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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
148151	BAA10g32560	A10	23356078	C	T	missense_variant	MODERATE	c.238C>T\|p.Pro80Ser	S23
148152	BAA10g32560	A10	23356894	G	A	missense_variant	MODERATE	c.695G>A\|p.Arg232Lys	S191
148153	BAA10g32560	A10	23357158	C	T	missense_variant	MODERATE	c.877C>T\|p.Leu293Phe	S10
148154	BAA10g32560	A10	23362103	G	A	downstream_gene_variant	MODIFIER	c.*4286G>A\|	S85
148155	BAA10g32570	A10	23363627	G	A	downstream_gene_variant	MODIFIER	c.*4892C>T\|	S70
148156	BAA10g32570	A10	23363659	G	A	downstream_gene_variant	MODIFIER	c.*4860C>T\|	S15 S156 S2 S3 S34 S4 S6
148157	BAA10g32570	A10	23365245	G	A	downstream_gene_variant	MODIFIER	c.*3274C>T\|	S4
148158	BAA10g32570	A10	23366794	C	T	downstream_gene_variant	MODIFIER	c.*1725G>A\|	S247
148159	BAA10g32570	A10	23366859	C	T	downstream_gene_variant	MODIFIER	c.*1660G>A\|	S302
148160	BAA10g32570	A10	23367232	C	T	downstream_gene_variant	MODIFIER	c.*1287G>A\|	S277
148161	BAA10g32570	A10	23367418	G	A	downstream_gene_variant	MODIFIER	c.*1101C>T\|	S270
148162	BAA10g32580	A10	23368153	G	A	upstream_gene_variant	MODIFIER	c.-4977G>A\|	S157 S166 S257
148163	BAA10g32580	A10	23373277	C	T	synonymous_variant	LOW	c.54C>T\|p.Val18Val	S268
148164	BAA10g32600	A10	23375074	C	T	upstream_gene_variant	MODIFIER	c.-4505C>T\|	S204
148165	BAA10g32590	A10	23375424	C	T	stop_gained	HIGH	c.888G>A\|p.Trp296*	S148 S30 S31
148166	BAA10g32590	A10	23375536	G	A	missense_variant	MODERATE	c.776C>T\|p.Ser259Phe	S57
148167	BAA10g32600	A10	23376351	G	A	upstream_gene_variant	MODIFIER	c.-3228G>A\|	S278
148168	BAA10g32590	A10	23377242	C	T	upstream_gene_variant	MODIFIER	c.-309G>A\|	S166
148169	BAA10g32590	A10	23379299	C	T	upstream_gene_variant	MODIFIER	c.-2366G>A\|	S232
148170	BAA10g32600	A10	23379933	G	A	missense_variant	MODERATE	c.118G>A\|p.Glu40Lys	S109
148171	BAA10g32590	A10	23380114	C	T	upstream_gene_variant	MODIFIER	c.-3181G>A\|	S190
148172	BAA10g32600	A10	23380398	G	A	missense_variant	MODERATE	c.220G>A\|p.Asp74Asn	S43
148173	BAA10g32600	A10	23380542	G	A	splice_acceptor_variant&intron_variant	HIGH	c.279-1G>A\|	S32
148174	BAA10g32600	A10	23380913	C	T	synonymous_variant	LOW	c.459C>T\|p.Leu153Leu	S112
148175	BAA10g32600	A10	23382100	G	A	downstream_gene_variant	MODIFIER	c.*910G>A\|	S139

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