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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g11170	A02	5052229	G	A	synonymous_variant	LOW	c.852C>T\|p.His284His	S179 S180 S183
2	BAA02g11170	A02	5052235	C	T	missense_variant	MODERATE	c.846G>A\|p.Met282Ile	S128
3	BAA02g11170	A02	5052238	C	T	synonymous_variant	LOW	c.843G>A\|p.Glu281Glu	S179 S180 S183
4	BAA02g11170	A02	5052241	A	T	synonymous_variant	LOW	c.840T>A\|p.Val280Val	S179 S180 S183
5	BAA02g11170	A02	5052250	G	C	synonymous_variant	LOW	c.831C>G\|p.Val277Val	S179 S183
6	BAA02g11170	A02	5052259	G	T	synonymous_variant	LOW	c.822C>A\|p.Thr274Thr	S178 S179 S183 S191
7	BAA02g11170	A02	5052541	C	T	synonymous_variant	LOW	c.540G>A\|p.Lys180Lys	S202
8	BAA02g11170	A02	5052746	G	A	missense_variant	MODERATE	c.425C>T\|p.Thr142Ile	S74
9	BAA02g11170	A02	5052998	C	T	stop_gained	HIGH	c.173G>A\|p.Trp58*	S172 S217
10	BAA02g11170	A02	5053408	G	A	upstream_gene_variant	MODIFIER	c.-238C>T\|	S158
11	BAA02g11170	A02	5054153	C	T	upstream_gene_variant	MODIFIER	c.-983G>A\|	S272
12	BAA02g11170	A02	5054599	G	A	upstream_gene_variant	MODIFIER	c.-1429C>T\|	S210 S225
13	BAA02g11170	A02	5055587	C	T	upstream_gene_variant	MODIFIER	c.-2417G>A\|	S257