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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA06g26190	A06	17953373	C	T	missense_variant	MODERATE	c.2623G>A\|p.Asp875Asn	S210
2	BAA06g26190	A06	17954007	G	A	synonymous_variant	LOW	c.2418C>T\|p.Leu806Leu	S246
3	BAA06g26190	A06	17954332	C	T	missense_variant	MODERATE	c.2264G>A\|p.Arg755Gln	S207
4	BAA06g26190	A06	17956680	C	T	missense_variant	MODERATE	c.799G>A\|p.Glu267Lys	S6
5	BAA06g26190	A06	17956725	C	T	missense_variant	MODERATE	c.754G>A\|p.Gly252Ser	S45
6	BAA06g26190	A06	17956867	C	T	splice_region_variant&intron_variant	LOW	c.677+5G>A\|	S301 S304
7	BAA06g26190	A06	17957288	G	A	synonymous_variant	LOW	c.261C>T\|p.Leu87Leu	S12
8	BAA06g26190	A06	17957688	C	T	upstream_gene_variant	MODIFIER	c.-60G>A\|	S245
9	BAA06g26190	A06	17958495	C	T	upstream_gene_variant	MODIFIER	c.-867G>A\|	S245
10	BAA06g26190	A06	17958520	C	T	upstream_gene_variant	MODIFIER	c.-892G>A\|	S178
11	BAA06g26190	A06	17958961	C	T	upstream_gene_variant	MODIFIER	c.-1333G>A\|	S126
12	BAA06g26190	A06	17959393	C	T	upstream_gene_variant	MODIFIER	c.-1765G>A\|	S148 S210
13	BAA06g26190	A06	17959412	C	T	upstream_gene_variant	MODIFIER	c.-1784G>A\|	S15 S2 S283 S3
14	BAA06g26190	A06	17960038	C	T	upstream_gene_variant	MODIFIER	c.-2410G>A\|	S232
15	BAA06g26190	A06	17961946	C	T	upstream_gene_variant	MODIFIER	c.-4318G>A\|	S288
16	BAA06g26190	A06	17962545	G	A	upstream_gene_variant	MODIFIER	c.-4917C>T\|	S261