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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
4601	BAA01g03690	A01	1682220	C	T	synonymous_variant	LOW	c.1419C>T\|p.Phe473Phe	S137
4602	BAA01g03690	A01	1682264	C	T	missense_variant	MODERATE	c.1463C>T\|p.Pro488Leu	S100
4603	BAA01g03690	A01	1682267	C	T	missense_variant	MODERATE	c.1466C>T\|p.Thr489Ile	S208 S219
4604	BAA01g03690	A01	1682408	G	A	missense_variant	MODERATE	c.1607G>A\|p.Gly536Glu	S159 S188 S243 S276 S298 S299
4605	BAA01g03690	A01	1683127	G	A	downstream_gene_variant	MODIFIER	c.*679G>A\|	S157 S163
4606	BAA01g03690	A01	1683228	G	A	downstream_gene_variant	MODIFIER	c.*780G>A\|	S263
4607	BAA01g03700	A01	1683291	C	T	missense_variant	MODERATE	c.1969G>A\|p.Glu657Lys	S69
4608	BAA01g03700	A01	1683621	G	A	missense_variant	MODERATE	c.1639C>T\|p.Leu547Phe	S32 S56
4609	BAA01g03700	A01	1683940	G	A	synonymous_variant	LOW	c.1320C>T\|p.Leu440Leu	S144
4610	BAA01g03700	A01	1684602	C	T	missense_variant	MODERATE	c.658G>A\|p.Glu220Lys	S249
4611	BAA01g03700	A01	1684774	C	T	synonymous_variant	LOW	c.486G>A\|p.Glu162Glu	S238
4612	BAA01g03700	A01	1685108	G	A	missense_variant	MODERATE	c.152C>T\|p.Ala51Val	S172 S217
4613	BAA01g03700	A01	1685118	G	A	missense_variant	MODERATE	c.142C>T\|p.Arg48Cys	S172 S217
4614	BAA01g03700	A01	1685406	C	T	upstream_gene_variant	MODIFIER	c.-147G>A\|	S267
4615	BAA01g03710	A01	1687046	C	T	synonymous_variant	LOW	c.1587G>A\|p.Lys529Lys	S68
4616	BAA01g03710	A01	1687412	C	T	missense_variant	MODERATE	c.1357G>A\|p.Asp453Asn	S43
4617	BAA01g03710	A01	1687570	C	T	missense_variant	MODERATE	c.1274G>A\|p.Ser425Asn	S100
4618	BAA01g03710	A01	1689180	C	T	synonymous_variant	LOW	c.384G>A\|p.Gln128Gln	S113 S19
4619	BAA01g03710	A01	1689457	C	T	synonymous_variant	LOW	c.177G>A\|p.Lys59Lys	S266
4620	BAA01g03710	A01	1691096	G	A	upstream_gene_variant	MODIFIER	c.-1463C>T\|	S295
4621	BAA01g03720	A01	1693228	C	T	missense_variant	MODERATE	c.1522C>T\|p.Leu508Phe	S211 S227
4622	BAA01g03720	A01	1694079	G	A	missense_variant	MODERATE	c.2057G>A\|p.Gly686Glu	S63
4623	BAA01g03720	A01	1694376	C	T	missense_variant	MODERATE	c.2191C>T\|p.Pro731Ser	S58
4624	BAA01g03720	A01	1694806	G	A	missense_variant	MODERATE	c.2500G>A\|p.Ala834Thr	S115
4625	BAA01g03720	A01	1695558	G	A	synonymous_variant	LOW	c.3060G>A\|p.Lys1020Lys	S177

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