ATP1A3 NM_152296.5(ATP1A3):c.154-5C>G

CI-VAR-00049638Explore in graph →NM_152296.5:c.154-5C>GClinVar 281502 rs191645384

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
281502	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Alternating hemiplegia of childhood 2; Dystonia 12; Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome; Developmental and epileptic encephalopathy 99; Malignant tumor of esophagus	germline	14	Feb 02, 2026	clinvar