280
30321	BAA01g21220	A01	10509301	C	T	upstream_gene_variant	MODIFIER	c.-4408G>A\|	S62
30322	BAA01g21230	A01	10512418	C	T	downstream_gene_variant	MODIFIER	c.*649G>A\|	S179
30323	BAA01g21230	A01	10513446	G	A	intron_variant	MODIFIER	c.1366-80C>T\|	S37
30324	BAA01g21230	A01	10513765	G	A	synonymous_variant	LOW	c.1320C>T\|p.Ser440Ser	S45
30325	BAA01g21230	A01	10515986	C	T	missense_variant	MODERATE	c.359G>A\|p.Arg120Lys	S215

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