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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
42501	BAA01g26300	A01	14625189	C	T	downstream_gene_variant	MODIFIER	c.*1380C>T\|	S77 S82
42502	BAA01g26300	A01	14625413	C	T	downstream_gene_variant	MODIFIER	c.*1604C>T\|	S198
42503	BAA01g26300	A01	14625791	G	A	downstream_gene_variant	MODIFIER	c.*1982G>A\|	S281
42504	BAA01g26300-BAA01g26310	A01	14630920	G	A	intergenic_region	MODIFIER	n.14630920G>A\|	S70
42505	BAA01g26310	A01	14633190	G	A	upstream_gene_variant	MODIFIER	c.-4029G>A\|	S116 S148 S295 S296 S30 S31 S54
42506	BAA01g26310	A01	14633613	C	T	upstream_gene_variant	MODIFIER	c.-3606C>T\|	S18
42507	BAA01g26310	A01	14634500	G	A	upstream_gene_variant	MODIFIER	c.-2719G>A\|	S203
42508	BAA01g26310	A01	14634597	C	T	upstream_gene_variant	MODIFIER	c.-2622C>T\|	S87
42509	BAA01g26310	A01	14634837	C	T	upstream_gene_variant	MODIFIER	c.-2382C>T\|	S176
42510	BAA01g26310	A01	14636890	G	A	upstream_gene_variant	MODIFIER	c.-329G>A\|	S59
42511	BAA01g26310	A01	14637889	G	A	synonymous_variant	LOW	c.312G>A\|p.Leu104Leu	S174 S216
42512	BAA01g26310	A01	14637975	G	A	intron_variant	MODIFIER	c.372+26G>A\|	S62
42513	BAA01g26310	A01	14638070	C	T	missense_variant	MODERATE	c.415C>T\|p.His139Tyr	S182
42514	BAA01g26310	A01	14638835	C	T	missense_variant	MODERATE	c.1112C>T\|p.Pro371Leu	S115
42515	BAA01g26310	A01	14638947	C	T	synonymous_variant	LOW	c.1224C>T\|p.Phe408Phe	S255
42516	BAA01g26310	A01	14639113	C	T	missense_variant	MODERATE	c.1390C>T\|p.Leu464Phe	S69
42517	BAA01g26310	A01	14639201	C	T	missense_variant	MODERATE	c.1478C>T\|p.Ala493Val	S231
42518	BAA01g26310	A01	14639713	G	A	downstream_gene_variant	MODIFIER	c.*142G>A\|	S159 S243 S276 S298 S299
42519	BAA01g26310	A01	14640095	G	A	downstream_gene_variant	MODIFIER	c.*524G>A\|	S278
42520	BAA01g26320	A01	14642593	G	A	upstream_gene_variant	MODIFIER	c.-2757G>A\|	S201
42521	BAA01g26320	A01	14643080	C	T	upstream_gene_variant	MODIFIER	c.-2270C>T\|	S140
42522	BAA01g26320	A01	14645322	C	T	upstream_gene_variant	MODIFIER	c.-28C>T\|	S179
42523	BAA01g26320	A01	14645454	G	A	synonymous_variant	LOW	c.105G>A\|p.Lys35Lys	S181
42524	BAA01g26320	A01	14645623	C	T	missense_variant	MODERATE	c.274C>T\|p.His92Tyr	S64
42525	BAA01g26320	A01	14645678	G	A	missense_variant	MODERATE	c.329G>A\|p.Arg110Lys	S138

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