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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
101251	BAA10g07160	A10	3993846	C	T	downstream_gene_variant	MODIFIER	c.*1034C>T\|	S271
101252	BAA10g07160	A10	3994757	C	T	downstream_gene_variant	MODIFIER	c.*1945C>T\|	S117
101253	BAA10g07160	A10	3995993	G	A	downstream_gene_variant	MODIFIER	c.*3181G>A\|	S178
101254	BAA10g07160	A10	3996589	G	A	downstream_gene_variant	MODIFIER	c.*3777G>A\|	S4
101255	BAA10g07160	A10	3997690	C	T	downstream_gene_variant	MODIFIER	c.*4878C>T\|	S11 S189
101256	BAA10g07160-BAA10g07170	A10	3997882	G	A	intergenic_region	MODIFIER	n.3997882G>A\|	S181
101257	BAA10g07160-BAA10g07170	A10	3998108	G	A	intergenic_region	MODIFIER	n.3998108G>A\|	S262
101258	BAA10g07170	A10	3998586	C	T	downstream_gene_variant	MODIFIER	c.*4663G>A\|	S56
101259	BAA10g07170	A10	3998607	C	T	downstream_gene_variant	MODIFIER	c.*4642G>A\|	S132 S137 S215 S89
101260	BAA10g07170	A10	3998672	C	T	downstream_gene_variant	MODIFIER	c.*4577G>A\|	S73 S91
101261	BAA10g07170	A10	3999641	C	T	downstream_gene_variant	MODIFIER	c.*3608G>A\|	S121
101262	BAA10g07170	A10	3999767	G	A	downstream_gene_variant	MODIFIER	c.*3482C>T\|	S128
101263	BAA10g07170	A10	4000161	G	A	downstream_gene_variant	MODIFIER	c.*3088C>T\|	S296
101264	BAA10g07170	A10	4000878	G	A	downstream_gene_variant	MODIFIER	c.*2371C>T\|	S128
101265	BAA10g07170	A10	4002920	C	T	downstream_gene_variant	MODIFIER	c.*329G>A\|	S144
101266	BAA10g07170	A10	4003304	G	A	missense_variant	MODERATE	c.1175C>T\|p.Pro392Leu	S308
101267	BAA10g07170	A10	4003551	C	T	missense_variant	MODERATE	c.928G>A\|p.Glu310Lys	S177
101268	BAA10g07170	A10	4003639	C	T	synonymous_variant	LOW	c.840G>A\|p.Pro280Pro	S282
101269	BAA10g07170	A10	4004612	C	T	synonymous_variant	LOW	c.159G>A\|p.Gln53Gln	S114
101270	BAA10g07170	A10	4004710	C	T	missense_variant	MODERATE	c.61G>A\|p.Asp21Asn	S202
101271	BAA10g07170	A10	4004827	G	A	upstream_gene_variant	MODIFIER	c.-57C>T\|	S174 S216 S241 S265 S27 S39
101272	BAA10g07170	A10	4005883	G	A	upstream_gene_variant	MODIFIER	c.-1113C>T\|	S20
101273	BAA10g07190	A10	4006157	C	T	stop_gained	HIGH	c.159G>A\|p.Trp53*	S270
101274	BAA10g07170	A10	4006648	C	T	upstream_gene_variant	MODIFIER	c.-1878G>A\|	S297
101275	BAA10g07170	A10	4007057	C	T	upstream_gene_variant	MODIFIER	c.-2287G>A\|	S23

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