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Gene | BRAF |
Variant | N20T |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | BRAF N20T does not lie within any known functional domains of the Braf protein (UniProt.org). N20T has been identified in sequencing studies (PMID: 29106415), but has not been biochemically characterized and therefore, its effect on Braf protein function is unknown (PubMed, Aug 2024). |
Associated Drug Resistance | |
Category Variants Paths |
BRAF mutant BRAF N20T |
Transcript | NM_004333.6 |
gDNA | chr7:g.140924645T>G |
cDNA | c.59A>C |
Protein | p.N20T |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_004333.6 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
XM_017012558 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001374258.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001378470.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
XM_047420769.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
XM_017012559.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
XM_017012558.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001378471.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
XM_005250045 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
XM_047420767.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001378469.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
XM_017012559.2 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_004333.5 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001378468.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001374244.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001378475.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001378467.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_004333 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001354609.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
XM_047420768.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001378474.1 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
NM_001354609.2 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
XM_017012559 | chr7:g.140924645T>G | c.59A>C | p.N20T | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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