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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
76801	BAA01g40580	A01	26879402	C	T	downstream_gene_variant	MODIFIER	c.*1419G>A\|	S37
76802	BAA01g40580	A01	26879720	C	T	downstream_gene_variant	MODIFIER	c.*1101G>A\|	S32
76803	BAA01g40580	A01	26879922	G	A	downstream_gene_variant	MODIFIER	c.*899C>T\|	S208 S219
76804	BAA01g40580	A01	26880134	G	A	downstream_gene_variant	MODIFIER	c.*687C>T\|	S202
76805	BAA01g40580	A01	26880669	C	T	downstream_gene_variant	MODIFIER	c.*152G>A\|	S237
76806	BAA01g40580	A01	26880998	C	T	intron_variant	MODIFIER	c.639+33G>A\|	S161
76807	BAA01g40580	A01	26881307	G	A	synonymous_variant	LOW	c.456C>T\|p.Asn152Asn	S298
76808	BAA01g40580	A01	26881460	G	A	intron_variant	MODIFIER	c.343-40C>T\|	S157 S163
76809	BAA01g40580	A01	26882303	C	T	upstream_gene_variant	MODIFIER	c.-444G>A\|	S293
76810	BAA01g40580	A01	26884707	G	A	upstream_gene_variant	MODIFIER	c.-2848C>T\|	S297
76811	BAA01g40590	A01	26886808	G	A	missense_variant	MODERATE	c.319C>T\|p.Leu107Phe	S163
76812	BAA01g40590	A01	26886838	C	T	missense_variant	MODERATE	c.289G>A\|p.Glu97Lys	S81 S85
76813	BAA01g40590	A01	26887017	G	A	missense_variant	MODERATE	c.110C>T\|p.Pro37Leu	S238
76814	BAA01g40590	A01	26888206	G	A	upstream_gene_variant	MODIFIER	c.-1080C>T\|	S159 S188 S243 S276 S298 S299
76815	BAA01g40590	A01	26888765	C	T	upstream_gene_variant	MODIFIER	c.-1639G>A\|	S281
76816	BAA01g40600	A01	26889513	G	A	synonymous_variant	LOW	c.4273C>T\|p.Leu1425Leu	S138
76817	BAA01g40600	A01	26889820	G	A	synonymous_variant	LOW	c.3966C>T\|p.Asp1322Asp	S139
76818	BAA01g40590	A01	26890913	C	T	upstream_gene_variant	MODIFIER	c.-3787G>A\|	S44
76819	BAA01g40600	A01	26891394	C	T	missense_variant	MODERATE	c.2980G>A\|p.Gly994Arg	S186
76820	BAA01g40600	A01	26891429	C	T	missense_variant	MODERATE	c.2945G>A\|p.Arg982His	S50
76821	BAA01g40600	A01	26891701	C	T	synonymous_variant	LOW	c.2673G>A\|p.Ala891Ala	S259
76822	BAA01g40600	A01	26891961	C	T	missense_variant	MODERATE	c.2413G>A\|p.Gly805Arg	S279
76823	BAA01g40600	A01	26891979	C	T	missense_variant	MODERATE	c.2395G>A\|p.Gly799Arg	S48
76824	BAA01g40600	A01	26892140	G	A	synonymous_variant	LOW	c.2322C>T\|p.Asp774Asp	S185
76825	BAA01g40610	A01	26892216	G	A	downstream_gene_variant	MODIFIER	c.*3701C>T\|	S299

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