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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
166951	BAA02g12920	A02	5770026	C	T	synonymous_variant	LOW	c.276C>T\|p.Leu92Leu	S194
166952	BAA02g12910	A02	5770507	G	A	upstream_gene_variant	MODIFIER	c.-2645C>T\|	S286
166953	BAA02g12910	A02	5770629	C	T	upstream_gene_variant	MODIFIER	c.-2767G>A\|	S71
166954	BAA02g12920	A02	5771169	C	T	missense_variant	MODERATE	c.880C>T\|p.Leu294Phe	S230
166955	BAA02g12910	A02	5772118	G	A	upstream_gene_variant	MODIFIER	c.-4256C>T\|	S161
166956	BAA02g12930	A02	5772279	C	T	missense_variant	MODERATE	c.1837G>A\|p.Val613Met	S185
166957	BAA02g12930	A02	5772776	G	A	synonymous_variant	LOW	c.1527C>T\|p.Tyr509Tyr	S148 S30 S31
166958	BAA02g12930	A02	5773403	G	A	splice_region_variant&intron_variant	LOW	c.1122+8C>T\|	S166
166959	BAA02g12920	A02	5774177	T	A	downstream_gene_variant	MODIFIER	c.*2946T>A\|	S273
166960	BAA02g12930	A02	5775284	G	A	synonymous_variant	LOW	c.321C>T\|p.Tyr107Tyr	S62
166961	BAA02g12930	A02	5775559	G	A	missense_variant	MODERATE	c.154C>T\|p.Leu52Phe	S72
166962	BAA02g12930	A02	5776034	G	A	upstream_gene_variant	MODIFIER	c.-206C>T\|	S79 S91
166963	BAA02g12930	A02	5776541	C	T	upstream_gene_variant	MODIFIER	c.-713G>A\|	S54
166964	BAA02g12930	A02	5778832	C	T	upstream_gene_variant	MODIFIER	c.-3004G>A\|	S115
166965	BAA02g12930	A02	5780053	G	A	upstream_gene_variant	MODIFIER	c.-4225C>T\|	S133 S202
166966	BAA02g12940	A02	5780962	G	A	upstream_gene_variant	MODIFIER	c.-4755G>A\|	S205
166967	BAA02g12940	A02	5781176	G	A	upstream_gene_variant	MODIFIER	c.-4541G>A\|	S105 S106
166968	BAA02g12940	A02	5781720	G	A	upstream_gene_variant	MODIFIER	c.-3997G>A\|	S282
166969	BAA02g12940	A02	5781852	G	A	upstream_gene_variant	MODIFIER	c.-3865G>A\|	S190
166970	BAA02g12940	A02	5782496	G	A	upstream_gene_variant	MODIFIER	c.-3221G>A\|	S104 S108 S109 S158 S208 S308 S76 S79 S85 S87 S89 S91 S93 S95 S96 S97 S99
166971	BAA02g12940	A02	5784604	G	A	upstream_gene_variant	MODIFIER	c.-1113G>A\|	S43
166972	BAA02g12940	A02	5785071	G	A	upstream_gene_variant	MODIFIER	c.-646G>A\|	S223
166973	BAA02g12960	A02	5786310	G	A	upstream_gene_variant	MODIFIER	c.-4494G>A\|	S287
166974	BAA02g12940	A02	5786599	G	A	stop_gained	HIGH	c.417G>A\|p.Trp139*	S132 S137 S138 S215 S237 S288 S89
166975	BAA02g12940	A02	5786708	G	A	missense_variant	MODERATE	c.526G>A\|p.Glu176Lys	S7

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