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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
71801	BAA01g37560	A01	25106574	G	A	upstream_gene_variant	MODIFIER	c.-4133C>T\|	S173
71802	BAA01g37560	A01	25106655	C	T	upstream_gene_variant	MODIFIER	c.-4214G>A\|	S257
71803	BAA01g37560	A01	25106963	C	T	upstream_gene_variant	MODIFIER	c.-4522G>A\|	S138 S215 S237 S288
71804	BAA01g37560	A01	25107030	C	T	upstream_gene_variant	MODIFIER	c.-4589G>A\|	S295
71805	BAA01g37580	A01	25107785	G	A	missense_variant	MODERATE	c.424G>A\|p.Val142Ile	S308
71806	BAA01g37590	A01	25109435	C	T	upstream_gene_variant	MODIFIER	c.-1283C>T\|	S211
71807	BAA01g37590	A01	25110013	C	T	upstream_gene_variant	MODIFIER	c.-705C>T\|	S183 S198
71808	BAA01g37590	A01	25110557	C	T	upstream_gene_variant	MODIFIER	c.-161C>T\|	S94
71809	BAA01g37590	A01	25110680	C	T	upstream_gene_variant	MODIFIER	c.-38C>T\|	S15 S34 S6
71810	BAA01g37590	A01	25110879	C	T	synonymous_variant	LOW	c.162C>T\|p.Leu54Leu	S269
71811	BAA01g37590	A01	25110885	C	T	synonymous_variant	LOW	c.168C>T\|p.Asn56Asn	S146
71812	BAA01g37590	A01	25110891	C	T	synonymous_variant	LOW	c.174C>T\|p.Ile58Ile	S205
71813	BAA01g37590	A01	25110934	A	C	missense_variant	MODERATE	c.217A>C\|p.Asn73His	S1 S109 S111 S132 S167 S187 S196 S2 S221 S230 S233 S246 S263 S291 S37 S46 S99
71814	BAA01g37590	A01	25111044	G	A	synonymous_variant	LOW	c.327G>A\|p.Glu109Glu	S38
71815	BAA01g37600	A01	25111442	C	T	upstream_gene_variant	MODIFIER	c.-3066C>T\|	S159 S187 S243 S276
71816	BAA01g37590	A01	25112173	C	T	missense_variant	MODERATE	c.1037C>T\|p.Thr346Ile	S198
71817	BAA01g37590	A01	25112889	G	A	missense_variant	MODERATE	c.1753G>A\|p.Glu585Lys	S234
71818	BAA01g37600	A01	25113771	G	A	upstream_gene_variant	MODIFIER	c.-737G>A\|	S245
71819	BAA01g37590	A01	25115078	G	A	downstream_gene_variant	MODIFIER	c.*1938G>A\|	S70
71820	BAA01g37600	A01	25116280	G	A	missense_variant	MODERATE	c.991G>A\|p.Glu331Lys	S110
71821	BAA01g37600	A01	25116704	C	T	synonymous_variant	LOW	c.1236C>T\|p.Asp412Asp	S77 S82
71822	BAA01g37600	A01	25116987	C	T	synonymous_variant	LOW	c.1434C>T\|p.Tyr478Tyr	S275
71823	BAA01g37590	A01	25117155	C	T	downstream_gene_variant	MODIFIER	c.*4015C>T\|	S59
71824	BAA01g37590	A01	25117920	G	A	downstream_gene_variant	MODIFIER	c.*4780G>A\|	S278
71825	BAA01g37610	A01	25119613	C	T	upstream_gene_variant	MODIFIER	c.-3976C>T\|	S20

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