HDAC4 NM_001378414.1(HDAC4):c.2371G>A (p.Ala791Thr)

CI-VAR-00049690Explore in graph →p.Ala791ThrNM_001378414.1:c.2371G>AClinVar 283520 rs61754648

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.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
283520	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Chromosome 2q37 deletion syndrome; HDAC4-related disorder; Acute myeloid leukemia; Malignant tumor of esophagus; Lung cancer; Familial cancer of breast	germline	8	Mar 01, 2026	clinvar