Variant · Snv
ALPK3 NM_020778.5(ALPK3):c.4130-1G>A
CI-VAR-00101733Explore in graph →NM_020778.5:c.4130-1G>AClinVar 548939 rs762110595
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 |
|---|---|---|---|---|---|---|---|---|
| 548939 | Likely pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Cardiomyopathy, familial hypertrophic 27; Cardiovascular phenotype; Lung cancer | germline | 7 | Jan 31, 2026 | clinvar |