Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Glu471Lys (p.E471K)
(
ENST00000649773.1,
ENST00000370225.4 )
ABCA4 p.Glu471Lys (p.E471K) ( ENST00000370225.4, ENST00000649773.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.1411G>A (p.Glu471Lys) AND Inborn genetic diseases
- ClinVar Allele ID
- 104942
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.1411G>A
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.1411G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2017-08-28
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000622340
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs