Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g39980	A02	33799540	C	T	missense_variant	MODERATE	c.2939G>A\|p.Ser980Asn	S133
2	BAA02g39980	A02	33800382	C	T	missense_variant	MODERATE	c.2405G>A\|p.Gly802Glu	S239
3	BAA02g39980	A02	33802691	C	T	missense_variant	MODERATE	c.1306G>A\|p.Ala436Thr	S1 S90
4	BAA02g39980	A02	33802834	C	T	splice_region_variant&intron_variant	LOW	c.1171-8G>A\|	S183 S198
5	BAA02g39980	A02	33803060	G	A	missense_variant	MODERATE	c.1034C>T\|p.Ser345Phe	S268
6	BAA02g39980	A02	33803271	C	T	splice_acceptor_variant&intron_variant	HIGH	c.913-1G>A\|	S15 S156 S3 S34
7	BAA02g39980	A02	33805082	C	T	missense_variant&splice_region_variant	MODERATE	c.645G>A\|p.Met215Ile	S259
8	BAA02g39980	A02	33808311	C	T	upstream_gene_variant	MODIFIER	c.-1773G>A\|	S201
9	BAA02g39980	A02	33810436	C	T	upstream_gene_variant	MODIFIER	c.-3898G>A\|	S98
10	BAA02g39980	A02	33811032	G	A	upstream_gene_variant	MODIFIER	c.-4494C>T\|	S84 S93