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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
137401	BAA10g23010	A10	19563400	G	A	upstream_gene_variant	MODIFIER	c.-3369C>T\|	S150 S303
137402	BAA10g23010	A10	19564989	G	T	upstream_gene_variant	MODIFIER	c.-4958C>A\|	S107 S118 S120 S144 S147 S174 S199 S211 S23 S233 S238 S247 S249 S274 S293 S30 S5 S75
137403	BAA10g23020	A10	19566129	G	A	missense_variant	MODERATE	c.1168G>A\|p.Asp390Asn	S109
137404	BAA10g23030	A10	19566858	G	A	upstream_gene_variant	MODIFIER	c.-2507G>A\|	S127
137405	BAA10g23030	A10	19568397	G	A	upstream_gene_variant	MODIFIER	c.-968G>A\|	S205
137406	BAA10g23030	A10	19568619	C	T	upstream_gene_variant	MODIFIER	c.-746C>T\|	S25
137407	BAA10g23030	A10	19569207	G	A	upstream_gene_variant	MODIFIER	c.-158G>A\|	S64
137408	BAA10g23030	A10	19569840	C	T	synonymous_variant	LOW	c.400C>T\|p.Leu134Leu	S97
137409	BAA10g23020	A10	19569864	T	C	downstream_gene_variant	MODIFIER	c.*3415T>C\|	S255
137410	BAA10g23020	A10	19570860	G	A	downstream_gene_variant	MODIFIER	c.*4411G>A\|	S88
137411	BAA10g23030	A10	19571733	C	T	missense_variant	MODERATE	c.1391C>T\|p.Ser464Phe	S169
137412	BAA10g23030	A10	19572604	C	T	missense_variant	MODERATE	c.2105C>T\|p.Pro702Leu	S97
137413	BAA10g23030	A10	19573547	G	A	synonymous_variant	LOW	c.2709G>A\|p.Lys903Lys	S69
137414	BAA10g23040	A10	19576448	G	A	upstream_gene_variant	MODIFIER	c.-1263G>A\|	S198
137415	BAA10g23040	A10	19577700	G	A	upstream_gene_variant	MODIFIER	c.-11G>A\|	S195
137416	BAA10g23040	A10	19577848	G	A	synonymous_variant	LOW	c.138G>A\|p.Arg46Arg	S1 S90
137417	BAA10g23040	A10	19577875	C	T	synonymous_variant	LOW	c.165C>T\|p.Thr55Thr	S281
137418	BAA10g23030	A10	19578417	G	A	downstream_gene_variant	MODIFIER	c.*4798G>A\|	S63
137419	BAA10g23040	A10	19579180	C	T	synonymous_variant	LOW	c.858C>T\|p.Ala286Ala	S150
137420	BAA10g23040	A10	19579409	G	A	missense_variant	MODERATE	c.991G>A\|p.Gly331Arg	S4
137421	BAA10g23040	A10	19579699	G	A	missense_variant	MODERATE	c.1162G>A\|p.Asp388Asn	S219 S72
137422	BAA10g23040	A10	19579890	C	T	downstream_gene_variant	MODIFIER	c.*75C>T\|	S183
137423	BAA10g23050	A10	19580929	C	T	missense_variant	MODERATE	c.179G>A\|p.Gly60Glu	S276
137424	BAA10g23050	A10	19581426	G	A	upstream_gene_variant	MODIFIER	c.-253C>T\|	S280
137425	BAA10g23050	A10	19581743	C	T	upstream_gene_variant	MODIFIER	c.-570G>A\|	S130

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