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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g11080	A09	6152615	C	T	missense_variant	MODERATE	c.290C>T\|p.Ser97Phe	S270
2	BAA09g11080	A09	6153578	G	A	missense_variant	MODERATE	c.1253G>A\|p.Arg418His	S210 S225
3	BAA09g11080	A09	6154585	C	T	missense_variant	MODERATE	c.1601C>T\|p.Ser534Leu	S237 S238 S288
4	BAA09g11080	A09	6154852	C	T	missense_variant	MODERATE	c.1868C>T\|p.Pro623Leu	S62
5	BAA09g11080	A09	6155483	C	T	downstream_gene_variant	MODIFIER	c.*351C>T\|	S208 S219
6	BAA09g11080	A09	6155762	G	A	downstream_gene_variant	MODIFIER	c.*630G>A\|	S200
7	BAA09g11080	A09	6156290	G	A	downstream_gene_variant	MODIFIER	c.*1158G>A\|	S192
8	BAA09g11080	A09	6156526	C	T	downstream_gene_variant	MODIFIER	c.*1394C>T\|	S132 S137 S215 S89
9	BAA09g11080	A09	6156578	C	T	downstream_gene_variant	MODIFIER	c.*1446C>T\|	S306
10	BAA09g11080	A09	6156776	C	T	downstream_gene_variant	MODIFIER	c.*1644C>T\|	S287
11	BAA09g11080	A09	6156822	G	A	downstream_gene_variant	MODIFIER	c.*1690G>A\|	S267
12	BAA09g11080	A09	6157151	C	T	downstream_gene_variant	MODIFIER	c.*2019C>T\|	S208 S219
13	BAA09g11080	A09	6157244	G	A	downstream_gene_variant	MODIFIER	c.*2112G>A\|	S89
14	BAA09g11080	A09	6157813	G	A	downstream_gene_variant	MODIFIER	c.*2681G>A\|	S144
15	BAA09g11080	A09	6158521	C	T	downstream_gene_variant	MODIFIER	c.*3389C>T\|	S179
16	BAA09g11080	A09	6158994	C	T	downstream_gene_variant	MODIFIER	c.*3862C>T\|	S179