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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1401	BAA01g01160	A01	483805	C	T	synonymous_variant	LOW	c.603C>T\|p.Asp201Asp	S179
1402	BAA01g01160	A01	485202	G	A	missense_variant	MODERATE	c.1465G>A\|p.Glu489Lys	S110 S298
1403	BAA01g01170	A01	486469	C	T	synonymous_variant	LOW	c.765G>A\|p.Lys255Lys	S208
1404	BAA01g01170	A01	486552	G	A	missense_variant	MODERATE	c.682C>T\|p.Pro228Ser	S296
1405	BAA01g01170	A01	487008	C	T	synonymous_variant	LOW	c.315G>A\|p.Thr105Thr	S1 S90
1406	BAA01g01170	A01	487697	C	T	upstream_gene_variant	MODIFIER	c.-309G>A\|	S48
1407	BAA01g01170	A01	487925	G	A	upstream_gene_variant	MODIFIER	c.-537C>T\|	S165
1408	BAA01g01170	A01	489134	G	A	upstream_gene_variant	MODIFIER	c.-1746C>T\|	S34
1409	BAA01g01180	A01	490917	C	T	missense_variant	MODERATE	c.610G>A\|p.Glu204Lys	S117
1410	BAA01g01180	A01	490937	G	A	missense_variant	MODERATE	c.590C>T\|p.Pro197Leu	S232
1411	BAA01g01180	A01	491114	C	T	missense_variant	MODERATE	c.413G>A\|p.Gly138Glu	S129 S132 S215
1412	BAA01g01180	A01	491263	G	A	synonymous_variant	LOW	c.264C>T\|p.Gly88Gly	S200
1413	BAA01g01170	A01	492334	A	G	upstream_gene_variant	MODIFIER	c.-4946T>C\|	S39
1414	BAA01g01180	A01	492865	C	T	upstream_gene_variant	MODIFIER	c.-1339G>A\|	S218
1415	BAA01g01180	A01	493163	G	A	upstream_gene_variant	MODIFIER	c.-1637C>T\|	S116 S148 S295 S30
1416	BAA01g01180	A01	493245	C	T	upstream_gene_variant	MODIFIER	c.-1719G>A\|	S273
1417	BAA01g01190	A01	493804	C	T	stop_gained	HIGH	c.1178G>A\|p.Trp393*	S157 S163
1418	BAA01g01190	A01	494108	C	T	missense_variant	MODERATE	c.874G>A\|p.Ala292Thr	S155 S211
1419	BAA01g01190	A01	494129	G	A	missense_variant	MODERATE	c.853C>T\|p.Pro285Ser	S136
1420	BAA01g01190	A01	494523	C	T	synonymous_variant	LOW	c.459G>A\|p.Leu153Leu	S25
1421	BAA01g01190	A01	494606	G	A	missense_variant	MODERATE	c.376C>T\|p.Pro126Ser	S95
1422	BAA01g01190	A01	494631	G	A	synonymous_variant	LOW	c.351C>T\|p.Ile117Ile	S70
1423	BAA01g01180	A01	496428	G	A	upstream_gene_variant	MODIFIER	c.-4902C>T\|	S148 S30 S31
1424	BAA01g01200	A01	497771	C	T	missense_variant	MODERATE	c.262G>A\|p.Asp88Asn	S38
1425	BAA01g01190	A01	497868	C	T	upstream_gene_variant	MODIFIER	c.-2887G>A\|	S164

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