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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g10890	A09	6028770	C	T	downstream_gene_variant	MODIFIER	c.*3608G>A\|	S200
2	BAA09g10890	A09	6031916	G	A	downstream_gene_variant	MODIFIER	c.*462C>T\|	S130
3	BAA09g10890	A09	6032166	C	T	downstream_gene_variant	MODIFIER	c.*212G>A\|	S15 S156 S2 S3
4	BAA09g10890	A09	6032451	C	T	missense_variant	MODERATE	c.1811G>A\|p.Gly604Glu	S302
5	BAA09g10890	A09	6032461	C	T	missense_variant	MODERATE	c.1801G>A\|p.Glu601Lys	S68
6	BAA09g10890	A09	6032704	C	T	missense_variant	MODERATE	c.1558G>A\|p.Val520Ile	S204
7	BAA09g10890	A09	6033023	C	T	intron_variant	MODIFIER	c.1306-67G>A\|	S202
8	BAA09g10890	A09	6034377	G	A	missense_variant	MODERATE	c.430C>T\|p.Leu144Phe	S159 S187 S243 S298 S299
9	BAA09g10890	A09	6034577	C	T	missense_variant	MODERATE	c.230G>A\|p.Gly77Glu	S302
10	BAA09g10890	A09	6035149	C	T	upstream_gene_variant	MODIFIER	c.-80G>A\|	S250
11	BAA09g10890	A09	6035844	G	A	upstream_gene_variant	MODIFIER	c.-775C>T\|	S44
12	BAA09g10890	A09	6038819	C	T	upstream_gene_variant	MODIFIER	c.-3750G>A\|	S133
13	BAA09g10890	A09	6039051	C	T	upstream_gene_variant	MODIFIER	c.-3982G>A\|	S53