PHF2 NM_005392.4(PHF2):c.1935C>T (p.Leu645=)

CI-VAR-00128217Explore in graph →p.Leu645=NM_005392.4:c.1935C>TClinVar 733486 rs138464551

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
733486	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Lung cancer; Familial cancer of breast; Sarcoma; Thyroid cancer, nonmedullary, 1; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Colon adenocarcinoma	germline	4	Jul 01, 2022	clinvar