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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
39401	BAA01g25240	A01	13595119	C	T	upstream_gene_variant	MODIFIER	c.-949G>A\|	S35
39402	BAA01g25240	A01	13596003	C	T	upstream_gene_variant	MODIFIER	c.-1833G>A\|	S223
39403	BAA01g25250	A01	13600664	G	A	upstream_gene_variant	MODIFIER	c.-2988G>A\|	S288
39404	BAA01g25250	A01	13600731	G	A	upstream_gene_variant	MODIFIER	c.-2921G>A\|	S7
39405	BAA01g25250	A01	13601412	C	T	upstream_gene_variant	MODIFIER	c.-2240C>T\|	S118
39406	BAA01g25250	A01	13602508	A	T	upstream_gene_variant	MODIFIER	c.-1144A>T\|	S279
39407	BAA01g25250	A01	13603867	C	T	synonymous_variant	LOW	c.216C>T\|p.Tyr72Tyr	S260
39408	BAA01g25250	A01	13604867	G	A	missense_variant	MODERATE	c.1216G>A\|p.Asp406Asn	S84 S93
39409	BAA01g25250	A01	13605454	G	A	synonymous_variant	LOW	c.1803G>A\|p.Glu601Glu	S262
39410	BAA01g25250	A01	13605475	C	T	synonymous_variant	LOW	c.1824C>T\|p.His608His	S46
39411	BAA01g25250	A01	13605646	C	T	synonymous_variant	LOW	c.1995C>T\|p.Phe665Phe	S9
39412	BAA01g25250	A01	13605969	G	A	missense_variant	MODERATE	c.2318G>A\|p.Gly773Glu	S236
39413	BAA01g25250	A01	13606032	C	T	missense_variant	MODERATE	c.2381C>T\|p.Ser794Phe	S159 S187 S188 S243 S276
39414	BAA01g25260	A01	13606621	G	A	upstream_gene_variant	MODIFIER	c.-4517G>A\|	S162
39415	BAA01g25260	A01	13608377	G	A	upstream_gene_variant	MODIFIER	c.-2761G>A\|	S284
39416	BAA01g25260	A01	13611107	C	T	upstream_gene_variant	MODIFIER	c.-31C>T\|	S289 S290
39417	BAA01g25260	A01	13612175	C	T	missense_variant	MODERATE	c.926C>T\|p.Pro309Leu	S20
39418	BAA01g25260	A01	13612341	C	T	synonymous_variant	LOW	c.1092C>T\|p.Phe364Phe	S130
39419	BAA01g25260	A01	13612509	C	T	synonymous_variant	LOW	c.1260C>T\|p.Ser420Ser	S35
39420	BAA01g25260	A01	13612848	C	T	missense_variant	MODERATE	c.1352C>T\|p.Ser451Leu	S289 S290
39421	BAA01g25260	A01	13612916	C	T	missense_variant	MODERATE	c.1420C>T\|p.Pro474Ser	S185
39422	BAA01g25260	A01	13613001	G	A	intron_variant	MODIFIER	c.1459-17G>A\|	S63
39423	BAA01g25260	A01	13613893	G	A	synonymous_variant	LOW	c.1953G>A\|p.Arg651Arg	S216
39424	BAA01g25260	A01	13613958	G	A	missense_variant	MODERATE	c.2018G>A\|p.Arg673Lys	S252
39425	BAA01g25260	A01	13614231	C	T	missense_variant	MODERATE	c.2291C>T\|p.Ser764Phe	S303

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