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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
128801	BAA10g16840	A10	16479241	C	T	upstream_gene_variant	MODIFIER	c.-113C>T\|	S256
128802	BAA10g16840	A10	16479440	G	A	synonymous_variant	LOW	c.87G>A\|p.Gln29Gln	S205
128803	BAA10g16840	A10	16479866	C	T	synonymous_variant	LOW	c.513C>T\|p.Val171Val	S149
128804	BAA10g16840	A10	16480200	C	T	missense_variant	MODERATE	c.847C>T\|p.Leu283Phe	S68
128805	BAA10g16840	A10	16480405	G	A	missense_variant	MODERATE	c.1052G>A\|p.Gly351Glu	S205
128806	BAA10g16840	A10	16480933	G	A	missense_variant	MODERATE	c.1580G>A\|p.Gly527Glu	S203
128807	BAA10g16850	A10	16482857	C	T	stop_gained	HIGH	c.828G>A\|p.Trp276*	S203
128808	BAA10g16850	A10	16484899	G	A	upstream_gene_variant	MODIFIER	c.-575C>T\|	S245
128809	BAA10g16860	A10	16485974	G	A	missense_variant	MODERATE	c.179C>T\|p.Ser60Phe	S167
128810	BAA10g16860	A10	16486165	C	T	splice_donor_variant&intron_variant	HIGH	c.123+1G>A\|	S281
128811	BAA10g16860	A10	16486267	C	T	missense_variant	MODERATE	c.22G>A\|p.Asp8Asn	S144
128812	BAA10g16850	A10	16487403	G	A	upstream_gene_variant	MODIFIER	c.-3079C>T\|	S36
128813	BAA10g16850	A10	16488995	A	C	upstream_gene_variant	MODIFIER	c.-4671T>G\|	S116 S13 S130 S150 S174 S206 S221 S228 S237 S251 S287 S50 S64 S66 S74 S87 S91
128814	BAA10g16860	A10	16491039	G	A	upstream_gene_variant	MODIFIER	c.-4751C>T\|	S34
128815	BAA10g16860-BAA10g16870	A10	16491439	G	C	intergenic_region	MODIFIER	n.16491439G>C\|	S148 S210 S30 S31
128816	BAA10g16860-BAA10g16870	A10	16492816	C	T	intergenic_region	MODIFIER	n.16492816C>T\|	S47
128817	BAA10g16860-BAA10g16870	A10	16494461	C	T	intergenic_region	MODIFIER	n.16494461C>T\|	S18
128818	BAA10g16860-BAA10g16870	A10	16494499	G	A	intergenic_region	MODIFIER	n.16494499G>A\|	S241
128819	BAA10g16860-BAA10g16870	A10	16494795	C	T	intergenic_region	MODIFIER	n.16494795C>T\|	S256
128820	BAA10g16860-BAA10g16870	A10	16496469	C	T	intergenic_region	MODIFIER	n.16496469C>T\|	S112
128821	BAA10g16860-BAA10g16870	A10	16496620	G	A	intergenic_region	MODIFIER	n.16496620G>A\|	S176
128822	BAA10g16870	A10	16498997	C	T	upstream_gene_variant	MODIFIER	c.-4621C>T\|	S150
128823	BAA10g16870	A10	16501293	G	A	upstream_gene_variant	MODIFIER	c.-2325G>A\|	S234
128824	BAA10g16870	A10	16501436	G	A	upstream_gene_variant	MODIFIER	c.-2182G>A\|	S148 S210 S30 S31
128825	BAA10g16870	A10	16501490	C	T	upstream_gene_variant	MODIFIER	c.-2128C>T\|	S123

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