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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g31440	A10	22933366	G	A	splice_region_variant&intron_variant	LOW	c.2883+7C>T\|	S118
2	BAA10g31440	A10	22933715	C	T	missense_variant	MODERATE	c.2635G>A\|p.Glu879Lys	S246
3	BAA10g31440	A10	22937025	G	A	missense_variant	MODERATE	c.1300C>T\|p.Pro434Ser	S70
4	BAA10g31440	A10	22937610	C	T	splice_region_variant&intron_variant	LOW	c.985-4G>A\|	S45
5	BAA10g31440	A10	22938888	C	T	stop_gained	HIGH	c.711G>A\|p.Trp237*	S160
6	BAA10g31440	A10	22940234	G	A	missense_variant	MODERATE	c.325C>T\|p.Arg109Trp	S35
7	BAA10g31440	A10	22940633	C	T	missense_variant	MODERATE	c.25G>A\|p.Ala9Thr	S148 S210 S30 S31
8	BAA10g31440	A10	22940859	C	T	upstream_gene_variant	MODIFIER	c.-202G>A\|	S190
9	BAA10g31440	A10	22941014	G	C	upstream_gene_variant	MODIFIER	c.-357C>G\|	S138 S172 S187 S194 S275 S293 S43 S53 S56 S61 S86
10	BAA10g31440	A10	22943359	G	A	upstream_gene_variant	MODIFIER	c.-2702C>T\|	S219 S72
11	BAA10g31440	A10	22943425	G	A	upstream_gene_variant	MODIFIER	c.-2768C>T\|	S241
12	BAA10g31440	A10	22945423	G	A	upstream_gene_variant	MODIFIER	c.-4766C>T\|	S71