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Gene | BRAF |
Variant | P367R |
Impact List | missense |
Protein Effect | gain of function |
Gene Variant Descriptions | BRAF P367R does not lie within any known functional domains within the Braf protein (UniProt.org). P367R confers a gain of function to the Braf protein as indicated by increased Erk phosphorylation in culture and tumor formation in animal models, and demonstrates resistance to Egfr inhibitors in culture (PMID: 27478040). |
Associated Drug Resistance | Y |
Category Variants Paths |
BRAF mutant BRAF act mut BRAF P367R BRAF mutant BRAF P367X BRAF P367R |
Transcript | NM_004333.6 |
gDNA | chr7:g.140794348G>C |
cDNA | c.1100C>G |
Protein | p.P367R |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001378474.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_001378468.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_001354609.2 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
XM_017012559 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
XM_017012558.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_001378469.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
XM_017012559.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
XM_005250045 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
XM_047420768.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
XM_047420769.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_004333.5 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
XM_047420767.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_001354609.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
XM_017012559.2 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_001378471.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_001374258.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_004333.6 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
XM_017012558 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_004333 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
NM_001374244.1 | chr7:g.140794348G>C | c.1100C>G | p.P367R | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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