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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
147951	BAA10g32360	A10	23286542	G	A	synonymous_variant	LOW	c.924G>A\|p.Lys308Lys	S178
147952	BAA10g32360	A10	23286627	C	T	missense_variant	MODERATE	c.1009C>T\|p.Pro337Ser	S188
147953	BAA10g32340	A10	23286876	C	T	upstream_gene_variant	MODIFIER	c.-4170G>A\|	S268
147954	BAA10g32360	A10	23287278	G	A	synonymous_variant	LOW	c.1314G>A\|p.Gly438Gly	S122
147955	BAA10g32370	A10	23288701	G	A	upstream_gene_variant	MODIFIER	c.-643G>A\|	S53
147956	BAA10g32370	A10	23289439	G	A	synonymous_variant	LOW	c.96G>A\|p.Gln32Gln	S260
147957	BAA10g32380	A10	23290578	C	T	upstream_gene_variant	MODIFIER	c.-2358C>T\|	S243
147958	BAA10g32370	A10	23291315	C	T	missense_variant	MODERATE	c.982C>T\|p.Pro328Ser	S144
147959	BAA10g32380	A10	23292540	G	A	upstream_gene_variant	MODIFIER	c.-396G>A\|	S284
147960	BAA10g32380	A10	23292728	C	T	upstream_gene_variant	MODIFIER	c.-208C>T\|	S282
147961	BAA10g32380	A10	23293120	G	A	missense_variant	MODERATE	c.185G>A\|p.Arg62Lys	S193
147962	BAA10g32380	A10	23293518	C	T	synonymous_variant	LOW	c.583C>T\|p.Leu195Leu	S19
147963	BAA10g32380	A10	23293545	G	A	missense_variant	MODERATE	c.610G>A\|p.Ala204Thr	S158
147964	BAA10g32380	A10	23293684	C	T	missense_variant	MODERATE	c.749C>T\|p.Ser250Phe	S78 S83
147965	BAA10g32380	A10	23293775	G	A	synonymous_variant	LOW	c.840G>A\|p.Ser280Ser	S217 S248
147966	BAA10g32390	A10	23294514	G	A	upstream_gene_variant	MODIFIER	c.-513G>A\|	S278
147967	BAA10g32390	A10	23296514	G	A	synonymous_variant	LOW	c.1488G>A\|p.Gly496Gly	S128
147968	BAA10g32390	A10	23296683	G	A	missense_variant	MODERATE	c.1657G>A\|p.Glu553Lys	S115
147969	BAA10g32400	A10	23297100	G	A	upstream_gene_variant	MODIFIER	c.-1040G>A\|	S183 S198
147970	BAA10g32400	A10	23297452	C	T	upstream_gene_variant	MODIFIER	c.-688C>T\|	S277
147971	BAA10g32390	A10	23300169	G	A	downstream_gene_variant	MODIFIER	c.*3166G>A\|	S157 S166 S257
147972	BAA10g32390	A10	23300441	T	A	downstream_gene_variant	MODIFIER	c.*3438T>A\|	S30
147973	BAA10g32410	A10	23300877	C	T	synonymous_variant	LOW	c.3366G>A\|p.Glu1122Glu	S279
147974	BAA10g32390	A10	23301010	G	A	downstream_gene_variant	MODIFIER	c.*4007G>A\|	S153 S213
147975	BAA10g32410	A10	23301704	C	T	missense_variant	MODERATE	c.2701G>A\|p.Val901Ile	S96

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