NM_000038.6(APC):c.7879T>A (p.Ser2627Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003153893.8
Allele description [Variation Report for NM_000038.6(APC):c.7879T>A (p.Ser2627Thr)]
NM_000038.6(APC):c.7879T>A (p.Ser2627Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024