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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA08g05170	A08	3864311	C	T	missense_variant	MODERATE	c.14C>T\|p.Ser5Phe	S292
2	BAA08g05170	A08	3865047	C	T	missense_variant	MODERATE	c.557C>T\|p.Ser186Phe	S126
3	BAA08g05170	A08	3865164	G	A	missense_variant	MODERATE	c.674G>A\|p.Gly225Asp	S128
4	BAA08g05170	A08	3868235	A	T	intron_variant	MODIFIER	c.1030-28A>T\|	S139 S15 S155 S189 S218 S275 S280 S4 S55 S67 S68 S72 S78 S89
5	BAA08g05170	A08	3869401	C	T	downstream_gene_variant	MODIFIER	c.*324C>T\|	S207
6	BAA08g05170	A08	3871102	G	A	downstream_gene_variant	MODIFIER	c.*2025G>A\|	S192
7	BAA08g05170	A08	3871237	G	A	downstream_gene_variant	MODIFIER	c.*2160G>A\|	S5
8	BAA08g05170	A08	3871653	G	A	downstream_gene_variant	MODIFIER	c.*2576G>A\|	S288
9	BAA08g05170	A08	3872267	G	A	downstream_gene_variant	MODIFIER	c.*3190G>A\|	S87
10	BAA08g05170	A08	3872311	C	T	downstream_gene_variant	MODIFIER	c.*3234C>T\|	S140
11	BAA08g05170	A08	3873638	C	T	downstream_gene_variant	MODIFIER	c.*4561C>T\|	S261
12	BAA08g05170	A08	3873780	C	T	downstream_gene_variant	MODIFIER	c.*4703C>T\|	S270