NOTCH3 NM_000435.3(NOTCH3):c.1725G>A (p.Thr575=)

CI-VAR-00047725Explore in graph →p.Thr575=NM_000435.3:c.1725G>AClinVar 256122 rs79926127

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
256122	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thyroid cancer, nonmedullary, 1; Lung cancer; Clear cell carcinoma of kidney; Melanoma; Cervical cancer	germline	14	May 01, 2026	clinvar