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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g26680	A09	17367452	C	T	synonymous_variant	LOW	c.1326G>A\|p.Leu442Leu	S151 S153 S157 S166 S167 S236 S262 S263
2	BAA09g26680	A09	17367516	G	A	missense_variant	MODERATE	c.1262C>T\|p.Ser421Phe	S122
3	BAA09g26680	A09	17367603	G	A	missense_variant	MODERATE	c.1175C>T\|p.Ala392Val	S170
4	BAA09g26680	A09	17367692	C	T	synonymous_variant	LOW	c.1086G>A\|p.Ser362Ser	S260
5	BAA09g26680	A09	17368785	G	A	missense_variant	MODERATE	c.641C>T\|p.Ala214Val	S100
6	BAA09g26680	A09	17371143	G	A	upstream_gene_variant	MODIFIER	c.-1042C>T\|	S28
7	BAA09g26680	A09	17372999	G	A	upstream_gene_variant	MODIFIER	c.-2898C>T\|	S295
8	BAA09g26680	A09	17374910	C	T	upstream_gene_variant	MODIFIER	c.-4809G>A\|	S135
9	BAA09g26680	A09	17374950	C	T	upstream_gene_variant	MODIFIER	c.-4849G>A\|	S71
10	BAA09g26680	A09	17374987	G	A	upstream_gene_variant	MODIFIER	c.-4886C>T\|	S65
11	BAA09g26680	A09	17375089	C	T	upstream_gene_variant	MODIFIER	c.-4988G>A\|	S43