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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA05g26200	A05	30882690	C	T	synonymous_variant	LOW	c.2994G>A\|p.Glu998Glu	S33
2	BAA05g26200	A05	30883037	C	T	stop_gained	HIGH	c.2826G>A\|p.Trp942*	S305
3	BAA05g26200	A05	30883234	G	A	missense_variant	MODERATE	c.2701C>T\|p.Leu901Phe	S34
4	BAA05g26200	A05	30884183	C	T	synonymous_variant	LOW	c.2091G>A\|p.Leu697Leu	S105 S106
5	BAA05g26200	A05	30884222	C	T	synonymous_variant	LOW	c.2052G>A\|p.Gln684Gln	S71
6	BAA05g26200	A05	30884248	C	T	missense_variant	MODERATE	c.2026G>A\|p.Glu676Lys	S65
7	BAA05g26200	A05	30884866	C	T	missense_variant	MODERATE	c.1807G>A\|p.Glu603Lys	S38
8	BAA05g26200	A05	30886358	G	A	missense_variant	MODERATE	c.931C>T\|p.Pro311Ser	S107
9	BAA05g26200	A05	30886797	C	T	missense_variant	MODERATE	c.728G>A\|p.Gly243Asp	S229
10	BAA05g26200	A05	30886932	C	T	missense_variant&splice_region_variant	MODERATE	c.700G>A\|p.Glu234Lys	S236
11	BAA05g26200	A05	30887955	G	A	missense_variant	MODERATE	c.77C>T\|p.Ser26Leu	S185
12	BAA05g26200	A05	30888079	C	T	upstream_gene_variant	MODIFIER	c.-48G>A\|	S162
13	BAA05g26200	A05	30891260	G	A	upstream_gene_variant	MODIFIER	c.-3229C>T\|	S64
14	BAA05g26200	A05	30891495	G	A	upstream_gene_variant	MODIFIER	c.-3464C>T\|	S156 S2 S213 S34 S4 S6
15	BAA05g26200	A05	30892378	G	A	upstream_gene_variant	MODIFIER	c.-4347C>T\|	S239