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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
56651	BAA01g30750	A01	19695340	G	A	missense_variant	MODERATE	c.1483C>T\|p.Pro495Ser	S129
56652	BAA01g30750	A01	19695447	C	T	missense_variant	MODERATE	c.1376G>A\|p.Gly459Glu	S111
56653	BAA01g30750	A01	19696199	C	T	synonymous_variant	LOW	c.624G>A\|p.Glu208Glu	S167
56654	BAA01g30750	A01	19696290	G	A	intron_variant	MODIFIER	c.575-42C>T\|	S197
56655	BAA01g30750	A01	19696686	G	A	intron_variant	MODIFIER	c.354+41C>T\|	S32
56656	BAA01g30750	A01	19700188	C	T	upstream_gene_variant	MODIFIER	c.-2783G>A\|	S240
56657	BAA01g30760	A01	19702601	G	A	downstream_gene_variant	MODIFIER	c.*939C>T\|	S36
56658	BAA01g30760	A01	19703477	C	T	downstream_gene_variant	MODIFIER	c.*63G>A\|	S213
56659	BAA01g30760	A01	19704788	G	A	missense_variant	MODERATE	c.1295C>T\|p.Ser432Phe	S72 S78
56660	BAA01g30760	A01	19706969	G	A	upstream_gene_variant	MODIFIER	c.-29C>T\|	S138
56661	BAA01g30760	A01	19707577	C	T	upstream_gene_variant	MODIFIER	c.-637G>A\|	S303
56662	BAA01g30760	A01	19708332	G	T	upstream_gene_variant	MODIFIER	c.-1392C>A\|	S48
56663	BAA01g30760	A01	19708545	C	T	upstream_gene_variant	MODIFIER	c.-1605G>A\|	S211 S227
56664	BAA01g30760	A01	19708687	G	A	upstream_gene_variant	MODIFIER	c.-1747C>T\|	S209
56665	BAA01g30760	A01	19711555	C	T	upstream_gene_variant	MODIFIER	c.-4615G>A\|	S73 S91
56666	BAA01g30770	A01	19712787	C	T	downstream_gene_variant	MODIFIER	c.*723G>A\|	S136
56667	BAA01g30770	A01	19712809	C	T	downstream_gene_variant	MODIFIER	c.*701G>A\|	S240
56668	BAA01g30770	A01	19712924	C	T	downstream_gene_variant	MODIFIER	c.*586G>A\|	S57
56669	BAA01g30770	A01	19713041	C	T	downstream_gene_variant	MODIFIER	c.*469G>A\|	S206 S26
56670	BAA01g30770	A01	19713865	C	T	intron_variant	MODIFIER	c.577-155G>A\|	S284
56671	BAA01g30770	A01	19713966	G	A	intron_variant	MODIFIER	c.577-256C>T\|	S149
56672	BAA01g30770	A01	19714491	G	A	intron_variant	MODIFIER	c.576+66C>T\|	S116
56673	BAA01g30770	A01	19715011	C	T	synonymous_variant	LOW	c.447G>A\|p.Lys149Lys	S303
56674	BAA01g30770	A01	19715041	C	T	synonymous_variant	LOW	c.417G>A\|p.Arg139Arg	S81 S85
56675	BAA01g30770	A01	19715088	C	T	missense_variant	MODERATE	c.370G>A\|p.Glu124Lys	S39

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