Variant · Snv
KRAS G12D
CI-VAR-00001606Explore in graph →NP_004976.2:p.Gly12AspNM_004985.4:c.35G>AClinVar 12582 CIViC 79 rs121913529
Curated evidence
Evidence by cancer (81 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
- 27010960
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Pancreatic Neoplasm9 | ||||||||
| KRAS G12D | (prognostic) | Prognostic | B | Supports Poor Outcome | 4 | accepted | EID1300In 219 patients with metastatic pancreatic ductal adenocarcinoma, a multivariate analysis identified KRAS G12D mutations as an independent predictor of poorer prognosis both in patients that have rece… (full text at CIViC) PMID 27010960 · Bournet et al., 2016 · Open in CIViC | civic |
| KRAS G12D | (prognostic) | Prognostic | D | Supports Poor Outcome | 4 | submitted | EID7171KRAS mutations are found in ∼90% of human pancreatic ductal adenocarcinomas. all mice with Kras G12D activation and Pten homozygous deletion succumbed to cancer by 3 weeks of age PMID 20807812 · Hill et al., 2010 · Open in CIViC | civic |
| KRAS G12D | ||||||||
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 |
|---|---|---|---|---|---|---|---|---|
| 12582 | Pathogenic/Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Carcinoma of pancreas; Epidermal nevus; Nevus sebaceous; Linear nevus sebaceous syndrome; Juvenile myelomonocytic leukemia; Non-small cell lung carcinoma; Ovarian neoplasm; Acute myeloid leukemia; RASopathy; Cerebral arteriovenous malformation; Vascular Tumors Including Pyogenic Granuloma; Primary low grade serous adenocarcinoma of ovary; Encephalocraniocutaneous lipomatosis; Capillary malformation-arteriovenous malformation 1; Gastric cancer; Congenital Pulmonary Airway Malformations; Atypical endometrial hyperplasia; Endometrial hyperplasia without atypia; Neoplasm; Cardiovascular phenotype; Adenocarcinoma of the large intestine; Ovarian mucinous adenocarcinoma; Precursor B-cell acute lymphoblastic leukemia; Diffuse midline glioma, H3 K27M-mutant; Colorectal cancer; Medulloblastoma non-WNT/non-SHH; Glioma; RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER 2, SOMATIC; Embryonal rhabdomyosarcoma; Papillary thyroid carcinoma; Alveolar rhabdomyosarcoma; Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype; KRAS-related disorder |