Annotation Detail
Information
- Associated Genes
- ZNF469
- Associated Variants
-
ZNF469 p.Pro900Leu (p.P900L)
(
ENST00000565624.3,
ENST00000437464.1 )
ZNF469 p.Pro900Leu (p.P900L) ( ENST00000437464.1, ENST00000565624.3 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001367624.2(ZNF469):c.2699C>T (p.Pro900Leu) AND not provided
- ClinVar Allele ID
- 132435
- ClinVar RefSeq Alternation Syntax
- NM_001367624.2:c.2699C>T
- Clinical Significance Description
- Benign/Likely benign
- Clinical Significance Last Update
- 2024-01-22
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000490000
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs