Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Trp855Ter (p.W855*)
(
ENST00000649773.1,
ENST00000370225.4 )
ABCA4 p.Trp855Ter (p.W855*) ( ENST00000370225.4, ENST00000649773.1 ) - Associated Disease
- Severe early-childhood-onset retinal dystrophy
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.2565G>A (p.Trp855Ter) AND Severe early-childhood-onset retinal dystrophy
- ClinVar Allele ID
- 22922
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.2343G>A
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.2565G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1998-01-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000008334
- ClinVar Disease
- Severe early-childhood-onset retinal dystrophy
- Observed Origin Sample
- germline
- Pubmed
- 9490294
Drugs