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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
132351	BAA10g19310	A10	17744084	G	A	downstream_gene_variant	MODIFIER	c.*27C>T\|	S112
132352	BAA10g19320	A10	17744294	G	A	downstream_gene_variant	MODIFIER	c.*3955C>T\|	S198
132353	BAA10g19320	A10	17744953	G	A	downstream_gene_variant	MODIFIER	c.*3296C>T\|	S289 S290
132354	BAA10g19320	A10	17745079	C	T	downstream_gene_variant	MODIFIER	c.*3170G>A\|	S84 S93
132355	BAA10g19310	A10	17745311	G	A	synonymous_variant	LOW	c.259C>T\|p.Leu87Leu	S218
132356	BAA10g19310	A10	17745403	C	T	splice_region_variant&intron_variant	LOW	c.174-7G>A\|	S116
132357	BAA10g19320	A10	17745668	C	T	downstream_gene_variant	MODIFIER	c.*2581G>A\|	S306 S308
132358	BAA10g19320	A10	17745907	C	T	downstream_gene_variant	MODIFIER	c.*2342G>A\|	S169 S173 S225 S73
132359	BAA10g19310	A10	17749817	C	T	upstream_gene_variant	MODIFIER	c.-3360G>A\|	S162
132360	BAA10g19330	A10	17750271	A	G	missense_variant	MODERATE	c.317T>C\|p.Ile106Thr	S94
132361	BAA10g19330	A10	17750471	G	A	synonymous_variant	LOW	c.117C>T\|p.Ala39Ala	S221
132362	BAA10g19330	A10	17750561	G	A	synonymous_variant	LOW	c.27C>T\|p.Pro9Pro	S207
132363	BAA10g19320	A10	17751617	C	T	upstream_gene_variant	MODIFIER	c.-2673G>A\|	S255
132364	BAA10g19340	A10	17752311	G	A	synonymous_variant	LOW	c.690G>A\|p.Glu230Glu	S113
132365	BAA10g19340	A10	17757036	G	A	downstream_gene_variant	MODIFIER	c.*3742G>A\|	S120
132366	BAA10g19340	A10	17757225	C	T	downstream_gene_variant	MODIFIER	c.*3931C>T\|	S148 S30 S31
132367	BAA10g19340	A10	17757747	G	A	downstream_gene_variant	MODIFIER	c.*4453G>A\|	S182
132368	BAA10g19350	A10	17758320	G	A	downstream_gene_variant	MODIFIER	c.*3199C>T\|	S59
132369	BAA10g19350	A10	17758529	G	A	downstream_gene_variant	MODIFIER	c.*2990C>T\|	S265
132370	BAA10g19350	A10	17764574	G	A	missense_variant	MODERATE	c.88C>T\|p.Pro30Ser	S62
132371	BAA10g19350	A10	17765401	C	T	upstream_gene_variant	MODIFIER	c.-740G>A\|	S266
132372	BAA10g19350	A10	17766487	G	A	upstream_gene_variant	MODIFIER	c.-1826C>T\|	S40 S49
132373	BAA10g19350	A10	17767303	T	A	upstream_gene_variant	MODIFIER	c.-2642A>T\|	S120 S121 S122 S174 S216 S23 S241 S265 S266 S27 S39 S55 S9
132374	BAA10g19350	A10	17768197	C	T	upstream_gene_variant	MODIFIER	c.-3536G>A\|	S11
132375	BAA10g19350	A10	17769023	C	T	upstream_gene_variant	MODIFIER	c.-4362G>A\|	S156

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