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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
138001	BAA10g23560	A10	19772707	G	A	upstream_gene_variant	MODIFIER	c.-556G>A\|	S280
138002	BAA10g23560	A10	19773683	G	A	intron_variant	MODIFIER	c.115-41G>A\|	S53
138003	BAA10g23560	A10	19774564	C	T	synonymous_variant	LOW	c.403C>T\|p.Leu135Leu	S68
138004	BAA10g23560	A10	19775079	C	T	intron_variant	MODIFIER	c.666+51C>T\|	S144
138005	BAA10g23560	A10	19775298	C	T	intron_variant	MODIFIER	c.721-9C>T\|	S286
138006	BAA10g23560	A10	19776922	C	T	downstream_gene_variant	MODIFIER	c.*1089C>T\|	S146
138007	BAA10g23560	A10	19777308	G	A	downstream_gene_variant	MODIFIER	c.*1475G>A\|	S202
138008	BAA10g23560	A10	19777486	G	A	downstream_gene_variant	MODIFIER	c.*1653G>A\|	S250
138009	BAA10g23560	A10	19777561	C	A	downstream_gene_variant	MODIFIER	c.*1728C>A\|	S259
138010	BAA10g23560	A10	19777722	C	T	downstream_gene_variant	MODIFIER	c.*1889C>T\|	S197
138011	BAA10g23560	A10	19777990	G	A	downstream_gene_variant	MODIFIER	c.*2157G>A\|	S117
138012	BAA10g23560	A10	19778168	C	T	downstream_gene_variant	MODIFIER	c.*2335C>T\|	S152 S203
138013	BAA10g23560	A10	19780052	C	T	downstream_gene_variant	MODIFIER	c.*4219C>T\|	S44
138014	BAA10g23560	A10	19780311	G	A	downstream_gene_variant	MODIFIER	c.*4478G>A\|	S128
138015	BAA10g23560-BAA10g23570	A10	19781153	C	T	intergenic_region	MODIFIER	n.19781153C>T\|	S306 S308
138016	BAA10g23560-BAA10g23570	A10	19783915	G	A	intergenic_region	MODIFIER	n.19783915G>A\|	S265
138017	BAA10g23570	A10	19785423	C	T	upstream_gene_variant	MODIFIER	c.-4802C>T\|	S189
138018	BAA10g23570	A10	19785825	A	G	upstream_gene_variant	MODIFIER	c.-4400A>G\|	S252
138019	BAA10g23570	A10	19789567	C	T	upstream_gene_variant	MODIFIER	c.-658C>T\|	S265 S39
138020	BAA10g23570	A10	19790844	C	T	missense_variant	MODERATE	c.620C>T\|p.Ala207Val	S148 S210 S30 S31
138021	BAA10g23580	A10	19792778	C	T	downstream_gene_variant	MODIFIER	c.*4100G>A\|	S292
138022	BAA10g23580	A10	19793056	C	T	downstream_gene_variant	MODIFIER	c.*3822G>A\|	S266
138023	BAA10g23580	A10	19793159	G	A	downstream_gene_variant	MODIFIER	c.*3719C>T\|	S293
138024	BAA10g23580	A10	19795266	A	T	downstream_gene_variant	MODIFIER	c.*1612T>A\|	S147 S199 S229 S257 S28
138025	BAA10g23570	A10	19796104	G	A	missense_variant	MODERATE	c.1091G>A\|p.Ser364Asn	S174

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