MYO7A NM_000260.4(MYO7A):c.468C>T (p.Ile156=)

CI-VAR-00008521Explore in graph →p.Ile156=NM_000260.4:c.468C>TClinVar 43252 rs12420129

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
43252	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive nonsyndromic hearing loss 2; Autosomal dominant nonsyndromic hearing loss 11; Usher syndrome type 1; Usher syndrome type 1B; Gastric cancer; Adrenocortical carcinoma, hereditary; Malignant tumor of esophagus	germline	13	Feb 04, 2026	clinvar