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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
14201	BAA01g11040	A01	5098011	C	T	missense_variant	MODERATE	c.1318C>T\|p.Arg440Cys	S155 S211
14202	BAA01g11040	A01	5099078	G	A	synonymous_variant	LOW	c.1593G>A\|p.Lys531Lys	S257
14203	BAA01g11060	A01	5099440	C	T	upstream_gene_variant	MODIFIER	c.-2025C>T\|	S148 S30 S31
14204	BAA01g11060	A01	5099539	C	T	upstream_gene_variant	MODIFIER	c.-1926C>T\|	S269
14205	BAA01g11050	A01	5100869	G	A	upstream_gene_variant	MODIFIER	c.-396C>T\|	S122 S127
14206	BAA01g11050	A01	5101248	G	A	upstream_gene_variant	MODIFIER	c.-775C>T\|	S103
14207	BAA01g11050	A01	5101338	G	A	upstream_gene_variant	MODIFIER	c.-865C>T\|	S15
14208	BAA01g11060	A01	5101823	G	A	missense_variant	MODERATE	c.262G>A\|p.Gly88Arg	S157 S163
14209	BAA01g11050	A01	5102109	G	A	upstream_gene_variant	MODIFIER	c.-1636C>T\|	S195
14210	BAA01g11050	A01	5103781	G	A	upstream_gene_variant	MODIFIER	c.-3308C>T\|	S10
14211	BAA01g11050	A01	5103821	C	T	upstream_gene_variant	MODIFIER	c.-3348G>A\|	S165 S211
14212	BAA01g11050	A01	5103929	G	A	upstream_gene_variant	MODIFIER	c.-3456C>T\|	S156
14213	BAA01g11080	A01	5104387	G	A	synonymous_variant	LOW	c.177G>A\|p.Ala59Ala	S165
14214	BAA01g11080	A01	5104710	T	A	missense_variant	MODERATE	c.500T>A\|p.Val167Asp	S209
14215	BAA01g11050	A01	5104957	C	T	upstream_gene_variant	MODIFIER	c.-4484G>A\|	S164
14216	BAA01g11050	A01	5105132	G	A	upstream_gene_variant	MODIFIER	c.-4659C>T\|	S110
14217	BAA01g11090	A01	5105258	C	T	missense_variant	MODERATE	c.6704G>A\|p.Arg2235Lys	S4
14218	BAA01g11090	A01	5105888	C	T	missense_variant	MODERATE	c.6074G>A\|p.Gly2025Glu	S13 S168 S278 S279 S64
14219	BAA01g11090	A01	5106795	G	A	missense_variant	MODERATE	c.5167C>T\|p.Pro1723Ser	S157 S163
14220	BAA01g11090	A01	5109139	G	A	synonymous_variant	LOW	c.2823C>T\|p.Ala941Ala	S183 S198
14221	BAA01g11090	A01	5110328	G	A	missense_variant	MODERATE	c.1634C>T\|p.Pro545Leu	S256
14222	BAA01g11090	A01	5110769	C	T	missense_variant	MODERATE	c.1193G>A\|p.Arg398Lys	S107
14223	BAA01g11090	A01	5110980	G	A	stop_gained	HIGH	c.982C>T\|p.Gln328*	S159 S188 S243 S276 S298 S299
14224	BAA01g11090	A01	5111096	C	T	missense_variant	MODERATE	c.866G>A\|p.Gly289Asp	S150
14225	BAA01g11090	A01	5111704	G	A	synonymous_variant	LOW	c.525C>T\|p.Asn175Asn	S236

Users can query the SNP information according to the gene ID.