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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
29201	BAA01g20600	A01	10170710	C	T	downstream_gene_variant	MODIFIER	c.*2893G>A\|	S82 S92
29202	BAA01g20600	A01	10171521	C	T	downstream_gene_variant	MODIFIER	c.*2082G>A\|	S104 S52
29203	BAA01g20600	A01	10171550	G	A	downstream_gene_variant	MODIFIER	c.*2053C>T\|	S59
29204	BAA01g20600	A01	10172624	G	A	downstream_gene_variant	MODIFIER	c.*979C>T\|	S126
29205	BAA01g20600	A01	10172758	G	A	downstream_gene_variant	MODIFIER	c.*845C>T\|	S23
29206	BAA01g20600	A01	10174690	G	A	missense_variant	MODERATE	c.731C>T\|p.Pro244Leu	S209
29207	BAA01g20600	A01	10175303	G	A	missense_variant	MODERATE	c.118C>T\|p.Pro40Ser	S14
29208	BAA01g20610	A01	10178247	G	A	missense_variant	MODERATE	c.1652C>T\|p.Ser551Phe	S234
29209	BAA01g20610	A01	10178341	G	A	missense_variant	MODERATE	c.1558C>T\|p.Pro520Ser	S247
29210	BAA01g20610	A01	10178350	G	A	missense_variant	MODERATE	c.1549C>T\|p.Pro517Ser	S263
29211	BAA01g20610	A01	10178506	G	A	missense_variant	MODERATE	c.1393C>T\|p.Pro465Ser	S159 S243 S298 S299
29212	BAA01g20610	A01	10179097	G	A	missense_variant	MODERATE	c.802C>T\|p.Pro268Ser	S155 S211
29213	BAA01g20600	A01	10179915	C	T	upstream_gene_variant	MODIFIER	c.-4495G>A\|	S63
29214	BAA01g20600	A01	10180169	G	A	upstream_gene_variant	MODIFIER	c.-4749C>T\|	S1 S90
29215	BAA01g20610	A01	10183270	G	A	upstream_gene_variant	MODIFIER	c.-3372C>T\|	S251
29216	BAA01g20610	A01	10184289	G	A	upstream_gene_variant	MODIFIER	c.-4391C>T\|	S174 S216 S241 S39
29217	BAA01g20630	A01	10187040	C	T	downstream_gene_variant	MODIFIER	c.*946G>A\|	S85
29218	BAA01g20630	A01	10187229	C	T	downstream_gene_variant	MODIFIER	c.*757G>A\|	S51
29219	BAA01g20630	A01	10188486	G	A	missense_variant	MODERATE	c.1291C>T\|p.Pro431Ser	S178
29220	BAA01g20630	A01	10188536	G	A	missense_variant	MODERATE	c.1241C>T\|p.Ser414Leu	S257
29221	BAA01g20630	A01	10188702	C	T	missense_variant	MODERATE	c.1075G>A\|p.Val359Ile	S242
29222	BAA01g20630	A01	10188951	G	A	missense_variant	MODERATE	c.826C>T\|p.Pro276Ser	S28
29223	BAA01g20630	A01	10189392	G	A	missense_variant	MODERATE	c.385C>T\|p.Pro129Ser	S172 S217
29224	BAA01g20630	A01	10189906	C	T	upstream_gene_variant	MODIFIER	c.-130G>A\|	S294
29225	BAA01g20630	A01	10190618	C	T	upstream_gene_variant	MODIFIER	c.-842G>A\|	S272

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