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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
4701	BAA01g03760	A01	1706831	C	T	missense_variant	MODERATE	c.292G>A\|p.Asp98Asn	S25
4702	BAA01g03760	A01	1706868	G	A	synonymous_variant	LOW	c.255C>T\|p.Leu85Leu	S32
4703	BAA01g03770	A01	1708298	G	A	missense_variant	MODERATE	c.337G>A\|p.Val113Ile	S263
4704	BAA01g03770	A01	1710161	G	A	missense_variant&splice_region_variant	MODERATE	c.1759G>A\|p.Glu587Lys	S156
4705	BAA01g03770	A01	1710640	G	A	missense_variant	MODERATE	c.1986G>A\|p.Met662Ile	S118
4706	BAA01g03770	A01	1711774	G	A	synonymous_variant	LOW	c.2514G>A\|p.Glu838Glu	S34
4707	BAA01g03770	A01	1711782	C	T	missense_variant	MODERATE	c.2522C>T\|p.Thr841Ile	S43
4708	BAA01g03770	A01	1711997	C	T	missense_variant	MODERATE	c.2641C>T\|p.Pro881Ser	S81 S85
4709	BAA01g03780	A01	1713011	C	T	downstream_gene_variant	MODIFIER	c.*1104G>A\|	S265
4710	BAA01g03780	A01	1713141	C	T	downstream_gene_variant	MODIFIER	c.*974G>A\|	S41
4711	BAA01g03770	A01	1713279	C	T	missense_variant	MODERATE	c.3193C>T\|p.Pro1065Ser	S47
4712	BAA01g03770	A01	1713771	G	A	downstream_gene_variant	MODIFIER	c.*122G>A\|	S230
4713	BAA01g03780	A01	1714261	G	A	missense_variant	MODERATE	c.169C>T\|p.Pro57Ser	S47
4714	BAA01g03780	A01	1715064	C	T	upstream_gene_variant	MODIFIER	c.-635G>A\|	S35
4715	BAA01g03780	A01	1715327	G	A	upstream_gene_variant	MODIFIER	c.-898C>T\|	S75
4716	BAA01g03790	A01	1716790	G	A	missense_variant	MODERATE	c.127C>T\|p.Pro43Ser	S56
4717	BAA01g03800	A01	1719024	G	A	missense_variant	MODERATE	c.214C>T\|p.Arg72Cys	S279
4718	BAA01g03790	A01	1720558	G	A	upstream_gene_variant	MODIFIER	c.-3642C>T\|	S202
4719	BAA01g03790	A01	1721447	C	T	upstream_gene_variant	MODIFIER	c.-4531G>A\|	S282
4720	BAA01g03790	A01	1721776	C	T	upstream_gene_variant	MODIFIER	c.-4860G>A\|	S78
4721	BAA01g03800	A01	1722700	G	T	upstream_gene_variant	MODIFIER	c.-3463C>A\|	S14 S153 S161 S170 S209 S230 S248 S249 S258 S286 S31 S70 S86
4722	BAA01g03800	A01	1722751	C	T	upstream_gene_variant	MODIFIER	c.-3514G>A\|	S71
4723	BAA01g03810	A01	1725850	C	T	stop_gained	HIGH	c.634C>T\|p.Gln212*	S185
4724	BAA01g03810	A01	1726237	C	T	downstream_gene_variant	MODIFIER	c.*307C>T\|	S277
4725	BAA01g03820	A01	1728000	G	A	upstream_gene_variant	MODIFIER	c.-987C>T\|	S118

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