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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
81201	BAA01g42950	A01	28431020	C	T	missense_variant	MODERATE	c.319G>A\|p.Ala107Thr	S305
81202	BAA01g42950	A01	28432205	G	A	upstream_gene_variant	MODIFIER	c.-653C>T\|	S278
81203	BAA01g42950	A01	28432380	C	T	upstream_gene_variant	MODIFIER	c.-828G>A\|	S132 S137 S215 S237 S288
81204	BAA01g42960	A01	28433048	C	T	missense_variant	MODERATE	c.92G>A\|p.Arg31Lys	S76
81205	BAA01g42950	A01	28435084	G	A	upstream_gene_variant	MODIFIER	c.-3532C>T\|	S53
81206	BAA01g42960	A01	28437443	G	A	upstream_gene_variant	MODIFIER	c.-4304C>T\|	S281
81207	BAA01g42960	A01	28437796	C	T	upstream_gene_variant	MODIFIER	c.-4657G>A\|	S74
81208	BAA01g42960	A01	28437976	C	T	upstream_gene_variant	MODIFIER	c.-4837G>A\|	S237
81209	BAA01g42960	A01	28438119	G	A	upstream_gene_variant	MODIFIER	c.-4980C>T\|	S139
81210	BAA01g42970	A01	28438437	C	T	downstream_gene_variant	MODIFIER	c.*398G>A\|	S210 S225
81211	BAA01g42970	A01	28439298	G	A	missense_variant	MODERATE	c.2813C>T\|p.Pro938Leu	S292
81212	BAA01g42970	A01	28439463	G	A	missense_variant	MODERATE	c.2648C>T\|p.Pro883Leu	S67
81213	BAA01g42970	A01	28439771	C	T	intron_variant	MODIFIER	c.2612-272G>A\|	S260
81214	BAA01g42970	A01	28440053	G	A	intron_variant	MODIFIER	c.2611+488C>T\|	S294
81215	BAA01g42970	A01	28442415	C	T	missense_variant	MODERATE	c.1103G>A\|p.Gly368Glu	S18
81216	BAA01g42970	A01	28442742	G	A	missense_variant	MODERATE	c.776C>T\|p.Thr259Ile	S193
81217	BAA01g42970	A01	28443331	C	T	intron_variant	MODIFIER	c.609+172G>A\|	S48
81218	BAA01g42970	A01	28444336	G	A	upstream_gene_variant	MODIFIER	c.-225C>T\|	S234
81219	BAA01g42970	A01	28444403	C	T	upstream_gene_variant	MODIFIER	c.-292G>A\|	S242
81220	BAA01g42970	A01	28444456	C	T	upstream_gene_variant	MODIFIER	c.-345G>A\|	S266
81221	BAA01g42970	A01	28445711	C	T	upstream_gene_variant	MODIFIER	c.-1600G>A\|	S136
81222	BAA01g42970	A01	28445815	G	A	upstream_gene_variant	MODIFIER	c.-1704C>T\|	S153 S157 S167 S236 S257 S262 S263
81223	BAA01g42970	A01	28446961	G	A	upstream_gene_variant	MODIFIER	c.-2850C>T\|	S262
81224	BAA01g42970	A01	28448403	C	T	upstream_gene_variant	MODIFIER	c.-4292G>A\|	S275
81225	BAA01g42980	A01	28450259	G	A	intron_variant	MODIFIER	c.325-253G>A\|	S278

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