Annotation Detail
Information
- Associated Genes
- ATP1A3
- Associated Variants
-
ATP1A3 p.Asn786Ser (p.N786S), ENSG00000285505 p.Asn773Ser (p.N773S)
(
ENST00000543770.5,
ENST00000545399.6,
ENST00000602133.5,
ENST00000648268.1 )
ATP1A3 p.Asn786Ser (p.N786S), ENSG00000285505 p.Asn773Ser (p.N773S) ( ENST00000543770.5, ENST00000545399.6, ENST00000602133.5, ENST00000648268.1 ) - Associated Disease
- dystonia 12
- Source Database
- ClinVar
- Description
- NM_152296.5(ATP1A3):c.2318A>G (p.Asn773Ser) AND Dystonia 12
- ClinVar Allele ID
- 170981
- ClinVar RefSeq Alternation Syntax
- NM_001256214.2:c.2357A>G
- ClinVar RefSeq Alternation Syntax
- NM_001256213.2:c.2351A>G
- ClinVar RefSeq Alternation Syntax
- NM_152296.5:c.2318A>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-08-23
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002514853
- ClinVar Disease
- Dystonia 12
- Observed Origin Sample
- germline
Drugs