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| Gene | HRAS |
| Variant | Q61X |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | HRAS Q61X indicates any HRAS missense mutation that results in replacement of the glutamine (Q) at amino acid 61 by a different amino acid. HRAS Q61 mutations are hotspot mutations that often result in decreased Hras GTPase activity, leading to activation of downstream signaling and transformation of cultured cells (PMID: 3510078, PMID: 26985062). |
| Associated Drug Resistance | |
| Category Variants Paths |
HRAS mutant HRAS Q61X |
| Transcript | NM_005343.4 |
| gDNA | chr11:g.533873_533875 |
| cDNA | c.181_183 |
| Protein | p.Q61 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_005343.4 | chr11:g.533873_533875 | c.181_183 | p.Q61 | RefSeq | GRCh38/hg38 |
| NM_005343 | chr11:g.533873_533875 | c.181_183 | p.Q61 | RefSeq | GRCh38/hg38 |
| NM_005343.3 | chr11:g.533873_533875 | c.181_183 | p.Q61 | RefSeq | GRCh38/hg38 |
| NM_001130442.3 | chr11:g.533873_533875 | c.181_183 | p.Q61 | RefSeq | GRCh38/hg38 |
| NM_176795.5 | chr11:g.533873_533875 | c.181_183 | p.Q61 | RefSeq | GRCh38/hg38 |
| NM_001130442 | chr11:g.533873_533875 | c.181_183 | p.Q61 | RefSeq | GRCh38/hg38 |
| NM_001130442.2 | chr11:g.533873_533875 | c.181_183 | p.Q61 | RefSeq | GRCh38/hg38 |
| NM_176795 | chr11:g.533873_533875 | c.181_183 | p.Q61 | RefSeq | GRCh38/hg38 |
| NM_176795.4 | chr11:g.533873_533875 | c.181_183 | p.Q61 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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