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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
119751	BAA10g11540	A10	13152222	C	T	downstream_gene_variant	MODIFIER	c.*3893C>T\|	S188
119752	BAA10g11540	A10	13152354	G	A	downstream_gene_variant	MODIFIER	c.*4025G>A\|	S198
119753	BAA10g11540	A10	13152552	G	A	downstream_gene_variant	MODIFIER	c.*4223G>A\|	S159 S243
119754	BAA10g11540-BAA10g11550	A10	13153783	C	T	intergenic_region	MODIFIER	n.13153783C>T\|	S210 S46
119755	BAA10g11540-BAA10g11550	A10	13155394	G	A	intergenic_region	MODIFIER	n.13155394G>A\|	S13 S140 S219 S279 S64 S72
119756	BAA10g11540-BAA10g11550	A10	13155638	G	A	intergenic_region	MODIFIER	n.13155638G>A\|	S216
119757	BAA10g11540-BAA10g11550	A10	13155878	C	T	intergenic_region	MODIFIER	n.13155878C>T\|	S149
119758	BAA10g11540-BAA10g11550	A10	13155974	C	T	intergenic_region	MODIFIER	n.13155974C>T\|	S177
119759	BAA10g11540-BAA10g11550	A10	13155976	C	T	intergenic_region	MODIFIER	n.13155976C>T\|	S199
119760	BAA10g11540-BAA10g11550	A10	13156637	G	A	intergenic_region	MODIFIER	n.13156637G>A\|	S155
119761	BAA10g11540-BAA10g11550	A10	13157125	G	A	intergenic_region	MODIFIER	n.13157125G>A\|	S148 S30 S31
119762	BAA10g11550	A10	13157334	A	T	upstream_gene_variant	MODIFIER	c.-4802A>T\|	S287
119763	BAA10g11550	A10	13158071	G	A	upstream_gene_variant	MODIFIER	c.-4065G>A\|	S226
119764	BAA10g11550	A10	13158074	C	T	upstream_gene_variant	MODIFIER	c.-4062C>T\|	S225 S73
119765	BAA10g11550	A10	13158571	C	T	upstream_gene_variant	MODIFIER	c.-3565C>T\|	S259
119766	BAA10g11550	A10	13158646	T	G	upstream_gene_variant	MODIFIER	c.-3490T>G\|	S251
119767	BAA10g11550	A10	13158648	T	C	upstream_gene_variant	MODIFIER	c.-3488T>C\|	S251
119768	BAA10g11550	A10	13159926	C	T	upstream_gene_variant	MODIFIER	c.-2210C>T\|	S61
119769	BAA10g11550	A10	13159929	C	T	upstream_gene_variant	MODIFIER	c.-2207C>T\|	S306 S308
119770	BAA10g11550	A10	13160159	C	T	upstream_gene_variant	MODIFIER	c.-1977C>T\|	S166
119771	BAA10g11550	A10	13162037	C	T	upstream_gene_variant	MODIFIER	c.-99C>T\|	S206 S26
119772	BAA10g11550	A10	13162358	G	A	missense_variant	MODERATE	c.142G>A\|p.Gly48Arg	S217
119773	BAA10g11550	A10	13162550	G	A	downstream_gene_variant	MODIFIER	c.*178G>A\|	S215
119774	BAA10g11550	A10	13162999	G	A	downstream_gene_variant	MODIFIER	c.*627G>A\|	S59
119775	BAA10g11560	A10	13164627	C	T	synonymous_variant	LOW	c.153G>A\|p.Lys51Lys	S237

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