TRPV4 NM_021625.5(TRPV4):c.2459-9T>G

CI-VAR-00047422Explore in graph →NM_021625.5:c.2459-9T>GClinVar 261418 rs115373018

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
261418	Benign	criteria provided, multiple submitters, no conflicts	2	Scapuloperoneal spinal muscular atrophy; Brachyrachia (short spine dysplasia); Neuronopathy, distal hereditary motor, autosomal dominant 8; Metatropic dysplasia; Spondylometaphyseal dysplasia, Kozlowski type; Charcot-Marie-Tooth disease axonal type 2C; Charcot-Marie-Tooth disease; Connective tissue disorder; Gastric cancer; Uterine corpus endometrial carcinoma; Uterine carcinosarcoma; Cholangiocarcinoma; Malignant tumor of esophagus; Lung cancer; Cervical cancer	germline	14	Feb 03, 2026	clinvar