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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g17420	A10	16751856	G	A	missense_variant	MODERATE	c.31G>A\|p.Gly11Ser	S166
2	BAA10g17420	A10	16755330	G	T	stop_gained	HIGH	c.544G>T\|p.Glu182*	S176 S209 S228 S282 S93
3	BAA10g17420	A10	16757313	G	A	intron_variant	MODIFIER	c.1531+197G>A\|	S178
4	BAA10g17420	A10	16757578	C	T	intron_variant	MODIFIER	c.1532-44C>T\|	S78 S83
5	BAA10g17420	A10	16758746	G	A	downstream_gene_variant	MODIFIER	c.*835G>A\|	S178
6	BAA10g17420	A10	16759478	G	A	downstream_gene_variant	MODIFIER	c.*1567G>A\|	S155 S211
7	BAA10g17420	A10	16760421	C	T	downstream_gene_variant	MODIFIER	c.*2510C>T\|	S235
8	BAA10g17420	A10	16760467	C	T	downstream_gene_variant	MODIFIER	c.*2556C>T\|	S281
9	BAA10g17420	A10	16760796	G	A	downstream_gene_variant	MODIFIER	c.*2885G>A\|	S159 S187 S188 S243 S276 S299
10	BAA10g17420	A10	16760999	C	T	downstream_gene_variant	MODIFIER	c.*3088C>T\|	S257
11	BAA10g17420	A10	16761596	G	A	downstream_gene_variant	MODIFIER	c.*3685G>A\|	S192 S243
12	BAA10g17420	A10	16761620	C	T	downstream_gene_variant	MODIFIER	c.*3709C>T\|	S48
13	BAA10g17420	A10	16761696	C	T	downstream_gene_variant	MODIFIER	c.*3785C>T\|	S243