VPS13B NM_152564.5(VPS13B):c.10065G>T (p.Ala3355=)

CI-VAR-00075469Explore in graph →p.Ala3355=NM_152564.5:c.10065G>TClinVar 459245 rs61753726

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
459245	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Cohen syndrome; Inborn genetic diseases; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Colon adenocarcinoma; Uterine carcinosarcoma; Thymoma; Thyroid cancer, nonmedullary, 1; Hepatocellular carcinoma; Cervical cancer	germline	13	Feb 04, 2026	clinvar