PLEC NM_201384.3(PLEC):c.9961G>A (p.Gly3321Arg)

CI-VAR-00020453Explore in graph →p.Gly3321ArgNM_201384.3:c.9961G>AClinVar 129918 rs34132016

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
129918	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Epidermolysis bullosa simplex 5B, with muscular dystrophy; Epidermolysis bullosa simplex 5C, with pyloric atresia; Autosomal recessive limb-girdle muscular dystrophy type 2Q; Epidermolysis bullosa simplex, Ogna type; Epidermolysis bullosa simplex with nail dystrophy; PLEC-related disorder; Thymoma; Thyroid cancer, nonmedullary, 1; Hepatocellular carcinoma; Cervical cancer	germline	13	Jun 01, 2026	clinvar