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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
147001	BAA10g31430	A10	22930907	G	A	upstream_gene_variant	MODIFIER	c.-32C>T\|	S278
147002	BAA10g31430	A10	22930915	C	T	upstream_gene_variant	MODIFIER	c.-40G>A\|	S1 S228 S244
147003	BAA10g31430	A10	22930952	G	C	upstream_gene_variant	MODIFIER	c.-77C>G\|	S105
147004	BAA10g31430	A10	22932806	C	T	upstream_gene_variant	MODIFIER	c.-1931G>A\|	S148 S210 S30 S31
147005	BAA10g31430	A10	22933309	C	T	upstream_gene_variant	MODIFIER	c.-2434G>A\|	S91
147006	BAA10g31440	A10	22933366	G	A	splice_region_variant&intron_variant	LOW	c.2883+7C>T\|	S118
147007	BAA10g31440	A10	22933715	C	T	missense_variant	MODERATE	c.2635G>A\|p.Glu879Lys	S246
147008	BAA10g31440	A10	22937025	G	A	missense_variant	MODERATE	c.1300C>T\|p.Pro434Ser	S70
147009	BAA10g31440	A10	22937610	C	T	splice_region_variant&intron_variant	LOW	c.985-4G>A\|	S45
147010	BAA10g31450	A10	22938676	G	A	downstream_gene_variant	MODIFIER	c.*4827C>T\|	S240
147011	BAA10g31450	A10	22938773	C	T	downstream_gene_variant	MODIFIER	c.*4730G>A\|	S78 S83
147012	BAA10g31440	A10	22938888	C	T	stop_gained	HIGH	c.711G>A\|p.Trp237*	S160
147013	BAA10g31440	A10	22940234	G	A	missense_variant	MODERATE	c.325C>T\|p.Arg109Trp	S35
147014	BAA10g31450	A10	22940363	C	T	downstream_gene_variant	MODIFIER	c.*3140G>A\|	S243
147015	BAA10g31440	A10	22940633	C	T	missense_variant	MODERATE	c.25G>A\|p.Ala9Thr	S148 S210 S30 S31
147016	BAA10g31440	A10	22940859	C	T	upstream_gene_variant	MODIFIER	c.-202G>A\|	S190
147017	BAA10g31440	A10	22941014	G	C	upstream_gene_variant	MODIFIER	c.-357C>G\|	S138 S172 S187 S194 S275 S293 S43 S53 S56 S61 S86
147018	BAA10g31440	A10	22943359	G	A	upstream_gene_variant	MODIFIER	c.-2702C>T\|	S219 S72
147019	BAA10g31440	A10	22943425	G	A	upstream_gene_variant	MODIFIER	c.-2768C>T\|	S241
147020	BAA10g31450	A10	22944317	G	A	missense_variant	MODERATE	c.683C>T\|p.Pro228Leu	S203
147021	BAA10g31450	A10	22944411	C	T	missense_variant	MODERATE	c.589G>A\|p.Val197Ile	S144
147022	BAA10g31450	A10	22945343	C	T	synonymous_variant	LOW	c.60G>A\|p.Leu20Leu	S279
147023	BAA10g31440	A10	22945423	G	A	upstream_gene_variant	MODIFIER	c.-4766C>T\|	S71
147024	BAA10g31450	A10	22945801	G	A	upstream_gene_variant	MODIFIER	c.-399C>T\|	S179
147025	BAA10g31450	A10	22946189	C	T	upstream_gene_variant	MODIFIER	c.-787G>A\|	S44

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