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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
132451	BAA10g19390	A10	17791313	C	T	upstream_gene_variant	MODIFIER	c.-582C>T\|	S186
132452	BAA10g19390	A10	17791864	C	T	upstream_gene_variant	MODIFIER	c.-31C>T\|	S5
132453	BAA10g19390	A10	17792271	G	A	missense_variant	MODERATE	c.196G>A\|p.Glu66Lys	S274
132454	BAA10g19400	A10	17792424	C	T	upstream_gene_variant	MODIFIER	c.-3672C>T\|	S162
132455	BAA10g19400	A10	17793014	G	A	upstream_gene_variant	MODIFIER	c.-3082G>A\|	S57
132456	BAA10g19390	A10	17793521	G	A	missense_variant	MODERATE	c.1114G>A\|p.Glu372Lys	S270
132457	BAA10g19400	A10	17794173	C	T	upstream_gene_variant	MODIFIER	c.-1923C>T\|	S153 S213
132458	BAA10g19400	A10	17794450	C	T	upstream_gene_variant	MODIFIER	c.-1646C>T\|	S189
132459	BAA10g19400	A10	17794718	A	G	upstream_gene_variant	MODIFIER	c.-1378A>G\|	S189
132460	BAA10g19400	A10	17795653	C	T	upstream_gene_variant	MODIFIER	c.-443C>T\|	S249
132461	BAA10g19400	A10	17795676	G	A	upstream_gene_variant	MODIFIER	c.-420G>A\|	S174
132462	BAA10g19410	A10	17797479	C	T	upstream_gene_variant	MODIFIER	c.-4816C>T\|	S152
132463	BAA10g19410	A10	17797565	C	T	upstream_gene_variant	MODIFIER	c.-4730C>T\|	S177
132464	BAA10g19410	A10	17797580	C	T	upstream_gene_variant	MODIFIER	c.-4715C>T\|	S60
132465	BAA10g19410	A10	17797610	G	A	upstream_gene_variant	MODIFIER	c.-4685G>A\|	S172 S217
132466	BAA10g19400	A10	17798400	G	A	missense_variant	MODERATE	c.961G>A\|p.Gly321Arg	S36
132467	BAA10g19400	A10	17799453	C	T	missense_variant	MODERATE	c.1309C>T\|p.Pro437Ser	S282
132468	BAA10g19410	A10	17800179	C	T	upstream_gene_variant	MODIFIER	c.-2116C>T\|	S299
132469	BAA10g19400	A10	17800656	G	A	missense_variant	MODERATE	c.2147G>A\|p.Gly716Glu	S131
132470	BAA10g19400	A10	17800677	C	T	missense_variant	MODERATE	c.2168C>T\|p.Thr723Ile	S146
132471	BAA10g19410	A10	17800853	C	A	upstream_gene_variant	MODIFIER	c.-1442C>A\|	S112 S12 S130 S131 S137 S164 S174 S185 S209 S215 S232 S244 S259 S262 S286 S301 S302 S78 S85
132472	BAA10g19410	A10	17801326	C	T	upstream_gene_variant	MODIFIER	c.-969C>T\|	S61
132473	BAA10g19410	A10	17801384	G	A	upstream_gene_variant	MODIFIER	c.-911G>A\|	S28
132474	BAA10g19410	A10	17801414	C	T	upstream_gene_variant	MODIFIER	c.-881C>T\|	S251
132475	BAA10g19410	A10	17802496	C	T	synonymous_variant	LOW	c.202C>T\|p.Leu68Leu	S301 S304

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