Annotation Detail
Information
- Associated Genes
- ATP1A3
- Associated Variants
-
ATP1A3 p.Leu770Pro (p.L770P), ENSG00000285505 p.Leu757Pro (p.L757P)
(
ENST00000543770.5,
ENST00000545399.6,
ENST00000602133.5,
ENST00000648268.1 )
ATP1A3 p.Leu770Pro (p.L770P), ENSG00000285505 p.Leu757Pro (p.L757P) ( ENST00000543770.5, ENST00000545399.6, ENST00000602133.5, ENST00000648268.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_152296.5(ATP1A3):c.2270T>C (p.Leu757Pro) AND not provided
- ClinVar Allele ID
- 170984
- ClinVar RefSeq Alternation Syntax
- NM_001256213.2:c.2303T>C
- ClinVar RefSeq Alternation Syntax
- NM_001256214.2:c.2309T>C
- ClinVar RefSeq Alternation Syntax
- NM_152296.5:c.2270T>C
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2020-08-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001781487
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs