RAB3GAP1 NM_012233.3(RAB3GAP1):c.669G>T (p.Leu223Phe)

CI-VAR-00020462Explore in graph →p.Leu223PheNM_012233.3:c.669G>TClinVar 130071 rs76927619

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
130071	Benign	criteria provided, multiple submitters, no conflicts	2	Warburg micro syndrome 1; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Sarcoma; Cervical cancer; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney	germline	9	Jan 06, 2026	clinvar