TPM3 NM_152263.4(TPM3):c.378-11A>T

CI-VAR-00332296Explore in graph →NM_152263.4:c.378-11A>TClinVar 2932970 rs374552223

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
2932970	Likely benign	criteria provided, single submitter	1	Congenital myopathy 4B, autosomal recessive; Congenital myopathy with fiber type disproportion; Familial cancer of breast	germline	2	Dec 09, 2025	clinvar