PIGG NM_001127178.3(PIGG):c.1967C>T (p.Ala656Val)

CI-VAR-00055918Explore in graph →p.Ala656ValNM_001127178.3:c.1967C>TClinVar 376924 rs61749092

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
376924	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Intellectual disability, autosomal recessive 53; Sarcoma; Clear cell carcinoma of kidney; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Lung cancer	germline	6	Feb 03, 2026	clinvar