NM_005359.6(SMAD4):c.955+6T>C AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 7, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003988038.1
Allele description [Variation Report for NM_005359.6(SMAD4):c.955+6T>C]
NM_005359.6(SMAD4):c.955+6T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024