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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
145451	BAA10g29990	A10	22379669	C	T	upstream_gene_variant	MODIFIER	c.-4904G>A\|	S186 S301 S304
145452	BAA10g30010	A10	22379980	C	T	missense_variant	MODERATE	c.262C>T\|p.Arg88Cys	S174 S27
145453	BAA10g30010	A10	22380130	G	A	missense_variant	MODERATE	c.412G>A\|p.Ala138Thr	S256
145454	BAA10g30010	A10	22380869	C	T	missense_variant	MODERATE	c.659C>T\|p.Pro220Leu	S221
145455	BAA10g30020	A10	22382997	G	A	missense_variant	MODERATE	c.443G>A\|p.Arg148His	S209
145456	BAA10g30020	A10	22383240	G	A	missense_variant	MODERATE	c.686G>A\|p.Gly229Glu	S212
145457	BAA10g30040	A10	22383346	G	A	upstream_gene_variant	MODIFIER	c.-3594G>A\|	S100
145458	BAA10g30040	A10	22383541	C	T	upstream_gene_variant	MODIFIER	c.-3399C>T\|	S251
145459	BAA10g30040	A10	22384167	C	T	upstream_gene_variant	MODIFIER	c.-2773C>T\|	S136
145460	BAA10g30030	A10	22384674	C	T	missense_variant	MODERATE	c.1051G>A\|p.Glu351Lys	S281
145461	BAA10g30030	A10	22384988	C	T	missense_variant	MODERATE	c.797G>A\|p.Arg266Lys	S185
145462	BAA10g30030	A10	22385065	C	T	synonymous_variant	LOW	c.720G>A\|p.Ala240Ala	S25
145463	BAA10g30030	A10	22385646	G	A	missense_variant	MODERATE	c.139C>T\|p.Leu47Phe	S69
145464	BAA10g30030	A10	22385869	G	A	upstream_gene_variant	MODIFIER	c.-85C>T\|	S183 S198
145465	BAA10g30040	A10	22387011	C	T	synonymous_variant	LOW	c.72C>T\|p.Phe24Phe	S33
145466	BAA10g30040	A10	22387142	G	A	missense_variant	MODERATE	c.116G>A\|p.Arg39Lys	S180
145467	BAA10g30040	A10	22387798	G	A	splice_acceptor_variant&intron_variant	HIGH	c.617-1G>A\|	S151
145468	BAA10g30040	A10	22387916	C	T	missense_variant	MODERATE	c.734C>T\|p.Ala245Val	S296
145469	BAA10g30040	A10	22388086	C	T	synonymous_variant	LOW	c.904C>T\|p.Leu302Leu	S206 S26
145470	BAA10g30040	A10	22388447	C	T	missense_variant	MODERATE	c.1265C>T\|p.Pro422Leu	S174 S265 S39
145471	BAA10g30030	A10	22389091	C	T	upstream_gene_variant	MODIFIER	c.-3307G>A\|	S244
145472	BAA10g30050	A10	22391248	C	T	missense_variant	MODERATE	c.1697C>T\|p.Pro566Leu	S112
145473	BAA10g30060	A10	22391446	C	T	upstream_gene_variant	MODIFIER	c.-443C>T\|	S157
145474	BAA10g30060	A10	22391905	G	A	missense_variant	MODERATE	c.17G>A\|p.Arg6Gln	S246
145475	BAA10g30060	A10	22391989	C	T	splice_region_variant&intron_variant	LOW	c.97+4C>T\|	S143

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