NM_005359.6(SMAD4):c.1492T>C (p.Leu498=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Aug 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000427335.8
Allele description [Variation Report for NM_005359.6(SMAD4):c.1492T>C (p.Leu498=)]
NM_005359.6(SMAD4):c.1492T>C (p.Leu498=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024