NM_015692.5(CPAMD8):c.4858C>G (p.Arg1620Gly) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000881944.4
Allele description [Variation Report for NM_015692.5(CPAMD8):c.4858C>G (p.Arg1620Gly)]
NM_015692.5(CPAMD8):c.4858C>G (p.Arg1620Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023