NM_014780.5(CUL7):c.1027C>T (p.Pro343Ser) AND 3M syndrome 1
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000347674.5
Allele description [Variation Report for NM_014780.5(CUL7):c.1027C>T (p.Pro343Ser)]
NM_014780.5(CUL7):c.1027C>T (p.Pro343Ser)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024