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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
69951	BAA01g36620	A01	24499594	C	T	synonymous_variant	LOW	c.252G>A\|p.Glu84Glu	S216
69952	BAA01g36620	A01	24500216	G	A	upstream_gene_variant	MODIFIER	c.-371C>T\|	S20
69953	BAA01g36620	A01	24500785	C	T	upstream_gene_variant	MODIFIER	c.-940G>A\|	S108
69954	BAA01g36630	A01	24501373	C	T	missense_variant	MODERATE	c.476G>A\|p.Arg159Gln	S9
69955	BAA01g36630	A01	24501382	C	T	missense_variant	MODERATE	c.467G>A\|p.Ser156Asn	S180 S231
69956	BAA01g36630	A01	24501482	C	T	missense_variant	MODERATE	c.367G>A\|p.Val123Met	S128
69957	BAA01g36620	A01	24502560	C	T	upstream_gene_variant	MODIFIER	c.-2715G>A\|	S208 S93
69958	BAA01g36630	A01	24506068	C	T	upstream_gene_variant	MODIFIER	c.-3132G>A\|	S112
69959	BAA01g36630	A01	24506464	C	T	upstream_gene_variant	MODIFIER	c.-3528G>A\|	S134
69960	BAA01g36630	A01	24506927	C	T	upstream_gene_variant	MODIFIER	c.-3991G>A\|	S302
69961	BAA01g36630	A01	24507859	C	T	upstream_gene_variant	MODIFIER	c.-4923G>A\|	S233
69962	BAA01g36640	A01	24508131	G	A	upstream_gene_variant	MODIFIER	c.-3186G>A\|	S163
69963	BAA01g36640	A01	24508154	G	A	upstream_gene_variant	MODIFIER	c.-3163G>A\|	S223
69964	BAA01g36640	A01	24508282	A	G	upstream_gene_variant	MODIFIER	c.-3035A>G\|	S189
69965	BAA01g36640	A01	24511155	C	T	upstream_gene_variant	MODIFIER	c.-162C>T\|	S201
69966	BAA01g36640	A01	24511459	C	T	missense_variant	MODERATE	c.143C>T\|p.Ser48Phe	S165 S211 S227
69967	BAA01g36650	A01	24513122	G	A	missense_variant	MODERATE	c.803C>T\|p.Pro268Leu	S20
69968	BAA01g36650	A01	24513603	C	T	missense_variant	MODERATE	c.322G>A\|p.Val108Met	S63
69969	BAA01g36650	A01	24513700	C	T	missense_variant	MODERATE	c.225G>A\|p.Met75Ile	S266
69970	BAA01g36650	A01	24514045	C	T	synonymous_variant	LOW	c.6G>A\|p.Lys2Lys	S240
69971	BAA01g36660	A01	24519318	G	A	missense_variant	MODERATE	c.856C>T\|p.Pro286Ser	S203
69972	BAA01g36660	A01	24519692	C	T	missense_variant	MODERATE	c.482G>A\|p.Arg161Gln	S115
69973	BAA01g36660	A01	24519726	C	T	missense_variant	MODERATE	c.448G>A\|p.Val150Met	S32
69974	BAA01g36660	A01	24519979	G	A	synonymous_variant	LOW	c.195C>T\|p.Leu65Leu	S207
69975	BAA01g36660	A01	24520396	C	T	upstream_gene_variant	MODIFIER	c.-223G>A\|	S216

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