PKD1 NM_001009944.3(PKD1):c.8440G>A (p.Gly2814Arg)

CI-VAR-00047554Explore in graph →p.Gly2814ArgNM_001009944.3:c.8440G>AClinVar 257021 rs149151043

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
257021	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Polycystic kidney disease, adult type; Autosomal dominant polycystic kidney disease; Polycystic kidney disease; PKD1-related disorder; Lung cancer; Ovarian serous cystadenocarcinoma; Cholangiocarcinoma	germline	14	Jun 30, 2026	clinvar