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Gene | HRAS |
Variant | G13R |
Impact List | missense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | HRAS G13R is hotspot mutation that lies within the GTP binding domain of the Hras protein (UniProt.org). G13R results in activation of Mapk and Pi3k signaling, increased cell proliferation in culture (PMID: 22683711), and is predicted to lead to a loss of Hras protein function based on the effects of other HRAS G13 mutations. |
Associated Drug Resistance | |
Category Variants Paths |
HRAS mutant HRAS act mut HRAS G13R HRAS mutant HRAS G13X HRAS G13R |
Transcript | NM_005343.4 |
gDNA | chr11:g.534286C>G |
cDNA | c.37G>C |
Protein | p.G13R |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_176795 | chr11:g.534286C>G | c.37G>C | p.G13R | RefSeq | GRCh38/hg38 |
NM_001130442.2 | chr11:g.534286C>G | c.37G>C | p.G13R | RefSeq | GRCh38/hg38 |
NM_005343.4 | chr11:g.534286C>G | c.37G>C | p.G13R | RefSeq | GRCh38/hg38 |
NM_176795.4 | chr11:g.534286C>G | c.37G>C | p.G13R | RefSeq | GRCh38/hg38 |
NM_001130442.3 | chr11:g.534286C>G | c.37G>C | p.G13R | RefSeq | GRCh38/hg38 |
NM_001130442 | chr11:g.534286C>G | c.37G>C | p.G13R | RefSeq | GRCh38/hg38 |
NM_005343 | chr11:g.534286C>G | c.37G>C | p.G13R | RefSeq | GRCh38/hg38 |
NM_176795.5 | chr11:g.534286C>G | c.37G>C | p.G13R | RefSeq | GRCh38/hg38 |
NM_005343.3 | chr11:g.534286C>G | c.37G>C | p.G13R | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
HRAS G13R | loss of function - predicted | MEK inhibitor (Pan) MEK1 Inhibitor MEK2 Inhibitor PI3K Inhibitor (Pan) PIK3CA inhibitor PIK3CB inhibitor PIK3CD inhibitor PIK3CG inhibitor RAS Inhibitor (Pan) |
HRAS G13R PTEN inact mut | ||
HRAS G13R PIK3CA H1047R | ||
ALK F1245Y HRAS G13R | ||
BRAF G466E HRAS G13R | ||
HRAS G13R PTEN loss |