NM_018249.6(CDK5RAP2):c.5388G>C (p.Arg1796=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000932664.7
Allele description [Variation Report for NM_018249.6(CDK5RAP2):c.5388G>C (p.Arg1796=)]
NM_018249.6(CDK5RAP2):c.5388G>C (p.Arg1796=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024