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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
111701	BAA10g08350	A10	10084127	G	A	intron_variant	MODIFIER	c.902-1217C>T\|	S234
111702	BAA10g08350	A10	10084569	C	T	intron_variant	MODIFIER	c.901+867G>A\|	S144
111703	BAA10g08350	A10	10085481	G	A	missense_variant	MODERATE	c.856C>T\|p.Pro286Ser	S221
111704	BAA10g08350	A10	10085865	C	T	missense_variant	MODERATE	c.472G>A\|p.Val158Ile	S188 S265
111705	BAA10g08350	A10	10086204	G	A	missense_variant	MODERATE	c.133C>T\|p.Pro45Ser	S172 S217
111706	BAA10g08350-BAA10g08360	A10	10092789	G	A	intergenic_region	MODIFIER	n.10092789G>A\|	S128
111707	BAA10g08350-BAA10g08360	A10	10094515	C	T	intergenic_region	MODIFIER	n.10094515C>T\|	S193
111708	BAA10g08350-BAA10g08360	A10	10095070	G	A	intergenic_region	MODIFIER	n.10095070G>A\|	S159 S187 S188 S243 S276
111709	BAA10g08360	A10	10095959	C	T	downstream_gene_variant	MODIFIER	c.*4504G>A\|	S191
111710	BAA10g08360	A10	10098801	C	T	downstream_gene_variant	MODIFIER	c.*1662G>A\|	S291
111711	BAA10g08360	A10	10099240	C	T	downstream_gene_variant	MODIFIER	c.*1223G>A\|	S269
111712	BAA10g08360	A10	10099935	G	A	downstream_gene_variant	MODIFIER	c.*528C>T\|	S71
111713	BAA10g08360	A10	10100346	C	T	downstream_gene_variant	MODIFIER	c.*117G>A\|	S183
111714	BAA10g08360	A10	10101062	G	T	missense_variant	MODERATE	c.4907C>A\|p.Pro1636Gln	S261
111715	BAA10g08360	A10	10101081	C	T	missense_variant	MODERATE	c.4888G>A\|p.Glu1630Lys	S42
111716	BAA10g08360	A10	10101308	C	T	missense_variant	MODERATE	c.4741G>A\|p.Asp1581Asn	S152
111717	BAA10g08360	A10	10102208	C	T	intron_variant	MODIFIER	c.4179+9G>A\|	S297
111718	BAA10g08360	A10	10102925	C	T	missense_variant	MODERATE	c.3619G>A\|p.Glu1207Lys	S185
111719	BAA10g08360	A10	10102930	G	A	missense_variant	MODERATE	c.3614C>T\|p.Pro1205Leu	S138
111720	BAA10g08360	A10	10104355	C	T	missense_variant	MODERATE	c.2428G>A\|p.Glu810Lys	S25
111721	BAA10g08360	A10	10104403	C	T	missense_variant	MODERATE	c.2380G>A\|p.Glu794Lys	S144
111722	BAA10g08360	A10	10105736	G	A	synonymous_variant	LOW	c.1212C>T\|p.Phe404Phe	S148 S210 S30 S31
111723	BAA10g08360	A10	10109318	G	A	upstream_gene_variant	MODIFIER	c.-2279C>T\|	S65
111724	BAA10g08360	A10	10110068	G	A	upstream_gene_variant	MODIFIER	c.-3029C>T\|	S178
111725	BAA10g08360	A10	10110294	C	T	upstream_gene_variant	MODIFIER	c.-3255G>A\|	S181

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