NM_020631.6(PLEKHG5):c.753C>T (p.Ser251=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 8, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000317714.3
Allele description [Variation Report for NM_020631.6(PLEKHG5):c.753C>T (p.Ser251=)]
NM_020631.6(PLEKHG5):c.753C>T (p.Ser251=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 16, 2024