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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

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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_001378470.1 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
XM_017012558 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
XM_047420769.1 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_001378474.1 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
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
XM_005250045 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
NM_004333 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
NM_001354609.1 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_001374244.1 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_001378468.1 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_004333.6 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
NM_001378469.1 chr7:g.140924645T>G c.59A>C p.N20T RefSeq GRCh38/hg38

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  • 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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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries