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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
87051	BAA01g46320	A01	30894964	G	A	intron_variant	MODIFIER	c.971-554C>T\|	S262
87052	BAA01g46320	A01	30895170	C	T	intron_variant	MODIFIER	c.971-760G>A\|	S266
87053	BAA01g46320	A01	30896278	C	T	intron_variant	MODIFIER	c.970+878G>A\|	S276
87054	BAA01g46320	A01	30897290	C	T	stop_gained	HIGH	c.927G>A\|p.Trp309*	S104 S52
87055	BAA01g46320	A01	30900024	C	T	upstream_gene_variant	MODIFIER	c.-1114G>A\|	S54
87056	BAA01g46320	A01	30900174	C	T	upstream_gene_variant	MODIFIER	c.-1264G>A\|	S210 S225
87057	BAA01g46320	A01	30901370	C	T	upstream_gene_variant	MODIFIER	c.-2460G>A\|	S4
87058	BAA01g46320	A01	30901682	G	A	upstream_gene_variant	MODIFIER	c.-2772C>T\|	S53
87059	BAA01g46320	A01	30901688	G	A	upstream_gene_variant	MODIFIER	c.-2778C>T\|	S302
87060	BAA01g46320	A01	30903106	G	A	upstream_gene_variant	MODIFIER	c.-4196C>T\|	S257
87061	BAA01g46320	A01	30903250	G	A	upstream_gene_variant	MODIFIER	c.-4340C>T\|	S169
87062	BAA01g46330	A01	30904303	C	T	missense_variant	MODERATE	c.1642G>A\|p.Asp548Asn	S18
87063	BAA01g46330	A01	30904505	C	T	synonymous_variant	LOW	c.1440G>A\|p.Lys480Lys	S15 S156 S3 S34 S4 S6
87064	BAA01g46330	A01	30905854	C	T	missense_variant	MODERATE	c.187G>A\|p.Ala63Thr	S267
87065	BAA01g46340	A01	30906209	C	T	upstream_gene_variant	MODIFIER	c.-2273C>T\|	S256
87066	BAA01g46340	A01	30906445	G	A	upstream_gene_variant	MODIFIER	c.-2037G>A\|	S295
87067	BAA01g46330	A01	30907234	C	T	upstream_gene_variant	MODIFIER	c.-658G>A\|	S168
87068	BAA01g46330	A01	30907319	G	A	upstream_gene_variant	MODIFIER	c.-743C>T\|	S298
87069	BAA01g46330	A01	30910293	C	T	upstream_gene_variant	MODIFIER	c.-3717G>A\|	S1 S90
87070	BAA01g46330	A01	30910667	C	T	upstream_gene_variant	MODIFIER	c.-4091G>A\|	S148 S210 S30 S31
87071	BAA01g46330	A01	30911136	C	T	upstream_gene_variant	MODIFIER	c.-4560G>A\|	S103
87072	BAA01g46340	A01	30911653	G	A	downstream_gene_variant	MODIFIER	c.*669G>A\|	S172 S217
87073	BAA01g46340	A01	30912156	G	A	downstream_gene_variant	MODIFIER	c.*1172G>A\|	S104
87074	BAA01g46350	A01	30912615	C	T	missense_variant	MODERATE	c.115G>A\|p.Gly39Ser	S63
87075	BAA01g46350	A01	30914752	C	T	upstream_gene_variant	MODIFIER	c.-2023G>A\|	S247

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