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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA06g20120	A06	10555720	G	A	synonymous_variant	LOW	c.1398C>T\|p.Tyr466Tyr	S131
2	BAA06g20120	A06	10556122	C	T	synonymous_variant	LOW	c.996G>A\|p.Glu332Glu	S192
3	BAA06g20120	A06	10556381	C	T	splice_region_variant&intron_variant	LOW	c.810+8G>A\|	S34
4	BAA06g20120	A06	10556392	G	A	synonymous_variant	LOW	c.807C>T\|p.Ile269Ile	S262
5	BAA06g20120	A06	10556645	C	T	missense_variant	MODERATE	c.554G>A\|p.Arg185Lys	S4
6	BAA06g20120	A06	10556781	C	T	missense_variant	MODERATE	c.418G>A\|p.Glu140Lys	S14
7	BAA06g20120	A06	10559010	G	A	upstream_gene_variant	MODIFIER	c.-1812C>T\|	S8
8	BAA06g20120	A06	10559561	G	A	upstream_gene_variant	MODIFIER	c.-2363C>T\|	S95
9	BAA06g20120	A06	10560975	C	T	upstream_gene_variant	MODIFIER	c.-3777G>A\|	S257
10	BAA06g20120	A06	10561034	G	T	upstream_gene_variant	MODIFIER	c.-3836C>A\|	S114 S119 S123 S133 S159 S169 S173 S225 S243 S298 S299 S73
11	BAA06g20120	A06	10561120	G	A	upstream_gene_variant	MODIFIER	c.-3922C>T\|	S59
12	BAA06g20120	A06	10561430	C	T	upstream_gene_variant	MODIFIER	c.-4232G>A\|	S109
13	BAA06g20120	A06	10561469	C	T	upstream_gene_variant	MODIFIER	c.-4271G>A\|	S74
14	BAA06g20120	A06	10561850	C	T	upstream_gene_variant	MODIFIER	c.-4652G>A\|	S144
15	BAA06g20120	A06	10561862	C	T	upstream_gene_variant	MODIFIER	c.-4664G>A\|	S298
16	BAA06g20120	A06	10562028	C	T	upstream_gene_variant	MODIFIER	c.-4830G>A\|	S148 S30 S31