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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
150951	BAA10g34890	A10	24391886	C	T	upstream_gene_variant	MODIFIER	c.-1253C>T\|	S306 S308
150952	BAA10g34890	A10	24392142	G	A	upstream_gene_variant	MODIFIER	c.-997G>A\|	S57
150953	BAA10g34890	A10	24393842	C	T	missense_variant	MODERATE	c.230C>T\|p.Pro77Leu	S96
150954	BAA10g34890	A10	24395441	T	G	missense_variant	MODERATE	c.958T>G\|p.Phe320Val	S152 S216 S235 S246 S256 S28 S287 S3 S35 S46 S58 S70 S79 S82 S94
150955	BAA10g34890	A10	24395938	G	A	missense_variant	MODERATE	c.1168G>A\|p.Val390Ile	S28
150956	BAA10g34890	A10	24396929	C	T	downstream_gene_variant	MODIFIER	c.*187C>T\|	S123
150957	BAA10g34920	A10	24397890	C	T	upstream_gene_variant	MODIFIER	c.-4221C>T\|	S143 S257
150958	BAA10g34920	A10	24397903	G	A	upstream_gene_variant	MODIFIER	c.-4208G>A\|	S116
150959	BAA10g34900	A10	24398541	C	T	missense_variant	MODERATE	c.818G>A\|p.Arg273Lys	S8
150960	BAA10g34900	A10	24400114	G	A	upstream_gene_variant	MODIFIER	c.-756C>T\|	S38
150961	BAA10g34900	A10	24400165	G	A	upstream_gene_variant	MODIFIER	c.-807C>T\|	S293
150962	BAA10g34920	A10	24402674	G	A	missense_variant	MODERATE	c.356G>A\|p.Ser119Asn	S162
150963	BAA10g34920	A10	24402888	C	T	synonymous_variant	LOW	c.570C>T\|p.Thr190Thr	S211 S227
150964	BAA10g34910	A10	24404755	C	T	upstream_gene_variant	MODIFIER	c.-3063G>A\|	S5
150965	BAA10g34910	A10	24405331	G	A	upstream_gene_variant	MODIFIER	c.-3639C>T\|	S12
150966	BAA10g34910	A10	24405476	G	A	upstream_gene_variant	MODIFIER	c.-3784C>T\|	S237
150967	BAA10g34910	A10	24405499	C	T	upstream_gene_variant	MODIFIER	c.-3807G>A\|	S302
150968	BAA10g34910	A10	24405700	C	T	upstream_gene_variant	MODIFIER	c.-4008G>A\|	S194
150969	BAA10g34910	A10	24405709	G	A	upstream_gene_variant	MODIFIER	c.-4017C>T\|	S178
150970	BAA10g34910	A10	24405837	G	A	upstream_gene_variant	MODIFIER	c.-4145C>T\|	S250
150971	BAA10g34910	A10	24405863	G	A	upstream_gene_variant	MODIFIER	c.-4171C>T\|	S159 S243
150972	BAA10g34910	A10	24405948	G	A	upstream_gene_variant	MODIFIER	c.-4256C>T\|	S115
150973	BAA10g34930	A10	24406513	G	A	missense_variant	MODERATE	c.236G>A\|p.Gly79Glu	S151
150974	BAA10g34920	A10	24406770	C	A	downstream_gene_variant	MODIFIER	c.*2165C>A\|	S264
150975	BAA10g34920	A10	24406901	C	T	downstream_gene_variant	MODIFIER	c.*2296C>T\|	S146

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