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Gene | BRAF |
Variant | P367S |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | BRAF P367S does not lie within any known functional domains of the Braf protein (UniProt.org). P367S results in increased transformation ability compared to wild-type Braf in one of two cell lines in culture (PMID: 29533785), but has not been biochemically characterized and therefore, its effect on Braf protein function is unknown (PubMed, Sep 2024). |
Associated Drug Resistance | |
Category Variants Paths |
BRAF mutant BRAF P367X BRAF P367S |
Transcript | NM_004333.6 |
gDNA | chr7:g.140794349G>A |
cDNA | c.1099C>T |
Protein | p.P367S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_005250045 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
XM_047420769.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_001378474.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
XM_017012559.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_004333.6 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_001354609.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_004333 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
XM_017012558.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_001378468.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
XM_017012559.2 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_001354609.2 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_001378469.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_001378471.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
XM_047420768.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_001374258.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
XM_017012559 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_001374244.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
NM_004333.5 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
XM_047420767.1 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
XM_017012558 | chr7:g.140794349G>A | c.1099C>T | p.P367S | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|---|---|---|---|---|---|
NCT03843775 | Phase Ib/II | Binimetinib + Encorafenib | A Study of Binimetinib and Encorafenib in Advanced BRAF Mutant Cancers | Completed | USA | 0 |