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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
22001	BAA01g15930	A01	7768329	G	A	upstream_gene_variant	MODIFIER	c.-2076C>T\|	S207
22002	BAA01g15950	A01	7770296	G	A	missense_variant	MODERATE	c.364G>A\|p.Asp122Asn	S237
22003	BAA01g15950	A01	7770321	G	A	missense_variant	MODERATE	c.389G>A\|p.Arg130Lys	S15 S3
22004	BAA01g15950	A01	7770693	C	T	missense_variant	MODERATE	c.479C>T\|p.Thr160Ile	S213
22005	BAA01g15950	A01	7770737	G	A	missense_variant	MODERATE	c.523G>A\|p.Asp175Asn	S165
22006	BAA01g15960	A01	7771792	C	T	upstream_gene_variant	MODIFIER	c.-227C>T\|	S289 S290
22007	BAA01g15940	A01	7773350	C	T	downstream_gene_variant	MODIFIER	c.*4502C>T\|	S125
22008	BAA01g15940	A01	7773753	G	A	downstream_gene_variant	MODIFIER	c.*4905G>A\|	S237
22009	BAA01g15960	A01	7774235	C	T	missense_variant	MODERATE	c.991C>T\|p.Leu331Phe	S299
22010	BAA01g15960	A01	7776501	C	T	splice_region_variant&synonymous_variant	LOW	c.2113C>T\|p.Leu705Leu	S135
22011	BAA01g15960	A01	7776605	G	A	downstream_gene_variant	MODIFIER	c.*60G>A\|	S228
22012	BAA01g15970	A01	7777379	C	T	missense_variant	MODERATE	c.542G>A\|p.Cys181Tyr	S2
22013	BAA01g15970	A01	7777468	C	T	synonymous_variant	LOW	c.453G>A\|p.Arg151Arg	S35
22014	BAA01g15970	A01	7778362	C	T	upstream_gene_variant	MODIFIER	c.-442G>A\|	S302
22015	BAA01g15970	A01	7780099	C	T	upstream_gene_variant	MODIFIER	c.-2179G>A\|	S100
22016	BAA01g15970	A01	7781001	C	T	upstream_gene_variant	MODIFIER	c.-3081G>A\|	S221
22017	BAA01g15980	A01	7783502	G	A	intron_variant	MODIFIER	c.394+63G>A\|	S293
22018	BAA01g15980	A01	7784683	C	T	synonymous_variant	LOW	c.1170C>T\|p.Ile390Ile	S8
22019	BAA01g15980	A01	7784881	C	T	synonymous_variant	LOW	c.1368C>T\|p.Leu456Leu	S296
22020	BAA01g15980	A01	7784955	C	T	missense_variant	MODERATE	c.1442C>T\|p.Ser481Phe	S221
22021	BAA01g15980	A01	7785031	G	A	missense_variant	MODERATE	c.1518G>A\|p.Met506Ile	S95
22022	BAA01g15980	A01	7785910	C	T	downstream_gene_variant	MODIFIER	c.*369C>T\|	S151 S157 S166 S167 S262 S263
22023	BAA01g15980	A01	7786203	G	A	downstream_gene_variant	MODIFIER	c.*662G>A\|	S165
22024	BAA01g15980	A01	7786831	C	T	downstream_gene_variant	MODIFIER	c.*1290C>T\|	S41
22025	BAA01g15980	A01	7786966	G	A	downstream_gene_variant	MODIFIER	c.*1425G>A\|	S298

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