Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Gly963AlafsTer14 (p.G963Afs*14)
(
ENST00000370225.4,
ENST00000649773.1 )
ABCA4 p.Gly963AlafsTer14 (p.G963Afs*14) ( ENST00000370225.4, ENST00000649773.1 ) - Associated Disease
- Severe early-childhood-onset retinal dystrophy
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.2888del (p.Gly963fs) AND Severe early-childhood-onset retinal dystrophy
- ClinVar Allele ID
- 22944
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.2888del
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.2664delG
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-05-31
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000986365
- ClinVar Disease
- Severe early-childhood-onset retinal dystrophy
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs