DCAF7 NM_005828.5(DCAF7):c.246C>T (p.Gly82=)

CI-VAR-00127246Explore in graph →p.Gly82=NM_005828.5:c.246C>TClinVar 782725 rs143007748

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
782725	Benign	criteria provided, multiple submitters, no conflicts	2	Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Gastric cancer; Acute myeloid leukemia; Cervical cancer; Thyroid cancer, nonmedullary, 1; Hepatocellular carcinoma	germline	3	Dec 31, 2019	clinvar