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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g47460	A02	38257295	G	A	missense_variant	MODERATE	c.640C>T\|p.Pro214Ser	S103
2	BAA02g47460	A02	38258031	C	T	synonymous_variant	LOW	c.378G>A\|p.Lys126Lys	S208 S93
3	BAA02g47460	A02	38258237	C	T	missense_variant	MODERATE	c.172G>A\|p.Glu58Lys	S33
4	BAA02g47460	A02	38258420	G	A	intron_variant	MODIFIER	c.68-79C>T\|	S99
5	BAA02g47460	A02	38258680	G	A	intron_variant	MODIFIER	c.67+43C>T\|	S174 S216
6	BAA02g47460	A02	38258704	C	T	intron_variant	MODIFIER	c.67+19G>A\|	S115 S117 S121 S122 S23 S297 S55
7	BAA02g47460	A02	38258833	G	A	upstream_gene_variant	MODIFIER	c.-44C>T\|	S148 S210 S31
8	BAA02g47460	A02	38261853	C	T	upstream_gene_variant	MODIFIER	c.-3064G>A\|	S136
9	BAA02g47460	A02	38261914	G	A	upstream_gene_variant	MODIFIER	c.-3125C>T\|	S226
10	BAA02g47460	A02	38262467	C	T	upstream_gene_variant	MODIFIER	c.-3678G>A\|	S205
11	BAA02g47460	A02	38262894	G	A	upstream_gene_variant	MODIFIER	c.-4105C>T\|	S225 S73
12	BAA02g47460	A02	38263022	G	A	upstream_gene_variant	MODIFIER	c.-4233C>T\|	S132 S137 S213 S215 S89
13	BAA02g47460	A02	38263307	C	T	upstream_gene_variant	MODIFIER	c.-4518G>A\|	S179
14	BAA02g47460	A02	38263428	C	T	upstream_gene_variant	MODIFIER	c.-4639G>A\|	S205
15	BAA02g47460	A02	38263440	C	T	upstream_gene_variant	MODIFIER	c.-4651G>A\|	S170
16	BAA02g47460	A02	38263446	C	T	upstream_gene_variant	MODIFIER	c.-4657G>A\|	S23
17	BAA02g47460	A02	38263610	G	A	upstream_gene_variant	MODIFIER	c.-4821C>T\|	S223