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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
83701	BAA01g44380	A01	29493568	C	T	upstream_gene_variant	MODIFIER	c.-1361G>A\|	S94
83702	BAA01g44380	A01	29493971	G	A	upstream_gene_variant	MODIFIER	c.-1764C>T\|	S250
83703	BAA01g44380	A01	29494580	C	T	upstream_gene_variant	MODIFIER	c.-2373G>A\|	S25
83704	BAA01g44380	A01	29495174	C	T	upstream_gene_variant	MODIFIER	c.-2967G>A\|	S47
83705	BAA01g44380	A01	29495386	G	A	upstream_gene_variant	MODIFIER	c.-3179C>T\|	S151 S153 S157 S167 S236 S262 S263
83706	BAA01g44380	A01	29495935	C	T	upstream_gene_variant	MODIFIER	c.-3728G>A\|	S42
83707	BAA01g44390	A01	29496019	C	T	missense_variant	MODERATE	c.866G>A\|p.Arg289Lys	S261
83708	BAA01g44390	A01	29496472	C	T	missense_variant	MODERATE	c.413G>A\|p.Gly138Glu	S206 S26
83709	BAA01g44390	A01	29496839	G	A	missense_variant	MODERATE	c.46C>T\|p.Pro16Ser	S262
83710	BAA01g44380	A01	29496888	C	T	upstream_gene_variant	MODIFIER	c.-4681G>A\|	S276
83711	BAA01g44380	A01	29497021	C	T	upstream_gene_variant	MODIFIER	c.-4814G>A\|	S171
83712	BAA01g44390	A01	29497562	G	A	upstream_gene_variant	MODIFIER	c.-678C>T\|	S280
83713	BAA01g44390	A01	29497905	C	T	upstream_gene_variant	MODIFIER	c.-1021G>A\|	S48
83714	BAA01g44390	A01	29498292	C	T	upstream_gene_variant	MODIFIER	c.-1408G>A\|	S77 S82
83715	BAA01g44400	A01	29499665	G	A	missense_variant	MODERATE	c.448G>A\|p.Asp150Asn	S135
83716	BAA01g44400	A01	29499744	C	T	missense_variant	MODERATE	c.527C>T\|p.Ser176Phe	S210 S225
83717	BAA01g44400	A01	29500252	G	A	synonymous_variant	LOW	c.1035G>A\|p.Lys345Lys	S296
83718	BAA01g44400	A01	29500394	C	T	missense_variant	MODERATE	c.1177C>T\|p.Arg393Trp	S189
83719	BAA01g44400	A01	29500564	C	T	missense_variant	MODERATE	c.1265C>T\|p.Pro422Leu	S128
83720	BAA01g44400	A01	29500875	G	A	splice_region_variant&intron_variant	LOW	c.1500+7G>A\|	S15
83721	BAA01g44390	A01	29501523	C	T	upstream_gene_variant	MODIFIER	c.-4639G>A\|	S54
83722	BAA01g44410	A01	29503283	C	T	missense_variant	MODERATE	c.370G>A\|p.Glu124Lys	S11
83723	BAA01g44420	A01	29503649	C	T	upstream_gene_variant	MODIFIER	c.-1728C>T\|	S45
83724	BAA01g44410	A01	29504114	C	T	missense_variant	MODERATE	c.100G>A\|p.Asp34Asn	S221
83725	BAA01g44410	A01	29504302	C	T	synonymous_variant	LOW	c.18G>A\|p.Leu6Leu	S303

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