NM_016953.4(PDE11A):c.1976G>A (p.Arg659Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004191062.1
Allele description [Variation Report for NM_016953.4(PDE11A):c.1976G>A (p.Arg659Gln)]
NM_016953.4(PDE11A):c.1976G>A (p.Arg659Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 25, 2024