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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
84251	BAA01g44690	A01	29725227	C	T	upstream_gene_variant	MODIFIER	c.-572C>T\|	S255
84252	BAA01g44700	A01	29726205	G	A	upstream_gene_variant	MODIFIER	c.-1009G>A\|	S143
84253	BAA01g44700	A01	29727302	C	T	splice_region_variant&intron_variant	LOW	c.81+8C>T\|	S39
84254	BAA01g44710	A01	29729087	G	A	upstream_gene_variant	MODIFIER	c.-613G>A\|	S43
84255	BAA01g44710	A01	29729514	C	T	upstream_gene_variant	MODIFIER	c.-186C>T\|	S107
84256	BAA01g44710	A01	29730419	G	A	synonymous_variant	LOW	c.720G>A\|p.Gln240Gln	S95
84257	BAA01g44710	A01	29730435	C	T	missense_variant	MODERATE	c.736C>T\|p.Pro246Ser	S56
84258	BAA01g44720	A01	29737338	G	A	synonymous_variant	LOW	c.915C>T\|p.His305His	S189
84259	BAA01g44720	A01	29737411	C	T	missense_variant	MODERATE	c.842G>A\|p.Gly281Glu	S35
84260	BAA01g44720	A01	29737570	G	A	missense_variant	MODERATE	c.683C>T\|p.Ser228Phe	S20
84261	BAA01g44720	A01	29737795	C	T	missense_variant	MODERATE	c.458G>A\|p.Gly153Glu	S210 S225
84262	BAA01g44720	A01	29738917	C	T	upstream_gene_variant	MODIFIER	c.-665G>A\|	S264
84263	BAA01g44720	A01	29739351	C	T	upstream_gene_variant	MODIFIER	c.-1099G>A\|	S19
84264	BAA01g44720	A01	29742720	C	T	upstream_gene_variant	MODIFIER	c.-4468G>A\|	S233
84265	BAA01g44720	A01	29743235	C	T	upstream_gene_variant	MODIFIER	c.-4983G>A\|	S153 S213
84266	BAA01g44730	A01	29743389	G	A	upstream_gene_variant	MODIFIER	c.-2058C>T\|	S262
84267	BAA01g44730	A01	29744622	C	T	upstream_gene_variant	MODIFIER	c.-3291G>A\|	S275
84268	BAA01g44740	A01	29747144	C	T	missense_variant	MODERATE	c.1051C>T\|p.Pro351Ser	S183 S198
84269	BAA01g44740	A01	29747310	C	T	missense_variant	MODERATE	c.1217C>T\|p.Thr406Ile	S16
84270	BAA01g44740	A01	29747427	C	T	missense_variant	MODERATE	c.1334C>T\|p.Ala445Val	S74
84271	BAA01g44740	A01	29747566	C	T	synonymous_variant	LOW	c.1473C>T\|p.Phe491Phe	S166
84272	BAA01g44740	A01	29747581	G	A	synonymous_variant	LOW	c.1488G>A\|p.Lys496Lys	S283
84273	BAA01g44740	A01	29747629	G	A	synonymous_variant	LOW	c.1536G>A\|p.Gln512Gln	S5
84274	BAA01g44740	A01	29747648	G	A	missense_variant	MODERATE	c.1555G>A\|p.Val519Met	S95
84275	BAA01g44750	A01	29750277	G	A	missense_variant	MODERATE	c.506C>T\|p.Pro169Leu	S113 S115 S117 S120 S9

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