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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g39200	A09	46845130	G	A	missense_variant	MODERATE	c.2684C>T\|p.Ser895Phe	S13
2	BAA09g39200	A09	46845342	G	A	synonymous_variant	LOW	c.2472C>T\|p.Phe824Phe	S166
3	BAA09g39200	A09	46845637	G	A	missense_variant	MODERATE	c.2177C>T\|p.Ser726Phe	S189
4	BAA09g39200	A09	46846835	G	A	missense_variant	MODERATE	c.1475C>T\|p.Ser492Phe	S187 S298
5	BAA09g39200	A09	46847541	C	T	missense_variant	MODERATE	c.1166G>A\|p.Arg389Gln	S282
6	BAA09g39200	A09	46848831	C	T	synonymous_variant	LOW	c.156G>A\|p.Arg52Arg	S168
7	BAA09g39200	A09	46849011	C	T	upstream_gene_variant	MODIFIER	c.-25G>A\|	S157 S163
8	BAA09g39200	A09	46849190	C	T	upstream_gene_variant	MODIFIER	c.-204G>A\|	S132 S137 S138 S192 S215 S237 S288
9	BAA09g39200	A09	46849317	G	A	upstream_gene_variant	MODIFIER	c.-331C>T\|	S161
10	BAA09g39200	A09	46849671	G	A	upstream_gene_variant	MODIFIER	c.-685C>T\|	S44
11	BAA09g39200	A09	46850825	C	T	upstream_gene_variant	MODIFIER	c.-1839G>A\|	S296
12	BAA09g39200	A09	46851032	C	T	upstream_gene_variant	MODIFIER	c.-2046G>A\|	S108
13	BAA09g39200	A09	46851426	G	A	upstream_gene_variant	MODIFIER	c.-2440C>T\|	S150
14	BAA09g39200	A09	46852612	C	T	upstream_gene_variant	MODIFIER	c.-3626G>A\|	S278
15	BAA09g39200	A09	46853492	C	T	upstream_gene_variant	MODIFIER	c.-4506G>A\|	S182
16	BAA09g39200	A09	46853592	G	A	upstream_gene_variant	MODIFIER	c.-4606C>T\|	S41