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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA06g17620	A06	8953641	C	T	upstream_gene_variant	MODIFIER	c.-286C>T\|	S202
2	BAA06g17620	A06	8955283	G	A	missense_variant	MODERATE	c.1357G>A\|p.Ala453Thr	S230
3	BAA06g17620	A06	8955715	G	A	missense_variant	MODERATE	c.1789G>A\|p.Glu597Lys	S1 S90
4	BAA06g17620	A06	8955800	C	T	missense_variant	MODERATE	c.1874C>T\|p.Ser625Phe	S142
5	BAA06g17620	A06	8956050	G	A	synonymous_variant	LOW	c.2124G>A\|p.Ala708Ala	S185
6	BAA06g17620	A06	8956107	G	A	synonymous_variant	LOW	c.2181G>A\|p.Glu727Glu	S182
7	BAA06g17620	A06	8956709	C	T	synonymous_variant	LOW	c.2598C>T\|p.Asp866Asp	S148 S210 S30 S31
8	BAA06g17620	A06	8957560	G	A	intron_variant	MODIFIER	c.3117+25G>A\|	S117 S248 S86
9	BAA06g17620	A06	8957923	G	A	missense_variant	MODERATE	c.3320G>A\|p.Gly1107Glu	S69
10	BAA06g17620	A06	8957938	C	T	missense_variant	MODERATE	c.3335C>T\|p.Pro1112Leu	S281
11	BAA06g17620	A06	8959777	C	T	downstream_gene_variant	MODIFIER	c.*850C>T\|	S80
12	BAA06g17620	A06	8960403	C	T	downstream_gene_variant	MODIFIER	c.*1476C>T\|	S278
13	BAA06g17620	A06	8960559	G	A	downstream_gene_variant	MODIFIER	c.*1632G>A\|	S206 S26
14	BAA06g17620	A06	8961434	G	A	downstream_gene_variant	MODIFIER	c.*2507G>A\|	S149
15	BAA06g17620	A06	8962009	G	A	downstream_gene_variant	MODIFIER	c.*3082G>A\|	S265
16	BAA06g17620	A06	8962371	G	A	downstream_gene_variant	MODIFIER	c.*3444G>A\|	S280