NM_005477.3(HCN4):c.1722C>T (p.Ser574=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000427645.1
Allele description [Variation Report for NM_005477.3(HCN4):c.1722C>T (p.Ser574=)]
NM_005477.3(HCN4):c.1722C>T (p.Ser574=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024