Annotation Detail
Information
- Associated Genes
- CFH
- Associated Variants
-
ENSG00000289697 p.Ala473= (p.A473=), CFH p.Ala473= (p.A473=)
(
ENST00000695969.1,
ENST00000695974.1,
ENST00000695971.1,
ENST00000695970.1,
ENST00000367429.9,
ENST00000695976.1,
ENST00000695984.1,
ENST00000695981.1,
ENST00000696027.1,
ENST00000696029.1,
ENST00000696028.1 )
ENSG00000289697 p.Ala473= (p.A473=), CFH p.Ala473= (p.A473=) ( ENST00000367429.9, ENST00000695969.1, ENST00000695970.1, ENST00000695971.1, ENST00000695974.1, ENST00000695976.1, ENST00000695981.1, ENST00000695984.1, ENST00000696027.1, ENST00000696028.1, ENST00000696029.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000186.4(CFH):c.1419G>A (p.Ala473=) AND not provided
- ClinVar Allele ID
- 279359
- ClinVar RefSeq Alternation Syntax
- NM_000186.4:c.1419G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-02-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001521611
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs