NM_006939.4(SOS2):c.432G>A (p.Leu144=) AND Noonan syndrome 9
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000792030.7
Allele description [Variation Report for NM_006939.4(SOS2):c.432G>A (p.Leu144=)]
NM_006939.4(SOS2):c.432G>A (p.Leu144=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024