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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA07g34990	A07	33276027	G	A	synonymous_variant	LOW	c.1686C>T\|p.Phe562Phe	S69
2	BAA07g34990	A07	33276801	C	T	synonymous_variant	LOW	c.912G>A\|p.Gln304Gln	S67
3	BAA07g34990	A07	33278687	G	A	intron_variant	MODIFIER	c.327+651C>T\|	S59
4	BAA07g34990	A07	33278818	C	T	intron_variant	MODIFIER	c.327+520G>A\|	S265
5	BAA07g34990	A07	33279333	G	A	splice_region_variant&intron_variant	LOW	c.327+5C>T\|	S133
6	BAA07g34990	A07	33279492	C	T	missense_variant	MODERATE	c.173G>A\|p.Arg58Lys	S174
7	BAA07g34990	A07	33280990	C	T	upstream_gene_variant	MODIFIER	c.-1057G>A\|	S159 S187 S188 S243 S298 S299
8	BAA07g34990	A07	33281511	C	T	upstream_gene_variant	MODIFIER	c.-1578G>A\|	S134
9	BAA07g34990	A07	33282644	G	A	upstream_gene_variant	MODIFIER	c.-2711C>T\|	S238
10	BAA07g34990	A07	33282699	C	T	upstream_gene_variant	MODIFIER	c.-2766G>A\|	S107
11	BAA07g34990	A07	33283720	C	T	upstream_gene_variant	MODIFIER	c.-3787G>A\|	S250