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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
150001	BAA10g34040	A10	24065571	G	A	upstream_gene_variant	MODIFIER	c.-4133C>T\|	S207
150002	BAA10g34060	A10	24066991	C	T	upstream_gene_variant	MODIFIER	c.-1624G>A\|	S210
150003	BAA10g34060	A10	24069031	A	G	upstream_gene_variant	MODIFIER	c.-3664T>C\|	S108 S119 S157 S161 S174 S182 S186 S198 S200 S209 S212 S247 S286 S293 S56 S64 S84 S94
150004	BAA10g34060	A10	24069693	C	T	upstream_gene_variant	MODIFIER	c.-4326G>A\|	S100
150005	BAA10g34080	A10	24070868	G	A	missense_variant	MODERATE	c.1142C>T\|p.Thr381Ile	S62
150006	BAA10g34080	A10	24071330	C	T	synonymous_variant	LOW	c.996G>A\|p.Ala332Ala	S210 S225
150007	BAA10g34080	A10	24071359	C	T	missense_variant	MODERATE	c.967G>A\|p.Ala323Thr	S5
150008	BAA10g34080	A10	24071680	C	T	missense_variant	MODERATE	c.646G>A\|p.Glu216Lys	S218
150009	BAA10g34080	A10	24071704	C	T	missense_variant	MODERATE	c.622G>A\|p.Ala208Thr	S87
150010	BAA10g34080	A10	24071774	C	T	synonymous_variant	LOW	c.552G>A\|p.Arg184Arg	S146
150011	BAA10g34080	A10	24072897	G	A	upstream_gene_variant	MODIFIER	c.-572C>T\|	S130
150012	BAA10g34080	A10	24073885	C	T	upstream_gene_variant	MODIFIER	c.-1560G>A\|	S222
150013	BAA10g34090	A10	24075995	G	A	missense_variant	MODERATE	c.799C>T\|p.Leu267Phe	S197
150014	BAA10g34090	A10	24076022	G	A	missense_variant	MODERATE	c.772C>T\|p.Pro258Ser	S298
150015	BAA10g34090	A10	24076127	C	T	missense_variant	MODERATE	c.667G>A\|p.Asp223Asn	S206 S26
150016	BAA10g34090	A10	24076317	C	T	synonymous_variant	LOW	c.477G>A\|p.Thr159Thr	S221
150017	BAA10g34090	A10	24076550	G	A	missense_variant	MODERATE	c.244C>T\|p.Leu82Phe	S1 S90
150018	BAA10g34100	A10	24077752	G	A	synonymous_variant	LOW	c.766C>T\|p.Leu256Leu	S152
150019	BAA10g34100	A10	24078786	C	T	stop_gained	HIGH	c.207G>A\|p.Trp69*	S117
150020	BAA10g34090	A10	24079058	G	A	upstream_gene_variant	MODIFIER	c.-2265C>T\|	S88
150021	BAA10g34110	A10	24079715	C	T	missense_variant	MODERATE	c.29C>T\|p.Ser10Phe	S282
150022	BAA10g34110	A10	24079872	C	T	synonymous_variant	LOW	c.186C>T\|p.Pro62Pro	S195
150023	BAA10g34110	A10	24081275	G	A	missense_variant	MODERATE	c.1096G>A\|p.Asp366Asn	S47
150024	BAA10g34110	A10	24081402	G	A	stop_gained	HIGH	c.1149G>A\|p.Trp383*	S37
150025	BAA10g34110	A10	24082274	G	A	missense_variant	MODERATE	c.1841G>A\|p.Arg614Lys	S130

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