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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
130651	BAA10g18180	A10	17132183	C	T	synonymous_variant	LOW	c.42G>A\|p.Pro14Pro	S98
130652	BAA10g18190	A10	17132630	C	T	missense_variant	MODERATE	c.929G>A\|p.Cys310Tyr	S2
130653	BAA10g18190	A10	17133066	C	T	missense_variant	MODERATE	c.493G>A\|p.Glu165Lys	S281
130654	BAA10g18190	A10	17133110	G	A	missense_variant	MODERATE	c.449C>T\|p.Ala150Val	S65
130655	BAA10g18190	A10	17133348	G	A	missense_variant	MODERATE	c.211C>T\|p.Pro71Ser	S132 S215 S89
130656	BAA10g18190	A10	17133364	G	A	synonymous_variant	LOW	c.195C>T\|p.Thr65Thr	S128
130657	BAA10g18190	A10	17133485	G	A	missense_variant	MODERATE	c.74C>T\|p.Pro25Leu	S113
130658	BAA10g18190	A10	17133521	G	A	missense_variant	MODERATE	c.38C>T\|p.Ser13Phe	S72 S78
130659	BAA10g18200	A10	17135166	C	T	synonymous_variant	LOW	c.606G>A\|p.Ala202Ala	S259
130660	BAA10g18170	A10	17135334	G	A	upstream_gene_variant	MODIFIER	c.-4480C>T\|	S160
130661	BAA10g18200	A10	17135792	G	A	synonymous_variant	LOW	c.186C>T\|p.Phe62Phe	S64
130662	BAA10g18180	A10	17137167	C	T	upstream_gene_variant	MODIFIER	c.-4943G>A\|	S298
130663	BAA10g18190	A10	17137595	G	A	upstream_gene_variant	MODIFIER	c.-4037C>T\|	S100
130664	BAA10g18190	A10	17138304	C	T	upstream_gene_variant	MODIFIER	c.-4746G>A\|	S130
130665	BAA10g18200	A10	17138804	C	T	upstream_gene_variant	MODIFIER	c.-2702G>A\|	S148 S30 S31
130666	BAA10g18200	A10	17139391	G	A	upstream_gene_variant	MODIFIER	c.-3289C>T\|	S289 S290
130667	BAA10g18200	A10	17140188	G	A	upstream_gene_variant	MODIFIER	c.-4086C>T\|	S239
130668	BAA10g18210	A10	17140994	G	A	synonymous_variant	LOW	c.147G>A\|p.Gln49Gln	S169 S75 S81
130669	BAA10g18220	A10	17142227	G	A	downstream_gene_variant	MODIFIER	c.*1106C>T\|	S169
130670	BAA10g18220	A10	17142457	G	A	downstream_gene_variant	MODIFIER	c.*876C>T\|	S138
130671	BAA10g18220	A10	17143403	G	A	missense_variant	MODERATE	c.473C>T\|p.Thr158Ile	S241
130672	BAA10g18230	A10	17143622	G	A	upstream_gene_variant	MODIFIER	c.-4755G>A\|	S73 S91
130673	BAA10g18230	A10	17143963	G	A	upstream_gene_variant	MODIFIER	c.-4414G>A\|	S208 S219
130674	BAA10g18220	A10	17144338	C	T	synonymous_variant	LOW	c.216G>A\|p.Glu72Glu	S168
130675	BAA10g18220	A10	17144543	C	T	missense_variant	MODERATE	c.11G>A\|p.Gly4Glu	S37

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