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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
47901	BAA01g27650	A01	16622852	C	T	downstream_gene_variant	MODIFIER	c.*2758G>A\|	S255
47902	BAA01g27640	A01	16624146	G	A	missense_variant	MODERATE	c.1072G>A\|p.Asp358Asn	S161 S228 S244 S289 S290
47903	BAA01g27650	A01	16625651	C	T	missense_variant	MODERATE	c.1954G>A\|p.Gly652Arg	S41
47904	BAA01g27640	A01	16626884	C	T	downstream_gene_variant	MODIFIER	c.*1915C>T\|	S156
47905	BAA01g27650	A01	16630492	C	T	upstream_gene_variant	MODIFIER	c.-807G>A\|	S166
47906	BAA01g27650	A01	16631098	G	A	upstream_gene_variant	MODIFIER	c.-1413C>T\|	S174 S27
47907	BAA01g27650	A01	16632027	G	A	upstream_gene_variant	MODIFIER	c.-2342C>T\|	S241
47908	BAA01g27660	A01	16638272	G	A	downstream_gene_variant	MODIFIER	c.*1475C>T\|	S74
47909	BAA01g27660	A01	16638554	G	A	downstream_gene_variant	MODIFIER	c.*1193C>T\|	S155 S211
47910	BAA01g27660	A01	16639407	G	A	downstream_gene_variant	MODIFIER	c.*340C>T\|	S188
47911	BAA01g27660	A01	16639845	C	T	missense_variant	MODERATE	c.1153G>A\|p.Glu385Lys	S264
47912	BAA01g27660	A01	16640197	G	A	intron_variant	MODIFIER	c.1104+211C>T\|	S172 S217
47913	BAA01g27660	A01	16640572	C	T	missense_variant	MODERATE	c.940G>A\|p.Asp314Asn	S222 S294
47914	BAA01g27660	A01	16640581	C	T	missense_variant	MODERATE	c.931G>A\|p.Asp311Asn	S104 S52
47915	BAA01g27660	A01	16640590	C	T	missense_variant	MODERATE	c.922G>A\|p.Asp308Asn	S148 S210
47916	BAA01g27660	A01	16640739	G	A	intron_variant	MODIFIER	c.871+15C>T\|	S306 S308
47917	BAA01g27660	A01	16640922	T	G	intron_variant	MODIFIER	c.843-140A>C\|	S28
47918	BAA01g27660	A01	16640923	C	T	intron_variant	MODIFIER	c.843-141G>A\|	S28
47919	BAA01g27660	A01	16640951	C	T	intron_variant	MODIFIER	c.843-169G>A\|	S25 S264
47920	BAA01g27660	A01	16641728	C	T	intron_variant	MODIFIER	c.711+227G>A\|	S295
47921	BAA01g27660	A01	16641825	C	T	intron_variant	MODIFIER	c.711+130G>A\|	S237
47922	BAA01g27660	A01	16642476	T	A	intron_variant	MODIFIER	c.405+192A>T\|	S111
47923	BAA01g27660	A01	16643085	C	T	intron_variant	MODIFIER	c.330+336G>A\|	S293
47924	BAA01g27660	A01	16643377	C	T	intron_variant	MODIFIER	c.330+44G>A\|	S107
47925	BAA01g27660	A01	16643517	G	A	synonymous_variant	LOW	c.234C>T\|p.Asp78Asp	S283

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