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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
8801	BAA01g07110	A01	3146166	G	A	synonymous_variant	LOW	c.232C>T\|p.Leu78Leu	S183 S198
8802	BAA01g07100	A01	3146852	C	T	upstream_gene_variant	MODIFIER	c.-3720G>A\|	S35
8803	BAA01g07100	A01	3147740	G	A	upstream_gene_variant	MODIFIER	c.-4608C>T\|	S274
8804	BAA01g07110	A01	3148750	C	T	upstream_gene_variant	MODIFIER	c.-2166G>A\|	S266
8805	BAA01g07110	A01	3150617	G	A	upstream_gene_variant	MODIFIER	c.-4033C>T\|	S183 S198 S286
8806	BAA01g07110	A01	3150865	G	A	upstream_gene_variant	MODIFIER	c.-4281C>T\|	S294
8807	BAA01g07120	A01	3154353	C	T	upstream_gene_variant	MODIFIER	c.-2964C>T\|	S61
8808	BAA01g07120	A01	3155088	C	G	upstream_gene_variant	MODIFIER	c.-2229C>G\|	S276
8809	BAA01g07120	A01	3155647	G	A	upstream_gene_variant	MODIFIER	c.-1670G>A\|	S195
8810	BAA01g07120	A01	3157322	G	A	synonymous_variant	LOW	c.6G>A\|p.Lys2Lys	S146
8811	BAA01g07120	A01	3157634	G	A	intron_variant	MODIFIER	c.127+191G>A\|	S121
8812	BAA01g07120	A01	3157639	G	A	intron_variant	MODIFIER	c.127+196G>A\|	S57
8813	BAA01g07120	A01	3159460	T	G	missense_variant	MODERATE	c.1206T>G\|p.Phe402Leu	S156 S157 S17 S243 S270
8814	BAA01g07120	A01	3160493	T	G	missense_variant	MODERATE	c.1661T>G\|p.Leu554Arg	S115 S129 S132 S185 S193 S222 S223 S237 S238 S239 S246 S251 S252 S259 S261 S276 S293
8815	BAA01g07120	A01	3160730	C	T	missense_variant	MODERATE	c.1898C>T\|p.Ala633Val	S42
8816	BAA01g07130	A01	3161280	C	T	upstream_gene_variant	MODIFIER	c.-1906C>T\|	S270
8817	BAA01g07130	A01	3161439	G	A	upstream_gene_variant	MODIFIER	c.-1747G>A\|	S10
8818	BAA01g07120	A01	3161530	G	A	synonymous_variant	LOW	c.2157G>A\|p.Arg719Arg	S103
8819	BAA01g07120	A01	3161857	G	A	synonymous_variant	LOW	c.2484G>A\|p.Pro828Pro	S23
8820	BAA01g07130	A01	3162252	C	T	upstream_gene_variant	MODIFIER	c.-934C>T\|	S42
8821	BAA01g07130	A01	3162564	C	T	upstream_gene_variant	MODIFIER	c.-622C>T\|	S198
8822	BAA01g07130	A01	3163171	G	A	upstream_gene_variant	MODIFIER	c.-15G>A\|	S91
8823	BAA01g07120	A01	3163344	G	A	downstream_gene_variant	MODIFIER	c.*1145G>A\|	S190
8824	BAA01g07130	A01	3163402	G	A	missense_variant	MODERATE	c.128G>A\|p.Gly43Glu	S162
8825	BAA01g07130	A01	3163464	G	A	missense_variant	MODERATE	c.190G>A\|p.Glu64Lys	S157 S163

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