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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA07g01470	A07	1026702	C	T	splice_acceptor_variant&intron_variant	HIGH	c.1297-1G>A\|	S79 S84
2	BAA07g01470	A07	1027255	G	A	synonymous_variant	LOW	c.1110C>T\|p.Cys370Cys	S40 S49
3	BAA07g01470	A07	1027523	G	A	synonymous_variant	LOW	c.1002C>T\|p.Tyr334Tyr	S140
4	BAA07g01470	A07	1029125	C	T	missense_variant	MODERATE	c.232G>A\|p.Gly78Ser	S13 S140 S219 S278 S72
5	BAA07g01470	A07	1029279	C	T	synonymous_variant	LOW	c.78G>A\|p.Arg26Arg	S261 S274 S303
6	BAA07g01470	A07	1029308	C	T	missense_variant	MODERATE	c.49G>A\|p.Gly17Ser	S103
7	BAA07g01470	A07	1029333	G	A	synonymous_variant	LOW	c.24C>T\|p.Gly8Gly	S262
8	BAA07g01470	A07	1029344	C	T	missense_variant	MODERATE	c.13G>A\|p.Asp5Asn	S79 S84
9	BAA07g01470	A07	1029797	G	A	upstream_gene_variant	MODIFIER	c.-441C>T\|	S273