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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g38600	A02	32880251	C	T	missense_variant	MODERATE	c.1252G>A\|p.Glu418Lys	S87
2	BAA02g38600	A02	32882027	C	T	missense_variant	MODERATE	c.848G>A\|p.Gly283Glu	S216
3	BAA02g38600	A02	32882085	C	T	missense_variant	MODERATE	c.790G>A\|p.Glu264Lys	S38
4	BAA02g38600	A02	32882749	C	T	synonymous_variant	LOW	c.126G>A\|p.Pro42Pro	S283
5	BAA02g38600	A02	32882941	G	T	upstream_gene_variant	MODIFIER	c.-67C>A\|	S140 S159 S163 S169 S173 S18 S186 S209 S213 S224 S26 S279 S291 S308 S61 S67 S68 S72
6	BAA02g38600	A02	32883327	G	A	upstream_gene_variant	MODIFIER	c.-453C>T\|	S113
7	BAA02g38600	A02	32884284	C	T	upstream_gene_variant	MODIFIER	c.-1410G>A\|	S233
8	BAA02g38600	A02	32885977	G	A	upstream_gene_variant	MODIFIER	c.-3103C>T\|	S232
9	BAA02g38600	A02	32885978	G	A	upstream_gene_variant	MODIFIER	c.-3104C>T\|	S133
10	BAA02g38600	A02	32887053	G	A	upstream_gene_variant	MODIFIER	c.-4179C>T\|	S113
11	BAA02g38600	A02	32887418	G	A	upstream_gene_variant	MODIFIER	c.-4544C>T\|	S199