Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Ala1038Val (p.A1038V)
(
ENST00000370225.4 )
ABCA4 p.Ala1038Val (p.A1038V) ( ENST00000370225.4 ) - Associated Disease
- ABCA4-related disorder
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.3113C>T (p.Ala1038Val) AND ABCA4-related disorder
- ClinVar Allele ID
- 22933
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.3113C>T
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.2891C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2024-01-16
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000778259
- ClinVar Disease
- ABCA4-related disorder
- Observed Origin Sample
- germline
Drugs