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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g18490	A01	9064874	C	T	synonymous_variant	LOW	c.1476G>A\|p.Gly492Gly	S260
2	BAA01g18490	A01	9065055	C	T	missense_variant	MODERATE	c.1295G>A\|p.Arg432Gln	S242
3	BAA01g18490	A01	9065139	C	T	missense_variant	MODERATE	c.1211G>A\|p.Arg404Gln	S117
4	BAA01g18490	A01	9065141	C	T	stop_gained	HIGH	c.1209G>A\|p.Trp403*	S264
5	BAA01g18490	A01	9065190	G	A	missense_variant	MODERATE	c.1160C>T\|p.Ser387Leu	S15 S156 S2 S213 S3 S4 S6
6	BAA01g18490	A01	9065279	C	T	synonymous_variant	LOW	c.1071G>A\|p.Val357Val	S176
7	BAA01g18490	A01	9065302	C	T	missense_variant	MODERATE	c.1048G>A\|p.Gly350Arg	S16
8	BAA01g18490	A01	9065723	G	A	synonymous_variant	LOW	c.840C>T\|p.Asn280Asn	S196
9	BAA01g18490	A01	9065755	C	T	missense_variant	MODERATE	c.808G>A\|p.Glu270Lys	S67
10	BAA01g18490	A01	9065894	G	A	synonymous_variant	LOW	c.669C>T\|p.Ile223Ile	S249
11	BAA01g18490	A01	9065899	C	T	missense_variant	MODERATE	c.664G>A\|p.Glu222Lys	S133
12	BAA01g18490	A01	9065953	G	A	synonymous_variant	LOW	c.610C>T\|p.Leu204Leu	S139
13	BAA01g18490	A01	9066993	G	A	synonymous_variant	LOW	c.28C>T\|p.Leu10Leu	S201
14	BAA01g18490	A01	9067200	G	A	upstream_gene_variant	MODIFIER	c.-180C>T\|	S124
15	BAA01g18490	A01	9069259	G	A	upstream_gene_variant	MODIFIER	c.-2239C>T\|	S149
16	BAA01g18490	A01	9069549	G	A	upstream_gene_variant	MODIFIER	c.-2529C>T\|	S87