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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA05g19800	A05	11983771	C	T	downstream_gene_variant	MODIFIER	c.*1008G>A\|	S117 S169
2	BAA05g19800	A05	11984139	C	T	downstream_gene_variant	MODIFIER	c.*640G>A\|	S195
3	BAA05g19800	A05	11984378	C	T	downstream_gene_variant	MODIFIER	c.*401G>A\|	S273
4	BAA05g19800	A05	11985221	G	A	missense_variant	MODERATE	c.1996C>T\|p.Leu666Phe	S245
5	BAA05g19800	A05	11985840	G	A	synonymous_variant	LOW	c.1377C>T\|p.Asn459Asn	S13
6	BAA05g19800	A05	11985915	C	T	synonymous_variant	LOW	c.1302G>A\|p.Arg434Arg	S61
7	BAA05g19800	A05	11986306	G	A	missense_variant	MODERATE	c.911C>T\|p.Pro304Leu	S282
8	BAA05g19800	A05	11986328	C	T	missense_variant	MODERATE	c.889G>A\|p.Asp297Asn	S193
9	BAA05g19800	A05	11986537	G	A	missense_variant	MODERATE	c.680C>T\|p.Ser227Leu	S114 S156
10	BAA05g19800	A05	11989168	G	A	missense_variant	MODERATE	c.410C>T\|p.Ser137Phe	S151 S263
11	BAA05g19800	A05	11989955	G	A	synonymous_variant	LOW	c.10C>T\|p.Leu4Leu	S116 S118 S295 S296
12	BAA05g19800	A05	11990376	C	T	upstream_gene_variant	MODIFIER	c.-412G>A\|	S45
13	BAA05g19800	A05	11991145	C	T	upstream_gene_variant	MODIFIER	c.-1181G>A\|	S117
14	BAA05g19800	A05	11991376	C	T	upstream_gene_variant	MODIFIER	c.-1412G>A\|	S262
15	BAA05g19800	A05	11992677	C	T	upstream_gene_variant	MODIFIER	c.-2713G>A\|	S2
16	BAA05g19800	A05	11993499	C	T	upstream_gene_variant	MODIFIER	c.-3535G>A\|	S273