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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
12651	BAA01g10050	A01	4533447	C	T	synonymous_variant	LOW	c.684G>A\|p.Gly228Gly	S267
12652	BAA01g10050	A01	4533558	G	A	synonymous_variant	LOW	c.573C>T\|p.Pro191Pro	S140
12653	BAA01g10050	A01	4533777	C	T	synonymous_variant	LOW	c.354G>A\|p.Gln118Gln	S51
12654	BAA01g10050	A01	4534073	G	A	missense_variant	MODERATE	c.58C>T\|p.Pro20Ser	S191
12655	BAA01g10040	A01	4535537	C	T	upstream_gene_variant	MODIFIER	c.-3505G>A\|	S270
12656	BAA01g10040	A01	4536176	G	A	upstream_gene_variant	MODIFIER	c.-4144C>T\|	S115
12657	BAA01g10040	A01	4536528	G	A	upstream_gene_variant	MODIFIER	c.-4496C>T\|	S221
12658	BAA01g10060	A01	4545862	C	T	synonymous_variant	LOW	c.1068G>A\|p.Glu356Glu	S64
12659	BAA01g10060	A01	4546638	C	T	missense_variant	MODERATE	c.551G>A\|p.Gly184Glu	S100
12660	BAA01g10060	A01	4547035	C	T	missense_variant	MODERATE	c.154G>A\|p.Ala52Thr	S107
12661	BAA01g10060	A01	4547859	G	A	upstream_gene_variant	MODIFIER	c.-152C>T\|	S159 S243
12662	BAA01g10060	A01	4548349	G	A	upstream_gene_variant	MODIFIER	c.-642C>T\|	S172 S217
12663	BAA01g10060	A01	4550235	C	T	upstream_gene_variant	MODIFIER	c.-2528G>A\|	S302
12664	BAA01g10060	A01	4551342	C	T	upstream_gene_variant	MODIFIER	c.-3635G>A\|	S166
12665	BAA01g10060	A01	4552125	G	A	upstream_gene_variant	MODIFIER	c.-4418C>T\|	S140 S168 S219 S72
12666	BAA01g10060	A01	4552386	G	A	upstream_gene_variant	MODIFIER	c.-4679C>T\|	S260
12667	BAA01g10070	A01	4553565	C	T	synonymous_variant	LOW	c.1530G>A\|p.Gln510Gln	S185
12668	BAA01g10070	A01	4553603	C	T	missense_variant	MODERATE	c.1492G>A\|p.Val498Ile	S208 S93
12669	BAA01g10070	A01	4553780	C	T	missense_variant	MODERATE	c.1315G>A\|p.Val439Met	S98
12670	BAA01g10070	A01	4553845	G	A	missense_variant	MODERATE	c.1250C>T\|p.Pro417Leu	S142
12671	BAA01g10070	A01	4553989	C	T	missense_variant	MODERATE	c.1106G>A\|p.Ser369Asn	S231
12672	BAA01g10070	A01	4554469	G	A	missense_variant	MODERATE	c.811C>T\|p.Leu271Phe	S217
12673	BAA01g10070	A01	4554617	C	T	splice_acceptor_variant&intron_variant	HIGH	c.664-1G>A\|	S252
12674	BAA01g10070	A01	4554735	C	T	missense_variant	MODERATE	c.631G>A\|p.Ala211Thr	S35
12675	BAA01g10070	A01	4555264	G	A	synonymous_variant	LOW	c.102C>T\|p.Thr34Thr	S95

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