Variant · Snv
HRAS G13R
CI-VAR-00001637Explore in graph →NP_005334.1:p.Gly13ArgNM_005343.3:c.37G>CClinVar 35554 CIViC 1393 rs104894228
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
- 22683711
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Neoplasm1 | ||||||||
| HRAS G13R | (oncogenic) | Oncogenic | D | Supports Oncogenicity | 5 | submitted | EID12906HRAS p.Gly13Arg (NM_005343.4:c.37G>C) causes increased proliferation, experiments were done in triplicates. PMID 22683711 · Groesser et al., 2012 · Open in CIViC | civic |
| Thyroid Gland Carcinoma1 | ||||||||
| HRAS G13R | Vemurafenib | Predictive | D | Supports Resistance | — | submitted | EID3853In an in vitro study, a C643 cell line expressing HRAS G13R demonstrated reduced sensitivity to vemurafenib treatment, compared to BRAF V600E expressing cells (8505C, SWI1736, BHT101 and BCPAP). Sensi… (full text at CIViC) PMID 19880792 · Salerno et al., 2010 · Open in CIViC | |
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 35554 | Pathogenic/Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Linear nevus sebaceous syndrome; Nevus sebaceous; Epidermal nevus; NEVUS SPILUS, SOMATIC; SPITZ NEVUS, SOMATIC; Lip and oral cavity carcinoma; Non-immune hydrops fetalis; Costello syndrome; Noonan syndrome and Noonan-related syndrome; cutaneous-skeletal hypophosphatemia syndrome; HRAS-related disorder; Ectomesenchymoma; Alveolar rhabdomyosarcoma; Embryonal rhabdomyosarcoma; Breast phyllodes tumor; HRAS-related disorders |