FOXP2 NM_014491.4(FOXP2):c.741C>T (p.Gly247=)

CI-VAR-00025875Explore in graph →p.Gly247=NM_014491.4:c.741C>TClinVar 167097 rs61732741

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
167097	Benign	criteria provided, multiple submitters, no conflicts	2	Childhood apraxia of speech; Inborn genetic diseases; FOXP2-related disorder; Thyroid cancer, nonmedullary, 1; Uterine carcinosarcoma; Malignant tumor of esophagus; Cervical cancer	germline	7	Dec 31, 2019	clinvar