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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
86601	BAA01g46040	A01	30688490	C	T	upstream_gene_variant	MODIFIER	c.-506C>T\|	S37
86602	BAA01g46030	A01	30690422	C	T	downstream_gene_variant	MODIFIER	c.*2393C>T\|	S294
86603	BAA01g46040	A01	30691216	C	T	missense_variant	MODERATE	c.857C>T\|p.Ser286Leu	S57
86604	BAA01g46030	A01	30691466	C	T	downstream_gene_variant	MODIFIER	c.*3437C>T\|	S161
86605	BAA01g46040	A01	30691656	C	T	missense_variant	MODERATE	c.1178C>T\|p.Ser393Phe	S186
86606	BAA01g46040	A01	30691693	C	T	synonymous_variant	LOW	c.1215C>T\|p.Ala405Ala	S97
86607	BAA01g46040	A01	30692469	C	T	missense_variant	MODERATE	c.1763C>T\|p.Ser588Phe	S128
86608	BAA01g46040	A01	30692659	G	A	synonymous_variant	LOW	c.1953G>A\|p.Arg651Arg	S10
86609	BAA01g46050	A01	30694108	C	T	missense_variant	MODERATE	c.730G>A\|p.Glu244Lys	S47
86610	BAA01g46060	A01	30694872	G	A	upstream_gene_variant	MODIFIER	c.-2060G>A\|	S175
86611	BAA01g46060	A01	30695411	C	T	upstream_gene_variant	MODIFIER	c.-1521C>T\|	S80
86612	BAA01g46050	A01	30695464	G	A	synonymous_variant	LOW	c.117C>T\|p.Thr39Thr	S71
86613	BAA01g46050	A01	30696406	C	T	upstream_gene_variant	MODIFIER	c.-826G>A\|	S142
86614	BAA01g46050	A01	30696520	G	A	upstream_gene_variant	MODIFIER	c.-940C>T\|	S251
86615	BAA01g46060	A01	30697049	C	A	missense_variant	MODERATE	c.118C>A\|p.Gln40Lys	S147
86616	BAA01g46060	A01	30697096	G	A	synonymous_variant	LOW	c.165G>A\|p.Gln55Gln	S209
86617	BAA01g46060	A01	30697905	G	A	missense_variant	MODERATE	c.764G>A\|p.Gly255Glu	S243 S299
86618	BAA01g46070	A01	30698715	C	T	missense_variant	MODERATE	c.1085G>A\|p.Gly362Glu	S156
86619	BAA01g46070	A01	30699016	C	T	missense_variant	MODERATE	c.784G>A\|p.Asp262Asn	S54
86620	BAA01g46070	A01	30699103	T	C	missense_variant	MODERATE	c.697A>G\|p.Lys233Glu	S162 S210 S220 S225 S229 S234
86621	BAA01g46070	A01	30699387	G	A	missense_variant	MODERATE	c.413C>T\|p.Ala138Val	S265
86622	BAA01g46050	A01	30699929	C	T	upstream_gene_variant	MODIFIER	c.-4349G>A\|	S221
86623	BAA01g46070	A01	30701762	C	T	synonymous_variant	LOW	c.195G>A\|p.Glu65Glu	S210
86624	BAA01g46070	A01	30701925	G	A	missense_variant	MODERATE	c.32C>T\|p.Ser11Phe	S224
86625	BAA01g46070	A01	30701990	G	A	upstream_gene_variant	MODIFIER	c.-34C>T\|	S185

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