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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g51250	A09	53704096	C	T	upstream_gene_variant	MODIFIER	c.-2241C>T\|	S289 S290
2	BAA09g51250	A09	53705177	C	T	upstream_gene_variant	MODIFIER	c.-1160C>T\|	S205
3	BAA09g51250	A09	53705295	G	A	upstream_gene_variant	MODIFIER	c.-1042G>A\|	S132 S137 S215 S89
4	BAA09g51250	A09	53705390	C	T	upstream_gene_variant	MODIFIER	c.-947C>T\|	S153 S157 S166 S257 S262
5	BAA09g51250	A09	53705692	G	A	upstream_gene_variant	MODIFIER	c.-645G>A\|	S166
6	BAA09g51250	A09	53706223	C	T	upstream_gene_variant	MODIFIER	c.-114C>T\|	S153 S157 S166 S257 S262
7	BAA09g51250	A09	53707297	G	A	missense_variant	MODERATE	c.281G>A\|p.Gly94Glu	S264
8	BAA09g51250	A09	53707786	C	T	missense_variant	MODERATE	c.596C>T\|p.Ala199Val	S286
9	BAA09g51250	A09	53707850	C	T	synonymous_variant	LOW	c.660C>T\|p.His220His	S273
10	BAA09g51250	A09	53708001	G	A	missense_variant	MODERATE	c.811G>A\|p.Asp271Asn	S1 S90
11	BAA09g51250	A09	53709583	C	T	downstream_gene_variant	MODIFIER	c.*1520C>T\|	S228
12	BAA09g51250	A09	53711073	C	T	downstream_gene_variant	MODIFIER	c.*3010C>T\|	S297
13	BAA09g51250	A09	53711915	G	A	downstream_gene_variant	MODIFIER	c.*3852G>A\|	S127
14	BAA09g51250	A09	53712058	G	A	downstream_gene_variant	MODIFIER	c.*3995G>A\|	S128