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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g42970	A01	28438437	C	T	downstream_gene_variant	MODIFIER	c.*398G>A\|	S210 S225
2	BAA01g42970	A01	28439298	G	A	missense_variant	MODERATE	c.2813C>T\|p.Pro938Leu	S292
3	BAA01g42970	A01	28439463	G	A	missense_variant	MODERATE	c.2648C>T\|p.Pro883Leu	S67
4	BAA01g42970	A01	28439771	C	T	intron_variant	MODIFIER	c.2612-272G>A\|	S260
5	BAA01g42970	A01	28440053	G	A	intron_variant	MODIFIER	c.2611+488C>T\|	S294
6	BAA01g42970	A01	28442415	C	T	missense_variant	MODERATE	c.1103G>A\|p.Gly368Glu	S18
7	BAA01g42970	A01	28442742	G	A	missense_variant	MODERATE	c.776C>T\|p.Thr259Ile	S193
8	BAA01g42970	A01	28443331	C	T	intron_variant	MODIFIER	c.609+172G>A\|	S48
9	BAA01g42970	A01	28444336	G	A	upstream_gene_variant	MODIFIER	c.-225C>T\|	S234
10	BAA01g42970	A01	28444403	C	T	upstream_gene_variant	MODIFIER	c.-292G>A\|	S242
11	BAA01g42970	A01	28444456	C	T	upstream_gene_variant	MODIFIER	c.-345G>A\|	S266
12	BAA01g42970	A01	28445711	C	T	upstream_gene_variant	MODIFIER	c.-1600G>A\|	S136
13	BAA01g42970	A01	28445815	G	A	upstream_gene_variant	MODIFIER	c.-1704C>T\|	S153 S157 S167 S236 S257 S262 S263
14	BAA01g42970	A01	28446961	G	A	upstream_gene_variant	MODIFIER	c.-2850C>T\|	S262
15	BAA01g42970	A01	28448403	C	T	upstream_gene_variant	MODIFIER	c.-4292G>A\|	S275