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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g33460	A10	23778208	C	T	synonymous_variant	LOW	c.1434G>A\|p.Arg478Arg	S60
2	BAA10g33460	A10	23778557	G	A	synonymous_variant	LOW	c.1257C>T\|p.Asn419Asn	S255
3	BAA10g33460	A10	23780595	C	T	missense_variant	MODERATE	c.323G>A\|p.Arg108Lys	S132
4	BAA10g33460	A10	23780661	C	T	missense_variant	MODERATE	c.257G>A\|p.Arg86Gln	S51
5	BAA10g33460	A10	23780706	C	T	missense_variant	MODERATE	c.212G>A\|p.Arg71Lys	S174 S216 S265 S27
6	BAA10g33460	A10	23782152	C	T	upstream_gene_variant	MODIFIER	c.-1235G>A\|	S89
7	BAA10g33460	A10	23782642	G	A	upstream_gene_variant	MODIFIER	c.-1725C>T\|	S132 S137 S215 S89
8	BAA10g33460	A10	23783134	G	A	upstream_gene_variant	MODIFIER	c.-2217C>T\|	S219 S72
9	BAA10g33460	A10	23783499	T	C	upstream_gene_variant	MODIFIER	c.-2582A>G\|	S217 S248
10	BAA10g33460	A10	23783588	G	A	upstream_gene_variant	MODIFIER	c.-2671C>T\|	S223
11	BAA10g33460	A10	23784063	C	T	upstream_gene_variant	MODIFIER	c.-3146G>A\|	S87
12	BAA10g33460	A10	23785555	C	T	upstream_gene_variant	MODIFIER	c.-4638G>A\|	S18
13	BAA10g33460	A10	23785817	C	T	upstream_gene_variant	MODIFIER	c.-4900G>A\|	S124