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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
150251	BAA10g34320	A10	24158642	C	T	missense_variant	MODERATE	c.748G>A\|p.Glu250Lys	S187
150252	BAA10g34320	A10	24158693	G	A	missense_variant	MODERATE	c.697C>T\|p.His233Tyr	S183 S198
150253	BAA10g34320	A10	24158724	G	A	synonymous_variant	LOW	c.666C>T\|p.Ile222Ile	S194 S69
150254	BAA10g34320	A10	24158800	C	T	missense_variant	MODERATE	c.590G>A\|p.Gly197Glu	S23
150255	BAA10g34320	A10	24159006	G	A	synonymous_variant	LOW	c.384C>T\|p.Leu128Leu	S264
150256	BAA10g34320	A10	24159147	G	A	synonymous_variant	LOW	c.243C>T\|p.Phe81Phe	S157 S163
150257	BAA10g34320	A10	24159608	C	T	synonymous_variant	LOW	c.117G>A\|p.Arg39Arg	S296
150258	BAA10g34320	A10	24159857	G	A	upstream_gene_variant	MODIFIER	c.-133C>T\|	S75 S81
150259	BAA10g34320	A10	24161215	C	T	upstream_gene_variant	MODIFIER	c.-1491G>A\|	S218
150260	BAA10g34320	A10	24164329	G	A	upstream_gene_variant	MODIFIER	c.-4605C>T\|	S160
150261	BAA10g34320	A10	24164626	C	T	upstream_gene_variant	MODIFIER	c.-4902G>A\|	S236
150262	BAA10g34330	A10	24166156	C	T	upstream_gene_variant	MODIFIER	c.-2385C>T\|	S44
150263	BAA10g34330	A10	24166295	C	T	upstream_gene_variant	MODIFIER	c.-2246C>T\|	S87
150264	BAA10g34340	A10	24168768	C	T	downstream_gene_variant	MODIFIER	c.*3055G>A\|	S18
150265	BAA10g34340	A10	24168782	G	A	downstream_gene_variant	MODIFIER	c.*3041C>T\|	S279
150266	BAA10g34330	A10	24169232	G	A	missense_variant	MODERATE	c.364G>A\|p.Glu122Lys	S159 S243
150267	BAA10g34330	A10	24169375	C	T	synonymous_variant	LOW	c.507C>T\|p.Ala169Ala	S230
150268	BAA10g34330	A10	24170054	G	A	missense_variant	MODERATE	c.1186G>A\|p.Asp396Asn	S130
150269	BAA10g34330	A10	24170485	G	A	synonymous_variant	LOW	c.1617G>A\|p.Lys539Lys	S273
150270	BAA10g34330	A10	24170494	G	A	synonymous_variant	LOW	c.1626G>A\|p.Val542Val	S92 S93
150271	BAA10g34330	A10	24170497	A	G	synonymous_variant	LOW	c.1629A>G\|p.Glu543Glu	S92 S93
150272	BAA10g34330	A10	24170498	G	T	missense_variant	MODERATE	c.1630G>T\|p.Ala544Ser	S92 S93
150273	BAA10g34330	A10	24170507	G	A	missense_variant	MODERATE	c.1639G>A\|p.Ala547Thr	S92 S93
150274	BAA10g34330	A10	24170509	T	G	synonymous_variant	LOW	c.1641T>G\|p.Ala547Ala	S92 S93
150275	BAA10g34330	A10	24170512	C	G	synonymous_variant	LOW	c.1644C>G\|p.Leu548Leu	S92 S93

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