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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g29850	A10	22308423	C	T	splice_region_variant&synonymous_variant	LOW	c.3267G>A\|p.Arg1089Arg	S6
2	BAA10g29850	A10	22308452	C	T	missense_variant	MODERATE	c.3238G>A\|p.Gly1080Arg	S92
3	BAA10g29850	A10	22309357	C	T	missense_variant	MODERATE	c.2885G>A\|p.Arg962Lys	S135
4	BAA10g29850	A10	22309571	C	T	missense_variant	MODERATE	c.2819G>A\|p.Gly940Glu	S225 S73
5	BAA10g29850	A10	22309811	G	A	missense_variant	MODERATE	c.2675C>T\|p.Pro892Leu	S160
6	BAA10g29850	A10	22310118	G	A	splice_region_variant&intron_variant	LOW	c.2562+8C>T\|	S284
7	BAA10g29850	A10	22311417	C	T	missense_variant	MODERATE	c.1918G>A\|p.Val640Ile	S211 S227
8	BAA10g29850	A10	22312045	C	T	missense_variant	MODERATE	c.1583G>A\|p.Arg528Lys	S281
9	BAA10g29850	A10	22312065	A	T	synonymous_variant	LOW	c.1563T>A\|p.Pro521Pro	S225 S270 S278 S291 S36 S59 S61 S98
10	BAA10g29850	A10	22312259	C	T	splice_region_variant&intron_variant	LOW	c.1466+8G>A\|	S38
11	BAA10g29850	A10	22313041	C	T	missense_variant	MODERATE	c.925G>A\|p.Glu309Lys	S87
12	BAA10g29850	A10	22313182	C	T	missense_variant	MODERATE	c.784G>A\|p.Asp262Asn	S42
13	BAA10g29850	A10	22314580	G	A	upstream_gene_variant	MODIFIER	c.-329C>T\|	S256