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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
139901	BAA10g25090	A10	20418000	C	T	synonymous_variant	LOW	c.952C>T\|p.Leu318Leu	S189
139902	BAA10g25090	A10	20420931	G	A	missense_variant	MODERATE	c.2731G>A\|p.Glu911Lys	S71
139903	BAA10g25090	A10	20421014	C	T	synonymous_variant	LOW	c.2814C>T\|p.Phe938Phe	S244
139904	BAA10g25090	A10	20422277	G	A	downstream_gene_variant	MODIFIER	c.*1063G>A\|	S289 S290
139905	BAA10g25100	A10	20422706	G	A	upstream_gene_variant	MODIFIER	c.-4611G>A\|	S202
139906	BAA10g25100	A10	20424224	G	A	upstream_gene_variant	MODIFIER	c.-3093G>A\|	S278
139907	BAA10g25100	A10	20424404	G	A	upstream_gene_variant	MODIFIER	c.-2913G>A\|	S28
139908	BAA10g25100	A10	20424702	G	A	upstream_gene_variant	MODIFIER	c.-2615G>A\|	S179
139909	BAA10g25100	A10	20424905	G	T	upstream_gene_variant	MODIFIER	c.-2412G>T\|	S177
139910	BAA10g25100	A10	20424988	G	A	upstream_gene_variant	MODIFIER	c.-2329G>A\|	S25
139911	BAA10g25100	A10	20427343	G	A	synonymous_variant	LOW	c.27G>A\|p.Gln9Gln	S28
139912	BAA10g25100	A10	20427963	G	A	intron_variant	MODIFIER	c.446+37G>A\|	S293
139913	BAA10g25100	A10	20428078	G	A	splice_donor_variant&intron_variant	HIGH	c.518+1G>A\|	S273
139914	BAA10g25110	A10	20428595	T	G	downstream_gene_variant	MODIFIER	c.*4428A>C\|	S119 S142 S20 S306 S67
139915	BAA10g25100	A10	20430230	C	T	downstream_gene_variant	MODIFIER	c.*206C>T\|	S133
139916	BAA10g25100	A10	20432493	G	A	downstream_gene_variant	MODIFIER	c.*2469G>A\|	S94
139917	BAA10g25100	A10	20433504	G	A	downstream_gene_variant	MODIFIER	c.*3480G>A\|	S151 S167 S236 S257 S262 S263
139918	BAA10g25110	A10	20433575	G	A	missense_variant	MODERATE	c.1292C>T\|p.Ser431Leu	S84 S93
139919	BAA10g25110	A10	20433646	C	T	synonymous_variant	LOW	c.1221G>A\|p.Ala407Ala	S162
139920	BAA10g25100	A10	20434036	G	A	downstream_gene_variant	MODIFIER	c.*4012G>A\|	S219 S72
139921	BAA10g25110	A10	20435695	T	A	synonymous_variant	LOW	c.762A>T\|p.Leu254Leu	S242
139922	BAA10g25120	A10	20437173	C	T	synonymous_variant	LOW	c.1071G>A\|p.Ser357Ser	S165
139923	BAA10g25120	A10	20437477	C	T	missense_variant	MODERATE	c.767G>A\|p.Ser256Asn	S133
139924	BAA10g25120	A10	20437888	C	T	missense_variant	MODERATE	c.356G>A\|p.Ser119Asn	S169
139925	BAA10g25120	A10	20438617	C	T	synonymous_variant	LOW	c.27G>A\|p.Lys9Lys	S10

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