CDH23 NM_022124.6(CDH23):c.4102_4103delinsTATCTTGAA (p.Thr1368fs) — variant · CancerIndex

Variant · Indel

CDH23 NM_022124.6(CDH23):c.4102_4103delinsTATCTTGAA (p.Thr1368fs)

CI-VAR-00363153Explore in graph →p.Thr1368fsNM_022124.6:c.4102_4103delinsTATCTTGAAClinVar 3596862

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
3596862	Likely pathogenic	criteria provided, single submitter	1	Pituitary adenoma 5, multiple types; Usher syndrome type 1D; Autosomal recessive nonsyndromic hearing loss 12	germline	1	Feb 29, 2024	clinvar