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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
115951	BAA10g10050	A10	11841309	G	A	intron_variant	MODIFIER	c.3216+172G>A\|	S192
115952	BAA10g10050	A10	11841533	C	T	missense_variant	MODERATE	c.3224C>T\|p.Ser1075Leu	S103
115953	BAA10g10060	A10	11842416	C	T	upstream_gene_variant	MODIFIER	c.-3950C>T\|	S19
115954	BAA10g10060	A10	11842439	C	T	upstream_gene_variant	MODIFIER	c.-3927C>T\|	S17
115955	BAA10g10060	A10	11842446	C	T	upstream_gene_variant	MODIFIER	c.-3920C>T\|	S61
115956	BAA10g10060	A10	11842554	C	T	upstream_gene_variant	MODIFIER	c.-3812C>T\|	S99
115957	BAA10g10060	A10	11842997	G	A	upstream_gene_variant	MODIFIER	c.-3369G>A\|	S48
115958	BAA10g10060	A10	11843515	C	T	upstream_gene_variant	MODIFIER	c.-2851C>T\|	S146
115959	BAA10g10060	A10	11844084	C	T	upstream_gene_variant	MODIFIER	c.-2282C>T\|	S225 S73
115960	BAA10g10060	A10	11846488	C	T	synonymous_variant	LOW	c.123C>T\|p.Thr41Thr	S117
115961	BAA10g10060	A10	11846501	C	T	missense_variant	MODERATE	c.136C>T\|p.Pro46Ser	S171
115962	BAA10g10060	A10	11847111	C	T	missense_variant	MODERATE	c.746C>T\|p.Ser249Phe	S53 S81 S82 S85 S92
115963	BAA10g10060	A10	11847576	C	T	downstream_gene_variant	MODIFIER	c.*178C>T\|	S34
115964	BAA10g10070	A10	11850267	T	G	upstream_gene_variant	MODIFIER	c.-784A>C\|	S110 S122 S123 S125 S165 S181 S19 S251 S275 S278 S288 S306 S5 S7 S77 S86
115965	BAA10g10070	A10	11850814	G	A	upstream_gene_variant	MODIFIER	c.-1331C>T\|	S296
115966	BAA10g10070	A10	11851074	C	T	upstream_gene_variant	MODIFIER	c.-1591G>A\|	S5
115967	BAA10g10070	A10	11851377	G	A	upstream_gene_variant	MODIFIER	c.-1894C>T\|	S262
115968	BAA10g10080	A10	11855246	G	A	upstream_gene_variant	MODIFIER	c.-3178G>A\|	S72
115969	BAA10g10080	A10	11855317	C	T	upstream_gene_variant	MODIFIER	c.-3107C>T\|	S152
115970	BAA10g10080	A10	11856471	C	T	upstream_gene_variant	MODIFIER	c.-1953C>T\|	S166
115971	BAA10g10080	A10	11856574	C	T	upstream_gene_variant	MODIFIER	c.-1850C>T\|	S208 S93
115972	BAA10g10080	A10	11856708	C	T	upstream_gene_variant	MODIFIER	c.-1716C>T\|	S56
115973	BAA10g10080	A10	11857853	G	A	upstream_gene_variant	MODIFIER	c.-571G>A\|	S296
115974	BAA10g10080	A10	11858202	C	T	upstream_gene_variant	MODIFIER	c.-222C>T\|	S270
115975	BAA10g10080	A10	11858749	C	T	intron_variant	MODIFIER	c.224+102C>T\|	S123

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