NM_020964.3(EPG5):c.151C>G (p.Leu51Val) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 17, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000826992.4
Allele description [Variation Report for NM_020964.3(EPG5):c.151C>G (p.Leu51Val)]
NM_020964.3(EPG5):c.151C>G (p.Leu51Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024