Annotation Detail
Information
- Associated Genes
- ATP1A3
- Associated Variants
-
ATP1A3 p.Arg769His (p.R769H), ENSG00000285505 p.Arg756His (p.R756H)
(
ENST00000543770.5,
ENST00000545399.6,
ENST00000602133.5,
ENST00000648268.1 )
ATP1A3 p.Arg769His (p.R769H), ENSG00000285505 p.Arg756His (p.R756H) ( ENST00000543770.5, ENST00000545399.6, ENST00000602133.5, ENST00000648268.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_152296.5(ATP1A3):c.2267G>A (p.Arg756His) AND not provided
- ClinVar Allele ID
- 170985
- ClinVar RefSeq Alternation Syntax
- NM_001256214.2:c.2306G>A
- ClinVar RefSeq Alternation Syntax
- NM_001256213.2:c.2300G>A
- ClinVar RefSeq Alternation Syntax
- NM_152296.5:c.2267G>A
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-09-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000489717
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs