Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@jax.org
Gene | BRAF |
Variant | Q262R |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | BRAF Q262R lies within the phorbol-ester/DAG-type zinc finger domain of the Braf protein (UniProt.org). Q262R has not been characterized in the scientific literature and therefore, its effect on Braf protein function is unknown (PubMed, Dec 2023). |
Associated Drug Resistance | |
Category Variants Paths |
BRAF mutant BRAF Q262R |
Transcript | NM_004333.6 |
gDNA | chr7:g.140801487T>C |
cDNA | c.785A>G |
Protein | p.Q262R |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_004333.5 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_001378469.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
XM_047420767.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_001354609.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_001374244.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
XM_005250045 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
XM_017012559.2 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_004333 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_001378474.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_001378468.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
XM_047420769.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
XM_017012558.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_001378471.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_001354609.2 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
XM_017012558 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
XM_017012559.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_001374258.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
NM_004333.6 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
XM_017012559 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
XM_047420768.1 | chr7:g.140801487T>C | c.785A>G | p.Q262R | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|