Variant · Snv
KRAS G13
CI-VAR-00001626Explore in graph →p.Gly13AspNM_004985.5:c.38G>AClinVar 12580 CIViC 80 rs112445441
Curated evidence
Evidence by cancer (4 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
- 21641636
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Colorectal Adenocarcinoma2 | ||||||||
| KRAS G12 OR KRAS G13 OR KRAS Q61 | (prognostic) | Prognostic | B | Supports Poor Outcome | 3 | submitted | EID11056The Medical Research Council (MRC) COIN trial consisted of patients with histologically confirmed adenocarcinoma of the colon or rectum, inoperable metastatic or locoregional measurable disease, and w… (full text at CIViC) PMID 21641636 · Maughan et al., 2011 · Open in CIViC | civic |
| KRAS G12 OR KRAS G13 OR KRAS Q61 | Cetuximab + ChemotherapyCombination | Predictive | B | Does Not Support Sensitivity Response | 4 | submitted | EID11055The Medical Research Council (MRC) COIN trial consisted of patients with histologically confirmed adenocarcinoma of the colon or rectum, inoperable metastatic or locoregional measurable disease, and w… (full text at CIViC) PMID 21641636 · | |
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 |
|---|---|---|---|---|---|---|---|---|
| 12580 | Pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Breast adenocarcinoma; Non-small cell lung carcinoma; Juvenile myelomonocytic leukemia; OCULOECTODERMAL SYNDROME, SOMATIC; Inborn genetic diseases; Nevus sebaceous; RASopathy; Noonan syndrome and Noonan-related syndrome; Encephalocraniocutaneous lipomatosis; KRAS-related disorder; Neoplasm; Melanoma; Acute myeloid leukemia; Malignant tumor of urinary bladder; Cervical cancer; Familial pancreatic carcinoma; Adenocarcinoma of the large intestine; Embryonal rhabdomyosarcoma; Diffuse midline glioma, H3 K27M-mutant; Colorectal cancer; RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER 2, SOMATIC |