NM_001127511.3(APC):c.-133C>G AND not specified
- Germline classification:
- 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:
- RCV000441233.14
Allele description [Variation Report for NM_001127511.3(APC):c.-133C>G]
NM_001127511.3(APC):c.-133C>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024