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| Gene | BRAF |
| Variant | A598X |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | BRAF A598X indicates any BRAF missense mutation that results in replacement of the alanine (A) at amino acid 598 by a different amino acid. |
| Associated Drug Resistance | |
| Category Variants Paths |
BRAF mutant BRAF A598X |
| Transcript | NM_004333.6 |
| gDNA | chr7:g.140753341_140753343 |
| cDNA | c.1792_1794 |
| Protein | p.A598 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001354609.1 | chr7:g.140753341_140753343 | c.1792_1794 | p.A598 | RefSeq | GRCh38/hg38 |
| NM_004333.6 | chr7:g.140753341_140753343 | c.1792_1794 | p.A598 | RefSeq | GRCh38/hg38 |
| NM_001354609.2 | chr7:g.140753341_140753343 | c.1792_1794 | p.A598 | RefSeq | GRCh38/hg38 |
| NM_001378474.1 | chr7:g.140753341_140753343 | c.1792_1794 | p.A598 | RefSeq | GRCh38/hg38 |
| NM_001378468.1 | chr7:g.140753341_140753343 | c.1792_1794 | p.A598 | RefSeq | GRCh38/hg38 |
| NM_004333.5 | chr7:g.140753341_140753343 | c.1792_1794 | p.A598 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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