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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA05g41840	A05	39819723	C	T	downstream_gene_variant	MODIFIER	c.*661G>A\|	S76
2	BAA05g41840	A05	39820593	G	A	missense_variant	MODERATE	c.1357C>T\|p.Pro453Ser	S34
3	BAA05g41840	A05	39821508	C	T	intron_variant	MODIFIER	c.645-47G>A\|	S241 S39
4	BAA05g41840	A05	39821715	C	T	intron_variant	MODIFIER	c.645-254G>A\|	S174 S216 S265 S27
5	BAA05g41840	A05	39821973	G	A	intron_variant	MODIFIER	c.644+154C>T\|	S32
6	BAA05g41840	A05	39822693	A	C	intron_variant	MODIFIER	c.252+73T>G\|	S148 S224 S234 S235 S282
7	BAA05g41840	A05	39822694	A	C	intron_variant	MODIFIER	c.252+72T>G\|	S148 S172 S224 S234 S235 S282
8	BAA05g41840	A05	39823777	C	T	upstream_gene_variant	MODIFIER	c.-760G>A\|	S283
9	BAA05g41840	A05	39823852	C	T	upstream_gene_variant	MODIFIER	c.-835G>A\|	S281 S282
10	BAA05g41840	A05	39823933	G	A	upstream_gene_variant	MODIFIER	c.-916C>T\|	S63
11	BAA05g41840	A05	39824390	C	T	upstream_gene_variant	MODIFIER	c.-1373G>A\|	S150
12	BAA05g41840	A05	39825925	C	T	upstream_gene_variant	MODIFIER	c.-2908G>A\|	S210 S225
13	BAA05g41840	A05	39826061	C	T	upstream_gene_variant	MODIFIER	c.-3044G>A\|	S232
14	BAA05g41840	A05	39826952	C	A	upstream_gene_variant	MODIFIER	c.-3935G>T\|	S256
15	BAA05g41840	A05	39827508	C	T	upstream_gene_variant	MODIFIER	c.-4491G>A\|	S265
16	BAA05g41840	A05	39827760	C	T	upstream_gene_variant	MODIFIER	c.-4743G>A\|	S192