NM_000038.6(APC):c.3876G>A (p.Thr1292=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001705547.9
Allele description [Variation Report for NM_000038.6(APC):c.3876G>A (p.Thr1292=)]
NM_000038.6(APC):c.3876G>A (p.Thr1292=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024