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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA06g19810	A06	10331460	C	T	upstream_gene_variant	MODIFIER	c.-407C>T\|	S120
2	BAA06g19810	A06	10331762	C	T	upstream_gene_variant	MODIFIER	c.-105C>T\|	S249
3	BAA06g19810	A06	10331909	C	T	missense_variant	MODERATE	c.43C>T\|p.Leu15Phe	S104 S52
4	BAA06g19810	A06	10332060	G	A	splice_donor_variant&intron_variant	HIGH	c.193+1G>A\|	S261 S77 S82
5	BAA06g19810	A06	10332465	C	T	intron_variant	MODIFIER	c.305+222C>T\|	S294
6	BAA06g19810	A06	10332561	G	A	intron_variant	MODIFIER	c.305+318G>A\|	S118
7	BAA06g19810	A06	10333022	C	T	intron_variant	MODIFIER	c.306-455C>T\|	S148 S210 S30 S31
8	BAA06g19810	A06	10333828	G	A	synonymous_variant	LOW	c.570G>A\|p.Gln190Gln	S25 S284
9	BAA06g19810	A06	10334536	G	A	stop_gained	HIGH	c.1014G>A\|p.Trp338*	S139
10	BAA06g19810	A06	10334709	C	T	missense_variant	MODERATE	c.1111C>T\|p.Pro371Ser	S286
11	BAA06g19810	A06	10334719	G	A	missense_variant	MODERATE	c.1121G>A\|p.Arg374Gln	S202
12	BAA06g19810	A06	10335209	C	T	missense_variant	MODERATE	c.1510C>T\|p.Leu504Phe	S244
13	BAA06g19810	A06	10335558	G	A	missense_variant	MODERATE	c.1766G>A\|p.Arg589Lys	S146
14	BAA06g19810	A06	10340035	C	T	downstream_gene_variant	MODIFIER	c.*4458C>T\|	S155 S211
15	BAA06g19810	A06	10340393	G	A	downstream_gene_variant	MODIFIER	c.*4816G>A\|	S244