RAD54L NM_003579.4(RAD54L):c.767-57G>T

CI-VAR-00239716Explore in graph →NM_003579.4:c.767-57G>TClinVar 1679090 rs61239976

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
1679090	Likely benign	criteria provided, multiple submitters, no conflicts	2	Hereditary breast ovarian cancer syndrome; Malignant tumor of esophagus; Lung cancer; Cervical cancer; Familial cancer of breast; Ovarian serous cystadenocarcinoma; Uterine corpus endometrial carcinoma	germline	3	Apr 19, 2022	clinvar