Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Thr829Met (p.T829M)
(
ENST00000649773.1,
ENST00000370225.4 )
ABCA4 p.Thr829Met (p.T829M) ( ENST00000370225.4, ENST00000649773.1 ) - Associated Disease
- ABCA4-related disorder
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.2486C>T (p.Thr829Met) AND ABCA4-related disorder
- ClinVar Allele ID
- 864870
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.2264C>T
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.2486C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2017-04-27
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001096536
- ClinVar Disease
- ABCA4-related disorder
- Observed Origin Sample
- germline
Drugs