CDH23 NM_022124.6(CDH23):c.4858G>A (p.Val1620Met)

CI-VAR-00008685Explore in graph →p.Val1620MetNM_022124.6:c.4858G>AClinVar 45957 rs41281330

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
45957	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Usher syndrome type 1D; Autosomal recessive nonsyndromic hearing loss 12; Usher syndrome type 1; Pituitary adenoma 5, multiple types; Colon adenocarcinoma; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Thymoma; Familial cancer of breast; Thyroid cancer, nonmedullary, 1	germline	16	Jun 01, 2026	clinvar