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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
145251	BAA10g29850	A10	22311417	C	T	missense_variant	MODERATE	c.1918G>A\|p.Val640Ile	S211 S227
145252	BAA10g29850	A10	22312045	C	T	missense_variant	MODERATE	c.1583G>A\|p.Arg528Lys	S281
145253	BAA10g29850	A10	22312065	A	T	synonymous_variant	LOW	c.1563T>A\|p.Pro521Pro	S225 S270 S278 S291 S36 S59 S61 S98
145254	BAA10g29850	A10	22312259	C	T	splice_region_variant&intron_variant	LOW	c.1466+8G>A\|	S38
145255	BAA10g29850	A10	22313041	C	T	missense_variant	MODERATE	c.925G>A\|p.Glu309Lys	S87
145256	BAA10g29850	A10	22313182	C	T	missense_variant	MODERATE	c.784G>A\|p.Asp262Asn	S42
145257	BAA10g29850	A10	22314580	G	A	upstream_gene_variant	MODIFIER	c.-329C>T\|	S256
145258	BAA10g29860	A10	22315888	C	T	missense_variant	MODERATE	c.46C>T\|p.Leu16Phe	S33
145259	BAA10g29860	A10	22317650	C	T	missense_variant	MODERATE	c.1270C>T\|p.His424Tyr	S133
145260	BAA10g29860	A10	22317689	G	A	missense_variant	MODERATE	c.1309G>A\|p.Val437Ile	S228
145261	BAA10g29860	A10	22317790	G	A	synonymous_variant	LOW	c.1410G>A\|p.Arg470Arg	S219 S72
145262	BAA10g29860	A10	22317812	G	A	missense_variant	MODERATE	c.1432G>A\|p.Asp478Asn	S140 S168 S278 S64
145263	BAA10g29860	A10	22318550	C	T	missense_variant	MODERATE	c.2170C>T\|p.Pro724Ser	S187
145264	BAA10g29860	A10	22318584	G	A	missense_variant	MODERATE	c.2204G>A\|p.Gly735Glu	S109
145265	BAA10g29860	A10	22318637	C	T	missense_variant	MODERATE	c.2257C>T\|p.Pro753Ser	S5
145266	BAA10g29860	A10	22319216	C	T	missense_variant	MODERATE	c.2570C>T\|p.Ala857Val	S107
145267	BAA10g29860	A10	22319821	G	A	splice_region_variant&synonymous_variant	LOW	c.2847G>A\|p.Gln949Gln	S179
145268	BAA10g29870	A10	22319849	C	T	downstream_gene_variant	MODIFIER	c.*2108G>A\|	S115
145269	BAA10g29860	A10	22320947	G	A	missense_variant	MODERATE	c.3370G>A\|p.Glu1124Lys	S263
145270	BAA10g29870	A10	22321052	G	A	downstream_gene_variant	MODIFIER	c.*905C>T\|	S279
145271	BAA10g29860	A10	22321334	C	T	downstream_gene_variant	MODIFIER	c.*89C>T\|	S292
145272	BAA10g29860	A10	22321704	G	A	downstream_gene_variant	MODIFIER	c.*459G>A\|	S125
145273	BAA10g29860	A10	22321885	G	A	downstream_gene_variant	MODIFIER	c.*640G>A\|	S75
145274	BAA10g29870	A10	22322397	G	A	missense_variant	MODERATE	c.928C>T\|p.Pro310Ser	S262
145275	BAA10g29870	A10	22323616	C	T	upstream_gene_variant	MODIFIER	c.-292G>A\|	S208

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