Variant · Snv
ACTL6A NM_004301.5(ACTL6A):c.1138T>G (p.Leu380Val)
CI-VAR-00308188Explore in graph →p.Leu380ValNM_004301.5:c.1138T>GClinVar 2672968 rs73883564
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 |
|---|---|---|---|---|---|---|---|---|
| 2672968 | Benign | criteria provided, single submitter | 1 | Familial pancreatic carcinoma; Ovarian serous cystadenocarcinoma | germline | 2 | Oct 01, 2023 | clinvar |