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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g46970	A09	51484613	C	T	upstream_gene_variant	MODIFIER	c.-4739C>T\|	S206 S5
2	BAA09g46970	A09	51484871	C	T	upstream_gene_variant	MODIFIER	c.-4481C>T\|	S293
3	BAA09g46970	A09	51487575	G	A	upstream_gene_variant	MODIFIER	c.-1777G>A\|	S189
4	BAA09g46970	A09	51488327	C	T	upstream_gene_variant	MODIFIER	c.-1025C>T\|	S61
5	BAA09g46970	A09	51488872	C	T	upstream_gene_variant	MODIFIER	c.-480C>T\|	S115
6	BAA09g46970	A09	51489376	C	T	synonymous_variant	LOW	c.25C>T\|p.Leu9Leu	S297
7	BAA09g46970	A09	51490589	C	T	missense_variant	MODERATE	c.643C>T\|p.Pro215Ser	S61
8	BAA09g46970	A09	51490701	G	A	missense_variant	MODERATE	c.755G>A\|p.Arg252Lys	S178
9	BAA09g46970	A09	51491553	C	T	missense_variant	MODERATE	c.1607C>T\|p.Ser536Phe	S119
10	BAA09g46970	A09	51491663	G	A	missense_variant	MODERATE	c.1717G>A\|p.Val573Ile	S71
11	BAA09g46970	A09	51492280	G	A	missense_variant	MODERATE	c.2149G>A\|p.Val717Ile	S73 S91
12	BAA09g46970	A09	51492560	G	A	missense_variant	MODERATE	c.2429G>A\|p.Arg810Lys	S165
13	BAA09g46970	A09	51492583	G	A	missense_variant	MODERATE	c.2452G>A\|p.Asp818Asn	S184
14	BAA09g46970	A09	51492594	G	A	synonymous_variant	LOW	c.2463G>A\|p.Glu821Glu	S130
15	BAA09g46970	A09	51492857	C	T	downstream_gene_variant	MODIFIER	c.*146C>T\|	S153 S157 S236 S257 S262