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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g31490	A10	22967688	C	T	missense_variant	MODERATE	c.2042G>A\|p.Arg681Lys	S13
2	BAA10g31490	A10	22967777	G	A	synonymous_variant	LOW	c.1953C>T\|p.Leu651Leu	S228
3	BAA10g31490	A10	22968298	C	T	missense_variant	MODERATE	c.1689G>A\|p.Met563Ile	S244
4	BAA10g31490	A10	22968305	C	T	missense_variant	MODERATE	c.1682G>A\|p.Gly561Glu	S146
5	BAA10g31490	A10	22969865	C	T	missense_variant	MODERATE	c.848G>A\|p.Gly283Glu	S305
6	BAA10g31490	A10	22969883	C	T	missense_variant	MODERATE	c.830G>A\|p.Cys277Tyr	S295
7	BAA10g31490	A10	22970112	C	T	synonymous_variant	LOW	c.696G>A\|p.Glu232Glu	S242
8	BAA10g31490	A10	22970178	C	T	stop_gained	HIGH	c.630G>A\|p.Trp210*	S200
9	BAA10g31490	A10	22970673	G	A	synonymous_variant	LOW	c.312C>T\|p.Asn104Asn	S15 S3
10	BAA10g31490	A10	22970726	G	A	missense_variant	MODERATE	c.259C>T\|p.Pro87Ser	S303
11	BAA10g31490	A10	22971045	G	A	upstream_gene_variant	MODIFIER	c.-61C>T\|	S151 S167 S236 S257 S262 S263
12	BAA10g31490	A10	22971115	C	T	upstream_gene_variant	MODIFIER	c.-131G>A\|	S260
13	BAA10g31490	A10	22972854	C	T	upstream_gene_variant	MODIFIER	c.-1870G>A\|	S157 S163
14	BAA10g31490	A10	22974471	C	T	upstream_gene_variant	MODIFIER	c.-3487G>A\|	S242
15	BAA10g31490	A10	22974510	C	T	upstream_gene_variant	MODIFIER	c.-3526G>A\|	S166