Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g37990	A01	25401476	G	A	downstream_gene_variant	MODIFIER	c.*279C>T\|	S42
2	BAA01g37990	A01	25401966	C	T	missense_variant	MODERATE	c.5342G>A\|p.Gly1781Glu	S67
3	BAA01g37990	A01	25403841	G	A	missense_variant	MODERATE	c.3932C>T\|p.Thr1311Ile	S45
4	BAA01g37990	A01	25404166	C	T	missense_variant	MODERATE	c.3677G>A\|p.Ser1226Asn	S19
5	BAA01g37990	A01	25404722	C	T	splice_region_variant&intron_variant	LOW	c.3353-8G>A\|	S174 S175 S27
6	BAA01g37990	A01	25407313	C	T	intron_variant	MODIFIER	c.1976-621G>A\|	S77
7	BAA01g37990	A01	25410911	G	A	synonymous_variant	LOW	c.1272C>T\|p.Phe424Phe	S17 S218 S268 S269
8	BAA01g37990	A01	25412257	C	T	missense_variant	MODERATE	c.661G>A\|p.Ala221Thr	S46
9	BAA01g37990	A01	25412751	C	T	synonymous_variant	LOW	c.342G>A\|p.Glu114Glu	S47
10	BAA01g37990	A01	25414011	C	T	upstream_gene_variant	MODIFIER	c.-630G>A\|	S12
11	BAA01g37990	A01	25414256	G	A	upstream_gene_variant	MODIFIER	c.-875C>T\|	S224
12	BAA01g37990	A01	25414795	C	T	upstream_gene_variant	MODIFIER	c.-1414G>A\|	S89
13	BAA01g37990	A01	25414926	C	T	upstream_gene_variant	MODIFIER	c.-1545G>A\|	S206 S26
14	BAA01g37990	A01	25415195	C	T	upstream_gene_variant	MODIFIER	c.-1814G>A\|	S174 S27
15	BAA01g37990	A01	25416761	G	A	upstream_gene_variant	MODIFIER	c.-3380C>T\|	S172 S217
16	BAA01g37990	A01	25417144	C	T	upstream_gene_variant	MODIFIER	c.-3763G>A\|	S212
17	BAA01g37990	A01	25418145	C	T	upstream_gene_variant	MODIFIER	c.-4764G>A\|	S274