NM_016953.4(PDE11A):c.2653G>A (p.Val885Met) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001763597.2
Allele description [Variation Report for NM_016953.4(PDE11A):c.2653G>A (p.Val885Met)]
NM_016953.4(PDE11A):c.2653G>A (p.Val885Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024