NM_001122630.2(CDKN1C):c.861A>C (p.Pro287=) AND Beckwith-Wiedemann syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001337868.6
Allele description [Variation Report for NM_001122630.2(CDKN1C):c.861A>C (p.Pro287=)]
NM_001122630.2(CDKN1C):c.861A>C (p.Pro287=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024