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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
145001	BAA10g29640	A10	22234350	G	A	synonymous_variant	LOW	c.1398G>A\|p.Glu466Glu	S59
145002	BAA10g29640	A10	22234510	C	T	missense_variant	MODERATE	c.1457C>T\|p.Ala486Val	S23
145003	BAA10g29650	A10	22234859	C	T	upstream_gene_variant	MODIFIER	c.-3431C>T\|	S235
145004	BAA10g29650	A10	22235536	C	T	upstream_gene_variant	MODIFIER	c.-2754C>T\|	S66
145005	BAA10g29640	A10	22235939	G	A	synonymous_variant	LOW	c.2190G>A\|p.Glu730Glu	S180
145006	BAA10g29640	A10	22236263	G	A	synonymous_variant	LOW	c.2439G>A\|p.Glu813Glu	S273
145007	BAA10g29650	A10	22236370	C	T	upstream_gene_variant	MODIFIER	c.-1920C>T\|	S38
145008	BAA10g29640	A10	22236481	G	A	missense_variant	MODERATE	c.2566G>A\|p.Glu856Lys	S279
145009	BAA10g29640	A10	22236767	C	T	synonymous_variant	LOW	c.2763C>T\|p.Phe921Phe	S305
145010	BAA10g29640	A10	22237739	T	A	missense_variant	MODERATE	c.3347T>A\|p.Leu1116Gln	S162
145011	BAA10g29650	A10	22239268	C	T	synonymous_variant	LOW	c.579C>T\|p.Asn193Asn	S82 S92
145012	BAA10g29660	A10	22239852	G	A	upstream_gene_variant	MODIFIER	c.-319G>A\|	S176
145013	BAA10g29660	A10	22240252	G	A	missense_variant	MODERATE	c.82G>A\|p.Glu28Lys	S262
145014	BAA10g29640	A10	22241717	G	A	downstream_gene_variant	MODIFIER	c.*3695G>A\|	S134
145015	BAA10g29640	A10	22241802	C	T	downstream_gene_variant	MODIFIER	c.*3780C>T\|	S224
145016	BAA10g29640	A10	22242463	C	T	downstream_gene_variant	MODIFIER	c.*4441C>T\|	S218
145017	BAA10g29690	A10	22243824	C	T	upstream_gene_variant	MODIFIER	c.-4283C>T\|	S242
145018	BAA10g29670	A10	22245479	G	A	upstream_gene_variant	MODIFIER	c.-1180C>T\|	S85
145019	BAA10g29680	A10	22246669	G	A	synonymous_variant	LOW	c.174C>T\|p.Ile58Ile	S113
145020	BAA10g29670	A10	22247171	G	T	upstream_gene_variant	MODIFIER	c.-2872C>A\|	S103 S106 S12 S121 S127 S134 S143 S154 S194 S200 S208 S212 S231 S262 S271 S302 S53 S54 S81
145021	BAA10g29670	A10	22247530	C	T	upstream_gene_variant	MODIFIER	c.-3231G>A\|	S19
145022	BAA10g29670	A10	22248038	G	A	upstream_gene_variant	MODIFIER	c.-3739C>T\|	S238
145023	BAA10g29690	A10	22248309	C	T	missense_variant	MODERATE	c.203C>T\|p.Pro68Leu	S133
145024	BAA10g29690	A10	22248626	C	T	synonymous_variant	LOW	c.439C>T\|p.Leu147Leu	S292
145025	BAA10g29670	A10	22248764	C	T	upstream_gene_variant	MODIFIER	c.-4465G>A\|	S246

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