NM_006939.4(SOS2):c.3830T>C (p.Leu1277Pro) AND Noonan syndrome 9
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000541220.10
Allele description [Variation Report for NM_006939.4(SOS2):c.3830T>C (p.Leu1277Pro)]
NM_006939.4(SOS2):c.3830T>C (p.Leu1277Pro)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024