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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA07g05740	A07	6375413	G	A	downstream_gene_variant	MODIFIER	c.*4652C>T\|	S198
2	BAA07g05740	A07	6375471	C	T	downstream_gene_variant	MODIFIER	c.*4594G>A\|	S33
3	BAA07g05740	A07	6375474	C	T	downstream_gene_variant	MODIFIER	c.*4591G>A\|	S110
4	BAA07g05740	A07	6376314	G	A	downstream_gene_variant	MODIFIER	c.*3751C>T\|	S161
5	BAA07g05740	A07	6376782	C	T	downstream_gene_variant	MODIFIER	c.*3283G>A\|	S291
6	BAA07g05740	A07	6376872	C	T	downstream_gene_variant	MODIFIER	c.*3193G>A\|	S142 S288
7	BAA07g05740	A07	6376960	C	T	downstream_gene_variant	MODIFIER	c.*3105G>A\|	S62
8	BAA07g05740	A07	6377249	G	A	downstream_gene_variant	MODIFIER	c.*2816C>T\|	S150
9	BAA07g05740	A07	6377578	G	A	downstream_gene_variant	MODIFIER	c.*2487C>T\|	S32
10	BAA07g05740	A07	6378687	T	G	downstream_gene_variant	MODIFIER	c.*1378A>C\|	S105 S15 S156 S160 S201 S209 S225 S251 S256 S28 S290 S296 S40 S72 S77 S81
11	BAA07g05740	A07	6378979	C	T	downstream_gene_variant	MODIFIER	c.*1086G>A\|	S92
12	BAA07g05740	A07	6379209	G	A	downstream_gene_variant	MODIFIER	c.*856C>T\|	S15 S156 S3 S4 S6
13	BAA07g05740	A07	6379322	G	A	downstream_gene_variant	MODIFIER	c.*743C>T\|	S249
14	BAA07g05740	A07	6379514	G	A	downstream_gene_variant	MODIFIER	c.*551C>T\|	S52
15	BAA07g05740	A07	6380083	C	T	synonymous_variant	LOW	c.3168G>A\|p.Gln1056Gln	S308
16	BAA07g05740	A07	6380095	C	T	synonymous_variant	LOW	c.3156G>A\|p.Lys1052Lys	S208 S219
17	BAA07g05740	A07	6380159	C	T	missense_variant	MODERATE	c.3092G>A\|p.Gly1031Glu	S182
18	BAA07g05740	A07	6380203	C	T	synonymous_variant	LOW	c.3048G>A\|p.Lys1016Lys	S184
19	BAA07g05740	A07	6380768	G	A	missense_variant	MODERATE	c.2815C>T\|p.Arg939Cys	S277
20	BAA07g05740	A07	6381059	C	T	missense_variant	MODERATE	c.2524G>A\|p.Asp842Asn	S245
21	BAA07g05740	A07	6382665	C	T	missense_variant	MODERATE	c.1765G>A\|p.Glu589Lys	S2
22	BAA07g05740	A07	6382678	C	T	synonymous_variant	LOW	c.1752G>A\|p.Val584Val	S33
23	BAA07g05740	A07	6383558	C	T	missense_variant	MODERATE	c.1444G>A\|p.Gly482Arg	S206 S26
24	BAA07g05740	A07	6383757	G	A	synonymous_variant	LOW	c.1245C>T\|p.Leu415Leu	S284
25	BAA07g05740	A07	6383762	G	A	missense_variant	MODERATE	c.1240C>T\|p.Pro414Ser	S166

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