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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
31051	BAA01g21630	A01	10743572	C	T	upstream_gene_variant	MODIFIER	c.-1811G>A\|	S51
31052	BAA01g21630	A01	10744424	C	T	upstream_gene_variant	MODIFIER	c.-2663G>A\|	S148 S30 S31
31053	BAA01g21630	A01	10744643	C	T	upstream_gene_variant	MODIFIER	c.-2882G>A\|	S36
31054	BAA01g21650	A01	10744849	C	T	missense_variant	MODERATE	c.247G>A\|p.Ala83Thr	S221
31055	BAA01g21650	A01	10744868	G	A	synonymous_variant	LOW	c.228C>T\|p.Asn76Asn	S180
31056	BAA01g21630	A01	10745571	C	T	upstream_gene_variant	MODIFIER	c.-3810G>A\|	S267
31057	BAA01g21630	A01	10745926	C	T	upstream_gene_variant	MODIFIER	c.-4165G>A\|	S185
31058	BAA01g21630	A01	10746030	C	T	upstream_gene_variant	MODIFIER	c.-4269G>A\|	S289 S290
31059	BAA01g21630	A01	10746584	C	T	upstream_gene_variant	MODIFIER	c.-4823G>A\|	S179
31060	BAA01g21630	A01	10746591	G	A	upstream_gene_variant	MODIFIER	c.-4830C>T\|	S43
31061	BAA01g21650	A01	10747357	C	T	upstream_gene_variant	MODIFIER	c.-2262G>A\|	S148 S30 S31
31062	BAA01g21650	A01	10747381	C	T	upstream_gene_variant	MODIFIER	c.-2286G>A\|	S205
31063	BAA01g21660	A01	10749107	G	A	missense_variant	MODERATE	c.712G>A\|p.Glu238Lys	S281
31064	BAA01g21660	A01	10749191	C	T	missense_variant	MODERATE	c.796C>T\|p.Leu266Phe	S44
31065	BAA01g21660	A01	10749291	G	A	missense_variant	MODERATE	c.896G>A\|p.Gly299Glu	S162
31066	BAA01g21660	A01	10749326	C	T	synonymous_variant	LOW	c.931C>T\|p.Leu311Leu	S65
31067	BAA01g21660	A01	10749527	G	A	missense_variant	MODERATE	c.1132G>A\|p.Glu378Lys	S94
31068	BAA01g21660	A01	10749744	C	T	splice_region_variant&intron_variant	LOW	c.1341+8C>T\|	S166
31069	BAA01g21650	A01	10749829	C	T	upstream_gene_variant	MODIFIER	c.-4734G>A\|	S171
31070	BAA01g21660	A01	10750870	G	A	downstream_gene_variant	MODIFIER	c.*911G>A\|	S7 S9
31071	BAA01g21660	A01	10751482	C	T	downstream_gene_variant	MODIFIER	c.*1523C>T\|	S136
31072	BAA01g21660	A01	10751632	G	A	downstream_gene_variant	MODIFIER	c.*1673G>A\|	S84 S93
31073	BAA01g21660	A01	10754809	C	T	downstream_gene_variant	MODIFIER	c.*4850C>T\|	S10
31074	BAA01g21670	A01	10758241	G	A	intron_variant	MODIFIER	c.184-5552G>A\|	S34
31075	BAA01g21670	A01	10760393	C	T	intron_variant	MODIFIER	c.184-3400C>T\|	S230

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