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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
133001	BAA10g19650	A10	17963530	C	T	missense_variant	MODERATE	c.1208G>A\|p.Gly403Glu	S73 S91
133002	BAA10g19650	A10	17963724	C	T	synonymous_variant	LOW	c.1014G>A\|p.Glu338Glu	S148 S30 S31
133003	BAA10g19660	A10	17964517	C	T	downstream_gene_variant	MODIFIER	c.*4689G>A\|	S54
133004	BAA10g19660	A10	17964876	C	T	downstream_gene_variant	MODIFIER	c.*4330G>A\|	S157 S163
133005	BAA10g19650	A10	17965166	G	A	synonymous_variant	LOW	c.612C>T\|p.Ser204Ser	S262
133006	BAA10g19660	A10	17965422	G	A	downstream_gene_variant	MODIFIER	c.*3784C>T\|	S1 S90
133007	BAA10g19660	A10	17965550	G	A	downstream_gene_variant	MODIFIER	c.*3656C>T\|	S118
133008	BAA10g19650	A10	17967063	G	A	upstream_gene_variant	MODIFIER	c.-171C>T\|	S239
133009	BAA10g19650	A10	17967624	G	A	upstream_gene_variant	MODIFIER	c.-732C>T\|	S219
133010	BAA10g19650	A10	17968388	G	A	upstream_gene_variant	MODIFIER	c.-1496C>T\|	S1 S113 S115 S117 S122 S161 S19 S228 S244 S251 S289 S290 S297 S305 S35 S5 S65 S8 S90
133011	BAA10g19660	A10	17969413	C	T	synonymous_variant	LOW	c.1518G>A\|p.Leu506Leu	S183
133012	BAA10g19660	A10	17969544	C	T	missense_variant	MODERATE	c.1387G>A\|p.Glu463Lys	S169
133013	BAA10g19660	A10	17969893	G	A	synonymous_variant	LOW	c.1038C>T\|p.Asn346Asn	S88
133014	BAA10g19650	A10	17970876	C	T	upstream_gene_variant	MODIFIER	c.-3984G>A\|	S96
133015	BAA10g19650	A10	17971061	C	T	upstream_gene_variant	MODIFIER	c.-4169G>A\|	S153 S213
133016	BAA10g19660	A10	17972688	C	T	stop_gained	HIGH	c.18G>A\|p.Trp6*	S119
133017	BAA10g19670	A10	17977905	G	A	downstream_gene_variant	MODIFIER	c.*1355C>T\|	S298
133018	BAA10g19670	A10	17978328	G	A	downstream_gene_variant	MODIFIER	c.*932C>T\|	S207
133019	BAA10g19670	A10	17978463	C	T	downstream_gene_variant	MODIFIER	c.*797G>A\|	S187
133020	BAA10g19670	A10	17978473	C	T	downstream_gene_variant	MODIFIER	c.*787G>A\|	S202
133021	BAA10g19670	A10	17978920	G	A	downstream_gene_variant	MODIFIER	c.*340C>T\|	S76
133022	BAA10g19670	A10	17978985	C	T	downstream_gene_variant	MODIFIER	c.*275G>A\|	S125
133023	BAA10g19670	A10	17979472	C	T	missense_variant	MODERATE	c.1510G>A\|p.Ala504Thr	S202
133024	BAA10g19670	A10	17979578	G	A	synonymous_variant	LOW	c.1404C>T\|p.Leu468Leu	S176
133025	BAA10g19670	A10	17979705	G	A	missense_variant	MODERATE	c.1277C>T\|p.Pro426Leu	S59

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