Annotation Detail
Information
- Associated Genes
- ATP1A3
- Associated Variants
-
ATP1A3 p.Thr626Met (p.T626M), ENSG00000285505 p.Thr613Met (p.T613M)
(
ENST00000543770.5,
ENST00000545399.6,
ENST00000602133.5,
ENST00000648268.1 )
ATP1A3 p.Thr626Met (p.T626M), ENSG00000285505 p.Thr613Met (p.T613M) ( ENST00000543770.5, ENST00000545399.6, ENST00000602133.5, ENST00000648268.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_152296.5(ATP1A3):c.1838C>T (p.Thr613Met) AND not provided
- ClinVar Allele ID
- 27948
- ClinVar RefSeq Alternation Syntax
- NM_152296.5:c.1838C>T
- ClinVar RefSeq Alternation Syntax
- NM_001256213.2:c.1871C>T
- ClinVar RefSeq Alternation Syntax
- NM_001256214.2:c.1877C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-05-15
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000726724
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs