Annotation Detail
Information
- Associated Genes
- HCN4
- Associated Variants
-
HCN4 p.Ser672= (p.S672=)
(
ENST00000261917.4 )
HCN4 p.Ser672= (p.S672=) ( ENST00000261917.4 ) - Source Database
- ClinVar
- Description
- NM_005477.3(HCN4):c.2016C>T (p.Ser672=) AND Cardiovascular phenotype
- ClinVar Allele ID
- 465159
- ClinVar RefSeq Alternation Syntax
- NM_005477.3:c.2016C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2021-09-02
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002420483
- Observed Origin Sample
- germline
Drugs