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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
164801	BAA02g11150	A02	5038871	C	T	downstream_gene_variant	MODIFIER	c.*3525G>A\|	S299
164802	BAA02g11150	A02	5038882	C	T	downstream_gene_variant	MODIFIER	c.*3514G>A\|	S262
164803	BAA02g11150	A02	5038941	C	T	downstream_gene_variant	MODIFIER	c.*3455G>A\|	S167
164804	BAA02g11150	A02	5040656	G	A	downstream_gene_variant	MODIFIER	c.*1740C>T\|	S41
164805	BAA02g11150	A02	5040875	C	T	downstream_gene_variant	MODIFIER	c.*1521G>A\|	S13
164806	BAA02g11150	A02	5043111	C	T	missense_variant	MODERATE	c.1937G>A\|p.Gly646Glu	S131
164807	BAA02g11150	A02	5043153	C	T	missense_variant	MODERATE	c.1895G>A\|p.Gly632Glu	S181
164808	BAA02g11150	A02	5043280	C	T	missense_variant	MODERATE	c.1768G>A\|p.Asp590Asn	S230
164809	BAA02g11150	A02	5043520	G	A	missense_variant	MODERATE	c.1528C>T\|p.Arg510Cys	S283
164810	BAA02g11150	A02	5044323	C	T	missense_variant	MODERATE	c.989G>A\|p.Arg330His	S40 S49
164811	BAA02g11150	A02	5044505	G	A	intron_variant	MODIFIER	c.931-124C>T\|	S206 S26
164812	BAA02g11150	A02	5046561	C	T	missense_variant	MODERATE	c.208G>A\|p.Asp70Asn	S152
164813	BAA02g11150	A02	5047968	C	T	upstream_gene_variant	MODIFIER	c.-719G>A\|	S193
164814	BAA02g11150	A02	5048407	C	T	upstream_gene_variant	MODIFIER	c.-1158G>A\|	S37
164815	BAA02g11150	A02	5048446	G	A	upstream_gene_variant	MODIFIER	c.-1197C>T\|	S289 S290
164816	BAA02g11150	A02	5049093	C	T	upstream_gene_variant	MODIFIER	c.-1844G>A\|	S257
164817	BAA02g11150	A02	5049162	G	A	upstream_gene_variant	MODIFIER	c.-1913C>T\|	S192
164818	BAA02g11150	A02	5050707	C	T	upstream_gene_variant	MODIFIER	c.-3458G>A\|	S44
164819	BAA02g11170	A02	5052229	G	A	synonymous_variant	LOW	c.852C>T\|p.His284His	S179 S180 S183
164820	BAA02g11170	A02	5052235	C	T	missense_variant	MODERATE	c.846G>A\|p.Met282Ile	S128
164821	BAA02g11170	A02	5052238	C	T	synonymous_variant	LOW	c.843G>A\|p.Glu281Glu	S179 S180 S183
164822	BAA02g11170	A02	5052241	A	T	synonymous_variant	LOW	c.840T>A\|p.Val280Val	S179 S180 S183
164823	BAA02g11170	A02	5052250	G	C	synonymous_variant	LOW	c.831C>G\|p.Val277Val	S179 S183
164824	BAA02g11170	A02	5052259	G	T	synonymous_variant	LOW	c.822C>A\|p.Thr274Thr	S178 S179 S183 S191
164825	BAA02g11170	A02	5052541	C	T	synonymous_variant	LOW	c.540G>A\|p.Lys180Lys	S202

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