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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
26651	BAA01g19000	A01	9320245	G	A	splice_region_variant&intron_variant	LOW	c.162+3C>T\|	S241
26652	BAA01g18980	A01	9320646	G	A	upstream_gene_variant	MODIFIER	c.-2995C>T\|	S274
26653	BAA01g19010	A01	9321151	G	A	synonymous_variant	LOW	c.2592C>T\|p.Leu864Leu	S13
26654	BAA01g19010	A01	9321381	G	A	splice_region_variant&intron_variant	LOW	c.2448+7C>T\|	S212
26655	BAA01g19010	A01	9321607	C	T	stop_gained	HIGH	c.2229G>A\|p.Trp743*	S182
26656	BAA01g19010	A01	9321728	C	T	missense_variant	MODERATE	c.2108G>A\|p.Arg703Lys	S144
26657	BAA01g19010	A01	9322149	C	T	missense_variant	MODERATE	c.1687G>A\|p.Val563Ile	S18
26658	BAA01g19010	A01	9322435	C	T	synonymous_variant	LOW	c.1401G>A\|p.Gly467Gly	S85
26659	BAA01g19010	A01	9322810	C	T	synonymous_variant	LOW	c.1026G>A\|p.Glu342Glu	S167
26660	BAA01g19000	A01	9323047	C	T	upstream_gene_variant	MODIFIER	c.-2552G>A\|	S111
26661	BAA01g19000	A01	9323513	C	T	upstream_gene_variant	MODIFIER	c.-3018G>A\|	S264
26662	BAA01g19000	A01	9323748	G	A	upstream_gene_variant	MODIFIER	c.-3253C>T\|	S8
26663	BAA01g19010	A01	9324096	C	T	missense_variant	MODERATE	c.478G>A\|p.Gly160Arg	S148 S210 S30 S31
26664	BAA01g19010	A01	9324118	C	T	synonymous_variant	LOW	c.456G>A\|p.Ala152Ala	S185
26665	BAA01g19010	A01	9324451	G	A	synonymous_variant	LOW	c.123C>T\|p.Phe41Phe	S1 S161 S90
26666	BAA01g19010	A01	9324491	G	A	missense_variant	MODERATE	c.83C>T\|p.Ser28Phe	S263
26667	BAA01g19010	A01	9324543	C	T	missense_variant	MODERATE	c.31G>A\|p.Ala11Thr	S155 S211
26668	BAA01g19000	A01	9324658	C	T	upstream_gene_variant	MODIFIER	c.-4163G>A\|	S117
26669	BAA01g19000	A01	9325411	C	T	upstream_gene_variant	MODIFIER	c.-4916G>A\|	S221
26670	BAA01g19010	A01	9325516	C	T	upstream_gene_variant	MODIFIER	c.-943G>A\|	S107
26671	BAA01g19030	A01	9326009	C	T	missense_variant	MODERATE	c.333G>A\|p.Met111Ile	S247
26672	BAA01g19010	A01	9326141	C	T	upstream_gene_variant	MODIFIER	c.-1568G>A\|	S256
26673	BAA01g19010	A01	9327620	C	T	upstream_gene_variant	MODIFIER	c.-3047G>A\|	S267
26674	BAA01g19010	A01	9328169	C	T	upstream_gene_variant	MODIFIER	c.-3596G>A\|	S114
26675	BAA01g19010	A01	9328995	G	A	upstream_gene_variant	MODIFIER	c.-4422C>T\|	S275

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