NM_000141.5(FGFR2):c.2424C>T (p.Cys808=) AND FGFR2-related craniosynostosis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 13, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001443694.4
Allele description [Variation Report for NM_000141.5(FGFR2):c.2424C>T (p.Cys808=)]
NM_000141.5(FGFR2):c.2424C>T (p.Cys808=)
Condition(s)
- Name:
- FGFR2-related craniosynostosis
- Identifiers:
- MedGen: CN231480
Assertion and evidence details
Last Updated: Dec 24, 2023