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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g07140	A01	3165248	C	T	missense_variant	MODERATE	c.3383G>A\|p.Gly1128Glu	S18
2	BAA01g07140	A01	3165449	C	T	splice_acceptor_variant&intron_variant	HIGH	c.3265-1G>A\|	S184
3	BAA01g07140	A01	3166539	C	T	stop_gained	HIGH	c.2849G>A\|p.Trp950*	S210
4	BAA01g07140	A01	3166779	G	A	missense_variant	MODERATE	c.2738C>T\|p.Thr913Ile	S116
5	BAA01g07140	A01	3167062	C	T	splice_region_variant&intron_variant	LOW	c.2661+7G>A\|	S113
6	BAA01g07140	A01	3167804	C	T	synonymous_variant	LOW	c.2490G>A\|p.Glu830Glu	S305
7	BAA01g07140	A01	3167836	C	T	missense_variant	MODERATE	c.2458G>A\|p.Asp820Asn	S256
8	BAA01g07140	A01	3168555	G	A	missense_variant	MODERATE	c.2177C>T\|p.Ala726Val	S201
9	BAA01g07140	A01	3169640	G	A	synonymous_variant	LOW	c.1354C>T\|p.Leu452Leu	S15 S153 S156 S2 S213 S3 S4 S6
10	BAA01g07140	A01	3169859	C	T	missense_variant	MODERATE	c.1250G>A\|p.Gly417Asp	S242
11	BAA01g07140	A01	3170218	G	A	missense_variant	MODERATE	c.968C>T\|p.Ser323Phe	S284
12	BAA01g07140	A01	3171080	C	T	missense_variant	MODERATE	c.173G>A\|p.Arg58Lys	S267
13	BAA01g07140	A01	3171099	C	T	missense_variant	MODERATE	c.154G>A\|p.Val52Ile	S25
14	BAA01g07140	A01	3176153	C	T	upstream_gene_variant	MODIFIER	c.-4768G>A\|	S187