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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
90801	BAA10g00870	A10	405247	C	T	missense_variant	MODERATE	c.391C>T\|p.Pro131Ser	S63
90802	BAA10g00870	A10	405518	G	A	intron_variant	MODIFIER	c.624+38G>A\|	S176
90803	BAA10g00870	A10	405608	G	A	intron_variant	MODIFIER	c.624+128G>A\|	S43
90804	BAA10g00870	A10	405882	G	A	intron_variant	MODIFIER	c.624+402G>A\|	S157 S163
90805	BAA10g00870	A10	406626	G	A	intron_variant	MODIFIER	c.625-635G>A\|	S125
90806	BAA10g00870	A10	407457	G	A	splice_region_variant&synonymous_variant	LOW	c.648G>A\|p.Arg216Arg	S234
90807	BAA10g00870	A10	407894	G	A	missense_variant	MODERATE	c.1085G>A\|p.Arg362Gln	S176
90808	BAA10g00870	A10	408297	G	A	missense_variant	MODERATE	c.1213G>A\|p.Asp405Asn	S180
90809	BAA10g00870	A10	408874	G	A	missense_variant	MODERATE	c.1595G>A\|p.Ser532Asn	S148 S210 S30
90810	BAA10g00870	A10	408897	G	A	missense_variant	MODERATE	c.1618G>A\|p.Asp540Asn	S256
90811	BAA10g00870	A10	409667	C	T	missense_variant	MODERATE	c.2105C>T\|p.Ser702Phe	S23
90812	BAA10g00880	A10	410220	G	A	upstream_gene_variant	MODIFIER	c.-1721G>A\|	S69
90813	BAA10g00880	A10	411021	C	T	upstream_gene_variant	MODIFIER	c.-920C>T\|	S185
90814	BAA10g00880	A10	411069	C	T	upstream_gene_variant	MODIFIER	c.-872C>T\|	S221
90815	BAA10g00880	A10	411858	C	T	upstream_gene_variant	MODIFIER	c.-83C>T\|	S244
90816	BAA10g00890	A10	412211	C	T	upstream_gene_variant	MODIFIER	c.-3783C>T\|	S132 S137 S89
90817	BAA10g00890	A10	412859	C	T	upstream_gene_variant	MODIFIER	c.-3135C>T\|	S270
90818	BAA10g00890	A10	413054	G	A	upstream_gene_variant	MODIFIER	c.-2940G>A\|	S136
90819	BAA10g00880	A10	413371	G	A	missense_variant	MODERATE	c.575G>A\|p.Gly192Glu	S3
90820	BAA10g00880	A10	414317	A	C	missense_variant	MODERATE	c.1069A>C\|p.Asn357His	S118 S12 S122 S128 S144 S164 S260 S266 S53 S8
90821	BAA10g00890	A10	415009	G	A	upstream_gene_variant	MODIFIER	c.-985G>A\|	S242
90822	BAA10g00890	A10	415837	C	T	upstream_gene_variant	MODIFIER	c.-157C>T\|	S52
90823	BAA10g00890	A10	416324	G	A	splice_region_variant&intron_variant	LOW	c.152-4G>A\|	S1 S293
90824	BAA10g00900	A10	416762	C	T	upstream_gene_variant	MODIFIER	c.-3166C>T\|	S37
90825	BAA10g00890	A10	417466	C	T	missense_variant	MODERATE	c.580C>T\|p.Pro194Ser	S8

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