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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
98901	BAA10g06250	A10	3218089	C	A	upstream_gene_variant	MODIFIER	c.-3453G>T\|	S191
98902	BAA10g06250	A10	3218991	C	A	upstream_gene_variant	MODIFIER	c.-4355G>T\|	S154 S159 S194 S199 S205 S207 S208 S213 S216 S220 S222 S226 S256 S44 S54 S61 S7 S82
98903	BAA10g06250	A10	3219108	G	A	upstream_gene_variant	MODIFIER	c.-4472C>T\|	S157 S163
98904	BAA10g06250	A10	3219217	C	T	upstream_gene_variant	MODIFIER	c.-4581G>A\|	S10
98905	BAA10g06250	A10	3219565	G	A	upstream_gene_variant	MODIFIER	c.-4929C>T\|	S75
98906	BAA10g06250	A10	3219589	A	T	upstream_gene_variant	MODIFIER	c.-4953T>A\|	S116 S118 S148 S30 S31 S54
98907	BAA10g06260	A10	3221940	C	A	upstream_gene_variant	MODIFIER	c.-2071C>A\|	S151 S184 S199 S200 S206 S215 S256 S263 S278 S6 S96
98908	BAA10g06260	A10	3221951	G	T	upstream_gene_variant	MODIFIER	c.-2060G>T\|	S137 S151 S184 S200 S250 S263 S96
98909	BAA10g06260	A10	3223157	C	A	upstream_gene_variant	MODIFIER	c.-854C>A\|	S246
98910	BAA10g06260	A10	3223552	A	T	upstream_gene_variant	MODIFIER	c.-459A>T\|	S1 S90
98911	BAA10g06260	A10	3223591	C	T	upstream_gene_variant	MODIFIER	c.-420C>T\|	S191
98912	BAA10g06260	A10	3224072	C	T	missense_variant	MODERATE	c.62C>T\|p.Ser21Phe	S196
98913	BAA10g06260	A10	3224283	G	A	stop_gained	HIGH	c.197G>A\|p.Trp66*	S236
98914	BAA10g06260	A10	3224389	G	A	synonymous_variant	LOW	c.303G>A\|p.Glu101Glu	S18
98915	BAA10g06260	A10	3224575	G	A	synonymous_variant	LOW	c.489G>A\|p.Glu163Glu	S226
98916	BAA10g06270	A10	3224850	G	A	upstream_gene_variant	MODIFIER	c.-450G>A\|	S291
98917	BAA10g06270	A10	3225181	G	A	upstream_gene_variant	MODIFIER	c.-119G>A\|	S99
98918	BAA10g06270	A10	3226818	G	A	missense_variant	MODERATE	c.529G>A\|p.Gly177Ser	S230
98919	BAA10g06260	A10	3226974	C	T	downstream_gene_variant	MODIFIER	c.*2237C>T\|	S146
98920	BAA10g06260	A10	3227945	G	A	downstream_gene_variant	MODIFIER	c.*3208G>A\|	S226
98921	BAA10g06280	A10	3229594	C	T	missense_variant	MODERATE	c.154G>A\|p.Asp52Asn	S40 S49
98922	BAA10g06280	A10	3229647	G	A	missense_variant	MODERATE	c.101C>T\|p.Thr34Met	S82 S92
98923	BAA10g06280	A10	3231156	C	T	upstream_gene_variant	MODIFIER	c.-1409G>A\|	S176
98924	BAA10g06280	A10	3232175	G	A	upstream_gene_variant	MODIFIER	c.-2428C>T\|	S198
98925	BAA10g06280	A10	3232614	G	A	upstream_gene_variant	MODIFIER	c.-2867C>T\|	S165 S211 S227

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