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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
86351	BAA01g45890	A01	30577506	C	T	downstream_gene_variant	MODIFIER	c.*2778C>T\|	S8
86352	BAA01g45890	A01	30577938	C	T	downstream_gene_variant	MODIFIER	c.*3210C>T\|	S288
86353	BAA01g45890	A01	30578204	G	A	downstream_gene_variant	MODIFIER	c.*3476G>A\|	S246
86354	BAA01g45910	A01	30580012	C	T	downstream_gene_variant	MODIFIER	c.*683G>A\|	S89
86355	BAA01g45910	A01	30580775	G	A	missense_variant	MODERATE	c.1240C>T\|p.Leu414Phe	S247
86356	BAA01g45910	A01	30582482	C	T	synonymous_variant	LOW	c.264G>A\|p.Lys88Lys	S210 S225
86357	BAA01g45910	A01	30583734	G	A	upstream_gene_variant	MODIFIER	c.-858C>T\|	S268
86358	BAA01g45910	A01	30584069	C	T	upstream_gene_variant	MODIFIER	c.-1193G>A\|	S302
86359	BAA01g45910	A01	30584458	C	T	upstream_gene_variant	MODIFIER	c.-1582G>A\|	S56
86360	BAA01g45910	A01	30584687	C	T	upstream_gene_variant	MODIFIER	c.-1811G>A\|	S162
86361	BAA01g45910	A01	30586637	C	T	upstream_gene_variant	MODIFIER	c.-3761G>A\|	S35
86362	BAA01g45930	A01	30589850	G	A	upstream_gene_variant	MODIFIER	c.-4673G>A\|	S108
86363	BAA01g45930	A01	30590593	G	A	upstream_gene_variant	MODIFIER	c.-3930G>A\|	S99
86364	BAA01g45930	A01	30590864	C	T	upstream_gene_variant	MODIFIER	c.-3659C>T\|	S103
86365	BAA01g45930	A01	30591306	C	T	upstream_gene_variant	MODIFIER	c.-3217C>T\|	S195
86366	BAA01g45930	A01	30591450	G	A	upstream_gene_variant	MODIFIER	c.-3073G>A\|	S153 S213
86367	BAA01g45930	A01	30591600	C	T	upstream_gene_variant	MODIFIER	c.-2923C>T\|	S128
86368	BAA01g45930	A01	30591946	G	T	upstream_gene_variant	MODIFIER	c.-2577G>T\|	S265
86369	BAA01g45930	A01	30592974	C	T	upstream_gene_variant	MODIFIER	c.-1549C>T\|	S206 S26
86370	BAA01g45930	A01	30593040	C	T	upstream_gene_variant	MODIFIER	c.-1483C>T\|	S247
86371	BAA01g45930	A01	30594538	G	A	missense_variant	MODERATE	c.16G>A\|p.Val6Met	S292
86372	BAA01g45930	A01	30594901	C	T	missense_variant	MODERATE	c.379C>T\|p.Leu127Phe	S171
86373	BAA01g45930	A01	30595675	G	A	missense_variant	MODERATE	c.1153G>A\|p.Asp385Asn	S250
86374	BAA01g45940	A01	30596735	C	T	missense_variant	MODERATE	c.182C>T\|p.Ser61Phe	S95
86375	BAA01g45940	A01	30596978	T	G	missense_variant	MODERATE	c.425T>G\|p.Leu142Trp	S105 S11 S262 S263 S283 S32 S56 S62 S83 S96

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