MYO7A NM_000260.4(MYO7A):c.687C>T (p.Gly229=)

CI-VAR-00008522Explore in graph →p.Gly229=NM_000260.4:c.687C>TClinVar 43339 rs371142158

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
43339	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Autosomal recessive nonsyndromic hearing loss 2; Autosomal dominant nonsyndromic hearing loss 11; Usher syndrome type 1; Usher syndrome type 1B; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Lung cancer	germline	9	Feb 02, 2026	clinvar