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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g47100	A09	51551497	C	T	upstream_gene_variant	MODIFIER	c.-1789C>T\|	S100
2	BAA09g47100	A09	51551701	G	A	upstream_gene_variant	MODIFIER	c.-1585G>A\|	S308
3	BAA09g47100	A09	51551737	G	A	upstream_gene_variant	MODIFIER	c.-1549G>A\|	S233
4	BAA09g47100	A09	51552031	G	A	upstream_gene_variant	MODIFIER	c.-1255G>A\|	S134
5	BAA09g47100	A09	51552456	C	T	upstream_gene_variant	MODIFIER	c.-830C>T\|	S109
6	BAA09g47100	A09	51553408	C	T	synonymous_variant	LOW	c.123C>T\|p.Val41Val	S220 S238 S267 S91
7	BAA09g47100	A09	51553426	T	C	synonymous_variant	LOW	c.141T>C\|p.Ala47Ala	S220 S238 S267 S91
8	BAA09g47100	A09	51553439	C	T	synonymous_variant	LOW	c.154C>T\|p.Leu52Leu	S220 S238 S267 S91
9	BAA09g47100	A09	51553441	G	A	synonymous_variant	LOW	c.156G>A\|p.Leu52Leu	S220 S238 S267 S91
10	BAA09g47100	A09	51553481	A	T	missense_variant	MODERATE	c.196A>T\|p.Thr66Ser	S238 S267 S91
11	BAA09g47100	A09	51553488	G	C	missense_variant	MODERATE	c.203G>C\|p.Ser68Thr	S238 S267 S91
12	BAA09g47100	A09	51553490	A	G	missense_variant	MODERATE	c.205A>G\|p.Thr69Ala	S238 S267 S91
13	BAA09g47100	A09	51553491	C	A	missense_variant	MODERATE	c.206C>A\|p.Thr69Asn	S238 S267 S91
14	BAA09g47100	A09	51553498	C	T	synonymous_variant	LOW	c.213C>T\|p.Gly71Gly	S238 S267 S91
15	BAA09g47100	A09	51553504	T	A	synonymous_variant	LOW	c.219T>A\|p.Val73Val	S238 S267 S91
16	BAA09g47100	A09	51553507	C	T	synonymous_variant	LOW	c.222C>T\|p.Asp74Asp	S238 S267 S91
17	BAA09g47100	A09	51553513	T	C	synonymous_variant	LOW	c.228T>C\|p.Gly76Gly	S238 S267 S91
18	BAA09g47100	A09	51553522	T	A	synonymous_variant	LOW	c.237T>A\|p.Gly79Gly	S238 S267 S91
19	BAA09g47100	A09	51553528	A	C	synonymous_variant	LOW	c.243A>C\|p.Leu81Leu	S267 S91
20	BAA09g47100	A09	51553543	T	C	synonymous_variant	LOW	c.258T>C\|p.Ala86Ala	S267 S91
21	BAA09g47100	A09	51553552	C	T	synonymous_variant	LOW	c.267C>T\|p.Gly89Gly	S267 S91
22	BAA09g47100	A09	51553567	T	C	synonymous_variant	LOW	c.282T>C\|p.Leu94Leu	S267 S91

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