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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
186901	BAA02g24010	A02	13107858	G	A	missense_variant	MODERATE	c.1157C>T\|p.Ser386Phe	S265
186902	BAA02g24010	A02	13108654	C	T	missense_variant	MODERATE	c.361G>A\|p.Asp121Asn	S116
186903	BAA02g24010	A02	13108759	G	A	synonymous_variant	LOW	c.256C>T\|p.Leu86Leu	S173
186904	BAA02g24010	A02	13108942	C	T	missense_variant	MODERATE	c.73G>A\|p.Val25Met	S175
186905	BAA02g24020	A02	13111476	G	A	synonymous_variant	LOW	c.2089C>T\|p.Leu697Leu	S67
186906	BAA02g24020	A02	13111722	C	T	missense_variant	MODERATE	c.1843G>A\|p.Glu615Lys	S171
186907	BAA02g24020	A02	13112131	G	A	synonymous_variant	LOW	c.1434C>T\|p.Asn478Asn	S223
186908	BAA02g24020	A02	13112142	C	T	missense_variant	MODERATE	c.1423G>A\|p.Glu475Lys	S192
186909	BAA02g24020	A02	13112446	C	T	synonymous_variant	LOW	c.1119G>A\|p.Glu373Glu	S240
186910	BAA02g24020	A02	13112515	C	T	synonymous_variant	LOW	c.1050G>A\|p.Lys350Lys	S160
186911	BAA02g24020	A02	13112652	C	T	missense_variant	MODERATE	c.913G>A\|p.Glu305Lys	S203
186912	BAA02g24020	A02	13113828	G	A	synonymous_variant	LOW	c.343C>T\|p.Leu115Leu	S200
186913	BAA02g24020	A02	13114033	C	T	missense_variant	MODERATE	c.138G>A\|p.Met46Ile	S18
186914	BAA02g24020	A02	13114099	C	T	synonymous_variant	LOW	c.72G>A\|p.Gln24Gln	S84 S93
186915	BAA02g24020	A02	13115292	C	T	upstream_gene_variant	MODIFIER	c.-1122G>A\|	S255
186916	BAA02g24030	A02	13115608	C	T	synonymous_variant	LOW	c.735G>A\|p.Glu245Glu	S32
186917	BAA02g24020	A02	13116553	G	A	upstream_gene_variant	MODIFIER	c.-2383C>T\|	S223
186918	BAA02g24040	A02	13116844	C	T	missense_variant	MODERATE	c.98C>T\|p.Ser33Phe	S135
186919	BAA02g24040	A02	13116936	C	T	missense_variant	MODERATE	c.190C>T\|p.Leu64Phe	S135
186920	BAA02g24040	A02	13116939	C	T	missense_variant	MODERATE	c.193C>T\|p.Leu65Phe	S97
186921	BAA02g24040	A02	13117228	C	G	missense_variant	MODERATE	c.482C>G\|p.Ala161Gly	S132 S134 S158 S166 S177 S181 S23 S246 S51 S71 S84 S90 S92
186922	BAA02g24030	A02	13119247	C	T	upstream_gene_variant	MODIFIER	c.-2815G>A\|	S174
186923	BAA02g24050	A02	13119801	G	A	missense_variant	MODERATE	c.484G>A\|p.Gly162Ser	S256
186924	BAA02g24030	A02	13120388	G	A	upstream_gene_variant	MODIFIER	c.-3956C>T\|	S7
186925	BAA02g24030	A02	13120652	C	T	upstream_gene_variant	MODIFIER	c.-4220G>A\|	S66

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