PKHD1 NM_138694.4(PKHD1):c.7921A>G (p.Thr2641Ala)

CI-VAR-00018278Explore in graph →p.Thr2641AlaNM_138694.4:c.7921A>GClinVar 96426 rs7766366

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
96426	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive polycystic kidney disease; Polycystic kidney disease; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma	germline	15	Jan 31, 2026	clinvar