CDAN1 NM_138477.4(CDAN1):c.1524A>G (p.Gln508=)

CI-VAR-00053855Explore in graph →p.Gln508=NM_138477.4:c.1524A>GClinVar 315947 rs147500837

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
315947	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Congenital dyserythropoietic anemia, type I; Clear cell carcinoma of kidney; Gastric cancer; Thyroid cancer, nonmedullary, 1; Sarcoma; Ovarian serous cystadenocarcinoma; Melanoma; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary; Lung cancer; Anemia, congenital dyserythropoietic, type 1a	germline	6	May 01, 2026	clinvar