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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g37560	A02	32150884	G	A	upstream_gene_variant	MODIFIER	c.-314G>A\|	S286
2	BAA02g37560	A02	32151394	C	T	missense_variant	MODERATE	c.197C>T\|p.Thr66Met	S189
3	BAA02g37560	A02	32151743	C	T	synonymous_variant	LOW	c.546C>T\|p.Asn182Asn	S25 S264
4	BAA02g37560	A02	32152371	C	T	stop_gained	HIGH	c.1174C>T\|p.Gln392*	S208 S219
5	BAA02g37560	A02	32152391	C	T	synonymous_variant	LOW	c.1194C>T\|p.Leu398Leu	S19
6	BAA02g37560	A02	32152503	G	A	missense_variant	MODERATE	c.1306G>A\|p.Ala436Thr	S169
7	BAA02g37560	A02	32152689	C	T	intron_variant	MODIFIER	c.1455+37C>T\|	S1 S113 S117 S122 S161 S19 S228 S244 S251 S266 S289 S290 S297 S305 S65 S8 S9 S90
8	BAA02g37560	A02	32153614	C	T	downstream_gene_variant	MODIFIER	c.*738C>T\|	S249
9	BAA02g37560	A02	32153673	C	T	downstream_gene_variant	MODIFIER	c.*797C>T\|	S216
10	BAA02g37560	A02	32153674	C	T	downstream_gene_variant	MODIFIER	c.*798C>T\|	S259
11	BAA02g37560	A02	32155066	G	A	downstream_gene_variant	MODIFIER	c.*2190G>A\|	S196
12	BAA02g37560	A02	32155090	C	T	downstream_gene_variant	MODIFIER	c.*2214C>T\|	S303