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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g47580	A09	51798635	G	A	synonymous_variant	LOW	c.1887C>T\|p.Asp629Asp	S90
2	BAA09g47580	A09	51798793	C	T	missense_variant	MODERATE	c.1826G>A\|p.Arg609Lys	S280
3	BAA09g47580	A09	51798836	G	A	missense_variant	MODERATE	c.1783C>T\|p.Leu595Phe	S128
4	BAA09g47580	A09	51799016	C	T	missense_variant	MODERATE	c.1753G>A\|p.Asp585Asn	S69
5	BAA09g47580	A09	51799577	G	A	missense_variant	MODERATE	c.1306C>T\|p.Leu436Phe	S166
6	BAA09g47580	A09	51799595	G	A	missense_variant&splice_region_variant	MODERATE	c.1288C>T\|p.Leu430Phe	S172 S217
7	BAA09g47580	A09	51799799	G	A	missense_variant	MODERATE	c.1253C>T\|p.Ser418Phe	S246
8	BAA09g47580	A09	51800929	T	G	splice_region_variant&intron_variant	LOW	c.900+3A>C\|	S110 S128 S130 S174 S195 S31 S65
9	BAA09g47580	A09	51802737	G	A	upstream_gene_variant	MODIFIER	c.-392C>T\|	S177
10	BAA09g47580	A09	51803582	C	T	upstream_gene_variant	MODIFIER	c.-1237G>A\|	S272
11	BAA09g47580	A09	51803741	C	T	upstream_gene_variant	MODIFIER	c.-1396G>A\|	S245
12	BAA09g47580	A09	51805139	G	T	upstream_gene_variant	MODIFIER	c.-2794C>A\|	S138
13	BAA09g47580	A09	51806005	C	T	upstream_gene_variant	MODIFIER	c.-3660G>A\|	S242
14	BAA09g47580	A09	51806035	C	T	upstream_gene_variant	MODIFIER	c.-3690G>A\|	S104 S105 S259 S45