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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
22401	BAA01g16280	A01	7897252	G	A	missense_variant&splice_region_variant	MODERATE	c.673G>A\|p.Glu225Lys	S188
22402	BAA01g16270	A01	7897330	G	A	upstream_gene_variant	MODIFIER	c.-4009C>T\|	S72 S78
22403	BAA01g16270	A01	7897543	C	T	upstream_gene_variant	MODIFIER	c.-4222G>A\|	S25
22404	BAA01g16280	A01	7897642	C	T	missense_variant	MODERATE	c.877C>T\|p.Pro293Ser	S53
22405	BAA01g16310	A01	7899606	G	A	upstream_gene_variant	MODIFIER	c.-4445G>A\|	S237
22406	BAA01g16310	A01	7899964	C	T	upstream_gene_variant	MODIFIER	c.-4087C>T\|	S171
22407	BAA01g16300	A01	7902146	C	T	synonymous_variant	LOW	c.513G>A\|p.Lys171Lys	S100
22408	BAA01g16300	A01	7902470	C	T	synonymous_variant	LOW	c.189G>A\|p.Lys63Lys	S47
22409	BAA01g16300	A01	7902708	C	A	upstream_gene_variant	MODIFIER	c.-50G>T\|	S136 S186 S275 S301 S304
22410	BAA01g16300	A01	7902723	G	A	upstream_gene_variant	MODIFIER	c.-65C>T\|	S34
22411	BAA01g16300	A01	7903353	C	T	upstream_gene_variant	MODIFIER	c.-695G>A\|	S7
22412	BAA01g16310	A01	7904757	C	T	missense_variant	MODERATE	c.431C>T\|p.Ser144Phe	S71
22413	BAA01g16320	A01	7905829	C	T	missense_variant	MODERATE	c.1285G>A\|p.Val429Ile	S260
22414	BAA01g16300	A01	7906387	G	A	upstream_gene_variant	MODIFIER	c.-3729C>T\|	S124
22415	BAA01g16320	A01	7906758	G	A	missense_variant	MODERATE	c.932C>T\|p.Pro311Leu	S287
22416	BAA01g16320	A01	7906772	C	T	synonymous_variant	LOW	c.918G>A\|p.Thr306Thr	S198
22417	BAA01g16320	A01	7906837	C	T	missense_variant	MODERATE	c.853G>A\|p.Asp285Asn	S100
22418	BAA01g16320	A01	7906904	C	T	synonymous_variant	LOW	c.786G>A\|p.Gln262Gln	S11
22419	BAA01g16320	A01	7908189	C	T	upstream_gene_variant	MODIFIER	c.-434G>A\|	S146
22420	BAA01g16320	A01	7908566	C	T	upstream_gene_variant	MODIFIER	c.-811G>A\|	S155
22421	BAA01g16330	A01	7912350	C	T	synonymous_variant	LOW	c.66C>T\|p.Ala22Ala	S65
22422	BAA01g16330	A01	7912814	G	A	missense_variant&splice_region_variant	MODERATE	c.298G>A\|p.Val100Ile	S32
22423	BAA01g16330	A01	7913173	G	A	missense_variant	MODERATE	c.509G>A\|p.Gly170Glu	S181 S217 S248
22424	BAA01g16330	A01	7913387	G	A	missense_variant	MODERATE	c.637G>A\|p.Asp213Asn	S209
22425	BAA01g16330	A01	7913519	C	T	intron_variant	MODIFIER	c.660+109C>T\|	S107

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