Variant · Snv
KRAS NM_033360.4(KRAS):c.64C>A (p.Gln22Lys)
CI-VAR-00055713Explore in graph →p.Gln22LysNM_033360.4:c.64C>AClinVar 376325 rs121913236
Curated evidence
Evidence by cancer (0 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.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- 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 |
|---|---|---|---|---|---|---|---|---|
| 376325 | Pathogenic/Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Linear nevus sebaceous syndrome; Vascular malformation; RASopathy; Neoplasm; Pilocytic astrocytoma; Embryonal rhabdomyosarcoma; Low grade glioma; High-grade astrocytoma with piloid features; KRAS-related disorder | germline/somatic | 7 | Feb 16, 2025 | clinvar |