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| Gene | BRAF |
| Variant | T599X |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | BRAF T599X indicates any BRAF missense mutation that results in replacement of the threonine (T) at amino acid 599 by a different amino acid. |
| Associated Drug Resistance | |
| Category Variants Paths |
BRAF mutant BRAF T599X |
| Transcript | NM_004333.6 |
| gDNA | chr7:g.140753338_140753340 |
| cDNA | c.1795_1797 |
| Protein | p.T599 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001378472.1 | chr7:g.140749326_140749328 | c.1795_1797 | p.T599 | RefSeq | GRCh38/hg38 |
| NM_004333.5 | chr7:g.140753338_140753340 | c.1795_1797 | p.T599 | RefSeq | GRCh38/hg38 |
| NM_001378473.1 | chr7:g.140749326_140749328 | c.1795_1797 | p.T599 | RefSeq | GRCh38/hg38 |
| NM_001378474.1 | chr7:g.140753338_140753340 | c.1795_1797 | p.T599 | RefSeq | GRCh38/hg38 |
| NM_001354609.1 | chr7:g.140753338_140753340 | c.1795_1797 | p.T599 | RefSeq | GRCh38/hg38 |
| NM_004333.6 | chr7:g.140753338_140753340 | c.1795_1797 | p.T599 | RefSeq | GRCh38/hg38 |
| NM_001378468.1 | chr7:g.140753338_140753340 | c.1795_1797 | p.T599 | RefSeq | GRCh38/hg38 |
| NM_001354609.2 | chr7:g.140753338_140753340 | c.1795_1797 | p.T599 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| BRAF T599X | unknown |