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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g19010	A01	9321151	G	A	synonymous_variant	LOW	c.2592C>T\|p.Leu864Leu	S13
2	BAA01g19010	A01	9321381	G	A	splice_region_variant&intron_variant	LOW	c.2448+7C>T\|	S212
3	BAA01g19010	A01	9321607	C	T	stop_gained	HIGH	c.2229G>A\|p.Trp743*	S182
4	BAA01g19010	A01	9321728	C	T	missense_variant	MODERATE	c.2108G>A\|p.Arg703Lys	S144
5	BAA01g19010	A01	9322149	C	T	missense_variant	MODERATE	c.1687G>A\|p.Val563Ile	S18
6	BAA01g19010	A01	9322435	C	T	synonymous_variant	LOW	c.1401G>A\|p.Gly467Gly	S85
7	BAA01g19010	A01	9322810	C	T	synonymous_variant	LOW	c.1026G>A\|p.Glu342Glu	S167
8	BAA01g19010	A01	9324096	C	T	missense_variant	MODERATE	c.478G>A\|p.Gly160Arg	S148 S210 S30 S31
9	BAA01g19010	A01	9324118	C	T	synonymous_variant	LOW	c.456G>A\|p.Ala152Ala	S185
10	BAA01g19010	A01	9324451	G	A	synonymous_variant	LOW	c.123C>T\|p.Phe41Phe	S1 S161 S90
11	BAA01g19010	A01	9324491	G	A	missense_variant	MODERATE	c.83C>T\|p.Ser28Phe	S263
12	BAA01g19010	A01	9324543	C	T	missense_variant	MODERATE	c.31G>A\|p.Ala11Thr	S155 S211
13	BAA01g19010	A01	9325516	C	T	upstream_gene_variant	MODIFIER	c.-943G>A\|	S107
14	BAA01g19010	A01	9326141	C	T	upstream_gene_variant	MODIFIER	c.-1568G>A\|	S256
15	BAA01g19010	A01	9327620	C	T	upstream_gene_variant	MODIFIER	c.-3047G>A\|	S267
16	BAA01g19010	A01	9328169	C	T	upstream_gene_variant	MODIFIER	c.-3596G>A\|	S114
17	BAA01g19010	A01	9328995	G	A	upstream_gene_variant	MODIFIER	c.-4422C>T\|	S275
18	BAA01g19010	A01	9329485	C	T	upstream_gene_variant	MODIFIER	c.-4912G>A\|	S208 S93