ATP13A2 NM_022089.4(ATP13A2):c.1617G>T (p.Leu539=)

CI-VAR-00020338Explore in graph →p.Leu539=NM_022089.4:c.1617G>TClinVar 128464 rs61739752

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
128464	Benign	criteria provided, multiple submitters, no conflicts	2	Kufor-Rakeb syndrome; Autosomal recessive spastic paraplegia type 78; Inborn genetic diseases; Colon adenocarcinoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Gastric cancer; Malignant tumor of esophagus; Lung cancer; Cervical cancer	germline	11	Jan 28, 2026	clinvar