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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
141201	BAA10g26200	A10	20883879	C	T	upstream_gene_variant	MODIFIER	c.-3928G>A\|	S107
141202	BAA10g26220	A10	20884343	C	T	synonymous_variant	LOW	c.414C>T\|p.Leu138Leu	S281
141203	BAA10g26210	A10	20885174	C	T	upstream_gene_variant	MODIFIER	c.-3333G>A\|	S189
141204	BAA10g26210	A10	20886415	C	T	upstream_gene_variant	MODIFIER	c.-4574G>A\|	S148 S210 S30 S31
141205	BAA10g26210	A10	20886828	C	T	upstream_gene_variant	MODIFIER	c.-4987G>A\|	S189
141206	BAA10g26230	A10	20886913	G	A	upstream_gene_variant	MODIFIER	c.-482G>A\|	S143
141207	BAA10g26230	A10	20887426	C	T	missense_variant	MODERATE	c.32C>T\|p.Ala11Val	S28
141208	BAA10g26230	A10	20887498	C	T	missense_variant	MODERATE	c.104C>T\|p.Ser35Leu	S153 S213
141209	BAA10g26220	A10	20888886	C	T	downstream_gene_variant	MODIFIER	c.*4198C>T\|	S180
141210	BAA10g26240	A10	20889123	C	T	missense_variant	MODERATE	c.439G>A\|p.Ala147Thr	S115
141211	BAA10g26240	A10	20889155	C	T	missense_variant	MODERATE	c.407G>A\|p.Arg136Gln	S115
141212	BAA10g26240	A10	20889204	G	A	missense_variant	MODERATE	c.358C>T\|p.Pro120Ser	S179
141213	BAA10g26220	A10	20889304	C	T	downstream_gene_variant	MODIFIER	c.*4616C>T\|	S42
141214	BAA10g26240	A10	20889574	C	T	missense_variant	MODERATE	c.157G>A\|p.Gly53Arg	S46
141215	BAA10g26240	A10	20890136	C	T	upstream_gene_variant	MODIFIER	c.-406G>A\|	S174 S216 S241 S27
141216	BAA10g26240	A10	20890179	G	A	upstream_gene_variant	MODIFIER	c.-449C>T\|	S279
141217	BAA10g26240	A10	20891214	C	T	upstream_gene_variant	MODIFIER	c.-1484G>A\|	S295
141218	BAA10g26240	A10	20891553	C	T	upstream_gene_variant	MODIFIER	c.-1823G>A\|	S204
141219	BAA10g26250	A10	20892671	G	A	missense_variant	MODERATE	c.1151C>T\|p.Ala384Val	S159 S243 S276 S298
141220	BAA10g26240	A10	20893497	G	A	upstream_gene_variant	MODIFIER	c.-3767C>T\|	S245
141221	BAA10g26250	A10	20895630	G	A	upstream_gene_variant	MODIFIER	c.-941C>T\|	S164
141222	BAA10g26260	A10	20897771	G	A	missense_variant	MODERATE	c.224G>A\|p.Arg75Gln	S165
141223	BAA10g26260	A10	20897902	G	A	missense_variant	MODERATE	c.262G>A\|p.Glu88Lys	S144
141224	BAA10g26260	A10	20898767	C	T	synonymous_variant	LOW	c.570C>T\|p.Ile190Ile	S282
141225	BAA10g26280	A10	20902544	C	T	upstream_gene_variant	MODIFIER	c.-1440C>T\|	S296

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