NM_173558.4(FGD2):c.1733A>T (p.Tyr578Phe) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004207089.1
Allele description [Variation Report for NM_173558.4(FGD2):c.1733A>T (p.Tyr578Phe)]
NM_173558.4(FGD2):c.1733A>T (p.Tyr578Phe)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 25, 2024