NM_000038.6(APC):c.5025T>G (p.Val1675=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002509311.8
Allele description [Variation Report for NM_000038.6(APC):c.5025T>G (p.Val1675=)]
NM_000038.6(APC):c.5025T>G (p.Val1675=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024