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Gene | BRAF |
Variant | G69S |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | BRAF G69S does not lie within any known functional domains of the Braf protein (UniProt.org). G69S results in increased transformation ability compared to wild-type Braf in one of two different cell lines in culture (PMID: 29533785), but has not been fully biochemically characterized and therefore, its effect on Braf protein function is unknown. |
Associated Drug Resistance | |
Category Variants Paths |
BRAF mutant BRAF G69S |
Transcript | NM_004333.6 |
gDNA | chr7:g.140850146C>T |
cDNA | c.205G>A |
Protein | p.G69S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017012559 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_004333.6 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
XM_047420767.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
XM_017012559.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
XM_005250045 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
XM_047420768.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001374258.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
XM_017012558 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001378469.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_004333 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001378474.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001378475.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
XM_017012559.2 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001378467.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001354609.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001354609.2 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
XM_017012558.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_004333.5 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001378468.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
XM_047420769.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001378471.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
NM_001374244.1 | chr7:g.140850146C>T | c.205G>A | p.G69S | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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