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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA07g07630	A07	16852909	A	G	missense_variant	MODERATE	c.3496T>C\|p.Cys1166Arg	S135
2	BAA07g07630	A07	16855693	G	A	intron_variant	MODIFIER	c.2265+39C>T\|	S237
3	BAA07g07630	A07	16855836	C	G	missense_variant&splice_region_variant	MODERATE	c.2161G>C\|p.Glu721Gln	S13 S140 S143 S164 S168 S173 S208 S219 S230 S278 S279 S302 S306 S308 S63 S72 S78
4	BAA07g07630	A07	16855909	C	T	intron_variant	MODIFIER	c.2161-73G>A\|	S20
5	BAA07g07630	A07	16855968	G	A	intron_variant	MODIFIER	c.2160+51C>T\|	S264
6	BAA07g07630	A07	16855972	C	T	intron_variant	MODIFIER	c.2160+47G>A\|	S296
7	BAA07g07630	A07	16856943	C	T	intron_variant	MODIFIER	c.1565-64G>A\|	S249
8	BAA07g07630	A07	16857301	C	T	synonymous_variant	LOW	c.1356G>A\|p.Leu452Leu	S262
9	BAA07g07630	A07	16857566	G	A	intron_variant	MODIFIER	c.1332+49C>T\|	S283
10	BAA07g07630	A07	16857885	C	T	intron_variant	MODIFIER	c.1227+17G>A\|	S187
11	BAA07g07630	A07	16858466	G	A	missense_variant	MODERATE	c.928C>T\|p.Leu310Phe	S251
12	BAA07g07630	A07	16858896	G	A	intron_variant	MODIFIER	c.561+37C>T\|	S265 S27 S39
13	BAA07g07630	A07	16859109	G	A	synonymous_variant	LOW	c.385C>T\|p.Leu129Leu	S106
14	BAA07g07630	A07	16860250	C	T	upstream_gene_variant	MODIFIER	c.-476G>A\|	S97
15	BAA07g07630	A07	16863375	G	A	upstream_gene_variant	MODIFIER	c.-3601C>T\|	S110
16	BAA07g07630	A07	16863642	G	A	upstream_gene_variant	MODIFIER	c.-3868C>T\|	S211 S227
17	BAA07g07630	A07	16864675	C	T	upstream_gene_variant	MODIFIER	c.-4901G>A\|	S242