TRPV4 NM_021625.5(TRPV4):c.81T>C (p.Gly27=)

CI-VAR-00043984Explore in graph →p.Gly27=NM_021625.5:c.81T>CClinVar 241389 rs34599967

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
241389	Benign	criteria provided, multiple submitters, no conflicts	2	Charcot-Marie-Tooth disease axonal type 2C; Metatropic dysplasia; Neuronopathy, distal hereditary motor, autosomal dominant 8; Brachyrachia (short spine dysplasia); Scapuloperoneal spinal muscular atrophy; Spondylometaphyseal dysplasia, Kozlowski type; Charcot-Marie-Tooth disease; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Sarcoma; Ovarian serous cystadenocarcinoma; Lung cancer; Thyroid cancer, nonmedullary, 1; Cervical cancer	germline	12	Feb 02, 2026	clinvar