ATR NM_001184.4(ATR):c.4835A>G (p.Asn1612Ser)

CI-VAR-00025075Explore in graph →p.Asn1612SerNM_001184.4:c.4835A>GClinVar 157989 rs55894265

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
157989	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Seckel syndrome 1; Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome; Uterine corpus endometrial carcinoma; Thyroid cancer, nonmedullary, 1; Malignant tumor of esophagus; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Thymoma; Hepatocellular carcinoma; Cervical cancer	germline	11	Feb 03, 2026	clinvar