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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
90201	BAA10g00290	A10	134812	G	A	upstream_gene_variant	MODIFIER	c.-2997C>T\|	S167 S236 S257 S262
90202	BAA10g00300	A10	134891	G	A	splice_region_variant&intron_variant	LOW	c.778-7C>T\|	S245
90203	BAA10g00300	A10	135612	C	T	splice_region_variant&intron_variant	LOW	c.457+5G>A\|	S187
90204	BAA10g00300	A10	136141	C	T	missense_variant	MODERATE	c.94G>A\|p.Ala32Thr	S206 S26
90205	BAA10g00300	A10	139096	C	T	upstream_gene_variant	MODIFIER	c.-2627G>A\|	S282
90206	BAA10g00310	A10	143010	G	A	missense_variant	MODERATE	c.545G>A\|p.Gly182Asp	S236
90207	BAA10g00330	A10	144262	G	A	upstream_gene_variant	MODIFIER	c.-3081G>A\|	S167
90208	BAA10g00320	A10	144631	G	A	missense_variant	MODERATE	c.151G>A\|p.Val51Ile	S264
90209	BAA10g00320	A10	145042	G	A	missense_variant	MODERATE	c.338G>A\|p.Ser113Asn	S263
90210	BAA10g00330	A10	145885	G	A	upstream_gene_variant	MODIFIER	c.-1458G>A\|	S138
90211	BAA10g00320	A10	146342	G	A	missense_variant	MODERATE	c.992G>A\|p.Arg331Lys	S94
90212	BAA10g00330	A10	146783	G	A	upstream_gene_variant	MODIFIER	c.-560G>A\|	S76
90213	BAA10g00330	A10	148478	G	A	synonymous_variant	LOW	c.693G>A\|p.Lys231Lys	S236
90214	BAA10g00330	A10	148747	G	A	synonymous_variant	LOW	c.882G>A\|p.Glu294Glu	S265
90215	BAA10g00330	A10	149038	G	A	synonymous_variant	LOW	c.1095G>A\|p.Glu365Glu	S34
90216	BAA10g00330	A10	149454	C	T	synonymous_variant	LOW	c.1443C>T\|p.Arg481Arg	S206 S26
90217	BAA10g00340	A10	149607	C	T	upstream_gene_variant	MODIFIER	c.-1980C>T\|	S95
90218	BAA10g00340	A10	150115	G	A	upstream_gene_variant	MODIFIER	c.-1472G>A\|	S158
90219	BAA10g00340	A10	150474	G	A	upstream_gene_variant	MODIFIER	c.-1113G>A\|	S161
90220	BAA10g00340	A10	151440	C	T	upstream_gene_variant	MODIFIER	c.-147C>T\|	S173
90221	BAA10g00340	A10	152200	C	T	synonymous_variant	LOW	c.156C>T\|p.Val52Val	S104 S52
90222	BAA10g00350	A10	152614	G	A	upstream_gene_variant	MODIFIER	c.-4016G>A\|	S125
90223	BAA10g00350	A10	156426	G	A	upstream_gene_variant	MODIFIER	c.-204G>A\|	S82 S92
90224	BAA10g00350	A10	157177	G	A	missense_variant	MODERATE	c.475G>A\|p.Asp159Asn	S216
90225	BAA10g00370	A10	157521	A	G	upstream_gene_variant	MODIFIER	c.-3910A>G\|	S111

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