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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA07g06730	A07	16066178	C	T	missense_variant	MODERATE	c.2720G>A\|p.Gly907Asp	S16
2	BAA07g06730	A07	16066867	G	A	missense_variant	MODERATE	c.2426C>T\|p.Ser809Phe	S115
3	BAA07g06730	A07	16066956	C	T	splice_region_variant&intron_variant	LOW	c.2341-4G>A\|	S205
4	BAA07g06730	A07	16067537	G	A	missense_variant	MODERATE	c.2078C>T\|p.Ser693Leu	S271
5	BAA07g06730	A07	16067654	C	T	missense_variant	MODERATE	c.2047G>A\|p.Val683Ile	S100
6	BAA07g06730	A07	16068741	G	A	missense_variant	MODERATE	c.1219C>T\|p.Pro407Ser	S71
7	BAA07g06730	A07	16068959	G	A	missense_variant	MODERATE	c.1001C>T\|p.Pro334Leu	S58
8	BAA07g06730	A07	16069210	C	T	synonymous_variant	LOW	c.750G>A\|p.Leu250Leu	S36
9	BAA07g06730	A07	16069220	G	A	missense_variant	MODERATE	c.740C>T\|p.Ala247Val	S89
10	BAA07g06730	A07	16069606	G	A	synonymous_variant	LOW	c.354C>T\|p.Phe118Phe	S80
11	BAA07g06730	A07	16070039	A	T	start_lost	HIGH	c.2T>A\|p.Met1?	S103 S106 S107 S136 S143 S144 S165 S182 S2 S201 S218 S281 S284 S38 S51 S76 S89
12	BAA07g06730	A07	16071156	C	T	upstream_gene_variant	MODIFIER	c.-1116G>A\|	S34
13	BAA07g06730	A07	16072260	C	T	upstream_gene_variant	MODIFIER	c.-2220G>A\|	S96
14	BAA07g06730	A07	16072388	C	T	upstream_gene_variant	MODIFIER	c.-2348G>A\|	S69
15	BAA07g06730	A07	16073798	C	T	upstream_gene_variant	MODIFIER	c.-3758G>A\|	S16
16	BAA07g06730	A07	16074752	C	T	upstream_gene_variant	MODIFIER	c.-4712G>A\|	S11