FLNA NM_001110556.2(FLNA):c.1314C>T (p.Gly438=)

CI-VAR-00094324Explore in graph →p.Gly438=NM_001110556.2:c.1314C>TClinVar 519877 rs372113435

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
519877	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Heterotopia, periventricular, X-linked dominant; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia; Melnick-Needles syndrome; Familial thoracic aortic aneurysm and aortic dissection; Thyroid cancer, nonmedullary, 1	germline	6	Jan 05, 2026	clinvar