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Gene | HRAS |
Variant | G13D |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | HRAS G13D is hotspot mutation that lies within the GTP nucleotide binding region of the Hras protein (UniProt.org). G13D results in decreased Hras GTPase activity and loss of response to GTPase-activating proteins, leading to activation of downstream signaling and senescence in cell culture (PMID: 24224811, PMID: 21850009). |
Associated Drug Resistance | |
Category Variants Paths |
HRAS mutant HRAS act mut HRAS G13D HRAS mutant HRAS G13X HRAS G13D |
Transcript | NM_005343.4 |
gDNA | chr11:g.534285C>T |
cDNA | c.38G>A |
Protein | p.G13D |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001130442.2 | chr11:g.534285C>T | c.38G>A | p.G13D | RefSeq | GRCh38/hg38 |
NM_176795.5 | chr11:g.534285C>T | c.38G>A | p.G13D | RefSeq | GRCh38/hg38 |
NM_176795.4 | chr11:g.534285C>T | c.38G>A | p.G13D | RefSeq | GRCh38/hg38 |
NM_001130442.3 | chr11:g.534285C>T | c.38G>A | p.G13D | RefSeq | GRCh38/hg38 |
NM_005343.4 | chr11:g.534285C>T | c.38G>A | p.G13D | RefSeq | GRCh38/hg38 |
NM_001130442 | chr11:g.534285C>T | c.38G>A | p.G13D | RefSeq | GRCh38/hg38 |
NM_176795 | chr11:g.534285C>T | c.38G>A | p.G13D | RefSeq | GRCh38/hg38 |
NM_005343 | chr11:g.534285C>T | c.38G>A | p.G13D | RefSeq | GRCh38/hg38 |
NM_005343.3 | chr11:g.534285C>T | c.38G>A | p.G13D | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
HRAS G13D | loss of function | MEK inhibitor (Pan) MEK1 Inhibitor MEK2 Inhibitor PI3K Inhibitor (Pan) PIK3CA inhibitor PIK3CB inhibitor PIK3CD inhibitor PIK3CG inhibitor RAS Inhibitor (Pan) |