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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g23190	A09	14643934	C	T	synonymous_variant	LOW	c.163C>T\|p.Leu55Leu	S144
2	BAA09g23190	A09	14644067	C	T	missense_variant	MODERATE	c.296C>T\|p.Pro99Leu	S159 S187 S188 S243 S276 S299
3	BAA09g23190	A09	14662317	G	A	intron_variant	MODIFIER	c.459-658G>A\|	S25 S264
4	BAA09g23190	A09	14662320	G	A	intron_variant	MODIFIER	c.459-655G>A\|	S152
5	BAA09g23190	A09	14662781	G	A	intron_variant	MODIFIER	c.459-194G>A\|	S166
6	BAA09g23190	A09	14663734	G	A	synonymous_variant	LOW	c.1218G>A\|p.Gln406Gln	S47
7	BAA09g23190	A09	14663776	G	A	synonymous_variant	LOW	c.1260G>A\|p.Lys420Lys	S15
8	BAA09g23190	A09	14664219	G	A	missense_variant	MODERATE	c.1580G>A\|p.Ser527Asn	S97
9	BAA09g23190	A09	14664451	G	A	synonymous_variant	LOW	c.1812G>A\|p.Lys604Lys	S308
10	BAA09g23190	A09	14666054	G	A	missense_variant	MODERATE	c.2482G>A\|p.Asp828Asn	S115