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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
88301	BAA01g47100	A01	31357911	G	A	synonymous_variant	LOW	c.702C>T\|p.Ile234Ile	S60
88302	BAA01g47100	A01	31358540	C	T	missense_variant	MODERATE	c.346G>A\|p.Ala116Thr	S187
88303	BAA01g47090	A01	31359406	C	T	upstream_gene_variant	MODIFIER	c.-3915G>A\|	S257
88304	BAA01g47110	A01	31360566	G	A	missense_variant	MODERATE	c.874G>A\|p.Glu292Lys	S46
88305	BAA01g47100	A01	31361130	C	T	upstream_gene_variant	MODIFIER	c.-1968G>A\|	S124
88306	BAA01g47120	A01	31361769	C	T	missense_variant	MODERATE	c.40C>T\|p.Leu14Phe	S152
88307	BAA01g47120	A01	31362333	G	A	missense_variant	MODERATE	c.344G>A\|p.Arg115Lys	S126
88308	BAA01g47120	A01	31362478	C	T	synonymous_variant	LOW	c.489C>T\|p.Leu163Leu	S202
88309	BAA01g47120	A01	31362756	G	A	synonymous_variant	LOW	c.684G>A\|p.Lys228Lys	S259
88310	BAA01g47100	A01	31363372	G	A	upstream_gene_variant	MODIFIER	c.-4210C>T\|	S171
88311	BAA01g47130	A01	31363717	C	T	missense_variant	MODERATE	c.98G>A\|p.Ser33Asn	S18
88312	BAA01g47140	A01	31364553	C	T	missense_variant	MODERATE	c.1168G>A\|p.Val390Met	S144
88313	BAA01g47140	A01	31366032	C	T	missense_variant	MODERATE	c.455G>A\|p.Gly152Glu	S58
88314	BAA01g47130	A01	31366437	C	T	upstream_gene_variant	MODIFIER	c.-2522G>A\|	S301 S304
88315	BAA01g47130	A01	31366921	C	T	upstream_gene_variant	MODIFIER	c.-3006G>A\|	S157
88316	BAA01g47130	A01	31367405	G	A	upstream_gene_variant	MODIFIER	c.-3490C>T\|	S188
88317	BAA01g47130	A01	31367427	G	A	upstream_gene_variant	MODIFIER	c.-3512C>T\|	S183 S198
88318	BAA01g47150	A01	31367768	C	T	missense_variant	MODERATE	c.265C>T\|p.Arg89Cys	S183 S58
88319	BAA01g47150	A01	31368407	C	T	synonymous_variant	LOW	c.453C>T\|p.Leu151Leu	S204
88320	BAA01g47140	A01	31368935	C	T	upstream_gene_variant	MODIFIER	c.-2210G>A\|	S197
88321	BAA01g47140	A01	31368999	C	T	upstream_gene_variant	MODIFIER	c.-2274G>A\|	S287
88322	BAA01g47160	A01	31369765	C	T	missense_variant	MODERATE	c.755G>A\|p.Arg252Lys	S79 S91
88323	BAA01g47160	A01	31369898	G	A	splice_region_variant&intron_variant	LOW	c.625-3C>T\|	S39
88324	BAA01g47160	A01	31370266	G	A	synonymous_variant	LOW	c.429C>T\|p.Phe143Phe	S120
88325	BAA01g47140	A01	31370948	C	T	upstream_gene_variant	MODIFIER	c.-4223G>A\|	S107

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