TTN NM_001267550.2(TTN):c.69145A>G (p.Ile23049Val)

CI-VAR-00008735Explore in graph →p.Ile23049ValNM_001267550.2:c.69145A>GClinVar 47271 rs72646881

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
47271	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Cardiovascular phenotype; Early-onset myopathy with fatal cardiomyopathy; Autosomal recessive limb-girdle muscular dystrophy type 2J; Dilated cardiomyopathy 1G; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Cardiomyopathy; Lung cancer; Gastric cancer; Thyroid cancer, nonmedullary, 1; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia	germline	18	Feb 03, 2026	clinvar