CDH23 NM_022124.6(CDH23):c.10021C>T (p.Arg3341Cys)

CI-VAR-00031865Explore in graph →p.Arg3341CysNM_022124.6:c.10021C>TClinVar 198640 rs370074117

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
198640	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Usher syndrome type 1; Usher syndrome type 1D; Pituitary adenoma 5, multiple types; Autosomal recessive nonsyndromic hearing loss 12; Inborn genetic diseases; Retinal dystrophy	germline	11	Nov 08, 2025	clinvar