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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g00770	A10	363581	C	T	missense_variant	MODERATE	c.29C>T\|p.Pro10Leu	S277
2	BAA10g00770	A10	366172	C	T	intron_variant	MODIFIER	c.253-1090C>T\|	S113
3	BAA10g00770	A10	366730	C	T	intron_variant	MODIFIER	c.253-532C>T\|	S155 S211
4	BAA10g00770	A10	366939	G	A	intron_variant	MODIFIER	c.253-323G>A\|	S95
5	BAA10g00770	A10	367048	C	T	intron_variant	MODIFIER	c.253-214C>T\|	S159 S243 S299
6	BAA10g00770	A10	367417	G	A	intron_variant	MODIFIER	c.325-73G>A\|	S15 S3
7	BAA10g00770	A10	367907	C	T	missense_variant	MODERATE	c.526C>T\|p.Leu176Phe	S98
8	BAA10g00770	A10	368448	G	A	splice_region_variant&intron_variant	LOW	c.783+5G>A\|	S158
9	BAA10g00770	A10	368851	C	T	synonymous_variant	LOW	c.969C>T\|p.Ile323Ile	S157