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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA05g14620	A05	7703131	C	T	missense_variant	MODERATE	c.1154G>A\|p.Arg385Lys	S198
2	BAA05g14620	A05	7703574	C	T	synonymous_variant	LOW	c.711G>A\|p.Lys237Lys	S249
3	BAA05g14620	A05	7703710	G	A	missense_variant	MODERATE	c.575C>T\|p.Ser192Phe	S4
4	BAA05g14620	A05	7703881	G	A	missense_variant	MODERATE	c.404C>T\|p.Ala135Val	S279
5	BAA05g14620	A05	7703970	G	A	synonymous_variant	LOW	c.315C>T\|p.Leu105Leu	S187
6	BAA05g14620	A05	7704708	C	T	upstream_gene_variant	MODIFIER	c.-424G>A\|	S255
7	BAA05g14620	A05	7704980	G	A	upstream_gene_variant	MODIFIER	c.-696C>T\|	S30
8	BAA05g14620	A05	7705455	C	T	upstream_gene_variant	MODIFIER	c.-1171G>A\|	S255
9	BAA05g14620	A05	7706448	G	A	upstream_gene_variant	MODIFIER	c.-2164C>T\|	S158
10	BAA05g14620	A05	7706624	G	T	upstream_gene_variant	MODIFIER	c.-2340C>A\|	S137 S215
11	BAA05g14620	A05	7707141	T	G	upstream_gene_variant	MODIFIER	c.-2857A>C\|	S128 S155 S166 S175 S198 S20 S230 S306 S8 S82
12	BAA05g14620	A05	7708316	C	T	upstream_gene_variant	MODIFIER	c.-4032G>A\|	S301 S304
13	BAA05g14620	A05	7708534	G	A	upstream_gene_variant	MODIFIER	c.-4250C>T\|	S11