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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA03g21860	A03	9918492	G	A	downstream_gene_variant	MODIFIER	c.*461C>T\|	S10
2	BAA03g21860	A03	9919271	G	A	synonymous_variant	LOW	c.3195C>T\|p.Val1065Val	S83 S88
3	BAA03g21860	A03	9919463	G	A	intron_variant	MODIFIER	c.3013-10C>T\|	S180
4	BAA03g21860	A03	9921040	C	T	intron_variant	MODIFIER	c.2212-368G>A\|	S43
5	BAA03g21860	A03	9921471	A	T	missense_variant	MODERATE	c.2190T>A\|p.Phe730Leu	S191
6	BAA03g21860	A03	9922827	G	A	intron_variant	MODIFIER	c.1441-18C>T\|	S130
7	BAA03g21860	A03	9924026	T	G	intron_variant	MODIFIER	c.909-235A>C\|	S124 S144 S193 S61
8	BAA03g21860	A03	9924028	T	G	intron_variant	MODIFIER	c.909-237A>C\|	S124 S126 S144 S159 S166 S193 S200 S28 S47 S61 S62 S63
9	BAA03g21860	A03	9925219	C	T	intron_variant	MODIFIER	c.337-115G>A\|	S259
10	BAA03g21860	A03	9926812	C	T	upstream_gene_variant	MODIFIER	c.-847G>A\|	S241
11	BAA03g21860	A03	9927258	G	A	upstream_gene_variant	MODIFIER	c.-1293C>T\|	S172 S259
12	BAA03g21860	A03	9928254	G	A	upstream_gene_variant	MODIFIER	c.-2289C>T\|	S175
13	BAA03g21860	A03	9928513	G	A	upstream_gene_variant	MODIFIER	c.-2548C>T\|	S162