DMD NM_004006.3(DMD):c.8729A>T (p.Glu2910Val)

CI-VAR-00005952Explore in graph →p.Glu2910ValNM_004006.3:c.8729A>TClinVar 11267 rs41305353

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
11267	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Duchenne muscular dystrophy; Cardiovascular phenotype; Dilated cardiomyopathy 3B; Dystrophin deficiency; Cardiomyopathy; Becker muscular dystrophy; Sarcoma; Thyroid cancer, nonmedullary, 1; Clear cell carcinoma of kidney; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Melanoma; Adrenocortical carcinoma, hereditary; Lung cancer; Cervical cancer	germline	22	Mar 27, 2026	clinvar