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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
133251	BAA10g19810	A10	18044320	G	A	synonymous_variant	LOW	c.1089G>A\|p.Arg363Arg	S202
133252	BAA10g19810	A10	18044647	G	A	synonymous_variant	LOW	c.1335G>A\|p.Gly445Gly	S262
133253	BAA10g19810	A10	18044665	G	A	stop_gained	HIGH	c.1353G>A\|p.Trp451*	S9
133254	BAA10g19810	A10	18044820	A	C	synonymous_variant	LOW	c.1437A>C\|p.Pro479Pro	S11 S143 S156 S159 S18 S208 S224 S263 S279 S287 S290 S292 S295 S30 S34 S49 S51
133255	BAA10g19810	A10	18045607	G	A	downstream_gene_variant	MODIFIER	c.*343G>A\|	S159 S243
133256	BAA10g19810	A10	18046137	G	A	downstream_gene_variant	MODIFIER	c.*873G>A\|	S74
133257	BAA10g19810	A10	18048614	G	A	downstream_gene_variant	MODIFIER	c.*3350G>A\|	S138
133258	BAA10g19810	A10	18049156	G	A	downstream_gene_variant	MODIFIER	c.*3892G>A\|	S79 S84
133259	BAA10g19820	A10	18050019	C	T	missense_variant	MODERATE	c.1700G>A\|p.Gly567Glu	S266
133260	BAA10g19820	A10	18050224	C	T	missense_variant	MODERATE	c.1495G>A\|p.Glu499Lys	S283
133261	BAA10g19820	A10	18050447	G	A	missense_variant	MODERATE	c.1360C>T\|p.Leu454Phe	S303
133262	BAA10g19820	A10	18050677	C	T	missense_variant	MODERATE	c.1211G>A\|p.Gly404Glu	S70
133263	BAA10g19820	A10	18051179	G	A	synonymous_variant	LOW	c.936C>T\|p.Leu312Leu	S234
133264	BAA10g19830	A10	18051962	C	T	downstream_gene_variant	MODIFIER	c.*4172G>A\|	S168
133265	BAA10g19830	A10	18051983	C	T	downstream_gene_variant	MODIFIER	c.*4151G>A\|	S308
133266	BAA10g19820	A10	18052340	C	T	splice_region_variant&synonymous_variant	LOW	c.708G>A\|p.Lys236Lys	S260
133267	BAA10g19820	A10	18053566	G	A	missense_variant	MODERATE	c.164C>T\|p.Ala55Val	S18
133268	BAA10g19830	A10	18056311	G	A	synonymous_variant	LOW	c.1008C>T\|p.Ile336Ile	S74
133269	BAA10g19830	A10	18056623	C	T	synonymous_variant	LOW	c.696G>A\|p.Leu232Leu	S19
133270	BAA10g19830	A10	18057147	C	T	missense_variant	MODERATE	c.281G>A\|p.Arg94Lys	S51
133271	BAA10g19830	A10	18057155	G	A	synonymous_variant	LOW	c.273C>T\|p.His91His	S79 S84
133272	BAA10g19840	A10	18058226	G	A	synonymous_variant	LOW	c.855C>T\|p.Tyr285Tyr	S64
133273	BAA10g19840	A10	18058366	C	T	missense_variant	MODERATE	c.715G>A\|p.Asp239Asn	S183
133274	BAA10g19830	A10	18059142	G	A	upstream_gene_variant	MODIFIER	c.-1715C>T\|	S280
133275	BAA10g19830	A10	18059459	G	A	upstream_gene_variant	MODIFIER	c.-2032C>T\|	S4

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