Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Ala192Thr (p.A192T)
(
ENST00000370225.4,
ENST00000649773.1 )
ABCA4 p.Ala192Thr (p.A192T) ( ENST00000370225.4, ENST00000649773.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.574G>A (p.Ala192Thr) AND not provided
- ClinVar Allele ID
- 105294
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.574G>A
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.574G>A
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2024-01-28
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000085759
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- not provided
Drugs