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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA07g00570	A07	287774	C	T	synonymous_variant	LOW	c.744C>T\|p.Asn248Asn	S173
2	BAA07g00570	A07	288158	G	A	synonymous_variant	LOW	c.1020G>A\|p.Glu340Glu	S204
3	BAA07g00570	A07	288219	C	T	missense_variant	MODERATE	c.1081C>T\|p.Arg361Cys	S70
4	BAA07g00570	A07	288267	C	T	synonymous_variant	LOW	c.1129C>T\|p.Leu377Leu	S18
5	BAA07g00570	A07	288595	G	A	missense_variant	MODERATE	c.1346G>A\|p.Gly449Glu	S209
6	BAA07g00570	A07	289270	G	A	missense_variant	MODERATE	c.1915G>A\|p.Glu639Lys	S122
7	BAA07g00570	A07	289457	C	T	missense_variant	MODERATE	c.2102C>T\|p.Ser701Leu	S41
8	BAA07g00570	A07	289564	G	A	missense_variant	MODERATE	c.2209G>A\|p.Gly737Ser	S159 S243 S299
9	BAA07g00570	A07	291315	G	A	downstream_gene_variant	MODIFIER	c.*1737G>A\|	S210
10	BAA07g00570	A07	291716	T	G	downstream_gene_variant	MODIFIER	c.*2138T>G\|	S123 S126 S166 S182 S241 S258 S292 S301 S47
11	BAA07g00570	A07	292084	G	A	downstream_gene_variant	MODIFIER	c.*2506G>A\|	S223
12	BAA07g00570	A07	293606	G	A	downstream_gene_variant	MODIFIER	c.*4028G>A\|	S125 S56
13	BAA07g00570	A07	294011	C	T	downstream_gene_variant	MODIFIER	c.*4433C>T\|	S114
14	BAA07g00570	A07	294024	G	A	downstream_gene_variant	MODIFIER	c.*4446G>A\|	S89
15	BAA07g00570	A07	294116	C	T	downstream_gene_variant	MODIFIER	c.*4538C>T\|	S104 S52
16	BAA07g00570	A07	294307	C	T	downstream_gene_variant	MODIFIER	c.*4729C>T\|	S298