Gene Variant Detail

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Gene BRAF
Variant P162S
Impact List missense
Protein Effect no effect - predicted
Gene Variant Descriptions BRAF P162S lies within the RBD domain of the Braf protein (UniProt.org). P162S has not been biochemically characterized, but results in similar cell proliferation and viability levels as wild-type Braf in culture (PMID: 29533785), and therefore, is predicted to have no effect on Braf protein function.
Associated Drug Resistance
Category Variants Paths

BRAF mutant BRAF P162S

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Transcript NM_004333.6
gDNA chr7:g.140834629G>A
cDNA c.484C>T
Protein p.P162S
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017012558.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
XM_017012559.2 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_001374258.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_001374244.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_001354609.2 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_004333.5 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_001378468.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
XM_047420769.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
XM_047420767.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_001354609.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_001378471.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
XM_017012559.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_004333 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_001378474.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
XM_017012559 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
XM_005250045 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_001378469.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
XM_047420768.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_004333.6 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
XM_017012558 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38
NM_001378467.1 chr7:g.140834629G>A c.484C>T p.P162S RefSeq GRCh38/hg38

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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