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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
74151	BAA01g38950	A01	25948383	C	T	missense_variant	MODERATE	c.670C>T\|p.Pro224Ser	S219 S72
74152	BAA01g38940	A01	25948955	C	T	upstream_gene_variant	MODIFIER	c.-3967G>A\|	S239
74153	BAA01g38940	A01	25949239	C	T	upstream_gene_variant	MODIFIER	c.-4251G>A\|	S242
74154	BAA01g38940	A01	25949621	G	A	upstream_gene_variant	MODIFIER	c.-4633C>T\|	S229
74155	BAA01g38960	A01	25950532	C	T	upstream_gene_variant	MODIFIER	c.-336C>T\|	S184
74156	BAA01g38960	A01	25951089	C	T	synonymous_variant	LOW	c.222C>T\|p.Val74Val	S213
74157	BAA01g38960	A01	25951406	C	T	missense_variant	MODERATE	c.539C>T\|p.Thr180Ile	S48
74158	BAA01g38980	A01	25953361	T	A	upstream_gene_variant	MODIFIER	c.-1732T>A\|	S10 S11 S248 S42 S71 S77
74159	BAA01g38970	A01	25954171	G	A	missense_variant	MODERATE	c.80C>T\|p.Ser27Phe	S181
74160	BAA01g38970	A01	25954658	C	T	upstream_gene_variant	MODIFIER	c.-408G>A\|	S23
74161	BAA01g38970	A01	25954715	C	T	upstream_gene_variant	MODIFIER	c.-465G>A\|	S28
74162	BAA01g38980	A01	25955345	G	A	missense_variant	MODERATE	c.179G>A\|p.Arg60Lys	S5
74163	BAA01g38980	A01	25955430	C	T	synonymous_variant	LOW	c.264C>T\|p.Asn88Asn	S32
74164	BAA01g38980	A01	25955527	C	T	stop_gained	HIGH	c.361C>T\|p.Gln121*	S219 S72
74165	BAA01g38970	A01	25955764	C	T	upstream_gene_variant	MODIFIER	c.-1514G>A\|	S167
74166	BAA01g38980	A01	25955856	G	A	stop_gained	HIGH	c.600G>A\|p.Trp200*	S265 S95
74167	BAA01g38990	A01	25956758	C	T	missense_variant	MODERATE	c.56C>T\|p.Ser19Phe	S146
74168	BAA01g38990	A01	25957091	C	T	missense_variant	MODERATE	c.389C>T\|p.Ser130Phe	S134
74169	BAA01g38990	A01	25957101	G	A	synonymous_variant	LOW	c.399G>A\|p.Gly133Gly	S125
74170	BAA01g38970	A01	25957835	C	T	upstream_gene_variant	MODIFIER	c.-3585G>A\|	S279
74171	BAA01g38970	A01	25958167	C	T	upstream_gene_variant	MODIFIER	c.-3917G>A\|	S182
74172	BAA01g38970	A01	25958340	C	T	upstream_gene_variant	MODIFIER	c.-4090G>A\|	S192
74173	BAA01g38970	A01	25958467	G	A	upstream_gene_variant	MODIFIER	c.-4217C>T\|	S238
74174	BAA01g39000	A01	25959344	C	T	synonymous_variant	LOW	c.951G>A\|p.Val317Val	S198
74175	BAA01g39000	A01	25959438	G	A	missense_variant	MODERATE	c.857C>T\|p.Ser286Phe	S259

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