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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g11090	A01	5105258	C	T	missense_variant	MODERATE	c.6704G>A\|p.Arg2235Lys	S4
2	BAA01g11090	A01	5105888	C	T	missense_variant	MODERATE	c.6074G>A\|p.Gly2025Glu	S13 S168 S278 S279 S64
3	BAA01g11090	A01	5106795	G	A	missense_variant	MODERATE	c.5167C>T\|p.Pro1723Ser	S157 S163
4	BAA01g11090	A01	5109139	G	A	synonymous_variant	LOW	c.2823C>T\|p.Ala941Ala	S183 S198
5	BAA01g11090	A01	5110328	G	A	missense_variant	MODERATE	c.1634C>T\|p.Pro545Leu	S256
6	BAA01g11090	A01	5110769	C	T	missense_variant	MODERATE	c.1193G>A\|p.Arg398Lys	S107
7	BAA01g11090	A01	5110980	G	A	stop_gained	HIGH	c.982C>T\|p.Gln328*	S159 S188 S243 S276 S298 S299
8	BAA01g11090	A01	5111096	C	T	missense_variant	MODERATE	c.866G>A\|p.Gly289Asp	S150
9	BAA01g11090	A01	5111704	G	A	synonymous_variant	LOW	c.525C>T\|p.Asn175Asn	S236
10	BAA01g11090	A01	5113259	C	T	upstream_gene_variant	MODIFIER	c.-443G>A\|	S136
11	BAA01g11090	A01	5116604	C	T	upstream_gene_variant	MODIFIER	c.-3788G>A\|	S70
12	BAA01g11090	A01	5116714	C	T	upstream_gene_variant	MODIFIER	c.-3898G>A\|	S80