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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
85201	BAA01g45150	A01	30087238	G	A	upstream_gene_variant	MODIFIER	c.-1914C>T\|	S163
85202	BAA01g45160	A01	30088481	G	A	missense_variant	MODERATE	c.947C>T\|p.Ala316Val	S84
85203	BAA01g45160	A01	30088912	C	T	missense_variant	MODERATE	c.704G>A\|p.Arg235Lys	S167
85204	BAA01g45160	A01	30089127	G	A	missense_variant	MODERATE	c.554C>T\|p.Pro185Leu	S122
85205	BAA01g45150	A01	30089926	C	T	upstream_gene_variant	MODIFIER	c.-4602G>A\|	S78
85206	BAA01g45160	A01	30091088	C	T	upstream_gene_variant	MODIFIER	c.-853G>A\|	S162
85207	BAA01g45170	A01	30094063	C	T	missense_variant	MODERATE	c.175C>T\|p.Pro59Ser	S264
85208	BAA01g45170	A01	30095369	G	A	missense_variant	MODERATE	c.682G>A\|p.Gly228Arg	S60
85209	BAA01g45170	A01	30095563	C	T	synonymous_variant	LOW	c.876C>T\|p.Leu292Leu	S60
85210	BAA01g45180	A01	30096313	C	T	missense_variant	MODERATE	c.358G>A\|p.Asp120Asn	S134
85211	BAA01g45180	A01	30097637	C	T	upstream_gene_variant	MODIFIER	c.-967G>A\|	S9
85212	BAA01g45180	A01	30100697	G	A	upstream_gene_variant	MODIFIER	c.-4027C>T\|	S218 S268
85213	BAA01g45190	A01	30101866	C	T	upstream_gene_variant	MODIFIER	c.-760G>A\|	S90
85214	BAA01g45200	A01	30102534	C	T	missense_variant	MODERATE	c.82G>A\|p.Val28Ile	S192
85215	BAA01g45190	A01	30102826	G	A	upstream_gene_variant	MODIFIER	c.-1720C>T\|	S86
85216	BAA01g45190	A01	30103371	C	T	upstream_gene_variant	MODIFIER	c.-2265G>A\|	S130
85217	BAA01g45190	A01	30103449	C	T	upstream_gene_variant	MODIFIER	c.-2343G>A\|	S279
85218	BAA01g45210	A01	30103966	C	T	missense_variant	MODERATE	c.1697G>A\|p.Arg566Lys	S273
85219	BAA01g45190	A01	30104615	C	T	upstream_gene_variant	MODIFIER	c.-3509G>A\|	S210 S225
85220	BAA01g45190	A01	30104657	G	A	upstream_gene_variant	MODIFIER	c.-3551C>T\|	S43
85221	BAA01g45210	A01	30105828	G	A	missense_variant	MODERATE	c.532C>T\|p.Pro178Ser	S10
85222	BAA01g45210-BAA01g45220	A01	30119448	G	A	intergenic_region	MODIFIER	n.30119448G>A\|	S146 S20 S235 S303 S43
85223	BAA01g45210-BAA01g45220	A01	30119477	T	A	intergenic_region	MODIFIER	n.30119477T>A\|	S146 S235 S259 S303
85224	BAA01g45210-BAA01g45220	A01	30119519	A	G	intergenic_region	MODIFIER	n.30119519A>G\|	S1 S128 S13 S186 S252 S283 S33 S41 S48 S61 S65 S69 S8 S85 S87 S88
85225	BAA01g45210-BAA01g45220	A01	30119559	A	T	intergenic_region	MODIFIER	n.30119559A>T\|	S160 S3 S305

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