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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g16820	A10	16459807	G	A	downstream_gene_variant	MODIFIER	c.*1164C>T\|	S9
2	BAA10g16820	A10	16460150	G	A	downstream_gene_variant	MODIFIER	c.*821C>T\|	S64
3	BAA10g16820	A10	16461870	C	T	missense_variant	MODERATE	c.811G>A\|p.Gly271Ser	S133
4	BAA10g16820	A10	16462171	G	A	missense_variant&splice_region_variant	MODERATE	c.665C>T\|p.Thr222Ile	S228
5	BAA10g16820	A10	16462381	G	A	missense_variant	MODERATE	c.532C>T\|p.Leu178Phe	S239 S33
6	BAA10g16820	A10	16463104	G	A	missense_variant	MODERATE	c.74C>T\|p.Ser25Phe	S289
7	BAA10g16820	A10	16464543	C	T	upstream_gene_variant	MODIFIER	c.-1366G>A\|	S51
8	BAA10g16820	A10	16465767	G	A	upstream_gene_variant	MODIFIER	c.-2590C>T\|	S166
9	BAA10g16820	A10	16465990	G	A	upstream_gene_variant	MODIFIER	c.-2813C>T\|	S261
10	BAA10g16820	A10	16466531	G	A	upstream_gene_variant	MODIFIER	c.-3354C>T\|	S208 S219
11	BAA10g16820	A10	16466975	A	T	upstream_gene_variant	MODIFIER	c.-3798T>A\|	S159 S165 S196 S20 S233 S245 S257 S287 S36 S41 S45 S67 S71 S73 S82
12	BAA10g16820	A10	16467537	C	T	upstream_gene_variant	MODIFIER	c.-4360G>A\|	S294
13	BAA10g16820	A10	16468066	C	T	upstream_gene_variant	MODIFIER	c.-4889G>A\|	S41