Variant · Snv
SOS1 NM_005633.4(SOS1):c.805A>G (p.Met269Val)
CI-VAR-00169529Explore in graph →p.Met269ValNM_005633.4:c.805A>GClinVar 981559 rs1671005559
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
- 2026-09-06
- 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 |
|---|---|---|---|---|---|---|---|---|
| 981559 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Noonan syndrome; Noonan syndrome 4; Cardiovascular phenotype; RASopathy; Lung cancer | germline | 7 | Nov 01, 2025 | clinvar |