ATR NM_001184.4(ATR):c.3702C>T (p.Phe1234=)

CI-VAR-00124270Explore in graph →p.Phe1234=NM_001184.4:c.3702C>TClinVar 696342 rs146222193

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
696342	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Inborn genetic diseases; Seckel syndrome 1; Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome	germline	4	Jan 06, 2026	clinvar