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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
87951	BAA01g46870-BAA01g46880	A01	31227793	G	A	intergenic_region	MODIFIER	n.31227793G>A\|	S299
87952	BAA01g46870-BAA01g46880	A01	31229274	G	A	intergenic_region	MODIFIER	n.31229274G>A\|	S124
87953	BAA01g46880	A01	31230620	C	T	downstream_gene_variant	MODIFIER	c.*4550G>A\|	S97
87954	BAA01g46880	A01	31230941	C	A	downstream_gene_variant	MODIFIER	c.*4229G>T\|	S108 S109 S120 S135 S174 S20 S208 S221 S260 S27 S41 S45 S74 S76 S83 S99
87955	BAA01g46880	A01	31230948	C	A	downstream_gene_variant	MODIFIER	c.*4222G>T\|	S108 S109 S120 S135 S174 S20 S221 S260 S27 S41 S45 S74 S76 S99
87956	BAA01g46880	A01	31230949	T	C	downstream_gene_variant	MODIFIER	c.*4221A>G\|	S108 S109 S120 S135 S174 S20 S221 S260 S27 S41 S45 S74 S76 S99
87957	BAA01g46880	A01	31230972	C	A	downstream_gene_variant	MODIFIER	c.*4198G>T\|	S108 S120 S174 S208 S221 S260 S27 S41 S45 S74 S76 S99
87958	BAA01g46880	A01	31230974	A	T	downstream_gene_variant	MODIFIER	c.*4196T>A\|	S1 S121 S151 S158 S223 S232 S236 S249 S288 S289 S33 S34 S90
87959	BAA01g46880	A01	31230981	T	A	downstream_gene_variant	MODIFIER	c.*4189A>T\|	S110 S151 S170 S178 S195 S196 S23 S263 S268 S274 S31 S32 S33 S53
87960	BAA01g46880	A01	31231814	C	T	downstream_gene_variant	MODIFIER	c.*3356G>A\|	S271
87961	BAA01g46880	A01	31232696	C	T	downstream_gene_variant	MODIFIER	c.*2474G>A\|	S239
87962	BAA01g46880	A01	31232804	C	T	downstream_gene_variant	MODIFIER	c.*2366G>A\|	S178
87963	BAA01g46880	A01	31234108	G	A	downstream_gene_variant	MODIFIER	c.*1062C>T\|	S278
87964	BAA01g46880	A01	31234168	C	T	downstream_gene_variant	MODIFIER	c.*1002G>A\|	S270
87965	BAA01g46880	A01	31234311	C	T	downstream_gene_variant	MODIFIER	c.*859G>A\|	S69
87966	BAA01g46880	A01	31234494	G	A	downstream_gene_variant	MODIFIER	c.*676C>T\|	S298
87967	BAA01g46880	A01	31234613	C	T	downstream_gene_variant	MODIFIER	c.*557G>A\|	S133
87968	BAA01g46880	A01	31235610	C	T	missense_variant	MODERATE	c.4102G>A\|p.Asp1368Asn	S39
87969	BAA01g46880	A01	31235797	G	A	synonymous_variant	LOW	c.3915C>T\|p.Phe1305Phe	S196
87970	BAA01g46880	A01	31235825	C	T	missense_variant	MODERATE	c.3887G>A\|p.Gly1296Asp	S303
87971	BAA01g46880	A01	31236345	G	A	missense_variant	MODERATE	c.3367C>T\|p.Leu1123Phe	S108
87972	BAA01g46880	A01	31236435	C	T	missense_variant	MODERATE	c.3277G>A\|p.Val1093Ile	S12
87973	BAA01g46880	A01	31236561	G	A	missense_variant	MODERATE	c.3151C>T\|p.Leu1051Phe	S265
87974	BAA01g46880	A01	31237338	G	A	missense_variant	MODERATE	c.2374C>T\|p.Leu792Phe	S53
87975	BAA01g46880	A01	31237387	C	T	synonymous_variant	LOW	c.2325G>A\|p.Glu775Glu	S208 S93

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