NM_005633.4(SOS1):c.73C>T (p.Pro25Ser) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002482943.1
Allele description [Variation Report for NM_005633.4(SOS1):c.73C>T (p.Pro25Ser)]
NM_005633.4(SOS1):c.73C>T (p.Pro25Ser)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024