ALPK3 NM_020778.5(ALPK3):c.3628C>T (p.Arg1210Trp)

CI-VAR-00057965Explore in graph →p.Arg1210TrpNM_020778.5:c.3628C>TClinVar 383786 rs55752937

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
383786	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Cardiovascular phenotype; Cardiomyopathy, familial hypertrophic 27; Malignant tumor of esophagus; Uterine corpus endometrial carcinoma; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Acute myeloid leukemia; Hepatocellular carcinoma; Lung cancer	germline	11	Feb 04, 2026	clinvar