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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g00220	A10	97623	C	T	missense_variant	MODERATE	c.2794G>A\|p.Asp932Asn	S73 S91
2	BAA10g00220	A10	98499	C	T	missense_variant	MODERATE	c.2350G>A\|p.Glu784Lys	S266
3	BAA10g00220	A10	98750	C	T	splice_region_variant&intron_variant	LOW	c.2194-8G>A\|	S142
4	BAA10g00220	A10	99578	C	T	synonymous_variant	LOW	c.1854G>A\|p.Leu618Leu	S184
5	BAA10g00220	A10	100192	C	T	missense_variant	MODERATE	c.1567G>A\|p.Glu523Lys	S146
6	BAA10g00220	A10	100332	C	T	synonymous_variant	LOW	c.1509G>A\|p.Gln503Gln	S15 S2 S4 S6
7	BAA10g00220	A10	100356	C	T	synonymous_variant	LOW	c.1485G>A\|p.Lys495Lys	S294
8	BAA10g00220	A10	100410	C	T	synonymous_variant	LOW	c.1431G>A\|p.Leu477Leu	S173
9	BAA10g00220	A10	100949	C	T	missense_variant	MODERATE	c.995G>A\|p.Arg332Lys	S105 S106
10	BAA10g00220	A10	102974	G	A	upstream_gene_variant	MODIFIER	c.-1031C>T\|	S128