NM_006939.4(SOS2):c.837C>T (p.Ser279=) AND Noonan syndrome 9
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jan 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000652824.10
Allele description [Variation Report for NM_006939.4(SOS2):c.837C>T (p.Ser279=)]
NM_006939.4(SOS2):c.837C>T (p.Ser279=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024