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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA05g31340	A05	34042874	C	T	upstream_gene_variant	MODIFIER	c.-4118C>T\|	S268
2	BAA05g31340	A05	34044491	C	T	upstream_gene_variant	MODIFIER	c.-2501C>T\|	S259
3	BAA05g31340	A05	34048265	G	A	intron_variant	MODIFIER	c.337+61G>A\|	S156
4	BAA05g31340	A05	34049000	G	A	missense_variant&splice_region_variant	MODERATE	c.643G>A\|p.Ala215Thr	S180
5	BAA05g31340	A05	34049117	G	A	missense_variant	MODERATE	c.682G>A\|p.Glu228Lys	S173
6	BAA05g31340	A05	34049234	C	T	missense_variant	MODERATE	c.728C>T\|p.Thr243Ile	S216
7	BAA05g31340	A05	34050718	C	T	intron_variant	MODIFIER	c.1306+32C>T\|	S15 S156 S2 S3 S4 S6
8	BAA05g31340	A05	34050871	C	T	intron_variant	MODIFIER	c.1357+50C>T\|	S235
9	BAA05g31340	A05	34051448	G	A	intron_variant	MODIFIER	c.1588-37G>A\|	S153 S2 S213 S34 S4 S6
10	BAA05g31340	A05	34051747	C	T	missense_variant	MODERATE	c.1850C>T\|p.Ala617Val	S128
11	BAA05g31340	A05	34051908	A	T	stop_gained	HIGH	c.2011A>T\|p.Lys671*	S62
12	BAA05g31340	A05	34052053	C	T	missense_variant	MODERATE	c.2156C>T\|p.Ala719Val	S204
13	BAA05g31340	A05	34052095	C	T	missense_variant	MODERATE	c.2198C>T\|p.Ala733Val	S36
14	BAA05g31340	A05	34052449	G	A	downstream_gene_variant	MODIFIER	c.*263G>A\|	S276
15	BAA05g31340	A05	34052792	C	T	downstream_gene_variant	MODIFIER	c.*606C>T\|	S13 S219 S279 S64 S72