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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
24701	BAA01g17860	A01	8689177	C	T	downstream_gene_variant	MODIFIER	c.*3241G>A\|	S259
24702	BAA01g17860	A01	8689299	G	A	downstream_gene_variant	MODIFIER	c.*3119C>T\|	S275
24703	BAA01g17870	A01	8690898	C	T	upstream_gene_variant	MODIFIER	c.-3699C>T\|	S136 S186 S275 S301 S304
24704	BAA01g17870	A01	8690979	G	A	upstream_gene_variant	MODIFIER	c.-3618G>A\|	S94
24705	BAA01g17870	A01	8692057	G	A	upstream_gene_variant	MODIFIER	c.-2540G>A\|	S47
24706	BAA01g17870	A01	8692070	C	T	upstream_gene_variant	MODIFIER	c.-2527C>T\|	S4
24707	BAA01g17860	A01	8692525	C	T	missense_variant	MODERATE	c.220G>A\|p.Glu74Lys	S289 S290
24708	BAA01g17860	A01	8693079	C	T	upstream_gene_variant	MODIFIER	c.-170G>A\|	S210 S225
24709	BAA01g17860	A01	8693399	C	T	upstream_gene_variant	MODIFIER	c.-490G>A\|	S134
24710	BAA01g17860	A01	8695587	C	T	upstream_gene_variant	MODIFIER	c.-2678G>A\|	S117
24711	BAA01g17860	A01	8695693	G	A	upstream_gene_variant	MODIFIER	c.-2784C>T\|	S275
24712	BAA01g17870	A01	8696417	G	A	missense_variant	MODERATE	c.638G>A\|p.Arg213Gln	S190
24713	BAA01g17880	A01	8697995	G	A	upstream_gene_variant	MODIFIER	c.-3344G>A\|	S187
24714	BAA01g17870	A01	8698759	C	T	missense_variant	MODERATE	c.2309C>T\|p.Ser770Phe	S160
24715	BAA01g17870	A01	8700003	C	T	missense_variant	MODERATE	c.3346C>T\|p.Pro1116Ser	S82 S92
24716	BAA01g17870	A01	8700253	G	A	missense_variant	MODERATE	c.3517G>A\|p.Asp1173Asn	S207
24717	BAA01g17880	A01	8701529	G	A	splice_region_variant&intron_variant	LOW	c.186+5G>A\|	S138
24718	BAA01g17880	A01	8701937	G	A	splice_region_variant&intron_variant	LOW	c.351+5G>A\|	S203
24719	BAA01g17880	A01	8702529	G	A	missense_variant	MODERATE	c.538G>A\|p.Ala180Thr	S240
24720	BAA01g17890	A01	8702597	G	A	upstream_gene_variant	MODIFIER	c.-3774G>A\|	S172 S217
24721	BAA01g17880	A01	8703133	C	T	splice_region_variant&intron_variant	LOW	c.646-3C>T\|	S215
24722	BAA01g17880	A01	8703190	G	A	missense_variant	MODERATE	c.700G>A\|p.Asp234Asn	S278
24723	BAA01g17890	A01	8703499	C	T	upstream_gene_variant	MODIFIER	c.-2872C>T\|	S166
24724	BAA01g17890	A01	8703700	G	A	upstream_gene_variant	MODIFIER	c.-2671G>A\|	S95
24725	BAA01g17880	A01	8704292	G	A	missense_variant	MODERATE	c.1204G>A\|p.Ala402Thr	S207

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