Variant · Snv
MAP2K1 NM_002755.4(MAP2K1):c.389A>G (p.Tyr130Cys)
CI-VAR-00006210Explore in graph →p.Tyr130CysNM_002755.4:c.389A>GClinVar 13351 rs121908595
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 |
|---|---|---|---|---|---|---|---|---|
| 13351 | Pathogenic | reviewed by expert panel | 3 | Cardiofaciocutaneous syndrome 3; Cardio-facio-cutaneous syndrome; RASopathy; Noonan syndrome 1; Melorheostosis; MAP2K1-related disorder; Cardiovascular phenotype; Neoplasm; Cardiofaciocutaneous syndrome 1 | germline/somatic | 38 | May 09, 2017 | clinvar |