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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
6601	BAA01g05460	A01	2408183	G	A	upstream_gene_variant	MODIFIER	c.-4878C>T\|	S295
6602	BAA01g05480	A01	2408607	C	T	missense_variant	MODERATE	c.220G>A\|p.Ala74Thr	S233
6603	BAA01g05480	A01	2409200	C	T	upstream_gene_variant	MODIFIER	c.-275G>A\|	S77 S82
6604	BAA01g05480	A01	2410138	G	A	upstream_gene_variant	MODIFIER	c.-1213C>T\|	S161
6605	BAA01g05480	A01	2410933	C	T	upstream_gene_variant	MODIFIER	c.-2008G>A\|	S168
6606	BAA01g05480	A01	2412119	C	T	upstream_gene_variant	MODIFIER	c.-3194G>A\|	S82 S92
6607	BAA01g05480	A01	2412180	G	T	upstream_gene_variant	MODIFIER	c.-3255C>A\|	S103 S138 S16 S172 S19 S241 S261 S287 S31 S50 S91 S92
6608	BAA01g05480	A01	2413904	C	T	upstream_gene_variant	MODIFIER	c.-4979G>A\|	S270
6609	BAA01g05490	A01	2415304	G	A	upstream_gene_variant	MODIFIER	c.-3869C>T\|	S129
6610	BAA01g05500	A01	2416126	C	T	missense_variant	MODERATE	c.728C>T\|p.Thr243Ile	S218
6611	BAA01g05520	A01	2417024	G	A	upstream_gene_variant	MODIFIER	c.-4468G>A\|	S262
6612	BAA01g05500	A01	2417342	G	A	missense_variant	MODERATE	c.1396G>A\|p.Ala466Thr	S172 S217
6613	BAA01g05510	A01	2419394	C	T	upstream_gene_variant	MODIFIER	c.-199G>A\|	S70
6614	BAA01g05510	A01	2421366	G	A	upstream_gene_variant	MODIFIER	c.-2171C>T\|	S177
6615	BAA01g05510	A01	2421435	G	A	upstream_gene_variant	MODIFIER	c.-2240C>T\|	S157 S163
6616	BAA01g05520	A01	2421767	G	A	synonymous_variant	LOW	c.276G>A\|p.Leu92Leu	S15 S3
6617	BAA01g05520	A01	2421928	G	A	missense_variant	MODERATE	c.437G>A\|p.Gly146Glu	S262
6618	BAA01g05520	A01	2421969	G	A	missense_variant	MODERATE	c.478G>A\|p.Glu160Lys	S161
6619	BAA01g05520	A01	2423369	G	A	synonymous_variant	LOW	c.1212G>A\|p.Glu404Glu	S271
6620	BAA01g05520	A01	2424881	G	A	synonymous_variant	LOW	c.2058G>A\|p.Arg686Arg	S83 S88
6621	BAA01g05520	A01	2425239	G	A	missense_variant	MODERATE	c.2326G>A\|p.Asp776Asn	S138
6622	BAA01g05520	A01	2426002	G	A	missense_variant	MODERATE	c.2899G>A\|p.Glu967Lys	S259
6623	BAA01g05520	A01	2426014	G	A	splice_region_variant&intron_variant	LOW	c.2906+5G>A\|	S9
6624	BAA01g05530	A01	2426820	C	T	downstream_gene_variant	MODIFIER	c.*2358G>A\|	S200
6625	BAA01g05520	A01	2427501	C	T	synonymous_variant	LOW	c.3816C>T\|p.Ile1272Ile	S166

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