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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA04g11190	A04	17117241	G	A	downstream_gene_variant	MODIFIER	c.*2305C>T\|	S169
2	BAA04g11190	A04	17117521	G	A	downstream_gene_variant	MODIFIER	c.*2025C>T\|	S95
3	BAA04g11190	A04	17118323	C	T	downstream_gene_variant	MODIFIER	c.*1223G>A\|	S113
4	BAA04g11190	A04	17118437	C	T	downstream_gene_variant	MODIFIER	c.*1109G>A\|	S51 S74
5	BAA04g11190	A04	17119451	C	T	downstream_gene_variant	MODIFIER	c.*95G>A\|	S192
6	BAA04g11190	A04	17119579	G	A	synonymous_variant	LOW	c.513C>T\|p.Ile171Ile	S220 S226 S238 S267 S91
7	BAA04g11190	A04	17119630	G	A	synonymous_variant	LOW	c.462C>T\|p.Ile154Ile	S14 S220 S226 S238 S267 S91
8	BAA04g11190	A04	17119639	G	A	synonymous_variant	LOW	c.453C>T\|p.Asn151Asn	S14 S220 S226 S238 S267 S91
9	BAA04g11190	A04	17119642	A	G	synonymous_variant	LOW	c.450T>C\|p.Pro150Pro	S14 S220 S226 S238 S267 S91
10	BAA04g11190	A04	17119652	G	T	missense_variant	MODERATE	c.440C>A\|p.Thr147Lys	S220 S226 S238 S267 S91
11	BAA04g11190	A04	17119654	T	C	synonymous_variant	LOW	c.438A>G\|p.Lys146Lys	S220 S226 S238 S267 S91
12	BAA04g11190	A04	17119665	G	C	missense_variant	MODERATE	c.427C>G\|p.Gln143Glu	S220 S226 S238 S267 S91
13	BAA04g11190	A04	17119666	G	C	synonymous_variant	LOW	c.426C>G\|p.Val142Val	S220 S226 S238 S267 S91
14	BAA04g11190	A04	17119687	A	G	synonymous_variant	LOW	c.405T>C\|p.Ser135Ser	S226 S238 S267
15	BAA04g11190	A04	17119699	T	A	synonymous_variant	LOW	c.393A>T\|p.Gly131Gly	S226 S238 S267
16	BAA04g11190	A04	17119753	G	T	synonymous_variant	LOW	c.339C>A\|p.Thr113Thr	S238 S267
17	BAA04g11190	A04	17119755	T	A	missense_variant	MODERATE	c.337A>T\|p.Thr113Ser	S238 S267
18	BAA04g11190	A04	17119757	C	T	missense_variant	MODERATE	c.335G>A\|p.Ser112Asn	S238 S267
19	BAA04g11190	A04	17119759	T	A	synonymous_variant	LOW	c.333A>T\|p.Gly111Gly	S238 S267
20	BAA04g11190	A04	17119774	A	C	synonymous_variant	LOW	c.318T>G\|p.Val106Val	S147 S238 S267
21	BAA04g11190	A04	17120144	G	A	intron_variant	MODIFIER	c.171+36C>T\|	S282
22	BAA04g11190	A04	17120202	C	T	missense_variant	MODERATE	c.149G>A\|p.Gly50Glu	S100
23	BAA04g11190	A04	17120390	C	T	upstream_gene_variant	MODIFIER	c.-40G>A\|	S115
24	BAA04g11190	A04	17121128	C	T	upstream_gene_variant	MODIFIER	c.-778G>A\|	S202
25	BAA04g11190	A04	17121807	G	A	upstream_gene_variant	MODIFIER	c.-1457C>T\|	S96

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