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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
48351	BAA01g27780	A01	16780383	C	T	upstream_gene_variant	MODIFIER	c.-2117G>A\|	S44
48352	BAA01g27780	A01	16782963	T	A	upstream_gene_variant	MODIFIER	c.-4697A>T\|	S124 S134 S257 S259 S262 S268 S280 S299 S301 S306
48353	BAA01g27780	A01	16782983	G	A	upstream_gene_variant	MODIFIER	c.-4717C>T\|	S109
48354	BAA01g27780	A01	16783078	G	T	upstream_gene_variant	MODIFIER	c.-4812C>A\|	S127 S132 S133 S144 S154 S170 S174 S183 S203 S209 S236 S297 S30 S305 S43 S47 S51 S78
48355	BAA01g27780-BAA01g27790	A01	16784246	G	A	intergenic_region	MODIFIER	n.16784246G>A\|	S94
48356	BAA01g27790	A01	16790215	C	T	downstream_gene_variant	MODIFIER	c.*12G>A\|	S183
48357	BAA01g27790	A01	16790511	C	T	stop_gained	HIGH	c.1298G>A\|p.Trp433*	S165
48358	BAA01g27800	A01	16790844	C	T	downstream_gene_variant	MODIFIER	c.*1325G>A\|	S168
48359	BAA01g27790	A01	16791238	C	T	missense_variant	MODERATE	c.641G>A\|p.Cys214Tyr	S195
48360	BAA01g27790	A01	16791544	G	A	missense_variant	MODERATE	c.335C>T\|p.Ser112Leu	S62
48361	BAA01g27800	A01	16792195	C	T	missense_variant	MODERATE	c.211G>A\|p.Ala71Thr	S256
48362	BAA01g27790	A01	16792410	C	T	upstream_gene_variant	MODIFIER	c.-532G>A\|	S82 S92
48363	BAA01g27790	A01	16792492	G	A	upstream_gene_variant	MODIFIER	c.-614C>T\|	S265
48364	BAA01g27790	A01	16792605	C	T	upstream_gene_variant	MODIFIER	c.-727G>A\|	S211
48365	BAA01g27790	A01	16793334	G	A	upstream_gene_variant	MODIFIER	c.-1456C>T\|	S116
48366	BAA01g27790	A01	16793784	C	T	upstream_gene_variant	MODIFIER	c.-1906G>A\|	S40 S49
48367	BAA01g27790	A01	16794182	C	T	upstream_gene_variant	MODIFIER	c.-2304G>A\|	S164
48368	BAA01g27790	A01	16794234	C	T	upstream_gene_variant	MODIFIER	c.-2356G>A\|	S69
48369	BAA01g27790	A01	16794462	A	G	upstream_gene_variant	MODIFIER	c.-2584T>C\|	S7
48370	BAA01g27790	A01	16794831	C	T	upstream_gene_variant	MODIFIER	c.-2953G>A\|	S162
48371	BAA01g27790	A01	16794871	C	T	upstream_gene_variant	MODIFIER	c.-2993G>A\|	S230 S38
48372	BAA01g27790	A01	16795091	G	A	upstream_gene_variant	MODIFIER	c.-3213C>T\|	S292
48373	BAA01g27790	A01	16796119	G	A	upstream_gene_variant	MODIFIER	c.-4241C>T\|	S278
48374	BAA01g27800	A01	16797172	G	A	upstream_gene_variant	MODIFIER	c.-4767C>T\|	S246
48375	BAA01g27800	A01	16797306	G	A	upstream_gene_variant	MODIFIER	c.-4901C>T\|	S263

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