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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
162951	BAA02g09790	A02	4318287	C	T	intron_variant	MODIFIER	c.738-80G>A\|	S117
162952	BAA02g09790	A02	4319348	C	T	splice_donor_variant&intron_variant	HIGH	c.268+1G>A\|	S230
162953	BAA02g09790	A02	4320067	C	T	upstream_gene_variant	MODIFIER	c.-372G>A\|	S261
162954	BAA02g09800	A02	4325102	C	T	downstream_gene_variant	MODIFIER	c.*1634G>A\|	S250
162955	BAA02g09800	A02	4326391	G	A	downstream_gene_variant	MODIFIER	c.*345C>T\|	S23
162956	BAA02g09800	A02	4326744	C	T	missense_variant	MODERATE	c.1600G>A\|p.Gly534Arg	S186
162957	BAA02g09800	A02	4328970	C	T	missense_variant	MODERATE	c.70G>A\|p.Gly24Arg	S128
162958	BAA02g09800	A02	4329301	G	A	upstream_gene_variant	MODIFIER	c.-262C>T\|	S45
162959	BAA02g09810	A02	4330592	C	T	missense_variant	MODERATE	c.1033G>A\|p.Gly345Ser	S277
162960	BAA02g09810	A02	4330764	C	T	synonymous_variant	LOW	c.861G>A\|p.Pro287Pro	S234
162961	BAA02g09810	A02	4331666	C	T	stop_gained	HIGH	c.90G>A\|p.Trp30*	S183 S198
162962	BAA02g09800	A02	4332135	G	A	upstream_gene_variant	MODIFIER	c.-3096C>T\|	S205
162963	BAA02g09800	A02	4332149	G	A	upstream_gene_variant	MODIFIER	c.-3110C>T\|	S132 S137 S138 S215 S237 S288 S89
162964	BAA02g09810	A02	4334112	A	C	upstream_gene_variant	MODIFIER	c.-2357T>G\|	S10 S105 S124 S125 S126 S138 S151 S160 S165 S177 S243 S38 S64 S76
162965	BAA02g09810	A02	4334518	C	T	upstream_gene_variant	MODIFIER	c.-2763G>A\|	S39
162966	BAA02g09830	A02	4335415	C	T	missense_variant	MODERATE	c.1414G>A\|p.Gly472Arg	S13
162967	BAA02g09830	A02	4335531	G	A	missense_variant	MODERATE	c.1298C>T\|p.Ala433Val	S276
162968	BAA02g09820	A02	4336781	G	A	upstream_gene_variant	MODIFIER	c.-3305C>T\|	S69
162969	BAA02g09820	A02	4337547	G	A	upstream_gene_variant	MODIFIER	c.-4071C>T\|	S173
162970	BAA02g09820	A02	4338022	A	C	upstream_gene_variant	MODIFIER	c.-4546T>G\|	S144
162971	BAA02g09840	A02	4339446	C	T	missense_variant	MODERATE	c.466C>T\|p.Pro156Ser	S200
162972	BAA02g09850	A02	4341226	G	A	missense_variant	MODERATE	c.623C>T\|p.Ala208Val	S210 S225
162973	BAA02g09850	A02	4341250	C	T	missense_variant	MODERATE	c.599G>A\|p.Arg200Lys	S240
162974	BAA02g09850	A02	4341764	C	T	missense_variant	MODERATE	c.343G>A\|p.Gly115Arg	S292
162975	BAA02g09830	A02	4342153	G	A	upstream_gene_variant	MODIFIER	c.-4137C>T\|	S256

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