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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
142601	BAA10g27430	A10	21404537	C	T	upstream_gene_variant	MODIFIER	c.-981G>A\|	S20
142602	BAA10g27430	A10	21404769	G	A	upstream_gene_variant	MODIFIER	c.-1213C>T\|	S18
142603	BAA10g27430	A10	21405068	G	A	upstream_gene_variant	MODIFIER	c.-1512C>T\|	S159 S243
142604	BAA10g27440	A10	21406087	G	A	synonymous_variant	LOW	c.162G>A\|p.Lys54Lys	S143
142605	BAA10g27440	A10	21406390	G	A	synonymous_variant	LOW	c.363G>A\|p.Lys121Lys	S136
142606	BAA10g27440	A10	21406462	G	A	splice_region_variant&intron_variant	LOW	c.430+5G>A\|	S239
142607	BAA10g27440	A10	21406872	C	T	missense_variant&splice_region_variant	MODERATE	c.553C>T\|p.Leu185Phe	S296
142608	BAA10g27430	A10	21407013	G	A	upstream_gene_variant	MODIFIER	c.-3457C>T\|	S130
142609	BAA10g27430	A10	21408289	C	T	upstream_gene_variant	MODIFIER	c.-4733G>A\|	S33
142610	BAA10g27440	A10	21408311	G	A	missense_variant	MODERATE	c.1264G>A\|p.Ala422Thr	S245
142611	BAA10g27450	A10	21409482	C	T	missense_variant&splice_region_variant	MODERATE	c.334G>A\|p.Val112Ile	S13 S168 S219 S279 S72
142612	BAA10g27450	A10	21410060	C	T	synonymous_variant	LOW	c.36G>A\|p.Lys12Lys	S19
142613	BAA10g27460	A10	21410751	G	A	missense_variant	MODERATE	c.295G>A\|p.Asp99Asn	S159 S243
142614	BAA10g27460	A10	21410796	G	A	missense_variant	MODERATE	c.340G>A\|p.Glu114Lys	S219 S72
142615	BAA10g27460	A10	21411139	C	T	missense_variant	MODERATE	c.598C>T\|p.Leu200Phe	S232
142616	BAA10g27460	A10	21411295	G	A	missense_variant	MODERATE	c.754G>A\|p.Glu252Lys	S112
142617	BAA10g27450	A10	21411449	C	T	upstream_gene_variant	MODIFIER	c.-1354G>A\|	S56
142618	BAA10g27450	A10	21411740	G	A	upstream_gene_variant	MODIFIER	c.-1645C>T\|	S94
142619	BAA10g27470	A10	21412600	G	A	splice_acceptor_variant&intron_variant	HIGH	c.98-1G>A\|	S109
142620	BAA10g27450	A10	21413091	C	T	upstream_gene_variant	MODIFIER	c.-2996G>A\|	S155 S211
142621	BAA10g27450	A10	21414039	T	A	upstream_gene_variant	MODIFIER	c.-3944A>T\|	S269
142622	BAA10g27450	A10	21414068	C	T	upstream_gene_variant	MODIFIER	c.-3973G>A\|	S286
142623	BAA10g27480	A10	21414367	G	A	missense_variant	MODERATE	c.206G>A\|p.Arg69Lys	S115
142624	BAA10g27480	A10	21414503	C	T	synonymous_variant	LOW	c.342C>T\|p.Ile114Ile	S104 S52
142625	BAA10g27480	A10	21414585	C	T	stop_gained	HIGH	c.424C>T\|p.Gln142*	S218

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