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Gene | HRAS |
Variant | N116I |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | HRAS N116I lies within a nucleotide-binding region of the Hras protein (UniProt.org). N116I results in a loss of intrinsic and GEF-stimulated GTPase activity, and is transforming in cell culture (PMID: 3487832, PMID: 8227029). |
Associated Drug Resistance | |
Category Variants Paths |
HRAS mutant HRAS act mut HRAS N116I |
Transcript | NM_005343.4 |
gDNA | chr11:g.533556T>A |
cDNA | c.347A>T |
Protein | p.N116I |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_176795.5 | chr11:g.533556T>A | c.347A>T | p.N116I | RefSeq | GRCh38/hg38 |
NM_005343 | chr11:g.533556T>A | c.347A>T | p.N116I | RefSeq | GRCh38/hg38 |
NM_176795 | chr11:g.533556T>A | c.347A>T | p.N116I | RefSeq | GRCh38/hg38 |
NM_005343.4 | chr11:g.533556T>A | c.347A>T | p.N116I | RefSeq | GRCh38/hg38 |
NM_001130442.2 | chr11:g.533556T>A | c.347A>T | p.N116I | RefSeq | GRCh38/hg38 |
NM_005343.3 | chr11:g.533556T>A | c.347A>T | p.N116I | RefSeq | GRCh38/hg38 |
NM_001130442 | chr11:g.533556T>A | c.347A>T | p.N116I | RefSeq | GRCh38/hg38 |
NM_001130442.3 | chr11:g.533556T>A | c.347A>T | p.N116I | RefSeq | GRCh38/hg38 |
NM_176795.4 | chr11:g.533556T>A | c.347A>T | p.N116I | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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