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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA08g05590	A08	4272276	C	T	upstream_gene_variant	MODIFIER	c.-4589C>T\|	S155 S211
2	BAA08g05590	A08	4273493	G	A	upstream_gene_variant	MODIFIER	c.-3372G>A\|	S62
3	BAA08g05590	A08	4274042	G	A	upstream_gene_variant	MODIFIER	c.-2823G>A\|	S200
4	BAA08g05590	A08	4274193	G	A	upstream_gene_variant	MODIFIER	c.-2672G>A\|	S199
5	BAA08g05590	A08	4274717	G	A	upstream_gene_variant	MODIFIER	c.-2148G>A\|	S274
6	BAA08g05590	A08	4274942	G	A	upstream_gene_variant	MODIFIER	c.-1923G>A\|	S35
7	BAA08g05590	A08	4275272	G	T	upstream_gene_variant	MODIFIER	c.-1593G>T\|	S12 S143 S194 S209 S224 S23 S247 S261 S41 S93
8	BAA08g05590	A08	4275389	C	T	upstream_gene_variant	MODIFIER	c.-1476C>T\|	S155 S211
9	BAA08g05590	A08	4275745	C	T	upstream_gene_variant	MODIFIER	c.-1120C>T\|	S82
10	BAA08g05590	A08	4276537	G	A	upstream_gene_variant	MODIFIER	c.-328G>A\|	S136
11	BAA08g05590	A08	4278759	C	T	intron_variant	MODIFIER	c.1653+16C>T\|	S131
12	BAA08g05590	A08	4279046	C	T	synonymous_variant	LOW	c.1662C>T\|p.Asp554Asp	S237
13	BAA08g05590	A08	4279085	C	T	synonymous_variant	LOW	c.1701C>T\|p.Leu567Leu	S60
14	BAA08g05590	A08	4279151	G	A	synonymous_variant	LOW	c.1767G>A\|p.Gln589Gln	S262
15	BAA08g05590	A08	4279210	G	A	missense_variant&splice_region_variant	MODERATE	c.1826G>A\|p.Cys609Tyr	S82 S92
16	BAA08g05590	A08	4279758	C	T	intron_variant	MODIFIER	c.2161-39C>T\|	S105 S106
17	BAA08g05590	A08	4280421	T	C	missense_variant	MODERATE	c.2522T>C\|p.Ile841Thr	S65
18	BAA08g05590	A08	4280589	G	A	missense_variant	MODERATE	c.2614G>A\|p.Gly872Arg	S174
19	BAA08g05590	A08	4281111	A	T	splice_acceptor_variant&intron_variant	HIGH	c.2763-2A>T\|	S107 S163 S176 S177 S204 S251 S255 S262 S283 S48 S64
20	BAA08g05590	A08	4282051	C	T	downstream_gene_variant	MODIFIER	c.*23C>T\|	S80
21	BAA08g05590	A08	4283337	C	T	downstream_gene_variant	MODIFIER	c.*1309C>T\|	S216
22	BAA08g05590	A08	4284608	C	T	downstream_gene_variant	MODIFIER	c.*2580C>T\|	S67
23	BAA08g05590	A08	4284616	C	T	downstream_gene_variant	MODIFIER	c.*2588C>T\|	S148 S210 S30 S31
24	BAA08g05590	A08	4284654	G	A	downstream_gene_variant	MODIFIER	c.*2626G>A\|	S8
25	BAA08g05590	A08	4284888	G	A	downstream_gene_variant	MODIFIER	c.*2860G>A\|	S261

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