PRKG1 NM_006258.4(PRKG1):c.845A>G (p.Asn282Ser)

CI-VAR-00057224Explore in graph →p.Asn282SerNM_006258.4:c.845A>GClinVar 381196 rs34997494

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
381196	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Aortic aneurysm, familial thoracic 8; Familial thoracic aortic aneurysm and aortic dissection; Malignant lymphoma, large B-cell, diffuse; Sarcoma; Uterine carcinosarcoma; Thymoma; Acute myeloid leukemia; Adrenocortical carcinoma, hereditary; Uterine corpus endometrial carcinoma; Colon adenocarcinoma	germline	11	Feb 04, 2026	clinvar