BRAF I592V
Gene Variant Detail

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Gene BRAF
Variant I592V
Impact List missense
Protein Effect unknown
Gene Variant Descriptions BRAF I592V lies within the protein kinase domain of the Braf protein (UniProt.org). I592V has been identified in sequencing studies (PMID: 24710085, PMID: 15331929), but has not been biochemically characterized and therefore, its effect on Braf protein function is unknown (PubMed, Dec 2025).
Associated Drug Resistance
Category Variants Paths

BRAF mutant BRAF I592V

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Transcript NM_004333.6
gDNA chr7:g.140753361T>C
cDNA c.1774A>G
Protein p.I592V
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001354609.1 chr7:g.140753361T>C c.1774A>G p.I592V RefSeq GRCh38/hg38
NM_001378468.1 chr7:g.140753361T>C c.1774A>G p.I592V RefSeq GRCh38/hg38
NM_004333.6 chr7:g.140753361T>C c.1774A>G p.I592V RefSeq GRCh38/hg38
NM_001378472.1 chr7:g.140749349T>C c.1774A>G p.I592V RefSeq GRCh38/hg38
NM_001378474.1 chr7:g.140753361T>C c.1774A>G p.I592V RefSeq GRCh38/hg38
NM_001354609.2 chr7:g.140753361T>C c.1774A>G p.I592V RefSeq GRCh38/hg38
NM_004333.5 chr7:g.140753361T>C c.1774A>G p.I592V RefSeq GRCh38/hg38
XM_005250045 chr7:g.140753361T>C c.1774A>G p.I592V RefSeq GRCh38/hg38
NM_004333 chr7:g.140753361T>C c.1774A>G p.I592V RefSeq GRCh38/hg38
NM_001378473.1 chr7:g.140749349T>C c.1774A>G p.I592V RefSeq GRCh38/hg38

Filtering

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  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References