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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g23600	A09	14985314	C	T	upstream_gene_variant	MODIFIER	c.-3813C>T\|	S259
2	BAA09g23600	A09	14986868	C	T	upstream_gene_variant	MODIFIER	c.-2259C>T\|	S213
3	BAA09g23600	A09	14988463	C	T	upstream_gene_variant	MODIFIER	c.-664C>T\|	S241
4	BAA09g23600	A09	14989178	G	A	missense_variant	MODERATE	c.52G>A\|p.Asp18Asn	S165 S211 S227
5	BAA09g23600	A09	14992140	G	A	missense_variant	MODERATE	c.1595G>A\|p.Gly532Asp	S104 S52
6	BAA09g23600	A09	14992238	G	A	missense_variant	MODERATE	c.1693G>A\|p.Gly565Arg	S87
7	BAA09g23600	A09	14992636	T	G	synonymous_variant	LOW	c.1971T>G\|p.Leu657Leu	S104 S133 S27 S280 S85
8	BAA09g23600	A09	14994027	G	A	splice_region_variant&intron_variant	LOW	c.2669+6G>A\|	S164
9	BAA09g23600	A09	14994328	G	A	missense_variant	MODERATE	c.2674G>A\|p.Glu892Lys	S216
10	BAA09g23600	A09	14994428	C	T	missense_variant	MODERATE	c.2774C>T\|p.Pro925Leu	S6
11	BAA09g23600	A09	14994706	G	A	missense_variant	MODERATE	c.2957G>A\|p.Gly986Asp	S125 S18
12	BAA09g23600	A09	14995368	C	T	missense_variant	MODERATE	c.3445C>T\|p.His1149Tyr	S11
13	BAA09g23600	A09	14995696	C	T	missense_variant	MODERATE	c.3680C>T\|p.Ala1227Val	S19
14	BAA09g23600	A09	14998048	C	T	downstream_gene_variant	MODIFIER	c.*1719C>T\|	S292
15	BAA09g23600	A09	14999303	G	A	downstream_gene_variant	MODIFIER	c.*2974G>A\|	S1 S90
16	BAA09g23600	A09	15001253	C	T	downstream_gene_variant	MODIFIER	c.*4924C>T\|	S296