CDAN1 NM_138477.4(CDAN1):c.2445C>T (p.Gly815=)

CI-VAR-00053728Explore in graph →p.Gly815=NM_138477.4:c.2445C>TClinVar 315933 rs114208791

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
315933	Benign	criteria provided, multiple submitters, no conflicts	2	Congenital dyserythropoietic anemia, type I; Anemia, congenital dyserythropoietic, type 1a; Uterine corpus endometrial carcinoma; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia; Lung cancer; Gastric cancer	germline	6	Jan 26, 2026	clinvar