DNMT3A NM_022552.5(DNMT3A):c.2644C>T (p.Arg882Cys)

CI-VAR-00055617Explore in graph →p.Arg882CysNM_022552.5:c.2644C>TClinVar 375882 rs377577594

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
375882	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Acute myeloid leukemia; Tatton-Brown-Rahman overgrowth syndrome; Inborn genetic diseases; Neurodevelopmental disorder; EBV-positive nodal T- and NK-cell lymphoma; DNMT3A-related disorder; Neoplasm; Heyn-Sproul-Jackson syndrome	germline/somatic	19	Feb 01, 2026	clinvar