ATP13A2 NM_022089.4(ATP13A2):c.881G>A (p.Arg294Gln)

CI-VAR-00020340Explore in graph →p.Arg294GlnNM_022089.4:c.881G>AClinVar 128476 rs56367069

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
128476	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Kufor-Rakeb syndrome; Autosomal recessive spastic paraplegia type 78; Inborn genetic diseases; Sarcoma; Ovarian serous cystadenocarcinoma; Thymoma; Thyroid cancer, nonmedullary, 1; Melanoma; Colon adenocarcinoma; Nonpapillary renal cell carcinoma; Cervical cancer; Clear cell carcinoma of kidney; Colorectal cancer; Lung cancer	germline	17	Jun 01, 2026	clinvar