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Gene | NRAS |
Variant | R167L |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | NRAS R167L lies within the hypervariable region of the Nras protein (UniProt.org). R167L has been identified in the scientific literature (PMID: 26343583), but has not been biochemically characterized and therefore, its effect on Nras protein function is unknown (PubMed, Dec 2024). |
Associated Drug Resistance | |
Category Variants Paths |
NRAS mutant NRAS R167L |
Transcript | NM_002524.5 |
gDNA | chr1:g.114708605C>A |
cDNA | c.500G>T |
Protein | p.R167L |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_002524 | chr1:g.114708605C>A | c.500G>T | p.R167L | RefSeq | GRCh38/hg38 |
NM_002524.5 | chr1:g.114708605C>A | c.500G>T | p.R167L | RefSeq | GRCh38/hg38 |
NM_002524.4 | chr1:g.114708605C>A | c.500G>T | p.R167L | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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