NM_018249.6(CDK5RAP2):c.5649A>G (p.Pro1883=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 29, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001821108.4
Allele description [Variation Report for NM_018249.6(CDK5RAP2):c.5649A>G (p.Pro1883=)]
NM_018249.6(CDK5RAP2):c.5649A>G (p.Pro1883=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024