Variant · Snv
KRAS A146P
CI-VAR-00000057Explore in graph →NP_004976.2:p.Ala146ProNM_004985.4:c.436G>CClinVar 375963 CIViC 905 rs121913527
Curated evidence
Evidence by cancer (11 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
- 41299036
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Colorectal Neoplasm9 | ||||||||
| KRAS A146P | (oncogenic) | Oncogenic | B | Supports Oncogenicity | 3 | submitted | EID13020In a systematic analysis of KRAS mutations across 2,280 KRAS-mutant colorectal cancer samples from three large clinical sequencing cohorts (DFCI, TCGA, MSKCC), KRAS A146P was confirmed as one of three… (full text at CIViC) PMID 41299036 · Navarro-Jiménez et al., 2025 · Open in CIViC | civic |
| KRAS A146P | (oncogenic) | Oncogenic | C | Supports Oncogenicity | 3 | submitted | EID13019Edkins et al. identified KRAS c.436G>C (p.A146P) in one primary colorectal cancer, PD1978a, during sequencing of two independent colorectal cancer cohorts. Normal DNA from the same individuals was ana… (full text at CIViC) PMID 16969076 · Edkins et al., 2006 · 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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 375963 | Pathogenic/Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Multiple myeloma; RASopathy; Autoimmune lymphoproliferative syndrome type 4; Encephalocraniocutaneous lipomatosis | germline/somatic | 4 | Jul 03, 2025 | clinvar |