Variant · Snv
PTEN NM_000314.8(PTEN):c.1161A>G (p.Pro387=)
CI-VAR-00056861Explore in graph →p.Pro387=NM_000314.8:c.1161A>GClinVar 391121 rs1057523975
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 |
|---|---|---|---|---|---|---|---|---|
| 391121 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | PTEN hamartoma tumor syndrome; Hereditary cancer-predisposing syndrome; Familial meningioma; Cowden syndrome 1; Macrocephaly-autism syndrome; Glioma susceptibility 2; Familial prostate cancer | germline | 9 | Jan 13, 2026 | clinvar |