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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
73151	BAA01g38320	A01	25571536	G	A	missense_variant	MODERATE	c.1282G>A\|p.Glu428Lys	S33
73152	BAA01g38330	A01	25571578	C	T	upstream_gene_variant	MODIFIER	c.-2531C>T\|	S161
73153	BAA01g38330	A01	25571647	T	A	upstream_gene_variant	MODIFIER	c.-2462T>A\|	S174 S27
73154	BAA01g38330	A01	25573899	C	T	upstream_gene_variant	MODIFIER	c.-210C>T\|	S128
73155	BAA01g38330	A01	25573926	C	T	upstream_gene_variant	MODIFIER	c.-183C>T\|	S157
73156	BAA01g38330	A01	25573929	C	T	upstream_gene_variant	MODIFIER	c.-180C>T\|	S198
73157	BAA01g38330	A01	25574475	G	A	missense_variant	MODERATE	c.367G>A\|p.Gly123Ser	S1 S90
73158	BAA01g38350	A01	25575238	G	A	upstream_gene_variant	MODIFIER	c.-2900G>A\|	S173
73159	BAA01g38340	A01	25575875	C	T	missense_variant	MODERATE	c.1879G>A\|p.Gly627Arg	S159 S243
73160	BAA01g38340	A01	25576184	C	T	missense_variant	MODERATE	c.1570G>A\|p.Gly524Ser	S103
73161	BAA01g38340	A01	25576327	C	T	missense_variant	MODERATE	c.1427G>A\|p.Ser476Asn	S92
73162	BAA01g38340	A01	25577258	C	T	missense_variant	MODERATE	c.496G>A\|p.Asp166Asn	S11
73163	BAA01g38340	A01	25577372	G	A	missense_variant	MODERATE	c.382C>T\|p.Leu128Phe	S260
73164	BAA01g38340	A01	25577510	C	T	missense_variant	MODERATE	c.244G>A\|p.Asp82Asn	S69
73165	BAA01g38350	A01	25578144	C	T	missense_variant	MODERATE	c.7C>T\|p.Leu3Phe	S186
73166	BAA01g38350	A01	25578257	C	T	synonymous_variant	LOW	c.120C>T\|p.Asp40Asp	S10
73167	BAA01g38350	A01	25578363	C	T	missense_variant	MODERATE	c.226C>T\|p.Pro76Ser	S239
73168	BAA01g38340	A01	25578471	C	T	upstream_gene_variant	MODIFIER	c.-718G>A\|	S301 S304
73169	BAA01g38340	A01	25578928	C	T	upstream_gene_variant	MODIFIER	c.-1175G>A\|	S120
73170	BAA01g38340	A01	25579171	C	T	upstream_gene_variant	MODIFIER	c.-1418G>A\|	S213
73171	BAA01g38350	A01	25579463	G	A	splice_acceptor_variant&intron_variant	HIGH	c.568-1G>A\|	S13
73172	BAA01g38350	A01	25579815	C	T	missense_variant	MODERATE	c.797C>T\|p.Ser266Phe	S50
73173	BAA01g38350	A01	25579885	G	A	synonymous_variant	LOW	c.867G>A\|p.Arg289Arg	S20
73174	BAA01g38350	A01	25579971	G	A	missense_variant	MODERATE	c.953G>A\|p.Arg318Lys	S153 S157 S236 S257 S262 S263
73175	BAA01g38350	A01	25580106	C	T	missense_variant	MODERATE	c.1088C>T\|p.Ser363Phe	S303

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