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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
129501	BAA10g17400	A10	16754820	G	A	downstream_gene_variant	MODIFIER	c.*4725G>A\|	S64
129502	BAA10g17420	A10	16755330	G	T	stop_gained	HIGH	c.544G>T\|p.Glu182*	S176 S209 S228 S282 S93
129503	BAA10g17420	A10	16757313	G	A	intron_variant	MODIFIER	c.1531+197G>A\|	S178
129504	BAA10g17420	A10	16757578	C	T	intron_variant	MODIFIER	c.1532-44C>T\|	S78 S83
129505	BAA10g17420	A10	16758746	G	A	downstream_gene_variant	MODIFIER	c.*835G>A\|	S178
129506	BAA10g17420	A10	16759478	G	A	downstream_gene_variant	MODIFIER	c.*1567G>A\|	S155 S211
129507	BAA10g17420	A10	16760421	C	T	downstream_gene_variant	MODIFIER	c.*2510C>T\|	S235
129508	BAA10g17420	A10	16760467	C	T	downstream_gene_variant	MODIFIER	c.*2556C>T\|	S281
129509	BAA10g17420	A10	16760796	G	A	downstream_gene_variant	MODIFIER	c.*2885G>A\|	S159 S187 S188 S243 S276 S299
129510	BAA10g17420	A10	16760999	C	T	downstream_gene_variant	MODIFIER	c.*3088C>T\|	S257
129511	BAA10g17420	A10	16761596	G	A	downstream_gene_variant	MODIFIER	c.*3685G>A\|	S192 S243
129512	BAA10g17420	A10	16761620	C	T	downstream_gene_variant	MODIFIER	c.*3709C>T\|	S48
129513	BAA10g17420	A10	16761696	C	T	downstream_gene_variant	MODIFIER	c.*3785C>T\|	S243
129514	BAA10g17420-BAA10g17430	A10	16763120	C	T	intergenic_region	MODIFIER	n.16763120C>T\|	S18
129515	BAA10g17430	A10	16765850	C	T	upstream_gene_variant	MODIFIER	c.-3757C>T\|	S5
129516	BAA10g17430	A10	16769581	G	A	upstream_gene_variant	MODIFIER	c.-26G>A\|	S5
129517	BAA10g17430	A10	16769803	C	T	missense_variant	MODERATE	c.131C>T\|p.Thr44Ile	S305
129518	BAA10g17430	A10	16770397	C	T	missense_variant	MODERATE	c.503C>T\|p.Ala168Val	S45
129519	BAA10g17430	A10	16770398	G	A	synonymous_variant	LOW	c.504G>A\|p.Ala168Ala	S129
129520	BAA10g17430	A10	16770796	C	T	missense_variant	MODERATE	c.677C>T\|p.Ala226Val	S18
129521	BAA10g17430	A10	16771933	G	A	missense_variant	MODERATE	c.1315G>A\|p.Asp439Asn	S184
129522	BAA10g17430	A10	16772329	C	T	synonymous_variant	LOW	c.1539C>T\|p.Asn513Asn	S6
129523	BAA10g17430	A10	16772780	G	A	missense_variant	MODERATE	c.1804G>A\|p.Asp602Asn	S88
129524	BAA10g17450	A10	16773189	G	A	upstream_gene_variant	MODIFIER	c.-2368G>A\|	S216
129525	BAA10g17450	A10	16774462	G	A	upstream_gene_variant	MODIFIER	c.-1095G>A\|	S105 S106

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