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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g21420	A01	10622272	G	A	upstream_gene_variant	MODIFIER	c.-4587G>A\|	S14
2	BAA01g21420	A01	10622295	C	T	upstream_gene_variant	MODIFIER	c.-4564C>T\|	S135
3	BAA01g21420	A01	10623684	C	T	upstream_gene_variant	MODIFIER	c.-3175C>T\|	S36
4	BAA01g21420	A01	10624504	C	T	upstream_gene_variant	MODIFIER	c.-2355C>T\|	S289 S290
5	BAA01g21420	A01	10627095	G	A	synonymous_variant	LOW	c.237G>A\|p.Ala79Ala	S160 S249
6	BAA01g21420	A01	10627531	C	T	missense_variant	MODERATE	c.673C>T\|p.Leu225Phe	S82 S92
7	BAA01g21420	A01	10627685	G	A	missense_variant	MODERATE	c.827G>A\|p.Gly276Glu	S132 S137 S138 S215 S288 S89
8	BAA01g21420	A01	10628062	G	A	missense_variant	MODERATE	c.1033G>A\|p.Gly345Arg	S57
9	BAA01g21420	A01	10628201	G	A	missense_variant	MODERATE	c.1172G>A\|p.Gly391Asp	S211 S227
10	BAA01g21420	A01	10629434	C	T	missense_variant	MODERATE	c.1519C>T\|p.Pro507Ser	S150
11	BAA01g21420	A01	10629530	C	T	missense_variant	MODERATE	c.1615C>T\|p.Pro539Ser	S36
12	BAA01g21420	A01	10629731	G	A	missense_variant	MODERATE	c.1816G>A\|p.Val606Ile	S6
13	BAA01g21420	A01	10631405	C	T	downstream_gene_variant	MODIFIER	c.*1167C>T\|	S35
14	BAA01g21420	A01	10632563	G	A	downstream_gene_variant	MODIFIER	c.*2325G>A\|	S163
15	BAA01g21420	A01	10633435	G	A	downstream_gene_variant	MODIFIER	c.*3197G>A\|	S281
16	BAA01g21420	A01	10634054	G	A	downstream_gene_variant	MODIFIER	c.*3816G>A\|	S144