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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
149001	BAA10g33200	A10	23683537	C	T	upstream_gene_variant	MODIFIER	c.-3982G>A\|	S282
149002	BAA10g33200	A10	23683552	C	A	upstream_gene_variant	MODIFIER	c.-3997G>T\|	S30
149003	BAA10g33220	A10	23684005	C	T	missense_variant	MODERATE	c.958G>A\|p.Glu320Lys	S192
149004	BAA10g33220	A10	23684143	C	T	missense_variant	MODERATE	c.820G>A\|p.Glu274Lys	S294
149005	BAA10g33220	A10	23685416	G	A	upstream_gene_variant	MODIFIER	c.-454C>T\|	S16
149006	BAA10g33230	A10	23685500	C	T	missense_variant	MODERATE	c.4795G>A\|p.Asp1599Asn	S125
149007	BAA10g33230	A10	23685548	C	T	missense_variant	MODERATE	c.4747G>A\|p.Glu1583Lys	S48
149008	BAA10g33230	A10	23685995	C	T	splice_region_variant&intron_variant	LOW	c.4538+3G>A\|	S13 S219 S279 S72
149009	BAA10g33230	A10	23686339	G	A	synonymous_variant	LOW	c.4287C>T\|p.Asp1429Asp	S298
149010	BAA10g33220	A10	23687470	C	T	upstream_gene_variant	MODIFIER	c.-2508G>A\|	S20
149011	BAA10g33230	A10	23687536	C	T	missense_variant	MODERATE	c.3542G>A\|p.Gly1181Glu	S204
149012	BAA10g33230	A10	23687557	G	A	missense_variant	MODERATE	c.3521C>T\|p.Ala1174Val	S298
149013	BAA10g33230	A10	23688070	C	T	missense_variant	MODERATE	c.3175G>A\|p.Asp1059Asn	S187
149014	BAA10g33230	A10	23688095	G	A	synonymous_variant	LOW	c.3150C>T\|p.Val1050Val	S178
149015	BAA10g33230	A10	23688480	C	T	missense_variant	MODERATE	c.2903G>A\|p.Arg968Lys	S36
149016	BAA10g33230	A10	23689028	G	A	missense_variant	MODERATE	c.2594C>T\|p.Thr865Ile	S179
149017	BAA10g33220	A10	23689772	G	A	upstream_gene_variant	MODIFIER	c.-4810C>T\|	S273
149018	BAA10g33230	A10	23690705	G	A	missense_variant	MODERATE	c.1439C>T\|p.Pro480Leu	S125
149019	BAA10g33230	A10	23691979	C	T	missense_variant	MODERATE	c.803G>A\|p.Gly268Glu	S11
149020	BAA10g33230	A10	23692916	G	A	missense_variant	MODERATE	c.161C>T\|p.Ser54Phe	S132 S137 S138 S215 S89
149021	BAA10g33230	A10	23693011	G	A	synonymous_variant	LOW	c.66C>T\|p.Leu22Leu	S130
149022	BAA10g33230	A10	23693712	C	T	upstream_gene_variant	MODIFIER	c.-636G>A\|	S148 S210 S30 S31
149023	BAA10g33240	A10	23694776	G	A	synonymous_variant	LOW	c.651C>T\|p.Val217Val	S99
149024	BAA10g33230	A10	23695627	C	T	upstream_gene_variant	MODIFIER	c.-2551G>A\|	S92
149025	BAA10g33230	A10	23696862	G	A	upstream_gene_variant	MODIFIER	c.-3786C>T\|	S172 S217

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