Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g06920	A10	3703682	G	A	downstream_gene_variant	MODIFIER	c.*4087C>T\|	S241
2	BAA10g06920	A10	3703792	C	T	downstream_gene_variant	MODIFIER	c.*3977G>A\|	S19
3	BAA10g06920	A10	3704725	G	A	downstream_gene_variant	MODIFIER	c.*3044C>T\|	S13 S140 S219 S278 S279 S64 S72
4	BAA10g06920	A10	3705119	G	A	downstream_gene_variant	MODIFIER	c.*2650C>T\|	S202
5	BAA10g06920	A10	3705144	C	T	downstream_gene_variant	MODIFIER	c.*2625G>A\|	S166
6	BAA10g06920	A10	3707931	G	A	synonymous_variant	LOW	c.1014C>T\|p.His338His	S80
7	BAA10g06920	A10	3708610	G	A	synonymous_variant	LOW	c.612C>T\|p.Phe204Phe	S55
8	BAA10g06920	A10	3708964	C	T	synonymous_variant	LOW	c.357G>A\|p.Lys119Lys	S126
9	BAA10g06920	A10	3709185	G	A	missense_variant	MODERATE	c.284C>T\|p.Ser95Phe	S18
10	BAA10g06920	A10	3709236	G	A	missense_variant	MODERATE	c.233C>T\|p.Ser78Phe	S59
11	BAA10g06920	A10	3709304	G	A	synonymous_variant	LOW	c.165C>T\|p.Pro55Pro	S171
12	BAA10g06920	A10	3709316	C	T	synonymous_variant	LOW	c.153G>A\|p.Glu51Glu	S308
13	BAA10g06920	A10	3709659	C	T	upstream_gene_variant	MODIFIER	c.-191G>A\|	S44
14	BAA10g06920	A10	3712562	C	T	upstream_gene_variant	MODIFIER	c.-3094G>A\|	S116
15	BAA10g06920	A10	3714193	G	A	upstream_gene_variant	MODIFIER	c.-4725C>T\|	S77