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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g40330	A02	34039993	C	T	missense_variant	MODERATE	c.1939G>A\|p.Gly647Ser	S179
2	BAA02g40330	A02	34040467	T	A	missense_variant	MODERATE	c.1465A>T\|p.Thr489Ser	S119 S176 S233 S262 S270 S280 S284 S30 S4 S7 S93
3	BAA02g40330	A02	34040507	C	T	synonymous_variant	LOW	c.1425G>A\|p.Gly475Gly	S140
4	BAA02g40330	A02	34040549	T	A	synonymous_variant	LOW	c.1383A>T\|p.Gly461Gly	S122 S131 S138 S145 S20 S218 S248 S293 S305
5	BAA02g40330	A02	34040593	T	A	missense_variant	MODERATE	c.1339A>T\|p.Thr447Ser	S140 S182 S223 S23 S247 S299 S306 S6
6	BAA02g40330	A02	34040800	C	T	missense_variant	MODERATE	c.1132G>A\|p.Gly378Ser	S217
7	BAA02g40330	A02	34040991	C	T	missense_variant	MODERATE	c.941G>A\|p.Gly314Asp	S112 S133
8	BAA02g40330	A02	34042221	G	A	upstream_gene_variant	MODIFIER	c.-180C>T\|	S297
9	BAA02g40330	A02	34042990	A	T	upstream_gene_variant	MODIFIER	c.-949T>A\|	S134
10	BAA02g40330	A02	34044580	C	T	upstream_gene_variant	MODIFIER	c.-2539G>A\|	S64
11	BAA02g40330	A02	34044974	G	A	upstream_gene_variant	MODIFIER	c.-2933C>T\|	S146
12	BAA02g40330	A02	34045094	G	A	upstream_gene_variant	MODIFIER	c.-3053C>T\|	S183
13	BAA02g40330	A02	34045398	G	A	upstream_gene_variant	MODIFIER	c.-3357C>T\|	S259
14	BAA02g40330	A02	34045899	C	T	upstream_gene_variant	MODIFIER	c.-3858G>A\|	S68
15	BAA02g40330	A02	34046247	G	A	upstream_gene_variant	MODIFIER	c.-4206C>T\|	S237
16	BAA02g40330	A02	34046891	C	T	upstream_gene_variant	MODIFIER	c.-4850G>A\|	S33
17	BAA02g40330	A02	34046945	C	T	upstream_gene_variant	MODIFIER	c.-4904G>A\|	S64