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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
97601	BAA10g05490	A10	2802786	C	T	missense_variant	MODERATE	c.520G>A\|p.Ala174Thr	S152
97602	BAA10g05500	A10	2803476	G	A	upstream_gene_variant	MODIFIER	c.-3772G>A\|	S86
97603	BAA10g05490	A10	2804076	C	T	missense_variant	MODERATE	c.34G>A\|p.Asp12Asn	S224
97604	BAA10g05490	A10	2804250	G	A	upstream_gene_variant	MODIFIER	c.-141C>T\|	S15 S3
97605	BAA10g05490	A10	2804377	G	A	upstream_gene_variant	MODIFIER	c.-268C>T\|	S283
97606	BAA10g05490	A10	2804599	G	A	upstream_gene_variant	MODIFIER	c.-490C>T\|	S261
97607	BAA10g05490	A10	2805394	C	T	upstream_gene_variant	MODIFIER	c.-1285G>A\|	S244
97608	BAA10g05490	A10	2806298	C	T	upstream_gene_variant	MODIFIER	c.-2189G>A\|	S10
97609	BAA10g05500	A10	2807422	C	T	missense_variant	MODERATE	c.175C>T\|p.Leu59Phe	S185
97610	BAA10g05500	A10	2807719	C	T	synonymous_variant	LOW	c.369C>T\|p.Val123Val	S249
97611	BAA10g05490	A10	2809045	C	T	upstream_gene_variant	MODIFIER	c.-4936G>A\|	S135
97612	BAA10g05510	A10	2809412	C	T	missense_variant	MODERATE	c.620G>A\|p.Arg207Lys	S135
97613	BAA10g05510	A10	2809455	G	A	missense_variant	MODERATE	c.577C>T\|p.Leu193Phe	S202
97614	BAA10g05510	A10	2811170	G	A	upstream_gene_variant	MODIFIER	c.-892C>T\|	S18
97615	BAA10g05510	A10	2811565	G	A	upstream_gene_variant	MODIFIER	c.-1287C>T\|	S75 S81
97616	BAA10g05510	A10	2811577	C	T	upstream_gene_variant	MODIFIER	c.-1299G>A\|	S104 S52
97617	BAA10g05520	A10	2812242	C	T	synonymous_variant	LOW	c.2670G>A\|p.Arg890Arg	S71
97618	BAA10g05520	A10	2812393	G	A	missense_variant	MODERATE	c.2519C>T\|p.Thr840Ile	S245
97619	BAA10g05520	A10	2814720	C	T	synonymous_variant	LOW	c.192G>A\|p.Arg64Arg	S206 S26
97620	BAA10g05530	A10	2815712	C	T	missense_variant	MODERATE	c.3298G>A\|p.Glu1100Lys	S270
97621	BAA10g05530	A10	2816179	C	T	missense_variant	MODERATE	c.2938G>A\|p.Gly980Arg	S298
97622	BAA10g05520	A10	2816741	G	A	upstream_gene_variant	MODIFIER	c.-1830C>T\|	S292
97623	BAA10g05530	A10	2817364	G	A	synonymous_variant	LOW	c.2424C>T\|p.Phe808Phe	S217 S248
97624	BAA10g05530	A10	2817377	C	T	missense_variant	MODERATE	c.2411G>A\|p.Gly804Glu	S161 S228 S289
97625	BAA10g05530	A10	2817463	C	T	synonymous_variant	LOW	c.2325G>A\|p.Arg775Arg	S210 S225

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