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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
105451	BAA10g08130	A10	5549044	C	T	upstream_gene_variant	MODIFIER	c.-1661C>T\|	S95
105452	BAA10g08130	A10	5549075	G	A	upstream_gene_variant	MODIFIER	c.-1630G>A\|	S296
105453	BAA10g08130	A10	5550212	G	A	upstream_gene_variant	MODIFIER	c.-493G>A\|	S107
105454	BAA10g08130	A10	5550539	C	T	upstream_gene_variant	MODIFIER	c.-166C>T\|	S132 S137 S89
105455	BAA10g08130	A10	5550608	G	A	upstream_gene_variant	MODIFIER	c.-97G>A\|	S11
105456	BAA10g08130	A10	5550785	G	A	synonymous_variant	LOW	c.81G>A\|p.Arg27Arg	S174 S216 S241 S265 S27 S39
105457	BAA10g08130	A10	5552921	C	T	missense_variant	MODERATE	c.1220C>T\|p.Pro407Leu	S181 S199
105458	BAA10g08130	A10	5555197	C	T	downstream_gene_variant	MODIFIER	c.*2013C>T\|	S166
105459	BAA10g08160	A10	5555879	G	A	upstream_gene_variant	MODIFIER	c.-4989G>A\|	S85
105460	BAA10g08160	A10	5555898	G	A	upstream_gene_variant	MODIFIER	c.-4970G>A\|	S208 S219
105461	BAA10g08160	A10	5556138	C	T	upstream_gene_variant	MODIFIER	c.-4730C>T\|	S155 S211
105462	BAA10g08160	A10	5556144	G	A	upstream_gene_variant	MODIFIER	c.-4724G>A\|	S25
105463	BAA10g08160	A10	5556298	G	A	upstream_gene_variant	MODIFIER	c.-4570G>A\|	S118 S67
105464	BAA10g08160	A10	5556699	C	T	upstream_gene_variant	MODIFIER	c.-4169C>T\|	S308
105465	BAA10g08160	A10	5556840	G	A	upstream_gene_variant	MODIFIER	c.-4028G>A\|	S273
105466	BAA10g08160	A10	5556871	G	A	upstream_gene_variant	MODIFIER	c.-3997G>A\|	S245
105467	BAA10g08140	A10	5557117	G	A	missense_variant	MODERATE	c.2738C>T\|p.Ser913Phe	S129
105468	BAA10g08140	A10	5557420	C	T	missense_variant	MODERATE	c.2435G>A\|p.Arg812Lys	S157 S247
105469	BAA10g08140	A10	5557730	G	A	missense_variant	MODERATE	c.2125C>T\|p.Pro709Ser	S157 S163
105470	BAA10g08140	A10	5557794	C	T	synonymous_variant	LOW	c.2061G>A\|p.Gly687Gly	S271
105471	BAA10g08140	A10	5557993	C	T	missense_variant	MODERATE	c.1862G>A\|p.Arg621Lys	S173
105472	BAA10g08140	A10	5558264	C	T	missense_variant	MODERATE	c.1591G>A\|p.Asp531Asn	S108
105473	BAA10g08140	A10	5558889	C	T	synonymous_variant	LOW	c.966G>A\|p.Lys322Lys	S67
105474	BAA10g08140	A10	5559003	G	A	synonymous_variant	LOW	c.852C>T\|p.Leu284Leu	S20
105475	BAA10g08140	A10	5559070	C	T	missense_variant	MODERATE	c.785G>A\|p.Arg262Lys	S108

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