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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA06g13410	A06	6675237	G	A	upstream_gene_variant	MODIFIER	c.-2283G>A\|	S81 S85
2	BAA06g13410	A06	6676672	C	T	upstream_gene_variant	MODIFIER	c.-848C>T\|	S10
3	BAA06g13410	A06	6677245	C	T	upstream_gene_variant	MODIFIER	c.-275C>T\|	S278
4	BAA06g13410	A06	6677312	C	T	upstream_gene_variant	MODIFIER	c.-208C>T\|	S195
5	BAA06g13410	A06	6678822	G	A	missense_variant	MODERATE	c.767G>A\|p.Gly256Asp	S45
6	BAA06g13410	A06	6678930	G	A	missense_variant	MODERATE	c.875G>A\|p.Gly292Glu	S174 S216 S241
7	BAA06g13410	A06	6679341	G	A	synonymous_variant	LOW	c.1113G>A\|p.Gln371Gln	S118
8	BAA06g13410	A06	6679832	C	T	missense_variant	MODERATE	c.1604C>T\|p.Ala535Val	S163
9	BAA06g13410	A06	6680258	C	T	missense_variant	MODERATE	c.2030C>T\|p.Ser677Phe	S148 S210 S30 S31
10	BAA06g13410	A06	6680732	C	T	missense_variant	MODERATE	c.2282C>T\|p.Thr761Ile	S175
11	BAA06g13410	A06	6681152	G	A	synonymous_variant	LOW	c.2610G>A\|p.Thr870Thr	S75 S81
12	BAA06g13410	A06	6681452	G	A	synonymous_variant	LOW	c.2754G>A\|p.Lys918Lys	S83 S88
13	BAA06g13410	A06	6681902	G	A	splice_acceptor_variant&intron_variant	HIGH	c.3034-1G>A\|	S25
14	BAA06g13410	A06	6681934	G	A	missense_variant	MODERATE	c.3065G>A\|p.Gly1022Asp	S297