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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
124451	BAA10g14020	A10	14881380	C	T	missense_variant	MODERATE	c.394C>T\|p.Pro132Ser	S56
124452	BAA10g14020	A10	14881707	C	T	synonymous_variant	LOW	c.639C>T\|p.Ser213Ser	S135
124453	BAA10g14020	A10	14882155	G	A	missense_variant	MODERATE	c.1087G>A\|p.Glu363Lys	S293
124454	BAA10g14020	A10	14882360	G	A	missense_variant	MODERATE	c.1292G>A\|p.Gly431Asp	S43
124455	BAA10g14020	A10	14883919	C	T	downstream_gene_variant	MODIFIER	c.*667C>T\|	S80
124456	BAA10g14020	A10	14884112	G	A	downstream_gene_variant	MODIFIER	c.*860G>A\|	S167
124457	BAA10g14030	A10	14884434	C	T	missense_variant	MODERATE	c.632G>A\|p.Gly211Glu	S297
124458	BAA10g14030	A10	14885955	G	A	upstream_gene_variant	MODIFIER	c.-452C>T\|	S234
124459	BAA10g14030	A10	14886054	G	A	upstream_gene_variant	MODIFIER	c.-551C>T\|	S112
124460	BAA10g14030	A10	14887350	C	T	upstream_gene_variant	MODIFIER	c.-1847G>A\|	S301 S304
124461	BAA10g14030	A10	14887955	G	A	upstream_gene_variant	MODIFIER	c.-2452C>T\|	S79 S91
124462	BAA10g14030	A10	14888279	G	A	upstream_gene_variant	MODIFIER	c.-2776C>T\|	S250
124463	BAA10g14030	A10	14889407	G	A	upstream_gene_variant	MODIFIER	c.-3904C>T\|	S35
124464	BAA10g14030	A10	14889437	C	T	upstream_gene_variant	MODIFIER	c.-3934G>A\|	S133
124465	BAA10g14030	A10	14889516	C	T	upstream_gene_variant	MODIFIER	c.-4013G>A\|	S200
124466	BAA10g14030	A10	14890044	G	A	upstream_gene_variant	MODIFIER	c.-4541C>T\|	S174 S216 S241 S265 S39
124467	BAA10g14030	A10	14890131	C	T	upstream_gene_variant	MODIFIER	c.-4628G>A\|	S246 S259
124468	BAA10g14040	A10	14891877	T	A	upstream_gene_variant	MODIFIER	c.-1226T>A\|	S1 S228 S244
124469	BAA10g14040	A10	14891927	C	T	upstream_gene_variant	MODIFIER	c.-1176C>T\|	S191
124470	BAA10g14040	A10	14892283	A	C	upstream_gene_variant	MODIFIER	c.-820A>C\|	S111 S131 S135 S172 S186 S204 S210 S218 S222 S223 S23 S247 S248 S252 S298 S36 S58 S61
124471	BAA10g14040	A10	14893753	G	A	intron_variant	MODIFIER	c.382+59G>A\|	S176
124472	BAA10g14040	A10	14895578	G	A	intron_variant	MODIFIER	c.949-23G>A\|	S278
124473	BAA10g14040	A10	14895813	C	T	intron_variant	MODIFIER	c.1110+51C>T\|	S153 S296
124474	BAA10g14040	A10	14896017	C	T	intron_variant	MODIFIER	c.1111-67C>T\|	S124
124475	BAA10g14040	A10	14896284	C	T	intron_variant	MODIFIER	c.1292+19C>T\|	S38

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