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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g01190	A01	493804	C	T	stop_gained	HIGH	c.1178G>A\|p.Trp393*	S157 S163
2	BAA01g01190	A01	494108	C	T	missense_variant	MODERATE	c.874G>A\|p.Ala292Thr	S155 S211
3	BAA01g01190	A01	494129	G	A	missense_variant	MODERATE	c.853C>T\|p.Pro285Ser	S136
4	BAA01g01190	A01	494523	C	T	synonymous_variant	LOW	c.459G>A\|p.Leu153Leu	S25
5	BAA01g01190	A01	494606	G	A	missense_variant	MODERATE	c.376C>T\|p.Pro126Ser	S95
6	BAA01g01190	A01	494631	G	A	synonymous_variant	LOW	c.351C>T\|p.Ile117Ile	S70
7	BAA01g01190	A01	497868	C	T	upstream_gene_variant	MODIFIER	c.-2887G>A\|	S164
8	BAA01g01190	A01	497927	G	A	upstream_gene_variant	MODIFIER	c.-2946C>T\|	S113 S115 S117 S120 S9
9	BAA01g01190	A01	498781	G	A	upstream_gene_variant	MODIFIER	c.-3800C>T\|	S161