CAPN3 NM_000070.3(CAPN3):c.318C>T (p.Cys106=)

CI-VAR-00017981Explore in graph →p.Cys106=NM_000070.3:c.318C>TClinVar 92416 rs117609395

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
92416	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive limb-girdle muscular dystrophy type 2A; Clear cell carcinoma of kidney; Gastric cancer; Ovarian serous cystadenocarcinoma; Melanoma; Malignant tumor of esophagus; Cervical cancer	germline	14	Jun 01, 2026	clinvar