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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g54680	A09	55208930	C	T	missense_variant	MODERATE	c.2816G>A\|p.Gly939Glu	S223
2	BAA09g54680	A09	55209260	G	A	missense_variant	MODERATE	c.2567C>T\|p.Ser856Phe	S135 S152 S273
3	BAA09g54680	A09	55210104	C	T	missense_variant	MODERATE	c.2332G>A\|p.Ala778Thr	S293
4	BAA09g54680	A09	55211138	C	T	missense_variant	MODERATE	c.1706G>A\|p.Gly569Glu	S124 S99
5	BAA09g54680	A09	55211202	C	T	missense_variant	MODERATE	c.1642G>A\|p.Glu548Lys	S130
6	BAA09g54680	A09	55212667	C	T	missense_variant	MODERATE	c.844G>A\|p.Asp282Asn	S139
7	BAA09g54680	A09	55214034	C	T	synonymous_variant	LOW	c.192G>A\|p.Ser64Ser	S120
8	BAA09g54680	A09	55214066	C	T	missense_variant	MODERATE	c.160G>A\|p.Glu54Lys	S132 S137 S215
9	BAA09g54680	A09	55214094	G	A	synonymous_variant	LOW	c.132C>T\|p.Phe44Phe	S249
10	BAA09g54680	A09	55215200	G	A	upstream_gene_variant	MODIFIER	c.-975C>T\|	S47
11	BAA09g54680	A09	55215270	C	T	upstream_gene_variant	MODIFIER	c.-1045G>A\|	S138
12	BAA09g54680	A09	55215393	C	T	upstream_gene_variant	MODIFIER	c.-1168G>A\|	S208 S219
13	BAA09g54680	A09	55216292	G	A	upstream_gene_variant	MODIFIER	c.-2067C>T\|	S107
14	BAA09g54680	A09	55216592	C	T	upstream_gene_variant	MODIFIER	c.-2367G>A\|	S13
15	BAA09g54680	A09	55216611	C	T	upstream_gene_variant	MODIFIER	c.-2386G>A\|	S232