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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA05g15960	A05	8714414	C	T	downstream_gene_variant	MODIFIER	c.*1635G>A\|	S206 S26
2	BAA05g15960	A05	8716788	G	A	synonymous_variant	LOW	c.1182C>T\|p.Leu394Leu	S173
3	BAA05g15960	A05	8719553	C	T	synonymous_variant	LOW	c.693G>A\|p.Arg231Arg	S18
4	BAA05g15960	A05	8719570	G	A	missense_variant	MODERATE	c.676C>T\|p.Pro226Ser	S109
5	BAA05g15960	A05	8719586	G	A	synonymous_variant	LOW	c.660C>T\|p.Phe220Phe	S32
6	BAA05g15960	A05	8720062	G	A	missense_variant	MODERATE	c.184C>T\|p.His62Tyr	S32
7	BAA05g15960	A05	8720271	T	G	upstream_gene_variant	MODIFIER	c.-26A>C\|	S100 S133 S175 S190 S20 S204 S272
8	BAA05g15960	A05	8720272	T	G	upstream_gene_variant	MODIFIER	c.-27A>C\|	S100 S133 S136 S175 S190 S20 S204 S272
9	BAA05g15960	A05	8720274	T	G	upstream_gene_variant	MODIFIER	c.-29A>C\|	S190 S20 S204 S272
10	BAA05g15960	A05	8720839	C	T	upstream_gene_variant	MODIFIER	c.-594G>A\|	S8
11	BAA05g15960	A05	8721606	C	T	upstream_gene_variant	MODIFIER	c.-1361G>A\|	S17
12	BAA05g15960	A05	8721928	G	A	upstream_gene_variant	MODIFIER	c.-1683C>T\|	S151 S263
13	BAA05g15960	A05	8722054	C	T	upstream_gene_variant	MODIFIER	c.-1809G>A\|	S295
14	BAA05g15960	A05	8722843	C	T	upstream_gene_variant	MODIFIER	c.-2598G>A\|	S181
15	BAA05g15960	A05	8723683	C	T	upstream_gene_variant	MODIFIER	c.-3438G>A\|	S143