Annotation Detail
Information
- Associated Genes
- ATP1A3
- Associated Variants
-
ATP1A3 p.Arg769Cys (p.R769C), ENSG00000285505 p.Arg756Cys (p.R756C)
(
ENST00000545399.6,
ENST00000602133.5,
ENST00000543770.5,
ENST00000648268.1 )
ATP1A3 p.Arg769Cys (p.R769C), ENSG00000285505 p.Arg756Cys (p.R756C) ( ENST00000543770.5, ENST00000545399.6, ENST00000602133.5, ENST00000648268.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_152296.5(ATP1A3):c.2266C>T (p.Arg756Cys) AND Inborn genetic diseases
- ClinVar Allele ID
- 413523
- ClinVar RefSeq Alternation Syntax
- NM_001256214.2:c.2305C>T
- ClinVar RefSeq Alternation Syntax
- NM_152296.5:c.2266C>T
- ClinVar RefSeq Alternation Syntax
- NM_001256213.2:c.2299C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2016-02-16
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000624914
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs