Variant · Snv
HRAS G13D
CI-VAR-00001633Explore in graph →NP_005334.1:p.Gly13AspNM_005343.3:c.38G>AClinVar 12604 CIViC 274 rs104894226
Curated evidence
Evidence by cancer (3 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 26561417
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Colorectal Neoplasm2 | ||||||||
| HRAS G13D | Cetuximab | Predictive | D | Supports Resistance | — | accepted | EID3852In an in vitro study, Colo-320, SW48, and CaCO2 cell lines expressing HRAS G13D mutation were associated with resistance to cetuximab treatment, as compared to Colo-320, SW48, and CaCO2 cells expressi… (full text at CIViC) PMID 26561417 · Boidot et al., 2016 · Open in CIViC | civic |
| HRAS G13D | Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor | Predictive | C | Supports Resistance | 3 | accepted | EID699Case report of a patient with metastatic colorectal carcinoma and a novel HRAS G13D mutation showed resistance to treatment with panitumumab. In vitro models of HRAS G13D confirmed resistance mechanis… (full text at CIViC) PMID 26561417 · Boidot et al., 2016 · | |
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 12604 | Pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Costello syndrome; RASopathy; Non-immune hydrops fetalis; Noonan syndrome and Noonan-related syndrome; Melanoma; Malignant tumor of urinary bladder; Embryonal rhabdomyosarcoma; HRAS-related disorder | germline/somatic | 20 | Oct 01, 2025 | clinvar |