Variant
NRAS G12/G13
CI-VAR-00001587Explore in graph →p.Gly13AspNM_002524.5:c.38G>AClinVar 13901 CIViC 596 rs121434596
Curated evidence
Evidence by cancer (1 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
- 27276561
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Acute Myeloid Leukemia1 | ||||||||
| NRAS G12/G13 | (prognostic) | Prognostic | B | Supports Better Outcome | 4 | accepted | EID1516Patients with a triple mutation of NPM1, DNMT3A, and NRAS (G12/13) (three-way interaction p=0.04) showed a relatively benign prognosis with an 8-year survival rate of 75% and a 10-year survival rate o… (full text at CIViC) PMID 27276561 · Papaemmanuil et al., 2016 · Open in CIViC | 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 |
|---|---|---|---|---|---|---|---|---|
| 13901 | Pathogenic/Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Juvenile myelomonocytic leukemia; Noonan syndrome 6; Autoimmune lymphoproliferative syndrome type 4; Acute megakaryoblastic leukemia in down syndrome; Neoplasm; RASopathy; Acute myeloid leukemia with NPM1 somatic mutations; Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype; Embryonal rhabdomyosarcoma; RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER 1, SOMATIC; NRAS-related disorder; Colorectal cancer; Melanoma; Acute myeloid leukemia |