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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g31890	A09	40416446	C	T	missense_variant	MODERATE	c.281C>T\|p.Ser94Phe	S250
2	BAA09g31890	A09	40416736	G	A	missense_variant	MODERATE	c.571G>A\|p.Val191Met	S197
3	BAA09g31890	A09	40416751	G	A	missense_variant	MODERATE	c.586G>A\|p.Glu196Lys	S40 S49
4	BAA09g31890	A09	40417145	C	T	missense_variant	MODERATE	c.980C>T\|p.Ala327Val	S235
5	BAA09g31890	A09	40417241	G	A	missense_variant	MODERATE	c.1076G>A\|p.Gly359Glu	S42
6	BAA09g31890	A09	40417404	G	A	synonymous_variant	LOW	c.1239G>A\|p.Ser413Ser	S79 S91
7	BAA09g31890	A09	40417729	G	A	missense_variant	MODERATE	c.1499G>A\|p.Ser500Asn	S34
8	BAA09g31890	A09	40418713	G	A	missense_variant	MODERATE	c.2078G>A\|p.Arg693Lys	S16
9	BAA09g31890	A09	40418847	G	A	missense_variant	MODERATE	c.2113G>A\|p.Gly705Arg	S107
10	BAA09g31890	A09	40418898	C	T	missense_variant	MODERATE	c.2164C>T\|p.His722Tyr	S255
11	BAA09g31890	A09	40420880	G	A	downstream_gene_variant	MODIFIER	c.*1809G>A\|	S172 S217
12	BAA09g31890	A09	40422552	C	T	downstream_gene_variant	MODIFIER	c.*3481C>T\|	S182
13	BAA09g31890	A09	40422874	G	A	downstream_gene_variant	MODIFIER	c.*3803G>A\|	S170
14	BAA09g31890	A09	40423133	T	G	downstream_gene_variant	MODIFIER	c.*4062T>G\|	S188
15	BAA09g31890	A09	40424062	G	A	downstream_gene_variant	MODIFIER	c.*4991G>A\|	S113 S115 S117 S120 S122 S266 S65 S8