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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g06480	A01	2898169	G	A	upstream_gene_variant	MODIFIER	c.-3362G>A\|	S75 S81
2	BAA01g06480	A01	2898179	G	A	upstream_gene_variant	MODIFIER	c.-3352G>A\|	S208 S219
3	BAA01g06480	A01	2899172	G	A	upstream_gene_variant	MODIFIER	c.-2359G>A\|	S124
4	BAA01g06480	A01	2899690	C	T	upstream_gene_variant	MODIFIER	c.-1841C>T\|	S223
5	BAA01g06480	A01	2900897	C	T	upstream_gene_variant	MODIFIER	c.-634C>T\|	S266
6	BAA01g06480	A01	2903111	C	T	intron_variant	MODIFIER	c.489-61C>T\|	S231
7	BAA01g06480	A01	2903409	C	T	missense_variant	MODERATE	c.652C>T\|p.Leu218Phe	S231
8	BAA01g06480	A01	2903556	G	A	missense_variant	MODERATE	c.799G>A\|p.Glu267Lys	S298
9	BAA01g06480	A01	2904299	G	A	missense_variant	MODERATE	c.1321G>A\|p.Glu441Lys	S274
10	BAA01g06480	A01	2904505	A	T	synonymous_variant	LOW	c.1527A>T\|p.Ser509Ser	S15 S153 S156 S2 S213 S3 S4 S6
11	BAA01g06480	A01	2904782	G	A	missense_variant	MODERATE	c.1804G>A\|p.Glu602Lys	S209
12	BAA01g06480	A01	2905488	G	A	splice_region_variant&intron_variant	LOW	c.2158-4G>A\|	S107
13	BAA01g06480	A01	2906165	G	A	intron_variant	MODIFIER	c.2405+24G>A\|	S12
14	BAA01g06480	A01	2906531	C	T	missense_variant	MODERATE	c.2579C>T\|p.Ser860Phe	S155 S211
15	BAA01g06480	A01	2906670	G	A	synonymous_variant	LOW	c.2718G>A\|p.Lys906Lys	S23
16	BAA01g06480	A01	2906762	G	A	downstream_gene_variant	MODIFIER	c.*80G>A\|	S190