Variant
KRAS G12/G13
CI-VAR-00001586Explore in graph →ClinVar 45122 CIViC 77 rs121913529
Curated evidence
Evidence by cancer (12 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
- 15696205
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Lung Non-Small Cell Carcinoma1 | ||||||||
| KRAS G12/G13 | Erlotinib + GefitinibSubstitutes | Predictive | B | Supports Resistance | 3 | accepted | EID35In 60 patients with NSCLC, Exon 2 KRAS mutations were associated with resistance to the EGFR kinase inhibitors gefitinib or erlotinib (9/38 refractory vs 0/21 sensitive patients; P=0.0201). PMID 15696205 · Pao et al., 2005 · Open in CIViC | civic |
| Malignant Colorectal Neoplasm9 | ||||||||
| KRAS G12/G13 | (prognostic) | Prognostic | B | Does Not Support Poor Outcome | 3 | accepted | EID2231In a retrospective study of 427 chemotherapy-refractory metastatic colorectal patients treated with either panitumumab monotherapy or best supportive care (BSC), KRAS codon 12 or 13 mutations were obs… (full text at 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 |
|---|---|---|---|---|---|---|---|---|
| 45122 | Pathogenic/Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Non-small cell lung carcinoma; Multiple myeloma; Gallbladder cancer; Lung cancer; KRAS-related disorder; Neoplasm; Pilocytic astrocytoma; High-grade astrocytoma with piloid features | germline/somatic | 11 | Oct 26, 2025 |