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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
151451	BAA02g00180	A02	125823	A	G	missense_variant	MODERATE	c.698T>C\|p.Met233Thr	S201 S213 S267
151452	BAA02g00180	A02	125831	A	C	synonymous_variant	LOW	c.690T>G\|p.Pro230Pro	S201 S213 S267
151453	BAA02g00180	A02	125839	A	C	missense_variant	MODERATE	c.682T>G\|p.Ser228Ala	S201 S213 S267
151454	BAA02g00180	A02	125849	A	T	synonymous_variant	LOW	c.672T>A\|p.Leu224Leu	S201 S213 S267
151455	BAA02g00180	A02	125858	G	A	synonymous_variant	LOW	c.663C>T\|p.Phe221Phe	S201 S213 S267
151456	BAA02g00180	A02	125864	T	C	synonymous_variant	LOW	c.657A>G\|p.Lys219Lys	S147 S201 S213 S267
151457	BAA02g00180	A02	125870	G	T	synonymous_variant	LOW	c.651C>A\|p.Gly217Gly	S147 S201 S213 S267
151458	BAA02g00180	A02	125873	A	G	synonymous_variant	LOW	c.648T>C\|p.Pro216Pro	S147 S201 S213 S267
151459	BAA02g00180	A02	125879	C	T	synonymous_variant	LOW	c.642G>A\|p.Leu214Leu	S147 S201 S213 S267
151460	BAA02g00180	A02	125891	A	C	synonymous_variant	LOW	c.630T>G\|p.Ser210Ser	S147 S201 S213 S267
151461	BAA02g00180	A02	125894	G	A	synonymous_variant	LOW	c.627C>T\|p.Asp209Asp	S147 S201 S213 S267
151462	BAA02g00180	A02	125903	A	G	synonymous_variant	LOW	c.618T>C\|p.Ala206Ala	S147 S201 S213 S267
151463	BAA02g00180	A02	125957	C	T	synonymous_variant	LOW	c.564G>A\|p.Thr188Thr	S201 S226 S239 S267 S91
151464	BAA02g00180	A02	125966	G	C	synonymous_variant	LOW	c.555C>G\|p.Ser185Ser	S201 S226 S239 S267 S91
151465	BAA02g00180	A02	125972	G	A	synonymous_variant	LOW	c.549C>T\|p.Pro183Pro	S201 S226 S239 S267 S91
151466	BAA02g00180	A02	125977	G	A	synonymous_variant	LOW	c.544C>T\|p.Leu182Leu	S201 S226 S239 S267 S91
151467	BAA02g00180	A02	126363	C	T	missense_variant	MODERATE	c.326G>A\|p.Gly109Glu	S61
151468	BAA02g00180	A02	126675	G	A	missense_variant	MODERATE	c.14C>T\|p.Pro5Leu	S64
151469	BAA02g00180	A02	127262	G	A	upstream_gene_variant	MODIFIER	c.-574C>T\|	S126
151470	BAA02g00190	A02	127446	G	A	synonymous_variant	LOW	c.2491C>T\|p.Leu831Leu	S149
151471	BAA02g00190	A02	128933	G	A	synonymous_variant	LOW	c.1719C>T\|p.Val573Val	S50
151472	BAA02g00180	A02	130527	C	T	upstream_gene_variant	MODIFIER	c.-3839G>A\|	S130
151473	BAA02g00190	A02	130713	G	A	synonymous_variant	LOW	c.375C>T\|p.Leu125Leu	S239
151474	BAA02g00190	A02	131050	G	A	synonymous_variant	LOW	c.216C>T\|p.Leu72Leu	S297
151475	BAA02g00190	A02	132904	A	T	upstream_gene_variant	MODIFIER	c.-1639T>A\|	S123 S125 S176 S197 S233 S240 S241 S26 S27 S32 S60 S66

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