Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Gly65Glu (p.G65E)
(
ENST00000370225.4,
ENST00000649773.1 )
ABCA4 p.Gly65Glu (p.G65E) ( ENST00000370225.4, ENST00000649773.1 ) - Associated Disease
- Severe early-childhood-onset retinal dystrophy
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.194G>A (p.Gly65Glu) AND Severe early-childhood-onset retinal dystrophy
- ClinVar Allele ID
- 104996
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.194G>A
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.194G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2016-01-01
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000132588
- ClinVar Disease
- Severe early-childhood-onset retinal dystrophy
- Observed Origin Sample
- germline
- Observed Origin Sample
- not provided
Drugs