NM_000038.6(APC):c.5118A>G (p.Ser1706=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 14, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000985307.2
Allele description [Variation Report for NM_000038.6(APC):c.5118A>G (p.Ser1706=)]
NM_000038.6(APC):c.5118A>G (p.Ser1706=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024